Motif 521 (n=194)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A3KN83 | SBNO1 | S811 | ochoa | Protein strawberry notch homolog 1 (Monocyte protein 3) (MOP-3) | Plays a crucial role in the regulation of neural stem cells (NSCs) proliferation. Enhances the phosphorylation of GSK3B through the PI3K-Akt signaling pathway, thereby upregulating the Wnt/beta-catenin signaling pathway and promoting the proliferation of NSCs. Improves ischemic stroke recovery while inhibiting neuroinflammation through small extracellular vesicles (sEVs)-mediated mechanism. Enhances the secretion of sEVs from NSCs, which in turn inhibit both the MAPK and NF-kappaB pathways in microglia. This inhibition suppresses the pro-inflammatory M1 polarization of microglia, promoting a shift towards the M2 anti-inflammatory phenotype, which is beneficial for reducing neuroinflammation. {ECO:0000250|UniProtKB:Q689Z5}. |
A6NKT7 | RGPD3 | S793 | ochoa | RanBP2-like and GRIP domain-containing protein 3 | None |
A6NKT7 | RGPD3 | S1591 | ochoa | RanBP2-like and GRIP domain-containing protein 3 | None |
O14639 | ABLIM1 | S363 | 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}. |
O14647 | CHD2 | S1785 | ochoa | Chromodomain-helicase-DNA-binding protein 2 (CHD-2) (EC 3.6.4.-) (ATP-dependent helicase CHD2) | ATP-dependent chromatin-remodeling factor that specifically binds to the promoter of target genes, leading to chromatin remodeling, possibly by promoting deposition of histone H3.3. Involved in myogenesis via interaction with MYOD1: binds to myogenic gene regulatory sequences and mediates incorporation of histone H3.3 prior to the onset of myogenic gene expression, promoting their expression (By similarity). {ECO:0000250}. |
O14686 | KMT2D | S1858 | ochoa | Histone-lysine N-methyltransferase 2D (Lysine N-methyltransferase 2D) (EC 2.1.1.364) (ALL1-related protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 2) | Histone methyltransferase that catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) (PubMed:25561738). Part of chromatin remodeling machinery predominantly forms H3K4me1 methylation marks at active chromatin sites where transcription and DNA repair take place (PubMed:17500065, PubMed:25561738). Acts as a coactivator for estrogen receptor by being recruited by ESR1, thereby activating transcription (PubMed:16603732). {ECO:0000269|PubMed:16603732, ECO:0000269|PubMed:17500065, ECO:0000269|PubMed:25561738}. |
O14715 | RGPD8 | S1590 | ochoa | RANBP2-like and GRIP domain-containing protein 8 (Ran-binding protein 2-like 3) (RanBP2-like 3) (RanBP2L3) | None |
O14920 | IKBKB | S679 | ochoa | Inhibitor of nuclear factor kappa-B kinase subunit beta (I-kappa-B-kinase beta) (IKK-B) (IKK-beta) (IkBKB) (EC 2.7.11.10) (I-kappa-B kinase 2) (IKK-2) (IKK2) (Nuclear factor NF-kappa-B inhibitor kinase beta) (NFKBIKB) (Serine/threonine protein kinase IKBKB) (EC 2.7.11.1) | Serine kinase that plays an essential role in the NF-kappa-B signaling pathway which is activated by multiple stimuli such as inflammatory cytokines, bacterial or viral products, DNA damages or other cellular stresses (PubMed:20434986, PubMed:20797629, PubMed:21138416, PubMed:30337470, PubMed:9346484). Acts as a part of the canonical IKK complex in the conventional pathway of NF-kappa-B activation (PubMed:9346484). Phosphorylates inhibitors of NF-kappa-B on 2 critical serine residues (PubMed:20434986, PubMed:20797629, PubMed:21138416, PubMed:9346484). These modifications allow polyubiquitination of the inhibitors and subsequent degradation by the proteasome (PubMed:20434986, PubMed:20797629, PubMed:21138416, PubMed:9346484). In turn, free NF-kappa-B is translocated into the nucleus and activates the transcription of hundreds of genes involved in immune response, growth control, or protection against apoptosis (PubMed:20434986, PubMed:20797629, PubMed:21138416, PubMed:9346484). In addition to the NF-kappa-B inhibitors, phosphorylates several other components of the signaling pathway including NEMO/IKBKG, NF-kappa-B subunits RELA and NFKB1, as well as IKK-related kinases TBK1 and IKBKE (PubMed:11297557, PubMed:14673179, PubMed:20410276, PubMed:21138416). IKK-related kinase phosphorylations may prevent the overproduction of inflammatory mediators since they exert a negative regulation on canonical IKKs (PubMed:11297557, PubMed:20410276, PubMed:21138416). Phosphorylates FOXO3, mediating the TNF-dependent inactivation of this pro-apoptotic transcription factor (PubMed:15084260). Also phosphorylates other substrates including NAA10, NCOA3, BCL10 and IRS1 (PubMed:17213322, PubMed:19716809). Phosphorylates RIPK1 at 'Ser-25' which represses its kinase activity and consequently prevents TNF-mediated RIPK1-dependent cell death (By similarity). Phosphorylates the C-terminus of IRF5, stimulating IRF5 homodimerization and translocation into the nucleus (PubMed:25326418). Following bacterial lipopolysaccharide (LPS)-induced TLR4 endocytosis, phosphorylates STAT1 at 'Thr-749' which restricts interferon signaling and anti-inflammatory responses and promotes innate inflammatory responses (PubMed:38621137). IKBKB-mediated phosphorylation of STAT1 at 'Thr-749' promotes binding of STAT1 to the ARID5A promoter, resulting in transcriptional activation of ARID5A and subsequent ARID5A-mediated stabilization of IL6 (PubMed:32209697). It also promotes binding of STAT1 to the IL12B promoter and activation of IL12B transcription (PubMed:32209697). {ECO:0000250|UniProtKB:O88351, ECO:0000269|PubMed:11297557, ECO:0000269|PubMed:14673179, ECO:0000269|PubMed:15084260, ECO:0000269|PubMed:17213322, ECO:0000269|PubMed:19716809, ECO:0000269|PubMed:20410276, ECO:0000269|PubMed:20434986, ECO:0000269|PubMed:20797629, ECO:0000269|PubMed:21138416, ECO:0000269|PubMed:25326418, ECO:0000269|PubMed:30337470, ECO:0000269|PubMed:32209697, ECO:0000269|PubMed:38621137, ECO:0000269|PubMed:9346484}. |
O15075 | DCLK1 | S330 | ochoa | Serine/threonine-protein kinase DCLK1 (EC 2.7.11.1) (Doublecortin domain-containing protein 3A) (Doublecortin-like and CAM kinase-like 1) (Doublecortin-like kinase 1) | Probable kinase that may be involved in a calcium-signaling pathway controlling neuronal migration in the developing brain. May also participate in functions of the mature nervous system. |
O15439 | ABCC4 | S661 | ochoa | ATP-binding cassette sub-family C member 4 (EC 7.6.2.-) (EC 7.6.2.2) (EC 7.6.2.3) (MRP/cMOAT-related ABC transporter) (Multi-specific organic anion transporter B) (MOAT-B) (Multidrug resistance-associated protein 4) | ATP-dependent transporter of the ATP-binding cassette (ABC) family that actively extrudes physiological compounds and xenobiotics from cells. Transports a range of endogenous molecules that have a key role in cellular communication and signaling, including cyclic nucleotides such as cyclic AMP (cAMP) and cyclic GMP (cGMP), bile acids, steroid conjugates, urate, and prostaglandins (PubMed:11856762, PubMed:12523936, PubMed:12835412, PubMed:12883481, PubMed:15364914, PubMed:15454390, PubMed:16282361, PubMed:17959747, PubMed:18300232, PubMed:26721430). Mediates the ATP-dependent efflux of glutathione conjugates such as leukotriene C4 (LTC4) and leukotriene B4 (LTB4) too. The presence of GSH is necessary for the ATP-dependent transport of LTB4, whereas GSH is not required for the transport of LTC4 (PubMed:17959747). Mediates the cotransport of bile acids with reduced glutathione (GSH) (PubMed:12523936, PubMed:12883481, PubMed:16282361). Transports a wide range of drugs and their metabolites, including anticancer, antiviral and antibiotics molecules (PubMed:11856762, PubMed:12105214, PubMed:15454390, PubMed:17344354, PubMed:18300232). Confers resistance to anticancer agents such as methotrexate (PubMed:11106685). {ECO:0000269|PubMed:11106685, ECO:0000269|PubMed:11856762, ECO:0000269|PubMed:12105214, ECO:0000269|PubMed:12523936, ECO:0000269|PubMed:12835412, ECO:0000269|PubMed:12883481, ECO:0000269|PubMed:15364914, ECO:0000269|PubMed:15454390, ECO:0000269|PubMed:16282361, ECO:0000269|PubMed:17344354, ECO:0000269|PubMed:17959747, ECO:0000269|PubMed:18300232, ECO:0000269|PubMed:26721430}. |
O15553 | MEFV | S345 | ochoa | Pyrin (Marenostrin) | Involved in the regulation of innate immunity and the inflammatory response in response to IFNG/IFN-gamma (PubMed:10807793, PubMed:11468188, PubMed:16037825, PubMed:16785446, PubMed:17431422, PubMed:17964261, PubMed:18577712, PubMed:19109554, PubMed:19584923, PubMed:26347139, PubMed:27030597, PubMed:28835462). Organizes autophagic machinery by serving as a platform for the assembly of ULK1, Beclin 1/BECN1, ATG16L1, and ATG8 family members and recognizes specific autophagy targets, thus coordinating target recognition with assembly of the autophagic apparatus and initiation of autophagy (PubMed:16785446, PubMed:17431422, PubMed:26347139). Acts as an autophagy receptor for the degradation of several inflammasome components, including CASP1, NLRP1 and NLRP3, hence preventing excessive IL1B- and IL18-mediated inflammation (PubMed:16785446, PubMed:17431422, PubMed:26347139). However, it can also have a positive effect in the inflammatory pathway, acting as an innate immune sensor that triggers PYCARD/ASC specks formation, caspase-1 activation, and IL1B and IL18 production (PubMed:16037825, PubMed:27030597, PubMed:28835462). Together with AIM2, also acts as a mediator of pyroptosis, necroptosis and apoptosis (PANoptosis), an integral part of host defense against pathogens, in response to bacterial infection (By similarity). It is required for PSTPIP1-induced PYCARD/ASC oligomerization and inflammasome formation (PubMed:10807793, PubMed:11468188, PubMed:17964261, PubMed:18577712, PubMed:19109554, PubMed:19584923). Recruits PSTPIP1 to inflammasomes, and is required for PSTPIP1 oligomerization (PubMed:10807793, PubMed:11468188, PubMed:17964261, PubMed:18577712, PubMed:19109554, PubMed:19584923). {ECO:0000250|UniProtKB:Q9JJ26, ECO:0000269|PubMed:10807793, ECO:0000269|PubMed:11468188, ECO:0000269|PubMed:16037825, ECO:0000269|PubMed:16785446, ECO:0000269|PubMed:17431422, ECO:0000269|PubMed:17964261, ECO:0000269|PubMed:18577712, ECO:0000269|PubMed:19109554, ECO:0000269|PubMed:19584923, ECO:0000269|PubMed:26347139, ECO:0000269|PubMed:27030597, ECO:0000269|PubMed:28835462}. |
O43399 | TPD52L2 | S145 | ochoa | Tumor protein D54 (hD54) (Tumor protein D52-like 2) | None |
O43474 | KLF4 | S240 | ochoa | Krueppel-like factor 4 (Epithelial zinc finger protein EZF) (Gut-enriched krueppel-like factor) | Transcription factor; can act both as activator and as repressor. Binds the 5'-CACCC-3' core sequence. Binds to the promoter region of its own gene and can activate its own transcription. Regulates the expression of key transcription factors during embryonic development. Plays an important role in maintaining embryonic stem cells, and in preventing their differentiation. Required for establishing the barrier function of the skin and for postnatal maturation and maintenance of the ocular surface. Involved in the differentiation of epithelial cells and may also function in skeletal and kidney development. Contributes to the down-regulation of p53/TP53 transcription. {ECO:0000269|PubMed:17308127, ECO:0000269|PubMed:20071344}. |
O43524 | FOXO3 | S421 | ochoa | Forkhead box protein O3 (AF6q21 protein) (Forkhead in rhabdomyosarcoma-like 1) | Transcriptional activator that recognizes and binds to the DNA sequence 5'-[AG]TAAA[TC]A-3' and regulates different processes, such as apoptosis and autophagy (PubMed:10102273, PubMed:16751106, PubMed:21329882, PubMed:30513302). Acts as a positive regulator of autophagy in skeletal muscle: in starved cells, enters the nucleus following dephosphorylation and binds the promoters of autophagy genes, such as GABARAP1L, MAP1LC3B and ATG12, thereby activating their expression, resulting in proteolysis of skeletal muscle proteins (By similarity). Triggers apoptosis in the absence of survival factors, including neuronal cell death upon oxidative stress (PubMed:10102273, PubMed:16751106). Participates in post-transcriptional regulation of MYC: following phosphorylation by MAPKAPK5, promotes induction of miR-34b and miR-34c expression, 2 post-transcriptional regulators of MYC that bind to the 3'UTR of MYC transcript and prevent its translation (PubMed:21329882). In response to metabolic stress, translocates into the mitochondria where it promotes mtDNA transcription (PubMed:23283301). In response to metabolic stress, translocates into the mitochondria where it promotes mtDNA transcription. Also acts as a key regulator of chondrogenic commitment of skeletal progenitor cells in response to lipid availability: when lipids levels are low, translocates to the nucleus and promotes expression of SOX9, which induces chondrogenic commitment and suppresses fatty acid oxidation (By similarity). Also acts as a key regulator of regulatory T-cells (Treg) differentiation by activating expression of FOXP3 (PubMed:30513302). {ECO:0000250|UniProtKB:Q9WVH4, ECO:0000269|PubMed:10102273, ECO:0000269|PubMed:16751106, ECO:0000269|PubMed:21329882, ECO:0000269|PubMed:23283301, ECO:0000269|PubMed:30513302}. |
O43524 | FOXO3 | S425 | ochoa|psp | Forkhead box protein O3 (AF6q21 protein) (Forkhead in rhabdomyosarcoma-like 1) | Transcriptional activator that recognizes and binds to the DNA sequence 5'-[AG]TAAA[TC]A-3' and regulates different processes, such as apoptosis and autophagy (PubMed:10102273, PubMed:16751106, PubMed:21329882, PubMed:30513302). Acts as a positive regulator of autophagy in skeletal muscle: in starved cells, enters the nucleus following dephosphorylation and binds the promoters of autophagy genes, such as GABARAP1L, MAP1LC3B and ATG12, thereby activating their expression, resulting in proteolysis of skeletal muscle proteins (By similarity). Triggers apoptosis in the absence of survival factors, including neuronal cell death upon oxidative stress (PubMed:10102273, PubMed:16751106). Participates in post-transcriptional regulation of MYC: following phosphorylation by MAPKAPK5, promotes induction of miR-34b and miR-34c expression, 2 post-transcriptional regulators of MYC that bind to the 3'UTR of MYC transcript and prevent its translation (PubMed:21329882). In response to metabolic stress, translocates into the mitochondria where it promotes mtDNA transcription (PubMed:23283301). In response to metabolic stress, translocates into the mitochondria where it promotes mtDNA transcription. Also acts as a key regulator of chondrogenic commitment of skeletal progenitor cells in response to lipid availability: when lipids levels are low, translocates to the nucleus and promotes expression of SOX9, which induces chondrogenic commitment and suppresses fatty acid oxidation (By similarity). Also acts as a key regulator of regulatory T-cells (Treg) differentiation by activating expression of FOXP3 (PubMed:30513302). {ECO:0000250|UniProtKB:Q9WVH4, ECO:0000269|PubMed:10102273, ECO:0000269|PubMed:16751106, ECO:0000269|PubMed:21329882, ECO:0000269|PubMed:23283301, ECO:0000269|PubMed:30513302}. |
O43524 | FOXO3 | S432 | ochoa | Forkhead box protein O3 (AF6q21 protein) (Forkhead in rhabdomyosarcoma-like 1) | Transcriptional activator that recognizes and binds to the DNA sequence 5'-[AG]TAAA[TC]A-3' and regulates different processes, such as apoptosis and autophagy (PubMed:10102273, PubMed:16751106, PubMed:21329882, PubMed:30513302). Acts as a positive regulator of autophagy in skeletal muscle: in starved cells, enters the nucleus following dephosphorylation and binds the promoters of autophagy genes, such as GABARAP1L, MAP1LC3B and ATG12, thereby activating their expression, resulting in proteolysis of skeletal muscle proteins (By similarity). Triggers apoptosis in the absence of survival factors, including neuronal cell death upon oxidative stress (PubMed:10102273, PubMed:16751106). Participates in post-transcriptional regulation of MYC: following phosphorylation by MAPKAPK5, promotes induction of miR-34b and miR-34c expression, 2 post-transcriptional regulators of MYC that bind to the 3'UTR of MYC transcript and prevent its translation (PubMed:21329882). In response to metabolic stress, translocates into the mitochondria where it promotes mtDNA transcription (PubMed:23283301). In response to metabolic stress, translocates into the mitochondria where it promotes mtDNA transcription. Also acts as a key regulator of chondrogenic commitment of skeletal progenitor cells in response to lipid availability: when lipids levels are low, translocates to the nucleus and promotes expression of SOX9, which induces chondrogenic commitment and suppresses fatty acid oxidation (By similarity). Also acts as a key regulator of regulatory T-cells (Treg) differentiation by activating expression of FOXP3 (PubMed:30513302). {ECO:0000250|UniProtKB:Q9WVH4, ECO:0000269|PubMed:10102273, ECO:0000269|PubMed:16751106, ECO:0000269|PubMed:21329882, ECO:0000269|PubMed:23283301, ECO:0000269|PubMed:30513302}. |
O43623 | SNAI2 | S100 | psp | Zinc finger protein SNAI2 (Neural crest transcription factor Slug) (Protein snail homolog 2) | Transcriptional repressor that modulates both activator-dependent and basal transcription. Involved in the generation and migration of neural crest cells. Plays a role in mediating RAF1-induced transcriptional repression of the TJ protein, occludin (OCLN) and subsequent oncogenic transformation of epithelial cells (By similarity). Represses BRCA2 expression by binding to its E2-box-containing silencer and recruiting CTBP1 and HDAC1 in breast cells. In epidermal keratinocytes, binds to the E-box in ITGA3 promoter and represses its transcription. Involved in the regulation of ITGB1 and ITGB4 expression and cell adhesion and proliferation in epidermal keratinocytes. Binds to E-box2 domain of BSG and activates its expression during TGFB1-induced epithelial-mesenchymal transition (EMT) in hepatocytes. Represses E-Cadherin/CDH1 transcription via E-box elements. Involved in osteoblast maturation. Binds to RUNX2 and SOC9 promoters and may act as a positive and negative transcription regulator, respectively, in osteoblasts. Binds to CXCL12 promoter via E-box regions in mesenchymal stem cells and osteoblasts. Plays an essential role in TWIST1-induced EMT and its ability to promote invasion and metastasis. {ECO:0000250, ECO:0000269|PubMed:10866665, ECO:0000269|PubMed:11912130, ECO:0000269|PubMed:15734731, ECO:0000269|PubMed:16707493, ECO:0000269|PubMed:19756381, ECO:0000269|PubMed:21182836}. |
O60271 | SPAG9 | S238 | ochoa | C-Jun-amino-terminal kinase-interacting protein 4 (JIP-4) (JNK-interacting protein 4) (Cancer/testis antigen 89) (CT89) (Human lung cancer oncogene 6 protein) (HLC-6) (JNK-associated leucine-zipper protein) (JLP) (Mitogen-activated protein kinase 8-interacting protein 4) (Proliferation-inducing protein 6) (Protein highly expressed in testis) (PHET) (Sperm surface protein) (Sperm-associated antigen 9) (Sperm-specific protein) (Sunday driver 1) | The JNK-interacting protein (JIP) group of scaffold proteins selectively mediates JNK signaling by aggregating specific components of the MAPK cascade to form a functional JNK signaling module (PubMed:14743216). Regulates lysosomal positioning by acting as an adapter protein which links PIP4P1-positive lysosomes to the dynein-dynactin complex (PubMed:29146937). Assists PIKFYVE selective functionality in microtubule-based endosome-to-TGN trafficking (By similarity). {ECO:0000250|UniProtKB:Q58A65, ECO:0000269|PubMed:14743216, ECO:0000269|PubMed:29146937}. |
O60307 | MAST3 | S43 | ochoa | Microtubule-associated serine/threonine-protein kinase 3 (EC 2.7.11.1) | None |
O60346 | PHLPP1 | S317 | ochoa|psp | PH domain leucine-rich repeat-containing protein phosphatase 1 (EC 3.1.3.16) (Pleckstrin homology domain-containing family E member 1) (PH domain-containing family E member 1) (Suprachiasmatic nucleus circadian oscillatory protein) (hSCOP) | Protein phosphatase involved in regulation of Akt and PKC signaling. Mediates dephosphorylation in the C-terminal domain hydrophobic motif of members of the AGC Ser/Thr protein kinase family; specifically acts on 'Ser-473' of AKT2 and AKT3, 'Ser-660' of PRKCB and 'Ser-657' of PRKCA (PubMed:15808505, PubMed:17386267, PubMed:18162466). Isoform 2 seems to have a major role in regulating Akt signaling in hippocampal neurons (By similarity). Akt regulates the balance between cell survival and apoptosis through a cascade that primarily alters the function of transcription factors that regulate pro- and antiapoptotic genes. Dephosphorylation of 'Ser-473' of Akt triggers apoptosis and suppression of tumor growth. Dephosphorylation of PRKCA and PRKCB leads to their destabilization and degradation (PubMed:18162466). Dephosphorylates STK4 on 'Thr-387' leading to STK4 activation and apoptosis (PubMed:20513427). Dephosphorylates RPS6KB1 and is involved in regulation of cap-dependent translation (PubMed:21986499). Inhibits cancer cell proliferation and may act as a tumor suppressor (PubMed:19079341). Dephosphorylates RAF1 inhibiting its kinase activity (PubMed:24530606). May act as a negative regulator of K-Ras signaling in membrane rafts (By similarity). Involved in the hippocampus-dependent long-term memory formation (By similarity). Involved in circadian control by regulating the consolidation of circadian periodicity after resetting (By similarity). Involved in development and function of regulatory T-cells (By similarity). {ECO:0000250|UniProtKB:Q8CHE4, ECO:0000250|UniProtKB:Q9WTR8, ECO:0000269|PubMed:15808505, ECO:0000269|PubMed:17386267, ECO:0000269|PubMed:18162466, ECO:0000269|PubMed:19079341, ECO:0000269|PubMed:21986499, ECO:0000269|PubMed:24530606}. |
O75122 | CLASP2 | S459 | ochoa | CLIP-associating protein 2 (Cytoplasmic linker-associated protein 2) (Protein Orbit homolog 2) (hOrbit2) | Microtubule plus-end tracking protein that promotes the stabilization of dynamic microtubules (PubMed:26003921). Involved in the nucleation of noncentrosomal microtubules originating from the trans-Golgi network (TGN). Required for the polarization of the cytoplasmic microtubule arrays in migrating cells towards the leading edge of the cell. May act at the cell cortex to enhance the frequency of rescue of depolymerizing microtubules by attaching their plus-ends to cortical platforms composed of ERC1 and PHLDB2 (PubMed:16824950). This cortical microtubule stabilizing activity is regulated at least in part by phosphatidylinositol 3-kinase signaling. Also performs a similar stabilizing function at the kinetochore which is essential for the bipolar alignment of chromosomes on the mitotic spindle (PubMed:16866869, PubMed:16914514). Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. {ECO:0000269|PubMed:11290329, ECO:0000269|PubMed:15631994, ECO:0000269|PubMed:16824950, ECO:0000269|PubMed:16866869, ECO:0000269|PubMed:16914514, ECO:0000269|PubMed:17543864, ECO:0000269|PubMed:20937854, ECO:0000269|PubMed:26003921}. |
O75122 | CLASP2 | S503 | ochoa | CLIP-associating protein 2 (Cytoplasmic linker-associated protein 2) (Protein Orbit homolog 2) (hOrbit2) | Microtubule plus-end tracking protein that promotes the stabilization of dynamic microtubules (PubMed:26003921). Involved in the nucleation of noncentrosomal microtubules originating from the trans-Golgi network (TGN). Required for the polarization of the cytoplasmic microtubule arrays in migrating cells towards the leading edge of the cell. May act at the cell cortex to enhance the frequency of rescue of depolymerizing microtubules by attaching their plus-ends to cortical platforms composed of ERC1 and PHLDB2 (PubMed:16824950). This cortical microtubule stabilizing activity is regulated at least in part by phosphatidylinositol 3-kinase signaling. Also performs a similar stabilizing function at the kinetochore which is essential for the bipolar alignment of chromosomes on the mitotic spindle (PubMed:16866869, PubMed:16914514). Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. {ECO:0000269|PubMed:11290329, ECO:0000269|PubMed:15631994, ECO:0000269|PubMed:16824950, ECO:0000269|PubMed:16866869, ECO:0000269|PubMed:16914514, ECO:0000269|PubMed:17543864, ECO:0000269|PubMed:20937854, ECO:0000269|PubMed:26003921}. |
O75376 | NCOR1 | Y2147 | ochoa | Nuclear receptor corepressor 1 (N-CoR) (N-CoR1) | Mediates transcriptional repression by certain nuclear receptors (PubMed:20812024). Part of a complex which promotes histone deacetylation and the formation of repressive chromatin structures which may impede the access of basal transcription factors. Participates in the transcriptional repressor activity produced by BCL6. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). Mediates the NR1D1-dependent repression and circadian regulation of TSHB expression (By similarity). The NCOR1-HDAC3 complex regulates the circadian expression of the core clock gene ARTNL/BMAL1 and the genes involved in lipid metabolism in the liver (By similarity). {ECO:0000250|UniProtKB:Q60974, ECO:0000269|PubMed:14527417, ECO:0000269|PubMed:20812024}. |
O75427 | LRCH4 | S517 | ochoa | Leucine-rich repeat and calponin homology domain-containing protein 4 (Leucine-rich repeat neuronal protein 4) (Leucine-rich neuronal protein) | Accessory protein that regulates signaling by multiple TLRs, acting as a broad-spanning regulator of the innate immune response. In macrophages, binds LPS and promotes proper docking of LPS in lipid raft membrane. May be required for lipid raft maintenance. {ECO:0000250|UniProtKB:Q921G6}. |
O75962 | TRIO | S2455 | ochoa | Triple functional domain protein (EC 2.7.11.1) (PTPRF-interacting protein) | Guanine nucleotide exchange factor (GEF) for RHOA and RAC1 GTPases (PubMed:22155786, PubMed:27418539, PubMed:8643598). Involved in coordinating actin remodeling, which is necessary for cell migration and growth (PubMed:10341202, PubMed:22155786). Plays a key role in the regulation of neurite outgrowth and lamellipodia formation (PubMed:32109419). In developing hippocampal neurons, limits dendrite formation, without affecting the establishment of axon polarity. Once dendrites are formed, involved in the control of synaptic function by regulating the endocytosis of AMPA-selective glutamate receptors (AMPARs) at CA1 excitatory synapses (By similarity). May act as a regulator of adipogenesis (By similarity). {ECO:0000250|UniProtKB:F1M0Z1, ECO:0000269|PubMed:10341202, ECO:0000269|PubMed:22155786, ECO:0000269|PubMed:27418539, ECO:0000269|PubMed:32109419, ECO:0000269|PubMed:8643598}. |
O75962 | TRIO | S2488 | ochoa | Triple functional domain protein (EC 2.7.11.1) (PTPRF-interacting protein) | Guanine nucleotide exchange factor (GEF) for RHOA and RAC1 GTPases (PubMed:22155786, PubMed:27418539, PubMed:8643598). Involved in coordinating actin remodeling, which is necessary for cell migration and growth (PubMed:10341202, PubMed:22155786). Plays a key role in the regulation of neurite outgrowth and lamellipodia formation (PubMed:32109419). In developing hippocampal neurons, limits dendrite formation, without affecting the establishment of axon polarity. Once dendrites are formed, involved in the control of synaptic function by regulating the endocytosis of AMPA-selective glutamate receptors (AMPARs) at CA1 excitatory synapses (By similarity). May act as a regulator of adipogenesis (By similarity). {ECO:0000250|UniProtKB:F1M0Z1, ECO:0000269|PubMed:10341202, ECO:0000269|PubMed:22155786, ECO:0000269|PubMed:27418539, ECO:0000269|PubMed:32109419, ECO:0000269|PubMed:8643598}. |
O75995 | SASH3 | S142 | ochoa | SAM and SH3 domain-containing protein 3 (SH3 protein expressed in lymphocytes homolog) | May function as a signaling adapter protein in lymphocytes. {ECO:0000250|UniProtKB:Q8K352}. |
O76080 | ZFAND5 | S54 | ochoa | AN1-type zinc finger protein 5 (Zinc finger A20 domain-containing protein 2) (Zinc finger protein 216) | Involved in protein degradation via the ubiquitin-proteasome system. May act by anchoring ubiquitinated proteins to the proteasome. Plays a role in ubiquitin-mediated protein degradation during muscle atrophy. Plays a role in the regulation of NF-kappa-B activation and apoptosis. Inhibits NF-kappa-B activation triggered by overexpression of RIPK1 and TRAF6 but not of RELA. Also inhibits tumor necrosis factor (TNF), IL-1 and TLR4-induced NF-kappa-B activation in a dose-dependent manner. Overexpression sensitizes cells to TNF-induced apoptosis. Is a potent inhibitory factor for osteoclast differentiation. {ECO:0000269|PubMed:14754897}. |
O94972 | TRIM37 | S801 | ochoa | E3 ubiquitin-protein ligase TRIM37 (EC 2.3.2.27) (Mulibrey nanism protein) (RING-type E3 ubiquitin transferase TRIM37) (Tripartite motif-containing protein 37) | E3 ubiquitin-protein ligase required to prevent centriole reduplication (PubMed:15885686, PubMed:23769972). Probably acts by ubiquitinating positive regulators of centriole reduplication (PubMed:23769972). Mediates monoubiquitination of 'Lys-119' of histone H2A (H2AK119Ub), a specific tag for epigenetic transcriptional repression: associates with some Polycomb group (PcG) multiprotein PRC2-like complex and mediates repression of target genes (PubMed:25470042). Also acts as a positive regulator of peroxisome import by mediating monoubiquitination of PEX5 at 'Lys-472': monoubiquitination promotes PEX5 stabilitation by preventing its polyubiquitination and degradation by the proteasome (PubMed:28724525). Has anti-HIV activity (PubMed:24317724). {ECO:0000269|PubMed:15885686, ECO:0000269|PubMed:23769972, ECO:0000269|PubMed:24317724, ECO:0000269|PubMed:25470042, ECO:0000269|PubMed:28724525}. |
O95049 | TJP3 | S323 | ochoa | Tight junction protein ZO-3 (Tight junction protein 3) (Zona occludens protein 3) (Zonula occludens protein 3) | TJP1, TJP2, and TJP3 are closely related scaffolding proteins that link tight junction (TJ) transmembrane proteins such as claudins, junctional adhesion molecules, and occludin to the actin cytoskeleton (PubMed:16129888). The tight junction acts to limit movement of substances through the paracellular space and as a boundary between the compositionally distinct apical and basolateral plasma membrane domains of epithelial and endothelial cells. Binds and recruits PATJ to tight junctions where it connects and stabilizes apical and lateral components of tight junctions (PubMed:16129888). Promotes cell-cycle progression through the sequestration of cyclin D1 (CCND1) at tight junctions during mitosis which prevents CCND1 degradation during M-phase and enables S-phase transition (PubMed:21411630). With TJP1 and TJP2, participates in the junctional retention and stability of the transcription factor DBPA, but is not involved in its shuttling to the nucleus (By similarity). Contrary to TJP2, TJP3 is dispensable for individual viability, embryonic development, epithelial differentiation, and the establishment of TJs, at least in the laboratory environment (By similarity). {ECO:0000250|UniProtKB:O62683, ECO:0000250|UniProtKB:Q9QXY1, ECO:0000269|PubMed:16129888, ECO:0000269|PubMed:21411630}. |
O95684 | CEP43 | S156 | ochoa | Centrosomal protein 43 (FGFR1 oncogene partner) | Required for anchoring microtubules to the centrosomes (PubMed:16314388, PubMed:28659385). Required for ciliation (PubMed:28625565, PubMed:28659385). {ECO:0000269|PubMed:16314388, ECO:0000269|PubMed:28625565, ECO:0000269|PubMed:28659385}. |
O95817 | BAG3 | S177 | ochoa | BAG family molecular chaperone regulator 3 (BAG-3) (Bcl-2-associated athanogene 3) (Bcl-2-binding protein Bis) (Docking protein CAIR-1) | Co-chaperone and adapter protein that connects different classes of molecular chaperones including heat shock proteins 70 (HSP70s), e.g. HSPA1A/HSP70 or HSPA8/HSC70, and small heat shock proteins (sHSPs), e.g. HSPB8 (PubMed:27884606, PubMed:30559338). Acts as a nucleotide-exchange factor (NEF) promoting the release of ADP from HSP70s, thereby triggering client protein release (PubMed:27884606, PubMed:30559338). Nucleotide release is mediated via BAG3 binding to the nucleotide-binding domain (NBD) of HSP70s, whereas client release is mediated via binding to the substrate-binding domain (SBD) (PubMed:27474739, PubMed:9873016). Has anti-apoptotic activity (PubMed:10597216). Plays a role in the HSF1 nucleocytoplasmic transport (PubMed:26159920). {ECO:0000269|PubMed:10597216, ECO:0000269|PubMed:24318877, ECO:0000269|PubMed:26159920, ECO:0000269|PubMed:27474739, ECO:0000269|PubMed:27884606, ECO:0000269|PubMed:30559338, ECO:0000269|PubMed:9873016}. |
O95863 | SNAI1 | S100 | psp | Zinc finger protein SNAI1 (Protein snail homolog 1) (Protein sna) | Involved in induction of the epithelial to mesenchymal transition (EMT), formation and maintenance of embryonic mesoderm, growth arrest, survival and cell migration (PubMed:10655587, PubMed:15647282, PubMed:20389281, PubMed:20562920, PubMed:21952048, PubMed:25827072). Binds to 3 E-boxes of the E-cadherin/CDH1 gene promoter and to the promoters of CLDN7 and KRT8 and, in association with histone demethylase KDM1A which it recruits to the promoters, causes a decrease in dimethylated H3K4 levels and represses transcription (PubMed:10655587, PubMed:20389281, PubMed:20562920). The N-terminal SNAG domain competes with histone H3 for the same binding site on the histone demethylase complex formed by KDM1A and RCOR1, and thereby inhibits demethylation of histone H3 at 'Lys-4' (in vitro) (PubMed:20389281, PubMed:21300290, PubMed:23721412). During EMT, involved with LOXL2 in negatively regulating pericentromeric heterochromatin transcription (PubMed:16096638). SNAI1 recruits LOXL2 to pericentromeric regions to oxidize histone H3 and repress transcription which leads to release of heterochromatin component CBX5/HP1A, enabling chromatin reorganization and acquisition of mesenchymal traits (By similarity). Associates with EGR1 and SP1 to mediate tetradecanoyl phorbol acetate (TPA)-induced up-regulation of CDKN2B, possibly by binding to the CDKN2B promoter region 5'-TCACA-3 (PubMed:20121949). In addition, may also activate the CDKN2B promoter by itself (PubMed:20121949). {ECO:0000250|UniProtKB:Q02085, ECO:0000269|PubMed:10655587, ECO:0000269|PubMed:15647282, ECO:0000269|PubMed:16096638, ECO:0000269|PubMed:20121949, ECO:0000269|PubMed:20389281, ECO:0000269|PubMed:20562920, ECO:0000269|PubMed:21300290, ECO:0000269|PubMed:21952048, ECO:0000269|PubMed:23721412, ECO:0000269|PubMed:25827072}. |
P02671 | FGA | S281 | ochoa | Fibrinogen alpha chain [Cleaved into: Fibrinopeptide A; Fibrinogen alpha chain] | Cleaved by the protease thrombin to yield monomers which, together with fibrinogen beta (FGB) and fibrinogen gamma (FGG), polymerize to form an insoluble fibrin matrix. Fibrin has a major function in hemostasis as one of the primary components of blood clots. In addition, functions during the early stages of wound repair to stabilize the lesion and guide cell migration during re-epithelialization. Was originally thought to be essential for platelet aggregation, based on in vitro studies using anticoagulated blood. However, subsequent studies have shown that it is not absolutely required for thrombus formation in vivo. Enhances expression of SELP in activated platelets via an ITGB3-dependent pathway. Maternal fibrinogen is essential for successful pregnancy. Fibrin deposition is also associated with infection, where it protects against IFNG-mediated hemorrhage. May also facilitate the immune response via both innate and T-cell mediated pathways. {ECO:0000250|UniProtKB:E9PV24}. |
P0DJD0 | RGPD1 | S783 | ochoa | RANBP2-like and GRIP domain-containing protein 1 (Ran-binding protein 2-like 6) (RanBP2-like 6) (RanBP2L6) | None |
P0DJD0 | RGPD1 | S1575 | ochoa | RANBP2-like and GRIP domain-containing protein 1 (Ran-binding protein 2-like 6) (RanBP2-like 6) (RanBP2L6) | None |
P0DJD1 | RGPD2 | S791 | ochoa | RANBP2-like and GRIP domain-containing protein 2 (Ran-binding protein 2-like 2) (RanBP2-like 2) (RanBP2L2) | None |
P0DJD1 | RGPD2 | S1583 | ochoa | RANBP2-like and GRIP domain-containing protein 2 (Ran-binding protein 2-like 2) (RanBP2-like 2) (RanBP2L2) | None |
P10071 | GLI3 | S660 | ochoa | Transcriptional activator GLI3 (GLI3 form of 190 kDa) (GLI3-190) (GLI3 full-length protein) (GLI3FL) [Cleaved into: Transcriptional repressor GLI3R (GLI3 C-terminally truncated form) (GLI3 form of 83 kDa) (GLI3-83)] | Has a dual function as a transcriptional activator and a repressor of the sonic hedgehog (Shh) pathway, and plays a role in limb development. The full-length GLI3 form (GLI3FL) after phosphorylation and nuclear translocation, acts as an activator (GLI3A) while GLI3R, its C-terminally truncated form, acts as a repressor. A proper balance between the GLI3 activator and the repressor GLI3R, rather than the repressor gradient itself or the activator/repressor ratio gradient, specifies limb digit number and identity. In concert with TRPS1, plays a role in regulating the size of the zone of distal chondrocytes, in restricting the zone of PTHLH expression in distal cells and in activating chondrocyte proliferation. Binds to the minimal GLI-consensus sequence 5'-GGGTGGTC-3'. {ECO:0000269|PubMed:10693759, ECO:0000269|PubMed:11238441, ECO:0000269|PubMed:17764085}. |
P10636 | MAPT | S512 | ochoa | Microtubule-associated protein tau (Neurofibrillary tangle protein) (Paired helical filament-tau) (PHF-tau) | Promotes microtubule assembly and stability, and might be involved in the establishment and maintenance of neuronal polarity (PubMed:21985311). The C-terminus binds axonal microtubules while the N-terminus binds neural plasma membrane components, suggesting that tau functions as a linker protein between both (PubMed:21985311, PubMed:32961270). Axonal polarity is predetermined by TAU/MAPT localization (in the neuronal cell) in the domain of the cell body defined by the centrosome. The short isoforms allow plasticity of the cytoskeleton whereas the longer isoforms may preferentially play a role in its stabilization. {ECO:0000269|PubMed:21985311, ECO:0000269|PubMed:32961270}. |
P10636 | MAPT | S717 | ochoa | Microtubule-associated protein tau (Neurofibrillary tangle protein) (Paired helical filament-tau) (PHF-tau) | Promotes microtubule assembly and stability, and might be involved in the establishment and maintenance of neuronal polarity (PubMed:21985311). The C-terminus binds axonal microtubules while the N-terminus binds neural plasma membrane components, suggesting that tau functions as a linker protein between both (PubMed:21985311, PubMed:32961270). Axonal polarity is predetermined by TAU/MAPT localization (in the neuronal cell) in the domain of the cell body defined by the centrosome. The short isoforms allow plasticity of the cytoskeleton whereas the longer isoforms may preferentially play a role in its stabilization. {ECO:0000269|PubMed:21985311, ECO:0000269|PubMed:32961270}. |
P11137 | MAP2 | S1786 | 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. |
P11274 | BCR | S367 | ochoa | Breakpoint cluster region protein (EC 2.7.11.1) (Renal carcinoma antigen NY-REN-26) | Protein with a unique structure having two opposing regulatory activities toward small GTP-binding proteins. The C-terminus is a GTPase-activating protein (GAP) domain which stimulates GTP hydrolysis by RAC1, RAC2 and CDC42. Accelerates the intrinsic rate of GTP hydrolysis of RAC1 or CDC42, leading to down-regulation of the active GTP-bound form (PubMed:17116687, PubMed:1903516, PubMed:7479768). The central Dbl homology (DH) domain functions as guanine nucleotide exchange factor (GEF) that modulates the GTPases CDC42, RHOA and RAC1. Promotes the conversion of CDC42, RHOA and RAC1 from the GDP-bound to the GTP-bound form (PubMed:23940119, PubMed:7479768). The amino terminus contains an intrinsic kinase activity (PubMed:1657398). Functions as an important negative regulator of neuronal RAC1 activity (By similarity). Regulates macrophage functions such as CSF1-directed motility and phagocytosis through the modulation of RAC1 activity (PubMed:17116687). Plays a major role as a RHOA GEF in keratinocytes being involved in focal adhesion formation and keratinocyte differentiation (PubMed:23940119). {ECO:0000250|UniProtKB:Q6PAJ1, ECO:0000269|PubMed:1657398, ECO:0000269|PubMed:17116687, ECO:0000269|PubMed:1903516, ECO:0000269|PubMed:23940119, ECO:0000269|PubMed:7479768}. |
P12270 | TPR | S2054 | ochoa | Nucleoprotein TPR (Megator) (NPC-associated intranuclear protein) (Translocated promoter region protein) | Component of the nuclear pore complex (NPC), a complex required for the trafficking across the nuclear envelope. Functions as a scaffolding element in the nuclear phase of the NPC essential for normal nucleocytoplasmic transport of proteins and mRNAs, plays a role in the establishment of nuclear-peripheral chromatin compartmentalization in interphase, and in the mitotic spindle checkpoint signaling during mitosis. Involved in the quality control and retention of unspliced mRNAs in the nucleus; in association with NUP153, regulates the nuclear export of unspliced mRNA species bearing constitutive transport element (CTE) in a NXF1- and KHDRBS1-independent manner. Negatively regulates both the association of CTE-containing mRNA with large polyribosomes and translation initiation. Does not play any role in Rev response element (RRE)-mediated export of unspliced mRNAs. Implicated in nuclear export of mRNAs transcribed from heat shock gene promoters; associates both with chromatin in the HSP70 promoter and with mRNAs transcribed from this promoter under stress-induced conditions. Modulates the nucleocytoplasmic transport of activated MAPK1/ERK2 and huntingtin/HTT and may serve as a docking site for the XPO1/CRM1-mediated nuclear export complex. According to some authors, plays a limited role in the regulation of nuclear protein export (PubMed:11952838, PubMed:22253824). Also plays a role as a structural and functional element of the perinuclear chromatin distribution; involved in the formation and/or maintenance of NPC-associated perinuclear heterochromatin exclusion zones (HEZs). Finally, acts as a spatial regulator of the spindle-assembly checkpoint (SAC) response ensuring a timely and effective recruitment of spindle checkpoint proteins like MAD1L1 and MAD2L1 to unattached kinetochore during the metaphase-anaphase transition before chromosome congression. Its N-terminus is involved in activation of oncogenic kinases. {ECO:0000269|PubMed:11952838, ECO:0000269|PubMed:15654337, ECO:0000269|PubMed:17897941, ECO:0000269|PubMed:18794356, ECO:0000269|PubMed:18981471, ECO:0000269|PubMed:19273613, ECO:0000269|PubMed:20133940, ECO:0000269|PubMed:20407419, ECO:0000269|PubMed:21613532, ECO:0000269|PubMed:22253824, ECO:0000269|PubMed:9864356}. |
P13807 | GYS1 | S649 | ochoa|psp | Glycogen [starch] synthase, muscle (EC 2.4.1.11) (Glycogen synthase 1) | Glycogen synthase participates in the glycogen biosynthetic process along with glycogenin and glycogen branching enzyme. Extends the primer composed of a few glucose units formed by glycogenin by adding new glucose units to it. In this context, glycogen synthase transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan. {ECO:0000269|PubMed:35835870}. |
P17661 | DES | S28 | ochoa|psp | Desmin | Muscle-specific type III intermediate filament essential for proper muscular structure and function. Plays a crucial role in maintaining the structure of sarcomeres, inter-connecting the Z-disks and forming the myofibrils, linking them not only to the sarcolemmal cytoskeleton, but also to the nucleus and mitochondria, thus providing strength for the muscle fiber during activity (PubMed:25358400). In adult striated muscle they form a fibrous network connecting myofibrils to each other and to the plasma membrane from the periphery of the Z-line structures (PubMed:24200904, PubMed:25394388, PubMed:26724190). May act as a sarcomeric microtubule-anchoring protein: specifically associates with detyrosinated tubulin-alpha chains, leading to buckled microtubules and mechanical resistance to contraction. Required for nuclear membrane integrity, via anchoring at the cell tip and nuclear envelope, resulting in maintenance of microtubule-derived intracellular mechanical forces (By similarity). Contributes to the transcriptional regulation of the NKX2-5 gene in cardiac progenitor cells during a short period of cardiomyogenesis and in cardiac side population stem cells in the adult. Plays a role in maintaining an optimal conformation of nebulette (NEB) on heart muscle sarcomeres to bind and recruit cardiac alpha-actin (By similarity). {ECO:0000250|UniProtKB:P31001, ECO:0000269|PubMed:24200904, ECO:0000269|PubMed:25394388, ECO:0000269|PubMed:26724190, ECO:0000303|PubMed:25358400}. |
P19484 | TFEB | S138 | ochoa|psp | Transcription factor EB (Class E basic helix-loop-helix protein 35) (bHLHe35) | Transcription factor that acts as a master regulator of lysosomal biogenesis, autophagy, lysosomal exocytosis, lipid catabolism, energy metabolism and immune response (PubMed:21617040, PubMed:22343943, PubMed:22576015, PubMed:22692423, PubMed:25720963, PubMed:30120233, PubMed:31672913, PubMed:32612235, PubMed:32753672, PubMed:35662396, PubMed:36697823, PubMed:36749723, PubMed:37079666). Specifically recognizes and binds E-box sequences (5'-CANNTG-3'); efficient DNA-binding requires dimerization with itself or with another MiT/TFE family member such as TFE3 or MITF (PubMed:1748288, PubMed:19556463, PubMed:29146937). Involved in the cellular response to amino acid availability by acting downstream of MTOR: in the presence of nutrients, TFEB phosphorylation by MTOR promotes its cytosolic retention and subsequent inactivation (PubMed:21617040, PubMed:22343943, PubMed:22576015, PubMed:22692423, PubMed:25720963, PubMed:32612235, PubMed:32753672, PubMed:35662396, PubMed:36697823). Upon starvation or lysosomal stress, inhibition of MTOR induces TFEB dephosphorylation, resulting in nuclear localization and transcription factor activity (PubMed:22343943, PubMed:22576015, PubMed:22692423, PubMed:25720963, PubMed:32612235, PubMed:32753672, PubMed:35662396, PubMed:36697823). Specifically recognizes and binds the CLEAR-box sequence (5'-GTCACGTGAC-3') present in the regulatory region of many lysosomal genes, leading to activate their expression, thereby playing a central role in expression of lysosomal genes (PubMed:19556463, PubMed:22692423). Regulates lysosomal positioning in response to nutrient deprivation by promoting the expression of PIP4P1 (PubMed:29146937). Acts as a positive regulator of autophagy by promoting expression of genes involved in autophagy (PubMed:21617040, PubMed:22576015, PubMed:23434374, PubMed:27278822). In association with TFE3, activates the expression of CD40L in T-cells, thereby playing a role in T-cell-dependent antibody responses in activated CD4(+) T-cells and thymus-dependent humoral immunity (By similarity). Specifically recognizes the gamma-E3 box, a subset of E-boxes, present in the heavy-chain immunoglobulin enhancer (PubMed:2115126). Plays a role in the signal transduction processes required for normal vascularization of the placenta (By similarity). Involved in the immune response to infection by the bacteria S.aureus, S.typhimurium or S.enterica: infection promotes itaconate production, leading to alkylation, resulting in nuclear localization and transcription factor activity (PubMed:35662396). Itaconate-mediated alkylation activates TFEB-dependent lysosomal biogenesis, facilitating the bacteria clearance during the antibacterial innate immune response (PubMed:35662396). In association with ACSS2, promotes the expression of genes involved in lysosome biogenesis and both autophagy upon glucose deprivation (PubMed:28552616). {ECO:0000250|UniProtKB:Q9R210, ECO:0000269|PubMed:1748288, ECO:0000269|PubMed:19556463, ECO:0000269|PubMed:2115126, ECO:0000269|PubMed:21617040, ECO:0000269|PubMed:22343943, ECO:0000269|PubMed:22576015, ECO:0000269|PubMed:22692423, ECO:0000269|PubMed:23434374, ECO:0000269|PubMed:25720963, ECO:0000269|PubMed:27278822, ECO:0000269|PubMed:28552616, ECO:0000269|PubMed:29146937, ECO:0000269|PubMed:30120233, ECO:0000269|PubMed:31672913, ECO:0000269|PubMed:32612235, ECO:0000269|PubMed:32753672, ECO:0000269|PubMed:35662396, ECO:0000269|PubMed:36697823, ECO:0000269|PubMed:36749723, ECO:0000269|PubMed:37079666}. |
P19838 | NFKB1 | S903 | ochoa|psp | Nuclear factor NF-kappa-B p105 subunit (DNA-binding factor KBF1) (EBP-1) (Nuclear factor of kappa light polypeptide gene enhancer in B-cells 1) [Cleaved into: Nuclear factor NF-kappa-B p50 subunit] | NF-kappa-B is a pleiotropic transcription factor present in almost all cell types and is the endpoint of a series of signal transduction events that are initiated by a vast array of stimuli related to many biological processes such as inflammation, immunity, differentiation, cell growth, tumorigenesis and apoptosis. NF-kappa-B is a homo- or heterodimeric complex formed by the Rel-like domain-containing proteins RELA/p65, RELB, NFKB1/p105, NFKB1/p50, REL and NFKB2/p52 and the heterodimeric p65-p50 complex appears to be most abundant one. The dimers bind at kappa-B sites in the DNA of their target genes and the individual dimers have distinct preferences for different kappa-B sites that they can bind with distinguishable affinity and specificity. Different dimer combinations act as transcriptional activators or repressors, respectively. NF-kappa-B is controlled by various mechanisms of post-translational modification and subcellular compartmentalization as well as by interactions with other cofactors or corepressors. NF-kappa-B complexes are held in the cytoplasm in an inactive state complexed with members of the NF-kappa-B inhibitor (I-kappa-B) family. In a conventional activation pathway, I-kappa-B is phosphorylated by I-kappa-B kinases (IKKs) in response to different activators, subsequently degraded thus liberating the active NF-kappa-B complex which translocates to the nucleus. NF-kappa-B heterodimeric p65-p50 and RelB-p50 complexes are transcriptional activators. The NF-kappa-B p50-p50 homodimer is a transcriptional repressor, but can act as a transcriptional activator when associated with BCL3. NFKB1 appears to have dual functions such as cytoplasmic retention of attached NF-kappa-B proteins by p105 and generation of p50 by a cotranslational processing. The proteasome-mediated process ensures the production of both p50 and p105 and preserves their independent function, although processing of NFKB1/p105 also appears to occur post-translationally. p50 binds to the kappa-B consensus sequence 5'-GGRNNYYCC-3', located in the enhancer region of genes involved in immune response and acute phase reactions. In a complex with MAP3K8, NFKB1/p105 represses MAP3K8-induced MAPK signaling; active MAP3K8 is released by proteasome-dependent degradation of NFKB1/p105. {ECO:0000269|PubMed:15485931, ECO:0000269|PubMed:1740106, ECO:0000269|PubMed:2203531, ECO:0000269|PubMed:2234062, ECO:0000269|PubMed:7830764}.; FUNCTION: [Nuclear factor NF-kappa-B p105 subunit]: P105 is the precursor of the active p50 subunit (Nuclear factor NF-kappa-B p50 subunit) of the nuclear factor NF-kappa-B (PubMed:1423592). Acts as a cytoplasmic retention of attached NF-kappa-B proteins by p105 (PubMed:1423592). {ECO:0000269|PubMed:1423592}.; FUNCTION: [Nuclear factor NF-kappa-B p50 subunit]: Constitutes the active form, which associates with RELA/p65 to form the NF-kappa-B p65-p50 complex to form a transcription factor (PubMed:1740106, PubMed:7830764). Together with RELA/p65, binds to the kappa-B consensus sequence 5'-GGRNNYYCC-3', located in the enhancer region of genes involved in immune response and acute phase reactions (PubMed:1740106, PubMed:7830764). {ECO:0000269|PubMed:1740106, ECO:0000269|PubMed:7830764}. |
P30291 | WEE1 | Y132 | ochoa | Wee1-like protein kinase (WEE1hu) (EC 2.7.10.2) (Wee1A kinase) | Acts as a negative regulator of entry into mitosis (G2 to M transition) by protecting the nucleus from cytoplasmically activated cyclin B1-complexed CDK1 before the onset of mitosis by mediating phosphorylation of CDK1 on 'Tyr-15' (PubMed:15070733, PubMed:7743995, PubMed:8348613, PubMed:8428596). Specifically phosphorylates and inactivates cyclin B1-complexed CDK1 reaching a maximum during G2 phase and a minimum as cells enter M phase (PubMed:7743995, PubMed:8348613, PubMed:8428596). Phosphorylation of cyclin B1-CDK1 occurs exclusively on 'Tyr-15' and phosphorylation of monomeric CDK1 does not occur (PubMed:7743995, PubMed:8348613, PubMed:8428596). Its activity increases during S and G2 phases and decreases at M phase when it is hyperphosphorylated (PubMed:7743995). A correlated decrease in protein level occurs at M/G1 phase, probably due to its degradation (PubMed:7743995). {ECO:0000269|PubMed:15070733, ECO:0000269|PubMed:7743995, ECO:0000269|PubMed:8348613, ECO:0000269|PubMed:8428596}. |
P35222 | CTNNB1 | S33 | psp | Catenin beta-1 (Beta-catenin) | Key downstream component of the canonical Wnt signaling pathway (PubMed:17524503, PubMed:18077326, PubMed:18086858, PubMed:18957423, PubMed:21262353, PubMed:22155184, PubMed:22647378, PubMed:22699938). In the absence of Wnt, forms a complex with AXIN1, AXIN2, APC, CSNK1A1 and GSK3B that promotes phosphorylation on N-terminal Ser and Thr residues and ubiquitination of CTNNB1 via BTRC and its subsequent degradation by the proteasome (PubMed:17524503, PubMed:18077326, PubMed:18086858, PubMed:18957423, PubMed:21262353, PubMed:22155184, PubMed:22647378, PubMed:22699938). In the presence of Wnt ligand, CTNNB1 is not ubiquitinated and accumulates in the nucleus, where it acts as a coactivator for transcription factors of the TCF/LEF family, leading to activate Wnt responsive genes (PubMed:17524503, PubMed:18077326, PubMed:18086858, PubMed:18957423, PubMed:21262353, PubMed:22155184, PubMed:22647378, PubMed:22699938). Also acts as a coactivator for other transcription factors, such as NR5A2 (PubMed:22187462). Promotes epithelial to mesenchymal transition/mesenchymal to epithelial transition (EMT/MET) via driving transcription of CTNNB1/TCF-target genes (PubMed:29910125). Involved in the regulation of cell adhesion, as component of an E-cadherin:catenin adhesion complex (By similarity). Acts as a negative regulator of centrosome cohesion (PubMed:18086858). Involved in the CDK2/PTPN6/CTNNB1/CEACAM1 pathway of insulin internalization (PubMed:21262353). Blocks anoikis of malignant kidney and intestinal epithelial cells and promotes their anchorage-independent growth by down-regulating DAPK2 (PubMed:18957423). Disrupts PML function and PML-NB formation by inhibiting RANBP2-mediated sumoylation of PML (PubMed:22155184). Promotes neurogenesis by maintaining sympathetic neuroblasts within the cell cycle (By similarity). Involved in chondrocyte differentiation via interaction with SOX9: SOX9-binding competes with the binding sites of TCF/LEF within CTNNB1, thereby inhibiting the Wnt signaling (By similarity). Acts as a positive regulator of odontoblast differentiation during mesenchymal tooth germ formation, via promoting the transcription of differentiation factors such as LEF1, BMP2 and BMP4 (By similarity). Activity is repressed in a MSX1-mediated manner at the bell stage of mesenchymal tooth germ formation which prevents premature differentiation of odontoblasts (By similarity). {ECO:0000250|UniProtKB:Q02248, ECO:0000269|PubMed:17524503, ECO:0000269|PubMed:18077326, ECO:0000269|PubMed:18086858, ECO:0000269|PubMed:18957423, ECO:0000269|PubMed:21262353, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22187462, ECO:0000269|PubMed:22647378, ECO:0000269|PubMed:22699938, ECO:0000269|PubMed:29910125}. |
P35568 | IRS1 | S341 | ochoa | Insulin receptor substrate 1 (IRS-1) | Signaling adapter protein that participates in the signal transduction from two prominent receptor tyrosine kinases, insulin receptor/INSR and insulin-like growth factor I receptor/IGF1R (PubMed:7541045, PubMed:33991522, PubMed:38625937). Plays therefore an important role in development, growth, glucose homeostasis as well as lipid metabolism (PubMed:19639489). Upon phosphorylation by the insulin receptor, functions as a signaling scaffold that propagates insulin action through binding to SH2 domain-containing proteins including the p85 regulatory subunit of PI3K, NCK1, NCK2, GRB2 or SHP2 (PubMed:11171109, PubMed:8265614). Recruitment of GRB2 leads to the activation of the guanine nucleotide exchange factor SOS1 which in turn triggers the Ras/Raf/MEK/MAPK signaling cascade (By similarity). Activation of the PI3K/AKT pathway is responsible for most of insulin metabolic effects in the cell, and the Ras/Raf/MEK/MAPK is involved in the regulation of gene expression and in cooperation with the PI3K pathway regulates cell growth and differentiation. Acts a positive regulator of the Wnt/beta-catenin signaling pathway through suppression of DVL2 autophagy-mediated degradation leading to cell proliferation (PubMed:24616100). {ECO:0000250|UniProtKB:P35570, ECO:0000269|PubMed:11171109, ECO:0000269|PubMed:16878150, ECO:0000269|PubMed:19639489, ECO:0000269|PubMed:38625937, ECO:0000269|PubMed:7541045, ECO:0000269|PubMed:8265614}. |
P35611 | ADD1 | S427 | ochoa | Alpha-adducin (Erythrocyte adducin subunit alpha) | Membrane-cytoskeleton-associated protein that promotes the assembly of the spectrin-actin network. Binds to calmodulin. |
P46821 | MAP1B | S1258 | ochoa | Microtubule-associated protein 1B (MAP-1B) [Cleaved into: MAP1B heavy chain; MAP1 light chain LC1] | Facilitates tyrosination of alpha-tubulin in neuronal microtubules (By similarity). Phosphorylated MAP1B is required for proper microtubule dynamics and plays a role in the cytoskeletal changes that accompany neuronal differentiation and neurite extension (PubMed:33268592). Possibly MAP1B binds to at least two tubulin subunits in the polymer, and this bridging of subunits might be involved in nucleating microtubule polymerization and in stabilizing microtubules. Acts as a positive cofactor in DAPK1-mediated autophagic vesicle formation and membrane blebbing. {ECO:0000250, ECO:0000269|PubMed:18195017, ECO:0000269|PubMed:33268592}. |
P49792 | RANBP2 | S792 | ochoa | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
P49792 | RANBP2 | S2566 | ochoa | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
P49815 | TSC2 | S1379 | ochoa | Tuberin (Tuberous sclerosis 2 protein) | Catalytic component of the TSC-TBC complex, a multiprotein complex that acts as a negative regulator of the canonical mTORC1 complex, an evolutionarily conserved central nutrient sensor that stimulates anabolic reactions and macromolecule biosynthesis to promote cellular biomass generation and growth (PubMed:12172553, PubMed:12271141, PubMed:12842888, PubMed:12906785, PubMed:15340059, PubMed:22819219, PubMed:24529379, PubMed:28215400, PubMed:33436626, PubMed:35772404). Within the TSC-TBC complex, TSC2 acts as a GTPase-activating protein (GAP) for the small GTPase RHEB, a direct activator of the protein kinase activity of mTORC1 (PubMed:12172553, PubMed:12820960, PubMed:12842888, PubMed:12906785, PubMed:15340059, PubMed:22819219, PubMed:24529379, PubMed:33436626). In absence of nutrients, the TSC-TBC complex inhibits mTORC1, thereby preventing phosphorylation of ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1) by the mTORC1 signaling (PubMed:12172553, PubMed:12271141, PubMed:12842888, PubMed:12906785, PubMed:22819219, PubMed:24529379, PubMed:28215400, PubMed:35772404). The TSC-TBC complex is inactivated in response to nutrients, relieving inhibition of mTORC1 (PubMed:12172553, PubMed:24529379). Involved in microtubule-mediated protein transport via its ability to regulate mTORC1 signaling (By similarity). Also stimulates the intrinsic GTPase activity of the Ras-related proteins RAP1A and RAB5 (By similarity). {ECO:0000250|UniProtKB:P49816, ECO:0000269|PubMed:12172553, ECO:0000269|PubMed:12271141, ECO:0000269|PubMed:12820960, ECO:0000269|PubMed:12842888, ECO:0000269|PubMed:12906785, ECO:0000269|PubMed:15340059, ECO:0000269|PubMed:22819219, ECO:0000269|PubMed:24529379, ECO:0000269|PubMed:28215400, ECO:0000269|PubMed:33436626, ECO:0000269|PubMed:35772404}. |
P56524 | HDAC4 | S632 | ochoa|psp | Histone deacetylase 4 (HD4) (EC 3.5.1.98) | Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation via its interaction with the myocyte enhancer factors such as MEF2A, MEF2C and MEF2D. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Deacetylates HSPA1A and HSPA1B at 'Lys-77' leading to their preferential binding to co-chaperone STUB1 (PubMed:27708256). {ECO:0000269|PubMed:10523670, ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:27708256}. |
P57682 | KLF3 | S74 | ochoa | Krueppel-like factor 3 (Basic krueppel-like factor) (CACCC-box-binding protein BKLF) (TEF-2) | Binds to the CACCC box of erythroid cell-expressed genes. May play a role in hematopoiesis (By similarity). {ECO:0000250}. |
P78310 | CXADR | S293 | ochoa|psp | Coxsackievirus and adenovirus receptor (CAR) (hCAR) (CVB3-binding protein) (Coxsackievirus B-adenovirus receptor) (HCVADR) | Component of the epithelial apical junction complex that may function as a homophilic cell adhesion molecule and is essential for tight junction integrity. Also involved in transepithelial migration of leukocytes through adhesive interactions with JAML a transmembrane protein of the plasma membrane of leukocytes. The interaction between both receptors also mediates the activation of gamma-delta T-cells, a subpopulation of T-cells residing in epithelia and involved in tissue homeostasis and repair. Upon epithelial CXADR-binding, JAML induces downstream cell signaling events in gamma-delta T-cells through PI3-kinase and MAP kinases. It results in proliferation and production of cytokines and growth factors by T-cells that in turn stimulate epithelial tissues repair. {ECO:0000269|PubMed:11734628, ECO:0000269|PubMed:12297051, ECO:0000269|PubMed:15800062, ECO:0000269|PubMed:19064666, ECO:0000269|PubMed:9096397}.; FUNCTION: (Microbial infection) Acts as a receptor for adenovirus type C. {ECO:0000269|PubMed:10567268, ECO:0000269|PubMed:10666333, ECO:0000269|PubMed:12297051, ECO:0000269|PubMed:9733828}.; FUNCTION: (Microbial infection) Acts as a receptor for Coxsackievirus B1 to B6. {ECO:0000269|PubMed:10814575, ECO:0000269|PubMed:14978041}. |
P78310 | CXADR | S297 | ochoa | Coxsackievirus and adenovirus receptor (CAR) (hCAR) (CVB3-binding protein) (Coxsackievirus B-adenovirus receptor) (HCVADR) | Component of the epithelial apical junction complex that may function as a homophilic cell adhesion molecule and is essential for tight junction integrity. Also involved in transepithelial migration of leukocytes through adhesive interactions with JAML a transmembrane protein of the plasma membrane of leukocytes. The interaction between both receptors also mediates the activation of gamma-delta T-cells, a subpopulation of T-cells residing in epithelia and involved in tissue homeostasis and repair. Upon epithelial CXADR-binding, JAML induces downstream cell signaling events in gamma-delta T-cells through PI3-kinase and MAP kinases. It results in proliferation and production of cytokines and growth factors by T-cells that in turn stimulate epithelial tissues repair. {ECO:0000269|PubMed:11734628, ECO:0000269|PubMed:12297051, ECO:0000269|PubMed:15800062, ECO:0000269|PubMed:19064666, ECO:0000269|PubMed:9096397}.; FUNCTION: (Microbial infection) Acts as a receptor for adenovirus type C. {ECO:0000269|PubMed:10567268, ECO:0000269|PubMed:10666333, ECO:0000269|PubMed:12297051, ECO:0000269|PubMed:9733828}.; FUNCTION: (Microbial infection) Acts as a receptor for Coxsackievirus B1 to B6. {ECO:0000269|PubMed:10814575, ECO:0000269|PubMed:14978041}. |
P78559 | MAP1A | S1214 | 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. |
P78559 | MAP1A | S1322 | 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. |
Q00536 | CDK16 | S82 | ochoa|psp | Cyclin-dependent kinase 16 (EC 2.7.11.22) (Cell division protein kinase 16) (PCTAIRE-motif protein kinase 1) (Serine/threonine-protein kinase PCTAIRE-1) | Protein kinase that plays a role in vesicle-mediated transport processes and exocytosis. Regulates GH1 release by brain neurons. Phosphorylates NSF, and thereby regulates NSF oligomerization. Required for normal spermatogenesis. Regulates neuron differentiation and dendrite development (By similarity). Plays a role in the regulation of insulin secretion in response to changes in blood glucose levels. Can phosphorylate CCNY at 'Ser-336' (in vitro). {ECO:0000250, ECO:0000269|PubMed:22184064, ECO:0000269|PubMed:22796189, ECO:0000269|PubMed:22798068}. |
Q01082 | SPTBN1 | S2165 | ochoa | Spectrin beta chain, non-erythrocytic 1 (Beta-II spectrin) (Fodrin beta chain) (Spectrin, non-erythroid beta chain 1) | Fodrin, which seems to be involved in secretion, interacts with calmodulin in a calcium-dependent manner and is thus candidate for the calcium-dependent movement of the cytoskeleton at the membrane. Plays a critical role in central nervous system development and function. {ECO:0000269|PubMed:34211179}. |
Q03164 | KMT2A | S3511 | 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}. |
Q04656 | ATP7A | S353 | ochoa | Copper-transporting ATPase 1 (EC 7.2.2.8) (Copper pump 1) (Menkes disease-associated protein) | ATP-driven copper (Cu(+)) ion pump that plays an important role in intracellular copper ion homeostasis (PubMed:10419525, PubMed:11092760, PubMed:28389643). Within a catalytic cycle, acquires Cu(+) ion from donor protein on the cytoplasmic side of the membrane and delivers it to acceptor protein on the lumenal side. The transfer of Cu(+) ion across the membrane is coupled to ATP hydrolysis and is associated with a transient phosphorylation that shifts the pump conformation from inward-facing to outward-facing state (PubMed:10419525, PubMed:19453293, PubMed:19917612, PubMed:28389643, PubMed:31283225). Under physiological conditions, at low cytosolic copper concentration, it is localized at the trans-Golgi network (TGN) where it transfers Cu(+) ions to cuproenzymes of the secretory pathway (PubMed:11092760, PubMed:28389643). Upon elevated cytosolic copper concentrations, it relocalizes to the plasma membrane where it is responsible for the export of excess Cu(+) ions (PubMed:10419525, PubMed:28389643). May play a dual role in neuron function and survival by regulating cooper efflux and neuronal transmission at the synapse as well as by supplying Cu(+) ions to enzymes such as PAM, TYR and SOD3 (By similarity) (PubMed:28389643). In the melanosomes of pigmented cells, provides copper cofactor to TYR to form an active TYR holoenzyme for melanin biosynthesis (By similarity). {ECO:0000250|UniProtKB:Q64430, ECO:0000269|PubMed:10419525, ECO:0000269|PubMed:11092760, ECO:0000269|PubMed:19453293, ECO:0000269|PubMed:19917612, ECO:0000269|PubMed:28389643, ECO:0000269|PubMed:31283225}. |
Q08495 | DMTN | S22 | ochoa | Dematin (Dematin actin-binding protein) (Erythrocyte membrane protein band 4.9) | Membrane-cytoskeleton-associated protein with F-actin-binding activity that induces F-actin bundles formation and stabilization. Its F-actin-bundling activity is reversibly regulated upon its phosphorylation by the cAMP-dependent protein kinase A (PKA). Binds to the erythrocyte membrane glucose transporter-1 SLC2A1/GLUT1, and hence stabilizes and attaches the spectrin-actin network to the erythrocytic plasma membrane. Plays a role in maintaining the functional integrity of PKA-activated erythrocyte shape and the membrane mechanical properties. Also plays a role as a modulator of actin dynamics in fibroblasts; acts as a negative regulator of the RhoA activation pathway. In platelets, functions as a regulator of internal calcium mobilization across the dense tubular system that affects platelet granule secretion pathways and aggregation. Also required for the formation of a diverse set of cell protrusions, such as filopodia and lamellipodia, necessary for platelet cell spreading, motility and migration. Acts as a tumor suppressor and inhibits malignant cell transformation. {ECO:0000269|PubMed:10565303, ECO:0000269|PubMed:11856323, ECO:0000269|PubMed:18347014, ECO:0000269|PubMed:19241372, ECO:0000269|PubMed:22927433, ECO:0000269|PubMed:23355471}. |
Q09666 | AHNAK | S212 | ochoa | Neuroblast differentiation-associated protein AHNAK (Desmoyokin) | May be required for neuronal cell differentiation. |
Q09666 | AHNAK | S216 | ochoa | Neuroblast differentiation-associated protein AHNAK (Desmoyokin) | May be required for neuronal cell differentiation. |
Q09666 | AHNAK | S5735 | ochoa | Neuroblast differentiation-associated protein AHNAK (Desmoyokin) | May be required for neuronal cell differentiation. |
Q12797 | ASPH | S20 | ochoa | Aspartyl/asparaginyl beta-hydroxylase (EC 1.14.11.16) (Aspartate beta-hydroxylase) (ASP beta-hydroxylase) (Peptide-aspartate beta-dioxygenase) | [Isoform 1]: Specifically hydroxylates an Asp or Asn residue in certain epidermal growth factor-like (EGF) domains of a number of proteins. {ECO:0000269|PubMed:11773073}.; FUNCTION: [Isoform 8]: Membrane-bound Ca(2+)-sensing protein, which is a structural component of the ER-plasma membrane junctions. Isoform 8 regulates the activity of Ca(+2) released-activated Ca(+2) (CRAC) channels in T-cells. {ECO:0000269|PubMed:22586105}. |
Q12888 | TP53BP1 | S1642 | ochoa | TP53-binding protein 1 (53BP1) (p53-binding protein 1) (p53BP1) | Double-strand break (DSB) repair protein involved in response to DNA damage, telomere dynamics and class-switch recombination (CSR) during antibody genesis (PubMed:12364621, PubMed:17190600, PubMed:21144835, PubMed:22553214, PubMed:23333306, PubMed:27153538, PubMed:28241136, PubMed:31135337, PubMed:37696958). Plays a key role in the repair of double-strand DNA breaks (DSBs) in response to DNA damage by promoting non-homologous end joining (NHEJ)-mediated repair of DSBs and specifically counteracting the function of the homologous recombination (HR) repair protein BRCA1 (PubMed:22553214, PubMed:23333306, PubMed:23727112, PubMed:27153538, PubMed:31135337). In response to DSBs, phosphorylation by ATM promotes interaction with RIF1 and dissociation from NUDT16L1/TIRR, leading to recruitment to DSBs sites (PubMed:28241136). Recruited to DSBs sites by recognizing and binding histone H2A monoubiquitinated at 'Lys-15' (H2AK15Ub) and histone H4 dimethylated at 'Lys-20' (H4K20me2), two histone marks that are present at DSBs sites (PubMed:17190600, PubMed:23760478, PubMed:27153538, PubMed:28241136). Required for immunoglobulin class-switch recombination (CSR) during antibody genesis, a process that involves the generation of DNA DSBs (PubMed:23345425). Participates in the repair and the orientation of the broken DNA ends during CSR (By similarity). In contrast, it is not required for classic NHEJ and V(D)J recombination (By similarity). Promotes NHEJ of dysfunctional telomeres via interaction with PAXIP1 (PubMed:23727112). {ECO:0000250|UniProtKB:P70399, ECO:0000269|PubMed:12364621, ECO:0000269|PubMed:17190600, ECO:0000269|PubMed:21144835, ECO:0000269|PubMed:22553214, ECO:0000269|PubMed:23333306, ECO:0000269|PubMed:23345425, ECO:0000269|PubMed:23727112, ECO:0000269|PubMed:23760478, ECO:0000269|PubMed:27153538, ECO:0000269|PubMed:28241136, ECO:0000269|PubMed:31135337, ECO:0000269|PubMed:37696958}. |
Q13191 | CBLB | S525 | ochoa | E3 ubiquitin-protein ligase CBL-B (EC 2.3.2.27) (Casitas B-lineage lymphoma proto-oncogene b) (RING finger protein 56) (RING-type E3 ubiquitin transferase CBL-B) (SH3-binding protein CBL-B) (Signal transduction protein CBL-B) | E3 ubiquitin-protein ligase which accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and transfers it to substrates, generally promoting their degradation by the proteasome. Negatively regulates TCR (T-cell receptor), BCR (B-cell receptor) and FCER1 (high affinity immunoglobulin epsilon receptor) signal transduction pathways. In naive T-cells, inhibits VAV1 activation upon TCR engagement and imposes a requirement for CD28 costimulation for proliferation and IL-2 production. Also acts by promoting PIK3R1/p85 ubiquitination, which impairs its recruitment to the TCR and subsequent activation. In activated T-cells, inhibits PLCG1 activation and calcium mobilization upon restimulation and promotes anergy. In B-cells, acts by ubiquitinating SYK and promoting its proteasomal degradation. Slightly promotes SRC ubiquitination. May be involved in EGFR ubiquitination and internalization. May be functionally coupled with the E2 ubiquitin-protein ligase UB2D3. In association with CBL, required for proper feedback inhibition of ciliary platelet-derived growth factor receptor-alpha (PDGFRA) signaling pathway via ubiquitination and internalization of PDGFRA (By similarity). {ECO:0000250|UniProtKB:Q3TTA7, ECO:0000269|PubMed:10022120, ECO:0000269|PubMed:10086340, ECO:0000269|PubMed:11087752, ECO:0000269|PubMed:11526404, ECO:0000269|PubMed:14661060, ECO:0000269|PubMed:20525694}. |
Q13247 | SRSF6 | S299 | ochoa | Serine/arginine-rich splicing factor 6 (Pre-mRNA-splicing factor SRP55) (Splicing factor, arginine/serine-rich 6) | Plays a role in constitutive splicing and modulates the selection of alternative splice sites. Plays a role in the alternative splicing of MAPT/Tau exon 10. Binds to alternative exons of TNC pre-mRNA and promotes the expression of alternatively spliced TNC. Plays a role in wound healing and in the regulation of keratinocyte differentiation and proliferation via its role in alternative splicing. {ECO:0000269|PubMed:12549914, ECO:0000269|PubMed:15009664, ECO:0000269|PubMed:22767602, ECO:0000269|PubMed:24440982}. |
Q13409 | DYNC1I2 | S97 | ochoa | Cytoplasmic dynein 1 intermediate chain 2 (Cytoplasmic dynein intermediate chain 2) (Dynein intermediate chain 2, cytosolic) (DH IC-2) | Acts as one of several non-catalytic accessory components of the cytoplasmic dynein 1 complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function (PubMed:31079899). Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules (PubMed:31079899). The intermediate chains mediate the binding of dynein to dynactin via its 150 kDa component (p150-glued) DCTN1 (By similarity). Involved in membrane-transport, such as Golgi apparatus, late endosomes and lysosomes (By similarity). {ECO:0000250|UniProtKB:Q62871, ECO:0000269|PubMed:31079899}. |
Q13428 | TCOF1 | S160 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q13501 | SQSTM1 | S287 | ochoa | Sequestosome-1 (EBI3-associated protein of 60 kDa) (EBIAP) (p60) (Phosphotyrosine-independent ligand for the Lck SH2 domain of 62 kDa) (Ubiquitin-binding protein p62) (p62) | Molecular adapter required for selective macroautophagy (aggrephagy) by acting as a bridge between polyubiquitinated proteins and autophagosomes (PubMed:15340068, PubMed:15953362, PubMed:16286508, PubMed:17580304, PubMed:20168092, PubMed:22017874, PubMed:22622177, PubMed:24128730, PubMed:28404643, PubMed:29343546, PubMed:29507397, PubMed:31857589, PubMed:33509017, PubMed:34471133, PubMed:34893540, PubMed:35831301, PubMed:37306101, PubMed:37802024). Promotes the recruitment of ubiquitinated cargo proteins to autophagosomes via multiple domains that bridge proteins and organelles in different steps (PubMed:16286508, PubMed:20168092, PubMed:22622177, PubMed:24128730, PubMed:28404643, PubMed:29343546, PubMed:29507397, PubMed:34893540, PubMed:37802024). SQSTM1 first mediates the assembly and removal of ubiquitinated proteins by undergoing liquid-liquid phase separation upon binding to ubiquitinated proteins via its UBA domain, leading to the formation of insoluble cytoplasmic inclusions, known as p62 bodies (PubMed:15911346, PubMed:20168092, PubMed:22017874, PubMed:24128730, PubMed:29343546, PubMed:29507397, PubMed:31857589, PubMed:37802024). SQSTM1 then interacts with ATG8 family proteins on autophagosomes via its LIR motif, leading to p62 body recruitment to autophagosomes, followed by autophagic clearance of ubiquitinated proteins (PubMed:16286508, PubMed:17580304, PubMed:20168092, PubMed:22622177, PubMed:24128730, PubMed:28404643, PubMed:37802024). SQSTM1 is itself degraded along with its ubiquitinated cargos (PubMed:16286508, PubMed:17580304, PubMed:37802024). Also required to recruit ubiquitinated proteins to PML bodies in the nucleus (PubMed:20168092). Also involved in autophagy of peroxisomes (pexophagy) in response to reactive oxygen species (ROS) by acting as a bridge between ubiquitinated PEX5 receptor and autophagosomes (PubMed:26344566). Acts as an activator of the NFE2L2/NRF2 pathway via interaction with KEAP1: interaction inactivates the BCR(KEAP1) complex by sequestering the complex in inclusion bodies, promoting nuclear accumulation of NFE2L2/NRF2 and subsequent expression of cytoprotective genes (PubMed:20452972, PubMed:28380357, PubMed:33393215, PubMed:37306101). Promotes relocalization of 'Lys-63'-linked ubiquitinated STING1 to autophagosomes (PubMed:29496741). Involved in endosome organization by retaining vesicles in the perinuclear cloud: following ubiquitination by RNF26, attracts specific vesicle-associated adapters, forming a molecular bridge that restrains cognate vesicles in the perinuclear region and organizes the endosomal pathway for efficient cargo transport (PubMed:27368102, PubMed:33472082). Sequesters tensin TNS2 into cytoplasmic puncta, promoting TNS2 ubiquitination and proteasomal degradation (PubMed:25101860). May regulate the activation of NFKB1 by TNF-alpha, nerve growth factor (NGF) and interleukin-1 (PubMed:10356400, PubMed:10747026, PubMed:11244088, PubMed:12471037, PubMed:16079148, PubMed:19931284). May play a role in titin/TTN downstream signaling in muscle cells (PubMed:15802564). Adapter that mediates the interaction between TRAF6 and CYLD (By similarity). {ECO:0000250|UniProtKB:Q64337, ECO:0000269|PubMed:10356400, ECO:0000269|PubMed:10747026, ECO:0000269|PubMed:11244088, ECO:0000269|PubMed:12471037, ECO:0000269|PubMed:15340068, ECO:0000269|PubMed:15802564, ECO:0000269|PubMed:15911346, ECO:0000269|PubMed:15953362, ECO:0000269|PubMed:16079148, ECO:0000269|PubMed:16286508, ECO:0000269|PubMed:17580304, ECO:0000269|PubMed:19931284, ECO:0000269|PubMed:20168092, ECO:0000269|PubMed:20452972, ECO:0000269|PubMed:22017874, ECO:0000269|PubMed:22622177, ECO:0000269|PubMed:24128730, ECO:0000269|PubMed:25101860, ECO:0000269|PubMed:26344566, ECO:0000269|PubMed:27368102, ECO:0000269|PubMed:28380357, ECO:0000269|PubMed:28404643, ECO:0000269|PubMed:29343546, ECO:0000269|PubMed:29496741, ECO:0000269|PubMed:29507397, ECO:0000269|PubMed:31857589, ECO:0000269|PubMed:33393215, ECO:0000269|PubMed:33472082, ECO:0000269|PubMed:33509017, ECO:0000269|PubMed:34471133, ECO:0000269|PubMed:34893540, ECO:0000269|PubMed:35831301, ECO:0000269|PubMed:37306101, ECO:0000269|PubMed:37802024}. |
Q13905 | RAPGEF1 | S345 | ochoa | Rap guanine nucleotide exchange factor 1 (CRK SH3-binding GNRP) (Guanine nucleotide-releasing factor 2) (Protein C3G) | Guanine nucleotide-releasing protein that binds to SH3 domain of CRK and GRB2/ASH. Transduces signals from CRK to activate RAS. Involved in cell branching and adhesion mediated by BCAR1-CRK-RAPGEF1 signaling and activation of RAP1 (PubMed:12432078). Plays a role in the establishment of basal endothelial barrier function. Plays a role in nerve growth factor (NGF)-induced sustained activation of Rap1 and neurite outgrowth. {ECO:0000269|PubMed:12432078, ECO:0000269|PubMed:17724123, ECO:0000269|PubMed:21840392, ECO:0000269|PubMed:7806500}. |
Q14162 | SCARF1 | S749 | ochoa | Scavenger receptor class F member 1 (Acetyl LDL receptor) (Scavenger receptor expressed by endothelial cells 1) (SREC-I) | Mediates the binding and degradation of acetylated low density lipoprotein (Ac-LDL). Mediates heterophilic interactions, suggesting a function as adhesion protein. Plays a role in the regulation of neurite-like outgrowth (By similarity). {ECO:0000250}. |
Q14244 | MAP7 | S165 | ochoa | Ensconsin (Epithelial microtubule-associated protein of 115 kDa) (E-MAP-115) (Microtubule-associated protein 7) (MAP-7) | Microtubule-stabilizing protein that may play an important role during reorganization of microtubules during polarization and differentiation of epithelial cells. Associates with microtubules in a dynamic manner. May play a role in the formation of intercellular contacts. Colocalization with TRPV4 results in the redistribution of TRPV4 toward the membrane and may link cytoskeletal microfilaments. {ECO:0000269|PubMed:11719555, ECO:0000269|PubMed:8408219, ECO:0000269|PubMed:9989799}. |
Q14687 | GSE1 | S80 | ochoa | Genetic suppressor element 1 | None |
Q14687 | GSE1 | T91 | ochoa | Genetic suppressor element 1 | None |
Q15746 | MYLK | S1772 | ochoa|psp | Myosin light chain kinase, smooth muscle (MLCK) (smMLCK) (EC 2.7.11.18) (Kinase-related protein) (KRP) (Telokin) [Cleaved into: Myosin light chain kinase, smooth muscle, deglutamylated form] | Calcium/calmodulin-dependent myosin light chain kinase implicated in smooth muscle contraction via phosphorylation of myosin light chains (MLC). Also regulates actin-myosin interaction through a non-kinase activity. Phosphorylates PTK2B/PYK2 and myosin light-chains. Involved in the inflammatory response (e.g. apoptosis, vascular permeability, leukocyte diapedesis), cell motility and morphology, airway hyperreactivity and other activities relevant to asthma. Required for tonic airway smooth muscle contraction that is necessary for physiological and asthmatic airway resistance. Necessary for gastrointestinal motility. Implicated in the regulation of endothelial as well as vascular permeability, probably via the regulation of cytoskeletal rearrangements. In the nervous system it has been shown to control the growth initiation of astrocytic processes in culture and to participate in transmitter release at synapses formed between cultured sympathetic ganglion cells. Critical participant in signaling sequences that result in fibroblast apoptosis. Plays a role in the regulation of epithelial cell survival. Required for epithelial wound healing, especially during actomyosin ring contraction during purse-string wound closure. Mediates RhoA-dependent membrane blebbing. Triggers TRPC5 channel activity in a calcium-dependent signaling, by inducing its subcellular localization at the plasma membrane. Promotes cell migration (including tumor cells) and tumor metastasis. PTK2B/PYK2 activation by phosphorylation mediates ITGB2 activation and is thus essential to trigger neutrophil transmigration during acute lung injury (ALI). May regulate optic nerve head astrocyte migration. Probably involved in mitotic cytoskeletal regulation. Regulates tight junction probably by modulating ZO-1 exchange in the perijunctional actomyosin ring. Mediates burn-induced microvascular barrier injury; triggers endothelial contraction in the development of microvascular hyperpermeability by phosphorylating MLC. Essential for intestinal barrier dysfunction. Mediates Giardia spp.-mediated reduced epithelial barrier function during giardiasis intestinal infection via reorganization of cytoskeletal F-actin and tight junctional ZO-1. Necessary for hypotonicity-induced Ca(2+) entry and subsequent activation of volume-sensitive organic osmolyte/anion channels (VSOAC) in cervical cancer cells. Responsible for high proliferative ability of breast cancer cells through anti-apoptosis. {ECO:0000269|PubMed:11113114, ECO:0000269|PubMed:11976941, ECO:0000269|PubMed:15020676, ECO:0000269|PubMed:15825080, ECO:0000269|PubMed:16284075, ECO:0000269|PubMed:16723733, ECO:0000269|PubMed:18587400, ECO:0000269|PubMed:18710790, ECO:0000269|PubMed:19826488, ECO:0000269|PubMed:20139351, ECO:0000269|PubMed:20181817, ECO:0000269|PubMed:20375339, ECO:0000269|PubMed:20453870}. |
Q16204 | CCDC6 | S363 | ochoa | Coiled-coil domain-containing protein 6 (Papillary thyroid carcinoma-encoded protein) (Protein H4) | None |
Q16204 | CCDC6 | S367 | ochoa | Coiled-coil domain-containing protein 6 (Papillary thyroid carcinoma-encoded protein) (Protein H4) | None |
Q16566 | CAMK4 | S356 | ochoa | Calcium/calmodulin-dependent protein kinase type IV (CaMK IV) (EC 2.7.11.17) (CaM kinase-GR) | Calcium/calmodulin-dependent protein kinase that operates in the calcium-triggered CaMKK-CaMK4 signaling cascade and regulates, mainly by phosphorylation, the activity of several transcription activators, such as CREB1, MEF2D, JUN and RORA, which play pivotal roles in immune response, inflammation, and memory consolidation. In the thymus, regulates the CD4(+)/CD8(+) double positive thymocytes selection threshold during T-cell ontogeny. In CD4 memory T-cells, is required to link T-cell antigen receptor (TCR) signaling to the production of IL2, IFNG and IL4 (through the regulation of CREB and MEF2). Regulates the differentiation and survival phases of osteoclasts and dendritic cells (DCs). Mediates DCs survival by linking TLR4 and the regulation of temporal expression of BCL2. Phosphorylates the transcription activator CREB1 on 'Ser-133' in hippocampal neuron nuclei and contribute to memory consolidation and long term potentiation (LTP) in the hippocampus. Can activate the MAP kinases MAPK1/ERK2, MAPK8/JNK1 and MAPK14/p38 and stimulate transcription through the phosphorylation of ELK1 and ATF2. Can also phosphorylate in vitro CREBBP, PRM2, MEF2A and STMN1/OP18. {ECO:0000269|PubMed:10617605, ECO:0000269|PubMed:17909078, ECO:0000269|PubMed:18829949, ECO:0000269|PubMed:7961813, ECO:0000269|PubMed:8065343, ECO:0000269|PubMed:8855261, ECO:0000269|PubMed:8980227, ECO:0000269|PubMed:9154845}. |
Q2LD37 | BLTP1 | S4304 | ochoa | Bridge-like lipid transfer protein family member 1 (Fragile site-associated protein) | Tube-forming lipid transport protein which provides phosphatidylethanolamine for glycosylphosphatidylinositol (GPI) anchor synthesis in the endoplasmic reticulum (Probable). Plays a role in endosomal trafficking and endosome recycling. Also involved in the actin cytoskeleton and cilia structural dynamics (PubMed:30906834). Acts as a regulator of phagocytosis (PubMed:31540829). {ECO:0000269|PubMed:30906834, ECO:0000269|PubMed:31540829, ECO:0000305|PubMed:35015055, ECO:0000305|PubMed:35491307}. |
Q4G0J3 | LARP7 | S254 | ochoa | La-related protein 7 (La ribonucleoprotein domain family member 7) (hLARP7) (P-TEFb-interaction protein for 7SK stability) (PIP7S) | RNA-binding protein that specifically binds distinct small nuclear RNA (snRNAs) and regulates their processing and function (PubMed:18249148, PubMed:32017898). Specifically binds the 7SK snRNA (7SK RNA) and acts as a core component of the 7SK ribonucleoprotein (RNP) complex, thereby acting as a negative regulator of transcription elongation by RNA polymerase II (PubMed:18249148, PubMed:18483487). The 7SK RNP complex sequesters the positive transcription elongation factor b (P-TEFb) in a large inactive 7SK RNP complex preventing RNA polymerase II phosphorylation and subsequent transcriptional elongation (PubMed:18249148, PubMed:18483487). The 7SK RNP complex also promotes snRNA gene transcription by RNA polymerase II via interaction with the little elongation complex (LEC) (PubMed:28254838). LARP7 specifically binds to the highly conserved 3'-terminal U-rich stretch of 7SK RNA; on stimulation, remains associated with 7SK RNA, whereas P-TEFb is released from the complex (PubMed:18281698, PubMed:18483487). LARP7 also acts as a regulator of mRNA splicing fidelity by promoting U6 snRNA processing (PubMed:32017898). Specifically binds U6 snRNAs and associates with a subset of box C/D RNP complexes: promotes U6 snRNA 2'-O-methylation by facilitating U6 snRNA loading into box C/D RNP complexes (PubMed:32017898). U6 snRNA 2'-O-methylation is required for mRNA splicing fidelity (PubMed:32017898). Binds U6 snRNAs with a 5'-CAGGG-3' sequence motif (PubMed:32017898). U6 snRNA processing is required for spermatogenesis (By similarity). {ECO:0000250|UniProtKB:Q05CL8, ECO:0000269|PubMed:18249148, ECO:0000269|PubMed:18281698, ECO:0000269|PubMed:18483487, ECO:0000269|PubMed:28254838, ECO:0000269|PubMed:32017898}. |
Q504U0 | C4orf46 | S26 | ochoa | Renal cancer differentiation gene 1 protein | None |
Q53GS7 | GLE1 | S92 | ochoa|psp | mRNA export factor GLE1 (hGLE1) (GLE1 RNA export mediator) (GLE1-like protein) (Nucleoporin GLE1) | Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC). {ECO:0000269|PubMed:12668658, ECO:0000269|PubMed:16000379, ECO:0000269|PubMed:9618489}. |
Q53H80 | AKIRIN2 | S121 | ochoa | Akirin-2 | Molecular adapter that acts as a bridge between a variety of multiprotein complexes, and which is involved in embryonic development, immunity, myogenesis and brain development (PubMed:34711951). Plays a key role in nuclear protein degradation by promoting import of proteasomes into the nucleus: directly binds to fully assembled 20S proteasomes at one end and to nuclear import receptor IPO9 at the other end, bridging them together and mediating the import of pre-assembled proteasome complexes through the nuclear pore (PubMed:34711951). Involved in innate immunity by regulating the production of interleukin-6 (IL6) downstream of Toll-like receptor (TLR): acts by bridging the NF-kappa-B inhibitor NFKBIZ and the SWI/SNF complex, leading to promote induction of IL6 (By similarity). Also involved in adaptive immunity by promoting B-cell activation (By similarity). Involved in brain development: required for the survival and proliferation of cerebral cortical progenitor cells (By similarity). Involved in myogenesis: required for skeletal muscle formation and skeletal development, possibly by regulating expression of muscle differentiation factors (By similarity). Also plays a role in facilitating interdigital tissue regression during limb development (By similarity). {ECO:0000250|UniProtKB:B1AXD8, ECO:0000269|PubMed:34711951}. |
Q5T200 | ZC3H13 | S329 | 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}. |
Q5THJ4 | VPS13D | S1038 | ochoa | Intermembrane lipid transfer protein VPS13D (Vacuolar protein sorting-associated protein 13D) | Mediates the transfer of lipids between membranes at organelle contact sites (By similarity). Functions in promoting mitochondrial clearance by mitochondrial autophagy (mitophagy), also possibly by positively regulating mitochondrial fission (PubMed:29307555, PubMed:29604224). Mitophagy plays an important role in regulating cell health and mitochondrial size and homeostasis. {ECO:0000250|UniProtKB:Q07878, ECO:0000269|PubMed:29307555, ECO:0000269|PubMed:29604224}. |
Q5VT52 | RPRD2 | S610 | ochoa | Regulation of nuclear pre-mRNA domain-containing protein 2 | None |
Q63HR2 | TNS2 | S996 | ochoa | Tensin-2 (EC 3.1.3.48) (C1 domain-containing phosphatase and tensin homolog) (C1-TEN) (Tensin-like C1 domain-containing phosphatase) | Tyrosine-protein phosphatase which regulates cell motility, proliferation and muscle-response to insulin (PubMed:15817639, PubMed:23401856). Phosphatase activity is mediated by binding to phosphatidylinositol-3,4,5-triphosphate (PtdIns(3,4,5)P3) via the SH2 domain (PubMed:30092354). In muscles and under catabolic conditions, dephosphorylates IRS1 leading to its degradation and muscle atrophy (PubMed:23401856, PubMed:30092354). Negatively regulates PI3K-AKT pathway activation (PubMed:15817639, PubMed:23401856, PubMed:30092354). Dephosphorylates nephrin NPHS1 in podocytes which regulates activity of the mTORC1 complex (PubMed:28955049). Under normal glucose conditions, NPHS1 outcompetes IRS1 for binding to phosphatidylinositol 3-kinase (PI3K) which balances mTORC1 activity but high glucose conditions lead to up-regulation of TNS2, increased NPHS1 dephosphorylation and activation of mTORC1, contributing to podocyte hypertrophy and proteinuria (PubMed:28955049). Required for correct podocyte morphology, podocyte-glomerular basement membrane interaction and integrity of the glomerular filtration barrier (By similarity). Enhances RHOA activation in the presence of DLC1 (PubMed:26427649). Plays a role in promoting DLC1-dependent remodeling of the extracellular matrix (PubMed:20069572). {ECO:0000250|UniProtKB:Q8CGB6, ECO:0000269|PubMed:15817639, ECO:0000269|PubMed:20069572, ECO:0000269|PubMed:23401856, ECO:0000269|PubMed:26427649, ECO:0000269|PubMed:28955049, ECO:0000269|PubMed:30092354}. |
Q658Y4 | FAM91A1 | T351 | ochoa | Protein FAM91A1 | As component of the WDR11 complex acts together with TBC1D23 to facilitate the golgin-mediated capture of vesicles generated using AP-1. {ECO:0000269|PubMed:29426865}. |
Q659A1 | ICE2 | S601 | ochoa | Little elongation complex subunit 2 (Interactor of little elongator complex ELL subunit 2) (NMDA receptor-regulated protein 2) | Component of the little elongation complex (LEC), a complex required to regulate small nuclear RNA (snRNA) gene transcription by RNA polymerase II and III. {ECO:0000269|PubMed:23932780}. |
Q68CZ2 | TNS3 | S683 | ochoa | Tensin-3 (EC 3.1.3.-) (Tensin-like SH2 domain-containing protein 1) (Tumor endothelial marker 6) | May act as a protein phosphatase and/or a lipid phosphatase (Probable). Involved in the dissociation of the integrin-tensin-actin complex (PubMed:17643115). EGF activates TNS4 and down-regulates TNS3 which results in capping the tail of ITGB1 (PubMed:17643115). Increases DOCK5 guanine nucleotide exchange activity towards Rac and plays a role in osteoclast podosome organization (By similarity). Enhances RHOA activation in the presence of DLC1 (PubMed:26427649). Required for growth factor-induced epithelial cell migration; growth factor stimulation induces TNS3 phosphorylation which changes its binding preference from DLC1 to the p85 regulatory subunit of the PI3K kinase complex, displacing PI3K inhibitor PTEN and resulting in translocation of the TNS3-p85 complex to the leading edge of migrating cells to promote RAC1 activation (PubMed:26166433). Meanwhile, PTEN switches binding preference from p85 to DLC1 and the PTEN-DLC1 complex translocates to the posterior of migrating cells to activate RHOA (PubMed:26166433). Acts as an adapter protein by bridging the association of scaffolding protein PEAK1 with integrins ITGB1, ITGB3 and ITGB5 which contributes to the promotion of cell migration (PubMed:35687021). Controls tonsil-derived mesenchymal stem cell proliferation and differentiation by regulating the activity of integrin ITGB1 (PubMed:31905841). {ECO:0000250|UniProtKB:Q5SSZ5, ECO:0000269|PubMed:17643115, ECO:0000269|PubMed:26166433, ECO:0000269|PubMed:26427649, ECO:0000269|PubMed:31905841, ECO:0000269|PubMed:35687021, ECO:0000305}. |
Q68CZ2 | TNS3 | S1119 | ochoa | Tensin-3 (EC 3.1.3.-) (Tensin-like SH2 domain-containing protein 1) (Tumor endothelial marker 6) | May act as a protein phosphatase and/or a lipid phosphatase (Probable). Involved in the dissociation of the integrin-tensin-actin complex (PubMed:17643115). EGF activates TNS4 and down-regulates TNS3 which results in capping the tail of ITGB1 (PubMed:17643115). Increases DOCK5 guanine nucleotide exchange activity towards Rac and plays a role in osteoclast podosome organization (By similarity). Enhances RHOA activation in the presence of DLC1 (PubMed:26427649). Required for growth factor-induced epithelial cell migration; growth factor stimulation induces TNS3 phosphorylation which changes its binding preference from DLC1 to the p85 regulatory subunit of the PI3K kinase complex, displacing PI3K inhibitor PTEN and resulting in translocation of the TNS3-p85 complex to the leading edge of migrating cells to promote RAC1 activation (PubMed:26166433). Meanwhile, PTEN switches binding preference from p85 to DLC1 and the PTEN-DLC1 complex translocates to the posterior of migrating cells to activate RHOA (PubMed:26166433). Acts as an adapter protein by bridging the association of scaffolding protein PEAK1 with integrins ITGB1, ITGB3 and ITGB5 which contributes to the promotion of cell migration (PubMed:35687021). Controls tonsil-derived mesenchymal stem cell proliferation and differentiation by regulating the activity of integrin ITGB1 (PubMed:31905841). {ECO:0000250|UniProtKB:Q5SSZ5, ECO:0000269|PubMed:17643115, ECO:0000269|PubMed:26166433, ECO:0000269|PubMed:26427649, ECO:0000269|PubMed:31905841, ECO:0000269|PubMed:35687021, ECO:0000305}. |
Q68EM7 | ARHGAP17 | S610 | ochoa | Rho GTPase-activating protein 17 (Rho-type GTPase-activating protein 17) (RhoGAP interacting with CIP4 homologs protein 1) (RICH-1) | Rho GTPase-activating protein involved in the maintenance of tight junction by regulating the activity of CDC42, thereby playing a central role in apical polarity of epithelial cells. Specifically acts as a GTPase activator for the CDC42 GTPase by converting it to an inactive GDP-bound state. The complex formed with AMOT acts by regulating the uptake of polarity proteins at tight junctions, possibly by deciding whether tight junction transmembrane proteins are recycled back to the plasma membrane or sent elsewhere. Participates in the Ca(2+)-dependent regulation of exocytosis, possibly by catalyzing GTPase activity of Rho family proteins and by inducing the reorganization of the cortical actin filaments. Acts as a GTPase activator in vitro for RAC1. {ECO:0000269|PubMed:11431473, ECO:0000269|PubMed:16678097}. |
Q6GQQ9 | OTUD7B | S453 | ochoa | OTU domain-containing protein 7B (EC 3.4.19.12) (Cellular zinc finger anti-NF-kappa-B protein) (Cezanne) (Zinc finger A20 domain-containing protein 1) (Zinc finger protein Cezanne) | Negative regulator of the non-canonical NF-kappa-B pathway that acts by mediating deubiquitination of TRAF3, an inhibitor of the NF-kappa-B pathway, thereby acting as a negative regulator of B-cell responses (PubMed:18178551). In response to non-canonical NF-kappa-B stimuli, deubiquitinates 'Lys-48'-linked polyubiquitin chains of TRAF3, preventing TRAF3 proteolysis and over-activation of non-canonical NF-kappa-B (By similarity). Negatively regulates mucosal immunity against infections (By similarity). Deubiquitinates ZAP70, and thereby regulates T cell receptor (TCR) signaling that leads to the activation of NF-kappa-B (PubMed:26903241). Plays a role in T cell homeostasis and is required for normal T cell responses, including production of IFNG and IL2 (By similarity). Mediates deubiquitination of EGFR (PubMed:22179831). Has deubiquitinating activity toward 'Lys-11', 'Lys-48' and 'Lys-63'-linked polyubiquitin chains (PubMed:11463333, PubMed:20622874, PubMed:23827681, PubMed:27732584). Has a much higher catalytic rate with 'Lys-11'-linked polyubiquitin chains (in vitro); however the physiological significance of these data are unsure (PubMed:27732584). Hydrolyzes both linear and branched forms of polyubiquitin (PubMed:12682062). Acts as a regulator of mTORC1 and mTORC2 assembly by mediating 'Lys-63'-linked deubiquitination of MLST8, thereby promoting assembly of the mTORC2 complex, while inibiting formation of the mTORC1 complex (PubMed:28489822). {ECO:0000250|UniProtKB:B2RUR8, ECO:0000269|PubMed:11463333, ECO:0000269|PubMed:12682062, ECO:0000269|PubMed:18178551, ECO:0000269|PubMed:20622874, ECO:0000269|PubMed:22179831, ECO:0000269|PubMed:23827681, ECO:0000269|PubMed:26903241, ECO:0000269|PubMed:27732584, ECO:0000269|PubMed:28489822}. |
Q6GQQ9 | OTUD7B | S471 | ochoa | OTU domain-containing protein 7B (EC 3.4.19.12) (Cellular zinc finger anti-NF-kappa-B protein) (Cezanne) (Zinc finger A20 domain-containing protein 1) (Zinc finger protein Cezanne) | Negative regulator of the non-canonical NF-kappa-B pathway that acts by mediating deubiquitination of TRAF3, an inhibitor of the NF-kappa-B pathway, thereby acting as a negative regulator of B-cell responses (PubMed:18178551). In response to non-canonical NF-kappa-B stimuli, deubiquitinates 'Lys-48'-linked polyubiquitin chains of TRAF3, preventing TRAF3 proteolysis and over-activation of non-canonical NF-kappa-B (By similarity). Negatively regulates mucosal immunity against infections (By similarity). Deubiquitinates ZAP70, and thereby regulates T cell receptor (TCR) signaling that leads to the activation of NF-kappa-B (PubMed:26903241). Plays a role in T cell homeostasis and is required for normal T cell responses, including production of IFNG and IL2 (By similarity). Mediates deubiquitination of EGFR (PubMed:22179831). Has deubiquitinating activity toward 'Lys-11', 'Lys-48' and 'Lys-63'-linked polyubiquitin chains (PubMed:11463333, PubMed:20622874, PubMed:23827681, PubMed:27732584). Has a much higher catalytic rate with 'Lys-11'-linked polyubiquitin chains (in vitro); however the physiological significance of these data are unsure (PubMed:27732584). Hydrolyzes both linear and branched forms of polyubiquitin (PubMed:12682062). Acts as a regulator of mTORC1 and mTORC2 assembly by mediating 'Lys-63'-linked deubiquitination of MLST8, thereby promoting assembly of the mTORC2 complex, while inibiting formation of the mTORC1 complex (PubMed:28489822). {ECO:0000250|UniProtKB:B2RUR8, ECO:0000269|PubMed:11463333, ECO:0000269|PubMed:12682062, ECO:0000269|PubMed:18178551, ECO:0000269|PubMed:20622874, ECO:0000269|PubMed:22179831, ECO:0000269|PubMed:23827681, ECO:0000269|PubMed:26903241, ECO:0000269|PubMed:27732584, ECO:0000269|PubMed:28489822}. |
Q6H8Q1 | ABLIM2 | S290 | ochoa | Actin-binding LIM protein 2 (abLIM-2) (Actin-binding LIM protein family member 2) | May act as scaffold protein. May stimulate ABRA activity and ABRA-dependent SRF transcriptional activity. {ECO:0000269|PubMed:17194709}. |
Q6JBY9 | RCSD1 | S116 | ochoa | CapZ-interacting protein (Protein kinase substrate CapZIP) (RCSD domain-containing protein 1) | Stress-induced phosphorylation of CAPZIP may regulate the ability of F-actin-capping protein to remodel actin filament assembly. {ECO:0000269|PubMed:15850461}. |
Q6P3S6 | FBXO42 | S583 | ochoa | F-box only protein 42 (Just one F-box and Kelch domain-containing protein) | Substrate-recognition component of some SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. Specifically recognizes p53/TP53, promoting its ubiquitination and degradation. {ECO:0000269|PubMed:19509332}. |
Q6P996 | PDXDC1 | S714 | ochoa | Pyridoxal-dependent decarboxylase domain-containing protein 1 (EC 4.1.1.-) | None |
Q6R327 | RICTOR | S1581 | ochoa | Rapamycin-insensitive companion of mTOR (AVO3 homolog) (hAVO3) | Component of the mechanistic target of rapamycin complex 2 (mTORC2), which transduces signals from growth factors to pathways involved in proliferation, cytoskeletal organization, lipogenesis and anabolic output (PubMed:15268862, PubMed:15718470, PubMed:19720745, PubMed:19995915, PubMed:21343617, PubMed:33158864, PubMed:35904232, PubMed:35926713). In response to growth factors, mTORC2 phosphorylates and activates AGC protein kinase family members, including AKT (AKT1, AKT2 and AKT3), PKC (PRKCA, PRKCB and PRKCE) and SGK1 (PubMed:19720745, PubMed:19935711, PubMed:19995915). In contrast to mTORC1, mTORC2 is nutrient-insensitive (PubMed:15467718, PubMed:21343617). Within the mTORC2 complex, RICTOR probably acts as a molecular adapter (PubMed:21343617, PubMed:33158864, PubMed:35926713). RICTOR is responsible for the FKBP12-rapamycin-insensitivity of mTORC2 (PubMed:33158864). mTORC2 plays a critical role in AKT1 activation by mediating phosphorylation of different sites depending on the context, such as 'Thr-450', 'Ser-473', 'Ser-477' or 'Thr-479', facilitating the phosphorylation of the activation loop of AKT1 on 'Thr-308' by PDPK1/PDK1 which is a prerequisite for full activation (PubMed:15718470, PubMed:19720745, PubMed:19935711, PubMed:35926713). mTORC2 catalyzes the phosphorylation of SGK1 at 'Ser-422' and of PRKCA on 'Ser-657' (By similarity). The mTORC2 complex also phosphorylates various proteins involved in insulin signaling, such as FBXW8 and IGF2BP1 (By similarity). mTORC2 acts upstream of Rho GTPases to regulate the actin cytoskeleton, probably by activating one or more Rho-type guanine nucleotide exchange factors (PubMed:15467718). mTORC2 promotes the serum-induced formation of stress-fibers or F-actin (PubMed:15467718). {ECO:0000250|UniProtKB:Q6QI06, ECO:0000269|PubMed:15268862, ECO:0000269|PubMed:15467718, ECO:0000269|PubMed:15718470, ECO:0000269|PubMed:19720745, ECO:0000269|PubMed:19935711, ECO:0000269|PubMed:19995915, ECO:0000269|PubMed:21343617, ECO:0000269|PubMed:33158864, ECO:0000269|PubMed:35904232, ECO:0000269|PubMed:35926713}. |
Q6UXY1 | BAIAP2L2 | S227 | 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}. |
Q6VN20 | RANBP10 | S365 | ochoa | Ran-binding protein 10 (RanBP10) | May act as an adapter protein to couple membrane receptors to intracellular signaling pathways (Probable). Core component of the CTLH E3 ubiquitin-protein ligase complex that selectively accepts ubiquitin from UBE2H and mediates ubiquitination and subsequent proteasomal degradation of the transcription factor HBP1 (PubMed:29911972). Enhances dihydrotestosterone-induced transactivation activity of AR, as well as dexamethasone-induced transactivation activity of NR3C1, but does not affect estrogen-induced transactivation (PubMed:18222118). Acts as a guanine nucleotide exchange factor (GEF) for RAN GTPase. May play an essential role in hemostasis and in maintaining microtubule dynamics with respect to both platelet shape and function (By similarity). {ECO:0000250|UniProtKB:Q6VN19, ECO:0000269|PubMed:18222118, ECO:0000269|PubMed:29911972, ECO:0000305}. |
Q6ZNJ1 | NBEAL2 | S1305 | ochoa | Neurobeachin-like protein 2 | Probably involved in thrombopoiesis. Plays a role in the development or secretion of alpha-granules, that contain several growth factors important for platelet biogenesis. {ECO:0000269|PubMed:21765411, ECO:0000269|PubMed:21765412}. |
Q6ZUT6 | CCDC9B | S407 | ochoa | Coiled-coil domain-containing protein 9B | None |
Q7Z3B3 | KANSL1 | S984 | 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}. |
Q7Z3J3 | RGPD4 | S793 | ochoa | RanBP2-like and GRIP domain-containing protein 4 | None |
Q7Z3J3 | RGPD4 | S1591 | ochoa | RanBP2-like and GRIP domain-containing protein 4 | None |
Q86UU0 | BCL9L | S938 | ochoa | B-cell CLL/lymphoma 9-like protein (B-cell lymphoma 9-like protein) (BCL9-like protein) (Protein BCL9-2) | Transcriptional regulator that acts as an activator. Promotes beta-catenin transcriptional activity. Plays a role in tumorigenesis. Enhances the neoplastic transforming activity of CTNNB1 (By similarity). {ECO:0000250}. |
Q86VP3 | PACS2 | S702 | ochoa | Phosphofurin acidic cluster sorting protein 2 (PACS-2) (PACS1-like protein) | Multifunctional sorting protein that controls the endoplasmic reticulum (ER)-mitochondria communication, including the apposition of mitochondria with the ER and ER homeostasis. In addition, in response to apoptotic inducer, translocates BIB to mitochondria, which initiates a sequence of events including the formation of mitochondrial truncated BID, the release of cytochrome c, the activation of caspase-3 thereby causing cell death. May also be involved in ion channel trafficking, directing acidic cluster-containing ion channels to distinct subcellular compartments. {ECO:0000269|PubMed:15692563, ECO:0000269|PubMed:15692567}. |
Q86X29 | LSR | S508 | ochoa | Lipolysis-stimulated lipoprotein receptor (Angulin-1) | Probable role in the clearance of triglyceride-rich lipoprotein from blood. Binds chylomicrons, LDL and VLDL in presence of free fatty acids and allows their subsequent uptake in the cells (By similarity). Maintains epithelial barrier function by recruiting MARVELD2/tricellulin to tricellular tight junctions (By similarity). {ECO:0000250|UniProtKB:Q99KG5, ECO:0000250|UniProtKB:Q9WU74}. |
Q86YD5 | LDLRAD3 | S309 | ochoa | Low-density lipoprotein receptor class A domain-containing protein 3 (LDLR class A domain-containing protein 3) | May influence APP processing, resulting in a decrease in sAPP-alpha production and increased amyloidogenic P3 peptide production. May regulate ITCH and NEDD4 E3 ligase activity and degradation (PubMed:26854353). {ECO:0000250, ECO:0000269|PubMed:26854353}.; FUNCTION: (Microbial infection) Acts as a receptor for Venezuelan equine encephalitis virus. {ECO:0000269|PubMed:33208938, ECO:0000269|PubMed:34646020, ECO:0000269|PubMed:34646021}. |
Q8IX07 | ZFPM1 | S487 | ochoa | Zinc finger protein ZFPM1 (Friend of GATA protein 1) (FOG-1) (Friend of GATA 1) (Zinc finger protein 89A) (Zinc finger protein multitype 1) | Transcription regulator that plays an essential role in erythroid and megakaryocytic cell differentiation. Essential cofactor that acts via the formation of a heterodimer with transcription factors of the GATA family GATA1, GATA2 and GATA3. Such heterodimer can both activate or repress transcriptional activity, depending on the cell and promoter context. The heterodimer formed with GATA proteins is essential to activate expression of genes such as NFE2, ITGA2B, alpha- and beta-globin, while it represses expression of KLF1. May be involved in regulation of some genes in gonads. May also be involved in cardiac development, in a non-redundant way with ZFPM2/FOG2 (By similarity). {ECO:0000250}. |
Q8IYB3 | SRRM1 | S777 | 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}. |
Q8IZD2 | KMT2E | S1355 | ochoa | Inactive histone-lysine N-methyltransferase 2E (Inactive lysine N-methyltransferase 2E) (Myeloid/lymphoid or mixed-lineage leukemia protein 5) | Associates with chromatin regions downstream of transcriptional start sites of active genes and thus regulates gene transcription (PubMed:23629655, PubMed:23798402, PubMed:24130829). Chromatin interaction is mediated via the binding to tri-methylated histone H3 at 'Lys-4' (H3K4me3) (PubMed:23798402, PubMed:24130829). Key regulator of hematopoiesis involved in terminal myeloid differentiation and in the regulation of hematopoietic stem cell (HSCs) self-renewal by a mechanism that involves DNA methylation (By similarity). Also acts as an important cell cycle regulator, participating in cell cycle regulatory network machinery at multiple cell cycle stages including G1/S transition, S phase progression and mitotic entry (PubMed:14718661, PubMed:18573682, PubMed:19264965, PubMed:23629655). Recruited to E2F1 responsive promoters by HCFC1 where it stimulates tri-methylation of histone H3 at 'Lys-4' and transcriptional activation and thereby facilitates G1 to S phase transition (PubMed:23629655). During myoblast differentiation, required to suppress inappropriate expression of S-phase-promoting genes and maintain expression of determination genes in quiescent cells (By similarity). {ECO:0000250|UniProtKB:Q3UG20, ECO:0000269|PubMed:14718661, ECO:0000269|PubMed:18573682, ECO:0000269|PubMed:23629655, ECO:0000269|PubMed:23798402, ECO:0000269|PubMed:24130829}.; FUNCTION: [Isoform NKp44L]: Cellular ligand for NCR2/NKp44, may play a role as a danger signal in cytotoxicity and NK-cell-mediated innate immunity. {ECO:0000269|PubMed:23958951}. |
Q8IZH2 | XRN1 | S1649 | ochoa | 5'-3' exoribonuclease 1 (EC 3.1.13.-) (Strand-exchange protein 1 homolog) | Major 5'-3' exoribonuclease involved in mRNA decay. Required for the 5'-3'-processing of the G4 tetraplex-containing DNA and RNA substrates. The kinetic of hydrolysis is faster for G4 RNA tetraplex than for G4 DNA tetraplex and monomeric RNA tetraplex. Binds to RNA and DNA (By similarity). Plays a role in replication-dependent histone mRNA degradation. May act as a tumor suppressor protein in osteogenic sarcoma (OGS). {ECO:0000250|UniProtKB:P97789, ECO:0000269|PubMed:18172165}. |
Q8IZP0 | ABI1 | S319 | ochoa | Abl interactor 1 (Abelson interactor 1) (Abi-1) (Abl-binding protein 4) (AblBP4) (Eps8 SH3 domain-binding protein) (Eps8-binding protein) (Nap1-binding protein) (Nap1BP) (Spectrin SH3 domain-binding protein 1) (e3B1) | May act in negative regulation of cell growth and transformation by interacting with nonreceptor tyrosine kinases ABL1 and/or ABL2. May play a role in regulation of EGF-induced Erk pathway activation. Involved in cytoskeletal reorganization and EGFR signaling. Together with EPS8 participates in transduction of signals from Ras to Rac. In vitro, a trimeric complex of ABI1, EPS8 and SOS1 exhibits Rac specific guanine nucleotide exchange factor (GEF) activity and ABI1 seems to act as an adapter in the complex. Regulates ABL1/c-Abl-mediated phosphorylation of ENAH. Recruits WASF1 to lamellipodia and there seems to regulate WASF1 protein level. In brain, seems to regulate the dendritic outgrowth and branching as well as to determine the shape and number of synaptic contacts of developing neurons. {ECO:0000269|PubMed:11003655, ECO:0000269|PubMed:18328268}. |
Q8N122 | RPTOR | S859 | ochoa|psp | Regulatory-associated protein of mTOR (Raptor) (p150 target of rapamycin (TOR)-scaffold protein) | Component of the mechanistic target of rapamycin complex 1 (mTORC1), an evolutionarily conserved central nutrient sensor that stimulates anabolic reactions and macromolecule biosynthesis to promote cellular biomass generation and growth (PubMed:12150925, PubMed:12150926, PubMed:12747827, PubMed:24403073, PubMed:26588989, PubMed:32561715, PubMed:37541260). In response to nutrients, growth factors or amino acids, mTORC1 is recruited to the lysosome membrane and promotes protein, lipid and nucleotide synthesis by phosphorylating several substrates, such as ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1) (PubMed:12150925, PubMed:12150926, PubMed:12747827, PubMed:24403073, PubMed:26588989, PubMed:37541260). In the same time, it inhibits catabolic pathways by phosphorylating the autophagy initiation components ULK1 and ATG13, as well as transcription factor TFEB, a master regulators of lysosomal biogenesis and autophagy (PubMed:12150925, PubMed:12150926, PubMed:12747827, PubMed:24403073, PubMed:32561715, PubMed:37541260). The mTORC1 complex is inhibited in response to starvation and amino acid depletion (PubMed:12150925, PubMed:12150926, PubMed:12747827, PubMed:24403073, PubMed:37541260). Within the mTORC1 complex, RPTOR acts both as a molecular adapter, which (1) mediates recruitment of mTORC1 to lysosomal membranes via interaction with small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD), and a (2) substrate-specific adapter, which promotes substrate specificity by binding to TOS motif-containing proteins and direct them towards the active site of the MTOR kinase domain for phosphorylation (PubMed:12747827, PubMed:24403073, PubMed:26588989, PubMed:37541260). mTORC1 complex regulates many cellular processes, such as odontoblast and osteoclast differentiation or neuronal transmission (By similarity). mTORC1 complex in excitatory neuronal transmission is required for the prosocial behavior induced by the psychoactive substance lysergic acid diethylamide (LSD) (By similarity). {ECO:0000250|UniProtKB:Q8K4Q0, ECO:0000269|PubMed:12150925, ECO:0000269|PubMed:12150926, ECO:0000269|PubMed:12747827, ECO:0000269|PubMed:24403073, ECO:0000269|PubMed:26588989, ECO:0000269|PubMed:32561715, ECO:0000269|PubMed:37541260}. |
Q8ND30 | PPFIBP2 | S483 | ochoa | Liprin-beta-2 (Protein tyrosine phosphatase receptor type f polypeptide-interacting protein-binding protein 2) (PTPRF-interacting protein-binding protein 2) | May regulate the disassembly of focal adhesions. Did not bind receptor-like tyrosine phosphatases type 2A. {ECO:0000269|PubMed:9624153}. |
Q8NEM7 | SUPT20H | S430 | ochoa | Transcription factor SPT20 homolog (p38-interacting protein) (p38IP) | Required for MAP kinase p38 (MAPK11, MAPK12, MAPK13 and/or MAPK14) activation during gastrulation. Required for down-regulation of E-cadherin during gastrulation by regulating E-cadherin protein level downstream from NCK-interacting kinase (NIK) and independently of the regulation of transcription by FGF signaling and Snail (By similarity). Required for starvation-induced ATG9A trafficking during autophagy. {ECO:0000250, ECO:0000269|PubMed:19893488}. |
Q8NHM5 | KDM2B | S828 | 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}. |
Q8TAP9 | MPLKIP | S97 | ochoa | M-phase-specific PLK1-interacting protein (TTD non-photosensitive 1 protein) | May play a role in maintenance of cell cycle integrity by regulating mitosis or cytokinesis. {ECO:0000269|PubMed:17310276}. |
Q8TBP0 | TBC1D16 | S122 | ochoa | TBC1 domain family member 16 | May act as a GTPase-activating protein for Rab family protein(s). |
Q8TDJ6 | DMXL2 | S949 | ochoa | DmX-like protein 2 (Rabconnectin-3) | May serve as a scaffold protein for MADD and RAB3GA on synaptic vesicles (PubMed:11809763). Plays a role in the brain as a key controller of neuronal and endocrine homeostatic processes (By similarity). {ECO:0000250|UniProtKB:Q8BPN8, ECO:0000269|PubMed:11809763}. |
Q8TEM1 | NUP210 | S1859 | ochoa | Nuclear pore membrane glycoprotein 210 (Nuclear pore protein gp210) (Nuclear envelope pore membrane protein POM 210) (POM210) (Nucleoporin Nup210) (Pore membrane protein of 210 kDa) | Nucleoporin essential for nuclear pore assembly and fusion, nuclear pore spacing, as well as structural integrity. {ECO:0000269|PubMed:14517331}. |
Q8TF72 | SHROOM3 | S974 | ochoa | Protein Shroom3 (Shroom-related protein) (hShrmL) | Controls cell shape changes in the neuroepithelium during neural tube closure. Induces apical constriction in epithelial cells by promoting the apical accumulation of F-actin and myosin II, and probably by bundling stress fibers (By similarity). Induces apicobasal cell elongation by redistributing gamma-tubulin and directing the assembly of robust apicobasal microtubule arrays (By similarity). {ECO:0000250|UniProtKB:Q27IV2, ECO:0000250|UniProtKB:Q9QXN0}. |
Q8WUM0 | NUP133 | S41 | ochoa | Nuclear pore complex protein Nup133 (133 kDa nucleoporin) (Nucleoporin Nup133) | Involved in poly(A)+ RNA transport. Involved in nephrogenesis (PubMed:30179222). {ECO:0000269|PubMed:11684705, ECO:0000269|PubMed:30179222}. |
Q8WX93 | PALLD | S759 | ochoa | Palladin (SIH002) (Sarcoma antigen NY-SAR-77) | Cytoskeletal protein required for organization of normal actin cytoskeleton. Roles in establishing cell morphology, motility, cell adhesion and cell-extracellular matrix interactions in a variety of cell types. May function as a scaffolding molecule with the potential to influence both actin polymerization and the assembly of existing actin filaments into higher-order arrays. Binds to proteins that bind to either monomeric or filamentous actin. Localizes at sites where active actin remodeling takes place, such as lamellipodia and membrane ruffles. Different isoforms may have functional differences. Involved in the control of morphological and cytoskeletal changes associated with dendritic cell maturation. Involved in targeting ACTN to specific subcellular foci. {ECO:0000269|PubMed:11598191, ECO:0000269|PubMed:15147863, ECO:0000269|PubMed:17537434}. |
Q8WYP5 | AHCTF1 | S1138 | ochoa | Protein ELYS (Embryonic large molecule derived from yolk sac) (Protein MEL-28) (Putative AT-hook-containing transcription factor 1) | Required for the assembly of a functional nuclear pore complex (NPC) on the surface of chromosomes as nuclei form at the end of mitosis. May initiate NPC assembly by binding to chromatin and recruiting the Nup107-160 subcomplex of the NPC. Also required for the localization of the Nup107-160 subcomplex of the NPC to the kinetochore during mitosis and for the completion of cytokinesis. {ECO:0000269|PubMed:17098863, ECO:0000269|PubMed:17235358}. |
Q92610 | ZNF592 | S687 | ochoa | Zinc finger protein 592 | May be involved in transcriptional regulation. {ECO:0000269|PubMed:20531441}. |
Q96CP6 | GRAMD1A | S267 | ochoa | Protein Aster-A (GRAM domain-containing protein 1A) | Cholesterol transporter that mediates non-vesicular transport of cholesterol from the plasma membrane (PM) to the endoplasmic reticulum (ER) (By similarity). Contains unique domains for binding cholesterol and the PM, thereby serving as a molecular bridge for the transfer of cholesterol from the PM to the ER (By similarity). Plays a crucial role in cholesterol homeostasis and has the unique ability to localize to the PM based on the level of membrane cholesterol (By similarity). In lipid-poor conditions localizes to the ER membrane and in response to excess cholesterol in the PM is recruited to the endoplasmic reticulum-plasma membrane contact sites (EPCS) which is mediated by the GRAM domain (By similarity). At the EPCS, the sterol-binding VASt/ASTER domain binds to the cholesterol in the PM and facilitates its transfer from the PM to ER (By similarity). May play a role in tumor progression (By similarity). Plays a role in autophagy regulation and is required for biogenesis of the autophagosome (PubMed:31222192). This function in autophagy requires its cholesterol-transfer activity (PubMed:31222192). {ECO:0000250|UniProtKB:Q8VEF1, ECO:0000269|PubMed:31222192}. |
Q96HC4 | PDLIM5 | S383 | ochoa | PDZ and LIM domain protein 5 (Enigma homolog) (Enigma-like PDZ and LIM domains protein) | May play an important role in the heart development by scaffolding PKC to the Z-disk region. May play a role in the regulation of cardiomyocyte expansion. Isoforms lacking the LIM domains may negatively modulate the scaffolding activity of isoform 1. Overexpression promotes the development of heart hypertrophy. Contributes to the regulation of dendritic spine morphogenesis in neurons. May be required to restrain postsynaptic growth of excitatory synapses. Isoform 1, but not isoform 2, expression favors spine thinning and elongation. {ECO:0000250|UniProtKB:Q62920}. |
Q96JM3 | CHAMP1 | S472 | ochoa | Chromosome alignment-maintaining phosphoprotein 1 (Zinc finger protein 828) | Required for proper alignment of chromosomes at metaphase and their accurate segregation during mitosis. Involved in the maintenance of spindle microtubules attachment to the kinetochore during sister chromatid biorientation. May recruit CENPE and CENPF to the kinetochore. {ECO:0000269|PubMed:21063390}. |
Q96JY6 | PDLIM2 | S120 | ochoa | PDZ and LIM domain protein 2 (PDZ-LIM protein mystique) | Probable adapter protein located at the actin cytoskeleton that promotes cell attachment. Necessary for the migratory capacity of epithelial cells. Overexpression enhances cell adhesion to collagen and fibronectin and suppresses anchorage independent growth. May contribute to tumor cell migratory capacity. {ECO:0000269|PubMed:15659642}. |
Q96PD2 | DCBLD2 | S720 | ochoa|psp | Discoidin, CUB and LCCL domain-containing protein 2 (CUB, LCCL and coagulation factor V/VIII-homology domains protein 1) (Endothelial and smooth muscle cell-derived neuropilin-like protein) | None |
Q96SI1 | KCTD15 | S31 | ochoa | BTB/POZ domain-containing protein KCTD15 (Potassium channel tetramerization domain-containing protein 15) | During embryonic development, it is involved in neural crest formation (By similarity). Inhibits AP2 transcriptional activity by interaction with its activation domain (PubMed:23382213). {ECO:0000250|UniProtKB:Q6DC02, ECO:0000269|PubMed:23382213}. |
Q99666 | RGPD5 | S1590 | ochoa | RANBP2-like and GRIP domain-containing protein 5/6 (Ran-binding protein 2-like 1/2) (RanBP2-like 1/2) (RanBP2L1) (RanBP2L2) (Sperm membrane protein BS-63) | None |
Q99700 | ATXN2 | S554 | ochoa | Ataxin-2 (Spinocerebellar ataxia type 2 protein) (Trinucleotide repeat-containing gene 13 protein) | Involved in EGFR trafficking, acting as negative regulator of endocytic EGFR internalization at the plasma membrane. {ECO:0000269|PubMed:18602463}. |
Q99700 | ATXN2 | S861 | ochoa | Ataxin-2 (Spinocerebellar ataxia type 2 protein) (Trinucleotide repeat-containing gene 13 protein) | Involved in EGFR trafficking, acting as negative regulator of endocytic EGFR internalization at the plasma membrane. {ECO:0000269|PubMed:18602463}. |
Q99959 | PKP2 | S293 | ochoa | Plakophilin-2 | A component of desmosome cell-cell junctions which are required for positive regulation of cellular adhesion (PubMed:25208567). Regulates focal adhesion turnover resulting in changes in focal adhesion size, cell adhesion and cell spreading, potentially via transcriptional modulation of beta-integrins (PubMed:23884246). Required to maintain gingival epithelial barrier function (PubMed:34368962). Important component of the desmosome that is also required for localization of desmosome component proteins such as DSC2, DSG2 and JUP to the desmosome cell-cell junction (PubMed:22781308, PubMed:25208567). Required for the formation of desmosome cell junctions in cardiomyocytes, thereby required for the correct formation of the heart, specifically trabeculation and formation of the atria walls (By similarity). Loss of desmosome cell junctions leads to mis-localization of DSP and DSG2 resulting in disruption of cell-cell adhesion and disordered intermediate filaments (By similarity). Modulates profibrotic gene expression in cardiomyocytes via regulation of DSP expression and subsequent activation of downstream TGFB1 and MAPK14/p38 MAPK signaling (By similarity). Required for cardiac sodium current propagation and electrical synchrony in cardiac myocytes, via ANK3 stabilization and modulation of SCN5A/Nav1.5 localization to cell-cell junctions (By similarity). Required for mitochondrial function, nuclear envelope integrity and positive regulation of SIRT3 transcription via maintaining DES localization at its nuclear envelope and cell tip anchoring points, and thereby preserving regulation of the transcriptional program (PubMed:35959657). Maintenance of nuclear envelope integrity protects against DNA damage and transcriptional dysregulation of genes, especially those involved in the electron transport chain, thereby preserving mitochondrial function and protecting against superoxide radical anion generation (PubMed:35959657). Binds single-stranded DNA (ssDNA) (PubMed:20613778). May regulate the localization of GJA1 to gap junctions in intercalated disks of the heart (PubMed:18662195). Involved in the inhibition of viral infection by influenza A viruses (IAV) (PubMed:28169297). Acts as a host restriction factor for IAV viral propagation, potentially via disrupting the interaction of IAV polymerase complex proteins (PubMed:28169297). {ECO:0000250|UniProtKB:F1M7L9, ECO:0000250|UniProtKB:Q9CQ73, ECO:0000269|PubMed:18662195, ECO:0000269|PubMed:20613778, ECO:0000269|PubMed:22781308, ECO:0000269|PubMed:23884246, ECO:0000269|PubMed:25208567, ECO:0000269|PubMed:28169297, ECO:0000269|PubMed:34368962, ECO:0000269|PubMed:35959657}. |
Q9BQE9 | BCL7B | S118 | ochoa | B-cell CLL/lymphoma 7 protein family member B (allergen Hom s 3) | Positive regulator of apoptosis. Plays a role in the Wnt signaling pathway, negatively regulating the expression of Wnt signaling components CTNNB1 and HMGA1 (PubMed:25569233). Involved in cell cycle progression, maintenance of the nuclear structure and stem cell differentiation (PubMed:25569233). May play a role in lung tumor development or progression (By similarity). {ECO:0000250|UniProtKB:Q921K9, ECO:0000269|PubMed:25569233}. |
Q9BX40 | LSM14B | S102 | ochoa | Protein LSM14 homolog B (RNA-associated protein 55B) (hRAP55B) | mRNA-binding protein essential for female fertility, oocyte meiotic maturation and the assembly of MARDO (mitochondria-associated ribonucleoprotein domain), a membraneless compartment that stores maternal mRNAs in oocytes. Ensures the proper accumulation and clearance of mRNAs essential for oocyte meiotic maturation and the normal progression from Meiosis I to Meiosis II in oocytes. Promotes the translation of some oogenesis-related mRNAs. Regulates the expression and/or localization of some key P-body proteins in oocytes. Essential for the assembly of the primordial follicle in the ovary. {ECO:0000250|UniProtKB:Q8CGC4}. |
Q9BXS6 | NUSAP1 | S247 | ochoa | Nucleolar and spindle-associated protein 1 (NuSAP) | Microtubule-associated protein with the capacity to bundle and stabilize microtubules (By similarity). May associate with chromosomes and promote the organization of mitotic spindle microtubules around them. {ECO:0000250, ECO:0000269|PubMed:12963707}. |
Q9BXS6 | NUSAP1 | S251 | ochoa | Nucleolar and spindle-associated protein 1 (NuSAP) | Microtubule-associated protein with the capacity to bundle and stabilize microtubules (By similarity). May associate with chromosomes and promote the organization of mitotic spindle microtubules around them. {ECO:0000250, ECO:0000269|PubMed:12963707}. |
Q9BZQ8 | NIBAN1 | S592 | ochoa | Protein Niban 1 (Cell growth-inhibiting gene 39 protein) (Protein FAM129A) | Regulates phosphorylation of a number of proteins involved in translation regulation including EIF2A, EIF4EBP1 and RPS6KB1. May be involved in the endoplasmic reticulum stress response (By similarity). {ECO:0000250}. |
Q9C0B5 | ZDHHC5 | S391 | ochoa | Palmitoyltransferase ZDHHC5 (EC 2.3.1.225) (Zinc finger DHHC domain-containing protein 5) (DHHC-5) (Zinc finger protein 375) | Palmitoyltransferase that catalyzes the addition of palmitate onto various protein substrates such as CTNND2, CD36, GSDMD, NLRP3, NOD1, NOD2, STAT3 and S1PR1 thus plays a role in various biological processes including cell adhesion, inflammation, fatty acid uptake, bacterial sensing or cardiac functions (PubMed:21820437, PubMed:29185452, PubMed:31402609, PubMed:31649195, PubMed:34293401, PubMed:38092000, PubMed:38530158, PubMed:38599239). Plays an important role in the regulation of synapse efficacy by mediating palmitoylation of delta-catenin/CTNND2, thereby increasing synaptic delivery and surface stabilization of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors (AMPARs) (PubMed:26334723). Under basal conditions, remains at the synaptic membrane through FYN-mediated phosphorylation that prevents association with endocytic proteins (PubMed:26334723). Neuronal activity enhances the internalization and trafficking of DHHC5 from spines to dendritic shafts where it palmitoylates delta-catenin/CTNND2 (PubMed:26334723). Regulates cell adhesion at the plasma membrane by palmitoylating GOLGA7B and DSG2 (PubMed:31402609). Plays a role in innate immune response by mediating the palmitoylation of NOD1 and NOD2 and their proper recruitment to the bacterial entry site and phagosomes (PubMed:31649195, PubMed:34293401). Also participates in fatty acid uptake by palmitoylating CD36 and thereby targeting it to the plasma membrane (PubMed:32958780). Upon binding of fatty acids to CD36, gets phosphorylated by LYN leading to inactivation and subsequent CD36 caveolar endocytosis (PubMed:32958780). Controls oligodendrocyte development by catalyzing STAT3 palmitoylation (By similarity). Acts as a regulator of inflammatory response by mediating palmitoylation of NLRP3 and GSDMD (PubMed:38092000, PubMed:38530158, PubMed:38599239). Palmitoylates NLRP3 to promote inflammasome assembly and activation (PubMed:38092000). Activates pyroptosis by catalyzing palmitoylation of gasdermin-D (GSDMD), thereby promoting membrane translocation and pore formation of GSDMD (PubMed:38530158, PubMed:38599239). {ECO:0000250|UniProtKB:Q8VDZ4, ECO:0000269|PubMed:21820437, ECO:0000269|PubMed:26334723, ECO:0000269|PubMed:29185452, ECO:0000269|PubMed:31402609, ECO:0000269|PubMed:31649195, ECO:0000269|PubMed:32958780, ECO:0000269|PubMed:34293401, ECO:0000269|PubMed:38092000, ECO:0000269|PubMed:38530158, ECO:0000269|PubMed:38599239}. |
Q9C0C2 | TNKS1BP1 | S297 | ochoa | 182 kDa tankyrase-1-binding protein | None |
Q9C0H2 | TTYH3 | S496 | ochoa | Protein tweety homolog 3 (hTTY3) (Volume-regulated anion channel subunit TTYH3) | Calcium-independent, swelling-dependent volume-regulated anion channel (VRAC-swell) which plays a pivotal role in the process of regulatory volume decrease (RVD) in the brain through the efflux of anions like chloride and organic osmolytes like glutamate (By similarity). Probable large-conductance Ca(2+)-activated chloride channel (PubMed:15010458). {ECO:0000250|UniProtKB:Q6P5F7, ECO:0000269|PubMed:15010458}. |
Q9GZV5 | WWTR1 | S307 | ochoa | WW domain-containing transcription regulator protein 1 (Transcriptional coactivator with PDZ-binding motif) | Transcriptional coactivator which acts as a downstream regulatory target in the Hippo signaling pathway that plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis (PubMed:11118213, PubMed:18227151, PubMed:23911299). The core of this pathway is composed of a kinase cascade wherein STK3/MST2 and STK4/MST1, in complex with its regulatory protein SAV1, phosphorylates and activates LATS1/2 in complex with its regulatory protein MOB1, which in turn phosphorylates and inactivates YAP1 oncoprotein and WWTR1/TAZ (PubMed:18227151). WWTR1 enhances PAX8 and NKX2-1/TTF1-dependent gene activation (PubMed:19010321). In conjunction with YAP1, involved in the regulation of TGFB1-dependent SMAD2 and SMAD3 nuclear accumulation (PubMed:18568018). Plays a key role in coupling SMADs to the transcriptional machinery such as the mediator complex (PubMed:18568018). Regulates embryonic stem-cell self-renewal, promotes cell proliferation and epithelial-mesenchymal transition (PubMed:18227151, PubMed:18568018). {ECO:0000269|PubMed:11118213, ECO:0000269|PubMed:18227151, ECO:0000269|PubMed:18568018, ECO:0000269|PubMed:19010321, ECO:0000269|PubMed:23911299}. |
Q9H1A4 | ANAPC1 | S518 | ochoa | Anaphase-promoting complex subunit 1 (APC1) (Cyclosome subunit 1) (Mitotic checkpoint regulator) (Testis-specific gene 24 protein) | Component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated E3 ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle (PubMed:18485873). The APC/C complex acts by mediating ubiquitination and subsequent degradation of target proteins: it mainly mediates the formation of 'Lys-11'-linked polyubiquitin chains and, to a lower extent, the formation of 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains (PubMed:18485873). The APC/C complex catalyzes assembly of branched 'Lys-11'-/'Lys-48'-linked branched ubiquitin chains on target proteins (PubMed:29033132). {ECO:0000269|PubMed:18485873, ECO:0000269|PubMed:29033132}. |
Q9H1K0 | RBSN | S215 | ochoa|psp | Rabenosyn-5 (110 kDa protein) (FYVE finger-containing Rab5 effector protein rabenosyn-5) (RAB effector RBSN) (Zinc finger FYVE domain-containing protein 20) | Rab4/Rab5 effector protein acting in early endocytic membrane fusion and membrane trafficking of recycling endosomes. Required for endosome fusion either homotypically or with clathrin coated vesicles. Plays a role in the lysosomal trafficking of CTSD/cathepsin D from the Golgi to lysosomes. Also promotes the recycling of transferrin directly from early endosomes to the plasma membrane. Binds phospholipid vesicles containing phosphatidylinositol 3-phosphate (PtdInsP3) (PubMed:11062261, PubMed:11788822, PubMed:15020713). Plays a role in the recycling of transferrin receptor to the plasma membrane (PubMed:22308388). {ECO:0000269|PubMed:11062261, ECO:0000269|PubMed:11788822, ECO:0000269|PubMed:15020713, ECO:0000269|PubMed:22308388}. |
Q9H1K0 | RBSN | S226 | ochoa | Rabenosyn-5 (110 kDa protein) (FYVE finger-containing Rab5 effector protein rabenosyn-5) (RAB effector RBSN) (Zinc finger FYVE domain-containing protein 20) | Rab4/Rab5 effector protein acting in early endocytic membrane fusion and membrane trafficking of recycling endosomes. Required for endosome fusion either homotypically or with clathrin coated vesicles. Plays a role in the lysosomal trafficking of CTSD/cathepsin D from the Golgi to lysosomes. Also promotes the recycling of transferrin directly from early endosomes to the plasma membrane. Binds phospholipid vesicles containing phosphatidylinositol 3-phosphate (PtdInsP3) (PubMed:11062261, PubMed:11788822, PubMed:15020713). Plays a role in the recycling of transferrin receptor to the plasma membrane (PubMed:22308388). {ECO:0000269|PubMed:11062261, ECO:0000269|PubMed:11788822, ECO:0000269|PubMed:15020713, ECO:0000269|PubMed:22308388}. |
Q9H6S0 | YTHDC2 | S1263 | ochoa | 3'-5' RNA helicase YTHDC2 (EC 3.6.4.13) (YTH domain-containing protein 2) (hYTHDC2) | 3'-5' RNA helicase that plays a key role in the male and female germline by promoting transition from mitotic to meiotic divisions in stem cells (PubMed:26318451, PubMed:29033321, PubMed:29970596). Specifically recognizes and binds N6-methyladenosine (m6A)-containing RNAs, a modification present at internal sites of mRNAs and some non-coding RNAs that plays a role in the efficiency of RNA processing and stability (PubMed:26318451, PubMed:29033321). Essential for ensuring a successful progression of the meiotic program in the germline by regulating the level of m6A-containing RNAs (By similarity). Acts by binding and promoting degradation of m6A-containing mRNAs: the 3'-5' RNA helicase activity is required for this process and RNA degradation may be mediated by XRN1 exoribonuclease (PubMed:29033321). Required for both spermatogenesis and oogenesis (By similarity). {ECO:0000250|UniProtKB:B2RR83, ECO:0000269|PubMed:26318451, ECO:0000269|PubMed:29033321, ECO:0000269|PubMed:29970596}. |
Q9H6S3 | EPS8L2 | S459 | ochoa | Epidermal growth factor receptor kinase substrate 8-like protein 2 (EPS8-like protein 2) (Epidermal growth factor receptor pathway substrate 8-related protein 2) (EPS8-related protein 2) | Stimulates guanine exchange activity of SOS1. May play a role in membrane ruffling and remodeling of the actin cytoskeleton. In the cochlea, is required for stereocilia maintenance in adult hair cells (By similarity). {ECO:0000250|UniProtKB:Q99K30, ECO:0000269|PubMed:14565974}. |
Q9H7D0 | DOCK5 | S1785 | ochoa | Dedicator of cytokinesis protein 5 | Guanine nucleotide exchange factor (GEF) for Rho and Rac. GEF proteins activate small GTPases by exchanging bound GDP for free GTP (By similarity). Along with DOCK1, mediates CRK/CRKL regulation of epithelial and endothelial cell spreading and migration on type IV collagen (PubMed:19004829). {ECO:0000250|UniProtKB:B2RY04, ECO:0000269|PubMed:19004829}. |
Q9NP08 | HMX1 | S133 | ochoa | Homeobox protein HMX1 (Homeobox protein H6) | DNA-binding protein that binds to the 5'-CAAG-3' core sequence. May function as a transcriptional repressor. Seems to act as a transcriptional antagonist of NKX2-5. May play an important role in the development of craniofacial structures such as the eye and ear. {ECO:0000269|PubMed:10206974}. |
Q9NQC7 | CYLD | S432 | psp | Ubiquitin carboxyl-terminal hydrolase CYLD (EC 3.4.19.12) (Deubiquitinating enzyme CYLD) (Ubiquitin thioesterase CYLD) (Ubiquitin-specific-processing protease CYLD) | Deubiquitinase that specifically cleaves 'Lys-63'- and linear 'Met-1'-linked polyubiquitin chains and is involved in NF-kappa-B activation and TNF-alpha-induced necroptosis (PubMed:18313383, PubMed:18636086, PubMed:26670046, PubMed:26997266, PubMed:27458237, PubMed:27591049, PubMed:27746020, PubMed:29291351, PubMed:32185393). Negatively regulates NF-kappa-B activation by deubiquitinating upstream signaling factors (PubMed:12917689, PubMed:12917691, PubMed:32185393). Contributes to the regulation of cell survival, proliferation and differentiation via its effects on NF-kappa-B activation (PubMed:12917690). Negative regulator of Wnt signaling (PubMed:20227366). Inhibits HDAC6 and thereby promotes acetylation of alpha-tubulin and stabilization of microtubules (PubMed:19893491). Plays a role in the regulation of microtubule dynamics, and thereby contributes to the regulation of cell proliferation, cell polarization, cell migration, and angiogenesis (PubMed:18222923, PubMed:20194890). Required for normal cell cycle progress and normal cytokinesis (PubMed:17495026, PubMed:19893491). Inhibits nuclear translocation of NF-kappa-B (PubMed:18636086). Plays a role in the regulation of inflammation and the innate immune response, via its effects on NF-kappa-B activation (PubMed:18636086). Dispensable for the maturation of intrathymic natural killer cells, but required for the continued survival of immature natural killer cells (By similarity). Negatively regulates TNFRSF11A signaling and osteoclastogenesis (By similarity). Involved in the regulation of ciliogenesis, allowing ciliary basal bodies to migrate and dock to the plasma membrane; this process does not depend on NF-kappa-B activation (By similarity). Ability to remove linear ('Met-1'-linked) polyubiquitin chains regulates innate immunity and TNF-alpha-induced necroptosis: recruited to the LUBAC complex via interaction with SPATA2 and restricts linear polyubiquitin formation on target proteins (PubMed:26670046, PubMed:26997266, PubMed:27458237, PubMed:27591049). Regulates innate immunity by restricting linear polyubiquitin formation on RIPK2 in response to NOD2 stimulation (PubMed:26997266). Involved in TNF-alpha-induced necroptosis by removing linear ('Met-1'-linked) polyubiquitin chains from RIPK1, thereby regulating the kinase activity of RIPK1 (By similarity). Negatively regulates intestinal inflammation by removing 'Lys-63' linked polyubiquitin chain of NLRP6, thereby reducing the interaction between NLRP6 and PYCARD/ASC and formation of the NLRP6 inflammasome (By similarity). Does not catalyze deubiquitination of heterotypic 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains (PubMed:27746020). Removes 'Lys-63' linked polyubiquitin chain of MAP3K7, which inhibits phosphorylation and blocks downstream activation of the JNK-p38 kinase cascades (PubMed:29291351). Also removes 'Lys-63'-linked polyubiquitin chains of MAP3K1 and MA3P3K3, which inhibit their interaction with MAP2K1 and MAP2K2 (PubMed:34497368). {ECO:0000250|UniProtKB:Q80TQ2, ECO:0000269|PubMed:12917689, ECO:0000269|PubMed:12917690, ECO:0000269|PubMed:12917691, ECO:0000269|PubMed:17495026, ECO:0000269|PubMed:18222923, ECO:0000269|PubMed:18313383, ECO:0000269|PubMed:18636086, ECO:0000269|PubMed:19893491, ECO:0000269|PubMed:20194890, ECO:0000269|PubMed:20227366, ECO:0000269|PubMed:26670046, ECO:0000269|PubMed:26997266, ECO:0000269|PubMed:27458237, ECO:0000269|PubMed:27591049, ECO:0000269|PubMed:27746020, ECO:0000269|PubMed:29291351, ECO:0000269|PubMed:32185393, ECO:0000269|PubMed:34497368}. |
Q9NYF8 | BCLAF1 | S272 | ochoa | Bcl-2-associated transcription factor 1 (Btf) (BCLAF1 and THRAP3 family member 1) | Death-promoting transcriptional repressor. May be involved in cyclin-D1/CCND1 mRNA stability through the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA. {ECO:0000269|PubMed:18794151}. |
Q9NYV4 | CDK12 | S261 | ochoa | Cyclin-dependent kinase 12 (EC 2.7.11.22) (EC 2.7.11.23) (Cdc2-related kinase, arginine/serine-rich) (CrkRS) (Cell division cycle 2-related protein kinase 7) (CDC2-related protein kinase 7) (Cell division protein kinase 12) (hCDK12) | Cyclin-dependent kinase that phosphorylates the C-terminal domain (CTD) of the large subunit of RNA polymerase II (POLR2A), thereby acting as a key regulator of transcription elongation. Regulates the expression of genes involved in DNA repair and is required for the maintenance of genomic stability. Preferentially phosphorylates 'Ser-5' in CTD repeats that are already phosphorylated at 'Ser-7', but can also phosphorylate 'Ser-2'. Required for RNA splicing, possibly by phosphorylating SRSF1/SF2. Involved in regulation of MAP kinase activity, possibly leading to affect the response to estrogen inhibitors. {ECO:0000269|PubMed:11683387, ECO:0000269|PubMed:19651820, ECO:0000269|PubMed:20952539, ECO:0000269|PubMed:22012619, ECO:0000269|PubMed:24662513}. |
Q9NYV4 | CDK12 | S287 | ochoa | Cyclin-dependent kinase 12 (EC 2.7.11.22) (EC 2.7.11.23) (Cdc2-related kinase, arginine/serine-rich) (CrkRS) (Cell division cycle 2-related protein kinase 7) (CDC2-related protein kinase 7) (Cell division protein kinase 12) (hCDK12) | Cyclin-dependent kinase that phosphorylates the C-terminal domain (CTD) of the large subunit of RNA polymerase II (POLR2A), thereby acting as a key regulator of transcription elongation. Regulates the expression of genes involved in DNA repair and is required for the maintenance of genomic stability. Preferentially phosphorylates 'Ser-5' in CTD repeats that are already phosphorylated at 'Ser-7', but can also phosphorylate 'Ser-2'. Required for RNA splicing, possibly by phosphorylating SRSF1/SF2. Involved in regulation of MAP kinase activity, possibly leading to affect the response to estrogen inhibitors. {ECO:0000269|PubMed:11683387, ECO:0000269|PubMed:19651820, ECO:0000269|PubMed:20952539, ECO:0000269|PubMed:22012619, ECO:0000269|PubMed:24662513}. |
Q9NYV4 | CDK12 | S316 | ochoa | Cyclin-dependent kinase 12 (EC 2.7.11.22) (EC 2.7.11.23) (Cdc2-related kinase, arginine/serine-rich) (CrkRS) (Cell division cycle 2-related protein kinase 7) (CDC2-related protein kinase 7) (Cell division protein kinase 12) (hCDK12) | Cyclin-dependent kinase that phosphorylates the C-terminal domain (CTD) of the large subunit of RNA polymerase II (POLR2A), thereby acting as a key regulator of transcription elongation. Regulates the expression of genes involved in DNA repair and is required for the maintenance of genomic stability. Preferentially phosphorylates 'Ser-5' in CTD repeats that are already phosphorylated at 'Ser-7', but can also phosphorylate 'Ser-2'. Required for RNA splicing, possibly by phosphorylating SRSF1/SF2. Involved in regulation of MAP kinase activity, possibly leading to affect the response to estrogen inhibitors. {ECO:0000269|PubMed:11683387, ECO:0000269|PubMed:19651820, ECO:0000269|PubMed:20952539, ECO:0000269|PubMed:22012619, ECO:0000269|PubMed:24662513}. |
Q9NZN8 | CNOT2 | S161 | 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}. |
Q9P0K1 | ADAM22 | S862 | ochoa | Disintegrin and metalloproteinase domain-containing protein 22 (ADAM 22) (Metalloproteinase-disintegrin ADAM22-3) (Metalloproteinase-like, disintegrin-like, and cysteine-rich protein 2) | Probable ligand for integrin in the brain. This is a non catalytic metalloprotease-like protein (PubMed:19692335). Involved in regulation of cell adhesion and spreading and in inhibition of cell proliferation. Neuronal receptor for LGI1. {ECO:0000269|PubMed:12589811, ECO:0000269|PubMed:15882968, ECO:0000269|PubMed:16385342, ECO:0000269|PubMed:19692335}. |
Q9P0K1 | ADAM22 | S866 | ochoa | Disintegrin and metalloproteinase domain-containing protein 22 (ADAM 22) (Metalloproteinase-disintegrin ADAM22-3) (Metalloproteinase-like, disintegrin-like, and cysteine-rich protein 2) | Probable ligand for integrin in the brain. This is a non catalytic metalloprotease-like protein (PubMed:19692335). Involved in regulation of cell adhesion and spreading and in inhibition of cell proliferation. Neuronal receptor for LGI1. {ECO:0000269|PubMed:12589811, ECO:0000269|PubMed:15882968, ECO:0000269|PubMed:16385342, ECO:0000269|PubMed:19692335}. |
Q9P0K7 | RAI14 | S286 | ochoa | Ankycorbin (Ankyrin repeat and coiled-coil structure-containing protein) (Novel retinal pigment epithelial cell protein) (Retinoic acid-induced protein 14) | Plays a role in actin regulation at the ectoplasmic specialization, a type of cell junction specific to testis. Important for establishment of sperm polarity and normal spermatid adhesion. May also promote integrity of Sertoli cell tight junctions at the blood-testis barrier. {ECO:0000250|UniProtKB:Q5U312}. |
Q9P206 | NHSL3 | S566 | ochoa | NHS-like protein 3 | Able to directly activate the TNF-NFkappaB signaling pathway. {ECO:0000269|PubMed:32854746}. |
Q9UBC2 | EPS15L1 | S246 | ochoa | Epidermal growth factor receptor substrate 15-like 1 (Eps15-related protein) (Eps15R) | Seems to be a constitutive component of clathrin-coated pits that is required for receptor-mediated endocytosis. Involved in endocytosis of integrin beta-1 (ITGB1) and transferrin receptor (TFR); internalization of ITGB1 as DAB2-dependent cargo but not TFR seems to require association with DAB2. {ECO:0000269|PubMed:22648170, ECO:0000269|PubMed:9407958}. |
Q9UBW5 | BIN2 | S259 | ochoa | Bridging integrator 2 (Breast cancer-associated protein 1) | Promotes cell motility and migration, probably via its interaction with the cell membrane and with podosome proteins that mediate interaction with the cytoskeleton. Modulates membrane curvature and mediates membrane tubulation. Plays a role in podosome formation. Inhibits phagocytosis. {ECO:0000269|PubMed:23285027}. |
Q9UBW5 | BIN2 | S273 | ochoa | Bridging integrator 2 (Breast cancer-associated protein 1) | Promotes cell motility and migration, probably via its interaction with the cell membrane and with podosome proteins that mediate interaction with the cytoskeleton. Modulates membrane curvature and mediates membrane tubulation. Plays a role in podosome formation. Inhibits phagocytosis. {ECO:0000269|PubMed:23285027}. |
Q9UBW5 | BIN2 | S429 | ochoa | Bridging integrator 2 (Breast cancer-associated protein 1) | Promotes cell motility and migration, probably via its interaction with the cell membrane and with podosome proteins that mediate interaction with the cytoskeleton. Modulates membrane curvature and mediates membrane tubulation. Plays a role in podosome formation. Inhibits phagocytosis. {ECO:0000269|PubMed:23285027}. |
Q9UBW5 | BIN2 | S440 | ochoa | Bridging integrator 2 (Breast cancer-associated protein 1) | Promotes cell motility and migration, probably via its interaction with the cell membrane and with podosome proteins that mediate interaction with the cytoskeleton. Modulates membrane curvature and mediates membrane tubulation. Plays a role in podosome formation. Inhibits phagocytosis. {ECO:0000269|PubMed:23285027}. |
Q9UDT6 | CLIP2 | S156 | ochoa | CAP-Gly domain-containing linker protein 2 (Cytoplasmic linker protein 115) (CLIP-115) (Cytoplasmic linker protein 2) (Williams-Beuren syndrome chromosomal region 3 protein) (Williams-Beuren syndrome chromosomal region 4 protein) | Seems to link microtubules to dendritic lamellar body (DLB), a membranous organelle predominantly present in bulbous dendritic appendages of neurons linked by dendrodendritic gap junctions. May operate in the control of brain-specific organelle translocations (By similarity). {ECO:0000250}. |
Q9UHV7 | MED13 | S2022 | ochoa | Mediator of RNA polymerase II transcription subunit 13 (Activator-recruited cofactor 250 kDa component) (ARC250) (Mediator complex subunit 13) (Thyroid hormone receptor-associated protein 1) (Thyroid hormone receptor-associated protein complex 240 kDa component) (Trap240) (Vitamin D3 receptor-interacting protein complex component DRIP250) (DRIP250) | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors. {ECO:0000269|PubMed:16595664}. |
Q9UI08 | EVL | S345 | ochoa | Ena/VASP-like protein (Ena/vasodilator-stimulated phosphoprotein-like) | Ena/VASP proteins are actin-associated proteins involved in a range of processes dependent on cytoskeleton remodeling and cell polarity such as axon guidance and lamellipodial and filopodial dynamics in migrating cells. EVL enhances actin nucleation and polymerization. |
Q9UJF2 | RASAL2 | S950 | ochoa | Ras GTPase-activating protein nGAP (RAS protein activator-like 2) | Inhibitory regulator of the Ras-cyclic AMP pathway. |
Q9UKI8 | TLK1 | S174 | ochoa | Serine/threonine-protein kinase tousled-like 1 (EC 2.7.11.1) (PKU-beta) (Tousled-like kinase 1) | Rapidly and transiently inhibited by phosphorylation following the generation of DNA double-stranded breaks during S-phase. This is cell cycle checkpoint and ATM-pathway dependent and appears to regulate processes involved in chromatin assembly. Isoform 3 phosphorylates and enhances the stability of the t-SNARE SNAP23, augmenting its assembly with syntaxin. Isoform 3 protects the cells from the ionizing radiation by facilitating the repair of DSBs. In vitro, phosphorylates histone H3 at 'Ser-10'. {ECO:0000269|PubMed:10523312, ECO:0000269|PubMed:10588641, ECO:0000269|PubMed:11314006, ECO:0000269|PubMed:11470414, ECO:0000269|PubMed:12660173, ECO:0000269|PubMed:9427565}. |
Q9UPA5 | BSN | S1488 | ochoa | Protein bassoon (Zinc finger protein 231) | Scaffold protein of the presynaptic cytomatrix at the active zone (CAZ) which is the place in the synapse where neurotransmitter is released (PubMed:12812759). After synthesis, participates in the formation of Golgi-derived membranous organelles termed Piccolo-Bassoon transport vesicles (PTVs) that are transported along axons to sites of nascent synaptic contacts (PubMed:19380881). At the presynaptic active zone, regulates the spatial organization of synaptic vesicle cluster, the protein complexes that execute membrane fusion and compensatory endocytosis (By similarity). Also functions in processes other than assembly such as the regulation of specific presynaptic protein ubiquitination by interacting with SIAH1 or the regulation of presynaptic autophagy by associating with ATG5 (By similarity). Also mediates synapse to nucleus communication leading to reconfiguration of gene expression by associating with the transcriptional corepressor CTBP1 and by subsequently reducing the size of its pool available for nuclear import (By similarity). Inhibits the activity of the proportion of DAO enzyme that localizes to the presynaptic active zone, which may modulate synaptic transmission (By similarity). {ECO:0000250|UniProtKB:O35078, ECO:0000250|UniProtKB:O88778, ECO:0000269|PubMed:12812759, ECO:0000269|PubMed:19380881}. |
Q9UPN3 | MACF1 | S7226 | psp | Microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5 (620 kDa actin-binding protein) (ABP620) (Actin cross-linking family protein 7) (Macrophin-1) (Trabeculin-alpha) | [Isoform 2]: F-actin-binding protein which plays a role in cross-linking actin to other cytoskeletal proteins and also binds to microtubules (PubMed:15265687, PubMed:20937854). Plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex (PubMed:20937854). Acts as a positive regulator of Wnt receptor signaling pathway and is involved in the translocation of AXIN1 and its associated complex (composed of APC, CTNNB1 and GSK3B) from the cytoplasm to the cell membrane (By similarity). Has actin-regulated ATPase activity and is essential for controlling focal adhesions (FAs) assembly and dynamics (By similarity). Interaction with CAMSAP3 at the minus ends of non-centrosomal microtubules tethers microtubules minus-ends to actin filaments, regulating focal adhesion size and cell migration (PubMed:27693509). May play role in delivery of transport vesicles containing GPI-linked proteins from the trans-Golgi network through its interaction with GOLGA4 (PubMed:15265687). Plays a key role in wound healing and epidermal cell migration (By similarity). Required for efficient upward migration of bulge cells in response to wounding and this function is primarily rooted in its ability to coordinate microtubule dynamics and polarize hair follicle stem cells (By similarity). As a regulator of actin and microtubule arrangement and stabilization, it plays an essential role in neurite outgrowth, branching and spine formation during brain development (By similarity). {ECO:0000250|UniProtKB:Q9QXZ0, ECO:0000269|PubMed:15265687, ECO:0000269|PubMed:20937854, ECO:0000269|PubMed:27693509}. |
Q9UPN3 | MACF1 | S7230 | ochoa|psp | Microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5 (620 kDa actin-binding protein) (ABP620) (Actin cross-linking family protein 7) (Macrophin-1) (Trabeculin-alpha) | [Isoform 2]: F-actin-binding protein which plays a role in cross-linking actin to other cytoskeletal proteins and also binds to microtubules (PubMed:15265687, PubMed:20937854). Plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex (PubMed:20937854). Acts as a positive regulator of Wnt receptor signaling pathway and is involved in the translocation of AXIN1 and its associated complex (composed of APC, CTNNB1 and GSK3B) from the cytoplasm to the cell membrane (By similarity). Has actin-regulated ATPase activity and is essential for controlling focal adhesions (FAs) assembly and dynamics (By similarity). Interaction with CAMSAP3 at the minus ends of non-centrosomal microtubules tethers microtubules minus-ends to actin filaments, regulating focal adhesion size and cell migration (PubMed:27693509). May play role in delivery of transport vesicles containing GPI-linked proteins from the trans-Golgi network through its interaction with GOLGA4 (PubMed:15265687). Plays a key role in wound healing and epidermal cell migration (By similarity). Required for efficient upward migration of bulge cells in response to wounding and this function is primarily rooted in its ability to coordinate microtubule dynamics and polarize hair follicle stem cells (By similarity). As a regulator of actin and microtubule arrangement and stabilization, it plays an essential role in neurite outgrowth, branching and spine formation during brain development (By similarity). {ECO:0000250|UniProtKB:Q9QXZ0, ECO:0000269|PubMed:15265687, ECO:0000269|PubMed:20937854, ECO:0000269|PubMed:27693509}. |
Q9UQ35 | SRRM2 | S950 | 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 | S1383 | 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 | S1451 | 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 | S2417 | 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}. |
Q9Y2W1 | THRAP3 | S306 | ochoa | Thyroid hormone receptor-associated protein 3 (BCLAF1 and THRAP3 family member 2) (Thyroid hormone receptor-associated protein complex 150 kDa component) (Trap150) | Involved in pre-mRNA splicing. Remains associated with spliced mRNA after splicing which probably involves interactions with the exon junction complex (EJC). Can trigger mRNA decay which seems to be independent of nonsense-mediated decay involving premature stop codons (PTC) recognition. May be involved in nuclear mRNA decay. Involved in regulation of signal-induced alternative splicing. During splicing of PTPRC/CD45 is proposed to sequester phosphorylated SFPQ from PTPRC/CD45 pre-mRNA in resting T-cells. Involved in cyclin-D1/CCND1 mRNA stability probably by acting as component of the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA. Involved in response to DNA damage. Is excluced from DNA damage sites in a manner that parallels transcription inhibition; the function may involve the SNARP complex. Initially thought to play a role in transcriptional coactivation through its association with the TRAP complex; however, it is not regarded as a stable Mediator complex subunit. Cooperatively with HELZ2, enhances the transcriptional activation mediated by PPARG, maybe through the stabilization of the PPARG binding to DNA in presence of ligand. May play a role in the terminal stage of adipocyte differentiation. Plays a role in the positive regulation of the circadian clock. Acts as a coactivator of the CLOCK-BMAL1 heterodimer and promotes its transcriptional activator activity and binding to circadian target genes (PubMed:24043798). {ECO:0000269|PubMed:20123736, ECO:0000269|PubMed:20932480, ECO:0000269|PubMed:22424773, ECO:0000269|PubMed:23525231, ECO:0000269|PubMed:24043798}. |
Q9Y2X7 | GIT1 | S581 | ochoa | ARF GTPase-activating protein GIT1 (ARF GAP GIT1) (Cool-associated and tyrosine-phosphorylated protein 1) (CAT-1) (CAT1) (G protein-coupled receptor kinase-interactor 1) (GRK-interacting protein 1) (p95-APP1) | GTPase-activating protein for ADP ribosylation factor family members, including ARF1. Multidomain scaffold protein that interacts with numerous proteins and therefore participates in many cellular functions, including receptor internalization, focal adhesion remodeling, and signaling by both G protein-coupled receptors and tyrosine kinase receptors (By similarity). Through PAK1 activation, positively regulates microtubule nucleation during interphase (PubMed:27012601). Plays a role in the regulation of cytokinesis; for this function, may act in a pathway also involving ENTR1 and PTPN13 (PubMed:23108400). May promote cell motility both by regulating focal complex dynamics and by local activation of RAC1 (PubMed:10938112, PubMed:11896197). May act as scaffold for MAPK1/3 signal transduction in focal adhesions. Recruits MAPK1/3/ERK1/2 to focal adhesions after EGF stimulation via a Src-dependent pathway, hence stimulating cell migration (PubMed:15923189). Plays a role in brain development and function. Involved in the regulation of spine density and synaptic plasticity that is required for processes involved in learning (By similarity). Plays an important role in dendritic spine morphogenesis and synapse formation (PubMed:12695502, PubMed:15800193). In hippocampal neurons, recruits guanine nucleotide exchange factors (GEFs), such as ARHGEF7/beta-PIX, to the synaptic membrane. These in turn locally activate RAC1, which is an essential step for spine morphogenesis and synapse formation (PubMed:12695502). May contribute to the organization of presynaptic active zones through oligomerization and formation of a Piccolo/PCLO-based protein network, which includes ARHGEF7/beta-PIX and FAK1 (By similarity). In neurons, through its interaction with liprin-alpha family members, may be required for AMPA receptor (GRIA2/3) proper targeting to the cell membrane (By similarity). In complex with GABA(A) receptors and ARHGEF7, plays a crucial role in regulating GABA(A) receptor synaptic stability, maintaining GPHN/gephyrin scaffolds and hence GABAergic inhibitory synaptic transmission, by locally coordinating RAC1 and PAK1 downstream effector activity, leading to F-actin stabilization (PubMed:25284783). May also be important for RAC1 downstream signaling pathway through PAK3 and regulation of neuronal inhibitory transmission at presynaptic input (By similarity). Required for successful bone regeneration during fracture healing (By similarity). The function in intramembranous ossification may, at least partly, exerted by macrophages in which GIT1 is a key negative regulator of redox homeostasis, IL1B production, and glycolysis, acting through the ERK1/2/NRF2/NFE2L2 axis (By similarity). May play a role in angiogenesis during fracture healing (By similarity). In this process, may regulate activation of the canonical NF-kappa-B signal in bone mesenchymal stem cells by enhancing the interaction between NEMO and 'Lys-63'-ubiquitinated RIPK1/RIP1, eventually leading to enhanced production of VEGFA and others angiogenic factors (PubMed:31502302). Essential for VEGF signaling through the activation of phospholipase C-gamma and ERK1/2, hence may control endothelial cell proliferation and angiogenesis (PubMed:19273721). {ECO:0000250|UniProtKB:Q68FF6, ECO:0000250|UniProtKB:Q9Z272, ECO:0000269|PubMed:10938112, ECO:0000269|PubMed:11896197, ECO:0000269|PubMed:12695502, ECO:0000269|PubMed:15800193, ECO:0000269|PubMed:15923189, ECO:0000269|PubMed:19273721, ECO:0000269|PubMed:23108400, ECO:0000269|PubMed:25284783, ECO:0000269|PubMed:27012601, ECO:0000269|PubMed:31502302}. |
Q9Y5K6 | CD2AP | S546 | ochoa | CD2-associated protein (Adapter protein CMS) (Cas ligand with multiple SH3 domains) | Seems to act as an adapter protein between membrane proteins and the actin cytoskeleton (PubMed:10339567). In collaboration with CBLC, modulates the rate of RET turnover and may act as regulatory checkpoint that limits the potency of GDNF on neuronal survival. Controls CBLC function, converting it from an inhibitor to a promoter of RET degradation (By similarity). May play a role in receptor clustering and cytoskeletal polarity in the junction between T-cell and antigen-presenting cell (By similarity). May anchor the podocyte slit diaphragm to the actin cytoskeleton in renal glomerolus. Also required for cytokinesis (PubMed:15800069). Plays a role in epithelial cell junctions formation (PubMed:22891260). {ECO:0000250|UniProtKB:F1LRS8, ECO:0000250|UniProtKB:Q9JLQ0, ECO:0000269|PubMed:10339567, ECO:0000269|PubMed:15800069, ECO:0000269|PubMed:22891260}. |
Q9Y5S2 | CDC42BPB | S1686 | ochoa|psp | Serine/threonine-protein kinase MRCK beta (EC 2.7.11.1) (CDC42-binding protein kinase beta) (CDC42BP-beta) (DMPK-like beta) (Myotonic dystrophy kinase-related CDC42-binding kinase beta) (MRCK beta) (Myotonic dystrophy protein kinase-like beta) | Serine/threonine-protein kinase which is an important downstream effector of CDC42 and plays a role in the regulation of cytoskeleton reorganization and cell migration. Regulates actin cytoskeletal reorganization via phosphorylation of PPP1R12C and MYL9/MLC2 (PubMed:21457715, PubMed:21949762). In concert with MYO18A and LURAP1, is involved in modulating lamellar actomyosin retrograde flow that is crucial to cell protrusion and migration (PubMed:18854160). Phosphorylates PPP1R12A (PubMed:21457715). In concert with FAM89B/LRAP25 mediates the targeting of LIMK1 to the lamellipodium resulting in its activation and subsequent phosphorylation of CFL1 which is important for lamellipodial F-actin regulation (By similarity). {ECO:0000250|UniProtKB:Q7TT50, ECO:0000269|PubMed:18854160, ECO:0000269|PubMed:21457715, ECO:0000269|PubMed:21949762}. |
Q96EP5 | DAZAP1 | S204 | Sugiyama | DAZ-associated protein 1 (Deleted in azoospermia-associated protein 1) | RNA-binding protein, which may be required during spermatogenesis. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 0.000034 | 4.463 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 0.000066 | 4.178 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 0.000696 | 3.158 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 0.000770 | 3.114 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 0.000770 | 3.114 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 0.000934 | 3.029 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 0.000934 | 3.029 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 0.001025 | 2.989 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 0.001226 | 2.912 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 0.001706 | 2.768 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 0.001843 | 2.734 |
R-HSA-209560 | NF-kB is activated and signals survival | 0.000630 | 3.201 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 0.001458 | 2.836 |
R-HSA-193639 | p75NTR signals via NF-kB | 0.001239 | 2.907 |
R-HSA-9675151 | Disorders of Developmental Biology | 0.001647 | 2.783 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 0.001452 | 2.838 |
R-HSA-418885 | DCC mediated attractive signaling | 0.001239 | 2.907 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 0.001025 | 2.989 |
R-HSA-180746 | Nuclear import of Rev protein | 0.001122 | 2.950 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 0.001843 | 2.734 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 0.001843 | 2.734 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 0.001575 | 2.803 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 0.001706 | 2.768 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 0.000830 | 3.081 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 0.001989 | 2.701 |
R-HSA-9609690 | HCMV Early Events | 0.002623 | 2.581 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 0.002835 | 2.547 |
R-HSA-73887 | Death Receptor Signaling | 0.002956 | 2.529 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 0.003029 | 2.519 |
R-HSA-9617828 | FOXO-mediated transcription of cell cycle genes | 0.003338 | 2.476 |
R-HSA-9758919 | Epithelial-Mesenchymal Transition (EMT) during gastrulation | 0.003549 | 2.450 |
R-HSA-5603029 | IkBA variant leads to EDA-ID | 0.003549 | 2.450 |
R-HSA-3371556 | Cellular response to heat stress | 0.003817 | 2.418 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 0.003860 | 2.413 |
R-HSA-141424 | Amplification of signal from the kinetochores | 0.003860 | 2.413 |
R-HSA-5674400 | Constitutive Signaling by AKT1 E17K in Cancer | 0.004072 | 2.390 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 0.005803 | 2.236 |
R-HSA-5357956 | TNFR1-induced NF-kappa-B signaling pathway | 0.005813 | 2.236 |
R-HSA-191859 | snRNP Assembly | 0.006443 | 2.191 |
R-HSA-194441 | Metabolism of non-coding RNA | 0.006443 | 2.191 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 0.006596 | 2.181 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 0.007128 | 2.147 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 0.007382 | 2.132 |
R-HSA-6784531 | tRNA processing in the nucleus | 0.007488 | 2.126 |
R-HSA-264870 | Caspase-mediated cleavage of cytoskeletal proteins | 0.007762 | 2.110 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 0.008230 | 2.085 |
R-HSA-168643 | Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signali... | 0.008243 | 2.084 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 0.008534 | 2.069 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 0.009046 | 2.044 |
R-HSA-9609646 | HCMV Infection | 0.009877 | 2.005 |
R-HSA-4839726 | Chromatin organization | 0.009674 | 2.014 |
R-HSA-162582 | Signal Transduction | 0.010529 | 1.978 |
R-HSA-5684264 | MAP3K8 (TPL2)-dependent MAPK1/3 activation | 0.016739 | 1.776 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 0.012639 | 1.898 |
R-HSA-2467813 | Separation of Sister Chromatids | 0.015184 | 1.819 |
R-HSA-9820841 | M-decay: degradation of maternal mRNAs by maternally stored factors | 0.015904 | 1.799 |
R-HSA-5260271 | Diseases of Immune System | 0.015047 | 1.823 |
R-HSA-5602358 | Diseases associated with the TLR signaling cascade | 0.015047 | 1.823 |
R-HSA-209543 | p75NTR recruits signalling complexes | 0.013414 | 1.872 |
R-HSA-9005895 | Pervasive developmental disorders | 0.013414 | 1.872 |
R-HSA-9697154 | Disorders of Nervous System Development | 0.013414 | 1.872 |
R-HSA-9005891 | Loss of function of MECP2 in Rett syndrome | 0.013414 | 1.872 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 0.011167 | 1.952 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 0.015904 | 1.799 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 0.016598 | 1.780 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 0.011758 | 1.930 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 0.010819 | 1.966 |
R-HSA-9856649 | Transcriptional and post-translational regulation of MITF-M expression and activ... | 0.011274 | 1.948 |
R-HSA-3214841 | PKMTs methylate histone lysines | 0.015904 | 1.799 |
R-HSA-8941326 | RUNX2 regulates bone development | 0.011890 | 1.925 |
R-HSA-74160 | Gene expression (Transcription) | 0.015003 | 1.824 |
R-HSA-69620 | Cell Cycle Checkpoints | 0.011610 | 1.935 |
R-HSA-1169408 | ISG15 antiviral mechanism | 0.013290 | 1.876 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 0.011804 | 1.928 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 0.017221 | 1.764 |
R-HSA-9006925 | Intracellular signaling by second messengers | 0.018196 | 1.740 |
R-HSA-1810476 | RIP-mediated NFkB activation via ZBP1 | 0.018520 | 1.732 |
R-HSA-9670621 | Defective Inhibition of DNA Recombination at Telomere | 0.021502 | 1.668 |
R-HSA-9673013 | Diseases of Telomere Maintenance | 0.021502 | 1.668 |
R-HSA-9006821 | Alternative Lengthening of Telomeres (ALT) | 0.021502 | 1.668 |
R-HSA-9670613 | Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations | 0.021502 | 1.668 |
R-HSA-9670615 | Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations | 0.021502 | 1.668 |
R-HSA-5357905 | Regulation of TNFR1 signaling | 0.021609 | 1.665 |
R-HSA-373752 | Netrin-1 signaling | 0.019599 | 1.708 |
R-HSA-75153 | Apoptotic execution phase | 0.021609 | 1.665 |
R-HSA-3247509 | Chromatin modifying enzymes | 0.021840 | 1.661 |
R-HSA-1257604 | PIP3 activates AKT signaling | 0.022647 | 1.645 |
R-HSA-9843745 | Adipogenesis | 0.022943 | 1.639 |
R-HSA-1839117 | Signaling by cytosolic FGFR1 fusion mutants | 0.026385 | 1.579 |
R-HSA-1606322 | ZBP1(DAI) mediated induction of type I IFNs | 0.026385 | 1.579 |
R-HSA-5603027 | IKBKG deficiency causes anhidrotic ectodermal dysplasia with immunodeficiency (E... | 0.032080 | 1.494 |
R-HSA-5602636 | IKBKB deficiency causes SCID | 0.032080 | 1.494 |
R-HSA-5357786 | TNFR1-induced proapoptotic signaling | 0.033016 | 1.481 |
R-HSA-75893 | TNF signaling | 0.033286 | 1.478 |
R-HSA-68877 | Mitotic Prometaphase | 0.029226 | 1.534 |
R-HSA-373753 | Nephrin family interactions | 0.030740 | 1.512 |
R-HSA-68886 | M Phase | 0.033026 | 1.481 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 0.031020 | 1.508 |
R-HSA-844456 | The NLRP3 inflammasome | 0.028529 | 1.545 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 0.031393 | 1.503 |
R-HSA-70171 | Glycolysis | 0.033775 | 1.471 |
R-HSA-1266738 | Developmental Biology | 0.035023 | 1.456 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 0.035944 | 1.444 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 0.037313 | 1.428 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 0.037663 | 1.424 |
R-HSA-350054 | Notch-HLH transcription pathway | 0.037759 | 1.423 |
R-HSA-6804115 | TP53 regulates transcription of additional cell cycle genes whose exact role in ... | 0.037759 | 1.423 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 0.038708 | 1.412 |
R-HSA-3828062 | Glycogen storage disease type 0 (muscle GYS1) | 0.042544 | 1.371 |
R-HSA-3814836 | Glycogen storage disease type XV (GYG1) | 0.042544 | 1.371 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 0.047960 | 1.319 |
R-HSA-933542 | TRAF6 mediated NF-kB activation | 0.042744 | 1.369 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 0.040727 | 1.390 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 0.047960 | 1.319 |
R-HSA-525793 | Myogenesis | 0.047960 | 1.319 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 0.050808 | 1.294 |
R-HSA-68882 | Mitotic Anaphase | 0.045209 | 1.345 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 0.045974 | 1.337 |
R-HSA-9610379 | HCMV Late Events | 0.043297 | 1.364 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 0.050808 | 1.294 |
R-HSA-429947 | Deadenylation of mRNA | 0.042744 | 1.369 |
R-HSA-1483249 | Inositol phosphate metabolism | 0.047313 | 1.325 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 0.049628 | 1.304 |
R-HSA-8953897 | Cellular responses to stimuli | 0.050769 | 1.294 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 0.041797 | 1.379 |
R-HSA-9700206 | Signaling by ALK in cancer | 0.041797 | 1.379 |
R-HSA-211000 | Gene Silencing by RNA | 0.041797 | 1.379 |
R-HSA-73857 | RNA Polymerase II Transcription | 0.051245 | 1.290 |
R-HSA-9944971 | Loss of Function of KMT2D in Kabuki Syndrome | 0.052896 | 1.277 |
R-HSA-9944997 | Loss of Function of KMT2D in MLL4 Complex Formation in Kabuki Syndrome | 0.052896 | 1.277 |
R-HSA-8952158 | RUNX3 regulates BCL2L11 (BIM) transcription | 0.063136 | 1.200 |
R-HSA-165181 | Inhibition of TSC complex formation by PKB | 0.063136 | 1.200 |
R-HSA-74713 | IRS activation | 0.073267 | 1.135 |
R-HSA-9673768 | Signaling by membrane-tethered fusions of PDGFRA or PDGFRB | 0.073267 | 1.135 |
R-HSA-9022535 | Loss of phosphorylation of MECP2 at T308 | 0.073267 | 1.135 |
R-HSA-9833576 | CDH11 homotypic and heterotypic interactions | 0.083288 | 1.079 |
R-HSA-9022537 | Loss of MECP2 binding ability to the NCoR/SMRT complex | 0.083288 | 1.079 |
R-HSA-8951430 | RUNX3 regulates WNT signaling | 0.103009 | 0.987 |
R-HSA-4411364 | Binding of TCF/LEF:CTNNB1 to target gene promoters | 0.103009 | 0.987 |
R-HSA-112412 | SOS-mediated signalling | 0.103009 | 0.987 |
R-HSA-3785653 | Myoclonic epilepsy of Lafora | 0.112710 | 0.948 |
R-HSA-8876493 | InlA-mediated entry of Listeria monocytogenes into host cells | 0.141194 | 0.850 |
R-HSA-9931512 | Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | 0.150484 | 0.823 |
R-HSA-5339716 | Signaling by GSK3beta mutants | 0.150484 | 0.823 |
R-HSA-4839743 | Signaling by CTNNB1 phospho-site mutants | 0.159675 | 0.797 |
R-HSA-3000484 | Scavenging by Class F Receptors | 0.159675 | 0.797 |
R-HSA-5358747 | CTNNB1 S33 mutants aren't phosphorylated | 0.159675 | 0.797 |
R-HSA-5358749 | CTNNB1 S37 mutants aren't phosphorylated | 0.159675 | 0.797 |
R-HSA-5358752 | CTNNB1 T41 mutants aren't phosphorylated | 0.159675 | 0.797 |
R-HSA-5358751 | CTNNB1 S45 mutants aren't phosphorylated | 0.159675 | 0.797 |
R-HSA-9027284 | Erythropoietin activates RAS | 0.186659 | 0.729 |
R-HSA-196299 | Beta-catenin phosphorylation cascade | 0.186659 | 0.729 |
R-HSA-390522 | Striated Muscle Contraction | 0.070893 | 1.149 |
R-HSA-354194 | GRB2:SOS provides linkage to MAPK signaling for Integrins | 0.195461 | 0.709 |
R-HSA-176412 | Phosphorylation of the APC/C | 0.195461 | 0.709 |
R-HSA-9687136 | Aberrant regulation of mitotic exit in cancer due to RB1 defects | 0.195461 | 0.709 |
R-HSA-72187 | mRNA 3'-end processing | 0.139100 | 0.857 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 0.180855 | 0.743 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 0.180855 | 0.743 |
R-HSA-8854518 | AURKA Activation by TPX2 | 0.192554 | 0.715 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 0.196027 | 0.708 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 0.196027 | 0.708 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 0.196027 | 0.708 |
R-HSA-3134973 | LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 0.073267 | 1.135 |
R-HSA-9762292 | Regulation of CDH11 function | 0.131802 | 0.880 |
R-HSA-198203 | PI3K/AKT activation | 0.131802 | 0.880 |
R-HSA-5682910 | LGI-ADAM interactions | 0.141194 | 0.850 |
R-HSA-5635851 | GLI proteins bind promoters of Hh responsive genes to promote transcription | 0.083288 | 1.079 |
R-HSA-9931521 | The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CL... | 0.204168 | 0.690 |
R-HSA-445989 | TAK1-dependent IKK and NF-kappa-B activation | 0.120922 | 0.917 |
R-HSA-1169091 | Activation of NF-kappaB in B cells | 0.135417 | 0.868 |
R-HSA-9614085 | FOXO-mediated transcription | 0.118925 | 0.925 |
R-HSA-442729 | CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | 0.112710 | 0.948 |
R-HSA-9614399 | Regulation of localization of FOXO transcription factors | 0.141194 | 0.850 |
R-HSA-9675126 | Diseases of mitotic cell cycle | 0.064872 | 1.188 |
R-HSA-1839124 | FGFR1 mutant receptor activation | 0.067860 | 1.168 |
R-HSA-2032785 | YAP1- and WWTR1 (TAZ)-stimulated gene expression | 0.177762 | 0.750 |
R-HSA-9758274 | Regulation of NF-kappa B signaling | 0.195461 | 0.709 |
R-HSA-8875513 | MET interacts with TNS proteins | 0.052896 | 1.277 |
R-HSA-69478 | G2/M DNA replication checkpoint | 0.093202 | 1.031 |
R-HSA-6803544 | Ion influx/efflux at host-pathogen interface | 0.131802 | 0.880 |
R-HSA-9933947 | Formation of the non-canonical BAF (ncBAF) complex | 0.168768 | 0.773 |
R-HSA-141430 | Inactivation of APC/C via direct inhibition of the APC/C complex | 0.204168 | 0.690 |
R-HSA-5655302 | Signaling by FGFR1 in disease | 0.099995 | 1.000 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 0.177004 | 0.752 |
R-HSA-1168372 | Downstream signaling events of B Cell Receptor (BCR) | 0.208300 | 0.681 |
R-HSA-111932 | CaMK IV-mediated phosphorylation of CREB | 0.131802 | 0.880 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 0.177004 | 0.752 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 0.185093 | 0.733 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 0.185093 | 0.733 |
R-HSA-165159 | MTOR signalling | 0.103407 | 0.985 |
R-HSA-9020702 | Interleukin-1 signaling | 0.123655 | 0.908 |
R-HSA-74749 | Signal attenuation | 0.131802 | 0.880 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 0.059036 | 1.229 |
R-HSA-9603381 | Activated NTRK3 signals through PI3K | 0.103009 | 0.987 |
R-HSA-8875555 | MET activates RAP1 and RAC1 | 0.131802 | 0.880 |
R-HSA-75035 | Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 0.168768 | 0.773 |
R-HSA-212165 | Epigenetic regulation of gene expression | 0.171879 | 0.765 |
R-HSA-8951671 | RUNX3 regulates YAP1-mediated transcription | 0.093202 | 1.031 |
R-HSA-8964046 | VLDL clearance | 0.103009 | 0.987 |
R-HSA-9619229 | Activation of RAC1 downstream of NMDARs | 0.122308 | 0.913 |
R-HSA-9623433 | NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | 0.150484 | 0.823 |
R-HSA-168927 | TICAM1, RIP1-mediated IKK complex recruitment | 0.186659 | 0.729 |
R-HSA-141405 | Inhibition of the proteolytic activity of APC/C required for the onset of anapha... | 0.204168 | 0.690 |
R-HSA-430039 | mRNA decay by 5' to 3' exoribonuclease | 0.204168 | 0.690 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 0.056190 | 1.250 |
R-HSA-9664873 | Pexophagy | 0.131802 | 0.880 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 0.067860 | 1.168 |
R-HSA-9842663 | Signaling by LTK | 0.159675 | 0.797 |
R-HSA-9818749 | Regulation of NFE2L2 gene expression | 0.093202 | 1.031 |
R-HSA-205043 | NRIF signals cell death from the nucleus | 0.177762 | 0.750 |
R-HSA-114608 | Platelet degranulation | 0.201552 | 0.696 |
R-HSA-9824585 | Regulation of MITF-M-dependent genes involved in pigmentation | 0.113830 | 0.944 |
R-HSA-438064 | Post NMDA receptor activation events | 0.087883 | 1.056 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 0.163755 | 0.786 |
R-HSA-8941284 | RUNX2 regulates chondrocyte maturation | 0.073267 | 1.135 |
R-HSA-5660668 | CLEC7A/inflammasome pathway | 0.083288 | 1.079 |
R-HSA-428890 | Role of ABL in ROBO-SLIT signaling | 0.103009 | 0.987 |
R-HSA-198693 | AKT phosphorylates targets in the nucleus | 0.122308 | 0.913 |
R-HSA-8951936 | RUNX3 regulates p14-ARF | 0.159675 | 0.797 |
R-HSA-937039 | IRAK1 recruits IKK complex | 0.159675 | 0.797 |
R-HSA-975144 | IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 0.159675 | 0.797 |
R-HSA-9796292 | Formation of axial mesoderm | 0.168768 | 0.773 |
R-HSA-450513 | Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 0.186659 | 0.729 |
R-HSA-8875878 | MET promotes cell motility | 0.086684 | 1.062 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 0.173118 | 0.762 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 0.207195 | 0.684 |
R-HSA-9659379 | Sensory processing of sound | 0.070054 | 1.155 |
R-HSA-9617629 | Regulation of FOXO transcriptional activity by acetylation | 0.159675 | 0.797 |
R-HSA-450294 | MAP kinase activation | 0.173118 | 0.762 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 0.157791 | 0.802 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 0.157791 | 0.802 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 0.067860 | 1.168 |
R-HSA-3134963 | DEx/H-box helicases activate type I IFN and inflammatory cytokines production | 0.073267 | 1.135 |
R-HSA-9764302 | Regulation of CDH19 Expression and Function | 0.083288 | 1.079 |
R-HSA-193692 | Regulated proteolysis of p75NTR | 0.122308 | 0.913 |
R-HSA-448706 | Interleukin-1 processing | 0.122308 | 0.913 |
R-HSA-933543 | NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 0.141194 | 0.850 |
R-HSA-8851805 | MET activates RAS signaling | 0.159675 | 0.797 |
R-HSA-9933937 | Formation of the canonical BAF (cBAF) complex | 0.177762 | 0.750 |
R-HSA-9933946 | Formation of the embryonic stem cell BAF (esBAF) complex | 0.186659 | 0.729 |
R-HSA-448424 | Interleukin-17 signaling | 0.208300 | 0.681 |
R-HSA-168898 | Toll-like Receptor Cascades | 0.196081 | 0.708 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 0.056938 | 1.245 |
R-HSA-2173795 | Downregulation of SMAD2/3:SMAD4 transcriptional activity | 0.064872 | 1.188 |
R-HSA-1500931 | Cell-Cell communication | 0.161032 | 0.793 |
R-HSA-69278 | Cell Cycle, Mitotic | 0.108502 | 0.965 |
R-HSA-1632852 | Macroautophagy | 0.094798 | 1.023 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 0.059193 | 1.228 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 0.154039 | 0.812 |
R-HSA-9660826 | Purinergic signaling in leishmaniasis infection | 0.117362 | 0.930 |
R-HSA-9664424 | Cell recruitment (pro-inflammatory response) | 0.117362 | 0.930 |
R-HSA-9860276 | SLC15A4:TASL-dependent IRF5 activation | 0.083288 | 1.079 |
R-HSA-8866904 | Negative regulation of activity of TFAP2 (AP-2) family transcription factors | 0.112710 | 0.948 |
R-HSA-8940973 | RUNX2 regulates osteoblast differentiation | 0.053395 | 1.273 |
R-HSA-5578768 | Physiological factors | 0.177762 | 0.750 |
R-HSA-9933939 | Formation of the polybromo-BAF (pBAF) complex | 0.177762 | 0.750 |
R-HSA-450385 | Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 0.186659 | 0.729 |
R-HSA-388844 | Receptor-type tyrosine-protein phosphatases | 0.195461 | 0.709 |
R-HSA-1640170 | Cell Cycle | 0.101398 | 0.994 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 0.126045 | 0.899 |
R-HSA-170968 | Frs2-mediated activation | 0.168768 | 0.773 |
R-HSA-397014 | Muscle contraction | 0.110224 | 0.958 |
R-HSA-9612973 | Autophagy | 0.122726 | 0.911 |
R-HSA-9764790 | Positive Regulation of CDH1 Gene Transcription | 0.131802 | 0.880 |
R-HSA-8854214 | TBC/RABGAPs | 0.106851 | 0.971 |
R-HSA-193648 | NRAGE signals death through JNK | 0.154039 | 0.812 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 0.120886 | 0.918 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 0.054088 | 1.267 |
R-HSA-5683057 | MAPK family signaling cascades | 0.211223 | 0.675 |
R-HSA-212436 | Generic Transcription Pathway | 0.132299 | 0.878 |
R-HSA-202403 | TCR signaling | 0.148278 | 0.829 |
R-HSA-5218920 | VEGFR2 mediated vascular permeability | 0.096615 | 1.015 |
R-HSA-9662361 | Sensory processing of sound by outer hair cells of the cochlea | 0.154039 | 0.812 |
R-HSA-936837 | Ion transport by P-type ATPases | 0.184743 | 0.733 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 0.161899 | 0.791 |
R-HSA-198323 | AKT phosphorylates targets in the cytosol | 0.159675 | 0.797 |
R-HSA-5223345 | Miscellaneous transport and binding events | 0.070893 | 1.149 |
R-HSA-168638 | NOD1/2 Signaling Pathway | 0.073969 | 1.131 |
R-HSA-622312 | Inflammasomes | 0.053395 | 1.273 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 0.054088 | 1.267 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 0.155752 | 0.808 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 0.111695 | 0.952 |
R-HSA-2586552 | Signaling by Leptin | 0.131802 | 0.880 |
R-HSA-169893 | Prolonged ERK activation events | 0.195461 | 0.709 |
R-HSA-351906 | Apoptotic cleavage of cell adhesion proteins | 0.112710 | 0.948 |
R-HSA-9711123 | Cellular response to chemical stress | 0.205623 | 0.687 |
R-HSA-6806834 | Signaling by MET | 0.071945 | 1.143 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 0.169270 | 0.771 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 0.107410 | 0.969 |
R-HSA-162909 | Host Interactions of HIV factors | 0.064796 | 1.188 |
R-HSA-2262752 | Cellular responses to stress | 0.101664 | 0.993 |
R-HSA-9860927 | Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZ... | 0.077088 | 1.113 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 0.187811 | 0.726 |
R-HSA-168255 | Influenza Infection | 0.170230 | 0.769 |
R-HSA-983712 | Ion channel transport | 0.191689 | 0.717 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 0.183179 | 0.737 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 0.134860 | 0.870 |
R-HSA-9762293 | Regulation of CDH11 gene transcription | 0.122308 | 0.913 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 0.177004 | 0.752 |
R-HSA-68875 | Mitotic Prophase | 0.059497 | 1.226 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 0.128121 | 0.892 |
R-HSA-70326 | Glucose metabolism | 0.055682 | 1.254 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 0.169270 | 0.771 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 0.169270 | 0.771 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 0.169270 | 0.771 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 0.169270 | 0.771 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 0.182386 | 0.739 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 0.166380 | 0.779 |
R-HSA-194138 | Signaling by VEGF | 0.196027 | 0.708 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 0.169270 | 0.771 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 0.098107 | 1.008 |
R-HSA-6791312 | TP53 Regulates Transcription of Cell Cycle Genes | 0.157821 | 0.802 |
R-HSA-72306 | tRNA processing | 0.151704 | 0.819 |
R-HSA-162587 | HIV Life Cycle | 0.124578 | 0.905 |
R-HSA-5619102 | SLC transporter disorders | 0.143733 | 0.842 |
R-HSA-9675108 | Nervous system development | 0.211416 | 0.675 |
R-HSA-372708 | p130Cas linkage to MAPK signaling for integrins | 0.212781 | 0.672 |
R-HSA-176407 | Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 0.212781 | 0.672 |
R-HSA-3229121 | Glycogen storage diseases | 0.212781 | 0.672 |
R-HSA-2028269 | Signaling by Hippo | 0.212781 | 0.672 |
R-HSA-9909505 | Modulation of host responses by IFN-stimulated genes | 0.212781 | 0.672 |
R-HSA-9694516 | SARS-CoV-2 Infection | 0.214638 | 0.668 |
R-HSA-389948 | Co-inhibition by PD-1 | 0.216216 | 0.665 |
R-HSA-9909396 | Circadian clock | 0.218342 | 0.661 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 0.220196 | 0.657 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 0.221169 | 0.655 |
R-HSA-9614657 | FOXO-mediated transcription of cell death genes | 0.221302 | 0.655 |
R-HSA-3928664 | Ephrin signaling | 0.221302 | 0.655 |
R-HSA-156711 | Polo-like kinase mediated events | 0.221302 | 0.655 |
R-HSA-8953854 | Metabolism of RNA | 0.222437 | 0.653 |
R-HSA-69473 | G2/M DNA damage checkpoint | 0.224174 | 0.649 |
R-HSA-1226099 | Signaling by FGFR in disease | 0.224174 | 0.649 |
R-HSA-380287 | Centrosome maturation | 0.228158 | 0.642 |
R-HSA-174048 | APC/C:Cdc20 mediated degradation of Cyclin B | 0.229731 | 0.639 |
R-HSA-9754189 | Germ layer formation at gastrulation | 0.229731 | 0.639 |
R-HSA-9834899 | Specification of the neural plate border | 0.229731 | 0.639 |
R-HSA-937041 | IKK complex recruitment mediated by RIP1 | 0.229731 | 0.639 |
R-HSA-912631 | Regulation of signaling by CBL | 0.229731 | 0.639 |
R-HSA-1980143 | Signaling by NOTCH1 | 0.232147 | 0.634 |
R-HSA-9934037 | Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | 0.238069 | 0.623 |
R-HSA-3322077 | Glycogen synthesis | 0.238069 | 0.623 |
R-HSA-9823730 | Formation of definitive endoderm | 0.238069 | 0.623 |
R-HSA-140875 | Common Pathway of Fibrin Clot Formation | 0.238069 | 0.623 |
R-HSA-9629569 | Protein hydroxylation | 0.238069 | 0.623 |
R-HSA-1181150 | Signaling by NODAL | 0.238069 | 0.623 |
R-HSA-416482 | G alpha (12/13) signalling events | 0.240137 | 0.620 |
R-HSA-6807070 | PTEN Regulation | 0.241152 | 0.618 |
R-HSA-179409 | APC-Cdc20 mediated degradation of Nek2A | 0.246318 | 0.609 |
R-HSA-5602498 | MyD88 deficiency (TLR2/4) | 0.246318 | 0.609 |
R-HSA-422085 | Synthesis, secretion, and deacylation of Ghrelin | 0.246318 | 0.609 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 0.248141 | 0.605 |
R-HSA-9856530 | High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR... | 0.248141 | 0.605 |
R-HSA-9833482 | PKR-mediated signaling | 0.248141 | 0.605 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 0.252147 | 0.598 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 0.253783 | 0.596 |
R-HSA-5603041 | IRAK4 deficiency (TLR2/4) | 0.254477 | 0.594 |
R-HSA-8876384 | Listeria monocytogenes entry into host cells | 0.254477 | 0.594 |
R-HSA-9617324 | Negative regulation of NMDA receptor-mediated neuronal transmission | 0.254477 | 0.594 |
R-HSA-9825892 | Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 0.254477 | 0.594 |
R-HSA-9034015 | Signaling by NTRK3 (TRKC) | 0.254477 | 0.594 |
R-HSA-9671555 | Signaling by PDGFR in disease | 0.254477 | 0.594 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 0.256154 | 0.591 |
R-HSA-418990 | Adherens junctions interactions | 0.260383 | 0.584 |
R-HSA-166208 | mTORC1-mediated signalling | 0.262549 | 0.581 |
R-HSA-8964038 | LDL clearance | 0.262549 | 0.581 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 0.264171 | 0.578 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 0.268181 | 0.572 |
R-HSA-6794362 | Protein-protein interactions at synapses | 0.268181 | 0.572 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 0.270178 | 0.568 |
R-HSA-9634638 | Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 0.270534 | 0.568 |
R-HSA-982772 | Growth hormone receptor signaling | 0.270534 | 0.568 |
R-HSA-9758941 | Gastrulation | 0.273104 | 0.564 |
R-HSA-422475 | Axon guidance | 0.274887 | 0.561 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 0.276199 | 0.559 |
R-HSA-381038 | XBP1(S) activates chaperone genes | 0.276199 | 0.559 |
R-HSA-913531 | Interferon Signaling | 0.277161 | 0.557 |
R-HSA-8862803 | Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's dis... | 0.278433 | 0.555 |
R-HSA-8863678 | Neurodegenerative Diseases | 0.278433 | 0.555 |
R-HSA-5621575 | CD209 (DC-SIGN) signaling | 0.278433 | 0.555 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 0.278967 | 0.554 |
R-HSA-162906 | HIV Infection | 0.281902 | 0.550 |
R-HSA-446652 | Interleukin-1 family signaling | 0.281903 | 0.550 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 0.284212 | 0.546 |
R-HSA-9663891 | Selective autophagy | 0.284212 | 0.546 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 0.286247 | 0.543 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 0.286247 | 0.543 |
R-HSA-3214842 | HDMs demethylate histones | 0.286247 | 0.543 |
R-HSA-9830364 | Formation of the nephric duct | 0.286247 | 0.543 |
R-HSA-1266695 | Interleukin-7 signaling | 0.286247 | 0.543 |
R-HSA-1236974 | ER-Phagosome pathway | 0.288216 | 0.540 |
R-HSA-1989781 | PPARA activates gene expression | 0.290728 | 0.537 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 0.292217 | 0.534 |
R-HSA-202424 | Downstream TCR signaling | 0.292217 | 0.534 |
R-HSA-9703465 | Signaling by FLT3 fusion proteins | 0.293977 | 0.532 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 0.296216 | 0.528 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 0.296623 | 0.528 |
R-HSA-381070 | IRE1alpha activates chaperones | 0.300211 | 0.523 |
R-HSA-445095 | Interaction between L1 and Ankyrins | 0.301623 | 0.521 |
R-HSA-4641262 | Disassembly of the destruction complex and recruitment of AXIN to the membrane | 0.301623 | 0.521 |
R-HSA-9734009 | Defective Intrinsic Pathway for Apoptosis | 0.301623 | 0.521 |
R-HSA-9841251 | Mitochondrial unfolded protein response (UPRmt) | 0.301623 | 0.521 |
R-HSA-389357 | CD28 dependent PI3K/Akt signaling | 0.301623 | 0.521 |
R-HSA-2682334 | EPH-Ephrin signaling | 0.304203 | 0.517 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 0.309188 | 0.510 |
R-HSA-5205685 | PINK1-PRKN Mediated Mitophagy | 0.309188 | 0.510 |
R-HSA-109581 | Apoptosis | 0.311389 | 0.507 |
R-HSA-9006335 | Signaling by Erythropoietin | 0.316670 | 0.499 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 0.324072 | 0.489 |
R-HSA-9687139 | Aberrant regulation of mitotic cell cycle due to RB1 defects | 0.324072 | 0.489 |
R-HSA-6807878 | COPI-mediated anterograde transport | 0.324094 | 0.489 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 0.324094 | 0.489 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 0.328056 | 0.484 |
R-HSA-5619115 | Disorders of transmembrane transporters | 0.330552 | 0.481 |
R-HSA-182971 | EGFR downregulation | 0.331395 | 0.480 |
R-HSA-936440 | Negative regulators of DDX58/IFIH1 signaling | 0.331395 | 0.480 |
R-HSA-186763 | Downstream signal transduction | 0.331395 | 0.480 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 0.332012 | 0.479 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 0.332012 | 0.479 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 0.332012 | 0.479 |
R-HSA-3214847 | HATs acetylate histones | 0.335962 | 0.474 |
R-HSA-4791275 | Signaling by WNT in cancer | 0.338638 | 0.470 |
R-HSA-421270 | Cell-cell junction organization | 0.340361 | 0.468 |
R-HSA-354192 | Integrin signaling | 0.345804 | 0.461 |
R-HSA-9930044 | Nuclear RNA decay | 0.345804 | 0.461 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 0.345804 | 0.461 |
R-HSA-9733709 | Cardiogenesis | 0.345804 | 0.461 |
R-HSA-9768727 | Regulation of CDH1 posttranslational processing and trafficking to plasma membra... | 0.352892 | 0.452 |
R-HSA-9619665 | EGR2 and SOX10-mediated initiation of Schwann cell myelination | 0.352892 | 0.452 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 0.359505 | 0.444 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 0.359505 | 0.444 |
R-HSA-9833110 | RSV-host interactions | 0.359505 | 0.444 |
R-HSA-5205647 | Mitophagy | 0.359904 | 0.444 |
R-HSA-5686938 | Regulation of TLR by endogenous ligand | 0.359904 | 0.444 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 0.363400 | 0.440 |
R-HSA-187687 | Signalling to ERKs | 0.366841 | 0.436 |
R-HSA-111933 | Calmodulin induced events | 0.373702 | 0.427 |
R-HSA-111997 | CaM pathway | 0.373702 | 0.427 |
R-HSA-9682385 | FLT3 signaling in disease | 0.373702 | 0.427 |
R-HSA-140877 | Formation of Fibrin Clot (Clotting Cascade) | 0.373702 | 0.427 |
R-HSA-6804757 | Regulation of TP53 Degradation | 0.373702 | 0.427 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 0.375032 | 0.426 |
R-HSA-2672351 | Stimuli-sensing channels | 0.375032 | 0.426 |
R-HSA-1236975 | Antigen processing-Cross presentation | 0.375032 | 0.426 |
R-HSA-1280218 | Adaptive Immune System | 0.376251 | 0.425 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 0.376339 | 0.424 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 0.378891 | 0.421 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 0.380490 | 0.420 |
R-HSA-2173796 | SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 0.380490 | 0.420 |
R-HSA-5689896 | Ovarian tumor domain proteases | 0.380490 | 0.420 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 0.382740 | 0.417 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 0.382740 | 0.417 |
R-HSA-69275 | G2/M Transition | 0.385131 | 0.414 |
R-HSA-452723 | Transcriptional regulation of pluripotent stem cells | 0.387204 | 0.412 |
R-HSA-453274 | Mitotic G2-G2/M phases | 0.390978 | 0.408 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 0.393847 | 0.405 |
R-HSA-381771 | Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 0.393847 | 0.405 |
R-HSA-8964043 | Plasma lipoprotein clearance | 0.393847 | 0.405 |
R-HSA-201556 | Signaling by ALK | 0.393847 | 0.405 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 0.393847 | 0.405 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 0.394224 | 0.404 |
R-HSA-9670095 | Inhibition of DNA recombination at telomere | 0.400417 | 0.397 |
R-HSA-9646399 | Aggrephagy | 0.400417 | 0.397 |
R-HSA-8982491 | Glycogen metabolism | 0.400417 | 0.397 |
R-HSA-1251985 | Nuclear signaling by ERBB4 | 0.400417 | 0.397 |
R-HSA-202433 | Generation of second messenger molecules | 0.400417 | 0.397 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 0.405611 | 0.392 |
R-HSA-446728 | Cell junction organization | 0.406537 | 0.391 |
R-HSA-9607240 | FLT3 Signaling | 0.406917 | 0.390 |
R-HSA-9694548 | Maturation of spike protein | 0.406917 | 0.390 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 0.408431 | 0.389 |
R-HSA-5610785 | GLI3 is processed to GLI3R by the proteasome | 0.413347 | 0.384 |
R-HSA-5674135 | MAP2K and MAPK activation | 0.413347 | 0.384 |
R-HSA-9656223 | Signaling by RAF1 mutants | 0.413347 | 0.384 |
R-HSA-9615017 | FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 0.413347 | 0.384 |
R-HSA-9007101 | Rab regulation of trafficking | 0.416896 | 0.380 |
R-HSA-1592230 | Mitochondrial biogenesis | 0.416896 | 0.380 |
R-HSA-2980736 | Peptide hormone metabolism | 0.416896 | 0.380 |
R-HSA-111996 | Ca-dependent events | 0.419707 | 0.377 |
R-HSA-400508 | Incretin synthesis, secretion, and inactivation | 0.419707 | 0.377 |
R-HSA-512988 | Interleukin-3, Interleukin-5 and GM-CSF signaling | 0.419707 | 0.377 |
R-HSA-3928662 | EPHB-mediated forward signaling | 0.432223 | 0.364 |
R-HSA-8864260 | Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 0.432223 | 0.364 |
R-HSA-5673001 | RAF/MAP kinase cascade | 0.433214 | 0.363 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 0.434073 | 0.362 |
R-HSA-9679506 | SARS-CoV Infections | 0.436081 | 0.360 |
R-HSA-76009 | Platelet Aggregation (Plug Formation) | 0.438380 | 0.358 |
R-HSA-9824272 | Somitogenesis | 0.438380 | 0.358 |
R-HSA-1489509 | DAG and IP3 signaling | 0.438380 | 0.358 |
R-HSA-72172 | mRNA Splicing | 0.440023 | 0.357 |
R-HSA-5357801 | Programmed Cell Death | 0.442865 | 0.354 |
R-HSA-72165 | mRNA Splicing - Minor Pathway | 0.444470 | 0.352 |
R-HSA-174084 | Autodegradation of Cdh1 by Cdh1:APC/C | 0.444470 | 0.352 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 0.444470 | 0.352 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 0.444470 | 0.352 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 0.444470 | 0.352 |
R-HSA-6802949 | Signaling by RAS mutants | 0.444470 | 0.352 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 0.447940 | 0.349 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 0.450026 | 0.347 |
R-HSA-174154 | APC/C:Cdc20 mediated degradation of Securin | 0.450495 | 0.346 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 0.456455 | 0.341 |
R-HSA-389356 | Co-stimulation by CD28 | 0.456455 | 0.341 |
R-HSA-69481 | G2/M Checkpoints | 0.457318 | 0.340 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 0.460913 | 0.336 |
R-HSA-9766229 | Degradation of CDH1 | 0.462351 | 0.335 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 0.462596 | 0.335 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 0.468063 | 0.330 |
R-HSA-5658442 | Regulation of RAS by GAPs | 0.468183 | 0.330 |
R-HSA-109704 | PI3K Cascade | 0.468183 | 0.330 |
R-HSA-9748787 | Azathioprine ADME | 0.468183 | 0.330 |
R-HSA-3371571 | HSF1-dependent transactivation | 0.473952 | 0.324 |
R-HSA-5576891 | Cardiac conduction | 0.475156 | 0.323 |
R-HSA-174184 | Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 0.479659 | 0.319 |
R-HSA-6794361 | Neurexins and neuroligins | 0.479659 | 0.319 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 0.479659 | 0.319 |
R-HSA-174178 | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins ... | 0.485304 | 0.314 |
R-HSA-179419 | APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of th... | 0.485304 | 0.314 |
R-HSA-9639288 | Amino acids regulate mTORC1 | 0.485304 | 0.314 |
R-HSA-445355 | Smooth Muscle Contraction | 0.485304 | 0.314 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 0.490888 | 0.309 |
R-HSA-176409 | APC/C:Cdc20 mediated degradation of mitotic proteins | 0.496413 | 0.304 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 0.496413 | 0.304 |
R-HSA-3214815 | HDACs deacetylate histones | 0.496413 | 0.304 |
R-HSA-9753281 | Paracetamol ADME | 0.496413 | 0.304 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 0.499528 | 0.301 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 0.501119 | 0.300 |
R-HSA-176814 | Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 0.501877 | 0.299 |
R-HSA-177929 | Signaling by EGFR | 0.501877 | 0.299 |
R-HSA-5578775 | Ion homeostasis | 0.501877 | 0.299 |
R-HSA-3299685 | Detoxification of Reactive Oxygen Species | 0.501877 | 0.299 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 0.506345 | 0.296 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 0.506358 | 0.296 |
R-HSA-9764561 | Regulation of CDH1 Function | 0.507283 | 0.295 |
R-HSA-112399 | IRS-mediated signalling | 0.507283 | 0.295 |
R-HSA-9029569 | NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflu... | 0.512630 | 0.290 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 0.517920 | 0.286 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 0.523152 | 0.281 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 0.526484 | 0.279 |
R-HSA-2428928 | IRS-related events triggered by IGF1R | 0.528328 | 0.277 |
R-HSA-9793380 | Formation of paraxial mesoderm | 0.528328 | 0.277 |
R-HSA-112043 | PLC beta mediated events | 0.528328 | 0.277 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 0.530583 | 0.275 |
R-HSA-1643685 | Disease | 0.532227 | 0.274 |
R-HSA-9707616 | Heme signaling | 0.533448 | 0.273 |
R-HSA-375165 | NCAM signaling for neurite out-growth | 0.533448 | 0.273 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 0.533448 | 0.273 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 0.533448 | 0.273 |
R-HSA-186797 | Signaling by PDGF | 0.533448 | 0.273 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 0.536339 | 0.271 |
R-HSA-166520 | Signaling by NTRKs | 0.539593 | 0.268 |
R-HSA-69242 | S Phase | 0.539593 | 0.268 |
R-HSA-74751 | Insulin receptor signalling cascade | 0.543523 | 0.265 |
R-HSA-2428924 | IGF1R signaling cascade | 0.543523 | 0.265 |
R-HSA-9856651 | MITF-M-dependent gene expression | 0.546054 | 0.263 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 0.548479 | 0.261 |
R-HSA-2404192 | Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 0.548479 | 0.261 |
R-HSA-449147 | Signaling by Interleukins | 0.556440 | 0.255 |
R-HSA-5693606 | DNA Double Strand Break Response | 0.558232 | 0.253 |
R-HSA-112040 | G-protein mediated events | 0.558232 | 0.253 |
R-HSA-9830369 | Kidney development | 0.558232 | 0.253 |
R-HSA-168256 | Immune System | 0.559202 | 0.252 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 0.563029 | 0.249 |
R-HSA-983705 | Signaling by the B Cell Receptor (BCR) | 0.571262 | 0.243 |
R-HSA-195253 | Degradation of beta-catenin by the destruction complex | 0.572469 | 0.242 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 0.572469 | 0.242 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 0.577112 | 0.239 |
R-HSA-453276 | Regulation of mitotic cell cycle | 0.577112 | 0.239 |
R-HSA-5632684 | Hedgehog 'on' state | 0.577112 | 0.239 |
R-HSA-9006936 | Signaling by TGFB family members | 0.577405 | 0.239 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 0.581706 | 0.235 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 0.581706 | 0.235 |
R-HSA-4086398 | Ca2+ pathway | 0.586249 | 0.232 |
R-HSA-69052 | Switching of origins to a post-replicative state | 0.586249 | 0.232 |
R-HSA-5663084 | Diseases of carbohydrate metabolism | 0.586249 | 0.232 |
R-HSA-1236394 | Signaling by ERBB4 | 0.590744 | 0.229 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 0.592292 | 0.227 |
R-HSA-9824446 | Viral Infection Pathways | 0.597613 | 0.224 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 0.603939 | 0.219 |
R-HSA-9694635 | Translation of Structural Proteins | 0.603939 | 0.219 |
R-HSA-383280 | Nuclear Receptor transcription pathway | 0.608243 | 0.216 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 0.608243 | 0.216 |
R-HSA-216083 | Integrin cell surface interactions | 0.608243 | 0.216 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 0.612913 | 0.213 |
R-HSA-112316 | Neuronal System | 0.616132 | 0.210 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 0.620877 | 0.207 |
R-HSA-977225 | Amyloid fiber formation | 0.620877 | 0.207 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 0.621367 | 0.207 |
R-HSA-9707564 | Cytoprotection by HMOX1 | 0.629073 | 0.201 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 0.633105 | 0.199 |
R-HSA-6802957 | Oncogenic MAPK signaling | 0.637094 | 0.196 |
R-HSA-9824443 | Parasitic Infection Pathways | 0.637179 | 0.196 |
R-HSA-9658195 | Leishmania infection | 0.637179 | 0.196 |
R-HSA-2559583 | Cellular Senescence | 0.638028 | 0.195 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 0.639400 | 0.194 |
R-HSA-163841 | Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | 0.644942 | 0.190 |
R-HSA-109582 | Hemostasis | 0.651379 | 0.186 |
R-HSA-9645723 | Diseases of programmed cell death | 0.652621 | 0.185 |
R-HSA-5617833 | Cilium Assembly | 0.664423 | 0.178 |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | 0.669513 | 0.174 |
R-HSA-74752 | Signaling by Insulin receptor | 0.671104 | 0.173 |
R-HSA-174824 | Plasma lipoprotein assembly, remodeling, and clearance | 0.671104 | 0.173 |
R-HSA-9772573 | Late SARS-CoV-2 Infection Events | 0.671104 | 0.173 |
R-HSA-195721 | Signaling by WNT | 0.673651 | 0.172 |
R-HSA-68867 | Assembly of the pre-replicative complex | 0.674682 | 0.171 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 0.678221 | 0.169 |
R-HSA-157579 | Telomere Maintenance | 0.691998 | 0.160 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 0.694040 | 0.159 |
R-HSA-8957275 | Post-translational protein phosphorylation | 0.695349 | 0.158 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 0.696408 | 0.157 |
R-HSA-376176 | Signaling by ROBO receptors | 0.696408 | 0.157 |
R-HSA-5610787 | Hedgehog 'off' state | 0.701944 | 0.154 |
R-HSA-382556 | ABC-family proteins mediated transport | 0.701944 | 0.154 |
R-HSA-9009391 | Extra-nuclear estrogen signaling | 0.705188 | 0.152 |
R-HSA-9842860 | Regulation of endogenous retroelements | 0.708397 | 0.150 |
R-HSA-111885 | Opioid Signalling | 0.714711 | 0.146 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 0.714711 | 0.146 |
R-HSA-112315 | Transmission across Chemical Synapses | 0.722307 | 0.141 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 0.723927 | 0.140 |
R-HSA-69239 | Synthesis of DNA | 0.726933 | 0.139 |
R-HSA-69002 | DNA Replication Pre-Initiation | 0.732848 | 0.135 |
R-HSA-6803157 | Antimicrobial peptides | 0.738635 | 0.132 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 0.747083 | 0.127 |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-l... | 0.749839 | 0.125 |
R-HSA-373760 | L1CAM interactions | 0.757926 | 0.120 |
R-HSA-5693538 | Homology Directed Repair | 0.763173 | 0.117 |
R-HSA-73886 | Chromosome Maintenance | 0.770833 | 0.113 |
R-HSA-157118 | Signaling by NOTCH | 0.775721 | 0.110 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 0.775801 | 0.110 |
R-HSA-2132295 | MHC class II antigen presentation | 0.775801 | 0.110 |
R-HSA-6809371 | Formation of the cornified envelope | 0.778245 | 0.109 |
R-HSA-69206 | G1/S Transition | 0.783054 | 0.106 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 0.801275 | 0.096 |
R-HSA-5688426 | Deubiquitination | 0.801709 | 0.096 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 0.811881 | 0.091 |
R-HSA-5358351 | Signaling by Hedgehog | 0.815965 | 0.088 |
R-HSA-416476 | G alpha (q) signalling events | 0.815995 | 0.088 |
R-HSA-9664407 | Parasite infection | 0.819960 | 0.086 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 0.819960 | 0.086 |
R-HSA-9664417 | Leishmania phagocytosis | 0.819960 | 0.086 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 0.821925 | 0.085 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 0.827693 | 0.082 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 0.833276 | 0.079 |
R-HSA-2173782 | Binding and Uptake of Ligands by Scavenger Receptors | 0.840440 | 0.075 |
R-HSA-5663205 | Infectious disease | 0.843461 | 0.074 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 0.845612 | 0.073 |
R-HSA-69306 | DNA Replication | 0.845612 | 0.073 |
R-HSA-9711097 | Cellular response to starvation | 0.853864 | 0.069 |
R-HSA-199991 | Membrane Trafficking | 0.855853 | 0.068 |
R-HSA-5633007 | Regulation of TP53 Activity | 0.857040 | 0.067 |
R-HSA-382551 | Transport of small molecules | 0.857824 | 0.067 |
R-HSA-168249 | Innate Immune System | 0.875548 | 0.058 |
R-HSA-5689880 | Ub-specific processing proteases | 0.877434 | 0.057 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 0.878775 | 0.056 |
R-HSA-9678108 | SARS-CoV-1 Infection | 0.880101 | 0.055 |
R-HSA-5653656 | Vesicle-mediated transport | 0.891186 | 0.050 |
R-HSA-6798695 | Neutrophil degranulation | 0.894384 | 0.048 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 0.908948 | 0.041 |
R-HSA-6805567 | Keratinization | 0.915707 | 0.038 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 0.922054 | 0.035 |
R-HSA-9748784 | Drug ADME | 0.926154 | 0.033 |
R-HSA-8951664 | Neddylation | 0.928558 | 0.032 |
R-HSA-597592 | Post-translational protein modification | 0.928591 | 0.032 |
R-HSA-198933 | Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 0.934595 | 0.029 |
R-HSA-8939211 | ESR-mediated signaling | 0.940124 | 0.027 |
R-HSA-202733 | Cell surface interactions at the vascular wall | 0.940124 | 0.027 |
R-HSA-446203 | Asparagine N-linked glycosylation | 0.954874 | 0.020 |
R-HSA-1474244 | Extracellular matrix organization | 0.978862 | 0.009 |
R-HSA-73894 | DNA Repair | 0.984689 | 0.007 |
R-HSA-9824439 | Bacterial Infection Pathways | 0.989160 | 0.005 |
R-HSA-418594 | G alpha (i) signalling events | 0.991033 | 0.004 |
R-HSA-388396 | GPCR downstream signalling | 0.992741 | 0.003 |
R-HSA-5668914 | Diseases of metabolism | 0.992829 | 0.003 |
R-HSA-392499 | Metabolism of proteins | 0.996370 | 0.002 |
R-HSA-372790 | Signaling by GPCR | 0.996617 | 0.001 |
R-HSA-9709957 | Sensory Perception | 0.999918 | 0.000 |
R-HSA-556833 | Metabolism of lipids | 0.999994 | 0.000 |
R-HSA-1430728 | Metabolism | 1.000000 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
GSK3A |
0.795 | 0.536 | 4 | 0.659 |
GSK3B |
0.783 | 0.508 | 4 | 0.661 |
CLK3 |
0.775 | 0.249 | 1 | 0.802 |
CLK2 |
0.765 | 0.230 | -3 | 0.688 |
KIS |
0.762 | 0.150 | 1 | 0.740 |
COT |
0.759 | 0.175 | 2 | 0.822 |
GRK1 |
0.759 | 0.264 | -2 | 0.819 |
NDR2 |
0.752 | 0.110 | -3 | 0.815 |
PIM3 |
0.752 | 0.126 | -3 | 0.795 |
MTOR |
0.752 | 0.147 | 1 | 0.707 |
MOS |
0.750 | 0.154 | 1 | 0.786 |
HIPK4 |
0.750 | 0.100 | 1 | 0.832 |
DYRK2 |
0.749 | 0.147 | 1 | 0.798 |
SRPK1 |
0.749 | 0.091 | -3 | 0.703 |
CDC7 |
0.748 | 0.084 | 1 | 0.736 |
SKMLCK |
0.746 | 0.141 | -2 | 0.874 |
GRK7 |
0.746 | 0.245 | 1 | 0.692 |
HIPK2 |
0.744 | 0.131 | 1 | 0.734 |
DYRK4 |
0.743 | 0.160 | 1 | 0.729 |
RSK2 |
0.742 | 0.104 | -3 | 0.714 |
CDK1 |
0.741 | 0.124 | 1 | 0.721 |
PIM1 |
0.740 | 0.107 | -3 | 0.726 |
GRK5 |
0.739 | 0.188 | -3 | 0.783 |
ATR |
0.739 | 0.076 | 1 | 0.761 |
NLK |
0.739 | 0.069 | 1 | 0.810 |
IKKB |
0.739 | 0.107 | -2 | 0.722 |
CLK4 |
0.739 | 0.122 | -3 | 0.687 |
CDK18 |
0.737 | 0.099 | 1 | 0.704 |
ERK5 |
0.737 | 0.073 | 1 | 0.797 |
CAMK2A |
0.737 | 0.168 | 2 | 0.747 |
PRPK |
0.736 | -0.008 | -1 | 0.789 |
CHAK2 |
0.735 | 0.068 | -1 | 0.792 |
CAMK2G |
0.735 | 0.108 | 2 | 0.741 |
CDK8 |
0.734 | 0.087 | 1 | 0.725 |
PRKD1 |
0.734 | 0.039 | -3 | 0.789 |
P90RSK |
0.734 | 0.070 | -3 | 0.718 |
CDK19 |
0.734 | 0.089 | 1 | 0.700 |
GRK6 |
0.734 | 0.203 | 1 | 0.728 |
JNK3 |
0.734 | 0.136 | 1 | 0.714 |
HIPK1 |
0.734 | 0.108 | 1 | 0.809 |
CDKL1 |
0.733 | 0.026 | -3 | 0.740 |
CAMK2B |
0.733 | 0.154 | 2 | 0.721 |
IKKA |
0.733 | 0.091 | -2 | 0.718 |
ICK |
0.733 | 0.070 | -3 | 0.784 |
CK1E |
0.733 | 0.108 | -3 | 0.549 |
JNK2 |
0.732 | 0.126 | 1 | 0.682 |
CAMK1B |
0.732 | 0.023 | -3 | 0.765 |
CDKL5 |
0.732 | 0.024 | -3 | 0.735 |
NDR1 |
0.732 | 0.014 | -3 | 0.774 |
PDHK4 |
0.731 | -0.009 | 1 | 0.736 |
LATS1 |
0.731 | 0.162 | -3 | 0.835 |
PRKX |
0.731 | 0.110 | -3 | 0.637 |
BMPR1B |
0.731 | 0.107 | 1 | 0.707 |
AURC |
0.730 | 0.054 | -2 | 0.665 |
SRPK2 |
0.730 | 0.043 | -3 | 0.627 |
PASK |
0.729 | 0.219 | -3 | 0.825 |
PKACG |
0.729 | 0.058 | -2 | 0.739 |
CLK1 |
0.729 | 0.092 | -3 | 0.659 |
FAM20C |
0.729 | 0.081 | 2 | 0.554 |
RAF1 |
0.729 | -0.033 | 1 | 0.695 |
CDK7 |
0.729 | 0.064 | 1 | 0.736 |
CDK13 |
0.729 | 0.090 | 1 | 0.717 |
RSK4 |
0.729 | 0.092 | -3 | 0.708 |
NUAK2 |
0.729 | 0.007 | -3 | 0.765 |
CK1D |
0.729 | 0.137 | -3 | 0.508 |
CDK5 |
0.728 | 0.077 | 1 | 0.759 |
LATS2 |
0.728 | 0.033 | -5 | 0.731 |
RIPK3 |
0.728 | 0.025 | 3 | 0.742 |
GRK4 |
0.728 | 0.119 | -2 | 0.842 |
SRPK3 |
0.728 | 0.046 | -3 | 0.671 |
MARK4 |
0.728 | -0.026 | 4 | 0.173 |
CAMK2D |
0.728 | 0.080 | -3 | 0.769 |
P38G |
0.727 | 0.097 | 1 | 0.648 |
PRKD2 |
0.727 | 0.025 | -3 | 0.724 |
DSTYK |
0.727 | -0.020 | 2 | 0.828 |
P38B |
0.727 | 0.109 | 1 | 0.711 |
PKACB |
0.726 | 0.070 | -2 | 0.678 |
CDK17 |
0.726 | 0.086 | 1 | 0.659 |
MSK1 |
0.726 | 0.096 | -3 | 0.691 |
BMPR2 |
0.725 | -0.068 | -2 | 0.869 |
WNK1 |
0.725 | -0.012 | -2 | 0.875 |
CK1A |
0.725 | 0.199 | -3 | 0.428 |
ERK1 |
0.725 | 0.097 | 1 | 0.697 |
GCN2 |
0.725 | -0.099 | 2 | 0.737 |
DAPK2 |
0.725 | 0.017 | -3 | 0.784 |
MST4 |
0.725 | -0.005 | 2 | 0.800 |
HUNK |
0.725 | -0.037 | 2 | 0.795 |
CK1A2 |
0.725 | 0.132 | -3 | 0.504 |
P38D |
0.725 | 0.120 | 1 | 0.666 |
CK1G1 |
0.725 | 0.119 | -3 | 0.537 |
MAPKAPK2 |
0.724 | 0.047 | -3 | 0.689 |
DYRK3 |
0.724 | 0.096 | 1 | 0.814 |
RSK3 |
0.724 | 0.009 | -3 | 0.701 |
CAMLCK |
0.723 | 0.014 | -2 | 0.840 |
NEK6 |
0.723 | -0.036 | -2 | 0.847 |
CDK3 |
0.723 | 0.088 | 1 | 0.679 |
DYRK1B |
0.723 | 0.095 | 1 | 0.747 |
TBK1 |
0.723 | -0.068 | 1 | 0.577 |
CDK12 |
0.723 | 0.083 | 1 | 0.690 |
CDK10 |
0.722 | 0.092 | 1 | 0.726 |
MLK1 |
0.722 | 0.010 | 2 | 0.755 |
P38A |
0.722 | 0.075 | 1 | 0.758 |
NIK |
0.722 | -0.032 | -3 | 0.787 |
MASTL |
0.722 | -0.009 | -2 | 0.799 |
DLK |
0.722 | 0.071 | 1 | 0.706 |
JNK1 |
0.721 | 0.132 | 1 | 0.690 |
PKN2 |
0.721 | -0.020 | -3 | 0.752 |
AMPKA1 |
0.721 | -0.034 | -3 | 0.782 |
IKKE |
0.721 | -0.046 | 1 | 0.570 |
CDK9 |
0.721 | 0.071 | 1 | 0.719 |
P70S6KB |
0.721 | 0.015 | -3 | 0.714 |
PKN3 |
0.720 | -0.034 | -3 | 0.763 |
CDK14 |
0.720 | 0.080 | 1 | 0.733 |
TGFBR1 |
0.720 | 0.072 | -2 | 0.824 |
TGFBR2 |
0.719 | -0.056 | -2 | 0.808 |
MSK2 |
0.719 | 0.034 | -3 | 0.698 |
DYRK1A |
0.719 | 0.064 | 1 | 0.762 |
ATM |
0.718 | 0.030 | 1 | 0.698 |
NEK7 |
0.718 | -0.062 | -3 | 0.766 |
PAK1 |
0.718 | 0.026 | -2 | 0.782 |
ALK4 |
0.717 | 0.044 | -2 | 0.846 |
CDK16 |
0.717 | 0.073 | 1 | 0.678 |
PKCB |
0.717 | -0.002 | 2 | 0.675 |
GRK2 |
0.717 | 0.080 | -2 | 0.730 |
MPSK1 |
0.717 | 0.111 | 1 | 0.797 |
ULK2 |
0.717 | -0.134 | 2 | 0.717 |
AMPKA2 |
0.717 | -0.022 | -3 | 0.753 |
ERK2 |
0.717 | 0.076 | 1 | 0.727 |
IRE1 |
0.716 | -0.049 | 1 | 0.739 |
SMG1 |
0.716 | 0.017 | 1 | 0.726 |
PDHK1 |
0.716 | -0.145 | 1 | 0.707 |
MNK1 |
0.716 | 0.021 | -2 | 0.789 |
MLK3 |
0.716 | -0.003 | 2 | 0.692 |
GRK3 |
0.716 | 0.124 | -2 | 0.702 |
TLK2 |
0.716 | 0.069 | 1 | 0.694 |
PKCD |
0.716 | -0.025 | 2 | 0.718 |
MAPKAPK3 |
0.716 | -0.018 | -3 | 0.720 |
MAK |
0.715 | 0.114 | -2 | 0.742 |
QSK |
0.715 | -0.036 | 4 | 0.146 |
RIPK1 |
0.715 | -0.024 | 1 | 0.723 |
CK2A1 |
0.715 | 0.194 | 1 | 0.629 |
TSSK1 |
0.715 | -0.037 | -3 | 0.809 |
DNAPK |
0.714 | 0.069 | 1 | 0.610 |
PRP4 |
0.714 | 0.072 | -3 | 0.742 |
HIPK3 |
0.714 | 0.054 | 1 | 0.762 |
MLK2 |
0.713 | -0.057 | 2 | 0.763 |
MNK2 |
0.713 | -0.012 | -2 | 0.781 |
TSSK2 |
0.713 | -0.036 | -5 | 0.787 |
PKCG |
0.713 | -0.029 | 2 | 0.690 |
MARK3 |
0.713 | -0.036 | 4 | 0.146 |
PKCZ |
0.713 | -0.013 | 2 | 0.712 |
BCKDK |
0.712 | -0.113 | -1 | 0.729 |
VRK2 |
0.712 | 0.045 | 1 | 0.797 |
ACVR2B |
0.712 | 0.052 | -2 | 0.806 |
NIM1 |
0.712 | -0.035 | 3 | 0.763 |
ANKRD3 |
0.712 | -0.047 | 1 | 0.739 |
GAK |
0.712 | 0.208 | 1 | 0.830 |
CK2A2 |
0.711 | 0.141 | 1 | 0.648 |
PKCA |
0.711 | -0.020 | 2 | 0.665 |
AKT2 |
0.711 | 0.020 | -3 | 0.626 |
ALK2 |
0.711 | 0.061 | -2 | 0.830 |
MYLK4 |
0.711 | 0.014 | -2 | 0.774 |
TTBK2 |
0.710 | -0.045 | 2 | 0.664 |
PKR |
0.710 | 0.002 | 1 | 0.764 |
CDK2 |
0.710 | 0.018 | 1 | 0.776 |
ULK1 |
0.710 | -0.096 | -3 | 0.721 |
AURB |
0.710 | 0.016 | -2 | 0.659 |
BMPR1A |
0.710 | 0.072 | 1 | 0.675 |
PLK1 |
0.709 | 0.053 | -2 | 0.776 |
DRAK1 |
0.709 | 0.039 | 1 | 0.667 |
ACVR2A |
0.709 | 0.037 | -2 | 0.792 |
PKG2 |
0.708 | 0.011 | -2 | 0.674 |
NEK9 |
0.708 | -0.096 | 2 | 0.757 |
MEK1 |
0.708 | -0.026 | 2 | 0.816 |
AURA |
0.708 | 0.033 | -2 | 0.636 |
PIM2 |
0.708 | 0.018 | -3 | 0.671 |
CAMK1G |
0.708 | 0.003 | -3 | 0.680 |
PAK3 |
0.708 | -0.031 | -2 | 0.773 |
DCAMKL1 |
0.707 | 0.018 | -3 | 0.723 |
CHAK1 |
0.707 | -0.055 | 2 | 0.730 |
MEKK3 |
0.706 | 0.085 | 1 | 0.675 |
CAMK4 |
0.706 | -0.057 | -3 | 0.735 |
MARK2 |
0.706 | -0.072 | 4 | 0.131 |
MST3 |
0.706 | 0.033 | 2 | 0.802 |
WNK3 |
0.706 | -0.178 | 1 | 0.690 |
QIK |
0.705 | -0.090 | -3 | 0.750 |
MLK4 |
0.705 | -0.029 | 2 | 0.673 |
PAK2 |
0.705 | -0.006 | -2 | 0.763 |
SIK |
0.705 | -0.047 | -3 | 0.687 |
MOK |
0.704 | 0.070 | 1 | 0.845 |
PKCH |
0.704 | -0.036 | 2 | 0.656 |
YSK4 |
0.704 | -0.032 | 1 | 0.628 |
PKACA |
0.703 | 0.037 | -2 | 0.631 |
SGK3 |
0.703 | -0.006 | -3 | 0.698 |
PRKD3 |
0.703 | -0.046 | -3 | 0.671 |
PLK3 |
0.702 | 0.031 | 2 | 0.736 |
BRSK1 |
0.701 | -0.056 | -3 | 0.720 |
PHKG1 |
0.700 | -0.091 | -3 | 0.762 |
DAPK1 |
0.700 | 0.070 | -3 | 0.714 |
IRE2 |
0.700 | -0.088 | 2 | 0.660 |
NUAK1 |
0.699 | -0.087 | -3 | 0.707 |
TAO3 |
0.698 | 0.016 | 1 | 0.668 |
PINK1 |
0.698 | -0.065 | 1 | 0.827 |
BRSK2 |
0.698 | -0.095 | -3 | 0.733 |
MEK5 |
0.697 | -0.066 | 2 | 0.775 |
MELK |
0.697 | -0.085 | -3 | 0.725 |
DAPK3 |
0.697 | 0.025 | -3 | 0.732 |
NEK5 |
0.697 | -0.045 | 1 | 0.728 |
TLK1 |
0.697 | -0.045 | -2 | 0.845 |
MARK1 |
0.697 | -0.083 | 4 | 0.144 |
NEK2 |
0.696 | -0.101 | 2 | 0.743 |
MAPKAPK5 |
0.696 | -0.039 | -3 | 0.654 |
SSTK |
0.695 | -0.058 | 4 | 0.136 |
PKCE |
0.695 | -0.009 | 2 | 0.671 |
PLK4 |
0.695 | -0.070 | 2 | 0.613 |
PAK6 |
0.694 | -0.029 | -2 | 0.688 |
BUB1 |
0.694 | 0.077 | -5 | 0.772 |
SMMLCK |
0.694 | -0.013 | -3 | 0.730 |
LKB1 |
0.694 | -0.025 | -3 | 0.777 |
MEKK2 |
0.694 | -0.039 | 2 | 0.740 |
CDK6 |
0.692 | 0.038 | 1 | 0.711 |
PERK |
0.692 | -0.099 | -2 | 0.827 |
GCK |
0.692 | 0.033 | 1 | 0.660 |
NEK11 |
0.692 | -0.037 | 1 | 0.650 |
WNK4 |
0.692 | -0.087 | -2 | 0.867 |
ZAK |
0.691 | -0.085 | 1 | 0.643 |
PLK2 |
0.691 | 0.067 | -3 | 0.654 |
ERK7 |
0.691 | -0.001 | 2 | 0.493 |
CHK1 |
0.691 | -0.068 | -3 | 0.756 |
AKT1 |
0.690 | -0.009 | -3 | 0.648 |
SGK1 |
0.690 | 0.032 | -3 | 0.561 |
DCAMKL2 |
0.690 | -0.040 | -3 | 0.722 |
P70S6K |
0.689 | -0.013 | -3 | 0.630 |
PKCI |
0.689 | -0.045 | 2 | 0.685 |
MEKK1 |
0.689 | -0.114 | 1 | 0.684 |
CAMK1D |
0.688 | -0.013 | -3 | 0.615 |
CDK4 |
0.687 | 0.033 | 1 | 0.690 |
IRAK4 |
0.687 | -0.117 | 1 | 0.715 |
PBK |
0.687 | 0.048 | 1 | 0.771 |
SNRK |
0.687 | -0.152 | 2 | 0.632 |
PKCT |
0.686 | -0.078 | 2 | 0.660 |
CK1G3 |
0.686 | 0.161 | -3 | 0.387 |
BRAF |
0.685 | -0.122 | -4 | 0.532 |
CAMKK2 |
0.685 | -0.028 | -2 | 0.718 |
PDK1 |
0.685 | -0.035 | 1 | 0.665 |
ROCK2 |
0.684 | 0.013 | -3 | 0.719 |
HRI |
0.684 | -0.163 | -2 | 0.836 |
HPK1 |
0.684 | 0.001 | 1 | 0.642 |
STK33 |
0.684 | -0.018 | 2 | 0.613 |
EEF2K |
0.684 | -0.009 | 3 | 0.793 |
MRCKA |
0.684 | 0.013 | -3 | 0.674 |
AKT3 |
0.683 | -0.005 | -3 | 0.587 |
PAK4 |
0.683 | -0.005 | -2 | 0.647 |
YANK3 |
0.682 | 0.017 | 2 | 0.428 |
CAMKK1 |
0.682 | -0.085 | -2 | 0.720 |
VRK1 |
0.682 | -0.038 | 2 | 0.779 |
MST2 |
0.682 | -0.040 | 1 | 0.663 |
NEK8 |
0.681 | -0.105 | 2 | 0.745 |
PAK5 |
0.681 | -0.033 | -2 | 0.641 |
CK1G2 |
0.681 | 0.157 | -3 | 0.467 |
LRRK2 |
0.680 | -0.059 | 2 | 0.776 |
TTBK1 |
0.679 | -0.085 | 2 | 0.593 |
MEKK6 |
0.679 | -0.127 | 1 | 0.669 |
MAP3K15 |
0.679 | -0.082 | 1 | 0.626 |
PDHK4_TYR |
0.678 | 0.277 | 2 | 0.836 |
TNIK |
0.678 | -0.054 | 3 | 0.841 |
MRCKB |
0.678 | -0.019 | -3 | 0.657 |
PDHK3_TYR |
0.678 | 0.271 | 4 | 0.260 |
TAO2 |
0.677 | -0.113 | 2 | 0.769 |
KHS2 |
0.677 | -0.006 | 1 | 0.649 |
DMPK1 |
0.677 | 0.017 | -3 | 0.681 |
MINK |
0.676 | -0.067 | 1 | 0.641 |
TAK1 |
0.675 | -0.022 | 1 | 0.669 |
HGK |
0.675 | -0.072 | 3 | 0.837 |
SLK |
0.675 | -0.036 | -2 | 0.694 |
CHK2 |
0.674 | -0.037 | -3 | 0.567 |
PHKG2 |
0.674 | -0.135 | -3 | 0.698 |
KHS1 |
0.674 | -0.045 | 1 | 0.633 |
SBK |
0.674 | 0.004 | -3 | 0.519 |
HASPIN |
0.673 | -0.003 | -1 | 0.670 |
NEK4 |
0.673 | -0.138 | 1 | 0.662 |
NEK1 |
0.672 | -0.095 | 1 | 0.689 |
MAP2K6_TYR |
0.672 | 0.213 | -1 | 0.809 |
CRIK |
0.671 | 0.017 | -3 | 0.662 |
MST1 |
0.670 | -0.079 | 1 | 0.646 |
CAMK1A |
0.670 | -0.042 | -3 | 0.589 |
LOK |
0.669 | -0.097 | -2 | 0.738 |
IRAK1 |
0.668 | -0.192 | -1 | 0.668 |
OSR1 |
0.668 | -0.035 | 2 | 0.764 |
MAP2K4_TYR |
0.667 | 0.149 | -1 | 0.805 |
ROCK1 |
0.667 | -0.014 | -3 | 0.670 |
PKN1 |
0.666 | -0.082 | -3 | 0.645 |
BIKE |
0.666 | 0.045 | 1 | 0.780 |
BMPR2_TYR |
0.666 | 0.110 | -1 | 0.788 |
PDHK1_TYR |
0.665 | 0.121 | -1 | 0.804 |
TTK |
0.665 | -0.037 | -2 | 0.815 |
YSK1 |
0.663 | -0.105 | 2 | 0.732 |
TESK1_TYR |
0.663 | -0.014 | 3 | 0.858 |
PKMYT1_TYR |
0.662 | 0.007 | 3 | 0.833 |
ALPHAK3 |
0.662 | 0.036 | -1 | 0.682 |
MEK2 |
0.661 | -0.176 | 2 | 0.764 |
PKG1 |
0.659 | -0.053 | -2 | 0.595 |
MAP2K7_TYR |
0.659 | -0.003 | 2 | 0.801 |
MYO3B |
0.658 | -0.073 | 2 | 0.754 |
AAK1 |
0.657 | 0.073 | 1 | 0.714 |
LIMK2_TYR |
0.656 | -0.039 | -3 | 0.812 |
YANK2 |
0.655 | 0.019 | 2 | 0.433 |
RIPK2 |
0.655 | -0.167 | 1 | 0.582 |
PINK1_TYR |
0.653 | -0.074 | 1 | 0.750 |
MYO3A |
0.650 | -0.092 | 1 | 0.672 |
ASK1 |
0.650 | -0.112 | 1 | 0.616 |
NEK3 |
0.648 | -0.206 | 1 | 0.624 |
FGR |
0.647 | -0.049 | 1 | 0.768 |
LIMK1_TYR |
0.647 | -0.122 | 2 | 0.774 |
DDR1 |
0.646 | -0.082 | 4 | 0.215 |
EPHB4 |
0.644 | -0.047 | -1 | 0.710 |
YES1 |
0.644 | -0.034 | -1 | 0.751 |
TXK |
0.644 | 0.001 | 1 | 0.730 |
EPHA6 |
0.644 | -0.092 | -1 | 0.742 |
TAO1 |
0.643 | -0.131 | 1 | 0.578 |
ABL2 |
0.643 | -0.057 | -1 | 0.706 |
RET |
0.643 | -0.140 | 1 | 0.688 |
TNK2 |
0.642 | -0.034 | 3 | 0.727 |
EPHA4 |
0.641 | -0.006 | 2 | 0.760 |
BLK |
0.641 | -0.007 | -1 | 0.729 |
FYN |
0.640 | 0.031 | -1 | 0.705 |
LCK |
0.640 | -0.046 | -1 | 0.723 |
MST1R |
0.639 | -0.189 | 3 | 0.796 |
ABL1 |
0.639 | -0.070 | -1 | 0.699 |
CSF1R |
0.638 | -0.117 | 3 | 0.775 |
DDR2 |
0.638 | 0.030 | 3 | 0.706 |
MET |
0.637 | -0.059 | 3 | 0.768 |
FER |
0.637 | -0.110 | 1 | 0.753 |
SRMS |
0.637 | -0.033 | 1 | 0.726 |
TYRO3 |
0.636 | -0.181 | 3 | 0.781 |
TYK2 |
0.636 | -0.200 | 1 | 0.675 |
STLK3 |
0.636 | -0.136 | 1 | 0.603 |
PTK2 |
0.636 | 0.049 | -1 | 0.682 |
HCK |
0.636 | -0.087 | -1 | 0.718 |
INSRR |
0.635 | -0.062 | 3 | 0.732 |
KIT |
0.635 | -0.075 | 3 | 0.774 |
ITK |
0.635 | -0.065 | -1 | 0.686 |
JAK2 |
0.635 | -0.156 | 1 | 0.663 |
ROS1 |
0.635 | -0.192 | 3 | 0.760 |
FLT1 |
0.635 | 0.012 | -1 | 0.715 |
SYK |
0.634 | 0.088 | -1 | 0.661 |
KDR |
0.634 | -0.089 | 3 | 0.738 |
EPHB1 |
0.634 | -0.049 | 1 | 0.705 |
JAK3 |
0.634 | -0.128 | 1 | 0.663 |
BMX |
0.631 | -0.034 | -1 | 0.609 |
EPHB3 |
0.631 | -0.075 | -1 | 0.688 |
FGFR2 |
0.631 | -0.126 | 3 | 0.775 |
WEE1_TYR |
0.631 | -0.061 | -1 | 0.651 |
TNK1 |
0.630 | -0.130 | 3 | 0.774 |
EPHB2 |
0.629 | -0.072 | -1 | 0.681 |
TNNI3K_TYR |
0.628 | -0.133 | 1 | 0.702 |
SRC |
0.628 | -0.021 | -1 | 0.701 |
EPHA3 |
0.626 | -0.069 | 2 | 0.722 |
FGFR3 |
0.626 | -0.073 | 3 | 0.746 |
MERTK |
0.626 | -0.100 | 3 | 0.762 |
ERBB2 |
0.625 | -0.089 | 1 | 0.655 |
PTK2B |
0.624 | -0.052 | -1 | 0.665 |
PDGFRB |
0.624 | -0.191 | 3 | 0.782 |
LYN |
0.624 | -0.077 | 3 | 0.704 |
NEK10_TYR |
0.623 | -0.126 | 1 | 0.551 |
TEC |
0.623 | -0.100 | -1 | 0.619 |
EPHA7 |
0.623 | -0.072 | 2 | 0.746 |
FLT3 |
0.622 | -0.196 | 3 | 0.769 |
JAK1 |
0.622 | -0.123 | 1 | 0.598 |
EPHA5 |
0.622 | -0.025 | 2 | 0.739 |
AXL |
0.622 | -0.149 | 3 | 0.762 |
TEK |
0.622 | -0.192 | 3 | 0.718 |
NTRK1 |
0.621 | -0.115 | -1 | 0.707 |
FGFR1 |
0.620 | -0.179 | 3 | 0.741 |
BTK |
0.620 | -0.167 | -1 | 0.654 |
MATK |
0.619 | -0.086 | -1 | 0.640 |
FRK |
0.619 | -0.119 | -1 | 0.724 |
PTK6 |
0.619 | -0.144 | -1 | 0.620 |
EGFR |
0.619 | -0.036 | 1 | 0.579 |
EPHA8 |
0.618 | -0.052 | -1 | 0.673 |
ERBB4 |
0.617 | -0.007 | 1 | 0.616 |
FLT4 |
0.617 | -0.122 | 3 | 0.738 |
PDGFRA |
0.617 | -0.223 | 3 | 0.782 |
FGFR4 |
0.616 | -0.033 | -1 | 0.650 |
ZAP70 |
0.616 | 0.038 | -1 | 0.605 |
INSR |
0.615 | -0.144 | 3 | 0.718 |
NTRK3 |
0.615 | -0.101 | -1 | 0.663 |
LTK |
0.614 | -0.147 | 3 | 0.717 |
ALK |
0.614 | -0.183 | 3 | 0.690 |
CSK |
0.613 | -0.080 | 2 | 0.743 |
EPHA2 |
0.613 | -0.029 | -1 | 0.634 |
EPHA1 |
0.612 | -0.178 | 3 | 0.752 |
NTRK2 |
0.609 | -0.184 | 3 | 0.728 |
IGF1R |
0.605 | -0.102 | 3 | 0.659 |
MUSK |
0.597 | -0.138 | 1 | 0.586 |
FES |
0.591 | -0.113 | -1 | 0.585 |