Motif 261 (n=134)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A0A6YYC7 | ZFP91-CNTF | S101 | ochoa | E3 ubiquitin-protein ligase ZFP91 (EC 2.3.2.27) (RING-type E3 ubiquitin transferase ZFP91) (Zinc finger protein 91 homolog) | Atypical E3 ubiquitin-protein ligase that mediates 'Lys-63'-linked ubiquitination of MAP3K14/NIK, leading to stabilize and activate MAP3K14/NIK. It thereby acts as an activator of the non-canonical NF-kappa-B2/NFKB2 pathway. May also play an important role in cell proliferation and/or anti-apoptosis. {ECO:0000256|ARBA:ARBA00054990}. |
A1L390 | PLEKHG3 | S1046 | ochoa | Pleckstrin homology domain-containing family G member 3 (PH domain-containing family G member 3) | Plays a role in controlling cell polarity and cell motility by selectively binding newly polymerized actin and activating RAC1 and CDC42 to enhance local actin polymerization. {ECO:0000269|PubMed:27555588}. |
A6NJT0 | UNCX | S449 | ochoa | Homeobox protein unc-4 homolog (Homeobox protein Uncx4.1) | Transcription factor involved in somitogenesis and neurogenesis. Required for the maintenance and differentiation of particular elements of the axial skeleton. May act upstream of PAX9. Plays a role in controlling the development of connections of hypothalamic neurons to pituitary elements, allowing central neurons to reach the peripheral blood circulation and to deliver hormones for control of peripheral functions (By similarity). {ECO:0000250}. |
B8ZZF3 | None | S322 | ochoa | Mediator of RNA polymerase II transcription subunit 26 (Cofactor required for Sp1 transcriptional activation subunit 7) (Mediator complex subunit 26) | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional pre-initiation complex with RNA polymerase II and the general transcription factors. {ECO:0000256|ARBA:ARBA00057523}. |
O00148 | DDX39A | S43 | ochoa | ATP-dependent RNA helicase DDX39A (EC 3.6.4.13) (DEAD box protein 39) (Nuclear RNA helicase URH49) | Helicase that plays an essential role in mRNA export and is involved in multiple steps in RNA metabolism including alternative splicing (PubMed:33941617, PubMed:38801080). Regulates nuclear mRNA export to the cytoplasm through association with ECD (PubMed:33941617). Also involved in spliceosomal uridine-rich small nuclear RNA (U snRNA) export by stimulating the RNA binding of adapter PHAX (PubMed:39011894). Plays a role in the negative regulation of type I IFN production by increasing the nuclear retention of antiviral transcripts and thus reducing their protein expression (PubMed:32393512). Independently of the interferon pathway, plays an antiviral role against alphaviruses by binding to a 5' conserved sequence element in the viral genomic RNA (PubMed:37949067). {ECO:0000269|PubMed:15047853, ECO:0000269|PubMed:17548965, ECO:0000269|PubMed:32393512, ECO:0000269|PubMed:33941617, ECO:0000269|PubMed:37949067, ECO:0000269|PubMed:38801080}. |
O00221 | NFKBIE | S183 | ochoa | NF-kappa-B inhibitor epsilon (NF-kappa-BIE) (I-kappa-B-epsilon) (IkB-E) (IkB-epsilon) (IkappaBepsilon) | Sequesters NF-kappa-B transcription factor complexes in the cytoplasm, thereby inhibiting their activity (PubMed:9315679). Sequestered complexes include NFKB1-RELA (p50-p65) and NFKB1-REL (p50-c-Rel) complexes (PubMed:9135156, PubMed:9315679). Limits B-cell activation in response to pathogens, and also plays an important role in B-cell development (By similarity). {ECO:0000250|UniProtKB:O54910, ECO:0000269|PubMed:9135156, ECO:0000269|PubMed:9315679}. |
O14639 | ABLIM1 | S458 | ochoa | Actin-binding LIM protein 1 (abLIM-1) (Actin-binding LIM protein family member 1) (Actin-binding double zinc finger protein) (LIMAB1) (Limatin) | May act as scaffold protein (By similarity). May play a role in the development of the retina. Has been suggested to play a role in axon guidance. {ECO:0000250, ECO:0000269|PubMed:9245787}. |
O14733 | MAP2K7 | S61 | ochoa | Dual specificity mitogen-activated protein kinase kinase 7 (MAP kinase kinase 7) (MAPKK 7) (EC 2.7.12.2) (JNK-activating kinase 2) (MAPK/ERK kinase 7) (MEK 7) (Stress-activated protein kinase kinase 4) (SAPK kinase 4) (SAPKK-4) (SAPKK4) (c-Jun N-terminal kinase kinase 2) (JNK kinase 2) (JNKK 2) | Dual specificity protein kinase which acts as an essential component of the MAP kinase signal transduction pathway. Essential component of the stress-activated protein kinase/c-Jun N-terminal kinase (SAP/JNK) signaling pathway. With MAP2K4/MKK4, is the one of the only known kinase to directly activate the stress-activated protein kinase/c-Jun N-terminal kinases MAPK8/JNK1, MAPK9/JNK2 and MAPK10/JNK3. MAP2K4/MKK4 and MAP2K7/MKK7 both activate the JNKs by phosphorylation, but they differ in their preference for the phosphorylation site in the Thr-Pro-Tyr motif. MAP2K4/MKK4 shows preference for phosphorylation of the Tyr residue and MAP2K7/MKK7 for the Thr residue. The monophosphorylation of JNKs on the Thr residue is sufficient to increase JNK activity indicating that MAP2K7/MKK7 is important to trigger JNK activity, while the additional phosphorylation of the Tyr residue by MAP2K4/MKK4 ensures optimal JNK activation. Has a specific role in JNK signal transduction pathway activated by pro-inflammatory cytokines. The MKK/JNK signaling pathway is also involved in mitochondrial death signaling pathway, including the release cytochrome c, leading to apoptosis. Part of a non-canonical MAPK signaling pathway, composed of the upstream MAP3K12 kinase and downstream MAP kinases MAPK1/ERK2 and MAPK3/ERK1, that enhances the AP-1-mediated transcription of APP in response to APOE (PubMed:28111074). {ECO:0000269|PubMed:28111074, ECO:0000269|PubMed:9312068, ECO:0000269|PubMed:9372971, ECO:0000269|PubMed:9535930, ECO:0000269|Ref.5}. |
O14827 | RASGRF2 | S854 | ochoa | Ras-specific guanine nucleotide-releasing factor 2 (Ras-GRF2) (Ras guanine nucleotide exchange factor 2) | Functions as a calcium-regulated nucleotide exchange factor activating both Ras and RAC1 through the exchange of bound GDP for GTP. Preferentially activates HRAS in vivo compared to RRAS based on their different types of prenylation. Functions in synaptic plasticity by contributing to the induction of long term potentiation. {ECO:0000269|PubMed:15128856}. |
O43166 | SIPA1L1 | Y1133 | ochoa | Signal-induced proliferation-associated 1-like protein 1 (SIPA1-like protein 1) (High-risk human papilloma viruses E6 oncoproteins targeted protein 1) (E6-targeted protein 1) | Stimulates the GTPase activity of RAP2A. Promotes reorganization of the actin cytoskeleton and recruits DLG4 to F-actin. Contributes to the regulation of dendritic spine morphogenesis (By similarity). {ECO:0000250}. |
O43439 | CBFA2T2 | S270 | ochoa | Protein CBFA2T2 (ETO homologous on chromosome 20) (MTG8-like protein) (MTG8-related protein 1) (Myeloid translocation-related protein 1) (p85) | Transcriptional corepressor which facilitates transcriptional repression via its association with DNA-binding transcription factors and recruitment of other corepressors and histone-modifying enzymes (PubMed:12559562, PubMed:15203199). Via association with PRDM14 is involved in regulation of embryonic stem cell (ESC) pluripotency (PubMed:27281218). Involved in primordial germ cell (PCG) formation. Stabilizes PRDM14 and OCT4 on chromatin in a homooligomerization-dependent manner (By similarity). Can repress the expression of MMP7 in a ZBTB33-dependent manner (PubMed:23251453). May function as a complex with the chimeric protein RUNX1/AML1-CBFA2T1/MTG8 (AML1-MTG8/ETO fusion protein) which is produced in acute myeloid leukemia with the chromosomal translocation t(8;21). May thus be involved in the repression of AML1-dependent transcription and the induction of G-CSF/CSF3-dependent cell growth. May be a tumor suppressor gene candidate involved in myeloid tumors with the deletion of the 20q11 region. Through heteromerization with CBFA2T3/MTG16 may be involved in regulation of the proliferation and the differentiation of erythroid progenitors by repressing the expression of TAL1 target genes (By similarity). Required for the maintenance of the secretory cell lineage in the small intestine. Can inhibit Notch signaling probably by association with RBPJ and may be involved in GFI1-mediated Paneth cell differentiation (By similarity). {ECO:0000250|UniProtKB:O70374, ECO:0000269|PubMed:23251453, ECO:0000303|PubMed:12559562, ECO:0000303|PubMed:15203199}. |
O43516 | WIPF1 | S244 | ochoa | WAS/WASL-interacting protein family member 1 (Protein PRPL-2) (Wiskott-Aldrich syndrome protein-interacting protein) (WASP-interacting protein) | Plays a role in the reorganization of the actin cytoskeleton. Contributes with NCK1 and GRB2 in the recruitment and activation of WASL. May participate in regulating the subcellular localization of WASL, resulting in the disassembly of stress fibers in favor of filopodia formation. Plays a role in the formation of cell ruffles (By similarity). Plays an important role in the intracellular motility of vaccinia virus by functioning as an adapter for recruiting WASL to vaccinia virus. {ECO:0000250, ECO:0000269|PubMed:10878810, ECO:0000269|PubMed:19910490, ECO:0000269|PubMed:9405671}. |
O60861 | GAS7 | S117 | ochoa | Growth arrest-specific protein 7 (GAS-7) | May play a role in promoting maturation and morphological differentiation of cerebellar neurons. |
O75151 | PHF2 | S905 | ochoa | Lysine-specific demethylase PHF2 (EC 1.14.11.-) (GRC5) (PHD finger protein 2) | Lysine demethylase that demethylates both histones and non-histone proteins (PubMed:20129925, PubMed:21167174, PubMed:21532585). Enzymatically inactive by itself, and becomes active following phosphorylation by PKA: forms a complex with ARID5B and mediates demethylation of methylated ARID5B (PubMed:21532585). Demethylation of ARID5B leads to target the PHF2-ARID5B complex to target promoters, where PHF2 mediates demethylation of dimethylated 'Lys-9' of histone H3 (H3K9me2), followed by transcription activation of target genes (PubMed:21532585). The PHF2-ARID5B complex acts as a coactivator of HNF4A in liver. PHF2 is recruited to trimethylated 'Lys-4' of histone H3 (H3K4me3) at rDNA promoters and promotes expression of rDNA (PubMed:21532585). Involved in the activation of toll-like receptor 4 (TLR4)-target inflammatory genes in macrophages by catalyzing the demethylation of trimethylated histone H4 lysine 20 (H4K20me3) at the gene promoters (By similarity). {ECO:0000250|UniProtKB:Q9WTU0, ECO:0000269|PubMed:20129925, ECO:0000269|PubMed:21167174, ECO:0000269|PubMed:21532585}. |
O75385 | ULK1 | S781 | ochoa | Serine/threonine-protein kinase ULK1 (EC 2.7.11.1) (Autophagy-related protein 1 homolog) (ATG1) (hATG1) (Unc-51-like kinase 1) | Serine/threonine-protein kinase involved in autophagy in response to starvation (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:23524951, PubMed:25040165, PubMed:29487085, PubMed:31123703). Acts upstream of phosphatidylinositol 3-kinase PIK3C3 to regulate the formation of autophagophores, the precursors of autophagosomes (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:25040165). Part of regulatory feedback loops in autophagy: acts both as a downstream effector and negative regulator of mammalian target of rapamycin complex 1 (mTORC1) via interaction with RPTOR (PubMed:21795849). Activated via phosphorylation by AMPK and also acts as a regulator of AMPK by mediating phosphorylation of AMPK subunits PRKAA1, PRKAB2 and PRKAG1, leading to negatively regulate AMPK activity (PubMed:21460634). May phosphorylate ATG13/KIAA0652 and RPTOR; however such data need additional evidences (PubMed:18936157). Plays a role early in neuronal differentiation and is required for granule cell axon formation (PubMed:11146101). Also phosphorylates SESN2 and SQSTM1 to regulate autophagy (PubMed:25040165, PubMed:37306101). Phosphorylates FLCN, promoting autophagy (PubMed:25126726). Phosphorylates AMBRA1 in response to autophagy induction, releasing AMBRA1 from the cytoskeletal docking site to induce autophagosome nucleation (PubMed:20921139). Phosphorylates ATG4B, leading to inhibit autophagy by decreasing both proteolytic activation and delipidation activities of ATG4B (PubMed:28821708). {ECO:0000269|PubMed:11146101, ECO:0000269|PubMed:18936157, ECO:0000269|PubMed:20921139, ECO:0000269|PubMed:21460634, ECO:0000269|PubMed:21795849, ECO:0000269|PubMed:23524951, ECO:0000269|PubMed:25040165, ECO:0000269|PubMed:25126726, ECO:0000269|PubMed:28821708, ECO:0000269|PubMed:29487085, ECO:0000269|PubMed:31123703, ECO:0000269|PubMed:37306101}. |
O75385 | ULK1 | S783 | ochoa | Serine/threonine-protein kinase ULK1 (EC 2.7.11.1) (Autophagy-related protein 1 homolog) (ATG1) (hATG1) (Unc-51-like kinase 1) | Serine/threonine-protein kinase involved in autophagy in response to starvation (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:23524951, PubMed:25040165, PubMed:29487085, PubMed:31123703). Acts upstream of phosphatidylinositol 3-kinase PIK3C3 to regulate the formation of autophagophores, the precursors of autophagosomes (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:25040165). Part of regulatory feedback loops in autophagy: acts both as a downstream effector and negative regulator of mammalian target of rapamycin complex 1 (mTORC1) via interaction with RPTOR (PubMed:21795849). Activated via phosphorylation by AMPK and also acts as a regulator of AMPK by mediating phosphorylation of AMPK subunits PRKAA1, PRKAB2 and PRKAG1, leading to negatively regulate AMPK activity (PubMed:21460634). May phosphorylate ATG13/KIAA0652 and RPTOR; however such data need additional evidences (PubMed:18936157). Plays a role early in neuronal differentiation and is required for granule cell axon formation (PubMed:11146101). Also phosphorylates SESN2 and SQSTM1 to regulate autophagy (PubMed:25040165, PubMed:37306101). Phosphorylates FLCN, promoting autophagy (PubMed:25126726). Phosphorylates AMBRA1 in response to autophagy induction, releasing AMBRA1 from the cytoskeletal docking site to induce autophagosome nucleation (PubMed:20921139). Phosphorylates ATG4B, leading to inhibit autophagy by decreasing both proteolytic activation and delipidation activities of ATG4B (PubMed:28821708). {ECO:0000269|PubMed:11146101, ECO:0000269|PubMed:18936157, ECO:0000269|PubMed:20921139, ECO:0000269|PubMed:21460634, ECO:0000269|PubMed:21795849, ECO:0000269|PubMed:23524951, ECO:0000269|PubMed:25040165, ECO:0000269|PubMed:25126726, ECO:0000269|PubMed:28821708, ECO:0000269|PubMed:29487085, ECO:0000269|PubMed:31123703, ECO:0000269|PubMed:37306101}. |
O75626 | PRDM1 | S342 | ochoa | PR domain zinc finger protein 1 (EC 2.1.1.-) (BLIMP-1) (Beta-interferon gene positive regulatory domain I-binding factor) (PR domain-containing protein 1) (Positive regulatory domain I-binding factor 1) (PRDI-BF1) (PRDI-binding factor 1) | Transcription factor that mediates a transcriptional program in various innate and adaptive immune tissue-resident lymphocyte T cell types such as tissue-resident memory T (Trm), natural killer (trNK) and natural killer T (NKT) cells and negatively regulates gene expression of proteins that promote the egress of tissue-resident T-cell populations from non-lymphoid organs. Plays a role in the development, retention and long-term establishment of adaptive and innate tissue-resident lymphocyte T cell types in non-lymphoid organs, such as the skin and gut, but also in other nonbarrier tissues like liver and kidney, and therefore may provide immediate immunological protection against reactivating infections or viral reinfection (By similarity). Binds specifically to the PRDI element in the promoter of the beta-interferon gene (PubMed:1851123). Drives the maturation of B-lymphocytes into Ig secreting cells (PubMed:12626569). Associates with the transcriptional repressor ZNF683 to chromatin at gene promoter regions (By similarity). Binds to the promoter and acts as a transcriptional repressor of IRF8, thereby promotes transcription of osteoclast differentiation factors such as NFATC1 and EEIG1 (By similarity). {ECO:0000250|UniProtKB:Q60636, ECO:0000269|PubMed:12626569, ECO:0000269|PubMed:1851123}. |
O75626 | PRDM1 | S355 | ochoa | PR domain zinc finger protein 1 (EC 2.1.1.-) (BLIMP-1) (Beta-interferon gene positive regulatory domain I-binding factor) (PR domain-containing protein 1) (Positive regulatory domain I-binding factor 1) (PRDI-BF1) (PRDI-binding factor 1) | Transcription factor that mediates a transcriptional program in various innate and adaptive immune tissue-resident lymphocyte T cell types such as tissue-resident memory T (Trm), natural killer (trNK) and natural killer T (NKT) cells and negatively regulates gene expression of proteins that promote the egress of tissue-resident T-cell populations from non-lymphoid organs. Plays a role in the development, retention and long-term establishment of adaptive and innate tissue-resident lymphocyte T cell types in non-lymphoid organs, such as the skin and gut, but also in other nonbarrier tissues like liver and kidney, and therefore may provide immediate immunological protection against reactivating infections or viral reinfection (By similarity). Binds specifically to the PRDI element in the promoter of the beta-interferon gene (PubMed:1851123). Drives the maturation of B-lymphocytes into Ig secreting cells (PubMed:12626569). Associates with the transcriptional repressor ZNF683 to chromatin at gene promoter regions (By similarity). Binds to the promoter and acts as a transcriptional repressor of IRF8, thereby promotes transcription of osteoclast differentiation factors such as NFATC1 and EEIG1 (By similarity). {ECO:0000250|UniProtKB:Q60636, ECO:0000269|PubMed:12626569, ECO:0000269|PubMed:1851123}. |
O75665 | OFD1 | S850 | ochoa | Centriole and centriolar satellite protein OFD1 (Oral-facial-digital syndrome 1 protein) (Protein 71-7A) | Component of the centrioles controlling mother and daughter centrioles length. Recruits to the centriole IFT88 and centriole distal appendage-specific proteins including CEP164 (By similarity). Involved in the biogenesis of the cilium, a centriole-associated function. The cilium is a cell surface projection found in many vertebrate cells required to transduce signals important for development and tissue homeostasis (PubMed:33934390). Plays an important role in development by regulating Wnt signaling and the specification of the left-right axis. Only OFD1 localized at the centriolar satellites is removed by autophagy, which is an important step in the ciliogenesis regulation (By similarity). {ECO:0000250|UniProtKB:Q80Z25, ECO:0000269|PubMed:33934390}. |
O94885 | SASH1 | S1031 | ochoa | SAM and SH3 domain-containing protein 1 (Proline-glutamate repeat-containing protein) | Is a positive regulator of NF-kappa-B signaling downstream of TLR4 activation. It acts as a scaffold molecule to assemble a molecular complex that includes TRAF6, MAP3K7, CHUK and IKBKB, thereby facilitating NF-kappa-B signaling activation (PubMed:23776175). Regulates TRAF6 and MAP3K7 ubiquitination (PubMed:23776175). Involved in the regulation of cell mobility (PubMed:23333244, PubMed:23776175, PubMed:25315659). Regulates lipolysaccharide (LPS)-induced endothelial cell migration (PubMed:23776175). Is involved in the regulation of skin pigmentation through the control of melanocyte migration in the epidermis (PubMed:23333244). {ECO:0000269|PubMed:23333244, ECO:0000269|PubMed:23776175, ECO:0000269|PubMed:25315659}. |
O94929 | ABLIM3 | S379 | ochoa | Actin-binding LIM protein 3 (abLIM-3) (Actin-binding LIM protein family member 3) | May act as scaffold protein. May stimulate ABRA activity and ABRA-dependent SRF transcriptional activity. {ECO:0000269|PubMed:17194709}. |
O95359 | TACC2 | S1796 | ochoa | Transforming acidic coiled-coil-containing protein 2 (Anti-Zuai-1) (AZU-1) | Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors (By similarity). May play a role in organizing centrosomal microtubules. May act as a tumor suppressor protein. May represent a tumor progression marker. {ECO:0000250, ECO:0000269|PubMed:10749935}. |
O95402 | MED26 | S314 | ochoa | Mediator of RNA polymerase II transcription subunit 26 (Activator-recruited cofactor 70 kDa component) (ARC70) (Cofactor required for Sp1 transcriptional activation subunit 7) (CRSP complex subunit 7) (Mediator complex subunit 26) (Transcriptional coactivator CRSP70) | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional pre-initiation complex with RNA polymerase II and the general transcription factors. |
P11137 | MAP2 | S1540 | ochoa | Microtubule-associated protein 2 (MAP-2) | The exact function of MAP2 is unknown but MAPs may stabilize the microtubules against depolymerization. They also seem to have a stiffening effect on microtubules. |
P15976 | GATA1 | S187 | psp | Erythroid transcription factor (Eryf1) (GATA-binding factor 1) (GATA-1) (GF-1) (NF-E1 DNA-binding protein) | Transcriptional activator or repressor which serves as a general switch factor for erythroid development (PubMed:35030251). It binds to DNA sites with the consensus sequence 5'-[AT]GATA[AG]-3' within regulatory regions of globin genes and of other genes expressed in erythroid cells. Activates the transcription of genes involved in erythroid differentiation of K562 erythroleukemia cells, including HBB, HBG1/2, ALAS2 and HMBS (PubMed:24245781). {ECO:0000269|PubMed:22235304, ECO:0000269|PubMed:24245781, ECO:0000269|PubMed:35030251}. |
P16144 | ITGB4 | S1521 | ochoa | Integrin beta-4 (GP150) (CD antigen CD104) | Integrin alpha-6/beta-4 is a receptor for laminin. Plays a critical structural role in the hemidesmosome of epithelial cells. Is required for the regulation of keratinocyte polarity and motility. ITGA6:ITGB4 binds to NRG1 (via EGF domain) and this binding is essential for NRG1-ERBB signaling (PubMed:20682778). ITGA6:ITGB4 binds to IGF1 and this binding is essential for IGF1 signaling (PubMed:22351760). ITGA6:ITGB4 binds to IGF2 and this binding is essential for IGF2 signaling (PubMed:28873464). {ECO:0000269|PubMed:12482924, ECO:0000269|PubMed:19403692, ECO:0000269|PubMed:20682778, ECO:0000269|PubMed:22351760, ECO:0000269|PubMed:28873464}. |
P23443 | RPS6KB1 | S447 | ochoa|psp | Ribosomal protein S6 kinase beta-1 (S6K-beta-1) (S6K1) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 1) (P70S6K1) (p70-S6K 1) (Ribosomal protein S6 kinase I) (Serine/threonine-protein kinase 14A) (p70 ribosomal S6 kinase alpha) (p70 S6 kinase alpha) (p70 S6K-alpha) (p70 S6KA) | Serine/threonine-protein kinase that acts downstream of mTOR signaling in response to growth factors and nutrients to promote cell proliferation, cell growth and cell cycle progression (PubMed:11500364, PubMed:12801526, PubMed:14673156, PubMed:15071500, PubMed:15341740, PubMed:16286006, PubMed:17052453, PubMed:17053147, PubMed:17936702, PubMed:18952604, PubMed:19085255, PubMed:19720745, PubMed:19935711, PubMed:19995915, PubMed:22017876, PubMed:23429703, PubMed:28178239). Regulates protein synthesis through phosphorylation of EIF4B, RPS6 and EEF2K, and contributes to cell survival by repressing the pro-apoptotic function of BAD (PubMed:11500364, PubMed:12801526, PubMed:14673156, PubMed:15071500, PubMed:15341740, PubMed:16286006, PubMed:17052453, PubMed:17053147, PubMed:17936702, PubMed:18952604, PubMed:19085255, PubMed:19720745, PubMed:19935711, PubMed:19995915, PubMed:22017876, PubMed:23429703, PubMed:28178239). Under conditions of nutrient depletion, the inactive form associates with the EIF3 translation initiation complex (PubMed:16286006). Upon mitogenic stimulation, phosphorylation by the mechanistic target of rapamycin complex 1 (mTORC1) leads to dissociation from the EIF3 complex and activation (PubMed:16286006). The active form then phosphorylates and activates several substrates in the pre-initiation complex, including the EIF2B complex and the cap-binding complex component EIF4B (PubMed:16286006). Also controls translation initiation by phosphorylating a negative regulator of EIF4A, PDCD4, targeting it for ubiquitination and subsequent proteolysis (PubMed:17053147). Promotes initiation of the pioneer round of protein synthesis by phosphorylating POLDIP3/SKAR (PubMed:15341740). In response to IGF1, activates translation elongation by phosphorylating EEF2 kinase (EEF2K), which leads to its inhibition and thus activation of EEF2 (PubMed:11500364). Also plays a role in feedback regulation of mTORC2 by mTORC1 by phosphorylating MAPKAP1/SIN1, MTOR and RICTOR, resulting in the inhibition of mTORC2 and AKT1 signaling (PubMed:15899889, PubMed:19720745, PubMed:19935711, PubMed:19995915). Also involved in feedback regulation of mTORC1 and mTORC2 by phosphorylating DEPTOR (PubMed:22017876). Mediates cell survival by phosphorylating the pro-apoptotic protein BAD and suppressing its pro-apoptotic function (By similarity). Phosphorylates mitochondrial URI1 leading to dissociation of a URI1-PPP1CC complex (PubMed:17936702). The free mitochondrial PPP1CC can then dephosphorylate RPS6KB1 at Thr-412, which is proposed to be a negative feedback mechanism for the RPS6KB1 anti-apoptotic function (PubMed:17936702). Mediates TNF-alpha-induced insulin resistance by phosphorylating IRS1 at multiple serine residues, resulting in accelerated degradation of IRS1 (PubMed:18952604). In cells lacking functional TSC1-2 complex, constitutively phosphorylates and inhibits GSK3B (PubMed:17052453). May be involved in cytoskeletal rearrangement through binding to neurabin (By similarity). Phosphorylates and activates the pyrimidine biosynthesis enzyme CAD, downstream of MTOR (PubMed:23429703). Following activation by mTORC1, phosphorylates EPRS and thereby plays a key role in fatty acid uptake by adipocytes and also most probably in interferon-gamma-induced translation inhibition (PubMed:28178239). {ECO:0000250|UniProtKB:P67999, ECO:0000250|UniProtKB:Q8BSK8, ECO:0000269|PubMed:11500364, ECO:0000269|PubMed:12801526, ECO:0000269|PubMed:14673156, ECO:0000269|PubMed:15071500, ECO:0000269|PubMed:15341740, ECO:0000269|PubMed:15899889, ECO:0000269|PubMed:16286006, ECO:0000269|PubMed:17052453, ECO:0000269|PubMed:17053147, ECO:0000269|PubMed:17936702, ECO:0000269|PubMed:18952604, ECO:0000269|PubMed:19085255, ECO:0000269|PubMed:19720745, ECO:0000269|PubMed:19935711, ECO:0000269|PubMed:19995915, ECO:0000269|PubMed:22017876, ECO:0000269|PubMed:23429703, ECO:0000269|PubMed:28178239}. |
P23588 | EIF4B | S504 | ochoa|psp | Eukaryotic translation initiation factor 4B (eIF-4B) | Required for the binding of mRNA to ribosomes. Functions in close association with EIF4-F and EIF4-A. Binds near the 5'-terminal cap of mRNA in presence of EIF-4F and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both EIF4-A and EIF4-F. |
P24864 | CCNE1 | S387 | ochoa|psp | G1/S-specific cyclin-E1 | Essential for the control of the cell cycle at the G1/S (start) transition. {ECO:0000269|PubMed:7739542}. |
P27448 | MARK3 | S546 | ochoa | MAP/microtubule affinity-regulating kinase 3 (EC 2.7.11.1) (C-TAK1) (cTAK1) (Cdc25C-associated protein kinase 1) (ELKL motif kinase 2) (EMK-2) (Protein kinase STK10) (Ser/Thr protein kinase PAR-1) (Par-1a) (Serine/threonine-protein kinase p78) | Serine/threonine-protein kinase (PubMed:16822840, PubMed:16980613, PubMed:23666762). Involved in the specific phosphorylation of microtubule-associated proteins for MAP2 and MAP4. Phosphorylates the microtubule-associated protein MAPT/TAU (PubMed:23666762). Phosphorylates CDC25C on 'Ser-216' (PubMed:12941695). 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 (PubMed:16980613). Regulates localization and activity of MITF by mediating its phosphorylation, promoting subsequent interaction between MITF and 14-3-3 and retention in the cytosol (PubMed:16822840). Negatively regulates the Hippo signaling pathway and antagonizes the phosphorylation of LATS1. Cooperates with DLG5 to inhibit the kinase activity of STK3/MST2 toward LATS1 (PubMed:28087714). Phosphorylates PKP2 and KSR1 (PubMed:12941695). {ECO:0000269|PubMed:12941695, ECO:0000269|PubMed:16822840, ECO:0000269|PubMed:16980613, ECO:0000269|PubMed:23666762, ECO:0000269|PubMed:28087714}. |
P27708 | CAD | T1906 | ochoa | Multifunctional protein CAD (Carbamoyl phosphate synthetase 2-aspartate transcarbamylase-dihydroorotase) [Includes: Glutamine-dependent carbamoyl phosphate synthase (EC 6.3.5.5); Glutamine amidotransferase (GATase) (GLNase) (EC 3.5.1.2); Ammonium-dependent carbamoyl phosphate synthase (CPS) (CPSase) (EC 6.3.4.16); Aspartate carbamoyltransferase (EC 2.1.3.2); Dihydroorotase (EC 3.5.2.3)] | Multifunctional protein that encodes the first 3 enzymatic activities of the de novo pyrimidine pathway: carbamoylphosphate synthetase (CPSase; EC 6.3.5.5), aspartate transcarbamylase (ATCase; EC 2.1.3.2) and dihydroorotase (DHOase; EC 3.5.2.3). The CPSase-function is accomplished in 2 steps, by a glutamine-dependent amidotransferase activity (GATase) that binds and cleaves glutamine to produce ammonia, followed by an ammonium-dependent carbamoyl phosphate synthetase, which reacts with the ammonia, hydrogencarbonate and ATP to form carbamoyl phosphate. The endogenously produced carbamoyl phosphate is sequestered and channeled to the ATCase active site. ATCase then catalyzes the formation of carbamoyl-L-aspartate from L-aspartate and carbamoyl phosphate. In the last step, DHOase catalyzes the cyclization of carbamoyl aspartate to dihydroorotate. {ECO:0000269|PubMed:24332717}. |
P27987 | ITPKB | S49 | ochoa | Inositol-trisphosphate 3-kinase B (EC 2.7.1.127) (Inositol 1,4,5-trisphosphate 3-kinase B) (IP3 3-kinase B) (IP3K B) (InsP 3-kinase B) | Catalyzes the phosphorylation of 1D-myo-inositol 1,4,5-trisphosphate (InsP3) into 1D-myo-inositol 1,3,4,5-tetrakisphosphate and participates to the regulation of calcium homeostasis. {ECO:0000269|PubMed:11846419, ECO:0000269|PubMed:12747803, ECO:0000269|PubMed:1654894}. |
P28290 | ITPRID2 | S759 | ochoa | Protein ITPRID2 (Cleavage signal-1 protein) (CS-1) (ITPR-interacting domain-containing protein 2) (Ki-ras-induced actin-interacting protein) (Sperm-specific antigen 2) | None |
P28749 | RBL1 | S988 | ochoa | Retinoblastoma-like protein 1 (107 kDa retinoblastoma-associated protein) (p107) (pRb1) | Key regulator of entry into cell division (PubMed:17671431). Directly involved in heterochromatin formation by maintaining overall chromatin structure and, in particular, that of constitutive heterochromatin by stabilizing histone methylation (By similarity). Recruits and targets histone methyltransferases KMT5B and KMT5C, leading to epigenetic transcriptional repression (By similarity). Controls histone H4 'Lys-20' trimethylation (By similarity). Probably acts as a transcription repressor by recruiting chromatin-modifying enzymes to promoters (By similarity). Potent inhibitor of E2F-mediated trans-activation (PubMed:8319904). May act as a tumor suppressor (PubMed:8319904). {ECO:0000250|UniProtKB:Q64701, ECO:0000269|PubMed:17671431, ECO:0000269|PubMed:8319904}. |
P38398 | BRCA1 | S1503 | ochoa | Breast cancer type 1 susceptibility protein (EC 2.3.2.27) (RING finger protein 53) (RING-type E3 ubiquitin transferase BRCA1) | E3 ubiquitin-protein ligase that specifically mediates the formation of 'Lys-6'-linked polyubiquitin chains and plays a central role in DNA repair by facilitating cellular responses to DNA damage (PubMed:10500182, PubMed:12887909, PubMed:12890688, PubMed:14976165, PubMed:16818604, PubMed:17525340, PubMed:19261748). It is unclear whether it also mediates the formation of other types of polyubiquitin chains (PubMed:12890688). The BRCA1-BARD1 heterodimer coordinates a diverse range of cellular pathways such as DNA damage repair, ubiquitination and transcriptional regulation to maintain genomic stability (PubMed:12890688, PubMed:14976165, PubMed:20351172). Regulates centrosomal microtubule nucleation (PubMed:18056443). Required for appropriate cell cycle arrests after ionizing irradiation in both the S-phase and the G2 phase of the cell cycle (PubMed:10724175, PubMed:11836499, PubMed:12183412, PubMed:19261748). Required for FANCD2 targeting to sites of DNA damage (PubMed:12887909). Inhibits lipid synthesis by binding to inactive phosphorylated ACACA and preventing its dephosphorylation (PubMed:16326698). Contributes to homologous recombination repair (HRR) via its direct interaction with PALB2, fine-tunes recombinational repair partly through its modulatory role in the PALB2-dependent loading of BRCA2-RAD51 repair machinery at DNA breaks (PubMed:19369211). Component of the BRCA1-RBBP8 complex which regulates CHEK1 activation and controls cell cycle G2/M checkpoints on DNA damage via BRCA1-mediated ubiquitination of RBBP8 (PubMed:16818604). Acts as a transcriptional activator (PubMed:20160719). {ECO:0000269|PubMed:10500182, ECO:0000269|PubMed:10724175, ECO:0000269|PubMed:11836499, ECO:0000269|PubMed:12183412, ECO:0000269|PubMed:12887909, ECO:0000269|PubMed:12890688, ECO:0000269|PubMed:14976165, ECO:0000269|PubMed:16326698, ECO:0000269|PubMed:16818604, ECO:0000269|PubMed:17525340, ECO:0000269|PubMed:18056443, ECO:0000269|PubMed:19261748, ECO:0000269|PubMed:19369211, ECO:0000269|PubMed:20160719, ECO:0000269|PubMed:20351172}. |
P42166 | TMPO | S442 | ochoa | Lamina-associated polypeptide 2, isoform alpha (Thymopoietin isoform alpha) (TP alpha) (Thymopoietin-related peptide isoform alpha) (TPRP isoform alpha) [Cleaved into: Thymopoietin (TP) (Splenin); Thymopentin (TP5)] | May be involved in the structural organization of the nucleus and in the post-mitotic nuclear assembly. Plays an important role, together with LMNA, in the nuclear anchorage of RB1.; FUNCTION: TP and TP5 may play a role in T-cell development and function. TP5 is an immunomodulating pentapeptide. |
P42702 | LIFR | S1050 | ochoa | Leukemia inhibitory factor receptor (LIF receptor) (LIF-R) (CD antigen CD118) | Signal-transducing molecule. May have a common pathway with IL6ST. The soluble form inhibits the biological activity of LIF by blocking its binding to receptors on target cells. |
P51825 | AFF1 | S212 | ochoa|psp | AF4/FMR2 family member 1 (ALL1-fused gene from chromosome 4 protein) (Protein AF-4) (Protein FEL) (Proto-oncogene AF4) | None |
P53814 | SMTN | S357 | ochoa | Smoothelin | Structural protein of the cytoskeleton. |
P78559 | MAP1A | S1160 | ochoa | Microtubule-associated protein 1A (MAP-1A) (Proliferation-related protein p80) [Cleaved into: MAP1A heavy chain; MAP1 light chain LC2] | Structural protein involved in the filamentous cross-bridging between microtubules and other skeletal elements. |
Q03164 | KMT2A | S3521 | ochoa | Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.364) (ALL-1) (CXXC-type zinc finger protein 7) (Cysteine methyltransferase KMT2A) (EC 2.1.1.-) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)] | Histone methyltransferase that plays an essential role in early development and hematopoiesis (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:26886794). Catalytic subunit of the MLL1/MLL complex, a multiprotein complex that mediates both methylation of 'Lys-4' of histone H3 (H3K4me) complex and acetylation of 'Lys-16' of histone H4 (H4K16ac) (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:24235145, PubMed:26886794). Catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) via a non-processive mechanism. Part of chromatin remodeling machinery predominantly forms H3K4me1 and H3K4me2 methylation marks at active chromatin sites where transcription and DNA repair take place (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:25561738, PubMed:26886794). Has weak methyltransferase activity by itself, and requires other component of the MLL1/MLL complex to obtain full methyltransferase activity (PubMed:19187761, PubMed:26886794). Has no activity toward histone H3 phosphorylated on 'Thr-3', less activity toward H3 dimethylated on 'Arg-8' or 'Lys-9', while it has higher activity toward H3 acetylated on 'Lys-9' (PubMed:19187761). Binds to unmethylated CpG elements in the promoter of target genes and helps maintain them in the nonmethylated state (PubMed:20010842). Required for transcriptional activation of HOXA9 (PubMed:12453419, PubMed:20010842, PubMed:20677832). Promotes PPP1R15A-induced apoptosis (PubMed:10490642). Plays a critical role in the control of circadian gene expression and is essential for the transcriptional activation mediated by the CLOCK-BMAL1 heterodimer (By similarity). Establishes a permissive chromatin state for circadian transcription by mediating a rhythmic methylation of 'Lys-4' of histone H3 (H3K4me) and this histone modification directs the circadian acetylation at H3K9 and H3K14 allowing the recruitment of CLOCK-BMAL1 to chromatin (By similarity). Also has auto-methylation activity on Cys-3882 in absence of histone H3 substrate (PubMed:24235145). {ECO:0000250|UniProtKB:P55200, ECO:0000269|PubMed:10490642, ECO:0000269|PubMed:12453419, ECO:0000269|PubMed:15960975, ECO:0000269|PubMed:19187761, ECO:0000269|PubMed:19556245, ECO:0000269|PubMed:20010842, ECO:0000269|PubMed:21220120, ECO:0000269|PubMed:24235145, ECO:0000269|PubMed:26886794, ECO:0000305|PubMed:20677832}. |
Q0JRZ9 | FCHO2 | S514 | ochoa | F-BAR domain only protein 2 | Functions in an early step of clathrin-mediated endocytosis. Has both a membrane binding/bending activity and the ability to recruit proteins essential to the formation of functional clathrin-coated pits. Has a lipid-binding activity with a preference for membranes enriched in phosphatidylserine and phosphoinositides (Pi(4,5) biphosphate) like the plasma membrane. Its membrane-bending activity might be important for the subsequent action of clathrin and adaptors in the formation of clathrin-coated vesicles. Involved in adaptor protein complex AP-2-dependent endocytosis of the transferrin receptor, it also functions in the AP-2-independent endocytosis of the LDL receptor. {ECO:0000269|PubMed:17540576, ECO:0000269|PubMed:20448150, ECO:0000269|PubMed:21762413, ECO:0000269|PubMed:22323290}. |
Q12893 | TMEM115 | S320 | ochoa | Transmembrane protein 115 (Placental protein 6) (Protein PL6) | May play a role in retrograde transport of proteins from the Golgi to the endoplasmic reticulum. May indirectly play a role in protein glycosylation in the Golgi. {ECO:0000269|PubMed:24806965}. |
Q13094 | LCP2 | S344 | ochoa | Lymphocyte cytosolic protein 2 (SH2 domain-containing leukocyte protein of 76 kDa) (SLP-76 tyrosine phosphoprotein) (SLP76) | Adapter protein primarily involved in signaling pathways within T-cells, as well as other immune cells such as platelets, mast cells, and natural killer (NK) cells (PubMed:11313406, PubMed:33159816). Plays a crucial role for transducing signal from the T-cell receptor (TCR) after antigen recognition leading to T-cell activation. Mechanistically, once phosphorylated by the kinase ZAP70, mediates interactions with the guanine-nucleotide exchange factor VAV1, the adapter protein NCK and the kinase ITK (PubMed:8673706, PubMed:8702662). In turn, stimulates the activation of PKC-theta/PRKCQ and NF-kappa-B transcriptional activity in response to CD3 and CD28 costimulation (PubMed:11313406). Also plays an essential role in AGER-induced signaling pathways including p38 MAPK and ERK1/2 activation leading to cytokine release and pro-inflammatory responses (PubMed:33436632). {ECO:0000269|PubMed:11313406, ECO:0000269|PubMed:33436632, ECO:0000269|PubMed:8673706, ECO:0000269|PubMed:8702662}. |
Q13207 | TBX2 | S342 | ochoa | T-box transcription factor TBX2 (T-box protein 2) | Transcription factor which acts as a transcriptional repressor (PubMed:11062467, PubMed:11111039, PubMed:12000749, PubMed:22844464, PubMed:30599067). May also function as a transcriptional activator (By similarity). Binds to the palindromic T site 5'-TTCACACCTAGGTGTGAA-3' DNA sequence, or a half-site, which are present in the regulatory region of several genes (PubMed:11111039, PubMed:12000749, PubMed:22844464, PubMed:30599067). Required for cardiac atrioventricular canal formation (PubMed:29726930). May cooperate with NKX2.5 to negatively modulate expression of NPPA/ANF in the atrioventricular canal (By similarity). May play a role as a positive regulator of TGFB2 expression, perhaps acting in concert with GATA4 in the developing outflow tract myocardium (By similarity). Plays a role in limb pattern formation (PubMed:29726930). Acts as a transcriptional repressor of ADAM10 gene expression, perhaps in concert with histone deacetylase HDAC1 as cofactor (PubMed:30599067). Involved in branching morphogenesis in both developing lungs and adult mammary glands, via negative modulation of target genes; acting redundantly with TBX3 (By similarity). Required, together with TBX3, to maintain cell proliferation in the embryonic lung mesenchyme; perhaps acting downstream of SHH, BMP and TGFbeta signaling (By similarity). Involved in modulating early inner ear development, acting independently of, and also redundantly with TBX3, in different subregions of the developing ear (By similarity). Acts as a negative regulator of PML function in cellular senescence (PubMed:22002537). Acts as a negative regulator of expression of CDKN1A/p21, IL33 and CCN4; repression of CDKN1A is enhanced in response to UV-induced stress, perhaps as a result of phosphorylation by p38 MAPK (By similarity). Negatively modulates expression of CDKN2A/p14ARF and CDH1/E-cadherin (PubMed:11062467, PubMed:12000749, PubMed:22844464). Plays a role in induction of the epithelial-mesenchymal transition (EMT) (PubMed:22844464). Plays a role in melanocyte proliferation, perhaps via regulation of cyclin CCND1 (By similarity). Involved in melanogenesis, acting via negative modulation of expression of DHICA oxidase/TYRP1 and P protein/OCA2 (By similarity). Involved in regulating retinal pigment epithelium (RPE) cell proliferation, perhaps via negatively modulating transcription of the transcription factor CEBPD (PubMed:28910203). {ECO:0000250|UniProtKB:Q60707, ECO:0000269|PubMed:11062467, ECO:0000269|PubMed:11111039, ECO:0000269|PubMed:12000749, ECO:0000269|PubMed:22002537, ECO:0000269|PubMed:22844464, ECO:0000269|PubMed:28910203, ECO:0000269|PubMed:29726930, ECO:0000269|PubMed:30599067}. |
Q13469 | NFATC2 | S814 | 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}. |
Q13838 | DDX39B | S44 | ochoa | Spliceosome RNA helicase DDX39B (EC 3.6.4.13) (56 kDa U2AF65-associated protein) (ATP-dependent RNA helicase p47) (DEAD box protein UAP56) (HLA-B-associated transcript 1 protein) | Involved in nuclear export of spliced and unspliced mRNA (PubMed:15833825, PubMed:15998806, PubMed:17190602). Component of the TREX complex which is thought to couple mRNA transcription, processing and nuclear export, and specifically associates with spliced mRNA and not with unspliced pre-mRNA (PubMed:15833825, PubMed:15998806, PubMed:17190602). The TREX complex is recruited to spliced mRNAs by a transcription-independent mechanism, binds to mRNA upstream of the exon-junction complex (EJC) and is recruited in a splicing- and cap-dependent manner to a region near the 5' end of the mRNA where it functions in mRNA export to the cytoplasm via the TAP/NXF1 pathway (PubMed:15833825, PubMed:15998806, PubMed:17190602). The THOC1-THOC2-THOC3 core complex alone is sufficient to promote ATPase activity of DDX39B; in the complex THOC2 is the only component that directly interacts with DDX39B (PubMed:33191911). Associates with SARNP/CIP29, which facilitates RNA binding of DDX39B and likely plays a role in mRNA export (PubMed:37578863). May undergo several rounds of ATP hydrolysis during assembly of TREX to drive subsequent loading of components such as ALYREF/THOC4 and CHTOP onto mRNA. Also associates with pre-mRNA independent of ALYREF/THOC4. Involved in the nuclear export of intronless mRNA; the ATP-bound form is proposed to recruit export adapter ALYREF/THOC4 to intronless mRNA; its ATPase activity is cooperatively stimulated by RNA and ALYREF/THOC4 and ATP hydrolysis is thought to trigger the dissociation from RNA to allow the association of ALYREF/THOC4 and the NXF1-NXT1 heterodimer. Involved in transcription elongation and genome stability. {ECO:0000269|PubMed:11675789, ECO:0000269|PubMed:15585580, ECO:0000269|PubMed:15833825, ECO:0000269|PubMed:15998806, ECO:0000269|PubMed:17190602, ECO:0000269|PubMed:17562711, ECO:0000269|PubMed:17984224, ECO:0000269|PubMed:20844015, ECO:0000269|PubMed:22144908, ECO:0000269|PubMed:23222130, ECO:0000269|PubMed:23299939, ECO:0000269|PubMed:33191911, ECO:0000269|PubMed:37578863, ECO:0000269|PubMed:9242493}.; FUNCTION: Splice factor that is required for the first ATP-dependent step in spliceosome assembly and for the interaction of U2 snRNP with the branchpoint. Has both RNA-stimulated ATP binding/hydrolysis activity and ATP-dependent RNA unwinding activity. Even with the stimulation of RNA, the ATPase activity is weak. Can only hydrolyze ATP but not other NTPs. The RNA stimulation of ATPase activity does not have a strong preference for the sequence and length of the RNA. However, ssRNA stimulates the ATPase activity much more strongly than dsRNA. Can unwind 5' or 3' overhangs or blunt end RNA duplexes in vitro. The ATPase and helicase activities are not influenced by U2AF2; the effect of ALYREF/THOC4 is reported conflictingly with [PubMed:23299939] reporting a stimulatory effect. {ECO:0000269|PubMed:23299939, ECO:0000269|PubMed:9242493}.; FUNCTION: (Microbial infection) The TREX complex is essential for the export of Kaposi's sarcoma-associated herpesvirus (KSHV) intronless mRNAs and infectious virus production. {ECO:0000269|PubMed:18974867}. |
Q14157 | UBAP2L | S416 | ochoa | Ubiquitin-associated protein 2-like (Protein NICE-4) (RNA polymerase II degradation factor UBAP2L) | Recruits the ubiquitination machinery to RNA polymerase II for polyubiquitination, removal and degradation, when the transcription-coupled nucleotide excision repair (TC-NER) machinery fails to resolve DNA damage (PubMed:35633597). Plays an important role in the activity of long-term repopulating hematopoietic stem cells (LT-HSCs) (By similarity). Is a regulator of stress granule assembly, required for their efficient formation (PubMed:29395067, PubMed:35977029). Required for proper brain development and neocortex lamination (By similarity). {ECO:0000250|UniProtKB:Q80X50, ECO:0000269|PubMed:29395067, ECO:0000269|PubMed:35633597}. |
Q14669 | TRIP12 | S997 | ochoa | E3 ubiquitin-protein ligase TRIP12 (EC 2.3.2.26) (E3 ubiquitin-protein ligase for Arf) (ULF) (HECT-type E3 ubiquitin transferase TRIP12) (Thyroid receptor-interacting protein 12) (TR-interacting protein 12) (TRIP-12) | E3 ubiquitin-protein ligase involved in ubiquitin fusion degradation (UFD) pathway and regulation of DNA repair (PubMed:19028681, PubMed:22884692). Part of the ubiquitin fusion degradation (UFD) pathway, a process that mediates ubiquitination of protein at their N-terminus, regardless of the presence of lysine residues in target proteins (PubMed:19028681). Acts as a key regulator of DNA damage response by acting as a suppressor of RNF168, an E3 ubiquitin-protein ligase that promotes accumulation of 'Lys-63'-linked histone H2A and H2AX at DNA damage sites, thereby acting as a guard against excessive spreading of ubiquitinated chromatin at damaged chromosomes (PubMed:22884692). In normal cells, mediates ubiquitination and degradation of isoform p19ARF/ARF of CDKN2A, a lysine-less tumor suppressor required for p53/TP53 activation under oncogenic stress (PubMed:20208519). In cancer cells, however, isoform p19ARF/ARF and TRIP12 are located in different cell compartments, preventing isoform p19ARF/ARF ubiquitination and degradation (PubMed:20208519). Does not mediate ubiquitination of isoform p16-INK4a of CDKN2A (PubMed:20208519). Also catalyzes ubiquitination of NAE1 and SMARCE1, leading to their degradation (PubMed:18627766). Ubiquitination and degradation of target proteins is regulated by interaction with proteins such as MYC, TRADD or SMARCC1, which disrupt the interaction between TRIP12 and target proteins (PubMed:20829358). Mediates ubiquitination of ASXL1: following binding to N(6)-methyladenosine methylated DNA, ASXL1 is ubiquitinated by TRIP12, leading to its degradation and subsequent inactivation of the PR-DUB complex (PubMed:30982744). {ECO:0000269|PubMed:18627766, ECO:0000269|PubMed:19028681, ECO:0000269|PubMed:20208519, ECO:0000269|PubMed:20829358, ECO:0000269|PubMed:22884692, ECO:0000269|PubMed:30982744}. |
Q14676 | MDC1 | S1570 | ochoa | Mediator of DNA damage checkpoint protein 1 (Nuclear factor with BRCT domains 1) | Histone reader protein required for checkpoint-mediated cell cycle arrest in response to DNA damage within both the S phase and G2/M phases of the cell cycle (PubMed:12475977, PubMed:12499369, PubMed:12551934, PubMed:12607003, PubMed:12607004, PubMed:12607005, PubMed:12611903, PubMed:14695167, PubMed:15201865, PubMed:15377652, PubMed:16049003, PubMed:16377563, PubMed:30898438). Specifically recognizes and binds histone H2AX phosphorylated at 'Ser-139', a marker of DNA damage, serving as a scaffold for the recruitment of DNA repair and signal transduction proteins to discrete foci of DNA damage sites (PubMed:12607005, PubMed:15201865, PubMed:16049003, PubMed:16377563, PubMed:30898438). Also required for downstream events subsequent to the recruitment of these proteins (PubMed:12607005, PubMed:15201865, PubMed:16049003, PubMed:16377563, PubMed:18582474). These include phosphorylation and activation of the ATM, CHEK1 and CHEK2 kinases, and stabilization of TP53/p53 and apoptosis (PubMed:12499369, PubMed:12551934, PubMed:12607004). ATM and CHEK2 may also be activated independently by a parallel pathway mediated by TP53BP1 (PubMed:12499369, PubMed:12551934, PubMed:12607004). Required for chromosomal stability during mitosis by promoting recruitment of TOPBP1 to DNA double strand breaks (DSBs): TOPBP1 forms filamentous assemblies that bridge MDC1 and tether broken chromosomes during mitosis (PubMed:30898438). Required for the repair of DSBs via homologous recombination by promoting recruitment of NBN component of the MRN complex to DSBs (PubMed:18411307, PubMed:18582474, PubMed:18583988, PubMed:18678890). {ECO:0000269|PubMed:12475977, ECO:0000269|PubMed:12499369, ECO:0000269|PubMed:12551934, ECO:0000269|PubMed:12607003, ECO:0000269|PubMed:12607004, ECO:0000269|PubMed:12607005, ECO:0000269|PubMed:12611903, ECO:0000269|PubMed:14695167, ECO:0000269|PubMed:15201865, ECO:0000269|PubMed:15377652, ECO:0000269|PubMed:16049003, ECO:0000269|PubMed:16377563, ECO:0000269|PubMed:18411307, ECO:0000269|PubMed:18582474, ECO:0000269|PubMed:18583988, ECO:0000269|PubMed:18678890, ECO:0000269|PubMed:30898438}. |
Q14764 | MVP | S873 | ochoa | Major vault protein (MVP) (Lung resistance-related protein) | Required for normal vault structure. Vaults are multi-subunit structures that may act as scaffolds for proteins involved in signal transduction. Vaults may also play a role in nucleo-cytoplasmic transport. Down-regulates IFNG-mediated STAT1 signaling and subsequent activation of JAK. Down-regulates SRC activity and signaling through MAP kinases. {ECO:0000269|PubMed:15133037, ECO:0000269|PubMed:16418217, ECO:0000269|PubMed:16441665}. |
Q14938 | NFIX | S268 | 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. |
Q14980 | NUMA1 | S1868 | ochoa | Nuclear mitotic apparatus protein 1 (Nuclear matrix protein-22) (NMP-22) (Nuclear mitotic apparatus protein) (NuMA protein) (SP-H antigen) | Microtubule (MT)-binding protein that plays a role in the formation and maintenance of the spindle poles and the alignement and the segregation of chromosomes during mitotic cell division (PubMed:17172455, PubMed:19255246, PubMed:24996901, PubMed:26195665, PubMed:27462074, PubMed:7769006). Functions to tether the minus ends of MTs at the spindle poles, which is critical for the establishment and maintenance of the spindle poles (PubMed:11956313, PubMed:12445386). Plays a role in the establishment of the mitotic spindle orientation during metaphase and elongation during anaphase in a dynein-dynactin-dependent manner (PubMed:23870127, PubMed:24109598, PubMed:24996901, PubMed:26765568). In metaphase, part of a ternary complex composed of GPSM2 and G(i) alpha proteins, that regulates the recruitment and anchorage of the dynein-dynactin complex in the mitotic cell cortex regions situated above the two spindle poles, and hence regulates the correct oritentation of the mitotic spindle (PubMed:22327364, PubMed:23027904, PubMed:23921553). During anaphase, mediates the recruitment and accumulation of the dynein-dynactin complex at the cell membrane of the polar cortical region through direct association with phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), and hence participates in the regulation of the spindle elongation and chromosome segregation (PubMed:22327364, PubMed:23921553, PubMed:24371089, PubMed:24996901). Also binds to other polyanionic phosphoinositides, such as phosphatidylinositol 3-phosphate (PIP), lysophosphatidic acid (LPA) and phosphatidylinositol triphosphate (PIP3), in vitro (PubMed:24371089, PubMed:24996901). Also required for proper orientation of the mitotic spindle during asymmetric cell divisions (PubMed:21816348). Plays a role in mitotic MT aster assembly (PubMed:11163243, PubMed:11229403, PubMed:12445386). Involved in anastral spindle assembly (PubMed:25657325). Positively regulates TNKS protein localization to spindle poles in mitosis (PubMed:16076287). Highly abundant component of the nuclear matrix where it may serve a non-mitotic structural role, occupies the majority of the nuclear volume (PubMed:10075938). Required for epidermal differentiation and hair follicle morphogenesis (By similarity). {ECO:0000250|UniProtKB:E9Q7G0, ECO:0000269|PubMed:11163243, ECO:0000269|PubMed:11229403, ECO:0000269|PubMed:11956313, ECO:0000269|PubMed:12445386, ECO:0000269|PubMed:16076287, ECO:0000269|PubMed:17172455, ECO:0000269|PubMed:19255246, ECO:0000269|PubMed:22327364, ECO:0000269|PubMed:23027904, ECO:0000269|PubMed:23870127, ECO:0000269|PubMed:23921553, ECO:0000269|PubMed:24109598, ECO:0000269|PubMed:24371089, ECO:0000269|PubMed:24996901, ECO:0000269|PubMed:25657325, ECO:0000269|PubMed:26195665, ECO:0000269|PubMed:26765568, ECO:0000269|PubMed:27462074, ECO:0000269|PubMed:7769006, ECO:0000305|PubMed:10075938, ECO:0000305|PubMed:21816348}. |
Q15596 | NCOA2 | S493 | ochoa|psp | Nuclear receptor coactivator 2 (NCoA-2) (Class E basic helix-loop-helix protein 75) (bHLHe75) (Transcriptional intermediary factor 2) (hTIF2) | Transcriptional coactivator for steroid receptors and nuclear receptors (PubMed:23508108, PubMed:8670870, PubMed:9430642, PubMed:22504882, PubMed:26553876). Coactivator of the steroid binding domain (AF-2) but not of the modulating N-terminal domain (AF-1) (PubMed:23508108, PubMed:8670870, PubMed:9430642). Required with NCOA1 to control energy balance between white and brown adipose tissues (PubMed:23508108, PubMed:8670870, PubMed:9430642). Critical regulator of glucose metabolism regulation, acts as a RORA coactivator to specifically modulate G6PC1 expression (PubMed:23508108, PubMed:8670870, PubMed:9430642). Involved in the positive regulation of the transcriptional activity of the glucocorticoid receptor NR3C1 by sumoylation enhancer RWDD3 (PubMed:23508108). Positively regulates the circadian clock by acting as a transcriptional coactivator for the CLOCK-BMAL1 heterodimer (By similarity). {ECO:0000250|UniProtKB:Q61026, ECO:0000269|PubMed:22504882, ECO:0000269|PubMed:23508108, ECO:0000269|PubMed:26553876, ECO:0000269|PubMed:8670870, ECO:0000269|PubMed:9430642}. |
Q15596 | NCOA2 | S499 | ochoa|psp | Nuclear receptor coactivator 2 (NCoA-2) (Class E basic helix-loop-helix protein 75) (bHLHe75) (Transcriptional intermediary factor 2) (hTIF2) | Transcriptional coactivator for steroid receptors and nuclear receptors (PubMed:23508108, PubMed:8670870, PubMed:9430642, PubMed:22504882, PubMed:26553876). Coactivator of the steroid binding domain (AF-2) but not of the modulating N-terminal domain (AF-1) (PubMed:23508108, PubMed:8670870, PubMed:9430642). Required with NCOA1 to control energy balance between white and brown adipose tissues (PubMed:23508108, PubMed:8670870, PubMed:9430642). Critical regulator of glucose metabolism regulation, acts as a RORA coactivator to specifically modulate G6PC1 expression (PubMed:23508108, PubMed:8670870, PubMed:9430642). Involved in the positive regulation of the transcriptional activity of the glucocorticoid receptor NR3C1 by sumoylation enhancer RWDD3 (PubMed:23508108). Positively regulates the circadian clock by acting as a transcriptional coactivator for the CLOCK-BMAL1 heterodimer (By similarity). {ECO:0000250|UniProtKB:Q61026, ECO:0000269|PubMed:22504882, ECO:0000269|PubMed:23508108, ECO:0000269|PubMed:26553876, ECO:0000269|PubMed:8670870, ECO:0000269|PubMed:9430642}. |
Q15751 | HERC1 | S2723 | ochoa | Probable E3 ubiquitin-protein ligase HERC1 (EC 2.3.2.26) (HECT domain and RCC1-like domain-containing protein 1) (HECT-type E3 ubiquitin transferase HERC1) (p532) (p619) | Involved in membrane trafficking via some guanine nucleotide exchange factor (GEF) activity and its ability to bind clathrin. Acts as a GEF for Arf and Rab, by exchanging bound GDP for free GTP. Binds phosphatidylinositol 4,5-bisphosphate, which is required for GEF activity. May also act as a E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. {ECO:0000269|PubMed:15642342, ECO:0000269|PubMed:8861955, ECO:0000269|PubMed:9233772}. |
Q16512 | PKN1 | S579 | ochoa | Serine/threonine-protein kinase N1 (EC 2.7.11.13) (Protease-activated kinase 1) (PAK-1) (Protein kinase C-like 1) (Protein kinase C-like PKN) (Protein kinase PKN-alpha) (Protein-kinase C-related kinase 1) (Serine-threonine protein kinase N) | PKC-related serine/threonine-protein kinase involved in various processes such as regulation of the intermediate filaments of the actin cytoskeleton, cell migration, tumor cell invasion and transcription regulation. Part of a signaling cascade that begins with the activation of the adrenergic receptor ADRA1B and leads to the activation of MAPK14. Regulates the cytoskeletal network by phosphorylating proteins such as VIM and neurofilament proteins NEFH, NEFL and NEFM, leading to inhibit their polymerization. Phosphorylates 'Ser-575', 'Ser-637' and 'Ser-669' of MAPT/Tau, lowering its ability to bind to microtubules, resulting in disruption of tubulin assembly. Acts as a key coactivator of androgen receptor (AR)-dependent transcription, by being recruited to AR target genes and specifically mediating phosphorylation of 'Thr-11' of histone H3 (H3T11ph), a specific tag for epigenetic transcriptional activation that promotes demethylation of histone H3 'Lys-9' (H3K9me) by KDM4C/JMJD2C. Phosphorylates HDAC5, HDAC7 and HDAC9, leading to impair their import in the nucleus. Phosphorylates 'Thr-38' of PPP1R14A, 'Ser-159', 'Ser-163' and 'Ser-170' of MARCKS, and GFAP. Able to phosphorylate RPS6 in vitro. {ECO:0000269|PubMed:11104762, ECO:0000269|PubMed:12514133, ECO:0000269|PubMed:17332740, ECO:0000269|PubMed:18066052, ECO:0000269|PubMed:20188095, ECO:0000269|PubMed:21224381, ECO:0000269|PubMed:21754995, ECO:0000269|PubMed:24248594, ECO:0000269|PubMed:8557118, ECO:0000269|PubMed:8621664, ECO:0000269|PubMed:9175763}. |
Q16666 | IFI16 | S166 | ochoa | Gamma-interferon-inducible protein 16 (Ifi-16) (Interferon-inducible myeloid differentiation transcriptional activator) | Binds double-stranded DNA. Binds preferentially to supercoiled DNA and cruciform DNA structures. Seems to be involved in transcriptional regulation. May function as a transcriptional repressor. Could have a role in the regulation of hematopoietic differentiation through activation of unknown target genes. Controls cellular proliferation by modulating the functions of cell cycle regulatory factors including p53/TP53 and the retinoblastoma protein. May be involved in TP53-mediated transcriptional activation by enhancing TP53 sequence-specific DNA binding and modulating TP53 phosphorylation status. Seems to be involved in energy-level-dependent activation of the ATM/ AMPK/TP53 pathway coupled to regulation of autophagy. May be involved in regulation of TP53-mediated cell death also involving BRCA1. May be involved in the senescence of prostate epithelial cells. Involved in innate immune response by recognizing viral dsDNA in the cytosol and probably in the nucleus. After binding to viral DNA in the cytoplasm recruits TMEM173/STING and mediates the induction of IFN-beta. Has anti-inflammatory activity and inhibits the activation of the AIM2 inflammasome, probably via association with AIM2. Proposed to bind viral DNA in the nucleus, such as of Kaposi's sarcoma-associated herpesvirus, and to induce the formation of nuclear caspase-1-activating inflammasome formation via association with PYCARD. Inhibits replication of herpesviruses such as human cytomegalovirus (HCMV) probably by interfering with promoter recruitment of members of the Sp1 family of transcription factors. Necessary to activate the IRF3 signaling cascade during human herpes simplex virus 1 (HHV-1) infection and promotes the assembly of heterochromatin on herpesviral DNA and inhibition of viral immediate-early gene expression and replication. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. {ECO:0000269|PubMed:11146555, ECO:0000269|PubMed:12894224, ECO:0000269|PubMed:14654789, ECO:0000269|PubMed:20890285, ECO:0000269|PubMed:21573174, ECO:0000269|PubMed:21575908, ECO:0000269|PubMed:22046441, ECO:0000269|PubMed:22291595, ECO:0000269|PubMed:23027953, ECO:0000269|PubMed:24198334, ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:9642285}.; FUNCTION: [Isoform IFI16-beta]: Isoform that specifically inhibits the AIM2 inflammasome (PubMed:30104205). Binds double-stranded DNA (dsDNA) in the cytoplasm, impeding its detection by AIM2 (PubMed:30104205). Also prevents the interaction between AIM2 and PYCARD/ASC via its interaction with AIM2, thereby inhibiting assembly of the AIM2 inflammasome (PubMed:30104205). This isoform also weakly induce production of type I interferon-beta (IFNB1) via its interaction with STING1 (PubMed:30104205). {ECO:0000269|PubMed:30104205}. |
Q3KQU3 | MAP7D1 | S460 | ochoa | MAP7 domain-containing protein 1 (Arginine/proline-rich coiled-coil domain-containing protein 1) (Proline/arginine-rich coiled-coil domain-containing protein 1) | Microtubule-stabilizing protein involved in the control of cell motility and neurite outgrowth. Facilitate microtubule stabilization through the maintenance of acetylated stable microtubules. {ECO:0000250|UniProtKB:A2AJI0}. |
Q5T200 | ZC3H13 | S378 | ochoa | Zinc finger CCCH domain-containing protein 13 | Associated component of the WMM complex, a complex that mediates N6-methyladenosine (m6A) methylation of RNAs, a modification that plays a role in the efficiency of mRNA splicing and RNA processing (PubMed:29507755). Acts as a key regulator of m6A methylation by promoting m6A methylation of mRNAs at the 3'-UTR (By similarity). Controls embryonic stem cells (ESCs) pluripotency via its role in m6A methylation (By similarity). In the WMM complex, anchors component of the MACOM subcomplex in the nucleus (By similarity). Also required for bridging WTAP to the RNA-binding component RBM15 (RBM15 or RBM15B) (By similarity). {ECO:0000250|UniProtKB:E9Q784}. |
Q641Q2 | WASHC2A | S996 | ochoa | WASH complex subunit 2A | Acts at least in part as component of the WASH core complex whose assembly at the surface of endosomes inhibits WASH nucleation-promoting factor (NPF) activity in recruiting and activating the Arp2/3 complex to induce actin polymerization and is involved in the fission of tubules that serve as transport intermediates during endosome sorting. Mediates the recruitment of the WASH core complex to endosome membranes via binding to phospholipids and VPS35 of the retromer CSC. Mediates the recruitment of the F-actin-capping protein dimer to the WASH core complex probably promoting localized F-actin polymerization needed for vesicle scission. Via its C-terminus binds various phospholipids, most strongly phosphatidylinositol 4-phosphate (PtdIns-(4)P), phosphatidylinositol 5-phosphate (PtdIns-(5)P) and phosphatidylinositol 3,5-bisphosphate (PtdIns-(3,5)P2). Involved in the endosome-to-plasma membrane trafficking and recycling of SNX27-retromer-dependent cargo proteins, such as GLUT1. Required for the association of DNAJC13, ENTR1, ANKRD50 with retromer CSC subunit VPS35. Required for the endosomal recruitment of CCC complex subunits COMMD1 and CCDC93 as well as the retriever complex subunit VPS35L. {ECO:0000269|PubMed:25355947, ECO:0000269|PubMed:28892079}. |
Q66K74 | MAP1S | S646 | ochoa | Microtubule-associated protein 1S (MAP-1S) (BPY2-interacting protein 1) (Microtubule-associated protein 8) (Variable charge Y chromosome 2-interacting protein 1) (VCY2-interacting protein 1) (VCY2IP-1) [Cleaved into: MAP1S heavy chain; MAP1S light chain] | Microtubule-associated protein that mediates aggregation of mitochondria resulting in cell death and genomic destruction (MAGD). Plays a role in anchoring the microtubule organizing center to the centrosomes. Binds to DNA. Plays a role in apoptosis. Involved in the formation of microtubule bundles (By similarity). {ECO:0000250, ECO:0000269|PubMed:15899810, ECO:0000269|PubMed:17234756}. |
Q674X7 | KAZN | S352 | ochoa | Kazrin | Component of the cornified envelope of keratinocytes. May be involved in the interplay between adherens junctions and desmosomes. The function in the nucleus is not known. {ECO:0000269|PubMed:15337775}. |
Q6PKG0 | LARP1 | S580 | ochoa | La-related protein 1 (La ribonucleoprotein domain family member 1) | RNA-binding protein that regulates the translation of specific target mRNA species downstream of the mTORC1 complex, in function of growth signals and nutrient availability (PubMed:20430826, PubMed:23711370, PubMed:24532714, PubMed:25940091, PubMed:28650797, PubMed:28673543, PubMed:29244122). Interacts on the one hand with the 3' poly-A tails that are present in all mRNA molecules, and on the other hand with the 7-methylguanosine cap structure of mRNAs containing a 5' terminal oligopyrimidine (5'TOP) motif, which is present in mRNAs encoding ribosomal proteins and several components of the translation machinery (PubMed:23711370, PubMed:25940091, PubMed:26206669, PubMed:28379136, PubMed:28650797, PubMed:29244122). The interaction with the 5' end of mRNAs containing a 5'TOP motif leads to translational repression by preventing the binding of EIF4G1 (PubMed:25940091, PubMed:28379136, PubMed:28650797, PubMed:29244122). When mTORC1 is activated, LARP1 is phosphorylated and dissociates from the 5' untranslated region (UTR) of mRNA (PubMed:25940091, PubMed:28650797). Does not prevent binding of EIF4G1 to mRNAs that lack a 5'TOP motif (PubMed:28379136). Interacts with the free 40S ribosome subunit and with ribosomes, both monosomes and polysomes (PubMed:20430826, PubMed:24532714, PubMed:25940091, PubMed:28673543). Under normal nutrient availability, interacts primarily with the 3' untranslated region (UTR) of mRNAs encoding ribosomal proteins and increases protein synthesis (PubMed:23711370, PubMed:28650797). Associates with actively translating ribosomes and stimulates translation of mRNAs containing a 5'TOP motif, thereby regulating protein synthesis, and as a consequence, cell growth and proliferation (PubMed:20430826, PubMed:24532714). Stabilizes mRNAs species with a 5'TOP motif, which is required to prevent apoptosis (PubMed:20430826, PubMed:23711370, PubMed:25940091, PubMed:28673543). {ECO:0000269|PubMed:20430826, ECO:0000269|PubMed:23711370, ECO:0000269|PubMed:24532714, ECO:0000269|PubMed:25940091, ECO:0000269|PubMed:26206669, ECO:0000269|PubMed:28379136, ECO:0000269|PubMed:28650797, ECO:0000269|PubMed:28673543, ECO:0000269|PubMed:29244122}.; FUNCTION: (Microbial infection) Positively regulates the replication of dengue virus (DENV). {ECO:0000269|PubMed:26735137}. |
Q6UB99 | ANKRD11 | S1891 | ochoa | Ankyrin repeat domain-containing protein 11 (Ankyrin repeat-containing cofactor 1) | Chromatin regulator which modulates histone acetylation and gene expression in neural precursor cells (By similarity). May recruit histone deacetylases (HDACs) to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation (PubMed:15184363). Has a role in proliferation and development of cortical neural precursors (PubMed:25556659). May also regulate bone homeostasis (By similarity). {ECO:0000250|UniProtKB:E9Q4F7, ECO:0000269|PubMed:15184363, ECO:0000269|PubMed:25556659}. |
Q6UXY1 | BAIAP2L2 | S231 | ochoa | BAR/IMD domain-containing adapter protein 2-like 2 (Brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2) (BAI1-associated protein 2-like protein 2) (Planar intestinal- and kidney-specific BAR domain protein) (Pinkbar) | Phosphoinositides-binding protein that induces the formation of planar or gently curved membrane structures. Binds to phosphoinositides, including to phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) headgroups. There seems to be no clear preference for a specific phosphoinositide (By similarity). {ECO:0000250}. |
Q6VY07 | PACS1 | S534 | ochoa | Phosphofurin acidic cluster sorting protein 1 (PACS-1) | Coat protein that is involved in the localization of trans-Golgi network (TGN) membrane proteins that contain acidic cluster sorting motifs. Controls the endosome-to-Golgi trafficking of furin and mannose-6-phosphate receptor by connecting the acidic-cluster-containing cytoplasmic domain of these molecules with the adapter-protein complex-1 (AP-1) of endosomal clathrin-coated membrane pits. Involved in HIV-1 nef-mediated removal of MHC-I from the cell surface to the TGN. Required for normal ER Ca2+ handling in lymphocytes. Together with WDR37, it plays an essential role in lymphocyte development, quiescence and survival. Required for stabilizing peripheral lymphocyte populations (By similarity). {ECO:0000250|UniProtKB:Q8K212, ECO:0000269|PubMed:11331585, ECO:0000269|PubMed:15692563}. |
Q71RC2 | LARP4 | S597 | ochoa | La-related protein 4 (La ribonucleoprotein domain family member 4) | RNA binding protein that binds to the poly-A tract of mRNA molecules (PubMed:21098120). Associates with the 40S ribosomal subunit and with polysomes (PubMed:21098120). Plays a role in the regulation of mRNA translation (PubMed:21098120). Plays a role in the regulation of cell morphology and cytoskeletal organization (PubMed:21834987, PubMed:27615744). {ECO:0000269|PubMed:21098120, ECO:0000269|PubMed:21834987, ECO:0000269|PubMed:27615744}. |
Q76L83 | ASXL2 | S530 | ochoa | Putative Polycomb group protein ASXL2 (Additional sex combs-like protein 2) | Putative Polycomb group (PcG) protein. PcG proteins act by forming multiprotein complexes, which are required to maintain the transcriptionally repressive state of homeotic genes throughout development. PcG proteins are not required to initiate repression, but to maintain it during later stages of development. They probably act via methylation of histones, rendering chromatin heritably changed in its expressibility (By similarity). Involved in transcriptional regulation mediated by ligand-bound nuclear hormone receptors, such as peroxisome proliferator-activated receptor gamma (PPARG). Acts as coactivator for PPARG and enhances its adipocyte differentiation-inducing activity; the function seems to involve differential recruitment of acetylated and methylated histone H3. Non-catalytic component of the PR-DUB complex, a complex that specifically mediates deubiquitination of histone H2A monoubiquitinated at 'Lys-119' (H2AK119ub1) (PubMed:30664650, PubMed:36180891). The PR-DUB complex is an epigenetic regulator of gene expression and acts as a transcriptional coactivator, affecting genes involved in development, cell communication, signaling, cell proliferation and cell viability (PubMed:30664650, PubMed:36180891). ASXL1, ASXL2 and ASXL3 function redundantly in the PR-DUB complex (By similarity) (PubMed:30664650). The ASXL proteins are essential for chromatin recruitment and transcriptional activation of associated genes (By similarity). ASXL1 and ASXL2 are important for BAP1 protein stability (PubMed:30664650). {ECO:0000250, ECO:0000250|UniProtKB:Q8BZ32, ECO:0000269|PubMed:21047783, ECO:0000269|PubMed:30664650, ECO:0000269|PubMed:36180891}. |
Q7RTP6 | MICAL3 | S1173 | ochoa | [F-actin]-monooxygenase MICAL3 (EC 1.14.13.225) (Molecule interacting with CasL protein 3) (MICAL-3) | Monooxygenase that promotes depolymerization of F-actin by mediating oxidation of specific methionine residues on actin to form methionine-sulfoxide, resulting in actin filament disassembly and preventing repolymerization. In the absence of actin, it also functions as a NADPH oxidase producing H(2)O(2). Seems to act as Rab effector protein and plays a role in vesicle trafficking. Involved in exocytic vesicles tethering and fusion: the monooxygenase activity is required for this process and implicates RAB8A associated with exocytotic vesicles. Required for cytokinesis. Contributes to stabilization and/or maturation of the intercellular bridge independently of its monooxygenase activity. Promotes recruitment of Rab8 and ERC1 to the intercellular bridge, and together these proteins are proposed to function in timely abscission. {ECO:0000269|PubMed:21596566, ECO:0000269|PubMed:24440334}. |
Q7Z3B3 | KANSL1 | S994 | ochoa | KAT8 regulatory NSL complex subunit 1 (MLL1/MLL complex subunit KANSL1) (MSL1 homolog 1) (hMSL1v1) (NSL complex protein NSL1) (Non-specific lethal 1 homolog) | Non-catalytic component of the NSL histone acetyltransferase complex, a multiprotein complex that mediates histone H4 acetylation at 'Lys-5'- and 'Lys-8' (H4K5ac and H4K8ac) at transcription start sites and promotes transcription initiation (PubMed:20018852, PubMed:22547026, PubMed:33657400). The NSL complex also acts as a regulator of gene expression in mitochondria (PubMed:27768893). In addition to its role in transcription, KANSL1 also plays an essential role in spindle assembly during mitosis (PubMed:26243146). Associates with microtubule ends and contributes to microtubule stability (PubMed:26243146). {ECO:0000269|PubMed:20018852, ECO:0000269|PubMed:22547026, ECO:0000269|PubMed:26243146, ECO:0000269|PubMed:27768893, ECO:0000269|PubMed:33657400}. |
Q7Z3K3 | POGZ | S274 | ochoa | Pogo transposable element with ZNF domain (Suppressor of hairy wing homolog 5) (Zinc finger protein 280E) (Zinc finger protein 635) | Plays a role in mitotic cell cycle progression and is involved in kinetochore assembly and mitotic sister chromatid cohesion. Probably through its association with CBX5 plays a role in mitotic chromosome segregation by regulating aurora kinase B/AURKB activation and AURKB and CBX5 dissociation from chromosome arms (PubMed:20562864). Promotes the repair of DNA double-strand breaks through the homologous recombination pathway (PubMed:26721387). {ECO:0000269|PubMed:20562864, ECO:0000269|PubMed:26721387}. |
Q7Z422 | SZRD1 | S74 | ochoa | SUZ RNA-binding domain-containing (SUZ domain-containing protein 1) (Putative MAPK-activating protein PM18/PM20/PM22) | None |
Q7Z6I6 | ARHGAP30 | S1043 | ochoa | Rho GTPase-activating protein 30 (Rho-type GTPase-activating protein 30) | GTPase-activating protein (GAP) for RAC1 and RHOA, but not for CDC42. {ECO:0000269|PubMed:21565175}. |
Q86UE8 | TLK2 | S117 | ochoa | Serine/threonine-protein kinase tousled-like 2 (EC 2.7.11.1) (HsHPK) (PKU-alpha) (Tousled-like kinase 2) | Serine/threonine-protein kinase involved in the process of chromatin assembly and probably also DNA replication, transcription, repair, and chromosome segregation (PubMed:10523312, PubMed:11470414, PubMed:12660173, PubMed:12955071, PubMed:29955062, PubMed:33323470, PubMed:9427565). Phosphorylates the chromatin assembly factors ASF1A and ASF1B (PubMed:11470414, PubMed:20016786, PubMed:29955062, PubMed:35136069). Phosphorylation of ASF1A prevents its proteasome-mediated degradation, thereby enhancing chromatin assembly (PubMed:20016786). Negative regulator of amino acid starvation-induced autophagy (PubMed:22354037). {ECO:0000269|PubMed:10523312, ECO:0000269|PubMed:11470414, ECO:0000269|PubMed:12660173, ECO:0000269|PubMed:12955071, ECO:0000269|PubMed:20016786, ECO:0000269|PubMed:22354037, ECO:0000269|PubMed:29955062, ECO:0000269|PubMed:33323470, ECO:0000269|PubMed:35136069, ECO:0000269|PubMed:9427565}. |
Q86WB0 | ZC3HC1 | S335 | 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}. |
Q86X51 | EZHIP | S465 | ochoa | EZH inhibitory protein | Inhibits PRC2/EED-EZH1 and PRC2/EED-EZH2 complex function by inhibiting EZH1/EZH2 methyltransferase activity, thereby causing down-regulation of histone H3 trimethylation on 'Lys-27' (H3K27me3) (PubMed:29909548, PubMed:30923826, PubMed:31086175, PubMed:31451685). Probably inhibits methyltransferase activity by limiting the stimulatory effect of cofactors such as AEBP2 and JARID2 (PubMed:30923826). Inhibits H3K27me3 deposition during spermatogenesis and oogenesis (By similarity). {ECO:0000250|UniProtKB:B1B0V2, ECO:0000269|PubMed:29909548, ECO:0000269|PubMed:30923826, ECO:0000269|PubMed:31086175, ECO:0000269|PubMed:31451685}. |
Q86YN6 | PPARGC1B | S390 | ochoa | Peroxisome proliferator-activated receptor gamma coactivator 1-beta (PGC-1-beta) (PPAR-gamma coactivator 1-beta) (PPARGC-1-beta) (PGC-1-related estrogen receptor alpha coactivator) | Plays a role of stimulator of transcription factors and nuclear receptors activities. Activates transcriptional activity of estrogen receptor alpha, nuclear respiratory factor 1 (NRF1) and glucocorticoid receptor in the presence of glucocorticoids. May play a role in constitutive non-adrenergic-mediated mitochondrial biogenesis as suggested by increased basal oxygen consumption and mitochondrial number when overexpressed. May be involved in fat oxidation and non-oxidative glucose metabolism and in the regulation of energy expenditure. Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner. {ECO:0000269|PubMed:11854298, ECO:0000269|PubMed:12678921, ECO:0000269|PubMed:15546003, ECO:0000269|PubMed:23836911}. |
Q8IVT2 | MISP | S400 | ochoa|psp | Mitotic interactor and substrate of PLK1 (Mitotic spindle positioning protein) | Plays a role in mitotic spindle orientation and mitotic progression. Regulates the distribution of dynactin at the cell cortex in a PLK1-dependent manner, thus stabilizing cortical and astral microtubule attachments required for proper mitotic spindle positioning. May link microtubules to the actin cytospkeleton and focal adhesions. May be required for directed cell migration and centrosome orientation. May also be necessary for proper stacking of the Golgi apparatus. {ECO:0000269|PubMed:23509069, ECO:0000269|PubMed:23574715}. |
Q8IWZ8 | SUGP1 | S344 | ochoa | SURP and G-patch domain-containing protein 1 (RNA-binding protein RBP) (Splicing factor 4) | Plays a role in pre-mRNA splicing. |
Q8IY63 | AMOTL1 | S906 | ochoa | Angiomotin-like protein 1 | Inhibits the Wnt/beta-catenin signaling pathway, probably by recruiting CTNNB1 to recycling endosomes and hence preventing its translocation to the nucleus. {ECO:0000269|PubMed:22362771}. |
Q8IY92 | SLX4 | S1342 | ochoa | Structure-specific endonuclease subunit SLX4 (BTB/POZ domain-containing protein 12) | Regulatory subunit that interacts with and increases the activity of different structure-specific endonucleases. Has several distinct roles in protecting genome stability by resolving diverse forms of deleterious DNA structures originating from replication and recombination intermediates and from DNA damage. Component of the SLX1-SLX4 structure-specific endonuclease that resolves DNA secondary structures generated during DNA repair and recombination. Has endonuclease activity towards branched DNA substrates, introducing single-strand cuts in duplex DNA close to junctions with ss-DNA. Has a preference for 5'-flap structures, and promotes symmetrical cleavage of static and migrating Holliday junctions (HJs). Resolves HJs by generating two pairs of ligatable, nicked duplex products. Interacts with the structure-specific ERCC4-ERCC1 endonuclease and promotes the cleavage of bubble structures. Interacts with the structure-specific MUS81-EME1 endonuclease and promotes the cleavage of 3'-flap and replication fork-like structures. SLX4 is required for recovery from alkylation-induced DNA damage and is involved in the resolution of DNA double-strand breaks. {ECO:0000269|PubMed:19595721, ECO:0000269|PubMed:19595722, ECO:0000269|PubMed:19596235, ECO:0000269|PubMed:19596236}. |
Q8IYB3 | SRRM1 | S420 | ochoa | Serine/arginine repetitive matrix protein 1 (SR-related nuclear matrix protein of 160 kDa) (SRm160) (Ser/Arg-related nuclear matrix protein) | Part of pre- and post-splicing multiprotein mRNP complexes. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). Involved in numerous pre-mRNA processing events. Promotes constitutive and exonic splicing enhancer (ESE)-dependent splicing activation by bridging together sequence-specific (SR family proteins, SFRS4, SFRS5 and TRA2B/SFRS10) and basal snRNP (SNRP70 and SNRPA1) factors of the spliceosome. Stimulates mRNA 3'-end cleavage independently of the formation of an exon junction complex. Binds both pre-mRNA and spliced mRNA 20-25 nt upstream of exon-exon junctions. Binds RNA and DNA with low sequence specificity and has similar preference for either double- or single-stranded nucleic acid substrates. {ECO:0000269|PubMed:10339552, ECO:0000269|PubMed:10668804, ECO:0000269|PubMed:11739730, ECO:0000269|PubMed:12600940, ECO:0000269|PubMed:12944400, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q8IZW8 | TNS4 | S248 | ochoa | Tensin-4 (C-terminal tensin-like protein) | Promotes EGF-induced cell migration by displacing tensin TNS3 from the cytoplasmic tail of integrin ITGB1 which results in dissociation of TNS3 from focal adhesions, disassembly of actin stress fibers and initiation of cell migration (PubMed:17643115). Suppresses ligand-induced degradation of EGFR by reducing EGFR ubiquitination in the presence of EGF (PubMed:23774213). Increases MET protein stability by inhibiting MET endocytosis and subsequent lysosomal degradation which leads to increased cell survival, proliferation and migration (PubMed:24814316). {ECO:0000269|PubMed:17643115, ECO:0000269|PubMed:23774213, ECO:0000269|PubMed:24814316}. |
Q8NDV7 | TNRC6A | S1585 | ochoa | Trinucleotide repeat-containing gene 6A protein (CAG repeat protein 26) (EMSY interactor protein) (GW182 autoantigen) (Protein GW1) (Glycine-tryptophan protein of 182 kDa) | Plays a role in RNA-mediated gene silencing by both micro-RNAs (miRNAs) and short interfering RNAs (siRNAs). Required for miRNA-dependent repression of translation and for siRNA-dependent endonucleolytic cleavage of complementary mRNAs by argonaute family proteins. As a scaffolding protein, associates with argonaute proteins bound to partially complementary mRNAs, and can simultaneously recruit CCR4-NOT and PAN deadenylase complexes. {ECO:0000269|PubMed:16284622, ECO:0000269|PubMed:16284623, ECO:0000269|PubMed:17596515, ECO:0000269|PubMed:17671087, ECO:0000269|PubMed:19056672, ECO:0000269|PubMed:19304925}. |
Q8NFH5 | NUP35 | S135 | ochoa | Nucleoporin NUP35 (35 kDa nucleoporin) (Mitotic phosphoprotein 44) (MP-44) (Nuclear pore complex protein Nup53) (Nucleoporin NUP53) | Functions as a component of the nuclear pore complex (NPC). NPC components, collectively referred to as nucleoporins (NUPs), can play the role of both NPC structural components and of docking or interaction partners for transiently associated nuclear transport factors. May play a role in the association of MAD1 with the NPC. {ECO:0000269|PubMed:15703211}. |
Q8NHM5 | KDM2B | S848 | ochoa | Lysine-specific demethylase 2B (EC 1.14.11.27) (CXXC-type zinc finger protein 2) (F-box and leucine-rich repeat protein 10) (F-box protein FBL10) (F-box/LRR-repeat protein 10) (JmjC domain-containing histone demethylation protein 1B) (Jumonji domain-containing EMSY-interactor methyltransferase motif protein) (Protein JEMMA) (Protein-containing CXXC domain 2) ([Histone-H3]-lysine-36 demethylase 1B) | Histone demethylase that demethylates 'Lys-4' and 'Lys-36' of histone H3, thereby playing a central role in histone code (PubMed:16362057, PubMed:17994099, PubMed:26237645). Preferentially demethylates trimethylated H3 'Lys-4' and dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys-36' (PubMed:16362057, PubMed:17994099, PubMed:26237645). Preferentially binds the transcribed region of ribosomal RNA and represses the transcription of ribosomal RNA genes which inhibits cell growth and proliferation (PubMed:16362057, PubMed:17994099). May also serve as a substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex (Probable). {ECO:0000269|PubMed:16362057, ECO:0000269|PubMed:17994099, ECO:0000269|PubMed:26237645, ECO:0000305}. |
Q8TBP0 | TBC1D16 | S126 | ochoa | TBC1 domain family member 16 | May act as a GTPase-activating protein for Rab family protein(s). |
Q8WWM7 | ATXN2L | S604 | 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}. |
Q92585 | MAML1 | S344 | ochoa | Mastermind-like protein 1 (Mam-1) | Acts as a transcriptional coactivator for NOTCH proteins. Has been shown to amplify NOTCH-induced transcription of HES1. Enhances phosphorylation and proteolytic turnover of the NOTCH intracellular domain in the nucleus through interaction with CDK8. Binds to CREBBP/CBP which promotes nucleosome acetylation at NOTCH enhancers and activates transcription. Induces phosphorylation and localization of CREBBP to nuclear foci. Plays a role in hematopoietic development by regulating NOTCH-mediated lymphoid cell fate decisions. {ECO:0000269|PubMed:11101851, ECO:0000269|PubMed:11390662, ECO:0000269|PubMed:12050117, ECO:0000269|PubMed:15546612, ECO:0000269|PubMed:17317671}. |
Q92615 | LARP4B | S599 | ochoa | La-related protein 4B (La ribonucleoprotein domain family member 4B) (La ribonucleoprotein domain family member 5) (La-related protein 5) | Stimulates mRNA translation. {ECO:0000269|PubMed:20573744}. |
Q96AC1 | FERMT2 | S181 | ochoa|psp | Fermitin family homolog 2 (Kindlin-2) (Mitogen-inducible gene 2 protein) (MIG-2) (Pleckstrin homology domain-containing family C member 1) (PH domain-containing family C member 1) | Scaffolding protein that enhances integrin activation mediated by TLN1 and/or TLN2, but activates integrins only weakly by itself. Binds to membranes enriched in phosphoinositides. Enhances integrin-mediated cell adhesion onto the extracellular matrix and cell spreading; this requires both its ability to interact with integrins and with phospholipid membranes. Required for the assembly of focal adhesions. Participates in the connection between extracellular matrix adhesion sites and the actin cytoskeleton and also in the orchestration of actin assembly and cell shape modulation. Recruits FBLIM1 to focal adhesions. Plays a role in the TGFB1 and integrin signaling pathways. Stabilizes active CTNNB1 and plays a role in the regulation of transcription mediated by CTNNB1 and TCF7L2/TCF4 and in Wnt signaling. {ECO:0000269|PubMed:12679033, ECO:0000269|PubMed:18458155, ECO:0000269|PubMed:21325030, ECO:0000269|PubMed:22030399, ECO:0000269|PubMed:22078565, ECO:0000269|PubMed:22699938}. |
Q96JP5 | ZFP91 | S101 | ochoa | E3 ubiquitin-protein ligase ZFP91 (EC 2.3.2.27) (RING-type E3 ubiquitin transferase ZFP91) (Zinc finger protein 757) (Zinc finger protein 91 homolog) (Zfp-91) | Atypical E3 ubiquitin-protein ligase that mediates 'Lys-63'-linked ubiquitination of MAP3K14/NIK, leading to stabilize and activate MAP3K14/NIK. It thereby acts as an activator of the non-canonical NF-kappa-B2/NFKB2 pathway. May also play an important role in cell proliferation and/or anti-apoptosis. {ECO:0000269|PubMed:12738986, ECO:0000269|PubMed:20682767}. |
Q96RE7 | NACC1 | S151 | ochoa | Nucleus accumbens-associated protein 1 (NAC-1) (BTB/POZ domain-containing protein 14B) | Functions as a transcriptional repressor. Seems to function as a transcriptional corepressor in neuronal cells through recruitment of HDAC3 and HDAC4. Contributes to tumor progression, and tumor cell proliferation and survival. This may be mediated at least in part through repressing transcriptional activity of GADD45GIP1. Required for recruiting the proteasome from the nucleus to the cytoplasm and dendritic spines. {ECO:0000269|PubMed:17130457, ECO:0000269|PubMed:17804717}. |
Q96RT1 | ERBIN | S1112 | ochoa | Erbin (Densin-180-like protein) (Erbb2-interacting protein) (Protein LAP2) | Acts as an adapter for the receptor ERBB2, in epithelia. By binding the unphosphorylated 'Tyr-1248' of receptor ERBB2, it may contribute to stabilize this unphosphorylated state (PubMed:16203728). Inhibits NOD2-dependent NF-kappa-B signaling and pro-inflammatory cytokine secretion (PubMed:16203728). {ECO:0000269|PubMed:10878805, ECO:0000269|PubMed:16203728}. |
Q99081 | TCF12 | S392 | ochoa | Transcription factor 12 (TCF-12) (Class B basic helix-loop-helix protein 20) (bHLHb20) (DNA-binding protein HTF4) (E-box-binding protein) (Transcription factor HTF-4) | Transcriptional regulator. Involved in the initiation of neuronal differentiation. Activates transcription by binding to the E box (5'-CANNTG-3') (By similarity). May be involved in the functional network that regulates the development of the GnRH axis (PubMed:32620954). {ECO:0000250|UniProtKB:Q61286, ECO:0000269|PubMed:32620954}. |
Q99501 | GAS2L1 | S492 | ochoa | GAS2-like protein 1 (GAS2-related protein on chromosome 22) (Growth arrest-specific protein 2-like 1) | Involved in the cross-linking of microtubules and microfilaments (PubMed:12584248, PubMed:24706950). Regulates microtubule dynamics and stability by interacting with microtubule plus-end tracking proteins, such as MAPRE1, to regulate microtubule growth along actin stress fibers (PubMed:24706950). {ECO:0000269|PubMed:12584248, ECO:0000269|PubMed:24706950}. |
Q99590 | SCAF11 | S802 | ochoa | Protein SCAF11 (CTD-associated SR protein 11) (Renal carcinoma antigen NY-REN-40) (SC35-interacting protein 1) (SR-related and CTD-associated factor 11) (SRSF2-interacting protein) (Serine/arginine-rich splicing factor 2-interacting protein) (Splicing factor, arginine/serine-rich 2-interacting protein) (Splicing regulatory protein 129) (SRrp129) | Plays a role in pre-mRNA alternative splicing by regulating spliceosome assembly. {ECO:0000269|PubMed:9447963}. |
Q9BV99 | LRRC61 | S188 | ochoa | Leucine-rich repeat-containing protein 61 | None |
Q9BY89 | KIAA1671 | S384 | ochoa | Uncharacterized protein KIAA1671 | None |
Q9BY89 | KIAA1671 | S1154 | ochoa | Uncharacterized protein KIAA1671 | None |
Q9C073 | FAM117A | S207 | ochoa | Protein FAM117A (C/EBP-induced protein) | None |
Q9GZU3 | TMEM39B | S53 | ochoa | Transmembrane protein 39B | May protect the cells against DNA damage caused by exposure to the cold-warming stress and facilitates tissue damage repair during the recovery phase. {ECO:0000250|UniProtKB:Q7ZW11}. |
Q9H0F6 | SHARPIN | S146 | ochoa|psp | Sharpin (Shank-associated RH domain-interacting protein) (Shank-interacting protein-like 1) (hSIPL1) | Component of the LUBAC complex which conjugates linear polyubiquitin chains in a head-to-tail manner to substrates and plays a key role in NF-kappa-B activation and regulation of inflammation (PubMed:21455173, PubMed:21455180, PubMed:21455181). LUBAC conjugates linear polyubiquitin to IKBKG and RIPK1 and is involved in activation of the canonical NF-kappa-B and the JNK signaling pathways (PubMed:21455173, PubMed:21455180, PubMed:21455181). Linear ubiquitination mediated by the LUBAC complex interferes with TNF-induced cell death and thereby prevents inflammation (PubMed:21455173, PubMed:21455180, PubMed:21455181). LUBAC is recruited to the TNF-R1 signaling complex (TNF-RSC) following polyubiquitination of TNF-RSC components by BIRC2 and/or BIRC3 and to conjugate linear polyubiquitin to IKBKG and possibly other components contributing to the stability of the complex (PubMed:21455173, PubMed:21455180, PubMed:21455181). The LUBAC complex is also involved in innate immunity by conjugating linear polyubiquitin chains at the surface of bacteria invading the cytosol to form the ubiquitin coat surrounding bacteria (PubMed:28481331). LUBAC is not able to initiate formation of the bacterial ubiquitin coat, and can only promote formation of linear polyubiquitins on pre-existing ubiquitin (PubMed:28481331). The bacterial ubiquitin coat acts as an 'eat-me' signal for xenophagy and promotes NF-kappa-B activation (PubMed:28481331). Together with OTULIN, the LUBAC complex regulates the canonical Wnt signaling during angiogenesis (PubMed:23708998). {ECO:0000269|PubMed:21455173, ECO:0000269|PubMed:21455180, ECO:0000269|PubMed:21455181, ECO:0000269|PubMed:23708998, ECO:0000269|PubMed:28481331}. |
Q9H7P6 | MVB12B | S207 | ochoa | Multivesicular body subunit 12B (ESCRT-I complex subunit MVB12B) (Protein FAM125B) | Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. |
Q9HB20 | PLEKHA3 | S250 | ochoa | Pleckstrin homology domain-containing family A member 3 (PH domain-containing family A member 3) (Phosphatidylinositol-four-phosphate adapter protein 1) (FAPP-1) (Phosphoinositol 4-phosphate adapter protein 1) | Plays a role in regulation of vesicular cargo transport from the trans-Golgi network (TGN) to the plasma membrane (PubMed:15107860). Regulates Golgi phosphatidylinositol 4-phosphate (PtdIns(4)P) levels and activates the PtdIns(4)P phosphatase activity of SACM1L when it binds PtdIns(4)P in 'trans' configuration (PubMed:30659099). Binds preferentially to PtdIns(4)P (PubMed:11001876, PubMed:15107860). Negatively regulates APOB secretion from hepatocytes (PubMed:30659099). {ECO:0000269|PubMed:11001876, ECO:0000269|PubMed:15107860, ECO:0000269|PubMed:30659099}. |
Q9HCD6 | TANC2 | S1744 | ochoa | Protein TANC2 (Tetratricopeptide repeat, ankyrin repeat and coiled-coil domain-containing protein 2) | Scaffolding protein in the dendritic spines which acts as immobile postsynaptic posts able to recruit KIF1A-driven dense core vesicles to dendritic spines. {ECO:0000269|PubMed:30021165}. |
Q9NQ75 | CASS4 | S249 | 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}. |
Q9NQW6 | ANLN | S362 | ochoa | Anillin | Required for cytokinesis (PubMed:16040610). Essential for the structural integrity of the cleavage furrow and for completion of cleavage furrow ingression. Plays a role in bleb assembly during metaphase and anaphase of mitosis (PubMed:23870127). May play a significant role in podocyte cell migration (PubMed:24676636). {ECO:0000269|PubMed:10931866, ECO:0000269|PubMed:12479805, ECO:0000269|PubMed:15496454, ECO:0000269|PubMed:16040610, ECO:0000269|PubMed:16357138, ECO:0000269|PubMed:23870127, ECO:0000269|PubMed:24676636}. |
Q9NRF2 | SH2B1 | S102 | ochoa | SH2B adapter protein 1 (Pro-rich, PH and SH2 domain-containing signaling mediator) (PSM) (SH2 domain-containing protein 1B) | Adapter protein for several members of the tyrosine kinase receptor family. Involved in multiple signaling pathways mediated by Janus kinase (JAK) and receptor tyrosine kinases, including the receptors of insulin (INS), insulin-like growth factor 1 (IGF1), nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), platelet-derived growth factor (PDGF) and fibroblast growth factors (FGFs). In growth hormone (GH) signaling, autophosphorylated ('Tyr-813') JAK2 recruits SH2B1, which in turn is phosphorylated by JAK2 on tyrosine residues. These phosphotyrosines form potential binding sites for other signaling proteins. GH also promotes serine/threonine phosphorylation of SH2B1 and these phosphorylated residues may serve to recruit other proteins to the GHR-JAK2-SH2B1 complexes, such as RAC1. In leptin (LEP) signaling, binds to and potentiates the activation of JAK2 by globally enhancing downstream pathways. In response to leptin, binds simultaneously to both, JAK2 and IRS1 or IRS2, thus mediating formation of a complex of JAK2, SH2B1 and IRS1 or IRS2. Mediates tyrosine phosphorylation of IRS1 and IRS2, resulting in activation of the PI 3-kinase pathway. Acts as a positive regulator of NGF-mediated activation of the Akt/Forkhead pathway; prolongs NGF-induced phosphorylation of AKT1 on 'Ser-473' and AKT1 enzymatic activity. Enhances the kinase activity of the cytokine receptor-associated tyrosine kinase JAK2 and of other receptor tyrosine kinases, such as FGFR3 and NTRK1. For JAK2, the mechanism seems to involve dimerization of both, SH2B1 and JAK2. Enhances RET phosphorylation and kinase activity. Isoforms seem to be differentially involved in IGF1 and PDGF-induced mitogenesis (By similarity). {ECO:0000250|UniProtKB:Q91ZM2, ECO:0000269|PubMed:11827956, ECO:0000269|PubMed:14565960, ECO:0000269|PubMed:15767667, ECO:0000269|PubMed:16569669, ECO:0000269|PubMed:17471236, ECO:0000269|PubMed:9694882, ECO:0000269|PubMed:9742218}. |
Q9NSY1 | BMP2K | S1141 | ochoa | BMP-2-inducible protein kinase (BIKe) (EC 2.7.11.1) | May be involved in osteoblast differentiation. {ECO:0000250|UniProtKB:Q91Z96}. |
Q9NYL2 | MAP3K20 | S733 | ochoa | Mitogen-activated protein kinase kinase kinase 20 (EC 2.7.11.25) (Human cervical cancer suppressor gene 4 protein) (HCCS-4) (Leucine zipper- and sterile alpha motif-containing kinase) (MLK-like mitogen-activated protein triple kinase) (Mitogen-activated protein kinase kinase kinase MLT) (Mixed lineage kinase 7) (Mixed lineage kinase-related kinase) (MLK-related kinase) (MRK) (Sterile alpha motif- and leucine zipper-containing kinase AZK) | Stress-activated component of a protein kinase signal transduction cascade that promotes programmed cell death in response to various stress, such as ribosomal stress, osmotic shock and ionizing radiation (PubMed:10924358, PubMed:11836244, PubMed:12220515, PubMed:14521931, PubMed:15350844, PubMed:15737997, PubMed:18331592, PubMed:20559024, PubMed:26999302, PubMed:32289254, PubMed:32610081, PubMed:35857590). Acts by catalyzing phosphorylation of MAP kinase kinases, leading to activation of the JNK (MAPK8/JNK1, MAPK9/JNK2 and/or MAPK10/JNK3) and MAP kinase p38 (MAPK11, MAPK12, MAPK13 and/or MAPK14) pathways (PubMed:11042189, PubMed:11836244, PubMed:12220515, PubMed:14521931, PubMed:15172994, PubMed:15737997, PubMed:32289254, PubMed:32610081, PubMed:35857590). Activates JNK through phosphorylation of MAP2K4/MKK4 and MAP2K7/MKK7, and MAP kinase p38 gamma (MAPK12) via phosphorylation of MAP2K3/MKK3 and MAP2K6/MKK6 (PubMed:11836244, PubMed:12220515). Involved in stress associated with adrenergic stimulation: contributes to cardiac decompensation during periods of acute cardiac stress (PubMed:15350844, PubMed:21224381, PubMed:27859413). May be involved in regulation of S and G2 cell cycle checkpoint by mediating phosphorylation of CHEK2 (PubMed:15342622). {ECO:0000269|PubMed:10924358, ECO:0000269|PubMed:11042189, ECO:0000269|PubMed:11836244, ECO:0000269|PubMed:12220515, ECO:0000269|PubMed:14521931, ECO:0000269|PubMed:15172994, ECO:0000269|PubMed:15342622, ECO:0000269|PubMed:15350844, ECO:0000269|PubMed:15737997, ECO:0000269|PubMed:18331592, ECO:0000269|PubMed:20559024, ECO:0000269|PubMed:21224381, ECO:0000269|PubMed:26999302, ECO:0000269|PubMed:27859413, ECO:0000269|PubMed:32289254, ECO:0000269|PubMed:32610081, ECO:0000269|PubMed:35857590}.; FUNCTION: [Isoform ZAKalpha]: Key component of the stress-activated protein kinase signaling cascade in response to ribotoxic stress or UV-B irradiation (PubMed:32289254, PubMed:32610081, PubMed:35857590). Acts as the proximal sensor of ribosome collisions during the ribotoxic stress response (RSR): directly binds to the ribosome by inserting its flexible C-terminus into the ribosomal intersubunit space, thereby acting as a sentinel for colliding ribosomes (PubMed:32289254, PubMed:32610081). Upon ribosome collisions, activates either the stress-activated protein kinase signal transduction cascade or the integrated stress response (ISR), leading to programmed cell death or cell survival, respectively (PubMed:32610081). Dangerous levels of ribosome collisions trigger the autophosphorylation and activation of MAP3K20, which dissociates from colliding ribosomes and phosphorylates MAP kinase kinases, leading to activation of the JNK and MAP kinase p38 pathways that promote programmed cell death (PubMed:32289254, PubMed:32610081). Less dangerous levels of ribosome collisions trigger the integrated stress response (ISR): MAP3K20 activates EIF2AK4/GCN2 independently of its protein-kinase activity, promoting EIF2AK4/GCN2-mediated phosphorylation of EIF2S1/eIF-2-alpha (PubMed:32610081). Also part of the stress-activated protein kinase signaling cascade triggering the NLRP1 inflammasome in response to UV-B irradiation: ribosome collisions activate MAP3K20, which directly phosphorylates NLRP1, leading to activation of the NLRP1 inflammasome and subsequent pyroptosis (PubMed:35857590). NLRP1 is also phosphorylated by MAP kinase p38 downstream of MAP3K20 (PubMed:35857590). Also acts as a histone kinase by phosphorylating histone H3 at 'Ser-28' (H3S28ph) (PubMed:15684425). {ECO:0000269|PubMed:15684425, ECO:0000269|PubMed:32289254, ECO:0000269|PubMed:32610081, ECO:0000269|PubMed:35857590}.; FUNCTION: [Isoform ZAKbeta]: Isoform that lacks the C-terminal region that mediates ribosome-binding: does not act as a sensor of ribosome collisions in response to ribotoxic stress (PubMed:32289254, PubMed:32610081, PubMed:35857590). May act as an antagonist of isoform ZAKalpha: interacts with isoform ZAKalpha, leading to decrease the expression of isoform ZAKalpha (PubMed:27859413). {ECO:0000269|PubMed:27859413, ECO:0000269|PubMed:32289254, ECO:0000269|PubMed:32610081, ECO:0000269|PubMed:35857590}. |
Q9NZN8 | CNOT2 | S126 | ochoa | CCR4-NOT transcription complex subunit 2 (CCR4-associated factor 2) | Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiation and general transcription regulation. Additional complex functions may be a consequence of its influence on mRNA expression. Required for the CCR4-NOT complex structural integrity. Can repress transcription and may link the CCR4-NOT complex to transcriptional regulation; the repressive function may specifically involve the N-Cor repressor complex containing HDAC3, NCOR1 and NCOR2. Involved in the maintenance of embryonic stem (ES) cell identity. {ECO:0000269|PubMed:14707134, ECO:0000269|PubMed:16712523, ECO:0000269|PubMed:21299754, ECO:0000269|PubMed:22367759}. |
Q9P206 | NHSL3 | S526 | ochoa | NHS-like protein 3 | Able to directly activate the TNF-NFkappaB signaling pathway. {ECO:0000269|PubMed:32854746}. |
Q9P266 | JCAD | S696 | ochoa | Junctional cadherin 5-associated protein (Junctional protein associated with coronary artery disease) (JCAD) | None |
Q9UBP9 | GULP1 | S229 | ochoa | PTB domain-containing engulfment adapter protein 1 (Cell death protein 6 homolog) (PTB domain adapter protein CED-6) (Protein GULP) | May function as an adapter protein. Required for efficient phagocytosis of apoptotic cells. Modulates cellular glycosphingolipid and cholesterol transport. May play a role in the internalization and endosomal trafficking of various LRP1 ligands, such as PSAP. Increases cellular levels of GTP-bound ARF6. {ECO:0000269|PubMed:10574763, ECO:0000269|PubMed:10574771, ECO:0000269|PubMed:16497666, ECO:0000269|PubMed:17398097}. |
Q9UBS0 | RPS6KB2 | S423 | ochoa|psp | Ribosomal protein S6 kinase beta-2 (S6K-beta-2) (S6K2) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 2) (P70S6K2) (p70-S6K 2) (S6 kinase-related kinase) (SRK) (Serine/threonine-protein kinase 14B) (p70 ribosomal S6 kinase beta) (S6K-beta) (p70 S6 kinase beta) (p70 S6K-beta) (p70 S6KB) (p70-beta) | Phosphorylates specifically ribosomal protein S6 (PubMed:29750193). Seems to act downstream of mTOR signaling in response to growth factors and nutrients to promote cell proliferation, cell growth and cell cycle progression in an alternative pathway regulated by MEAK7 (PubMed:29750193). {ECO:0000269|PubMed:29750193}. |
Q9UGJ0 | PRKAG2 | S71 | ochoa | 5'-AMP-activated protein kinase subunit gamma-2 (AMPK gamma2) (AMPK subunit gamma-2) (H91620p) | AMP/ATP-binding subunit of AMP-activated protein kinase (AMPK), an energy sensor protein kinase that plays a key role in regulating cellular energy metabolism (PubMed:14722619, PubMed:24563466). In response to reduction of intracellular ATP levels, AMPK activates energy-producing pathways and inhibits energy-consuming processes: inhibits protein, carbohydrate and lipid biosynthesis, as well as cell growth and proliferation (PubMed:14722619, PubMed:24563466). AMPK acts via direct phosphorylation of metabolic enzymes, and by longer-term effects via phosphorylation of transcription regulators (PubMed:14722619, PubMed:24563466). Also acts as a regulator of cellular polarity by remodeling the actin cytoskeleton; probably by indirectly activating myosin (PubMed:14722619, PubMed:24563466). Gamma non-catalytic subunit mediates binding to AMP, ADP and ATP, leading to activate or inhibit AMPK: AMP-binding results in allosteric activation of alpha catalytic subunit (PRKAA1 or PRKAA2) both by inducing phosphorylation and preventing dephosphorylation of catalytic subunits (PubMed:14722619, PubMed:24563466). ADP also stimulates phosphorylation, without stimulating already phosphorylated catalytic subunit (PubMed:14722619, PubMed:24563466). ATP promotes dephosphorylation of catalytic subunit, rendering the AMPK enzyme inactive (PubMed:14722619, PubMed:24563466). {ECO:0000269|PubMed:14722619, ECO:0000269|PubMed:24563466}. |
Q9UH99 | SUN2 | S38 | ochoa | SUN domain-containing protein 2 (Protein unc-84 homolog B) (Rab5-interacting protein) (Rab5IP) (Sad1/unc-84 protein-like 2) | As a component of the LINC (LInker of Nucleoskeleton and Cytoskeleton) complex, involved in the connection between the nuclear lamina and the cytoskeleton. The nucleocytoplasmic interactions established by the LINC complex play an important role in the transmission of mechanical forces across the nuclear envelope and in nuclear movement and positioning. Specifically, SYNE2 and SUN2 assemble in arrays of transmembrane actin-associated nuclear (TAN) lines which are bound to F-actin cables and couple the nucleus to retrograde actin flow during actin-dependent nuclear movement. Required for interkinetic nuclear migration (INM) and essential for nucleokinesis and centrosome-nucleus coupling during radial neuronal migration in the cerebral cortex and during glial migration. Required for nuclear migration in retinal photoreceptor progenitors implicating association with cytoplasmic dynein-dynactin and kinesin motor complexes, and probably B-type lamins; SUN1 and SUN2 seem to act redundantly. The SUN1/2:KASH5 LINC complex couples telomeres to microtubules during meiosis; SUN1 and SUN2 seem to act at least partial redundantly. Anchors chromosome movement in the prophase of meiosis and is involved in selective gene expression of coding and non-coding RNAs needed for gametogenesis. Required for telomere attachment to nuclear envelope and gametogenesis. May also function on endocytic vesicles as a receptor for RAB5-GDP and participate in the activation of RAB5. {ECO:0000250|UniProtKB:Q8BJS4, ECO:0000269|PubMed:18396275, ECO:0000305}. |
Q9ULH1 | ASAP1 | S785 | ochoa | Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 (130 kDa phosphatidylinositol 4,5-bisphosphate-dependent ARF1 GTPase-activating protein) (ADP-ribosylation factor-directed GTPase-activating protein 1) (ARF GTPase-activating protein 1) (Development and differentiation-enhancing factor 1) (DEF-1) (Differentiation-enhancing factor 1) (PIP2-dependent ARF1 GAP) | Possesses phosphatidylinositol 4,5-bisphosphate-dependent GTPase-activating protein activity for ARF1 (ADP ribosylation factor 1) and ARF5 and a lesser activity towards ARF6. May coordinate membrane trafficking with cell growth or actin cytoskeleton remodeling by binding to both SRC and PIP2. May function as a signal transduction protein involved in the differentiation of fibroblasts into adipocytes and possibly other cell types. Part of the ciliary targeting complex containing Rab11, ASAP1, Rabin8/RAB3IP, RAB11FIP3 and ARF4, which direct preciliary vesicle trafficking to mother centriole and ciliogenesis initiation (PubMed:25673879). {ECO:0000250, ECO:0000269|PubMed:20393563, ECO:0000269|PubMed:25673879}. |
Q9UQ35 | SRRM2 | S421 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S437 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S857 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S937 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S1404 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S1502 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S1675 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9Y2U8 | LEMD3 | S402 | ochoa|psp | Inner nuclear membrane protein Man1 (LEM domain-containing protein 3) | Can function as a specific repressor of TGF-beta, activin, and BMP signaling through its interaction with the R-SMAD proteins. Antagonizes TGF-beta-induced cell proliferation arrest. {ECO:0000269|PubMed:15601644, ECO:0000269|PubMed:15647271}. |
Q9Y4E8 | USP15 | S242 | ochoa | Ubiquitin carboxyl-terminal hydrolase 15 (EC 3.4.19.12) (Deubiquitinating enzyme 15) (Ubiquitin thioesterase 15) (Ubiquitin-specific-processing protease 15) (Unph-2) (Unph4) | Hydrolase that removes conjugated ubiquitin from target proteins and regulates various pathways such as the TGF-beta receptor signaling, NF-kappa-B and RNF41/NRDP1-PRKN pathways (PubMed:16005295, PubMed:17318178, PubMed:19576224, PubMed:19826004, PubMed:21947082, PubMed:22344298, PubMed:24852371). Acts as a key regulator of TGF-beta receptor signaling pathway, but the precise mechanism is still unclear: according to a report, acts by promoting deubiquitination of monoubiquitinated R-SMADs (SMAD1, SMAD2 and/or SMAD3), thereby alleviating inhibition of R-SMADs and promoting activation of TGF-beta target genes (PubMed:21947082). According to another reports, regulates the TGF-beta receptor signaling pathway by mediating deubiquitination and stabilization of TGFBR1, leading to an enhanced TGF-beta signal (PubMed:22344298). Able to mediate deubiquitination of monoubiquitinated substrates, 'Lys-27'-, 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains (PubMed:33093067). May also regulate gene expression and/or DNA repair through the deubiquitination of histone H2B (PubMed:24526689). Acts as an inhibitor of mitophagy by counteracting the action of parkin (PRKN): hydrolyzes cleavage of 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains attached by parkin on target proteins such as MFN2, thereby reducing parkin's ability to drive mitophagy (PubMed:24852371). Acts as an associated component of COP9 signalosome complex (CSN) and regulates different pathways via this association: regulates NF-kappa-B by mediating deubiquitination of NFKBIA and deubiquitinates substrates bound to VCP (PubMed:16005295, PubMed:17318178, PubMed:19576224, PubMed:19826004). Involved in endosome organization by mediating deubiquitination of SQSTM1: ubiquitinated SQSTM1 forms a molecular bridge that restrains cognate vesicles in the perinuclear region and its deubiquitination releases target vesicles for fast transport into the cell periphery (PubMed:27368102). Acts as a negative regulator of antifungal immunity by mediating 'Lys-27'-linked deubiquitination of CARD9, thereby inactivating CARD9 (PubMed:33093067). {ECO:0000269|PubMed:16005295, ECO:0000269|PubMed:17318178, ECO:0000269|PubMed:19576224, ECO:0000269|PubMed:19826004, ECO:0000269|PubMed:21947082, ECO:0000269|PubMed:22344298, ECO:0000269|PubMed:24526689, ECO:0000269|PubMed:24852371, ECO:0000269|PubMed:27368102, ECO:0000269|PubMed:33093067}.; FUNCTION: (Microbial infection) Protects APC and human papillomavirus type 16 protein E6 against degradation via the ubiquitin proteasome pathway. {ECO:0000269|PubMed:19553310}. |
Q9Y6Q9 | NCOA3 | S569 | ochoa | Nuclear receptor coactivator 3 (NCoA-3) (EC 2.3.1.48) (ACTR) (Amplified in breast cancer 1 protein) (AIB-1) (CBP-interacting protein) (pCIP) (Class E basic helix-loop-helix protein 42) (bHLHe42) (Receptor-associated coactivator 3) (RAC-3) (Steroid receptor coactivator protein 3) (SRC-3) (Thyroid hormone receptor activator molecule 1) (TRAM-1) | Nuclear receptor coactivator that directly binds nuclear receptors and stimulates the transcriptional activities in a hormone-dependent fashion. Plays a central role in creating a multisubunit coactivator complex, which probably acts via remodeling of chromatin. Involved in the coactivation of different nuclear receptors, such as for steroids (GR and ER), retinoids (RARs and RXRs), thyroid hormone (TRs), vitamin D3 (VDR) and prostanoids (PPARs). Displays histone acetyltransferase activity. Also involved in the coactivation of the NF-kappa-B pathway via its interaction with the NFKB1 subunit. |
Q9Y285 | FARSA | S199 | Sugiyama | Phenylalanine--tRNA ligase alpha subunit (EC 6.1.1.20) (CML33) (Phenylalanyl-tRNA synthetase alpha subunit) (PheRS) | None |
O75676 | RPS6KA4 | S700 | Sugiyama | Ribosomal protein S6 kinase alpha-4 (S6K-alpha-4) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 4) (Nuclear mitogen- and stress-activated protein kinase 2) (Ribosomal protein kinase B) (RSKB) | Serine/threonine-protein kinase that is required for the mitogen or stress-induced phosphorylation of the transcription factors CREB1 and ATF1 and for the regulation of the transcription factor RELA, and that contributes to gene activation by histone phosphorylation and functions in the regulation of inflammatory genes. Phosphorylates CREB1 and ATF1 in response to mitogenic or stress stimuli such as UV-C irradiation, epidermal growth factor (EGF) and anisomycin. Plays an essential role in the control of RELA transcriptional activity in response to TNF. Phosphorylates 'Ser-10' of histone H3 in response to mitogenics, stress stimuli and EGF, which results in the transcriptional activation of several immediate early genes, including proto-oncogenes c-fos/FOS and c-jun/JUN. May also phosphorylate 'Ser-28' of histone H3. Mediates the mitogen- and stress-induced phosphorylation of high mobility group protein 1 (HMGN1/HMG14). In lipopolysaccharide-stimulated primary macrophages, acts downstream of the Toll-like receptor TLR4 to limit the production of pro-inflammatory cytokines. Functions probably by inducing transcription of the MAP kinase phosphatase DUSP1 and the anti-inflammatory cytokine interleukin 10 (IL10), via CREB1 and ATF1 transcription factors. {ECO:0000269|PubMed:11035004, ECO:0000269|PubMed:12773393, ECO:0000269|PubMed:9792677}. |
P08151 | GLI1 | S608 | GPS6 | Zinc finger protein GLI1 (Glioma-associated oncogene) (Oncogene GLI) | Acts as a transcriptional activator (PubMed:10806483, PubMed:19706761, PubMed:19878745, PubMed:24076122, PubMed:24217340, PubMed:24311597). Binds to the DNA consensus sequence 5'-GACCACCCA-3' (PubMed:2105456, PubMed:24217340, PubMed:8378770). Regulates the transcription of specific genes during normal development (PubMed:19706761). Plays a role in craniofacial development and digital development, as well as development of the central nervous system and gastrointestinal tract. Mediates SHH signaling (PubMed:19706761, PubMed:28973407). Plays a role in cell proliferation and differentiation via its role in SHH signaling (PubMed:11238441, PubMed:28973407). {ECO:0000269|PubMed:10806483, ECO:0000269|PubMed:11238441, ECO:0000269|PubMed:19706761, ECO:0000269|PubMed:19878745, ECO:0000269|PubMed:2105456, ECO:0000269|PubMed:24076122, ECO:0000269|PubMed:24217340, ECO:0000269|PubMed:24311597, ECO:0000269|PubMed:28973407, ECO:0000269|PubMed:8378770}.; FUNCTION: [Isoform 2]: Acts as a transcriptional activator, but activates a different set of genes than isoform 1. Activates expression of CD24, unlike isoform 1. Mediates SHH signaling. Promotes cancer cell migration. {ECO:0000269|PubMed:19706761}. |
Q9NRA0 | SPHK2 | S393 | Sugiyama | Sphingosine kinase 2 (SK 2) (SPK 2) (EC 2.7.1.91) | Catalyzes the phosphorylation of sphingosine to form sphingosine-1-phosphate (SPP), a lipid mediator with both intra- and extracellular functions. Also acts on D-erythro-dihydrosphingosine, D-erythro-sphingosine and L-threo-dihydrosphingosine. Binds phosphoinositides (PubMed:12954646, PubMed:19168031). In contrast to prosurvival SPHK1, has a positive effect on intracellular ceramide levels, inhibits cells growth and enhances apoptosis (PubMed:16118219). In mitochondria, is important for cytochrome-c oxidase assembly and mitochondrial respiration. The SPP produced in mitochondria binds PHB2 and modulates the regulation via PHB2 of complex IV assembly and respiration (PubMed:20959514). In nucleus, plays a role in epigenetic regulation of gene expression. Interacts with HDAC1 and HDAC2 and, through SPP production, inhibits their enzymatic activity, preventing the removal of acetyl groups from lysine residues with histones. Up-regulates acetylation of histone H3-K9, histone H4-K5 and histone H2B-K12 (PubMed:19729656). In nucleus, may have an inhibitory effect on DNA synthesis and cell cycle (PubMed:12954646, PubMed:16103110). In mast cells, is the main regulator of SPP production which mediates calcium influx, NF-kappa-B activation, cytokine production, such as TNF and IL6, and degranulation of mast cells (By similarity). In dopaminergic neurons, is involved in promoting mitochondrial functions regulating ATP and ROS levels (By similarity). Also involved in the regulation of glucose and lipid metabolism (By similarity). {ECO:0000250|UniProtKB:Q9JIA7, ECO:0000269|PubMed:12954646, ECO:0000269|PubMed:16103110, ECO:0000269|PubMed:16118219, ECO:0000269|PubMed:19168031, ECO:0000269|PubMed:19729656, ECO:0000269|PubMed:20959514}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-9827857 | Specification of primordial germ cells | 0.000045 | 4.349 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 0.000114 | 3.944 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 0.000089 | 4.053 |
R-HSA-6804754 | Regulation of TP53 Expression | 0.000579 | 3.238 |
R-HSA-74160 | Gene expression (Transcription) | 0.000755 | 3.122 |
R-HSA-8939247 | RUNX1 regulates transcription of genes involved in interleukin signaling | 0.001742 | 2.759 |
R-HSA-1474165 | Reproduction | 0.001789 | 2.748 |
R-HSA-5635851 | GLI proteins bind promoters of Hh responsive genes to promote transcription | 0.002262 | 2.645 |
R-HSA-429947 | Deadenylation of mRNA | 0.002344 | 2.630 |
R-HSA-6791312 | TP53 Regulates Transcription of Cell Cycle Genes | 0.002565 | 2.591 |
R-HSA-73857 | RNA Polymerase II Transcription | 0.003149 | 2.502 |
R-HSA-2025928 | Calcineurin activates NFAT | 0.004977 | 2.303 |
R-HSA-1538133 | G0 and Early G1 | 0.004532 | 2.344 |
R-HSA-9825895 | Regulation of MITF-M-dependent genes involved in DNA replication, damage repair ... | 0.004206 | 2.376 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 0.005567 | 2.254 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 0.005766 | 2.239 |
R-HSA-69205 | G1/S-Specific Transcription | 0.006365 | 2.196 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 0.007998 | 2.097 |
R-HSA-9820841 | M-decay: degradation of maternal mRNAs by maternally stored factors | 0.008583 | 2.066 |
R-HSA-212436 | Generic Transcription Pathway | 0.008499 | 2.071 |
R-HSA-165159 | MTOR signalling | 0.009581 | 2.019 |
R-HSA-5607763 | CLEC7A (Dectin-1) induces NFAT activation | 0.010827 | 1.965 |
R-HSA-9701898 | STAT3 nuclear events downstream of ALK signaling | 0.011996 | 1.921 |
R-HSA-418885 | DCC mediated attractive signaling | 0.011996 | 1.921 |
R-HSA-9699150 | Defective DNA double strand break response due to BARD1 loss of function | 0.017117 | 1.767 |
R-HSA-9663199 | Defective DNA double strand break response due to BRCA1 loss of function | 0.017117 | 1.767 |
R-HSA-72187 | mRNA 3'-end processing | 0.015562 | 1.808 |
R-HSA-4419969 | Depolymerization of the Nuclear Lamina | 0.017190 | 1.765 |
R-HSA-9856651 | MITF-M-dependent gene expression | 0.015752 | 1.803 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 0.016180 | 1.791 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 0.017248 | 1.763 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 0.019183 | 1.717 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 0.020752 | 1.683 |
R-HSA-1362277 | Transcription of E2F targets under negative control by DREAM complex | 0.020085 | 1.697 |
R-HSA-9665230 | Drug resistance in ERBB2 KD mutants | 0.033943 | 1.469 |
R-HSA-9652282 | Drug-mediated inhibition of ERBB2 signaling | 0.033943 | 1.469 |
R-HSA-9665246 | Resistance of ERBB2 KD mutants to neratinib | 0.033943 | 1.469 |
R-HSA-9665737 | Drug resistance in ERBB2 TMD/JMD mutants | 0.033943 | 1.469 |
R-HSA-9665245 | Resistance of ERBB2 KD mutants to tesevatinib | 0.033943 | 1.469 |
R-HSA-9665251 | Resistance of ERBB2 KD mutants to lapatinib | 0.033943 | 1.469 |
R-HSA-9665244 | Resistance of ERBB2 KD mutants to sapitinib | 0.033943 | 1.469 |
R-HSA-9665250 | Resistance of ERBB2 KD mutants to AEE788 | 0.033943 | 1.469 |
R-HSA-9665233 | Resistance of ERBB2 KD mutants to trastuzumab | 0.033943 | 1.469 |
R-HSA-9665247 | Resistance of ERBB2 KD mutants to osimertinib | 0.033943 | 1.469 |
R-HSA-9665249 | Resistance of ERBB2 KD mutants to afatinib | 0.033943 | 1.469 |
R-HSA-9839394 | TGFBR3 expression | 0.029868 | 1.525 |
R-HSA-166208 | mTORC1-mediated signalling | 0.024777 | 1.606 |
R-HSA-1168372 | Downstream signaling events of B Cell Receptor (BCR) | 0.030600 | 1.514 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 0.028656 | 1.543 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 0.022388 | 1.650 |
R-HSA-3214842 | HDMs demethylate histones | 0.029868 | 1.525 |
R-HSA-68875 | Mitotic Prophase | 0.029509 | 1.530 |
R-HSA-2995383 | Initiation of Nuclear Envelope (NE) Reformation | 0.023167 | 1.635 |
R-HSA-1640170 | Cell Cycle | 0.024504 | 1.611 |
R-HSA-162582 | Signal Transduction | 0.026681 | 1.574 |
R-HSA-9825892 | Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 0.023167 | 1.635 |
R-HSA-6804115 | TP53 regulates transcription of additional cell cycle genes whose exact role in ... | 0.024777 | 1.606 |
R-HSA-9843745 | Adipogenesis | 0.039295 | 1.406 |
R-HSA-69200 | Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 ... | 0.050482 | 1.297 |
R-HSA-8849470 | PTK6 Regulates Cell Cycle | 0.066741 | 1.176 |
R-HSA-446107 | Type I hemidesmosome assembly | 0.090612 | 1.043 |
R-HSA-9768778 | Regulation of NPAS4 mRNA translation | 0.090612 | 1.043 |
R-HSA-9759811 | Regulation of CDH11 mRNA translation by microRNAs | 0.113877 | 0.944 |
R-HSA-9931512 | Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | 0.121500 | 0.915 |
R-HSA-2197563 | NOTCH2 intracellular domain regulates transcription | 0.129058 | 0.889 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 0.129058 | 0.889 |
R-HSA-9661069 | Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 0.136551 | 0.865 |
R-HSA-8948700 | Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 0.151346 | 0.820 |
R-HSA-1362300 | Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL... | 0.158649 | 0.800 |
R-HSA-5625886 | Activated PKN1 stimulates transcription of AR (androgen receptor) regulated gene... | 0.065196 | 1.186 |
R-HSA-9709603 | Impaired BRCA2 binding to PALB2 | 0.187241 | 0.728 |
R-HSA-9909620 | Regulation of PD-L1(CD274) translation | 0.194237 | 0.712 |
R-HSA-9701193 | Defective homologous recombination repair (HRR) due to PALB2 loss of function | 0.194237 | 0.712 |
R-HSA-9701192 | Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 0.194237 | 0.712 |
R-HSA-9704646 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.194237 | 0.712 |
R-HSA-9704331 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.194237 | 0.712 |
R-HSA-442982 | Ras activation upon Ca2+ influx through NMDA receptor | 0.208051 | 0.682 |
R-HSA-8943723 | Regulation of PTEN mRNA translation | 0.221629 | 0.654 |
R-HSA-5693554 | Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SD... | 0.234976 | 0.629 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 0.254571 | 0.594 |
R-HSA-9709570 | Impaired BRCA2 binding to RAD51 | 0.260992 | 0.583 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 0.267358 | 0.573 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 0.273669 | 0.563 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 0.273669 | 0.563 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 0.286129 | 0.543 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 0.286129 | 0.543 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 0.292280 | 0.534 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 0.304424 | 0.517 |
R-HSA-1989781 | PPARA activates gene expression | 0.063791 | 1.195 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 0.204493 | 0.689 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 0.065944 | 1.181 |
R-HSA-9013508 | NOTCH3 Intracellular Domain Regulates Transcription | 0.267358 | 0.573 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 0.113710 | 0.944 |
R-HSA-9013695 | NOTCH4 Intracellular Domain Regulates Transcription | 0.201174 | 0.696 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 0.241564 | 0.617 |
R-HSA-140342 | Apoptosis induced DNA fragmentation | 0.106189 | 0.974 |
R-HSA-5620916 | VxPx cargo-targeting to cilium | 0.194237 | 0.712 |
R-HSA-9675136 | Diseases of DNA Double-Strand Break Repair | 0.298378 | 0.525 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 0.121598 | 0.915 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 0.121598 | 0.915 |
R-HSA-164940 | Nef mediated downregulation of MHC class I complex cell surface expression | 0.090612 | 1.043 |
R-HSA-163680 | AMPK inhibits chREBP transcriptional activation activity | 0.098434 | 1.007 |
R-HSA-9931521 | The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CL... | 0.165889 | 0.780 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 0.046014 | 1.337 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 0.114535 | 0.941 |
R-HSA-8941856 | RUNX3 regulates NOTCH signaling | 0.129058 | 0.889 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 0.267358 | 0.573 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 0.121598 | 0.915 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 0.179610 | 0.746 |
R-HSA-5693537 | Resolution of D-Loop Structures | 0.047312 | 1.325 |
R-HSA-426496 | Post-transcriptional silencing by small RNAs | 0.058647 | 1.232 |
R-HSA-9764562 | Regulation of CDH1 mRNA translation by microRNAs | 0.143980 | 0.842 |
R-HSA-5693568 | Resolution of D-loop Structures through Holliday Junction Intermediates | 0.045225 | 1.345 |
R-HSA-450321 | JNK (c-Jun kinases) phosphorylation and activation mediated by activated human ... | 0.201174 | 0.696 |
R-HSA-1221632 | Meiotic synapsis | 0.098079 | 1.008 |
R-HSA-5685938 | HDR through Single Strand Annealing (SSA) | 0.286129 | 0.543 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 0.316361 | 0.500 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 0.096387 | 1.016 |
R-HSA-2871809 | FCERI mediated Ca+2 mobilization | 0.101593 | 0.993 |
R-HSA-72172 | mRNA Splicing | 0.129781 | 0.887 |
R-HSA-5357956 | TNFR1-induced NF-kappa-B signaling pathway | 0.248096 | 0.605 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 0.152260 | 0.817 |
R-HSA-5693606 | DNA Double Strand Break Response | 0.137461 | 0.862 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 0.137461 | 0.862 |
R-HSA-5673000 | RAF activation | 0.298378 | 0.525 |
R-HSA-8934593 | Regulation of RUNX1 Expression and Activity | 0.241564 | 0.617 |
R-HSA-5693538 | Homology Directed Repair | 0.106909 | 0.971 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 0.184467 | 0.734 |
R-HSA-2424491 | DAP12 signaling | 0.267358 | 0.573 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 0.066192 | 1.179 |
R-HSA-8875513 | MET interacts with TNS proteins | 0.042248 | 1.374 |
R-HSA-2151209 | Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 0.106189 | 0.974 |
R-HSA-9634285 | Constitutive Signaling by Overexpressed ERBB2 | 0.129058 | 0.889 |
R-HSA-174490 | Membrane binding and targetting of GAG proteins | 0.136551 | 0.865 |
R-HSA-9659787 | Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 0.136551 | 0.865 |
R-HSA-73980 | RNA Polymerase III Transcription Termination | 0.180185 | 0.744 |
R-HSA-350054 | Notch-HLH transcription pathway | 0.214869 | 0.668 |
R-HSA-917729 | Endosomal Sorting Complex Required For Transport (ESCRT) | 0.260992 | 0.583 |
R-HSA-162588 | Budding and maturation of HIV virion | 0.273669 | 0.563 |
R-HSA-390471 | Association of TriC/CCT with target proteins during biosynthesis | 0.292280 | 0.534 |
R-HSA-9701190 | Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 0.298378 | 0.525 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 0.316361 | 0.500 |
R-HSA-2871796 | FCERI mediated MAPK activation | 0.290203 | 0.537 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 0.046090 | 1.336 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 0.213924 | 0.670 |
R-HSA-6788467 | IL-6-type cytokine receptor ligand interactions | 0.136551 | 0.865 |
R-HSA-500753 | Pyrimidine biosynthesis | 0.187241 | 0.728 |
R-HSA-1980145 | Signaling by NOTCH2 | 0.298378 | 0.525 |
R-HSA-1227990 | Signaling by ERBB2 in Cancer | 0.267358 | 0.573 |
R-HSA-174495 | Synthesis And Processing Of GAG, GAGPOL Polyproteins | 0.143980 | 0.842 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 0.292280 | 0.534 |
R-HSA-5693579 | Homologous DNA Pairing and Strand Exchange | 0.322253 | 0.492 |
R-HSA-5632684 | Hedgehog 'on' state | 0.149275 | 0.826 |
R-HSA-1500620 | Meiosis | 0.191997 | 0.717 |
R-HSA-5357905 | Regulation of TNFR1 signaling | 0.079848 | 1.098 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 0.293383 | 0.533 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 0.054572 | 1.263 |
R-HSA-9706019 | RHOBTB3 ATPase cycle | 0.113877 | 0.944 |
R-HSA-5357786 | TNFR1-induced proapoptotic signaling | 0.201174 | 0.696 |
R-HSA-9615710 | Late endosomal microautophagy | 0.260992 | 0.583 |
R-HSA-9687139 | Aberrant regulation of mitotic cell cycle due to RB1 defects | 0.267358 | 0.573 |
R-HSA-75893 | TNF signaling | 0.106220 | 0.974 |
R-HSA-5610787 | Hedgehog 'off' state | 0.072130 | 1.142 |
R-HSA-212165 | Epigenetic regulation of gene expression | 0.176315 | 0.754 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 0.084940 | 1.071 |
R-HSA-9665686 | Signaling by ERBB2 TMD/JMD mutants | 0.228331 | 0.641 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 0.228747 | 0.641 |
R-HSA-8934903 | Receptor Mediated Mitophagy | 0.106189 | 0.974 |
R-HSA-442742 | CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 0.286129 | 0.543 |
R-HSA-180746 | Nuclear import of Rev protein | 0.298378 | 0.525 |
R-HSA-5693616 | Presynaptic phase of homologous DNA pairing and strand exchange | 0.304424 | 0.517 |
R-HSA-5358351 | Signaling by Hedgehog | 0.150958 | 0.821 |
R-HSA-69206 | G1/S Transition | 0.121598 | 0.915 |
R-HSA-389948 | Co-inhibition by PD-1 | 0.293479 | 0.532 |
R-HSA-5689603 | UCH proteinases | 0.164315 | 0.784 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 0.172029 | 0.764 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 0.051589 | 1.287 |
R-HSA-9665348 | Signaling by ERBB2 ECD mutants | 0.180185 | 0.744 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 0.126791 | 0.897 |
R-HSA-9839373 | Signaling by TGFBR3 | 0.079848 | 1.098 |
R-HSA-198693 | AKT phosphorylates targets in the nucleus | 0.098434 | 1.007 |
R-HSA-210744 | Regulation of gene expression in late stage (branching morphogenesis) pancreatic... | 0.158649 | 0.800 |
R-HSA-69473 | G2/M DNA damage checkpoint | 0.158266 | 0.801 |
R-HSA-9018519 | Estrogen-dependent gene expression | 0.146918 | 0.833 |
R-HSA-9664565 | Signaling by ERBB2 KD Mutants | 0.260992 | 0.583 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 0.286129 | 0.543 |
R-HSA-9613354 | Lipophagy | 0.098434 | 1.007 |
R-HSA-3270619 | IRF3-mediated induction of type I IFN | 0.151346 | 0.820 |
R-HSA-164938 | Nef-mediates down modulation of cell surface receptors by recruiting them to cla... | 0.173068 | 0.762 |
R-HSA-9824594 | Regulation of MITF-M-dependent genes involved in apoptosis | 0.201174 | 0.696 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 0.241564 | 0.617 |
R-HSA-9675126 | Diseases of mitotic cell cycle | 0.279926 | 0.553 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 0.322253 | 0.492 |
R-HSA-1592230 | Mitochondrial biogenesis | 0.105125 | 0.978 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 0.179610 | 0.746 |
R-HSA-6804114 | TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 0.165889 | 0.780 |
R-HSA-9768759 | Regulation of NPAS4 gene expression | 0.173068 | 0.762 |
R-HSA-69236 | G1 Phase | 0.074856 | 1.126 |
R-HSA-69231 | Cyclin D associated events in G1 | 0.074856 | 1.126 |
R-HSA-6783589 | Interleukin-6 family signaling | 0.228331 | 0.641 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 0.116005 | 0.936 |
R-HSA-73887 | Death Receptor Signaling | 0.186625 | 0.729 |
R-HSA-5689901 | Metalloprotease DUBs | 0.241564 | 0.617 |
R-HSA-2586552 | Signaling by Leptin | 0.106189 | 0.974 |
R-HSA-6794361 | Neurexins and neuroligins | 0.095407 | 1.020 |
R-HSA-2559585 | Oncogene Induced Senescence | 0.304424 | 0.517 |
R-HSA-69278 | Cell Cycle, Mitotic | 0.068860 | 1.162 |
R-HSA-8877330 | RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | 0.136551 | 0.865 |
R-HSA-164952 | The role of Nef in HIV-1 replication and disease pathogenesis | 0.221629 | 0.654 |
R-HSA-8953854 | Metabolism of RNA | 0.320501 | 0.494 |
R-HSA-1170546 | Prolactin receptor signaling | 0.143980 | 0.842 |
R-HSA-8854214 | TBC/RABGAPs | 0.072400 | 1.140 |
R-HSA-525793 | Myogenesis | 0.241564 | 0.617 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 0.260992 | 0.583 |
R-HSA-8863795 | Downregulation of ERBB2 signaling | 0.267358 | 0.573 |
R-HSA-1483249 | Inositol phosphate metabolism | 0.290203 | 0.537 |
R-HSA-9612973 | Autophagy | 0.190960 | 0.719 |
R-HSA-2028269 | Signaling by Hippo | 0.173068 | 0.762 |
R-HSA-3214847 | HATs acetylate histones | 0.245611 | 0.610 |
R-HSA-983705 | Signaling by the B Cell Receptor (BCR) | 0.195321 | 0.709 |
R-HSA-438064 | Post NMDA receptor activation events | 0.201360 | 0.696 |
R-HSA-175474 | Assembly Of The HIV Virion | 0.208051 | 0.682 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 0.041333 | 1.384 |
R-HSA-2173796 | SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 0.316361 | 0.500 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 0.191997 | 0.717 |
R-HSA-211000 | Gene Silencing by RNA | 0.274282 | 0.562 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 0.286129 | 0.543 |
R-HSA-114604 | GPVI-mediated activation cascade | 0.310418 | 0.508 |
R-HSA-159418 | Recycling of bile acids and salts | 0.286129 | 0.543 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 0.302912 | 0.519 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 0.060537 | 1.218 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 0.267358 | 0.573 |
R-HSA-3247509 | Chromatin modifying enzymes | 0.070142 | 1.154 |
R-HSA-1834941 | STING mediated induction of host immune responses | 0.187241 | 0.728 |
R-HSA-446728 | Cell junction organization | 0.257112 | 0.590 |
R-HSA-68886 | M Phase | 0.269271 | 0.570 |
R-HSA-446353 | Cell-extracellular matrix interactions | 0.151346 | 0.820 |
R-HSA-200425 | Carnitine shuttle | 0.221629 | 0.654 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 0.255162 | 0.593 |
R-HSA-6794362 | Protein-protein interactions at synapses | 0.191997 | 0.717 |
R-HSA-5205647 | Mitophagy | 0.298378 | 0.525 |
R-HSA-4839726 | Chromatin organization | 0.084658 | 1.072 |
R-HSA-9007101 | Rab regulation of trafficking | 0.312419 | 0.505 |
R-HSA-193807 | Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 0.248096 | 0.605 |
R-HSA-1855204 | Synthesis of IP3 and IP4 in the cytosol | 0.286129 | 0.543 |
R-HSA-8875878 | MET promotes cell motility | 0.322253 | 0.492 |
R-HSA-749476 | RNA Polymerase III Abortive And Retractive Initiation | 0.310418 | 0.508 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 0.198233 | 0.703 |
R-HSA-9006936 | Signaling by TGFB family members | 0.069245 | 1.160 |
R-HSA-2173788 | Downregulation of TGF-beta receptor signaling | 0.214869 | 0.668 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 0.255162 | 0.593 |
R-HSA-3000170 | Syndecan interactions | 0.221629 | 0.654 |
R-HSA-3000157 | Laminin interactions | 0.234976 | 0.629 |
R-HSA-5633007 | Regulation of TP53 Activity | 0.069245 | 1.160 |
R-HSA-8953750 | Transcriptional Regulation by E2F6 | 0.060537 | 1.218 |
R-HSA-6804116 | TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 0.158649 | 0.800 |
R-HSA-5674400 | Constitutive Signaling by AKT1 E17K in Cancer | 0.221629 | 0.654 |
R-HSA-1368108 | BMAL1:CLOCK,NPAS2 activates circadian expression | 0.298378 | 0.525 |
R-HSA-2559583 | Cellular Senescence | 0.247001 | 0.607 |
R-HSA-1266738 | Developmental Biology | 0.179780 | 0.745 |
R-HSA-9663891 | Selective autophagy | 0.204493 | 0.689 |
R-HSA-5210891 | Uptake and function of anthrax toxins | 0.173068 | 0.762 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 0.239251 | 0.621 |
R-HSA-201556 | Signaling by ALK | 0.060537 | 1.218 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 0.236075 | 0.627 |
R-HSA-74158 | RNA Polymerase III Transcription | 0.310418 | 0.508 |
R-HSA-982772 | Growth hormone receptor signaling | 0.221629 | 0.654 |
R-HSA-373752 | Netrin-1 signaling | 0.074856 | 1.126 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 0.328094 | 0.484 |
R-HSA-9725554 | Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | 0.328094 | 0.484 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 0.328094 | 0.484 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 0.328094 | 0.484 |
R-HSA-1500931 | Cell-Cell communication | 0.330205 | 0.481 |
R-HSA-68882 | Mitotic Anaphase | 0.333444 | 0.477 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 0.333886 | 0.476 |
R-HSA-202433 | Generation of second messenger molecules | 0.333886 | 0.476 |
R-HSA-9844594 | Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | 0.333886 | 0.476 |
R-HSA-9843743 | Transcriptional regulation of brown and beige adipocyte differentiation | 0.333886 | 0.476 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 0.333886 | 0.476 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 0.333886 | 0.476 |
R-HSA-162909 | Host Interactions of HIV factors | 0.334489 | 0.476 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 0.335797 | 0.474 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 0.339628 | 0.469 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 0.339628 | 0.469 |
R-HSA-3214841 | PKMTs methylate histone lysines | 0.339628 | 0.469 |
R-HSA-5610780 | Degradation of GLI1 by the proteasome | 0.345321 | 0.462 |
R-HSA-5674135 | MAP2K and MAPK activation | 0.345321 | 0.462 |
R-HSA-9656223 | Signaling by RAF1 mutants | 0.345321 | 0.462 |
R-HSA-5675221 | Negative regulation of MAPK pathway | 0.345321 | 0.462 |
R-HSA-69481 | G2/M Checkpoints | 0.347012 | 0.460 |
R-HSA-379716 | Cytosolic tRNA aminoacylation | 0.350965 | 0.455 |
R-HSA-2173789 | TGF-beta receptor signaling activates SMADs | 0.356560 | 0.448 |
R-HSA-162906 | HIV Infection | 0.359297 | 0.445 |
R-HSA-187577 | SCF(Skp2)-mediated degradation of p27/p21 | 0.362108 | 0.441 |
R-HSA-2172127 | DAP12 interactions | 0.362108 | 0.441 |
R-HSA-9909396 | Circadian clock | 0.365649 | 0.437 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 0.367609 | 0.435 |
R-HSA-6783310 | Fanconi Anemia Pathway | 0.367609 | 0.435 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 0.373062 | 0.428 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 0.373062 | 0.428 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 0.373062 | 0.428 |
R-HSA-6802949 | Signaling by RAS mutants | 0.373062 | 0.428 |
R-HSA-9675135 | Diseases of DNA repair | 0.373062 | 0.428 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 0.373062 | 0.428 |
R-HSA-75153 | Apoptotic execution phase | 0.373062 | 0.428 |
R-HSA-437239 | Recycling pathway of L1 | 0.378469 | 0.422 |
R-HSA-8939211 | ESR-mediated signaling | 0.382684 | 0.417 |
R-HSA-9725371 | Nuclear events stimulated by ALK signaling in cancer | 0.383829 | 0.416 |
R-HSA-9031628 | NGF-stimulated transcription | 0.383829 | 0.416 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 0.389143 | 0.410 |
R-HSA-69563 | p53-Dependent G1 DNA Damage Response | 0.389143 | 0.410 |
R-HSA-69580 | p53-Dependent G1/S DNA damage checkpoint | 0.389143 | 0.410 |
R-HSA-5683057 | MAPK family signaling cascades | 0.390757 | 0.408 |
R-HSA-1632852 | Macroautophagy | 0.396247 | 0.402 |
R-HSA-1169091 | Activation of NF-kappaB in B cells | 0.399636 | 0.398 |
R-HSA-912446 | Meiotic recombination | 0.399636 | 0.398 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 0.402288 | 0.395 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 0.402288 | 0.395 |
R-HSA-9931269 | AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | 0.404815 | 0.393 |
R-HSA-9634815 | Transcriptional Regulation by NPAS4 | 0.404815 | 0.393 |
R-HSA-5339562 | Uptake and actions of bacterial toxins | 0.404815 | 0.393 |
R-HSA-445355 | Smooth Muscle Contraction | 0.409950 | 0.387 |
R-HSA-8956320 | Nucleotide biosynthesis | 0.409950 | 0.387 |
R-HSA-72649 | Translation initiation complex formation | 0.415041 | 0.382 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 0.415041 | 0.382 |
R-HSA-9012852 | Signaling by NOTCH3 | 0.420088 | 0.377 |
R-HSA-5688426 | Deubiquitination | 0.424269 | 0.372 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 0.425092 | 0.372 |
R-HSA-193648 | NRAGE signals death through JNK | 0.425092 | 0.372 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 0.425092 | 0.372 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 0.426554 | 0.370 |
R-HSA-69620 | Cell Cycle Checkpoints | 0.431114 | 0.365 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 0.434971 | 0.362 |
R-HSA-9029569 | NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflu... | 0.434971 | 0.362 |
R-HSA-191859 | snRNP Assembly | 0.439847 | 0.357 |
R-HSA-194441 | Metabolism of non-coding RNA | 0.439847 | 0.357 |
R-HSA-186712 | Regulation of beta-cell development | 0.439847 | 0.357 |
R-HSA-2022090 | Assembly of collagen fibrils and other multimeric structures | 0.439847 | 0.357 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 0.444682 | 0.352 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 0.444682 | 0.352 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 0.444682 | 0.352 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 0.444682 | 0.352 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 0.444682 | 0.352 |
R-HSA-1227986 | Signaling by ERBB2 | 0.444682 | 0.352 |
R-HSA-1660661 | Sphingolipid de novo biosynthesis | 0.444682 | 0.352 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 0.444682 | 0.352 |
R-HSA-379724 | tRNA Aminoacylation | 0.444682 | 0.352 |
R-HSA-9610379 | HCMV Late Events | 0.446642 | 0.350 |
R-HSA-162587 | HIV Life Cycle | 0.446642 | 0.350 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 0.449475 | 0.347 |
R-HSA-211976 | Endogenous sterols | 0.449475 | 0.347 |
R-HSA-9793380 | Formation of paraxial mesoderm | 0.449475 | 0.347 |
R-HSA-8939902 | Regulation of RUNX2 expression and activity | 0.449475 | 0.347 |
R-HSA-450294 | MAP kinase activation | 0.449475 | 0.347 |
R-HSA-6784531 | tRNA processing in the nucleus | 0.454227 | 0.343 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 0.454227 | 0.343 |
R-HSA-9707616 | Heme signaling | 0.454227 | 0.343 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 0.454227 | 0.343 |
R-HSA-1660499 | Synthesis of PIPs at the plasma membrane | 0.454227 | 0.343 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 0.458938 | 0.338 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 0.458938 | 0.338 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 0.458938 | 0.338 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 0.458938 | 0.338 |
R-HSA-8848021 | Signaling by PTK6 | 0.458938 | 0.338 |
R-HSA-69615 | G1/S DNA Damage Checkpoints | 0.458938 | 0.338 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 0.468240 | 0.330 |
R-HSA-8854518 | AURKA Activation by TPX2 | 0.472832 | 0.325 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 0.472832 | 0.325 |
R-HSA-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 0.477383 | 0.321 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 0.489122 | 0.311 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 0.490806 | 0.309 |
R-HSA-448424 | Interleukin-17 signaling | 0.490806 | 0.309 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 0.490806 | 0.309 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 0.490806 | 0.309 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 0.493749 | 0.306 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 0.494633 | 0.306 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 0.494633 | 0.306 |
R-HSA-5620920 | Cargo trafficking to the periciliary membrane | 0.495204 | 0.305 |
R-HSA-9856649 | Transcriptional and post-translational regulation of MITF-M expression and activ... | 0.495204 | 0.305 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 0.499564 | 0.301 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 0.499564 | 0.301 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 0.500106 | 0.301 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 0.503887 | 0.298 |
R-HSA-69052 | Switching of origins to a post-replicative state | 0.503887 | 0.298 |
R-HSA-4086398 | Ca2+ pathway | 0.503887 | 0.298 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 0.503887 | 0.298 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 0.503887 | 0.298 |
R-HSA-9013694 | Signaling by NOTCH4 | 0.508172 | 0.294 |
R-HSA-380287 | Centrosome maturation | 0.512421 | 0.290 |
R-HSA-1169408 | ISG15 antiviral mechanism | 0.512421 | 0.290 |
R-HSA-3000171 | Non-integrin membrane-ECM interactions | 0.512421 | 0.290 |
R-HSA-1980143 | Signaling by NOTCH1 | 0.516633 | 0.287 |
R-HSA-199991 | Membrane Trafficking | 0.520233 | 0.284 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 0.520810 | 0.283 |
R-HSA-416482 | G alpha (12/13) signalling events | 0.524950 | 0.280 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 0.529055 | 0.276 |
R-HSA-6806834 | Signaling by MET | 0.533125 | 0.273 |
R-HSA-5617833 | Cilium Assembly | 0.539934 | 0.268 |
R-HSA-9707564 | Cytoprotection by HMOX1 | 0.545125 | 0.264 |
R-HSA-68877 | Mitotic Prometaphase | 0.547635 | 0.262 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 0.549057 | 0.260 |
R-HSA-6802957 | Oncogenic MAPK signaling | 0.552955 | 0.257 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 0.555247 | 0.256 |
R-HSA-8876198 | RAB GEFs exchange GTP for GDP on RABs | 0.556820 | 0.254 |
R-HSA-9909615 | Regulation of PD-L1(CD274) Post-translational modification | 0.556820 | 0.254 |
R-HSA-390466 | Chaperonin-mediated protein folding | 0.564450 | 0.248 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 0.575651 | 0.240 |
R-HSA-1280218 | Adaptive Immune System | 0.577069 | 0.239 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 0.579321 | 0.237 |
R-HSA-391251 | Protein folding | 0.586566 | 0.232 |
R-HSA-1474290 | Collagen formation | 0.593687 | 0.226 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 0.596666 | 0.224 |
R-HSA-6807878 | COPI-mediated anterograde transport | 0.604142 | 0.219 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 0.607567 | 0.216 |
R-HSA-418990 | Adherens junctions interactions | 0.610585 | 0.214 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 0.610962 | 0.214 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 0.610962 | 0.214 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 0.610962 | 0.214 |
R-HSA-112316 | Neuronal System | 0.611946 | 0.213 |
R-HSA-192105 | Synthesis of bile acids and bile salts | 0.614329 | 0.212 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 0.614329 | 0.212 |
R-HSA-70171 | Glycolysis | 0.617666 | 0.209 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 0.624256 | 0.205 |
R-HSA-1483255 | PI Metabolism | 0.624256 | 0.205 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 0.630732 | 0.200 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 0.632972 | 0.199 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 0.633929 | 0.198 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 0.633929 | 0.198 |
R-HSA-9833110 | RSV-host interactions | 0.633929 | 0.198 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 0.637098 | 0.196 |
R-HSA-73894 | DNA Repair | 0.639663 | 0.194 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 0.642855 | 0.192 |
R-HSA-69239 | Synthesis of DNA | 0.643355 | 0.192 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 0.643355 | 0.192 |
R-HSA-9700206 | Signaling by ALK in cancer | 0.643355 | 0.192 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 0.644933 | 0.190 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 0.646443 | 0.189 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 0.646443 | 0.189 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 0.646443 | 0.189 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 0.646443 | 0.189 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 0.649505 | 0.187 |
R-HSA-202403 | TCR signaling | 0.652540 | 0.185 |
R-HSA-194068 | Bile acid and bile salt metabolism | 0.652540 | 0.185 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 0.652540 | 0.185 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 0.652540 | 0.185 |
R-HSA-157118 | Signaling by NOTCH | 0.658507 | 0.181 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 0.661490 | 0.179 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 0.670211 | 0.174 |
R-HSA-72613 | Eukaryotic Translation Initiation | 0.675901 | 0.170 |
R-HSA-72737 | Cap-dependent Translation Initiation | 0.675901 | 0.170 |
R-HSA-373760 | L1CAM interactions | 0.675901 | 0.170 |
R-HSA-9609646 | HCMV Infection | 0.678694 | 0.168 |
R-HSA-70326 | Glucose metabolism | 0.678709 | 0.168 |
R-HSA-421270 | Cell-cell junction organization | 0.680658 | 0.167 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 0.681493 | 0.167 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 0.684253 | 0.165 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 0.684253 | 0.165 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 0.684253 | 0.165 |
R-HSA-3371556 | Cellular response to heat stress | 0.689702 | 0.161 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 0.692392 | 0.160 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 0.692392 | 0.160 |
R-HSA-6809371 | Formation of the cornified envelope | 0.697701 | 0.156 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 0.710581 | 0.148 |
R-HSA-9711123 | Cellular response to chemical stress | 0.712588 | 0.147 |
R-HSA-5653656 | Vesicle-mediated transport | 0.725708 | 0.139 |
R-HSA-163685 | Integration of energy metabolism | 0.734728 | 0.134 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 0.734728 | 0.134 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 0.736854 | 0.133 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 0.737030 | 0.133 |
R-HSA-6807070 | PTEN Regulation | 0.741574 | 0.130 |
R-HSA-9664417 | Leishmania phagocytosis | 0.743817 | 0.129 |
R-HSA-9664407 | Parasite infection | 0.743817 | 0.129 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 0.743817 | 0.129 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 0.746040 | 0.127 |
R-HSA-5673001 | RAF/MAP kinase cascade | 0.748324 | 0.126 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 0.752597 | 0.123 |
R-HSA-1257604 | PIP3 activates AKT signaling | 0.757815 | 0.120 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 0.759366 | 0.120 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 0.761077 | 0.119 |
R-HSA-69242 | S Phase | 0.763152 | 0.117 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 0.763152 | 0.117 |
R-HSA-166520 | Signaling by NTRKs | 0.763152 | 0.117 |
R-HSA-9758941 | Gastrulation | 0.765209 | 0.116 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 0.769270 | 0.114 |
R-HSA-69306 | DNA Replication | 0.773261 | 0.112 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 0.775230 | 0.111 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 0.777183 | 0.109 |
R-HSA-109581 | Apoptosis | 0.790388 | 0.102 |
R-HSA-112315 | Transmission across Chemical Synapses | 0.798137 | 0.098 |
R-HSA-211897 | Cytochrome P450 - arranged by substrate type | 0.799342 | 0.097 |
R-HSA-5619102 | SLC transporter disorders | 0.799342 | 0.097 |
R-HSA-72306 | tRNA processing | 0.806230 | 0.094 |
R-HSA-5689880 | Ub-specific processing proteases | 0.811242 | 0.091 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 0.812884 | 0.090 |
R-HSA-168255 | Influenza Infection | 0.820883 | 0.086 |
R-HSA-9006925 | Intracellular signaling by second messengers | 0.822030 | 0.085 |
R-HSA-9694516 | SARS-CoV-2 Infection | 0.830178 | 0.081 |
R-HSA-69275 | G2/M Transition | 0.831515 | 0.080 |
R-HSA-453274 | Mitotic G2-G2/M phases | 0.834435 | 0.079 |
R-HSA-168898 | Toll-like Receptor Cascades | 0.838723 | 0.076 |
R-HSA-9609690 | HCMV Early Events | 0.845624 | 0.073 |
R-HSA-428157 | Sphingolipid metabolism | 0.852233 | 0.069 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 0.853520 | 0.069 |
R-HSA-5357801 | Programmed Cell Death | 0.858560 | 0.066 |
R-HSA-6805567 | Keratinization | 0.859793 | 0.066 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 0.866110 | 0.062 |
R-HSA-397014 | Muscle contraction | 0.866969 | 0.062 |
R-HSA-422475 | Axon guidance | 0.869996 | 0.060 |
R-HSA-8951664 | Neddylation | 0.877055 | 0.057 |
R-HSA-2262752 | Cellular responses to stress | 0.890400 | 0.050 |
R-HSA-15869 | Metabolism of nucleotides | 0.892205 | 0.050 |
R-HSA-9675108 | Nervous system development | 0.896082 | 0.048 |
R-HSA-5619115 | Disorders of transmembrane transporters | 0.902123 | 0.045 |
R-HSA-72766 | Translation | 0.902805 | 0.044 |
R-HSA-9734767 | Developmental Cell Lineages | 0.914954 | 0.039 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 0.922791 | 0.035 |
R-HSA-211945 | Phase I - Functionalization of compounds | 0.925460 | 0.034 |
R-HSA-9824443 | Parasitic Infection Pathways | 0.927401 | 0.033 |
R-HSA-9658195 | Leishmania infection | 0.927401 | 0.033 |
R-HSA-1483257 | Phospholipid metabolism | 0.935816 | 0.029 |
R-HSA-195721 | Signaling by WNT | 0.937489 | 0.028 |
R-HSA-8953897 | Cellular responses to stimuli | 0.942065 | 0.026 |
R-HSA-8957322 | Metabolism of steroids | 0.950291 | 0.022 |
R-HSA-168249 | Innate Immune System | 0.951694 | 0.022 |
R-HSA-1474244 | Extracellular matrix organization | 0.953268 | 0.021 |
R-HSA-9679506 | SARS-CoV Infections | 0.961055 | 0.017 |
R-HSA-913531 | Interferon Signaling | 0.970748 | 0.013 |
R-HSA-109582 | Hemostasis | 0.972033 | 0.012 |
R-HSA-9824439 | Bacterial Infection Pathways | 0.972506 | 0.012 |
R-HSA-9824446 | Viral Infection Pathways | 0.973131 | 0.012 |
R-HSA-8978868 | Fatty acid metabolism | 0.976351 | 0.010 |
R-HSA-449147 | Signaling by Interleukins | 0.977014 | 0.010 |
R-HSA-168256 | Immune System | 0.977819 | 0.010 |
R-HSA-556833 | Metabolism of lipids | 0.979290 | 0.009 |
R-HSA-446203 | Asparagine N-linked glycosylation | 0.979298 | 0.009 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 0.984559 | 0.007 |
R-HSA-6798695 | Neutrophil degranulation | 0.984832 | 0.007 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 0.986971 | 0.006 |
R-HSA-211859 | Biological oxidations | 0.991578 | 0.004 |
R-HSA-597592 | Post-translational protein modification | 0.992271 | 0.003 |
R-HSA-5663205 | Infectious disease | 0.993623 | 0.003 |
R-HSA-1643685 | Disease | 0.995772 | 0.002 |
R-HSA-392499 | Metabolism of proteins | 0.998483 | 0.001 |
R-HSA-388396 | GPCR downstream signalling | 0.999122 | 0.000 |
R-HSA-372790 | Signaling by GPCR | 0.999588 | 0.000 |
R-HSA-1430728 | Metabolism | 1.000000 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
KIS |
0.862 | 0.666 | 1 | 0.917 |
HIPK2 |
0.845 | 0.641 | 1 | 0.922 |
CDK18 |
0.845 | 0.685 | 1 | 0.934 |
CDK1 |
0.844 | 0.669 | 1 | 0.919 |
CDK19 |
0.843 | 0.654 | 1 | 0.935 |
P38G |
0.842 | 0.706 | 1 | 0.928 |
P38D |
0.841 | 0.703 | 1 | 0.950 |
CDK8 |
0.841 | 0.655 | 1 | 0.926 |
ERK1 |
0.841 | 0.684 | 1 | 0.933 |
P38B |
0.840 | 0.702 | 1 | 0.921 |
JNK2 |
0.839 | 0.710 | 1 | 0.935 |
CDK17 |
0.838 | 0.683 | 1 | 0.922 |
JNK3 |
0.837 | 0.703 | 1 | 0.928 |
CDK3 |
0.836 | 0.604 | 1 | 0.929 |
DYRK2 |
0.835 | 0.609 | 1 | 0.892 |
CDK7 |
0.834 | 0.640 | 1 | 0.933 |
CLK3 |
0.833 | 0.424 | 1 | 0.751 |
CDK13 |
0.832 | 0.649 | 1 | 0.935 |
CDK5 |
0.831 | 0.636 | 1 | 0.920 |
CDK12 |
0.830 | 0.652 | 1 | 0.936 |
P38A |
0.828 | 0.665 | 1 | 0.906 |
HIPK1 |
0.828 | 0.573 | 1 | 0.888 |
DYRK4 |
0.828 | 0.619 | 1 | 0.931 |
HIPK4 |
0.827 | 0.421 | 1 | 0.774 |
ERK2 |
0.826 | 0.659 | 1 | 0.915 |
CDK16 |
0.826 | 0.643 | 1 | 0.928 |
NLK |
0.825 | 0.582 | 1 | 0.791 |
CDK14 |
0.823 | 0.644 | 1 | 0.922 |
CDK10 |
0.821 | 0.604 | 1 | 0.926 |
JNK1 |
0.820 | 0.632 | 1 | 0.923 |
ERK5 |
0.819 | 0.352 | 1 | 0.724 |
CDK9 |
0.818 | 0.615 | 1 | 0.931 |
DYRK1B |
0.818 | 0.576 | 1 | 0.911 |
SRPK1 |
0.817 | 0.271 | -3 | 0.678 |
MTOR |
0.817 | 0.244 | 1 | 0.606 |
HIPK3 |
0.816 | 0.546 | 1 | 0.874 |
DYRK1A |
0.814 | 0.490 | 1 | 0.883 |
COT |
0.811 | 0.018 | 2 | 0.845 |
CDK6 |
0.810 | 0.616 | 1 | 0.931 |
CDK2 |
0.810 | 0.483 | 1 | 0.857 |
MAK |
0.809 | 0.458 | -2 | 0.802 |
CLK2 |
0.807 | 0.339 | -3 | 0.667 |
ICK |
0.806 | 0.304 | -3 | 0.762 |
MOS |
0.806 | 0.083 | 1 | 0.528 |
DYRK3 |
0.805 | 0.437 | 1 | 0.858 |
CDK4 |
0.805 | 0.622 | 1 | 0.940 |
PRP4 |
0.805 | 0.394 | -3 | 0.741 |
CLK4 |
0.805 | 0.302 | -3 | 0.684 |
CDC7 |
0.802 | -0.044 | 1 | 0.469 |
CDKL5 |
0.801 | 0.134 | -3 | 0.708 |
IKKB |
0.801 | -0.070 | -2 | 0.707 |
SRPK2 |
0.801 | 0.193 | -3 | 0.592 |
CDKL1 |
0.800 | 0.104 | -3 | 0.722 |
SRPK3 |
0.800 | 0.186 | -3 | 0.660 |
CLK1 |
0.799 | 0.307 | -3 | 0.649 |
GRK1 |
0.798 | 0.077 | -2 | 0.777 |
ATR |
0.798 | -0.009 | 1 | 0.523 |
PRPK |
0.797 | -0.083 | -1 | 0.849 |
SKMLCK |
0.796 | 0.045 | -2 | 0.848 |
PIM3 |
0.795 | -0.026 | -3 | 0.774 |
RAF1 |
0.795 | -0.106 | 1 | 0.486 |
TBK1 |
0.794 | -0.107 | 1 | 0.437 |
CK1E |
0.792 | 0.171 | -3 | 0.768 |
CK1D |
0.792 | 0.207 | -3 | 0.734 |
NDR2 |
0.792 | -0.036 | -3 | 0.786 |
GRK5 |
0.791 | -0.040 | -3 | 0.867 |
BMPR2 |
0.791 | -0.126 | -2 | 0.820 |
IKKE |
0.791 | -0.120 | 1 | 0.433 |
PDHK4 |
0.790 | -0.186 | 1 | 0.544 |
PRKD1 |
0.790 | 0.006 | -3 | 0.746 |
IKKA |
0.789 | -0.047 | -2 | 0.686 |
MLK1 |
0.788 | -0.075 | 2 | 0.783 |
RIPK3 |
0.788 | -0.066 | 3 | 0.721 |
MST4 |
0.787 | -0.035 | 2 | 0.834 |
CAMK1B |
0.786 | -0.061 | -3 | 0.778 |
AURC |
0.786 | 0.051 | -2 | 0.673 |
GRK7 |
0.786 | 0.058 | 1 | 0.455 |
MOK |
0.786 | 0.378 | 1 | 0.815 |
BMPR1B |
0.786 | 0.029 | 1 | 0.415 |
CHAK2 |
0.785 | -0.051 | -1 | 0.848 |
CAMLCK |
0.785 | -0.002 | -2 | 0.833 |
PRKD2 |
0.785 | 0.000 | -3 | 0.677 |
GCN2 |
0.785 | -0.201 | 2 | 0.782 |
WNK1 |
0.784 | -0.085 | -2 | 0.859 |
CK1A2 |
0.784 | 0.176 | -3 | 0.730 |
NIK |
0.784 | -0.076 | -3 | 0.809 |
PDHK1 |
0.783 | -0.195 | 1 | 0.525 |
DSTYK |
0.783 | -0.156 | 2 | 0.847 |
NDR1 |
0.783 | -0.075 | -3 | 0.758 |
RSK2 |
0.783 | -0.022 | -3 | 0.675 |
CAMK2G |
0.782 | -0.112 | 2 | 0.782 |
ERK7 |
0.781 | 0.212 | 2 | 0.516 |
PIM1 |
0.781 | -0.006 | -3 | 0.719 |
CK1G1 |
0.781 | 0.122 | -3 | 0.749 |
DAPK2 |
0.781 | -0.038 | -3 | 0.785 |
MLK3 |
0.780 | -0.020 | 2 | 0.701 |
MPSK1 |
0.780 | 0.132 | 1 | 0.548 |
NEK6 |
0.780 | -0.113 | -2 | 0.770 |
GRK6 |
0.780 | -0.061 | 1 | 0.453 |
TGFBR2 |
0.780 | -0.098 | -2 | 0.727 |
PKACG |
0.779 | -0.029 | -2 | 0.724 |
IRE1 |
0.779 | -0.069 | 1 | 0.470 |
PKN2 |
0.779 | -0.068 | -3 | 0.772 |
SMG1 |
0.779 | -0.033 | 1 | 0.500 |
GRK4 |
0.779 | -0.074 | -2 | 0.773 |
NUAK2 |
0.779 | -0.054 | -3 | 0.765 |
BCKDK |
0.778 | -0.147 | -1 | 0.800 |
DLK |
0.778 | -0.120 | 1 | 0.476 |
ULK2 |
0.778 | -0.230 | 2 | 0.770 |
MLK2 |
0.777 | -0.083 | 2 | 0.796 |
PKN3 |
0.777 | -0.093 | -3 | 0.751 |
PAK1 |
0.777 | -0.023 | -2 | 0.810 |
P90RSK |
0.776 | -0.042 | -3 | 0.680 |
GSK3A |
0.776 | 0.175 | 4 | 0.409 |
NEK7 |
0.776 | -0.203 | -3 | 0.791 |
WNK3 |
0.776 | -0.202 | 1 | 0.487 |
MASTL |
0.776 | -0.168 | -2 | 0.761 |
PKACB |
0.775 | 0.026 | -2 | 0.676 |
AMPKA1 |
0.775 | -0.094 | -3 | 0.781 |
RSK3 |
0.774 | -0.055 | -3 | 0.672 |
MARK4 |
0.774 | -0.098 | 4 | 0.834 |
RIPK1 |
0.774 | -0.166 | 1 | 0.458 |
VRK2 |
0.774 | 0.049 | 1 | 0.577 |
ANKRD3 |
0.774 | -0.145 | 1 | 0.500 |
PAK3 |
0.774 | -0.049 | -2 | 0.799 |
PKCD |
0.774 | -0.052 | 2 | 0.749 |
TSSK2 |
0.773 | -0.071 | -5 | 0.684 |
P70S6KB |
0.773 | -0.057 | -3 | 0.701 |
ALK4 |
0.772 | -0.052 | -2 | 0.778 |
TTBK2 |
0.772 | -0.148 | 2 | 0.674 |
TSSK1 |
0.771 | -0.054 | -3 | 0.793 |
LATS2 |
0.771 | -0.089 | -5 | 0.577 |
HUNK |
0.771 | -0.187 | 2 | 0.791 |
TLK2 |
0.771 | -0.075 | 1 | 0.475 |
ATM |
0.771 | -0.074 | 1 | 0.465 |
PKR |
0.770 | -0.076 | 1 | 0.503 |
MAPKAPK2 |
0.770 | -0.050 | -3 | 0.644 |
PINK1 |
0.770 | 0.081 | 1 | 0.662 |
MLK4 |
0.770 | -0.064 | 2 | 0.696 |
AURB |
0.770 | 0.007 | -2 | 0.667 |
MAPKAPK3 |
0.769 | -0.096 | -3 | 0.687 |
ACVR2B |
0.769 | -0.050 | -2 | 0.731 |
TGFBR1 |
0.769 | -0.048 | -2 | 0.744 |
FAM20C |
0.769 | -0.019 | 2 | 0.586 |
YSK4 |
0.769 | -0.123 | 1 | 0.452 |
GRK2 |
0.769 | -0.031 | -2 | 0.679 |
MST3 |
0.769 | 0.012 | 2 | 0.809 |
PAK2 |
0.769 | -0.050 | -2 | 0.793 |
PKCA |
0.768 | -0.033 | 2 | 0.687 |
DNAPK |
0.768 | -0.035 | 1 | 0.466 |
MNK2 |
0.768 | -0.030 | -2 | 0.767 |
PRKD3 |
0.768 | -0.045 | -3 | 0.655 |
LATS1 |
0.768 | -0.031 | -3 | 0.778 |
ULK1 |
0.768 | -0.223 | -3 | 0.761 |
AMPKA2 |
0.768 | -0.088 | -3 | 0.741 |
MEK1 |
0.768 | -0.106 | 2 | 0.823 |
AKT2 |
0.768 | 0.004 | -3 | 0.601 |
PKG2 |
0.767 | -0.009 | -2 | 0.675 |
IRE2 |
0.767 | -0.087 | 2 | 0.728 |
NEK9 |
0.767 | -0.214 | 2 | 0.810 |
PKCB |
0.767 | -0.054 | 2 | 0.697 |
ACVR2A |
0.767 | -0.065 | -2 | 0.722 |
PRKX |
0.767 | 0.014 | -3 | 0.610 |
NIM1 |
0.766 | -0.129 | 3 | 0.727 |
CAMK2D |
0.766 | -0.136 | -3 | 0.753 |
MSK2 |
0.766 | -0.064 | -3 | 0.677 |
MYLK4 |
0.765 | -0.034 | -2 | 0.773 |
PKCG |
0.765 | -0.065 | 2 | 0.692 |
MEKK3 |
0.765 | -0.081 | 1 | 0.471 |
MSK1 |
0.765 | -0.026 | -3 | 0.674 |
PAK6 |
0.765 | -0.019 | -2 | 0.736 |
RSK4 |
0.765 | -0.030 | -3 | 0.659 |
MNK1 |
0.764 | -0.029 | -2 | 0.768 |
AURA |
0.764 | -0.004 | -2 | 0.642 |
PHKG1 |
0.763 | -0.102 | -3 | 0.751 |
CAMK4 |
0.763 | -0.143 | -3 | 0.746 |
PIM2 |
0.763 | -0.018 | -3 | 0.651 |
QSK |
0.763 | -0.069 | 4 | 0.819 |
PKCZ |
0.763 | -0.073 | 2 | 0.748 |
MEKK2 |
0.763 | -0.063 | 2 | 0.781 |
SGK3 |
0.763 | -0.036 | -3 | 0.686 |
ALK2 |
0.762 | -0.065 | -2 | 0.750 |
BMPR1A |
0.762 | -0.026 | 1 | 0.392 |
GAK |
0.761 | 0.036 | 1 | 0.549 |
MEK5 |
0.761 | -0.129 | 2 | 0.809 |
GSK3B |
0.761 | 0.046 | 4 | 0.402 |
QIK |
0.761 | -0.146 | -3 | 0.755 |
TAO3 |
0.761 | -0.034 | 1 | 0.492 |
CHAK1 |
0.760 | -0.151 | 2 | 0.763 |
PASK |
0.760 | -0.027 | -3 | 0.810 |
CAMK2A |
0.759 | -0.063 | 2 | 0.766 |
GRK3 |
0.759 | -0.018 | -2 | 0.643 |
NEK2 |
0.759 | -0.162 | 2 | 0.788 |
LKB1 |
0.758 | 0.020 | -3 | 0.783 |
MEKK1 |
0.758 | -0.132 | 1 | 0.486 |
PLK1 |
0.758 | -0.174 | -2 | 0.703 |
CK1A |
0.758 | 0.150 | -3 | 0.662 |
ZAK |
0.757 | -0.130 | 1 | 0.440 |
CAMK2B |
0.757 | -0.101 | 2 | 0.752 |
MELK |
0.757 | -0.130 | -3 | 0.709 |
TLK1 |
0.756 | -0.115 | -2 | 0.758 |
WNK4 |
0.756 | -0.142 | -2 | 0.852 |
PKCH |
0.756 | -0.108 | 2 | 0.684 |
SSTK |
0.755 | -0.041 | 4 | 0.811 |
AKT1 |
0.755 | -0.012 | -3 | 0.619 |
NEK5 |
0.755 | -0.121 | 1 | 0.492 |
GCK |
0.755 | -0.017 | 1 | 0.485 |
BUB1 |
0.755 | 0.067 | -5 | 0.664 |
SIK |
0.755 | -0.099 | -3 | 0.678 |
IRAK4 |
0.754 | -0.124 | 1 | 0.462 |
BRAF |
0.754 | -0.132 | -4 | 0.789 |
MARK3 |
0.754 | -0.073 | 4 | 0.774 |
PLK4 |
0.753 | -0.145 | 2 | 0.630 |
PKACA |
0.753 | -0.010 | -2 | 0.633 |
PERK |
0.753 | -0.173 | -2 | 0.761 |
NUAK1 |
0.753 | -0.127 | -3 | 0.693 |
NEK11 |
0.752 | -0.105 | 1 | 0.473 |
DCAMKL1 |
0.752 | -0.092 | -3 | 0.703 |
HPK1 |
0.751 | -0.014 | 1 | 0.474 |
PDK1 |
0.751 | -0.071 | 1 | 0.483 |
TNIK |
0.751 | 0.001 | 3 | 0.834 |
BRSK1 |
0.751 | -0.122 | -3 | 0.708 |
PAK5 |
0.751 | -0.036 | -2 | 0.679 |
BRSK2 |
0.751 | -0.143 | -3 | 0.726 |
HRI |
0.750 | -0.205 | -2 | 0.783 |
DRAK1 |
0.750 | -0.156 | 1 | 0.385 |
MARK2 |
0.750 | -0.099 | 4 | 0.738 |
HGK |
0.750 | -0.037 | 3 | 0.831 |
PLK3 |
0.749 | -0.159 | 2 | 0.750 |
MINK |
0.749 | -0.057 | 1 | 0.469 |
TAK1 |
0.749 | -0.065 | 1 | 0.482 |
CK2A2 |
0.749 | -0.033 | 1 | 0.369 |
SMMLCK |
0.749 | -0.070 | -3 | 0.731 |
SNRK |
0.748 | -0.199 | 2 | 0.682 |
MEKK6 |
0.748 | -0.088 | 1 | 0.491 |
TAO2 |
0.748 | -0.088 | 2 | 0.810 |
MAP3K15 |
0.747 | -0.069 | 1 | 0.453 |
KHS1 |
0.747 | 0.002 | 1 | 0.478 |
PKCT |
0.747 | -0.090 | 2 | 0.695 |
DAPK3 |
0.747 | -0.036 | -3 | 0.723 |
CHK1 |
0.747 | -0.159 | -3 | 0.729 |
AKT3 |
0.747 | -0.000 | -3 | 0.546 |
KHS2 |
0.747 | 0.011 | 1 | 0.489 |
NEK8 |
0.746 | -0.155 | 2 | 0.793 |
PBK |
0.746 | -0.004 | 1 | 0.521 |
CAMK1G |
0.746 | -0.111 | -3 | 0.665 |
PAK4 |
0.746 | -0.027 | -2 | 0.678 |
PKCE |
0.745 | -0.038 | 2 | 0.678 |
MAPKAPK5 |
0.745 | -0.162 | -3 | 0.623 |
MST2 |
0.745 | -0.098 | 1 | 0.476 |
PKCI |
0.744 | -0.073 | 2 | 0.716 |
TTBK1 |
0.744 | -0.167 | 2 | 0.597 |
P70S6K |
0.744 | -0.086 | -3 | 0.608 |
CAMKK1 |
0.744 | -0.178 | -2 | 0.695 |
MARK1 |
0.743 | -0.132 | 4 | 0.790 |
EEF2K |
0.743 | -0.066 | 3 | 0.796 |
LOK |
0.743 | -0.072 | -2 | 0.715 |
SGK1 |
0.742 | -0.007 | -3 | 0.527 |
CK2A1 |
0.742 | -0.035 | 1 | 0.350 |
LRRK2 |
0.742 | -0.073 | 2 | 0.822 |
SLK |
0.741 | -0.069 | -2 | 0.668 |
HASPIN |
0.741 | 0.026 | -1 | 0.718 |
PHKG2 |
0.741 | -0.139 | -3 | 0.707 |
NEK4 |
0.741 | -0.152 | 1 | 0.472 |
CAMKK2 |
0.740 | -0.140 | -2 | 0.693 |
DAPK1 |
0.740 | -0.045 | -3 | 0.715 |
ROCK2 |
0.740 | -0.021 | -3 | 0.711 |
SBK |
0.740 | 0.048 | -3 | 0.469 |
DCAMKL2 |
0.740 | -0.122 | -3 | 0.710 |
IRAK1 |
0.738 | -0.244 | -1 | 0.785 |
MRCKB |
0.738 | -0.032 | -3 | 0.650 |
OSR1 |
0.737 | -0.017 | 2 | 0.785 |
MST1 |
0.736 | -0.110 | 1 | 0.463 |
CK1G3 |
0.736 | 0.132 | -3 | 0.623 |
PDHK3_TYR |
0.735 | 0.156 | 4 | 0.875 |
CHK2 |
0.735 | -0.065 | -3 | 0.541 |
VRK1 |
0.734 | -0.161 | 2 | 0.818 |
NEK1 |
0.734 | -0.148 | 1 | 0.466 |
DMPK1 |
0.733 | 0.004 | -3 | 0.670 |
CAMK1D |
0.733 | -0.093 | -3 | 0.591 |
MRCKA |
0.733 | -0.054 | -3 | 0.660 |
TTK |
0.733 | -0.021 | -2 | 0.733 |
YSK1 |
0.733 | -0.113 | 2 | 0.784 |
PKN1 |
0.732 | -0.088 | -3 | 0.623 |
YANK3 |
0.731 | -0.007 | 2 | 0.382 |
PDHK4_TYR |
0.731 | 0.129 | 2 | 0.870 |
STK33 |
0.730 | -0.138 | 2 | 0.592 |
PLK2 |
0.730 | -0.089 | -3 | 0.754 |
BIKE |
0.730 | -0.004 | 1 | 0.504 |
MAP2K6_TYR |
0.728 | 0.094 | -1 | 0.869 |
MAP2K4_TYR |
0.728 | 0.074 | -1 | 0.864 |
CRIK |
0.727 | -0.024 | -3 | 0.616 |
MEK2 |
0.726 | -0.217 | 2 | 0.799 |
TESK1_TYR |
0.726 | 0.031 | 3 | 0.834 |
ALPHAK3 |
0.726 | -0.044 | -1 | 0.760 |
MYO3B |
0.725 | -0.056 | 2 | 0.798 |
PKG1 |
0.725 | -0.054 | -2 | 0.609 |
CAMK1A |
0.725 | -0.066 | -3 | 0.566 |
PDHK1_TYR |
0.725 | 0.036 | -1 | 0.869 |
ROCK1 |
0.725 | -0.039 | -3 | 0.664 |
PKMYT1_TYR |
0.725 | 0.065 | 3 | 0.806 |
ASK1 |
0.724 | -0.089 | 1 | 0.443 |
BMPR2_TYR |
0.724 | 0.048 | -1 | 0.869 |
RIPK2 |
0.724 | -0.239 | 1 | 0.414 |
MYO3A |
0.724 | -0.067 | 1 | 0.470 |
LIMK2_TYR |
0.723 | 0.084 | -3 | 0.808 |
AAK1 |
0.722 | 0.034 | 1 | 0.473 |
MAP2K7_TYR |
0.721 | -0.084 | 2 | 0.843 |
NEK3 |
0.719 | -0.175 | 1 | 0.471 |
PINK1_TYR |
0.716 | -0.135 | 1 | 0.525 |
TAO1 |
0.715 | -0.115 | 1 | 0.443 |
CK1G2 |
0.715 | 0.098 | -3 | 0.695 |
CSF1R |
0.714 | -0.013 | 3 | 0.753 |
ABL2 |
0.714 | -0.013 | -1 | 0.802 |
RET |
0.713 | -0.103 | 1 | 0.493 |
ABL1 |
0.713 | -0.012 | -1 | 0.800 |
TXK |
0.712 | -0.008 | 1 | 0.453 |
JAK2 |
0.712 | -0.074 | 1 | 0.498 |
LCK |
0.711 | 0.002 | -1 | 0.837 |
FGR |
0.711 | -0.066 | 1 | 0.499 |
MST1R |
0.711 | -0.080 | 3 | 0.766 |
YES1 |
0.711 | -0.044 | -1 | 0.842 |
LIMK1_TYR |
0.710 | -0.082 | 2 | 0.832 |
BLK |
0.710 | 0.014 | -1 | 0.828 |
STLK3 |
0.710 | -0.141 | 1 | 0.428 |
EPHA6 |
0.709 | -0.065 | -1 | 0.846 |
TYRO3 |
0.709 | -0.114 | 3 | 0.744 |
ROS1 |
0.709 | -0.098 | 3 | 0.710 |
TYK2 |
0.708 | -0.176 | 1 | 0.485 |
EPHB4 |
0.708 | -0.074 | -1 | 0.816 |
KIT |
0.707 | -0.046 | 3 | 0.759 |
HCK |
0.707 | -0.065 | -1 | 0.836 |
TNK2 |
0.706 | -0.060 | 3 | 0.723 |
KDR |
0.705 | -0.030 | 3 | 0.723 |
FER |
0.705 | -0.137 | 1 | 0.496 |
MET |
0.705 | -0.027 | 3 | 0.746 |
JAK3 |
0.704 | -0.093 | 1 | 0.468 |
YANK2 |
0.704 | -0.012 | 2 | 0.389 |
FGFR2 |
0.704 | -0.047 | 3 | 0.754 |
FYN |
0.703 | -0.001 | -1 | 0.823 |
DDR1 |
0.702 | -0.151 | 4 | 0.802 |
NEK10_TYR |
0.701 | -0.108 | 1 | 0.447 |
ITK |
0.701 | -0.105 | -1 | 0.819 |
FLT1 |
0.700 | -0.042 | -1 | 0.822 |
INSRR |
0.700 | -0.112 | 3 | 0.695 |
TNNI3K_TYR |
0.700 | -0.056 | 1 | 0.511 |
SRMS |
0.699 | -0.124 | 1 | 0.457 |
TNK1 |
0.699 | -0.076 | 3 | 0.729 |
JAK1 |
0.699 | -0.078 | 1 | 0.448 |
FLT3 |
0.698 | -0.145 | 3 | 0.752 |
FGFR1 |
0.697 | -0.077 | 3 | 0.708 |
EPHA4 |
0.697 | -0.090 | 2 | 0.749 |
MERTK |
0.696 | -0.100 | 3 | 0.733 |
FGFR3 |
0.696 | -0.037 | 3 | 0.729 |
TEK |
0.696 | -0.065 | 3 | 0.688 |
WEE1_TYR |
0.695 | -0.078 | -1 | 0.760 |
PDGFRB |
0.695 | -0.188 | 3 | 0.755 |
BMX |
0.694 | -0.079 | -1 | 0.731 |
AXL |
0.694 | -0.134 | 3 | 0.734 |
EPHB1 |
0.693 | -0.165 | 1 | 0.453 |
LYN |
0.692 | -0.084 | 3 | 0.678 |
SRC |
0.692 | -0.053 | -1 | 0.810 |
TEC |
0.692 | -0.121 | -1 | 0.750 |
EPHB3 |
0.692 | -0.147 | -1 | 0.803 |
EPHB2 |
0.692 | -0.128 | -1 | 0.791 |
ERBB2 |
0.692 | -0.121 | 1 | 0.435 |
SYK |
0.691 | 0.008 | -1 | 0.772 |
FRK |
0.690 | -0.100 | -1 | 0.827 |
BTK |
0.690 | -0.193 | -1 | 0.796 |
PTK2 |
0.690 | 0.004 | -1 | 0.811 |
MATK |
0.689 | -0.070 | -1 | 0.717 |
FGFR4 |
0.688 | -0.055 | -1 | 0.747 |
PTK6 |
0.688 | -0.184 | -1 | 0.756 |
PDGFRA |
0.687 | -0.219 | 3 | 0.753 |
ALK |
0.686 | -0.159 | 3 | 0.650 |
EGFR |
0.686 | -0.081 | 1 | 0.371 |
EPHA7 |
0.686 | -0.118 | 2 | 0.750 |
DDR2 |
0.685 | -0.054 | 3 | 0.684 |
EPHA3 |
0.684 | -0.138 | 2 | 0.726 |
EPHA1 |
0.684 | -0.134 | 3 | 0.726 |
ZAP70 |
0.683 | 0.029 | -1 | 0.702 |
FLT4 |
0.683 | -0.153 | 3 | 0.712 |
INSR |
0.683 | -0.156 | 3 | 0.674 |
NTRK3 |
0.683 | -0.134 | -1 | 0.759 |
PTK2B |
0.683 | -0.098 | -1 | 0.773 |
LTK |
0.683 | -0.174 | 3 | 0.676 |
NTRK1 |
0.682 | -0.213 | -1 | 0.810 |
NTRK2 |
0.681 | -0.212 | 3 | 0.719 |
ERBB4 |
0.680 | -0.041 | 1 | 0.375 |
EPHA8 |
0.680 | -0.101 | -1 | 0.793 |
CSK |
0.680 | -0.132 | 2 | 0.754 |
EPHA5 |
0.677 | -0.138 | 2 | 0.736 |
EPHA2 |
0.670 | -0.112 | -1 | 0.763 |
IGF1R |
0.669 | -0.137 | 3 | 0.617 |
MUSK |
0.667 | -0.158 | 1 | 0.369 |
FES |
0.659 | -0.135 | -1 | 0.713 |