Motif 879 (n=107)
Position-wise Probabilities
Download
uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A1B0GU03 | None | S333 | ochoa | Cathepsin D (EC 3.4.23.5) | None |
O00141 | SGK1 | S56 | ochoa | Serine/threonine-protein kinase Sgk1 (EC 2.7.11.1) (Serum/glucocorticoid-regulated kinase 1) | Serine/threonine-protein kinase which is involved in the regulation of a wide variety of ion channels, membrane transporters, cellular enzymes, transcription factors, neuronal excitability, cell growth, proliferation, survival, migration and apoptosis. Plays an important role in cellular stress response. Contributes to regulation of renal Na(+) retention, renal K(+) elimination, salt appetite, gastric acid secretion, intestinal Na(+)/H(+) exchange and nutrient transport, insulin-dependent salt sensitivity of blood pressure, salt sensitivity of peripheral glucose uptake, cardiac repolarization and memory consolidation. Up-regulates Na(+) channels: SCNN1A/ENAC, SCN5A and ASIC1/ACCN2, K(+) channels: KCNJ1/ROMK1, KCNA1-5, KCNQ1-5 and KCNE1, epithelial Ca(2+) channels: TRPV5 and TRPV6, chloride channels: BSND, CLCN2 and CFTR, glutamate transporters: SLC1A3/EAAT1, SLC1A2 /EAAT2, SLC1A1/EAAT3, SLC1A6/EAAT4 and SLC1A7/EAAT5, amino acid transporters: SLC1A5/ASCT2, SLC38A1/SN1 and SLC6A19, creatine transporter: SLC6A8, Na(+)/dicarboxylate cotransporter: SLC13A2/NADC1, Na(+)-dependent phosphate cotransporter: SLC34A2/NAPI-2B, glutamate receptor: GRIK2/GLUR6. Up-regulates carriers: SLC9A3/NHE3, SLC12A1/NKCC2, SLC12A3/NCC, SLC5A3/SMIT, SLC2A1/GLUT1, SLC5A1/SGLT1 and SLC15A2/PEPT2. Regulates enzymes: GSK3A/B, PMM2 and Na(+)/K(+) ATPase, and transcription factors: CTNNB1 and nuclear factor NF-kappa-B. Stimulates sodium transport into epithelial cells by enhancing the stability and expression of SCNN1A/ENAC. This is achieved by phosphorylating the NEDD4L ubiquitin E3 ligase, promoting its interaction with 14-3-3 proteins, thereby preventing it from binding to SCNN1A/ENAC and targeting it for degradation. Regulates store-operated Ca(+2) entry (SOCE) by stimulating ORAI1 and STIM1. Regulates KCNJ1/ROMK1 directly via its phosphorylation or indirectly via increased interaction with SLC9A3R2/NHERF2. Phosphorylates MDM2 and activates MDM2-dependent ubiquitination of p53/TP53. Phosphorylates MAPT/TAU and mediates microtubule depolymerization and neurite formation in hippocampal neurons. Phosphorylates SLC2A4/GLUT4 and up-regulates its activity. Phosphorylates APBB1/FE65 and promotes its localization to the nucleus. Phosphorylates MAPK1/ERK2 and activates it by enhancing its interaction with MAP2K1/MEK1 and MAP2K2/MEK2. Phosphorylates FBXW7 and plays an inhibitory role in the NOTCH1 signaling. Phosphorylates FOXO1 resulting in its relocalization from the nucleus to the cytoplasm. Phosphorylates FOXO3, promoting its exit from the nucleus and interference with FOXO3-dependent transcription. Phosphorylates BRAF and MAP3K3/MEKK3 and inhibits their activity. Phosphorylates SLC9A3/NHE3 in response to dexamethasone, resulting in its activation and increased localization at the cell membrane. Phosphorylates CREB1. Necessary for vascular remodeling during angiogenesis. Sustained high levels and activity may contribute to conditions such as hypertension and diabetic nephropathy. Isoform 2 exhibited a greater effect on cell plasma membrane expression of SCNN1A/ENAC and Na(+) transport than isoform 1. {ECO:0000269|PubMed:11154281, ECO:0000269|PubMed:11410590, ECO:0000269|PubMed:11696533, ECO:0000269|PubMed:12397388, ECO:0000269|PubMed:12590200, ECO:0000269|PubMed:12634932, ECO:0000269|PubMed:12650886, ECO:0000269|PubMed:12761204, ECO:0000269|PubMed:12911626, ECO:0000269|PubMed:14623317, ECO:0000269|PubMed:14706641, ECO:0000269|PubMed:15040001, ECO:0000269|PubMed:15044175, ECO:0000269|PubMed:15234985, ECO:0000269|PubMed:15319523, ECO:0000269|PubMed:15496163, ECO:0000269|PubMed:15733869, ECO:0000269|PubMed:15737648, ECO:0000269|PubMed:15845389, ECO:0000269|PubMed:15888551, ECO:0000269|PubMed:16036218, ECO:0000269|PubMed:16443776, ECO:0000269|PubMed:16982696, ECO:0000269|PubMed:17382906, ECO:0000269|PubMed:18005662, ECO:0000269|PubMed:18304449, ECO:0000269|PubMed:18753299, ECO:0000269|PubMed:19447520, ECO:0000269|PubMed:19756449, ECO:0000269|PubMed:20511718, ECO:0000269|PubMed:20730100, ECO:0000269|PubMed:21865597}. |
O00425 | IGF2BP3 | S438 | ochoa | Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2 mRNA-binding protein 3) (IMP-3) (IGF-II mRNA-binding protein 3) (KH domain-containing protein overexpressed in cancer) (hKOC) (VICKZ family member 3) | RNA-binding factor that may recruit target transcripts to cytoplasmic protein-RNA complexes (mRNPs). This transcript 'caging' into mRNPs allows mRNA transport and transient storage. It also modulates the rate and location at which target transcripts encounter the translational apparatus and shields them from endonuclease attacks or microRNA-mediated degradation. Preferentially binds to N6-methyladenosine (m6A)-containing mRNAs and increases their stability (PubMed:29476152). Binds to the 3'-UTR of CD44 mRNA and stabilizes it, hence promotes cell adhesion and invadopodia formation in cancer cells. Binds to beta-actin/ACTB and MYC transcripts. Increases MYC mRNA stability by binding to the coding region instability determinant (CRD) and binding is enhanced by m6A-modification of the CRD (PubMed:29476152). Binds to the 5'-UTR of the insulin-like growth factor 2 (IGF2) mRNAs. {ECO:0000269|PubMed:16541107, ECO:0000269|PubMed:23640942, ECO:0000269|PubMed:29476152}. |
O15550 | KDM6A | S775 | ochoa | Lysine-specific demethylase 6A (EC 1.14.11.68) (Histone demethylase UTX) (Ubiquitously-transcribed TPR protein on the X chromosome) (Ubiquitously-transcribed X chromosome tetratricopeptide repeat protein) ([histone H3]-trimethyl-L-lysine(27) demethylase 6A) | Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code (PubMed:17713478, PubMed:17761849, PubMed:17851529). Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-27' (PubMed:17713478, PubMed:17761849, PubMed:17851529). Plays a central role in regulation of posterior development, by regulating HOX gene expression (PubMed:17851529). Demethylation of 'Lys-27' of histone H3 is concomitant with methylation of 'Lys-4' of histone H3, and regulates the recruitment of the PRC1 complex and monoubiquitination of histone H2A (PubMed:17761849). Plays a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression (By similarity). {ECO:0000250|UniProtKB:O70546, ECO:0000269|PubMed:17713478, ECO:0000269|PubMed:17761849, ECO:0000269|PubMed:17851529, ECO:0000269|PubMed:18003914}. |
O43294 | TGFB1I1 | S68 | ochoa | Transforming growth factor beta-1-induced transcript 1 protein (Androgen receptor coactivator 55 kDa protein) (Androgen receptor-associated protein of 55 kDa) (Hydrogen peroxide-inducible clone 5 protein) (Hic-5) | Functions as a molecular adapter coordinating multiple protein-protein interactions at the focal adhesion complex and in the nucleus. Links various intracellular signaling modules to plasma membrane receptors and regulates the Wnt and TGFB signaling pathways. May also regulate SLC6A3 and SLC6A4 targeting to the plasma membrane hence regulating their activity. In the nucleus, functions as a nuclear receptor coactivator regulating glucocorticoid, androgen, mineralocorticoid and progesterone receptor transcriptional activity. May play a role in the processes of cell growth, proliferation, migration, differentiation and senescence. May have a zinc-dependent DNA-binding activity. {ECO:0000269|PubMed:10075738, ECO:0000269|PubMed:11463817, ECO:0000269|PubMed:11856738, ECO:0000269|PubMed:12177201, ECO:0000269|PubMed:12445807, ECO:0000269|PubMed:12700349, ECO:0000269|PubMed:15211577, ECO:0000269|PubMed:15561701, ECO:0000269|PubMed:16141357, ECO:0000269|PubMed:16624805, ECO:0000269|PubMed:16803896, ECO:0000269|PubMed:16849583, ECO:0000269|PubMed:17166536, ECO:0000269|PubMed:17233630, ECO:0000269|PubMed:9032249}. |
O43711 | TLX3 | S26 | ochoa | T-cell leukemia homeobox protein 3 (Homeobox protein Hox-11L2) | None |
O43823 | AKAP8 | S91 | ochoa | A-kinase anchor protein 8 (AKAP-8) (A-kinase anchor protein 95 kDa) (AKAP 95) | Anchoring protein that mediates the subcellular compartmentation of cAMP-dependent protein kinase (PKA type II) (PubMed:9473338). Acts as an anchor for a PKA-signaling complex onto mitotic chromosomes, which is required for maintenance of chromosomes in a condensed form throughout mitosis. Recruits condensin complex subunit NCAPD2 to chromosomes required for chromatin condensation; the function appears to be independent from PKA-anchoring (PubMed:10601332, PubMed:10791967, PubMed:11964380). May help to deliver cyclin D/E to CDK4 to facilitate cell cycle progression (PubMed:14641107). Required for cell cycle G2/M transition and histone deacetylation during mitosis. In mitotic cells recruits HDAC3 to the vicinity of chromatin leading to deacetylation and subsequent phosphorylation at 'Ser-10' of histone H3; in this function may act redundantly with AKAP8L (PubMed:16980585). Involved in nuclear retention of RPS6KA1 upon ERK activation thus inducing cell proliferation (PubMed:22130794). May be involved in regulation of DNA replication by acting as scaffold for MCM2 (PubMed:12740381). Enhances HMT activity of the KMT2 family MLL4/WBP7 complex and is involved in transcriptional regulation. In a teratocarcinoma cell line is involved in retinoic acid-mediated induction of developmental genes implicating H3 'Lys-4' methylation (PubMed:23995757). May be involved in recruitment of active CASP3 to the nucleus in apoptotic cells (PubMed:16227597). May act as a carrier protein of GJA1 for its transport to the nucleus (PubMed:26880274). May play a repressive role in the regulation of rDNA transcription. Preferentially binds GC-rich DNA in vitro. In cells, associates with ribosomal RNA (rRNA) chromatin, preferentially with rRNA promoter and transcribed regions (PubMed:26683827). Involved in modulation of Toll-like receptor signaling. Required for the cAMP-dependent suppression of TNF-alpha in early stages of LPS-induced macrophage activation; the function probably implicates targeting of PKA to NFKB1 (By similarity). {ECO:0000250|UniProtKB:Q63014, ECO:0000250|UniProtKB:Q9DBR0, ECO:0000269|PubMed:10601332, ECO:0000269|PubMed:10791967, ECO:0000269|PubMed:11964380, ECO:0000269|PubMed:16980585, ECO:0000269|PubMed:22130794, ECO:0000269|PubMed:26683827, ECO:0000269|PubMed:26880274, ECO:0000305|PubMed:14641107, ECO:0000305|PubMed:9473338}. |
O95644 | NFATC1 | S335 | psp | Nuclear factor of activated T-cells, cytoplasmic 1 (NF-ATc1) (NFATc1) (NFAT transcription complex cytosolic component) (NF-ATc) (NFATc) | Plays a role in the inducible expression of cytokine genes in T-cells, especially in the induction of the IL-2 or IL-4 gene transcription. Also controls gene expression in embryonic cardiac cells. Could regulate not only the activation and proliferation but also the differentiation and programmed death of T-lymphocytes as well as lymphoid and non-lymphoid cells (PubMed:10358178). Required for osteoclastogenesis and regulates many genes important for osteoclast differentiation and function (By similarity). {ECO:0000250|UniProtKB:O88942, ECO:0000269|PubMed:10358178}. |
P05186 | ALPL | S110 | ochoa | Alkaline phosphatase, tissue-nonspecific isozyme (AP-TNAP) (TNS-ALP) (TNSALP) (EC 3.1.3.1) (Alkaline phosphatase liver/bone/kidney isozyme) (Phosphoamidase) (Phosphocreatine phosphatase) (EC 3.9.1.1) | Alkaline phosphatase that metabolizes various phosphate compounds and plays a key role in skeletal mineralization and adaptive thermogenesis (PubMed:12162492, PubMed:23688511, PubMed:25982064). Has broad substrate specificity and can hydrolyze a considerable variety of compounds: however, only a few substrates, such as diphosphate (inorganic pyrophosphate; PPi), pyridoxal 5'-phosphate (PLP) and N-phosphocreatine are natural substrates (PubMed:12162492, PubMed:2220817). Plays an essential role in skeletal and dental mineralization via its ability to hydrolyze extracellular diphosphate, a potent mineralization inhibitor, to phosphate: it thereby promotes hydroxyapatite crystal formation and increases inorganic phosphate concentration (PubMed:23688511, PubMed:25982064). Acts in a non-redundant manner with PHOSPHO1 in skeletal mineralization: while PHOSPHO1 mediates the initiation of hydroxyapatite crystallization in the matrix vesicles (MVs), ALPL/TNAP catalyzes the spread of hydroxyapatite crystallization in the extracellular matrix (By similarity). Also promotes dephosphorylation of osteopontin (SSP1), an inhibitor of hydroxyapatite crystallization in its phosphorylated state; it is however unclear whether ALPL/TNAP mediates SSP1 dephosphorylation via a direct or indirect manner (By similarity). Catalyzes dephosphorylation of PLP to pyridoxal (PL), the transportable form of vitamin B6, in order to provide a sufficient amount of PLP in the brain, an essential cofactor for enzymes catalyzing the synthesis of diverse neurotransmitters (PubMed:20049532, PubMed:2220817). Additionally, also able to mediate ATP degradation in a stepwise manner to adenosine, thereby regulating the availability of ligands for purinergic receptors (By similarity). Also capable of dephosphorylating microbial products, such as lipopolysaccharides (LPS) as well as other phosphorylated small-molecules, such as poly-inosine:cytosine (poly I:C) (PubMed:28448526). Acts as a key regulator of adaptive thermogenesis as part of the futile creatine cycle: localizes to the mitochondria of thermogenic fat cells and acts by mediating hydrolysis of N-phosphocreatine to initiate a futile cycle of creatine dephosphorylation and phosphorylation (By similarity). During the futile creatine cycle, creatine and N-phosphocreatine are in a futile cycle, which dissipates the high energy charge of N-phosphocreatine as heat without performing any mechanical or chemical work (By similarity). {ECO:0000250|UniProtKB:P09242, ECO:0000269|PubMed:12162492, ECO:0000269|PubMed:20049532, ECO:0000269|PubMed:2220817, ECO:0000269|PubMed:23688511, ECO:0000269|PubMed:25982064, ECO:0000269|PubMed:28448526}. |
P05187 | ALPP | S114 | 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}. |
P07339 | CTSD | S333 | ochoa | Cathepsin D (EC 3.4.23.5) [Cleaved into: Cathepsin D light chain; Cathepsin D heavy chain] | Acid protease active in intracellular protein breakdown. Plays a role in APP processing following cleavage and activation by ADAM30 which leads to APP degradation (PubMed:27333034). Involved in the pathogenesis of several diseases such as breast cancer and possibly Alzheimer disease. {ECO:0000269|PubMed:27333034}. |
P09923 | ALPI | S111 | ochoa | Intestinal-type alkaline phosphatase (IAP) (Intestinal alkaline phosphatase) (EC 3.1.3.1) | Alkaline phosphatase that can hydrolyze various phosphate compounds. {ECO:0000250|UniProtKB:P15693}. |
P10696 | ALPG | S111 | 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}. |
P11831 | SRF | S446 | psp | Serum response factor (SRF) | SRF is a transcription factor that binds to the serum response element (SRE), a short sequence of dyad symmetry located 300 bp to the 5' of the site of transcription initiation of some genes (such as FOS). Together with MRTFA transcription coactivator, controls expression of genes regulating the cytoskeleton during development, morphogenesis and cell migration. The SRF-MRTFA complex activity responds to Rho GTPase-induced changes in cellular globular actin (G-actin) concentration, thereby coupling cytoskeletal gene expression to cytoskeletal dynamics. Required for cardiac differentiation and maturation. {ECO:0000250|UniProtKB:Q9JM73}. |
P13688 | CEACAM1 | S494 | psp | Cell adhesion molecule CEACAM1 (Biliary glycoprotein 1) (BGP-1) (Carcinoembryonic antigen-related cell adhesion molecule 1) (CEA cell adhesion molecule 1) (CD antigen CD66a) | [Isoform 1]: Cell adhesion protein that mediates homophilic cell adhesion in a calcium-independent manner (By similarity). Plays a role as coinhibitory receptor in immune response, insulin action and also functions as an activator during angiogenesis (PubMed:18424730, PubMed:23696226, PubMed:25363763). Its coinhibitory receptor function is phosphorylation- and PTPN6 -dependent, which in turn, suppress signal transduction of associated receptors by dephosphorylation of their downstream effectors. Plays a role in immune response, of T cells, natural killer (NK) and neutrophils (PubMed:18424730, PubMed:23696226). Upon TCR/CD3 complex stimulation, inhibits TCR-mediated cytotoxicity by blocking granule exocytosis by mediating homophilic binding to adjacent cells, allowing interaction with and phosphorylation by LCK and interaction with the TCR/CD3 complex which recruits PTPN6 resulting in dephosphorylation of CD247 and ZAP70 (PubMed:18424730). Also inhibits T cell proliferation and cytokine production through inhibition of JNK cascade and plays a crucial role in regulating autoimmunity and anti-tumor immunity by inhibiting T cell through its interaction with HAVCR2 (PubMed:25363763). Upon natural killer (NK) cells activation, inhibit KLRK1-mediated cytolysis of CEACAM1-bearing tumor cells by trans-homophilic interactions with CEACAM1 on the target cell and lead to cis-interaction between CEACAM1 and KLRK1, allowing PTPN6 recruitment and then VAV1 dephosphorylation (PubMed:23696226). Upon neutrophils activation negatively regulates IL1B production by recruiting PTPN6 to a SYK-TLR4-CEACAM1 complex, that dephosphorylates SYK, reducing the production of reactive oxygen species (ROS) and lysosome disruption, which in turn, reduces the activity of the inflammasome. Down-regulates neutrophil production by acting as a coinhibitory receptor for CSF3R by down-regulating the CSF3R-STAT3 pathway through recruitment of PTPN6 that dephosphorylates CSF3R (By similarity). Also regulates insulin action by promoting INS clearance and regulating lipogenesis in liver through regulating insulin signaling (By similarity). Upon INS stimulation, undergoes phosphorylation by INSR leading to INS clearance by increasing receptor-mediated insulin endocytosis. This inernalization promotes interaction with FASN leading to receptor-mediated insulin degradation and to reduction of FASN activity leading to negative regulation of fatty acid synthesis. INSR-mediated phosphorylation also provokes a down-regulation of cell proliferation through SHC1 interaction resulting in decrease coupling of SHC1 to the MAPK3/ERK1-MAPK1/ERK2 and phosphatidylinositol 3-kinase pathways (By similarity). Functions as activator in angiogenesis by promoting blood vessel remodeling through endothelial cell differentiation and migration and in arteriogenesis by increasing the number of collateral arteries and collateral vessel calibers after ischemia. Also regulates vascular permeability through the VEGFR2 signaling pathway resulting in control of nitric oxide production (By similarity). Down-regulates cell growth in response to EGF through its interaction with SHC1 that mediates interaction with EGFR resulting in decrease coupling of SHC1 to the MAPK3/ERK1-MAPK1/ERK2 pathway (By similarity). Negatively regulates platelet aggregation by decreasing platelet adhesion on type I collagen through the GPVI-FcRgamma complex (By similarity). Inhibits cell migration and cell scattering through interaction with FLNA; interferes with the interaction of FLNA with RALA (PubMed:16291724). Mediates bile acid transport activity in a phosphorylation dependent manner (By similarity). Negatively regulates osteoclastogenesis (By similarity). {ECO:0000250|UniProtKB:P16573, ECO:0000250|UniProtKB:P31809, ECO:0000269|PubMed:16291724, ECO:0000269|PubMed:18424730, ECO:0000269|PubMed:23696226, ECO:0000269|PubMed:25363763}.; FUNCTION: [Isoform 8]: Cell adhesion protein that mediates homophilic cell adhesion in a calcium-independent manner (By similarity). Promotes populations of T cells regulating IgA production and secretion associated with control of the commensal microbiota and resistance to enteropathogens (By similarity). {ECO:0000250|UniProtKB:P16573, ECO:0000250|UniProtKB:P31809}. |
P14859 | POU2F1 | S167 | psp | POU domain, class 2, transcription factor 1 (NF-A1) (Octamer-binding protein 1) (Oct-1) (Octamer-binding transcription factor 1) (OTF-1) | Transcription factor that binds to the octamer motif (5'-ATTTGCAT-3') and activates the promoters of the genes for some small nuclear RNAs (snRNA) and of genes such as those for histone H2B and immunoglobulins. Modulates transcription transactivation by NR3C1, AR and PGR. {ECO:0000269|PubMed:10480874, ECO:0000269|PubMed:1684878, ECO:0000269|PubMed:7859290}.; FUNCTION: (Microbial infection) In case of human herpes simplex virus (HSV) infection, POU2F1 forms a multiprotein-DNA complex with the viral transactivator protein VP16 and HCFC1 thereby enabling the transcription of the viral immediate early genes. {ECO:0000305|PubMed:12826401}. |
P17947 | SPI1 | S112 | ochoa | Transcription factor PU.1 (31 kDa-transforming protein) | Pioneer transcription factor, which controls hematopoietic cell fate by decompacting stem cell heterochromatin and allowing other transcription factors to enter otherwise inaccessible genomic sites. Once in open chromatin, can directly control gene expression by binding genetic regulatory elements and can also more broadly influence transcription by recruiting transcription factors, such as interferon regulatory factors (IRFs), to otherwise inaccessible genomic regions (PubMed:23658224, PubMed:33951726). Transcriptionally activates genes important for myeloid and lymphoid lineages, such as CSF1R (By similarity). Transcriptional activation from certain promoters, possibly containing low affinity binding sites, is achieved cooperatively with other transcription factors. FCER1A transactivation is achieved in cooperation with GATA1 (By similarity). May be particularly important for the pro- to pre-B cell transition (PubMed:33951726). Binds (via the ETS domain) onto the purine-rich DNA core sequence 5'-GAGGAA-3', also known as the PU-box (PubMed:33951726). In vitro can bind RNA and interfere with pre-mRNA splicing (By similarity). {ECO:0000250|UniProtKB:P17433, ECO:0000250|UniProtKB:Q6BDS1, ECO:0000269|PubMed:23658224, ECO:0000269|PubMed:33951726}. |
P22681 | CBL | S866 | psp | E3 ubiquitin-protein ligase CBL (EC 2.3.2.27) (Casitas B-lineage lymphoma proto-oncogene) (Proto-oncogene c-Cbl) (RING finger protein 55) (RING-type E3 ubiquitin transferase CBL) (Signal transduction protein CBL) | E3 ubiquitin-protein ligase that acts as a negative regulator of many signaling pathways by mediating ubiquitination of cell surface receptors (PubMed:10514377, PubMed:11896602, PubMed:14661060, PubMed:14739300, PubMed:15190072, PubMed:17509076, PubMed:18374639, PubMed:19689429, PubMed:21596750, PubMed:28381567). Accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and then transfers it to substrates promoting their degradation by the proteasome (PubMed:10514377, PubMed:14661060, PubMed:14739300, PubMed:17094949, PubMed:17509076, PubMed:17974561). Recognizes activated receptor tyrosine kinases, including KIT, FLT1, FGFR1, FGFR2, PDGFRA, PDGFRB, CSF1R, EPHA8 and KDR and mediates their ubiquitination to terminate signaling (PubMed:15190072, PubMed:18374639, PubMed:21596750). Recognizes membrane-bound HCK, SRC and other kinases of the SRC family and mediates their ubiquitination and degradation (PubMed:11896602). Ubiquitinates EGFR and SPRY2 (PubMed:17094949, PubMed:17974561). Ubiquitinates NECTIN1 following association between NECTIN1 and herpes simplex virus 1/HHV-1 envelope glycoprotein D, leading to NECTIN1 removal from cell surface (PubMed:28381567). Participates in signal transduction in hematopoietic cells. Plays an important role in the regulation of osteoblast differentiation and apoptosis (PubMed:15190072, PubMed:18374639). Essential for osteoclastic bone resorption (PubMed:14739300). The 'Tyr-731' phosphorylated form induces the activation and recruitment of phosphatidylinositol 3-kinase to the cell membrane in a signaling pathway that is critical for osteoclast function (PubMed:14739300). May be functionally coupled with the E2 ubiquitin-protein ligase UB2D3. In association with CBLB, required for proper feedback inhibition of ciliary platelet-derived growth factor receptor-alpha (PDGFRA) signaling pathway via ubiquitination and internalization of PDGFRA (By similarity). {ECO:0000250|UniProtKB:P22682, ECO:0000269|PubMed:10514377, ECO:0000269|PubMed:11896602, ECO:0000269|PubMed:14661060, ECO:0000269|PubMed:14739300, ECO:0000269|PubMed:15190072, ECO:0000269|PubMed:17094949, ECO:0000269|PubMed:17509076, ECO:0000269|PubMed:17974561, ECO:0000269|PubMed:18374639, ECO:0000269|PubMed:19689429, ECO:0000269|PubMed:21596750, ECO:0000269|PubMed:28381567}. |
P27816 | MAP4 | S742 | ochoa | Microtubule-associated protein 4 (MAP-4) | Non-neuronal microtubule-associated protein. Promotes microtubule assembly. {ECO:0000269|PubMed:10791892, ECO:0000269|PubMed:34782749}. |
P31785 | IL2RG | S326 | ochoa | Cytokine receptor common subunit gamma (Interleukin-2 receptor subunit gamma) (IL-2 receptor subunit gamma) (IL-2R subunit gamma) (IL-2RG) (gammaC) (p64) (CD antigen CD132) | Common subunit for the receptors for a variety of interleukins. Probably in association with IL15RA, involved in the stimulation of neutrophil phagocytosis by IL15 (PubMed:15123770). {ECO:0000269|PubMed:15123770}. |
P31948 | STIP1 | S42 | ochoa | Stress-induced-phosphoprotein 1 (STI1) (Hsc70/Hsp90-organizing protein) (Hop) (Renal carcinoma antigen NY-REN-11) (Transformation-sensitive protein IEF SSP 3521) | Acts as a co-chaperone for HSP90AA1 (PubMed:27353360). Mediates the association of the molecular chaperones HSPA8/HSC70 and HSP90 (By similarity). {ECO:0000250|UniProtKB:O35814, ECO:0000303|PubMed:27353360}. |
P32119 | PRDX2 | S76 | psp | Peroxiredoxin-2 (EC 1.11.1.24) (Natural killer cell-enhancing factor B) (NKEF-B) (PRP) (Thiol-specific antioxidant protein) (TSA) (Thioredoxin peroxidase 1) (Thioredoxin-dependent peroxide reductase 1) (Thioredoxin-dependent peroxiredoxin 2) | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides and as sensor of hydrogen peroxide-mediated signaling events. Might participate in the signaling cascades of growth factors and tumor necrosis factor-alpha by regulating the intracellular concentrations of H(2)O(2). {ECO:0000269|PubMed:9497357}. |
P35573 | AGL | S672 | ochoa | Glycogen debranching enzyme (Glycogen debrancher) [Includes: 4-alpha-glucanotransferase (EC 2.4.1.25) (Oligo-1,4-1,4-glucantransferase); Amylo-alpha-1,6-glucosidase (Amylo-1,6-glucosidase) (EC 3.2.1.33) (Dextrin 6-alpha-D-glucosidase)] | Multifunctional enzyme acting as 1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glycosyltransferase and amylo-1,6-glucosidase in glycogen degradation. |
P40763 | STAT3 | S701 | ochoa | Signal transducer and activator of transcription 3 (Acute-phase response factor) | Signal transducer and transcription activator that mediates cellular responses to interleukins, KITLG/SCF, LEP and other growth factors (PubMed:10688651, PubMed:12359225, PubMed:12873986, PubMed:15194700, PubMed:15653507, PubMed:16285960, PubMed:17344214, PubMed:18242580, PubMed:18782771, PubMed:22306293, PubMed:23084476, PubMed:28262505, PubMed:32929201, PubMed:38404237). Once activated, recruits coactivators, such as NCOA1 or MED1, to the promoter region of the target gene (PubMed:15653507, PubMed:16285960, PubMed:17344214, PubMed:18782771, PubMed:28262505, PubMed:32929201). May mediate cellular responses to activated FGFR1, FGFR2, FGFR3 and FGFR4 (PubMed:12873986). Upon activation of IL6ST/gp130 signaling by interleukin-6 (IL6), binds to the IL6-responsive elements identified in the promoters of various acute-phase protein genes (PubMed:12359225). Activated by IL31 through IL31RA (PubMed:15194700). Acts as a regulator of inflammatory response by regulating differentiation of naive CD4(+) T-cells into T-helper Th17 or regulatory T-cells (Treg): acetylation promotes its transcription activity and cell differentiation while deacetylation and oxidation of lysine residues by LOXL3 inhibits differentiation (PubMed:28065600, PubMed:28262505). Involved in cell cycle regulation by inducing the expression of key genes for the progression from G1 to S phase, such as CCND1 (PubMed:17344214). Mediates the effects of LEP on melanocortin production, body energy homeostasis and lactation (By similarity). May play an apoptotic role by transctivating BIRC5 expression under LEP activation (PubMed:18242580). Cytoplasmic STAT3 represses macroautophagy by inhibiting EIF2AK2/PKR activity (PubMed:23084476). Plays a crucial role in basal beta cell functions, such as regulation of insulin secretion (By similarity). Following JAK/STAT signaling activation and as part of a complex with NFATC3 and NFATC4, binds to the alpha-beta E4 promoter region of CRYAB and activates transcription in cardiomyocytes (By similarity). {ECO:0000250|UniProtKB:P42227, ECO:0000269|PubMed:10688651, ECO:0000269|PubMed:12359225, ECO:0000269|PubMed:12873986, ECO:0000269|PubMed:15194700, ECO:0000269|PubMed:15653507, ECO:0000269|PubMed:16285960, ECO:0000269|PubMed:17344214, ECO:0000269|PubMed:18242580, ECO:0000269|PubMed:18782771, ECO:0000269|PubMed:22306293, ECO:0000269|PubMed:23084476, ECO:0000269|PubMed:28065600, ECO:0000269|PubMed:28262505, ECO:0000269|PubMed:32929201, ECO:0000269|PubMed:38404237}. |
P48634 | PRRC2A | S119 | ochoa | Protein PRRC2A (HLA-B-associated transcript 2) (Large proline-rich protein BAT2) (Proline-rich and coiled-coil-containing protein 2A) (Protein G2) | May play a role in the regulation of pre-mRNA splicing. {ECO:0000269|PubMed:14667819}. |
P51610 | HCFC1 | S1490 | ochoa | Host cell factor 1 (HCF) (HCF-1) (C1 factor) (CFF) (VCAF) (VP16 accessory protein) [Cleaved into: HCF N-terminal chain 1; HCF N-terminal chain 2; HCF N-terminal chain 3; HCF N-terminal chain 4; HCF N-terminal chain 5; HCF N-terminal chain 6; HCF C-terminal chain 1; HCF C-terminal chain 2; HCF C-terminal chain 3; HCF C-terminal chain 4; HCF C-terminal chain 5; HCF C-terminal chain 6] | Transcriptional coregulator (By similarity). Serves as a scaffold protein, bridging interactions between transcription factors, including THAP11 and ZNF143, and transcriptional coregulators (PubMed:26416877). Involved in control of the cell cycle (PubMed:10629049, PubMed:10779346, PubMed:15190068, PubMed:16624878, PubMed:23629655). Also antagonizes transactivation by ZBTB17 and GABP2; represses ZBTB17 activation of the p15(INK4b) promoter and inhibits its ability to recruit p300 (PubMed:10675337, PubMed:12244100). Coactivator for EGR2 and GABP2 (PubMed:12244100, PubMed:14532282). Tethers the chromatin modifying Set1/Ash2 histone H3 'Lys-4' methyltransferase (H3K4me) and Sin3 histone deacetylase (HDAC) complexes (involved in the activation and repression of transcription, respectively) together (PubMed:12670868). Component of a THAP1/THAP3-HCFC1-OGT complex that is required for the regulation of the transcriptional activity of RRM1 (PubMed:20200153). As part of the NSL complex it may be involved in acetylation of nucleosomal histone H4 on several lysine residues (PubMed:20018852). Recruits KMT2E/MLL5 to E2F1 responsive promoters promoting transcriptional activation and thereby facilitates G1 to S phase transition (PubMed:23629655). Modulates expression of homeobox protein PDX1, perhaps acting in concert with transcription factor E2F1, thereby regulating pancreatic beta-cell growth and glucose-stimulated insulin secretion (By similarity). May negatively modulate transcriptional activity of FOXO3 (By similarity). {ECO:0000250|UniProtKB:D3ZN95, ECO:0000269|PubMed:10629049, ECO:0000269|PubMed:10675337, ECO:0000269|PubMed:10779346, ECO:0000269|PubMed:12244100, ECO:0000269|PubMed:12670868, ECO:0000269|PubMed:14532282, ECO:0000269|PubMed:15190068, ECO:0000269|PubMed:16624878, ECO:0000269|PubMed:20018852, ECO:0000269|PubMed:20200153, ECO:0000269|PubMed:23629655, ECO:0000269|PubMed:26416877}.; FUNCTION: (Microbial infection) In case of human herpes simplex virus (HSV) infection, HCFC1 forms a multiprotein-DNA complex with the viral transactivator protein VP16 and POU2F1 thereby enabling the transcription of the viral immediate early genes. {ECO:0000269|PubMed:10629049, ECO:0000269|PubMed:17578910}. |
P53992 | SEC24C | S218 | ochoa | Protein transport protein Sec24C (SEC24-related protein C) | Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules for their transport to the Golgi complex (PubMed:10214955, PubMed:17499046, PubMed:18843296, PubMed:20427317). Plays a central role in cargo selection within the COPII complex and together with SEC24D may have a different specificity compared to SEC24A and SEC24B (PubMed:17499046, PubMed:18843296, PubMed:20427317). May more specifically package GPI-anchored proteins through the cargo receptor TMED10 (PubMed:20427317). May also be specific for IxM motif-containing cargos like the SNAREs GOSR2 and STX5 (PubMed:18843296). {ECO:0000269|PubMed:10214955, ECO:0000269|PubMed:17499046, ECO:0000269|PubMed:18843296, ECO:0000269|PubMed:20427317}. |
Q00872 | MYBPC1 | S550 | ochoa | Myosin-binding protein C, slow-type (Slow MyBP-C) (C-protein, skeletal muscle slow isoform) | Thick filament-associated protein located in the crossbridge region of vertebrate striated muscle a bands. Slow skeletal protein that binds to both myosin and actin (PubMed:31025394, PubMed:31264822). In vitro, binds to native thin filaments and modifies the activity of actin-activated myosin ATPase. May modulate muscle contraction or may play a more structural role. {ECO:0000269|PubMed:31025394, ECO:0000269|PubMed:31264822}. |
Q00978 | IRF9 | S253 | psp | Interferon regulatory factor 9 (IRF-9) (IFN-alpha-responsive transcription factor subunit) (ISGF3 p48 subunit) (Interferon-stimulated gene factor 3 gamma) (ISGF-3 gamma) (Transcriptional regulator ISGF3 subunit gamma) | Transcription factor that plays an essential role in anti-viral immunity. It mediates signaling by type I IFNs (IFN-alpha and IFN-beta). Following type I IFN binding to cell surface receptors, Jak kinases (TYK2 and JAK1) are activated, leading to tyrosine phosphorylation of STAT1 and STAT2. IRF9/ISGF3G associates with the phosphorylated STAT1:STAT2 dimer to form a complex termed ISGF3 transcription factor, that enters the nucleus. ISGF3 binds to the IFN stimulated response element (ISRE) to activate the transcription of interferon stimulated genes, which drive the cell in an antiviral state. {ECO:0000269|PubMed:30143481}. |
Q02086 | SP2 | S25 | ochoa | Transcription factor Sp2 | Binds to GC box promoters elements and selectively activates mRNA synthesis from genes that contain functional recognition sites. |
Q02446 | SP4 | S38 | ochoa | Transcription factor Sp4 (SPR-1) | Binds to GT and GC boxes promoters elements. Probable transcriptional activator. |
Q03252 | LMNB2 | S552 | ochoa | Lamin-B2 | Lamins are intermediate filament proteins that assemble into a filamentous meshwork, and which constitute the major components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane (PubMed:33033404). Lamins provide a framework for the nuclear envelope, bridging the nuclear envelope and chromatin, thereby playing an important role in nuclear assembly, chromatin organization, nuclear membrane and telomere dynamics (PubMed:33033404). The structural integrity of the lamina is strictly controlled by the cell cycle, as seen by the disintegration and formation of the nuclear envelope in prophase and telophase, respectively (PubMed:33033404). {ECO:0000269|PubMed:33033404}. |
Q10571 | MN1 | S1073 | ochoa | Transcriptional activator MN1 (Probable tumor suppressor protein MN1) | Transcriptional activator which specifically regulates expression of TBX22 in the posterior region of the developing palate. Required during later stages of palate development for growth and medial fusion of the palatal shelves. Promotes maturation and normal function of calvarial osteoblasts, including expression of the osteoclastogenic cytokine TNFSF11/RANKL. Necessary for normal development of the membranous bones of the skull (By similarity). May play a role in tumor suppression (Probable). {ECO:0000250|UniProtKB:D3YWE6, ECO:0000305|PubMed:7731706}. |
Q12834 | CDC20 | S104 | ochoa | Cell division cycle protein 20 homolog (p55CDC) | Substrate-specific adapter of the anaphase promoting complex/cyclosome (APC/C) complex that confers substrate specificity by binding to substrates and targeting them to the APC/C complex for ubiquitination and degradation (PubMed:9734353, PubMed:27030811, PubMed:29343641). Recognizes and binds the destruction box (D box) on protein substrates (PubMed:29343641). Involved in the metaphase/anaphase transition of cell cycle (PubMed:32666501). Is regulated by MAD2L1: in metaphase the MAD2L1-CDC20-APC/C ternary complex is inactive and in anaphase the CDC20-APC/C binary complex is active in degrading substrates (PubMed:9811605, PubMed:9637688). The CDC20-APC/C complex positively regulates the formation of synaptic vesicle clustering at active zone to the presynaptic membrane in postmitotic neurons (By similarity). CDC20-APC/C-induced degradation of NEUROD2 induces presynaptic differentiation (By similarity). The CDC20-APC/C complex promotes proper dilation formation and radial migration by degrading CCDC41 (By similarity). {ECO:0000250|UniProtKB:Q9JJ66, ECO:0000269|PubMed:27030811, ECO:0000269|PubMed:29343641, ECO:0000269|PubMed:32666501, ECO:0000269|PubMed:9637688, ECO:0000269|PubMed:9734353, ECO:0000269|PubMed:9811605}. |
Q13177 | PAK2 | S141 | ochoa|psp | Serine/threonine-protein kinase PAK 2 (EC 2.7.11.1) (Gamma-PAK) (PAK65) (S6/H4 kinase) (p21-activated kinase 2) (PAK-2) (p58) [Cleaved into: PAK-2p27 (p27); PAK-2p34 (p34) (C-t-PAK2)] | Serine/threonine protein kinase that plays a role in a variety of different signaling pathways including cytoskeleton regulation, cell motility, cell cycle progression, apoptosis or proliferation (PubMed:12853446, PubMed:16617111, PubMed:19273597, PubMed:19923322, PubMed:33693784, PubMed:7744004, PubMed:9171063). Acts as a downstream effector of the small GTPases CDC42 and RAC1 (PubMed:7744004). Activation by the binding of active CDC42 and RAC1 results in a conformational change and a subsequent autophosphorylation on several serine and/or threonine residues (PubMed:7744004). Full-length PAK2 stimulates cell survival and cell growth (PubMed:7744004). Phosphorylates MAPK4 and MAPK6 and activates the downstream target MAPKAPK5, a regulator of F-actin polymerization and cell migration (PubMed:21317288). Phosphorylates JUN and plays an important role in EGF-induced cell proliferation (PubMed:21177766). Phosphorylates many other substrates including histone H4 to promote assembly of H3.3 and H4 into nucleosomes, BAD, ribosomal protein S6, or MBP (PubMed:21724829). Phosphorylates CASP7, thereby preventing its activity (PubMed:21555521, PubMed:27889207). Additionally, associates with ARHGEF7 and GIT1 to perform kinase-independent functions such as spindle orientation control during mitosis (PubMed:19273597, PubMed:19923322). On the other hand, apoptotic stimuli such as DNA damage lead to caspase-mediated cleavage of PAK2, generating PAK-2p34, an active p34 fragment that translocates to the nucleus and promotes cellular apoptosis involving the JNK signaling pathway (PubMed:12853446, PubMed:16617111, PubMed:9171063). Caspase-activated PAK2 phosphorylates MKNK1 and reduces cellular translation (PubMed:15234964). {ECO:0000269|PubMed:12853446, ECO:0000269|PubMed:15234964, ECO:0000269|PubMed:16617111, ECO:0000269|PubMed:19273597, ECO:0000269|PubMed:19923322, ECO:0000269|PubMed:21177766, ECO:0000269|PubMed:21317288, ECO:0000269|PubMed:21555521, ECO:0000269|PubMed:21724829, ECO:0000269|PubMed:27889207, ECO:0000269|PubMed:33693784, ECO:0000269|PubMed:7744004, ECO:0000269|PubMed:9171063}. |
Q13330 | MTA1 | S53 | ochoa | Metastasis-associated protein MTA1 | Transcriptional coregulator which can act as both a transcriptional corepressor and coactivator (PubMed:16617102, PubMed:17671180, PubMed:17922032, PubMed:21965678, PubMed:24413532). Acts as a component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin (PubMed:16428440, PubMed:28977666). In the NuRD complex, regulates transcription of its targets by modifying the acetylation status of the target chromatin and cofactor accessibility to the target DNA (PubMed:17671180). In conjunction with other components of NuRD, acts as a transcriptional corepressor of BRCA1, ESR1, TFF1 and CDKN1A (PubMed:17922032, PubMed:24413532). Acts as a transcriptional coactivator of BCAS3, and SUMO2, independent of the NuRD complex (PubMed:16617102, PubMed:17671180, PubMed:21965678). Stimulates the expression of WNT1 by inhibiting the expression of its transcriptional corepressor SIX3 (By similarity). Regulates p53-dependent and -independent DNA repair processes following genotoxic stress (PubMed:19837670). Regulates the stability and function of p53/TP53 by inhibiting its ubiquitination by COP1 and MDM2 thereby regulating the p53-dependent DNA repair (PubMed:19837670). Plays a role in the regulation of the circadian clock and is essential for the generation and maintenance of circadian rhythms under constant light and for normal entrainment of behavior to light-dark (LD) cycles (By similarity). Positively regulates the CLOCK-BMAL1 heterodimer mediated transcriptional activation of its own transcription and the transcription of CRY1 (By similarity). Regulates deacetylation of BMAL1 by regulating SIRT1 expression, resulting in derepressing CRY1-mediated transcription repression (By similarity). With TFCP2L1, promotes establishment and maintenance of pluripotency in embryonic stem cells (ESCs) and inhibits endoderm differentiation (By similarity). {ECO:0000250|UniProtKB:Q8K4B0, ECO:0000269|PubMed:16428440, ECO:0000269|PubMed:16617102, ECO:0000269|PubMed:17671180, ECO:0000269|PubMed:17922032, ECO:0000269|PubMed:19837670, ECO:0000269|PubMed:21965678, ECO:0000269|PubMed:24413532}.; FUNCTION: [Isoform Short]: Binds to ESR1 and sequesters it in the cytoplasm and enhances its non-genomic responses. {ECO:0000269|PubMed:15077195}. |
Q13469 | NFATC2 | S367 | ochoa | Nuclear factor of activated T-cells, cytoplasmic 2 (NF-ATc2) (NFATc2) (NFAT pre-existing subunit) (NF-ATp) (T-cell transcription factor NFAT1) | Plays a role in the inducible expression of cytokine genes in T-cells, especially in the induction of the IL-2, IL-3, IL-4, TNF-alpha or GM-CSF (PubMed:15790681). Promotes invasive migration through the activation of GPC6 expression and WNT5A signaling pathway (PubMed:21871017). Is involved in the negative regulation of chondrogenesis (PubMed:35789258). Recruited by AKAP5 to ORAI1 pore-forming subunit of CRAC channels in Ca(2+) signaling microdomains where store-operated Ca(2+) influx is coupled to calmodulin and calcineurin signaling and activation of NFAT-dependent transcriptional responses. {ECO:0000250|UniProtKB:Q60591, ECO:0000269|PubMed:15790681, ECO:0000269|PubMed:21871017, ECO:0000269|PubMed:35789258}. |
Q13938 | CAPS | S40 | ochoa | Calcyphosin (Calcyphosine) | Calcium-binding protein. May play a role in cellular signaling events (Potential). {ECO:0000305}. |
Q14686 | NCOA6 | S1231 | ochoa | Nuclear receptor coactivator 6 (Activating signal cointegrator 2) (ASC-2) (Amplified in breast cancer protein 3) (Cancer-amplified transcriptional coactivator ASC-2) (Nuclear receptor coactivator RAP250) (NRC RAP250) (Nuclear receptor-activating protein, 250 kDa) (Peroxisome proliferator-activated receptor-interacting protein) (PPAR-interacting protein) (PRIP) (Thyroid hormone receptor-binding protein) | Nuclear receptor coactivator that directly binds nuclear receptors and stimulates the transcriptional activities in a hormone-dependent fashion. Coactivates expression in an agonist- and AF2-dependent manner. Involved in the coactivation of different nuclear receptors, such as for steroids (GR and ERs), retinoids (RARs and RXRs), thyroid hormone (TRs), vitamin D3 (VDR) and prostanoids (PPARs). Probably functions as a general coactivator, rather than just a nuclear receptor coactivator. May also be involved in the coactivation of the NF-kappa-B pathway. May coactivate expression via a remodeling of chromatin and its interaction with histone acetyltransferase proteins. |
Q14938 | NFIX | S231 | ochoa | Nuclear factor 1 X-type (NF1-X) (Nuclear factor 1/X) (CCAAT-box-binding transcription factor) (CTF) (Nuclear factor I/X) (NF-I/X) (NFI-X) (TGGCA-binding protein) | Recognizes and binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3' present in viral and cellular promoters and in the origin of replication of adenovirus type 2. These proteins are individually capable of activating transcription and replication. |
Q14999 | CUL7 | S329 | ochoa | Cullin-7 (CUL-7) | Core component of the 3M and Cul7-RING(FBXW8) complexes, which mediate the ubiquitination and subsequent proteasomal degradation of target proteins (PubMed:12481031, PubMed:12904573, PubMed:21572988, PubMed:21737058, PubMed:24793695, PubMed:35982156). Core component of the 3M complex, a complex required to regulate microtubule dynamics and genome integrity (PubMed:21572988, PubMed:21737058, PubMed:24793695). It is unclear how the 3M complex regulates microtubules, it could act by controlling the level of a microtubule stabilizer (PubMed:24793695). The Cul7-RING(FBXW8) complex alone lacks ubiquitination activity and does not promote polyubiquitination and proteasomal degradation of p53/TP53 (PubMed:16547496, PubMed:17332328, PubMed:35982156). However it mediates recruitment of p53/TP53 for ubiquitination by neddylated CUL1-RBX1 (PubMed:35982156). Interaction with CUL9 is required to inhibit CUL9 activity and ubiquitination of BIRC5 (PubMed:24793696). The Cul7-RING(FBXW8) complex also mediates ubiquitination and consequent degradation of target proteins such as GORASP1, IRS1 and MAP4K1/HPK1 (PubMed:21572988, PubMed:24362026). Ubiquitination of GORASP1 regulates Golgi morphogenesis and dendrite patterning in brain (PubMed:21572988). Mediates ubiquitination and degradation of IRS1 in a mTOR-dependent manner: the Cul7-RING(FBXW8) complex recognizes and binds IRS1 previously phosphorylated by S6 kinase (RPS6KB1 or RPS6KB2) (PubMed:18498745). The Cul7-RING(FBXW8) complex also mediates ubiquitination of MAP4K1/HPK1: recognizes and binds autophosphorylated MAP4K1/HPK1, leading to its degradation, thereby affecting cell proliferation and differentiation (PubMed:24362026). Acts as a regulator in trophoblast cell epithelial-mesenchymal transition and placental development (PubMed:20139075). While the Cul7-RING(FBXW8) and the 3M complexes are associated and involved in common processes, CUL7 and the Cul7-RING(FBXW8) complex may have additional functions. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation. {ECO:0000269|PubMed:12481031, ECO:0000269|PubMed:12904573, ECO:0000269|PubMed:16547496, ECO:0000269|PubMed:17332328, ECO:0000269|PubMed:18498745, ECO:0000269|PubMed:20139075, ECO:0000269|PubMed:21572988, ECO:0000269|PubMed:21737058, ECO:0000269|PubMed:24362026, ECO:0000269|PubMed:24793695, ECO:0000269|PubMed:24793696, ECO:0000269|PubMed:35982156}. |
Q15365 | PCBP1 | S223 | ochoa | Poly(rC)-binding protein 1 (Alpha-CP1) (Heterogeneous nuclear ribonucleoprotein E1) (hnRNP E1) (Nucleic acid-binding protein SUB2.3) | Single-stranded nucleic acid binding protein that binds preferentially to oligo dC (PubMed:15731341, PubMed:7556077, PubMed:7607214, PubMed:8152927). Together with PCBP2, required for erythropoiesis, possibly by regulating mRNA splicing (By similarity). {ECO:0000250|UniProtKB:P60335, ECO:0000269|PubMed:15731341, ECO:0000269|PubMed:7556077, ECO:0000269|PubMed:7607214, ECO:0000269|PubMed:8152927}.; FUNCTION: (Microbial infection) In case of infection by poliovirus, plays a role in initiation of viral RNA replication in concert with the viral protein 3CD. {ECO:0000269|PubMed:12414943}. |
Q15911 | ZFHX3 | S2515 | ochoa | Zinc finger homeobox protein 3 (AT motif-binding factor 1) (AT-binding transcription factor 1) (Alpha-fetoprotein enhancer-binding protein) (Zinc finger homeodomain protein 3) (ZFH-3) | Transcriptional regulator which can act as an activator or a repressor. Inhibits the enhancer element of the AFP gene by binding to its AT-rich core sequence. In concert with SMAD-dependent TGF-beta signaling can repress the transcription of AFP via its interaction with SMAD2/3 (PubMed:25105025). Regulates the circadian locomotor rhythms via transcriptional activation of neuropeptidergic genes which are essential for intercellular synchrony and rhythm amplitude in the suprachiasmatic nucleus (SCN) of the brain (By similarity). Regulator of myoblasts differentiation through the binding to the AT-rich sequence of MYF6 promoter and promoter repression (PubMed:11312261). Down-regulates the MUC5AC promoter in gastric cancer (PubMed:17330845). In association with RUNX3, up-regulates CDKN1A promoter activity following TGF-beta stimulation (PubMed:20599712). Inhibits estrogen receptor (ESR1) function by selectively competing with coactivator NCOA3 for binding to ESR1 in ESR1-positive breast cancer cells (PubMed:20720010). {ECO:0000250|UniProtKB:Q61329, ECO:0000269|PubMed:11312261, ECO:0000269|PubMed:17330845, ECO:0000269|PubMed:20599712, ECO:0000269|PubMed:20720010, ECO:0000269|PubMed:25105025}. |
Q16656 | NRF1 | S102 | psp | Nuclear respiratory factor 1 (NRF-1) (Alpha palindromic-binding protein) (Alpha-pal) | Transcription factor that activates the expression of the EIF2S1 (EIF2-alpha) gene. Links the transcriptional modulation of key metabolic genes to cellular growth and development. Implicated in the control of nuclear genes required for respiration, heme biosynthesis, and mitochondrial DNA transcription and replication. |
Q38SD2 | LRRK1 | S1817 | psp | Leucine-rich repeat serine/threonine-protein kinase 1 (EC 2.7.11.1) | Serine/threonine-protein kinase which phosphorylates RAB proteins involved in intracellular trafficking (PubMed:36040231). Phosphorylates RAB7A; this activity is dependent on protein kinase C (PKC) activation (PubMed:36040231, PubMed:37558661, PubMed:37857821). Plays a role in the negative regulation of bone mass, acting through the maturation of osteoclasts (By similarity). {ECO:0000250|UniProtKB:Q3UHC2, ECO:0000269|PubMed:36040231, ECO:0000269|PubMed:37558661, ECO:0000269|PubMed:37857821}. |
Q5JTC6 | AMER1 | S683 | psp | APC membrane recruitment protein 1 (Amer1) (Protein FAM123B) (Wilms tumor gene on the X chromosome protein) | Regulator of the canonical Wnt signaling pathway. Acts by specifically binding phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), translocating to the cell membrane and interacting with key regulators of the canonical Wnt signaling pathway, such as components of the beta-catenin destruction complex. Acts both as a positive and negative regulator of the Wnt signaling pathway, depending on the context: acts as a positive regulator by promoting LRP6 phosphorylation. Also acts as a negative regulator by acting as a scaffold protein for the beta-catenin destruction complex and promoting stabilization of Axin at the cell membrane. Promotes CTNNB1 ubiquitination and degradation. Involved in kidney development. {ECO:0000269|PubMed:17510365, ECO:0000269|PubMed:17925383, ECO:0000269|PubMed:19416806, ECO:0000269|PubMed:21304492, ECO:0000269|PubMed:21498506}. |
Q5SY16 | NOL9 | S249 | ochoa | Polynucleotide 5'-hydroxyl-kinase NOL9 (EC 2.7.1.78) (Nucleolar protein 9) | Polynucleotide kinase that can phosphorylate the 5'-hydroxyl groups of single-stranded and double-stranded RNA and DNA substrates (PubMed:21063389). Involved in rRNA processing and its kinase activity is required for the processing of the 32S precursor into 5.8S and 28S rRNAs, more specifically for the generation of the major 5.8S(S) form (PubMed:21063389). Required for the efficient pre-rRNA processing of internal transcribed spacer 2 (ITS2) (PubMed:21063389). Associates with LAS1L to form an ITS2 pre-rRNA endonuclease-kinase complex and is responsible for the transport of this complex into the nucleolus (PubMed:31288032). {ECO:0000269|PubMed:21063389, ECO:0000269|PubMed:31288032}. |
Q5XUX1 | FBXW9 | S51 | ochoa | F-box/WD repeat-containing protein 9 (F-box and WD-40 domain-containing protein 9) | Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. {ECO:0000250}. |
Q68CZ2 | TNS3 | S602 | 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}. |
Q6AI12 | ANKRD40 | S202 | ochoa | Ankyrin repeat domain-containing protein 40 | None |
Q6AI12 | ANKRD40 | S214 | ochoa | Ankyrin repeat domain-containing protein 40 | None |
Q6F5E8 | CARMIL2 | S1270 | ochoa | Capping protein, Arp2/3 and myosin-I linker protein 2 (Capping protein regulator and myosin 1 linker 2) (F-actin-uncapping protein RLTPR) (Leucine-rich repeat-containing protein 16C) (RGD, leucine-rich repeat, tropomodulin and proline-rich-containing protein) | Cell membrane-cytoskeleton-associated protein that plays a role in the regulation of actin polymerization at the barbed end of actin filaments. Prevents F-actin heterodimeric capping protein (CP) activity at the leading edges of migrating cells, and hence generates uncapped barbed ends and enhances actin polymerization (PubMed:26466680). Plays a role in cell protrusion formations; involved in cell polarity, lamellipodial assembly, membrane ruffling and macropinosome formations (PubMed:19846667, PubMed:26466680, PubMed:26578515). Involved as well in cell migration and invadopodia formation during wound healing (PubMed:19846667, PubMed:26466680, PubMed:26578515). Required for CD28-mediated stimulation of NF-kappa-B signaling, involved in naive T cells activation, maturation into T memory cells, and differentiation into T helper and T regulatory cells (PubMed:27647348, PubMed:27647349, PubMed:28112205). {ECO:0000269|PubMed:19846667, ECO:0000269|PubMed:26466680, ECO:0000269|PubMed:26578515, ECO:0000269|PubMed:27647348, ECO:0000269|PubMed:27647349, ECO:0000269|PubMed:28112205}. |
Q6P1N0 | CC2D1A | S118 | ochoa | Coiled-coil and C2 domain-containing protein 1A (Akt kinase-interacting protein 1) (Five prime repressor element under dual repression-binding protein 1) (FRE under dual repression-binding protein 1) (Freud-1) (Putative NF-kappa-B-activating protein 023N) | Transcription factor that binds specifically to the DRE (dual repressor element) and represses HTR1A gene transcription in neuronal cells. The combination of calcium and ATP specifically inactivates the binding with FRE. May play a role in the altered regulation of HTR1A associated with anxiety and major depression. Mediates HDAC-independent repression of HTR1A promoter in neuronal cell. Performs essential function in controlling functional maturation of synapses (By similarity). Plays distinct roles depending on its localization. When cytoplasmic, acts as a scaffold protein in the PI3K/PDK1/AKT pathway. Repressor of HTR1A when nuclear. In the centrosome, regulates spindle pole localization of the cohesin subunit SCC1/RAD21, thereby mediating centriole cohesion during mitosis. {ECO:0000250, ECO:0000269|PubMed:20171170}. |
Q70J99 | UNC13D | S784 | ochoa | Protein unc-13 homolog D (Munc13-4) | Plays a role in cytotoxic granule exocytosis in lymphocytes. Required for both granule maturation and granule docking and priming at the immunologic synapse. Regulates assembly of recycling and late endosomal structures, leading to the formation of an endosomal exocytic compartment that fuses with perforin-containing granules at the immunologic synapse and licences them for exocytosis. Regulates Ca(2+)-dependent secretory lysosome exocytosis in mast cells. {ECO:0000269|PubMed:15548590, ECO:0000269|PubMed:17237785}. |
Q76FK4 | NOL8 | S273 | ochoa | Nucleolar protein 8 (Nucleolar protein Nop132) | Plays an essential role in the survival of diffuse-type gastric cancer cells. Acts as a nucleolar anchoring protein for DDX47. May be involved in regulation of gene expression at the post-transcriptional level or in ribosome biogenesis in cancer cells. {ECO:0000269|PubMed:14660641, ECO:0000269|PubMed:15132771, ECO:0000269|PubMed:16963496}. |
Q7KZI7 | MARK2 | S537 | ochoa | Serine/threonine-protein kinase MARK2 (EC 2.7.11.1) (EC 2.7.11.26) (ELKL motif kinase 1) (EMK-1) (MAP/microtubule affinity-regulating kinase 2) (PAR1 homolog) (PAR1 homolog b) (Par-1b) (Par1b) | Serine/threonine-protein kinase (PubMed:23666762). Involved in cell polarity and microtubule dynamics regulation. Phosphorylates CRTC2/TORC2, DCX, HDAC7, KIF13B, MAP2, MAP4 and RAB11FIP2. Phosphorylates the microtubule-associated protein MAPT/TAU (PubMed:23666762). Plays a key role in cell polarity by phosphorylating the microtubule-associated proteins MAP2, MAP4 and MAPT/TAU at KXGS motifs, causing detachment from microtubules, and their disassembly. Regulates epithelial cell polarity by phosphorylating RAB11FIP2. Involved in the regulation of neuronal migration through its dual activities in regulating cellular polarity and microtubule dynamics, possibly by phosphorylating and regulating DCX. Regulates axogenesis by phosphorylating KIF13B, promoting interaction between KIF13B and 14-3-3 and inhibiting microtubule-dependent accumulation of KIF13B. Also required for neurite outgrowth and establishment of neuronal polarity. Regulates localization and activity of some histone deacetylases by mediating phosphorylation of HDAC7, promoting subsequent interaction between HDAC7 and 14-3-3 and export from the nucleus. Also acts as a positive regulator of the Wnt signaling pathway, probably by mediating phosphorylation of dishevelled proteins (DVL1, DVL2 and/or DVL3). Modulates the developmental decision to build a columnar versus a hepatic epithelial cell apparently by promoting a switch from a direct to a transcytotic mode of apical protein delivery. Essential for the asymmetric development of membrane domains of polarized epithelial cells. {ECO:0000269|PubMed:11433294, ECO:0000269|PubMed:12429843, ECO:0000269|PubMed:14976552, ECO:0000269|PubMed:15158914, ECO:0000269|PubMed:15324659, ECO:0000269|PubMed:15365179, ECO:0000269|PubMed:16775013, ECO:0000269|PubMed:16980613, ECO:0000269|PubMed:18626018, ECO:0000269|PubMed:20194617, ECO:0000269|PubMed:23666762}. |
Q7Z434 | MAVS | S285 | ochoa | Mitochondrial antiviral-signaling protein (MAVS) (CARD adapter inducing interferon beta) (Cardif) (Interferon beta promoter stimulator protein 1) (IPS-1) (Putative NF-kappa-B-activating protein 031N) (Virus-induced-signaling adapter) (VISA) | Adapter required for innate immune defense against viruses (PubMed:16125763, PubMed:16127453, PubMed:16153868, PubMed:16177806, PubMed:19631370, PubMed:20127681, PubMed:20451243, PubMed:21170385, PubMed:23087404, PubMed:27992402, PubMed:33139700, PubMed:37582970). Acts downstream of DHX33, RIGI and IFIH1/MDA5, which detect intracellular dsRNA produced during viral replication, to coordinate pathways leading to the activation of NF-kappa-B, IRF3 and IRF7, and to the subsequent induction of antiviral cytokines such as IFNB and RANTES (CCL5) (PubMed:16125763, PubMed:16127453, PubMed:16153868, PubMed:16177806, PubMed:19631370, PubMed:20127681, PubMed:20451243, PubMed:20628368, PubMed:21170385, PubMed:23087404, PubMed:25636800, PubMed:27736772, PubMed:33110251). Peroxisomal and mitochondrial MAVS act sequentially to create an antiviral cellular state (PubMed:20451243). Upon viral infection, peroxisomal MAVS induces the rapid interferon-independent expression of defense factors that provide short-term protection, whereas mitochondrial MAVS activates an interferon-dependent signaling pathway with delayed kinetics, which amplifies and stabilizes the antiviral response (PubMed:20451243). May activate the same pathways following detection of extracellular dsRNA by TLR3 (PubMed:16153868). May protect cells from apoptosis (PubMed:16125763). Involved in NLRP3 inflammasome activation by mediating NLRP3 recruitment to mitochondria (PubMed:23582325). {ECO:0000269|PubMed:16125763, ECO:0000269|PubMed:16127453, ECO:0000269|PubMed:16153868, ECO:0000269|PubMed:16177806, ECO:0000269|PubMed:19631370, ECO:0000269|PubMed:20127681, ECO:0000269|PubMed:20451243, ECO:0000269|PubMed:20628368, ECO:0000269|PubMed:21170385, ECO:0000269|PubMed:23087404, ECO:0000269|PubMed:23582325, ECO:0000269|PubMed:25636800, ECO:0000269|PubMed:27736772, ECO:0000269|PubMed:27992402, ECO:0000269|PubMed:33110251, ECO:0000269|PubMed:33139700, ECO:0000269|PubMed:37582970}. |
Q86WB0 | ZC3HC1 | S161 | ochoa | Zinc finger C3HC-type protein 1 (Nuclear-interacting partner of ALK) (hNIPA) (Nuclear-interacting partner of anaplastic lymphoma kinase) | Required for proper positioning of a substantial amount of TPR at the nuclear basket (NB) through interaction with TPR. {ECO:0000269|PubMed:34440706}. |
Q8IX15 | HOMEZ | S315 | ochoa | Homeobox and leucine zipper protein Homez (Homeodomain leucine zipper-containing factor) | May function as a transcriptional regulator. |
Q8N163 | CCAR2 | S117 | ochoa | Cell cycle and apoptosis regulator protein 2 (Cell division cycle and apoptosis regulator protein 2) (DBIRD complex subunit KIAA1967) (Deleted in breast cancer gene 1 protein) (DBC-1) (DBC.1) (NET35) (p30 DBC) | Core component of the DBIRD complex, a multiprotein complex that acts at the interface between core mRNP particles and RNA polymerase II (RNAPII) and integrates transcript elongation with the regulation of alternative splicing: the DBIRD complex affects local transcript elongation rates and alternative splicing of a large set of exons embedded in (A + T)-rich DNA regions (PubMed:22446626). Inhibits SIRT1 deacetylase activity leading to increasing levels of p53/TP53 acetylation and p53-mediated apoptosis (PubMed:18235501, PubMed:18235502, PubMed:23352644). Inhibits SUV39H1 methyltransferase activity (PubMed:19218236). Mediates ligand-dependent transcriptional activation by nuclear hormone receptors (PubMed:19131338). Plays a critical role in maintaining genomic stability and cellular integrity following UV-induced genotoxic stress (PubMed:23398316). Regulates the circadian expression of the core clock components NR1D1 and BMAL1 (PubMed:23398316). Enhances the transcriptional repressor activity of NR1D1 through stabilization of NR1D1 protein levels by preventing its ubiquitination and subsequent degradation (PubMed:23398316). Represses the ligand-dependent transcriptional activation function of ESR2 (PubMed:20074560). Acts as a regulator of PCK1 expression and gluconeogenesis by a mechanism that involves, at least in part, both NR1D1 and SIRT1 (PubMed:24415752). Negatively regulates the deacetylase activity of HDAC3 and can alter its subcellular localization (PubMed:21030595). Positively regulates the beta-catenin pathway (canonical Wnt signaling pathway) and is required for MCC-mediated repression of the beta-catenin pathway (PubMed:24824780). Represses ligand-dependent transcriptional activation function of NR1H2 and NR1H3 and inhibits the interaction of SIRT1 with NR1H3 (PubMed:25661920). Plays an important role in tumor suppression through p53/TP53 regulation; stabilizes p53/TP53 by affecting its interaction with ubiquitin ligase MDM2 (PubMed:25732823). Represses the transcriptional activator activity of BRCA1 (PubMed:20160719). Inhibits SIRT1 in a CHEK2 and PSEM3-dependent manner and inhibits the activity of CHEK2 in vitro (PubMed:25361978). {ECO:0000269|PubMed:18235501, ECO:0000269|PubMed:18235502, ECO:0000269|PubMed:19131338, ECO:0000269|PubMed:19218236, ECO:0000269|PubMed:20074560, ECO:0000269|PubMed:20160719, ECO:0000269|PubMed:21030595, ECO:0000269|PubMed:22446626, ECO:0000269|PubMed:23352644, ECO:0000269|PubMed:23398316, ECO:0000269|PubMed:24415752, ECO:0000269|PubMed:24824780, ECO:0000269|PubMed:25361978, ECO:0000269|PubMed:25661920, ECO:0000269|PubMed:25732823}. |
Q8N201 | INTS1 | S81 | ochoa | Integrator complex subunit 1 (Int1) | Component of the integrator complex, a multiprotein complex that terminates RNA polymerase II (Pol II) transcription in the promoter-proximal region of genes (PubMed:25201415, PubMed:33243860, PubMed:38570683). The integrator complex provides a quality checkpoint during transcription elongation by driving premature transcription termination of transcripts that are unfavorably configured for transcriptional elongation: the complex terminates transcription by (1) catalyzing dephosphorylation of the C-terminal domain (CTD) of Pol II subunit POLR2A/RPB1 and SUPT5H/SPT5, (2) degrading the exiting nascent RNA transcript via endonuclease activity and (3) promoting the release of Pol II from bound DNA (PubMed:33243860). The integrator complex is also involved in terminating the synthesis of non-coding Pol II transcripts, such as enhancer RNAs (eRNAs), small nuclear RNAs (snRNAs), telomerase RNAs and long non-coding RNAs (lncRNAs) (PubMed:16239144, PubMed:26308897, PubMed:30737432). Within the integrator complex, INTS1 is involved in the post-termination step: INTS1 displaces INTS3 and the SOSS factors, allowing the integrator complex to return to the closed conformation, ready to bind to the paused elongation complex for another termination cycle (PubMed:38570683). Mediates recruitment of cytoplasmic dynein to the nuclear envelope, probably as component of the integrator complex (PubMed:23904267). {ECO:0000269|PubMed:16239144, ECO:0000269|PubMed:23904267, ECO:0000269|PubMed:25201415, ECO:0000269|PubMed:26308897, ECO:0000269|PubMed:30737432, ECO:0000269|PubMed:33243860, ECO:0000269|PubMed:38570683}. |
Q8NDX5 | PHC3 | S661 | ochoa | Polyhomeotic-like protein 3 (Early development regulatory protein 3) (Homolog of polyhomeotic 3) (hPH3) | Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. {ECO:0000269|PubMed:12167701}. |
Q8TCG1 | CIP2A | S572 | ochoa | Protein CIP2A (Cancerous inhibitor of PP2A) (p90 autoantigen) | Acts as an inhibitor of protein phosphatase PP2A (PubMed:17632056). Promotes anchorage-independent cell growth and tumor formation by preventing dephosphorylation of MYC, thereby stabilizing MYC in human malignancies (PubMed:17632056). Together with TOPBP1, plays an essential role in the response to genome instability generated by the presence of acentric chromosome fragments derived from shattered chromosomes within micronuclei (PubMed:35121901, PubMed:35842428, PubMed:37165191, PubMed:37316668). Micronuclei, which are frequently found in cancer cells, consist of chromatin surrounded by their own nuclear membrane: following breakdown of the micronuclear envelope, a process associated with chromothripsis, the CIP2A-TOPBP1 complex tethers chromosome fragments during mitosis to ensure clustered segregation of the fragments to a single daughter cell nucleus, facilitating re-ligation with limited chromosome scattering and loss (PubMed:37165191, PubMed:37316668). {ECO:0000269|PubMed:17632056, ECO:0000269|PubMed:35121901, ECO:0000269|PubMed:35842428, ECO:0000269|PubMed:37165191, ECO:0000269|PubMed:37316668}. |
Q8TER5 | ARHGEF40 | S409 | ochoa | Rho guanine nucleotide exchange factor 40 (Protein SOLO) | May act as a guanine nucleotide exchange factor (GEF). {ECO:0000250}. |
Q8TES7 | FBF1 | S494 | ochoa | Fas-binding factor 1 (FBF-1) (Protein albatross) | Keratin-binding protein required for epithelial cell polarization. Involved in apical junction complex (AJC) assembly via its interaction with PARD3. Required for ciliogenesis. {ECO:0000269|PubMed:18838552, ECO:0000269|PubMed:23348840}. |
Q8TF76 | HASPIN | S185 | psp | Serine/threonine-protein kinase haspin (EC 2.7.11.1) (Germ cell-specific gene 2 protein) (H-haspin) (Haploid germ cell-specific nuclear protein kinase) | Serine/threonine-protein kinase that phosphorylates histone H3 at 'Thr-3' (H3T3ph) during mitosis. May act through H3T3ph to both position and modulate activation of AURKB and other components of the chromosomal passenger complex (CPC) at centromeres to ensure proper chromatid cohesion, metaphase alignment and normal progression through the cell cycle. {ECO:0000269|PubMed:11228240, ECO:0000269|PubMed:15681610, ECO:0000269|PubMed:17084365, ECO:0000269|PubMed:20705812, ECO:0000269|PubMed:20929775}. |
Q8WUA7 | TBC1D22A | S21 | ochoa | TBC1 domain family member 22A | May act as a GTPase-activating protein for Rab family protein(s). {ECO:0000250}. |
Q8WWM7 | ATXN2L | S937 | ochoa | Ataxin-2-like protein (Ataxin-2 domain protein) (Ataxin-2-related protein) | Involved in the regulation of stress granule and P-body formation. {ECO:0000269|PubMed:23209657}. |
Q8WYP5 | AHCTF1 | S2123 | ochoa | Protein ELYS (Embryonic large molecule derived from yolk sac) (Protein MEL-28) (Putative AT-hook-containing transcription factor 1) | Required for the assembly of a functional nuclear pore complex (NPC) on the surface of chromosomes as nuclei form at the end of mitosis. May initiate NPC assembly by binding to chromatin and recruiting the Nup107-160 subcomplex of the NPC. Also required for the localization of the Nup107-160 subcomplex of the NPC to the kinetochore during mitosis and for the completion of cytokinesis. {ECO:0000269|PubMed:17098863, ECO:0000269|PubMed:17235358}. |
Q8WZA9 | IRGQ | S44 | ochoa | Immunity-related GTPase family Q protein | Autophagy receptor that specifically promotes clearance of misfolded MHC class I molecules by targeting them to the lysosome for degradation (PubMed:39481378). Acts as a molecular adapter that specifically recognizes and binds (1) misfolded MHC class I molecules following their ubiquitination, as well as (2) autophagy-related proteins, promoting the recruitment of misfolded MHC class I molecules to autophagy machinery for degradation (PubMed:39481378). Degradation of misfolded MHC class I molecules is essential to prevent accumulation of defective MHC class I complexes at the surface of CD8(+) T-cells and prevent a stronger T-cell-mediated response (PubMed:39481378). In contrast to other members of the family, does not show GTPase activity (PubMed:39481378). {ECO:0000269|PubMed:39481378}. |
Q92545 | TMEM131 | S1495 | ochoa | Transmembrane protein 131 (Protein RW1) | Collagen binding transmembrane protein involved in collagen secretion by recruiting the ER-to-Golgi transport complex TRAPPIII (PubMed:32095531). May play a role in the immune response to viral infection. {ECO:0000250, ECO:0000269|PubMed:32095531}. |
Q92574 | TSC1 | S673 | ochoa | Hamartin (Tuberous sclerosis 1 protein) | Non-catalytic component of the TSC-TBC complex, a multiprotein complex that acts as a negative regulator of the canonical mTORC1 complex, an evolutionarily conserved central nutrient sensor that stimulates anabolic reactions and macromolecule biosynthesis to promote cellular biomass generation and growth (PubMed:12172553, PubMed:12271141, PubMed:12906785, PubMed:15340059, PubMed:24529379, PubMed:28215400). The TSC-TBC complex acts as a GTPase-activating protein (GAP) for the small GTPase RHEB, a direct activator of the protein kinase activity of mTORC1 (PubMed:12906785, PubMed:15340059, PubMed:24529379). In absence of nutrients, the TSC-TBC complex inhibits mTORC1, thereby preventing phosphorylation of ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1) by the mTORC1 signaling (PubMed:12271141, PubMed:24529379, PubMed:28215400, PubMed:33215753). The TSC-TBC complex is inactivated in response to nutrients, relieving inhibition of mTORC1 (PubMed:12172553, PubMed:24529379). Within the TSC-TBC complex, TSC1 stabilizes TSC2 and prevents TSC2 self-aggregation (PubMed:10585443, PubMed:28215400). Acts as a tumor suppressor (PubMed:9242607). Involved in microtubule-mediated protein transport via its ability to regulate mTORC1 signaling (By similarity). Also acts as a co-chaperone for HSP90AA1 facilitating HSP90AA1 chaperoning of protein clients such as kinases, TSC2 and glucocorticoid receptor NR3C1 (PubMed:29127155). Increases ATP binding to HSP90AA1 and inhibits HSP90AA1 ATPase activity (PubMed:29127155). Competes with the activating co-chaperone AHSA1 for binding to HSP90AA1, thereby providing a reciprocal regulatory mechanism for chaperoning of client proteins (PubMed:29127155). Recruits TSC2 to HSP90AA1 and stabilizes TSC2 by preventing the interaction between TSC2 and ubiquitin ligase HERC1 (PubMed:16464865, PubMed:29127155). {ECO:0000250|UniProtKB:Q9Z136, ECO:0000269|PubMed:10585443, ECO:0000269|PubMed:12172553, ECO:0000269|PubMed:12271141, ECO:0000269|PubMed:12906785, ECO:0000269|PubMed:15340059, ECO:0000269|PubMed:16464865, ECO:0000269|PubMed:24529379, ECO:0000269|PubMed:28215400, ECO:0000269|PubMed:29127155, ECO:0000269|PubMed:33215753, ECO:0000269|PubMed:9242607}. |
Q96BT3 | CENPT | S201 | ochoa|psp | Centromere protein T (CENP-T) (Interphase centromere complex protein 22) | 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. Part of a nucleosome-associated complex that binds specifically to histone H3-containing nucleosomes at the centromere, as opposed to nucleosomes containing CENPA. Component of the heterotetrameric CENP-T-W-S-X complex that binds and supercoils DNA, and plays an important role in kinetochore assembly. CENPT has a fundamental role in kinetochore assembly and function. It is one of the inner kinetochore proteins, with most further proteins binding downstream. Required for normal chromosome organization and normal progress through mitosis. {ECO:0000269|PubMed:16716197, ECO:0000269|PubMed:21529714, ECO:0000269|PubMed:21695110}. |
Q96DX4 | RSPRY1 | S55 | ochoa | RING finger and SPRY domain-containing protein 1 | None |
Q96F07 | CYFIP2 | S927 | ochoa | Cytoplasmic FMR1-interacting protein 2 (p53-inducible protein 121) | Involved in T-cell adhesion and p53/TP53-dependent induction of apoptosis. Does not bind RNA. As component of the WAVE1 complex, required for BDNF-NTRK2 endocytic trafficking and signaling from early endosomes (By similarity). {ECO:0000250|UniProtKB:Q5SQX6, ECO:0000269|PubMed:10449408, ECO:0000269|PubMed:15048733, ECO:0000269|PubMed:17245118}. |
Q96GX5 | MASTL | S217 | ochoa | Serine/threonine-protein kinase greatwall (GW) (GWL) (hGWL) (EC 2.7.11.1) (Microtubule-associated serine/threonine-protein kinase-like) (MAST-L) | Serine/threonine kinase that plays a key role in M phase by acting as a regulator of mitosis entry and maintenance (PubMed:19680222). Acts by promoting the inactivation of protein phosphatase 2A (PP2A) during M phase: does not directly inhibit PP2A but acts by mediating phosphorylation and subsequent activation of ARPP19 and ENSA at 'Ser-62' and 'Ser-67', respectively (PubMed:38123684). ARPP19 and ENSA are phosphatase inhibitors that specifically inhibit the PPP2R2D (PR55-delta) subunit of PP2A. Inactivation of PP2A during M phase is essential to keep cyclin-B1-CDK1 activity high (PubMed:20818157). Following DNA damage, it is also involved in checkpoint recovery by being inhibited. Phosphorylates histone protein in vitro; however such activity is unsure in vivo. May be involved in megakaryocyte differentiation. {ECO:0000269|PubMed:12890928, ECO:0000269|PubMed:19680222, ECO:0000269|PubMed:19793917, ECO:0000269|PubMed:20538976, ECO:0000269|PubMed:20818157, ECO:0000269|PubMed:38123684}. |
Q96J92 | WNK4 | S1022 | psp | Serine/threonine-protein kinase WNK4 (EC 2.7.11.1) (Protein kinase lysine-deficient 4) (Protein kinase with no lysine 4) | Serine/threonine-protein kinase component of the WNK4-SPAK/OSR1 kinase cascade, which acts as a key regulator of ion transport in the distal nephron and blood pressure (By similarity). The WNK4-SPAK/OSR1 kinase cascade is composed of WNK4, which mediates phosphorylation and activation of downstream kinases OXSR1/OSR1 and STK39/SPAK (PubMed:16832045). Following activation, OXSR1/OSR1 and STK39/SPAK catalyze phosphorylation of ion cotransporters, such as SLC12A1/NKCC2, SLC12A2/NKCC1, SLC12A3/NCC, SLC12A5/KCC2 or SLC12A6/KCC3, regulating their activity (PubMed:16832045, PubMed:22989884). Acts as a molecular switch that regulates the balance between renal salt reabsorption and K(+) secretion by modulating the activities of renal transporters and channels, including the Na-Cl cotransporter SLC12A3/NCC and the K(+) channel, KCNJ1/ROMK (By similarity). Regulates NaCl reabsorption in the distal nephron by activating the thiazide-sensitive Na-Cl cotransporter SLC12A3/NCC in distal convoluted tubule cells of kidney: activates SLC12A3/NCC in a OXSR1/OSR1- and STK39/SPAK-dependent process (By similarity). Also acts as a scaffold protein independently of its protein kinase activity: negatively regulates cell membrane localization of various transporters and channels (CFTR, KCNJ1/ROMK, SLC4A4, SLC26A9 and TRPV4) by clathrin-dependent endocytosis (By similarity). Also inhibits the activity of the epithelial Na(+) channel (ENaC) SCNN1A, SCNN1B, SCNN1D in a inase-independent mechanism (By similarity). May also phosphorylate NEDD4L (PubMed:20525693). {ECO:0000250|UniProtKB:Q80UE6, ECO:0000269|PubMed:16832045, ECO:0000269|PubMed:20525693, ECO:0000269|PubMed:22989884}. |
Q96L91 | EP400 | S3132 | ochoa | E1A-binding protein p400 (EC 3.6.4.-) (CAG repeat protein 32) (Domino homolog) (hDomino) (Trinucleotide repeat-containing gene 12 protein) (p400 kDa SWI2/SNF2-related protein) | Component of the NuA4 histone acetyltransferase complex which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histones H4 and H2A. This modification may both alter nucleosome - DNA interactions and promote interaction of the modified histones with other proteins which positively regulate transcription. May be required for transcriptional activation of E2F1 and MYC target genes during cellular proliferation. The NuA4 complex ATPase and helicase activities seem to be, at least in part, contributed by the association of RUVBL1 and RUVBL2 with EP400. May regulate ZNF42 transcription activity. Component of a SWR1-like complex that specifically mediates the removal of histone H2A.Z/H2AZ1 from the nucleosome. {ECO:0000269|PubMed:14966270, ECO:0000269|PubMed:24463511}. |
Q96MG2 | JSRP1 | S166 | ochoa | Junctional sarcoplasmic reticulum protein 1 (Junctional-face membrane protein of 45 kDa homolog) (JP-45) | Involved in skeletal muscle excitation/contraction coupling (EC), probably acting as a regulator of the voltage-sensitive calcium channel CACNA1S. EC is a physiological process whereby an electrical signal (depolarization of the plasma membrane) is converted into a chemical signal, a calcium gradient, by the opening of ryanodine receptor calcium release channels. May regulate CACNA1S membrane targeting and activity. {ECO:0000269|PubMed:22927026}. |
Q96QS3 | ARX | S174 | psp | Homeobox protein ARX (Aristaless-related homeobox) | Transcription factor (PubMed:22194193, PubMed:31691806). Binds to specific sequence motif 5'-TAATTA-3' in regulatory elements of target genes, such as histone demethylase KDM5C (PubMed:22194193, PubMed:31691806). Positively modulates transcription of KDM5C (PubMed:31691806). Activates expression of KDM5C synergistically with histone lysine demethylase PHF8 and perhaps in competition with transcription regulator ZNF711; synergy may be related to enrichment of histone H3K4me3 in regulatory elements (PubMed:31691806). Required for normal brain development (PubMed:11889467, PubMed:12379852, PubMed:14722918). Plays a role in neuronal proliferation, interneuronal migration and differentiation in the embryonic forebrain (By similarity). May also be involved in axonal guidance in the floor plate (By similarity). {ECO:0000250|UniProtKB:O35085, ECO:0000269|PubMed:11889467, ECO:0000269|PubMed:12379852, ECO:0000269|PubMed:14722918, ECO:0000269|PubMed:22194193, ECO:0000269|PubMed:31691806}. |
Q99708 | RBBP8 | S243 | ochoa | DNA endonuclease RBBP8 (EC 3.1.-.-) (CtBP-interacting protein) (CtIP) (Retinoblastoma-binding protein 8) (RBBP-8) (Retinoblastoma-interacting protein and myosin-like) (RIM) (Sporulation in the absence of SPO11 protein 2 homolog) (SAE2) | Endonuclease that cooperates with the MRE11-RAD50-NBN (MRN) complex in DNA-end resection, the first step of double-strand break (DSB) repair through the homologous recombination (HR) pathway (PubMed:17965729, PubMed:19202191, PubMed:19759395, PubMed:20064462, PubMed:23273981, PubMed:26721387, PubMed:27814491, PubMed:27889449, PubMed:30787182). HR is restricted to S and G2 phases of the cell cycle and preferentially repairs DSBs resulting from replication fork collapse (PubMed:17965729, PubMed:19202191, PubMed:23273981, PubMed:27814491, PubMed:27889449, PubMed:30787182). Key determinant of DSB repair pathway choice, as it commits cells to HR by preventing classical non-homologous end-joining (NHEJ) (PubMed:19202191). Specifically promotes the endonuclease activity of the MRN complex to clear DNA ends containing protein adducts: recruited to DSBs by NBN following phosphorylation by CDK1, and promotes the endonuclease activity of MRE11 to clear protein-DNA adducts and generate clean double-strand break ends (PubMed:27814491, PubMed:27889449, PubMed:30787182, PubMed:33836577). Functions downstream of the MRN complex and ATM, promotes ATR activation and its recruitment to DSBs in the S/G2 phase facilitating the generation of ssDNA (PubMed:16581787, PubMed:17965729, PubMed:19759395, PubMed:20064462). Component of the BRCA1-RBBP8 complex that regulates CHEK1 activation and controls cell cycle G2/M checkpoints on DNA damage (PubMed:15485915, PubMed:16818604). During immunoglobulin heavy chain class-switch recombination, promotes microhomology-mediated alternative end joining (A-NHEJ) and plays an essential role in chromosomal translocations (By similarity). Binds preferentially to DNA Y-junctions and to DNA substrates with blocked ends and promotes intermolecular DNA bridging (PubMed:30601117). {ECO:0000250|UniProtKB:Q80YR6, ECO:0000269|PubMed:15485915, ECO:0000269|PubMed:16581787, ECO:0000269|PubMed:16818604, ECO:0000269|PubMed:17965729, ECO:0000269|PubMed:19202191, ECO:0000269|PubMed:19759395, ECO:0000269|PubMed:20064462, ECO:0000269|PubMed:23273981, ECO:0000269|PubMed:26721387, ECO:0000269|PubMed:27814491, ECO:0000269|PubMed:27889449, ECO:0000269|PubMed:30601117, ECO:0000269|PubMed:30787182, ECO:0000269|PubMed:33836577}. |
Q9BSJ5 | MTNAP1 | S442 | ochoa | Mitochondrial nucleoid-associated protein 1 (Cell migration-inducing gene 3 protein) (Human lung cancer oncogene 8 protein) (HLC-8) (Protein C17orf80) | Critical regulator of mitochondrial DNA (mtDNA) abundance (PubMed:37676315). Binds dsDNA throughout the mitochondrial genome without sequence specificity and controls mtDNA copy number by promoting its replication (PubMed:37676315). Also plays important roles in mitochondrial metabolism and cell proliferation (PubMed:37676315). {ECO:0000269|PubMed:37676315}. |
Q9BX66 | SORBS1 | S143 | ochoa | Sorbin and SH3 domain-containing protein 1 (Ponsin) (SH3 domain protein 5) (SH3P12) (c-Cbl-associated protein) (CAP) | Plays a role in tyrosine phosphorylation of CBL by linking CBL to the insulin receptor. Required for insulin-stimulated glucose transport. Involved in formation of actin stress fibers and focal adhesions (By similarity). {ECO:0000250|UniProtKB:Q62417}. |
Q9C0D6 | FHDC1 | S723 | ochoa | FH2 domain-containing protein 1 (Inverted formin-1) | Microtubule-associated formin which regulates both actin and microtubule dynamics. Induces microtubule acetylation and stabilization and actin stress fiber formation (PubMed:18815276). Regulates Golgi ribbon formation (PubMed:26564798). Required for normal cilia assembly. Early in cilia assembly, may assist in the maturation and positioning of the centrosome/basal body, and once cilia assembly has initiated, may also promote cilia elongation by inhibiting disassembly (PubMed:29742020). {ECO:0000269|PubMed:18815276, ECO:0000269|PubMed:26564798, ECO:0000269|PubMed:29742020}. |
Q9H792 | PEAK1 | S1005 | 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}. |
Q9HCD5 | NCOA5 | S416 | ochoa | Nuclear receptor coactivator 5 (NCoA-5) (Coactivator independent of AF-2) (CIA) | Nuclear receptor coregulator that can have both coactivator and corepressor functions. Interacts with nuclear receptors for steroids (ESR1 and ESR2) independently of the steroid binding domain (AF-2) of the ESR receptors, and with the orphan nuclear receptor NR1D2. Involved in the coactivation of nuclear steroid receptors (ER) as well as the corepression of MYC in response to 17-beta-estradiol (E2). {ECO:0000269|PubMed:15073177}. |
Q9HCJ0 | TNRC6C | S714 | ochoa | Trinucleotide repeat-containing gene 6C protein | Plays a role in RNA-mediated gene silencing by micro-RNAs (miRNAs). Required for miRNA-dependent translational repression of complementary mRNAs by argonaute family proteins. As scaffoldng protein associates with argonaute proteins bound to partially complementary mRNAs and simultaneously can recruit CCR4-NOT and PAN deadenylase complexes. {ECO:0000269|PubMed:19304925, ECO:0000269|PubMed:21981923, ECO:0000269|PubMed:21984184, ECO:0000269|PubMed:21984185}. |
Q9NQ75 | CASS4 | S232 | ochoa | Cas scaffolding protein family member 4 (HEF-like protein) (HEF1-EFS-p130Cas-like protein) (HEPL) | Docking protein that plays a role in tyrosine kinase-based signaling related to cell adhesion and cell spreading. Regulates PTK2/FAK1 activity, focal adhesion integrity, and cell spreading. {ECO:0000269|PubMed:18256281}. |
Q9NQV6 | PRDM10 | S803 | ochoa | PR domain zinc finger protein 10 (PR domain-containing protein 10) (Tristanin) | Transcriptional activator, essential for early embryonic development and survival of embryonic stem cells (ESCs) (By similarity). Supports cell growth and survival during early development by transcriptionally activating the expression of the translation initiation factor EIF3B, to sustain global translation (By similarity). Activates the transcription of FLNC (PubMed:36440963). {ECO:0000250|UniProtKB:Q3UTQ7, ECO:0000269|PubMed:36440963}. |
Q9UBU3 | GHRL | S41 | psp | Appetite-regulating hormone (Growth hormone secretagogue) (Growth hormone-releasing peptide) (Motilin-related peptide) (Protein M46) [Cleaved into: Ghrelin-27; Ghrelin-28 (Ghrelin); Obestatin] | [Ghrelin-27]: Ghrelin is the ligand for growth hormone secretagogue receptor type 1 (GHSR) (PubMed:10604470). Induces the release of growth hormone from the pituitary (PubMed:10604470). Has an appetite-stimulating effect, induces adiposity and stimulates gastric acid secretion. Involved in growth regulation. {ECO:0000269|PubMed:10604470}.; FUNCTION: [Ghrelin-28]: Ghrelin is the ligand for growth hormone secretagogue receptor type 1 (GHSR) (PubMed:10604470). Induces the release of growth hormone from the pituitary (PubMed:10604470). Has an appetite-stimulating effect, induces adiposity and stimulates gastric acid secretion. Involved in growth regulation. {ECO:0000269|PubMed:10604470}.; FUNCTION: [Obestatin]: May be the ligand for GPR39. May have an appetite-reducing effect resulting in decreased food intake. May reduce gastric emptying activity and jejunal motility (By similarity). {ECO:0000250}. |
Q9UBY9 | HSPB7 | S49 | ochoa | Heat shock protein beta-7 (HspB7) (Cardiovascular heat shock protein) (cvHsp) | None |
Q9UHR6 | ZNHIT2 | S165 | ochoa | Zinc finger HIT domain-containing protein 2 (Protein FON) | May act as a bridging factor mediating the interaction between the R2TP/Prefoldin-like (R2TP/PFDL) complex and U5 small nuclear ribonucleoprotein (U5 snRNP) (PubMed:28561026). Required for the interaction of R2TP complex subunit RPAP3 and prefoldin-like subunit URI1 with U5 snRNP proteins EFTUD2 and PRPF8 (PubMed:28561026). May play a role in regulating the composition of the U5 snRNP complex (PubMed:28561026). {ECO:0000269|PubMed:28561026}. |
Q9UHX1 | PUF60 | S41 | ochoa | Poly(U)-binding-splicing factor PUF60 (60 kDa poly(U)-binding-splicing factor) (FUSE-binding protein-interacting repressor) (FBP-interacting repressor) (Ro-binding protein 1) (RoBP1) (Siah-binding protein 1) (Siah-BP1) | DNA- and RNA-binding protein, involved in several nuclear processes such as pre-mRNA splicing, apoptosis and transcription regulation. In association with FUBP1 regulates MYC transcription at the P2 promoter through the core-TFIIH basal transcription factor. Acts as a transcriptional repressor through the core-TFIIH basal transcription factor. Represses FUBP1-induced transcriptional activation but not basal transcription. Decreases ERCC3 helicase activity. Does not repress TFIIH-mediated transcription in xeroderma pigmentosum complementation group B (XPB) cells. Is also involved in pre-mRNA splicing. Promotes splicing of an intron with weak 3'-splice site and pyrimidine tract in a cooperative manner with U2AF2. Involved in apoptosis induction when overexpressed in HeLa cells. Isoform 6 failed to repress MYC transcription and inhibited FIR-induced apoptosis in colorectal cancer. Isoform 6 may contribute to tumor progression by enabling increased MYC expression and greater resistance to apoptosis in tumors than in normal cells. Modulates alternative splicing of several mRNAs. Binds to relaxed DNA of active promoter regions. Binds to the pyrimidine tract and 3'-splice site regions of pre-mRNA; binding is enhanced in presence of U2AF2. Binds to Y5 RNA in association with RO60. Binds to poly(U) RNA. {ECO:0000269|PubMed:10606266, ECO:0000269|PubMed:10882074, ECO:0000269|PubMed:11239393, ECO:0000269|PubMed:16452196, ECO:0000269|PubMed:16628215, ECO:0000269|PubMed:17579712}. |
Q9UMS6 | SYNPO2 | S804 | ochoa | Synaptopodin-2 (Genethonin-2) (Myopodin) | Has an actin-binding and actin-bundling activity. Can induce the formation of F-actin networks in an isoform-specific manner (PubMed:23225103, PubMed:24005909). At the sarcomeric Z lines is proposed to act as adapter protein that links nascent myofibers to the sarcolemma via ZYX and may play a role in early assembly and stabilization of the Z lines. Involved in autophagosome formation. May play a role in chaperone-assisted selective autophagy (CASA) involved in Z lines maintenance in striated muscle under mechanical tension; may link the client-processing CASA chaperone machinery to a membrane-tethering and fusion complex providing autophagosome membranes (By similarity). Involved in regulation of cell migration (PubMed:22915763, PubMed:25883213). May be a tumor suppressor (PubMed:16885336). {ECO:0000250|UniProtKB:D4A702, ECO:0000250|UniProtKB:Q91YE8, ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:23225103, ECO:0000269|PubMed:24005909, ECO:0000269|PubMed:25883213, ECO:0000305|PubMed:16885336, ECO:0000305|PubMed:20554076}.; FUNCTION: [Isoform 1]: Involved in regulation of cell migration. Can induce formation of thick, irregular actin bundles in the cell body. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 2]: Involved in regulation of cell migration. Can induce long, well-organized actin bundles frequently orientated in parallel along the long axis of the cell showing characteristics of contractile ventral stress fibers. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 3]: Involved in regulation of cell migration. Can induce an amorphous actin meshwork throughout the cell body containing a mixture of long and short, randomly organized thick and thin actin bundles. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 4]: Can induce long, well-organized actin bundles frequently orientated in parallel along the long axis of the cell showing characteristics of contractile ventral stress fibers. {ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 5]: Involved in regulation of cell migration in part dependent on the Rho-ROCK cascade; can promote formation of nascent focal adhesions, actin bundles at the leading cell edge and lamellipodia (PubMed:22915763, PubMed:25883213). Can induce formation of thick, irregular actin bundles in the cell body; the induced actin network is associated with enhanced cell migration in vitro. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909, ECO:0000269|PubMed:25883213}. |
Q9UMS6 | SYNPO2 | S847 | ochoa | Synaptopodin-2 (Genethonin-2) (Myopodin) | Has an actin-binding and actin-bundling activity. Can induce the formation of F-actin networks in an isoform-specific manner (PubMed:23225103, PubMed:24005909). At the sarcomeric Z lines is proposed to act as adapter protein that links nascent myofibers to the sarcolemma via ZYX and may play a role in early assembly and stabilization of the Z lines. Involved in autophagosome formation. May play a role in chaperone-assisted selective autophagy (CASA) involved in Z lines maintenance in striated muscle under mechanical tension; may link the client-processing CASA chaperone machinery to a membrane-tethering and fusion complex providing autophagosome membranes (By similarity). Involved in regulation of cell migration (PubMed:22915763, PubMed:25883213). May be a tumor suppressor (PubMed:16885336). {ECO:0000250|UniProtKB:D4A702, ECO:0000250|UniProtKB:Q91YE8, ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:23225103, ECO:0000269|PubMed:24005909, ECO:0000269|PubMed:25883213, ECO:0000305|PubMed:16885336, ECO:0000305|PubMed:20554076}.; FUNCTION: [Isoform 1]: Involved in regulation of cell migration. Can induce formation of thick, irregular actin bundles in the cell body. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 2]: Involved in regulation of cell migration. Can induce long, well-organized actin bundles frequently orientated in parallel along the long axis of the cell showing characteristics of contractile ventral stress fibers. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 3]: Involved in regulation of cell migration. Can induce an amorphous actin meshwork throughout the cell body containing a mixture of long and short, randomly organized thick and thin actin bundles. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 4]: Can induce long, well-organized actin bundles frequently orientated in parallel along the long axis of the cell showing characteristics of contractile ventral stress fibers. {ECO:0000269|PubMed:24005909}.; FUNCTION: [Isoform 5]: Involved in regulation of cell migration in part dependent on the Rho-ROCK cascade; can promote formation of nascent focal adhesions, actin bundles at the leading cell edge and lamellipodia (PubMed:22915763, PubMed:25883213). Can induce formation of thick, irregular actin bundles in the cell body; the induced actin network is associated with enhanced cell migration in vitro. {ECO:0000269|PubMed:22915763, ECO:0000269|PubMed:24005909, ECO:0000269|PubMed:25883213}. |
Q9UPS6 | SETD1B | S375 | ochoa | Histone-lysine N-methyltransferase SETD1B (EC 2.1.1.364) (Lysine N-methyltransferase 2G) (SET domain-containing protein 1B) (hSET1B) | Histone methyltransferase that catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) via a non-processive mechanism (PubMed:17355966, PubMed:25561738). Part of chromatin remodeling machinery, forms H3K4me1, H3K4me2 and H3K4me3 methylation marks at active chromatin sites where transcription and DNA repair take place (PubMed:17355966, PubMed:25561738). Plays an essential role in regulating the transcriptional programming of multipotent hematopoietic progenitor cells and lymphoid lineage specification during hematopoiesis (By similarity). {ECO:0000250|UniProtKB:Q8CFT2, ECO:0000269|PubMed:17355966, ECO:0000269|PubMed:25561738}. |
Q9Y2H2 | INPP5F | S881 | ochoa | Phosphatidylinositide phosphatase SAC2 (EC 3.1.3.25) (Inositol polyphosphate 5-phosphatase F) (Sac domain-containing inositol phosphatase 2) (Sac domain-containing phosphoinositide 4-phosphatase 2) (hSAC2) | Inositol 4-phosphatase which mainly acts on phosphatidylinositol 4-phosphate. May be functionally linked to OCRL, which converts phosphatidylinositol 4,5-bisphosphate to phosphatidylinositol, for a sequential dephosphorylation of phosphatidylinositol 4,5-bisphosphate at the 5 and 4 position of inositol, thus playing an important role in the endocytic recycling (PubMed:25869669). Regulator of TF:TFRC and integrins recycling pathway, is also involved in cell migration mechanisms (PubMed:25869669). Modulates AKT/GSK3B pathway by decreasing AKT and GSK3B phosphorylation (PubMed:17322895). Negatively regulates STAT3 signaling pathway through inhibition of STAT3 phosphorylation and translocation to the nucleus (PubMed:25476455). Functionally important modulator of cardiac myocyte size and of the cardiac response to stress (By similarity). May play a role as negative regulator of axon regeneration after central nervous system injuries (By similarity). {ECO:0000250|UniProtKB:Q8CDA1, ECO:0000269|PubMed:17322895, ECO:0000269|PubMed:25476455, ECO:0000269|PubMed:25869669}. |
Q9Y3Q8 | TSC22D4 | S150 | ochoa | TSC22 domain family protein 4 (TSC22-related-inducible leucine zipper protein 2) | Binds DNA and acts as a transcriptional repressor (PubMed:10488076). Involved in the regulation of systematic glucose homeostasis and insulin sensitivity, via transcriptional repression of downstream insulin signaling targets such as OBP2A/LCN13 (By similarity). Acts as a negative regulator of lipogenic gene expression in hepatocytes and thereby mediates the control of very low-density lipoprotein release (PubMed:23307490). May play a role in neurite elongation and survival (By similarity). {ECO:0000250|UniProtKB:Q9EQN3, ECO:0000269|PubMed:10488076, ECO:0000269|PubMed:23307490}. |
P35998 | PSMC2 | S89 | Sugiyama | 26S proteasome regulatory subunit 7 (26S proteasome AAA-ATPase subunit RPT1) (Proteasome 26S subunit ATPase 2) | Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. PSMC2 belongs to the heterohexameric ring of AAA (ATPases associated with diverse cellular activities) proteins that unfolds ubiquitinated target proteins that are concurrently translocated into a proteolytic chamber and degraded into peptides. {ECO:0000269|PubMed:1317798, ECO:0000269|PubMed:28539385, ECO:0000269|PubMed:9295362}. |
P31327 | CPS1 | S819 | Sugiyama | Carbamoyl-phosphate synthase [ammonia], mitochondrial (EC 6.3.4.16) (Carbamoyl-phosphate synthetase I) (CPSase I) | Involved in the urea cycle of ureotelic animals where the enzyme plays an important role in removing excess ammonia from the cell. |
P31939 | ATIC | S202 | Sugiyama | Bifunctional purine biosynthesis protein ATIC (AICAR transformylase/inosine monophosphate cyclohydrolase) (ATIC) [Cleaved into: Bifunctional purine biosynthesis protein ATIC, N-terminally processed] [Includes: Phosphoribosylaminoimidazolecarboxamide formyltransferase (EC 2.1.2.3) (5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase) (AICAR formyltransferase) (AICAR transformylase); Inosine 5'-monophosphate cyclohydrolase (IMP cyclohydrolase) (EC 3.5.4.10) (IMP synthase) (Inosinicase)] | Bifunctional enzyme that catalyzes the last two steps of purine biosynthesis (PubMed:11948179, PubMed:14756554). Acts as a transformylase that incorporates a formyl group to the AMP analog AICAR (5-amino-1-(5-phospho-beta-D-ribosyl)imidazole-4-carboxamide) to produce the intermediate formyl-AICAR (FAICAR) (PubMed:10985775, PubMed:11948179, PubMed:9378707). Can use both 10-formyldihydrofolate and 10-formyltetrahydrofolate as the formyl donor in this reaction (PubMed:10985775). Also catalyzes the cyclization of FAICAR to inosine monophosphate (IMP) (PubMed:11948179, PubMed:14756554). Is able to convert thio-AICAR to 6-mercaptopurine ribonucleotide, an inhibitor of purine biosynthesis used in the treatment of human leukemias (PubMed:10985775). Promotes insulin receptor/INSR autophosphorylation and is involved in INSR internalization (PubMed:25687571). {ECO:0000269|PubMed:10985775, ECO:0000269|PubMed:11948179, ECO:0000269|PubMed:14756554, ECO:0000269|PubMed:25687571, ECO:0000269|PubMed:9378707}. |
O75689 | ADAP1 | S87 | SIGNOR|iPTMNet|EPSD|PSP | Arf-GAP with dual PH domain-containing protein 1 (Centaurin-alpha-1) (Cnt-a1) (Putative MAPK-activating protein PM25) | GTPase-activating protein for the ADP ribosylation factor family (Probable). Binds phosphatidylinositol 3,4,5-trisphosphate (PtdInsP3) and inositol 1,3,4,5-tetrakisphosphate (InsP4). Regulates the incorporation of CD63 and CD9 into multivesicular bodies (PubMed:38682696). {ECO:0000269|PubMed:10448098, ECO:0000269|PubMed:38682696, ECO:0000303|PubMed:10333475, ECO:0000305}. |
Q6ZN44 | UNC5A | S352 | SIGNOR | Netrin receptor UNC5A (Protein unc-5 homolog 1) (Protein unc-5 homolog A) | Receptor for netrin required for axon guidance. Functions in the netrin signaling pathway and promotes neurite outgrowth in response to NTN1. Mediates axon repulsion of neuronal growth cones in the developing nervous system in response to netrin. Axon repulsion in growth cones may be mediated by its association with DCC that may trigger signaling for repulsion. It also acts as a dependence receptor required for apoptosis induction when not associated with netrin ligand. {ECO:0000250|UniProtKB:O08721}. |
P51813 | BMX | S381 | 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}. |
P51957 | NEK4 | S379 | Sugiyama | Serine/threonine-protein kinase Nek4 (EC 2.7.11.1) (Never in mitosis A-related kinase 4) (NimA-related protein kinase 4) (Serine/threonine-protein kinase 2) (Serine/threonine-protein kinase NRK2) | Protein kinase that seems to act exclusively upon threonine residues (By similarity). Required for normal entry into proliferative arrest after a limited number of cell divisions, also called replicative senescence. Required for normal cell cycle arrest in response to double-stranded DNA damage. {ECO:0000250|UniProtKB:Q9Z1J2, ECO:0000269|PubMed:22851694}. |
Q92793 | CREBBP | S302 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CREB-binding protein (Histone lysine acetyltransferase CREBBP) (EC 2.3.1.48) (Protein lactyltransferas CREBBP) (EC 2.3.1.-) (Protein-lysine acetyltransferase CREBBP) (EC 2.3.1.-) | Acetylates histones, giving a specific tag for transcriptional activation (PubMed:21131905, PubMed:24616510). Mediates acetylation of histone H3 at 'Lys-18' and 'Lys-27' (H3K18ac and H3K27ac, respectively) (PubMed:21131905). Also acetylates non-histone proteins, like DDX21, FBL, IRF2, MAFG, NCOA3, POLR1E/PAF53 and FOXO1 (PubMed:10490106, PubMed:11154691, PubMed:12738767, PubMed:12929931, PubMed:24207024, PubMed:28790157, PubMed:30540930, PubMed:35675826, PubMed:9707565). Binds specifically to phosphorylated CREB and enhances its transcriptional activity toward cAMP-responsive genes. Acts as a coactivator of ALX1. Acts as a circadian transcriptional coactivator which enhances the activity of the circadian transcriptional activators: NPAS2-BMAL1 and CLOCK-BMAL1 heterodimers (PubMed:14645221). Acetylates PCNA; acetylation promotes removal of chromatin-bound PCNA and its degradation during nucleotide excision repair (NER) (PubMed:24939902). Acetylates POLR1E/PAF53, leading to decreased association of RNA polymerase I with the rDNA promoter region and coding region (PubMed:24207024). Acetylates DDX21, thereby inhibiting DDX21 helicase activity (PubMed:28790157). Acetylates FBL, preventing methylation of 'Gln-105' of histone H2A (H2AQ104me) (PubMed:30540930). In addition to protein acetyltransferase, can use different acyl-CoA substrates, such as lactoyl-CoA, and is able to mediate protein lactylation (PubMed:38128537). Catalyzes lactylation of MRE11 in response to DNA damage, thereby promoting DNA double-strand breaks (DSBs) via homologous recombination (HR) (PubMed:38128537). Functions as a transcriptional coactivator for SMAD4 in the TGF-beta signaling pathway (PubMed:25514493). {ECO:0000269|PubMed:10490106, ECO:0000269|PubMed:11154691, ECO:0000269|PubMed:12738767, ECO:0000269|PubMed:12929931, ECO:0000269|PubMed:14645221, ECO:0000269|PubMed:21131905, ECO:0000269|PubMed:24207024, ECO:0000269|PubMed:24616510, ECO:0000269|PubMed:24939902, ECO:0000269|PubMed:25514493, ECO:0000269|PubMed:28790157, ECO:0000269|PubMed:30540930, ECO:0000269|PubMed:35675826, ECO:0000269|PubMed:38128537, ECO:0000269|PubMed:9707565}. |
Q9BVC4 | MLST8 | S43 | Sugiyama | Target of rapamycin complex subunit LST8 (TORC subunit LST8) (G protein beta subunit-like) (Gable) (Protein GbetaL) (Mammalian lethal with SEC13 protein 8) (mLST8) | Subunit of both mTORC1 and mTORC2, which regulates cell growth and survival in response to nutrient and hormonal signals (PubMed:12718876, PubMed:15268862, PubMed:15467718, PubMed:24403073, PubMed:28489822). mTORC1 is activated in response to growth factors or amino acids (PubMed:12718876, PubMed:15268862, PubMed:15467718, PubMed:24403073). In response to nutrients, mTORC1 is recruited to the lysosome membrane and promotes protein, lipid and nucleotide synthesis by phosphorylating several substrates, such as ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1) (PubMed:12718876, PubMed:15268862, PubMed:15467718, PubMed:24403073). In the same time, it inhibits catabolic pathways by phosphorylating the autophagy initiation components ULK1 and ATG13, as well as transcription factor TFEB, a master regulators of lysosomal biogenesis and autophagy (PubMed:24403073). The mTORC1 complex is inhibited in response to starvation and amino acid depletion (PubMed:24403073). Within mTORC1, MLST8 interacts directly with MTOR and enhances its kinase activity (PubMed:12718876). In nutrient-poor conditions, stabilizes the MTOR-RPTOR interaction and favors RPTOR-mediated inhibition of MTOR activity (PubMed:12718876). As part of the mTORC2 complex, transduces signals from growth factors to pathways involved in proliferation, cytoskeletal organization, lipogenesis and anabolic output (PubMed:15467718, PubMed:35926713). mTORC2 is also activated by growth factors, but seems to be nutrient-insensitive (PubMed:15467718, PubMed:35926713). In response to growth factors, mTORC2 phosphorylates and activates AGC protein kinase family members, including AKT (AKT1, AKT2 and AKT3), PKC (PRKCA, PRKCB and PRKCE) and SGK1 (PubMed:15467718, PubMed:35926713). mTORC2 functions upstream of Rho GTPases to regulate the actin cytoskeleton, probably by activating one or more Rho-type guanine nucleotide exchange factors (PubMed:15467718). mTORC2 promotes the serum-induced formation of stress-fibers or F-actin (PubMed:15467718). mTORC2 plays a critical role in AKT1 activation by mediating phosphorylation of different sites depending on the context, such as 'Thr-450', 'Ser-473', 'Ser-477' or 'Thr-479', facilitating the phosphorylation of the activation loop of AKT1 on 'Thr-308' by PDPK1/PDK1 which is a prerequisite for full activation (PubMed:15467718). mTORC2 regulates the phosphorylation of SGK1 at 'Ser-422' (PubMed:15467718). mTORC2 also modulates the phosphorylation of PRKCA on 'Ser-657' (PubMed:15467718). Within mTORC2, MLST8 acts as a bridge between MAPKAP1/SIN1 and MTOR (PubMed:31085701). {ECO:0000269|PubMed:12718876, ECO:0000269|PubMed:15268862, ECO:0000269|PubMed:15467718, ECO:0000269|PubMed:24403073, ECO:0000269|PubMed:28489822, ECO:0000269|PubMed:31085701, ECO:0000269|PubMed:35926713}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-9701898 | STAT3 nuclear events downstream of ALK signaling | 0.000514 | 3.289 |
R-HSA-2025928 | Calcineurin activates NFAT | 0.000135 | 3.870 |
R-HSA-5607763 | CLEC7A (Dectin-1) induces NFAT activation | 0.000439 | 3.357 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 0.000393 | 3.406 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 0.000805 | 3.094 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 0.000881 | 3.055 |
R-HSA-422085 | Synthesis, secretion, and deacylation of Ghrelin | 0.001264 | 2.898 |
R-HSA-9854909 | Regulation of MITF-M dependent genes involved in invasion | 0.001504 | 2.823 |
R-HSA-9018519 | Estrogen-dependent gene expression | 0.001548 | 2.810 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 0.001813 | 2.741 |
R-HSA-9020958 | Interleukin-21 signaling | 0.004305 | 2.366 |
R-HSA-8985947 | Interleukin-9 signaling | 0.003637 | 2.439 |
R-HSA-1592230 | Mitochondrial biogenesis | 0.004264 | 2.370 |
R-HSA-1168372 | Downstream signaling events of B Cell Receptor (BCR) | 0.003749 | 2.426 |
R-HSA-2262752 | Cellular responses to stress | 0.004001 | 2.398 |
R-HSA-3247509 | Chromatin modifying enzymes | 0.004570 | 2.340 |
R-HSA-8939211 | ESR-mediated signaling | 0.004865 | 2.313 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 0.004474 | 2.349 |
R-HSA-4839748 | Signaling by AMER1 mutants | 0.006623 | 2.179 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 0.005493 | 2.260 |
R-HSA-201556 | Signaling by ALK | 0.006233 | 2.205 |
R-HSA-4839726 | Chromatin organization | 0.006194 | 2.208 |
R-HSA-8953750 | Transcriptional Regulation by E2F6 | 0.006233 | 2.205 |
R-HSA-5467343 | Deletions in the AMER1 gene destabilize the destruction complex | 0.007979 | 2.098 |
R-HSA-9818030 | NFE2L2 regulating tumorigenic genes | 0.008419 | 2.075 |
R-HSA-8983432 | Interleukin-15 signaling | 0.007496 | 2.125 |
R-HSA-6807070 | PTEN Regulation | 0.008729 | 2.059 |
R-HSA-1059683 | Interleukin-6 signaling | 0.008419 | 2.075 |
R-HSA-9711123 | Cellular response to chemical stress | 0.008828 | 2.054 |
R-HSA-918233 | TRAF3-dependent IRF activation pathway | 0.012582 | 1.900 |
R-HSA-9725371 | Nuclear events stimulated by ALK signaling in cancer | 0.010617 | 1.974 |
R-HSA-8953897 | Cellular responses to stimuli | 0.012050 | 1.919 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 0.011348 | 1.945 |
R-HSA-2892247 | POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | 0.012582 | 1.900 |
R-HSA-9634815 | Transcriptional Regulation by NPAS4 | 0.012761 | 1.894 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 0.011131 | 1.953 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 0.012869 | 1.890 |
R-HSA-211728 | Regulation of PAK-2p34 activity by PS-GAP/RHG10 | 0.015895 | 1.799 |
R-HSA-211736 | Stimulation of the cell death response by PAK-2p34 | 0.031540 | 1.501 |
R-HSA-8875791 | MET activates STAT3 | 0.039269 | 1.406 |
R-HSA-198745 | Signalling to STAT3 | 0.039269 | 1.406 |
R-HSA-9818035 | NFE2L2 regulating ER-stress associated genes | 0.046937 | 1.328 |
R-HSA-9818026 | NFE2L2 regulating inflammation associated genes | 0.054545 | 1.263 |
R-HSA-9706377 | FLT3 signaling by CBL mutants | 0.054545 | 1.263 |
R-HSA-176417 | Phosphorylation of Emi1 | 0.062092 | 1.207 |
R-HSA-9768778 | Regulation of NPAS4 mRNA translation | 0.084377 | 1.074 |
R-HSA-9818032 | NFE2L2 regulating MDR associated enzymes | 0.091688 | 1.038 |
R-HSA-933543 | NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 0.106136 | 0.974 |
R-HSA-9759811 | Regulation of CDH11 mRNA translation by microRNAs | 0.106136 | 0.974 |
R-HSA-5467340 | AXIN missense mutants destabilize the destruction complex | 0.106136 | 0.974 |
R-HSA-5467348 | Truncations of AMER1 destabilize the destruction complex | 0.106136 | 0.974 |
R-HSA-5467337 | APC truncation mutants have impaired AXIN binding | 0.106136 | 0.974 |
R-HSA-9931512 | Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | 0.113275 | 0.946 |
R-HSA-5339716 | Signaling by GSK3beta mutants | 0.113275 | 0.946 |
R-HSA-4839743 | Signaling by CTNNB1 phospho-site mutants | 0.120357 | 0.920 |
R-HSA-5358749 | CTNNB1 S37 mutants aren't phosphorylated | 0.120357 | 0.920 |
R-HSA-5358751 | CTNNB1 S45 mutants aren't phosphorylated | 0.120357 | 0.920 |
R-HSA-5358752 | CTNNB1 T41 mutants aren't phosphorylated | 0.120357 | 0.920 |
R-HSA-5358747 | CTNNB1 S33 mutants aren't phosphorylated | 0.120357 | 0.920 |
R-HSA-5685939 | HDR through MMEJ (alt-NHEJ) | 0.127382 | 0.895 |
R-HSA-211733 | Regulation of activated PAK-2p34 by proteasome mediated degradation | 0.035962 | 1.444 |
R-HSA-8948700 | Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 0.141267 | 0.850 |
R-HSA-196299 | Beta-catenin phosphorylation cascade | 0.141267 | 0.850 |
R-HSA-174113 | SCF-beta-TrCP mediated degradation of Emi1 | 0.045165 | 1.345 |
R-HSA-141405 | Inhibition of the proteolytic activity of APC/C required for the onset of anapha... | 0.154933 | 0.810 |
R-HSA-141430 | Inactivation of APC/C via direct inhibition of the APC/C complex | 0.154933 | 0.810 |
R-HSA-912631 | Regulation of signaling by CBL | 0.175028 | 0.757 |
R-HSA-174048 | APC/C:Cdc20 mediated degradation of Cyclin B | 0.175028 | 0.757 |
R-HSA-9709603 | Impaired BRCA2 binding to PALB2 | 0.175028 | 0.757 |
R-HSA-9909620 | Regulation of PD-L1(CD274) translation | 0.181620 | 0.741 |
R-HSA-9701193 | Defective homologous recombination repair (HRR) due to PALB2 loss of function | 0.181620 | 0.741 |
R-HSA-9704646 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.181620 | 0.741 |
R-HSA-9701192 | Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 0.181620 | 0.741 |
R-HSA-9704331 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.181620 | 0.741 |
R-HSA-179409 | APC-Cdc20 mediated degradation of Nek2A | 0.188160 | 0.725 |
R-HSA-174154 | APC/C:Cdc20 mediated degradation of Securin | 0.072486 | 1.140 |
R-HSA-76071 | RNA Polymerase III Transcription Initiation From Type 3 Promoter | 0.201085 | 0.697 |
R-HSA-8943723 | Regulation of PTEN mRNA translation | 0.207471 | 0.683 |
R-HSA-912526 | Interleukin receptor SHC signaling | 0.207471 | 0.683 |
R-HSA-174184 | Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 0.084106 | 1.075 |
R-HSA-179419 | APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of th... | 0.086495 | 1.063 |
R-HSA-5693554 | Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SD... | 0.220091 | 0.657 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 0.040421 | 1.393 |
R-HSA-141424 | Amplification of signal from the kinetochores | 0.040421 | 1.393 |
R-HSA-176409 | APC/C:Cdc20 mediated degradation of mitotic proteins | 0.091332 | 1.039 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 0.041489 | 1.382 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 0.060467 | 1.218 |
R-HSA-1989781 | PPARA activates gene expression | 0.051179 | 1.291 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 0.052953 | 1.276 |
R-HSA-176814 | Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 0.093781 | 1.028 |
R-HSA-933541 | TRAF6 mediated IRF7 activation | 0.049064 | 1.309 |
R-HSA-169911 | Regulation of Apoptosis | 0.045165 | 1.345 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 0.226326 | 0.645 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 0.103168 | 0.986 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 0.103168 | 0.986 |
R-HSA-451927 | Interleukin-2 family signaling | 0.055132 | 1.259 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 0.103168 | 0.986 |
R-HSA-2465910 | MASTL Facilitates Mitotic Progression | 0.091688 | 1.038 |
R-HSA-9839394 | TGFBR3 expression | 0.026036 | 1.584 |
R-HSA-9931521 | The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CL... | 0.154933 | 0.810 |
R-HSA-8941856 | RUNX3 regulates NOTCH signaling | 0.120357 | 0.920 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 0.132532 | 0.878 |
R-HSA-453276 | Regulation of mitotic cell cycle | 0.132532 | 0.878 |
R-HSA-6798695 | Neutrophil degranulation | 0.186121 | 0.730 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 0.205879 | 0.686 |
R-HSA-8849474 | PTK6 Activates STAT3 | 0.054545 | 1.263 |
R-HSA-426496 | Post-transcriptional silencing by small RNAs | 0.054545 | 1.263 |
R-HSA-9764562 | Regulation of CDH1 mRNA translation by microRNAs | 0.134352 | 0.872 |
R-HSA-174178 | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins ... | 0.086495 | 1.063 |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | 0.028050 | 1.552 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 0.108851 | 0.963 |
R-HSA-8875360 | InlB-mediated entry of Listeria monocytogenes into host cell | 0.141267 | 0.850 |
R-HSA-2467813 | Separation of Sister Chromatids | 0.059426 | 1.226 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 0.095112 | 1.022 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 0.067100 | 1.173 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 0.067100 | 1.173 |
R-HSA-9020558 | Interleukin-2 signaling | 0.106136 | 0.974 |
R-HSA-8934593 | Regulation of RUNX1 Expression and Activity | 0.226326 | 0.645 |
R-HSA-1234158 | Regulation of gene expression by Hypoxia-inducible Factor | 0.113275 | 0.946 |
R-HSA-195253 | Degradation of beta-catenin by the destruction complex | 0.025292 | 1.597 |
R-HSA-4791275 | Signaling by WNT in cancer | 0.037738 | 1.423 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 0.224153 | 0.649 |
R-HSA-5689603 | UCH proteinases | 0.146153 | 0.835 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 0.211714 | 0.674 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 0.015836 | 1.800 |
R-HSA-8875513 | MET interacts with TNS proteins | 0.039269 | 1.406 |
R-HSA-165181 | Inhibition of TSC complex formation by PKB | 0.046937 | 1.328 |
R-HSA-418886 | Netrin mediated repulsion signals | 0.077008 | 1.113 |
R-HSA-9020933 | Interleukin-23 signaling | 0.084377 | 1.074 |
R-HSA-4839744 | Signaling by APC mutants | 0.106136 | 0.974 |
R-HSA-9818028 | NFE2L2 regulates pentose phosphate pathway genes | 0.113275 | 0.946 |
R-HSA-4839735 | Signaling by AXIN mutants | 0.113275 | 0.946 |
R-HSA-2559584 | Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 0.127382 | 0.895 |
R-HSA-399954 | Sema3A PAK dependent Axon repulsion | 0.141267 | 0.850 |
R-HSA-390471 | Association of TriC/CCT with target proteins during biosynthesis | 0.041388 | 1.383 |
R-HSA-9680350 | Signaling by CSF1 (M-CSF) in myeloid cells | 0.043261 | 1.364 |
R-HSA-73980 | RNA Polymerase III Transcription Termination | 0.168383 | 0.774 |
R-HSA-350054 | Notch-HLH transcription pathway | 0.201085 | 0.697 |
R-HSA-933542 | TRAF6 mediated NF-kB activation | 0.213806 | 0.670 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 0.047730 | 1.321 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 0.019854 | 1.702 |
R-HSA-8854691 | Interleukin-20 family signaling | 0.207471 | 0.683 |
R-HSA-1266695 | Interleukin-7 signaling | 0.026036 | 1.584 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 0.191376 | 0.718 |
R-HSA-9843745 | Adipogenesis | 0.114884 | 0.940 |
R-HSA-9700206 | Signaling by ALK in cancer | 0.015836 | 1.800 |
R-HSA-9617629 | Regulation of FOXO transcriptional activity by acetylation | 0.120357 | 0.920 |
R-HSA-9705462 | Inactivation of CSF3 (G-CSF) signaling | 0.194649 | 0.711 |
R-HSA-8939246 | RUNX1 regulates transcription of genes involved in differentiation of myeloid ce... | 0.084377 | 1.074 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 0.034220 | 1.466 |
R-HSA-6807004 | Negative regulation of MET activity | 0.181620 | 0.741 |
R-HSA-165159 | MTOR signalling | 0.061448 | 1.211 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 0.019136 | 1.718 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 0.226326 | 0.645 |
R-HSA-8876384 | Listeria monocytogenes entry into host cells | 0.194649 | 0.711 |
R-HSA-1257604 | PIP3 activates AKT signaling | 0.041938 | 1.377 |
R-HSA-9768759 | Regulation of NPAS4 gene expression | 0.013737 | 1.862 |
R-HSA-9670439 | Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT m... | 0.201085 | 0.697 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 0.124510 | 0.905 |
R-HSA-212165 | Epigenetic regulation of gene expression | 0.058620 | 1.232 |
R-HSA-512988 | Interleukin-3, Interleukin-5 and GM-CSF signaling | 0.061448 | 1.211 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 0.068339 | 1.165 |
R-HSA-8941855 | RUNX3 regulates CDKN1A transcription | 0.062092 | 1.207 |
R-HSA-428359 | Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RN... | 0.098941 | 1.005 |
R-HSA-9833109 | Evasion by RSV of host interferon responses | 0.035962 | 1.444 |
R-HSA-176407 | Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 0.161685 | 0.791 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 0.017744 | 1.751 |
R-HSA-5218920 | VEGFR2 mediated vascular permeability | 0.057210 | 1.243 |
R-HSA-9909396 | Circadian clock | 0.116598 | 0.933 |
R-HSA-8951664 | Neddylation | 0.129171 | 0.889 |
R-HSA-445355 | Smooth Muscle Contraction | 0.086495 | 1.063 |
R-HSA-389948 | Co-inhibition by PD-1 | 0.100160 | 0.999 |
R-HSA-749476 | RNA Polymerase III Abortive And Retractive Initiation | 0.047100 | 1.327 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 0.095112 | 1.022 |
R-HSA-449147 | Signaling by Interleukins | 0.075951 | 1.119 |
R-HSA-9818749 | Regulation of NFE2L2 gene expression | 0.069579 | 1.158 |
R-HSA-4641262 | Disassembly of the destruction complex and recruitment of AXIN to the membrane | 0.232512 | 0.634 |
R-HSA-9006925 | Intracellular signaling by second messengers | 0.071921 | 1.143 |
R-HSA-68882 | Mitotic Anaphase | 0.122291 | 0.913 |
R-HSA-74158 | RNA Polymerase III Transcription | 0.047100 | 1.327 |
R-HSA-5621575 | CD209 (DC-SIGN) signaling | 0.024509 | 1.611 |
R-HSA-1295596 | Spry regulation of FGF signaling | 0.141267 | 0.850 |
R-HSA-3928664 | Ephrin signaling | 0.168383 | 0.774 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 0.123654 | 0.908 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 0.056667 | 1.247 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 0.038327 | 1.416 |
R-HSA-2586552 | Signaling by Leptin | 0.098941 | 1.005 |
R-HSA-2559585 | Oncogene Induced Senescence | 0.045165 | 1.345 |
R-HSA-9839373 | Signaling by TGFBR3 | 0.070230 | 1.153 |
R-HSA-8849469 | PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | 0.084377 | 1.074 |
R-HSA-418889 | Caspase activation via Dependence Receptors in the absence of ligand | 0.091688 | 1.038 |
R-HSA-8866907 | Activation of the TFAP2 (AP-2) family of transcription factors | 0.091688 | 1.038 |
R-HSA-9020956 | Interleukin-27 signaling | 0.098941 | 1.005 |
R-HSA-428540 | Activation of RAC1 | 0.113275 | 0.946 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 0.032512 | 1.488 |
R-HSA-9945266 | Differentiation of T cells | 0.148127 | 0.829 |
R-HSA-9942503 | Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | 0.148127 | 0.829 |
R-HSA-9706369 | Negative regulation of FLT3 | 0.148127 | 0.829 |
R-HSA-210744 | Regulation of gene expression in late stage (branching morphogenesis) pancreatic... | 0.148127 | 0.829 |
R-HSA-1566977 | Fibronectin matrix formation | 0.154933 | 0.810 |
R-HSA-166208 | mTORC1-mediated signalling | 0.201085 | 0.697 |
R-HSA-3371571 | HSF1-dependent transactivation | 0.081739 | 1.088 |
R-HSA-1234174 | Cellular response to hypoxia | 0.116613 | 0.933 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 0.024282 | 1.615 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 0.224137 | 0.649 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 0.168123 | 0.774 |
R-HSA-9768777 | Regulation of NPAS4 gene transcription | 0.091688 | 1.038 |
R-HSA-9031628 | NGF-stimulated transcription | 0.074765 | 1.126 |
R-HSA-9762293 | Regulation of CDH11 gene transcription | 0.091688 | 1.038 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 0.039547 | 1.403 |
R-HSA-6783589 | Interleukin-6 family signaling | 0.024509 | 1.611 |
R-HSA-3134973 | LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 0.054545 | 1.263 |
R-HSA-164944 | Nef and signal transduction | 0.069579 | 1.158 |
R-HSA-111453 | BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members | 0.084377 | 1.074 |
R-HSA-9614657 | FOXO-mediated transcription of cell death genes | 0.168383 | 0.774 |
R-HSA-9824594 | Regulation of MITF-M-dependent genes involved in apoptosis | 0.188160 | 0.725 |
R-HSA-3214847 | HATs acetylate histones | 0.059179 | 1.228 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 0.074051 | 1.130 |
R-HSA-6806834 | Signaling by MET | 0.034312 | 1.465 |
R-HSA-68886 | M Phase | 0.222688 | 0.652 |
R-HSA-2871809 | FCERI mediated Ca+2 mobilization | 0.085807 | 1.066 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 0.020079 | 1.697 |
R-HSA-69620 | Cell Cycle Checkpoints | 0.073743 | 1.132 |
R-HSA-3371556 | Cellular response to heat stress | 0.095112 | 1.022 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 0.056644 | 1.247 |
R-HSA-389359 | CD28 dependent Vav1 pathway | 0.127382 | 0.895 |
R-HSA-9634638 | Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 0.207471 | 0.683 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 0.119231 | 0.924 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 0.135232 | 0.869 |
R-HSA-195721 | Signaling by WNT | 0.043561 | 1.361 |
R-HSA-168256 | Immune System | 0.080390 | 1.095 |
R-HSA-9669938 | Signaling by KIT in disease | 0.201085 | 0.697 |
R-HSA-8848021 | Signaling by PTK6 | 0.111423 | 0.953 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 0.111423 | 0.953 |
R-HSA-8877330 | RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | 0.127382 | 0.895 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 0.039367 | 1.405 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 0.229310 | 0.640 |
R-HSA-2980736 | Peptide hormone metabolism | 0.021634 | 1.665 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 0.137883 | 0.860 |
R-HSA-4086398 | Ca2+ pathway | 0.137945 | 0.860 |
R-HSA-9764790 | Positive Regulation of CDH1 Gene Transcription | 0.098941 | 1.005 |
R-HSA-9673770 | Signaling by PDGFRA extracellular domain mutants | 0.141267 | 0.850 |
R-HSA-9735871 | SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 0.141267 | 0.850 |
R-HSA-9673767 | Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 0.141267 | 0.850 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 0.085807 | 1.066 |
R-HSA-2559583 | Cellular Senescence | 0.022549 | 1.647 |
R-HSA-74160 | Gene expression (Transcription) | 0.014766 | 1.831 |
R-HSA-1280218 | Adaptive Immune System | 0.047239 | 1.326 |
R-HSA-447115 | Interleukin-12 family signaling | 0.042571 | 1.371 |
R-HSA-1236382 | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 0.188160 | 0.725 |
R-HSA-5637815 | Signaling by Ligand-Responsive EGFR Variants in Cancer | 0.188160 | 0.725 |
R-HSA-1433557 | Signaling by SCF-KIT | 0.063606 | 1.197 |
R-HSA-194138 | Signaling by VEGF | 0.103168 | 0.986 |
R-HSA-1433559 | Regulation of KIT signaling | 0.134352 | 0.872 |
R-HSA-70221 | Glycogen breakdown (glycogenolysis) | 0.220091 | 0.657 |
R-HSA-70635 | Urea cycle | 0.226326 | 0.645 |
R-HSA-3214842 | HDMs demethylate histones | 0.026036 | 1.584 |
R-HSA-9819196 | Zygotic genome activation (ZGA) | 0.188160 | 0.725 |
R-HSA-5357769 | Caspase activation via extrinsic apoptotic signalling pathway | 0.226326 | 0.645 |
R-HSA-5688426 | Deubiquitination | 0.179876 | 0.745 |
R-HSA-8984722 | Interleukin-35 Signalling | 0.120357 | 0.920 |
R-HSA-452723 | Transcriptional regulation of pluripotent stem cells | 0.051058 | 1.292 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 0.035175 | 1.454 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 0.034220 | 1.466 |
R-HSA-9013695 | NOTCH4 Intracellular Domain Regulates Transcription | 0.188160 | 0.725 |
R-HSA-389357 | CD28 dependent PI3K/Akt signaling | 0.232512 | 0.634 |
R-HSA-162582 | Signal Transduction | 0.059417 | 1.226 |
R-HSA-73857 | RNA Polymerase II Transcription | 0.055585 | 1.255 |
R-HSA-389356 | Co-stimulation by CD28 | 0.074765 | 1.126 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 0.047041 | 1.328 |
R-HSA-9793380 | Formation of paraxial mesoderm | 0.106296 | 0.973 |
R-HSA-212436 | Generic Transcription Pathway | 0.078133 | 1.107 |
R-HSA-6804757 | Regulation of TP53 Degradation | 0.047100 | 1.327 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 0.053081 | 1.275 |
R-HSA-9013694 | Signaling by NOTCH4 | 0.140669 | 0.852 |
R-HSA-9833482 | PKR-mediated signaling | 0.157248 | 0.803 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 0.220726 | 0.656 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 0.125308 | 0.902 |
R-HSA-1643713 | Signaling by EGFR in Cancer | 0.226326 | 0.645 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 0.033784 | 1.471 |
R-HSA-2022377 | Metabolism of Angiotensinogen to Angiotensins | 0.194649 | 0.711 |
R-HSA-9707564 | Cytoprotection by HMOX1 | 0.037302 | 1.428 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 0.108129 | 0.966 |
R-HSA-9006936 | Signaling by TGFB family members | 0.172022 | 0.764 |
R-HSA-75153 | Apoptotic execution phase | 0.070230 | 1.153 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 0.053081 | 1.275 |
R-HSA-109581 | Apoptosis | 0.015366 | 1.813 |
R-HSA-9671555 | Signaling by PDGFR in disease | 0.194649 | 0.711 |
R-HSA-168249 | Innate Immune System | 0.193119 | 0.714 |
R-HSA-6803204 | TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 0.232512 | 0.634 |
R-HSA-1660516 | Synthesis of PIPs at the early endosome membrane | 0.220091 | 0.657 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 0.200066 | 0.699 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 0.200066 | 0.699 |
R-HSA-9733709 | Cardiogenesis | 0.039547 | 1.403 |
R-HSA-1839117 | Signaling by cytosolic FGFR1 fusion mutants | 0.168383 | 0.774 |
R-HSA-982772 | Growth hormone receptor signaling | 0.207471 | 0.683 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 0.214637 | 0.668 |
R-HSA-983705 | Signaling by the B Cell Receptor (BCR) | 0.053853 | 1.269 |
R-HSA-163125 | Post-translational modification: synthesis of GPI-anchored proteins | 0.067100 | 1.173 |
R-HSA-5357801 | Programmed Cell Death | 0.035466 | 1.450 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 0.118242 | 0.927 |
R-HSA-1251985 | Nuclear signaling by ERBB4 | 0.055132 | 1.259 |
R-HSA-1368108 | BMAL1:CLOCK,NPAS2 activates circadian expression | 0.043261 | 1.364 |
R-HSA-5637812 | Signaling by EGFRvIII in Cancer | 0.161685 | 0.791 |
R-HSA-5637810 | Constitutive Signaling by EGFRvIII | 0.161685 | 0.791 |
R-HSA-5674400 | Constitutive Signaling by AKT1 E17K in Cancer | 0.207471 | 0.683 |
R-HSA-166520 | Signaling by NTRKs | 0.148991 | 0.827 |
R-HSA-390466 | Chaperonin-mediated protein folding | 0.179880 | 0.745 |
R-HSA-164952 | The role of Nef in HIV-1 replication and disease pathogenesis | 0.207471 | 0.683 |
R-HSA-9841251 | Mitochondrial unfolded protein response (UPRmt) | 0.029201 | 1.535 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 0.096662 | 1.015 |
R-HSA-8863678 | Neurodegenerative Diseases | 0.213806 | 0.670 |
R-HSA-8862803 | Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's dis... | 0.213806 | 0.670 |
R-HSA-9856651 | MITF-M-dependent gene expression | 0.152756 | 0.816 |
R-HSA-9734009 | Defective Intrinsic Pathway for Apoptosis | 0.232512 | 0.634 |
R-HSA-5633007 | Regulation of TP53 Activity | 0.172022 | 0.764 |
R-HSA-9707616 | Heme signaling | 0.108851 | 0.963 |
R-HSA-1236394 | Signaling by ERBB4 | 0.140669 | 0.852 |
R-HSA-391251 | Protein folding | 0.197161 | 0.705 |
R-HSA-8950505 | Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulati... | 0.116613 | 0.933 |
R-HSA-1483255 | PI Metabolism | 0.229310 | 0.640 |
R-HSA-381038 | XBP1(S) activates chaperone genes | 0.177023 | 0.752 |
R-HSA-381070 | IRE1alpha activates chaperones | 0.194266 | 0.712 |
R-HSA-9020591 | Interleukin-12 signaling | 0.146153 | 0.835 |
R-HSA-9833110 | RSV-host interactions | 0.238147 | 0.623 |
R-HSA-5654732 | Negative regulation of FGFR3 signaling | 0.238648 | 0.622 |
R-HSA-77387 | Insulin receptor recycling | 0.238648 | 0.622 |
R-HSA-68877 | Mitotic Prometaphase | 0.241799 | 0.617 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 0.244049 | 0.613 |
R-HSA-9709570 | Impaired BRCA2 binding to RAD51 | 0.244736 | 0.611 |
R-HSA-9674555 | Signaling by CSF3 (G-CSF) | 0.244736 | 0.611 |
R-HSA-5654733 | Negative regulation of FGFR4 signaling | 0.244736 | 0.611 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 0.248187 | 0.605 |
R-HSA-2672351 | Stimuli-sensing channels | 0.249957 | 0.602 |
R-HSA-76046 | RNA Polymerase III Transcription Initiation | 0.250775 | 0.601 |
R-HSA-9013508 | NOTCH3 Intracellular Domain Regulates Transcription | 0.250775 | 0.601 |
R-HSA-9008059 | Interleukin-37 signaling | 0.250775 | 0.601 |
R-HSA-202403 | TCR signaling | 0.255870 | 0.592 |
R-HSA-182971 | EGFR downregulation | 0.256767 | 0.590 |
R-HSA-936440 | Negative regulators of DDX58/IFIH1 signaling | 0.256767 | 0.590 |
R-HSA-5694530 | Cargo concentration in the ER | 0.256767 | 0.590 |
R-HSA-186763 | Downstream signal transduction | 0.256767 | 0.590 |
R-HSA-350562 | Regulation of ornithine decarboxylase (ODC) | 0.262711 | 0.581 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 0.262711 | 0.581 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 0.264744 | 0.577 |
R-HSA-5685938 | HDR through Single Strand Annealing (SSA) | 0.268608 | 0.571 |
R-HSA-5693568 | Resolution of D-loop Structures through Holliday Junction Intermediates | 0.268608 | 0.571 |
R-HSA-5654726 | Negative regulation of FGFR1 signaling | 0.268608 | 0.571 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 0.268608 | 0.571 |
R-HSA-8939243 | RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not kno... | 0.268608 | 0.571 |
R-HSA-1839124 | FGFR1 mutant receptor activation | 0.268608 | 0.571 |
R-HSA-390522 | Striated Muscle Contraction | 0.274458 | 0.562 |
R-HSA-5693537 | Resolution of D-Loop Structures | 0.274458 | 0.562 |
R-HSA-9818027 | NFE2L2 regulating anti-oxidant/detoxification enzymes | 0.274458 | 0.562 |
R-HSA-180534 | Vpu mediated degradation of CD4 | 0.274458 | 0.562 |
R-HSA-909733 | Interferon alpha/beta signaling | 0.276577 | 0.558 |
R-HSA-9675136 | Diseases of DNA Double-Strand Break Repair | 0.280261 | 0.552 |
R-HSA-9701190 | Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 0.280261 | 0.552 |
R-HSA-5654727 | Negative regulation of FGFR2 signaling | 0.280261 | 0.552 |
R-HSA-983170 | Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 0.280261 | 0.552 |
R-HSA-349425 | Autodegradation of the E3 ubiquitin ligase COP1 | 0.280261 | 0.552 |
R-HSA-75815 | Ubiquitin-dependent degradation of Cyclin D | 0.280261 | 0.552 |
R-HSA-9768919 | NPAS4 regulates expression of target genes | 0.280261 | 0.552 |
R-HSA-397014 | Muscle contraction | 0.284817 | 0.545 |
R-HSA-8854050 | FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 0.286019 | 0.544 |
R-HSA-5693616 | Presynaptic phase of homologous DNA pairing and strand exchange | 0.286019 | 0.544 |
R-HSA-450408 | AUF1 (hnRNP D0) binds and destabilizes mRNA | 0.291731 | 0.535 |
R-HSA-180585 | Vif-mediated degradation of APOBEC3G | 0.291731 | 0.535 |
R-HSA-9682385 | FLT3 signaling in disease | 0.291731 | 0.535 |
R-HSA-4641258 | Degradation of DVL | 0.297397 | 0.527 |
R-HSA-4641257 | Degradation of AXIN | 0.297397 | 0.527 |
R-HSA-9762114 | GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 0.297397 | 0.527 |
R-HSA-2173796 | SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 0.297397 | 0.527 |
R-HSA-5689896 | Ovarian tumor domain proteases | 0.297397 | 0.527 |
R-HSA-8957322 | Metabolism of steroids | 0.297639 | 0.526 |
R-HSA-418990 | Adherens junctions interactions | 0.297868 | 0.526 |
R-HSA-2132295 | MHC class II antigen presentation | 0.300205 | 0.523 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 0.300205 | 0.523 |
R-HSA-5693579 | Homologous DNA Pairing and Strand Exchange | 0.303019 | 0.519 |
R-HSA-8875878 | MET promotes cell motility | 0.303019 | 0.519 |
R-HSA-162909 | Host Interactions of HIV factors | 0.303152 | 0.518 |
R-HSA-1236978 | Cross-presentation of soluble exogenous antigens (endosomes) | 0.308595 | 0.511 |
R-HSA-9929356 | GSK3B-mediated proteasomal degradation of PD-L1(CD274) | 0.308595 | 0.511 |
R-HSA-69541 | Stabilization of p53 | 0.308595 | 0.511 |
R-HSA-1266738 | Developmental Biology | 0.311174 | 0.507 |
R-HSA-427389 | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 0.314128 | 0.503 |
R-HSA-9843743 | Transcriptional regulation of brown and beige adipocyte differentiation | 0.314128 | 0.503 |
R-HSA-9844594 | Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | 0.314128 | 0.503 |
R-HSA-3371568 | Attenuation phase | 0.314128 | 0.503 |
R-HSA-9604323 | Negative regulation of NOTCH4 signaling | 0.314128 | 0.503 |
R-HSA-8941858 | Regulation of RUNX3 expression and activity | 0.314128 | 0.503 |
R-HSA-202433 | Generation of second messenger molecules | 0.314128 | 0.503 |
R-HSA-8982491 | Glycogen metabolism | 0.314128 | 0.503 |
R-HSA-69481 | G2/M Checkpoints | 0.314915 | 0.502 |
R-HSA-3214841 | PKMTs methylate histone lysines | 0.319617 | 0.495 |
R-HSA-5362768 | Hh mutants are degraded by ERAD | 0.319617 | 0.495 |
R-HSA-9929491 | SPOP-mediated proteasomal degradation of PD-L1(CD274) | 0.319617 | 0.495 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 0.319617 | 0.495 |
R-HSA-73817 | Purine ribonucleoside monophosphate biosynthesis | 0.319617 | 0.495 |
R-HSA-5676590 | NIK-->noncanonical NF-kB signaling | 0.319617 | 0.495 |
R-HSA-9821002 | Chromatin modifications during the maternal to zygotic transition (MZT) | 0.319617 | 0.495 |
R-HSA-9607240 | FLT3 Signaling | 0.319617 | 0.495 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 0.319693 | 0.495 |
R-HSA-9932298 | Degradation of CRY and PER proteins | 0.325062 | 0.488 |
R-HSA-5610780 | Degradation of GLI1 by the proteasome | 0.325062 | 0.488 |
R-HSA-5610785 | GLI3 is processed to GLI3R by the proteasome | 0.325062 | 0.488 |
R-HSA-5610783 | Degradation of GLI2 by the proteasome | 0.325062 | 0.488 |
R-HSA-6811438 | Intra-Golgi traffic | 0.325062 | 0.488 |
R-HSA-5655302 | Signaling by FGFR1 in disease | 0.325062 | 0.488 |
R-HSA-73762 | RNA Polymerase I Transcription Initiation | 0.330464 | 0.481 |
R-HSA-5387390 | Hh mutants abrogate ligand secretion | 0.335822 | 0.474 |
R-HSA-5654743 | Signaling by FGFR4 | 0.335822 | 0.474 |
R-HSA-8854214 | TBC/RABGAPs | 0.335822 | 0.474 |
R-HSA-2173789 | TGF-beta receptor signaling activates SMADs | 0.335822 | 0.474 |
R-HSA-5683057 | MAPK family signaling cascades | 0.339165 | 0.470 |
R-HSA-202733 | Cell surface interactions at the vascular wall | 0.339360 | 0.469 |
R-HSA-9907900 | Proteasome assembly | 0.341139 | 0.467 |
R-HSA-187577 | SCF(Skp2)-mediated degradation of p27/p21 | 0.341139 | 0.467 |
R-HSA-373752 | Netrin-1 signaling | 0.341139 | 0.467 |
R-HSA-5683826 | Surfactant metabolism | 0.341139 | 0.467 |
R-HSA-8864260 | Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 0.341139 | 0.467 |
R-HSA-157118 | Signaling by NOTCH | 0.345911 | 0.461 |
R-HSA-774815 | Nucleosome assembly | 0.346413 | 0.460 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 0.346413 | 0.460 |
R-HSA-4608870 | Asymmetric localization of PCP proteins | 0.346413 | 0.460 |
R-HSA-5678895 | Defective CFTR causes cystic fibrosis | 0.346413 | 0.460 |
R-HSA-5654741 | Signaling by FGFR3 | 0.346413 | 0.460 |
R-HSA-5607761 | Dectin-1 mediated noncanonical NF-kB signaling | 0.346413 | 0.460 |
R-HSA-69613 | p53-Independent G1/S DNA Damage Checkpoint | 0.346413 | 0.460 |
R-HSA-69601 | Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | 0.346413 | 0.460 |
R-HSA-9824272 | Somitogenesis | 0.346413 | 0.460 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 0.349913 | 0.456 |
R-HSA-174084 | Autodegradation of Cdh1 by Cdh1:APC/C | 0.351645 | 0.454 |
R-HSA-9675135 | Diseases of DNA repair | 0.351645 | 0.454 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 0.355693 | 0.449 |
R-HSA-1632852 | Macroautophagy | 0.361454 | 0.442 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 0.367094 | 0.435 |
R-HSA-9766229 | Degradation of CDH1 | 0.367094 | 0.435 |
R-HSA-69563 | p53-Dependent G1 DNA Damage Response | 0.367094 | 0.435 |
R-HSA-69580 | p53-Dependent G1/S DNA damage checkpoint | 0.367094 | 0.435 |
R-HSA-421270 | Cell-cell junction organization | 0.369876 | 0.432 |
R-HSA-5658442 | Regulation of RAS by GAPs | 0.372162 | 0.429 |
R-HSA-912446 | Meiotic recombination | 0.377189 | 0.423 |
R-HSA-1169091 | Activation of NF-kappaB in B cells | 0.377189 | 0.423 |
R-HSA-1234176 | Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 0.377189 | 0.423 |
R-HSA-5358346 | Hedgehog ligand biogenesis | 0.377189 | 0.423 |
R-HSA-68949 | Orc1 removal from chromatin | 0.382177 | 0.418 |
R-HSA-9931269 | AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | 0.382177 | 0.418 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 0.382177 | 0.418 |
R-HSA-9639288 | Amino acids regulate mTORC1 | 0.387125 | 0.412 |
R-HSA-8956320 | Nucleotide biosynthesis | 0.387125 | 0.412 |
R-HSA-8948751 | Regulation of PTEN stability and activity | 0.387125 | 0.412 |
R-HSA-9758941 | Gastrulation | 0.387135 | 0.412 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 0.392034 | 0.407 |
R-HSA-446652 | Interleukin-1 family signaling | 0.395598 | 0.403 |
R-HSA-3214815 | HDACs deacetylate histones | 0.396904 | 0.401 |
R-HSA-9012852 | Signaling by NOTCH3 | 0.396904 | 0.401 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 0.401211 | 0.397 |
R-HSA-177929 | Signaling by EGFR | 0.401735 | 0.396 |
R-HSA-193648 | NRAGE signals death through JNK | 0.401735 | 0.396 |
R-HSA-5654736 | Signaling by FGFR1 | 0.401735 | 0.396 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 0.401735 | 0.396 |
R-HSA-8935690 | Digestion | 0.401735 | 0.396 |
R-HSA-3299685 | Detoxification of Reactive Oxygen Species | 0.401735 | 0.396 |
R-HSA-109606 | Intrinsic Pathway for Apoptosis | 0.401735 | 0.396 |
R-HSA-913531 | Interferon Signaling | 0.406237 | 0.391 |
R-HSA-9764561 | Regulation of CDH1 Function | 0.406527 | 0.391 |
R-HSA-1483166 | Synthesis of PA | 0.406527 | 0.391 |
R-HSA-9612973 | Autophagy | 0.406799 | 0.391 |
R-HSA-9029569 | NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflu... | 0.411282 | 0.386 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 0.411282 | 0.386 |
R-HSA-877300 | Interferon gamma signaling | 0.415135 | 0.382 |
R-HSA-186712 | Regulation of beta-cell development | 0.415999 | 0.381 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 0.420678 | 0.376 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 0.420678 | 0.376 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 0.420678 | 0.376 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 0.420678 | 0.376 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 0.420678 | 0.376 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 0.420678 | 0.376 |
R-HSA-351202 | Metabolism of polyamines | 0.420678 | 0.376 |
R-HSA-8939902 | Regulation of RUNX2 expression and activity | 0.425320 | 0.371 |
R-HSA-1442490 | Collagen degradation | 0.425320 | 0.371 |
R-HSA-446728 | Cell junction organization | 0.427903 | 0.369 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 0.429925 | 0.367 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 0.429925 | 0.367 |
R-HSA-186797 | Signaling by PDGF | 0.429925 | 0.367 |
R-HSA-1660499 | Synthesis of PIPs at the plasma membrane | 0.429925 | 0.367 |
R-HSA-373755 | Semaphorin interactions | 0.434494 | 0.362 |
R-HSA-69615 | G1/S DNA Damage Checkpoints | 0.434494 | 0.362 |
R-HSA-8963743 | Digestion and absorption | 0.434494 | 0.362 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 0.452407 | 0.344 |
R-HSA-5689880 | Ub-specific processing proteases | 0.455910 | 0.341 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 0.456797 | 0.340 |
R-HSA-9678108 | SARS-CoV-1 Infection | 0.461225 | 0.336 |
R-HSA-1483257 | Phospholipid metabolism | 0.463505 | 0.334 |
R-HSA-204005 | COPII-mediated vesicle transport | 0.465472 | 0.332 |
R-HSA-9843940 | Regulation of endogenous retroelements by KRAB-ZFP proteins | 0.465472 | 0.332 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 0.465472 | 0.332 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 0.465472 | 0.332 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 0.465472 | 0.332 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 0.469758 | 0.328 |
R-HSA-9856649 | Transcriptional and post-translational regulation of MITF-M expression and activ... | 0.469758 | 0.328 |
R-HSA-5632684 | Hedgehog 'on' state | 0.469758 | 0.328 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 0.474009 | 0.324 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 0.474009 | 0.324 |
R-HSA-69052 | Switching of origins to a post-replicative state | 0.478227 | 0.320 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 0.478227 | 0.320 |
R-HSA-597592 | Post-translational protein modification | 0.479938 | 0.319 |
R-HSA-69473 | G2/M DNA damage checkpoint | 0.482411 | 0.317 |
R-HSA-1226099 | Signaling by FGFR in disease | 0.482411 | 0.317 |
R-HSA-392499 | Metabolism of proteins | 0.485230 | 0.314 |
R-HSA-5633008 | TP53 Regulates Transcription of Cell Death Genes | 0.486562 | 0.313 |
R-HSA-1980143 | Signaling by NOTCH1 | 0.490680 | 0.309 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 0.490680 | 0.309 |
R-HSA-9679506 | SARS-CoV Infections | 0.491537 | 0.308 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 0.494765 | 0.306 |
R-HSA-983712 | Ion channel transport | 0.497572 | 0.303 |
R-HSA-6783783 | Interleukin-10 signaling | 0.498818 | 0.302 |
R-HSA-73864 | RNA Polymerase I Transcription | 0.498818 | 0.302 |
R-HSA-416482 | G alpha (12/13) signalling events | 0.498818 | 0.302 |
R-HSA-5619084 | ABC transporter disorders | 0.498818 | 0.302 |
R-HSA-4086400 | PCP/CE pathway | 0.498818 | 0.302 |
R-HSA-9925561 | Developmental Lineage of Pancreatic Acinar Cells | 0.502839 | 0.299 |
R-HSA-1500931 | Cell-Cell communication | 0.506124 | 0.296 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 0.506827 | 0.295 |
R-HSA-5654738 | Signaling by FGFR2 | 0.506827 | 0.295 |
R-HSA-9856530 | High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR... | 0.506827 | 0.295 |
R-HSA-69278 | Cell Cycle, Mitotic | 0.508250 | 0.294 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 0.510174 | 0.292 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 0.510784 | 0.292 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 0.514709 | 0.288 |
R-HSA-5668541 | TNFR2 non-canonical NF-kB pathway | 0.518603 | 0.285 |
R-HSA-1500620 | Meiosis | 0.526298 | 0.279 |
R-HSA-9909615 | Regulation of PD-L1(CD274) Post-translational modification | 0.530099 | 0.276 |
R-HSA-1640170 | Cell Cycle | 0.531495 | 0.275 |
R-HSA-376176 | Signaling by ROBO receptors | 0.532337 | 0.274 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 0.533871 | 0.273 |
R-HSA-72172 | mRNA Splicing | 0.537169 | 0.270 |
R-HSA-9645723 | Diseases of programmed cell death | 0.541323 | 0.267 |
R-HSA-1236974 | ER-Phagosome pathway | 0.545005 | 0.264 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 0.548658 | 0.261 |
R-HSA-202424 | Downstream TCR signaling | 0.548658 | 0.261 |
R-HSA-2682334 | EPH-Ephrin signaling | 0.559442 | 0.252 |
R-HSA-74752 | Signaling by Insulin receptor | 0.559442 | 0.252 |
R-HSA-68867 | Assembly of the pre-replicative complex | 0.562980 | 0.250 |
R-HSA-9694516 | SARS-CoV-2 Infection | 0.569408 | 0.245 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 0.573424 | 0.242 |
R-HSA-190236 | Signaling by FGFR | 0.583621 | 0.234 |
R-HSA-9614085 | FOXO-mediated transcription | 0.586966 | 0.231 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 0.586966 | 0.231 |
R-HSA-162906 | HIV Infection | 0.590267 | 0.229 |
R-HSA-5610787 | Hedgehog 'off' state | 0.590284 | 0.229 |
R-HSA-382556 | ABC-family proteins mediated transport | 0.590284 | 0.229 |
R-HSA-9009391 | Extra-nuclear estrogen signaling | 0.593576 | 0.227 |
R-HSA-9020702 | Interleukin-1 signaling | 0.593576 | 0.227 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 0.596842 | 0.224 |
R-HSA-9842860 | Regulation of endogenous retroelements | 0.596842 | 0.224 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 0.603295 | 0.219 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 0.603295 | 0.219 |
R-HSA-69239 | Synthesis of DNA | 0.615895 | 0.210 |
R-HSA-211000 | Gene Silencing by RNA | 0.615895 | 0.210 |
R-HSA-1236975 | Antigen processing-Cross presentation | 0.618983 | 0.208 |
R-HSA-69002 | DNA Replication Pre-Initiation | 0.622046 | 0.206 |
R-HSA-6803157 | Antimicrobial peptides | 0.628099 | 0.202 |
R-HSA-2871796 | FCERI mediated MAPK activation | 0.631089 | 0.200 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 0.636998 | 0.196 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 0.636998 | 0.196 |
R-HSA-9007101 | Rab regulation of trafficking | 0.651363 | 0.186 |
R-HSA-5693538 | Homology Directed Repair | 0.654167 | 0.184 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 0.654167 | 0.184 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 0.656950 | 0.182 |
R-HSA-68875 | Mitotic Prophase | 0.659710 | 0.181 |
R-HSA-73886 | Chromosome Maintenance | 0.662448 | 0.179 |
R-HSA-69206 | G1/S Transition | 0.675813 | 0.170 |
R-HSA-1474165 | Reproduction | 0.691159 | 0.160 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 0.693379 | 0.159 |
R-HSA-1474228 | Degradation of the extracellular matrix | 0.696113 | 0.157 |
R-HSA-5673001 | RAF/MAP kinase cascade | 0.710585 | 0.148 |
R-HSA-9948299 | Ribosome-associated quality control | 0.712838 | 0.147 |
R-HSA-5358351 | Signaling by Hedgehog | 0.712838 | 0.147 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 0.717446 | 0.144 |
R-HSA-9664417 | Leishmania phagocytosis | 0.717446 | 0.144 |
R-HSA-9664407 | Parasite infection | 0.717446 | 0.144 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 0.719723 | 0.143 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 0.722148 | 0.141 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 0.726444 | 0.139 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 0.728649 | 0.137 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 0.733006 | 0.135 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 0.735158 | 0.134 |
R-HSA-69242 | S Phase | 0.737293 | 0.132 |
R-HSA-9679191 | Potential therapeutics for SARS | 0.741512 | 0.130 |
R-HSA-9820448 | Developmental Cell Lineages of the Exocrine Pancreas | 0.745664 | 0.127 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 0.745664 | 0.127 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 0.747715 | 0.126 |
R-HSA-69306 | DNA Replication | 0.747715 | 0.126 |
R-HSA-73887 | Death Receptor Signaling | 0.749749 | 0.125 |
R-HSA-9711097 | Cellular response to starvation | 0.757726 | 0.120 |
R-HSA-1474244 | Extracellular matrix organization | 0.774293 | 0.111 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 0.781948 | 0.107 |
R-HSA-199991 | Membrane Trafficking | 0.787861 | 0.104 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 0.788906 | 0.103 |
R-HSA-69275 | G2/M Transition | 0.808484 | 0.092 |
R-HSA-375276 | Peptide ligand-binding receptors | 0.808484 | 0.092 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 0.811567 | 0.091 |
R-HSA-453274 | Mitotic G2-G2/M phases | 0.811567 | 0.091 |
R-HSA-5617833 | Cilium Assembly | 0.814601 | 0.089 |
R-HSA-9824446 | Viral Infection Pathways | 0.820540 | 0.086 |
R-HSA-8953854 | Metabolism of RNA | 0.821106 | 0.086 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 0.829058 | 0.081 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 0.831813 | 0.080 |
R-HSA-1483206 | Glycerophospholipid biosynthesis | 0.833173 | 0.079 |
R-HSA-422475 | Axon guidance | 0.835202 | 0.078 |
R-HSA-9675108 | Nervous system development | 0.865319 | 0.063 |
R-HSA-72312 | rRNA processing | 0.869283 | 0.061 |
R-HSA-15869 | Metabolism of nucleotides | 0.873470 | 0.059 |
R-HSA-5619115 | Disorders of transmembrane transporters | 0.884311 | 0.053 |
R-HSA-1643685 | Disease | 0.894807 | 0.048 |
R-HSA-9734767 | Developmental Cell Lineages | 0.898455 | 0.047 |
R-HSA-416476 | G alpha (q) signalling events | 0.899279 | 0.046 |
R-HSA-5653656 | Vesicle-mediated transport | 0.903526 | 0.044 |
R-HSA-9824443 | Parasitic Infection Pathways | 0.912324 | 0.040 |
R-HSA-9658195 | Leishmania infection | 0.912324 | 0.040 |
R-HSA-556833 | Metabolism of lipids | 0.924471 | 0.034 |
R-HSA-5663205 | Infectious disease | 0.939245 | 0.027 |
R-HSA-73894 | DNA Repair | 0.954070 | 0.020 |
R-HSA-109582 | Hemostasis | 0.958950 | 0.018 |
R-HSA-9824439 | Bacterial Infection Pathways | 0.964394 | 0.016 |
R-HSA-373076 | Class A/1 (Rhodopsin-like receptors) | 0.965546 | 0.015 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 0.965882 | 0.015 |
R-HSA-446203 | Asparagine N-linked glycosylation | 0.972637 | 0.012 |
R-HSA-72766 | Translation | 0.974171 | 0.011 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 0.979156 | 0.009 |
R-HSA-382551 | Transport of small molecules | 0.988448 | 0.005 |
R-HSA-388396 | GPCR downstream signalling | 0.988781 | 0.005 |
R-HSA-500792 | GPCR ligand binding | 0.993137 | 0.003 |
R-HSA-372790 | Signaling by GPCR | 0.993902 | 0.003 |
R-HSA-1430728 | Metabolism | 0.999990 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
COT |
0.852 | 0.040 | 2 | 0.870 |
HIPK4 |
0.852 | 0.319 | 1 | 0.781 |
CLK3 |
0.850 | 0.204 | 1 | 0.833 |
PRKD1 |
0.849 | 0.189 | -3 | 0.788 |
PIM3 |
0.847 | 0.091 | -3 | 0.797 |
CDKL5 |
0.847 | 0.220 | -3 | 0.752 |
NDR2 |
0.846 | 0.099 | -3 | 0.810 |
PRKD2 |
0.843 | 0.157 | -3 | 0.727 |
CDKL1 |
0.842 | 0.146 | -3 | 0.753 |
PRPK |
0.841 | -0.017 | -1 | 0.842 |
CDC7 |
0.841 | 0.009 | 1 | 0.852 |
ERK5 |
0.841 | 0.132 | 1 | 0.810 |
MOS |
0.840 | 0.064 | 1 | 0.870 |
TBK1 |
0.840 | 0.041 | 1 | 0.771 |
ICK |
0.839 | 0.227 | -3 | 0.793 |
RAF1 |
0.838 | -0.035 | 1 | 0.860 |
KIS |
0.838 | 0.178 | 1 | 0.701 |
NLK |
0.838 | 0.054 | 1 | 0.836 |
NDR1 |
0.836 | 0.032 | -3 | 0.796 |
GCN2 |
0.836 | -0.051 | 2 | 0.775 |
SRPK1 |
0.836 | 0.100 | -3 | 0.699 |
ATR |
0.835 | 0.062 | 1 | 0.861 |
RIPK3 |
0.835 | -0.012 | 3 | 0.656 |
RSK2 |
0.835 | 0.054 | -3 | 0.729 |
WNK1 |
0.835 | 0.021 | -2 | 0.852 |
MTOR |
0.834 | -0.063 | 1 | 0.799 |
SKMLCK |
0.834 | 0.044 | -2 | 0.815 |
CAMK1B |
0.834 | -0.023 | -3 | 0.807 |
IKKE |
0.833 | -0.022 | 1 | 0.765 |
CDK8 |
0.833 | 0.142 | 1 | 0.677 |
ULK2 |
0.833 | -0.098 | 2 | 0.773 |
DSTYK |
0.832 | -0.073 | 2 | 0.882 |
BMPR2 |
0.832 | -0.072 | -2 | 0.823 |
CDK19 |
0.832 | 0.167 | 1 | 0.636 |
PIM1 |
0.832 | 0.065 | -3 | 0.736 |
PDHK4 |
0.832 | -0.194 | 1 | 0.865 |
DYRK2 |
0.832 | 0.170 | 1 | 0.692 |
PKN3 |
0.831 | -0.005 | -3 | 0.781 |
P90RSK |
0.831 | 0.028 | -3 | 0.726 |
CAMLCK |
0.831 | 0.019 | -2 | 0.811 |
IKKB |
0.830 | -0.119 | -2 | 0.696 |
PDHK1 |
0.830 | -0.103 | 1 | 0.867 |
TGFBR2 |
0.830 | -0.026 | -2 | 0.696 |
PKCD |
0.830 | 0.055 | 2 | 0.794 |
MAPKAPK3 |
0.830 | 0.061 | -3 | 0.739 |
AURC |
0.830 | 0.070 | -2 | 0.634 |
CHAK2 |
0.830 | 0.022 | -1 | 0.784 |
RSK3 |
0.830 | 0.028 | -3 | 0.714 |
SRPK2 |
0.830 | 0.088 | -3 | 0.625 |
NIK |
0.829 | -0.017 | -3 | 0.827 |
PKN2 |
0.829 | -0.003 | -3 | 0.789 |
MLK2 |
0.829 | 0.095 | 2 | 0.809 |
CDK7 |
0.828 | 0.104 | 1 | 0.673 |
MST4 |
0.828 | -0.003 | 2 | 0.844 |
P70S6KB |
0.828 | 0.033 | -3 | 0.747 |
NUAK2 |
0.827 | -0.036 | -3 | 0.791 |
NEK6 |
0.827 | -0.035 | -2 | 0.779 |
CAMK2D |
0.827 | -0.011 | -3 | 0.798 |
PKACG |
0.826 | 0.023 | -2 | 0.721 |
DAPK2 |
0.826 | 0.001 | -3 | 0.817 |
LATS2 |
0.826 | 0.005 | -5 | 0.789 |
IRE2 |
0.826 | 0.038 | 2 | 0.759 |
MLK1 |
0.826 | -0.054 | 2 | 0.818 |
WNK3 |
0.826 | -0.118 | 1 | 0.835 |
MAPKAPK2 |
0.826 | 0.053 | -3 | 0.701 |
CDK18 |
0.826 | 0.146 | 1 | 0.595 |
AMPKA1 |
0.825 | -0.035 | -3 | 0.809 |
CAMK2G |
0.825 | -0.137 | 2 | 0.795 |
TSSK2 |
0.824 | -0.010 | -5 | 0.875 |
MARK4 |
0.824 | -0.072 | 4 | 0.779 |
PRKD3 |
0.824 | 0.063 | -3 | 0.683 |
PKCA |
0.824 | 0.065 | 2 | 0.740 |
TSSK1 |
0.823 | 0.010 | -3 | 0.830 |
P38A |
0.823 | 0.177 | 1 | 0.701 |
CDK5 |
0.823 | 0.094 | 1 | 0.687 |
P38B |
0.823 | 0.190 | 1 | 0.629 |
IKKA |
0.822 | -0.040 | -2 | 0.688 |
GRK5 |
0.822 | -0.125 | -3 | 0.820 |
HIPK2 |
0.822 | 0.188 | 1 | 0.599 |
IRE1 |
0.822 | -0.026 | 1 | 0.807 |
MLK3 |
0.822 | 0.040 | 2 | 0.755 |
NEK7 |
0.821 | -0.166 | -3 | 0.778 |
ULK1 |
0.821 | -0.136 | -3 | 0.756 |
PKCB |
0.821 | 0.036 | 2 | 0.750 |
AMPKA2 |
0.821 | -0.026 | -3 | 0.780 |
PAK3 |
0.821 | -0.005 | -2 | 0.761 |
PAK1 |
0.821 | 0.010 | -2 | 0.771 |
SRPK3 |
0.820 | 0.052 | -3 | 0.664 |
PKG2 |
0.820 | 0.056 | -2 | 0.665 |
DLK |
0.820 | -0.065 | 1 | 0.868 |
MASTL |
0.820 | -0.187 | -2 | 0.775 |
MNK2 |
0.820 | 0.009 | -2 | 0.755 |
PKACB |
0.820 | 0.058 | -2 | 0.647 |
PKCG |
0.820 | 0.017 | 2 | 0.754 |
BCKDK |
0.819 | -0.143 | -1 | 0.753 |
LATS1 |
0.819 | 0.068 | -3 | 0.832 |
NEK9 |
0.819 | -0.099 | 2 | 0.821 |
RSK4 |
0.819 | 0.046 | -3 | 0.706 |
CDK1 |
0.818 | 0.080 | 1 | 0.622 |
PHKG1 |
0.818 | -0.008 | -3 | 0.778 |
CAMK4 |
0.818 | -0.066 | -3 | 0.774 |
HIPK1 |
0.818 | 0.137 | 1 | 0.712 |
DYRK1A |
0.818 | 0.145 | 1 | 0.734 |
HUNK |
0.817 | -0.201 | 2 | 0.806 |
RIPK1 |
0.817 | -0.161 | 1 | 0.834 |
MELK |
0.817 | -0.033 | -3 | 0.762 |
NIM1 |
0.817 | -0.094 | 3 | 0.672 |
GRK1 |
0.817 | -0.028 | -2 | 0.726 |
CAMK2A |
0.817 | 0.004 | 2 | 0.774 |
PIM2 |
0.817 | 0.068 | -3 | 0.701 |
ERK1 |
0.817 | 0.135 | 1 | 0.618 |
ANKRD3 |
0.817 | -0.114 | 1 | 0.883 |
CLK1 |
0.816 | 0.068 | -3 | 0.688 |
AURB |
0.816 | 0.017 | -2 | 0.628 |
CLK4 |
0.816 | 0.055 | -3 | 0.710 |
MSK2 |
0.815 | -0.035 | -3 | 0.692 |
CAMK2B |
0.815 | -0.016 | 2 | 0.754 |
CDK17 |
0.815 | 0.093 | 1 | 0.540 |
JNK2 |
0.815 | 0.084 | 1 | 0.616 |
NUAK1 |
0.815 | -0.062 | -3 | 0.740 |
CDK13 |
0.815 | 0.038 | 1 | 0.641 |
CLK2 |
0.814 | 0.109 | -3 | 0.696 |
HIPK3 |
0.814 | 0.130 | 1 | 0.712 |
VRK2 |
0.814 | -0.027 | 1 | 0.895 |
PKR |
0.814 | -0.003 | 1 | 0.855 |
YSK4 |
0.814 | -0.028 | 1 | 0.804 |
MPSK1 |
0.814 | 0.231 | 1 | 0.793 |
MNK1 |
0.814 | -0.007 | -2 | 0.764 |
PAK6 |
0.813 | 0.027 | -2 | 0.682 |
DYRK4 |
0.813 | 0.140 | 1 | 0.617 |
PKCZ |
0.813 | -0.012 | 2 | 0.777 |
P38D |
0.813 | 0.159 | 1 | 0.565 |
BMPR1B |
0.812 | 0.020 | 1 | 0.809 |
MSK1 |
0.812 | -0.004 | -3 | 0.705 |
MLK4 |
0.812 | -0.028 | 2 | 0.728 |
ATM |
0.812 | -0.033 | 1 | 0.802 |
SGK3 |
0.812 | 0.029 | -3 | 0.726 |
PAK2 |
0.812 | -0.030 | -2 | 0.751 |
QSK |
0.812 | -0.062 | 4 | 0.761 |
GRK4 |
0.812 | -0.141 | -2 | 0.750 |
GRK6 |
0.812 | -0.151 | 1 | 0.852 |
MYLK4 |
0.811 | -0.033 | -2 | 0.726 |
CHK1 |
0.811 | 0.010 | -3 | 0.803 |
AKT2 |
0.811 | 0.026 | -3 | 0.637 |
PRP4 |
0.811 | 0.098 | -3 | 0.697 |
PKCH |
0.811 | -0.024 | 2 | 0.732 |
ALK4 |
0.811 | -0.058 | -2 | 0.738 |
TGFBR1 |
0.810 | -0.027 | -2 | 0.702 |
QIK |
0.810 | -0.126 | -3 | 0.789 |
CDK2 |
0.810 | 0.003 | 1 | 0.705 |
CDK16 |
0.810 | 0.116 | 1 | 0.556 |
MAK |
0.810 | 0.277 | -2 | 0.909 |
PRKX |
0.810 | 0.046 | -3 | 0.648 |
CHAK1 |
0.810 | -0.084 | 2 | 0.759 |
NEK2 |
0.809 | -0.062 | 2 | 0.800 |
JNK3 |
0.809 | 0.037 | 1 | 0.646 |
CDK14 |
0.809 | 0.077 | 1 | 0.641 |
SIK |
0.809 | -0.064 | -3 | 0.710 |
DNAPK |
0.809 | 0.015 | 1 | 0.732 |
P38G |
0.808 | 0.076 | 1 | 0.537 |
CDK3 |
0.808 | 0.072 | 1 | 0.559 |
CDK9 |
0.808 | 0.017 | 1 | 0.648 |
BUB1 |
0.808 | 0.284 | -5 | 0.832 |
FAM20C |
0.808 | -0.020 | 2 | 0.595 |
ERK2 |
0.808 | 0.051 | 1 | 0.661 |
AURA |
0.807 | -0.007 | -2 | 0.589 |
BRSK2 |
0.807 | -0.093 | -3 | 0.766 |
MEK1 |
0.807 | -0.166 | 2 | 0.818 |
TTBK2 |
0.806 | -0.192 | 2 | 0.699 |
CDK10 |
0.806 | 0.081 | 1 | 0.626 |
CDK12 |
0.806 | 0.025 | 1 | 0.614 |
SMG1 |
0.806 | -0.050 | 1 | 0.813 |
SNRK |
0.806 | -0.151 | 2 | 0.693 |
TLK2 |
0.805 | -0.042 | 1 | 0.817 |
PLK1 |
0.805 | -0.144 | -2 | 0.726 |
DYRK1B |
0.805 | 0.089 | 1 | 0.644 |
MST3 |
0.805 | 0.016 | 2 | 0.845 |
MARK3 |
0.804 | -0.077 | 4 | 0.714 |
BRSK1 |
0.804 | -0.093 | -3 | 0.737 |
WNK4 |
0.804 | -0.057 | -2 | 0.849 |
ZAK |
0.804 | -0.052 | 1 | 0.842 |
PKACA |
0.804 | 0.029 | -2 | 0.604 |
DYRK3 |
0.804 | 0.074 | 1 | 0.718 |
AKT1 |
0.803 | 0.021 | -3 | 0.663 |
IRAK4 |
0.803 | -0.063 | 1 | 0.824 |
HRI |
0.803 | -0.112 | -2 | 0.779 |
BRAF |
0.803 | -0.062 | -4 | 0.820 |
MAPKAPK5 |
0.803 | -0.073 | -3 | 0.668 |
ACVR2A |
0.802 | -0.067 | -2 | 0.693 |
ACVR2B |
0.802 | -0.061 | -2 | 0.703 |
MEKK1 |
0.802 | -0.082 | 1 | 0.863 |
MARK2 |
0.802 | -0.093 | 4 | 0.683 |
P70S6K |
0.802 | -0.001 | -3 | 0.661 |
PKCT |
0.802 | -0.023 | 2 | 0.738 |
PASK |
0.802 | 0.035 | -3 | 0.814 |
DRAK1 |
0.802 | -0.085 | 1 | 0.772 |
SSTK |
0.801 | -0.034 | 4 | 0.760 |
SMMLCK |
0.801 | -0.032 | -3 | 0.765 |
NEK5 |
0.801 | -0.047 | 1 | 0.851 |
PHKG2 |
0.801 | -0.049 | -3 | 0.744 |
ALK2 |
0.800 | -0.073 | -2 | 0.710 |
PERK |
0.800 | -0.087 | -2 | 0.750 |
CAMK1G |
0.799 | -0.077 | -3 | 0.703 |
GRK7 |
0.799 | -0.049 | 1 | 0.764 |
MOK |
0.799 | 0.193 | 1 | 0.720 |
MEK5 |
0.799 | -0.193 | 2 | 0.810 |
DCAMKL1 |
0.799 | -0.059 | -3 | 0.735 |
PLK4 |
0.798 | -0.128 | 2 | 0.628 |
LKB1 |
0.797 | 0.047 | -3 | 0.777 |
MARK1 |
0.797 | -0.121 | 4 | 0.738 |
TAO3 |
0.796 | -0.019 | 1 | 0.822 |
MEKK2 |
0.796 | -0.124 | 2 | 0.792 |
PKCE |
0.796 | 0.012 | 2 | 0.740 |
CAMKK2 |
0.795 | 0.018 | -2 | 0.719 |
PKCI |
0.795 | -0.037 | 2 | 0.748 |
CAMKK1 |
0.795 | -0.056 | -2 | 0.715 |
PLK3 |
0.795 | -0.158 | 2 | 0.758 |
TLK1 |
0.795 | -0.098 | -2 | 0.729 |
ERK7 |
0.795 | 0.045 | 2 | 0.551 |
CK1E |
0.795 | -0.049 | -3 | 0.496 |
CDK6 |
0.795 | 0.058 | 1 | 0.621 |
MEKK6 |
0.793 | 0.015 | 1 | 0.838 |
PINK1 |
0.793 | -0.165 | 1 | 0.822 |
AKT3 |
0.793 | 0.029 | -3 | 0.582 |
GRK2 |
0.793 | -0.107 | -2 | 0.653 |
CDK4 |
0.793 | 0.059 | 1 | 0.598 |
PAK5 |
0.793 | -0.023 | -2 | 0.619 |
CAMK1D |
0.793 | -0.030 | -3 | 0.632 |
BMPR1A |
0.792 | -0.034 | 1 | 0.792 |
GCK |
0.792 | 0.027 | 1 | 0.819 |
TAO2 |
0.792 | -0.046 | 2 | 0.844 |
MEKK3 |
0.792 | -0.223 | 1 | 0.839 |
HGK |
0.792 | 0.016 | 3 | 0.785 |
DCAMKL2 |
0.791 | -0.087 | -3 | 0.754 |
NEK4 |
0.791 | -0.044 | 1 | 0.822 |
MAP3K15 |
0.791 | 0.025 | 1 | 0.812 |
EEF2K |
0.791 | 0.005 | 3 | 0.715 |
TNIK |
0.791 | 0.042 | 3 | 0.779 |
GSK3B |
0.790 | -0.044 | 4 | 0.351 |
ROCK2 |
0.790 | 0.067 | -3 | 0.748 |
DAPK3 |
0.790 | -0.016 | -3 | 0.746 |
PKN1 |
0.790 | -0.032 | -3 | 0.676 |
NEK11 |
0.790 | -0.121 | 1 | 0.825 |
MRCKA |
0.790 | 0.030 | -3 | 0.709 |
LOK |
0.789 | 0.028 | -2 | 0.737 |
MST2 |
0.789 | -0.016 | 1 | 0.839 |
PAK4 |
0.789 | -0.025 | -2 | 0.623 |
NEK8 |
0.789 | -0.148 | 2 | 0.821 |
GAK |
0.788 | -0.031 | 1 | 0.853 |
GSK3A |
0.788 | -0.017 | 4 | 0.359 |
KHS1 |
0.788 | 0.056 | 1 | 0.801 |
IRAK1 |
0.787 | -0.219 | -1 | 0.703 |
MRCKB |
0.787 | 0.017 | -3 | 0.688 |
MINK |
0.787 | -0.032 | 1 | 0.823 |
PBK |
0.786 | 0.079 | 1 | 0.781 |
VRK1 |
0.786 | -0.041 | 2 | 0.848 |
NEK1 |
0.785 | -0.017 | 1 | 0.827 |
JNK1 |
0.785 | 0.012 | 1 | 0.592 |
CHK2 |
0.785 | -0.019 | -3 | 0.585 |
HPK1 |
0.785 | -0.023 | 1 | 0.803 |
SGK1 |
0.785 | 0.016 | -3 | 0.570 |
MST1 |
0.784 | 0.001 | 1 | 0.820 |
CK1D |
0.784 | -0.060 | -3 | 0.452 |
SBK |
0.783 | 0.021 | -3 | 0.526 |
KHS2 |
0.783 | 0.027 | 1 | 0.809 |
TTBK1 |
0.782 | -0.171 | 2 | 0.626 |
CAMK1A |
0.782 | -0.023 | -3 | 0.600 |
LRRK2 |
0.782 | -0.112 | 2 | 0.836 |
PDK1 |
0.782 | -0.126 | 1 | 0.799 |
TAK1 |
0.781 | -0.107 | 1 | 0.842 |
CK1G1 |
0.781 | -0.096 | -3 | 0.482 |
PKG1 |
0.780 | -0.005 | -2 | 0.584 |
SLK |
0.780 | -0.023 | -2 | 0.681 |
DAPK1 |
0.780 | -0.046 | -3 | 0.723 |
CK1A2 |
0.780 | -0.068 | -3 | 0.447 |
DMPK1 |
0.780 | 0.038 | -3 | 0.708 |
YSK1 |
0.779 | -0.042 | 2 | 0.801 |
RIPK2 |
0.777 | -0.199 | 1 | 0.795 |
ROCK1 |
0.776 | 0.029 | -3 | 0.706 |
CK2A2 |
0.775 | -0.053 | 1 | 0.712 |
PDHK3_TYR |
0.775 | 0.187 | 4 | 0.820 |
STK33 |
0.775 | -0.155 | 2 | 0.610 |
GRK3 |
0.774 | -0.124 | -2 | 0.598 |
CRIK |
0.774 | 0.037 | -3 | 0.673 |
NEK3 |
0.772 | -0.092 | 1 | 0.805 |
MEK2 |
0.770 | -0.204 | 2 | 0.785 |
OSR1 |
0.770 | -0.012 | 2 | 0.774 |
MYO3B |
0.769 | 0.000 | 2 | 0.817 |
HASPIN |
0.769 | -0.025 | -1 | 0.598 |
TESK1_TYR |
0.769 | 0.078 | 3 | 0.788 |
PLK2 |
0.769 | -0.109 | -3 | 0.694 |
PKMYT1_TYR |
0.768 | 0.074 | 3 | 0.765 |
TTK |
0.768 | -0.073 | -2 | 0.734 |
LIMK2_TYR |
0.766 | 0.131 | -3 | 0.855 |
CK2A1 |
0.765 | -0.066 | 1 | 0.691 |
BIKE |
0.765 | 0.028 | 1 | 0.733 |
ASK1 |
0.765 | -0.057 | 1 | 0.802 |
MYO3A |
0.764 | -0.048 | 1 | 0.809 |
EPHB4 |
0.764 | 0.153 | -1 | 0.826 |
EPHA6 |
0.764 | 0.094 | -1 | 0.834 |
MAP2K4_TYR |
0.763 | -0.008 | -1 | 0.849 |
RET |
0.763 | 0.087 | 1 | 0.830 |
PDHK4_TYR |
0.763 | 0.013 | 2 | 0.866 |
ABL2 |
0.762 | 0.209 | -1 | 0.812 |
TAO1 |
0.762 | -0.053 | 1 | 0.764 |
TYRO3 |
0.761 | 0.031 | 3 | 0.728 |
MAP2K6_TYR |
0.761 | -0.047 | -1 | 0.854 |
ROS1 |
0.761 | 0.023 | 3 | 0.683 |
MST1R |
0.760 | 0.054 | 3 | 0.731 |
TNNI3K_TYR |
0.760 | 0.136 | 1 | 0.879 |
PDHK1_TYR |
0.760 | -0.013 | -1 | 0.867 |
MAP2K7_TYR |
0.759 | -0.167 | 2 | 0.850 |
JAK2 |
0.759 | 0.082 | 1 | 0.837 |
CSF1R |
0.759 | 0.062 | 3 | 0.723 |
ABL1 |
0.758 | 0.190 | -1 | 0.806 |
BMPR2_TYR |
0.757 | -0.056 | -1 | 0.834 |
ALPHAK3 |
0.756 | -0.070 | -1 | 0.782 |
ITK |
0.756 | 0.077 | -1 | 0.774 |
TYK2 |
0.756 | -0.054 | 1 | 0.832 |
LIMK1_TYR |
0.756 | -0.064 | 2 | 0.842 |
PINK1_TYR |
0.756 | -0.166 | 1 | 0.846 |
TXK |
0.754 | 0.079 | 1 | 0.865 |
TNK2 |
0.754 | 0.054 | 3 | 0.667 |
JAK3 |
0.754 | -0.004 | 1 | 0.814 |
FGR |
0.754 | -0.007 | 1 | 0.869 |
DDR1 |
0.753 | -0.063 | 4 | 0.741 |
YANK3 |
0.752 | -0.093 | 2 | 0.406 |
PDGFRB |
0.752 | -0.005 | 3 | 0.721 |
EPHB1 |
0.752 | 0.042 | 1 | 0.881 |
EPHB3 |
0.751 | 0.057 | -1 | 0.809 |
EPHB2 |
0.751 | 0.076 | -1 | 0.820 |
YES1 |
0.750 | -0.024 | -1 | 0.824 |
EPHA4 |
0.750 | 0.038 | 2 | 0.769 |
FLT3 |
0.750 | -0.013 | 3 | 0.726 |
KIT |
0.750 | -0.004 | 3 | 0.727 |
LCK |
0.749 | 0.033 | -1 | 0.811 |
JAK1 |
0.749 | 0.030 | 1 | 0.788 |
AAK1 |
0.749 | 0.059 | 1 | 0.627 |
FER |
0.749 | -0.069 | 1 | 0.879 |
TNK1 |
0.749 | 0.023 | 3 | 0.715 |
INSRR |
0.748 | -0.075 | 3 | 0.657 |
KDR |
0.748 | -0.023 | 3 | 0.673 |
STLK3 |
0.748 | -0.144 | 1 | 0.804 |
HCK |
0.747 | -0.042 | -1 | 0.804 |
FGFR2 |
0.747 | -0.076 | 3 | 0.694 |
BMX |
0.746 | 0.017 | -1 | 0.719 |
SRMS |
0.746 | -0.014 | 1 | 0.872 |
AXL |
0.746 | -0.023 | 3 | 0.696 |
FGFR1 |
0.746 | -0.054 | 3 | 0.671 |
TEK |
0.746 | -0.071 | 3 | 0.660 |
MET |
0.745 | 0.016 | 3 | 0.720 |
PDGFRA |
0.745 | -0.040 | 3 | 0.723 |
MERTK |
0.745 | 0.002 | 3 | 0.701 |
ALK |
0.744 | -0.053 | 3 | 0.630 |
CK1A |
0.743 | -0.094 | -3 | 0.361 |
PTK2B |
0.743 | 0.100 | -1 | 0.773 |
TEC |
0.741 | -0.040 | -1 | 0.716 |
LTK |
0.741 | -0.051 | 3 | 0.650 |
BLK |
0.741 | -0.010 | -1 | 0.805 |
DDR2 |
0.741 | 0.025 | 3 | 0.632 |
NEK10_TYR |
0.740 | -0.057 | 1 | 0.682 |
EPHA7 |
0.740 | -0.006 | 2 | 0.767 |
EPHA3 |
0.740 | -0.016 | 2 | 0.746 |
INSR |
0.739 | -0.070 | 3 | 0.645 |
EPHA1 |
0.738 | -0.013 | 3 | 0.695 |
WEE1_TYR |
0.738 | -0.071 | -1 | 0.734 |
NTRK2 |
0.737 | -0.095 | 3 | 0.681 |
BTK |
0.736 | -0.133 | -1 | 0.733 |
FLT4 |
0.736 | -0.097 | 3 | 0.667 |
FLT1 |
0.736 | -0.060 | -1 | 0.834 |
LYN |
0.735 | -0.049 | 3 | 0.655 |
NTRK1 |
0.735 | -0.119 | -1 | 0.828 |
FYN |
0.735 | -0.027 | -1 | 0.785 |
FRK |
0.734 | -0.057 | -1 | 0.810 |
PTK6 |
0.734 | -0.125 | -1 | 0.734 |
FGFR3 |
0.733 | -0.124 | 3 | 0.668 |
EPHA5 |
0.733 | -0.004 | 2 | 0.756 |
NTRK3 |
0.732 | -0.070 | -1 | 0.795 |
ERBB2 |
0.731 | -0.140 | 1 | 0.778 |
MATK |
0.730 | -0.062 | -1 | 0.764 |
CSK |
0.729 | -0.046 | 2 | 0.774 |
EPHA8 |
0.726 | -0.058 | -1 | 0.779 |
SRC |
0.724 | -0.088 | -1 | 0.788 |
EPHA2 |
0.722 | -0.020 | -1 | 0.766 |
MUSK |
0.720 | -0.082 | 1 | 0.671 |
PTK2 |
0.720 | -0.007 | -1 | 0.760 |
EGFR |
0.720 | -0.093 | 1 | 0.698 |
FGFR4 |
0.719 | -0.091 | -1 | 0.802 |
IGF1R |
0.719 | -0.116 | 3 | 0.597 |
YANK2 |
0.717 | -0.122 | 2 | 0.416 |
SYK |
0.716 | -0.037 | -1 | 0.777 |
CK1G3 |
0.714 | -0.128 | -3 | 0.314 |
ERBB4 |
0.710 | -0.088 | 1 | 0.713 |
FES |
0.704 | -0.119 | -1 | 0.711 |
ZAP70 |
0.702 | -0.006 | -1 | 0.707 |
CK1G2 |
0.697 | -0.132 | -3 | 0.402 |