Motif 1002 (n=147)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
O14523 | C2CD2L | T670 | ochoa | Phospholipid transfer protein C2CD2L (C2 domain-containing protein 2-like) (C2CD2-like) (Transmembrane protein 24) | Lipid-binding protein that transports phosphatidylinositol, the precursor of phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), from its site of synthesis in the endoplasmic reticulum to the cell membrane (PubMed:28209843). It thereby maintains the pool of cell membrane phosphoinositides, which are degraded during phospholipase C (PLC) signaling (PubMed:28209843). Plays a key role in the coordination of Ca(2+) and phosphoinositide signaling: localizes to sites of contact between the endoplasmic reticulum and the cell membrane, where it tethers the two bilayers (PubMed:28209843). In response to elevation of cytosolic Ca(2+), it is phosphorylated at its C-terminus and dissociates from the cell membrane, abolishing phosphatidylinositol transport to the cell membrane (PubMed:28209843). Positively regulates insulin secretion in response to glucose: phosphatidylinositol transfer to the cell membrane allows replenishment of PI(4,5)P2 pools and calcium channel opening, priming a new population of insulin granules (PubMed:28209843). {ECO:0000269|PubMed:28209843}. |
O14976 | GAK | T329 | ochoa | Cyclin-G-associated kinase (EC 2.7.11.1) (DnaJ homolog subfamily C member 26) | Associates with cyclin G and CDK5. Seems to act as an auxilin homolog that is involved in the uncoating of clathrin-coated vesicles by Hsc70 in non-neuronal cells. Expression oscillates slightly during the cell cycle, peaking at G1 (PubMed:10625686). May play a role in clathrin-mediated endocytosis and intracellular trafficking, and in the dynamics of clathrin assembly/disassembly (PubMed:18489706). {ECO:0000269|PubMed:10625686, ECO:0000269|PubMed:18489706}. |
O15173 | PGRMC2 | T93 | ochoa | Membrane-associated progesterone receptor component 2 (Progesterone membrane-binding protein) (Steroid receptor protein DG6) | Required for the maintenance of uterine histoarchitecture and normal female reproductive lifespan (By similarity). May serve as a universal non-classical progesterone receptor in the uterus (Probable). Intracellular heme chaperone required for delivery of labile, or signaling heme, to the nucleus (By similarity). Plays a role in adipocyte function and systemic glucose homeostasis (PubMed:28111073). In brown fat, which has a high demand for heme, delivery of labile heme in the nucleus regulates the activity of heme-responsive transcriptional repressors such as NR1D1 and BACH1 (By similarity). {ECO:0000250|UniProtKB:Q80UU9, ECO:0000269|PubMed:28111073, ECO:0000305|PubMed:28396637}. |
O15409 | FOXP2 | T458 | ochoa | Forkhead box protein P2 (CAG repeat protein 44) (Trinucleotide repeat-containing gene 10 protein) | Transcriptional repressor that may play a role in the specification and differentiation of lung epithelium. May also play a role in developing neural, gastrointestinal and cardiovascular tissues. Can act with CTBP1 to synergistically repress transcription but CTPBP1 is not essential. Plays a role in synapse formation by regulating SRPX2 levels. Involved in neural mechanisms mediating the development of speech and language. |
O43310 | CTIF | T302 | ochoa | CBP80/20-dependent translation initiation factor | Specifically required for the pioneer round of mRNA translation mediated by the cap-binding complex (CBC), that takes place during or right after mRNA export via the nuclear pore complex (NPC). Acts via its interaction with the NCBP1/CBP80 component of the CBC complex and recruits the 40S small subunit of the ribosome via eIF3. In contrast, it is not involved in steady state translation, that takes place when the CBC complex is replaced by cytoplasmic cap-binding protein eIF4E. Also required for nonsense-mediated mRNA decay (NMD), the pioneer round of mRNA translation mediated by the cap-binding complex playing a central role in nonsense-mediated mRNA decay (NMD). {ECO:0000269|PubMed:19648179}. |
O75037 | KIF21B | T1244 | ochoa | Kinesin-like protein KIF21B | Plus-end directed microtubule-dependent motor protein which displays processive activity. Is involved in regulation of microtubule dynamics, synapse function and neuronal morphology, including dendritic tree branching and spine formation. Plays a role in lerning and memory. Involved in delivery of gamma-aminobutyric acid (GABA(A)) receptor to cell surface. {ECO:0000250|UniProtKB:Q9QXL1}. |
O75132 | ZBED4 | T627 | ochoa | Zinc finger BED domain-containing protein 4 | Transcriptional regulator that binds to poly-guanine tracts in gene promoters and activates transcription (By similarity). Able to bind single- and double-stranded DNA and RNA (By similarity). {ECO:0000250|UniProtKB:Q80WQ9}. |
O75363 | BCAS1 | T66 | ochoa | Breast carcinoma-amplified sequence 1 (Amplified and overexpressed in breast cancer) (Novel amplified in breast cancer 1) | Required for myelination. {ECO:0000250|UniProtKB:Q80YN3}. |
O75369 | FLNB | T935 | 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. |
O75369 | FLNB | T1031 | 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. |
O75581 | LRP6 | T1493 | ochoa|psp | Low-density lipoprotein receptor-related protein 6 (LRP-6) | Component of the Wnt-Fzd-LRP5-LRP6 complex that triggers beta-catenin signaling through inducing aggregation of receptor-ligand complexes into ribosome-sized signalosomes (PubMed:11357136, PubMed:11448771, PubMed:15778503, PubMed:16341017, PubMed:16513652, PubMed:17326769, PubMed:17400545, PubMed:19107203, PubMed:19293931, PubMed:19801552, PubMed:28341812). Cell-surface coreceptor of Wnt/beta-catenin signaling, which plays a pivotal role in bone formation (PubMed:11357136, PubMed:11448771, PubMed:15778503, PubMed:16341017, PubMed:16513652, PubMed:17326769, PubMed:17400545, PubMed:19107203, PubMed:19293931, PubMed:19801552, PubMed:28341812). The Wnt-induced Fzd/LRP6 coreceptor complex recruits DVL1 polymers to the plasma membrane which, in turn, recruits the AXIN1/GSK3B-complex to the cell surface promoting the formation of signalosomes and inhibiting AXIN1/GSK3-mediated phosphorylation and destruction of beta-catenin (PubMed:16513652). Required for posterior patterning of the epiblast during gastrulation (By similarity). {ECO:0000250|UniProtKB:O88572, ECO:0000269|PubMed:11357136, ECO:0000269|PubMed:11448771, ECO:0000269|PubMed:15778503, ECO:0000269|PubMed:16341017, ECO:0000269|PubMed:16513652, ECO:0000269|PubMed:17326769, ECO:0000269|PubMed:17400545, ECO:0000269|PubMed:19107203, ECO:0000269|PubMed:19293931, ECO:0000269|PubMed:19801552, ECO:0000269|PubMed:28341812}. |
O76061 | STC2 | T254 | ochoa | Stanniocalcin-2 (STC-2) (Stanniocalcin-related protein) (STC-related protein) (STCRP) | Has an anti-hypocalcemic action on calcium and phosphate homeostasis. |
P05187 | ALPP | T117 | ochoa | Alkaline phosphatase, placental type (EC 3.1.3.1) (Alkaline phosphatase Regan isozyme) (Placental alkaline phosphatase 1) (PLAP-1) | Alkaline phosphatase that can hydrolyze various phosphate compounds. {ECO:0000269|PubMed:1939159, ECO:0000269|PubMed:25775211}. |
P0DPH7 | TUBA3C | T51 | ochoa | Tubulin alpha-3C chain (EC 3.6.5.-) (Alpha-tubulin 2) (Alpha-tubulin 3C) (Tubulin alpha-2 chain) [Cleaved into: Detyrosinated tubulin alpha-3C chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
P0DPH7 | TUBA3C | T94 | ochoa | Tubulin alpha-3C chain (EC 3.6.5.-) (Alpha-tubulin 2) (Alpha-tubulin 3C) (Tubulin alpha-2 chain) [Cleaved into: Detyrosinated tubulin alpha-3C chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
P0DPH8 | TUBA3D | T51 | ochoa | Tubulin alpha-3D chain (EC 3.6.5.-) (Alpha-tubulin 3D) [Cleaved into: Detyrosinated tubulin alpha-3D chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
P0DPH8 | TUBA3D | T94 | ochoa | Tubulin alpha-3D chain (EC 3.6.5.-) (Alpha-tubulin 3D) [Cleaved into: Detyrosinated tubulin alpha-3D chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
P10244 | MYBL2 | T396 | ochoa | Myb-related protein B (B-Myb) (Myb-like protein 2) | Transcription factor involved in the regulation of cell survival, proliferation, and differentiation. Transactivates the expression of the CLU gene. {ECO:0000269|PubMed:10770937}. |
P10589 | NR2F1 | T66 | ochoa | COUP transcription factor 1 (COUP-TF1) (COUP transcription factor I) (COUP-TF I) (Nuclear receptor subfamily 2 group F member 1) (V-erbA-related protein 3) (EAR-3) | Coup (chicken ovalbumin upstream promoter) transcription factor binds to the ovalbumin promoter and, in conjunction with another protein (S300-II) stimulates initiation of transcription. Binds to both direct repeats and palindromes of the 5'-AGGTCA-3' motif. Represses transcriptional activity of LHCG. {ECO:0000269|PubMed:10644740, ECO:0000269|PubMed:11682620}. |
P10696 | ALPG | T114 | ochoa | Alkaline phosphatase, germ cell type (EC 3.1.3.1) (ALP-1) (Alkaline phosphatase Nagao isozyme) (Alkaline phosphatase, placental-like) (Germ cell alkaline phosphatase) (GCAP) (Placental alkaline phosphatase-like) (PLAP-like) | Alkaline phosphatase that can hydrolyze various phosphate compounds. {ECO:0000269|PubMed:1939159}. |
P15260 | IFNGR1 | T330 | ochoa | Interferon gamma receptor 1 (IFN-gamma receptor 1) (IFN-gamma-R1) (CDw119) (Interferon gamma receptor alpha-chain) (IFN-gamma-R-alpha) (CD antigen CD119) | Receptor subunit for interferon gamma/INFG that plays crucial roles in antimicrobial, antiviral, and antitumor responses by activating effector immune cells and enhancing antigen presentation (PubMed:20015550). Associates with transmembrane accessory factor IFNGR2 to form a functional receptor (PubMed:10986460, PubMed:2971451, PubMed:7615558, PubMed:7617032, PubMed:7673114). Upon ligand binding, the intracellular domain of IFNGR1 opens out to allow association of downstream signaling components JAK1 and JAK2. In turn, activated JAK1 phosphorylates IFNGR1 to form a docking site for STAT1. Subsequent phosphorylation of STAT1 leads to dimerization, translocation to the nucleus, and stimulation of target gene transcription (PubMed:28883123). STAT3 can also be activated in a similar manner although activation seems weaker. IFNGR1 intracellular domain phosphorylation also provides a docking site for SOCS1 that regulates the JAK-STAT pathway by competing with STAT1 binding to IFNGR1 (By similarity). {ECO:0000250|UniProtKB:P15261, ECO:0000269|PubMed:10986460, ECO:0000269|PubMed:20015550, ECO:0000269|PubMed:28883123, ECO:0000269|PubMed:2971451, ECO:0000269|PubMed:7615558, ECO:0000269|PubMed:7617032, ECO:0000269|PubMed:7673114}. |
P17096 | HMGA1 | T39 | ochoa | High mobility group protein HMG-I/HMG-Y (HMG-I(Y)) (High mobility group AT-hook protein 1) (High mobility group protein A1) (High mobility group protein R) | HMG-I/Y bind preferentially to the minor groove of A+T rich regions in double-stranded DNA. It is suggested that these proteins could function in nucleosome phasing and in the 3'-end processing of mRNA transcripts. They are also involved in the transcription regulation of genes containing, or in close proximity to A+T-rich regions. |
P19438 | TNFRSF1A | T353 | ochoa | Tumor necrosis factor receptor superfamily member 1A (Tumor necrosis factor receptor 1) (TNF-R1) (Tumor necrosis factor receptor type I) (TNF-RI) (TNFR-I) (p55) (p60) (CD antigen CD120a) [Cleaved into: Tumor necrosis factor receptor superfamily member 1A, membrane form; Tumor necrosis factor-binding protein 1 (TBPI)] | Receptor for TNFSF2/TNF-alpha and homotrimeric TNFSF1/lymphotoxin-alpha. The adapter molecule FADD recruits caspase-8 to the activated receptor. The resulting death-inducing signaling complex (DISC) performs caspase-8 proteolytic activation which initiates the subsequent cascade of caspases (aspartate-specific cysteine proteases) mediating apoptosis. Contributes to the induction of non-cytocidal TNF effects including anti-viral state and activation of the acid sphingomyelinase. |
P21291 | CSRP1 | T101 | ochoa | Cysteine and glycine-rich protein 1 (Cysteine-rich protein 1) (CRP) (CRP1) (Epididymis luminal protein 141) (HEL-141) | Could play a role in neuronal development. |
P21796 | VDAC1 | T107 | ochoa|psp | Non-selective voltage-gated ion channel VDAC1 (Outer mitochondrial membrane protein porin 1) (Plasmalemmal porin) (Porin 31HL) (Porin 31HM) (Voltage-dependent anion-selective channel protein 1) (VDAC-1) (hVDAC1) | Non-selective voltage-gated ion channel that mediates the transport of anions and cations through the mitochondrion outer membrane and plasma membrane (PubMed:10661876, PubMed:11845315, PubMed:18755977, PubMed:30061676, PubMed:8420959). The channel at the outer mitochondrial membrane allows diffusion of small hydrophilic molecules; in the plasma membrane it is involved in cell volume regulation and apoptosis (PubMed:10661876, PubMed:11845315, PubMed:18755977, PubMed:8420959). It adopts an open conformation at low or zero membrane potential and a closed conformation at potentials above 30-40 mV (PubMed:10661876, PubMed:18755977, PubMed:8420959). The open state has a weak anion selectivity whereas the closed state is cation-selective (PubMed:18755977, PubMed:8420959). Binds various signaling molecules, including the sphingolipid ceramide, the phospholipid phosphatidylcholine, and the sterols cholesterol and oxysterol (PubMed:18755977, PubMed:31015432). In depolarized mitochondria, acts downstream of PRKN and PINK1 to promote mitophagy or prevent apoptosis; polyubiquitination by PRKN promotes mitophagy, while monoubiquitination by PRKN decreases mitochondrial calcium influx which ultimately inhibits apoptosis (PubMed:32047033). May participate in the formation of the permeability transition pore complex (PTPC) responsible for the release of mitochondrial products that triggers apoptosis (PubMed:15033708, PubMed:25296756). May mediate ATP export from cells (PubMed:30061676). Part of a complex composed of HSPA9, ITPR1 and VDAC1 that regulates mitochondrial calcium-dependent apoptosis by facilitating calcium transport from the ER lumen to the mitochondria intermembrane space thus providing calcium for the downstream calcium channel MCU that directly releases it into mitochondria matrix (By similarity). Mediates cytochrome c efflux (PubMed:20230784). {ECO:0000250|UniProtKB:Q60932, ECO:0000269|PubMed:10661876, ECO:0000269|PubMed:11845315, ECO:0000269|PubMed:15033708, ECO:0000269|PubMed:18755977, ECO:0000269|PubMed:20230784, ECO:0000269|PubMed:25296756, ECO:0000269|PubMed:30061676, ECO:0000269|PubMed:31015432, ECO:0000269|PubMed:32047033, ECO:0000269|PubMed:8420959}.; FUNCTION: Catalyzes the scrambling of phospholipids across the outer mitochondrial membrane; the mechanism is unrelated to channel activity and is capable of translocating both anionic and zwitterionic phospholipids. {ECO:0000269|PubMed:38065946}. |
P29474 | NOS3 | T60 | ochoa | Nitric oxide synthase 3 (EC 1.14.13.39) (Constitutive NOS) (cNOS) (EC-NOS) (NOS type III) (NOSIII) (Nitric oxide synthase, endothelial) (Endothelial NOS) (eNOS) | Produces nitric oxide (NO) which is implicated in vascular smooth muscle relaxation through a cGMP-mediated signal transduction pathway (PubMed:1378832). NO mediates vascular endothelial growth factor (VEGF)-induced angiogenesis in coronary vessels and promotes blood clotting through the activation of platelets. {ECO:0000269|PubMed:1378832}.; FUNCTION: [Isoform eNOS13C]: Lacks eNOS activity, dominant-negative form that may down-regulate eNOS activity by forming heterodimers with isoform 1. |
P31943 | HNRNPH1 | T107 | ochoa | Heterogeneous nuclear ribonucleoprotein H (hnRNP H) [Cleaved into: Heterogeneous nuclear ribonucleoprotein H, N-terminally processed] | This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Mediates pre-mRNA alternative splicing regulation. Inhibits, together with CUGBP1, insulin receptor (IR) pre-mRNA exon 11 inclusion in myoblast. Binds to the IR RNA. Binds poly(RG). {ECO:0000269|PubMed:11003644, ECO:0000269|PubMed:16946708}. |
P32519 | ELF1 | T190 | ochoa | ETS-related transcription factor Elf-1 (E74-like factor 1) | Transcription factor that activates the LYN and BLK promoters. Appears to be required for the T-cell-receptor-mediated trans activation of HIV-2 gene expression. Binds specifically to two purine-rich motifs in the HIV-2 enhancer. {ECO:0000269|PubMed:8756667}. |
P33241 | LSP1 | T196 | ochoa | Lymphocyte-specific protein 1 (47 kDa actin-binding protein) (52 kDa phosphoprotein) (pp52) (Lymphocyte-specific antigen WP34) | May play a role in mediating neutrophil activation and chemotaxis. {ECO:0000250}. |
P35568 | IRS1 | T351 | ochoa | Insulin receptor substrate 1 (IRS-1) | Signaling adapter protein that participates in the signal transduction from two prominent receptor tyrosine kinases, insulin receptor/INSR and insulin-like growth factor I receptor/IGF1R (PubMed:7541045, PubMed:33991522, PubMed:38625937). Plays therefore an important role in development, growth, glucose homeostasis as well as lipid metabolism (PubMed:19639489). Upon phosphorylation by the insulin receptor, functions as a signaling scaffold that propagates insulin action through binding to SH2 domain-containing proteins including the p85 regulatory subunit of PI3K, NCK1, NCK2, GRB2 or SHP2 (PubMed:11171109, PubMed:8265614). Recruitment of GRB2 leads to the activation of the guanine nucleotide exchange factor SOS1 which in turn triggers the Ras/Raf/MEK/MAPK signaling cascade (By similarity). Activation of the PI3K/AKT pathway is responsible for most of insulin metabolic effects in the cell, and the Ras/Raf/MEK/MAPK is involved in the regulation of gene expression and in cooperation with the PI3K pathway regulates cell growth and differentiation. Acts a positive regulator of the Wnt/beta-catenin signaling pathway through suppression of DVL2 autophagy-mediated degradation leading to cell proliferation (PubMed:24616100). {ECO:0000250|UniProtKB:P35570, ECO:0000269|PubMed:11171109, ECO:0000269|PubMed:16878150, ECO:0000269|PubMed:19639489, ECO:0000269|PubMed:38625937, ECO:0000269|PubMed:7541045, ECO:0000269|PubMed:8265614}. |
P35869 | AHR | T697 | psp | Aryl hydrocarbon receptor (Ah receptor) (AhR) (Class E basic helix-loop-helix protein 76) (bHLHe76) | Ligand-activated transcription factor that enables cells to adapt to changing conditions by sensing compounds from the environment, diet, microbiome and cellular metabolism, and which plays important roles in development, immunity and cancer (PubMed:23275542, PubMed:30373764, PubMed:32818467, PubMed:7961644). Upon ligand binding, translocates into the nucleus, where it heterodimerizes with ARNT and induces transcription by binding to xenobiotic response elements (XRE) (PubMed:23275542, PubMed:30373764, PubMed:7961644). Regulates a variety of biological processes, including angiogenesis, hematopoiesis, drug and lipid metabolism, cell motility and immune modulation (PubMed:12213388). Xenobiotics can act as ligands: upon xenobiotic-binding, activates the expression of multiple phase I and II xenobiotic chemical metabolizing enzyme genes (such as the CYP1A1 gene) (PubMed:7961644, PubMed:33193710). Mediates biochemical and toxic effects of halogenated aromatic hydrocarbons (PubMed:34521881, PubMed:7961644). Next to xenobiotics, natural ligands derived from plants, microbiota, and endogenous metabolism are potent AHR agonists (PubMed:18076143). Tryptophan (Trp) derivatives constitute an important class of endogenous AHR ligands (PubMed:32818467, PubMed:32866000). Acts as a negative regulator of anti-tumor immunity: indoles and kynurenic acid generated by Trp catabolism act as ligand and activate AHR, thereby promoting AHR-driven cancer cell motility and suppressing adaptive immunity (PubMed:32818467). Regulates the circadian clock by inhibiting the basal and circadian expression of the core circadian component PER1 (PubMed:28602820). Inhibits PER1 by repressing the CLOCK-BMAL1 heterodimer mediated transcriptional activation of PER1 (PubMed:28602820). The heterodimer ARNT:AHR binds to core DNA sequence 5'-TGCGTG-3' within the dioxin response element (DRE) of target gene promoters and activates their transcription (PubMed:28602820). {ECO:0000269|PubMed:23275542, ECO:0000269|PubMed:28602820, ECO:0000269|PubMed:30373764, ECO:0000269|PubMed:32818467, ECO:0000269|PubMed:32866000, ECO:0000269|PubMed:33193710, ECO:0000269|PubMed:34521881, ECO:0000269|PubMed:7961644, ECO:0000303|PubMed:12213388, ECO:0000303|PubMed:18076143}. |
P42858 | HTT | T2654 | ochoa | Huntingtin (Huntington disease protein) (HD protein) [Cleaved into: Huntingtin, myristoylated N-terminal fragment] | [Huntingtin]: May play a role in microtubule-mediated transport or vesicle function.; FUNCTION: [Huntingtin, myristoylated N-terminal fragment]: Promotes the formation of autophagic vesicles. {ECO:0000269|PubMed:24459296}. |
P45880 | VDAC2 | T118 | ochoa | Non-selective voltage-gated ion channel VDAC2 (VDAC-2) (hVDAC2) (Outer mitochondrial membrane protein porin 2) | Non-selective voltage-gated ion channel that mediates the transport of anions and cations through the mitochondrion outer membrane and plasma membrane (PubMed:8420959). The channel adopts an open conformation at zero mV and a closed conformation at both positive and negative potentials (PubMed:8420959). There are two populations of channels; the main that functions in a lower open-state conductance with lower ion selectivity, that switch, in a voltage-dependent manner, from the open to a low-conducting 'closed' state and the other that has a normal ion selectivity in the typical high conductance, 'open' state (PubMed:8420959). Binds various lipids, including the sphingolipid ceramide, the phospholipid phosphatidylcholine, and the sterols cholesterol and oxysterol (PubMed:31015432). Binding of ceramide promotes the mitochondrial outer membrane permeabilization (MOMP) apoptotic pathway (PubMed:31015432). {ECO:0000269|PubMed:31015432, ECO:0000269|PubMed:8420959}.; FUNCTION: Catalyzes the scrambling of phospholipids across the outer mitochondrial membrane; the mechanism is unrelated to channel activity and is capable of translocating both anionic and zwitterionic phospholipids. {ECO:0000269|PubMed:38065946}. |
P49757 | NUMB | T250 | ochoa | Protein numb homolog (h-Numb) (Protein S171) | Regulates clathrin-mediated receptor endocytosis (PubMed:18657069). Plays a role in the process of neurogenesis (By similarity). Required throughout embryonic neurogenesis to maintain neural progenitor cells, also called radial glial cells (RGCs), by allowing their daughter cells to choose progenitor over neuronal cell fate (By similarity). Not required for the proliferation of neural progenitor cells before the onset of neurogenesis. Also involved postnatally in the subventricular zone (SVZ) neurogenesis by regulating SVZ neuroblasts survival and ependymal wall integrity (By similarity). May also mediate local repair of brain ventricular wall damage (By similarity). {ECO:0000250|UniProtKB:Q9QZS3, ECO:0000269|PubMed:18657069}. |
P49815 | TSC2 | T667 | ochoa | Tuberin (Tuberous sclerosis 2 protein) | 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:12842888, PubMed:12906785, PubMed:15340059, PubMed:22819219, PubMed:24529379, PubMed:28215400, PubMed:33436626, PubMed:35772404). Within the TSC-TBC complex, TSC2 acts as a GTPase-activating protein (GAP) for the small GTPase RHEB, a direct activator of the protein kinase activity of mTORC1 (PubMed:12172553, PubMed:12820960, PubMed:12842888, PubMed:12906785, PubMed:15340059, PubMed:22819219, PubMed:24529379, PubMed:33436626). 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:12172553, PubMed:12271141, PubMed:12842888, PubMed:12906785, PubMed:22819219, PubMed:24529379, PubMed:28215400, PubMed:35772404). The TSC-TBC complex is inactivated in response to nutrients, relieving inhibition of mTORC1 (PubMed:12172553, PubMed:24529379). Involved in microtubule-mediated protein transport via its ability to regulate mTORC1 signaling (By similarity). Also stimulates the intrinsic GTPase activity of the Ras-related proteins RAP1A and RAB5 (By similarity). {ECO:0000250|UniProtKB:P49816, ECO:0000269|PubMed:12172553, ECO:0000269|PubMed:12271141, ECO:0000269|PubMed:12820960, ECO:0000269|PubMed:12842888, ECO:0000269|PubMed:12906785, ECO:0000269|PubMed:15340059, ECO:0000269|PubMed:22819219, ECO:0000269|PubMed:24529379, ECO:0000269|PubMed:28215400, ECO:0000269|PubMed:33436626, ECO:0000269|PubMed:35772404}. |
P55196 | AFDN | T249 | ochoa | Afadin (ALL1-fused gene from chromosome 6 protein) (Protein AF-6) (Afadin adherens junction formation factor) | Belongs to an adhesion system, probably together with the E-cadherin-catenin system, which plays a role in the organization of homotypic, interneuronal and heterotypic cell-cell adherens junctions (AJs) (By similarity). Nectin- and actin-filament-binding protein that connects nectin to the actin cytoskeleton (PubMed:11024295). May play a key role in the organization of epithelial structures of the embryonic ectoderm (By similarity). Essential for the organization of adherens junctions (PubMed:30463011). {ECO:0000250|UniProtKB:O35889, ECO:0000250|UniProtKB:Q9QZQ1, ECO:0000269|PubMed:11024295, ECO:0000269|PubMed:30463011}. |
P55795 | HNRNPH2 | T107 | ochoa | Heterogeneous nuclear ribonucleoprotein H2 (hnRNP H2) (FTP-3) (Heterogeneous nuclear ribonucleoprotein H') (hnRNP H') [Cleaved into: Heterogeneous nuclear ribonucleoprotein H2, N-terminally processed] | This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Binds poly(RG). |
P58012 | FOXL2 | T329 | psp | Forkhead box protein L2 | Transcriptional regulator. Critical factor essential for ovary differentiation and maintenance, and repression of the genetic program for somatic testis determination. Prevents trans-differentiation of ovary to testis through transcriptional repression of the Sertoli cell-promoting gene SOX9 (By similarity). Has apoptotic activity in ovarian cells. Suppresses ESR1-mediated transcription of PTGS2/COX2 stimulated by tamoxifen (By similarity). Is a regulator of CYP19 expression (By similarity). Participates in SMAD3-dependent transcription of FST via the intronic SMAD-binding element (By similarity). Is a transcriptional repressor of STAR. Activates SIRT1 transcription under cellular stress conditions. Activates transcription of OSR2. {ECO:0000250, ECO:0000269|PubMed:16153597, ECO:0000269|PubMed:19010791, ECO:0000269|PubMed:19429596, ECO:0000269|PubMed:19744555}. |
P68363 | TUBA1B | T51 | ochoa | Tubulin alpha-1B chain (EC 3.6.5.-) (Alpha-tubulin ubiquitous) (Tubulin K-alpha-1) (Tubulin alpha-ubiquitous chain) [Cleaved into: Detyrosinated tubulin alpha-1B chain] | Tubulin is the major constituent of microtubules, protein filaments consisting of alpha- and beta-tubulin heterodimers (PubMed:38305685, PubMed:34996871, PubMed:38609661). Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms (PubMed:38305685, PubMed:34996871, PubMed:38609661). Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin (PubMed:34996871, PubMed:38609661). {ECO:0000269|PubMed:34996871, ECO:0000269|PubMed:38305685, ECO:0000269|PubMed:38609661}. |
P68363 | TUBA1B | T94 | ochoa | Tubulin alpha-1B chain (EC 3.6.5.-) (Alpha-tubulin ubiquitous) (Tubulin K-alpha-1) (Tubulin alpha-ubiquitous chain) [Cleaved into: Detyrosinated tubulin alpha-1B chain] | Tubulin is the major constituent of microtubules, protein filaments consisting of alpha- and beta-tubulin heterodimers (PubMed:38305685, PubMed:34996871, PubMed:38609661). Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms (PubMed:38305685, PubMed:34996871, PubMed:38609661). Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin (PubMed:34996871, PubMed:38609661). {ECO:0000269|PubMed:34996871, ECO:0000269|PubMed:38305685, ECO:0000269|PubMed:38609661}. |
P68366 | TUBA4A | T94 | ochoa | Tubulin alpha-4A chain (EC 3.6.5.-) (Alpha-tubulin 1) (Testis-specific alpha-tubulin) (Tubulin H2-alpha) (Tubulin alpha-1 chain) | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q01082 | SPTBN1 | T2335 | ochoa | Spectrin beta chain, non-erythrocytic 1 (Beta-II spectrin) (Fodrin beta chain) (Spectrin, non-erythroid beta chain 1) | Fodrin, which seems to be involved in secretion, interacts with calmodulin in a calcium-dependent manner and is thus candidate for the calcium-dependent movement of the cytoskeleton at the membrane. Plays a critical role in central nervous system development and function. {ECO:0000269|PubMed:34211179}. |
Q01094 | E2F1 | T344 | ochoa | Transcription factor E2F1 (E2F-1) (PBR3) (Retinoblastoma-associated protein 1) (RBAP-1) (Retinoblastoma-binding protein 3) (RBBP-3) (pRB-binding protein E2F-1) | Transcription activator that binds DNA cooperatively with DP proteins through the E2 recognition site, 5'-TTTC[CG]CGC-3' found in the promoter region of a number of genes whose products are involved in cell cycle regulation or in DNA replication (PubMed:10675335, PubMed:12717439, PubMed:17050006, PubMed:17704056, PubMed:18625225, PubMed:28992046). The DRTF1/E2F complex functions in the control of cell-cycle progression from G1 to S phase (PubMed:10675335, PubMed:12717439, PubMed:17704056). E2F1 binds preferentially RB1 in a cell-cycle dependent manner (PubMed:10675335, PubMed:12717439, PubMed:17704056). It can mediate both cell proliferation and TP53/p53-dependent apoptosis (PubMed:8170954). Blocks adipocyte differentiation by binding to specific promoters repressing CEBPA binding to its target gene promoters (PubMed:20176812). Directly activates transcription of PEG10 (PubMed:17050006, PubMed:18625225, PubMed:28992046). Positively regulates transcription of RRP1B (PubMed:20040599). {ECO:0000269|PubMed:10675335, ECO:0000269|PubMed:12717439, ECO:0000269|PubMed:17050006, ECO:0000269|PubMed:17704056, ECO:0000269|PubMed:18625225, ECO:0000269|PubMed:20040599, ECO:0000269|PubMed:20176812, ECO:0000269|PubMed:28992046, ECO:0000269|PubMed:8170954}. |
Q01130 | SRSF2 | T29 | ochoa | Serine/arginine-rich splicing factor 2 (Protein PR264) (Splicing component, 35 kDa) (Splicing factor SC35) (SC-35) (Splicing factor, arginine/serine-rich 2) | Necessary for the splicing of pre-mRNA. It is required for formation of the earliest ATP-dependent splicing complex and interacts with spliceosomal components bound to both the 5'- and 3'-splice sites during spliceosome assembly. It also is required for ATP-dependent interactions of both U1 and U2 snRNPs with pre-mRNA. Interacts with other spliceosomal components, via the RS domains, to form a bridge between the 5'- and 3'-splice site binding components, U1 snRNP and U2AF. Binds to purine-rich RNA sequences, either 5'-AGSAGAGTA-3' (S=C or G) or 5'-GTTCGAGTA-3'. Can bind to beta-globin mRNA and commit it to the splicing pathway. The phosphorylated form (by SRPK2) is required for cellular apoptosis in response to cisplatin treatment. {ECO:0000269|PubMed:19592491, ECO:0000269|PubMed:21157427}. |
Q02880 | TOP2B | T1403 | ochoa | DNA topoisomerase 2-beta (EC 5.6.2.2) (DNA topoisomerase II, beta isozyme) | Key decatenating enzyme that alters DNA topology by binding to two double-stranded DNA molecules, generating a double-stranded break in one of the strands, passing the intact strand through the broken strand, and religating the broken strand. Plays a role in B-cell differentiation. {ECO:0000269|PubMed:10684600, ECO:0000269|PubMed:31409799, ECO:0000269|PubMed:32128574}. |
Q02952 | AKAP12 | T289 | 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). |
Q02952 | AKAP12 | T1730 | 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). |
Q04637 | EIF4G1 | T211 | ochoa | Eukaryotic translation initiation factor 4 gamma 1 (eIF-4-gamma 1) (eIF-4G 1) (eIF-4G1) (p220) | Component of the protein complex eIF4F, which is involved in the recognition of the mRNA cap, ATP-dependent unwinding of 5'-terminal secondary structure and recruitment of mRNA to the ribosome (PubMed:29987188). Exists in two complexes, either with EIF1 or with EIF4E (mutually exclusive) (PubMed:29987188). Together with EIF1, is required for leaky scanning, in particular for avoiding cap-proximal start codon (PubMed:29987188). Together with EIF4E, antagonizes the scanning promoted by EIF1-EIF4G1 and locates the start codon (through a TISU element) without scanning (PubMed:29987188). As a member of the eIF4F complex, required for endoplasmic reticulum stress-induced ATF4 mRNA translation (PubMed:29062139). {ECO:0000269|PubMed:29062139, ECO:0000269|PubMed:29987188}. |
Q08AD1 | CAMSAP2 | T614 | ochoa | Calmodulin-regulated spectrin-associated protein 2 (Calmodulin-regulated spectrin-associated protein 1-like protein 1) | Key microtubule-organizing protein that specifically binds the minus-end of non-centrosomal microtubules and regulates their dynamics and organization (PubMed:23169647, PubMed:24486153, PubMed:24706919). Specifically recognizes growing microtubule minus-ends and autonomously decorates and stabilizes microtubule lattice formed by microtubule minus-end polymerization (PubMed:24486153, PubMed:24706919). Acts on free microtubule minus-ends that are not capped by microtubule-nucleating proteins or other factors and protects microtubule minus-ends from depolymerization (PubMed:24486153, PubMed:24706919). In addition, it also reduces the velocity of microtubule polymerization (PubMed:24486153, PubMed:24706919). Through the microtubule cytoskeleton, also regulates the organization of cellular organelles including the Golgi and the early endosomes (PubMed:27666745). Essential for the tethering, but not for nucleation of non-centrosomal microtubules at the Golgi: together with Golgi-associated proteins AKAP9 and PDE4DIP, required to tether non-centrosomal minus-end microtubules to the Golgi, an important step for polarized cell movement (PubMed:27666745). Also acts as a regulator of neuronal polarity and development: localizes to non-centrosomal microtubule minus-ends in neurons and stabilizes non-centrosomal microtubules, which is required for neuronal polarity, axon specification and dendritic branch formation (PubMed:24908486). Through the microtubule cytoskeleton, regulates the autophagosome transport (PubMed:28726242). {ECO:0000269|PubMed:23169647, ECO:0000269|PubMed:24486153, ECO:0000269|PubMed:24706919, ECO:0000269|PubMed:24908486, ECO:0000269|PubMed:27666745, ECO:0000269|PubMed:28726242}. |
Q12830 | BPTF | T2101 | ochoa | Nucleosome-remodeling factor subunit BPTF (Bromodomain and PHD finger-containing transcription factor) (Fetal Alz-50 clone 1 protein) (Fetal Alzheimer antigen) | Regulatory subunit of the ATP-dependent NURF-1 and NURF-5 ISWI chromatin remodeling complexes, which form ordered nucleosome arrays on chromatin and facilitate access to DNA during DNA-templated processes such as DNA replication, transcription, and repair (PubMed:14609955, PubMed:28801535). The NURF-1 ISWI chromatin remodeling complex has a lower ATP hydrolysis rate than the NURF-5 ISWI chromatin remodeling complex (PubMed:28801535). Within the NURF-1 ISWI chromatin-remodeling complex, binds to the promoters of En1 and En2 to positively regulate their expression and promote brain development (PubMed:14609955). Histone-binding protein which binds to H3 tails trimethylated on 'Lys-4' (H3K4me3), which mark transcription start sites of active genes (PubMed:16728976, PubMed:16728978). Binds to histone H3 tails dimethylated on 'Lys-4' (H3K4Me2) to a lesser extent (PubMed:16728976, PubMed:16728978, PubMed:18042461). May also regulate transcription through direct binding to DNA or transcription factors (PubMed:10575013). {ECO:0000269|PubMed:10575013, ECO:0000269|PubMed:14609955, ECO:0000269|PubMed:16728976, ECO:0000269|PubMed:16728978, ECO:0000269|PubMed:18042461, ECO:0000269|PubMed:28801535}. |
Q13045 | FLII | T409 | ochoa | Protein flightless-1 homolog | Is a regulator of actin polymerization, required for proper myofibril organization and regulation of the length of sarcomeric thin filaments (By similarity). It also plays a role in the assembly of cardiomyocyte cell adhesion complexes (By similarity). Regulates cytoskeletal rearrangements involved in cytokinesis and cell migration, by inhibiting Rac1-dependent paxillin phosphorylation (By similarity). May play a role as coactivator in transcriptional activation by hormone-activated nuclear receptors (NR) and acts in cooperation with NCOA2 and CARM1 (PubMed:14966289). Involved in estrogen hormone signaling. {ECO:0000250|UniProtKB:Q9JJ28, ECO:0000269|PubMed:14966289}. |
Q13112 | CHAF1B | T432 | ochoa | Chromatin assembly factor 1 subunit B (CAF-1 subunit B) (Chromatin assembly factor I p60 subunit) (CAF-I 60 kDa subunit) (CAF-I p60) (M-phase phosphoprotein 7) | Acts as a component of the histone chaperone complex chromatin assembly factor 1 (CAF-1), which assembles histone octamers onto DNA during replication and repair. CAF-1 performs the first step of the nucleosome assembly process, bringing newly synthesized histones H3 and H4 to replicating DNA; histones H2A/H2B can bind to this chromatin precursor subsequent to DNA replication to complete the histone octamer. {ECO:0000269|PubMed:9813080}. |
Q13428 | TCOF1 | T1260 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q14135 | VGLL4 | T203 | ochoa | Transcription cofactor vestigial-like protein 4 (Vgl-4) | May act as a specific coactivator for the mammalian TEFs. {ECO:0000250}. |
Q14511 | NEDD9 | T185 | ochoa | Enhancer of filamentation 1 (hEF1) (CRK-associated substrate-related protein) (CAS-L) (CasL) (Cas scaffolding protein family member 2) (CASS2) (Neural precursor cell expressed developmentally down-regulated protein 9) (NEDD-9) (Renal carcinoma antigen NY-REN-12) (p105) [Cleaved into: Enhancer of filamentation 1 p55] | Scaffolding protein which plays a central coordinating role for tyrosine-kinase-based signaling related to cell adhesion (PubMed:24574519). As a focal adhesion protein, plays a role in embryonic fibroblast migration (By similarity). May play an important role in integrin beta-1 or B cell antigen receptor (BCR) mediated signaling in B- and T-cells. Integrin beta-1 stimulation leads to recruitment of various proteins including CRKL and SHPTP2 to the tyrosine phosphorylated form (PubMed:9020138). Promotes adhesion and migration of lymphocytes; as a result required for the correct migration of lymphocytes to the spleen and other secondary lymphoid organs (PubMed:17174122). Plays a role in the organization of T-cell F-actin cortical cytoskeleton and the centralization of T-cell receptor microclusters at the immunological synapse (By similarity). Negatively regulates cilia outgrowth in polarized cysts (By similarity). Modulates cilia disassembly via activation of AURKA-mediated phosphorylation of HDAC6 and subsequent deacetylation of alpha-tubulin (PubMed:17604723). Positively regulates RANKL-induced osteoclastogenesis (By similarity). Required for the maintenance of hippocampal dendritic spines in the dentate gyrus and CA1 regions, thereby involved in spatial learning and memory (By similarity). {ECO:0000250|UniProtKB:A0A8I3PDQ1, ECO:0000250|UniProtKB:O35177, ECO:0000269|PubMed:17174122, ECO:0000269|PubMed:17604723, ECO:0000269|PubMed:24574519, ECO:0000269|PubMed:9020138}. |
Q14653 | IRF3 | T253 | psp | Interferon regulatory factor 3 (IRF-3) | Key transcriptional regulator of type I interferon (IFN)-dependent immune responses which plays a critical role in the innate immune response against DNA and RNA viruses (PubMed:22394562, PubMed:24049179, PubMed:25636800, PubMed:27302953, PubMed:31340999, PubMed:36603579, PubMed:8524823). Regulates the transcription of type I IFN genes (IFN-alpha and IFN-beta) and IFN-stimulated genes (ISG) by binding to an interferon-stimulated response element (ISRE) in their promoters (PubMed:11846977, PubMed:16846591, PubMed:16979567, PubMed:20049431, PubMed:32972995, PubMed:36603579, PubMed:8524823). Acts as a more potent activator of the IFN-beta (IFNB) gene than the IFN-alpha (IFNA) gene and plays a critical role in both the early and late phases of the IFNA/B gene induction (PubMed:16846591, PubMed:16979567, PubMed:20049431, PubMed:36603579). Found in an inactive form in the cytoplasm of uninfected cells and following viral infection, double-stranded RNA (dsRNA), or toll-like receptor (TLR) signaling, is phosphorylated by IKBKE and TBK1 kinases (PubMed:22394562, PubMed:25636800, PubMed:27302953, PubMed:36603579). This induces a conformational change, leading to its dimerization and nuclear localization and association with CREB binding protein (CREBBP) to form dsRNA-activated factor 1 (DRAF1), a complex which activates the transcription of the type I IFN and ISG genes (PubMed:16154084, PubMed:27302953, PubMed:33440148, PubMed:36603579). Can activate distinct gene expression programs in macrophages and can induce significant apoptosis in primary macrophages (PubMed:16846591). In response to Sendai virus infection, is recruited by TOMM70:HSP90AA1 to mitochondrion and forms an apoptosis complex TOMM70:HSP90AA1:IRF3:BAX inducing apoptosis (PubMed:25609812). Key transcription factor regulating the IFN response during SARS-CoV-2 infection (PubMed:33440148). {ECO:0000269|PubMed:16154084, ECO:0000269|PubMed:22394562, ECO:0000269|PubMed:24049179, ECO:0000269|PubMed:25609812, ECO:0000269|PubMed:25636800, ECO:0000269|PubMed:27302953, ECO:0000269|PubMed:31340999, ECO:0000269|PubMed:31413131, ECO:0000269|PubMed:32972995, ECO:0000269|PubMed:33440148, ECO:0000269|PubMed:36603579, ECO:0000269|PubMed:8524823, ECO:0000303|PubMed:11846977, ECO:0000303|PubMed:16846591, ECO:0000303|PubMed:16979567, ECO:0000303|PubMed:20049431}. |
Q14847 | LASP1 | T166 | ochoa | LIM and SH3 domain protein 1 (LASP-1) (Metastatic lymph node gene 50 protein) (MLN 50) | Plays an important role in the regulation of dynamic actin-based, cytoskeletal activities. Agonist-dependent changes in LASP1 phosphorylation may also serve to regulate actin-associated ion transport activities, not only in the parietal cell but also in certain other F-actin-rich secretory epithelial cell types (By similarity). {ECO:0000250}. |
Q15691 | MAPRE1 | T154 | ochoa|psp | Microtubule-associated protein RP/EB family member 1 (APC-binding protein EB1) (End-binding protein 1) (EB1) | Plus-end tracking protein (+TIP) that binds to the plus-end of microtubules and regulates the dynamics of the microtubule cytoskeleton (PubMed:12388762, PubMed:16109370, PubMed:19632184, PubMed:21646404, PubMed:23001180, PubMed:28726242, PubMed:28814570, PubMed:34608293). Recruits other +TIP proteins to microtubules by binding to a conserved Ser-X-Leu-Pro (SXLP) motif in their polypeptide chains (PubMed:19632184, PubMed:36592928). Promotes cytoplasmic microtubule nucleation and elongation (PubMed:12388762, PubMed:16109370, PubMed:19632184, PubMed:21646404, PubMed:28726242, PubMed:28814570). Involved in mitotic spindle positioning by stabilizing microtubules and promoting dynamic connection between astral microtubules and the cortex during mitotic chromosome segregation (PubMed:12388762, PubMed:34608293). Assists chromosome alignment in metaphase by recruiting the SKA complex to the spindle and stabilizing its interactions with microtubule bundles (K-fibers) (PubMed:27225956, PubMed:36592928). Also acts as a regulator of minus-end microtubule organization: interacts with the complex formed by AKAP9 and PDE4DIP, leading to recruit CAMSAP2 to the Golgi apparatus, thereby tethering non-centrosomal minus-end microtubules to the Golgi, an important step for polarized cell movement (PubMed:28814570). Promotes elongation of CAMSAP2-decorated microtubule stretches on the minus-end of microtubules (PubMed:28814570). Acts as a regulator of autophagosome transport via interaction with CAMSAP2 (PubMed:28726242). Functions downstream of Rho GTPases and DIAPH1 in stable microtubule formation (By similarity). May play a role in cell migration (By similarity). {ECO:0000250|UniProtKB:Q61166, ECO:0000269|PubMed:12388762, ECO:0000269|PubMed:16109370, ECO:0000269|PubMed:19632184, ECO:0000269|PubMed:21646404, ECO:0000269|PubMed:23001180, ECO:0000269|PubMed:27225956, ECO:0000269|PubMed:28726242, ECO:0000269|PubMed:28814570, ECO:0000269|PubMed:34608293, ECO:0000269|PubMed:36592928}. |
Q15776 | ZKSCAN8 | T166 | ochoa | Zinc finger protein with KRAB and SCAN domains 8 (LD5-1) (Zinc finger protein 192) | May be involved in transcriptional regulation. |
Q16799 | RTN1 | T338 | ochoa | Reticulon-1 (Neuroendocrine-specific protein) | Inhibits amyloid precursor protein processing, probably by blocking BACE1 activity. {ECO:0000269|PubMed:15286784}. |
Q2KHM9 | KIAA0753 | T193 | ochoa | Protein moonraker (MNR) (OFD1- and FOPNL-interacting protein) | Involved in centriole duplication (PubMed:24613305, PubMed:26297806). Positively regulates CEP63 centrosomal localization (PubMed:24613305, PubMed:26297806). Required for WDR62 centrosomal localization and promotes the centrosomal localization of CDK2 (PubMed:24613305, PubMed:26297806). May play a role in cilium assembly. {ECO:0000269|PubMed:24613305, ECO:0000269|PubMed:26297806, ECO:0000269|PubMed:28220259}. |
Q3KR16 | PLEKHG6 | T540 | ochoa | Pleckstrin homology domain-containing family G member 6 (PH domain-containing family G member 6) (Myosin-interacting guanine nucleotide exchange factor) (MyoGEF) | Guanine nucleotide exchange factor activating the small GTPase RHOA, which, in turn, induces myosin filament formation. Also activates RHOG. Does not activate RAC1, or to a much lower extent than RHOA and RHOG. Part of a functional unit, involving PLEKHG6, MYH10 and RHOA, at the cleavage furrow to advance furrow ingression during cytokinesis. In epithelial cells, required for the formation of microvilli and membrane ruffles on the apical pole. Along with EZR, required for normal macropinocytosis. {ECO:0000269|PubMed:16721066, ECO:0000269|PubMed:17881735}. |
Q4VCS5 | AMOT | T717 | ochoa | Angiomotin | Plays a central role in tight junction maintenance via the complex formed with ARHGAP17, which acts by regulating the uptake of polarity proteins at tight junctions. Appears to regulate endothelial cell migration and tube formation. May also play a role in the assembly of endothelial cell-cell junctions. Repressor of YAP1 and WWTR1/TAZ transcription of target genes, potentially via regulation of Hippo signaling-mediated phosphorylation of YAP1 which results in its recruitment to tight junctions (PubMed:21205866). {ECO:0000269|PubMed:11257124, ECO:0000269|PubMed:16678097, ECO:0000269|PubMed:21205866}. |
Q53H80 | AKIRIN2 | T128 | ochoa | Akirin-2 | Molecular adapter that acts as a bridge between a variety of multiprotein complexes, and which is involved in embryonic development, immunity, myogenesis and brain development (PubMed:34711951). Plays a key role in nuclear protein degradation by promoting import of proteasomes into the nucleus: directly binds to fully assembled 20S proteasomes at one end and to nuclear import receptor IPO9 at the other end, bridging them together and mediating the import of pre-assembled proteasome complexes through the nuclear pore (PubMed:34711951). Involved in innate immunity by regulating the production of interleukin-6 (IL6) downstream of Toll-like receptor (TLR): acts by bridging the NF-kappa-B inhibitor NFKBIZ and the SWI/SNF complex, leading to promote induction of IL6 (By similarity). Also involved in adaptive immunity by promoting B-cell activation (By similarity). Involved in brain development: required for the survival and proliferation of cerebral cortical progenitor cells (By similarity). Involved in myogenesis: required for skeletal muscle formation and skeletal development, possibly by regulating expression of muscle differentiation factors (By similarity). Also plays a role in facilitating interdigital tissue regression during limb development (By similarity). {ECO:0000250|UniProtKB:B1AXD8, ECO:0000269|PubMed:34711951}. |
Q5H9R7 | PPP6R3 | T669 | ochoa | Serine/threonine-protein phosphatase 6 regulatory subunit 3 (SAPS domain family member 3) (Sporulation-induced transcript 4-associated protein SAPL) | Regulatory subunit of protein phosphatase 6 (PP6). May function as a scaffolding PP6 subunit. May have an important role in maintaining immune self-tolerance. {ECO:0000269|PubMed:11401438, ECO:0000269|PubMed:16769727}. |
Q5JSP0 | FGD3 | T139 | ochoa | FYVE, RhoGEF and PH domain-containing protein 3 (Zinc finger FYVE domain-containing protein 5) | Promotes the formation of filopodia. May activate CDC42, a member of the Ras-like family of Rho- and Rac proteins, by exchanging bound GDP for free GTP. Plays a role in regulating the actin cytoskeleton and cell shape (By similarity). {ECO:0000250}. |
Q5SRE5 | NUP188 | T1712 | ochoa | Nucleoporin NUP188 (hNup188) | Component of the nuclear pore complex (NPC), a complex required for the trafficking across the nuclear envelope (Probable). Required for proper protein transport into the nucleus (PubMed:32275884). {ECO:0000269|PubMed:32275884, ECO:0000305|PubMed:32275884}. |
Q5UIP0 | RIF1 | T986 | ochoa | Telomere-associated protein RIF1 (Rap1-interacting factor 1 homolog) | Key regulator of TP53BP1 that plays a key role in the repair of double-strand DNA breaks (DSBs) in response to DNA damage: acts by promoting non-homologous end joining (NHEJ)-mediated repair of DSBs (PubMed:15342490, PubMed:28241136). In response to DNA damage, interacts with ATM-phosphorylated TP53BP1 (PubMed:23333306, PubMed:28241136). Interaction with TP53BP1 leads to dissociate the interaction between NUDT16L1/TIRR and TP53BP1, thereby unmasking the tandem Tudor-like domain of TP53BP1 and allowing recruitment to DNA DSBs (PubMed:28241136). Once recruited to DSBs, RIF1 and TP53BP1 act by promoting NHEJ-mediated repair of DSBs (PubMed:23333306). In the same time, RIF1 and TP53BP1 specifically counteract the function of BRCA1 by blocking DSBs resection via homologous recombination (HR) during G1 phase (PubMed:23333306). Also required for immunoglobulin class-switch recombination (CSR) during antibody genesis, a process that involves the generation of DNA DSBs (By similarity). Promotes NHEJ of dysfunctional telomeres (By similarity). {ECO:0000250|UniProtKB:Q6PR54, ECO:0000269|PubMed:15342490, ECO:0000269|PubMed:23333306, ECO:0000269|PubMed:28241136}. |
Q5VZL5 | ZMYM4 | T220 | ochoa | Zinc finger MYM-type protein 4 (Zinc finger protein 262) | Plays a role in the regulation of cell morphology and cytoskeletal organization. {ECO:0000269|PubMed:21834987}. |
Q641Q2 | WASHC2A | T707 | ochoa | WASH complex subunit 2A | Acts at least in part as component of the WASH core complex whose assembly at the surface of endosomes inhibits WASH nucleation-promoting factor (NPF) activity in recruiting and activating the Arp2/3 complex to induce actin polymerization and is involved in the fission of tubules that serve as transport intermediates during endosome sorting. Mediates the recruitment of the WASH core complex to endosome membranes via binding to phospholipids and VPS35 of the retromer CSC. Mediates the recruitment of the F-actin-capping protein dimer to the WASH core complex probably promoting localized F-actin polymerization needed for vesicle scission. Via its C-terminus binds various phospholipids, most strongly phosphatidylinositol 4-phosphate (PtdIns-(4)P), phosphatidylinositol 5-phosphate (PtdIns-(5)P) and phosphatidylinositol 3,5-bisphosphate (PtdIns-(3,5)P2). Involved in the endosome-to-plasma membrane trafficking and recycling of SNX27-retromer-dependent cargo proteins, such as GLUT1. Required for the association of DNAJC13, ENTR1, ANKRD50 with retromer CSC subunit VPS35. Required for the endosomal recruitment of CCC complex subunits COMMD1 and CCDC93 as well as the retriever complex subunit VPS35L. {ECO:0000269|PubMed:25355947, ECO:0000269|PubMed:28892079}. |
Q68CZ2 | TNS3 | T1296 | ochoa | Tensin-3 (EC 3.1.3.-) (Tensin-like SH2 domain-containing protein 1) (Tumor endothelial marker 6) | May act as a protein phosphatase and/or a lipid phosphatase (Probable). Involved in the dissociation of the integrin-tensin-actin complex (PubMed:17643115). EGF activates TNS4 and down-regulates TNS3 which results in capping the tail of ITGB1 (PubMed:17643115). Increases DOCK5 guanine nucleotide exchange activity towards Rac and plays a role in osteoclast podosome organization (By similarity). Enhances RHOA activation in the presence of DLC1 (PubMed:26427649). Required for growth factor-induced epithelial cell migration; growth factor stimulation induces TNS3 phosphorylation which changes its binding preference from DLC1 to the p85 regulatory subunit of the PI3K kinase complex, displacing PI3K inhibitor PTEN and resulting in translocation of the TNS3-p85 complex to the leading edge of migrating cells to promote RAC1 activation (PubMed:26166433). Meanwhile, PTEN switches binding preference from p85 to DLC1 and the PTEN-DLC1 complex translocates to the posterior of migrating cells to activate RHOA (PubMed:26166433). Acts as an adapter protein by bridging the association of scaffolding protein PEAK1 with integrins ITGB1, ITGB3 and ITGB5 which contributes to the promotion of cell migration (PubMed:35687021). Controls tonsil-derived mesenchymal stem cell proliferation and differentiation by regulating the activity of integrin ITGB1 (PubMed:31905841). {ECO:0000250|UniProtKB:Q5SSZ5, ECO:0000269|PubMed:17643115, ECO:0000269|PubMed:26166433, ECO:0000269|PubMed:26427649, ECO:0000269|PubMed:31905841, ECO:0000269|PubMed:35687021, ECO:0000305}. |
Q6IAA8 | LAMTOR1 | T30 | ochoa | Ragulator complex protein LAMTOR1 (Late endosomal/lysosomal adaptor and MAPK and MTOR activator 1) (Lipid raft adaptor protein p18) (Protein associated with DRMs and endosomes) (p27Kip1-releasing factor from RhoA) (p27RF-Rho) | Key component of the Ragulator complex, a multiprotein complex involved in amino acid sensing and activation of mTORC1, a signaling complex promoting cell growth in response to growth factors, energy levels, and amino acids (PubMed:20381137, PubMed:22980980, PubMed:29158492). Activated by amino acids through a mechanism involving the lysosomal V-ATPase, the Ragulator plays a dual role for the small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD): it (1) acts as a guanine nucleotide exchange factor (GEF), activating the small GTPases Rag and (2) mediates recruitment of Rag GTPases to the lysosome membrane (PubMed:22980980, PubMed:28935770, PubMed:29158492, PubMed:30181260, PubMed:31001086, PubMed:32686708, PubMed:36476874). Activated Ragulator and Rag GTPases function as a scaffold recruiting mTORC1 to lysosomes where it is in turn activated (PubMed:20381137, PubMed:22980980, PubMed:29158492). LAMTOR1 is directly responsible for anchoring the Ragulator complex to the lysosomal membrane (PubMed:31001086, PubMed:32686708). LAMTOR1 wraps around the other subunits of the Ragulator complex to hold them in place and interacts with the Rag GTPases, thereby playing a key role in the recruitment of the mTORC1 complex to lysosomes (PubMed:28935770, PubMed:29107538, PubMed:29123114, PubMed:29285400). Also involved in the control of embryonic stem cells differentiation via non-canonical RagC/RRAGC and RagD/RRAGD activation: together with FLCN, it is necessary to recruit and activate RagC/RRAGC and RagD/RRAGD at the lysosomes, and to induce exit of embryonic stem cells from pluripotency via non-canonical, mTOR-independent TFE3 inactivation (By similarity). Also required for late endosomes/lysosomes biogenesis it may regulate both the recycling of receptors through endosomes and the MAPK signaling pathway through recruitment of some of its components to late endosomes (PubMed:20381137, PubMed:22980980). May be involved in cholesterol homeostasis regulating LDL uptake and cholesterol release from late endosomes/lysosomes (PubMed:20544018). May also play a role in RHOA activation (PubMed:19654316). {ECO:0000250|UniProtKB:Q9CQ22, ECO:0000269|PubMed:19654316, ECO:0000269|PubMed:20381137, ECO:0000269|PubMed:20544018, ECO:0000269|PubMed:22980980, ECO:0000269|PubMed:28935770, ECO:0000269|PubMed:29107538, ECO:0000269|PubMed:29123114, ECO:0000269|PubMed:29158492, ECO:0000269|PubMed:29285400, ECO:0000269|PubMed:30181260, ECO:0000269|PubMed:31001086, ECO:0000269|PubMed:32686708, ECO:0000269|PubMed:36476874}. |
Q6JBY9 | RCSD1 | T287 | ochoa | CapZ-interacting protein (Protein kinase substrate CapZIP) (RCSD domain-containing protein 1) | Stress-induced phosphorylation of CAPZIP may regulate the ability of F-actin-capping protein to remodel actin filament assembly. {ECO:0000269|PubMed:15850461}. |
Q6NYC8 | PPP1R18 | T493 | ochoa | Phostensin (Protein phosphatase 1 F-actin cytoskeleton-targeting subunit) (Protein phosphatase 1 regulatory subunit 18) | [Isoform 1]: May target protein phosphatase 1 to F-actin cytoskeleton. {ECO:0000269|PubMed:24434620}.; FUNCTION: [Isoform 4]: May target protein phosphatase 1 to F-actin cytoskeleton. {ECO:0000269|PubMed:17374523}. |
Q6P4F7 | ARHGAP11A | T562 | ochoa | Rho GTPase-activating protein 11A (Rho-type GTPase-activating protein 11A) | GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state. {ECO:0000269|PubMed:27957544}. |
Q6P4R8 | NFRKB | T899 | ochoa | Nuclear factor related to kappa-B-binding protein (DNA-binding protein R kappa-B) (INO80 complex subunit G) | Binds to the DNA consensus sequence 5'-GGGGAATCTCC-3'. {ECO:0000269|PubMed:18922472}.; FUNCTION: Putative regulatory component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair. Modulates the deubiquitinase activity of UCHL5 in the INO80 complex. {ECO:0000269|PubMed:18922472}. |
Q6P5Z2 | PKN3 | T869 | ochoa | Serine/threonine-protein kinase N3 (EC 2.7.11.13) (Protein kinase PKN-beta) (Protein-kinase C-related kinase 3) | Contributes to invasiveness in malignant prostate cancer. {ECO:0000269|PubMed:15282551}. |
Q6PEY2 | TUBA3E | T51 | ochoa | Tubulin alpha-3E chain (EC 3.6.5.-) (Alpha-tubulin 3E) [Cleaved into: Detyrosinated tubulin alpha-3E chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q6PJG6 | BRAT1 | T745 | ochoa | Integrator complex assembly factor BRAT1 (BRCA1-associated ATM activator 1) (BRCA1-associated protein required for ATM activation protein 1) | Component of a multiprotein complex required for the assembly of the RNA endonuclease module of the integrator complex (PubMed:39032489, PubMed:39032490). Associates with INTS9 and INTS11 in the cytoplasm and blocks the active site of INTS11 to inhibit the endonuclease activity of INTS11 before formation of the full integrator complex (PubMed:39032489, PubMed:39032490). Following dissociation of WDR73 of the complex, BRAT1 facilitates the nuclear import of the INTS9-INTS11 heterodimer (PubMed:39032489). In the nucleus, INTS4 is integrated to the INTS9-INTS11 heterodimer and BRAT1 is released from the mature RNA endonuclease module by inositol hexakisphosphate (InsP6) (PubMed:39032489). BRAT1 is also involved in DNA damage response; activates kinases ATM, SMC1A and PRKDC by modulating their phosphorylation status following ionizing radiation (IR) stress (PubMed:16452482, PubMed:22977523). Plays a role in regulating mitochondrial function and cell proliferation (PubMed:25070371). Required for protein stability of MTOR and MTOR-related proteins, and cell cycle progress by growth factors (PubMed:25657994). {ECO:0000269|PubMed:16452482, ECO:0000269|PubMed:22977523, ECO:0000269|PubMed:25070371, ECO:0000269|PubMed:25657994, ECO:0000269|PubMed:39032489, ECO:0000269|PubMed:39032490}. |
Q6ZRV2 | FAM83H | T414 | ochoa | Protein FAM83H | May play a major role in the structural organization and calcification of developing enamel (PubMed:18252228). May play a role in keratin cytoskeleton disassembly by recruiting CSNK1A1 to keratin filaments. Thereby, it may regulate epithelial cell migration (PubMed:23902688). {ECO:0000269|PubMed:18252228, ECO:0000269|PubMed:23902688}. |
Q71F23 | CENPU | T110 | ochoa | Centromere protein U (CENP-U) (Centromere protein of 50 kDa) (CENP-50) (Interphase centromere complex protein 24) (KSHV latent nuclear antigen-interacting protein 1) (MLF1-interacting protein) (Polo-box-interacting protein 1) | Component of the CENPA-NAC (nucleosome-associated) complex, a complex that plays a central role in assembly of kinetochore proteins, mitotic progression and chromosome segregation. The CENPA-NAC complex recruits the CENPA-CAD (nucleosome distal) complex and may be involved in incorporation of newly synthesized CENPA into centromeres. Plays an important role in the correct PLK1 localization to the mitotic kinetochores. A scaffold protein responsible for the initial recruitment and maintenance of the kinetochore PLK1 population until its degradation. Involved in transcriptional repression. {ECO:0000269|PubMed:12941884, ECO:0000269|PubMed:16716197, ECO:0000269|PubMed:17081991}. |
Q71U36 | TUBA1A | T51 | ochoa | Tubulin alpha-1A chain (EC 3.6.5.-) (Alpha-tubulin 3) (Tubulin B-alpha-1) (Tubulin alpha-3 chain) [Cleaved into: Detyrosinated tubulin alpha-1A chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q71U36 | TUBA1A | T94 | ochoa | Tubulin alpha-1A chain (EC 3.6.5.-) (Alpha-tubulin 3) (Tubulin B-alpha-1) (Tubulin alpha-3 chain) [Cleaved into: Detyrosinated tubulin alpha-1A chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q7KZF4 | SND1 | T429 | ochoa|psp | Staphylococcal nuclease domain-containing protein 1 (EC 3.1.31.1) (100 kDa coactivator) (EBNA2 coactivator p100) (Tudor domain-containing protein 11) (p100 co-activator) | Endonuclease that mediates miRNA decay of both protein-free and AGO2-loaded miRNAs (PubMed:18453631, PubMed:28546213). As part of its function in miRNA decay, regulates mRNAs involved in G1-to-S phase transition (PubMed:28546213). Functions as a bridging factor between STAT6 and the basal transcription factor (PubMed:12234934). Plays a role in PIM1 regulation of MYB activity (PubMed:9809063). Functions as a transcriptional coactivator for STAT5 (By similarity). {ECO:0000250|UniProtKB:Q78PY7, ECO:0000269|PubMed:12234934, ECO:0000269|PubMed:18453631, ECO:0000269|PubMed:28546213, ECO:0000269|PubMed:9809063}.; FUNCTION: (Microbial infection) Functions as a transcriptional coactivator for the Epstein-Barr virus nuclear antigen 2 (EBNA2). {ECO:0000269|PubMed:7651391}.; FUNCTION: (Microbial infection) Promotes SARS-CoV-2 RNA synthesis by binding to negative-sense RNA and the viral protein nsp9. {ECO:0000269|PubMed:37794589}. |
Q7L2J0 | MEPCE | T243 | ochoa | 7SK snRNA methylphosphate capping enzyme (MePCE) (EC 2.1.1.-) (Bicoid-interacting protein 3 homolog) (Bin3 homolog) | S-adenosyl-L-methionine-dependent methyltransferase that adds a methylphosphate cap at the 5'-end of 7SK snRNA (7SK RNA), leading to stabilize it (PubMed:17643375, PubMed:19906723, PubMed:30559425). Also has a non-enzymatic function as part of the 7SK RNP complex: the 7SK RNP complex sequesters the positive transcription elongation factor b (P-TEFb) in a large inactive 7SK RNP complex preventing RNA polymerase II phosphorylation and subsequent transcriptional elongation (PubMed:17643375). The 7SK RNP complex also promotes snRNA gene transcription by RNA polymerase II via interaction with the little elongation complex (LEC) (PubMed:28254838). In the 7SK RNP complex, MEPCE is required to stabilize 7SK RNA and facilitate the assembly of 7SK RNP complex (PubMed:19906723, PubMed:38100593). MEPCE has a non-enzymatic function in the 7SK RNP complex; interaction with LARP7 within the 7SK RNP complex occluding its catalytic center (PubMed:19906723). Also required for stability of U6 snRNAs (PubMed:38100593). {ECO:0000269|PubMed:17643375, ECO:0000269|PubMed:19906723, ECO:0000269|PubMed:28254838, ECO:0000269|PubMed:30559425, ECO:0000269|PubMed:38100593}. |
Q7Z2K8 | GPRIN1 | T392 | ochoa | G protein-regulated inducer of neurite outgrowth 1 (GRIN1) | May be involved in neurite outgrowth. {ECO:0000250}. |
Q7Z2Z1 | TICRR | T1677 | ochoa | Treslin (TopBP1-interacting checkpoint and replication regulator) (TopBP1-interacting, replication-stimulating protein) | Regulator of DNA replication and S/M and G2/M checkpoints. Regulates the triggering of DNA replication initiation via its interaction with TOPBP1 by participating in CDK2-mediated loading of CDC45L onto replication origins. Required for the transition from pre-replication complex (pre-RC) to pre-initiation complex (pre-IC). Required to prevent mitotic entry after treatment with ionizing radiation. {ECO:0000269|PubMed:20116089}. |
Q7Z591 | AKNA | T938 | ochoa | Microtubule organization protein AKNA (AT-hook-containing transcription factor) | Centrosomal protein that plays a key role in cell delamination by regulating microtubule organization (By similarity). Required for the delamination and retention of neural stem cells from the subventricular zone during neurogenesis (By similarity). Also regulates the epithelial-to-mesenchymal transition in other epithelial cells (By similarity). Acts by increasing centrosomal microtubule nucleation and recruiting nucleation factors and minus-end stabilizers, thereby destabilizing microtubules at the adherens junctions and mediating constriction of the apical endfoot (By similarity). In addition, may also act as a transcription factor that specifically activates the expression of the CD40 receptor and its ligand CD40L/CD154, two cell surface molecules on lymphocytes that are critical for antigen-dependent-B-cell development (PubMed:11268217). Binds to A/T-rich promoters (PubMed:11268217). It is unclear how it can both act as a microtubule organizer and as a transcription factor; additional evidences are required to reconcile these two apparently contradictory functions (Probable). {ECO:0000250|UniProtKB:Q80VW7, ECO:0000269|PubMed:11268217, ECO:0000305}. |
Q7Z5L9 | IRF2BP2 | T412 | ochoa | Interferon regulatory factor 2-binding protein 2 (IRF-2-binding protein 2) (IRF-2BP2) | Acts as a transcriptional corepressor in a IRF2-dependent manner; this repression is not mediated by histone deacetylase activities (PubMed:12799427). Represses the NFAT1-dependent transactivation of NFAT-responsive promoters (PubMed:21576369). Acts as a coactivator of VEGFA expression in cardiac and skeletal muscles (PubMed:20702774). Plays a role in immature B-cell differentiation (PubMed:27016798). {ECO:0000269|PubMed:12799427, ECO:0000269|PubMed:20702774, ECO:0000269|PubMed:21576369, ECO:0000269|PubMed:27016798}. |
Q7Z6Z7 | HUWE1 | T2746 | ochoa | E3 ubiquitin-protein ligase HUWE1 (EC 2.3.2.26) (ARF-binding protein 1) (ARF-BP1) (HECT, UBA and WWE domain-containing protein 1) (HECT-type E3 ubiquitin transferase HUWE1) (Homologous to E6AP carboxyl terminus homologous protein 9) (HectH9) (Large structure of UREB1) (LASU1) (Mcl-1 ubiquitin ligase E3) (Mule) (Upstream regulatory element-binding protein 1) (URE-B1) (URE-binding protein 1) | E3 ubiquitin-protein ligase which mediates ubiquitination and subsequent proteasomal degradation of target proteins (PubMed:15567145, PubMed:15767685, PubMed:15989957, PubMed:17567951, PubMed:18488021, PubMed:19037095, PubMed:19713937, PubMed:20534529, PubMed:30217973). Regulates apoptosis by catalyzing the polyubiquitination and degradation of MCL1 (PubMed:15989957). Mediates monoubiquitination of DNA polymerase beta (POLB) at 'Lys-41', 'Lys-61' and 'Lys-81', thereby playing a role in base-excision repair (PubMed:19713937). Also ubiquitinates the p53/TP53 tumor suppressor and core histones including H1, H2A, H2B, H3 and H4 (PubMed:15567145, PubMed:15767685, PubMed:15989956). Ubiquitinates MFN2 to negatively regulate mitochondrial fusion in response to decreased stearoylation of TFRC (PubMed:26214738). Ubiquitination of MFN2 also takes place following induction of mitophagy; AMBRA1 acts as a cofactor for HUWE1-mediated ubiquitination (PubMed:30217973). Regulates neural differentiation and proliferation by catalyzing the polyubiquitination and degradation of MYCN (PubMed:18488021). May regulate abundance of CDC6 after DNA damage by polyubiquitinating and targeting CDC6 to degradation (PubMed:17567951). Mediates polyubiquitination of isoform 2 of PA2G4 (PubMed:19037095). Acts in concert with MYCBP2 to regulate the circadian clock gene expression by promoting the lithium-induced ubiquination and degradation of NR1D1 (PubMed:20534529). Binds to an upstream initiator-like sequence in the preprodynorphin gene (By similarity). Mediates HAPSTR1 degradation, but is also a required cofactor in the pathway by which HAPSTR1 governs stress signaling (PubMed:35776542). Acts as a regulator of the JNK and NF-kappa-B signaling pathways by mediating assembly of heterotypic 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains that are then recognized by TAB2: HUWE1 mediates branching of 'Lys-48'-linked chains of substrates initially modified with 'Lys-63'-linked conjugates by TRAF6 (PubMed:27746020). 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains protect 'Lys-63'-linkages from CYLD deubiquitination (PubMed:27746020). Ubiquitinates PPARA in hepatocytes (By similarity). {ECO:0000250|UniProtKB:P51593, ECO:0000250|UniProtKB:Q7TMY8, ECO:0000269|PubMed:15567145, ECO:0000269|PubMed:15767685, ECO:0000269|PubMed:15989956, ECO:0000269|PubMed:15989957, ECO:0000269|PubMed:17567951, ECO:0000269|PubMed:18488021, ECO:0000269|PubMed:19037095, ECO:0000269|PubMed:19713937, ECO:0000269|PubMed:20534529, ECO:0000269|PubMed:26214738, ECO:0000269|PubMed:27746020, ECO:0000269|PubMed:30217973, ECO:0000269|PubMed:35776542}. |
Q86UP2 | KTN1 | T1316 | ochoa | Kinectin (CG-1 antigen) (Kinesin receptor) | Receptor for kinesin thus involved in kinesin-driven vesicle motility. Accumulates in integrin-based adhesion complexes (IAC) upon integrin aggregation by fibronectin. |
Q86XP3 | DDX42 | T757 | ochoa | ATP-dependent RNA helicase DDX42 (EC 3.6.4.13) (DEAD box protein 42) (RNA helicase-like protein) (RHELP) (RNA helicase-related protein) (RNAHP) (SF3b DEAD box protein) (Splicing factor 3B-associated 125 kDa protein) (SF3b125) | ATP-dependent RNA helicase that binds to partially double-stranded RNAs (dsRNAs) in order to unwind RNA secondary structures (PubMed:16397294). Unwinding is promoted in the presence of single-strand binding proteins (PubMed:16397294). Also mediates RNA duplex formation thereby displacing the single-strand RNA binding protein (PubMed:16397294). ATP and ADP modulate its activity: ATP binding and hydrolysis by DDX42 triggers RNA strand separation, whereas the ADP-bound form of the protein triggers annealing of complementary RNA strands (PubMed:16397294). Required for assembly of the 17S U2 SnRNP complex of the spliceosome, a large ribonucleoprotein complex that removes introns from transcribed pre-mRNAs: DDX42 associates transiently with the SF3B subcomplex of the 17S U2 SnRNP complex and is released after fulfilling its role in the assembly of 17S U2 SnRNP (PubMed:12234937, PubMed:36797247). Involved in the survival of cells by interacting with TP53BP2 and thereby counteracting the apoptosis-stimulating activity of TP53BP2 (PubMed:19377511). Relocalizes TP53BP2 to the cytoplasm (PubMed:19377511). {ECO:0000269|PubMed:12234937, ECO:0000269|PubMed:16397294, ECO:0000269|PubMed:19377511, ECO:0000269|PubMed:36797247}. |
Q8IVH2 | FOXP4 | T276 | ochoa | Forkhead box protein P4 (Fork head-related protein-like A) | Transcriptional repressor that represses lung-specific expression. {ECO:0000250}. |
Q8IWB9 | TEX2 | T269 | 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}. |
Q8IXJ9 | ASXL1 | T469 | ochoa | Polycomb group protein ASXL1 (Additional sex combs-like protein 1) | Probable Polycomb group (PcG) protein involved in transcriptional regulation mediated by ligand-bound nuclear hormone receptors, such as retinoic acid receptors (RARs) and peroxisome proliferator-activated receptor gamma (PPARG) (PubMed:16606617). Acts as a coactivator of RARA and RXRA through association with NCOA1 (PubMed:16606617). Acts as a corepressor for PPARG and suppresses its adipocyte differentiation-inducing activity (By similarity). Non-catalytic component of the PR-DUB complex, a complex that specifically mediates deubiquitination of histone H2A monoubiquitinated at 'Lys-119' (H2AK119ub1) (PubMed:20436459, PubMed:30664650, PubMed:36180891). Acts as a sensor of N(6)-methyladenine methylation on DNA (6mA): recognizes and binds 6mA DNA, leading to its ubiquitination and degradation by TRIP12, thereby inactivating the PR-DUB complex and regulating Polycomb silencing (PubMed:30982744). The PR-DUB complex is an epigenetic regulator of gene expression and acts as a transcriptional coactivator, affecting genes involved in development, cell communication, signaling, cell proliferation and cell viability (PubMed:30664650, PubMed:36180891). ASXL1, ASXL2 and ASXL3 function redundantly in the PR-DUB complex (By similarity) (PubMed:30664650). The ASXL proteins are essential for chromatin recruitment and transcriptional activation of associated genes (By similarity). ASXL1 and ASXL2 are important for BAP1 protein stability (PubMed:30664650). Together with BAP1, negatively regulates epithelial-mesenchymal transition (EMT) of trophoblast stem cells during placental development by regulating genes involved in epithelial cell integrity, cell adhesion and cytoskeletal organization (PubMed:34170818). {ECO:0000250|UniProtKB:P59598, ECO:0000269|PubMed:16606617, ECO:0000269|PubMed:20436459, ECO:0000269|PubMed:30664650, ECO:0000269|PubMed:30982744, ECO:0000269|PubMed:34170818, ECO:0000269|PubMed:36180891}. |
Q8N302 | AGGF1 | T341 | ochoa | Angiogenic factor with G patch and FHA domains 1 (Angiogenic factor VG5Q) (hVG5Q) (G patch domain-containing protein 7) (Vasculogenesis gene on 5q protein) | Promotes angiogenesis and the proliferation of endothelial cells. Able to bind to endothelial cells and promote cell proliferation, suggesting that it may act in an autocrine fashion. {ECO:0000269|PubMed:14961121}. |
Q8N5F7 | NKAP | T298 | ochoa | NF-kappa-B-activating protein | Acts as a transcriptional repressor (PubMed:14550261, PubMed:19409814, PubMed:31587868). Plays a role as a transcriptional corepressor of the Notch-mediated signaling required for T-cell development (PubMed:19409814). Also involved in the TNF and IL-1 induced NF-kappa-B activation. Associates with chromatin at the Notch-regulated SKP2 promoter. {ECO:0000269|PubMed:14550261, ECO:0000269|PubMed:19409814, ECO:0000269|PubMed:31587868}. |
Q8N8Z6 | DCBLD1 | T692 | ochoa | Discoidin, CUB and LCCL domain-containing protein 1 | None |
Q8TD55 | PLEKHO2 | T442 | ochoa | Pleckstrin homology domain-containing family O member 2 (PH domain-containing family O member 2) (Pleckstrin homology domain-containing family Q member 1) (PH domain-containing family Q member 1) | None |
Q8TDY4 | ASAP3 | T732 | ochoa | Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3 (Development and differentiation-enhancing factor-like 1) (Protein up-regulated in liver cancer 1) | Promotes cell proliferation. {ECO:0000269|PubMed:14654939}. |
Q8TEW8 | PARD3B | T341 | ochoa | Partitioning defective 3 homolog B (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 19 protein) (PAR3-beta) (Partitioning defective 3-like protein) (PAR3-L protein) | Putative adapter protein involved in asymmetrical cell division and cell polarization processes. May play a role in the formation of epithelial tight junctions. |
Q8WUY3 | PRUNE2 | T1792 | ochoa | Protein prune homolog 2 (BNIP2 motif-containing molecule at the C-terminal region 1) | May play an important role in regulating differentiation, survival and aggressiveness of the tumor cells. {ECO:0000269|PubMed:16288218}. |
Q8WXI9 | GATAD2B | T489 | ochoa | Transcriptional repressor p66-beta (GATA zinc finger domain-containing protein 2B) (p66/p68) | Transcriptional repressor (PubMed:12183469, PubMed:16415179). Acts as a component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin (PubMed:16428440, PubMed:28977666). Enhances MBD2-mediated repression (PubMed:12183469, PubMed:16415179). Efficient repression requires the presence of GATAD2A (PubMed:16415179). Targets MBD3 to discrete loci in the nucleus (PubMed:11756549). May play a role in synapse development (PubMed:23644463). {ECO:0000269|PubMed:11756549, ECO:0000269|PubMed:12183469, ECO:0000269|PubMed:16415179, ECO:0000269|PubMed:16428440, ECO:0000269|PubMed:23644463, ECO:0000269|PubMed:28977666}. |
Q92797 | SYMPK | T1246 | ochoa | Symplekin | Scaffold protein that functions as a component of a multimolecular complex involved in histone mRNA 3'-end processing. Specific component of the tight junction (TJ) plaque, but might not be an exclusively junctional component. May have a house-keeping rule. Is involved in pre-mRNA polyadenylation. Enhances SSU72 phosphatase activity. {ECO:0000269|PubMed:16230528, ECO:0000269|PubMed:20861839}. |
Q92844 | TANK | T260 | ochoa | TRAF family member-associated NF-kappa-B activator (TRAF-interacting protein) (I-TRAF) | Adapter protein involved in I-kappa-B-kinase (IKK) regulation which constitutively binds TBK1 and IKBKE playing a role in antiviral innate immunity. Acts as a regulator of TRAF function by maintaining them in a latent state. Blocks TRAF2 binding to LMP1 and inhibits LMP1-mediated NF-kappa-B activation. Negatively regulates NF-kappaB signaling and cell survival upon DNA damage (PubMed:25861989). Plays a role as an adapter to assemble ZC3H12A, USP10 in a deubiquitination complex which plays a negative feedback response to attenuate NF-kappaB activation through the deubiquitination of IKBKG or TRAF6 in response to interleukin-1-beta (IL1B) stimulation or upon DNA damage (PubMed:25861989). Promotes UBP10-induced deubiquitination of TRAF6 in response to DNA damage (PubMed:25861989). May control negatively TRAF2-mediated NF-kappa-B activation signaled by CD40, TNFR1 and TNFR2. {ECO:0000269|PubMed:12133833, ECO:0000269|PubMed:21931631, ECO:0000269|PubMed:25861989}. |
Q92934 | BAD | T137 | psp | Bcl2-associated agonist of cell death (BAD) (Bcl-2-binding component 6) (Bcl-2-like protein 8) (Bcl2-L-8) (Bcl-xL/Bcl-2-associated death promoter) (Bcl2 antagonist of cell death) | Promotes cell death. Successfully competes for the binding to Bcl-X(L), Bcl-2 and Bcl-W, thereby affecting the level of heterodimerization of these proteins with BAX. Can reverse the death repressor activity of Bcl-X(L), but not that of Bcl-2 (By similarity). Appears to act as a link between growth factor receptor signaling and the apoptotic pathways. {ECO:0000250}. |
Q93009 | USP7 | T966 | ochoa | Ubiquitin carboxyl-terminal hydrolase 7 (EC 3.4.19.12) (Deubiquitinating enzyme 7) (Herpesvirus-associated ubiquitin-specific protease) (Ubiquitin thioesterase 7) (Ubiquitin-specific-processing protease 7) | Hydrolase that deubiquitinates target proteins such as ARMC5, FOXO4, DEPTOR, KAT5, p53/TP53, MDM2, ERCC6, DNMT1, UHRF1, PTEN, KMT2E/MLL5 and DAXX (PubMed:11923872, PubMed:15053880, PubMed:16964248, PubMed:18716620, PubMed:25283148, PubMed:25865756, PubMed:26678539, PubMed:28655758, PubMed:33544460, PubMed:35216969). Together with DAXX, prevents MDM2 self-ubiquitination and enhances the E3 ligase activity of MDM2 towards p53/TP53, thereby promoting p53/TP53 ubiquitination and proteasomal degradation (PubMed:15053880, PubMed:16845383, PubMed:18566590, PubMed:20153724). Deubiquitinates p53/TP53, preventing degradation of p53/TP53, and enhances p53/TP53-dependent transcription regulation, cell growth repression and apoptosis (PubMed:25283148). Deubiquitinates p53/TP53 and MDM2 and strongly stabilizes p53/TP53 even in the presence of excess MDM2, and also induces p53/TP53-dependent cell growth repression and apoptosis (PubMed:11923872, PubMed:26786098). Deubiquitination of FOXO4 in presence of hydrogen peroxide is not dependent on p53/TP53 and inhibits FOXO4-induced transcriptional activity (PubMed:16964248). In association with DAXX, is involved in the deubiquitination and translocation of PTEN from the nucleus to the cytoplasm, both processes that are counteracted by PML (PubMed:18716620). Deubiquitinates KMT2E/MLL5 preventing KMT2E/MLL5 proteasomal-mediated degradation (PubMed:26678539). Involved in cell proliferation during early embryonic development. Involved in transcription-coupled nucleotide excision repair (TC-NER) in response to UV damage: recruited to DNA damage sites following interaction with KIAA1530/UVSSA and promotes deubiquitination of ERCC6, preventing UV-induced degradation of ERCC6 (PubMed:22466611, PubMed:22466612). Involved in maintenance of DNA methylation via its interaction with UHRF1 and DNMT1: acts by mediating deubiquitination of UHRF1 and DNMT1, preventing their degradation and promoting DNA methylation by DNMT1 (PubMed:21745816, PubMed:22411829). Deubiquitinates alkylation repair enzyme ALKBH3. OTUD4 recruits USP7 and USP9X to stabilize ALKBH3, thereby promoting the repair of alkylated DNA lesions (PubMed:25944111). Acts as a chromatin regulator via its association with the Polycomb group (PcG) multiprotein PRC1-like complex; may act by deubiquitinating components of the PRC1-like complex (PubMed:20601937). Able to mediate deubiquitination of histone H2B; it is however unsure whether this activity takes place in vivo (PubMed:20601937). Exhibits a preference towards 'Lys-48'-linked ubiquitin chains (PubMed:22689415). Increases regulatory T-cells (Treg) suppressive capacity by deubiquitinating and stabilizing the transcription factor FOXP3 which is crucial for Treg cell function (PubMed:23973222). Plays a role in the maintenance of the circadian clock periodicity via deubiquitination and stabilization of the CRY1 and CRY2 proteins (PubMed:27123980). Deubiquitinates REST, thereby stabilizing REST and promoting the maintenance of neural progenitor cells (PubMed:21258371). Deubiquitinates SIRT7, inhibiting SIRT7 histone deacetylase activity and regulating gluconeogenesis (PubMed:28655758). Involved in the regulation of WASH-dependent actin polymerization at the surface of endosomes and the regulation of endosomal protein recycling (PubMed:26365382). It maintains optimal WASH complex activity and precise F-actin levels via deubiquitination of TRIM27 and WASHC1 (PubMed:26365382). Mediates the deubiquitination of phosphorylated DEPTOR, promoting its stability and leading to decreased mTORC1 signaling (PubMed:35216969). {ECO:0000269|PubMed:11923872, ECO:0000269|PubMed:15053880, ECO:0000269|PubMed:16845383, ECO:0000269|PubMed:16964248, ECO:0000269|PubMed:18566590, ECO:0000269|PubMed:18716620, ECO:0000269|PubMed:20153724, ECO:0000269|PubMed:20601937, ECO:0000269|PubMed:21258371, ECO:0000269|PubMed:21745816, ECO:0000269|PubMed:22411829, ECO:0000269|PubMed:22466611, ECO:0000269|PubMed:22466612, ECO:0000269|PubMed:22689415, ECO:0000269|PubMed:23973222, ECO:0000269|PubMed:25283148, ECO:0000269|PubMed:25865756, ECO:0000269|PubMed:25944111, ECO:0000269|PubMed:26365382, ECO:0000269|PubMed:26678539, ECO:0000269|PubMed:26786098, ECO:0000269|PubMed:27123980, ECO:0000269|PubMed:28655758, ECO:0000269|PubMed:33544460, ECO:0000269|PubMed:35216969}.; FUNCTION: (Microbial infection) Contributes to the overall stabilization and trans-activation capability of the herpesvirus 1 trans-acting transcriptional protein ICP0/VMW110 during HSV-1 infection. {ECO:0000269|PubMed:14506283, ECO:0000269|PubMed:16160161, ECO:0000269|PubMed:18590780}.; FUNCTION: (Microbial infection) Upon infection with Epstein-Barr virus, the interaction with viral EBNA1 increases the association of USP7 with PML proteins, which is required for the polyubiquitylation and degradation of PML. {ECO:0000269|PubMed:20719947, ECO:0000269|PubMed:24216761}. |
Q96C57 | CUSTOS | T182 | ochoa | Protein CUSTOS | Plays a role in the regulation of Wnt signaling pathway during early development. {ECO:0000250|UniProtKB:A9C3N6}. |
Q96II8 | LRCH3 | Y595 | ochoa | DISP complex protein LRCH3 (Leucine-rich repeat and calponin homology domain-containing protein 3) | As part of the DISP complex, may regulate the association of septins with actin and thereby regulate the actin cytoskeleton. {ECO:0000269|PubMed:29467281}. |
Q96M96 | FGD4 | T144 | ochoa | FYVE, RhoGEF and PH domain-containing protein 4 (Actin filament-binding protein frabin) (FGD1-related F-actin-binding protein) (Zinc finger FYVE domain-containing protein 6) | Activates CDC42, a member of the Ras-like family of Rho- and Rac proteins, by exchanging bound GDP for free GTP. Plays a role in regulating the actin cytoskeleton and cell shape. Activates MAPK8 (By similarity). {ECO:0000250, ECO:0000269|PubMed:15133042}. |
Q96NU1 | SAMD11 | T643 | ochoa | Sterile alpha motif domain-containing protein 11 (SAM domain-containing protein 11) | Component of a Polycomb group (PcG) multiprotein PRC1-like complex, essential for establishing rod photoreceptor cell identity and function by silencing nonrod gene expression in developing rod photoreceptor cells. {ECO:0000250|UniProtKB:Q1RNF8}. |
Q96PE2 | ARHGEF17 | T530 | ochoa | Rho guanine nucleotide exchange factor 17 (164 kDa Rho-specific guanine-nucleotide exchange factor) (p164-RhoGEF) (p164RhoGEF) (Tumor endothelial marker 4) | Acts as a guanine nucleotide exchange factor (GEF) for RhoA GTPases. {ECO:0000269|PubMed:12071859}. |
Q9BQE3 | TUBA1C | T51 | ochoa | Tubulin alpha-1C chain (EC 3.6.5.-) (Alpha-tubulin 6) (Tubulin alpha-6 chain) [Cleaved into: Detyrosinated tubulin alpha-1C chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q9BQE3 | TUBA1C | T94 | ochoa | Tubulin alpha-1C chain (EC 3.6.5.-) (Alpha-tubulin 6) (Tubulin alpha-6 chain) [Cleaved into: Detyrosinated tubulin alpha-1C chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q9BW04 | SARG | T465 | ochoa | Specifically androgen-regulated gene protein | Putative androgen-specific receptor. {ECO:0000269|PubMed:15525603}. |
Q9BXK5 | BCL2L13 | T374 | ochoa | Bcl-2-like protein 13 (Bcl2-L-13) (Bcl-rambo) (Protein Mil1) | May promote the activation of caspase-3 and apoptosis. |
Q9BXS5 | AP1M1 | T152 | ochoa | AP-1 complex subunit mu-1 (AP-mu chain family member mu1A) (Adaptor protein complex AP-1 subunit mu-1) (Adaptor-related protein complex 1 subunit mu-1) (Clathrin assembly protein complex 1 mu-1 medium chain 1) (Clathrin coat assembly protein AP47) (Clathrin coat-associated protein AP47) (Golgi adaptor HA1/AP1 adaptin mu-1 subunit) (Mu-adaptin 1) (Mu1A-adaptin) | Subunit of clathrin-associated adaptor protein complex 1 that plays a role in protein sorting in the trans-Golgi network (TGN) and endosomes. The AP complexes mediate the recruitment of clathrin to membranes and the recognition of sorting signals within the cytosolic tails of transmembrane cargo molecules. |
Q9C0C2 | TNKS1BP1 | T501 | ochoa | 182 kDa tankyrase-1-binding protein | None |
Q9C0D5 | TANC1 | T347 | 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}. |
Q9H3D4 | TP63 | T625 | ochoa | Tumor protein 63 (p63) (Chronic ulcerative stomatitis protein) (CUSP) (Keratinocyte transcription factor KET) (Transformation-related protein 63) (TP63) (Tumor protein p73-like) (p73L) (p40) (p51) | Acts as a sequence specific DNA binding transcriptional activator or repressor. The isoforms contain a varying set of transactivation and auto-regulating transactivation inhibiting domains thus showing an isoform specific activity. Isoform 2 activates RIPK4 transcription. May be required in conjunction with TP73/p73 for initiation of p53/TP53 dependent apoptosis in response to genotoxic insults and the presence of activated oncogenes. Involved in Notch signaling by probably inducing JAG1 and JAG2. Plays a role in the regulation of epithelial morphogenesis. The ratio of DeltaN-type and TA*-type isoforms may govern the maintenance of epithelial stem cell compartments and regulate the initiation of epithelial stratification from the undifferentiated embryonal ectoderm. Required for limb formation from the apical ectodermal ridge. Activates transcription of the p21 promoter. {ECO:0000269|PubMed:11641404, ECO:0000269|PubMed:12374749, ECO:0000269|PubMed:12446779, ECO:0000269|PubMed:12446784, ECO:0000269|PubMed:20123734, ECO:0000269|PubMed:22197488, ECO:0000269|PubMed:9774969}. |
Q9H792 | PEAK1 | T822 | ochoa | Inactive tyrosine-protein kinase PEAK1 (Pseudopodium-enriched atypical kinase 1) (Sugen kinase 269) (Tyrosine-protein kinase SgK269) | Probable catalytically inactive kinase. Scaffolding protein that regulates the cytoskeleton to control cell spreading and migration by modulating focal adhesion dynamics (PubMed:20534451, PubMed:23105102, PubMed:35687021). Acts as a scaffold for mediating EGFR signaling (PubMed:23846654). {ECO:0000269|PubMed:20534451, ECO:0000269|PubMed:23105102, ECO:0000269|PubMed:23846654, ECO:0000269|PubMed:35687021}. |
Q9H8K7 | PAAT | T427 | ochoa | ATPase PAAT (EC 3.6.1.-) (Protein associated with ABC transporters) (PAAT) | ATPase that regulates mitochondrial ABC transporters ABCB7, ABCB8/MITOSUR and ABCB10 (PubMed:25063848). Regulates mitochondrial ferric concentration and heme biosynthesis and plays a role in the maintenance of mitochondrial homeostasis and cell survival (PubMed:25063848). {ECO:0000269|PubMed:25063848}. |
Q9HCE1 | MOV10 | T972 | ochoa | Helicase MOV-10 (EC 3.6.4.13) (Armitage homolog) (Moloney leukemia virus 10 protein) | 5' to 3' RNA helicase that is involved in a number of cellular roles ranging from mRNA metabolism and translation, modulation of viral infectivity, inhibition of retrotransposition, or regulation of synaptic transmission (PubMed:23093941). Plays an important role in innate antiviral immunity by promoting type I interferon production (PubMed:27016603, PubMed:27974568, PubMed:35157734). Mechanistically, specifically uses IKKepsilon/IKBKE as the mediator kinase for IRF3 activation (PubMed:27016603, PubMed:35157734). Blocks HIV-1 virus replication at a post-entry step (PubMed:20215113). Counteracts HIV-1 Vif-mediated degradation of APOBEC3G through its helicase activity by interfering with the ubiquitin-proteasome pathway (PubMed:29258557). Also inhibits hepatitis B virus/HBV replication by interacting with HBV RNA and thereby inhibiting the early step of viral reverse transcription (PubMed:31722967). Contributes to UPF1 mRNA target degradation by translocation along 3' UTRs (PubMed:24726324). Required for microRNA (miRNA)-mediated gene silencing by the RNA-induced silencing complex (RISC). Required for both miRNA-mediated translational repression and miRNA-mediated cleavage of complementary mRNAs by RISC (PubMed:16289642, PubMed:17507929, PubMed:22791714). In cooperation with FMR1, regulates miRNA-mediated translational repression by AGO2 (PubMed:25464849). Restricts retrotransposition of long interspersed element-1 (LINE-1) in cooperation with TUT4 and TUT7 counteracting the RNA chaperonne activity of L1RE1 (PubMed:23093941, PubMed:30122351). Facilitates LINE-1 uridylation by TUT4 and TUT7 (PubMed:30122351). Required for embryonic viability and for normal central nervous system development and function. Plays two critical roles in early brain development: suppresses retroelements in the nucleus by directly inhibiting cDNA synthesis, while regulates cytoskeletal mRNAs to influence neurite outgrowth in the cytosol (By similarity). May function as a messenger ribonucleoprotein (mRNP) clearance factor (PubMed:24726324). {ECO:0000250|UniProtKB:P23249, ECO:0000269|PubMed:16289642, ECO:0000269|PubMed:17507929, ECO:0000269|PubMed:20215113, ECO:0000269|PubMed:22791714, ECO:0000269|PubMed:23093941, ECO:0000269|PubMed:24726324, ECO:0000269|PubMed:25464849, ECO:0000269|PubMed:27016603, ECO:0000269|PubMed:27974568, ECO:0000269|PubMed:29258557, ECO:0000269|PubMed:30122351, ECO:0000269|PubMed:31722967, ECO:0000269|PubMed:35157734}.; FUNCTION: (Microbial infection) Required for RNA-directed transcription and replication of the human hepatitis delta virus (HDV). Interacts with small capped HDV RNAs derived from genomic hairpin structures that mark the initiation sites of RNA-dependent HDV RNA transcription. {ECO:0000269|PubMed:18552826}. |
Q9NP66 | HMG20A | T108 | ochoa | High mobility group protein 20A (HMG box-containing protein 20A) (HMG domain-containing protein 1) (HMG domain-containing protein HMGX1) | Plays a role in neuronal differentiation as chromatin-associated protein. Acts as inhibitor of HMG20B. Overcomes the repressive effects of the neuronal silencer REST and induces the activation of neuronal-specific genes. Involved in the recruitment of the histone methyltransferase KMT2A/MLL1 and consequent increased methylation of histone H3 lysine 4 (By similarity). {ECO:0000250}. |
Q9NTJ3 | SMC4 | T44 | ochoa | Structural maintenance of chromosomes protein 4 (SMC protein 4) (SMC-4) (Chromosome-associated polypeptide C) (hCAP-C) (XCAP-C homolog) | Central component of the condensin complex, a complex required for conversion of interphase chromatin into mitotic-like condense chromosomes. The condensin complex probably introduces positive supercoils into relaxed DNA in the presence of type I topoisomerases and converts nicked DNA into positive knotted forms in the presence of type II topoisomerases. {ECO:0000269|PubMed:11136719}. |
Q9NY65 | TUBA8 | T94 | ochoa | Tubulin alpha-8 chain (EC 3.6.5.-) (Alpha-tubulin 8) (Tubulin alpha chain-like 2) [Cleaved into: Dephenylalaninated tubulin alpha-8 chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q9NYD6 | HOXC10 | T244 | ochoa | Homeobox protein Hox-C10 (Homeobox protein Hox-3I) | Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. |
Q9P206 | NHSL3 | T932 | ochoa | NHS-like protein 3 | Able to directly activate the TNF-NFkappaB signaling pathway. {ECO:0000269|PubMed:32854746}. |
Q9UBP9 | GULP1 | T214 | ochoa | PTB domain-containing engulfment adapter protein 1 (Cell death protein 6 homolog) (PTB domain adapter protein CED-6) (Protein GULP) | May function as an adapter protein. Required for efficient phagocytosis of apoptotic cells. Modulates cellular glycosphingolipid and cholesterol transport. May play a role in the internalization and endosomal trafficking of various LRP1 ligands, such as PSAP. Increases cellular levels of GTP-bound ARF6. {ECO:0000269|PubMed:10574763, ECO:0000269|PubMed:10574771, ECO:0000269|PubMed:16497666, ECO:0000269|PubMed:17398097}. |
Q9UK61 | TASOR | T982 | ochoa | Protein TASOR (CTCL tumor antigen se89-1) (Retinoblastoma-associated protein RAP140) (Transgene activation suppressor protein) | Component of the HUSH complex, a multiprotein complex that mediates epigenetic repression (PubMed:26022416, PubMed:28581500). The HUSH complex is recruited to genomic loci rich in H3K9me3 and is required to maintain transcriptional silencing by promoting recruitment of SETDB1, a histone methyltransferase that mediates further deposition of H3K9me3, as well as MORC2 (PubMed:26022416, PubMed:28581500). Also represses L1 retrotransposons in collaboration with MORC2 and, probably, SETDB1, the silencing is dependent of repressive epigenetic modifications, such as H3K9me3 mark. Silencing events often occur within introns of transcriptionally active genes, and lead to the down-regulation of host gene expression (PubMed:29211708). The HUSH complex is also involved in the silencing of unintegrated retroviral DNA by being recruited by ZNF638: some part of the retroviral DNA formed immediately after infection remains unintegrated in the host genome and is transcriptionally repressed (PubMed:30487602). Plays a crucial role in early embryonic development (By similarity). Involved in the organization of spindle poles and spindle apparatus assembly during zygotic division (By similarity). Plays an important role in maintaining epiblast fitness or potency (By similarity). {ECO:0000250|UniProtKB:Q69ZR9, ECO:0000269|PubMed:26022416, ECO:0000269|PubMed:28581500, ECO:0000269|PubMed:29211708, ECO:0000269|PubMed:30487602}. |
Q9UKA4 | AKAP11 | T1583 | ochoa | A-kinase anchor protein 11 (AKAP-11) (A-kinase anchor protein 220 kDa) (AKAP 220) (hAKAP220) (Protein kinase A-anchoring protein 11) (PRKA11) | Binds to type II regulatory subunits of protein kinase A and anchors/targets them. |
Q9UKS6 | PACSIN3 | T347 | ochoa | Protein kinase C and casein kinase substrate in neurons protein 3 (SH3 domain-containing protein 6511) | Plays a role in endocytosis and regulates internalization of plasma membrane proteins. Overexpression impairs internalization of SLC2A1/GLUT1 and TRPV4 and increases the levels of SLC2A1/GLUT1 and TRPV4 at the cell membrane. Inhibits the TRPV4 calcium channel activity (By similarity). {ECO:0000250, ECO:0000269|PubMed:11082044}. |
Q9UKS7 | IKZF2 | T372 | ochoa | Zinc finger protein Helios (Ikaros family zinc finger protein 2) | Transcriptional regulator required for outer hair cells (OHC) maturation and, consequently, for hearing. {ECO:0000250|UniProtKB:P81183}. |
Q9ULR3 | PPM1H | T224 | ochoa | Protein phosphatase 1H (EC 3.1.3.16) | Dephosphorylates CDKN1B at 'Thr-187', thus removing a signal for proteasomal degradation. {ECO:0000269|PubMed:22586611}. |
Q9UN81 | L1RE1 | T30 | ochoa | LINE-1 retrotransposable element ORF1 protein (L1ORF1p) (LINE retrotransposable element 1) (LINE1 retrotransposable element 1) | Nucleic acid-binding protein which is essential for retrotransposition of LINE-1 elements in the genome. Functions as a nucleic acid chaperone binding its own transcript and therefore preferentially mobilizing the transcript from which they are encoded. {ECO:0000269|PubMed:11158327, ECO:0000269|PubMed:21937507, ECO:0000269|PubMed:28806172, ECO:0000269|PubMed:30122351, ECO:0000269|PubMed:8945518}. |
Q9UPN4 | CEP131 | T117 | ochoa | Centrosomal protein of 131 kDa (5-azacytidine-induced protein 1) (Pre-acrosome localization protein 1) | Component of centriolar satellites contributing to the building of a complex and dynamic network required to regulate cilia/flagellum formation (PubMed:17954613, PubMed:24185901). In proliferating cells, MIB1-mediated ubiquitination induces its sequestration within centriolar satellites, precluding untimely cilia formation initiation (PubMed:24121310). In contrast, during normal and ultraviolet or heat shock cellular stress-induced ciliogenesis, its non-ubiquitinated form is rapidly displaced from centriolar satellites and recruited to centrosome/basal bodies in a microtubule- and p38 MAPK-dependent manner (PubMed:24121310, PubMed:26616734). Also acts as a negative regulator of BBSome ciliary trafficking (PubMed:24550735). Plays a role in sperm flagellar formation; may be involved in the regulation of intraflagellar transport (IFT) and/or intramanchette (IMT) trafficking, which are important for axoneme extension and/or cargo delivery to the nascent sperm tail (By similarity). Required for optimal cell proliferation and cell cycle progression; may play a role in the regulation of genome stability in non-ciliogenic cells (PubMed:22797915, PubMed:26297806). Involved in centriole duplication (By similarity). Required for CEP152, WDR62 and CEP63 centrosomal localization and promotes the centrosomal localization of CDK2 (PubMed:26297806). Essential for maintaining proper centriolar satellite integrity (PubMed:30804208). {ECO:0000250|UniProtKB:Q62036, ECO:0000269|PubMed:17954613, ECO:0000269|PubMed:22797915, ECO:0000269|PubMed:24121310, ECO:0000269|PubMed:24185901, ECO:0000269|PubMed:24550735, ECO:0000269|PubMed:26297806, ECO:0000269|PubMed:26616734, ECO:0000269|PubMed:30804208}. |
Q9UQP3 | TNN | T941 | ochoa | Tenascin-N (TN-N) (Tenascin-W) (TN-W) | Extracellular matrix protein that seems to be a ligand for ITGA8:ITGB1, ITGAV:ITGB1 and ITGA4:ITGB1 (By similarity) (PubMed:17909022). Involved in neurite outgrowth and cell migration in hippocampal explants (By similarity). During endochondral bone formation, inhibits proliferation and differentiation of proteoblasts mediated by canonical WNT signaling (By similarity). In tumors, stimulates angiogenesis by elongation, migration and sprouting of endothelial cells (PubMed:19884327). Expressed in most mammary tumors, may facilitate tumorigenesis by supporting the migratory behavior of breast cancer cells (PubMed:17909022). {ECO:0000250|UniProtKB:Q80YX1, ECO:0000250|UniProtKB:Q80Z71, ECO:0000269|PubMed:17909022, ECO:0000269|PubMed:19884327}. |
Q9Y2X9 | ZNF281 | T654 | ochoa | Zinc finger protein 281 (GC-box-binding zinc finger protein 1) (Transcription factor ZBP-99) (Zinc finger DNA-binding protein 99) | Transcription repressor that plays a role in regulation of embryonic stem cells (ESCs) differentiation. Required for ESCs differentiation and acts by mediating autorepression of NANOG in ESCs: binds to the NANOG promoter and promotes association of NANOG protein to its own promoter and recruits the NuRD complex, which deacetylates histones. Not required for establishement and maintenance of ESCs (By similarity). Represses the transcription of a number of genes including GAST, ODC1 and VIM. Binds to the G-rich box in the enhancer region of these genes. {ECO:0000250, ECO:0000269|PubMed:10448078, ECO:0000269|PubMed:12771217}. |
Q9Y4A5 | TRRAP | T1631 | ochoa | Transformation/transcription domain-associated protein (350/400 kDa PCAF-associated factor) (PAF350/400) (STAF40) (Tra1 homolog) | Adapter protein, which is found in various multiprotein chromatin complexes with histone acetyltransferase activity (HAT), which gives a specific tag for epigenetic transcription activation. Component of the NuA4 histone acetyltransferase complex which is responsible for acetylation of nucleosomal histones H4 and H2A. Plays a central role in MYC transcription activation, and also participates in cell transformation by MYC. Required for p53/TP53-, E2F1- and E2F4-mediated transcription activation. Also involved in transcription activation mediated by the adenovirus E1A, a viral oncoprotein that deregulates transcription of key genes. Probably acts by linking transcription factors such as E1A, MYC or E2F1 to HAT complexes such as STAGA thereby allowing transcription activation. Probably not required in the steps following histone acetylation in processes of transcription activation. May be required for the mitotic checkpoint and normal cell cycle progression. Component of a SWR1-like complex that specifically mediates the removal of histone H2A.Z/H2AZ1 from the nucleosome. May play a role in the formation and maintenance of the auditory system (By similarity). {ECO:0000250|UniProtKB:A0A0R4ITC5, ECO:0000269|PubMed:11418595, ECO:0000269|PubMed:12138177, ECO:0000269|PubMed:12660246, ECO:0000269|PubMed:12743606, ECO:0000269|PubMed:14966270, ECO:0000269|PubMed:17967892, ECO:0000269|PubMed:24463511, ECO:0000269|PubMed:9708738}. |
Q9Y613 | FHOD1 | T489 | ochoa | FH1/FH2 domain-containing protein 1 (Formin homolog overexpressed in spleen 1) (FHOS) (Formin homology 2 domain-containing protein 1) | Required for the assembly of F-actin structures, such as stress fibers. Depends on the Rho-ROCK cascade for its activity. Contributes to the coordination of microtubules with actin fibers and plays a role in cell elongation. Acts synergistically with ROCK1 to promote SRC-dependent non-apoptotic plasma membrane blebbing. {ECO:0000269|PubMed:14576350, ECO:0000269|PubMed:15878344, ECO:0000269|PubMed:18694941}. |
Q9Y6A5 | TACC3 | T437 | ochoa | Transforming acidic coiled-coil-containing protein 3 (ERIC-1) | Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors (By similarity). Acts as a component of the TACC3/ch-TOG/clathrin complex proposed to contribute to stabilization of kinetochore fibers of the mitotic spindle by acting as inter-microtubule bridge. The TACC3/ch-TOG/clathrin complex is required for the maintenance of kinetochore fiber tension (PubMed:21297582, PubMed:23532825). May be involved in the control of cell growth and differentiation. May contribute to cancer (PubMed:14767476). {ECO:0000250|UniProtKB:Q9JJ11, ECO:0000269|PubMed:14767476, ECO:0000269|PubMed:21297582, ECO:0000269|PubMed:23532825}. |
P08865 | RPSA | T82 | Sugiyama | Small ribosomal subunit protein uS2 (37 kDa laminin receptor precursor) (37LRP) (37/67 kDa laminin receptor) (LRP/LR) (40S ribosomal protein SA) (67 kDa laminin receptor) (67LR) (Colon carcinoma laminin-binding protein) (Laminin receptor 1) (LamR) (Laminin-binding protein precursor p40) (LBP/p40) (Multidrug resistance-associated protein MGr1-Ag) (NEM/1CHD4) | Required for the assembly and/or stability of the 40S ribosomal subunit. Required for the processing of the 20S rRNA-precursor to mature 18S rRNA in a late step of the maturation of 40S ribosomal subunits. Also functions as a cell surface receptor for laminin. Plays a role in cell adhesion to the basement membrane and in the consequent activation of signaling transduction pathways. May play a role in cell fate determination and tissue morphogenesis. Acts as a PPP1R16B-dependent substrate of PPP1CA. {ECO:0000255|HAMAP-Rule:MF_03016, ECO:0000269|PubMed:16263087, ECO:0000269|PubMed:6300843}.; FUNCTION: (Microbial infection) Acts as a receptor for the Adeno-associated viruses 2,3,8 and 9. {ECO:0000269|PubMed:16973587}.; FUNCTION: (Microbial infection) Acts as a receptor for the Dengue virus. {ECO:0000269|PubMed:15507651}.; FUNCTION: (Microbial infection) Acts as a receptor for the Sindbis virus. {ECO:0000269|PubMed:1385835}.; FUNCTION: (Microbial infection) Acts as a receptor for the Venezuelan equine encephalitis virus. {ECO:0000269|PubMed:1385835}.; FUNCTION: (Microbial infection) Acts as a receptor for the pathogenic prion protein. {ECO:0000269|PubMed:11689427, ECO:0000269|PubMed:9396609}.; FUNCTION: (Microbial infection) Acts as a receptor for bacteria. {ECO:0000269|PubMed:15516338}. |
P30101 | PDIA3 | T120 | Sugiyama | Protein disulfide-isomerase A3 (EC 5.3.4.1) (58 kDa glucose-regulated protein) (58 kDa microsomal protein) (p58) (Disulfide isomerase ER-60) (Endoplasmic reticulum resident protein 57) (ER protein 57) (ERp57) (Endoplasmic reticulum resident protein 60) (ER protein 60) (ERp60) | Protein disulfide isomerase that catalyzes the formation, isomerization, and reduction or oxidation of disulfide bonds in client proteins and functions as a protein folding chaperone (PubMed:11825568, PubMed:16193070, PubMed:27897272, PubMed:36104323, PubMed:7487104). Core component of the major histocompatibility complex class I (MHC I) peptide loading complex where it functions as an essential folding chaperone for TAPBP. Through TAPBP, assists the dynamic assembly of the MHC I complex with high affinity antigens in the endoplasmic reticulum. Therefore, plays a crucial role in the presentation of antigens to cytotoxic T cells in adaptive immunity (PubMed:35948544, PubMed:36104323). {ECO:0000269|PubMed:11825568, ECO:0000269|PubMed:16193070, ECO:0000269|PubMed:27897272, ECO:0000269|PubMed:35948544, ECO:0000269|PubMed:36104323, ECO:0000269|PubMed:7487104}. |
P62829 | RPL23 | T118 | Sugiyama | Large ribosomal subunit protein uL14 (60S ribosomal protein L17) (60S ribosomal protein L23) | 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}. |
P51813 | BMX | T190 | Sugiyama | Cytoplasmic tyrosine-protein kinase BMX (EC 2.7.10.2) (Bone marrow tyrosine kinase gene in chromosome X protein) (Epithelial and endothelial tyrosine kinase) (ETK) (NTK38) | Non-receptor tyrosine kinase that plays central but diverse modulatory roles in various signaling processes involved in the regulation of actin reorganization, cell migration, cell proliferation and survival, cell adhesion, and apoptosis. Participates in signal transduction stimulated by growth factor receptors, cytokine receptors, G-protein coupled receptors, antigen receptors and integrins. Induces tyrosine phosphorylation of BCAR1 in response to integrin regulation. Activation of BMX by integrins is mediated by PTK2/FAK1, a key mediator of integrin signaling events leading to the regulation of actin cytoskeleton and cell motility. Plays a critical role in TNF-induced angiogenesis, and implicated in the signaling of TEK and FLT1 receptors, 2 important receptor families essential for angiogenesis. Required for the phosphorylation and activation of STAT3, a transcription factor involved in cell differentiation. Also involved in interleukin-6 (IL6) induced differentiation. Also plays a role in programming adaptive cytoprotection against extracellular stress in different cell systems, salivary epithelial cells, brain endothelial cells, and dermal fibroblasts. May be involved in regulation of endocytosis through its interaction with an endosomal protein RUFY1. May also play a role in the growth and differentiation of hematopoietic cells; as well as in signal transduction in endocardial and arterial endothelial cells. {ECO:0000269|PubMed:10688651, ECO:0000269|PubMed:11331870, ECO:0000269|PubMed:12370298, ECO:0000269|PubMed:12832404, ECO:0000269|PubMed:15788485, ECO:0000269|PubMed:18292575, ECO:0000269|PubMed:9520419}. |
P12956 | XRCC6 | T541 | Sugiyama | X-ray repair cross-complementing protein 6 (EC 3.6.4.-) (EC 4.2.99.-) (5'-deoxyribose-5-phosphate lyase Ku70) (5'-dRP lyase Ku70) (70 kDa subunit of Ku antigen) (ATP-dependent DNA helicase 2 subunit 1) (ATP-dependent DNA helicase II 70 kDa subunit) (CTC box-binding factor 75 kDa subunit) (CTC75) (CTCBF) (DNA repair protein XRCC6) (Lupus Ku autoantigen protein p70) (Ku70) (Thyroid-lupus autoantigen) (TLAA) (X-ray repair complementing defective repair in Chinese hamster cells 6) | 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:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). Required for double-strand break repair and V(D)J recombination (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). Also has a role in chromosome translocation (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). Has a role in chromosome translocation (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). 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:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). It works in the 3'-5' direction (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). 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:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). Binding to DNA may be mediated by XRCC6 (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). 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:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). The XRCC5-XRRC6 dimer is probably involved in stabilizing broken DNA ends and bringing them together (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). The assembly of the DNA-PK complex to DNA ends is required for the NHEJ ligation step (PubMed:11493912, PubMed:12145306, PubMed:20493174, PubMed:2466842, PubMed:7957065, PubMed:8621488, PubMed:9742108). 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). 5'-dRP lyase activity 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). 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). Negatively regulates apoptosis by interacting with BAX and sequestering it from the mitochondria (PubMed:15023334). Might have deubiquitination activity, acting on BAX (PubMed:18362350). {ECO:0000269|PubMed:11493912, ECO:0000269|PubMed:12145306, ECO:0000269|PubMed:15023334, ECO:0000269|PubMed:18362350, ECO:0000269|PubMed:20383123, ECO:0000269|PubMed:20493174, ECO:0000269|PubMed:2466842, ECO:0000269|PubMed:28712728, ECO:0000269|PubMed:7957065, ECO:0000269|PubMed:8621488, ECO:0000269|PubMed:9742108}. |
P14598 | NCF1 | T133 | SIGNOR|EPSD|PSP | Neutrophil cytosol factor 1 (NCF-1) (47 kDa autosomal chronic granulomatous disease protein) (47 kDa neutrophil oxidase factor) (NCF-47K) (Neutrophil NADPH oxidase factor 1) (Nox organizer 2) (Nox-organizing protein 2) (SH3 and PX domain-containing protein 1A) (p47-phox) | Subunit of the phagocyte NADPH oxidase complex that mediates the transfer of electrons from cytosolic NADPH to O2 to produce the superoxide anion (O2(-)) (PubMed:2547247, PubMed:2550933, PubMed:38355798). In the activated complex, electrons are first transferred from NADPH to flavin adenine dinucleotide (FAD) and subsequently transferred via two heme molecules to molecular oxygen, producing superoxide through an outer-sphere reaction (PubMed:38355798). Activation of the NADPH oxidase complex is initiated by the assembly of cytosolic subunits of the NADPH oxidase complex with the core NADPH oxidase complex to form a complex at the plasma membrane or phagosomal membrane (PubMed:38355798). This activation process is initiated by phosphorylation dependent binding of the cytosolic NCF1/p47-phox subunit to the C-terminus of CYBA/p22-phox (PubMed:12732142, PubMed:19801500). {ECO:0000269|PubMed:12732142, ECO:0000269|PubMed:19801500, ECO:0000269|PubMed:2547247, ECO:0000269|PubMed:2550933, ECO:0000269|PubMed:38355798}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-190840 | Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 8.560064e-11 | 10.068 |
R-HSA-190872 | Transport of connexons to the plasma membrane | 1.211442e-10 | 9.917 |
R-HSA-389977 | Post-chaperonin tubulin folding pathway | 2.321500e-10 | 9.634 |
R-HSA-389960 | Formation of tubulin folding intermediates by CCT/TriC | 9.575117e-10 | 9.019 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 2.520863e-09 | 8.598 |
R-HSA-389958 | Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 4.836059e-09 | 8.316 |
R-HSA-437239 | Recycling pathway of L1 | 5.671535e-09 | 8.246 |
R-HSA-9668328 | Sealing of the nuclear envelope (NE) by ESCRT-III | 7.247179e-09 | 8.140 |
R-HSA-190861 | Gap junction assembly | 1.063403e-08 | 7.973 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 2.226260e-08 | 7.652 |
R-HSA-453274 | Mitotic G2-G2/M phases | 2.472968e-08 | 7.607 |
R-HSA-9646399 | Aggrephagy | 3.016755e-08 | 7.520 |
R-HSA-983189 | Kinesins | 3.433827e-08 | 7.464 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 4.383441e-08 | 7.358 |
R-HSA-9609736 | Assembly and cell surface presentation of NMDA receptors | 4.140990e-08 | 7.383 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 5.933962e-08 | 7.227 |
R-HSA-9663891 | Selective autophagy | 5.933962e-08 | 7.227 |
R-HSA-190828 | Gap junction trafficking | 6.497275e-08 | 7.187 |
R-HSA-1632852 | Macroautophagy | 7.485960e-08 | 7.126 |
R-HSA-8955332 | Carboxyterminal post-translational modifications of tubulin | 9.926059e-08 | 7.003 |
R-HSA-157858 | Gap junction trafficking and regulation | 1.299140e-07 | 6.886 |
R-HSA-9612973 | Autophagy | 2.081523e-07 | 6.682 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 2.752525e-07 | 6.560 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 2.957422e-07 | 6.529 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 4.425730e-07 | 6.354 |
R-HSA-373760 | L1CAM interactions | 8.409449e-07 | 6.075 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 1.176128e-06 | 5.930 |
R-HSA-69275 | G2/M Transition | 1.146482e-06 | 5.941 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 1.108240e-06 | 5.955 |
R-HSA-6807878 | COPI-mediated anterograde transport | 1.465818e-06 | 5.834 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 1.465818e-06 | 5.834 |
R-HSA-5620920 | Cargo trafficking to the periciliary membrane | 1.473425e-06 | 5.832 |
R-HSA-68877 | Mitotic Prometaphase | 1.617083e-06 | 5.791 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 1.770042e-06 | 5.752 |
R-HSA-9833482 | PKR-mediated signaling | 3.241487e-06 | 5.489 |
R-HSA-390466 | Chaperonin-mediated protein folding | 6.084755e-06 | 5.216 |
R-HSA-438064 | Post NMDA receptor activation events | 6.084755e-06 | 5.216 |
R-HSA-69278 | Cell Cycle, Mitotic | 6.324396e-06 | 5.199 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 6.803131e-06 | 5.167 |
R-HSA-391251 | Protein folding | 9.403234e-06 | 5.027 |
R-HSA-2132295 | MHC class II antigen presentation | 1.055284e-05 | 4.977 |
R-HSA-389957 | Prefoldin mediated transfer of substrate to CCT/TriC | 1.195563e-05 | 4.922 |
R-HSA-913531 | Interferon Signaling | 1.329407e-05 | 4.876 |
R-HSA-2467813 | Separation of Sister Chromatids | 1.572975e-05 | 4.803 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 1.929328e-05 | 4.715 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 1.947740e-05 | 4.710 |
R-HSA-5620924 | Intraflagellar transport | 2.290293e-05 | 4.640 |
R-HSA-68882 | Mitotic Anaphase | 2.654390e-05 | 4.576 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 2.757503e-05 | 4.559 |
R-HSA-1640170 | Cell Cycle | 3.795417e-05 | 4.421 |
R-HSA-5617833 | Cilium Assembly | 5.003744e-05 | 4.301 |
R-HSA-1362300 | Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL... | 5.231879e-05 | 4.281 |
R-HSA-9609690 | HCMV Early Events | 6.315580e-05 | 4.200 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 7.344070e-05 | 4.134 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 7.909569e-05 | 4.102 |
R-HSA-5610787 | Hedgehog 'off' state | 1.323778e-04 | 3.878 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 1.502913e-04 | 3.823 |
R-HSA-68886 | M Phase | 2.035367e-04 | 3.691 |
R-HSA-9609646 | HCMV Infection | 3.890899e-04 | 3.410 |
R-HSA-1538133 | G0 and Early G1 | 5.942394e-04 | 3.226 |
R-HSA-5358351 | Signaling by Hedgehog | 9.571410e-04 | 3.019 |
R-HSA-199991 | Membrane Trafficking | 1.030693e-03 | 2.987 |
R-HSA-1169408 | ISG15 antiviral mechanism | 1.499808e-03 | 2.824 |
R-HSA-422475 | Axon guidance | 1.561950e-03 | 2.806 |
R-HSA-5660489 | MTF1 activates gene expression | 1.677317e-03 | 2.775 |
R-HSA-68911 | G2 Phase | 2.268297e-03 | 2.644 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 2.177217e-03 | 2.662 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 2.305909e-03 | 2.637 |
R-HSA-8949215 | Mitochondrial calcium ion transport | 2.549678e-03 | 2.594 |
R-HSA-9675108 | Nervous system development | 2.775217e-03 | 2.557 |
R-HSA-8869496 | TFAP2A acts as a transcriptional repressor during retinoic acid induced cell dif... | 3.701503e-03 | 2.432 |
R-HSA-193648 | NRAGE signals death through JNK | 3.925199e-03 | 2.406 |
R-HSA-139915 | Activation of PUMA and translocation to mitochondria | 4.540367e-03 | 2.343 |
R-HSA-446203 | Asparagine N-linked glycosylation | 4.782578e-03 | 2.320 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 5.639285e-03 | 2.249 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 5.639285e-03 | 2.249 |
R-HSA-114452 | Activation of BH3-only proteins | 5.666357e-03 | 2.247 |
R-HSA-8953897 | Cellular responses to stimuli | 5.595336e-03 | 2.252 |
R-HSA-8854518 | AURKA Activation by TPX2 | 6.505746e-03 | 2.187 |
R-HSA-112315 | Transmission across Chemical Synapses | 7.395236e-03 | 2.131 |
R-HSA-164843 | 2-LTR circle formation | 7.526350e-03 | 2.123 |
R-HSA-5653656 | Vesicle-mediated transport | 8.247798e-03 | 2.084 |
R-HSA-2559585 | Oncogene Induced Senescence | 8.620760e-03 | 2.064 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 8.859985e-03 | 2.053 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 8.859985e-03 | 2.053 |
R-HSA-380287 | Centrosome maturation | 9.622292e-03 | 2.017 |
R-HSA-9013973 | TICAM1-dependent activation of IRF3/IRF7 | 9.892265e-03 | 2.005 |
R-HSA-162592 | Integration of provirus | 9.892265e-03 | 2.005 |
R-HSA-9661069 | Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 1.254398e-02 | 1.902 |
R-HSA-9659787 | Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 1.254398e-02 | 1.902 |
R-HSA-198323 | AKT phosphorylates targets in the cytosol | 1.118315e-02 | 1.951 |
R-HSA-162582 | Signal Transduction | 1.285293e-02 | 1.891 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 1.357690e-02 | 1.867 |
R-HSA-165159 | MTOR signalling | 1.374020e-02 | 1.862 |
R-HSA-2262752 | Cellular responses to stress | 1.465022e-02 | 1.834 |
R-HSA-3270619 | IRF3-mediated induction of type I IFN | 1.546957e-02 | 1.811 |
R-HSA-6804116 | TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 1.703142e-02 | 1.769 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 1.727626e-02 | 1.763 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 1.785109e-02 | 1.748 |
R-HSA-936964 | Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | 1.865742e-02 | 1.729 |
R-HSA-5660526 | Response to metal ions | 1.865742e-02 | 1.729 |
R-HSA-5688426 | Deubiquitination | 2.009650e-02 | 1.697 |
R-HSA-9827857 | Specification of primordial germ cells | 2.034618e-02 | 1.692 |
R-HSA-1362277 | Transcription of E2F targets under negative control by DREAM complex | 2.577533e-02 | 1.589 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 2.407424e-02 | 1.618 |
R-HSA-162594 | Early Phase of HIV Life Cycle | 2.770157e-02 | 1.557 |
R-HSA-73887 | Death Receptor Signaling | 2.872615e-02 | 1.542 |
R-HSA-1834941 | STING mediated induction of host immune responses | 2.390648e-02 | 1.621 |
R-HSA-109606 | Intrinsic Pathway for Apoptosis | 2.609794e-02 | 1.583 |
R-HSA-6791312 | TP53 Regulates Transcription of Cell Cycle Genes | 2.714846e-02 | 1.566 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 2.425800e-02 | 1.615 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 2.347999e-02 | 1.629 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 2.979864e-02 | 1.526 |
R-HSA-166208 | mTORC1-mediated signalling | 3.172103e-02 | 1.499 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 3.189648e-02 | 1.496 |
R-HSA-5674400 | Constitutive Signaling by AKT1 E17K in Cancer | 3.381173e-02 | 1.471 |
R-HSA-9824446 | Viral Infection Pathways | 3.514478e-02 | 1.454 |
R-HSA-429947 | Deadenylation of mRNA | 3.595476e-02 | 1.444 |
R-HSA-1257604 | PIP3 activates AKT signaling | 3.778559e-02 | 1.423 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 3.891599e-02 | 1.410 |
R-HSA-9022699 | MECP2 regulates neuronal receptors and channels | 4.039294e-02 | 1.394 |
R-HSA-597592 | Post-translational protein modification | 4.171210e-02 | 1.380 |
R-HSA-5689880 | Ub-specific processing proteases | 4.272152e-02 | 1.369 |
R-HSA-5205685 | PINK1-PRKN Mediated Mitophagy | 4.502607e-02 | 1.347 |
R-HSA-5626978 | TNFR1-mediated ceramide production | 5.753327e-02 | 1.240 |
R-HSA-165181 | Inhibition of TSC complex formation by PKB | 5.753327e-02 | 1.240 |
R-HSA-9927432 | Developmental Lineage of Mammary Gland Myoepithelial Cells | 4.741285e-02 | 1.324 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 6.049509e-02 | 1.218 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 6.118121e-02 | 1.213 |
R-HSA-8875513 | MET interacts with TNS proteins | 4.817811e-02 | 1.317 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 4.984494e-02 | 1.302 |
R-HSA-111448 | Activation of NOXA and translocation to mitochondria | 5.753327e-02 | 1.240 |
R-HSA-9687139 | Aberrant regulation of mitotic cell cycle due to RB1 defects | 4.984494e-02 | 1.302 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 5.740202e-02 | 1.241 |
R-HSA-9675126 | Diseases of mitotic cell cycle | 5.484060e-02 | 1.261 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 4.741285e-02 | 1.324 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 5.740202e-02 | 1.241 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 5.293793e-02 | 1.276 |
R-HSA-416482 | G alpha (12/13) signalling events | 5.427286e-02 | 1.265 |
R-HSA-112316 | Neuronal System | 5.460920e-02 | 1.263 |
R-HSA-5205647 | Mitophagy | 6.264672e-02 | 1.203 |
R-HSA-74713 | IRS activation | 6.679705e-02 | 1.175 |
R-HSA-203754 | NOSIP mediated eNOS trafficking | 6.679705e-02 | 1.175 |
R-HSA-1606341 | IRF3 mediated activation of type 1 IFN | 6.679705e-02 | 1.175 |
R-HSA-8939247 | RUNX1 regulates transcription of genes involved in interleukin signaling | 6.679705e-02 | 1.175 |
R-HSA-8939245 | RUNX1 regulates transcription of genes involved in BCR signaling | 6.679705e-02 | 1.175 |
R-HSA-3134973 | LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 6.679705e-02 | 1.175 |
R-HSA-9006925 | Intracellular signaling by second messengers | 6.893453e-02 | 1.162 |
R-HSA-6807070 | PTEN Regulation | 6.987715e-02 | 1.156 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 7.080310e-02 | 1.150 |
R-HSA-933541 | TRAF6 mediated IRF7 activation | 7.080310e-02 | 1.150 |
R-HSA-72172 | mRNA Splicing | 7.240453e-02 | 1.140 |
R-HSA-5340588 | Signaling by RNF43 mutants | 7.597035e-02 | 1.119 |
R-HSA-8937144 | Aryl hydrocarbon receptor signalling | 7.597035e-02 | 1.119 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 7.642199e-02 | 1.117 |
R-HSA-9725554 | Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | 7.642199e-02 | 1.117 |
R-HSA-8953750 | Transcriptional Regulation by E2F6 | 7.642199e-02 | 1.117 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 7.742303e-02 | 1.111 |
R-HSA-177539 | Autointegration results in viral DNA circles | 8.505404e-02 | 1.070 |
R-HSA-203641 | NOSTRIN mediated eNOS trafficking | 9.404898e-02 | 1.027 |
R-HSA-9732724 | IFNG signaling activates MAPKs | 9.404898e-02 | 1.027 |
R-HSA-112412 | SOS-mediated signalling | 9.404898e-02 | 1.027 |
R-HSA-9828211 | Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | 1.029560e-01 | 0.987 |
R-HSA-9768778 | Regulation of NPAS4 mRNA translation | 1.029560e-01 | 0.987 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 7.928294e-02 | 1.101 |
R-HSA-72165 | mRNA Splicing - Minor Pathway | 1.001858e-01 | 0.999 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 1.064135e-01 | 0.973 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 7.921932e-02 | 1.101 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 1.165921e-01 | 0.933 |
R-HSA-164940 | Nef mediated downregulation of MHC class I complex cell surface expression | 1.029560e-01 | 0.987 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 1.165921e-01 | 0.933 |
R-HSA-9820841 | M-decay: degradation of maternal mRNAs by maternally stored factors | 8.217697e-02 | 1.085 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 7.928294e-02 | 1.101 |
R-HSA-9603381 | Activated NTRK3 signals through PI3K | 9.404898e-02 | 1.027 |
R-HSA-111453 | BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members | 1.029560e-01 | 0.987 |
R-HSA-175567 | Integration of viral DNA into host genomic DNA | 8.505404e-02 | 1.070 |
R-HSA-8948747 | Regulation of PTEN localization | 9.404898e-02 | 1.027 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 1.021397e-01 | 0.991 |
R-HSA-157118 | Signaling by NOTCH | 1.163553e-01 | 0.934 |
R-HSA-109581 | Apoptosis | 1.039990e-01 | 0.983 |
R-HSA-69236 | G1 Phase | 9.406590e-02 | 1.027 |
R-HSA-69231 | Cyclin D associated events in G1 | 9.406590e-02 | 1.027 |
R-HSA-8864260 | Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 9.406590e-02 | 1.027 |
R-HSA-72187 | mRNA 3'-end processing | 1.191670e-01 | 0.924 |
R-HSA-198203 | PI3K/AKT activation | 1.205099e-01 | 0.919 |
R-HSA-74749 | Signal attenuation | 1.205099e-01 | 0.919 |
R-HSA-1236973 | Cross-presentation of particulate exogenous antigens (phagosomes) | 1.205099e-01 | 0.919 |
R-HSA-2586552 | Signaling by Leptin | 1.205099e-01 | 0.919 |
R-HSA-9762292 | Regulation of CDH11 function | 1.205099e-01 | 0.919 |
R-HSA-9764790 | Positive Regulation of CDH1 Gene Transcription | 1.205099e-01 | 0.919 |
R-HSA-432722 | Golgi Associated Vesicle Biogenesis | 1.224129e-01 | 0.912 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 1.251766e-01 | 0.902 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 1.251766e-01 | 0.902 |
R-HSA-72649 | Translation initiation complex formation | 1.256803e-01 | 0.901 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 1.273578e-01 | 0.895 |
R-HSA-9759811 | Regulation of CDH11 mRNA translation by microRNAs | 1.291585e-01 | 0.889 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 1.322768e-01 | 0.879 |
R-HSA-2559583 | Cellular Senescence | 1.354552e-01 | 0.868 |
R-HSA-2514853 | Condensation of Prometaphase Chromosomes | 1.377224e-01 | 0.861 |
R-HSA-9824878 | Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | 1.377224e-01 | 0.861 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 1.462027e-01 | 0.835 |
R-HSA-8948700 | Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 1.711496e-01 | 0.767 |
R-HSA-111447 | Activation of BAD and translocation to mitochondria | 1.711496e-01 | 0.767 |
R-HSA-77595 | Processing of Intronless Pre-mRNAs | 1.873770e-01 | 0.727 |
R-HSA-9909620 | Regulation of PD-L1(CD274) translation | 2.188907e-01 | 0.660 |
R-HSA-9938206 | Developmental Lineage of Mammary Stem Cells | 2.417263e-01 | 0.617 |
R-HSA-8943723 | Regulation of PTEN mRNA translation | 2.491897e-01 | 0.603 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 1.628421e-01 | 0.788 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 1.909493e-01 | 0.719 |
R-HSA-141424 | Amplification of signal from the kinetochores | 2.377542e-01 | 0.624 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 2.377542e-01 | 0.624 |
R-HSA-9954714 | PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | 2.595880e-01 | 0.586 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 1.389508e-01 | 0.857 |
R-HSA-156902 | Peptide chain elongation | 2.486628e-01 | 0.604 |
R-HSA-6803529 | FGFR2 alternative splicing | 2.417263e-01 | 0.617 |
R-HSA-877300 | Interferon gamma signaling | 2.550398e-01 | 0.593 |
R-HSA-72737 | Cap-dependent Translation Initiation | 1.384646e-01 | 0.859 |
R-HSA-72613 | Eukaryotic Translation Initiation | 1.384646e-01 | 0.859 |
R-HSA-9764562 | Regulation of CDH1 mRNA translation by microRNAs | 1.629155e-01 | 0.788 |
R-HSA-918233 | TRAF3-dependent IRF activation pathway | 1.873770e-01 | 0.727 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 1.873986e-01 | 0.727 |
R-HSA-9703465 | Signaling by FLT3 fusion proteins | 2.711449e-01 | 0.567 |
R-HSA-3772470 | Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 1.377224e-01 | 0.861 |
R-HSA-8934593 | Regulation of RUNX1 Expression and Activity | 2.711449e-01 | 0.567 |
R-HSA-380615 | Serotonin clearance from the synaptic cleft | 1.462027e-01 | 0.835 |
R-HSA-877312 | Regulation of IFNG signaling | 1.462027e-01 | 0.835 |
R-HSA-2559584 | Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 1.546002e-01 | 0.811 |
R-HSA-4641263 | Regulation of FZD by ubiquitination | 1.953719e-01 | 0.709 |
R-HSA-75067 | Processing of Capped Intronless Pre-mRNA | 2.565802e-01 | 0.591 |
R-HSA-9839394 | TGFBR3 expression | 2.638983e-01 | 0.579 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 1.490951e-01 | 0.827 |
R-HSA-199992 | trans-Golgi Network Vesicle Budding | 1.873986e-01 | 0.727 |
R-HSA-156842 | Eukaryotic Translation Elongation | 2.668754e-01 | 0.574 |
R-HSA-9711097 | Cellular response to starvation | 2.524035e-01 | 0.598 |
R-HSA-156711 | Polo-like kinase mediated events | 2.032887e-01 | 0.692 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 1.423151e-01 | 0.847 |
R-HSA-1606322 | ZBP1(DAI) mediated induction of type I IFNs | 2.032887e-01 | 0.692 |
R-HSA-113501 | Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 1.377224e-01 | 0.861 |
R-HSA-180689 | APOBEC3G mediated resistance to HIV-1 infection | 1.377224e-01 | 0.861 |
R-HSA-5357786 | TNFR1-induced proapoptotic signaling | 2.265775e-01 | 0.645 |
R-HSA-9842663 | Signaling by LTK | 1.462027e-01 | 0.835 |
R-HSA-6803211 | TP53 Regulates Transcription of Death Receptors and Ligands | 1.629155e-01 | 0.788 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 2.445198e-01 | 0.612 |
R-HSA-5689603 | UCH proteinases | 2.016539e-01 | 0.695 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 1.456968e-01 | 0.837 |
R-HSA-113510 | E2F mediated regulation of DNA replication | 2.111280e-01 | 0.675 |
R-HSA-8953854 | Metabolism of RNA | 2.266638e-01 | 0.645 |
R-HSA-3134975 | Regulation of innate immune responses to cytosolic DNA | 1.873770e-01 | 0.727 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 1.803263e-01 | 0.744 |
R-HSA-6803205 | TP53 regulates transcription of several additional cell death genes whose specif... | 2.417263e-01 | 0.617 |
R-HSA-6804759 | Regulation of TP53 Activity through Association with Co-factors | 1.546002e-01 | 0.811 |
R-HSA-164938 | Nef-mediates down modulation of cell surface receptors by recruiting them to cla... | 1.953719e-01 | 0.709 |
R-HSA-9824594 | Regulation of MITF-M-dependent genes involved in apoptosis | 2.265775e-01 | 0.645 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 2.711449e-01 | 0.567 |
R-HSA-162909 | Host Interactions of HIV factors | 1.568837e-01 | 0.804 |
R-HSA-9768759 | Regulation of NPAS4 gene expression | 1.953719e-01 | 0.709 |
R-HSA-164952 | The role of Nef in HIV-1 replication and disease pathogenesis | 2.491897e-01 | 0.603 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 1.429974e-01 | 0.845 |
R-HSA-162906 | HIV Infection | 2.285149e-01 | 0.641 |
R-HSA-2028269 | Signaling by Hippo | 1.953719e-01 | 0.709 |
R-HSA-162587 | HIV Life Cycle | 2.497712e-01 | 0.602 |
R-HSA-6803207 | TP53 Regulates Transcription of Caspase Activators and Caspases | 1.793031e-01 | 0.746 |
R-HSA-6802957 | Oncogenic MAPK signaling | 2.341234e-01 | 0.631 |
R-HSA-9034015 | Signaling by NTRK3 (TRKC) | 2.341891e-01 | 0.630 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 2.366779e-01 | 0.626 |
R-HSA-2122948 | Activated NOTCH1 Transmits Signal to the Nucleus | 2.711449e-01 | 0.567 |
R-HSA-1280218 | Adaptive Immune System | 1.704189e-01 | 0.768 |
R-HSA-418990 | Adherens junctions interactions | 2.098865e-01 | 0.678 |
R-HSA-5357801 | Programmed Cell Death | 1.838257e-01 | 0.736 |
R-HSA-373753 | Nephrin family interactions | 2.188907e-01 | 0.660 |
R-HSA-5669034 | TNFs bind their physiological receptors | 2.565802e-01 | 0.591 |
R-HSA-6804115 | TP53 regulates transcription of additional cell cycle genes whose exact role in ... | 2.417263e-01 | 0.617 |
R-HSA-1500931 | Cell-Cell communication | 2.393004e-01 | 0.621 |
R-HSA-9013507 | NOTCH3 Activation and Transmission of Signal to the Nucleus | 2.417263e-01 | 0.617 |
R-HSA-6783783 | Interleukin-10 signaling | 2.088288e-01 | 0.680 |
R-HSA-5633007 | Regulation of TP53 Activity | 2.576802e-01 | 0.589 |
R-HSA-9690406 | Transcriptional regulation of testis differentiation | 1.873770e-01 | 0.727 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 1.622589e-01 | 0.790 |
R-HSA-1222556 | ROS and RNS production in phagocytes | 1.945091e-01 | 0.711 |
R-HSA-1266695 | Interleukin-7 signaling | 2.638983e-01 | 0.579 |
R-HSA-982772 | Growth hormone receptor signaling | 2.491897e-01 | 0.603 |
R-HSA-109582 | Hemostasis | 2.736164e-01 | 0.563 |
R-HSA-9954716 | ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ri... | 2.778056e-01 | 0.556 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 2.778056e-01 | 0.556 |
R-HSA-5357956 | TNFR1-induced NF-kappa-B signaling pathway | 2.783206e-01 | 0.555 |
R-HSA-3928663 | EPHA-mediated growth cone collapse | 2.783206e-01 | 0.555 |
R-HSA-4641262 | Disassembly of the destruction complex and recruitment of AXIN to the membrane | 2.783206e-01 | 0.555 |
R-HSA-445095 | Interaction between L1 and Ankyrins | 2.783206e-01 | 0.555 |
R-HSA-6803204 | TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 2.783206e-01 | 0.555 |
R-HSA-8866652 | Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 2.783206e-01 | 0.555 |
R-HSA-421270 | Cell-cell junction organization | 2.799747e-01 | 0.553 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 2.814473e-01 | 0.551 |
R-HSA-72764 | Eukaryotic Translation Termination | 2.814473e-01 | 0.551 |
R-HSA-392499 | Metabolism of proteins | 2.833367e-01 | 0.548 |
R-HSA-171319 | Telomere Extension By Telomerase | 2.854260e-01 | 0.545 |
R-HSA-5620971 | Pyroptosis | 2.854260e-01 | 0.545 |
R-HSA-8957275 | Post-translational protein phosphorylation | 2.923629e-01 | 0.534 |
R-HSA-392154 | Nitric oxide stimulates guanylate cyclase | 2.924620e-01 | 0.534 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 2.994291e-01 | 0.524 |
R-HSA-1474151 | Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 2.994291e-01 | 0.524 |
R-HSA-112311 | Neurotransmitter clearance | 2.994291e-01 | 0.524 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 2.996289e-01 | 0.523 |
R-HSA-1266738 | Developmental Biology | 3.003443e-01 | 0.522 |
R-HSA-2408557 | Selenocysteine synthesis | 3.032576e-01 | 0.518 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 3.063280e-01 | 0.514 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 3.063280e-01 | 0.514 |
R-HSA-9833109 | Evasion by RSV of host interferon responses | 3.063280e-01 | 0.514 |
R-HSA-936440 | Negative regulators of DDX58/IFIH1 signaling | 3.063280e-01 | 0.514 |
R-HSA-9734767 | Developmental Cell Lineages | 3.063864e-01 | 0.514 |
R-HSA-9842860 | Regulation of endogenous retroelements | 3.068831e-01 | 0.513 |
R-HSA-192823 | Viral mRNA Translation | 3.105050e-01 | 0.508 |
R-HSA-168255 | Influenza Infection | 3.110771e-01 | 0.507 |
R-HSA-4791275 | Signaling by WNT in cancer | 3.131594e-01 | 0.504 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 3.131594e-01 | 0.504 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 3.141232e-01 | 0.503 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 3.199239e-01 | 0.495 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 3.199239e-01 | 0.495 |
R-HSA-6804758 | Regulation of TP53 Activity through Acetylation | 3.199239e-01 | 0.495 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 3.199239e-01 | 0.495 |
R-HSA-5696398 | Nucleotide Excision Repair | 3.213471e-01 | 0.493 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 3.213471e-01 | 0.493 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 3.249523e-01 | 0.488 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 3.266223e-01 | 0.486 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 3.266223e-01 | 0.486 |
R-HSA-5696394 | DNA Damage Recognition in GG-NER | 3.266223e-01 | 0.486 |
R-HSA-1799339 | SRP-dependent cotranslational protein targeting to membrane | 3.285526e-01 | 0.483 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 3.285526e-01 | 0.483 |
R-HSA-9700206 | Signaling by ALK in cancer | 3.285526e-01 | 0.483 |
R-HSA-1236975 | Antigen processing-Cross presentation | 3.321479e-01 | 0.479 |
R-HSA-9843970 | Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | 3.332550e-01 | 0.477 |
R-HSA-203615 | eNOS activation | 3.332550e-01 | 0.477 |
R-HSA-9735869 | SARS-CoV-1 modulates host translation machinery | 3.332550e-01 | 0.477 |
R-HSA-983170 | Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 3.332550e-01 | 0.477 |
R-HSA-180746 | Nuclear import of Rev protein | 3.332550e-01 | 0.477 |
R-HSA-901042 | Calnexin/calreticulin cycle | 3.332550e-01 | 0.477 |
R-HSA-73857 | RNA Polymerase II Transcription | 3.333464e-01 | 0.477 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 3.393220e-01 | 0.469 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 3.393220e-01 | 0.469 |
R-HSA-446728 | Cell junction organization | 3.397455e-01 | 0.469 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 3.398229e-01 | 0.469 |
R-HSA-69205 | G1/S-Specific Transcription | 3.463264e-01 | 0.461 |
R-HSA-432720 | Lysosome Vesicle Biogenesis | 3.463264e-01 | 0.461 |
R-HSA-450408 | AUF1 (hnRNP D0) binds and destabilizes mRNA | 3.463264e-01 | 0.461 |
R-HSA-9682385 | FLT3 signaling in disease | 3.463264e-01 | 0.461 |
R-HSA-6804757 | Regulation of TP53 Degradation | 3.463264e-01 | 0.461 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 3.567671e-01 | 0.448 |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-l... | 3.571515e-01 | 0.447 |
R-HSA-202131 | Metabolism of nitric oxide: NOS3 activation and regulation | 3.591431e-01 | 0.445 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 3.591431e-01 | 0.445 |
R-HSA-8875878 | MET promotes cell motility | 3.591431e-01 | 0.445 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 3.642363e-01 | 0.439 |
R-HSA-909733 | Interferon alpha/beta signaling | 3.642363e-01 | 0.439 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 3.654575e-01 | 0.437 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 3.654575e-01 | 0.437 |
R-HSA-201556 | Signaling by ALK | 3.654575e-01 | 0.437 |
R-HSA-427389 | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 3.717101e-01 | 0.430 |
R-HSA-9843743 | Transcriptional regulation of brown and beige adipocyte differentiation | 3.717101e-01 | 0.430 |
R-HSA-9844594 | Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | 3.717101e-01 | 0.430 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 3.717101e-01 | 0.430 |
R-HSA-9604323 | Negative regulation of NOTCH4 signaling | 3.717101e-01 | 0.430 |
R-HSA-376176 | Signaling by ROBO receptors | 3.754990e-01 | 0.425 |
R-HSA-5218920 | VEGFR2 mediated vascular permeability | 3.779014e-01 | 0.423 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 3.779014e-01 | 0.423 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 3.779014e-01 | 0.423 |
R-HSA-68875 | Mitotic Prophase | 3.818164e-01 | 0.418 |
R-HSA-5610780 | Degradation of GLI1 by the proteasome | 3.840321e-01 | 0.416 |
R-HSA-6811438 | Intra-Golgi traffic | 3.840321e-01 | 0.416 |
R-HSA-442660 | SLC-mediated transport of neurotransmitters | 3.840321e-01 | 0.416 |
R-HSA-212436 | Generic Transcription Pathway | 3.851592e-01 | 0.414 |
R-HSA-73886 | Chromosome Maintenance | 3.853083e-01 | 0.414 |
R-HSA-9927418 | Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 3.901028e-01 | 0.409 |
R-HSA-73762 | RNA Polymerase I Transcription Initiation | 3.901028e-01 | 0.409 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 3.922666e-01 | 0.406 |
R-HSA-8854214 | TBC/RABGAPs | 3.961140e-01 | 0.402 |
R-HSA-194138 | Signaling by VEGF | 4.026376e-01 | 0.395 |
R-HSA-74160 | Gene expression (Transcription) | 4.075210e-01 | 0.390 |
R-HSA-774815 | Nucleosome assembly | 4.079604e-01 | 0.389 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 4.079604e-01 | 0.389 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 4.079604e-01 | 0.389 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 4.137967e-01 | 0.383 |
R-HSA-5357905 | Regulation of TNFR1 signaling | 4.137967e-01 | 0.383 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 4.137967e-01 | 0.383 |
R-HSA-6781823 | Formation of TC-NER Pre-Incision Complex | 4.137967e-01 | 0.383 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 4.137967e-01 | 0.383 |
R-HSA-9839373 | Signaling by TGFBR3 | 4.137967e-01 | 0.383 |
R-HSA-75153 | Apoptotic execution phase | 4.137967e-01 | 0.383 |
R-HSA-168256 | Immune System | 4.148814e-01 | 0.382 |
R-HSA-3928665 | EPH-ephrin mediated repulsion of cells | 4.195758e-01 | 0.377 |
R-HSA-1474165 | Reproduction | 4.231256e-01 | 0.374 |
R-HSA-9725371 | Nuclear events stimulated by ALK signaling in cancer | 4.252983e-01 | 0.371 |
R-HSA-5663205 | Infectious disease | 4.261166e-01 | 0.370 |
R-HSA-532668 | N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 4.309647e-01 | 0.366 |
R-HSA-109704 | PI3K Cascade | 4.365756e-01 | 0.360 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 4.438720e-01 | 0.353 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 4.476330e-01 | 0.349 |
R-HSA-9634815 | Transcriptional Regulation by NPAS4 | 4.476330e-01 | 0.349 |
R-HSA-9639288 | Amino acids regulate mTORC1 | 4.530806e-01 | 0.344 |
R-HSA-9948299 | Ribosome-associated quality control | 4.531667e-01 | 0.344 |
R-HSA-9754678 | SARS-CoV-2 modulates host translation machinery | 4.584748e-01 | 0.339 |
R-HSA-3214815 | HDACs deacetylate histones | 4.638161e-01 | 0.334 |
R-HSA-9012852 | Signaling by NOTCH3 | 4.638161e-01 | 0.334 |
R-HSA-6782210 | Gap-filling DNA repair synthesis and ligation in TC-NER | 4.691050e-01 | 0.329 |
R-HSA-75893 | TNF signaling | 4.691050e-01 | 0.329 |
R-HSA-9662361 | Sensory processing of sound by outer hair cells of the cochlea | 4.691050e-01 | 0.329 |
R-HSA-3299685 | Detoxification of Reactive Oxygen Species | 4.691050e-01 | 0.329 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 4.694709e-01 | 0.328 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 4.726973e-01 | 0.325 |
R-HSA-112399 | IRS-mediated signalling | 4.743421e-01 | 0.324 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 4.743421e-01 | 0.324 |
R-HSA-6782135 | Dual incision in TC-NER | 4.795279e-01 | 0.319 |
R-HSA-9029569 | NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflu... | 4.795279e-01 | 0.319 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 4.795279e-01 | 0.319 |
R-HSA-194441 | Metabolism of non-coding RNA | 4.846628e-01 | 0.315 |
R-HSA-191859 | snRNP Assembly | 4.846628e-01 | 0.315 |
R-HSA-180786 | Extension of Telomeres | 4.846628e-01 | 0.315 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 4.886516e-01 | 0.311 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 4.897474e-01 | 0.310 |
R-HSA-2428928 | IRS-related events triggered by IGF1R | 4.947821e-01 | 0.306 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 4.947821e-01 | 0.306 |
R-HSA-211976 | Endogenous sterols | 4.947821e-01 | 0.306 |
R-HSA-9679191 | Potential therapeutics for SARS | 4.949491e-01 | 0.305 |
R-HSA-375165 | NCAM signaling for neurite out-growth | 4.997675e-01 | 0.301 |
R-HSA-6784531 | tRNA processing in the nucleus | 4.997675e-01 | 0.301 |
R-HSA-9707616 | Heme signaling | 4.997675e-01 | 0.301 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 4.997675e-01 | 0.301 |
R-HSA-1268020 | Mitochondrial protein import | 4.997675e-01 | 0.301 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 4.997675e-01 | 0.301 |
R-HSA-1660499 | Synthesis of PIPs at the plasma membrane | 4.997675e-01 | 0.301 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 5.043036e-01 | 0.297 |
R-HSA-74751 | Insulin receptor signalling cascade | 5.095920e-01 | 0.293 |
R-HSA-2428924 | IGF1R signaling cascade | 5.095920e-01 | 0.293 |
R-HSA-211981 | Xenobiotics | 5.095920e-01 | 0.293 |
R-HSA-6798695 | Neutrophil degranulation | 5.110368e-01 | 0.292 |
R-HSA-2404192 | Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 5.144321e-01 | 0.289 |
R-HSA-9610379 | HCMV Late Events | 5.166021e-01 | 0.287 |
R-HSA-73894 | DNA Repair | 5.185221e-01 | 0.285 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 5.286694e-01 | 0.277 |
R-HSA-5218859 | Regulated Necrosis | 5.286694e-01 | 0.277 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 5.286694e-01 | 0.277 |
R-HSA-2408522 | Selenoamino acid metabolism | 5.376364e-01 | 0.270 |
R-HSA-9843940 | Regulation of endogenous retroelements by KRAB-ZFP proteins | 5.379298e-01 | 0.269 |
R-HSA-204005 | COPII-mediated vesicle transport | 5.379298e-01 | 0.269 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 5.379298e-01 | 0.269 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 5.379298e-01 | 0.269 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 5.424919e-01 | 0.266 |
R-HSA-5632684 | Hedgehog 'on' state | 5.424919e-01 | 0.266 |
R-HSA-3000178 | ECM proteoglycans | 5.424919e-01 | 0.266 |
R-HSA-8978934 | Metabolism of cofactors | 5.424919e-01 | 0.266 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 5.470093e-01 | 0.262 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 5.470093e-01 | 0.262 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 5.470093e-01 | 0.262 |
R-HSA-1643685 | Disease | 5.474070e-01 | 0.262 |
R-HSA-4086398 | Ca2+ pathway | 5.514823e-01 | 0.258 |
R-HSA-9013694 | Signaling by NOTCH4 | 5.559115e-01 | 0.255 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 5.580379e-01 | 0.253 |
R-HSA-6781827 | Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 5.602971e-01 | 0.252 |
R-HSA-5633008 | TP53 Regulates Transcription of Cell Death Genes | 5.602971e-01 | 0.252 |
R-HSA-8852135 | Protein ubiquitination | 5.602971e-01 | 0.252 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 5.646398e-01 | 0.248 |
R-HSA-1980143 | Signaling by NOTCH1 | 5.646398e-01 | 0.248 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 5.665850e-01 | 0.247 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 5.665850e-01 | 0.247 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 5.668559e-01 | 0.247 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 5.689398e-01 | 0.245 |
R-HSA-9678108 | SARS-CoV-1 Infection | 5.722172e-01 | 0.242 |
R-HSA-383280 | Nuclear Receptor transcription pathway | 5.731976e-01 | 0.242 |
R-HSA-73864 | RNA Polymerase I Transcription | 5.731976e-01 | 0.242 |
R-HSA-9659379 | Sensory processing of sound | 5.774136e-01 | 0.239 |
R-HSA-9856530 | High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR... | 5.815883e-01 | 0.235 |
R-HSA-5654738 | Signaling by FGFR2 | 5.815883e-01 | 0.235 |
R-HSA-6806834 | Signaling by MET | 5.815883e-01 | 0.235 |
R-HSA-5668541 | TNFR2 non-canonical NF-kB pathway | 5.938678e-01 | 0.226 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 5.942167e-01 | 0.226 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 5.978809e-01 | 0.223 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 6.018546e-01 | 0.221 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 6.075351e-01 | 0.216 |
R-HSA-195721 | Signaling by WNT | 6.098417e-01 | 0.215 |
R-HSA-70268 | Pyruvate metabolism | 6.135430e-01 | 0.212 |
R-HSA-168898 | Toll-like Receptor Cascades | 6.153669e-01 | 0.211 |
R-HSA-1236974 | ER-Phagosome pathway | 6.211452e-01 | 0.207 |
R-HSA-74752 | Signaling by Insulin receptor | 6.359066e-01 | 0.197 |
R-HSA-2682334 | EPH-Ephrin signaling | 6.359066e-01 | 0.197 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 6.430715e-01 | 0.192 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 6.500963e-01 | 0.187 |
R-HSA-157579 | Telomere Maintenance | 6.569837e-01 | 0.182 |
R-HSA-190236 | Signaling by FGFR | 6.603767e-01 | 0.180 |
R-HSA-3214847 | HATs acetylate histones | 6.637363e-01 | 0.178 |
R-HSA-70171 | Glycolysis | 6.670630e-01 | 0.176 |
R-HSA-9009391 | Extra-nuclear estrogen signaling | 6.703569e-01 | 0.174 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 6.736184e-01 | 0.172 |
R-HSA-1483255 | PI Metabolism | 6.736184e-01 | 0.172 |
R-HSA-9679506 | SARS-CoV Infections | 6.754702e-01 | 0.170 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 6.800456e-01 | 0.167 |
R-HSA-9833110 | RSV-host interactions | 6.832118e-01 | 0.165 |
R-HSA-163125 | Post-translational modification: synthesis of GPI-anchored proteins | 6.832118e-01 | 0.165 |
R-HSA-418346 | Platelet homeostasis | 6.894513e-01 | 0.161 |
R-HSA-211000 | Gene Silencing by RNA | 6.925250e-01 | 0.160 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 7.001696e-01 | 0.155 |
R-HSA-5683057 | MAPK family signaling cascades | 7.047105e-01 | 0.152 |
R-HSA-1483249 | Inositol phosphate metabolism | 7.074462e-01 | 0.150 |
R-HSA-9694516 | SARS-CoV-2 Infection | 7.081833e-01 | 0.150 |
R-HSA-72312 | rRNA processing | 7.127020e-01 | 0.147 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 7.132111e-01 | 0.147 |
R-HSA-3247509 | Chromatin modifying enzymes | 7.167817e-01 | 0.145 |
R-HSA-8939211 | ESR-mediated signaling | 7.228104e-01 | 0.141 |
R-HSA-70326 | Glucose metabolism | 7.271344e-01 | 0.138 |
R-HSA-9007101 | Rab regulation of trafficking | 7.271344e-01 | 0.138 |
R-HSA-3371556 | Cellular response to heat stress | 7.377876e-01 | 0.132 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 7.429582e-01 | 0.129 |
R-HSA-4839726 | Chromatin organization | 7.458584e-01 | 0.127 |
R-HSA-69206 | G1/S Transition | 7.505247e-01 | 0.125 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 7.537926e-01 | 0.123 |
R-HSA-114608 | Platelet degranulation | 7.554456e-01 | 0.122 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 7.578698e-01 | 0.120 |
R-HSA-69620 | Cell Cycle Checkpoints | 7.620564e-01 | 0.118 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 7.626468e-01 | 0.118 |
R-HSA-9843745 | Adipogenesis | 7.673300e-01 | 0.115 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 7.719215e-01 | 0.112 |
R-HSA-9018519 | Estrogen-dependent gene expression | 7.808360e-01 | 0.107 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 7.808360e-01 | 0.107 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 7.830100e-01 | 0.106 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 7.956111e-01 | 0.099 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 8.009636e-01 | 0.096 |
R-HSA-166520 | Signaling by NTRKs | 8.074848e-01 | 0.093 |
R-HSA-69242 | S Phase | 8.074848e-01 | 0.093 |
R-HSA-5673001 | RAF/MAP kinase cascade | 8.112056e-01 | 0.091 |
R-HSA-9856651 | MITF-M-dependent gene expression | 8.112884e-01 | 0.091 |
R-HSA-9609507 | Protein localization | 8.168541e-01 | 0.088 |
R-HSA-1989781 | PPARA activates gene expression | 8.204736e-01 | 0.086 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 8.209782e-01 | 0.086 |
R-HSA-72766 | Translation | 8.239399e-01 | 0.084 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 8.240221e-01 | 0.084 |
R-HSA-9006936 | Signaling by TGFB family members | 8.292145e-01 | 0.081 |
R-HSA-211897 | Cytochrome P450 - arranged by substrate type | 8.407456e-01 | 0.075 |
R-HSA-5619102 | SLC transporter disorders | 8.407456e-01 | 0.075 |
R-HSA-72306 | tRNA processing | 8.469839e-01 | 0.072 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 8.500114e-01 | 0.071 |
R-HSA-212165 | Epigenetic regulation of gene expression | 8.545752e-01 | 0.068 |
R-HSA-389948 | Co-inhibition by PD-1 | 8.866450e-01 | 0.052 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 8.939168e-01 | 0.049 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 9.014739e-01 | 0.045 |
R-HSA-168249 | Innate Immune System | 9.234921e-01 | 0.035 |
R-HSA-5619115 | Disorders of transmembrane transporters | 9.299427e-01 | 0.032 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 9.359974e-01 | 0.029 |
R-HSA-9711123 | Cellular response to chemical stress | 9.432688e-01 | 0.025 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 9.465904e-01 | 0.024 |
R-HSA-211945 | Phase I - Functionalization of compounds | 9.486967e-01 | 0.023 |
R-HSA-449147 | Signaling by Interleukins | 9.559645e-01 | 0.020 |
R-HSA-1483257 | Phospholipid metabolism | 9.567654e-01 | 0.019 |
R-HSA-1474244 | Extracellular matrix organization | 9.699256e-01 | 0.013 |
R-HSA-1428517 | Aerobic respiration and respiratory electron transport | 9.728140e-01 | 0.012 |
R-HSA-196854 | Metabolism of vitamins and cofactors | 9.784533e-01 | 0.009 |
R-HSA-425407 | SLC-mediated transmembrane transport | 9.847293e-01 | 0.007 |
R-HSA-388396 | GPCR downstream signalling | 9.862377e-01 | 0.006 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 9.878913e-01 | 0.005 |
R-HSA-382551 | Transport of small molecules | 9.905192e-01 | 0.004 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 9.915269e-01 | 0.004 |
R-HSA-372790 | Signaling by GPCR | 9.930184e-01 | 0.003 |
R-HSA-211859 | Biological oxidations | 9.957645e-01 | 0.002 |
R-HSA-556833 | Metabolism of lipids | 9.999972e-01 | 0.000 |
R-HSA-9709957 | Sensory Perception | 9.999976e-01 | 0.000 |
R-HSA-1430728 | Metabolism | 1.000000e+00 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
GAK |
0.742 | 0.091 | 1 | 0.835 |
MPSK1 |
0.732 | 0.248 | 1 | 0.754 |
MAK |
0.731 | 0.274 | -2 | 0.849 |
TAK1 |
0.729 | 0.018 | 1 | 0.739 |
GCK |
0.728 | 0.045 | 1 | 0.715 |
P38B |
0.724 | 0.178 | 1 | 0.556 |
LKB1 |
0.722 | 0.030 | -3 | 0.350 |
CK1D |
0.722 | 0.390 | -3 | 0.732 |
PKR |
0.722 | -0.007 | 1 | 0.766 |
VRK2 |
0.721 | -0.052 | 1 | 0.780 |
TNIK |
0.721 | 0.007 | 3 | 0.772 |
ALPHAK3 |
0.721 | 0.069 | -1 | 0.705 |
BMPR1B |
0.721 | 0.127 | 1 | 0.821 |
MST2 |
0.721 | -0.005 | 1 | 0.723 |
MOS |
0.719 | 0.151 | 1 | 0.835 |
P38A |
0.719 | 0.173 | 1 | 0.621 |
MINK |
0.719 | -0.018 | 1 | 0.700 |
OSR1 |
0.719 | 0.022 | 2 | 0.767 |
EEF2K |
0.718 | 0.033 | 3 | 0.727 |
VRK1 |
0.718 | -0.040 | 2 | 0.789 |
KHS1 |
0.718 | 0.015 | 1 | 0.678 |
TTK |
0.718 | 0.014 | -2 | 0.449 |
CAMKK2 |
0.718 | -0.048 | -2 | 0.492 |
PASK |
0.717 | 0.041 | -3 | 0.375 |
ICK |
0.717 | 0.203 | -3 | 0.327 |
MEK1 |
0.717 | 0.009 | 2 | 0.787 |
MST1 |
0.717 | -0.024 | 1 | 0.699 |
TAO3 |
0.717 | 0.025 | 1 | 0.698 |
CAMKK1 |
0.716 | -0.063 | -2 | 0.477 |
NEK1 |
0.716 | -0.071 | 1 | 0.720 |
LRRK2 |
0.716 | -0.089 | 2 | 0.831 |
GRK7 |
0.715 | 0.148 | 1 | 0.722 |
NEK5 |
0.715 | -0.030 | 1 | 0.758 |
PBK |
0.715 | 0.039 | 1 | 0.782 |
KHS2 |
0.715 | 0.008 | 1 | 0.692 |
HPK1 |
0.714 | -0.007 | 1 | 0.693 |
ASK1 |
0.714 | -0.043 | 1 | 0.648 |
MEKK2 |
0.713 | 0.017 | 2 | 0.771 |
MST3 |
0.713 | 0.042 | 2 | 0.835 |
CK1A2 |
0.713 | 0.381 | -3 | 0.726 |
PRP4 |
0.713 | 0.024 | -3 | 0.326 |
CDKL1 |
0.713 | 0.113 | -3 | 0.307 |
MAP3K15 |
0.712 | 0.012 | 1 | 0.662 |
HGK |
0.712 | -0.033 | 3 | 0.765 |
ALK4 |
0.712 | -0.000 | -2 | 0.455 |
DLK |
0.712 | 0.064 | 1 | 0.753 |
BMPR2 |
0.712 | -0.056 | -2 | 0.526 |
BIKE |
0.712 | 0.026 | 1 | 0.755 |
BRAF |
0.711 | -0.076 | -4 | 0.765 |
MYO3B |
0.711 | -0.035 | 2 | 0.825 |
DAPK2 |
0.711 | -0.050 | -3 | 0.337 |
PDK1 |
0.710 | -0.068 | 1 | 0.708 |
ATR |
0.710 | 0.059 | 1 | 0.755 |
CK1E |
0.709 | 0.404 | -3 | 0.721 |
ALK2 |
0.709 | 0.011 | -2 | 0.424 |
NIK |
0.709 | -0.080 | -3 | 0.359 |
TAO2 |
0.708 | -0.077 | 2 | 0.838 |
MEK5 |
0.708 | -0.087 | 2 | 0.791 |
PRPK |
0.708 | 0.013 | -1 | 0.792 |
JNK2 |
0.708 | 0.066 | 1 | 0.507 |
ACVR2B |
0.707 | 0.039 | -2 | 0.420 |
CAMLCK |
0.706 | -0.046 | -2 | 0.530 |
BMPR1A |
0.706 | 0.072 | 1 | 0.797 |
MYO3A |
0.706 | -0.054 | 1 | 0.673 |
LATS1 |
0.706 | -0.027 | -3 | 0.332 |
GRK6 |
0.705 | 0.138 | 1 | 0.794 |
MLK2 |
0.705 | 0.075 | 2 | 0.802 |
P38D |
0.705 | 0.101 | 1 | 0.466 |
YSK4 |
0.705 | -0.031 | 1 | 0.680 |
CDKL5 |
0.704 | 0.186 | -3 | 0.292 |
JNK3 |
0.704 | 0.045 | 1 | 0.544 |
AAK1 |
0.704 | 0.047 | 1 | 0.673 |
DAPK3 |
0.704 | -0.052 | -3 | 0.323 |
GRK5 |
0.704 | 0.138 | -3 | 0.469 |
ERK5 |
0.704 | 0.131 | 1 | 0.782 |
NEK11 |
0.704 | -0.040 | 1 | 0.692 |
MEKK1 |
0.704 | -0.068 | 1 | 0.709 |
TGFBR1 |
0.704 | 0.003 | -2 | 0.423 |
NEK4 |
0.703 | -0.085 | 1 | 0.698 |
SKMLCK |
0.703 | 0.049 | -2 | 0.548 |
MEKK6 |
0.703 | -0.065 | 1 | 0.709 |
NEK8 |
0.703 | -0.082 | 2 | 0.806 |
MOK |
0.702 | 0.153 | 1 | 0.673 |
ACVR2A |
0.702 | 0.029 | -2 | 0.408 |
STLK3 |
0.701 | -0.094 | 1 | 0.643 |
MEKK3 |
0.701 | -0.002 | 1 | 0.717 |
ROCK2 |
0.701 | -0.043 | -3 | 0.308 |
DMPK1 |
0.701 | -0.053 | -3 | 0.294 |
COT |
0.701 | 0.141 | 2 | 0.832 |
ANKRD3 |
0.701 | -0.106 | 1 | 0.777 |
YSK1 |
0.700 | -0.077 | 2 | 0.804 |
PIM1 |
0.700 | 0.024 | -3 | 0.339 |
ERK1 |
0.699 | 0.134 | 1 | 0.537 |
PIM3 |
0.698 | 0.051 | -3 | 0.349 |
GRK1 |
0.698 | 0.178 | -2 | 0.480 |
NLK |
0.698 | 0.005 | 1 | 0.716 |
CAMK1B |
0.698 | -0.073 | -3 | 0.337 |
GRK2 |
0.698 | 0.088 | -2 | 0.408 |
RAF1 |
0.697 | 0.011 | 1 | 0.760 |
CDC7 |
0.697 | 0.158 | 1 | 0.829 |
CLK3 |
0.697 | 0.110 | 1 | 0.744 |
CHAK2 |
0.697 | 0.068 | -1 | 0.742 |
MLK1 |
0.696 | 0.081 | 2 | 0.796 |
ZAK |
0.696 | -0.055 | 1 | 0.684 |
HIPK1 |
0.696 | 0.047 | 1 | 0.616 |
MEK2 |
0.696 | -0.170 | 2 | 0.765 |
P38G |
0.695 | 0.070 | 1 | 0.446 |
LOK |
0.695 | -0.078 | -2 | 0.487 |
TLK2 |
0.695 | -0.005 | 1 | 0.702 |
SLK |
0.694 | -0.047 | -2 | 0.465 |
CDK1 |
0.692 | 0.081 | 1 | 0.538 |
DAPK1 |
0.692 | -0.058 | -3 | 0.325 |
HIPK4 |
0.691 | 0.161 | 1 | 0.682 |
MLK3 |
0.691 | 0.097 | 2 | 0.739 |
BUB1 |
0.690 | 0.013 | -5 | 0.550 |
SMMLCK |
0.690 | -0.109 | -3 | 0.307 |
MLK4 |
0.690 | 0.089 | 2 | 0.697 |
NEK9 |
0.689 | -0.082 | 2 | 0.816 |
PIM2 |
0.688 | -0.034 | -3 | 0.267 |
CAMK2G |
0.688 | -0.035 | 2 | 0.774 |
DYRK2 |
0.688 | 0.057 | 1 | 0.601 |
DYRK1A |
0.687 | 0.079 | 1 | 0.613 |
MTOR |
0.687 | 0.106 | 1 | 0.679 |
CDK5 |
0.687 | 0.070 | 1 | 0.594 |
MASTL |
0.687 | -0.090 | -2 | 0.528 |
ERK2 |
0.687 | 0.048 | 1 | 0.564 |
PERK |
0.686 | -0.115 | -2 | 0.467 |
JNK1 |
0.685 | 0.037 | 1 | 0.504 |
PLK1 |
0.685 | -0.078 | -2 | 0.450 |
HIPK2 |
0.685 | 0.104 | 1 | 0.510 |
TLK1 |
0.683 | -0.042 | -2 | 0.442 |
DSTYK |
0.683 | -0.051 | 2 | 0.859 |
TAO1 |
0.683 | -0.090 | 1 | 0.609 |
GRK3 |
0.682 | 0.111 | -2 | 0.369 |
PDHK4 |
0.682 | -0.138 | 1 | 0.757 |
ROCK1 |
0.681 | -0.075 | -3 | 0.284 |
ERK7 |
0.680 | 0.043 | 2 | 0.556 |
NEK2 |
0.680 | -0.115 | 2 | 0.806 |
CDK18 |
0.680 | 0.096 | 1 | 0.510 |
CK1G3 |
0.679 | 0.297 | -3 | 0.716 |
RIPK3 |
0.679 | 0.007 | 3 | 0.637 |
PDHK1 |
0.679 | -0.158 | 1 | 0.736 |
CRIK |
0.679 | -0.071 | -3 | 0.256 |
DNAPK |
0.679 | -0.006 | 1 | 0.603 |
HASPIN |
0.679 | -0.005 | -1 | 0.569 |
PKN3 |
0.679 | -0.071 | -3 | 0.321 |
CDK8 |
0.679 | 0.112 | 1 | 0.552 |
HIPK3 |
0.679 | 0.022 | 1 | 0.596 |
PKCD |
0.678 | -0.030 | 2 | 0.774 |
GRK4 |
0.678 | 0.091 | -2 | 0.466 |
WNK1 |
0.678 | -0.049 | -2 | 0.585 |
TSSK2 |
0.678 | -0.064 | -5 | 0.555 |
PINK1 |
0.678 | -0.131 | 1 | 0.740 |
P70S6KB |
0.678 | -0.067 | -3 | 0.296 |
SMG1 |
0.677 | -0.015 | 1 | 0.705 |
HRI |
0.677 | -0.169 | -2 | 0.485 |
GSK3A |
0.677 | 0.048 | 4 | 0.433 |
MRCKA |
0.677 | -0.082 | -3 | 0.283 |
CHK1 |
0.677 | -0.131 | -3 | 0.287 |
WNK4 |
0.677 | -0.104 | -2 | 0.599 |
DRAK1 |
0.677 | -0.039 | 1 | 0.757 |
IRAK4 |
0.676 | -0.071 | 1 | 0.727 |
TBK1 |
0.675 | 0.038 | 1 | 0.635 |
SGK1 |
0.675 | -0.051 | -3 | 0.221 |
MRCKB |
0.675 | -0.073 | -3 | 0.269 |
IKKA |
0.675 | 0.051 | -2 | 0.475 |
RIPK1 |
0.675 | -0.108 | 1 | 0.736 |
CDK3 |
0.675 | 0.058 | 1 | 0.480 |
PLK2 |
0.675 | -0.017 | -3 | 0.352 |
SGK3 |
0.674 | -0.060 | -3 | 0.285 |
IKKB |
0.674 | 0.014 | -2 | 0.464 |
ATM |
0.674 | -0.012 | 1 | 0.701 |
DYRK1B |
0.673 | 0.009 | 1 | 0.549 |
PLK3 |
0.673 | -0.067 | 2 | 0.719 |
CDK16 |
0.673 | 0.062 | 1 | 0.473 |
AMPKA1 |
0.673 | -0.085 | -3 | 0.341 |
CDK14 |
0.673 | 0.024 | 1 | 0.546 |
CHAK1 |
0.673 | -0.047 | 2 | 0.786 |
CDK17 |
0.672 | 0.053 | 1 | 0.454 |
AKT2 |
0.672 | -0.054 | -3 | 0.251 |
MST4 |
0.672 | -0.042 | 2 | 0.853 |
DCAMKL1 |
0.671 | -0.106 | -3 | 0.298 |
PKN2 |
0.671 | -0.073 | -3 | 0.346 |
NUAK2 |
0.671 | -0.081 | -3 | 0.344 |
NEK7 |
0.671 | -0.110 | -3 | 0.371 |
MYLK4 |
0.671 | -0.057 | -2 | 0.450 |
NEK6 |
0.670 | -0.053 | -2 | 0.506 |
PAK1 |
0.670 | -0.026 | -2 | 0.519 |
CAMK2D |
0.670 | -0.079 | -3 | 0.315 |
DYRK3 |
0.669 | -0.008 | 1 | 0.616 |
CDK19 |
0.669 | 0.120 | 1 | 0.517 |
RSK2 |
0.669 | -0.041 | -3 | 0.271 |
CK2A2 |
0.669 | 0.082 | 1 | 0.753 |
NEK3 |
0.668 | -0.186 | 1 | 0.655 |
CK1A |
0.668 | 0.347 | -3 | 0.727 |
YANK3 |
0.668 | 0.094 | 2 | 0.374 |
DYRK4 |
0.668 | 0.034 | 1 | 0.525 |
IKKE |
0.668 | -0.019 | 1 | 0.626 |
MARK4 |
0.668 | -0.084 | 4 | 0.802 |
CLK4 |
0.668 | -0.045 | -3 | 0.303 |
TSSK1 |
0.667 | -0.061 | -3 | 0.334 |
SRPK1 |
0.667 | -0.015 | -3 | 0.286 |
PAK2 |
0.667 | -0.059 | -2 | 0.503 |
GSK3B |
0.667 | 0.003 | 4 | 0.420 |
PKCA |
0.667 | -0.012 | 2 | 0.730 |
CK1G1 |
0.667 | 0.333 | -3 | 0.698 |
CDK2 |
0.667 | -0.005 | 1 | 0.619 |
CDK6 |
0.667 | 0.008 | 1 | 0.524 |
CAMK2B |
0.667 | -0.026 | 2 | 0.737 |
MAPKAPK3 |
0.666 | -0.065 | -3 | 0.279 |
PKCZ |
0.666 | -0.036 | 2 | 0.769 |
YANK2 |
0.666 | 0.102 | 2 | 0.384 |
TTBK2 |
0.666 | -0.020 | 2 | 0.671 |
RSK4 |
0.665 | -0.024 | -3 | 0.276 |
ULK2 |
0.665 | -0.140 | 2 | 0.749 |
HUNK |
0.665 | -0.138 | 2 | 0.752 |
CAMK2A |
0.664 | -0.023 | 2 | 0.763 |
PRKD1 |
0.664 | -0.008 | -3 | 0.288 |
CDK4 |
0.663 | 0.003 | 1 | 0.494 |
P90RSK |
0.663 | -0.060 | -3 | 0.274 |
CDK7 |
0.663 | 0.053 | 1 | 0.569 |
SRPK3 |
0.663 | -0.047 | -3 | 0.290 |
MAPKAPK2 |
0.663 | -0.011 | -3 | 0.273 |
TGFBR2 |
0.663 | -0.100 | -2 | 0.415 |
AMPKA2 |
0.663 | -0.080 | -3 | 0.317 |
CDK13 |
0.663 | 0.005 | 1 | 0.538 |
NDR1 |
0.663 | -0.065 | -3 | 0.331 |
PKACB |
0.663 | -0.020 | -2 | 0.390 |
PDHK3_TYR |
0.662 | 0.190 | 4 | 0.900 |
CHK2 |
0.662 | -0.091 | -3 | 0.220 |
CAMK1D |
0.662 | -0.087 | -3 | 0.238 |
SBK |
0.662 | -0.057 | -3 | 0.184 |
AKT1 |
0.662 | -0.065 | -3 | 0.261 |
IRE1 |
0.661 | -0.032 | 1 | 0.725 |
NDR2 |
0.661 | 0.012 | -3 | 0.345 |
MSK1 |
0.660 | -0.054 | -3 | 0.286 |
CK2A1 |
0.660 | 0.075 | 1 | 0.732 |
PKCB |
0.660 | -0.028 | 2 | 0.735 |
WNK3 |
0.660 | -0.155 | 1 | 0.721 |
AURB |
0.659 | -0.050 | -2 | 0.386 |
PKACG |
0.659 | -0.054 | -2 | 0.446 |
IRE2 |
0.659 | -0.056 | 2 | 0.722 |
DCAMKL2 |
0.658 | -0.127 | -3 | 0.292 |
PDHK1_TYR |
0.658 | 0.184 | -1 | 0.815 |
PDHK4_TYR |
0.658 | 0.154 | 2 | 0.852 |
BCKDK |
0.658 | -0.045 | -1 | 0.779 |
PAK3 |
0.658 | -0.070 | -2 | 0.503 |
AURA |
0.658 | -0.037 | -2 | 0.363 |
MAP2K6_TYR |
0.658 | 0.155 | -1 | 0.808 |
CAMK4 |
0.658 | -0.128 | -3 | 0.336 |
MAP2K4_TYR |
0.658 | 0.134 | -1 | 0.809 |
CK1G2 |
0.657 | 0.233 | -3 | 0.714 |
CLK2 |
0.657 | -0.001 | -3 | 0.291 |
CDK12 |
0.657 | -0.000 | 1 | 0.506 |
PKCG |
0.657 | -0.030 | 2 | 0.734 |
KIS |
0.657 | 0.099 | 1 | 0.580 |
AURC |
0.657 | -0.011 | -2 | 0.388 |
PKCH |
0.656 | -0.084 | 2 | 0.713 |
PRKD2 |
0.656 | -0.029 | -3 | 0.267 |
CDK10 |
0.656 | 0.014 | 1 | 0.536 |
MELK |
0.654 | -0.133 | -3 | 0.287 |
PKG2 |
0.654 | -0.064 | -2 | 0.401 |
QSK |
0.653 | -0.074 | 4 | 0.769 |
MSK2 |
0.653 | -0.074 | -3 | 0.296 |
TXK |
0.653 | 0.150 | 1 | 0.841 |
PRKD3 |
0.653 | -0.086 | -3 | 0.250 |
LATS2 |
0.653 | -0.063 | -5 | 0.505 |
CLK1 |
0.652 | -0.058 | -3 | 0.265 |
STK33 |
0.652 | -0.093 | 2 | 0.585 |
PKCE |
0.652 | -0.055 | 2 | 0.724 |
GCN2 |
0.651 | -0.098 | 2 | 0.767 |
NIM1 |
0.651 | -0.108 | 3 | 0.679 |
RSK3 |
0.651 | -0.077 | -3 | 0.258 |
EPHB4 |
0.650 | 0.111 | -1 | 0.809 |
CAMK1A |
0.650 | -0.074 | -3 | 0.227 |
IRAK1 |
0.650 | -0.217 | -1 | 0.653 |
MARK2 |
0.650 | -0.101 | 4 | 0.696 |
QIK |
0.649 | -0.150 | -3 | 0.326 |
AKT3 |
0.649 | -0.050 | -3 | 0.230 |
BMPR2_TYR |
0.649 | 0.012 | -1 | 0.798 |
FAM20C |
0.649 | 0.047 | 2 | 0.555 |
ABL2 |
0.649 | 0.123 | -1 | 0.761 |
TESK1_TYR |
0.649 | 0.009 | 3 | 0.798 |
PKACA |
0.649 | -0.053 | -2 | 0.354 |
FGR |
0.648 | 0.103 | 1 | 0.840 |
CAMK1G |
0.648 | -0.109 | -3 | 0.286 |
ULK1 |
0.648 | -0.152 | -3 | 0.353 |
CDK9 |
0.647 | -0.040 | 1 | 0.545 |
P70S6K |
0.647 | -0.100 | -3 | 0.241 |
PRKX |
0.647 | -0.020 | -3 | 0.273 |
ABL1 |
0.647 | 0.125 | -1 | 0.755 |
MARK3 |
0.647 | -0.076 | 4 | 0.721 |
SRPK2 |
0.647 | -0.040 | -3 | 0.250 |
PKCI |
0.645 | -0.095 | 2 | 0.734 |
MAP2K7_TYR |
0.645 | -0.052 | 2 | 0.832 |
MARK1 |
0.645 | -0.121 | 4 | 0.747 |
RIPK2 |
0.645 | -0.212 | 1 | 0.639 |
MNK1 |
0.644 | -0.080 | -2 | 0.487 |
SSTK |
0.643 | -0.096 | 4 | 0.755 |
PKMYT1_TYR |
0.643 | -0.055 | 3 | 0.767 |
PKCT |
0.643 | -0.093 | 2 | 0.721 |
YES1 |
0.643 | 0.065 | -1 | 0.790 |
MNK2 |
0.643 | -0.066 | -2 | 0.491 |
EPHA6 |
0.642 | 0.018 | -1 | 0.818 |
LIMK2_TYR |
0.641 | -0.016 | -3 | 0.338 |
SIK |
0.641 | -0.100 | -3 | 0.290 |
PINK1_TYR |
0.641 | -0.084 | 1 | 0.761 |
PLK4 |
0.641 | -0.108 | 2 | 0.577 |
FER |
0.641 | 0.032 | 1 | 0.842 |
BLK |
0.640 | 0.083 | -1 | 0.781 |
LCK |
0.639 | 0.073 | -1 | 0.774 |
EPHA4 |
0.638 | 0.029 | 2 | 0.725 |
NUAK1 |
0.638 | -0.118 | -3 | 0.288 |
EPHB2 |
0.638 | 0.057 | -1 | 0.792 |
FYN |
0.638 | 0.087 | -1 | 0.754 |
EPHB3 |
0.637 | 0.043 | -1 | 0.808 |
CSF1R |
0.637 | 0.061 | 3 | 0.699 |
RET |
0.637 | -0.019 | 1 | 0.703 |
PHKG1 |
0.637 | -0.090 | -3 | 0.335 |
SRMS |
0.636 | 0.033 | 1 | 0.825 |
HCK |
0.635 | 0.024 | -1 | 0.771 |
EPHB1 |
0.635 | 0.013 | 1 | 0.806 |
TTBK1 |
0.634 | -0.083 | 2 | 0.593 |
PAK6 |
0.634 | -0.056 | -2 | 0.457 |
ROS1 |
0.633 | -0.008 | 3 | 0.654 |
TYRO3 |
0.633 | -0.025 | 3 | 0.693 |
JAK2 |
0.633 | -0.021 | 1 | 0.691 |
TNK2 |
0.633 | 0.031 | 3 | 0.672 |
ITK |
0.632 | 0.014 | -1 | 0.738 |
MET |
0.632 | 0.059 | 3 | 0.696 |
INSRR |
0.632 | 0.007 | 3 | 0.633 |
KIT |
0.631 | 0.031 | 3 | 0.702 |
MAPKAPK5 |
0.631 | -0.142 | -3 | 0.262 |
TYK2 |
0.631 | -0.092 | 1 | 0.701 |
SYK |
0.631 | 0.085 | -1 | 0.724 |
LIMK1_TYR |
0.630 | -0.133 | 2 | 0.832 |
MST1R |
0.630 | -0.052 | 3 | 0.713 |
MERTK |
0.629 | 0.028 | 3 | 0.683 |
PKN1 |
0.629 | -0.104 | -3 | 0.252 |
PTK2 |
0.629 | 0.066 | -1 | 0.726 |
DDR1 |
0.629 | -0.083 | 4 | 0.812 |
BMX |
0.628 | 0.029 | -1 | 0.674 |
BRSK1 |
0.628 | -0.102 | -3 | 0.293 |
JAK3 |
0.627 | -0.043 | 1 | 0.692 |
EPHA7 |
0.626 | 0.011 | 2 | 0.729 |
FLT1 |
0.626 | 0.019 | -1 | 0.774 |
SRC |
0.625 | 0.045 | -1 | 0.763 |
SNRK |
0.625 | -0.188 | 2 | 0.659 |
EPHA3 |
0.624 | -0.016 | 2 | 0.702 |
BRSK2 |
0.624 | -0.124 | -3 | 0.303 |
LYN |
0.623 | 0.007 | 3 | 0.616 |
KDR |
0.623 | -0.029 | 3 | 0.658 |
TEC |
0.623 | -0.015 | -1 | 0.702 |
MATK |
0.623 | 0.012 | -1 | 0.685 |
TNNI3K_TYR |
0.622 | -0.029 | 1 | 0.729 |
EPHA5 |
0.622 | 0.008 | 2 | 0.705 |
JAK1 |
0.622 | -0.030 | 1 | 0.633 |
PTK2B |
0.622 | 0.021 | -1 | 0.741 |
BTK |
0.621 | -0.063 | -1 | 0.708 |
EPHA8 |
0.620 | 0.006 | -1 | 0.784 |
PTK6 |
0.620 | -0.066 | -1 | 0.690 |
PDGFRB |
0.620 | -0.090 | 3 | 0.700 |
PAK5 |
0.620 | -0.075 | -2 | 0.419 |
FLT3 |
0.619 | -0.072 | 3 | 0.693 |
FGFR2 |
0.619 | -0.074 | 3 | 0.695 |
AXL |
0.619 | -0.044 | 3 | 0.672 |
NTRK1 |
0.619 | -0.070 | -1 | 0.776 |
FRK |
0.618 | -0.004 | -1 | 0.791 |
NTRK3 |
0.618 | -0.026 | -1 | 0.747 |
LTK |
0.618 | -0.052 | 3 | 0.646 |
ALK |
0.617 | -0.054 | 3 | 0.613 |
NEK10_TYR |
0.617 | -0.088 | 1 | 0.569 |
DDR2 |
0.616 | 0.004 | 3 | 0.630 |
CSK |
0.616 | 0.019 | 2 | 0.732 |
TNK1 |
0.616 | -0.063 | 3 | 0.681 |
WEE1_TYR |
0.615 | -0.057 | -1 | 0.679 |
ERBB2 |
0.615 | -0.047 | 1 | 0.684 |
PHKG2 |
0.615 | -0.136 | -3 | 0.295 |
EGFR |
0.615 | -0.009 | 1 | 0.602 |
INSR |
0.614 | -0.040 | 3 | 0.608 |
EPHA1 |
0.614 | -0.036 | 3 | 0.667 |
ZAP70 |
0.613 | 0.074 | -1 | 0.643 |
FGFR4 |
0.613 | 0.006 | -1 | 0.726 |
FGFR3 |
0.612 | -0.053 | 3 | 0.663 |
PDGFRA |
0.611 | -0.125 | 3 | 0.700 |
NTRK2 |
0.610 | -0.110 | 3 | 0.644 |
FGFR1 |
0.609 | -0.122 | 3 | 0.660 |
PAK4 |
0.609 | -0.064 | -2 | 0.422 |
TEK |
0.609 | -0.141 | 3 | 0.626 |
ERBB4 |
0.608 | 0.025 | 1 | 0.647 |
EPHA2 |
0.606 | -0.029 | -1 | 0.740 |
FLT4 |
0.605 | -0.109 | 3 | 0.651 |
IGF1R |
0.603 | -0.030 | 3 | 0.549 |
PKG1 |
0.603 | -0.110 | -2 | 0.325 |
FES |
0.596 | -0.020 | -1 | 0.662 |
MUSK |
0.591 | -0.106 | 1 | 0.600 |