Motif 897 (n=237)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A0B4J203 | None | S112 | ochoa | receptor protein-tyrosine kinase (EC 2.7.10.1) | None |
A0A0C4DFX4 | None | S549 | ochoa | Snf2 related CREBBP activator protein | None |
A2RTX5 | TARS3 | S675 | ochoa | Threonine--tRNA ligase 2, cytoplasmic (EC 6.1.1.3) (Threonyl-tRNA synthetase) (ThrRS) (Threonyl-tRNA synthetase protein 3) | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction: threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr). Also edits incorrectly charged tRNA(Thr) via its editing domain, at the post-transfer stage. {ECO:0000250|UniProtKB:Q8BLY2}. |
A6NKT7 | RGPD3 | S1472 | ochoa | RanBP2-like and GRIP domain-containing protein 3 | None |
O00186 | STXBP3 | S508 | ochoa | Syntaxin-binding protein 3 (Platelet Sec1 protein) (PSP) (Protein unc-18 homolog 3) (Unc18-3) (Protein unc-18 homolog C) (Unc-18C) | Together with STX4 and VAMP2, may play a role in insulin-dependent movement of GLUT4 and in docking/fusion of intracellular GLUT4-containing vesicles with the cell surface in adipocytes. {ECO:0000250}. |
O00622 | CCN1 | S205 | ochoa | CCN family member 1 (Cellular communication network factor 1) (Cysteine-rich angiogenic inducer 61) (Insulin-like growth factor-binding protein 10) (IBP-10) (IGF-binding protein 10) (IGFBP-10) (Protein CYR61) (Protein GIG1) | Promotes cell proliferation, chemotaxis, angiogenesis and cell adhesion. Appears to play a role in wound healing by up-regulating, in skin fibroblasts, the expression of a number of genes involved in angiogenesis, inflammation and matrix remodeling including VEGA-A, VEGA-C, MMP1, MMP3, TIMP1, uPA, PAI-1 and integrins alpha-3 and alpha-5. CCN1-mediated gene regulation is dependent on heparin-binding. Down-regulates the expression of alpha-1 and alpha-2 subunits of collagen type-1. Promotes cell adhesion and adhesive signaling through integrin alpha-6/beta-1, cell migration through integrin alpha-v/beta-5 and cell proliferation through integrin alpha-v/beta-3. {ECO:0000269|PubMed:11584015}. |
O14715 | RGPD8 | S1471 | ochoa | RANBP2-like and GRIP domain-containing protein 8 (Ran-binding protein 2-like 3) (RanBP2-like 3) (RanBP2L3) | None |
O15054 | KDM6B | S971 | ochoa | Lysine-specific demethylase 6B (EC 1.14.11.68) (JmjC domain-containing protein 3) (Jumonji domain-containing protein 3) (Lysine demethylase 6B) ([histone H3]-trimethyl-L-lysine(27) demethylase 6B) | Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code (PubMed:17713478, PubMed:17825402, PubMed:17851529, PubMed:18003914). Demethylates trimethylated and dimethylated H3 'Lys-27' (PubMed:17713478, PubMed:17825402, PubMed:17851529, PubMed:18003914). Plays a central role in regulation of posterior development, by regulating HOX gene expression (PubMed:17851529). Involved in inflammatory response by participating in macrophage differentiation in case of inflammation by regulating gene expression and macrophage differentiation (PubMed:17825402). Plays a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression by acting as a link between T-box factors and the SMARCA4-containing SWI/SNF remodeling complex (By similarity). {ECO:0000250|UniProtKB:Q5NCY0, ECO:0000269|PubMed:17713478, ECO:0000269|PubMed:17825402, ECO:0000269|PubMed:17851529, ECO:0000269|PubMed:18003914, ECO:0000269|PubMed:28262558}. |
O15511 | ARPC5 | S77 | psp | Actin-related protein 2/3 complex subunit 5 (Arp2/3 complex 16 kDa subunit) (p16-ARC) | Component of the Arp2/3 complex, a multiprotein complex that mediates actin polymerization upon stimulation by nucleation-promoting factor (NPF) (PubMed:9230079). The Arp2/3 complex mediates the formation of branched actin networks in the cytoplasm, providing the force for cell motility (PubMed:9230079). In addition to its role in the cytoplasmic cytoskeleton, the Arp2/3 complex also promotes actin polymerization in the nucleus, thereby regulating gene transcription and repair of damaged DNA (PubMed:29925947). The Arp2/3 complex promotes homologous recombination (HR) repair in response to DNA damage by promoting nuclear actin polymerization, leading to drive motility of double-strand breaks (DSBs) (PubMed:29925947). {ECO:0000269|PubMed:29925947, ECO:0000269|PubMed:9230079}. |
O43295 | SRGAP3 | S919 | ochoa | SLIT-ROBO Rho GTPase-activating protein 3 (srGAP3) (Mental disorder-associated GAP) (Rho GTPase-activating protein 14) (WAVE-associated Rac GTPase-activating protein) (WRP) | GTPase-activating protein for RAC1 and perhaps Cdc42, but not for RhoA small GTPase. May attenuate RAC1 signaling in neurons. {ECO:0000269|PubMed:12195014, ECO:0000269|PubMed:12447388}. |
O43390 | HNRNPR | S252 | ochoa | Heterogeneous nuclear ribonucleoprotein R (hnRNP R) | Component of ribonucleosomes, which are complexes of at least 20 other different heterogeneous nuclear ribonucleoproteins (hnRNP). hnRNP play an important role in processing of precursor mRNA in the nucleus. |
O43829 | ZBTB14 | S233 | ochoa | Zinc finger and BTB domain-containing protein 14 (Zinc finger protein 161 homolog) (Zfp-161) (Zinc finger protein 478) (Zinc finger protein 5 homolog) (ZF5) (Zfp-5) (hZF5) | Transcriptional activator of the dopamine transporter (DAT), binding it's promoter at the consensus sequence 5'-CCTGCACAGTTCACGGA-3'. Binds to 5'-d(GCC)(n)-3' trinucleotide repeats in promoter regions and acts as a repressor of the FMR1 gene. Transcriptional repressor of MYC and thymidine kinase promoters. {ECO:0000269|PubMed:17714511}. |
O60341 | KDM1A | S683 | psp | Lysine-specific histone demethylase 1A (EC 1.14.99.66) (BRAF35-HDAC complex protein BHC110) (Flavin-containing amine oxidase domain-containing protein 2) ([histone H3]-dimethyl-L-lysine(4) FAD-dependent demethylase 1A) | Histone demethylase that can demethylate both 'Lys-4' (H3K4me) and 'Lys-9' (H3K9me) of histone H3, thereby acting as a coactivator or a corepressor, depending on the context (PubMed:15620353, PubMed:15811342, PubMed:16079794, PubMed:16079795, PubMed:16140033, PubMed:16223729, PubMed:27292636). Acts by oxidizing the substrate by FAD to generate the corresponding imine that is subsequently hydrolyzed (PubMed:15620353, PubMed:15811342, PubMed:16079794, PubMed:21300290). Acts as a corepressor by mediating demethylation of H3K4me, a specific tag for epigenetic transcriptional activation. Demethylates both mono- (H3K4me1) and di-methylated (H3K4me2) H3K4me (PubMed:15620353, PubMed:20389281, PubMed:21300290, PubMed:23721412). May play a role in the repression of neuronal genes. Alone, it is unable to demethylate H3K4me on nucleosomes and requires the presence of RCOR1/CoREST to achieve such activity (PubMed:16079794, PubMed:16140033, PubMed:16885027, PubMed:21300290, PubMed:23721412). Also acts as a coactivator of androgen receptor (AR)-dependent transcription, by being recruited to AR target genes and mediating demethylation of H3K9me, a specific tag for epigenetic transcriptional repression. The presence of PRKCB in AR-containing complexes, which mediates phosphorylation of 'Thr-6' of histone H3 (H3T6ph), a specific tag that prevents demethylation H3K4me, prevents H3K4me demethylase activity of KDM1A (PubMed:16079795). Demethylates di-methylated 'Lys-370' of p53/TP53 which prevents interaction of p53/TP53 with TP53BP1 and represses p53/TP53-mediated transcriptional activation. Demethylates and stabilizes the DNA methylase DNMT1 (PubMed:29691401). Demethylates methylated 'Lys-42' and methylated 'Lys-117' of SOX2 (PubMed:29358331). Required for gastrulation during embryogenesis. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development (PubMed:16079794, PubMed:16140033). Facilitates epithelial-to-mesenchymal transition by acting as an effector of SNAI1-mediated transcription repression of epithelial markers E-cadherin/CDH1, CDN7 and KRT8 (PubMed:20562920, PubMed:27292636). Required for the maintenance of the silenced state of the SNAI1 target genes E-cadherin/CDH1 and CDN7 (PubMed:20389281). Required for the repression of GIPR expression (PubMed:34655521, PubMed:34906447). {ECO:0000269|PubMed:12032298, ECO:0000269|PubMed:15620353, ECO:0000269|PubMed:15811342, ECO:0000269|PubMed:16079794, ECO:0000269|PubMed:16079795, ECO:0000269|PubMed:16140033, ECO:0000269|PubMed:16223729, ECO:0000269|PubMed:16885027, ECO:0000269|PubMed:16956976, ECO:0000269|PubMed:17805299, ECO:0000269|PubMed:20228790, ECO:0000269|PubMed:20389281, ECO:0000269|PubMed:20562920, ECO:0000269|PubMed:21300290, ECO:0000269|PubMed:23721412, ECO:0000269|PubMed:27292636, ECO:0000269|PubMed:29358331, ECO:0000269|PubMed:29691401, ECO:0000269|PubMed:34655521, ECO:0000269|PubMed:34906447}. |
O60506 | SYNCRIP | S249 | ochoa | Heterogeneous nuclear ribonucleoprotein Q (hnRNP Q) (Glycine- and tyrosine-rich RNA-binding protein) (GRY-RBP) (NS1-associated protein 1) (Synaptotagmin-binding, cytoplasmic RNA-interacting protein) | Heterogenous nuclear ribonucleoprotein (hnRNP) implicated in mRNA processing mechanisms. Component of the CRD-mediated complex that promotes MYC mRNA stability. Isoform 1, isoform 2 and isoform 3 are associated in vitro with pre-mRNA, splicing intermediates and mature mRNA protein complexes. Isoform 1 binds to apoB mRNA AU-rich sequences. Isoform 1 is part of the APOB mRNA editosome complex and may modulate the postranscriptional C to U RNA-editing of the APOB mRNA through either by binding to A1CF (APOBEC1 complementation factor), to APOBEC1 or to RNA itself. May be involved in translationally coupled mRNA turnover. Implicated with other RNA-binding proteins in the cytoplasmic deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of instability (mCRD) domain. Interacts in vitro preferentially with poly(A) and poly(U) RNA sequences. Isoform 3 may be involved in cytoplasmic vesicle-based mRNA transport through interaction with synaptotagmins. Component of the GAIT (gamma interferon-activated inhibitor of translation) complex which mediates interferon-gamma-induced transcript-selective translation inhibition in inflammation processes. Upon interferon-gamma activation assembles into the GAIT complex which binds to stem loop-containing GAIT elements in the 3'-UTR of diverse inflammatory mRNAs (such as ceruplasmin) and suppresses their translation; seems not to be essential for GAIT complex function. {ECO:0000269|PubMed:11051545, ECO:0000269|PubMed:11134005, ECO:0000269|PubMed:11352648, ECO:0000269|PubMed:11574476, ECO:0000269|PubMed:19029303, ECO:0000269|PubMed:23071094}. |
O60506 | SYNCRIP | S587 | ochoa | Heterogeneous nuclear ribonucleoprotein Q (hnRNP Q) (Glycine- and tyrosine-rich RNA-binding protein) (GRY-RBP) (NS1-associated protein 1) (Synaptotagmin-binding, cytoplasmic RNA-interacting protein) | Heterogenous nuclear ribonucleoprotein (hnRNP) implicated in mRNA processing mechanisms. Component of the CRD-mediated complex that promotes MYC mRNA stability. Isoform 1, isoform 2 and isoform 3 are associated in vitro with pre-mRNA, splicing intermediates and mature mRNA protein complexes. Isoform 1 binds to apoB mRNA AU-rich sequences. Isoform 1 is part of the APOB mRNA editosome complex and may modulate the postranscriptional C to U RNA-editing of the APOB mRNA through either by binding to A1CF (APOBEC1 complementation factor), to APOBEC1 or to RNA itself. May be involved in translationally coupled mRNA turnover. Implicated with other RNA-binding proteins in the cytoplasmic deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of instability (mCRD) domain. Interacts in vitro preferentially with poly(A) and poly(U) RNA sequences. Isoform 3 may be involved in cytoplasmic vesicle-based mRNA transport through interaction with synaptotagmins. Component of the GAIT (gamma interferon-activated inhibitor of translation) complex which mediates interferon-gamma-induced transcript-selective translation inhibition in inflammation processes. Upon interferon-gamma activation assembles into the GAIT complex which binds to stem loop-containing GAIT elements in the 3'-UTR of diverse inflammatory mRNAs (such as ceruplasmin) and suppresses their translation; seems not to be essential for GAIT complex function. {ECO:0000269|PubMed:11051545, ECO:0000269|PubMed:11134005, ECO:0000269|PubMed:11352648, ECO:0000269|PubMed:11574476, ECO:0000269|PubMed:19029303, ECO:0000269|PubMed:23071094}. |
O60664 | PLIN3 | S179 | ochoa | Perilipin-3 (47 kDa mannose 6-phosphate receptor-binding protein) (47 kDa MPR-binding protein) (Cargo selection protein TIP47) (Mannose-6-phosphate receptor-binding protein 1) (Placental protein 17) (PP17) | Structural component of lipid droplets, which is required for the formation and maintenance of lipid storage droplets (PubMed:34077757). Required for the transport of mannose 6-phosphate receptors (MPR) from endosomes to the trans-Golgi network (PubMed:9590177). {ECO:0000269|PubMed:34077757, ECO:0000269|PubMed:9590177}. |
O60716 | CTNND1 | S895 | ochoa | Catenin delta-1 (Cadherin-associated Src substrate) (CAS) (p120 catenin) (p120(ctn)) (p120(cas)) | Key regulator of cell-cell adhesion that associates with and regulates the cell adhesion properties of both C-, E- and N-cadherins, being critical for their surface stability (PubMed:14610055, PubMed:20371349). Promotes localization and retention of DSG3 at cell-cell junctions, via its interaction with DSG3 (PubMed:18343367). Beside cell-cell adhesion, regulates gene transcription through several transcription factors including ZBTB33/Kaiso2 and GLIS2, and the activity of Rho family GTPases and downstream cytoskeletal dynamics (PubMed:10207085, PubMed:20371349). Implicated both in cell transformation by SRC and in ligand-induced receptor signaling through the EGF, PDGF, CSF-1 and ERBB2 receptors (PubMed:17344476). {ECO:0000269|PubMed:10207085, ECO:0000269|PubMed:14610055, ECO:0000269|PubMed:17344476, ECO:0000269|PubMed:18343367, ECO:0000269|PubMed:20371349}. |
O75167 | PHACTR2 | S23 | ochoa | Phosphatase and actin regulator 2 | None |
O75369 | FLNB | S1433 | ochoa | Filamin-B (FLN-B) (ABP-278) (ABP-280 homolog) (Actin-binding-like protein) (Beta-filamin) (Filamin homolog 1) (Fh1) (Filamin-3) (Thyroid autoantigen) (Truncated actin-binding protein) (Truncated ABP) | Connects cell membrane constituents to the actin cytoskeleton. May promote orthogonal branching of actin filaments and links actin filaments to membrane glycoproteins. Anchors various transmembrane proteins to the actin cytoskeleton. Interaction with FLNA may allow neuroblast migration from the ventricular zone into the cortical plate. Various interactions and localizations of isoforms affect myotube morphology and myogenesis. Isoform 6 accelerates muscle differentiation in vitro. |
O75376 | NCOR1 | S1381 | ochoa | Nuclear receptor corepressor 1 (N-CoR) (N-CoR1) | Mediates transcriptional repression by certain nuclear receptors (PubMed:20812024). Part of a complex which promotes histone deacetylation and the formation of repressive chromatin structures which may impede the access of basal transcription factors. Participates in the transcriptional repressor activity produced by BCL6. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). Mediates the NR1D1-dependent repression and circadian regulation of TSHB expression (By similarity). The NCOR1-HDAC3 complex regulates the circadian expression of the core clock gene ARTNL/BMAL1 and the genes involved in lipid metabolism in the liver (By similarity). {ECO:0000250|UniProtKB:Q60974, ECO:0000269|PubMed:14527417, ECO:0000269|PubMed:20812024}. |
O75762 | TRPA1 | S428 | psp | Transient receptor potential cation channel subfamily A member 1 (Ankyrin-like with transmembrane domains protein 1) (Transformation-sensitive protein p120) (p120) (Wasabi receptor) | Ligand-activated Ca(2+)-permeable, nonselective cation channel involved in pain detection and possibly also in cold perception, oxygen concentration perception, cough, itch, and inner ear function (PubMed:17259981, PubMed:21195050, PubMed:21873995, PubMed:23199233, PubMed:25389312, PubMed:33152265). Has a relatively high Ca(2+) selectivity, with a preference for divalent over monovalent cations (Ca(2+) > Ba(2+) > Mg(2+) > NH4(+) > Li(+) > K(+)), the influx of cation into the cytoplasm leads to membrane depolarization (PubMed:19202543, PubMed:21195050). Has a central role in the pain response to endogenous inflammatory mediators, such as bradykinin and to a diverse array of irritants. Activated by a large variety of structurally unrelated electrophilic and non-electrophilic chemical compounds, such as allylthiocyanate (AITC) from mustard oil or wasabi, cinnamaldehyde, diallyl disulfide (DADS) from garlic, and acrolein, an environmental irritant (PubMed:20547126, PubMed:25389312, PubMed:27241698, PubMed:30878828). Electrophilic ligands activate TRPA1 by interacting with critical N-terminal Cys residues in a covalent manner (PubMed:17164327, PubMed:27241698, PubMed:31866091, PubMed:32641835). Non-electrophile agonists bind at distinct sites in the transmembrane domain to promote channel activation (PubMed:33152265). Also acts as an ionotropic cannabinoid receptor by being activated by delta(9)-tetrahydrocannabinol (THC), the psychoactive component of marijuana (PubMed:25389312). May be a component for the mechanosensitive transduction channel of hair cells in inner ear, thereby participating in the perception of sounds (By similarity). {ECO:0000250|UniProtKB:Q8BLA8, ECO:0000269|PubMed:17164327, ECO:0000269|PubMed:17259981, ECO:0000269|PubMed:19202543, ECO:0000269|PubMed:20547126, ECO:0000269|PubMed:21195050, ECO:0000269|PubMed:21873995, ECO:0000269|PubMed:23199233, ECO:0000269|PubMed:25389312, ECO:0000269|PubMed:27241698, ECO:0000269|PubMed:30878828, ECO:0000269|PubMed:31866091, ECO:0000269|PubMed:32641835, ECO:0000269|PubMed:33152265}. |
O75821 | EIF3G | S264 | ochoa | Eukaryotic translation initiation factor 3 subunit G (eIF3g) (Eukaryotic translation initiation factor 3 RNA-binding subunit) (eIF-3 RNA-binding subunit) (Eukaryotic translation initiation factor 3 subunit 4) (eIF-3-delta) (eIF3 p42) (eIF3 p44) | RNA-binding component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis (PubMed:17581632, PubMed:25849773, PubMed:27462815). The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation (PubMed:17581632). The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression (PubMed:25849773). This subunit can bind 18S rRNA. {ECO:0000255|HAMAP-Rule:MF_03006, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815}.; FUNCTION: (Microbial infection) In case of FCV infection, plays a role in the ribosomal termination-reinitiation event leading to the translation of VP2 (PubMed:18056426). {ECO:0000269|PubMed:18056426}. |
O95376 | ARIH2 | S335 | ochoa | E3 ubiquitin-protein ligase ARIH2 (ARI-2) (Protein ariadne-2 homolog) (EC 2.3.2.31) (Triad1 protein) | E3 ubiquitin-protein ligase, which catalyzes ubiquitination of target proteins together with ubiquitin-conjugating enzyme E2 UBE2L3 (PubMed:16118314, PubMed:17646546, PubMed:19340006, PubMed:24076655, PubMed:33268465, PubMed:34518685, PubMed:38418882). Acts as an atypical E3 ubiquitin-protein ligase by working together with cullin-5-RING ubiquitin ligase complex (ECS complex, also named CRL5 complex) and initiating ubiquitination of ECS substrates: associates with ECS complex and specifically mediates addition of the first ubiquitin on ECS targets (PubMed:33268465, PubMed:34518685, PubMed:38418882). The initial ubiquitin is then elongated (PubMed:33268465). E3 ubiquitin-protein ligase activity is activated upon binding to neddylated form of the cullin-5 (CUL5) component of the ECS complex (PubMed:24076655). Together with the ECS(ASB9) complex, catalyzes ubiquitination of CKB (PubMed:33268465). Promotes ubiquitination of DCUN1D1 (PubMed:30587576). Mediates 'Lys-6', 'Lys-48'- and 'Lys-63'-linked polyubiquitination (PubMed:16118314, PubMed:17646546, PubMed:19340006). May play a role in myelopoiesis (PubMed:19340006). {ECO:0000269|PubMed:16118314, ECO:0000269|PubMed:17646546, ECO:0000269|PubMed:19340006, ECO:0000269|PubMed:24076655, ECO:0000269|PubMed:30587576, ECO:0000269|PubMed:33268465, ECO:0000269|PubMed:34518685, ECO:0000269|PubMed:38418882}.; FUNCTION: (Microbial infection) Following infection by HIV-1 virus, acts together with a cullin-5-RING E3 ubiquitin-protein ligase complex (ECS complex) hijacked by the HIV-1 Vif protein, to catalyze ubiquitination and degradation of APOBEC3F and APOBEC3G. {ECO:0000269|PubMed:31253590, ECO:0000269|PubMed:36754086}. |
O95822 | MLYCD | S471 | ochoa | Malonyl-CoA decarboxylase, mitochondrial (MCD) (EC 4.1.1.9) | Catalyzes the conversion of malonyl-CoA to acetyl-CoA. In the fatty acid biosynthesis MCD selectively removes malonyl-CoA and thus assures that methyl-malonyl-CoA is the only chain elongating substrate for fatty acid synthase and that fatty acids with multiple methyl side chains are produced. In peroxisomes it may be involved in degrading intraperoxisomal malonyl-CoA, which is generated by the peroxisomal beta-oxidation of odd chain-length dicarboxylic fatty acids. Plays a role in the metabolic balance between glucose and lipid oxidation in muscle independent of alterations in insulin signaling. May play a role in controlling the extent of ischemic injury by promoting glucose oxidation. {ECO:0000269|PubMed:10455107, ECO:0000269|PubMed:15003260, ECO:0000269|PubMed:18314420, ECO:0000269|PubMed:23482565}. |
O96028 | NSD2 | S437 | ochoa | Histone-lysine N-methyltransferase NSD2 (EC 2.1.1.357) (Multiple myeloma SET domain-containing protein) (MMSET) (Nuclear SET domain-containing protein 2) (Protein trithorax-5) (Wolf-Hirschhorn syndrome candidate 1 protein) | Histone methyltransferase which specifically dimethylates nucleosomal histone H3 at 'Lys-36' (H3K36me2) (PubMed:19808676, PubMed:22099308, PubMed:27571355, PubMed:29728617, PubMed:33941880). Also monomethylates nucleosomal histone H3 at 'Lys-36' (H3K36me) in vitro (PubMed:22099308). Does not trimethylate nucleosomal histone H3 at 'Lys-36' (H3K36me3) (PubMed:22099308). However, specifically trimethylates histone H3 at 'Lys-36' (H3K36me3) at euchromatic regions in embryonic stem (ES) cells (By similarity). By methylating histone H3 at 'Lys-36', involved in the regulation of gene transcription during various biological processes (PubMed:16115125, PubMed:22099308, PubMed:29728617). In ES cells, associates with developmental transcription factors such as SALL1 and represses inappropriate gene transcription mediated by histone deacetylation (By similarity). During heart development, associates with transcription factor NKX2-5 to repress transcription of NKX2-5 target genes (By similarity). Plays an essential role in adipogenesis, by regulating expression of genes involved in pre-adipocyte differentiation (PubMed:29728617). During T-cell receptor (TCR) and CD28-mediated T-cell activation, promotes the transcription of transcription factor BCL6 which is required for follicular helper T (Tfh) cell differentiation (By similarity). During B-cell development, required for the generation of the B1 lineage (By similarity). During B2 cell activation, may contribute to the control of isotype class switch recombination (CRS), splenic germinal center formation, and the humoral immune response (By similarity). Plays a role in class switch recombination of the immunoglobulin heavy chain (IgH) locus during B-cell activation (By similarity). By regulating the methylation of histone H3 at 'Lys-36' and histone H4 at 'Lys-20' at the IgH locus, involved in TP53BP1 recruitment to the IgH switch region and promotes the transcription of IgA (By similarity). {ECO:0000250|UniProtKB:Q8BVE8, ECO:0000269|PubMed:16115125, ECO:0000269|PubMed:19808676, ECO:0000269|PubMed:22099308, ECO:0000269|PubMed:27571355, ECO:0000269|PubMed:29728617, ECO:0000269|PubMed:33941880}.; FUNCTION: [Isoform 1]: Histone methyltransferase which specifically dimethylates nucleosomal histone H3 at 'Lys-36' (H3K36me2). {ECO:0000269|PubMed:22099308}.; FUNCTION: [Isoform 4]: Histone methyltransferase which specifically dimethylates nucleosomal histone H3 at 'Lys-36' (H3K36me2) (PubMed:22099308). Methylation of histone H3 at 'Lys-27' is controversial (PubMed:18172012, PubMed:22099308). Mono-, di- or tri-methylates histone H3 at 'Lys-27' (H3K27me, H3K27me2 and H3K27me3) (PubMed:18172012). Does not methylate histone H3 at 'Lys-27' (PubMed:22099308). May act as a transcription regulator that binds DNA and suppresses IL5 transcription through HDAC recruitment (PubMed:11152655, PubMed:18172012). {ECO:0000269|PubMed:11152655, ECO:0000269|PubMed:18172012, ECO:0000269|PubMed:22099308}. |
P00338 | LDHA | S161 | ochoa|psp | L-lactate dehydrogenase A chain (LDH-A) (EC 1.1.1.27) (Cell proliferation-inducing gene 19 protein) (LDH muscle subunit) (LDH-M) (Renal carcinoma antigen NY-REN-59) | Interconverts simultaneously and stereospecifically pyruvate and lactate with concomitant interconversion of NADH and NAD(+). {ECO:0000269|PubMed:11276087}. |
P00367 | GLUD1 | S370 | psp | Glutamate dehydrogenase 1, mitochondrial (GDH 1) (EC 1.4.1.3) | Mitochondrial glutamate dehydrogenase that catalyzes the conversion of L-glutamate into alpha-ketoglutarate. Plays a key role in glutamine anaplerosis by producing alpha-ketoglutarate, an important intermediate in the tricarboxylic acid cycle (PubMed:11032875, PubMed:11254391, PubMed:16023112, PubMed:16959573). Plays a role in insulin homeostasis (PubMed:11297618, PubMed:9571255). May be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate (By similarity). {ECO:0000250|UniProtKB:P10860, ECO:0000269|PubMed:11032875, ECO:0000269|PubMed:11254391, ECO:0000269|PubMed:11297618, ECO:0000269|PubMed:16023112, ECO:0000269|PubMed:16959573, ECO:0000269|PubMed:9571255}. |
P00558 | PGK1 | S115 | ochoa | Phosphoglycerate kinase 1 (EC 2.7.11.1) (EC 2.7.2.3) (Cell migration-inducing gene 10 protein) (Primer recognition protein 2) (PRP 2) | Catalyzes one of the two ATP producing reactions in the glycolytic pathway via the reversible conversion of 1,3-diphosphoglycerate to 3-phosphoglycerate (PubMed:30323285, PubMed:7391028). Both L- and D- forms of purine and pyrimidine nucleotides can be used as substrates, but the activity is much lower on pyrimidines (PubMed:18463139). In addition to its role as a glycolytic enzyme, it seems that PGK1 acts as a polymerase alpha cofactor protein (primer recognition protein) (PubMed:2324090). Acts as a protein kinase when localized to the mitochondrion where it phosphorylates pyruvate dehydrogenase kinase PDK1 to inhibit pyruvate dehydrogenase complex activity and suppress the formation of acetyl-coenzyme A from pyruvate, and consequently inhibit oxidative phosphorylation and promote glycolysis (PubMed:26942675, PubMed:36849569). May play a role in sperm motility (PubMed:26677959). {ECO:0000269|PubMed:18463139, ECO:0000269|PubMed:2324090, ECO:0000269|PubMed:26677959, ECO:0000269|PubMed:26942675, ECO:0000269|PubMed:30323285, ECO:0000269|PubMed:36849569, ECO:0000269|PubMed:7391028}. |
P00918 | CA2 | S151 | ochoa | Carbonic anhydrase 2 (EC 4.2.1.1) (Carbonate dehydratase II) (Carbonic anhydrase C) (CAC) (Carbonic anhydrase II) (CA-II) (Cyanamide hydratase CA2) (EC 4.2.1.69) | Catalyzes the reversible hydration of carbon dioxide (PubMed:11327835, PubMed:11802772, PubMed:11831900, PubMed:12056894, PubMed:12171926, PubMed:1336460, PubMed:14736236, PubMed:15300855, PubMed:15453828, PubMed:15667203, PubMed:15865431, PubMed:16106378, PubMed:16214338, PubMed:16290146, PubMed:16686544, PubMed:16759856, PubMed:16807956, PubMed:17127057, PubMed:17251017, PubMed:17314045, PubMed:17330962, PubMed:17346964, PubMed:17540563, PubMed:17588751, PubMed:17705204, PubMed:18024029, PubMed:18162396, PubMed:18266323, PubMed:18374572, PubMed:18481843, PubMed:18618712, PubMed:18640037, PubMed:18942852, PubMed:1909891, PubMed:1910042, PubMed:19170619, PubMed:19186056, PubMed:19206230, PubMed:19520834, PubMed:19778001, PubMed:7761440, PubMed:7901850, PubMed:8218160, PubMed:8262987, PubMed:8399159, PubMed:8451242, PubMed:8485129, PubMed:8639494, PubMed:9265618, PubMed:9398308). Can also hydrate cyanamide to urea (PubMed:10550681, PubMed:11015219). Stimulates the chloride-bicarbonate exchange activity of SLC26A6 (PubMed:15990874). Essential for bone resorption and osteoclast differentiation (PubMed:15300855). Involved in the regulation of fluid secretion into the anterior chamber of the eye. Contributes to intracellular pH regulation in the duodenal upper villous epithelium during proton-coupled peptide absorption. {ECO:0000269|PubMed:10550681, ECO:0000269|PubMed:11015219, ECO:0000269|PubMed:11327835, ECO:0000269|PubMed:11802772, ECO:0000269|PubMed:11831900, ECO:0000269|PubMed:12056894, ECO:0000269|PubMed:12171926, ECO:0000269|PubMed:1336460, ECO:0000269|PubMed:14736236, ECO:0000269|PubMed:15300855, ECO:0000269|PubMed:15453828, ECO:0000269|PubMed:15667203, ECO:0000269|PubMed:15865431, ECO:0000269|PubMed:15990874, ECO:0000269|PubMed:16106378, ECO:0000269|PubMed:16214338, ECO:0000269|PubMed:16290146, ECO:0000269|PubMed:16686544, ECO:0000269|PubMed:16759856, ECO:0000269|PubMed:16807956, ECO:0000269|PubMed:17127057, ECO:0000269|PubMed:17251017, ECO:0000269|PubMed:17314045, ECO:0000269|PubMed:17330962, ECO:0000269|PubMed:17346964, ECO:0000269|PubMed:17540563, ECO:0000269|PubMed:17588751, ECO:0000269|PubMed:17705204, ECO:0000269|PubMed:18024029, ECO:0000269|PubMed:18162396, ECO:0000269|PubMed:18266323, ECO:0000269|PubMed:18374572, ECO:0000269|PubMed:18481843, ECO:0000269|PubMed:18618712, ECO:0000269|PubMed:18640037, ECO:0000269|PubMed:18942852, ECO:0000269|PubMed:1909891, ECO:0000269|PubMed:1910042, ECO:0000269|PubMed:19170619, ECO:0000269|PubMed:19186056, ECO:0000269|PubMed:19206230, ECO:0000269|PubMed:19520834, ECO:0000269|PubMed:19778001, ECO:0000269|PubMed:7761440, ECO:0000269|PubMed:7901850, ECO:0000269|PubMed:8218160, ECO:0000269|PubMed:8262987, ECO:0000269|PubMed:8399159, ECO:0000269|PubMed:8451242, ECO:0000269|PubMed:8485129, ECO:0000269|PubMed:8639494, ECO:0000269|PubMed:9265618, ECO:0000269|PubMed:9398308}. |
P02671 | FGA | S609 | ochoa|psp | Fibrinogen alpha chain [Cleaved into: Fibrinopeptide A; Fibrinogen alpha chain] | Cleaved by the protease thrombin to yield monomers which, together with fibrinogen beta (FGB) and fibrinogen gamma (FGG), polymerize to form an insoluble fibrin matrix. Fibrin has a major function in hemostasis as one of the primary components of blood clots. In addition, functions during the early stages of wound repair to stabilize the lesion and guide cell migration during re-epithelialization. Was originally thought to be essential for platelet aggregation, based on in vitro studies using anticoagulated blood. However, subsequent studies have shown that it is not absolutely required for thrombus formation in vivo. Enhances expression of SELP in activated platelets via an ITGB3-dependent pathway. Maternal fibrinogen is essential for successful pregnancy. Fibrin deposition is also associated with infection, where it protects against IFNG-mediated hemorrhage. May also facilitate the immune response via both innate and T-cell mediated pathways. {ECO:0000250|UniProtKB:E9PV24}. |
P04049 | RAF1 | S357 | ochoa|psp | RAF proto-oncogene serine/threonine-protein kinase (EC 2.7.11.1) (Proto-oncogene c-RAF) (cRaf) (Raf-1) | Serine/threonine-protein kinase that acts as a regulatory link between the membrane-associated Ras GTPases and the MAPK/ERK cascade, and this critical regulatory link functions as a switch determining cell fate decisions including proliferation, differentiation, apoptosis, survival and oncogenic transformation. RAF1 activation initiates a mitogen-activated protein kinase (MAPK) cascade that comprises a sequential phosphorylation of the dual-specific MAPK kinases (MAP2K1/MEK1 and MAP2K2/MEK2) and the extracellular signal-regulated kinases (MAPK3/ERK1 and MAPK1/ERK2). The phosphorylated form of RAF1 (on residues Ser-338 and Ser-339, by PAK1) phosphorylates BAD/Bcl2-antagonist of cell death at 'Ser-75'. Phosphorylates adenylyl cyclases: ADCY2, ADCY5 and ADCY6, resulting in their activation. Phosphorylates PPP1R12A resulting in inhibition of the phosphatase activity. Phosphorylates TNNT2/cardiac muscle troponin T. Can promote NF-kB activation and inhibit signal transducers involved in motility (ROCK2), apoptosis (MAP3K5/ASK1 and STK3/MST2), proliferation and angiogenesis (RB1). Can protect cells from apoptosis also by translocating to the mitochondria where it binds BCL2 and displaces BAD/Bcl2-antagonist of cell death. Regulates Rho signaling and migration, and is required for normal wound healing. Plays a role in the oncogenic transformation of epithelial cells via repression of the TJ protein, occludin (OCLN) by inducing the up-regulation of a transcriptional repressor SNAI2/SLUG, which induces down-regulation of OCLN. Restricts caspase activation in response to selected stimuli, notably Fas stimulation, pathogen-mediated macrophage apoptosis, and erythroid differentiation. {ECO:0000269|PubMed:11427728, ECO:0000269|PubMed:11719507, ECO:0000269|PubMed:15385642, ECO:0000269|PubMed:15618521, ECO:0000269|PubMed:15849194, ECO:0000269|PubMed:16892053, ECO:0000269|PubMed:16924233, ECO:0000269|PubMed:9360956}. |
P04075 | ALDOA | S39 | ochoa | Fructose-bisphosphate aldolase A (EC 4.1.2.13) (Lung cancer antigen NY-LU-1) (Muscle-type aldolase) | Catalyzes the reversible conversion of beta-D-fructose 1,6-bisphosphate (FBP) into two triose phosphate and plays a key role in glycolysis and gluconeogenesis (PubMed:14766013). In addition, may also function as scaffolding protein (By similarity). {ECO:0000250, ECO:0000269|PubMed:14766013}. |
P06748 | NPM1 | S106 | ochoa|psp | Nucleophosmin (NPM) (Nucleolar phosphoprotein B23) (Nucleolar protein NO38) (Numatrin) | Involved in diverse cellular processes such as ribosome biogenesis, centrosome duplication, protein chaperoning, histone assembly, cell proliferation, and regulation of tumor suppressors p53/TP53 and ARF. Binds ribosome presumably to drive ribosome nuclear export. Associated with nucleolar ribonucleoprotein structures and bind single-stranded nucleic acids. Acts as a chaperonin for the core histones H3, H2B and H4. Stimulates APEX1 endonuclease activity on apurinic/apyrimidinic (AP) double-stranded DNA but inhibits APEX1 endonuclease activity on AP single-stranded RNA. May exert a control of APEX1 endonuclease activity within nucleoli devoted to repair AP on rDNA and the removal of oxidized rRNA molecules. In concert with BRCA2, regulates centrosome duplication. Regulates centriole duplication: phosphorylation by PLK2 is able to trigger centriole replication. Negatively regulates the activation of EIF2AK2/PKR and suppresses apoptosis through inhibition of EIF2AK2/PKR autophosphorylation. Antagonizes the inhibitory effect of ATF5 on cell proliferation and relieves ATF5-induced G2/M blockade (PubMed:22528486). In complex with MYC enhances the transcription of MYC target genes (PubMed:25956029). May act as chaperonin or cotransporter in the nucleolar localization of transcription termination factor TTF1 (By similarity). {ECO:0000250|UniProtKB:Q61937, ECO:0000269|PubMed:12882984, ECO:0000269|PubMed:16107701, ECO:0000269|PubMed:17015463, ECO:0000269|PubMed:18809582, ECO:0000269|PubMed:19188445, ECO:0000269|PubMed:20352051, ECO:0000269|PubMed:21084279, ECO:0000269|PubMed:22002061, ECO:0000269|PubMed:22528486, ECO:0000269|PubMed:25956029}. |
P07195 | LDHB | S162 | ochoa|psp | L-lactate dehydrogenase B chain (LDH-B) (EC 1.1.1.27) (LDH heart subunit) (LDH-H) (Renal carcinoma antigen NY-REN-46) | Interconverts simultaneously and stereospecifically pyruvate and lactate with concomitant interconversion of NADH and NAD(+). {ECO:0000269|PubMed:27618187}. |
P07864 | LDHC | S161 | ochoa | L-lactate dehydrogenase C chain (LDH-C) (EC 1.1.1.27) (Cancer/testis antigen 32) (CT32) (LDH testis subunit) (LDH-X) | Possible role in sperm motility. |
P07900 | HSP90AA1 | S169 | ochoa | Heat shock protein HSP 90-alpha (EC 3.6.4.10) (Heat shock 86 kDa) (HSP 86) (HSP86) (Heat shock protein family C member 1) (Lipopolysaccharide-associated protein 2) (LAP-2) (LPS-associated protein 2) (Renal carcinoma antigen NY-REN-38) | Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle that is linked to its ATPase activity which is essential for its chaperone activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:11274138, PubMed:12526792, PubMed:15577939, PubMed:15937123, PubMed:27353360, PubMed:29127155). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself (PubMed:29127155). Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:26991466, PubMed:27295069). Plays a critical role in mitochondrial import, delivers preproteins to the mitochondrial import receptor TOMM70 (PubMed:12526792). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels (PubMed:25973397). In the first place, they alter the steady-state levels of certain transcription factors in response to various physiological cues (PubMed:25973397). Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment (PubMed:25973397). Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes (PubMed:11276205). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Mediates the association of TOMM70 with IRF3 or TBK1 in mitochondrial outer membrane which promotes host antiviral response (PubMed:20628368, PubMed:25609812). {ECO:0000269|PubMed:11274138, ECO:0000269|PubMed:11276205, ECO:0000269|PubMed:12526792, ECO:0000269|PubMed:15577939, ECO:0000269|PubMed:15937123, ECO:0000269|PubMed:20628368, ECO:0000269|PubMed:24613385, ECO:0000269|PubMed:25609812, ECO:0000269|PubMed:27353360, ECO:0000269|PubMed:29127155, ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466, ECO:0000303|PubMed:27295069}.; FUNCTION: (Microbial infection) Seems to interfere with N.meningitidis NadA-mediated invasion of human cells. Decreasing HSP90 levels increases adhesion and entry of E.coli expressing NadA into human Chang cells; increasing its levels leads to decreased adhesion and invasion. {ECO:0000305|PubMed:22066472}. |
P08238 | HSP90AB1 | S164 | ochoa | Heat shock protein HSP 90-beta (HSP 90) (Heat shock 84 kDa) (HSP 84) (HSP84) (Heat shock protein family C member 3) | Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle linked to its ATPase activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:16478993, PubMed:19696785). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself. Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:26991466, PubMed:27295069). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels. They first alter the steady-state levels of certain transcription factors in response to various physiological cues. Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment. Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Promotes cell differentiation by chaperoning BIRC2 and thereby protecting from auto-ubiquitination and degradation by the proteasomal machinery (PubMed:18239673). Main chaperone involved in the phosphorylation/activation of the STAT1 by chaperoning both JAK2 and PRKCE under heat shock and in turn, activates its own transcription (PubMed:20353823). Involved in the translocation into ERGIC (endoplasmic reticulum-Golgi intermediate compartment) of leaderless cargos (lacking the secretion signal sequence) such as the interleukin 1/IL-1; the translocation process is mediated by the cargo receptor TMED10 (PubMed:32272059). {ECO:0000269|PubMed:16478993, ECO:0000269|PubMed:18239673, ECO:0000269|PubMed:19696785, ECO:0000269|PubMed:20353823, ECO:0000269|PubMed:24613385, ECO:0000269|PubMed:32272059, ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466, ECO:0000303|PubMed:27295069}.; FUNCTION: (Microbial infection) Binding to N.meningitidis NadA stimulates monocytes (PubMed:21949862). Seems to interfere with N.meningitidis NadA-mediated invasion of human cells (Probable). {ECO:0000269|PubMed:21949862, ECO:0000305|PubMed:22066472}. |
P09467 | FBP1 | S63 | psp | Fructose-1,6-bisphosphatase 1 (FBPase 1) (EC 3.1.3.11) (D-fructose-1,6-bisphosphate 1-phosphohydrolase 1) (Liver FBPase) | Catalyzes the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate in the presence of divalent cations, acting as a rate-limiting enzyme in gluconeogenesis. Plays a role in regulating glucose sensing and insulin secretion of pancreatic beta-cells. Appears to modulate glycerol gluconeogenesis in liver. Important regulator of appetite and adiposity; increased expression of the protein in liver after nutrient excess increases circulating satiety hormones and reduces appetite-stimulating neuropeptides and thus seems to provide a feedback mechanism to limit weight gain. {ECO:0000269|PubMed:16497803, ECO:0000269|PubMed:18375435, ECO:0000269|PubMed:22517657}. |
P09651 | HNRNPA1 | S142 | ochoa | Heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) (Helix-destabilizing protein) (Single-strand RNA-binding protein) (hnRNP core protein A1) [Cleaved into: Heterogeneous nuclear ribonucleoprotein A1, N-terminally processed] | Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and modulation of splice site selection (PubMed:17371836). Plays a role in the splicing of pyruvate kinase PKM by binding repressively to sequences flanking PKM exon 9, inhibiting exon 9 inclusion and resulting in exon 10 inclusion and production of the PKM M2 isoform (PubMed:20010808). Binds to the IRES and thereby inhibits the translation of the apoptosis protease activating factor APAF1 (PubMed:31498791). May bind to specific miRNA hairpins (PubMed:28431233). {ECO:0000269|PubMed:17371836, ECO:0000269|PubMed:20010808, ECO:0000269|PubMed:28431233, ECO:0000269|PubMed:31498791}.; FUNCTION: (Microbial infection) May play a role in HCV RNA replication. {ECO:0000269|PubMed:17229681}.; FUNCTION: (Microbial infection) Cleavage by Enterovirus 71 protease 3C results in increased translation of apoptosis protease activating factor APAF1, leading to apoptosis. {ECO:0000269|PubMed:17229681}. |
P09972 | ALDOC | S39 | ochoa | Fructose-bisphosphate aldolase C (EC 4.1.2.13) (Brain-type aldolase) | None |
P0C7U0 | ELFN1 | S461 | ochoa | Protein ELFN1 (Extracellular leucine-rich repeat and fibronectin type-III domain-containing protein 1) (Protein phosphatase 1 regulatory subunit 28) | Postsynaptic protein that regulates circuit dynamics in the central nervous system by modulating the temporal dynamics of interneuron recruitment. Specifically present in excitatory synapses onto oriens-lacunosum molecular (OLM) interneurons and acts as a regulator of presynaptic release probability to direct the formation of highly facilitating pyramidal-OLM synapses (By similarity). Inhibits phosphatase activity of protein phosphatase 1 (PP1) complexes. {ECO:0000250, ECO:0000269|PubMed:19389623}. |
P0DJD0 | RGPD1 | S1456 | ochoa | RANBP2-like and GRIP domain-containing protein 1 (Ran-binding protein 2-like 6) (RanBP2-like 6) (RanBP2L6) | None |
P0DJD1 | RGPD2 | S1464 | ochoa | RANBP2-like and GRIP domain-containing protein 2 (Ran-binding protein 2-like 2) (RanBP2-like 2) (RanBP2L2) | None |
P10809 | HSPD1 | S488 | ochoa | 60 kDa heat shock protein, mitochondrial (EC 5.6.1.7) (60 kDa chaperonin) (Chaperonin 60) (CPN60) (Heat shock protein 60) (HSP-60) (Hsp60) (Heat shock protein family D member 1) (HuCHA60) (Mitochondrial matrix protein P1) (P60 lymphocyte protein) | Chaperonin implicated in mitochondrial protein import and macromolecular assembly. Together with Hsp10, facilitates the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix (PubMed:11422376, PubMed:1346131). The functional units of these chaperonins consist of heptameric rings of the large subunit Hsp60, which function as a back-to-back double ring. In a cyclic reaction, Hsp60 ring complexes bind one unfolded substrate protein per ring, followed by the binding of ATP and association with 2 heptameric rings of the co-chaperonin Hsp10. This leads to sequestration of the substrate protein in the inner cavity of Hsp60 where, for a certain period of time, it can fold undisturbed by other cell components. Synchronous hydrolysis of ATP in all Hsp60 subunits results in the dissociation of the chaperonin rings and the release of ADP and the folded substrate protein (Probable). {ECO:0000269|PubMed:11422376, ECO:0000269|PubMed:1346131, ECO:0000305|PubMed:25918392}. |
P11274 | BCR | S429 | ochoa | Breakpoint cluster region protein (EC 2.7.11.1) (Renal carcinoma antigen NY-REN-26) | Protein with a unique structure having two opposing regulatory activities toward small GTP-binding proteins. The C-terminus is a GTPase-activating protein (GAP) domain which stimulates GTP hydrolysis by RAC1, RAC2 and CDC42. Accelerates the intrinsic rate of GTP hydrolysis of RAC1 or CDC42, leading to down-regulation of the active GTP-bound form (PubMed:17116687, PubMed:1903516, PubMed:7479768). The central Dbl homology (DH) domain functions as guanine nucleotide exchange factor (GEF) that modulates the GTPases CDC42, RHOA and RAC1. Promotes the conversion of CDC42, RHOA and RAC1 from the GDP-bound to the GTP-bound form (PubMed:23940119, PubMed:7479768). The amino terminus contains an intrinsic kinase activity (PubMed:1657398). Functions as an important negative regulator of neuronal RAC1 activity (By similarity). Regulates macrophage functions such as CSF1-directed motility and phagocytosis through the modulation of RAC1 activity (PubMed:17116687). Plays a major role as a RHOA GEF in keratinocytes being involved in focal adhesion formation and keratinocyte differentiation (PubMed:23940119). {ECO:0000250|UniProtKB:Q6PAJ1, ECO:0000269|PubMed:1657398, ECO:0000269|PubMed:17116687, ECO:0000269|PubMed:1903516, ECO:0000269|PubMed:23940119, ECO:0000269|PubMed:7479768}. |
P13010 | XRCC5 | S255 | ochoa | X-ray repair cross-complementing protein 5 (EC 3.6.4.-) (86 kDa subunit of Ku antigen) (ATP-dependent DNA helicase 2 subunit 2) (ATP-dependent DNA helicase II 80 kDa subunit) (CTC box-binding factor 85 kDa subunit) (CTC85) (CTCBF) (DNA repair protein XRCC5) (Ku80) (Ku86) (Lupus Ku autoantigen protein p86) (Nuclear factor IV) (Thyroid-lupus autoantigen) (TLAA) (X-ray repair complementing defective repair in Chinese hamster cells 5 (double-strand-break rejoining)) | Single-stranded DNA-dependent ATP-dependent helicase that plays a key role in DNA non-homologous end joining (NHEJ) by recruiting DNA-PK to DNA (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). Required for double-strand break repair and V(D)J recombination (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). Also has a role in chromosome translocation (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). The DNA helicase II complex binds preferentially to fork-like ends of double-stranded DNA in a cell cycle-dependent manner (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). It works in the 3'-5' direction (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). During NHEJ, the XRCC5-XRRC6 dimer performs the recognition step: it recognizes and binds to the broken ends of the DNA and protects them from further resection (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). Binding to DNA may be mediated by XRCC6 (PubMed:11493912, PubMed:12145306, PubMed:7957065, PubMed:8621488). The XRCC5-XRRC6 dimer acts as a regulatory subunit of the DNA-dependent protein kinase complex DNA-PK by increasing the affinity of the catalytic subunit PRKDC to DNA by 100-fold (PubMed:11493912, PubMed:12145306, PubMed:20383123, PubMed:7957065, PubMed:8621488). The XRCC5-XRRC6 dimer is probably involved in stabilizing broken DNA ends and bringing them together (PubMed:12145306, PubMed:20383123, PubMed:7957065, PubMed:8621488). The assembly of the DNA-PK complex to DNA ends is required for the NHEJ ligation step (PubMed:12145306, PubMed:20383123, PubMed:7957065, PubMed:8621488). The XRCC5-XRRC6 dimer probably also acts as a 5'-deoxyribose-5-phosphate lyase (5'-dRP lyase), by catalyzing the beta-elimination of the 5' deoxyribose-5-phosphate at an abasic site near double-strand breaks (PubMed:20383123). XRCC5 probably acts as the catalytic subunit of 5'-dRP activity, and allows to 'clean' the termini of abasic sites, a class of nucleotide damage commonly associated with strand breaks, before such broken ends can be joined (PubMed:20383123). The XRCC5-XRRC6 dimer together with APEX1 acts as a negative regulator of transcription (PubMed:8621488). In association with NAA15, the XRCC5-XRRC6 dimer binds to the osteocalcin promoter and activates osteocalcin expression (PubMed:12145306). As part of the DNA-PK complex, involved in the early steps of ribosome assembly by promoting the processing of precursor rRNA into mature 18S rRNA in the small-subunit processome (PubMed:32103174). Binding to U3 small nucleolar RNA, recruits PRKDC and XRCC5/Ku86 to the small-subunit processome (PubMed:32103174). Plays a role in the regulation of DNA virus-mediated innate immune response by assembling into the HDP-RNP complex, a complex that serves as a platform for IRF3 phosphorylation and subsequent innate immune response activation through the cGAS-STING pathway (PubMed:28712728). {ECO:0000269|PubMed:11493912, ECO:0000269|PubMed:12145306, ECO:0000269|PubMed:20383123, ECO:0000269|PubMed:28712728, ECO:0000269|PubMed:32103174, ECO:0000269|PubMed:7957065, ECO:0000269|PubMed:8621488}. |
P15056 | BRAF | S465 | ochoa|psp | Serine/threonine-protein kinase B-raf (EC 2.7.11.1) (Proto-oncogene B-Raf) (p94) (v-Raf murine sarcoma viral oncogene homolog B1) | Protein kinase involved in the transduction of mitogenic signals from the cell membrane to the nucleus (Probable). Phosphorylates MAP2K1, and thereby activates the MAP kinase signal transduction pathway (PubMed:21441910, PubMed:29433126). Phosphorylates PFKFB2 (PubMed:36402789). May play a role in the postsynaptic responses of hippocampal neurons (PubMed:1508179). {ECO:0000269|PubMed:1508179, ECO:0000269|PubMed:21441910, ECO:0000269|PubMed:29433126, ECO:0000269|PubMed:36402789, ECO:0000305}. |
P15923 | TCF3 | S156 | ochoa | Transcription factor E2-alpha (Class B basic helix-loop-helix protein 21) (bHLHb21) (Immunoglobulin enhancer-binding factor E12/E47) (Immunoglobulin transcription factor 1) (Kappa-E2-binding factor) (Transcription factor 3) (TCF-3) (Transcription factor ITF-1) | Transcriptional regulator involved in the initiation of neuronal differentiation and mesenchymal to epithelial transition (By similarity). Heterodimers between TCF3 and tissue-specific basic helix-loop-helix (bHLH) proteins play major roles in determining tissue-specific cell fate during embryogenesis, like muscle or early B-cell differentiation (By similarity). Together with TCF15, required for the mesenchymal to epithelial transition (By similarity). Dimers bind DNA on E-box motifs: 5'-CANNTG-3' (By similarity). Binds to the kappa-E2 site in the kappa immunoglobulin gene enhancer (PubMed:2493990). Binds to IEB1 and IEB2, which are short DNA sequences in the insulin gene transcription control region (By similarity). {ECO:0000250|UniProtKB:P15806, ECO:0000269|PubMed:2493990}.; FUNCTION: [Isoform E47]: Facilitates ATOH7 binding to DNA at the consensus sequence 5'-CAGGTG-3', and positively regulates transcriptional activity. {ECO:0000269|PubMed:31696227}. |
P17677 | GAP43 | S96 | ochoa | Neuromodulin (Axonal membrane protein GAP-43) (Growth-associated protein 43) (Neural phosphoprotein B-50) (pp46) | This protein is associated with nerve growth. It is a major component of the motile 'growth cones' that form the tips of elongating axons. Plays a role in axonal and dendritic filopodia induction. {ECO:0000269|PubMed:14978216, ECO:0000269|PubMed:21152083}. |
P17844 | DDX5 | S24 | ochoa | Probable ATP-dependent RNA helicase DDX5 (EC 3.6.4.13) (DEAD box protein 5) (RNA helicase p68) | Involved in the alternative regulation of pre-mRNA splicing; its RNA helicase activity is necessary for increasing tau exon 10 inclusion and occurs in a RBM4-dependent manner. Binds to the tau pre-mRNA in the stem-loop region downstream of exon 10. The rate of ATP hydrolysis is highly stimulated by single-stranded RNA. Involved in transcriptional regulation; the function is independent of the RNA helicase activity. Transcriptional coactivator for androgen receptor AR but probably not ESR1. Synergizes with DDX17 and SRA1 RNA to activate MYOD1 transcriptional activity and involved in skeletal muscle differentiation. Transcriptional coactivator for p53/TP53 and involved in p53/TP53 transcriptional response to DNA damage and p53/TP53-dependent apoptosis. Transcriptional coactivator for RUNX2 and involved in regulation of osteoblast differentiation. Acts as a transcriptional repressor in a promoter-specific manner; the function probably involves association with histone deacetylases, such as HDAC1. As component of a large PER complex is involved in the inhibition of 3' transcriptional termination of circadian target genes such as PER1 and NR1D1 and the control of the circadian rhythms. {ECO:0000269|PubMed:12527917, ECO:0000269|PubMed:15298701, ECO:0000269|PubMed:15660129, ECO:0000269|PubMed:17011493, ECO:0000269|PubMed:17960593, ECO:0000269|PubMed:18829551, ECO:0000269|PubMed:19718048, ECO:0000269|PubMed:21343338}. |
P19367 | HK1 | S124 | psp | Hexokinase-1 (EC 2.7.1.1) (Brain form hexokinase) (Hexokinase type I) (HK I) (Hexokinase-A) | Catalyzes the phosphorylation of various hexoses, such as D-glucose, D-glucosamine, D-fructose, D-mannose and 2-deoxy-D-glucose, to hexose 6-phosphate (D-glucose 6-phosphate, D-glucosamine 6-phosphate, D-fructose 6-phosphate, D-mannose 6-phosphate and 2-deoxy-D-glucose 6-phosphate, respectively) (PubMed:1637300, PubMed:25316723, PubMed:27374331). Does not phosphorylate N-acetyl-D-glucosamine (PubMed:27374331). Mediates the initial step of glycolysis by catalyzing phosphorylation of D-glucose to D-glucose 6-phosphate (By similarity). Involved in innate immunity and inflammation by acting as a pattern recognition receptor for bacterial peptidoglycan (PubMed:27374331). When released in the cytosol, N-acetyl-D-glucosamine component of bacterial peptidoglycan inhibits the hexokinase activity of HK1 and causes its dissociation from mitochondrial outer membrane, thereby activating the NLRP3 inflammasome (PubMed:27374331). {ECO:0000250|UniProtKB:P05708, ECO:0000269|PubMed:1637300, ECO:0000269|PubMed:25316723, ECO:0000269|PubMed:27374331}. |
P20340 | RAB6A | S117 | ochoa | Ras-related protein Rab-6A (Rab-6) (EC 3.6.5.2) | The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes (PubMed:25962623). Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different sets of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion (PubMed:25962623). RAB6A acts as a regulator of COPI-independent retrograde transport from the Golgi apparatus towards the endoplasmic reticulum (ER) (PubMed:25962623). Has a low GTPase activity (PubMed:25962623). Recruits VPS13B to the Golgi membrane (PubMed:25492866). Plays a role in neuron projection development (Probable). {ECO:0000269|PubMed:25492866, ECO:0000269|PubMed:25962623, ECO:0000305|PubMed:25492866}. |
P20929 | NEB | S437 | ochoa | Nebulin | This giant muscle protein may be involved in maintaining the structural integrity of sarcomeres and the membrane system associated with the myofibrils. Binds and stabilize F-actin. |
P21333 | FLNA | S2292 | ochoa|psp | Filamin-A (FLN-A) (Actin-binding protein 280) (ABP-280) (Alpha-filamin) (Endothelial actin-binding protein) (Filamin-1) (Non-muscle filamin) | Promotes orthogonal branching of actin filaments and links actin filaments to membrane glycoproteins. Anchors various transmembrane proteins to the actin cytoskeleton and serves as a scaffold for a wide range of cytoplasmic signaling proteins. Interaction with FLNB may allow neuroblast migration from the ventricular zone into the cortical plate. Tethers cell surface-localized furin, modulates its rate of internalization and directs its intracellular trafficking (By similarity). Involved in ciliogenesis. Plays a role in cell-cell contacts and adherens junctions during the development of blood vessels, heart and brain organs. Plays a role in platelets morphology through interaction with SYK that regulates ITAM- and ITAM-like-containing receptor signaling, resulting in by platelet cytoskeleton organization maintenance (By similarity). During the axon guidance process, required for growth cone collapse induced by SEMA3A-mediated stimulation of neurons (PubMed:25358863). {ECO:0000250, ECO:0000250|UniProtKB:Q8BTM8, ECO:0000269|PubMed:22121117, ECO:0000269|PubMed:25358863}. |
P21333 | FLNA | S2494 | ochoa | Filamin-A (FLN-A) (Actin-binding protein 280) (ABP-280) (Alpha-filamin) (Endothelial actin-binding protein) (Filamin-1) (Non-muscle filamin) | Promotes orthogonal branching of actin filaments and links actin filaments to membrane glycoproteins. Anchors various transmembrane proteins to the actin cytoskeleton and serves as a scaffold for a wide range of cytoplasmic signaling proteins. Interaction with FLNB may allow neuroblast migration from the ventricular zone into the cortical plate. Tethers cell surface-localized furin, modulates its rate of internalization and directs its intracellular trafficking (By similarity). Involved in ciliogenesis. Plays a role in cell-cell contacts and adherens junctions during the development of blood vessels, heart and brain organs. Plays a role in platelets morphology through interaction with SYK that regulates ITAM- and ITAM-like-containing receptor signaling, resulting in by platelet cytoskeleton organization maintenance (By similarity). During the axon guidance process, required for growth cone collapse induced by SEMA3A-mediated stimulation of neurons (PubMed:25358863). {ECO:0000250, ECO:0000250|UniProtKB:Q8BTM8, ECO:0000269|PubMed:22121117, ECO:0000269|PubMed:25358863}. |
P25786 | PSMA1 | S114 | ochoa | Proteasome subunit alpha type-1 (30 kDa prosomal protein) (PROS-30) (Macropain subunit C2) (Multicatalytic endopeptidase complex subunit C2) (Proteasome component C2) (Proteasome nu chain) (Proteasome subunit alpha-6) (alpha-6) | Component of the 20S core proteasome complex involved in the proteolytic degradation of most intracellular proteins. This complex plays numerous essential roles within the cell by associating with different regulatory particles. Associated with two 19S regulatory particles, forms the 26S proteasome and thus participates in the ATP-dependent degradation of ubiquitinated proteins. The 26S proteasome plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins that could impair cellular functions, and by removing proteins whose functions are no longer required. Associated with the PA200 or PA28, the 20S proteasome mediates ubiquitin-independent protein degradation. This type of proteolysis is required in several pathways including spermatogenesis (20S-PA200 complex) or generation of a subset of MHC class I-presented antigenic peptides (20S-PA28 complex). {ECO:0000269|PubMed:15244466, ECO:0000269|PubMed:27176742, ECO:0000269|PubMed:8610016}. |
P26639 | TARS1 | S596 | ochoa | Threonine--tRNA ligase 1, cytoplasmic (EC 6.1.1.3) (Threonyl-tRNA synthetase) (ThrRS) (Threonyl-tRNA synthetase 1) | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction: threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) (PubMed:25824639, PubMed:31374204). Also edits incorrectly charged tRNA(Thr) via its editing domain, at the post-transfer stage (By similarity). {ECO:0000250|UniProtKB:Q9D0R2, ECO:0000269|PubMed:25824639, ECO:0000269|PubMed:31374204}. |
P27708 | CAD | S1321 | ochoa | Multifunctional protein CAD (Carbamoyl phosphate synthetase 2-aspartate transcarbamylase-dihydroorotase) [Includes: Glutamine-dependent carbamoyl phosphate synthase (EC 6.3.5.5); Glutamine amidotransferase (GATase) (GLNase) (EC 3.5.1.2); Ammonium-dependent carbamoyl phosphate synthase (CPS) (CPSase) (EC 6.3.4.16); Aspartate carbamoyltransferase (EC 2.1.3.2); Dihydroorotase (EC 3.5.2.3)] | Multifunctional protein that encodes the first 3 enzymatic activities of the de novo pyrimidine pathway: carbamoylphosphate synthetase (CPSase; EC 6.3.5.5), aspartate transcarbamylase (ATCase; EC 2.1.3.2) and dihydroorotase (DHOase; EC 3.5.2.3). The CPSase-function is accomplished in 2 steps, by a glutamine-dependent amidotransferase activity (GATase) that binds and cleaves glutamine to produce ammonia, followed by an ammonium-dependent carbamoyl phosphate synthetase, which reacts with the ammonia, hydrogencarbonate and ATP to form carbamoyl phosphate. The endogenously produced carbamoyl phosphate is sequestered and channeled to the ATCase active site. ATCase then catalyzes the formation of carbamoyl-L-aspartate from L-aspartate and carbamoyl phosphate. In the last step, DHOase catalyzes the cyclization of carbamoyl aspartate to dihydroorotate. {ECO:0000269|PubMed:24332717}. |
P28072 | PSMB6 | S58 | ochoa | Proteasome subunit beta type-6 (EC 3.4.25.1) (Macropain delta chain) (Multicatalytic endopeptidase complex delta chain) (Proteasome delta chain) (Proteasome subunit Y) (Proteasome subunit beta-1) (beta-1) | Component of the 20S core proteasome complex involved in the proteolytic degradation of most intracellular proteins. This complex plays numerous essential roles within the cell by associating with different regulatory particles. Associated with two 19S regulatory particles, forms the 26S proteasome and thus participates in the ATP-dependent degradation of ubiquitinated proteins. The 26S proteasome plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins that could impair cellular functions, and by removing proteins whose functions are no longer required. Associated with the PA200 or PA28, the 20S proteasome mediates ubiquitin-independent protein degradation. This type of proteolysis is required in several pathways including spermatogenesis (20S-PA200 complex) or generation of a subset of MHC class I-presented antigenic peptides (20S-PA28 complex). Within the 20S core complex, PSMB6 displays a peptidylglutamyl-hydrolizing activity also termed postacidic or caspase-like activity, meaning that the peptides bond hydrolysis occurs directly after acidic residues. {ECO:0000269|PubMed:15244466, ECO:0000269|PubMed:27176742, ECO:0000269|PubMed:8610016}. |
P29218 | IMPA1 | S165 | ochoa | Inositol monophosphatase 1 (IMP 1) (IMPase 1) (EC 3.1.3.25) (D-galactose 1-phosphate phosphatase) (EC 3.1.3.94) (Inositol-1(or 4)-monophosphatase 1) (Lithium-sensitive myo-inositol monophosphatase A1) | Phosphatase involved in the dephosphorylation of myo-inositol monophosphates to generate myo-inositol (PubMed:17068342, PubMed:8718889, PubMed:9462881). Is also able to dephosphorylate scyllo-inositol-phosphate, myo-inositol 1,4-diphosphate, scyllo-inositol-1,3-diphosphate and scyllo-inositol-1,4-diphosphate (PubMed:17068342). Also dephosphorylates in vitro other sugar-phosphates including D-galactose-1-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate and 2'-AMP (PubMed:17068342, PubMed:8718889, PubMed:9462881). Responsible for the provision of inositol required for synthesis of phosphatidylinositols and polyphosphoinositides, and involved in maintaining normal brain function (PubMed:26416544, PubMed:8718889). Has been implicated as the pharmacological target for lithium (Li(+)) action in brain, which is used to treat bipolar affective disorder (PubMed:17068342). Is equally active with 1D-myo-inositol 1-phosphate, 1D-myo-inositol 3-phosphate and D-galactose 1-phosphate (PubMed:9462881). {ECO:0000269|PubMed:17068342, ECO:0000269|PubMed:26416544, ECO:0000269|PubMed:8718889, ECO:0000269|PubMed:9462881}. |
P30291 | WEE1 | S312 | ochoa|psp | Wee1-like protein kinase (WEE1hu) (EC 2.7.10.2) (Wee1A kinase) | Acts as a negative regulator of entry into mitosis (G2 to M transition) by protecting the nucleus from cytoplasmically activated cyclin B1-complexed CDK1 before the onset of mitosis by mediating phosphorylation of CDK1 on 'Tyr-15' (PubMed:15070733, PubMed:7743995, PubMed:8348613, PubMed:8428596). Specifically phosphorylates and inactivates cyclin B1-complexed CDK1 reaching a maximum during G2 phase and a minimum as cells enter M phase (PubMed:7743995, PubMed:8348613, PubMed:8428596). Phosphorylation of cyclin B1-CDK1 occurs exclusively on 'Tyr-15' and phosphorylation of monomeric CDK1 does not occur (PubMed:7743995, PubMed:8348613, PubMed:8428596). Its activity increases during S and G2 phases and decreases at M phase when it is hyperphosphorylated (PubMed:7743995). A correlated decrease in protein level occurs at M/G1 phase, probably due to its degradation (PubMed:7743995). {ECO:0000269|PubMed:15070733, ECO:0000269|PubMed:7743995, ECO:0000269|PubMed:8348613, ECO:0000269|PubMed:8428596}. |
P35250 | RFC2 | S30 | ochoa | Replication factor C subunit 2 (Activator 1 40 kDa subunit) (A1 40 kDa subunit) (Activator 1 subunit 2) (Replication factor C 40 kDa subunit) (RF-C 40 kDa subunit) (RFC40) | Subunit of the replication factor C (RFC) complex which acts during elongation of primed DNA templates by DNA polymerases delta and epsilon, and is necessary for ATP-dependent loading of proliferating cell nuclear antigen (PCNA) onto primed DNA (PubMed:9488738). This subunit binds ATP (By similarity). {ECO:0000250, ECO:0000269|PubMed:9488738}. |
P35348 | ADRA1A | S381 | psp | Alpha-1A adrenergic receptor (Alpha-1A adrenoreceptor) (Alpha-1A adrenoceptor) (Alpha-1C adrenergic receptor) (Alpha-adrenergic receptor 1c) | This alpha-adrenergic receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. Its effect is mediated by G(q) and G(11) proteins. Nuclear ADRA1A-ADRA1B heterooligomers regulate phenylephrine(PE)-stimulated ERK signaling in cardiac myocytes. {ECO:0000269|PubMed:18802028, ECO:0000269|PubMed:22120526}. |
P35580 | MYH10 | S641 | ochoa | Myosin-10 (Cellular myosin heavy chain, type B) (Myosin heavy chain 10) (Myosin heavy chain, non-muscle IIb) (Non-muscle myosin heavy chain B) (NMMHC-B) (Non-muscle myosin heavy chain IIb) (NMMHC II-b) (NMMHC-IIB) | Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. Involved with LARP6 in the stabilization of type I collagen mRNAs for CO1A1 and CO1A2. During cell spreading, plays an important role in cytoskeleton reorganization, focal contacts formation (in the central part but not the margins of spreading cells), and lamellipodial extension; this function is mechanically antagonized by MYH9. {ECO:0000269|PubMed:20052411, ECO:0000269|PubMed:20603131}.; FUNCTION: (Microbial infection) Acts as a receptor for herpes simplex virus 1/HHV-1 envelope glycoprotein B. {ECO:0000305|PubMed:25428876, ECO:0000305|PubMed:39048823}. |
P36382 | GJA5 | S122 | ochoa | Gap junction alpha-5 protein (Connexin-40) (Cx40) | One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. |
P37840 | SNCA | S42 | ochoa | Alpha-synuclein (Non-A beta component of AD amyloid) (Non-A4 component of amyloid precursor) (NACP) | Neuronal protein that plays several roles in synaptic activity such as regulation of synaptic vesicle trafficking and subsequent neurotransmitter release (PubMed:20798282, PubMed:26442590, PubMed:28288128, PubMed:30404828). Participates as a monomer in synaptic vesicle exocytosis by enhancing vesicle priming, fusion and dilation of exocytotic fusion pores (PubMed:28288128, PubMed:30404828). Mechanistically, acts by increasing local Ca(2+) release from microdomains which is essential for the enhancement of ATP-induced exocytosis (PubMed:30404828). Also acts as a molecular chaperone in its multimeric membrane-bound state, assisting in the folding of synaptic fusion components called SNAREs (Soluble NSF Attachment Protein REceptors) at presynaptic plasma membrane in conjunction with cysteine string protein-alpha/DNAJC5 (PubMed:20798282). This chaperone activity is important to sustain normal SNARE-complex assembly during aging (PubMed:20798282). Also plays a role in the regulation of the dopamine neurotransmission by associating with the dopamine transporter (DAT1) and thereby modulating its activity (PubMed:26442590). {ECO:0000269|PubMed:20798282, ECO:0000269|PubMed:26442590, ECO:0000269|PubMed:28288128, ECO:0000269|PubMed:30404828}. |
P41279 | MAP3K8 | S141 | ochoa | Mitogen-activated protein kinase kinase kinase 8 (EC 2.7.11.25) (Cancer Osaka thyroid oncogene) (Proto-oncogene c-Cot) (Serine/threonine-protein kinase cot) (Tumor progression locus 2) (TPL-2) | Required for lipopolysaccharide (LPS)-induced, TLR4-mediated activation of the MAPK/ERK pathway in macrophages, thus being critical for production of the pro-inflammatory cytokine TNF-alpha (TNF) during immune responses. Involved in the regulation of T-helper cell differentiation and IFNG expression in T-cells. Involved in mediating host resistance to bacterial infection through negative regulation of type I interferon (IFN) production. In vitro, activates MAPK/ERK pathway in response to IL1 in an IRAK1-independent manner, leading to up-regulation of IL8 and CCL4. Transduces CD40 and TNFRSF1A signals that activate ERK in B-cells and macrophages, and thus may play a role in the regulation of immunoglobulin production. May also play a role in the transduction of TNF signals that activate JNK and NF-kappa-B in some cell types. In adipocytes, activates MAPK/ERK pathway in an IKBKB-dependent manner in response to IL1B and TNF, but not insulin, leading to induction of lipolysis. Plays a role in the cell cycle. Isoform 1 shows some transforming activity, although it is much weaker than that of the activated oncogenic variant. {ECO:0000269|PubMed:11342626, ECO:0000269|PubMed:12667451, ECO:0000269|PubMed:15169888, ECO:0000269|PubMed:16371247, ECO:0000269|PubMed:1833717, ECO:0000269|PubMed:19001140, ECO:0000269|PubMed:19808894}. |
P49257 | LMAN1 | S425 | ochoa | Protein ERGIC-53 (ER-Golgi intermediate compartment 53 kDa protein) (Gp58) (Intracellular mannose-specific lectin MR60) (Lectin mannose-binding 1) | Mannose-specific lectin. May recognize sugar residues of glycoproteins, glycolipids, or glycosylphosphatidyl inositol anchors and may be involved in the sorting or recycling of proteins, lipids, or both. The LMAN1-MCFD2 complex forms a specific cargo receptor for the ER-to-Golgi transport of selected proteins. {ECO:0000269|PubMed:12717434, ECO:0000269|PubMed:13130098}. |
P49792 | RANBP2 | S1495 | ochoa | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
P49792 | RANBP2 | S2447 | ochoa | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
P49848 | TAF6 | S602 | ochoa | Transcription initiation factor TFIID subunit 6 (RNA polymerase II TBP-associated factor subunit E) (Transcription initiation factor TFIID 70 kDa subunit) (TAF(II)70) (TAFII-70) (TAFII70) (Transcription initiation factor TFIID 80 kDa subunit) (TAF(II)80) (TAFII-80) (TAFII80) | The TFIID basal transcription factor complex plays a major role in the initiation of RNA polymerase II (Pol II)-dependent transcription (PubMed:33795473). TFIID recognizes and binds promoters with or without a TATA box via its subunit TBP, a TATA-box-binding protein, and promotes assembly of the pre-initiation complex (PIC) (PubMed:33795473). The TFIID complex consists of TBP and TBP-associated factors (TAFs), including TAF1, TAF2, TAF3, TAF4, TAF5, TAF6, TAF7, TAF8, TAF9, TAF10, TAF11, TAF12 and TAF13 (PubMed:33795473). The TFIID complex structure can be divided into 3 modules TFIID-A, TFIID-B, and TFIID-C (PubMed:33795473). TAF6 homodimer connects TFIID modules, forming a rigid core (PubMed:33795473). {ECO:0000269|PubMed:33795473}.; FUNCTION: [Isoform 4]: Transcriptional regulator which acts primarily as a positive regulator of transcription (PubMed:20096117, PubMed:29358700). Recruited to the promoters of a number of genes including GADD45A and CDKN1A/p21, leading to transcriptional up-regulation and subsequent induction of apoptosis (PubMed:11583621). Also up-regulates expression of other genes including GCNA/ACRC, HES1 and IFFO1 (PubMed:18628956). In contrast, down-regulates transcription of MDM2 (PubMed:11583621). Acts as a transcriptional coactivator to enhance transcription of TP53/p53-responsive genes such as DUSP1 (PubMed:20096117). Can also activate transcription and apoptosis independently of TP53 (PubMed:18628956). Drives apoptosis via the intrinsic apoptotic pathway by up-regulating apoptosis effectors such as BCL2L11/BIM and PMAIP1/NOXA (PubMed:29358700). {ECO:0000269|PubMed:11583621, ECO:0000269|PubMed:18628956, ECO:0000269|PubMed:20096117, ECO:0000269|PubMed:29358700}. |
P50748 | KNTC1 | S1034 | ochoa | Kinetochore-associated protein 1 (Rough deal homolog) (HsROD) (Rod) (hRod) | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores (PubMed:11146660, PubMed:11590237, PubMed:15824131). Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex. {ECO:0000269|PubMed:11146660, ECO:0000269|PubMed:11590237, ECO:0000269|PubMed:15824131, ECO:0000305}. |
P50993 | ATP1A2 | S464 | ochoa | Sodium/potassium-transporting ATPase subunit alpha-2 (Na(+)/K(+) ATPase alpha-2 subunit) (EC 7.2.2.13) (Sodium pump subunit alpha-2) | This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium, providing the energy for active transport of various nutrients. {ECO:0000269|PubMed:33880529}. |
P51531 | SMARCA2 | S698 | ochoa | SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 2 (SAMRCA2) (EC 3.6.4.-) (BRG1-associated factor 190B) (BAF190B) (Probable global transcription activator SNF2L2) (Protein brahma homolog) (hBRM) (SNF2-alpha) | ATPase involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner. Binds DNA non-specifically (PubMed:15075294, PubMed:22952240, PubMed:26601204). Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a postmitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to postmitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity). {ECO:0000250|UniProtKB:Q6DIC0, ECO:0000269|PubMed:15075294, ECO:0000303|PubMed:22952240, ECO:0000303|PubMed:26601204}. |
P51608 | MECP2 | S164 | ochoa|psp | Methyl-CpG-binding protein 2 (MeCp-2 protein) (MeCp2) | Chromosomal protein that binds to methylated DNA. It can bind specifically to a single methyl-CpG pair. It is not influenced by sequences flanking the methyl-CpGs. Mediates transcriptional repression through interaction with histone deacetylase and the corepressor SIN3A. Binds both 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC)-containing DNA, with a preference for 5-methylcytosine (5mC). {ECO:0000250|UniProtKB:Q9Z2D6}. |
P51825 | AFF1 | S717 | ochoa | AF4/FMR2 family member 1 (ALL1-fused gene from chromosome 4 protein) (Protein AF-4) (Protein FEL) (Proto-oncogene AF4) | None |
P52565 | ARHGDIA | S148 | ochoa | Rho GDP-dissociation inhibitor 1 (Rho GDI 1) (Rho-GDI alpha) | Controls Rho proteins homeostasis. Regulates the GDP/GTP exchange reaction of the Rho proteins by inhibiting the dissociation of GDP from them, and the subsequent binding of GTP to them. Retains Rho proteins such as CDC42, RAC1 and RHOA in an inactive cytosolic pool, regulating their stability and protecting them from degradation. Actively involved in the recycling and distribution of activated Rho GTPases in the cell, mediates extraction from membranes of both inactive and activated molecules due its exceptionally high affinity for prenylated forms. Through the modulation of Rho proteins, may play a role in cell motility regulation. In glioma cells, inhibits cell migration and invasion by mediating the signals of SEMA5A and PLXNB3 that lead to inactivation of RAC1. {ECO:0000269|PubMed:20400958, ECO:0000269|PubMed:23434736}. |
P52566 | ARHGDIB | S145 | ochoa | Rho GDP-dissociation inhibitor 2 (Rho GDI 2) (Ly-GDI) (Rho-GDI beta) | Regulates the GDP/GTP exchange reaction of the Rho proteins by inhibiting the dissociation of GDP from them, and the subsequent binding of GTP to them (PubMed:7512369, PubMed:8356058). Regulates reorganization of the actin cytoskeleton mediated by Rho family members (PubMed:8262133). {ECO:0000269|PubMed:7512369, ECO:0000269|PubMed:8262133, ECO:0000269|PubMed:8356058}. |
P53007 | SLC25A1 | S94 | ochoa | Tricarboxylate transport protein, mitochondrial (Citrate transport protein) (CTP) (Mitochondrial citrate carrier) (CIC) (Solute carrier family 25 member 1) (Tricarboxylate carrier protein) | Mitochondrial electroneutral antiporter that exports citrate from the mitochondria into the cytosol in exchange for malate (PubMed:26870663, PubMed:29031613, PubMed:29238895, PubMed:39881208). Also able to mediate the exchange of citrate for isocitrate, phosphoenolpyruvate, cis-aconitate and to a lesser extent trans-aconitate, maleate and succinate (PubMed:29031613). In the cytoplasm, citrate plays important roles in fatty acid and sterol synthesis, regulation of glycolysis, protein acetylation, and other physiopathological processes (PubMed:29031613, PubMed:29238895, PubMed:39881208). {ECO:0000269|PubMed:26870663, ECO:0000269|PubMed:29031613, ECO:0000269|PubMed:29238895, ECO:0000269|PubMed:39881208}. |
P54296 | MYOM2 | S553 | ochoa | Myomesin-2 (165 kDa connectin-associated protein) (165 kDa titin-associated protein) (M-protein) (Myomesin family member 2) | Major component of the vertebrate myofibrillar M band. Binds myosin, titin, and light meromyosin. This binding is dose dependent. |
P54296 | MYOM2 | S555 | ochoa | Myomesin-2 (165 kDa connectin-associated protein) (165 kDa titin-associated protein) (M-protein) (Myomesin family member 2) | Major component of the vertebrate myofibrillar M band. Binds myosin, titin, and light meromyosin. This binding is dose dependent. |
P54760 | EPHB4 | S911 | ochoa | Ephrin type-B receptor 4 (EC 2.7.10.1) (Hepatoma transmembrane kinase) (Tyrosine-protein kinase TYRO11) | Receptor tyrosine kinase which binds promiscuously transmembrane ephrin-B family ligands residing on adjacent cells, leading to contact-dependent bidirectional signaling into neighboring cells. The signaling pathway downstream of the receptor is referred to as forward signaling while the signaling pathway downstream of the ephrin ligand is referred to as reverse signaling. Together with its cognate ligand/functional ligand EFNB2 it is involved in the regulation of cell adhesion and migration, and plays a central role in heart morphogenesis, angiogenesis and blood vessel remodeling and permeability. EPHB4-mediated forward signaling controls cellular repulsion and segregation from EFNB2-expressing cells. {ECO:0000269|PubMed:12734395, ECO:0000269|PubMed:16424904, ECO:0000269|PubMed:27400125, ECO:0000269|PubMed:30578106}. |
P56470 | LGALS4 | S258 | ochoa | Galectin-4 (Gal-4) (Antigen NY-CO-27) (L-36 lactose-binding protein) (L36LBP) (Lactose-binding lectin 4) | Galectin that binds lactose and a related range of sugars. May be involved in the assembly of adherens junctions. |
P57721 | PCBP3 | S143 | ochoa | Poly(rC)-binding protein 3 (Alpha-CP3) (PCBP3-overlapping transcript) (PCBP3-overlapping transcript 1) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC. {ECO:0000250}. |
P61513 | RPL37A | S59 | ochoa | Large ribosomal subunit protein eL43 (60S ribosomal protein L37a) | Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547}. |
P61978 | HNRNPK | S401 | ochoa | Heterogeneous nuclear ribonucleoprotein K (hnRNP K) (Transformation up-regulated nuclear protein) (TUNP) | One of the major pre-mRNA-binding proteins. Binds tenaciously to poly(C) sequences. Likely to play a role in the nuclear metabolism of hnRNAs, particularly for pre-mRNAs that contain cytidine-rich sequences. Can also bind poly(C) single-stranded DNA. Plays an important role in p53/TP53 response to DNA damage, acting at the level of both transcription activation and repression. When sumoylated, acts as a transcriptional coactivator of p53/TP53, playing a role in p21/CDKN1A and 14-3-3 sigma/SFN induction (By similarity). As far as transcription repression is concerned, acts by interacting with long intergenic RNA p21 (lincRNA-p21), a non-coding RNA induced by p53/TP53. This interaction is necessary for the induction of apoptosis, but not cell cycle arrest. As part of a ribonucleoprotein complex composed at least of ZNF827, HNRNPL and the circular RNA circZNF827 that nucleates the complex on chromatin, may negatively regulate the transcription of genes involved in neuronal differentiation (PubMed:33174841). {ECO:0000250, ECO:0000269|PubMed:16360036, ECO:0000269|PubMed:20673990, ECO:0000269|PubMed:22825850, ECO:0000269|PubMed:33174841}. |
P61978 | HNRNPK | S430 | ochoa | Heterogeneous nuclear ribonucleoprotein K (hnRNP K) (Transformation up-regulated nuclear protein) (TUNP) | One of the major pre-mRNA-binding proteins. Binds tenaciously to poly(C) sequences. Likely to play a role in the nuclear metabolism of hnRNAs, particularly for pre-mRNAs that contain cytidine-rich sequences. Can also bind poly(C) single-stranded DNA. Plays an important role in p53/TP53 response to DNA damage, acting at the level of both transcription activation and repression. When sumoylated, acts as a transcriptional coactivator of p53/TP53, playing a role in p21/CDKN1A and 14-3-3 sigma/SFN induction (By similarity). As far as transcription repression is concerned, acts by interacting with long intergenic RNA p21 (lincRNA-p21), a non-coding RNA induced by p53/TP53. This interaction is necessary for the induction of apoptosis, but not cell cycle arrest. As part of a ribonucleoprotein complex composed at least of ZNF827, HNRNPL and the circular RNA circZNF827 that nucleates the complex on chromatin, may negatively regulate the transcription of genes involved in neuronal differentiation (PubMed:33174841). {ECO:0000250, ECO:0000269|PubMed:16360036, ECO:0000269|PubMed:20673990, ECO:0000269|PubMed:22825850, ECO:0000269|PubMed:33174841}. |
P78347 | GTF2I | S710 | ochoa | General transcription factor II-I (GTFII-I) (TFII-I) (Bruton tyrosine kinase-associated protein 135) (BAP-135) (BTK-associated protein 135) (SRF-Phox1-interacting protein) (SPIN) (Williams-Beuren syndrome chromosomal region 6 protein) | Interacts with the basal transcription machinery by coordinating the formation of a multiprotein complex at the C-FOS promoter, and linking specific signal responsive activator complexes. Promotes the formation of stable high-order complexes of SRF and PHOX1 and interacts cooperatively with PHOX1 to promote serum-inducible transcription of a reporter gene deriven by the C-FOS serum response element (SRE). Acts as a coregulator for USF1 by binding independently two promoter elements, a pyrimidine-rich initiator (Inr) and an upstream E-box. Required for the formation of functional ARID3A DNA-binding complexes and for activation of immunoglobulin heavy-chain transcription upon B-lymphocyte activation. {ECO:0000269|PubMed:10373551, ECO:0000269|PubMed:11373296, ECO:0000269|PubMed:16738337}. |
P78362 | SRPK2 | S608 | ochoa | SRSF protein kinase 2 (EC 2.7.11.1) (SFRS protein kinase 2) (Serine/arginine-rich protein-specific kinase 2) (SR-protein-specific kinase 2) [Cleaved into: SRSF protein kinase 2 N-terminal; SRSF protein kinase 2 C-terminal] | Serine/arginine-rich protein-specific kinase which specifically phosphorylates its substrates at serine residues located in regions rich in arginine/serine dipeptides, known as RS domains and is involved in the phosphorylation of SR splicing factors and the regulation of splicing (PubMed:18559500, PubMed:21056976, PubMed:9472028). Promotes neuronal apoptosis by up-regulating cyclin-D1 (CCND1) expression (PubMed:19592491). This is done by the phosphorylation of SRSF2, leading to the suppression of p53/TP53 phosphorylation thereby relieving the repressive effect of p53/TP53 on cyclin-D1 (CCND1) expression (PubMed:21205200). Phosphorylates ACIN1, and redistributes it from the nuclear speckles to the nucleoplasm, resulting in cyclin A1 but not cyclin A2 up-regulation (PubMed:18559500). Plays an essential role in spliceosomal B complex formation via the phosphorylation of DDX23/PRP28 (PubMed:18425142). Probably by phosphorylating DDX23, leads to the suppression of incorrect R-loops formed during transcription; R-loops are composed of a DNA:RNA hybrid and the associated non-template single-stranded DNA (PubMed:28076779). Can mediate hepatitis B virus (HBV) core protein phosphorylation (PubMed:12134018). Plays a negative role in the regulation of HBV replication through a mechanism not involving the phosphorylation of the core protein but by reducing the packaging efficiency of the pregenomic RNA (pgRNA) without affecting the formation of the viral core particles (PubMed:16122776). {ECO:0000269|PubMed:12134018, ECO:0000269|PubMed:16122776, ECO:0000269|PubMed:18425142, ECO:0000269|PubMed:18559500, ECO:0000269|PubMed:19592491, ECO:0000269|PubMed:21056976, ECO:0000269|PubMed:21205200, ECO:0000269|PubMed:28076779, ECO:0000269|PubMed:9472028}. |
P98160 | HSPG2 | S4277 | ochoa | Basement membrane-specific heparan sulfate proteoglycan core protein (HSPG) (Perlecan) (PLC) [Cleaved into: Endorepellin; LG3 peptide] | Integral component of basement membranes. Component of the glomerular basement membrane (GBM), responsible for the fixed negative electrostatic membrane charge, and which provides a barrier which is both size- and charge-selective. It serves as an attachment substrate for cells. Plays essential roles in vascularization. Critical for normal heart development and for regulating the vascular response to injury. Also required for avascular cartilage development.; FUNCTION: [Endorepellin]: Anti-angiogenic and anti-tumor peptide that inhibits endothelial cell migration, collagen-induced endothelial tube morphogenesis and blood vessel growth in the chorioallantoic membrane. Blocks endothelial cell adhesion to fibronectin and type I collagen. Anti-tumor agent in neovascularization. Interaction with its ligand, integrin alpha2/beta1, is required for the anti-angiogenic properties. Evokes a reduction in phosphorylation of receptor tyrosine kinases via alpha2/beta1 integrin-mediated activation of the tyrosine phosphatase, PTPN6.; FUNCTION: [LG3 peptide]: Has anti-angiogenic properties that require binding of calcium ions for full activity. |
Q00577 | PURA | S182 | ochoa | Transcriptional activator protein Pur-alpha (Purine-rich single-stranded DNA-binding protein alpha) | This is a probable transcription activator that specifically binds the purine-rich single strand of the PUR element located upstream of the MYC gene (PubMed:1448097, PubMed:20976240). May play a role in the initiation of DNA replication and in recombination. {ECO:0000269|PubMed:1448097, ECO:0000269|PubMed:20976240}. |
Q02790 | FKBP4 | S229 | ochoa | Peptidyl-prolyl cis-trans isomerase FKBP4 (PPIase FKBP4) (EC 5.2.1.8) (51 kDa FK506-binding protein) (FKBP51) (52 kDa FK506-binding protein) (52 kDa FKBP) (FKBP-52) (59 kDa immunophilin) (p59) (FK506-binding protein 4) (FKBP-4) (FKBP59) (HSP-binding immunophilin) (HBI) (Immunophilin FKBP52) (Rotamase) [Cleaved into: Peptidyl-prolyl cis-trans isomerase FKBP4, N-terminally processed] | Immunophilin protein with PPIase and co-chaperone activities. Component of steroid receptors heterocomplexes through interaction with heat-shock protein 90 (HSP90). May play a role in the intracellular trafficking of heterooligomeric forms of steroid hormone receptors between cytoplasm and nuclear compartments. The isomerase activity controls neuronal growth cones via regulation of TRPC1 channel opening. Also acts as a regulator of microtubule dynamics by inhibiting MAPT/TAU ability to promote microtubule assembly. May have a protective role against oxidative stress in mitochondria. {ECO:0000269|PubMed:1279700, ECO:0000269|PubMed:1376003, ECO:0000269|PubMed:19945390, ECO:0000269|PubMed:21730050, ECO:0000269|PubMed:2378870}. |
Q02952 | AKAP12 | S787 | ochoa | A-kinase anchor protein 12 (AKAP-12) (A-kinase anchor protein 250 kDa) (AKAP 250) (Gravin) (Myasthenia gravis autoantigen) | Anchoring protein that mediates the subcellular compartmentation of protein kinase A (PKA) and protein kinase C (PKC). |
Q03001 | DST | S2502 | ochoa | Dystonin (230 kDa bullous pemphigoid antigen) (230/240 kDa bullous pemphigoid antigen) (Bullous pemphigoid antigen 1) (BPA) (Bullous pemphigoid antigen) (Dystonia musculorum protein) (Hemidesmosomal plaque protein) | Cytoskeletal linker protein. Acts as an integrator of intermediate filaments, actin and microtubule cytoskeleton networks. Required for anchoring either intermediate filaments to the actin cytoskeleton in neural and muscle cells or keratin-containing intermediate filaments to hemidesmosomes in epithelial cells. The proteins may self-aggregate to form filaments or a two-dimensional mesh. Regulates the organization and stability of the microtubule network of sensory neurons to allow axonal transport. Mediates docking of the dynein/dynactin motor complex to vesicle cargos for retrograde axonal transport through its interaction with TMEM108 and DCTN1 (By similarity). {ECO:0000250|UniProtKB:Q91ZU6}.; FUNCTION: [Isoform 3]: Plays a structural role in the assembly of hemidesmosomes of epithelial cells; anchors keratin-containing intermediate filaments to the inner plaque of hemidesmosomes. Required for the regulation of keratinocyte polarity and motility; mediates integrin ITGB4 regulation of RAC1 activity.; FUNCTION: [Isoform 6]: Required for bundling actin filaments around the nucleus. {ECO:0000250, ECO:0000269|PubMed:10428034, ECO:0000269|PubMed:12482924, ECO:0000269|PubMed:19403692}.; FUNCTION: [Isoform 7]: Regulates the organization and stability of the microtubule network of sensory neurons to allow axonal transport. |
Q03164 | KMT2A | S897 | ochoa | Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.364) (ALL-1) (CXXC-type zinc finger protein 7) (Cysteine methyltransferase KMT2A) (EC 2.1.1.-) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)] | Histone methyltransferase that plays an essential role in early development and hematopoiesis (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:26886794). Catalytic subunit of the MLL1/MLL complex, a multiprotein complex that mediates both methylation of 'Lys-4' of histone H3 (H3K4me) complex and acetylation of 'Lys-16' of histone H4 (H4K16ac) (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:24235145, PubMed:26886794). Catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) via a non-processive mechanism. Part of chromatin remodeling machinery predominantly forms H3K4me1 and H3K4me2 methylation marks at active chromatin sites where transcription and DNA repair take place (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:25561738, PubMed:26886794). Has weak methyltransferase activity by itself, and requires other component of the MLL1/MLL complex to obtain full methyltransferase activity (PubMed:19187761, PubMed:26886794). Has no activity toward histone H3 phosphorylated on 'Thr-3', less activity toward H3 dimethylated on 'Arg-8' or 'Lys-9', while it has higher activity toward H3 acetylated on 'Lys-9' (PubMed:19187761). Binds to unmethylated CpG elements in the promoter of target genes and helps maintain them in the nonmethylated state (PubMed:20010842). Required for transcriptional activation of HOXA9 (PubMed:12453419, PubMed:20010842, PubMed:20677832). Promotes PPP1R15A-induced apoptosis (PubMed:10490642). Plays a critical role in the control of circadian gene expression and is essential for the transcriptional activation mediated by the CLOCK-BMAL1 heterodimer (By similarity). Establishes a permissive chromatin state for circadian transcription by mediating a rhythmic methylation of 'Lys-4' of histone H3 (H3K4me) and this histone modification directs the circadian acetylation at H3K9 and H3K14 allowing the recruitment of CLOCK-BMAL1 to chromatin (By similarity). Also has auto-methylation activity on Cys-3882 in absence of histone H3 substrate (PubMed:24235145). {ECO:0000250|UniProtKB:P55200, ECO:0000269|PubMed:10490642, ECO:0000269|PubMed:12453419, ECO:0000269|PubMed:15960975, ECO:0000269|PubMed:19187761, ECO:0000269|PubMed:19556245, ECO:0000269|PubMed:20010842, ECO:0000269|PubMed:21220120, ECO:0000269|PubMed:24235145, ECO:0000269|PubMed:26886794, ECO:0000305|PubMed:20677832}. |
Q03164 | KMT2A | S2420 | ochoa | Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.364) (ALL-1) (CXXC-type zinc finger protein 7) (Cysteine methyltransferase KMT2A) (EC 2.1.1.-) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)] | Histone methyltransferase that plays an essential role in early development and hematopoiesis (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:26886794). Catalytic subunit of the MLL1/MLL complex, a multiprotein complex that mediates both methylation of 'Lys-4' of histone H3 (H3K4me) complex and acetylation of 'Lys-16' of histone H4 (H4K16ac) (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:24235145, PubMed:26886794). Catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) via a non-processive mechanism. Part of chromatin remodeling machinery predominantly forms H3K4me1 and H3K4me2 methylation marks at active chromatin sites where transcription and DNA repair take place (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:25561738, PubMed:26886794). Has weak methyltransferase activity by itself, and requires other component of the MLL1/MLL complex to obtain full methyltransferase activity (PubMed:19187761, PubMed:26886794). Has no activity toward histone H3 phosphorylated on 'Thr-3', less activity toward H3 dimethylated on 'Arg-8' or 'Lys-9', while it has higher activity toward H3 acetylated on 'Lys-9' (PubMed:19187761). Binds to unmethylated CpG elements in the promoter of target genes and helps maintain them in the nonmethylated state (PubMed:20010842). Required for transcriptional activation of HOXA9 (PubMed:12453419, PubMed:20010842, PubMed:20677832). Promotes PPP1R15A-induced apoptosis (PubMed:10490642). Plays a critical role in the control of circadian gene expression and is essential for the transcriptional activation mediated by the CLOCK-BMAL1 heterodimer (By similarity). Establishes a permissive chromatin state for circadian transcription by mediating a rhythmic methylation of 'Lys-4' of histone H3 (H3K4me) and this histone modification directs the circadian acetylation at H3K9 and H3K14 allowing the recruitment of CLOCK-BMAL1 to chromatin (By similarity). Also has auto-methylation activity on Cys-3882 in absence of histone H3 substrate (PubMed:24235145). {ECO:0000250|UniProtKB:P55200, ECO:0000269|PubMed:10490642, ECO:0000269|PubMed:12453419, ECO:0000269|PubMed:15960975, ECO:0000269|PubMed:19187761, ECO:0000269|PubMed:19556245, ECO:0000269|PubMed:20010842, ECO:0000269|PubMed:21220120, ECO:0000269|PubMed:24235145, ECO:0000269|PubMed:26886794, ECO:0000305|PubMed:20677832}. |
Q05397 | PTK2 | S850 | ochoa | Focal adhesion kinase 1 (FADK 1) (EC 2.7.10.2) (Focal adhesion kinase-related nonkinase) (FRNK) (Protein phosphatase 1 regulatory subunit 71) (PPP1R71) (Protein-tyrosine kinase 2) (p125FAK) (pp125FAK) | Non-receptor protein-tyrosine kinase that plays an essential role in regulating cell migration, adhesion, spreading, reorganization of the actin cytoskeleton, formation and disassembly of focal adhesions and cell protrusions, cell cycle progression, cell proliferation and apoptosis. Required for early embryonic development and placenta development. Required for embryonic angiogenesis, normal cardiomyocyte migration and proliferation, and normal heart development. Regulates axon growth and neuronal cell migration, axon branching and synapse formation; required for normal development of the nervous system. Plays a role in osteogenesis and differentiation of osteoblasts. Functions in integrin signal transduction, but also in signaling downstream of numerous growth factor receptors, G-protein coupled receptors (GPCR), EPHA2, netrin receptors and LDL receptors. Forms multisubunit signaling complexes with SRC and SRC family members upon activation; this leads to the phosphorylation of additional tyrosine residues, creating binding sites for scaffold proteins, effectors and substrates. Regulates numerous signaling pathways. Promotes activation of phosphatidylinositol 3-kinase and the AKT1 signaling cascade. Promotes activation of MAPK1/ERK2, MAPK3/ERK1 and the MAP kinase signaling cascade. Promotes localized and transient activation of guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs), and thereby modulates the activity of Rho family GTPases. Signaling via CAS family members mediates activation of RAC1. Phosphorylates NEDD9 following integrin stimulation (PubMed:9360983). Recruits the ubiquitin ligase MDM2 to P53/TP53 in the nucleus, and thereby regulates P53/TP53 activity, P53/TP53 ubiquitination and proteasomal degradation. Phosphorylates SRC; this increases SRC kinase activity. Phosphorylates ACTN1, ARHGEF7, GRB7, RET and WASL. Promotes phosphorylation of PXN and STAT1; most likely PXN and STAT1 are phosphorylated by a SRC family kinase that is recruited to autophosphorylated PTK2/FAK1, rather than by PTK2/FAK1 itself. Promotes phosphorylation of BCAR1; GIT2 and SHC1; this requires both SRC and PTK2/FAK1. Promotes phosphorylation of BMX and PIK3R1. Isoform 6 (FRNK) does not contain a kinase domain and inhibits PTK2/FAK1 phosphorylation and signaling. Its enhanced expression can attenuate the nuclear accumulation of LPXN and limit its ability to enhance serum response factor (SRF)-dependent gene transcription. {ECO:0000269|PubMed:10655584, ECO:0000269|PubMed:11331870, ECO:0000269|PubMed:11980671, ECO:0000269|PubMed:15166238, ECO:0000269|PubMed:15561106, ECO:0000269|PubMed:15895076, ECO:0000269|PubMed:16919435, ECO:0000269|PubMed:16927379, ECO:0000269|PubMed:17395594, ECO:0000269|PubMed:17431114, ECO:0000269|PubMed:17968709, ECO:0000269|PubMed:18006843, ECO:0000269|PubMed:18206965, ECO:0000269|PubMed:18256281, ECO:0000269|PubMed:18292575, ECO:0000269|PubMed:18497331, ECO:0000269|PubMed:18677107, ECO:0000269|PubMed:19138410, ECO:0000269|PubMed:19147981, ECO:0000269|PubMed:19224453, ECO:0000269|PubMed:20332118, ECO:0000269|PubMed:20495381, ECO:0000269|PubMed:21454698, ECO:0000269|PubMed:9360983}.; FUNCTION: [Isoform 6]: Isoform 6 (FRNK) does not contain a kinase domain and inhibits PTK2/FAK1 phosphorylation and signaling. Its enhanced expression can attenuate the nuclear accumulation of LPXN and limit its ability to enhance serum response factor (SRF)-dependent gene transcription. {ECO:0000269|PubMed:20109444}. |
Q06187 | BTK | S55 | ochoa | Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) | Non-receptor tyrosine kinase indispensable for B lymphocyte development, differentiation and signaling (PubMed:19290921). Binding of antigen to the B-cell antigen receptor (BCR) triggers signaling that ultimately leads to B-cell activation (PubMed:19290921). After BCR engagement and activation at the plasma membrane, phosphorylates PLCG2 at several sites, igniting the downstream signaling pathway through calcium mobilization, followed by activation of the protein kinase C (PKC) family members (PubMed:11606584). PLCG2 phosphorylation is performed in close cooperation with the adapter protein B-cell linker protein BLNK (PubMed:11606584). BTK acts as a platform to bring together a diverse array of signaling proteins and is implicated in cytokine receptor signaling pathways (PubMed:16517732, PubMed:17932028). Plays an important role in the function of immune cells of innate as well as adaptive immunity, as a component of the Toll-like receptors (TLR) pathway (PubMed:16517732). The TLR pathway acts as a primary surveillance system for the detection of pathogens and are crucial to the activation of host defense (PubMed:16517732). Especially, is a critical molecule in regulating TLR9 activation in splenic B-cells (PubMed:16517732, PubMed:17932028). Within the TLR pathway, induces tyrosine phosphorylation of TIRAP which leads to TIRAP degradation (PubMed:16415872). BTK also plays a critical role in transcription regulation (PubMed:19290921). Induces the activity of NF-kappa-B, which is involved in regulating the expression of hundreds of genes (PubMed:19290921). BTK is involved on the signaling pathway linking TLR8 and TLR9 to NF-kappa-B (PubMed:19290921). Acts as an activator of NLRP3 inflammasome assembly by mediating phosphorylation of NLRP3 (PubMed:34554188). Transiently phosphorylates transcription factor GTF2I on tyrosine residues in response to BCR (PubMed:9012831). GTF2I then translocates to the nucleus to bind regulatory enhancer elements to modulate gene expression (PubMed:9012831). ARID3A and NFAT are other transcriptional target of BTK (PubMed:16738337). BTK is required for the formation of functional ARID3A DNA-binding complexes (PubMed:16738337). There is however no evidence that BTK itself binds directly to DNA (PubMed:16738337). BTK has a dual role in the regulation of apoptosis (PubMed:9751072). Plays a role in STING1-mediated induction of type I interferon (IFN) response by phosphorylating DDX41 (PubMed:25704810). {ECO:0000269|PubMed:11606584, ECO:0000269|PubMed:16415872, ECO:0000269|PubMed:16517732, ECO:0000269|PubMed:16738337, ECO:0000269|PubMed:17932028, ECO:0000269|PubMed:25704810, ECO:0000269|PubMed:34554188, ECO:0000269|PubMed:9012831, ECO:0000303|PubMed:19290921, ECO:0000303|PubMed:9751072}. |
Q06210 | GFPT1 | S235 | psp | Glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 (EC 2.6.1.16) (D-fructose-6-phosphate amidotransferase 1) (Glutamine:fructose-6-phosphate amidotransferase 1) (GFAT 1) (GFAT1) (Hexosephosphate aminotransferase 1) | Controls the flux of glucose into the hexosamine pathway. Most likely involved in regulating the availability of precursors for N- and O-linked glycosylation of proteins. Regulates the circadian expression of clock genes BMAL1 and CRY1 (By similarity). Has a role in fine tuning the metabolic fluctuations of cytosolic UDP-GlcNAc and its effects on hyaluronan synthesis that occur during tissue remodeling (PubMed:26887390). {ECO:0000250|UniProtKB:P47856, ECO:0000269|PubMed:26887390}. |
Q09666 | AHNAK | S407 | ochoa | Neuroblast differentiation-associated protein AHNAK (Desmoyokin) | May be required for neuronal cell differentiation. |
Q12774 | ARHGEF5 | S199 | ochoa | Rho guanine nucleotide exchange factor 5 (Ephexin-3) (Guanine nucleotide regulatory protein TIM) (Oncogene TIM) (Transforming immortalized mammary oncogene) (p60 TIM) | Guanine nucleotide exchange factor which activates Rho GTPases (PubMed:15601624). Strongly activates RHOA (PubMed:15601624). Also strongly activates RHOB, weakly activates RHOC and RHOG and shows no effect on RHOD, RHOV, RHOQ or RAC1 (By similarity). Involved in regulation of cell shape and actin cytoskeletal organization (PubMed:15601624). Plays a role in actin organization by generating a loss of actin stress fibers and the formation of membrane ruffles and filopodia (PubMed:14662653). Required for SRC-induced podosome formation (By similarity). Involved in positive regulation of immature dendritic cell migration (By similarity). {ECO:0000250|UniProtKB:E9Q7D5, ECO:0000269|PubMed:14662653, ECO:0000269|PubMed:15601624}. |
Q12923 | PTPN13 | S348 | ochoa | Tyrosine-protein phosphatase non-receptor type 13 (EC 3.1.3.48) (Fas-associated protein-tyrosine phosphatase 1) (FAP-1) (PTP-BAS) (Protein-tyrosine phosphatase 1E) (PTP-E1) (hPTPE1) (Protein-tyrosine phosphatase PTPL1) | Tyrosine phosphatase which negatively regulates FAS-induced apoptosis and NGFR-mediated pro-apoptotic signaling (PubMed:15611135). May regulate phosphoinositide 3-kinase (PI3K) signaling through dephosphorylation of PIK3R2 (PubMed:23604317). {ECO:0000269|PubMed:15611135, ECO:0000269|PubMed:23604317}. |
Q13033 | STRN3 | S214 | ochoa | Striatin-3 (Cell cycle autoantigen SG2NA) (S/G2 antigen) | Calmodulin-binding scaffolding protein which is the center of the striatin-interacting phosphatase and kinase (STRIPAK) complexes (PubMed:18782753, PubMed:30622739, PubMed:33633399). STRIPAK complexes have critical roles in protein (de)phosphorylation and are regulators of multiple signaling pathways including Hippo, MAPK, nuclear receptor and cytoskeleton remodeling. Different types of STRIPAK complexes are involved in a variety of biological processes such as cell growth, differentiation, apoptosis, metabolism and immune regulation (Probable). {ECO:0000269|PubMed:18782753, ECO:0000269|PubMed:30622739, ECO:0000269|PubMed:33633399, ECO:0000305|PubMed:26876214}. |
Q13123 | IK | S417 | ochoa | Protein Red (Cytokine IK) (IK factor) (Protein RER) | Involved in pre-mRNA splicing as a component of the spliceosome (PubMed:28781166). Auxiliary spliceosomal protein that regulates selection of alternative splice sites in a small set of target pre-mRNA species (Probable). Required for normal mitotic cell cycle progression (PubMed:22351768, PubMed:24252166). Recruits MAD1L1 and MAD2L1 to kinetochores, and is required to trigger the spindle assembly checkpoint (PubMed:22351768). Required for normal accumulation of SMU1 (PubMed:24945353). {ECO:0000269|PubMed:22351768, ECO:0000269|PubMed:24252166, ECO:0000269|PubMed:24945353, ECO:0000269|PubMed:28781166, ECO:0000305}.; FUNCTION: (Microbial infection) Required, together with SMU1, for normal splicing of influenza A virus NS1 pre-mRNA, which is required for the production of the exportin NS2 and for the production of influenza A virus particles. Not required for the production of VSV virus particles. {ECO:0000269|PubMed:24945353}. |
Q13201 | MMRN1 | S884 | ochoa | Multimerin-1 (EMILIN-4) (Elastin microfibril interface located protein 4) (Elastin microfibril interfacer 4) (Endothelial cell multimerin) [Cleaved into: Platelet glycoprotein Ia*; 155 kDa platelet multimerin (p-155) (p155)] | Carrier protein for platelet (but not plasma) factor V/Va. Plays a role in the storage and stabilization of factor V in platelets. Upon release following platelet activation, may limit platelet and plasma factor Va-dependent thrombin generation. Ligand for integrin alpha-IIb/beta-3 and integrin alpha-V/beta-3 on activated platelets, and may function as an extracellular matrix or adhesive protein. {ECO:0000269|PubMed:16363244, ECO:0000269|PubMed:19132231, ECO:0000269|PubMed:7629143}. |
Q13573 | SNW1 | S481 | ochoa | SNW domain-containing protein 1 (Nuclear protein SkiP) (Nuclear receptor coactivator NCoA-62) (Ski-interacting protein) | Involved in pre-mRNA splicing as component of the spliceosome (PubMed:11991638, PubMed:28076346, PubMed:28502770). As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). Required for the specific splicing of CDKN1A pre-mRNA; the function probably involves the recruitment of U2AF2 to the mRNA. May recruit PPIL1 to the spliceosome. May be involved in cyclin-D1/CCND1 mRNA stability through the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA. Involved in transcriptional regulation. Modulates TGF-beta-mediated transcription via association with SMAD proteins, MYOD1-mediated transcription via association with PABPN1, RB1-mediated transcriptional repression, and retinoid-X receptor (RXR)- and vitamin D receptor (VDR)-dependent gene transcription in a cell line-specific manner probably involving coactivators NCOA1 and GRIP1. Is involved in NOTCH1-mediated transcriptional activation. Binds to multimerized forms of Notch intracellular domain (NICD) and is proposed to recruit transcriptional coactivators such as MAML1 to form an intermediate preactivation complex which associates with DNA-bound CBF-1/RBPJ to form a transcriptional activation complex by releasing SNW1 and redundant NOTCH1 NICD. {ECO:0000269|PubMed:10644367, ECO:0000269|PubMed:11278756, ECO:0000269|PubMed:11371506, ECO:0000269|PubMed:11514567, ECO:0000269|PubMed:11991638, ECO:0000269|PubMed:12840015, ECO:0000269|PubMed:14985122, ECO:0000269|PubMed:15194481, ECO:0000269|PubMed:15905409, ECO:0000269|PubMed:18794151, ECO:0000269|PubMed:19818711, ECO:0000269|PubMed:21245387, ECO:0000269|PubMed:21460037, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:9632709, ECO:0000305|PubMed:33509932}.; FUNCTION: (Microbial infection) Is recruited by HIV-1 Tat to Tat:P-TEFb:TAR RNA complexes and is involved in Tat transcription by recruitment of MYC, MEN1 and TRRAP to the HIV promoter. {ECO:0000269|PubMed:15905409, ECO:0000269|PubMed:19818711}.; FUNCTION: (Microbial infection) Proposed to be involved in transcriptional activation by EBV EBNA2 of CBF-1/RBPJ-repressed promoters. {ECO:0000269|PubMed:10644367}. |
Q13621 | SLC12A1 | S120 | psp | Solute carrier family 12 member 1 (Bumetanide-sensitive sodium-(potassium)-chloride cotransporter 1) (BSC1) (Kidney-specific Na-K-Cl symporter) (Na-K-2Cl cotransporter 2) (NKCC2) | Renal sodium, potassium and chloride ion cotransporter that mediates the transepithelial NaCl reabsorption in the thick ascending limb and plays an essential role in the urinary concentration and volume regulation (PubMed:21321328). Electrically silent transporter system (By similarity). {ECO:0000250|UniProtKB:P55014, ECO:0000250|UniProtKB:P55016, ECO:0000269|PubMed:21321328}. |
Q14244 | MAP7 | S282 | ochoa | Ensconsin (Epithelial microtubule-associated protein of 115 kDa) (E-MAP-115) (Microtubule-associated protein 7) (MAP-7) | Microtubule-stabilizing protein that may play an important role during reorganization of microtubules during polarization and differentiation of epithelial cells. Associates with microtubules in a dynamic manner. May play a role in the formation of intercellular contacts. Colocalization with TRPV4 results in the redistribution of TRPV4 toward the membrane and may link cytoskeletal microfilaments. {ECO:0000269|PubMed:11719555, ECO:0000269|PubMed:8408219, ECO:0000269|PubMed:9989799}. |
Q14566 | MCM6 | S219 | ochoa | DNA replication licensing factor MCM6 (EC 3.6.4.12) (p105MCM) | Acts as a component of the MCM2-7 complex (MCM complex) which is the replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. Core component of CDC45-MCM-GINS (CMG) helicase, the molecular machine that unwinds template DNA during replication, and around which the replisome is built (PubMed:16899510, PubMed:32453425, PubMed:34694004, PubMed:34700328, PubMed:35585232, PubMed:9305914). The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity (PubMed:32453425). {ECO:0000269|PubMed:16899510, ECO:0000269|PubMed:32453425, ECO:0000269|PubMed:34694004, ECO:0000269|PubMed:34700328, ECO:0000269|PubMed:35585232, ECO:0000269|PubMed:9305914}. |
Q14568 | HSP90AA2P | S169 | ochoa | Heat shock protein HSP 90-alpha A2 (Heat shock 90 kDa protein 1 alpha-like 3) (Heat shock protein HSP 90-alpha A2 pseudogene) (Heat shock protein family C member 2) | Putative molecular chaperone that may promote the maturation, structural maintenance and proper regulation of specific target proteins. {ECO:0000250}. |
Q14684 | RRP1B | S624 | ochoa | Ribosomal RNA processing protein 1 homolog B (RRP1-like protein B) | Positively regulates DNA damage-induced apoptosis by acting as a transcriptional coactivator of proapoptotic target genes of the transcriptional activator E2F1 (PubMed:20040599). Likely to play a role in ribosome biogenesis by targeting serine/threonine protein phosphatase PP1 to the nucleolus (PubMed:20926688). Involved in regulation of mRNA splicing (By similarity). Inhibits SIPA1 GTPase activity (By similarity). Involved in regulating expression of extracellular matrix genes (By similarity). Associates with chromatin and may play a role in modulating chromatin structure (PubMed:19710015). {ECO:0000250|UniProtKB:Q91YK2, ECO:0000269|PubMed:19710015, ECO:0000269|PubMed:20040599, ECO:0000269|PubMed:20926688}.; FUNCTION: (Microbial infection) Following influenza A virus (IAV) infection, promotes viral mRNA transcription by facilitating the binding of IAV RNA-directed RNA polymerase to capped mRNA. {ECO:0000269|PubMed:26311876}. |
Q14980 | NUMA1 | S1105 | ochoa | Nuclear mitotic apparatus protein 1 (Nuclear matrix protein-22) (NMP-22) (Nuclear mitotic apparatus protein) (NuMA protein) (SP-H antigen) | Microtubule (MT)-binding protein that plays a role in the formation and maintenance of the spindle poles and the alignement and the segregation of chromosomes during mitotic cell division (PubMed:17172455, PubMed:19255246, PubMed:24996901, PubMed:26195665, PubMed:27462074, PubMed:7769006). Functions to tether the minus ends of MTs at the spindle poles, which is critical for the establishment and maintenance of the spindle poles (PubMed:11956313, PubMed:12445386). Plays a role in the establishment of the mitotic spindle orientation during metaphase and elongation during anaphase in a dynein-dynactin-dependent manner (PubMed:23870127, PubMed:24109598, PubMed:24996901, PubMed:26765568). In metaphase, part of a ternary complex composed of GPSM2 and G(i) alpha proteins, that regulates the recruitment and anchorage of the dynein-dynactin complex in the mitotic cell cortex regions situated above the two spindle poles, and hence regulates the correct oritentation of the mitotic spindle (PubMed:22327364, PubMed:23027904, PubMed:23921553). During anaphase, mediates the recruitment and accumulation of the dynein-dynactin complex at the cell membrane of the polar cortical region through direct association with phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), and hence participates in the regulation of the spindle elongation and chromosome segregation (PubMed:22327364, PubMed:23921553, PubMed:24371089, PubMed:24996901). Also binds to other polyanionic phosphoinositides, such as phosphatidylinositol 3-phosphate (PIP), lysophosphatidic acid (LPA) and phosphatidylinositol triphosphate (PIP3), in vitro (PubMed:24371089, PubMed:24996901). Also required for proper orientation of the mitotic spindle during asymmetric cell divisions (PubMed:21816348). Plays a role in mitotic MT aster assembly (PubMed:11163243, PubMed:11229403, PubMed:12445386). Involved in anastral spindle assembly (PubMed:25657325). Positively regulates TNKS protein localization to spindle poles in mitosis (PubMed:16076287). Highly abundant component of the nuclear matrix where it may serve a non-mitotic structural role, occupies the majority of the nuclear volume (PubMed:10075938). Required for epidermal differentiation and hair follicle morphogenesis (By similarity). {ECO:0000250|UniProtKB:E9Q7G0, ECO:0000269|PubMed:11163243, ECO:0000269|PubMed:11229403, ECO:0000269|PubMed:11956313, ECO:0000269|PubMed:12445386, ECO:0000269|PubMed:16076287, ECO:0000269|PubMed:17172455, ECO:0000269|PubMed:19255246, ECO:0000269|PubMed:22327364, ECO:0000269|PubMed:23027904, ECO:0000269|PubMed:23870127, ECO:0000269|PubMed:23921553, ECO:0000269|PubMed:24109598, ECO:0000269|PubMed:24371089, ECO:0000269|PubMed:24996901, ECO:0000269|PubMed:25657325, ECO:0000269|PubMed:26195665, ECO:0000269|PubMed:26765568, ECO:0000269|PubMed:27462074, ECO:0000269|PubMed:7769006, ECO:0000305|PubMed:10075938, ECO:0000305|PubMed:21816348}. |
Q14D04 | VEPH1 | S420 | ochoa | Ventricular zone-expressed PH domain-containing protein homolog 1 (Protein melted) | Interacts with TGF-beta receptor type-1 (TGFBR1) and inhibits dissociation of activated SMAD2 from TGFBR1, impeding its nuclear accumulation and resulting in impaired TGF-beta signaling. May also affect FOXO, Hippo and Wnt signaling. {ECO:0000269|PubMed:26039994}. |
Q15052 | ARHGEF6 | S678 | ochoa | Rho guanine nucleotide exchange factor 6 (Alpha-Pix) (COOL-2) (PAK-interacting exchange factor alpha) (Rac/Cdc42 guanine nucleotide exchange factor 6) | Acts as a RAC1 guanine nucleotide exchange factor (GEF). |
Q15286 | RAB35 | S36 | ochoa | Ras-related protein Rab-35 (EC 3.6.5.2) (GTP-binding protein RAY) (Ras-related protein Rab-1C) | The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different sets of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion (PubMed:30905672). RAB35 is involved in the process of endocytosis and is an essential rate-limiting regulator of the fast recycling pathway back to the plasma membrane (PubMed:21951725). During cytokinesis, required for the postfurrowing terminal steps, namely for intercellular bridge stability and abscission, possibly by controlling phosphatidylinositol 4,5-bis phosphate (PIP2) and SEPT2 localization at the intercellular bridge (PubMed:16950109). May indirectly regulate neurite outgrowth. Together with TBC1D13 may be involved in regulation of insulin-induced glucose transporter SLC2A4/GLUT4 translocation to the plasma membrane in adipocytes (By similarity). {ECO:0000250|UniProtKB:Q6PHN9, ECO:0000269|PubMed:16950109, ECO:0000269|PubMed:21951725, ECO:0000269|PubMed:30905672}. |
Q15303 | ERBB4 | S726 | ochoa | Receptor tyrosine-protein kinase erbB-4 (EC 2.7.10.1) (Proto-oncogene-like protein c-ErbB-4) (Tyrosine kinase-type cell surface receptor HER4) (p180erbB4) [Cleaved into: ERBB4 intracellular domain (4ICD) (E4ICD) (s80HER4)] | Tyrosine-protein kinase that plays an essential role as cell surface receptor for neuregulins and EGF family members and regulates development of the heart, the central nervous system and the mammary gland, gene transcription, cell proliferation, differentiation, migration and apoptosis. Required for normal cardiac muscle differentiation during embryonic development, and for postnatal cardiomyocyte proliferation. Required for normal development of the embryonic central nervous system, especially for normal neural crest cell migration and normal axon guidance. Required for mammary gland differentiation, induction of milk proteins and lactation. Acts as cell-surface receptor for the neuregulins NRG1, NRG2, NRG3 and NRG4 and the EGF family members BTC, EREG and HBEGF. Ligand binding triggers receptor dimerization and autophosphorylation at specific tyrosine residues that then serve as binding sites for scaffold proteins and effectors. Ligand specificity and signaling is modulated by alternative splicing, proteolytic processing, and by the formation of heterodimers with other ERBB family members, thereby creating multiple combinations of intracellular phosphotyrosines that trigger ligand- and context-specific cellular responses. Mediates phosphorylation of SHC1 and activation of the MAP kinases MAPK1/ERK2 and MAPK3/ERK1. Isoform JM-A CYT-1 and isoform JM-B CYT-1 phosphorylate PIK3R1, leading to the activation of phosphatidylinositol 3-kinase and AKT1 and protect cells against apoptosis. Isoform JM-A CYT-1 and isoform JM-B CYT-1 mediate reorganization of the actin cytoskeleton and promote cell migration in response to NRG1. Isoform JM-A CYT-2 and isoform JM-B CYT-2 lack the phosphotyrosine that mediates interaction with PIK3R1, and hence do not phosphorylate PIK3R1, do not protect cells against apoptosis, and do not promote reorganization of the actin cytoskeleton and cell migration. Proteolytic processing of isoform JM-A CYT-1 and isoform JM-A CYT-2 gives rise to the corresponding soluble intracellular domains (4ICD) that translocate to the nucleus, promote nuclear import of STAT5A, activation of STAT5A, mammary epithelium differentiation, cell proliferation and activation of gene expression. The ERBB4 soluble intracellular domains (4ICD) colocalize with STAT5A at the CSN2 promoter to regulate transcription of milk proteins during lactation. The ERBB4 soluble intracellular domains can also translocate to mitochondria and promote apoptosis. {ECO:0000269|PubMed:10348342, ECO:0000269|PubMed:10353604, ECO:0000269|PubMed:10358079, ECO:0000269|PubMed:10722704, ECO:0000269|PubMed:10867024, ECO:0000269|PubMed:11178955, ECO:0000269|PubMed:11390655, ECO:0000269|PubMed:12807903, ECO:0000269|PubMed:15534001, ECO:0000269|PubMed:15746097, ECO:0000269|PubMed:16251361, ECO:0000269|PubMed:16778220, ECO:0000269|PubMed:16837552, ECO:0000269|PubMed:17486069, ECO:0000269|PubMed:17638867, ECO:0000269|PubMed:19098003, ECO:0000269|PubMed:20858735, ECO:0000269|PubMed:8383326, ECO:0000269|PubMed:8617750, ECO:0000269|PubMed:9135143, ECO:0000269|PubMed:9168115, ECO:0000269|PubMed:9334263}. |
Q15365 | PCBP1 | S111 | ochoa | Poly(rC)-binding protein 1 (Alpha-CP1) (Heterogeneous nuclear ribonucleoprotein E1) (hnRNP E1) (Nucleic acid-binding protein SUB2.3) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC (PubMed:15731341, PubMed:7556077, PubMed:7607214, PubMed:8152927). Together with PCBP2, required for erythropoiesis, possibly by regulating mRNA splicing (By similarity). {ECO:0000250|UniProtKB:P60335, ECO:0000269|PubMed:15731341, ECO:0000269|PubMed:7556077, ECO:0000269|PubMed:7607214, ECO:0000269|PubMed:8152927}.; FUNCTION: (Microbial infection) In case of infection by poliovirus, plays a role in initiation of viral RNA replication in concert with the viral protein 3CD. {ECO:0000269|PubMed:12414943}. |
Q15365 | PCBP1 | S322 | ochoa | Poly(rC)-binding protein 1 (Alpha-CP1) (Heterogeneous nuclear ribonucleoprotein E1) (hnRNP E1) (Nucleic acid-binding protein SUB2.3) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC (PubMed:15731341, PubMed:7556077, PubMed:7607214, PubMed:8152927). Together with PCBP2, required for erythropoiesis, possibly by regulating mRNA splicing (By similarity). {ECO:0000250|UniProtKB:P60335, ECO:0000269|PubMed:15731341, ECO:0000269|PubMed:7556077, ECO:0000269|PubMed:7607214, ECO:0000269|PubMed:8152927}.; FUNCTION: (Microbial infection) In case of infection by poliovirus, plays a role in initiation of viral RNA replication in concert with the viral protein 3CD. {ECO:0000269|PubMed:12414943}. |
Q15366 | PCBP2 | S111 | ochoa | Poly(rC)-binding protein 2 (Alpha-CP2) (Heterogeneous nuclear ribonucleoprotein E2) (hnRNP E2) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC (PubMed:12414943, PubMed:7607214). Major cellular poly(rC)-binding protein (PubMed:12414943). Also binds poly(rU) (PubMed:12414943). Acts as a negative regulator of antiviral signaling (PubMed:19881509, PubMed:35322803). Negatively regulates cellular antiviral responses mediated by MAVS signaling (PubMed:19881509). It acts as an adapter between MAVS and the E3 ubiquitin ligase ITCH, therefore triggering MAVS ubiquitination and degradation (PubMed:19881509). Negativeley regulates the cGAS-STING pathway via interaction with CGAS, preventing the formation of liquid-like droplets in which CGAS is activated (PubMed:35322803). Together with PCBP1, required for erythropoiesis, possibly by regulating mRNA splicing (By similarity). {ECO:0000250|UniProtKB:Q61990, ECO:0000269|PubMed:12414943, ECO:0000269|PubMed:19881509, ECO:0000269|PubMed:35322803, ECO:0000269|PubMed:7607214}.; FUNCTION: (Microbial infection) In case of infection by poliovirus, binds to the viral internal ribosome entry site (IRES) and stimulates the IRES-mediated translation (PubMed:12414943, PubMed:24371074). Also plays a role in initiation of viral RNA replication in concert with the viral protein 3CD (PubMed:12414943). {ECO:0000269|PubMed:12414943, ECO:0000269|PubMed:24371074}. |
Q15648 | MED1 | S207 | ochoa | Mediator of RNA polymerase II transcription subunit 1 (Activator-recruited cofactor 205 kDa component) (ARC205) (Mediator complex subunit 1) (Peroxisome proliferator-activated receptor-binding protein) (PBP) (PPAR-binding protein) (Thyroid hormone receptor-associated protein complex 220 kDa component) (Trap220) (Thyroid receptor-interacting protein 2) (TR-interacting protein 2) (TRIP-2) (Vitamin D receptor-interacting protein complex component DRIP205) (p53 regulatory protein RB18A) | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors (PubMed:10406464, PubMed:11867769, PubMed:12037571, PubMed:12218053, PubMed:12556447, PubMed:14636573, PubMed:15340084, PubMed:15471764, PubMed:15989967, PubMed:16574658, PubMed:9653119). Acts as a coactivator for GATA1-mediated transcriptional activation during erythroid differentiation of K562 erythroleukemia cells (PubMed:24245781). {ECO:0000269|PubMed:10406464, ECO:0000269|PubMed:11867769, ECO:0000269|PubMed:12037571, ECO:0000269|PubMed:12218053, ECO:0000269|PubMed:12556447, ECO:0000269|PubMed:14636573, ECO:0000269|PubMed:15340084, ECO:0000269|PubMed:15471764, ECO:0000269|PubMed:15989967, ECO:0000269|PubMed:16574658, ECO:0000269|PubMed:24245781, ECO:0000269|PubMed:9653119}. |
Q16143 | SNCB | S42 | ochoa | Beta-synuclein | Non-amyloid component of senile plaques found in Alzheimer disease. Could act as a regulator of SNCA aggregation process. Protects neurons from staurosporine and 6-hydroxy dopamine (6OHDA)-stimulated caspase activation in a p53/TP53-dependent manner. Contributes to restore the SNCA anti-apoptotic function abolished by 6OHDA. Not found in the Lewy bodies associated with Parkinson disease. |
Q32P51 | HNRNPA1L2 | S142 | ochoa | Heterogeneous nuclear ribonucleoprotein A1-like 2 (hnRNP A1-like 2) (hnRNP core protein A1-like 2) | Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and may modulate splice site selection. {ECO:0000250}. |
Q4KMP7 | TBC1D10B | S318 | ochoa | TBC1 domain family member 10B (Rab27A-GAP-beta) | Acts as a GTPase-activating protein for RAB3A, RAB22A, RAB27A, and RAB35. Does not act on RAB2A and RAB6A. {ECO:0000269|PubMed:16923811, ECO:0000269|PubMed:19077034}. |
Q53F19 | NCBP3 | S73 | ochoa | Nuclear cap-binding protein subunit 3 (Protein ELG) | Associates with NCBP1/CBP80 to form an alternative cap-binding complex (CBC) which plays a key role in mRNA export. NCBP3 serves as adapter protein linking the capped RNAs (m7GpppG-capped RNA) to NCBP1/CBP80. Unlike the conventional CBC with NCBP2 which binds both small nuclear RNA (snRNA) and messenger (mRNA) and is involved in their export from the nucleus, the alternative CBC with NCBP3 does not bind snRNA and associates only with mRNA thereby playing a role in only mRNA export. The alternative CBC is particularly important in cellular stress situations such as virus infections and the NCBP3 activity is critical to inhibit virus growth (PubMed:26382858). {ECO:0000269|PubMed:26382858}. |
Q53GG5 | PDLIM3 | S264 | ochoa | PDZ and LIM domain protein 3 (Actinin-associated LIM protein) (Alpha-actinin-2-associated LIM protein) | May play a role in the organization of actin filament arrays within muscle cells. {ECO:0000250}. |
Q5PRF9 | SAMD4B | S299 | ochoa | Protein Smaug homolog 2 (Smaug 2) (hSmaug2) (Sterile alpha motif domain-containing protein 4B) (SAM domain-containing protein 4B) | Has transcriptional repressor activity. Overexpression inhibits the transcriptional activities of AP-1, p53/TP53 and CDKN1A. {ECO:0000269|PubMed:20510020}. |
Q5R3F8 | ELFN2 | S451 | ochoa | Protein phosphatase 1 regulatory subunit 29 (Extracellular leucine-rich repeat and fibronectin type III domain-containing protein 2) (Leucine-rich repeat and fibronectin type-III domain-containing protein 6) (Leucine-rich repeat-containing protein 62) | Inhibits phosphatase activity of protein phosphatase 1 (PP1) complexes. {ECO:0000269|PubMed:19389623}. |
Q5T0W9 | FAM83B | S514 | ochoa | Protein FAM83B | Probable proto-oncogene that functions in the epidermal growth factor receptor/EGFR signaling pathway. Activates both the EGFR itself and downstream RAS/MAPK and PI3K/AKT/TOR signaling cascades. {ECO:0000269|PubMed:22886302, ECO:0000269|PubMed:23676467, ECO:0000269|PubMed:23912460}. |
Q5T200 | ZC3H13 | S1232 | ochoa | Zinc finger CCCH domain-containing protein 13 | Associated component of the WMM complex, a complex that mediates N6-methyladenosine (m6A) methylation of RNAs, a modification that plays a role in the efficiency of mRNA splicing and RNA processing (PubMed:29507755). Acts as a key regulator of m6A methylation by promoting m6A methylation of mRNAs at the 3'-UTR (By similarity). Controls embryonic stem cells (ESCs) pluripotency via its role in m6A methylation (By similarity). In the WMM complex, anchors component of the MACOM subcomplex in the nucleus (By similarity). Also required for bridging WTAP to the RNA-binding component RBM15 (RBM15 or RBM15B) (By similarity). {ECO:0000250|UniProtKB:E9Q784}. |
Q5VST9 | OBSCN | S2326 | ochoa | Obscurin (EC 2.7.11.1) (Obscurin-RhoGEF) (Obscurin-myosin light chain kinase) (Obscurin-MLCK) | Structural component of striated muscles which plays a role in myofibrillogenesis. Probably involved in the assembly of myosin into sarcomeric A bands in striated muscle (PubMed:11448995, PubMed:16205939). Has serine/threonine protein kinase activity and phosphorylates N-cadherin CDH2 and sodium/potassium-transporting ATPase subunit ATP1B1 (By similarity). Binds (via the PH domain) strongly to phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P2) and phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), and to a lesser extent to phosphatidylinositol 3-phosphate (PtdIns(3)P), phosphatidylinositol 4-phosphate (PtdIns(4)P), phosphatidylinositol 5-phosphate (PtdIns(5)P) and phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P3) (PubMed:28826662). {ECO:0000250|UniProtKB:A2AAJ9, ECO:0000269|PubMed:11448995, ECO:0000269|PubMed:16205939, ECO:0000269|PubMed:28826662}. |
Q5VT52 | RPRD2 | S381 | ochoa | Regulation of nuclear pre-mRNA domain-containing protein 2 | None |
Q5VZ89 | DENND4C | S538 | ochoa | DENN domain-containing protein 4C | Guanine nucleotide exchange factor (GEF) activating RAB10. Promotes the exchange of GDP to GTP, converting inactive GDP-bound RAB10 into its active GTP-bound form. Thereby, stimulates SLC2A4/GLUT4 glucose transporter-enriched vesicles delivery to the plasma membrane in response to insulin. {ECO:0000269|PubMed:20937701}. |
Q658Y4 | FAM91A1 | S686 | ochoa | Protein FAM91A1 | As component of the WDR11 complex acts together with TBC1D23 to facilitate the golgin-mediated capture of vesicles generated using AP-1. {ECO:0000269|PubMed:29426865}. |
Q6GQQ9 | OTUD7B | S508 | ochoa | OTU domain-containing protein 7B (EC 3.4.19.12) (Cellular zinc finger anti-NF-kappa-B protein) (Cezanne) (Zinc finger A20 domain-containing protein 1) (Zinc finger protein Cezanne) | Negative regulator of the non-canonical NF-kappa-B pathway that acts by mediating deubiquitination of TRAF3, an inhibitor of the NF-kappa-B pathway, thereby acting as a negative regulator of B-cell responses (PubMed:18178551). In response to non-canonical NF-kappa-B stimuli, deubiquitinates 'Lys-48'-linked polyubiquitin chains of TRAF3, preventing TRAF3 proteolysis and over-activation of non-canonical NF-kappa-B (By similarity). Negatively regulates mucosal immunity against infections (By similarity). Deubiquitinates ZAP70, and thereby regulates T cell receptor (TCR) signaling that leads to the activation of NF-kappa-B (PubMed:26903241). Plays a role in T cell homeostasis and is required for normal T cell responses, including production of IFNG and IL2 (By similarity). Mediates deubiquitination of EGFR (PubMed:22179831). Has deubiquitinating activity toward 'Lys-11', 'Lys-48' and 'Lys-63'-linked polyubiquitin chains (PubMed:11463333, PubMed:20622874, PubMed:23827681, PubMed:27732584). Has a much higher catalytic rate with 'Lys-11'-linked polyubiquitin chains (in vitro); however the physiological significance of these data are unsure (PubMed:27732584). Hydrolyzes both linear and branched forms of polyubiquitin (PubMed:12682062). Acts as a regulator of mTORC1 and mTORC2 assembly by mediating 'Lys-63'-linked deubiquitination of MLST8, thereby promoting assembly of the mTORC2 complex, while inibiting formation of the mTORC1 complex (PubMed:28489822). {ECO:0000250|UniProtKB:B2RUR8, ECO:0000269|PubMed:11463333, ECO:0000269|PubMed:12682062, ECO:0000269|PubMed:18178551, ECO:0000269|PubMed:20622874, ECO:0000269|PubMed:22179831, ECO:0000269|PubMed:23827681, ECO:0000269|PubMed:26903241, ECO:0000269|PubMed:27732584, ECO:0000269|PubMed:28489822}. |
Q6UN15 | FIP1L1 | S112 | ochoa | Pre-mRNA 3'-end-processing factor FIP1 (hFip1) (FIP1-like 1 protein) (Factor interacting with PAP) (Rearranged in hypereosinophilia) | Component of the cleavage and polyadenylation specificity factor (CPSF) complex that plays a key role in pre-mRNA 3'-end formation, recognizing the AAUAAA signal sequence and interacting with poly(A) polymerase and other factors to bring about cleavage and poly(A) addition. FIP1L1 contributes to poly(A) site recognition and stimulates poly(A) addition. Binds to U-rich RNA sequence elements surrounding the poly(A) site. May act to tether poly(A) polymerase to the CPSF complex. {ECO:0000269|PubMed:14749727}. |
Q6ZMR3 | LDHAL6A | S161 | ochoa | L-lactate dehydrogenase A-like 6A (LDHA-like protein 6A) (EC 1.1.1.27) | Catalyzes the interconversion of L-lactate and pyruvate with nicotinamide adenine dinucleotide NAD(+) as a coenzyme (PubMed:18351441). Significantly increases the transcriptional activity of JUN, when overexpressed. {ECO:0000269|PubMed:18351441}. |
Q6ZNB6 | NFXL1 | S331 | ochoa | NF-X1-type zinc finger protein NFXL1 (Ovarian zinc finger protein) (hOZFP) | None |
Q6ZRS2 | SRCAP | S568 | ochoa | Helicase SRCAP (EC 3.6.4.-) (Domino homolog 2) (Snf2-related CBP activator) | Catalytic component of the SRCAP complex which mediates the ATP-dependent exchange of histone H2AZ/H2B dimers for nucleosomal H2A/H2B, leading to transcriptional regulation of selected genes by chromatin remodeling. Acts as a coactivator for CREB-mediated transcription, steroid receptor-mediated transcription, and Notch-mediated transcription. {ECO:0000269|PubMed:10347196, ECO:0000269|PubMed:11522779, ECO:0000269|PubMed:14500758, ECO:0000269|PubMed:16024792, ECO:0000269|PubMed:16634648, ECO:0000269|PubMed:17617668}. |
Q709C8 | VPS13C | S3641 | ochoa | Intermembrane lipid transfer protein VPS13C (Vacuolar protein sorting-associated protein 13C) | Mediates the transfer of lipids between membranes at organelle contact sites (By similarity). Necessary for proper mitochondrial function and maintenance of mitochondrial transmembrane potential (PubMed:26942284). Involved in the regulation of PINK1/PRKN-mediated mitophagy in response to mitochondrial depolarization (PubMed:26942284). {ECO:0000250|UniProtKB:Q07878, ECO:0000269|PubMed:26942284}. |
Q7Z3J3 | RGPD4 | S1472 | ochoa | RanBP2-like and GRIP domain-containing protein 4 | None |
Q86U42 | PABPN1 | S197 | ochoa | Polyadenylate-binding protein 2 (PABP-2) (Poly(A)-binding protein 2) (Nuclear poly(A)-binding protein 1) (Poly(A)-binding protein II) (PABII) (Polyadenylate-binding nuclear protein 1) | Involved in the 3'-end formation of mRNA precursors (pre-mRNA) by the addition of a poly(A) tail of 200-250 nt to the upstream cleavage product (By similarity). Stimulates poly(A) polymerase (PAPOLA) conferring processivity on the poly(A) tail elongation reaction and also controls the poly(A) tail length (By similarity). Increases the affinity of poly(A) polymerase for RNA (By similarity). Is also present at various stages of mRNA metabolism including nucleocytoplasmic trafficking and nonsense-mediated decay (NMD) of mRNA. Cooperates with SKIP to synergistically activate E-box-mediated transcription through MYOD1 and may regulate the expression of muscle-specific genes (PubMed:11371506). Binds to poly(A) and to poly(G) with high affinity (By similarity). May protect the poly(A) tail from degradation (By similarity). Subunit of the trimeric poly(A) tail exosome targeting (PAXT) complex, a complex that directs a subset of long and polyadenylated poly(A) RNAs for exosomal degradation. The RNA exosome is fundamental for the degradation of RNA in eukaryotic nuclei. Substrate targeting is facilitated by its cofactor MTREX, which links to RNA-binding protein adapters (PubMed:27871484). {ECO:0000250|UniProtKB:Q28165, ECO:0000269|PubMed:11371506, ECO:0000269|PubMed:27871484}. |
Q86U86 | PBRM1 | S605 | ochoa | Protein polybromo-1 (hPB1) (BRG1-associated factor 180) (BAF180) (Polybromo-1D) | Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Required for the stability of the SWI/SNF chromatin remodeling complex SWI/SNF-B (PBAF). Acts as a negative regulator of cell proliferation. {ECO:0000269|PubMed:21248752, ECO:0000303|PubMed:22952240, ECO:0000303|PubMed:26601204}. |
Q86XL3 | ANKLE2 | S339 | ochoa | Ankyrin repeat and LEM domain-containing protein 2 (LEM domain-containing protein 4) | Involved in mitotic nuclear envelope reassembly by promoting dephosphorylation of BAF/BANF1 during mitotic exit (PubMed:22770216). Coordinates the control of BAF/BANF1 dephosphorylation by inhibiting VRK1 kinase and promoting dephosphorylation of BAF/BANF1 by protein phosphatase 2A (PP2A), thereby facilitating nuclear envelope assembly (PubMed:22770216). May regulate nuclear localization of VRK1 in non-dividing cells (PubMed:31735666). It is unclear whether it acts as a real PP2A regulatory subunit or whether it is involved in recruitment of the PP2A complex (PubMed:22770216). Involved in brain development (PubMed:25259927). {ECO:0000269|PubMed:22770216, ECO:0000269|PubMed:25259927, ECO:0000269|PubMed:31735666}. |
Q8IWB9 | TEX2 | S388 | ochoa | Testis-expressed protein 2 (Transmembrane protein 96) | During endoplasmic reticulum (ER) stress or when cellular ceramide levels increase, may induce contacts between the ER and medial-Golgi complex to facilitate non-vesicular transport of ceramides from the ER to the Golgi complex where they are converted to complex sphingolipids, preventing toxic ceramide accumulation. {ECO:0000269|PubMed:28011845}. |
Q8N1F7 | NUP93 | S66 | ochoa | Nuclear pore complex protein Nup93 (93 kDa nucleoporin) (Nucleoporin Nup93) | Plays a role in the nuclear pore complex (NPC) assembly and/or maintenance (PubMed:9348540). May anchor nucleoporins, but not NUP153 and TPR, to the NPC. During renal development, regulates podocyte migration and proliferation through SMAD4 signaling (PubMed:26878725). {ECO:0000269|PubMed:15229283, ECO:0000269|PubMed:15703211, ECO:0000269|PubMed:26878725, ECO:0000269|PubMed:9348540}. |
Q8N3R9 | PALS1 | S245 | ochoa | Protein PALS1 (MAGUK p55 subfamily member 5) (Membrane protein, palmitoylated 5) (Protein associated with Lin-7 1) | Plays a role in tight junction biogenesis and in the establishment of cell polarity in epithelial cells (PubMed:16678097, PubMed:25385611). Also involved in adherens junction biogenesis by ensuring correct localization of the exocyst complex protein EXOC4/SEC8 which allows trafficking of adherens junction structural component CDH1 to the cell surface (By similarity). Plays a role through its interaction with CDH5 in vascular lumen formation and endothelial membrane polarity (PubMed:27466317). Required during embryonic and postnatal retinal development (By similarity). Required for the maintenance of cerebellar progenitor cells in an undifferentiated proliferative state, preventing premature differentiation, and is required for cerebellar histogenesis, fissure formation, cerebellar layer organization and cortical development (By similarity). Plays a role in neuronal progenitor cell survival, potentially via promotion of mTOR signaling (By similarity). Plays a role in the radial and longitudinal extension of the myelin sheath in Schwann cells (By similarity). May modulate SC6A1/GAT1-mediated GABA uptake by stabilizing the transporter (By similarity). Plays a role in the T-cell receptor-mediated activation of NF-kappa-B (PubMed:21479189). Required for localization of EZR to the apical membrane of parietal cells and may play a role in the dynamic remodeling of the apical cytoskeleton (By similarity). Required for the normal polarized localization of the vesicular marker STX4 (By similarity). Required for the correct trafficking of the myelin proteins PMP22 and MAG (By similarity). Involved in promoting phosphorylation and cytoplasmic retention of transcriptional coactivators YAP1 and WWTR1/TAZ which leads to suppression of TGFB1-dependent transcription of target genes such as CCN2/CTGF, SERPINE1/PAI1, SNAI1/SNAIL1 and SMAD7 (By similarity). {ECO:0000250|UniProtKB:B4F7E7, ECO:0000250|UniProtKB:Q9JLB2, ECO:0000269|PubMed:16678097, ECO:0000269|PubMed:21479189, ECO:0000269|PubMed:25385611, ECO:0000269|PubMed:27466317}.; FUNCTION: (Microbial infection) Acts as an interaction partner for human coronaviruses SARS-CoV and, probably, SARS-CoV-2 envelope protein E which results in delayed formation of tight junctions and disregulation of cell polarity. {ECO:0000269|PubMed:20861307, ECO:0000303|PubMed:32891874}. |
Q8N4C6 | NIN | S1157 | ochoa | Ninein (hNinein) (Glycogen synthase kinase 3 beta-interacting protein) (GSK3B-interacting protein) | Centrosomal protein required in the positioning and anchorage of the microtubule minus-end in epithelial cells (PubMed:15190203, PubMed:23386061). May also act as a centrosome maturation factor (PubMed:11956314). May play a role in microtubule nucleation, by recruiting the gamma-tubulin ring complex to the centrosome (PubMed:15190203). Overexpression does not perturb nucleation or elongation of microtubules but suppresses release of microtubules (PubMed:15190203). Required for centriole organization and microtubule anchoring at the mother centriole (PubMed:23386061). {ECO:0000269|PubMed:11956314, ECO:0000269|PubMed:15190203, ECO:0000269|PubMed:23386061}. |
Q8N4X5 | AFAP1L2 | S309 | ochoa | Actin filament-associated protein 1-like 2 (AFAP1-like protein 2) | May play a role in a signaling cascade by enhancing the kinase activity of SRC. Contributes to SRC-regulated transcription activation. {ECO:0000269|PubMed:17412687}. |
Q8N556 | AFAP1 | S510 | ochoa | Actin filament-associated protein 1 (110 kDa actin filament-associated protein) (AFAP-110) | Can cross-link actin filaments into both network and bundle structures (By similarity). May modulate changes in actin filament integrity and induce lamellipodia formation. May function as an adapter molecule that links other proteins, such as SRC and PKC to the actin cytoskeleton. Seems to play a role in the development and progression of prostate adenocarcinoma by regulating cell-matrix adhesions and migration in the cancer cells. {ECO:0000250, ECO:0000269|PubMed:15485829}. |
Q8NEY8 | PPHLN1 | S48 | ochoa | Periphilin-1 (CDC7 expression repressor) (CR) (Gastric cancer antigen Ga50) | Component of the HUSH complex, a multiprotein complex that mediates epigenetic repression. The HUSH complex is recruited to genomic loci rich in H3K9me3 and is probably required to maintain transcriptional silencing by promoting recruitment of SETDB1, a histone methyltransferase that mediates further deposition of H3K9me3. In the HUSH complex, contributes to the maintenance of the complex at chromatin (PubMed:26022416). Acts as a transcriptional corepressor and regulates the cell cycle, probably via the HUSH complex (PubMed:15474462, PubMed:17963697). The HUSH complex is also involved in the silencing of unintegrated retroviral DNA: some part of the retroviral DNA formed immediately after infection remains unintegrated in the host genome and is transcriptionally repressed (PubMed:30487602). May be involved in epithelial differentiation by contributing to epidermal integrity and barrier formation (PubMed:12853457). {ECO:0000269|PubMed:15474462, ECO:0000269|PubMed:17963697, ECO:0000269|PubMed:26022416, ECO:0000269|PubMed:30487602, ECO:0000305|PubMed:12853457}. |
Q8NFM4 | ADCY4 | S253 | ochoa | Adenylate cyclase type 4 (EC 4.6.1.1) (ATP pyrophosphate-lyase 4) (Adenylate cyclase type IV) (Adenylyl cyclase 4) | Catalyzes the formation of the signaling molecule cAMP in response to G-protein signaling. {ECO:0000250|UniProtKB:P26770}. |
Q8TED9 | AFAP1L1 | S385 | ochoa | Actin filament-associated protein 1-like 1 (AFAP1-like protein 1) | May be involved in podosome and invadosome formation. {ECO:0000269|PubMed:21333378}. |
Q8WUH6 | TMEM263 | S23 | ochoa | Transmembrane protein 263 | May play a role in bone development. {ECO:0000269|PubMed:34238371}. |
Q8WUX1 | SLC38A5 | S36 | ochoa | Sodium-coupled neutral amino acid transporter 5 (Solute carrier family 38 member 5) (System N transporter 2) | Symporter that cotransports neutral amino acids and sodium ions, coupled to an H(+) antiporter activity (PubMed:11243884). Releases L-glutamine and glycine from astroglial cells and may participate in the glutamate/GABA-L-glutamine cycle and the NMDA receptors activation (By similarity). In addition, contributes significantly to L-glutamine uptake in retina, namely in ganglion and Mueller cells therefore, participates in the retinal glutamate-glutamine cycle (By similarity). The transport activity is pH sensitive and Li(+) tolerant (PubMed:11243884). Moreover functions in both direction and is associated with large uncoupled fluxes of protons (By similarity). The transport is electroneutral coupled to the cotransport of 1 Na(+) and the antiport of 1 H(+) (By similarity). May have a particular importance for modulation of net hepatic glutamine flux (By similarity). {ECO:0000250|UniProtKB:A2VCW5, ECO:0000250|UniProtKB:Q3U1J0, ECO:0000269|PubMed:11243884}. |
Q8WVV4 | POF1B | S156 | ochoa | Protein POF1B (Premature ovarian failure protein 1B) | Plays a key role in the organization of epithelial monolayers by regulating the actin cytoskeleton. May be involved in ovary development. {ECO:0000269|PubMed:16773570, ECO:0000269|PubMed:21940798}. |
Q8WWI1 | LMO7 | S919 | ochoa | LIM domain only protein 7 (LMO-7) (F-box only protein 20) (LOMP) | None |
Q8WXE9 | STON2 | S272 | ochoa | Stonin-2 (Stoned B) | Adapter protein involved in endocytic machinery. Involved in the synaptic vesicle recycling. May facilitate clathrin-coated vesicle uncoating. {ECO:0000269|PubMed:11381094, ECO:0000269|PubMed:11454741, ECO:0000269|PubMed:21102408}. |
Q92574 | TSC1 | S1080 | ochoa | Hamartin (Tuberous sclerosis 1 protein) | Non-catalytic component of the TSC-TBC complex, a multiprotein complex that acts as a negative regulator of the canonical mTORC1 complex, an evolutionarily conserved central nutrient sensor that stimulates anabolic reactions and macromolecule biosynthesis to promote cellular biomass generation and growth (PubMed:12172553, PubMed:12271141, PubMed:12906785, PubMed:15340059, PubMed:24529379, PubMed:28215400). The TSC-TBC complex acts as a GTPase-activating protein (GAP) for the small GTPase RHEB, a direct activator of the protein kinase activity of mTORC1 (PubMed:12906785, PubMed:15340059, PubMed:24529379). In absence of nutrients, the TSC-TBC complex inhibits mTORC1, thereby preventing phosphorylation of ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1) by the mTORC1 signaling (PubMed:12271141, PubMed:24529379, PubMed:28215400, PubMed:33215753). The TSC-TBC complex is inactivated in response to nutrients, relieving inhibition of mTORC1 (PubMed:12172553, PubMed:24529379). Within the TSC-TBC complex, TSC1 stabilizes TSC2 and prevents TSC2 self-aggregation (PubMed:10585443, PubMed:28215400). Acts as a tumor suppressor (PubMed:9242607). Involved in microtubule-mediated protein transport via its ability to regulate mTORC1 signaling (By similarity). Also acts as a co-chaperone for HSP90AA1 facilitating HSP90AA1 chaperoning of protein clients such as kinases, TSC2 and glucocorticoid receptor NR3C1 (PubMed:29127155). Increases ATP binding to HSP90AA1 and inhibits HSP90AA1 ATPase activity (PubMed:29127155). Competes with the activating co-chaperone AHSA1 for binding to HSP90AA1, thereby providing a reciprocal regulatory mechanism for chaperoning of client proteins (PubMed:29127155). Recruits TSC2 to HSP90AA1 and stabilizes TSC2 by preventing the interaction between TSC2 and ubiquitin ligase HERC1 (PubMed:16464865, PubMed:29127155). {ECO:0000250|UniProtKB:Q9Z136, ECO:0000269|PubMed:10585443, ECO:0000269|PubMed:12172553, ECO:0000269|PubMed:12271141, ECO:0000269|PubMed:12906785, ECO:0000269|PubMed:15340059, ECO:0000269|PubMed:16464865, ECO:0000269|PubMed:24529379, ECO:0000269|PubMed:28215400, ECO:0000269|PubMed:29127155, ECO:0000269|PubMed:33215753, ECO:0000269|PubMed:9242607}. |
Q92667 | AKAP1 | S600 | ochoa | A-kinase anchor protein 1, mitochondrial (A-kinase anchor protein 149 kDa) (AKAP 149) (Dual specificity A-kinase-anchoring protein 1) (D-AKAP-1) (Protein kinase A-anchoring protein 1) (PRKA1) (Spermatid A-kinase anchor protein 84) (S-AKAP84) | Binds to type I and II regulatory subunits of protein kinase A and anchors them to the cytoplasmic face of the mitochondrial outer membrane (By similarity). Involved in mitochondrial-mediated antiviral innate immunity (PubMed:31522117). Promotes translocation of NDUFS1 into mitochondria to regulate mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) activity (By similarity). {ECO:0000250|UniProtKB:O08715, ECO:0000269|PubMed:31522117}. |
Q96CN7 | ISOC1 | S166 | ochoa | Isochorismatase domain-containing protein 1 | None |
Q96D71 | REPS1 | S307 | ochoa | RalBP1-associated Eps domain-containing protein 1 (RalBP1-interacting protein 1) | May coordinate the cellular actions of activated EGF receptors and Ral-GTPases. {ECO:0000250}. |
Q96EI5 | TCEAL4 | S108 | ochoa | Transcription elongation factor A protein-like 4 (TCEA-like protein 4) (Transcription elongation factor S-II protein-like 4) | May be involved in transcriptional regulation. |
Q96FV2 | SCRN2 | S55 | ochoa | Secernin-2 | None |
Q96K76 | USP47 | S865 | ochoa | Ubiquitin carboxyl-terminal hydrolase 47 (EC 3.4.19.12) (Deubiquitinating enzyme 47) (Ubiquitin thioesterase 47) (Ubiquitin-specific-processing protease 47) | Ubiquitin-specific protease that specifically deubiquitinates monoubiquitinated DNA polymerase beta (POLB), stabilizing POLB thereby playing a role in base-excision repair (BER). Acts as a regulator of cell growth and genome integrity. May also indirectly regulate CDC25A expression at a transcriptional level. {ECO:0000269|PubMed:19966869, ECO:0000269|PubMed:21362556}. |
Q96ME7 | ZNF512 | S94 | ochoa | Zinc finger protein 512 | May be involved in transcriptional regulation. |
Q96PU5 | NEDD4L | S428 | psp | E3 ubiquitin-protein ligase NEDD4-like (EC 2.3.2.26) (EC 2.3.2.36) (HECT-type E3 ubiquitin transferase NED4L) (NEDD4.2) (Nedd4-2) | E3 ubiquitin-protein ligase that mediates the polyubiquitination of lysine and cysteine residues on target proteins and is thereby implicated in the regulation of various signaling pathways including autophagy, innate immunity or DNA repair (PubMed:20064473, PubMed:31959741, PubMed:33608556). Inhibits TGF-beta signaling by triggering SMAD2 and TGFBR1 ubiquitination and proteasome-dependent degradation (PubMed:15496141). Downregulates autophagy and cell growth by ubiquitinating and reducing cellular ULK1 or ASCT2 levels (PubMed:28820317, PubMed:31959741). Promotes ubiquitination and internalization of various plasma membrane channels such as ENaC, SCN2A/Nav1.2, SCN3A/Nav1.3, SCN5A/Nav1.5, SCN9A/Nav1.7, SCN10A/Nav1.8, KCNA3/Kv1.3, KCNH2, EAAT1, KCNQ2/Kv7.2, KCNQ3/Kv7.3 or CLC5 (PubMed:26363003, PubMed:27445338). Promotes ubiquitination and degradation of SGK1 and TNK2. Ubiquitinates BRAT1 and this ubiquitination is enhanced in the presence of NDFIP1 (PubMed:25631046). Plays a role in dendrite formation by melanocytes (PubMed:23999003). Involved in the regulation of TOR signaling (PubMed:27694961). Ubiquitinates and regulates protein levels of NTRK1 once this one is activated by NGF (PubMed:27445338). Plays a role in antiviral innate immunity by catalyzing 'Lys-29'-linked cysteine ubiquitination of TRAF3, resulting in enhanced 'Lys-48' and 'Lys-63'-linked ubiquitination of TRAF3 (PubMed:33608556). Ubiquitinates TTYH2 and TTYH3 and regulates protein levels of TTYH2 (PubMed:18577513). {ECO:0000250|UniProtKB:Q8CFI0, ECO:0000269|PubMed:12911626, ECO:0000269|PubMed:15040001, ECO:0000269|PubMed:15217910, ECO:0000269|PubMed:15489223, ECO:0000269|PubMed:15496141, ECO:0000269|PubMed:15576372, ECO:0000269|PubMed:18577513, ECO:0000269|PubMed:19144635, ECO:0000269|PubMed:23999003, ECO:0000269|PubMed:25631046, ECO:0000269|PubMed:26363003, ECO:0000269|PubMed:27445338, ECO:0000269|PubMed:27694961, ECO:0000269|PubMed:33608556}. |
Q96RL1 | UIMC1 | S597 | ochoa | BRCA1-A complex subunit RAP80 (Receptor-associated protein 80) (Retinoid X receptor-interacting protein 110) (Ubiquitin interaction motif-containing protein 1) | Ubiquitin-binding protein (PubMed:24627472). Specifically recognizes and binds 'Lys-63'-linked ubiquitin (PubMed:19328070, Ref.38). Plays a central role in the BRCA1-A complex by specifically binding 'Lys-63'-linked ubiquitinated histones H2A and H2AX at DNA lesions sites, leading to target the BRCA1-BARD1 heterodimer to sites of DNA damage at double-strand breaks (DSBs). The BRCA1-A complex also possesses deubiquitinase activity that specifically removes 'Lys-63'-linked ubiquitin on histones H2A and H2AX. Also weakly binds monoubiquitin but with much less affinity than 'Lys-63'-linked ubiquitin. May interact with monoubiquitinated histones H2A and H2B; the relevance of such results is however unclear in vivo. Does not bind Lys-48'-linked ubiquitin. May indirectly act as a transcriptional repressor by inhibiting the interaction of NR6A1 with the corepressor NCOR1. {ECO:0000269|PubMed:12080054, ECO:0000269|PubMed:17525340, ECO:0000269|PubMed:17525341, ECO:0000269|PubMed:17525342, ECO:0000269|PubMed:17621610, ECO:0000269|PubMed:17643121, ECO:0000269|PubMed:19015238, ECO:0000269|PubMed:19202061, ECO:0000269|PubMed:19261748, ECO:0000269|PubMed:19328070, ECO:0000269|PubMed:24627472, ECO:0000269|Ref.38}. |
Q99569 | PKP4 | S162 | ochoa | Plakophilin-4 (p0071) | Plays a role as a regulator of Rho activity during cytokinesis. May play a role in junctional plaques. {ECO:0000269|PubMed:17115030}. |
Q99626 | CDX2 | S179 | ochoa | Homeobox protein CDX-2 (CDX-3) (Caudal-type homeobox protein 2) | Transcription factor which regulates the transcription of multiple genes expressed in the intestinal epithelium (By similarity). Binds to the promoter of the intestinal sucrase-isomaltase SI and activates SI transcription (By similarity). Binds to the DNA sequence 5'-ATAAAAACTTAT-3' in the promoter region of VDR and activates VDR transcription (By similarity). Binds to and activates transcription of LPH (By similarity). Activates transcription of CLDN2 and intestinal mucin MUC2 (By similarity). Binds to the 5'-AATTTTTTACAACACCT-3' DNA sequence in the promoter region of CA1 and activates CA1 transcription (By similarity). Important in broad range of functions from early differentiation to maintenance of the intestinal epithelial lining of both the small and large intestine. Binds preferentially to methylated DNA (PubMed:28473536). {ECO:0000250|UniProtKB:P43241, ECO:0000250|UniProtKB:Q04649, ECO:0000269|PubMed:28473536}. |
Q99666 | RGPD5 | S1471 | ochoa | RANBP2-like and GRIP domain-containing protein 5/6 (Ran-binding protein 2-like 1/2) (RanBP2-like 1/2) (RanBP2L1) (RanBP2L2) (Sperm membrane protein BS-63) | None |
Q99973 | TEP1 | S2353 | ochoa | Telomerase protein component 1 (Telomerase-associated protein 1) (Telomerase protein 1) (p240) (p80 telomerase homolog) | Component of the telomerase ribonucleoprotein complex that is essential for the replication of chromosome termini (PubMed:19179534). Also a component of the ribonucleoprotein vaults particle, a multi-subunit structure involved in nucleo-cytoplasmic transport (By similarity). Responsible for the localizing and stabilizing vault RNA (vRNA) association in the vault ribonucleoprotein particle. Binds to TERC (By similarity). {ECO:0000250|UniProtKB:P97499, ECO:0000269|PubMed:19179534}. |
Q9BQ89 | FAM110A | S243 | ochoa | Protein FAM110A | None |
Q9BRQ6 | CHCHD6 | S126 | ochoa | MICOS complex subunit MIC25 (Coiled-coil-helix cristae morphology protein 1) (Coiled-coil-helix-coiled-coil-helix domain-containing protein 6) | Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. {ECO:0000269|PubMed:22228767}. |
Q9BTE3 | MCMBP | S193 | ochoa | Mini-chromosome maintenance complex-binding protein (MCM-BP) (MCM-binding protein) | Associated component of the MCM complex that acts as a regulator of DNA replication. Binds to the MCM complex during late S phase and promotes the disassembly of the MCM complex from chromatin, thereby acting as a key regulator of pre-replication complex (pre-RC) unloading from replicated DNA. Can dissociate the MCM complex without addition of ATP; probably acts by destabilizing interactions of each individual subunits of the MCM complex. Required for sister chromatid cohesion. {ECO:0000269|PubMed:20090939, ECO:0000269|PubMed:21196493}. |
Q9BZ29 | DOCK9 | S170 | ochoa | Dedicator of cytokinesis protein 9 (Cdc42 guanine nucleotide exchange factor zizimin-1) (Zizimin-1) | Guanine nucleotide-exchange factor (GEF) that activates CDC42 by exchanging bound GDP for free GTP. Overexpression induces filopodia formation. {ECO:0000269|PubMed:12172552, ECO:0000269|PubMed:19745154}. |
Q9C026 | TRIM9 | S80 | psp | E3 ubiquitin-protein ligase TRIM9 (EC 2.3.2.27) (RING finger protein 91) (RING-type E3 ubiquitin transferase TRIM9) (Tripartite motif-containing protein 9) | E3 ubiquitin-protein ligase which ubiquitinates itself in cooperation with an E2 enzyme UBE2D2/UBC4 and serves as a targeting signal for proteasomal degradation. May play a role in regulation of neuronal functions and may also participate in the formation or breakdown of abnormal inclusions in neurodegenerative disorders. May act as a regulator of synaptic vesicle exocytosis by controlling the availability of SNAP25 for the SNARE complex formation. {ECO:0000269|PubMed:20085810}. |
Q9C040 | TRIM2 | S375 | ochoa | Tripartite motif-containing protein 2 (EC 2.3.2.27) (E3 ubiquitin-protein ligase TRIM2) (RING finger protein 86) (RING-type E3 ubiquitin transferase TRIM2) | UBE2D1-dependent E3 ubiquitin-protein ligase that mediates the ubiquitination of NEFL and of phosphorylated BCL2L11. Plays a neuroprotective function. May play a role in neuronal rapid ischemic tolerance. Plays a role in antiviral immunity and limits New World arenavirus infection independently of its ubiquitin ligase activity (PubMed:24068738). {ECO:0000250|UniProtKB:Q9ESN6, ECO:0000269|PubMed:24068738}. |
Q9C0B0 | UNK | S411 | ochoa | RING finger protein unkempt homolog (Zinc finger CCCH domain-containing protein 5) | Sequence-specific RNA-binding protein which plays an important role in the establishment and maintenance of the early morphology of cortical neurons during embryonic development. Acts as a translation repressor and controls a translationally regulated cell morphology program to ensure proper structuring of the nervous system. Translational control depends on recognition of its binding element within target mRNAs which consists of a mandatory UAG trimer upstream of a U/A-rich motif. Associated with polysomes (PubMed:25737280). {ECO:0000269|PubMed:25737280}. |
Q9C0D5 | TANC1 | S1542 | ochoa | Protein TANC1 (Tetratricopeptide repeat, ankyrin repeat and coiled-coil domain-containing protein 1) | May be a scaffold component in the postsynaptic density. {ECO:0000250}. |
Q9H0E9 | BRD8 | S383 | ochoa | Bromodomain-containing protein 8 (Skeletal muscle abundant protein) (Skeletal muscle abundant protein 2) (Thyroid hormone receptor coactivating protein of 120 kDa) (TrCP120) (p120) | May act as a coactivator during transcriptional activation by hormone-activated nuclear receptors (NR). Isoform 2 stimulates transcriptional activation by AR/DHTR, ESR1/NR3A1, RXRA/NR2B1 and THRB/ERBA2. At least isoform 1 and isoform 2 are components of the NuA4 histone acetyltransferase (HAT) complex which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histones H4 and H2A. This modification may both alter nucleosome - DNA interactions and promote interaction of the modified histones with other proteins which positively regulate transcription. This complex may be required for the activation of transcriptional programs associated with oncogene and proto-oncogene mediated growth induction, tumor suppressor mediated growth arrest and replicative senescence, apoptosis, and DNA repair. NuA4 may also play a direct role in DNA repair when recruited to sites of DNA damage. Component of a SWR1-like complex that specifically mediates the removal of histone H2A.Z/H2AZ1 from the nucleosome. {ECO:0000269|PubMed:10517671, ECO:0000269|PubMed:14966270, ECO:0000269|PubMed:24463511}. |
Q9H2G2 | SLK | S667 | ochoa | STE20-like serine/threonine-protein kinase (STE20-like kinase) (hSLK) (EC 2.7.11.1) (CTCL tumor antigen se20-9) (STE20-related serine/threonine-protein kinase) (STE20-related kinase) (Serine/threonine-protein kinase 2) | Mediates apoptosis and actin stress fiber dissolution. {ECO:0000250}. |
Q9H845 | ACAD9 | S187 | ochoa | Complex I assembly factor ACAD9, mitochondrial (Acyl-CoA dehydrogenase family member 9) (ACAD-9) (EC 1.3.8.-) | As part of the MCIA complex, primarily participates in the assembly of the mitochondrial complex I and therefore plays a role in oxidative phosphorylation (PubMed:20816094, PubMed:24158852, PubMed:32320651). This moonlighting protein also has a dehydrogenase activity toward a broad range of substrates with greater specificity for long-chain unsaturated acyl-CoAs (PubMed:12359260, PubMed:16020546, PubMed:21237683, PubMed:24158852). However, in vivo, it does not seem to play a primary role in fatty acid oxidation (PubMed:20816094, PubMed:24158852). In addition, the function in complex I assembly is independent of the dehydrogenase activity of the protein (PubMed:24158852). {ECO:0000269|PubMed:12359260, ECO:0000269|PubMed:16020546, ECO:0000269|PubMed:20816094, ECO:0000269|PubMed:21237683, ECO:0000269|PubMed:24158852, ECO:0000269|PubMed:32320651}. |
Q9H9B1 | EHMT1 | S38 | ochoa | Histone-lysine N-methyltransferase EHMT1 (EC 2.1.1.-) (EC 2.1.1.367) (Euchromatic histone-lysine N-methyltransferase 1) (Eu-HMTase1) (G9a-like protein 1) (GLP) (GLP1) (Histone H3-K9 methyltransferase 5) (H3-K9-HMTase 5) (Lysine N-methyltransferase 1D) | Histone methyltransferase that specifically mono- and dimethylates 'Lys-9' of histone H3 (H3K9me1 and H3K9me2, respectively) in euchromatin. H3K9me represents a specific tag for epigenetic transcriptional repression by recruiting HP1 proteins to methylated histones. Also weakly methylates 'Lys-27' of histone H3 (H3K27me). Also required for DNA methylation, the histone methyltransferase activity is not required for DNA methylation, suggesting that these 2 activities function independently. Probably targeted to histone H3 by different DNA-binding proteins like E2F6, MGA, MAX and/or DP1. During G0 phase, it probably contributes to silencing of MYC- and E2F-responsive genes, suggesting a role in G0/G1 transition in cell cycle. In addition to the histone methyltransferase activity, also methylates non-histone proteins: mediates dimethylation of 'Lys-373' of p53/TP53. Represses the expression of mitochondrial function-related genes, perhaps by occupying their promoter regions, working in concert with probable chromatin reader BAZ2B (By similarity). {ECO:0000250|UniProtKB:Q5DW34, ECO:0000269|PubMed:12004135, ECO:0000269|PubMed:20118233}. |
Q9NP79 | VTA1 | S281 | ochoa | Vacuolar protein sorting-associated protein VTA1 homolog (Dopamine-responsive gene 1 protein) (DRG-1) (LYST-interacting protein 5) (LIP5) (SKD1-binding protein 1) (SBP1) | Involved in the endosomal multivesicular bodies (MVB) pathway. MVBs contain intraluminal vesicles (ILVs) that are generated by invagination and scission from the limiting membrane of the endosome and mostly are delivered to lysosomes enabling degradation of membrane proteins, such as stimulated growth factor receptors, lysosomal enzymes and lipids. Thought to be a cofactor of VPS4A/B, which catalyzes disassembles membrane-associated ESCRT-III assemblies. Involved in the sorting and down-regulation of EGFR (By similarity). Involved in HIV-1 budding. {ECO:0000250, ECO:0000269|PubMed:15644320}. |
Q9NQG5 | RPRD1B | S164 | ochoa | Regulation of nuclear pre-mRNA domain-containing protein 1B (Cell cycle-related and expression-elevated protein in tumor) | Interacts with phosphorylated C-terminal heptapeptide repeat domain (CTD) of the largest RNA polymerase II subunit POLR2A, and participates in dephosphorylation of the CTD by RPAP2. Transcriptional regulator which enhances expression of CCND1. Promotes binding of RNA polymerase II to the CCDN1 promoter and to the termination region before the poly-A site but decreases its binding after the poly-A site. Prevents RNA polymerase II from reading through the 3' end termination site and may allow it to be recruited back to the promoter through promotion of the formation of a chromatin loop. Also enhances the transcription of a number of other cell cycle-related genes including CDK2, CDK4, CDK6 and cyclin-E but not CDKN1A, CDKN1B or cyclin-A. Promotes cell proliferation. {ECO:0000269|PubMed:22231121, ECO:0000269|PubMed:22264791, ECO:0000269|PubMed:24399136, ECO:0000269|PubMed:24997600}. |
Q9NRW1 | RAB6B | S117 | ochoa | Ras-related protein Rab-6B (EC 3.6.5.2) | The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between active GTP-bound and inactive GDP-bound states. In their active state, drive transport of vesicular carriers from donor organelles to acceptor organelles to regulate the membrane traffic that maintains organelle identity and morphology (By similarity). Recruits VPS13B to the Golgi membrane (PubMed:25492866). Regulates the compacted morphology of the Golgi (PubMed:26209634). Seems to have a role in retrograde membrane traffic at the level of the Golgi complex. May function in retrograde transport in neuronal cells (PubMed:17707369). Plays a role in neuron projection development (PubMed:25492866). {ECO:0000250|UniProtKB:P20340, ECO:0000269|PubMed:17707369, ECO:0000269|PubMed:25492866, ECO:0000269|PubMed:26209634}. |
Q9NV58 | RNF19A | S599 | ochoa | E3 ubiquitin-protein ligase RNF19A (EC 2.3.2.31) (Double ring-finger protein) (Dorfin) (RING finger protein 19A) (p38) | E3 ubiquitin-protein ligase which accepts ubiquitin from E2 ubiquitin-conjugating enzymes UBE2L3 and UBE2L6 in the form of a thioester and then directly transfers the ubiquitin to targeted substrates, such as SNCAIP or CASR. Specifically ubiquitinates pathogenic SOD1 variants, which leads to their proteasomal degradation and to neuronal protection. {ECO:0000269|PubMed:11237715, ECO:0000269|PubMed:12145308, ECO:0000269|PubMed:12750386, ECO:0000269|PubMed:15456787, ECO:0000269|PubMed:16513638}. |
Q9NWS0 | PIH1D1 | S173 | ochoa | PIH1 domain-containing protein 1 (Nucleolar protein 17 homolog) | Involved in the assembly of C/D box small nucleolar ribonucleoprotein (snoRNP) particles (PubMed:17636026). Recruits the SWI/SNF complex to the core promoter of rRNA genes and enhances pre-rRNA transcription (PubMed:22368283, PubMed:24036451). Mediates interaction of TELO2 with the R2TP complex which is necessary for the stability of MTOR and SMG1 (PubMed:20864032). Positively regulates the assembly and activity of the mTORC1 complex (PubMed:24036451). {ECO:0000269|PubMed:17636026, ECO:0000269|PubMed:20864032, ECO:0000269|PubMed:22368283, ECO:0000269|PubMed:24036451}. |
Q9NY57 | STK32B | S378 | ochoa | Serine/threonine-protein kinase 32B (EC 2.7.11.1) (Yet another novel kinase 2) | None |
Q9NY61 | AATF | S55 | ochoa | Protein AATF (Apoptosis-antagonizing transcription factor) (Rb-binding protein Che-1) | Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome (PubMed:34516797). May function as a general inhibitor of the histone deacetylase HDAC1. Binding to the pocket region of RB1 may displace HDAC1 from RB1/E2F complexes, leading to activation of E2F target genes and cell cycle progression. Conversely, displacement of HDAC1 from SP1 bound to the CDKN1A promoter leads to increased expression of this CDK inhibitor and blocks cell cycle progression. Also antagonizes PAWR mediated induction of aberrant amyloid peptide production in Alzheimer disease (presenile and senile dementia), although the molecular basis for this phenomenon has not been described to date. {ECO:0000269|PubMed:12450794, ECO:0000269|PubMed:12847090, ECO:0000269|PubMed:14627703, ECO:0000269|PubMed:15207272, ECO:0000269|PubMed:34516797}. |
Q9NYM9 | BET1L | S70 | ochoa | BET1-like protein (Golgi SNARE with a size of 15 kDa) (GOS-15) (GS15) (Vesicle transport protein GOS15) | Vesicle SNARE required for targeting and fusion of retrograde transport vesicles with the Golgi complex. Required for the integrity of the Golgi complex (By similarity). {ECO:0000250|UniProtKB:O35152}. |
Q9NYP7 | ELOVL5 | S273 | ochoa | Very long chain fatty acid elongase 5 (EC 2.3.1.199) (3-keto acyl-CoA synthase ELOVL5) (ELOVL fatty acid elongase 5) (ELOVL FA elongase 5) (Elongation of very long chain fatty acids protein 5) (Fatty acid elongase 1) (hELO1) (Very long chain 3-ketoacyl-CoA synthase 5) (Very long chain 3-oxoacyl-CoA synthase 5) | Catalyzes the first and rate-limiting reaction of the four reactions that constitute the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids (VLCFAs) per cycle. Condensing enzyme that acts specifically toward polyunsaturated acyl-CoA with the higher activity toward C18:3(n-6) acyl-CoA. May participate in the production of monounsaturated and of polyunsaturated VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators (By similarity) (PubMed:10970790, PubMed:20937905). In conditions where the essential linoleic and alpha linoleic fatty acids are lacking it is also involved in the synthesis of Mead acid from oleic acid (By similarity). {ECO:0000250|UniProtKB:Q8BHI7, ECO:0000255|HAMAP-Rule:MF_03205, ECO:0000269|PubMed:10970790, ECO:0000269|PubMed:20937905}. |
Q9P260 | RELCH | S45 | ochoa | RAB11-binding protein RELCH (LisH domain and HEAT repeat-containing protein KIAA1468) (RAB11 binding and LisH domain, coiled-coil and HEAT repeat-containing) (RAB11-binding protein containing LisH, coiled-coil, and HEAT repeats) | Regulates intracellular cholesterol distribution from recycling endosomes to the trans-Golgi network through interactions with RAB11 and OSBP (PubMed:29514919). Functions in membrane tethering and promotes OSBP-mediated cholesterol transfer between RAB11-bound recycling endosomes and OSBP-bound Golgi-like membranes (PubMed:29514919). {ECO:0000269|PubMed:29514919}. |
Q9UGP8 | SEC63 | S466 | ochoa | Translocation protein SEC63 homolog (DnaJ homolog subfamily C member 23) | Mediates cotranslational and post-translational transport of certain precursor polypeptides across endoplasmic reticulum (ER) (PubMed:22375059, PubMed:29719251). Proposed to play an auxiliary role in recognition of precursors with short and apolar signal peptides. May cooperate with SEC62 and HSPA5/BiP to facilitate targeting of small presecretory proteins into the SEC61 channel-forming translocon complex, triggering channel opening for polypeptide translocation to the ER lumen (PubMed:29719251). Required for efficient PKD1/Polycystin-1 biogenesis and trafficking to the plasma membrane of the primary cilia (By similarity). {ECO:0000250|UniProtKB:Q8VHE0, ECO:0000269|PubMed:22375059, ECO:0000269|PubMed:29719251}. |
Q9UHK0 | NUFIP1 | S312 | ochoa | FMR1-interacting protein NUFIP1 (Nuclear FMR1-interacting protein 1) (Nuclear FMRP-interacting protein 1) | Binds RNA. {ECO:0000269|PubMed:10556305}. |
Q9UII2 | ATP5IF1 | S27 | psp | ATPase inhibitor, mitochondrial (ATP synthase F1 subunit epsilon) (Inhibitor of F(1)F(o)-ATPase) (IF(1)) (IF1) | Endogenous F(1)F(o)-ATPase inhibitor limiting ATP depletion when the mitochondrial membrane potential falls below a threshold and the F(1)F(o)-ATP synthase starts hydrolyzing ATP to pump protons out of the mitochondrial matrix. Required to avoid the consumption of cellular ATP when the F(1)F(o)-ATP synthase enzyme acts as an ATP hydrolase. Indirectly acts as a regulator of heme synthesis in erythroid tissues: regulates heme synthesis by modulating the mitochondrial pH and redox potential, allowing FECH to efficiently catalyze the incorporation of iron into protoporphyrin IX to produce heme. {ECO:0000269|PubMed:12110673, ECO:0000269|PubMed:15528193, ECO:0000269|PubMed:19559621, ECO:0000269|PubMed:23135403}. |
Q9UKE5 | TNIK | S896 | ochoa | TRAF2 and NCK-interacting protein kinase (EC 2.7.11.1) | Serine/threonine kinase that acts as an essential activator of the Wnt signaling pathway. Recruited to promoters of Wnt target genes and required to activate their expression. May act by phosphorylating TCF4/TCF7L2. Appears to act upstream of the JUN N-terminal pathway. May play a role in the response to environmental stress. Part of a signaling complex composed of NEDD4, RAP2A and TNIK which regulates neuronal dendrite extension and arborization during development. More generally, it may play a role in cytoskeletal rearrangements and regulate cell spreading. Phosphorylates SMAD1 on Thr-322. Activator of the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. MAP4Ks act in parallel to and are partially redundant with STK3/MST2 and STK4/MST2 in the phosphorylation and activation of LATS1/2, and establish MAP4Ks as components of the expanded Hippo pathway (PubMed:26437443). {ECO:0000269|PubMed:10521462, ECO:0000269|PubMed:15342639, ECO:0000269|PubMed:19061864, ECO:0000269|PubMed:19816403, ECO:0000269|PubMed:20159449, ECO:0000269|PubMed:21690388, ECO:0000269|PubMed:26437443}. |
Q9Y250 | LZTS1 | S117 | ochoa | Leucine zipper putative tumor suppressor 1 (F37/esophageal cancer-related gene-coding leucine-zipper motif) (Fez1) | Involved in the regulation of cell growth. May stabilize the active CDC2-cyclin B1 complex and thereby contribute to the regulation of the cell cycle and the prevention of uncontrolled cell proliferation. May act as a tumor suppressor. {ECO:0000269|PubMed:10097140, ECO:0000269|PubMed:11464283, ECO:0000269|PubMed:11504921}. |
Q9Y3T6 | R3HCC1 | S236 | ochoa | R3H and coiled-coil domain-containing protein 1 | None |
Q9Y4F5 | CEP170B | S1356 | ochoa | Centrosomal protein of 170 kDa protein B (Centrosomal protein 170B) (Cep170B) | Plays a role in microtubule organization. {ECO:0000250|UniProtKB:Q5SW79}. |
Q9Y4L1 | HYOU1 | S634 | ochoa | Hypoxia up-regulated protein 1 (150 kDa oxygen-regulated protein) (ORP-150) (170 kDa glucose-regulated protein) (GRP-170) (Heat shock protein family H member 4) | Has a pivotal role in cytoprotective cellular mechanisms triggered by oxygen deprivation. Promotes HSPA5/BiP-mediated ATP nucleotide exchange and thereby activates the unfolded protein response (UPR) pathway in the presence of endoplasmic reticulum stress (By similarity). May play a role as a molecular chaperone and participate in protein folding. {ECO:0000250|UniProtKB:Q9JKR6, ECO:0000269|PubMed:10037731}. |
Q9Y520 | PRRC2C | S653 | ochoa | Protein PRRC2C (BAT2 domain-containing protein 1) (HBV X-transactivated gene 2 protein) (HBV XAg-transactivated protein 2) (HLA-B-associated transcript 2-like 2) (Proline-rich and coiled-coil-containing protein 2C) | Required for efficient formation of stress granules. {ECO:0000269|PubMed:29395067}. |
Q9Y6N7 | ROBO1 | S1157 | ochoa | Roundabout homolog 1 (Deleted in U twenty twenty) (H-Robo-1) | Receptor for SLIT1 and SLIT2 that mediates cellular responses to molecular guidance cues in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development (PubMed:10102268, PubMed:24560577). Interaction with the intracellular domain of FLRT3 mediates axon attraction towards cells expressing NTN1 (PubMed:24560577). In axon growth cones, the silencing of the attractive effect of NTN1 by SLIT2 may require the formation of a ROBO1-DCC complex (By similarity). Plays a role in the regulation of cell migration via its interaction with MYO9B; inhibits MYO9B-mediated stimulation of RHOA GTPase activity, and thereby leads to increased levels of active, GTP-bound RHOA (PubMed:26529257). May be required for lung development (By similarity). {ECO:0000250|UniProtKB:O89026, ECO:0000269|PubMed:10102268, ECO:0000269|PubMed:24560577, ECO:0000269|PubMed:26529257, ECO:0000305}. |
P36871 | PGM1 | S483 | Sugiyama | Phosphoglucomutase-1 (PGM 1) (EC 5.4.2.2) (Glucose phosphomutase 1) | Catalyzes the reversible isomerization of alpha-D-glucose 1-phosphate to alpha-D-glucose 6-phosphate (PubMed:15378030, PubMed:25288802). The mechanism proceeds via the intermediate compound alpha-D-glucose 1,6-bisphosphate (Probable) (PubMed:25288802). This enzyme participates in both the breakdown and synthesis of glucose (PubMed:17924679, PubMed:25288802). {ECO:0000269|PubMed:15378030, ECO:0000269|PubMed:17924679, ECO:0000269|PubMed:25288802, ECO:0000305|PubMed:15378030}. |
P57721 | PCBP3 | S59 | Sugiyama | Poly(rC)-binding protein 3 (Alpha-CP3) (PCBP3-overlapping transcript) (PCBP3-overlapping transcript 1) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC. {ECO:0000250}. |
P57723 | PCBP4 | S31 | Sugiyama | Poly(rC)-binding protein 4 (Alpha-CP4) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC. {ECO:0000250}. |
Q15365 | PCBP1 | S27 | Sugiyama | Poly(rC)-binding protein 1 (Alpha-CP1) (Heterogeneous nuclear ribonucleoprotein E1) (hnRNP E1) (Nucleic acid-binding protein SUB2.3) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC (PubMed:15731341, PubMed:7556077, PubMed:7607214, PubMed:8152927). Together with PCBP2, required for erythropoiesis, possibly by regulating mRNA splicing (By similarity). {ECO:0000250|UniProtKB:P60335, ECO:0000269|PubMed:15731341, ECO:0000269|PubMed:7556077, ECO:0000269|PubMed:7607214, ECO:0000269|PubMed:8152927}.; FUNCTION: (Microbial infection) In case of infection by poliovirus, plays a role in initiation of viral RNA replication in concert with the viral protein 3CD. {ECO:0000269|PubMed:12414943}. |
Q15366 | PCBP2 | S27 | Sugiyama | Poly(rC)-binding protein 2 (Alpha-CP2) (Heterogeneous nuclear ribonucleoprotein E2) (hnRNP E2) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC (PubMed:12414943, PubMed:7607214). Major cellular poly(rC)-binding protein (PubMed:12414943). Also binds poly(rU) (PubMed:12414943). Acts as a negative regulator of antiviral signaling (PubMed:19881509, PubMed:35322803). Negatively regulates cellular antiviral responses mediated by MAVS signaling (PubMed:19881509). It acts as an adapter between MAVS and the E3 ubiquitin ligase ITCH, therefore triggering MAVS ubiquitination and degradation (PubMed:19881509). Negativeley regulates the cGAS-STING pathway via interaction with CGAS, preventing the formation of liquid-like droplets in which CGAS is activated (PubMed:35322803). Together with PCBP1, required for erythropoiesis, possibly by regulating mRNA splicing (By similarity). {ECO:0000250|UniProtKB:Q61990, ECO:0000269|PubMed:12414943, ECO:0000269|PubMed:19881509, ECO:0000269|PubMed:35322803, ECO:0000269|PubMed:7607214}.; FUNCTION: (Microbial infection) In case of infection by poliovirus, binds to the viral internal ribosome entry site (IRES) and stimulates the IRES-mediated translation (PubMed:12414943, PubMed:24371074). Also plays a role in initiation of viral RNA replication in concert with the viral protein 3CD (PubMed:12414943). {ECO:0000269|PubMed:12414943, ECO:0000269|PubMed:24371074}. |
P35606 | COPB2 | S350 | Sugiyama | Coatomer subunit beta' (Beta'-coat protein) (Beta'-COP) (p102) | The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. In mammals, the coatomer can only be recruited by membranes associated to ADP-ribosylation factors (ARFs), which are small GTP-binding proteins; the complex also influences the Golgi structural integrity, as well as the processing, activity, and endocytic recycling of LDL receptors. {ECO:0000269|PubMed:34450031}.; FUNCTION: This coatomer complex protein, essential for Golgi budding and vesicular trafficking, is a selective binding protein (RACK) for protein kinase C, epsilon type. It binds to Golgi membranes in a GTP-dependent manner (By similarity). {ECO:0000250}. |
Q7RTV0 | PHF5A | S53 | Sugiyama | PHD finger-like domain-containing protein 5A (PHD finger-like domain protein 5A) (Splicing factor 3B-associated 14 kDa protein) (SF3b14b) | Component of the 17S U2 SnRNP complex of the spliceosome, a large ribonucleoprotein complex that removes introns from transcribed pre-mRNAs (PubMed:12234937, PubMed:27720643, PubMed:28541300, PubMed:32494006, PubMed:34822310). The 17S U2 SnRNP complex (1) directly participates in early spliceosome assembly and (2) mediates recognition of the intron branch site during pre-mRNA splicing by promoting the selection of the pre-mRNA branch-site adenosine, the nucleophile for the first step of splicing (PubMed:12234937, PubMed:32494006, PubMed:34822310). Within the 17S U2 SnRNP complex, PHF5A is part of the SF3B subcomplex, which is required for 'A' complex assembly formed by the stable binding of U2 snRNP to the branchpoint sequence in pre-mRNA (PubMed:12234937, PubMed:27720643). Sequence independent binding of SF3A and SF3B subcomplexes upstream of the branch site is essential, it may anchor U2 snRNP to the pre-mRNA (PubMed:12234937). Also acts as a component of the minor spliceosome, which is involved in the splicing of U12-type introns in pre-mRNAs (PubMed:15146077, PubMed:33509932). Also involved in elongation by RNA polymerase II as part of the PAF1 complex (PAF1C) (By similarity). PAF1C is required for maintenance of embryonic stem cell (ESC) self-renewal and cellular reprogramming of stem cells (By similarity). Maintains pluripotency by recruiting and stabilizing PAF1C on pluripotency genes loci, and by regulating the expression of the pluripotency genes (By similarity). Regulates the deposition of elongation-associated histone modifications, including dimethylated histone H3 'Lys-79' (H3K79me2) and trimethylated histone H3 'Lys-36' (H3K36me3), on PAF1C targets, self-renewal and pluripotency genes (By similarity). Regulates RNA polymerase II promoter-proximal pause release of the PAF1C targets and self-renewal genes, and the levels of elongating ('Ser-2' phosphorylated) RNA polymerase II in their gene bodies (By similarity). Regulates muscle specification in adult stem cells by stabilizing PAF1C in chromatin to promote myogenic differentiation (By similarity). Acts as a transcriptional regulator by binding to the GJA1/Cx43 promoter and enhancing its up-regulation by ESR1/ER-alpha (By similarity). {ECO:0000250|UniProtKB:P83870, ECO:0000250|UniProtKB:P83871, ECO:0000269|PubMed:12234937, ECO:0000269|PubMed:15146077, ECO:0000269|PubMed:27720643, ECO:0000269|PubMed:28541300, ECO:0000269|PubMed:32494006, ECO:0000269|PubMed:33509932, ECO:0000269|PubMed:34822310}. |
Q02809 | PLOD1 | S342 | Sugiyama | Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 (EC 1.14.11.4) (Lysyl hydroxylase 1) (LH1) | Part of a complex composed of PLOD1, P3H3 and P3H4 that catalyzes hydroxylation of lysine residues in collagen alpha chains and is required for normal assembly and cross-linkling of collagen fibrils (By similarity). Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens (PubMed:10686424, PubMed:15854030, PubMed:8621606). These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links (Probable). {ECO:0000250|UniProtKB:Q9R0E2, ECO:0000269|PubMed:10686424, ECO:0000269|PubMed:15854030, ECO:0000269|PubMed:8621606, ECO:0000305}. |
O75582 | RPS6KA5 | S436 | Sugiyama | Ribosomal protein S6 kinase alpha-5 (S6K-alpha-5) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 5) (Nuclear mitogen- and stress-activated protein kinase 1) (RSK-like protein kinase) (RSKL) | Serine/threonine-protein kinase that is required for the mitogen or stress-induced phosphorylation of the transcription factors CREB1 and ATF1 and for the regulation of the transcription factors RELA, STAT3 and ETV1/ER81, and that contributes to gene activation by histone phosphorylation and functions in the regulation of inflammatory genes (PubMed:11909979, PubMed:12569367, PubMed:12763138, PubMed:18511904, PubMed:9687510, PubMed:9873047). Phosphorylates CREB1 and ATF1 in response to mitogenic or stress stimuli such as UV-C irradiation, epidermal growth factor (EGF) and anisomycin (PubMed:11909979, PubMed:9873047). Plays an essential role in the control of RELA transcriptional activity in response to TNF and upon glucocorticoid, associates in the cytoplasm with the glucocorticoid receptor NR3C1 and contributes to RELA inhibition and repression of inflammatory gene expression (PubMed:12628924, PubMed:18511904). In skeletal myoblasts is required for phosphorylation of RELA at 'Ser-276' during oxidative stress (PubMed:12628924). In erythropoietin-stimulated cells, is necessary for the 'Ser-727' phosphorylation of STAT3 and regulation of its transcriptional potential (PubMed:12763138). Phosphorylates ETV1/ER81 at 'Ser-191' and 'Ser-216', and thereby regulates its ability to stimulate transcription, which may be important during development and breast tumor formation (PubMed:12569367). Directly represses transcription via phosphorylation of 'Ser-1' of histone H2A (PubMed:15010469). Phosphorylates 'Ser-10' of histone H3 in response to mitogenics, stress stimuli and EGF, which results in the transcriptional activation of several immediate early genes, including proto-oncogenes c-fos/FOS and c-jun/JUN (PubMed:12773393). May also phosphorylate 'Ser-28' of histone H3 (PubMed:12773393). Mediates the mitogen- and stress-induced phosphorylation of high mobility group protein 1 (HMGN1/HMG14) (PubMed:12773393). In lipopolysaccharide-stimulated primary macrophages, acts downstream of the Toll-like receptor TLR4 to limit the production of pro-inflammatory cytokines (By similarity). Functions probably by inducing transcription of the MAP kinase phosphatase DUSP1 and the anti-inflammatory cytokine interleukin 10 (IL10), via CREB1 and ATF1 transcription factors (By similarity). Plays a role in neuronal cell death by mediating the downstream effects of excitotoxic injury (By similarity). Phosphorylates TRIM7 at 'Ser-107' in response to growth factor signaling via the MEK/ERK pathway, thereby stimulating its ubiquitin ligase activity (PubMed:25851810). {ECO:0000250|UniProtKB:Q8C050, ECO:0000269|PubMed:11909979, ECO:0000269|PubMed:12569367, ECO:0000269|PubMed:12628924, ECO:0000269|PubMed:12763138, ECO:0000269|PubMed:12773393, ECO:0000269|PubMed:15010469, ECO:0000269|PubMed:18511904, ECO:0000269|PubMed:25851810, ECO:0000269|PubMed:9687510, ECO:0000269|PubMed:9873047}. |
O75676 | RPS6KA4 | S421 | Sugiyama | Ribosomal protein S6 kinase alpha-4 (S6K-alpha-4) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 4) (Nuclear mitogen- and stress-activated protein kinase 2) (Ribosomal protein kinase B) (RSKB) | Serine/threonine-protein kinase that is required for the mitogen or stress-induced phosphorylation of the transcription factors CREB1 and ATF1 and for the regulation of the transcription factor RELA, and that contributes to gene activation by histone phosphorylation and functions in the regulation of inflammatory genes. Phosphorylates CREB1 and ATF1 in response to mitogenic or stress stimuli such as UV-C irradiation, epidermal growth factor (EGF) and anisomycin. Plays an essential role in the control of RELA transcriptional activity in response to TNF. Phosphorylates 'Ser-10' of histone H3 in response to mitogenics, stress stimuli and EGF, which results in the transcriptional activation of several immediate early genes, including proto-oncogenes c-fos/FOS and c-jun/JUN. May also phosphorylate 'Ser-28' of histone H3. Mediates the mitogen- and stress-induced phosphorylation of high mobility group protein 1 (HMGN1/HMG14). In lipopolysaccharide-stimulated primary macrophages, acts downstream of the Toll-like receptor TLR4 to limit the production of pro-inflammatory cytokines. Functions probably by inducing transcription of the MAP kinase phosphatase DUSP1 and the anti-inflammatory cytokine interleukin 10 (IL10), via CREB1 and ATF1 transcription factors. {ECO:0000269|PubMed:11035004, ECO:0000269|PubMed:12773393, ECO:0000269|PubMed:9792677}. |
P68104 | EEF1A1 | S53 | SIGNOR | Elongation factor 1-alpha 1 (EF-1-alpha-1) (EC 3.6.5.-) (Elongation factor Tu) (EF-Tu) (Eukaryotic elongation factor 1 A-1) (eEF1A-1) (Leukocyte receptor cluster member 7) | Translation elongation factor that catalyzes the GTP-dependent binding of aminoacyl-tRNA (aa-tRNA) to the A-site of ribosomes during the elongation phase of protein synthesis (PubMed:26593721, PubMed:26651998, PubMed:36123449, PubMed:36264623, PubMed:36638793). Base pairing between the mRNA codon and the aa-tRNA anticodon promotes GTP hydrolysis, releasing the aa-tRNA from EEF1A1 and allowing its accommodation into the ribosome (PubMed:26593721, PubMed:26651998, PubMed:36123449, PubMed:36264623, PubMed:36638793). The growing protein chain is subsequently transferred from the P-site peptidyl tRNA to the A-site aa-tRNA, extending it by one amino acid through ribosome-catalyzed peptide bond formation (PubMed:26593721, PubMed:26651998, PubMed:36123449, PubMed:36264623). Also plays a role in the positive regulation of IFNG transcription in T-helper 1 cells as part of an IFNG promoter-binding complex with TXK and PARP1 (PubMed:17177976). Also plays a role in cytoskeleton organization by promoting actin bundling (By similarity). {ECO:0000250|UniProtKB:P68105, ECO:0000269|PubMed:17177976, ECO:0000269|PubMed:26593721, ECO:0000269|PubMed:26651998, ECO:0000269|PubMed:36123449, ECO:0000269|PubMed:36264623, ECO:0000269|PubMed:36638793}.; FUNCTION: (Microbial infection) Required for the translation of viral proteins and viral replication during human coronavirus SARS-CoV-2 infection. {ECO:0000269|PubMed:33495306}. |
Q05639 | EEF1A2 | S53 | SIGNOR | Elongation factor 1-alpha 2 (EF-1-alpha-2) (EC 3.6.5.-) (Eukaryotic elongation factor 1 A-2) (eEF1A-2) (Statin-S1) | Translation elongation factor that catalyzes the GTP-dependent binding of aminoacyl-tRNA (aa-tRNA) to the A-site of ribosomes during the elongation phase of protein synthesis. Base pairing between the mRNA codon and the aa-tRNA anticodon promotes GTP hydrolysis, releasing the aa-tRNA from EEF1A1 and allowing its accommodation into the ribosome (By similarity). The growing protein chain is subsequently transferred from the P-site peptidyl tRNA to the A-site aa-tRNA, extending it by one amino acid through ribosome-catalyzed peptide bond formation (By similarity). {ECO:0000250|UniProtKB:P68104, ECO:0000250|UniProtKB:Q71V39}. |
P06493 | CDK1 | S178 | Sugiyama | Cyclin-dependent kinase 1 (CDK1) (EC 2.7.11.22) (EC 2.7.11.23) (Cell division control protein 2 homolog) (Cell division protein kinase 1) (p34 protein kinase) | Plays a key role in the control of the eukaryotic cell cycle by modulating the centrosome cycle as well as mitotic onset; promotes G2-M transition via association with multiple interphase cyclins (PubMed:16407259, PubMed:16933150, PubMed:17459720, PubMed:18356527, PubMed:19509060, PubMed:19917720, PubMed:20171170, PubMed:20935635, PubMed:20937773, PubMed:21063390, PubMed:2188730, PubMed:23355470, PubMed:2344612, PubMed:23601106, PubMed:23602554, PubMed:25556658, PubMed:26829474, PubMed:27814491, PubMed:30139873, PubMed:30704899). Phosphorylates PARVA/actopaxin, APC, AMPH, APC, BARD1, Bcl-xL/BCL2L1, BRCA2, CALD1, CASP8, CDC7, CDC20, CDC25A, CDC25C, CC2D1A, CENPA, CSNK2 proteins/CKII, FZR1/CDH1, CDK7, CEBPB, CHAMP1, DMD/dystrophin, EEF1 proteins/EF-1, EZH2, KIF11/EG5, EGFR, FANCG, FOS, GFAP, GOLGA2/GM130, GRASP1, UBE2A/hHR6A, HIST1H1 proteins/histone H1, HMGA1, HIVEP3/KRC, KAT5, LMNA, LMNB, LBR, MKI67, LATS1, MAP1B, MAP4, MARCKS, MCM2, MCM4, MKLP1, MLST8, MYB, NEFH, NFIC, NPC/nuclear pore complex, PITPNM1/NIR2, NPM1, NCL, NUCKS1, NPM1/numatrin, ORC1, PRKAR2A, EEF1E1/p18, EIF3F/p47, p53/TP53, NONO/p54NRB, PAPOLA, PLEC/plectin, RB1, TPPP, UL40/R2, RAB4A, RAP1GAP, RBBP8/CtIP, RCC1, RPS6KB1/S6K1, KHDRBS1/SAM68, ESPL1, SKI, BIRC5/survivin, STIP1, TEX14, beta-tubulins, MAPT/TAU, NEDD1, VIM/vimentin, TK1, FOXO1, RUNX1/AML1, SAMHD1, SIRT2, CGAS and RUNX2 (PubMed:16407259, PubMed:16933150, PubMed:17459720, PubMed:18356527, PubMed:19202191, PubMed:19509060, PubMed:19917720, PubMed:20171170, PubMed:20935635, PubMed:20937773, PubMed:21063390, PubMed:2188730, PubMed:23355470, PubMed:2344612, PubMed:23601106, PubMed:23602554, PubMed:25012651, PubMed:25556658, PubMed:26829474, PubMed:27814491, PubMed:30704899, PubMed:32351706, PubMed:34741373). CDK1/CDC2-cyclin-B controls pronuclear union in interphase fertilized eggs (PubMed:18480403, PubMed:20360007). Essential for early stages of embryonic development (PubMed:18480403, PubMed:20360007). During G2 and early mitosis, CDC25A/B/C-mediated dephosphorylation activates CDK1/cyclin complexes which phosphorylate several substrates that trigger at least centrosome separation, Golgi dynamics, nuclear envelope breakdown and chromosome condensation (PubMed:18480403, PubMed:20360007, PubMed:2188730, PubMed:2344612, PubMed:30139873). Once chromosomes are condensed and aligned at the metaphase plate, CDK1 activity is switched off by WEE1- and PKMYT1-mediated phosphorylation to allow sister chromatid separation, chromosome decondensation, reformation of the nuclear envelope and cytokinesis (PubMed:18480403, PubMed:20360007). Phosphorylates KRT5 during prometaphase and metaphase (By similarity). Inactivated by PKR/EIF2AK2- and WEE1-mediated phosphorylation upon DNA damage to stop cell cycle and genome replication at the G2 checkpoint thus facilitating DNA repair (PubMed:20360007). Reactivated after successful DNA repair through WIP1-dependent signaling leading to CDC25A/B/C-mediated dephosphorylation and restoring cell cycle progression (PubMed:20395957). Catalyzes lamin (LMNA, LMNB1 and LMNB2) phosphorylation at the onset of mitosis, promoting nuclear envelope breakdown (PubMed:2188730, PubMed:2344612, PubMed:37788673). In proliferating cells, CDK1-mediated FOXO1 phosphorylation at the G2-M phase represses FOXO1 interaction with 14-3-3 proteins and thereby promotes FOXO1 nuclear accumulation and transcription factor activity, leading to cell death of postmitotic neurons (PubMed:18356527). The phosphorylation of beta-tubulins regulates microtubule dynamics during mitosis (PubMed:16371510). NEDD1 phosphorylation promotes PLK1-mediated NEDD1 phosphorylation and subsequent targeting of the gamma-tubulin ring complex (gTuRC) to the centrosome, an important step for spindle formation (PubMed:19509060). In addition, CC2D1A phosphorylation regulates CC2D1A spindle pole localization and association with SCC1/RAD21 and centriole cohesion during mitosis (PubMed:20171170). The phosphorylation of Bcl-xL/BCL2L1 after prolongated G2 arrest upon DNA damage triggers apoptosis (PubMed:19917720). In contrast, CASP8 phosphorylation during mitosis prevents its activation by proteolysis and subsequent apoptosis (PubMed:20937773). This phosphorylation occurs in cancer cell lines, as well as in primary breast tissues and lymphocytes (PubMed:20937773). EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing (PubMed:20935635). CALD1 phosphorylation promotes Schwann cell migration during peripheral nerve regeneration (By similarity). CDK1-cyclin-B complex phosphorylates NCKAP5L and mediates its dissociation from centrosomes during mitosis (PubMed:26549230). Regulates the amplitude of the cyclic expression of the core clock gene BMAL1 by phosphorylating its transcriptional repressor NR1D1, and this phosphorylation is necessary for SCF(FBXW7)-mediated ubiquitination and proteasomal degradation of NR1D1 (PubMed:27238018). Phosphorylates EML3 at 'Thr-881' which is essential for its interaction with HAUS augmin-like complex and TUBG1 (PubMed:30723163). Phosphorylates CGAS during mitosis, leading to its inhibition, thereby preventing CGAS activation by self DNA during mitosis (PubMed:32351706). Phosphorylates SKA3 on multiple sites during mitosis which promotes SKA3 binding to the NDC80 complex and anchoring of the SKA complex to kinetochores, to enable stable attachment of mitotic spindle microtubules to kinetochores (PubMed:28479321, PubMed:31804178, PubMed:32491969). {ECO:0000250|UniProtKB:P11440, ECO:0000250|UniProtKB:P39951, ECO:0000269|PubMed:16371510, ECO:0000269|PubMed:16407259, ECO:0000269|PubMed:16933150, ECO:0000269|PubMed:17459720, ECO:0000269|PubMed:18356527, ECO:0000269|PubMed:18480403, ECO:0000269|PubMed:19202191, ECO:0000269|PubMed:19509060, ECO:0000269|PubMed:19917720, ECO:0000269|PubMed:20171170, ECO:0000269|PubMed:20360007, ECO:0000269|PubMed:20395957, ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:20937773, ECO:0000269|PubMed:21063390, ECO:0000269|PubMed:2188730, ECO:0000269|PubMed:23355470, ECO:0000269|PubMed:2344612, ECO:0000269|PubMed:23601106, ECO:0000269|PubMed:23602554, ECO:0000269|PubMed:25012651, ECO:0000269|PubMed:25556658, ECO:0000269|PubMed:26549230, ECO:0000269|PubMed:26829474, ECO:0000269|PubMed:27238018, ECO:0000269|PubMed:27814491, ECO:0000269|PubMed:28479321, ECO:0000269|PubMed:30139873, ECO:0000269|PubMed:30704899, ECO:0000269|PubMed:30723163, ECO:0000269|PubMed:31804178, ECO:0000269|PubMed:32351706, ECO:0000269|PubMed:32491969, ECO:0000269|PubMed:34741373, ECO:0000269|PubMed:37788673}.; FUNCTION: (Microbial infection) Acts as a receptor for hepatitis C virus (HCV) in hepatocytes and facilitates its cell entry. {ECO:0000269|PubMed:21516087}. |
P16234 | PDGFRA | S601 | Sugiyama | Platelet-derived growth factor receptor alpha (PDGF-R-alpha) (PDGFR-alpha) (EC 2.7.10.1) (Alpha platelet-derived growth factor receptor) (Alpha-type platelet-derived growth factor receptor) (CD140 antigen-like family member A) (CD140a antigen) (Platelet-derived growth factor alpha receptor) (Platelet-derived growth factor receptor 2) (PDGFR-2) (CD antigen CD140a) | Tyrosine-protein kinase that acts as a cell-surface receptor for PDGFA, PDGFB and PDGFC and plays an essential role in the regulation of embryonic development, cell proliferation, survival and chemotaxis. Depending on the context, promotes or inhibits cell proliferation and cell migration. Plays an important role in the differentiation of bone marrow-derived mesenchymal stem cells. Required for normal skeleton development and cephalic closure during embryonic development. Required for normal development of the mucosa lining the gastrointestinal tract, and for recruitment of mesenchymal cells and normal development of intestinal villi. Plays a role in cell migration and chemotaxis in wound healing. Plays a role in platelet activation, secretion of agonists from platelet granules, and in thrombin-induced platelet aggregation. Binding of its cognate ligands - homodimeric PDGFA, homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB or homodimeric PDGFC -leads to the activation of several signaling cascades; the response depends on the nature of the bound ligand and is modulated by the formation of heterodimers between PDGFRA and PDGFRB. Phosphorylates PIK3R1, PLCG1, and PTPN11. Activation of PLCG1 leads to the production of the cellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate, mobilization of cytosolic Ca(2+) and the activation of protein kinase C. Phosphorylates PIK3R1, the regulatory subunit of phosphatidylinositol 3-kinase, and thereby mediates activation of the AKT1 signaling pathway. Mediates activation of HRAS and of the MAP kinases MAPK1/ERK2 and/or MAPK3/ERK1. Promotes activation of STAT family members STAT1, STAT3 and STAT5A and/or STAT5B. Receptor signaling is down-regulated by protein phosphatases that dephosphorylate the receptor and its down-stream effectors, and by rapid internalization of the activated receptor. {ECO:0000269|PubMed:10734113, ECO:0000269|PubMed:10947961, ECO:0000269|PubMed:11297552, ECO:0000269|PubMed:12522257, ECO:0000269|PubMed:1646396, ECO:0000269|PubMed:17087943, ECO:0000269|PubMed:1709159, ECO:0000269|PubMed:17141222, ECO:0000269|PubMed:20972453, ECO:0000269|PubMed:21224473, ECO:0000269|PubMed:21596750, ECO:0000269|PubMed:2554309, ECO:0000269|PubMed:8188664, ECO:0000269|PubMed:8760137, ECO:0000269|PubMed:8943348}. |
P36888 | FLT3 | S618 | Sugiyama | Receptor-type tyrosine-protein kinase FLT3 (EC 2.7.10.1) (FL cytokine receptor) (Fetal liver kinase-2) (FLK-2) (Fms-like tyrosine kinase 3) (FLT-3) (Stem cell tyrosine kinase 1) (STK-1) (CD antigen CD135) | Tyrosine-protein kinase that acts as a cell-surface receptor for the cytokine FLT3LG and regulates differentiation, proliferation and survival of hematopoietic progenitor cells and of dendritic cells. Promotes phosphorylation of SHC1 and AKT1, and activation of the downstream effector MTOR. Promotes activation of RAS signaling and phosphorylation of downstream kinases, including MAPK1/ERK2 and/or MAPK3/ERK1. Promotes phosphorylation of FES, FER, PTPN6/SHP, PTPN11/SHP-2, PLCG1, and STAT5A and/or STAT5B. Activation of wild-type FLT3 causes only marginal activation of STAT5A or STAT5B. Mutations that cause constitutive kinase activity promote cell proliferation and resistance to apoptosis via the activation of multiple signaling pathways. {ECO:0000269|PubMed:10080542, ECO:0000269|PubMed:11090077, ECO:0000269|PubMed:14504097, ECO:0000269|PubMed:16266983, ECO:0000269|PubMed:16627759, ECO:0000269|PubMed:18490735, ECO:0000269|PubMed:20111072, ECO:0000269|PubMed:21067588, ECO:0000269|PubMed:21262971, ECO:0000269|PubMed:21516120, ECO:0000269|PubMed:7507245}. |
P24752 | ACAT1 | S69 | Sugiyama | Acetyl-CoA acetyltransferase, mitochondrial (EC 2.3.1.9) (Acetoacetyl-CoA thiolase) (T2) | This is one of the enzymes that catalyzes the last step of the mitochondrial beta-oxidation pathway, an aerobic process breaking down fatty acids into acetyl-CoA (PubMed:1715688, PubMed:7728148, PubMed:9744475). Using free coenzyme A/CoA, catalyzes the thiolytic cleavage of medium- to long-chain 3-oxoacyl-CoAs into acetyl-CoA and a fatty acyl-CoA shortened by two carbon atoms (PubMed:1715688, PubMed:7728148, PubMed:9744475). The activity of the enzyme is reversible and it can also catalyze the condensation of two acetyl-CoA molecules into acetoacetyl-CoA (PubMed:17371050). Thereby, it plays a major role in ketone body metabolism (PubMed:1715688, PubMed:17371050, PubMed:7728148, PubMed:9744475). {ECO:0000269|PubMed:1715688, ECO:0000269|PubMed:17371050, ECO:0000269|PubMed:7728148, ECO:0000269|PubMed:9744475}. |
Q92626 | PXDN | S1300 | Sugiyama | Peroxidasin homolog (EC 1.11.2.-) (Melanoma-associated antigen MG50) (Peroxidasin 1) (hsPxd01) (Vascular peroxidase 1) (p53-responsive gene 2 protein) [Cleaved into: PXDN active fragment] | Catalyzes the two-electron oxidation of bromide by hydrogen peroxide and generates hypobromite as a reactive intermediate which mediates the formation of sulfilimine cross-links between methionine and hydroxylysine residues within an uncross-linked collagen IV/COL4A1 NC1 hexamer (PubMed:18929642, PubMed:19590037, PubMed:22842973, PubMed:25708780, PubMed:25713063, PubMed:27697841, PubMed:28154175, PubMed:34679700). In turns, directly contributes to the collagen IV network-dependent fibronectin/FN and laminin assembly, which is required for full extracellular matrix (ECM)-mediated signaling (PubMed:19590037, PubMed:32543734, PubMed:34679700). Thus, sulfilimine cross-links are essential for growth factor-induced cell proliferation and survival in endothelial cells, an event essential to basement membrane integrity (PubMed:32543734). In addition, through the bromide oxidation, may promote tubulogenesis and induce angiogenesis through ERK1/2, Akt, and FAK pathways (PubMed:25713063). Moreover brominates alpha2 collagen IV chain/COL4A2 at 'Tyr-1485' and leads to bromine enrichment of the basement membranes (PubMed:32571911). In vitro, can also catalyze the two-electron oxidation of thiocyanate and iodide and these two substrates could effectively compete with bromide and thus inhibit the formation of sulfilimine bonds (PubMed:28154175). Binds laminins (PubMed:32485152). May play a role in the organization of eyeball structure and lens development during eye development (By similarity). {ECO:0000250|UniProtKB:Q3UQ28, ECO:0000269|PubMed:18929642, ECO:0000269|PubMed:19590037, ECO:0000269|PubMed:22842973, ECO:0000269|PubMed:25708780, ECO:0000269|PubMed:25713063, ECO:0000269|PubMed:27697841, ECO:0000269|PubMed:28154175, ECO:0000269|PubMed:32485152, ECO:0000269|PubMed:32543734, ECO:0000269|PubMed:32571911, ECO:0000269|PubMed:34679700}. |
Q9NZV7 | ZIM2 | S158 | Sugiyama | Zinc finger imprinted 2 (Zinc finger protein 656) | May be involved in transcriptional regulation. |
P14866 | HNRNPL | S471 | Sugiyama | Heterogeneous nuclear ribonucleoprotein L (hnRNP L) | Splicing factor binding to exonic or intronic sites and acting as either an activator or repressor of exon inclusion. Exhibits a binding preference for CA-rich elements (PubMed:11809897, PubMed:22570490, PubMed:24164894, PubMed:25623890, PubMed:26051023). Component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes and associated with most nascent transcripts (PubMed:2687284). Associates, together with APEX1, to the negative calcium responsive element (nCaRE) B2 of the APEX2 promoter (PubMed:11809897). As part of a ribonucleoprotein complex composed at least of ZNF827, HNRNPK and the circular RNA circZNF827 that nucleates the complex on chromatin, may negatively regulate the transcription of genes involved in neuronal differentiation (PubMed:33174841). Regulates alternative splicing of a core group of genes involved in neuronal differentiation, likely by mediating H3K36me3-coupled transcription elongation and co-transcriptional RNA processing via interaction with CHD8. {ECO:0000269|PubMed:11809897, ECO:0000269|PubMed:22570490, ECO:0000269|PubMed:25623890, ECO:0000269|PubMed:26051023, ECO:0000269|PubMed:2687284, ECO:0000269|PubMed:33174841, ECO:0000269|PubMed:36537238}. |
Q12952 | FOXL1 | S174 | Sugiyama | Forkhead box protein L1 (Forkhead-related protein FKHL11) (Forkhead-related transcription factor 7) (FREAC-7) | Transcription factor required for proper proliferation and differentiation in the gastrointestinal epithelium. Target gene of the hedgehog (Hh) signaling pathway via GLI2 and GLI3 transcription factors (By similarity). {ECO:0000250}. |
P48736 | PIK3CG | S496 | Sugiyama | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform (PI3-kinase subunit gamma) (PI3K-gamma) (PI3Kgamma) (PtdIns-3-kinase subunit gamma) (EC 2.7.1.137) (EC 2.7.1.153) (EC 2.7.1.154) (Phosphatidylinositol 4,5-bisphosphate 3-kinase 110 kDa catalytic subunit gamma) (PtdIns-3-kinase subunit p110-gamma) (p110gamma) (Phosphoinositide-3-kinase catalytic gamma polypeptide) (Serine/threonine protein kinase PIK3CG) (EC 2.7.11.1) (p120-PI3K) | Phosphoinositide-3-kinase (PI3K) that phosphorylates PtdIns(4,5)P2 (Phosphatidylinositol 4,5-bisphosphate) to generate phosphatidylinositol 3,4,5-trisphosphate (PIP3). PIP3 plays a key role by recruiting PH domain-containing proteins to the membrane, including AKT1 and PDPK1, activating signaling cascades involved in cell growth, survival, proliferation, motility and morphology. Links G-protein coupled receptor activation to PIP3 production. Involved in immune, inflammatory and allergic responses. Modulates leukocyte chemotaxis to inflammatory sites and in response to chemoattractant agents. May control leukocyte polarization and migration by regulating the spatial accumulation of PIP3 and by regulating the organization of F-actin formation and integrin-based adhesion at the leading edge. Controls motility of dendritic cells. Together with PIK3CD is involved in natural killer (NK) cell development and migration towards the sites of inflammation. Participates in T-lymphocyte migration. Regulates T-lymphocyte proliferation, activation, and cytokine production. Together with PIK3CD participates in T-lymphocyte development. Required for B-lymphocyte development and signaling. Together with PIK3CD participates in neutrophil respiratory burst. Together with PIK3CD is involved in neutrophil chemotaxis and extravasation. Together with PIK3CB promotes platelet aggregation and thrombosis. Regulates alpha-IIb/beta-3 integrins (ITGA2B/ ITGB3) adhesive function in platelets downstream of P2Y12 through a lipid kinase activity-independent mechanism. May have also a lipid kinase activity-dependent function in platelet aggregation. Involved in endothelial progenitor cell migration. Negative regulator of cardiac contractility. Modulates cardiac contractility by anchoring protein kinase A (PKA) and PDE3B activation, reducing cAMP levels. Regulates cardiac contractility also by promoting beta-adrenergic receptor internalization by binding to GRK2 and by non-muscle tropomyosin phosphorylation. Also has serine/threonine protein kinase activity: both lipid and protein kinase activities are required for beta-adrenergic receptor endocytosis. May also have a scaffolding role in modulating cardiac contractility. Contributes to cardiac hypertrophy under pathological stress. Through simultaneous binding of PDE3B to RAPGEF3 and PIK3R6 is assembled in a signaling complex in which the PI3K gamma complex is activated by RAPGEF3 and which is involved in angiogenesis. In neutrophils, participates in a phospholipase C-activating N-formyl peptide-activated GPCR (G protein-coupled receptor) signaling pathway downstream of RASGRP4-mediated Ras-activation, to promote neutrophil functional responses (By similarity). {ECO:0000250|UniProtKB:Q9JHG7, ECO:0000269|PubMed:11277933, ECO:0000269|PubMed:12163475, ECO:0000269|PubMed:15135396, ECO:0000269|PubMed:15294162, ECO:0000269|PubMed:16094730, ECO:0000269|PubMed:16123124, ECO:0000269|PubMed:21393242, ECO:0000269|PubMed:31554793, ECO:0000269|PubMed:33054089, ECO:0000269|PubMed:7624799}. |
O60829 | PAGE4 | S79 | EPSD|PSP | P antigen family member 4 (PAGE-4) (G antigen family C member 1) (PAGE-1) | Intrinsically disordered protein that potentiates the transcriptional activator activity of JUN (PubMed:24263171, PubMed:28289210). Protects cells from stress-induced apoptosis by inhibiting reactive oxygen species (ROS) production and via regulation of the MAPK signaling pathway (PubMed:21357425, PubMed:25374899, PubMed:30658679). {ECO:0000269|PubMed:21357425, ECO:0000269|PubMed:24263171, ECO:0000269|PubMed:25374899, ECO:0000269|PubMed:28289210, ECO:0000269|PubMed:30658679}. |
P51812 | RPS6KA3 | S432 | Sugiyama | Ribosomal protein S6 kinase alpha-3 (S6K-alpha-3) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 3) (p90-RSK 3) (p90RSK3) (Insulin-stimulated protein kinase 1) (ISPK-1) (MAP kinase-activated protein kinase 1b) (MAPK-activated protein kinase 1b) (MAPKAP kinase 1b) (MAPKAPK-1b) (Ribosomal S6 kinase 2) (RSK-2) (pp90RSK2) | Serine/threonine-protein kinase that acts downstream of ERK (MAPK1/ERK2 and MAPK3/ERK1) signaling and mediates mitogenic and stress-induced activation of the transcription factors CREB1, ETV1/ER81 and NR4A1/NUR77, regulates translation through RPS6 and EIF4B phosphorylation, and mediates cellular proliferation, survival, and differentiation by modulating mTOR signaling and repressing pro-apoptotic function of BAD and DAPK1 (PubMed:16213824, PubMed:16223362, PubMed:17360704, PubMed:9770464). In fibroblast, is required for EGF-stimulated phosphorylation of CREB1 and histone H3 at 'Ser-10', which results in the subsequent transcriptional activation of several immediate-early genes (PubMed:10436156, PubMed:9770464). In response to mitogenic stimulation (EGF and PMA), phosphorylates and activates NR4A1/NUR77 and ETV1/ER81 transcription factors and the cofactor CREBBP (PubMed:16223362). Upon insulin-derived signal, acts indirectly on the transcription regulation of several genes by phosphorylating GSK3B at 'Ser-9' and inhibiting its activity (PubMed:8250835). Phosphorylates RPS6 in response to serum or EGF via an mTOR-independent mechanism and promotes translation initiation by facilitating assembly of the preinitiation complex (PubMed:17360704). In response to insulin, phosphorylates EIF4B, enhancing EIF4B affinity for the EIF3 complex and stimulating cap-dependent translation (PubMed:18508509, PubMed:18813292). Is involved in the mTOR nutrient-sensing pathway by directly phosphorylating TSC2 at 'Ser-1798', which potently inhibits TSC2 ability to suppress mTOR signaling, and mediates phosphorylation of RPTOR, which regulates mTORC1 activity and may promote rapamycin-sensitive signaling independently of the PI3K/AKT pathway (PubMed:18722121). Mediates cell survival by phosphorylating the pro-apoptotic proteins BAD and DAPK1 and suppressing their pro-apoptotic function (PubMed:16213824). Promotes the survival of hepatic stellate cells by phosphorylating CEBPB in response to the hepatotoxin carbon tetrachloride (CCl4) (PubMed:18508509, PubMed:18813292). Is involved in cell cycle regulation by phosphorylating the CDK inhibitor CDKN1B, which promotes CDKN1B association with 14-3-3 proteins and prevents its translocation to the nucleus and inhibition of G1 progression (By similarity). In LPS-stimulated dendritic cells, is involved in TLR4-induced macropinocytosis, and in myeloma cells, acts as effector of FGFR3-mediated transformation signaling, after direct phosphorylation at Tyr-529 by FGFR3 (By similarity). Negatively regulates EGF-induced MAPK1/3 phosphorylation via phosphorylation of SOS1 (By similarity). Phosphorylates SOS1 at 'Ser-1134' and 'Ser-1161' that create YWHAB and YWHAE binding sites and which contribute to the negative regulation of MAPK1/3 phosphorylation (By similarity). Phosphorylates EPHA2 at 'Ser-897', the RPS6KA-EPHA2 signaling pathway controls cell migration (PubMed:26158630). Acts as a regulator of osteoblast differentiation by mediating phosphorylation of ATF4, thereby promoting ATF4 transactivation activity (By similarity). {ECO:0000250|UniProtKB:P18654, ECO:0000269|PubMed:10436156, ECO:0000269|PubMed:16213824, ECO:0000269|PubMed:16223362, ECO:0000269|PubMed:17360704, ECO:0000269|PubMed:18722121, ECO:0000269|PubMed:26158630, ECO:0000269|PubMed:8250835, ECO:0000269|PubMed:9770464, ECO:0000303|PubMed:18508509, ECO:0000303|PubMed:18813292}. |
Q15349 | RPS6KA2 | S425 | Sugiyama | Ribosomal protein S6 kinase alpha-2 (S6K-alpha-2) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 2) (p90-RSK 2) (p90RSK2) (MAP kinase-activated protein kinase 1c) (MAPK-activated protein kinase 1c) (MAPKAP kinase 1c) (MAPKAPK-1c) (Ribosomal S6 kinase 3) (RSK-3) (pp90RSK3) | Serine/threonine-protein kinase that acts downstream of ERK (MAPK1/ERK2 and MAPK3/ERK1) signaling and mediates mitogenic and stress-induced activation of transcription factors, regulates translation, and mediates cellular proliferation, survival, and differentiation. May function as tumor suppressor in epithelial ovarian cancer cells. {ECO:0000269|PubMed:16878154, ECO:0000269|PubMed:7623830}. |
Q9UK32 | RPS6KA6 | S436 | Sugiyama | Ribosomal protein S6 kinase alpha-6 (S6K-alpha-6) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 6) (p90-RSK 6) (p90RSK6) (Ribosomal S6 kinase 4) (RSK-4) (pp90RSK4) | Constitutively active serine/threonine-protein kinase that exhibits growth-factor-independent kinase activity and that may participate in p53/TP53-dependent cell growth arrest signaling and play an inhibitory role during embryogenesis. {ECO:0000269|PubMed:15042092, ECO:0000269|PubMed:15632195}. |
Q03112 | MECOM | S1037 | SIGNOR | Histone-lysine N-methyltransferase MECOM (EC 2.1.1.367) (Ecotropic virus integration site 1 protein homolog) (EVI-1) (MDS1 and EVI1 complex locus protein) (Myelodysplasia syndrome 1 protein) (Myelodysplasia syndrome-associated protein 1) | [Isoform 1]: Functions as a transcriptional regulator binding to DNA sequences in the promoter region of target genes and regulating positively or negatively their expression. Oncogene which plays a role in development, cell proliferation and differentiation. May also play a role in apoptosis through regulation of the JNK and TGF-beta signaling. Involved in hematopoiesis. {ECO:0000269|PubMed:10856240, ECO:0000269|PubMed:11568182, ECO:0000269|PubMed:15897867, ECO:0000269|PubMed:16462766, ECO:0000269|PubMed:19767769, ECO:0000269|PubMed:9665135}.; FUNCTION: [Isoform 7]: Displays histone methyltransferase activity and monomethylates 'Lys-9' of histone H3 (H3K9me1) in vitro. Probably catalyzes the monomethylation of free histone H3 in the cytoplasm which is then transported to the nucleus and incorporated into nucleosomes where SUV39H methyltransferases use it as a substrate to catalyze histone H3 'Lys-9' trimethylation. Likely to be one of the primary histone methyltransferases along with PRDM16 that direct cytoplasmic H3K9me1 methylation. {ECO:0000250|UniProtKB:P14404}. |
Q00536 | CDK16 | S336 | SIGNOR | Cyclin-dependent kinase 16 (EC 2.7.11.22) (Cell division protein kinase 16) (PCTAIRE-motif protein kinase 1) (Serine/threonine-protein kinase PCTAIRE-1) | Protein kinase that plays a role in vesicle-mediated transport processes and exocytosis. Regulates GH1 release by brain neurons. Phosphorylates NSF, and thereby regulates NSF oligomerization. Required for normal spermatogenesis. Regulates neuron differentiation and dendrite development (By similarity). Plays a role in the regulation of insulin secretion in response to changes in blood glucose levels. Can phosphorylate CCNY at 'Ser-336' (in vitro). {ECO:0000250, ECO:0000269|PubMed:22184064, ECO:0000269|PubMed:22796189, ECO:0000269|PubMed:22798068}. |
Q15139 | PRKD1 | S460 | Sugiyama | Serine/threonine-protein kinase D1 (EC 2.7.11.13) (Protein kinase C mu type) (Protein kinase D) (nPKC-D1) (nPKC-mu) | Serine/threonine-protein kinase that converts transient diacylglycerol (DAG) signals into prolonged physiological effects downstream of PKC, and is involved in the regulation of MAPK8/JNK1 and Ras signaling, Golgi membrane integrity and trafficking, cell survival through NF-kappa-B activation, cell migration, cell differentiation by mediating HDAC7 nuclear export, cell proliferation via MAPK1/3 (ERK1/2) signaling, and plays a role in cardiac hypertrophy, VEGFA-induced angiogenesis, genotoxic-induced apoptosis and flagellin-stimulated inflammatory response (PubMed:10764790, PubMed:12505989, PubMed:12637538, PubMed:17442957, PubMed:18509061, PubMed:19135240, PubMed:19211839). Phosphorylates the epidermal growth factor receptor (EGFR) on dual threonine residues, which leads to the suppression of epidermal growth factor (EGF)-induced MAPK8/JNK1 activation and subsequent JUN phosphorylation (PubMed:10523301). Phosphorylates RIN1, inducing RIN1 binding to 14-3-3 proteins YWHAB, YWHAE and YWHAZ and increased competition with RAF1 for binding to GTP-bound form of Ras proteins (NRAS, HRAS and KRAS). Acts downstream of the heterotrimeric G-protein beta/gamma-subunit complex to maintain the structural integrity of the Golgi membranes, and is required for protein transport along the secretory pathway. In the trans-Golgi network (TGN), regulates the fission of transport vesicles that are on their way to the plasma membrane. May act by activating the lipid kinase phosphatidylinositol 4-kinase beta (PI4KB) at the TGN for the local synthesis of phosphorylated inositol lipids, which induces a sequential production of DAG, phosphatidic acid (PA) and lyso-PA (LPA) that are necessary for membrane fission and generation of specific transport carriers to the cell surface. Under oxidative stress, is phosphorylated at Tyr-463 via SRC-ABL1 and contributes to cell survival by activating IKK complex and subsequent nuclear translocation and activation of NFKB1 (PubMed:12505989). Involved in cell migration by regulating integrin alpha-5/beta-3 recycling and promoting its recruitment in newly forming focal adhesion. In osteoblast differentiation, mediates the bone morphogenetic protein 2 (BMP2)-induced nuclear export of HDAC7, which results in the inhibition of HDAC7 transcriptional repression of RUNX2 (PubMed:18509061). In neurons, plays an important role in neuronal polarity by regulating the biogenesis of TGN-derived dendritic vesicles, and is involved in the maintenance of dendritic arborization and Golgi structure in hippocampal cells. May potentiate mitogenesis induced by the neuropeptide bombesin or vasopressin by mediating an increase in the duration of MAPK1/3 (ERK1/2) signaling, which leads to accumulation of immediate-early gene products including FOS that stimulate cell cycle progression. Plays an important role in the proliferative response induced by low calcium in keratinocytes, through sustained activation of MAPK1/3 (ERK1/2) pathway. Downstream of novel PKC signaling, plays a role in cardiac hypertrophy by phosphorylating HDAC5, which in turn triggers XPO1/CRM1-dependent nuclear export of HDAC5, MEF2A transcriptional activation and induction of downstream target genes that promote myocyte hypertrophy and pathological cardiac remodeling (PubMed:18332134). Mediates cardiac troponin I (TNNI3) phosphorylation at the PKA sites, which results in reduced myofilament calcium sensitivity, and accelerated crossbridge cycling kinetics. The PRKD1-HDAC5 pathway is also involved in angiogenesis by mediating VEGFA-induced specific subset of gene expression, cell migration, and tube formation (PubMed:19211839). In response to VEGFA, is necessary and required for HDAC7 phosphorylation which induces HDAC7 nuclear export and endothelial cell proliferation and migration. During apoptosis induced by cytarabine and other genotoxic agents, PRKD1 is cleaved by caspase-3 at Asp-378, resulting in activation of its kinase function and increased sensitivity of cells to the cytotoxic effects of genotoxic agents (PubMed:10764790). In epithelial cells, is required for transducing flagellin-stimulated inflammatory responses by binding and phosphorylating TLR5, which contributes to MAPK14/p38 activation and production of inflammatory cytokines (PubMed:17442957). Acts as an activator of NLRP3 inflammasome assembly by mediating phosphorylation of NLRP3 (By similarity). May play a role in inflammatory response by mediating activation of NF-kappa-B. May be involved in pain transmission by directly modulating TRPV1 receptor (PubMed:15471852). Plays a role in activated KRAS-mediated stabilization of ZNF304 in colorectal cancer (CRC) cells (PubMed:24623306). Regulates nuclear translocation of transcription factor TFEB in macrophages upon live S.enterica infection (By similarity). {ECO:0000250|UniProtKB:Q62101, ECO:0000269|PubMed:10523301, ECO:0000269|PubMed:10764790, ECO:0000269|PubMed:12505989, ECO:0000269|PubMed:12637538, ECO:0000269|PubMed:15471852, ECO:0000269|PubMed:17442957, ECO:0000269|PubMed:18332134, ECO:0000269|PubMed:18509061, ECO:0000269|PubMed:19135240, ECO:0000269|PubMed:19211839, ECO:0000269|PubMed:24623306}. |
P10636 | MAPT | S622 | SIGNOR | Microtubule-associated protein tau (Neurofibrillary tangle protein) (Paired helical filament-tau) (PHF-tau) | Promotes microtubule assembly and stability, and might be involved in the establishment and maintenance of neuronal polarity (PubMed:21985311). The C-terminus binds axonal microtubules while the N-terminus binds neural plasma membrane components, suggesting that tau functions as a linker protein between both (PubMed:21985311, PubMed:32961270). Axonal polarity is predetermined by TAU/MAPT localization (in the neuronal cell) in the domain of the cell body defined by the centrosome. The short isoforms allow plasticity of the cytoskeleton whereas the longer isoforms may preferentially play a role in its stabilization. {ECO:0000269|PubMed:21985311, ECO:0000269|PubMed:32961270}. |
P62913 | RPL11 | S51 | Sugiyama | Large ribosomal subunit protein uL5 (60S ribosomal protein L11) (CLL-associated antigen KW-12) | Component of the ribosome, a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:19191325, PubMed:32669547). The small ribosomal subunit (SSU) binds messenger RNAs (mRNAs) and translates the encoded message by selecting cognate aminoacyl-transfer RNA (tRNA) molecules (PubMed:19191325, PubMed:32669547). The large subunit (LSU) contains the ribosomal catalytic site termed the peptidyl transferase center (PTC), which catalyzes the formation of peptide bonds, thereby polymerizing the amino acids delivered by tRNAs into a polypeptide chain (PubMed:19191325, PubMed:32669547). The nascent polypeptides leave the ribosome through a tunnel in the LSU and interact with protein factors that function in enzymatic processing, targeting, and the membrane insertion of nascent chains at the exit of the ribosomal tunnel (PubMed:19191325, PubMed:32669547). As part of the 5S RNP/5S ribonucleoprotein particle it is an essential component of the LSU, required for its formation and the maturation of rRNAs (PubMed:12962325, PubMed:19061985, PubMed:24120868). It also couples ribosome biogenesis to p53/TP53 activation. As part of the 5S RNP it accumulates in the nucleoplasm and inhibits MDM2, when ribosome biogenesis is perturbed, mediating the stabilization and the activation of TP53 (PubMed:24120868). Promotes nucleolar location of PML (By similarity). {ECO:0000250|UniProtKB:Q9CXW4, ECO:0000269|PubMed:12962325, ECO:0000269|PubMed:19061985, ECO:0000269|PubMed:19191325, ECO:0000269|PubMed:24120868, ECO:0000269|PubMed:32669547}. |
Q8NBP7 | PCSK9 | S666 | GPS6 | Proprotein convertase subtilisin/kexin type 9 (EC 3.4.21.-) (Neural apoptosis-regulated convertase 1) (NARC-1) (Proprotein convertase 9) (PC9) (Subtilisin/kexin-like protease PC9) | Crucial player in the regulation of plasma cholesterol homeostasis. Binds to low-density lipid receptor family members: low density lipoprotein receptor (LDLR), very low density lipoprotein receptor (VLDLR), apolipoprotein E receptor (LRP1/APOER) and apolipoprotein receptor 2 (LRP8/APOER2), and promotes their degradation in intracellular acidic compartments (PubMed:18039658). Acts via a non-proteolytic mechanism to enhance the degradation of the hepatic LDLR through a clathrin LDLRAP1/ARH-mediated pathway. May prevent the recycling of LDLR from endosomes to the cell surface or direct it to lysosomes for degradation. Can induce ubiquitination of LDLR leading to its subsequent degradation (PubMed:17461796, PubMed:18197702, PubMed:18799458, PubMed:22074827). Inhibits intracellular degradation of APOB via the autophagosome/lysosome pathway in a LDLR-independent manner. Involved in the disposal of non-acetylated intermediates of BACE1 in the early secretory pathway (PubMed:18660751). Inhibits epithelial Na(+) channel (ENaC)-mediated Na(+) absorption by reducing ENaC surface expression primarily by increasing its proteasomal degradation. Regulates neuronal apoptosis via modulation of LRP8/APOER2 levels and related anti-apoptotic signaling pathways. {ECO:0000269|PubMed:17461796, ECO:0000269|PubMed:18039658, ECO:0000269|PubMed:18197702, ECO:0000269|PubMed:18660751, ECO:0000269|PubMed:18799458, ECO:0000269|PubMed:22074827, ECO:0000269|PubMed:22493497, ECO:0000269|PubMed:22580899}. |
O14980 | XPO1 | S690 | Sugiyama | Exportin-1 (Exp1) (Chromosome region maintenance 1 protein homolog) | Mediates the nuclear export of cellular proteins (cargos) bearing a leucine-rich nuclear export signal (NES) and of RNAs. In the nucleus, in association with RANBP3, binds cooperatively to the NES on its target protein and to the GTPase RAN in its active GTP-bound form (Ran-GTP). Docking of this complex to the nuclear pore complex (NPC) is mediated through binding to nucleoporins. Upon transit of a nuclear export complex into the cytoplasm, disassembling of the complex and hydrolysis of Ran-GTP to Ran-GDP (induced by RANBP1 and RANGAP1, respectively) cause release of the cargo from the export receptor. The directionality of nuclear export is thought to be conferred by an asymmetric distribution of the GTP- and GDP-bound forms of Ran between the cytoplasm and nucleus. Involved in U3 snoRNA transport from Cajal bodies to nucleoli. Binds to late precursor U3 snoRNA bearing a TMG cap. {ECO:0000269|PubMed:15574332, ECO:0000269|PubMed:20921223, ECO:0000269|PubMed:9311922, ECO:0000269|PubMed:9323133}.; FUNCTION: (Microbial infection) Mediates the export of unspliced or incompletely spliced RNAs out of the nucleus from different viruses including HIV-1, HTLV-1 and influenza A. Interacts with, and mediates the nuclear export of HIV-1 Rev and HTLV-1 Rex proteins. Involved in HTLV-1 Rex multimerization. {ECO:0000269|PubMed:14612415, ECO:0000269|PubMed:9837918}. |
Q13011 | ECH1 | S240 | Sugiyama | Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial (EC 5.3.3.-) | Isomerization of 3-trans,5-cis-dienoyl-CoA to 2-trans,4-trans-dienoyl-CoA. {ECO:0000250|UniProtKB:Q62651}. |
P49005 | POLD2 | S75 | Sugiyama | DNA polymerase delta subunit 2 (DNA polymerase delta subunit p50) | Accessory component of both the DNA polymerase delta complex and the DNA polymerase zeta complex (PubMed:17317665, PubMed:22801543, PubMed:24449906). As a component of the trimeric and tetrameric DNA polymerase delta complexes (Pol-delta3 and Pol-delta4, respectively), plays a role in high fidelity genome replication, including in lagging strand synthesis, and repair (PubMed:12403614, PubMed:16510448, PubMed:19074196, PubMed:20334433, PubMed:24035200). Pol-delta3 and Pol-delta4 are characterized by the absence or the presence of POLD4. They exhibit differences in catalytic activity. Most notably, Pol-delta3 shows higher proofreading activity than Pol-delta4 (PubMed:19074196, PubMed:20334433). Although both Pol-delta3 and Pol-delta4 process Okazaki fragments in vitro, Pol-delta3 may also be better suited to fulfill this task, exhibiting near-absence of strand displacement activity compared to Pol-delta4 and stalling on encounter with the 5'-blocking oligonucleotides. Pol-delta3 idling process may avoid the formation of a gap, while maintaining a nick that can be readily ligated (PubMed:24035200). Along with DNA polymerase kappa, DNA polymerase delta carries out approximately half of nucleotide excision repair (NER) synthesis following UV irradiation (PubMed:20227374). Under conditions of DNA replication stress, required for the repair of broken replication forks through break-induced replication (BIR) (PubMed:24310611). Involved in the translesion synthesis (TLS) of templates carrying O6-methylguanine or abasic sites performed by Pol-delta4, independently of DNA polymerase zeta (REV3L) or eta (POLH). Facilitates abasic site bypass by DNA polymerase delta by promoting extension from the nucleotide inserted opposite the lesion. Also involved in TLS as a component of the DNA polymerase zeta complex (PubMed:24449906). Along with POLD3, dramatically increases the efficiency and processivity of DNA synthesis of the DNA polymerase zeta complex compared to the minimal zeta complex, consisting of only REV3L and REV7 (PubMed:24449906). {ECO:0000269|PubMed:12403614, ECO:0000269|PubMed:16510448, ECO:0000269|PubMed:19074196, ECO:0000269|PubMed:20227374, ECO:0000269|PubMed:20334433, ECO:0000269|PubMed:24035200, ECO:0000269|PubMed:24310611, ECO:0000269|PubMed:24449906}. |
Download
reactome_id | name | p | -log10_p |
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R-HSA-9022534 | Loss of MECP2 binding ability to 5hmC-DNA | 0.000536 | 3.271 |
R-HSA-9022537 | Loss of MECP2 binding ability to the NCoR/SMRT complex | 0.000349 | 3.458 |
R-HSA-8869496 | TFAP2A acts as a transcriptional repressor during retinoic acid induced cell dif... | 0.000490 | 3.309 |
R-HSA-69478 | G2/M DNA replication checkpoint | 0.000490 | 3.309 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 0.000537 | 3.270 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 0.000556 | 3.255 |
R-HSA-199920 | CREB phosphorylation | 0.000490 | 3.309 |
R-HSA-1362300 | Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL... | 0.000380 | 3.420 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 0.000106 | 3.974 |
R-HSA-422475 | Axon guidance | 0.000573 | 3.242 |
R-HSA-8953897 | Cellular responses to stimuli | 0.000516 | 3.287 |
R-HSA-9613829 | Chaperone Mediated Autophagy | 0.000639 | 3.194 |
R-HSA-69481 | G2/M Checkpoints | 0.000701 | 3.154 |
R-HSA-1253288 | Downregulation of ERBB4 signaling | 0.000874 | 3.059 |
R-HSA-444257 | RSK activation | 0.000874 | 3.059 |
R-HSA-69620 | Cell Cycle Checkpoints | 0.000879 | 3.056 |
R-HSA-1251985 | Nuclear signaling by ERBB4 | 0.001226 | 2.911 |
R-HSA-9675108 | Nervous system development | 0.001257 | 2.901 |
R-HSA-438064 | Post NMDA receptor activation events | 0.001238 | 2.907 |
R-HSA-9824446 | Viral Infection Pathways | 0.001534 | 2.814 |
R-HSA-9665686 | Signaling by ERBB2 TMD/JMD mutants | 0.001690 | 2.772 |
R-HSA-8854214 | TBC/RABGAPs | 0.001749 | 2.757 |
R-HSA-9005895 | Pervasive developmental disorders | 0.002531 | 2.597 |
R-HSA-9697154 | Disorders of Nervous System Development | 0.002531 | 2.597 |
R-HSA-9005891 | Loss of function of MECP2 in Rett syndrome | 0.002531 | 2.597 |
R-HSA-2262752 | Cellular responses to stress | 0.002358 | 2.628 |
R-HSA-437239 | Recycling pathway of L1 | 0.002419 | 2.616 |
R-HSA-69473 | G2/M DNA damage checkpoint | 0.002686 | 2.571 |
R-HSA-9022538 | Loss of MECP2 binding ability to 5mC-DNA | 0.003241 | 2.489 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 0.003283 | 2.484 |
R-HSA-1227990 | Signaling by ERBB2 in Cancer | 0.003245 | 2.489 |
R-HSA-9664565 | Signaling by ERBB2 KD Mutants | 0.002937 | 2.532 |
R-HSA-75035 | Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 0.002999 | 2.523 |
R-HSA-162906 | HIV Infection | 0.003112 | 2.507 |
R-HSA-8863795 | Downregulation of ERBB2 signaling | 0.003245 | 2.489 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 0.003063 | 2.514 |
R-HSA-8847993 | ERBB2 Activates PTK6 Signaling | 0.003517 | 2.454 |
R-HSA-416482 | G alpha (12/13) signalling events | 0.003386 | 2.470 |
R-HSA-1538133 | G0 and Early G1 | 0.003927 | 2.406 |
R-HSA-9022927 | MECP2 regulates transcription of genes involved in GABA signaling | 0.004617 | 2.336 |
R-HSA-6785631 | ERBB2 Regulates Cell Motility | 0.004086 | 2.389 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 0.004301 | 2.366 |
R-HSA-72172 | mRNA Splicing | 0.004647 | 2.333 |
R-HSA-5660489 | MTF1 activates gene expression | 0.004617 | 2.336 |
R-HSA-6804116 | TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 0.004709 | 2.327 |
R-HSA-9018519 | Estrogen-dependent gene expression | 0.004402 | 2.356 |
R-HSA-6791312 | TP53 Regulates Transcription of Cell Cycle Genes | 0.004884 | 2.311 |
R-HSA-1250347 | SHC1 events in ERBB4 signaling | 0.005385 | 2.269 |
R-HSA-9675151 | Disorders of Developmental Biology | 0.005385 | 2.269 |
R-HSA-1963640 | GRB2 events in ERBB2 signaling | 0.005385 | 2.269 |
R-HSA-1640170 | Cell Cycle | 0.005418 | 2.266 |
R-HSA-3371511 | HSF1 activation | 0.006039 | 2.219 |
R-HSA-9022535 | Loss of phosphorylation of MECP2 at T308 | 0.006217 | 2.206 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 0.006924 | 2.160 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 0.006622 | 2.179 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 0.006583 | 2.182 |
R-HSA-70326 | Glucose metabolism | 0.006728 | 2.172 |
R-HSA-168255 | Influenza Infection | 0.006335 | 2.198 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 0.009058 | 2.043 |
R-HSA-3371568 | Attenuation phase | 0.008191 | 2.087 |
R-HSA-156842 | Eukaryotic Translation Elongation | 0.007590 | 2.120 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 0.008191 | 2.087 |
R-HSA-5674499 | Negative feedback regulation of MAPK pathway | 0.008032 | 2.095 |
R-HSA-3214841 | PKMTs methylate histone lysines | 0.008798 | 2.056 |
R-HSA-3371556 | Cellular response to heat stress | 0.007862 | 2.104 |
R-HSA-198753 | ERK/MAPK targets | 0.009622 | 2.017 |
R-HSA-162587 | HIV Life Cycle | 0.009497 | 2.022 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 0.007125 | 2.147 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 0.008073 | 2.093 |
R-HSA-69206 | G1/S Transition | 0.009469 | 2.024 |
R-HSA-5683057 | MAPK family signaling cascades | 0.009013 | 2.045 |
R-HSA-162582 | Signal Transduction | 0.007800 | 2.108 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 0.008622 | 2.064 |
R-HSA-69278 | Cell Cycle, Mitotic | 0.009807 | 2.008 |
R-HSA-3247509 | Chromatin modifying enzymes | 0.010683 | 1.971 |
R-HSA-9702506 | Drug resistance of FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9674415 | Drug resistance of PDGFR mutants | 0.016445 | 1.784 |
R-HSA-9674428 | PDGFR mutants bind TKIs | 0.016445 | 1.784 |
R-HSA-9702509 | FLT3 mutants bind TKIs | 0.016445 | 1.784 |
R-HSA-9703009 | tamatinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702624 | sorafenib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702632 | sunitinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702600 | midostaurin-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702998 | linifanib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9674396 | Imatinib-resistant PDGFR mutants | 0.016445 | 1.784 |
R-HSA-9702596 | lestaurtinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702614 | ponatinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9674404 | Sorafenib-resistant PDGFR mutants | 0.016445 | 1.784 |
R-HSA-9674403 | Regorafenib-resistant PDGFR mutants | 0.016445 | 1.784 |
R-HSA-9702605 | pexidartinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702636 | tandutinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702590 | gilteritinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702577 | semaxanib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702581 | crenolanib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702569 | KW2449-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9702620 | quizartinib-resistant FLT3 mutants | 0.016445 | 1.784 |
R-HSA-9674401 | Sunitinib-resistant PDGFR mutants | 0.016445 | 1.784 |
R-HSA-9022707 | MECP2 regulates transcription factors | 0.012281 | 1.911 |
R-HSA-9726840 | SHOC2 M1731 mutant abolishes MRAS complex function | 0.012281 | 1.911 |
R-HSA-9660537 | Signaling by MRAS-complex mutants | 0.014700 | 1.833 |
R-HSA-9726842 | Gain-of-function MRAS complexes activate RAF signaling | 0.014700 | 1.833 |
R-HSA-428543 | Inactivation of CDC42 and RAC1 | 0.017306 | 1.762 |
R-HSA-1236394 | Signaling by ERBB4 | 0.012473 | 1.904 |
R-HSA-69239 | Synthesis of DNA | 0.015226 | 1.817 |
R-HSA-3371571 | HSF1-dependent transactivation | 0.017467 | 1.758 |
R-HSA-376176 | Signaling by ROBO receptors | 0.012672 | 1.897 |
R-HSA-1257604 | PIP3 activates AKT signaling | 0.017164 | 1.765 |
R-HSA-5673001 | RAF/MAP kinase cascade | 0.015124 | 1.820 |
R-HSA-430116 | GP1b-IX-V activation signalling | 0.017306 | 1.762 |
R-HSA-4839726 | Chromatin organization | 0.015349 | 1.814 |
R-HSA-390696 | Adrenoceptors | 0.014700 | 1.833 |
R-HSA-8939211 | ESR-mediated signaling | 0.011517 | 1.939 |
R-HSA-70171 | Glycolysis | 0.011166 | 1.952 |
R-HSA-5336415 | Uptake and function of diphtheria toxin | 0.012281 | 1.911 |
R-HSA-9834752 | Respiratory syncytial virus genome replication | 0.017306 | 1.762 |
R-HSA-69580 | p53-Dependent G1/S DNA damage checkpoint | 0.015606 | 1.807 |
R-HSA-69563 | p53-Dependent G1 DNA Damage Response | 0.015606 | 1.807 |
R-HSA-70263 | Gluconeogenesis | 0.014725 | 1.832 |
R-HSA-9620244 | Long-term potentiation | 0.015359 | 1.814 |
R-HSA-9679506 | SARS-CoV Infections | 0.016674 | 1.778 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 0.018349 | 1.736 |
R-HSA-174184 | Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 0.018447 | 1.734 |
R-HSA-68949 | Orc1 removal from chromatin | 0.018447 | 1.734 |
R-HSA-9022702 | MECP2 regulates transcription of neuronal ligands | 0.020093 | 1.697 |
R-HSA-176409 | APC/C:Cdc20 mediated degradation of mitotic proteins | 0.021589 | 1.666 |
R-HSA-179419 | APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of th... | 0.019460 | 1.711 |
R-HSA-450282 | MAPK targets/ Nuclear events mediated by MAP kinases | 0.021071 | 1.676 |
R-HSA-9006925 | Intracellular signaling by second messengers | 0.018879 | 1.724 |
R-HSA-9820962 | Assembly and release of respiratory syncytial virus (RSV) virions | 0.020093 | 1.697 |
R-HSA-2559583 | Cellular Senescence | 0.019052 | 1.720 |
R-HSA-1643685 | Disease | 0.019705 | 1.705 |
R-HSA-69242 | S Phase | 0.021881 | 1.660 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 0.021881 | 1.660 |
R-HSA-69275 | G2/M Transition | 0.022245 | 1.653 |
R-HSA-373760 | L1CAM interactions | 0.022336 | 1.651 |
R-HSA-1250196 | SHC1 events in ERBB2 signaling | 0.022657 | 1.645 |
R-HSA-176814 | Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 0.022704 | 1.644 |
R-HSA-193648 | NRAGE signals death through JNK | 0.022704 | 1.644 |
R-HSA-9007101 | Rab regulation of trafficking | 0.023076 | 1.637 |
R-HSA-9679191 | Potential therapeutics for SARS | 0.023157 | 1.635 |
R-HSA-453274 | Mitotic G2-G2/M phases | 0.023389 | 1.631 |
R-HSA-156902 | Peptide chain elongation | 0.023742 | 1.624 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 0.023833 | 1.623 |
R-HSA-1250342 | PI3K events in ERBB4 signaling | 0.026181 | 1.582 |
R-HSA-69190 | DNA strand elongation | 0.026019 | 1.585 |
R-HSA-397795 | G-protein beta:gamma signalling | 0.027794 | 1.556 |
R-HSA-442742 | CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 0.027794 | 1.556 |
R-HSA-1227986 | Signaling by ERBB2 | 0.027514 | 1.560 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 0.024607 | 1.609 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 0.024607 | 1.609 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 0.027027 | 1.568 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 0.027027 | 1.568 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 0.026568 | 1.576 |
R-HSA-162909 | Host Interactions of HIV factors | 0.028725 | 1.542 |
R-HSA-2173795 | Downregulation of SMAD2/3:SMAD4 transcriptional activity | 0.026019 | 1.585 |
R-HSA-450294 | MAP kinase activation | 0.028804 | 1.541 |
R-HSA-69109 | Leading Strand Synthesis | 0.029470 | 1.531 |
R-HSA-69091 | Polymerase switching | 0.029470 | 1.531 |
R-HSA-3000484 | Scavenging by Class F Receptors | 0.029470 | 1.531 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 0.030130 | 1.521 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 0.030708 | 1.513 |
R-HSA-69615 | G1/S DNA Damage Checkpoints | 0.031491 | 1.502 |
R-HSA-180746 | Nuclear import of Rev protein | 0.031534 | 1.501 |
R-HSA-9692912 | SARS-CoV-1 targets PDZ proteins in cell-cell junction | 0.032620 | 1.487 |
R-HSA-5602566 | TICAM1 deficiency - HSE | 0.032620 | 1.487 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 0.032910 | 1.483 |
R-HSA-1475029 | Reversible hydration of carbon dioxide | 0.032913 | 1.483 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 0.033498 | 1.475 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 0.037612 | 1.425 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 0.039762 | 1.401 |
R-HSA-399954 | Sema3A PAK dependent Axon repulsion | 0.040243 | 1.395 |
R-HSA-5689896 | Ovarian tumor domain proteases | 0.037612 | 1.425 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 0.039321 | 1.405 |
R-HSA-446353 | Cell-extracellular matrix interactions | 0.040243 | 1.395 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 0.035218 | 1.453 |
R-HSA-9933939 | Formation of the polybromo-BAF (pBAF) complex | 0.036506 | 1.438 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 0.037604 | 1.425 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 0.041324 | 1.384 |
R-HSA-5663205 | Infectious disease | 0.039302 | 1.406 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 0.041972 | 1.377 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 0.041972 | 1.377 |
R-HSA-9820965 | Respiratory syncytial virus (RSV) genome replication, transcription and translat... | 0.041972 | 1.377 |
R-HSA-448424 | Interleukin-17 signaling | 0.042020 | 1.377 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 0.042020 | 1.377 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 0.043668 | 1.360 |
R-HSA-453276 | Regulation of mitotic cell cycle | 0.043668 | 1.360 |
R-HSA-5609974 | Defective PGM1 causes PGM1-CDG | 0.048530 | 1.314 |
R-HSA-5602571 | TRAF3 deficiency - HSE | 0.048530 | 1.314 |
R-HSA-5619056 | Defective HK1 causes hexokinase deficiency (HK deficiency) | 0.048530 | 1.314 |
R-HSA-9915355 | Beta-ketothiolase deficiency | 0.048530 | 1.314 |
R-HSA-5674404 | PTEN Loss of Function in Cancer | 0.048530 | 1.314 |
R-HSA-4085023 | Defective GFPT1 causes CMSTA1 | 0.048530 | 1.314 |
R-HSA-354194 | GRB2:SOS provides linkage to MAPK signaling for Integrins | 0.044116 | 1.355 |
R-HSA-77595 | Processing of Intronless Pre-mRNAs | 0.048122 | 1.318 |
R-HSA-9912633 | Antigen processing: Ub, ATP-independent proteasomal degradation | 0.048122 | 1.318 |
R-HSA-372708 | p130Cas linkage to MAPK signaling for integrins | 0.052255 | 1.282 |
R-HSA-5651801 | PCNA-Dependent Long Patch Base Excision Repair | 0.056509 | 1.248 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 0.044243 | 1.354 |
R-HSA-9656223 | Signaling by RAF1 mutants | 0.048965 | 1.310 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 0.051056 | 1.292 |
R-HSA-9948299 | Ribosome-associated quality control | 0.046023 | 1.337 |
R-HSA-5674135 | MAP2K and MAPK activation | 0.048965 | 1.310 |
R-HSA-3928662 | EPHB-mediated forward signaling | 0.056489 | 1.248 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 0.051056 | 1.292 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 0.045351 | 1.343 |
R-HSA-187577 | SCF(Skp2)-mediated degradation of p27/p21 | 0.056489 | 1.248 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 0.049600 | 1.305 |
R-HSA-6807070 | PTEN Regulation | 0.047205 | 1.326 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 0.054045 | 1.267 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 0.046761 | 1.330 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 0.054045 | 1.267 |
R-HSA-9636667 | Manipulation of host energy metabolism | 0.048530 | 1.314 |
R-HSA-168315 | Inhibition of Host mRNA Processing and RNA Silencing | 0.048530 | 1.314 |
R-HSA-69052 | Switching of origins to a post-replicative state | 0.047071 | 1.327 |
R-HSA-9700206 | Signaling by ALK in cancer | 0.049600 | 1.305 |
R-HSA-5260271 | Diseases of Immune System | 0.044243 | 1.354 |
R-HSA-5602358 | Diseases associated with the TLR signaling cascade | 0.044243 | 1.354 |
R-HSA-68882 | Mitotic Anaphase | 0.044860 | 1.348 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 0.045774 | 1.339 |
R-HSA-1963642 | PI3K events in ERBB2 signaling | 0.052255 | 1.282 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 0.051056 | 1.292 |
R-HSA-8953854 | Metabolism of RNA | 0.048821 | 1.311 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 0.058488 | 1.233 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 0.052538 | 1.280 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 0.056585 | 1.247 |
R-HSA-1500931 | Cell-Cell communication | 0.055597 | 1.255 |
R-HSA-73933 | Resolution of Abasic Sites (AP sites) | 0.046575 | 1.332 |
R-HSA-8864260 | Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 0.056489 | 1.248 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 0.048168 | 1.317 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 0.047071 | 1.327 |
R-HSA-9926550 | Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adh... | 0.056509 | 1.248 |
R-HSA-5660526 | Response to metal ions | 0.048122 | 1.318 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 0.058713 | 1.231 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 0.059112 | 1.228 |
R-HSA-9833482 | PKR-mediated signaling | 0.060107 | 1.221 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 0.060320 | 1.220 |
R-HSA-881907 | Gastrin-CREB signalling pathway via PKC and MAPK | 0.060880 | 1.216 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 0.061791 | 1.209 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 0.061791 | 1.209 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 0.061791 | 1.209 |
R-HSA-6802949 | Signaling by RAS mutants | 0.061791 | 1.209 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 0.061791 | 1.209 |
R-HSA-75153 | Apoptotic execution phase | 0.061791 | 1.209 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 0.062111 | 1.207 |
R-HSA-446728 | Cell junction organization | 0.062518 | 1.204 |
R-HSA-168898 | Toll-like Receptor Cascades | 0.062649 | 1.203 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 0.063606 | 1.197 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 0.064149 | 1.193 |
R-HSA-9665230 | Drug resistance in ERBB2 KD mutants | 0.064179 | 1.193 |
R-HSA-9652282 | Drug-mediated inhibition of ERBB2 signaling | 0.064179 | 1.193 |
R-HSA-8985801 | Regulation of cortical dendrite branching | 0.064179 | 1.193 |
R-HSA-9665246 | Resistance of ERBB2 KD mutants to neratinib | 0.064179 | 1.193 |
R-HSA-9665251 | Resistance of ERBB2 KD mutants to lapatinib | 0.064179 | 1.193 |
R-HSA-9665233 | Resistance of ERBB2 KD mutants to trastuzumab | 0.064179 | 1.193 |
R-HSA-9665249 | Resistance of ERBB2 KD mutants to afatinib | 0.064179 | 1.193 |
R-HSA-9665245 | Resistance of ERBB2 KD mutants to tesevatinib | 0.064179 | 1.193 |
R-HSA-9665247 | Resistance of ERBB2 KD mutants to osimertinib | 0.064179 | 1.193 |
R-HSA-9665737 | Drug resistance in ERBB2 TMD/JMD mutants | 0.064179 | 1.193 |
R-HSA-9665250 | Resistance of ERBB2 KD mutants to AEE788 | 0.064179 | 1.193 |
R-HSA-9665244 | Resistance of ERBB2 KD mutants to sapitinib | 0.064179 | 1.193 |
R-HSA-5619104 | Defective SLC12A1 causes Bartter syndrome 1 (BS1) | 0.064179 | 1.193 |
R-HSA-6811440 | Retrograde transport at the Trans-Golgi-Network | 0.064526 | 1.190 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 0.064928 | 1.188 |
R-HSA-72613 | Eukaryotic Translation Initiation | 0.066992 | 1.174 |
R-HSA-72737 | Cap-dependent Translation Initiation | 0.066992 | 1.174 |
R-HSA-69306 | DNA Replication | 0.067196 | 1.173 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 0.067196 | 1.173 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 0.067316 | 1.172 |
R-HSA-9725371 | Nuclear events stimulated by ALK signaling in cancer | 0.067316 | 1.172 |
R-HSA-209563 | Axonal growth stimulation | 0.079572 | 1.099 |
R-HSA-9673766 | Signaling by cytosolic PDGFRA and PDGFRB fusion proteins | 0.079572 | 1.099 |
R-HSA-9706374 | FLT3 signaling through SRC family kinases | 0.094713 | 1.024 |
R-HSA-9013957 | TLR3-mediated TICAM1-dependent programmed cell death | 0.094713 | 1.024 |
R-HSA-5602498 | MyD88 deficiency (TLR2/4) | 0.069951 | 1.155 |
R-HSA-5696397 | Gap-filling DNA repair synthesis and ligation in GG-NER | 0.074642 | 1.127 |
R-HSA-5603041 | IRAK4 deficiency (TLR2/4) | 0.074642 | 1.127 |
R-HSA-350054 | Notch-HLH transcription pathway | 0.079430 | 1.100 |
R-HSA-9022699 | MECP2 regulates neuronal receptors and channels | 0.099471 | 1.002 |
R-HSA-9954714 | PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | 0.086414 | 1.063 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 0.088823 | 1.051 |
R-HSA-9954716 | ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ri... | 0.098778 | 1.005 |
R-HSA-8948751 | Regulation of PTEN stability and activity | 0.082066 | 1.086 |
R-HSA-9671555 | Signaling by PDGFR in disease | 0.074642 | 1.127 |
R-HSA-69186 | Lagging Strand Synthesis | 0.069951 | 1.155 |
R-HSA-110314 | Recognition of DNA damage by PCNA-containing replication complex | 0.089281 | 1.049 |
R-HSA-174411 | Polymerase switching on the C-strand of the telomere | 0.094336 | 1.025 |
R-HSA-2682334 | EPH-Ephrin signaling | 0.091264 | 1.040 |
R-HSA-2995383 | Initiation of Nuclear Envelope (NE) Reformation | 0.074642 | 1.127 |
R-HSA-72764 | Eukaryotic Translation Termination | 0.101345 | 0.994 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 0.068330 | 1.165 |
R-HSA-9705677 | SARS-CoV-2 targets PDZ proteins in cell-cell junction | 0.094713 | 1.024 |
R-HSA-165181 | Inhibition of TSC complex formation by PKB | 0.094713 | 1.024 |
R-HSA-75067 | Processing of Capped Intronless Pre-mRNA | 0.089281 | 1.049 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 0.085170 | 1.070 |
R-HSA-9764561 | Regulation of CDH1 Function | 0.094775 | 1.023 |
R-HSA-69895 | Transcriptional activation of cell cycle inhibitor p21 | 0.094713 | 1.024 |
R-HSA-69560 | Transcriptional activation of p53 responsive genes | 0.094713 | 1.024 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 0.094775 | 1.023 |
R-HSA-5621575 | CD209 (DC-SIGN) signaling | 0.089281 | 1.049 |
R-HSA-199991 | Membrane Trafficking | 0.093054 | 1.031 |
R-HSA-110373 | Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 0.099471 | 1.002 |
R-HSA-8964038 | LDL clearance | 0.079430 | 1.100 |
R-HSA-9766229 | Degradation of CDH1 | 0.070161 | 1.154 |
R-HSA-1236974 | ER-Phagosome pathway | 0.081693 | 1.088 |
R-HSA-114608 | Platelet degranulation | 0.089358 | 1.049 |
R-HSA-5693538 | Homology Directed Repair | 0.070476 | 1.152 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 0.094336 | 1.025 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 0.094336 | 1.025 |
R-HSA-3214842 | HDMs demethylate histones | 0.094336 | 1.025 |
R-HSA-74160 | Gene expression (Transcription) | 0.084349 | 1.074 |
R-HSA-2173788 | Downregulation of TGF-beta receptor signaling | 0.079430 | 1.100 |
R-HSA-9837999 | Mitochondrial protein degradation | 0.096242 | 1.017 |
R-HSA-9634638 | Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 0.084311 | 1.074 |
R-HSA-8876198 | RAB GEFs exchange GTP for GDP on RABs | 0.072649 | 1.139 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 0.079615 | 1.099 |
R-HSA-5688426 | Deubiquitination | 0.089795 | 1.047 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 0.091525 | 1.038 |
R-HSA-913531 | Interferon Signaling | 0.075925 | 1.120 |
R-HSA-109581 | Apoptosis | 0.081235 | 1.090 |
R-HSA-70268 | Pyruvate metabolism | 0.077104 | 1.113 |
R-HSA-73887 | Death Receptor Signaling | 0.068681 | 1.163 |
R-HSA-5357801 | Programmed Cell Death | 0.083102 | 1.080 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 0.070473 | 1.152 |
R-HSA-9830364 | Formation of the nephric duct | 0.094336 | 1.025 |
R-HSA-381038 | XBP1(S) activates chaperone genes | 0.074860 | 1.126 |
R-HSA-381070 | IRE1alpha activates chaperones | 0.088823 | 1.051 |
R-HSA-180786 | Extension of Telomeres | 0.101413 | 0.994 |
R-HSA-9909396 | Circadian clock | 0.101827 | 0.992 |
R-HSA-1266738 | Developmental Biology | 0.101951 | 0.992 |
R-HSA-389357 | CD28 dependent PI3K/Akt signaling | 0.104682 | 0.980 |
R-HSA-9841251 | Mitochondrial unfolded protein response (UPRmt) | 0.104682 | 0.980 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 0.104801 | 0.980 |
R-HSA-8873719 | RAB geranylgeranylation | 0.104801 | 0.980 |
R-HSA-9678108 | SARS-CoV-1 Infection | 0.106071 | 0.974 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 0.106571 | 0.972 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 0.106571 | 0.972 |
R-HSA-9793380 | Formation of paraxial mesoderm | 0.108233 | 0.966 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 0.109229 | 0.962 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 0.109229 | 0.962 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 0.109229 | 0.962 |
R-HSA-68911 | G2 Phase | 0.109605 | 0.960 |
R-HSA-9706377 | FLT3 signaling by CBL mutants | 0.109605 | 0.960 |
R-HSA-9833576 | CDH11 homotypic and heterotypic interactions | 0.124254 | 0.906 |
R-HSA-8985586 | SLIT2:ROBO1 increases RHOA activity | 0.124254 | 0.906 |
R-HSA-9645135 | STAT5 Activation | 0.138662 | 0.858 |
R-HSA-113507 | E2F-enabled inhibition of pre-replication complex formation | 0.138662 | 0.858 |
R-HSA-4411364 | Binding of TCF/LEF:CTNNB1 to target gene promoters | 0.152834 | 0.816 |
R-HSA-428890 | Role of ABL in ROBO-SLIT signaling | 0.152834 | 0.816 |
R-HSA-8948747 | Regulation of PTEN localization | 0.152834 | 0.816 |
R-HSA-2562578 | TRIF-mediated programmed cell death | 0.152834 | 0.816 |
R-HSA-9732724 | IFNG signaling activates MAPKs | 0.152834 | 0.816 |
R-HSA-9828211 | Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | 0.166774 | 0.778 |
R-HSA-9613354 | Lipophagy | 0.180486 | 0.744 |
R-HSA-9700645 | ALK mutants bind TKIs | 0.180486 | 0.744 |
R-HSA-9014325 | TICAM1,TRAF6-dependent induction of TAK1 complex | 0.193972 | 0.712 |
R-HSA-164843 | 2-LTR circle formation | 0.193972 | 0.712 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 0.120736 | 0.918 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 0.126215 | 0.899 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 0.126215 | 0.899 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 0.137343 | 0.862 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 0.137343 | 0.862 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 0.142986 | 0.845 |
R-HSA-9843970 | Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | 0.148677 | 0.828 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 0.122382 | 0.912 |
R-HSA-192823 | Viral mRNA Translation | 0.122956 | 0.910 |
R-HSA-1799339 | SRP-dependent cotranslational protein targeting to membrane | 0.137377 | 0.862 |
R-HSA-141424 | Amplification of signal from the kinetochores | 0.205666 | 0.687 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 0.205666 | 0.687 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 0.218490 | 0.661 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 0.188857 | 0.724 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 0.133413 | 0.875 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 0.204389 | 0.690 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 0.204389 | 0.690 |
R-HSA-6802957 | Oncogenic MAPK signaling | 0.201431 | 0.696 |
R-HSA-5656169 | Termination of translesion DNA synthesis | 0.115318 | 0.938 |
R-HSA-110313 | Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA templa... | 0.189617 | 0.722 |
R-HSA-140342 | Apoptosis induced DNA fragmentation | 0.193972 | 0.712 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 0.152444 | 0.817 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 0.204389 | 0.690 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 0.209922 | 0.678 |
R-HSA-9762292 | Regulation of CDH11 function | 0.193972 | 0.712 |
R-HSA-8876493 | InlA-mediated entry of Listeria monocytogenes into host cells | 0.207238 | 0.684 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 0.152444 | 0.817 |
R-HSA-174417 | Telomere C-strand (Lagging Strand) Synthesis | 0.195589 | 0.709 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 0.177751 | 0.750 |
R-HSA-5673000 | RAF activation | 0.148677 | 0.828 |
R-HSA-9735869 | SARS-CoV-1 modulates host translation machinery | 0.148677 | 0.828 |
R-HSA-5696400 | Dual Incision in GG-NER | 0.148677 | 0.828 |
R-HSA-354192 | Integrin signaling | 0.137343 | 0.862 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 0.159509 | 0.797 |
R-HSA-8937144 | Aryl hydrocarbon receptor signalling | 0.124254 | 0.906 |
R-HSA-8951430 | RUNX3 regulates WNT signaling | 0.152834 | 0.816 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 0.120736 | 0.918 |
R-HSA-76009 | Platelet Aggregation (Plug Formation) | 0.219690 | 0.658 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 0.132161 | 0.879 |
R-HSA-9907900 | Proteasome assembly | 0.213638 | 0.670 |
R-HSA-176417 | Phosphorylation of Emi1 | 0.124254 | 0.906 |
R-HSA-114516 | Disinhibition of SNARE formation | 0.152834 | 0.816 |
R-HSA-446107 | Type I hemidesmosome assembly | 0.166774 | 0.778 |
R-HSA-9927354 | Co-stimulation by ICOS | 0.166774 | 0.778 |
R-HSA-193697 | p75NTR regulates axonogenesis | 0.180486 | 0.744 |
R-HSA-176974 | Unwinding of DNA | 0.180486 | 0.744 |
R-HSA-192905 | vRNP Assembly | 0.207238 | 0.684 |
R-HSA-162588 | Budding and maturation of HIV virion | 0.126215 | 0.899 |
R-HSA-211733 | Regulation of activated PAK-2p34 by proteasome mediated degradation | 0.126215 | 0.899 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 0.166010 | 0.780 |
R-HSA-9707616 | Heme signaling | 0.111708 | 0.952 |
R-HSA-73886 | Chromosome Maintenance | 0.187609 | 0.727 |
R-HSA-5218920 | VEGFR2 mediated vascular permeability | 0.189617 | 0.722 |
R-HSA-176187 | Activation of ATR in response to replication stress | 0.137343 | 0.862 |
R-HSA-212165 | Epigenetic regulation of gene expression | 0.212350 | 0.673 |
R-HSA-428542 | Regulation of commissural axon pathfinding by SLIT and ROBO | 0.180486 | 0.744 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 0.142986 | 0.845 |
R-HSA-68877 | Mitotic Prometaphase | 0.143078 | 0.844 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 0.187609 | 0.727 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 0.124410 | 0.905 |
R-HSA-2467813 | Separation of Sister Chromatids | 0.186771 | 0.729 |
R-HSA-72766 | Translation | 0.216687 | 0.664 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 0.166010 | 0.780 |
R-HSA-5675221 | Negative regulation of MAPK pathway | 0.195589 | 0.709 |
R-HSA-187706 | Signalling to p38 via RIT and RIN | 0.124254 | 0.906 |
R-HSA-193634 | Axonal growth inhibition (RHOA activation) | 0.166774 | 0.778 |
R-HSA-170984 | ARMS-mediated activation | 0.180486 | 0.744 |
R-HSA-77108 | Utilization of Ketone Bodies | 0.207238 | 0.684 |
R-HSA-9706019 | RHOBTB3 ATPase cycle | 0.207238 | 0.684 |
R-HSA-350562 | Regulation of ornithine decarboxylase (ODC) | 0.131752 | 0.880 |
R-HSA-8854050 | FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 0.154414 | 0.811 |
R-HSA-174113 | SCF-beta-TrCP mediated degradation of Emi1 | 0.154414 | 0.811 |
R-HSA-9932298 | Degradation of CRY and PER proteins | 0.195589 | 0.709 |
R-HSA-5610780 | Degradation of GLI1 by the proteasome | 0.195589 | 0.709 |
R-HSA-373752 | Netrin-1 signaling | 0.213638 | 0.670 |
R-HSA-68886 | M Phase | 0.136072 | 0.866 |
R-HSA-5653656 | Vesicle-mediated transport | 0.149326 | 0.826 |
R-HSA-68875 | Mitotic Prophase | 0.184308 | 0.734 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 0.180592 | 0.743 |
R-HSA-450520 | HuR (ELAVL1) binds and stabilizes mRNA | 0.180486 | 0.744 |
R-HSA-4641258 | Degradation of DVL | 0.166010 | 0.780 |
R-HSA-1236978 | Cross-presentation of soluble exogenous antigens (endosomes) | 0.177751 | 0.750 |
R-HSA-2408557 | Selenocysteine synthesis | 0.117379 | 0.930 |
R-HSA-977225 | Amyloid fiber formation | 0.184712 | 0.734 |
R-HSA-195253 | Degradation of beta-catenin by the destruction complex | 0.140952 | 0.851 |
R-HSA-2980767 | Activation of NIMA Kinases NEK9, NEK6, NEK7 | 0.138662 | 0.858 |
R-HSA-426117 | Cation-coupled Chloride cotransporters | 0.152834 | 0.816 |
R-HSA-2465910 | MASTL Facilitates Mitotic Progression | 0.180486 | 0.744 |
R-HSA-110056 | MAPK3 (ERK1) activation | 0.193972 | 0.712 |
R-HSA-450408 | AUF1 (hnRNP D0) binds and destabilizes mRNA | 0.160192 | 0.795 |
R-HSA-180585 | Vif-mediated degradation of APOBEC3G | 0.160192 | 0.795 |
R-HSA-4641257 | Degradation of AXIN | 0.166010 | 0.780 |
R-HSA-9762114 | GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 0.166010 | 0.780 |
R-HSA-8964043 | Plasma lipoprotein clearance | 0.177751 | 0.750 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 0.183670 | 0.736 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 0.189617 | 0.722 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 0.125786 | 0.900 |
R-HSA-9612973 | Autophagy | 0.164825 | 0.783 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 0.137594 | 0.861 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 0.218539 | 0.660 |
R-HSA-73857 | RNA Polymerase II Transcription | 0.116334 | 0.934 |
R-HSA-446388 | Regulation of cytoskeletal remodeling and cell spreading by IPP complex componen... | 0.124254 | 0.906 |
R-HSA-9764302 | Regulation of CDH19 Expression and Function | 0.124254 | 0.906 |
R-HSA-8939243 | RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not kno... | 0.137343 | 0.862 |
R-HSA-180534 | Vpu mediated degradation of CD4 | 0.142986 | 0.845 |
R-HSA-349425 | Autodegradation of the E3 ubiquitin ligase COP1 | 0.148677 | 0.828 |
R-HSA-75815 | Ubiquitin-dependent degradation of Cyclin D | 0.148677 | 0.828 |
R-HSA-169911 | Regulation of Apoptosis | 0.154414 | 0.811 |
R-HSA-5610783 | Degradation of GLI2 by the proteasome | 0.195589 | 0.709 |
R-HSA-5610785 | GLI3 is processed to GLI3R by the proteasome | 0.195589 | 0.709 |
R-HSA-1236975 | Antigen processing-Cross presentation | 0.140341 | 0.853 |
R-HSA-1483249 | Inositol phosphate metabolism | 0.152444 | 0.817 |
R-HSA-212436 | Generic Transcription Pathway | 0.179769 | 0.745 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 0.120154 | 0.920 |
R-HSA-9604323 | Negative regulation of NOTCH4 signaling | 0.183670 | 0.736 |
R-HSA-9929491 | SPOP-mediated proteasomal degradation of PD-L1(CD274) | 0.189617 | 0.722 |
R-HSA-5362768 | Hh mutants are degraded by ERAD | 0.189617 | 0.722 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 0.215583 | 0.666 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 0.215583 | 0.666 |
R-HSA-1660499 | Synthesis of PIPs at the plasma membrane | 0.111708 | 0.952 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 0.214663 | 0.668 |
R-HSA-2892245 | POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | 0.152834 | 0.816 |
R-HSA-9929356 | GSK3B-mediated proteasomal degradation of PD-L1(CD274) | 0.177751 | 0.750 |
R-HSA-5387390 | Hh mutants abrogate ligand secretion | 0.207602 | 0.683 |
R-HSA-4608870 | Asymmetric localization of PCP proteins | 0.219690 | 0.658 |
R-HSA-1592230 | Mitochondrial biogenesis | 0.174525 | 0.758 |
R-HSA-2173789 | TGF-beta receptor signaling activates SMADs | 0.207602 | 0.683 |
R-HSA-3214858 | RMTs methylate histone arginines | 0.213638 | 0.670 |
R-HSA-110357 | Displacement of DNA glycosylase by APEX1 | 0.152834 | 0.816 |
R-HSA-5609975 | Diseases associated with glycosylation precursor biosynthesis | 0.137343 | 0.862 |
R-HSA-5678895 | Defective CFTR causes cystic fibrosis | 0.219690 | 0.658 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 0.148631 | 0.828 |
R-HSA-1169408 | ISG15 antiviral mechanism | 0.160395 | 0.795 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 0.184712 | 0.734 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 0.148631 | 0.828 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 0.209922 | 0.678 |
R-HSA-8941858 | Regulation of RUNX3 expression and activity | 0.183670 | 0.736 |
R-HSA-5676590 | NIK-->noncanonical NF-kB signaling | 0.189617 | 0.722 |
R-HSA-5607761 | Dectin-1 mediated noncanonical NF-kB signaling | 0.219690 | 0.658 |
R-HSA-446652 | Interleukin-1 family signaling | 0.154265 | 0.812 |
R-HSA-9006936 | Signaling by TGFB family members | 0.175666 | 0.755 |
R-HSA-264870 | Caspase-mediated cleavage of cytoskeletal proteins | 0.180486 | 0.744 |
R-HSA-9013694 | Signaling by NOTCH4 | 0.156442 | 0.806 |
R-HSA-5689880 | Ub-specific processing proteases | 0.215583 | 0.666 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 0.204547 | 0.689 |
R-HSA-69613 | p53-Independent G1/S DNA Damage Checkpoint | 0.219690 | 0.658 |
R-HSA-69601 | Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | 0.219690 | 0.658 |
R-HSA-375280 | Amine ligand-binding receptors | 0.213638 | 0.670 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 0.112841 | 0.948 |
R-HSA-5632684 | Hedgehog 'on' state | 0.144775 | 0.839 |
R-HSA-112315 | Transmission across Chemical Synapses | 0.212350 | 0.673 |
R-HSA-373755 | Semaphorin interactions | 0.115225 | 0.938 |
R-HSA-9008059 | Interleukin-37 signaling | 0.120736 | 0.918 |
R-HSA-69205 | G1/S-Specific Transcription | 0.160192 | 0.795 |
R-HSA-69541 | Stabilization of p53 | 0.177751 | 0.750 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 0.115114 | 0.939 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 0.131752 | 0.880 |
R-HSA-9824272 | Somitogenesis | 0.219690 | 0.658 |
R-HSA-5633007 | Regulation of TP53 Activity | 0.175666 | 0.755 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 0.115225 | 0.938 |
R-HSA-8848021 | Signaling by PTK6 | 0.115225 | 0.938 |
R-HSA-6804757 | Regulation of TP53 Degradation | 0.160192 | 0.795 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 0.177751 | 0.750 |
R-HSA-428540 | Activation of RAC1 | 0.220285 | 0.657 |
R-HSA-9824878 | Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | 0.220285 | 0.657 |
R-HSA-9931512 | Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | 0.220285 | 0.657 |
R-HSA-9013973 | TICAM1-dependent activation of IRF3/IRF7 | 0.220285 | 0.657 |
R-HSA-9623433 | NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | 0.220285 | 0.657 |
R-HSA-2514853 | Condensation of Prometaphase Chromosomes | 0.220285 | 0.657 |
R-HSA-162592 | Integration of provirus | 0.220285 | 0.657 |
R-HSA-174084 | Autodegradation of Cdh1 by Cdh1:APC/C | 0.225756 | 0.646 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 0.226178 | 0.646 |
R-HSA-73884 | Base Excision Repair | 0.227129 | 0.644 |
R-HSA-202424 | Downstream TCR signaling | 0.227129 | 0.644 |
R-HSA-174154 | APC/C:Cdc20 mediated degradation of Securin | 0.231834 | 0.635 |
R-HSA-3656253 | Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 0.233119 | 0.632 |
R-HSA-3656237 | Defective EXT2 causes exostoses 2 | 0.233119 | 0.632 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 0.233119 | 0.632 |
R-HSA-8866427 | VLDLR internalisation and degradation | 0.233119 | 0.632 |
R-HSA-4641265 | Repression of WNT target genes | 0.233119 | 0.632 |
R-HSA-8941856 | RUNX3 regulates NOTCH signaling | 0.233119 | 0.632 |
R-HSA-9027276 | Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 0.233119 | 0.632 |
R-HSA-9634285 | Constitutive Signaling by Overexpressed ERBB2 | 0.233119 | 0.632 |
R-HSA-446205 | Synthesis of GDP-mannose | 0.233119 | 0.632 |
R-HSA-1247673 | Erythrocytes take up oxygen and release carbon dioxide | 0.233119 | 0.632 |
R-HSA-8983711 | OAS antiviral response | 0.233119 | 0.632 |
R-HSA-389356 | Co-stimulation by CD28 | 0.237923 | 0.624 |
R-HSA-73893 | DNA Damage Bypass | 0.244020 | 0.613 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 0.244020 | 0.613 |
R-HSA-68867 | Assembly of the pre-replicative complex | 0.244593 | 0.612 |
R-HSA-170660 | Adenylate cyclase activating pathway | 0.245743 | 0.610 |
R-HSA-9933947 | Formation of the non-canonical BAF (ncBAF) complex | 0.245743 | 0.610 |
R-HSA-170968 | Frs2-mediated activation | 0.245743 | 0.610 |
R-HSA-162658 | Golgi Cisternae Pericentriolar Stack Reorganization | 0.245743 | 0.610 |
R-HSA-9682706 | Replication of the SARS-CoV-1 genome | 0.245743 | 0.610 |
R-HSA-1474290 | Collagen formation | 0.248993 | 0.604 |
R-HSA-5658442 | Regulation of RAS by GAPs | 0.250123 | 0.602 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 0.253405 | 0.596 |
R-HSA-1169091 | Activation of NF-kappaB in B cells | 0.256231 | 0.591 |
R-HSA-1234176 | Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 0.256231 | 0.591 |
R-HSA-5358346 | Hedgehog ligand biogenesis | 0.256231 | 0.591 |
R-HSA-5358351 | Signaling by Hedgehog | 0.257037 | 0.590 |
R-HSA-5684264 | MAP3K8 (TPL2)-dependent MAPK1/3 activation | 0.258159 | 0.588 |
R-HSA-69166 | Removal of the Flap Intermediate | 0.258159 | 0.588 |
R-HSA-9933937 | Formation of the canonical BAF (cBAF) complex | 0.258159 | 0.588 |
R-HSA-975163 | IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 0.258159 | 0.588 |
R-HSA-391160 | Signal regulatory protein family interactions | 0.258159 | 0.588 |
R-HSA-9679514 | SARS-CoV-1 Genome Replication and Transcription | 0.258159 | 0.588 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 0.260646 | 0.584 |
R-HSA-72187 | mRNA 3'-end processing | 0.262341 | 0.581 |
R-HSA-9931269 | AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | 0.262341 | 0.581 |
R-HSA-5339562 | Uptake and actions of bacterial toxins | 0.262341 | 0.581 |
R-HSA-983712 | Ion channel transport | 0.264248 | 0.578 |
R-HSA-157579 | Telomere Maintenance | 0.266706 | 0.574 |
R-HSA-174178 | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins ... | 0.268452 | 0.571 |
R-HSA-9673767 | Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 0.270372 | 0.568 |
R-HSA-9673770 | Signaling by PDGFRA extracellular domain mutants | 0.270372 | 0.568 |
R-HSA-937072 | TRAF6-mediated induction of TAK1 complex within TLR4 complex | 0.270372 | 0.568 |
R-HSA-170670 | Adenylate cyclase inhibitory pathway | 0.270372 | 0.568 |
R-HSA-8964315 | G beta:gamma signalling through BTK | 0.270372 | 0.568 |
R-HSA-168927 | TICAM1, RIP1-mediated IKK complex recruitment | 0.270372 | 0.568 |
R-HSA-69183 | Processive synthesis on the lagging strand | 0.270372 | 0.568 |
R-HSA-418885 | DCC mediated attractive signaling | 0.270372 | 0.568 |
R-HSA-110312 | Translesion synthesis by REV1 | 0.270372 | 0.568 |
R-HSA-1810476 | RIP-mediated NFkB activation via ZBP1 | 0.270372 | 0.568 |
R-HSA-8876725 | Protein methylation | 0.270372 | 0.568 |
R-HSA-3270619 | IRF3-mediated induction of type I IFN | 0.270372 | 0.568 |
R-HSA-1295596 | Spry regulation of FGF signaling | 0.270372 | 0.568 |
R-HSA-9694516 | SARS-CoV-2 Infection | 0.271014 | 0.567 |
R-HSA-8957275 | Post-translational protein phosphorylation | 0.271159 | 0.567 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 0.275174 | 0.560 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 0.280087 | 0.553 |
R-HSA-5610787 | Hedgehog 'off' state | 0.280087 | 0.553 |
R-HSA-3214815 | HDACs deacetylate histones | 0.280670 | 0.552 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 0.280670 | 0.552 |
R-HSA-9706369 | Negative regulation of FLT3 | 0.282384 | 0.549 |
R-HSA-5656121 | Translesion synthesis by POLI | 0.282384 | 0.549 |
R-HSA-176412 | Phosphorylation of the APC/C | 0.282384 | 0.549 |
R-HSA-169893 | Prolonged ERK activation events | 0.282384 | 0.549 |
R-HSA-210744 | Regulation of gene expression in late stage (branching morphogenesis) pancreatic... | 0.282384 | 0.549 |
R-HSA-5635838 | Activation of SMO | 0.282384 | 0.549 |
R-HSA-140534 | Caspase activation via Death Receptors in the presence of ligand | 0.282384 | 0.549 |
R-HSA-5619115 | Disorders of transmembrane transporters | 0.283844 | 0.547 |
R-HSA-9009391 | Extra-nuclear estrogen signaling | 0.284562 | 0.546 |
R-HSA-9020702 | Interleukin-1 signaling | 0.284562 | 0.546 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 0.286294 | 0.543 |
R-HSA-6782210 | Gap-filling DNA repair synthesis and ligation in TC-NER | 0.286775 | 0.542 |
R-HSA-5578775 | Ion homeostasis | 0.286775 | 0.542 |
R-HSA-9842860 | Regulation of endogenous retroelements | 0.289043 | 0.539 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 0.289043 | 0.539 |
R-HSA-1483255 | PI Metabolism | 0.289043 | 0.539 |
R-HSA-8964616 | G beta:gamma signalling through CDC42 | 0.294200 | 0.531 |
R-HSA-5655862 | Translesion synthesis by POLK | 0.294200 | 0.531 |
R-HSA-4420332 | Defective B3GALT6 causes EDSP2 and SEMDJL1 | 0.294200 | 0.531 |
R-HSA-3560783 | Defective B4GALT7 causes EDS, progeroid type | 0.294200 | 0.531 |
R-HSA-936964 | Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | 0.294200 | 0.531 |
R-HSA-9931521 | The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CL... | 0.294200 | 0.531 |
R-HSA-9702518 | STAT5 activation downstream of FLT3 ITD mutants | 0.294200 | 0.531 |
R-HSA-70370 | Galactose catabolism | 0.294200 | 0.531 |
R-HSA-6804114 | TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 0.294200 | 0.531 |
R-HSA-421270 | Cell-cell junction organization | 0.295199 | 0.530 |
R-HSA-166520 | Signaling by NTRKs | 0.297206 | 0.527 |
R-HSA-6782135 | Dual incision in TC-NER | 0.298965 | 0.524 |
R-HSA-9029569 | NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflu... | 0.298965 | 0.524 |
R-HSA-9772572 | Early SARS-CoV-2 Infection Events | 0.298965 | 0.524 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 0.299046 | 0.524 |
R-HSA-9758941 | Gastrulation | 0.300901 | 0.522 |
R-HSA-9856651 | MITF-M-dependent gene expression | 0.304601 | 0.516 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 0.305048 | 0.516 |
R-HSA-191859 | snRNP Assembly | 0.305048 | 0.516 |
R-HSA-194441 | Metabolism of non-coding RNA | 0.305048 | 0.516 |
R-HSA-9033241 | Peroxisomal protein import | 0.305048 | 0.516 |
R-HSA-2022090 | Assembly of collagen fibrils and other multimeric structures | 0.305048 | 0.516 |
R-HSA-5637812 | Signaling by EGFRvIII in Cancer | 0.305822 | 0.515 |
R-HSA-5637810 | Constitutive Signaling by EGFRvIII | 0.305822 | 0.515 |
R-HSA-174437 | Removal of the Flap Intermediate from the C-strand | 0.305822 | 0.515 |
R-HSA-3560801 | Defective B3GAT3 causes JDSSDHD | 0.305822 | 0.515 |
R-HSA-5358606 | Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 0.305822 | 0.515 |
R-HSA-5358565 | Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 0.305822 | 0.515 |
R-HSA-9694686 | Replication of the SARS-CoV-2 genome | 0.305822 | 0.515 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 0.309516 | 0.509 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 0.311122 | 0.507 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 0.311122 | 0.507 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 0.311122 | 0.507 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 0.311122 | 0.507 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 0.311122 | 0.507 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 0.311122 | 0.507 |
R-HSA-351202 | Metabolism of polyamines | 0.311122 | 0.507 |
R-HSA-211000 | Gene Silencing by RNA | 0.316018 | 0.500 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 0.317184 | 0.499 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 0.317184 | 0.499 |
R-HSA-8939902 | Regulation of RUNX2 expression and activity | 0.317184 | 0.499 |
R-HSA-3928664 | Ephrin signaling | 0.317252 | 0.499 |
R-HSA-1839117 | Signaling by cytosolic FGFR1 fusion mutants | 0.317252 | 0.499 |
R-HSA-164378 | PKA activation in glucagon signalling | 0.317252 | 0.499 |
R-HSA-4419969 | Depolymerization of the Nuclear Lamina | 0.317252 | 0.499 |
R-HSA-9665348 | Signaling by ERBB2 ECD mutants | 0.317252 | 0.499 |
R-HSA-428643 | Organic anion transport by SLC5/17/25 transporters | 0.317252 | 0.499 |
R-HSA-163615 | PKA activation | 0.317252 | 0.499 |
R-HSA-1606322 | ZBP1(DAI) mediated induction of type I IFNs | 0.317252 | 0.499 |
R-HSA-6804760 | Regulation of TP53 Activity through Methylation | 0.317252 | 0.499 |
R-HSA-156711 | Polo-like kinase mediated events | 0.317252 | 0.499 |
R-HSA-5358508 | Mismatch Repair | 0.317252 | 0.499 |
R-HSA-2672351 | Stimuli-sensing channels | 0.320522 | 0.494 |
R-HSA-375165 | NCAM signaling for neurite out-growth | 0.323234 | 0.490 |
R-HSA-6784531 | tRNA processing in the nucleus | 0.323234 | 0.490 |
R-HSA-69002 | DNA Replication Pre-Initiation | 0.325026 | 0.488 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 0.325026 | 0.488 |
R-HSA-937041 | IKK complex recruitment mediated by RIP1 | 0.328496 | 0.483 |
R-HSA-174048 | APC/C:Cdc20 mediated degradation of Cyclin B | 0.328496 | 0.483 |
R-HSA-110320 | Translesion Synthesis by POLH | 0.328496 | 0.483 |
R-HSA-500753 | Pyrimidine biosynthesis | 0.328496 | 0.483 |
R-HSA-1237044 | Erythrocytes take up carbon dioxide and release oxygen | 0.328496 | 0.483 |
R-HSA-113510 | E2F mediated regulation of DNA replication | 0.328496 | 0.483 |
R-HSA-844456 | The NLRP3 inflammasome | 0.328496 | 0.483 |
R-HSA-1480926 | O2/CO2 exchange in erythrocytes | 0.328496 | 0.483 |
R-HSA-392517 | Rap1 signalling | 0.328496 | 0.483 |
R-HSA-9834899 | Specification of the neural plate border | 0.328496 | 0.483 |
R-HSA-1912420 | Pre-NOTCH Processing in Golgi | 0.328496 | 0.483 |
R-HSA-9856532 | Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | 0.328496 | 0.483 |
R-HSA-2243919 | Crosslinking of collagen fibrils | 0.328496 | 0.483 |
R-HSA-9694631 | Maturation of nucleoprotein | 0.328496 | 0.483 |
R-HSA-1834941 | STING mediated induction of host immune responses | 0.328496 | 0.483 |
R-HSA-9694682 | SARS-CoV-2 Genome Replication and Transcription | 0.328496 | 0.483 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 0.329271 | 0.482 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 0.329271 | 0.482 |
R-HSA-202403 | TCR signaling | 0.329531 | 0.482 |
R-HSA-9711097 | Cellular response to starvation | 0.334348 | 0.476 |
R-HSA-936837 | Ion transport by P-type ATPases | 0.335293 | 0.475 |
R-HSA-9934037 | Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | 0.339555 | 0.469 |
R-HSA-416572 | Sema4D induced cell migration and growth-cone collapse | 0.339555 | 0.469 |
R-HSA-140875 | Common Pathway of Fibrin Clot Formation | 0.339555 | 0.469 |
R-HSA-77111 | Synthesis of Ketone Bodies | 0.339555 | 0.469 |
R-HSA-3322077 | Glycogen synthesis | 0.339555 | 0.469 |
R-HSA-1234174 | Cellular response to hypoxia | 0.341299 | 0.467 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 0.344283 | 0.463 |
R-HSA-8854518 | AURKA Activation by TPX2 | 0.347288 | 0.459 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 0.347288 | 0.459 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 0.347539 | 0.459 |
R-HSA-5637815 | Signaling by Ligand-Responsive EGFR Variants in Cancer | 0.350432 | 0.455 |
R-HSA-1236382 | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 0.350432 | 0.455 |
R-HSA-5357786 | TNFR1-induced proapoptotic signaling | 0.350432 | 0.455 |
R-HSA-111931 | PKA-mediated phosphorylation of CREB | 0.350432 | 0.455 |
R-HSA-9013695 | NOTCH4 Intracellular Domain Regulates Transcription | 0.350432 | 0.455 |
R-HSA-162594 | Early Phase of HIV Life Cycle | 0.350432 | 0.455 |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-l... | 0.352035 | 0.453 |
R-HSA-5693606 | DNA Double Strand Break Response | 0.353259 | 0.452 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 0.353259 | 0.452 |
R-HSA-9830369 | Kidney development | 0.353259 | 0.452 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 0.356527 | 0.448 |
R-HSA-2408522 | Selenoamino acid metabolism | 0.356753 | 0.448 |
R-HSA-167172 | Transcription of the HIV genome | 0.359211 | 0.445 |
R-HSA-418990 | Adherens junctions interactions | 0.360576 | 0.443 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 0.361016 | 0.442 |
R-HSA-9694614 | Attachment and Entry | 0.361131 | 0.442 |
R-HSA-8876384 | Listeria monocytogenes entry into host cells | 0.361131 | 0.442 |
R-HSA-9825892 | Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 0.361131 | 0.442 |
R-HSA-8949215 | Mitochondrial calcium ion transport | 0.361131 | 0.442 |
R-HSA-9617828 | FOXO-mediated transcription of cell cycle genes | 0.361131 | 0.442 |
R-HSA-9925563 | Developmental Lineage of Pancreatic Ductal Cells | 0.365143 | 0.438 |
R-HSA-5619102 | SLC transporter disorders | 0.367959 | 0.434 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 0.371053 | 0.431 |
R-HSA-1168372 | Downstream signaling events of B Cell Receptor (BCR) | 0.371053 | 0.431 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 0.371053 | 0.431 |
R-HSA-6803529 | FGFR2 alternative splicing | 0.371655 | 0.430 |
R-HSA-112409 | RAF-independent MAPK1/3 activation | 0.371655 | 0.430 |
R-HSA-6804115 | TP53 regulates transcription of additional cell cycle genes whose exact role in ... | 0.371655 | 0.430 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 0.378918 | 0.421 |
R-HSA-392451 | G beta:gamma signalling through PI3Kgamma | 0.382005 | 0.418 |
R-HSA-74182 | Ketone body metabolism | 0.382005 | 0.418 |
R-HSA-446210 | Synthesis of UDP-N-acetyl-glucosamine | 0.382005 | 0.418 |
R-HSA-8943723 | Regulation of PTEN mRNA translation | 0.382005 | 0.418 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 0.382809 | 0.417 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 0.382882 | 0.417 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 0.386608 | 0.413 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 0.388651 | 0.410 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 0.388651 | 0.410 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 0.390330 | 0.409 |
R-HSA-9703648 | Signaling by FLT3 ITD and TKD mutants | 0.392186 | 0.407 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 0.392205 | 0.406 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 0.393205 | 0.405 |
R-HSA-674695 | RNA Polymerase II Pre-transcription Events | 0.394469 | 0.404 |
R-HSA-6798695 | Neutrophil degranulation | 0.396901 | 0.401 |
R-HSA-380287 | Centrosome maturation | 0.400262 | 0.398 |
R-HSA-6781827 | Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 0.400262 | 0.398 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 0.401479 | 0.396 |
R-HSA-420029 | Tight junction interactions | 0.402200 | 0.396 |
R-HSA-9839394 | TGFBR3 expression | 0.402200 | 0.396 |
R-HSA-3000157 | Laminin interactions | 0.402200 | 0.396 |
R-HSA-400685 | Sema4D in semaphorin signaling | 0.402200 | 0.396 |
R-HSA-5601884 | PIWI-interacting RNA (piRNA) biogenesis | 0.402200 | 0.396 |
R-HSA-70221 | Glycogen breakdown (glycogenolysis) | 0.402200 | 0.396 |
R-HSA-1980143 | Signaling by NOTCH1 | 0.406029 | 0.391 |
R-HSA-5689603 | UCH proteinases | 0.406029 | 0.391 |
R-HSA-194138 | Signaling by VEGF | 0.409974 | 0.387 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 0.411769 | 0.385 |
R-HSA-8874081 | MET activates PTK2 signaling | 0.412049 | 0.385 |
R-HSA-1643713 | Signaling by EGFR in Cancer | 0.412049 | 0.385 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 0.412049 | 0.385 |
R-HSA-3295583 | TRP channels | 0.412049 | 0.385 |
R-HSA-1855183 | Synthesis of IP2, IP, and Ins in the cytosol | 0.412049 | 0.385 |
R-HSA-525793 | Myogenesis | 0.412049 | 0.385 |
R-HSA-2046105 | Linoleic acid (LA) metabolism | 0.412049 | 0.385 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 0.412049 | 0.385 |
R-HSA-5689901 | Metalloprotease DUBs | 0.412049 | 0.385 |
R-HSA-9865118 | Diseases of branched-chain amino acid catabolism | 0.412049 | 0.385 |
R-HSA-5357769 | Caspase activation via extrinsic apoptotic signalling pathway | 0.412049 | 0.385 |
R-HSA-383280 | Nuclear Receptor transcription pathway | 0.417482 | 0.379 |
R-HSA-216083 | Integrin cell surface interactions | 0.417482 | 0.379 |
R-HSA-5619084 | ABC transporter disorders | 0.417482 | 0.379 |
R-HSA-4086400 | PCP/CE pathway | 0.417482 | 0.379 |
R-HSA-174414 | Processive synthesis on the C-strand of the telomere | 0.421737 | 0.375 |
R-HSA-167243 | Tat-mediated HIV elongation arrest and recovery | 0.421737 | 0.375 |
R-HSA-167238 | Pausing and recovery of Tat-mediated HIV elongation | 0.421737 | 0.375 |
R-HSA-8949613 | Cristae formation | 0.421737 | 0.375 |
R-HSA-5357956 | TNFR1-induced NF-kappa-B signaling pathway | 0.421737 | 0.375 |
R-HSA-3928663 | EPHA-mediated growth cone collapse | 0.421737 | 0.375 |
R-HSA-9828806 | Maturation of hRSV A proteins | 0.421737 | 0.375 |
R-HSA-5654738 | Signaling by FGFR2 | 0.428822 | 0.368 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 0.431014 | 0.366 |
R-HSA-167287 | HIV elongation arrest and recovery | 0.431266 | 0.365 |
R-HSA-167290 | Pausing and recovery of HIV elongation | 0.431266 | 0.365 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 0.431266 | 0.365 |
R-HSA-171319 | Telomere Extension By Telomerase | 0.431266 | 0.365 |
R-HSA-622312 | Inflammasomes | 0.431266 | 0.365 |
R-HSA-5654732 | Negative regulation of FGFR3 signaling | 0.431266 | 0.365 |
R-HSA-157118 | Signaling by NOTCH | 0.432174 | 0.364 |
R-HSA-9615710 | Late endosomal microautophagy | 0.440638 | 0.356 |
R-HSA-9709570 | Impaired BRCA2 binding to RAD51 | 0.440638 | 0.356 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 0.440638 | 0.356 |
R-HSA-917729 | Endosomal Sorting Complex Required For Transport (ESCRT) | 0.440638 | 0.356 |
R-HSA-9006335 | Signaling by Erythropoietin | 0.440638 | 0.356 |
R-HSA-5654733 | Negative regulation of FGFR4 signaling | 0.440638 | 0.356 |
R-HSA-73894 | DNA Repair | 0.442445 | 0.354 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 0.444864 | 0.352 |
R-HSA-5668541 | TNFR2 non-canonical NF-kB pathway | 0.445613 | 0.351 |
R-HSA-9707564 | Cytoprotection by HMOX1 | 0.445613 | 0.351 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 0.449281 | 0.347 |
R-HSA-68962 | Activation of the pre-replicative complex | 0.449856 | 0.347 |
R-HSA-2424491 | DAP12 signaling | 0.449856 | 0.347 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 0.449856 | 0.347 |
R-HSA-9013508 | NOTCH3 Intracellular Domain Regulates Transcription | 0.449856 | 0.347 |
R-HSA-1474151 | Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 0.449856 | 0.347 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 0.451149 | 0.346 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 0.451149 | 0.346 |
R-HSA-186763 | Downstream signal transduction | 0.458923 | 0.338 |
R-HSA-5694530 | Cargo concentration in the ER | 0.458923 | 0.338 |
R-HSA-936440 | Negative regulators of DDX58/IFIH1 signaling | 0.458923 | 0.338 |
R-HSA-9820960 | Respiratory syncytial virus (RSV) attachment and entry | 0.458923 | 0.338 |
R-HSA-9913351 | Formation of the dystrophin-glycoprotein complex (DGC) | 0.458923 | 0.338 |
R-HSA-9909615 | Regulation of PD-L1(CD274) Post-translational modification | 0.462126 | 0.335 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 0.466258 | 0.331 |
R-HSA-2024096 | HS-GAG degradation | 0.467841 | 0.330 |
R-HSA-5685938 | HDR through Single Strand Annealing (SSA) | 0.476613 | 0.322 |
R-HSA-1839124 | FGFR1 mutant receptor activation | 0.476613 | 0.322 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 0.476613 | 0.322 |
R-HSA-9930044 | Nuclear RNA decay | 0.476613 | 0.322 |
R-HSA-5654726 | Negative regulation of FGFR1 signaling | 0.476613 | 0.322 |
R-HSA-5675482 | Regulation of necroptotic cell death | 0.476613 | 0.322 |
R-HSA-1855204 | Synthesis of IP3 and IP4 in the cytosol | 0.476613 | 0.322 |
R-HSA-392499 | Metabolism of proteins | 0.477830 | 0.321 |
R-HSA-9663891 | Selective autophagy | 0.478349 | 0.320 |
R-HSA-9664407 | Parasite infection | 0.483109 | 0.316 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 0.483109 | 0.316 |
R-HSA-9664417 | Leishmania phagocytosis | 0.483109 | 0.316 |
R-HSA-390522 | Striated Muscle Contraction | 0.485241 | 0.314 |
R-HSA-163359 | Glucagon signaling in metabolic regulation | 0.485241 | 0.314 |
R-HSA-8964539 | Glutamate and glutamine metabolism | 0.485241 | 0.314 |
R-HSA-1632852 | Macroautophagy | 0.487283 | 0.312 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 0.488997 | 0.311 |
R-HSA-389948 | Co-inhibition by PD-1 | 0.492306 | 0.308 |
R-HSA-1971475 | Glycosaminoglycan-protein linkage region biosynthesis | 0.493726 | 0.307 |
R-HSA-203615 | eNOS activation | 0.493726 | 0.307 |
R-HSA-9701190 | Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 0.493726 | 0.307 |
R-HSA-5654727 | Negative regulation of FGFR2 signaling | 0.493726 | 0.307 |
R-HSA-9675136 | Diseases of DNA Double-Strand Break Repair | 0.493726 | 0.307 |
R-HSA-110328 | Recognition and association of DNA glycosylase with site containing an affected ... | 0.493726 | 0.307 |
R-HSA-5686938 | Regulation of TLR by endogenous ligand | 0.493726 | 0.307 |
R-HSA-190861 | Gap junction assembly | 0.493726 | 0.307 |
R-HSA-1368108 | BMAL1:CLOCK,NPAS2 activates circadian expression | 0.493726 | 0.307 |
R-HSA-9768919 | NPAS4 regulates expression of target genes | 0.493726 | 0.307 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 0.495633 | 0.305 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 0.499706 | 0.301 |
R-HSA-187687 | Signalling to ERKs | 0.502073 | 0.299 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 0.502073 | 0.299 |
R-HSA-5693616 | Presynaptic phase of homologous DNA pairing and strand exchange | 0.502073 | 0.299 |
R-HSA-9860927 | Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZ... | 0.502073 | 0.299 |
R-HSA-174824 | Plasma lipoprotein assembly, remodeling, and clearance | 0.504713 | 0.297 |
R-HSA-416476 | G alpha (q) signalling events | 0.508208 | 0.294 |
R-HSA-2022928 | HS-GAG biosynthesis | 0.510282 | 0.292 |
R-HSA-9682385 | FLT3 signaling in disease | 0.510282 | 0.292 |
R-HSA-114604 | GPVI-mediated activation cascade | 0.510282 | 0.292 |
R-HSA-140877 | Formation of Fibrin Clot (Clotting Cascade) | 0.510282 | 0.292 |
R-HSA-163560 | Triglyceride catabolism | 0.510282 | 0.292 |
R-HSA-111933 | Calmodulin induced events | 0.510282 | 0.292 |
R-HSA-111997 | CaM pathway | 0.510282 | 0.292 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 0.516030 | 0.287 |
R-HSA-390247 | Beta-oxidation of very long chain fatty acids | 0.518357 | 0.285 |
R-HSA-8875878 | MET promotes cell motility | 0.526299 | 0.279 |
R-HSA-202131 | Metabolism of nitric oxide: NOS3 activation and regulation | 0.526299 | 0.279 |
R-HSA-2046106 | alpha-linolenic acid (ALA) metabolism | 0.526299 | 0.279 |
R-HSA-5693579 | Homologous DNA Pairing and Strand Exchange | 0.526299 | 0.279 |
R-HSA-5213460 | RIPK1-mediated regulated necrosis | 0.526299 | 0.279 |
R-HSA-9958790 | SLC-mediated transport of inorganic anions | 0.526299 | 0.279 |
R-HSA-452723 | Transcriptional regulation of pluripotent stem cells | 0.526299 | 0.279 |
R-HSA-6807878 | COPI-mediated anterograde transport | 0.530202 | 0.276 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 0.530202 | 0.276 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 0.530202 | 0.276 |
R-HSA-167200 | Formation of HIV-1 elongation complex containing HIV-1 Tat | 0.534110 | 0.272 |
R-HSA-381771 | Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 0.534110 | 0.272 |
R-HSA-8953750 | Transcriptional Regulation by E2F6 | 0.534110 | 0.272 |
R-HSA-9820448 | Developmental Cell Lineages of the Exocrine Pancreas | 0.536029 | 0.271 |
R-HSA-397014 | Muscle contraction | 0.537274 | 0.270 |
R-HSA-9609507 | Protein localization | 0.539973 | 0.268 |
R-HSA-190236 | Signaling by FGFR | 0.540146 | 0.267 |
R-HSA-73779 | RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 0.541793 | 0.266 |
R-HSA-167246 | Tat-mediated elongation of the HIV-1 transcript | 0.541793 | 0.266 |
R-HSA-167152 | Formation of HIV elongation complex in the absence of HIV Tat | 0.541793 | 0.266 |
R-HSA-167169 | HIV Transcription Elongation | 0.541793 | 0.266 |
R-HSA-9646399 | Aggrephagy | 0.541793 | 0.266 |
R-HSA-9854311 | Maturation of TCA enzymes and regulation of TCA cycle | 0.541793 | 0.266 |
R-HSA-8982491 | Glycogen metabolism | 0.541793 | 0.266 |
R-HSA-9607240 | FLT3 Signaling | 0.549350 | 0.260 |
R-HSA-5625886 | Activated PKN1 stimulates transcription of AR (androgen receptor) regulated gene... | 0.549350 | 0.260 |
R-HSA-9821002 | Chromatin modifications during the maternal to zygotic transition (MZT) | 0.549350 | 0.260 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 0.549350 | 0.260 |
R-HSA-382556 | ABC-family proteins mediated transport | 0.549944 | 0.260 |
R-HSA-1428517 | Aerobic respiration and respiratory electron transport | 0.553815 | 0.257 |
R-HSA-9610379 | HCMV Late Events | 0.555554 | 0.255 |
R-HSA-167161 | HIV Transcription Initiation | 0.556783 | 0.254 |
R-HSA-75953 | RNA Polymerase II Transcription Initiation | 0.556783 | 0.254 |
R-HSA-167162 | RNA Polymerase II HIV Promoter Escape | 0.556783 | 0.254 |
R-HSA-6811438 | Intra-Golgi traffic | 0.556783 | 0.254 |
R-HSA-5655302 | Signaling by FGFR1 in disease | 0.556783 | 0.254 |
R-HSA-983705 | Signaling by the B Cell Receptor (BCR) | 0.559400 | 0.252 |
R-HSA-9824443 | Parasitic Infection Pathways | 0.559537 | 0.252 |
R-HSA-9658195 | Leishmania infection | 0.559537 | 0.252 |
R-HSA-877300 | Interferon gamma signaling | 0.563226 | 0.249 |
R-HSA-991365 | Activation of GABAB receptors | 0.564094 | 0.249 |
R-HSA-977444 | GABA B receptor activation | 0.564094 | 0.249 |
R-HSA-165159 | MTOR signalling | 0.564094 | 0.249 |
R-HSA-110329 | Cleavage of the damaged pyrimidine | 0.564094 | 0.249 |
R-HSA-73928 | Depyrimidination | 0.564094 | 0.249 |
R-HSA-400508 | Incretin synthesis, secretion, and inactivation | 0.564094 | 0.249 |
R-HSA-379716 | Cytosolic tRNA aminoacylation | 0.564094 | 0.249 |
R-HSA-111996 | Ca-dependent events | 0.564094 | 0.249 |
R-HSA-112316 | Neuronal System | 0.564365 | 0.248 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 0.569097 | 0.245 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 0.569097 | 0.245 |
R-HSA-73776 | RNA Polymerase II Promoter Escape | 0.571284 | 0.243 |
R-HSA-75876 | Synthesis of very long-chain fatty acyl-CoAs | 0.571284 | 0.243 |
R-HSA-5654743 | Signaling by FGFR4 | 0.571284 | 0.243 |
R-HSA-9637690 | Response of Mtb to phagocytosis | 0.571284 | 0.243 |
R-HSA-9833110 | RSV-host interactions | 0.573793 | 0.241 |
R-HSA-109582 | Hemostasis | 0.578243 | 0.238 |
R-HSA-2172127 | DAP12 interactions | 0.578356 | 0.238 |
R-HSA-190828 | Gap junction trafficking | 0.578356 | 0.238 |
R-HSA-5696398 | Nucleotide Excision Repair | 0.578452 | 0.238 |
R-HSA-76042 | RNA Polymerase II Transcription Initiation And Promoter Clearance | 0.585312 | 0.233 |
R-HSA-774815 | Nucleosome assembly | 0.585312 | 0.233 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 0.585312 | 0.233 |
R-HSA-3560782 | Diseases associated with glycosaminoglycan metabolism | 0.585312 | 0.233 |
R-HSA-9824585 | Regulation of MITF-M-dependent genes involved in pigmentation | 0.585312 | 0.233 |
R-HSA-9660821 | ADORA2B mediated anti-inflammatory cytokines production | 0.585312 | 0.233 |
R-HSA-432040 | Vasopressin regulates renal water homeostasis via Aquaporins | 0.585312 | 0.233 |
R-HSA-5654741 | Signaling by FGFR3 | 0.585312 | 0.233 |
R-HSA-1489509 | DAG and IP3 signaling | 0.585312 | 0.233 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 0.592154 | 0.228 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 0.592154 | 0.228 |
R-HSA-9664424 | Cell recruitment (pro-inflammatory response) | 0.592154 | 0.228 |
R-HSA-9660826 | Purinergic signaling in leishmaniasis infection | 0.592154 | 0.228 |
R-HSA-9861718 | Regulation of pyruvate metabolism | 0.592154 | 0.228 |
R-HSA-9839373 | Signaling by TGFBR3 | 0.592154 | 0.228 |
R-HSA-9675135 | Diseases of DNA repair | 0.592154 | 0.228 |
R-HSA-5357905 | Regulation of TNFR1 signaling | 0.592154 | 0.228 |
R-HSA-597592 | Post-translational protein modification | 0.597384 | 0.224 |
R-HSA-3928665 | EPH-ephrin mediated repulsion of cells | 0.598883 | 0.223 |
R-HSA-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 0.598883 | 0.223 |
R-HSA-72312 | rRNA processing | 0.602308 | 0.220 |
R-HSA-9634597 | GPER1 signaling | 0.605502 | 0.218 |
R-HSA-168256 | Immune System | 0.608827 | 0.216 |
R-HSA-157858 | Gap junction trafficking and regulation | 0.612012 | 0.213 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 0.614377 | 0.212 |
R-HSA-109704 | PI3K Cascade | 0.618414 | 0.209 |
R-HSA-70895 | Branched-chain amino acid catabolism | 0.624712 | 0.204 |
R-HSA-112382 | Formation of RNA Pol II elongation complex | 0.630906 | 0.200 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 0.630906 | 0.200 |
R-HSA-9634815 | Transcriptional Regulation by NPAS4 | 0.630906 | 0.200 |
R-HSA-449147 | Signaling by Interleukins | 0.631349 | 0.200 |
R-HSA-75955 | RNA Polymerase II Transcription Elongation | 0.636998 | 0.196 |
R-HSA-445355 | Smooth Muscle Contraction | 0.636998 | 0.196 |
R-HSA-8956320 | Nucleotide biosynthesis | 0.636998 | 0.196 |
R-HSA-72649 | Translation initiation complex formation | 0.642990 | 0.192 |
R-HSA-73929 | Base-Excision Repair, AP Site Formation | 0.642990 | 0.192 |
R-HSA-418597 | G alpha (z) signalling events | 0.648883 | 0.188 |
R-HSA-9012852 | Signaling by NOTCH3 | 0.648883 | 0.188 |
R-HSA-168249 | Innate Immune System | 0.651796 | 0.186 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 0.654680 | 0.184 |
R-HSA-75893 | TNF signaling | 0.654680 | 0.184 |
R-HSA-5654736 | Signaling by FGFR1 | 0.654680 | 0.184 |
R-HSA-177929 | Signaling by EGFR | 0.654680 | 0.184 |
R-HSA-3781865 | Diseases of glycosylation | 0.655330 | 0.184 |
R-HSA-9609646 | HCMV Infection | 0.655899 | 0.183 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 0.655937 | 0.183 |
R-HSA-112399 | IRS-mediated signalling | 0.660381 | 0.180 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 0.663808 | 0.178 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 0.665988 | 0.177 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 0.665988 | 0.177 |
R-HSA-1638091 | Heparan sulfate/heparin (HS-GAG) metabolism | 0.671503 | 0.173 |
R-HSA-8979227 | Triglyceride metabolism | 0.671503 | 0.173 |
R-HSA-186712 | Regulation of beta-cell development | 0.671503 | 0.173 |
R-HSA-352230 | Amino acid transport across the plasma membrane | 0.671503 | 0.173 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 0.676928 | 0.169 |
R-HSA-977443 | GABA receptor activation | 0.676928 | 0.169 |
R-HSA-1660661 | Sphingolipid de novo biosynthesis | 0.676928 | 0.169 |
R-HSA-379724 | tRNA Aminoacylation | 0.676928 | 0.169 |
R-HSA-2428928 | IRS-related events triggered by IGF1R | 0.682263 | 0.166 |
R-HSA-445717 | Aquaporin-mediated transport | 0.682263 | 0.166 |
R-HSA-112043 | PLC beta mediated events | 0.682263 | 0.166 |
R-HSA-186797 | Signaling by PDGF | 0.687510 | 0.163 |
R-HSA-1268020 | Mitochondrial protein import | 0.687510 | 0.163 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 0.687510 | 0.163 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 0.687510 | 0.163 |
R-HSA-6799198 | Complex I biogenesis | 0.692671 | 0.159 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 0.692671 | 0.159 |
R-HSA-9609690 | HCMV Early Events | 0.692874 | 0.159 |
R-HSA-1474244 | Extracellular matrix organization | 0.692952 | 0.159 |
R-HSA-382551 | Transport of small molecules | 0.694458 | 0.158 |
R-HSA-1280218 | Adaptive Immune System | 0.696163 | 0.157 |
R-HSA-168643 | Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signali... | 0.697747 | 0.156 |
R-HSA-2428924 | IGF1R signaling cascade | 0.697747 | 0.156 |
R-HSA-74751 | Insulin receptor signalling cascade | 0.697747 | 0.156 |
R-HSA-9843745 | Adipogenesis | 0.701010 | 0.154 |
R-HSA-5576891 | Cardiac conduction | 0.701010 | 0.154 |
R-HSA-446219 | Synthesis of substrates in N-glycan biosythesis | 0.701010 | 0.154 |
R-HSA-2404192 | Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 0.702740 | 0.153 |
R-HSA-9711123 | Cellular response to chemical stress | 0.704452 | 0.152 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 0.710461 | 0.148 |
R-HSA-112040 | G-protein mediated events | 0.712480 | 0.147 |
R-HSA-9958863 | SLC-mediated transport of amino acids | 0.712480 | 0.147 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 0.713316 | 0.147 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 0.717230 | 0.144 |
R-HSA-1650814 | Collagen biosynthesis and modifying enzymes | 0.717230 | 0.144 |
R-HSA-5218859 | Regulated Necrosis | 0.717230 | 0.144 |
R-HSA-204005 | COPII-mediated vesicle transport | 0.726497 | 0.139 |
R-HSA-75105 | Fatty acyl-CoA biosynthesis | 0.726497 | 0.139 |
R-HSA-975634 | Retinoid metabolism and transport | 0.731016 | 0.136 |
R-HSA-8978934 | Metabolism of cofactors | 0.731016 | 0.136 |
R-HSA-9856649 | Transcriptional and post-translational regulation of MITF-M expression and activ... | 0.731016 | 0.136 |
R-HSA-3000178 | ECM proteoglycans | 0.731016 | 0.136 |
R-HSA-4086398 | Ca2+ pathway | 0.739833 | 0.131 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 0.739833 | 0.131 |
R-HSA-1226099 | Signaling by FGFR in disease | 0.744133 | 0.128 |
R-HSA-3000171 | Non-integrin membrane-ECM interactions | 0.748362 | 0.126 |
R-HSA-71403 | Citric acid cycle (TCA cycle) | 0.748362 | 0.126 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 0.750362 | 0.125 |
R-HSA-9694635 | Translation of Structural Proteins | 0.756612 | 0.121 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 0.760635 | 0.119 |
R-HSA-9955298 | SLC-mediated transport of organic anions | 0.760635 | 0.119 |
R-HSA-8951664 | Neddylation | 0.763511 | 0.117 |
R-HSA-9925561 | Developmental Lineage of Pancreatic Acinar Cells | 0.764592 | 0.117 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 0.764592 | 0.117 |
R-HSA-2173782 | Binding and Uptake of Ligands by Scavenger Receptors | 0.768060 | 0.115 |
R-HSA-6806834 | Signaling by MET | 0.768485 | 0.114 |
R-HSA-9856530 | High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR... | 0.768485 | 0.114 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 0.770902 | 0.113 |
R-HSA-6806667 | Metabolism of fat-soluble vitamins | 0.772312 | 0.112 |
R-HSA-195721 | Signaling by WNT | 0.774023 | 0.111 |
R-HSA-1989781 | PPARA activates gene expression | 0.781968 | 0.107 |
R-HSA-390918 | Peroxisomal lipid metabolism | 0.783422 | 0.106 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 0.787323 | 0.104 |
R-HSA-446193 | Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, L... | 0.787323 | 0.104 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 0.810477 | 0.091 |
R-HSA-74752 | Signaling by Insulin receptor | 0.816697 | 0.088 |
R-HSA-9772573 | Late SARS-CoV-2 Infection Events | 0.816697 | 0.088 |
R-HSA-983695 | Antigen activates B Cell Receptor (BCR) leading to generation of second messenge... | 0.819731 | 0.086 |
R-HSA-72306 | tRNA processing | 0.821675 | 0.085 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 0.831372 | 0.080 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 0.834079 | 0.079 |
R-HSA-3214847 | HATs acetylate histones | 0.839609 | 0.076 |
R-HSA-9614085 | FOXO-mediated transcription | 0.839609 | 0.076 |
R-HSA-9734767 | Developmental Cell Lineages | 0.849329 | 0.071 |
R-HSA-388396 | GPCR downstream signalling | 0.852418 | 0.069 |
R-HSA-111885 | Opioid Signalling | 0.852456 | 0.069 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 0.854900 | 0.068 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 0.854900 | 0.068 |
R-HSA-446203 | Asparagine N-linked glycosylation | 0.859876 | 0.066 |
R-HSA-5617833 | Cilium Assembly | 0.862146 | 0.064 |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | 0.865694 | 0.063 |
R-HSA-2871809 | FCERI mediated Ca+2 mobilization | 0.883228 | 0.054 |
R-HSA-2980736 | Peptide hormone metabolism | 0.887067 | 0.052 |
R-HSA-9635486 | Infection with Mycobacterium tuberculosis | 0.894373 | 0.048 |
R-HSA-1483257 | Phospholipid metabolism | 0.895239 | 0.048 |
R-HSA-6809371 | Formation of the cornified envelope | 0.899541 | 0.046 |
R-HSA-9664323 | FCGR3A-mediated IL10 synthesis | 0.904457 | 0.044 |
R-HSA-9824439 | Bacterial Infection Pathways | 0.910877 | 0.041 |
R-HSA-1474228 | Degradation of the extracellular matrix | 0.915017 | 0.039 |
R-HSA-372790 | Signaling by GPCR | 0.920386 | 0.036 |
R-HSA-163685 | Integration of energy metabolism | 0.921839 | 0.035 |
R-HSA-5173105 | O-linked glycosylation | 0.923137 | 0.035 |
R-HSA-2187338 | Visual phototransduction | 0.936068 | 0.029 |
R-HSA-5668914 | Diseases of metabolism | 0.940503 | 0.027 |
R-HSA-418555 | G alpha (s) signalling events | 0.957958 | 0.019 |
R-HSA-9662851 | Anti-inflammatory response favouring Leishmania parasite infection | 0.959345 | 0.018 |
R-HSA-9664433 | Leishmania parasite growth and survival | 0.959345 | 0.018 |
R-HSA-611105 | Respiratory electron transport | 0.962618 | 0.017 |
R-HSA-425407 | SLC-mediated transmembrane transport | 0.970272 | 0.013 |
R-HSA-1630316 | Glycosaminoglycan metabolism | 0.970942 | 0.013 |
R-HSA-428157 | Sphingolipid metabolism | 0.974598 | 0.011 |
R-HSA-6805567 | Keratinization | 0.977035 | 0.010 |
R-HSA-15869 | Metabolism of nucleotides | 0.986140 | 0.006 |
R-HSA-196854 | Metabolism of vitamins and cofactors | 0.988041 | 0.005 |
R-HSA-373076 | Class A/1 (Rhodopsin-like receptors) | 0.992433 | 0.003 |
R-HSA-211945 | Phase I - Functionalization of compounds | 0.993176 | 0.003 |
R-HSA-8978868 | Fatty acid metabolism | 0.993764 | 0.003 |
R-HSA-8957322 | Metabolism of steroids | 0.996866 | 0.001 |
R-HSA-418594 | G alpha (i) signalling events | 0.999248 | 0.000 |
R-HSA-500792 | GPCR ligand binding | 0.999617 | 0.000 |
R-HSA-556833 | Metabolism of lipids | 0.999872 | 0.000 |
R-HSA-211859 | Biological oxidations | 0.999896 | 0.000 |
R-HSA-1430728 | Metabolism | 0.999927 | 0.000 |
R-HSA-9709957 | Sensory Perception | 1.000000 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
COT |
0.830 | 0.126 | 2 | 0.874 |
MTOR |
0.826 | 0.346 | 1 | 0.823 |
MST4 |
0.823 | 0.245 | 2 | 0.860 |
ULK2 |
0.817 | 0.055 | 2 | 0.790 |
GCN2 |
0.815 | 0.001 | 2 | 0.783 |
NIM1 |
0.814 | 0.351 | 3 | 0.760 |
PRPK |
0.814 | 0.045 | -1 | 0.199 |
RAF1 |
0.812 | 0.017 | 1 | 0.895 |
DSTYK |
0.812 | -0.005 | 2 | 0.867 |
PKCD |
0.811 | 0.155 | 2 | 0.790 |
TBK1 |
0.811 | -0.004 | 1 | 0.837 |
CLK3 |
0.811 | 0.083 | 1 | 0.791 |
CDC7 |
0.809 | 0.007 | 1 | 0.807 |
NEK6 |
0.809 | -0.000 | -2 | 0.875 |
NDR2 |
0.809 | 0.074 | -3 | 0.804 |
PDHK1 |
0.807 | -0.005 | 1 | 0.908 |
WNK1 |
0.807 | 0.049 | -2 | 0.887 |
PKCA |
0.807 | 0.184 | 2 | 0.736 |
IKKE |
0.807 | -0.036 | 1 | 0.829 |
IKKB |
0.807 | -0.091 | -2 | 0.829 |
CDKL1 |
0.806 | 0.076 | -3 | 0.761 |
MOS |
0.806 | -0.012 | 1 | 0.857 |
BMPR2 |
0.806 | -0.055 | -2 | 0.913 |
NLK |
0.806 | 0.013 | 1 | 0.812 |
PIM3 |
0.806 | 0.006 | -3 | 0.794 |
PDHK4 |
0.805 | -0.025 | 1 | 0.889 |
PRKD1 |
0.805 | 0.019 | -3 | 0.788 |
MARK4 |
0.805 | 0.194 | 4 | 0.847 |
NDR1 |
0.804 | 0.058 | -3 | 0.793 |
BCKDK |
0.804 | 0.000 | -1 | 0.226 |
TGFBR2 |
0.804 | -0.003 | -2 | 0.808 |
PKN2 |
0.804 | 0.077 | -3 | 0.800 |
CHAK2 |
0.803 | -0.037 | -1 | 0.119 |
ULK1 |
0.802 | -0.048 | -3 | 0.823 |
NEK7 |
0.802 | -0.067 | -3 | 0.843 |
PKCG |
0.802 | 0.136 | 2 | 0.747 |
RSK3 |
0.802 | 0.035 | -3 | 0.723 |
ATR |
0.802 | 0.025 | 1 | 0.852 |
ERK5 |
0.802 | 0.005 | 1 | 0.781 |
NUAK2 |
0.802 | 0.057 | -3 | 0.791 |
NEK9 |
0.801 | -0.002 | 2 | 0.838 |
CDKL5 |
0.801 | 0.047 | -3 | 0.750 |
IRE1 |
0.801 | 0.028 | 1 | 0.847 |
NIK |
0.801 | 0.040 | -3 | 0.857 |
PKN3 |
0.800 | 0.020 | -3 | 0.794 |
AMPKA1 |
0.800 | 0.067 | -3 | 0.816 |
MLK1 |
0.799 | -0.062 | 2 | 0.815 |
CAMK1B |
0.799 | -0.028 | -3 | 0.825 |
PKCB |
0.799 | 0.114 | 2 | 0.741 |
RSK2 |
0.799 | 0.026 | -3 | 0.717 |
IRE2 |
0.799 | 0.043 | 2 | 0.774 |
SRPK1 |
0.799 | 0.043 | -3 | 0.699 |
PRKD2 |
0.798 | -0.005 | -3 | 0.718 |
CDK5 |
0.798 | 0.109 | 1 | 0.632 |
MNK2 |
0.798 | 0.041 | -2 | 0.798 |
IKKA |
0.797 | -0.036 | -2 | 0.811 |
PKACG |
0.797 | 0.033 | -2 | 0.749 |
WNK3 |
0.796 | -0.110 | 1 | 0.886 |
RIPK3 |
0.796 | -0.094 | 3 | 0.734 |
P90RSK |
0.795 | 0.012 | -3 | 0.722 |
HIPK4 |
0.795 | 0.021 | 1 | 0.750 |
SIK |
0.795 | 0.149 | -3 | 0.705 |
CAMLCK |
0.794 | -0.019 | -2 | 0.872 |
MLK3 |
0.794 | -0.005 | 2 | 0.744 |
CAMK2G |
0.794 | -0.084 | 2 | 0.785 |
AMPKA2 |
0.794 | 0.050 | -3 | 0.775 |
NEK2 |
0.794 | 0.027 | 2 | 0.810 |
QSK |
0.794 | 0.164 | 4 | 0.833 |
HUNK |
0.794 | -0.045 | 2 | 0.827 |
MLK2 |
0.794 | -0.044 | 2 | 0.807 |
CDK8 |
0.794 | 0.026 | 1 | 0.607 |
PKCZ |
0.794 | 0.058 | 2 | 0.781 |
QIK |
0.794 | 0.147 | -3 | 0.796 |
MASTL |
0.794 | 0.012 | -2 | 0.851 |
TSSK1 |
0.793 | 0.030 | -3 | 0.840 |
PIM1 |
0.793 | 0.022 | -3 | 0.724 |
MPSK1 |
0.793 | 0.259 | 1 | 0.839 |
SKMLCK |
0.793 | -0.013 | -2 | 0.858 |
AURC |
0.793 | 0.013 | -2 | 0.651 |
ICK |
0.793 | 0.033 | -3 | 0.795 |
SRPK2 |
0.793 | 0.032 | -3 | 0.613 |
PKR |
0.792 | 0.037 | 1 | 0.890 |
SGK3 |
0.792 | 0.098 | -3 | 0.718 |
P70S6KB |
0.792 | -0.018 | -3 | 0.746 |
KIS |
0.791 | 0.019 | 1 | 0.652 |
MNK1 |
0.791 | 0.043 | -2 | 0.814 |
PKCH |
0.791 | 0.074 | 2 | 0.733 |
GRK5 |
0.791 | -0.126 | -3 | 0.858 |
DAPK2 |
0.791 | -0.026 | -3 | 0.836 |
CDK19 |
0.790 | 0.036 | 1 | 0.564 |
LATS2 |
0.790 | -0.029 | -5 | 0.740 |
CAMK2D |
0.790 | -0.013 | -3 | 0.809 |
PLK4 |
0.789 | 0.114 | 2 | 0.649 |
DNAPK |
0.789 | 0.100 | 1 | 0.757 |
PAK3 |
0.788 | -0.033 | -2 | 0.802 |
CDK18 |
0.788 | 0.074 | 1 | 0.538 |
RIPK1 |
0.788 | -0.096 | 1 | 0.877 |
YSK4 |
0.788 | -0.010 | 1 | 0.846 |
CDK7 |
0.788 | -0.006 | 1 | 0.611 |
PAK1 |
0.788 | -0.019 | -2 | 0.792 |
SRPK3 |
0.788 | 0.038 | -3 | 0.673 |
CHAK1 |
0.788 | -0.062 | 2 | 0.777 |
MAPKAPK3 |
0.787 | -0.060 | -3 | 0.729 |
ANKRD3 |
0.787 | -0.111 | 1 | 0.920 |
PKCT |
0.787 | 0.097 | 2 | 0.739 |
TAO3 |
0.787 | 0.200 | 1 | 0.852 |
CDK13 |
0.787 | 0.026 | 1 | 0.585 |
NUAK1 |
0.787 | 0.002 | -3 | 0.738 |
MST3 |
0.786 | 0.184 | 2 | 0.843 |
FAM20C |
0.786 | 0.024 | 2 | 0.586 |
TSSK2 |
0.786 | -0.038 | -5 | 0.801 |
CDK2 |
0.786 | 0.065 | 1 | 0.660 |
MELK |
0.786 | -0.031 | -3 | 0.757 |
PAK6 |
0.786 | -0.004 | -2 | 0.736 |
ATM |
0.786 | -0.028 | 1 | 0.789 |
PHKG1 |
0.786 | -0.021 | -3 | 0.779 |
CDK1 |
0.785 | 0.048 | 1 | 0.549 |
AKT2 |
0.785 | 0.036 | -3 | 0.621 |
TTBK2 |
0.785 | -0.119 | 2 | 0.713 |
LATS1 |
0.784 | 0.029 | -3 | 0.821 |
GRK1 |
0.784 | -0.065 | -2 | 0.802 |
MEKK1 |
0.784 | 0.073 | 1 | 0.898 |
PRKD3 |
0.784 | -0.031 | -3 | 0.688 |
MARK3 |
0.784 | 0.121 | 4 | 0.776 |
VRK2 |
0.784 | -0.002 | 1 | 0.905 |
DLK |
0.784 | -0.152 | 1 | 0.875 |
IRAK4 |
0.784 | 0.002 | 1 | 0.870 |
MLK4 |
0.784 | -0.057 | 2 | 0.714 |
ZAK |
0.784 | 0.061 | 1 | 0.871 |
CLK1 |
0.784 | 0.030 | -3 | 0.680 |
HRI |
0.783 | -0.063 | -2 | 0.885 |
GRK4 |
0.783 | -0.121 | -2 | 0.833 |
CDK3 |
0.783 | 0.090 | 1 | 0.494 |
PKACB |
0.783 | 0.044 | -2 | 0.670 |
WNK4 |
0.783 | 0.033 | -2 | 0.884 |
P38A |
0.783 | 0.041 | 1 | 0.656 |
TGFBR1 |
0.782 | -0.010 | -2 | 0.824 |
TNIK |
0.782 | 0.235 | 3 | 0.919 |
AKT1 |
0.782 | 0.057 | -3 | 0.641 |
CDK12 |
0.782 | 0.032 | 1 | 0.556 |
SMG1 |
0.782 | -0.053 | 1 | 0.807 |
ALK4 |
0.781 | -0.048 | -2 | 0.857 |
GRK6 |
0.781 | -0.121 | 1 | 0.858 |
DYRK2 |
0.781 | 0.010 | 1 | 0.642 |
DCAMKL1 |
0.781 | 0.073 | -3 | 0.732 |
HGK |
0.781 | 0.210 | 3 | 0.916 |
RSK4 |
0.781 | 0.012 | -3 | 0.679 |
PKG2 |
0.781 | -0.005 | -2 | 0.684 |
MEK1 |
0.781 | 0.001 | 2 | 0.826 |
BRAF |
0.780 | 0.015 | -4 | 0.844 |
AURB |
0.780 | -0.017 | -2 | 0.648 |
PKCI |
0.780 | 0.069 | 2 | 0.753 |
PIM2 |
0.780 | 0.020 | -3 | 0.687 |
MARK2 |
0.780 | 0.109 | 4 | 0.743 |
PERK |
0.780 | -0.071 | -2 | 0.872 |
CLK4 |
0.779 | 0.007 | -3 | 0.703 |
GRK7 |
0.779 | 0.049 | 1 | 0.790 |
BMPR1B |
0.779 | -0.014 | 1 | 0.745 |
CAMK4 |
0.779 | -0.089 | -3 | 0.771 |
NEK5 |
0.779 | 0.014 | 1 | 0.895 |
MAPKAPK2 |
0.779 | -0.041 | -3 | 0.671 |
MSK2 |
0.779 | -0.033 | -3 | 0.690 |
CLK2 |
0.779 | 0.081 | -3 | 0.689 |
TAO2 |
0.779 | 0.134 | 2 | 0.850 |
JNK2 |
0.779 | 0.028 | 1 | 0.551 |
MEKK2 |
0.778 | 0.088 | 2 | 0.796 |
BRSK2 |
0.778 | -0.010 | -3 | 0.774 |
PRP4 |
0.778 | 0.044 | -3 | 0.835 |
CDK17 |
0.778 | 0.041 | 1 | 0.477 |
PHKG2 |
0.778 | 0.012 | -3 | 0.746 |
CDK9 |
0.778 | 0.004 | 1 | 0.597 |
MINK |
0.778 | 0.209 | 1 | 0.866 |
PKCE |
0.777 | 0.096 | 2 | 0.739 |
PAK2 |
0.777 | -0.058 | -2 | 0.782 |
TLK2 |
0.777 | -0.057 | 1 | 0.838 |
PLK1 |
0.776 | -0.118 | -2 | 0.826 |
JNK3 |
0.776 | 0.008 | 1 | 0.592 |
PINK1 |
0.776 | -0.047 | 1 | 0.827 |
MAP3K15 |
0.776 | 0.233 | 1 | 0.854 |
MARK1 |
0.775 | 0.088 | 4 | 0.806 |
IRAK1 |
0.775 | -0.088 | -1 | 0.109 |
HIPK1 |
0.775 | 0.027 | 1 | 0.669 |
P38B |
0.775 | 0.019 | 1 | 0.573 |
PRKX |
0.775 | 0.032 | -3 | 0.608 |
MEK5 |
0.774 | -0.015 | 2 | 0.815 |
P38G |
0.774 | 0.018 | 1 | 0.466 |
ACVR2B |
0.774 | -0.066 | -2 | 0.833 |
EEF2K |
0.774 | 0.114 | 3 | 0.901 |
CHK1 |
0.774 | -0.044 | -3 | 0.802 |
NEK4 |
0.774 | 0.083 | 1 | 0.874 |
ACVR2A |
0.774 | -0.066 | -2 | 0.819 |
MEKK6 |
0.773 | 0.194 | 1 | 0.859 |
CDK14 |
0.773 | 0.061 | 1 | 0.595 |
CDK16 |
0.773 | 0.068 | 1 | 0.499 |
KHS1 |
0.773 | 0.203 | 1 | 0.850 |
ERK1 |
0.773 | -0.006 | 1 | 0.563 |
CDK10 |
0.772 | 0.054 | 1 | 0.574 |
MEKK3 |
0.772 | -0.026 | 1 | 0.862 |
BRSK1 |
0.772 | -0.030 | -3 | 0.746 |
YSK1 |
0.772 | 0.205 | 2 | 0.809 |
CAMK2B |
0.772 | -0.052 | 2 | 0.741 |
AURA |
0.771 | -0.026 | -2 | 0.605 |
PLK3 |
0.771 | -0.094 | 2 | 0.755 |
KHS2 |
0.771 | 0.206 | 1 | 0.848 |
CAMKK1 |
0.771 | -0.040 | -2 | 0.841 |
CDK6 |
0.771 | 0.056 | 1 | 0.576 |
SNRK |
0.771 | -0.105 | 2 | 0.684 |
LKB1 |
0.771 | 0.028 | -3 | 0.850 |
AKT3 |
0.771 | 0.047 | -3 | 0.554 |
GCK |
0.770 | 0.148 | 1 | 0.843 |
HIPK3 |
0.770 | 0.001 | 1 | 0.684 |
NEK1 |
0.770 | 0.126 | 1 | 0.885 |
HIPK2 |
0.770 | 0.011 | 1 | 0.540 |
MSK1 |
0.769 | -0.037 | -3 | 0.699 |
ALK2 |
0.769 | -0.070 | -2 | 0.831 |
DCAMKL2 |
0.769 | 0.008 | -3 | 0.754 |
NEK11 |
0.769 | 0.065 | 1 | 0.862 |
PDK1 |
0.769 | 0.067 | 1 | 0.860 |
HPK1 |
0.768 | 0.155 | 1 | 0.833 |
MST2 |
0.768 | 0.074 | 1 | 0.868 |
PAK5 |
0.768 | -0.027 | -2 | 0.655 |
CAMKK2 |
0.768 | -0.030 | -2 | 0.842 |
PKACA |
0.768 | 0.018 | -2 | 0.623 |
P70S6K |
0.767 | -0.038 | -3 | 0.652 |
LOK |
0.767 | 0.019 | -2 | 0.824 |
CAMK2A |
0.767 | -0.078 | 2 | 0.755 |
MYLK4 |
0.767 | -0.075 | -2 | 0.779 |
DRAK1 |
0.767 | -0.083 | 1 | 0.759 |
ERK2 |
0.766 | -0.048 | 1 | 0.609 |
PBK |
0.766 | 0.119 | 1 | 0.842 |
NEK3 |
0.766 | 0.092 | 1 | 0.850 |
P38D |
0.766 | 0.006 | 1 | 0.495 |
SSTK |
0.765 | -0.036 | 4 | 0.830 |
MAPKAPK5 |
0.765 | -0.121 | -3 | 0.672 |
DYRK1A |
0.765 | -0.020 | 1 | 0.694 |
NEK8 |
0.764 | -0.091 | 2 | 0.823 |
PKN1 |
0.764 | 0.008 | -3 | 0.665 |
SMMLCK |
0.764 | -0.035 | -3 | 0.775 |
CAMK1G |
0.764 | -0.051 | -3 | 0.702 |
MST1 |
0.764 | 0.058 | 1 | 0.864 |
TTBK1 |
0.764 | -0.116 | 2 | 0.640 |
SGK1 |
0.763 | 0.056 | -3 | 0.539 |
LRRK2 |
0.763 | 0.046 | 2 | 0.845 |
PAK4 |
0.762 | -0.033 | -2 | 0.649 |
GAK |
0.762 | 0.042 | 1 | 0.894 |
ERK7 |
0.762 | 0.001 | 2 | 0.526 |
TLK1 |
0.762 | -0.127 | -2 | 0.838 |
BUB1 |
0.762 | 0.025 | -5 | 0.740 |
CDK4 |
0.761 | 0.017 | 1 | 0.543 |
CK1G1 |
0.761 | -0.001 | -3 | 0.499 |
MAK |
0.761 | 0.081 | -2 | 0.764 |
MRCKB |
0.760 | 0.016 | -3 | 0.680 |
DYRK3 |
0.760 | -0.003 | 1 | 0.678 |
MYO3B |
0.760 | 0.163 | 2 | 0.824 |
BMPR1A |
0.760 | -0.042 | 1 | 0.730 |
ROCK2 |
0.760 | 0.044 | -3 | 0.735 |
CK1E |
0.758 | -0.038 | -3 | 0.500 |
DYRK1B |
0.758 | -0.013 | 1 | 0.590 |
MRCKA |
0.758 | 0.015 | -3 | 0.696 |
MEK2 |
0.758 | 0.018 | 2 | 0.804 |
GRK2 |
0.757 | -0.094 | -2 | 0.740 |
DYRK4 |
0.757 | -0.003 | 1 | 0.553 |
HASPIN |
0.757 | 0.000 | -1 | 0.128 |
TAO1 |
0.756 | 0.103 | 1 | 0.812 |
MYO3A |
0.756 | 0.165 | 1 | 0.854 |
VRK1 |
0.755 | -0.067 | 2 | 0.868 |
TAK1 |
0.755 | -0.088 | 1 | 0.870 |
STK33 |
0.755 | -0.069 | 2 | 0.620 |
SLK |
0.755 | -0.050 | -2 | 0.766 |
MOK |
0.754 | 0.049 | 1 | 0.685 |
JNK1 |
0.752 | -0.005 | 1 | 0.533 |
PASK |
0.751 | -0.099 | -3 | 0.815 |
DAPK3 |
0.751 | -0.035 | -3 | 0.743 |
CAMK1D |
0.751 | -0.059 | -3 | 0.620 |
RIPK2 |
0.750 | -0.115 | 1 | 0.838 |
GSK3B |
0.750 | -0.032 | 4 | 0.390 |
CHK2 |
0.750 | -0.037 | -3 | 0.561 |
OSR1 |
0.749 | 0.004 | 2 | 0.784 |
CK1D |
0.748 | -0.046 | -3 | 0.445 |
PLK2 |
0.747 | -0.045 | -3 | 0.838 |
CK1A2 |
0.747 | -0.041 | -3 | 0.441 |
GSK3A |
0.747 | -0.006 | 4 | 0.400 |
ASK1 |
0.747 | 0.097 | 1 | 0.844 |
ROCK1 |
0.747 | 0.023 | -3 | 0.696 |
DMPK1 |
0.746 | 0.032 | -3 | 0.696 |
PKMYT1_TYR |
0.745 | 0.326 | 3 | 0.850 |
BIKE |
0.744 | 0.068 | 1 | 0.798 |
PKG1 |
0.744 | -0.037 | -2 | 0.610 |
CAMK1A |
0.743 | -0.047 | -3 | 0.585 |
CK2A2 |
0.741 | -0.065 | 1 | 0.644 |
GRK3 |
0.741 | -0.094 | -2 | 0.683 |
SBK |
0.741 | -0.010 | -3 | 0.493 |
DAPK1 |
0.740 | -0.056 | -3 | 0.724 |
CRIK |
0.740 | 0.010 | -3 | 0.641 |
TTK |
0.739 | -0.039 | -2 | 0.819 |
PDHK3_TYR |
0.737 | 0.024 | 4 | 0.920 |
MAP2K4_TYR |
0.737 | 0.143 | -1 | 0.238 |
LIMK2_TYR |
0.735 | 0.078 | -3 | 0.883 |
AAK1 |
0.734 | 0.113 | 1 | 0.695 |
TESK1_TYR |
0.734 | -0.004 | 3 | 0.876 |
TYK2 |
0.734 | 0.040 | 1 | 0.888 |
ALPHAK3 |
0.733 | -0.076 | -1 | 0.147 |
TNNI3K_TYR |
0.732 | 0.110 | 1 | 0.891 |
BMPR2_TYR |
0.732 | 0.003 | -1 | 0.212 |
MAP2K7_TYR |
0.732 | 0.044 | 2 | 0.848 |
JAK2 |
0.730 | 0.012 | 1 | 0.881 |
LIMK1_TYR |
0.730 | 0.058 | 2 | 0.851 |
PINK1_TYR |
0.730 | -0.017 | 1 | 0.869 |
MAP2K6_TYR |
0.730 | 0.006 | -1 | 0.214 |
ABL2 |
0.729 | -0.040 | -1 | 0.122 |
JAK1 |
0.729 | 0.095 | 1 | 0.844 |
EPHA6 |
0.729 | -0.075 | -1 | 0.127 |
ROS1 |
0.728 | -0.018 | 3 | 0.794 |
CK2A1 |
0.727 | -0.083 | 1 | 0.618 |
MST1R |
0.727 | -0.079 | 3 | 0.815 |
CSF1R |
0.726 | -0.045 | 3 | 0.803 |
RET |
0.726 | -0.114 | 1 | 0.879 |
TYRO3 |
0.726 | -0.086 | 3 | 0.827 |
ABL1 |
0.726 | -0.045 | -1 | 0.125 |
EPHB4 |
0.725 | -0.106 | -1 | 0.124 |
LCK |
0.724 | -0.032 | -1 | 0.108 |
PDHK4_TYR |
0.724 | -0.051 | 2 | 0.855 |
YANK3 |
0.724 | -0.040 | 2 | 0.406 |
YES1 |
0.723 | -0.048 | -1 | 0.134 |
HCK |
0.723 | -0.077 | -1 | 0.115 |
TNK1 |
0.723 | 0.010 | 3 | 0.798 |
ITK |
0.722 | -0.070 | -1 | 0.107 |
PDHK1_TYR |
0.722 | -0.117 | -1 | 0.182 |
STLK3 |
0.722 | -0.111 | 1 | 0.837 |
FLT3 |
0.721 | -0.061 | 3 | 0.827 |
TNK2 |
0.721 | -0.045 | 3 | 0.755 |
WEE1_TYR |
0.720 | -0.027 | -1 | 0.122 |
JAK3 |
0.720 | -0.094 | 1 | 0.848 |
BLK |
0.720 | -0.028 | -1 | 0.116 |
PDGFRB |
0.720 | -0.086 | 3 | 0.822 |
FGR |
0.719 | -0.087 | 1 | 0.895 |
TXK |
0.718 | -0.063 | 1 | 0.818 |
BMX |
0.718 | -0.084 | -1 | 0.080 |
DDR1 |
0.717 | -0.116 | 4 | 0.842 |
BTK |
0.717 | -0.125 | -1 | 0.091 |
NEK10_TYR |
0.717 | -0.005 | 1 | 0.735 |
KIT |
0.716 | -0.101 | 3 | 0.805 |
PDGFRA |
0.715 | -0.090 | 3 | 0.834 |
TEC |
0.715 | -0.107 | -1 | 0.086 |
FER |
0.714 | -0.163 | 1 | 0.878 |
SRMS |
0.713 | -0.136 | 1 | 0.862 |
EPHB2 |
0.713 | -0.129 | -1 | 0.107 |
EPHB1 |
0.713 | -0.153 | 1 | 0.870 |
PTK6 |
0.713 | -0.149 | -1 | 0.092 |
KDR |
0.712 | -0.094 | 3 | 0.749 |
EPHB3 |
0.712 | -0.146 | -1 | 0.106 |
LYN |
0.712 | -0.069 | 3 | 0.747 |
AXL |
0.712 | -0.136 | 3 | 0.758 |
INSRR |
0.711 | -0.136 | 3 | 0.741 |
FYN |
0.710 | -0.060 | -1 | 0.107 |
ALK |
0.710 | -0.123 | 3 | 0.733 |
TEK |
0.710 | -0.127 | 3 | 0.752 |
FGFR1 |
0.710 | -0.119 | 3 | 0.752 |
MERTK |
0.710 | -0.135 | 3 | 0.756 |
EPHA4 |
0.709 | -0.107 | 2 | 0.759 |
LTK |
0.709 | -0.123 | 3 | 0.743 |
FRK |
0.709 | -0.098 | -1 | 0.105 |
FGFR2 |
0.708 | -0.153 | 3 | 0.760 |
MET |
0.707 | -0.120 | 3 | 0.780 |
NTRK2 |
0.706 | -0.141 | 3 | 0.757 |
NTRK1 |
0.706 | -0.146 | -1 | 0.143 |
EPHA7 |
0.704 | -0.126 | 2 | 0.763 |
EPHA1 |
0.703 | -0.141 | 3 | 0.761 |
SRC |
0.703 | -0.070 | -1 | 0.116 |
MATK |
0.703 | -0.101 | -1 | 0.102 |
NTRK3 |
0.703 | -0.119 | -1 | 0.126 |
CK1A |
0.703 | -0.070 | -3 | 0.354 |
ERBB2 |
0.703 | -0.128 | 1 | 0.836 |
FLT1 |
0.703 | -0.137 | -1 | 0.140 |
INSR |
0.702 | -0.128 | 3 | 0.729 |
MUSK |
0.702 | -0.071 | 1 | 0.748 |
FLT4 |
0.702 | -0.139 | 3 | 0.744 |
EPHA3 |
0.701 | -0.145 | 2 | 0.734 |
PTK2B |
0.701 | -0.105 | -1 | 0.094 |
CSK |
0.697 | -0.119 | 2 | 0.767 |
DDR2 |
0.696 | -0.073 | 3 | 0.720 |
EGFR |
0.696 | -0.086 | 1 | 0.754 |
FGFR3 |
0.695 | -0.169 | 3 | 0.731 |
FGFR4 |
0.695 | -0.105 | -1 | 0.120 |
EPHA8 |
0.694 | -0.131 | -1 | 0.100 |
EPHA5 |
0.693 | -0.149 | 2 | 0.738 |
YANK2 |
0.693 | -0.050 | 2 | 0.416 |
PTK2 |
0.691 | -0.091 | -1 | 0.136 |
EPHA2 |
0.687 | -0.134 | -1 | 0.100 |
IGF1R |
0.686 | -0.136 | 3 | 0.667 |
SYK |
0.686 | -0.115 | -1 | 0.115 |
CK1G3 |
0.683 | -0.083 | -3 | 0.306 |
ERBB4 |
0.678 | -0.090 | 1 | 0.738 |
FES |
0.678 | -0.140 | -1 | 0.080 |
ZAP70 |
0.673 | -0.076 | -1 | 0.116 |
CK1G2 |
0.665 | -0.090 | -3 | 0.409 |