Motif 387 (n=112)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A087WTJ2 | GIMAP1-GIMAP5 | S424 | ochoa | GIMAP1-GIMAP5 readthrough | None |
A0A0C4DFX4 | None | S3034 | ochoa | Snf2 related CREBBP activator protein | None |
A8CG34 | POM121C | S328 | ochoa | Nuclear envelope pore membrane protein POM 121C (Nuclear pore membrane protein 121-2) (POM121-2) (Pore membrane protein of 121 kDa C) | Essential component of the nuclear pore complex (NPC). The repeat-containing domain may be involved in anchoring components of the pore complex to the pore membrane. When overexpressed in cells induces the formation of cytoplasmic annulate lamellae (AL). {ECO:0000269|PubMed:17900573}. |
O00273 | DFFA | S257 | ochoa | DNA fragmentation factor subunit alpha (DNA fragmentation factor 45 kDa subunit) (DFF-45) (Inhibitor of CAD) (ICAD) | Inhibitor of the caspase-activated DNase (DFF40). |
O14686 | KMT2D | S3202 | 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}. |
O14874 | BCKDK | S360 | ochoa | Branched-chain alpha-ketoacid dehydrogenase kinase (BCKDH kinase) (BCKDHKIN) (BDK) (EC 2.7.11.1) ([3-methyl-2-oxobutanoate dehydrogenase [lipoamide]] kinase, mitochondrial) (EC 2.7.11.4) | Serine/threonine-protein kinase component of macronutrients metabolism. Forms a functional kinase and phosphatase pair with PPM1K, serving as a metabolic regulatory node that coordinates branched-chain amino acids (BCAAs) with glucose and lipid metabolism via two distinct phosphoprotein targets: mitochondrial BCKDHA subunit of the branched-chain alpha-ketoacid dehydrogenase (BCKDH) complex and cytosolic ACLY, a lipogenic enzyme of Krebs cycle (PubMed:24449431, PubMed:29779826, PubMed:37558654). Phosphorylates and inactivates mitochondrial BCKDH complex a multisubunit complex consisting of three multimeric components each involved in different steps of BCAA catabolism: E1 composed of BCKDHA and BCKDHB, E2 core composed of DBT monomers, and E3 composed of DLD monomers. Associates with the E2 component of BCKDH complex and phosphorylates BCKDHA on Ser-337, leading to conformational changes that interrupt substrate channeling between E1 and E2 and inactivates the BCKDH complex (PubMed:29779826, PubMed:37558654). Phosphorylates ACLY on Ser-455 in response to changes in cellular carbohydrate abundance such as occurs during fasting to feeding metabolic transition. Refeeding stimulates MLXIPL/ChREBP transcription factor, leading to increased BCKDK to PPM1K expression ratio, phosphorylation and activation of ACLY that ultimately results in the generation of malonyl-CoA and oxaloacetate immediate substrates of de novo lipogenesis and glucogenesis, respectively (PubMed:29779826). Recognizes phosphosites having SxxE/D canonical motif (PubMed:29779826). {ECO:0000269|PubMed:24449431, ECO:0000269|PubMed:29779826, ECO:0000269|PubMed:37558654}. |
O15055 | PER2 | S696 | psp | Period circadian protein homolog 2 (hPER2) (Circadian clock protein PERIOD 2) | Transcriptional repressor which forms a core component of the circadian clock. The circadian clock, an internal time-keeping system, regulates various physiological processes through the generation of approximately 24 hour circadian rhythms in gene expression, which are translated into rhythms in metabolism and behavior. It is derived from the Latin roots 'circa' (about) and 'diem' (day) and acts as an important regulator of a wide array of physiological functions including metabolism, sleep, body temperature, blood pressure, endocrine, immune, cardiovascular, and renal function. Consists of two major components: the central clock, residing in the suprachiasmatic nucleus (SCN) of the brain, and the peripheral clocks that are present in nearly every tissue and organ system. Both the central and peripheral clocks can be reset by environmental cues, also known as Zeitgebers (German for 'timegivers'). The predominant Zeitgeber for the central clock is light, which is sensed by retina and signals directly to the SCN. The central clock entrains the peripheral clocks through neuronal and hormonal signals, body temperature and feeding-related cues, aligning all clocks with the external light/dark cycle. Circadian rhythms allow an organism to achieve temporal homeostasis with its environment at the molecular level by regulating gene expression to create a peak of protein expression once every 24 hours to control when a particular physiological process is most active with respect to the solar day. Transcription and translation of core clock components (CLOCK, NPAS2, BMAL1, BMAL2, PER1, PER2, PER3, CRY1 and CRY2) plays a critical role in rhythm generation, whereas delays imposed by post-translational modifications (PTMs) are important for determining the period (tau) of the rhythms (tau refers to the period of a rhythm and is the length, in time, of one complete cycle). A diurnal rhythm is synchronized with the day/night cycle, while the ultradian and infradian rhythms have a period shorter and longer than 24 hours, respectively. Disruptions in the circadian rhythms contribute to the pathology of cardiovascular diseases, cancer, metabolic syndrome and aging. A transcription/translation feedback loop (TTFL) forms the core of the molecular circadian clock mechanism. Transcription factors, CLOCK or NPAS2 and BMAL1 or BMAL2, form the positive limb of the feedback loop, act in the form of a heterodimer and activate the transcription of core clock genes and clock-controlled genes (involved in key metabolic processes), harboring E-box elements (5'-CACGTG-3') within their promoters. The core clock genes: PER1/2/3 and CRY1/2 which are transcriptional repressors form the negative limb of the feedback loop and interact with the CLOCK|NPAS2-BMAL1|BMAL2 heterodimer inhibiting its activity and thereby negatively regulating their own expression. This heterodimer also activates nuclear receptors NR1D1/2 and RORA/B/G, which form a second feedback loop and which activate and repress BMAL1 transcription, respectively. PER1 and PER2 proteins transport CRY1 and CRY2 into the nucleus with appropriate circadian timing, but also contribute directly to repression of clock-controlled target genes through interaction with several classes of RNA-binding proteins, helicases and others transcriptional repressors. PER appears to regulate circadian control of transcription by at least three different modes. First, interacts directly with the CLOCK-BMAL1 at the tail end of the nascent transcript peak to recruit complexes containing the SIN3-HDAC that remodel chromatin to repress transcription. Second, brings H3K9 methyltransferases such as SUV39H1 and SUV39H2 to the E-box elements of the circadian target genes, like PER2 itself or PER1. The recruitment of each repressive modifier to the DNA seems to be very precisely temporally orchestrated by the large PER complex, the deacetylases acting before than the methyltransferases. Additionally, large PER complexes are also recruited to the target genes 3' termination site through interactions with RNA-binding proteins and helicases that may play a role in transcription termination to regulate transcription independently of CLOCK-BMAL1 interactions. Recruitment of large PER complexes to the elongating polymerase at PER and CRY termination sites inhibited SETX action, impeding RNA polymerase II release and thereby repressing transcriptional reinitiation. May propagate clock information to metabolic pathways via the interaction with nuclear receptors. Coactivator of PPARA and corepressor of NR1D1, binds rhythmically at the promoter of nuclear receptors target genes like BMAL1 or G6PC1. Directly and specifically represses PPARG proadipogenic activity by blocking PPARG recruitment to target promoters and thereby inhibiting transcriptional activation. Required for fatty acid and lipid metabolism, is involved as well in the regulation of circulating insulin levels. Plays an important role in the maintenance of cardiovascular functions through the regulation of NO and vasodilatatory prostaglandins production in aortas. Controls circadian glutamate uptake in synaptic vesicles through the regulation of VGLUT1 expression. May also be involved in the regulation of inflammatory processes. Represses the CLOCK-BMAL1 induced transcription of BHLHE40/DEC1 and ATF4. Negatively regulates the formation of the TIMELESS-CRY1 complex by competing with TIMELESS for binding to CRY1. {ECO:0000250|UniProtKB:O54943}. |
O15355 | PPM1G | S243 | ochoa | Protein phosphatase 1G (EC 3.1.3.16) (Protein phosphatase 1C) (Protein phosphatase 2C isoform gamma) (PP2C-gamma) (Protein phosphatase magnesium-dependent 1 gamma) | None |
O15503 | INSIG1 | S43 | psp | Insulin-induced gene 1 protein (INSIG-1) | Oxysterol-binding protein that mediates feedback control of cholesterol synthesis by controlling both endoplasmic reticulum to Golgi transport of SCAP and degradation of HMGCR (PubMed:12202038, PubMed:12535518, PubMed:16168377, PubMed:16399501, PubMed:16606821, PubMed:32322062). Acts as a negative regulator of cholesterol biosynthesis by mediating the retention of the SCAP-SREBP complex in the endoplasmic reticulum, thereby blocking the processing of sterol regulatory element-binding proteins (SREBPs) SREBF1/SREBP1 and SREBF2/SREBP2 (PubMed:12202038, PubMed:16399501, PubMed:26311497, PubMed:32322062). Binds oxysterol, including 25-hydroxycholesterol, regulating interaction with SCAP and retention of the SCAP-SREBP complex in the endoplasmic reticulum (PubMed:32322062). In presence of oxysterol, interacts with SCAP, retaining the SCAP-SREBP complex in the endoplasmic reticulum, thereby preventing SCAP from escorting SREBF1/SREBP1 and SREBF2/SREBP2 to the Golgi (PubMed:15899885, PubMed:32322062). Sterol deprivation or phosphorylation by PCK1 reduce oxysterol-binding, disrupting the interaction between INSIG1 and SCAP, thereby promoting Golgi transport of the SCAP-SREBP complex, followed by processing and nuclear translocation of SREBF1/SREBP1 and SREBF2/SREBP2 (PubMed:26311497, PubMed:32322062). Also regulates cholesterol synthesis by regulating degradation of HMGCR: initiates the sterol-mediated ubiquitin-mediated endoplasmic reticulum-associated degradation (ERAD) of HMGCR via recruitment of the reductase to the ubiquitin ligases AMFR/gp78 and/or RNF139 (PubMed:12535518, PubMed:16168377, PubMed:22143767). Also regulates degradation of SOAT2/ACAT2 when the lipid levels are low: initiates the ubiquitin-mediated degradation of SOAT2/ACAT2 via recruitment of the ubiquitin ligases AMFR/gp78 (PubMed:28604676). {ECO:0000269|PubMed:12202038, ECO:0000269|PubMed:12535518, ECO:0000269|PubMed:15899885, ECO:0000269|PubMed:16168377, ECO:0000269|PubMed:16399501, ECO:0000269|PubMed:16606821, ECO:0000269|PubMed:22143767, ECO:0000269|PubMed:26311497, ECO:0000269|PubMed:28604676, ECO:0000269|PubMed:32322062}. |
O60299 | LZTS3 | S647 | ochoa | Leucine zipper putative tumor suppressor 3 (ProSAP-interacting protein 1) (ProSAPiP1) | May be involved in promoting the maturation of dendritic spines, probably via regulating SIPA1L1 levels at the postsynaptic density of synapses. {ECO:0000250|UniProtKB:Q8K1Q4}. |
O60361 | NME2P1 | S110 | ochoa | Putative nucleoside diphosphate kinase (NDK) (NDP kinase) (EC 2.7.4.6) | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity). {ECO:0000250}. |
O75150 | RNF40 | S528 | ochoa | E3 ubiquitin-protein ligase BRE1B (BRE1-B) (EC 2.3.2.27) (95 kDa retinoblastoma-associated protein) (RBP95) (RING finger protein 40) (RING-type E3 ubiquitin transferase BRE1B) | Component of the RNF20/40 E3 ubiquitin-protein ligase complex that mediates monoubiquitination of 'Lys-120' of histone H2B (H2BK120ub1). H2BK120ub1 gives a specific tag for epigenetic transcriptional activation and is also prerequisite for histone H3 'Lys-4' and 'Lys-79' methylation (H3K4me and H3K79me, respectively). It thereby plays a central role in histone code and gene regulation. The RNF20/40 complex forms a H2B ubiquitin ligase complex in cooperation with the E2 enzyme UBE2A or UBE2B; reports about the cooperation with UBE2E1/UBCH are contradictory. Required for transcriptional activation of Hox genes. {ECO:0000269|PubMed:16307923, ECO:0000269|PubMed:19410543}.; FUNCTION: (Microbial infection) Promotes the human herpesvirus 8 (KSHV) lytic cycle by inducing the expression of lytic viral genes including the latency switch gene RTA/ORF50. {ECO:0000269|PubMed:37888983}. |
O75815 | BCAR3 | S317 | ochoa | Breast cancer anti-estrogen resistance protein 3 (Novel SH2-containing protein 2) (SH2 domain-containing protein 3B) | Acts as an adapter protein downstream of several growth factor receptors to promote cell proliferation, migration, and redistribution of actin fibers (PubMed:24216110). Specifically involved in INS/insulin signaling pathway by mediating MAPK1/ERK2-MAPK3/ERK1 activation and DNA synthesis (PubMed:24216110). Promotes insulin-mediated membrane ruffling (By similarity). In response to vasoconstrictor peptide EDN1, involved in the activation of RAP1 downstream of PTK2B via interaction with phosphorylated BCAR1 (PubMed:19086031). Inhibits cell migration and invasion via regulation of TGFB-mediated matrix digestion, actin filament rearrangement, and inhibition of invadopodia activity (By similarity). May inhibit TGFB-SMAD signaling, via facilitating BCAR1 and SMAD2 and/or SMAD3 interaction (By similarity). Regulates EGF-induced DNA synthesis (PubMed:18722344). Required for the maintenance of ocular lens morphology and structural integrity, potentially via regulation of focal adhesion complex signaling (By similarity). Acts upstream of PTPRA to regulate the localization of BCAR1 and PTPRA to focal adhesions, via regulation of SRC-mediated phosphorylation of PTPRA (By similarity). Positively regulates integrin-induced tyrosine phosphorylation of BCAR1 (By similarity). Acts as a guanine nucleotide exchange factor (GEF) for small GTPases RALA, RAP1A and RRAS (By similarity). However, in a contrasting study, lacks GEF activity towards RAP1 (PubMed:22081014). {ECO:0000250|UniProtKB:D3ZAZ5, ECO:0000250|UniProtKB:Q9QZK2, ECO:0000269|PubMed:18722344, ECO:0000269|PubMed:19086031, ECO:0000269|PubMed:22081014, ECO:0000269|PubMed:24216110}. |
O75943 | RAD17 | S656 | psp | Cell cycle checkpoint protein RAD17 (hRad17) (RF-C/activator 1 homolog) | Essential for sustained cell growth, maintenance of chromosomal stability, and ATR-dependent checkpoint activation upon DNA damage (PubMed:10208430, PubMed:11418864, PubMed:11687627, PubMed:11799063, PubMed:12672690, PubMed:14624239, PubMed:15235112). Has a weak ATPase activity required for binding to chromatin (PubMed:10208430, PubMed:11418864, PubMed:11687627, PubMed:11799063, PubMed:12672690, PubMed:14624239, PubMed:15235112). Participates in the recruitment of the 9-1-1 (RAD1-RAD9-HUS1) complex and RHNO1 onto chromatin, and in CHEK1 activation (PubMed:21659603). Involved in homologous recombination by mediating recruitment of the MRN complex to DNA damage sites (PubMed:24534091). May also serve as a sensor of DNA replication progression (PubMed:12578958, PubMed:14500819, PubMed:15538388). {ECO:0000269|PubMed:10208430, ECO:0000269|PubMed:11418864, ECO:0000269|PubMed:11687627, ECO:0000269|PubMed:11799063, ECO:0000269|PubMed:12578958, ECO:0000269|PubMed:12672690, ECO:0000269|PubMed:14500819, ECO:0000269|PubMed:14624239, ECO:0000269|PubMed:15235112, ECO:0000269|PubMed:15538388, ECO:0000269|PubMed:21659603, ECO:0000269|PubMed:24534091}. |
O94972 | TRIM37 | S808 | 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}. |
O94992 | HEXIM1 | S69 | ochoa | Protein HEXIM1 (Cardiac lineage protein 1) (Estrogen down-regulated gene 1 protein) (Hexamethylene bis-acetamide-inducible protein 1) (Menage a quatre protein 1) | Transcriptional regulator which functions as a general RNA polymerase II transcription inhibitor (PubMed:14580347, PubMed:15201869, PubMed:15713661). Core component of the 7SK RNP complex: in cooperation with 7SK snRNA sequesters P-TEFb in a large inactive 7SK snRNP complex preventing RNA polymerase II phosphorylation and subsequent transcriptional elongation (PubMed:12832472, PubMed:14580347, PubMed:15201869, PubMed:15713661). May also regulate NF-kappa-B, ESR1, NR3C1 and CIITA-dependent transcriptional activity (PubMed:15940264, PubMed:15941832, PubMed:17088550). Plays a role in the regulation of DNA virus-mediated innate immune response by assembling into the HDP-RNP complex, a complex that serves as a platform for IRF3 phosphorylation and subsequent innate immune response activation through the cGAS-STING pathway (PubMed:28712728). {ECO:0000269|PubMed:12581153, ECO:0000269|PubMed:12832472, ECO:0000269|PubMed:14580347, ECO:0000269|PubMed:15201869, ECO:0000269|PubMed:15713661, ECO:0000269|PubMed:15940264, ECO:0000269|PubMed:15941832, ECO:0000269|PubMed:17088550, ECO:0000269|PubMed:28712728}. |
O95071 | UBR5 | S174 | ochoa|psp | E3 ubiquitin-protein ligase UBR5 (EC 2.3.2.26) (E3 ubiquitin-protein ligase, HECT domain-containing 1) (Hyperplastic discs protein homolog) (hHYD) (Progestin-induced protein) | E3 ubiquitin-protein ligase involved in different protein quality control pathways in the cytoplasm and nucleus (PubMed:29033132, PubMed:33208877, PubMed:37478846, PubMed:37478862). Mainly acts as a ubiquitin chain elongator that extends pre-ubiquitinated substrates (PubMed:29033132, PubMed:37409633). Component of the N-end rule pathway: ubiquitinates proteins bearing specific N-terminal residues that are destabilizing according to the N-end rule, leading to their degradation (By similarity). Recognizes type-1 N-degrons, containing positively charged amino acids (Arg, Lys and His) (By similarity). Together with UBR4, part of a cytoplasm protein quality control pathway that prevents protein aggregation by catalyzing assembly of heterotypic 'Lys-11'-/'Lys-48'-linked branched ubiquitin chains on aggregated proteins, leading to substrate recognition by the segregase p97/VCP and degradation by the proteasome: UBR5 is probably branching multiple 'Lys-48'-linked chains of substrates initially modified with mixed conjugates by UBR4 (PubMed:29033132). Together with ITCH, catalyzes 'Lys-48'-/'Lys-63'-branched ubiquitination of TXNIP, leading to its degradation: UBR5 mediates branching of 'Lys-48'-linked chains of substrates initially modified with 'Lys-63'-linked conjugates by ITCH (PubMed:29378950). Catalytic component of a nuclear protein quality control pathway that mediates ubiquitination and degradation of unpaired transcription factors (i.e. transcription factors that are not assembled into functional multiprotein complexes): specifically recognizes and binds degrons that are not accessible when transcription regulators are associated with their coactivators (PubMed:37478846, PubMed:37478862). Ubiquitinates various unpaired transcription regulator (MYC, SUPT4H1, SUPT5H, CDC20 and MCRS1), as well as ligand-bound nuclear receptors (ESR1, NR1H3, NR3C1, PGR, RARA, RXRA AND VDR) that are not associated with their nuclear receptor coactivators (NCOAs) (PubMed:33208877, PubMed:37478846, PubMed:37478862). Involved in maturation and/or transcriptional regulation of mRNA by mediating polyubiquitination and activation of CDK9 (PubMed:21127351). Also acts as a regulator of DNA damage response by acting as a suppressor of RNF168, an E3 ubiquitin-protein ligase that promotes accumulation of 'Lys-63'-linked histone H2A and H2AX at DNA damage sites, thereby acting as a guard against excessive spreading of ubiquitinated chromatin at damaged chromosomes (PubMed:22884692). Regulates DNA topoisomerase II binding protein (TopBP1) in the DNA damage response (PubMed:11714696). Ubiquitinates acetylated PCK1 (PubMed:21726808). Acts as a positive regulator of the canonical Wnt signaling pathway by mediating (1) ubiquitination and stabilization of CTNNB1, and (2) 'Lys-48'-linked ubiquitination and degradation of TLE3 (PubMed:21118991, PubMed:28689657). Promotes disassembly of the mitotic checkpoint complex (MCC) from the APC/C complex by catalyzing ubiquitination of BUB1B, BUB3 and CDC20 (PubMed:35217622). Plays an essential role in extraembryonic development (By similarity). Required for the maintenance of skeletal tissue homeostasis by acting as an inhibitor of hedgehog (HH) signaling (By similarity). {ECO:0000250|UniProtKB:Q80TP3, ECO:0000269|PubMed:11714696, ECO:0000269|PubMed:21118991, ECO:0000269|PubMed:21127351, ECO:0000269|PubMed:21726808, ECO:0000269|PubMed:22884692, ECO:0000269|PubMed:28689657, ECO:0000269|PubMed:29033132, ECO:0000269|PubMed:29378950, ECO:0000269|PubMed:33208877, ECO:0000269|PubMed:35217622, ECO:0000269|PubMed:37409633, ECO:0000269|PubMed:37478846, ECO:0000269|PubMed:37478862}. |
O95674 | CDS2 | S41 | ochoa | Phosphatidate cytidylyltransferase 2 (EC 2.7.7.41) (CDP-DAG synthase 2) (CDP-DG synthase 2) (CDP-diacylglycerol synthase 2) (CDS 2) (CDP-diglyceride pyrophosphorylase 2) (CDP-diglyceride synthase 2) (CTP:phosphatidate cytidylyltransferase 2) | Catalyzes the conversion of phosphatidic acid (PA) to CDP-diacylglycerol (CDP-DAG), an essential intermediate in the synthesis of phosphatidylglycerol, cardiolipin and phosphatidylinositol (PubMed:25375833). Exhibits specificity for the nature of the acyl chains at the sn-1 and sn-2 positions in the substrate, PA and the preferred acyl chain composition is 1-stearoyl-2-arachidonoyl-sn-phosphatidic acid (PubMed:25375833). Plays an important role in regulating the growth and maturation of lipid droplets which are storage organelles at the center of lipid and energy homeostasis (PubMed:26946540, PubMed:31548309). {ECO:0000269|PubMed:25375833, ECO:0000269|PubMed:26946540, ECO:0000269|PubMed:31548309}. |
P06127 | CD5 | S454 | ochoa | T-cell surface glycoprotein CD5 (Lymphocyte antigen T1/Leu-1) (CD antigen CD5) | Lymphoid-specific receptor expressed by all T-cells and in a subset of B-cells known as B1a cells. Plays a role in the regulation of TCR and BCR signaling, thymocyte selection, T-cell effector differentiation and immune tolerance. Acts by interacting with several ligands expressed on B-cells such as CD5L or CD72 and thereby plays an important role in contact-mediated, T-dependent B-cell activation and in the maintenance of regulatory T and B-cell homeostasis. Functions as a negative regulator of TCR signaling during thymocyte development by associating with several signaling proteins including LCK, CD3Z chain, PI3K or CBL (PubMed:1384049, PubMed:1385158). Mechanistically, co-engagement of CD3 with CD5 enhances phosphorylated CBL recruitment leading to increased VAV1 phosphorylation and degradation (PubMed:23376399). Modulates B-cell biology through ERK1/2 activation in a Ca(2+)-dependent pathway via the non-selective Ca(2+) channel TRPC1, leading to IL-10 production (PubMed:27499044). {ECO:0000250|UniProtKB:P13379, ECO:0000269|PubMed:1384049, ECO:0000269|PubMed:1385158, ECO:0000269|PubMed:23376399, ECO:0000269|PubMed:27499044}. |
P12830 | CDH1 | S793 | ochoa | Cadherin-1 (CAM 120/80) (Epithelial cadherin) (E-cadherin) (Uvomorulin) (CD antigen CD324) [Cleaved into: E-Cad/CTF1; E-Cad/CTF2; E-Cad/CTF3] | Cadherins are calcium-dependent cell adhesion proteins (PubMed:11976333). They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. CDH1 is involved in mechanisms regulating cell-cell adhesions, mobility and proliferation of epithelial cells (PubMed:11976333). Promotes organization of radial actin fiber structure and cellular response to contractile forces, via its interaction with AMOTL2 which facilitates anchoring of radial actin fibers to CDH1 junction complexes at the cell membrane (By similarity). Plays a role in the early stages of desmosome cell-cell junction formation via facilitating the recruitment of DSG2 and DSP to desmosome plaques (PubMed:29999492). Has a potent invasive suppressor role. It is a ligand for integrin alpha-E/beta-7. {ECO:0000250|UniProtKB:F1PAA9, ECO:0000269|PubMed:11976333, ECO:0000269|PubMed:16417575, ECO:0000269|PubMed:29999492}.; FUNCTION: E-Cad/CTF2 promotes non-amyloidogenic degradation of Abeta precursors. Has a strong inhibitory effect on APP C99 and C83 production. {ECO:0000269|PubMed:16417575}.; FUNCTION: (Microbial infection) Serves as a receptor for Listeria monocytogenes; internalin A (InlA) binds to this protein and promotes uptake of the bacteria. {ECO:0000269|PubMed:10406800, ECO:0000269|PubMed:17540170, ECO:0000269|PubMed:8601315}. |
P15036 | ETS2 | S225 | psp | Protein C-ets-2 | Transcription factor activating transcription. Binds specifically the DNA GGAA/T core motif (Ets-binding site or EBS) in gene promoters and stimulates transcription. {ECO:0000269|PubMed:11909962}. |
P15056 | BRAF | S405 | ochoa | Serine/threonine-protein kinase B-raf (EC 2.7.11.1) (Proto-oncogene B-Raf) (p94) (v-Raf murine sarcoma viral oncogene homolog B1) | Protein kinase involved in the transduction of mitogenic signals from the cell membrane to the nucleus (Probable). Phosphorylates MAP2K1, and thereby activates the MAP kinase signal transduction pathway (PubMed:21441910, PubMed:29433126). Phosphorylates PFKFB2 (PubMed:36402789). May play a role in the postsynaptic responses of hippocampal neurons (PubMed:1508179). {ECO:0000269|PubMed:1508179, ECO:0000269|PubMed:21441910, ECO:0000269|PubMed:29433126, ECO:0000269|PubMed:36402789, ECO:0000305}. |
P15336 | ATF2 | S310 | ochoa | Cyclic AMP-dependent transcription factor ATF-2 (cAMP-dependent transcription factor ATF-2) (Activating transcription factor 2) (Cyclic AMP-responsive element-binding protein 2) (CREB-2) (cAMP-responsive element-binding protein 2) (HB16) (cAMP response element-binding protein CRE-BP1) | Transcriptional activator which regulates the transcription of various genes, including those involved in anti-apoptosis, cell growth, and DNA damage response. Dependent on its binding partner, binds to CRE (cAMP response element) consensus sequences (5'-TGACGTCA-3') or to AP-1 (activator protein 1) consensus sequences (5'-TGACTCA-3'). In the nucleus, contributes to global transcription and the DNA damage response, in addition to specific transcriptional activities that are related to cell development, proliferation and death. In the cytoplasm, interacts with and perturbs HK1- and VDAC1-containing complexes at the mitochondrial outer membrane, thereby impairing mitochondrial membrane potential, inducing mitochondrial leakage and promoting cell death. The phosphorylated form (mediated by ATM) plays a role in the DNA damage response and is involved in the ionizing radiation (IR)-induced S phase checkpoint control and in the recruitment of the MRN complex into the IR-induced foci (IRIF). Exhibits histone acetyltransferase (HAT) activity which specifically acetylates histones H2B and H4 in vitro (PubMed:10821277). In concert with CUL3 and RBX1, promotes the degradation of KAT5 thereby attenuating its ability to acetylate and activate ATM. Can elicit oncogenic or tumor suppressor activities depending on the tissue or cell type. {ECO:0000269|PubMed:10821277, ECO:0000269|PubMed:15916964, ECO:0000269|PubMed:18397884, ECO:0000269|PubMed:22304920}. |
P15531 | NME1 | S125 | ochoa | Nucleoside diphosphate kinase A (NDK A) (NDP kinase A) (EC 2.7.4.6) (Granzyme A-activated DNase) (GAAD) (Metastasis inhibition factor nm23) (NM23-H1) (Tumor metastatic process-associated protein) | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate. Possesses nucleoside-diphosphate kinase, serine/threonine-specific protein kinase, geranyl and farnesyl pyrophosphate kinase, histidine protein kinase and 3'-5' exonuclease activities. Involved in cell proliferation, differentiation and development, signal transduction, G protein-coupled receptor endocytosis, and gene expression. Required for neural development including neural patterning and cell fate determination. During GZMA-mediated cell death, works in concert with TREX1. NME1 nicks one strand of DNA and TREX1 removes bases from the free 3' end to enhance DNA damage and prevent DNA end reannealing and rapid repair. {ECO:0000269|PubMed:12628186, ECO:0000269|PubMed:16818237, ECO:0000269|PubMed:8810265}. |
P16144 | ITGB4 | S1084 | ochoa | Integrin beta-4 (GP150) (CD antigen CD104) | Integrin alpha-6/beta-4 is a receptor for laminin. Plays a critical structural role in the hemidesmosome of epithelial cells. Is required for the regulation of keratinocyte polarity and motility. ITGA6:ITGB4 binds to NRG1 (via EGF domain) and this binding is essential for NRG1-ERBB signaling (PubMed:20682778). ITGA6:ITGB4 binds to IGF1 and this binding is essential for IGF1 signaling (PubMed:22351760). ITGA6:ITGB4 binds to IGF2 and this binding is essential for IGF2 signaling (PubMed:28873464). {ECO:0000269|PubMed:12482924, ECO:0000269|PubMed:19403692, ECO:0000269|PubMed:20682778, ECO:0000269|PubMed:22351760, ECO:0000269|PubMed:28873464}. |
P16157 | ANK1 | S960 | ochoa | Ankyrin-1 (ANK-1) (Ankyrin-R) (Erythrocyte ankyrin) | Component of the ankyrin-1 complex, a multiprotein complex involved in the stability and shape of the erythrocyte membrane (PubMed:35835865). Attaches integral membrane proteins to cytoskeletal elements; binds to the erythrocyte membrane protein band 4.2, to Na-K ATPase, to the lymphocyte membrane protein GP85, and to the cytoskeletal proteins fodrin, tubulin, vimentin and desmin. Erythrocyte ankyrins also link spectrin (beta chain) to the cytoplasmic domain of the erythrocytes anion exchange protein; they retain most or all of these binding functions. {ECO:0000269|PubMed:12456646, ECO:0000269|PubMed:35835865}.; FUNCTION: [Isoform Mu17]: Together with obscurin in skeletal muscle may provide a molecular link between the sarcoplasmic reticulum and myofibrils. {ECO:0000269|PubMed:12527750}. |
P17600 | SYN1 | S513 | ochoa | Synapsin-1 (Brain protein 4.1) (Synapsin I) | Neuronal phosphoprotein that coats synaptic vesicles, and binds to the cytoskeleton. Acts as a regulator of synaptic vesicles trafficking, involved in the control of neurotransmitter release at the pre-synaptic terminal (PubMed:21441247, PubMed:23406870). Also involved in the regulation of axon outgrowth and synaptogenesis (By similarity). The complex formed with NOS1 and CAPON proteins is necessary for specific nitric-oxid functions at a presynaptic level (By similarity). {ECO:0000250|UniProtKB:O88935, ECO:0000250|UniProtKB:P09951, ECO:0000269|PubMed:21441247, ECO:0000269|PubMed:23406870}. |
P19838 | NFKB1 | S80 | 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}. |
P22392 | NME2 | S125 | ochoa | Nucleoside diphosphate kinase B (NDK B) (NDP kinase B) (EC 2.7.4.6) (C-myc purine-binding transcription factor PUF) (Histidine protein kinase NDKB) (EC 2.7.13.3) (nm23-H2) | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity). Negatively regulates Rho activity by interacting with AKAP13/LBC (PubMed:15249197). Acts as a transcriptional activator of the MYC gene; binds DNA non-specifically (PubMed:19435876, PubMed:8392752). Binds to both single-stranded guanine- and cytosine-rich strands within the nuclease hypersensitive element (NHE) III(1) region of the MYC gene promoter. Does not bind to duplex NHE III(1) (PubMed:19435876). Has G-quadruplex (G4) DNA-binding activity, which is independent of its nucleotide-binding and kinase activity. Binds both folded and unfolded G4 with similar low nanomolar affinities. Stabilizes folded G4s regardless of whether they are prefolded or not (PubMed:25679041). Exhibits histidine protein kinase activity (PubMed:20946858). {ECO:0000250|UniProtKB:P36010, ECO:0000269|PubMed:15249197, ECO:0000269|PubMed:19435876, ECO:0000269|PubMed:20946858, ECO:0000269|PubMed:25679041, ECO:0000269|PubMed:8392752}. |
P22681 | CBL | S619 | ochoa|psp | E3 ubiquitin-protein ligase CBL (EC 2.3.2.27) (Casitas B-lineage lymphoma proto-oncogene) (Proto-oncogene c-Cbl) (RING finger protein 55) (RING-type E3 ubiquitin transferase CBL) (Signal transduction protein CBL) | E3 ubiquitin-protein ligase that acts as a negative regulator of many signaling pathways by mediating ubiquitination of cell surface receptors (PubMed:10514377, PubMed:11896602, PubMed:14661060, PubMed:14739300, PubMed:15190072, PubMed:17509076, PubMed:18374639, PubMed:19689429, PubMed:21596750, PubMed:28381567). Accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and then transfers it to substrates promoting their degradation by the proteasome (PubMed:10514377, PubMed:14661060, PubMed:14739300, PubMed:17094949, PubMed:17509076, PubMed:17974561). Recognizes activated receptor tyrosine kinases, including KIT, FLT1, FGFR1, FGFR2, PDGFRA, PDGFRB, CSF1R, EPHA8 and KDR and mediates their ubiquitination to terminate signaling (PubMed:15190072, PubMed:18374639, PubMed:21596750). Recognizes membrane-bound HCK, SRC and other kinases of the SRC family and mediates their ubiquitination and degradation (PubMed:11896602). Ubiquitinates EGFR and SPRY2 (PubMed:17094949, PubMed:17974561). Ubiquitinates NECTIN1 following association between NECTIN1 and herpes simplex virus 1/HHV-1 envelope glycoprotein D, leading to NECTIN1 removal from cell surface (PubMed:28381567). Participates in signal transduction in hematopoietic cells. Plays an important role in the regulation of osteoblast differentiation and apoptosis (PubMed:15190072, PubMed:18374639). Essential for osteoclastic bone resorption (PubMed:14739300). The 'Tyr-731' phosphorylated form induces the activation and recruitment of phosphatidylinositol 3-kinase to the cell membrane in a signaling pathway that is critical for osteoclast function (PubMed:14739300). May be functionally coupled with the E2 ubiquitin-protein ligase UB2D3. In association with CBLB, required for proper feedback inhibition of ciliary platelet-derived growth factor receptor-alpha (PDGFRA) signaling pathway via ubiquitination and internalization of PDGFRA (By similarity). {ECO:0000250|UniProtKB:P22682, ECO:0000269|PubMed:10514377, ECO:0000269|PubMed:11896602, ECO:0000269|PubMed:14661060, ECO:0000269|PubMed:14739300, ECO:0000269|PubMed:15190072, ECO:0000269|PubMed:17094949, ECO:0000269|PubMed:17509076, ECO:0000269|PubMed:17974561, ECO:0000269|PubMed:18374639, ECO:0000269|PubMed:19689429, ECO:0000269|PubMed:21596750, ECO:0000269|PubMed:28381567}. |
P41162 | ETV3 | S365 | ochoa | ETS translocation variant 3 (ETS domain transcriptional repressor PE1) (PE-1) (Mitogenic Ets transcriptional suppressor) | Transcriptional repressor that contribute to growth arrest during terminal macrophage differentiation by repressing target genes involved in Ras-dependent proliferation. Represses MMP1 promoter activity. {ECO:0000269|PubMed:12007404}. |
P43243 | MATR3 | S37 | ochoa | Matrin-3 | May play a role in transcription or may interact with other nuclear matrix proteins to form the internal fibrogranular network. In association with the SFPQ-NONO heteromer may play a role in nuclear retention of defective RNAs. Plays a role in the regulation of DNA virus-mediated innate immune response by assembling into the HDP-RNP complex, a complex that serves as a platform for IRF3 phosphorylation and subsequent innate immune response activation through the cGAS-STING pathway (PubMed:28712728). Binds to N6-methyladenosine (m6A)-containing mRNAs and contributes to MYC stability by binding to m6A-containing MYC mRNAs (PubMed:32245947). May bind to specific miRNA hairpins (PubMed:28431233). {ECO:0000269|PubMed:11525732, ECO:0000269|PubMed:28431233, ECO:0000269|PubMed:28712728, ECO:0000269|PubMed:32245947}. |
P46109 | CRKL | S184 | ochoa | Crk-like protein | May mediate the transduction of intracellular signals. |
P46939 | UTRN | S2226 | ochoa | Utrophin (Dystrophin-related protein 1) (DRP-1) | May play a role in anchoring the cytoskeleton to the plasma membrane. {ECO:0000250}. |
P51116 | FXR2 | S516 | ochoa | RNA-binding protein FXR2 (FXR2P) (FMR1 autosomal homolog 2) | mRNA-binding protein that acts as a regulator of mRNAs translation and/or stability, and which is required for adult hippocampal neurogenesis (By similarity). Specifically binds to AU-rich elements (AREs) in the 3'-UTR of target mRNAs (By similarity). Promotes formation of some phase-separated membraneless compartment by undergoing liquid-liquid phase separation upon binding to AREs-containing mRNAs: mRNAs storage into membraneless compartments regulates their translation and/or stability (By similarity). Acts as a regulator of adult hippocampal neurogenesis by regulating translation and/or stability of NOG mRNA, thereby preventing NOG protein expression in the dentate gyrus (By similarity). {ECO:0000250|UniProtKB:Q61584, ECO:0000250|UniProtKB:Q9WVR4}. |
P56524 | HDAC4 | S467 | 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}. |
P56524 | HDAC4 | S636 | ochoa | 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}. |
Q01082 | SPTBN1 | S2319 | 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}. |
Q01860 | POU5F1 | S93 | psp | POU domain, class 5, transcription factor 1 (Octamer-binding protein 3) (Oct-3) (Octamer-binding protein 4) (Oct-4) (Octamer-binding transcription factor 3) (OTF-3) | Transcription factor that binds to the octamer motif (5'-ATTTGCAT-3'). Forms a trimeric complex with SOX2 or SOX15 on DNA and controls the expression of a number of genes involved in embryonic development such as YES1, FGF4, UTF1 and ZFP206. Critical for early embryogenesis and for embryonic stem cell pluripotency. {ECO:0000269|PubMed:18035408}. |
Q02086 | SP2 | S30 | ochoa | Transcription factor Sp2 | Binds to GC box promoters elements and selectively activates mRNA synthesis from genes that contain functional recognition sites. |
Q02446 | SP4 | S43 | ochoa | Transcription factor Sp4 (SPR-1) | Binds to GT and GC boxes promoters elements. Probable transcriptional activator. |
Q03252 | LMNB2 | S541 | ochoa | Lamin-B2 | Lamins are intermediate filament proteins that assemble into a filamentous meshwork, and which constitute the major components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane (PubMed:33033404). Lamins provide a framework for the nuclear envelope, bridging the nuclear envelope and chromatin, thereby playing an important role in nuclear assembly, chromatin organization, nuclear membrane and telomere dynamics (PubMed:33033404). The structural integrity of the lamina is strictly controlled by the cell cycle, as seen by the disintegration and formation of the nuclear envelope in prophase and telophase, respectively (PubMed:33033404). {ECO:0000269|PubMed:33033404}. |
Q07157 | TJP1 | S1142 | ochoa | Tight junction protein 1 (Tight junction protein ZO-1) (Zona occludens protein 1) (Zonula occludens protein 1) | 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:7798316, PubMed:9792688). Forms a multistranded TJP1/ZO1 condensate which elongates to form a tight junction belt, the belt is anchored at the apical cell membrane via interaction with PATJ (By similarity). 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. Necessary for lumenogenesis, and particularly efficient epithelial polarization and barrier formation (By similarity). Plays a role in the regulation of cell migration by targeting CDC42BPB to the leading edge of migrating cells (PubMed:21240187). Plays an important role in podosome formation and associated function, thus regulating cell adhesion and matrix remodeling (PubMed:20930113). With TJP2 and TJP3, participates in the junctional retention and stability of the transcription factor DBPA, but is not involved in its shuttling to the nucleus (By similarity). May play a role in mediating cell morphology changes during ameloblast differentiation via its role in tight junctions (By similarity). {ECO:0000250|UniProtKB:O97758, ECO:0000250|UniProtKB:P39447, ECO:0000269|PubMed:20930113, ECO:0000269|PubMed:21240187}. |
Q12802 | AKAP13 | S1229 | ochoa | A-kinase anchor protein 13 (AKAP-13) (AKAP-Lbc) (Breast cancer nuclear receptor-binding auxiliary protein) (Guanine nucleotide exchange factor Lbc) (Human thyroid-anchoring protein 31) (Lymphoid blast crisis oncogene) (LBC oncogene) (Non-oncogenic Rho GTPase-specific GTP exchange factor) (Protein kinase A-anchoring protein 13) (PRKA13) (p47) | Scaffold protein that plays an important role in assembling signaling complexes downstream of several types of G protein-coupled receptors. Activates RHOA in response to signaling via G protein-coupled receptors via its function as Rho guanine nucleotide exchange factor (PubMed:11546812, PubMed:15229649, PubMed:23090968, PubMed:24993829, PubMed:25186459). May also activate other Rho family members (PubMed:11546812). Part of a kinase signaling complex that links ADRA1A and ADRA1B adrenergic receptor signaling to the activation of downstream p38 MAP kinases, such as MAPK11 and MAPK14 (PubMed:17537920, PubMed:21224381, PubMed:23716597). Part of a signaling complex that links ADRA1B signaling to the activation of RHOA and IKBKB/IKKB, leading to increased NF-kappa-B transcriptional activity (PubMed:23090968). Part of a RHOA-dependent signaling cascade that mediates responses to lysophosphatidic acid (LPA), a signaling molecule that activates G-protein coupled receptors and potentiates transcriptional activation of the glucocorticoid receptor NR3C1 (PubMed:16469733). Part of a signaling cascade that stimulates MEF2C-dependent gene expression in response to lysophosphatidic acid (LPA) (By similarity). Part of a signaling pathway that activates MAPK11 and/or MAPK14 and leads to increased transcription activation of the estrogen receptors ESR1 and ESR2 (PubMed:11579095, PubMed:9627117). Part of a signaling cascade that links cAMP and EGFR signaling to BRAF signaling and to PKA-mediated phosphorylation of KSR1, leading to the activation of downstream MAP kinases, such as MAPK1 or MAPK3 (PubMed:21102438). Functions as a scaffold protein that anchors cAMP-dependent protein kinase (PKA) and PRKD1. This promotes activation of PRKD1, leading to increased phosphorylation of HDAC5 and ultimately cardiomyocyte hypertrophy (By similarity). Has no guanine nucleotide exchange activity on CDC42, Ras or Rac (PubMed:11546812). Required for normal embryonic heart development, and in particular for normal sarcomere formation in the developing cardiomyocytes (By similarity). Plays a role in cardiomyocyte growth and cardiac hypertrophy in response to activation of the beta-adrenergic receptor by phenylephrine or isoproterenol (PubMed:17537920, PubMed:23090968). Required for normal adaptive cardiac hypertrophy in response to pressure overload (PubMed:23716597). Plays a role in osteogenesis (By similarity). {ECO:0000250|UniProtKB:E9Q394, ECO:0000269|PubMed:11546812, ECO:0000269|PubMed:11579095, ECO:0000269|PubMed:17537920, ECO:0000269|PubMed:21224381, ECO:0000269|PubMed:23716597, ECO:0000269|PubMed:24993829, ECO:0000269|PubMed:25186459, ECO:0000269|PubMed:9627117, ECO:0000269|PubMed:9891067}. |
Q13459 | MYO9B | S1261 | ochoa | Unconventional myosin-IXb (Unconventional myosin-9b) | Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Binds actin with high affinity both in the absence and presence of ATP and its mechanochemical activity is inhibited by calcium ions (PubMed:9490638). Also acts as a GTPase activator for RHOA (PubMed:26529257, PubMed:9490638). Plays a role in the regulation of cell migration via its role as RHOA GTPase activator. This is regulated by its interaction with the SLIT2 receptor ROBO1; interaction with ROBO1 impairs interaction with RHOA and subsequent activation of RHOA GTPase activity, and thereby leads to increased levels of active, GTP-bound RHOA (PubMed:26529257). {ECO:0000269|PubMed:26529257, ECO:0000269|PubMed:9490638}. |
Q13625 | TP53BP2 | S361 | ochoa|psp | Apoptosis-stimulating of p53 protein 2 (Bcl2-binding protein) (Bbp) (Renal carcinoma antigen NY-REN-51) (Tumor suppressor p53-binding protein 2) (53BP2) (p53-binding protein 2) (p53BP2) | Regulator that plays a central role in regulation of apoptosis and cell growth via its interactions with proteins such as TP53 (PubMed:12524540). Regulates TP53 by enhancing the DNA binding and transactivation function of TP53 on the promoters of proapoptotic genes in vivo. Inhibits the ability of NAE1 to conjugate NEDD8 to CUL1, and thereby decreases NAE1 ability to induce apoptosis. Impedes cell cycle progression at G2/M. Its apoptosis-stimulating activity is inhibited by its interaction with DDX42. {ECO:0000269|PubMed:11684014, ECO:0000269|PubMed:12524540, ECO:0000269|PubMed:12694406, ECO:0000269|PubMed:19377511}. |
Q14689 | DIP2A | S154 | ochoa | Disco-interacting protein 2 homolog A (DIP2 homolog A) (EC 6.2.1.1) | Catalyzes the de novo synthesis of acetyl-CoA in vitro (By similarity). Promotes acetylation of CTTN, possibly by providing the acetyl donor, ensuring correct dendritic spine morphology and synaptic transmission (By similarity). Binds to follistatin-related protein FSTL1 and may act as a cell surface receptor for FSTL1, contributing to AKT activation and subsequent FSTL1-induced survival and function of endothelial cells and cardiac myocytes (PubMed:20054002). {ECO:0000250|UniProtKB:Q8BWT5, ECO:0000269|PubMed:20054002}. |
Q14847 | LASP1 | S167 | ochoa | LIM and SH3 domain protein 1 (LASP-1) (Metastatic lymph node gene 50 protein) (MLN 50) | Plays an important role in the regulation of dynamic actin-based, cytoskeletal activities. Agonist-dependent changes in LASP1 phosphorylation may also serve to regulate actin-associated ion transport activities, not only in the parietal cell but also in certain other F-actin-rich secretory epithelial cell types (By similarity). {ECO:0000250}. |
Q14980 | NUMA1 | S2096 | ochoa | Nuclear mitotic apparatus protein 1 (Nuclear matrix protein-22) (NMP-22) (Nuclear mitotic apparatus protein) (NuMA protein) (SP-H antigen) | Microtubule (MT)-binding protein that plays a role in the formation and maintenance of the spindle poles and the alignement and the segregation of chromosomes during mitotic cell division (PubMed:17172455, PubMed:19255246, PubMed:24996901, PubMed:26195665, PubMed:27462074, PubMed:7769006). Functions to tether the minus ends of MTs at the spindle poles, which is critical for the establishment and maintenance of the spindle poles (PubMed:11956313, PubMed:12445386). Plays a role in the establishment of the mitotic spindle orientation during metaphase and elongation during anaphase in a dynein-dynactin-dependent manner (PubMed:23870127, PubMed:24109598, PubMed:24996901, PubMed:26765568). In metaphase, part of a ternary complex composed of GPSM2 and G(i) alpha proteins, that regulates the recruitment and anchorage of the dynein-dynactin complex in the mitotic cell cortex regions situated above the two spindle poles, and hence regulates the correct oritentation of the mitotic spindle (PubMed:22327364, PubMed:23027904, PubMed:23921553). During anaphase, mediates the recruitment and accumulation of the dynein-dynactin complex at the cell membrane of the polar cortical region through direct association with phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), and hence participates in the regulation of the spindle elongation and chromosome segregation (PubMed:22327364, PubMed:23921553, PubMed:24371089, PubMed:24996901). Also binds to other polyanionic phosphoinositides, such as phosphatidylinositol 3-phosphate (PIP), lysophosphatidic acid (LPA) and phosphatidylinositol triphosphate (PIP3), in vitro (PubMed:24371089, PubMed:24996901). Also required for proper orientation of the mitotic spindle during asymmetric cell divisions (PubMed:21816348). Plays a role in mitotic MT aster assembly (PubMed:11163243, PubMed:11229403, PubMed:12445386). Involved in anastral spindle assembly (PubMed:25657325). Positively regulates TNKS protein localization to spindle poles in mitosis (PubMed:16076287). Highly abundant component of the nuclear matrix where it may serve a non-mitotic structural role, occupies the majority of the nuclear volume (PubMed:10075938). Required for epidermal differentiation and hair follicle morphogenesis (By similarity). {ECO:0000250|UniProtKB:E9Q7G0, ECO:0000269|PubMed:11163243, ECO:0000269|PubMed:11229403, ECO:0000269|PubMed:11956313, ECO:0000269|PubMed:12445386, ECO:0000269|PubMed:16076287, ECO:0000269|PubMed:17172455, ECO:0000269|PubMed:19255246, ECO:0000269|PubMed:22327364, ECO:0000269|PubMed:23027904, ECO:0000269|PubMed:23870127, ECO:0000269|PubMed:23921553, ECO:0000269|PubMed:24109598, ECO:0000269|PubMed:24371089, ECO:0000269|PubMed:24996901, ECO:0000269|PubMed:25657325, ECO:0000269|PubMed:26195665, ECO:0000269|PubMed:26765568, ECO:0000269|PubMed:27462074, ECO:0000269|PubMed:7769006, ECO:0000305|PubMed:10075938, ECO:0000305|PubMed:21816348}. |
Q15361 | TTF1 | S253 | ochoa | Transcription termination factor 1 (TTF-1) (RNA polymerase I termination factor) (Transcription termination factor I) (TTF-I) | Multifunctional nucleolar protein that terminates ribosomal gene transcription, mediates replication fork arrest and regulates RNA polymerase I transcription on chromatin. Plays a dual role in rDNA regulation, being involved in both activation and silencing of rDNA transcription. Interaction with BAZ2A/TIP5 recovers DNA-binding activity. {ECO:0000250|UniProtKB:Q62187, ECO:0000269|PubMed:7597036}. |
Q15772 | SPEG | S2037 | ochoa | Striated muscle preferentially expressed protein kinase (EC 2.7.11.1) (Aortic preferentially expressed protein 1) (APEG-1) | Isoform 3 may have a role in regulating the growth and differentiation of arterial smooth muscle cells. |
Q16825 | PTPN21 | S484 | ochoa | Tyrosine-protein phosphatase non-receptor type 21 (EC 3.1.3.48) (Protein-tyrosine phosphatase D1) | None |
Q2TAZ0 | ATG2A | S1453 | ochoa | Autophagy-related protein 2 homolog A | Lipid transfer protein involved in autophagosome assembly (PubMed:28561066, PubMed:30952800, PubMed:31271352). Tethers the edge of the isolation membrane (IM) to the endoplasmic reticulum (ER) and mediates direct lipid transfer from ER to IM for IM expansion (PubMed:30952800, PubMed:31271352). Binds to the ER exit site (ERES), which is the membrane source for autophagosome formation, and extracts phospholipids from the membrane source and transfers them to ATG9 (ATG9A or ATG9B) to the IM for membrane expansion (PubMed:30952800, PubMed:31271352). Lipid transfer activity is enhanced by WIPI1 and WDR45/WIPI4, which promote ATG2A-association with phosphatidylinositol 3-monophosphate (PI3P)-containing membranes (PubMed:31271352). Also regulates lipid droplets morphology and distribution within the cell (PubMed:22219374, PubMed:28561066). {ECO:0000269|PubMed:22219374, ECO:0000269|PubMed:28561066, ECO:0000269|PubMed:30952800, ECO:0000269|PubMed:31271352}. |
Q58A45 | PAN3 | S191 | ochoa | PAN2-PAN3 deadenylation complex subunit PAN3 (PAB1P-dependent poly(A)-specific ribonuclease) (Poly(A)-nuclease deadenylation complex subunit 3) (PAN deadenylation complex subunit 3) | Regulatory subunit of the poly(A)-nuclease (PAN) deadenylation complex, one of two cytoplasmic mRNA deadenylases involved in general and miRNA-mediated mRNA turnover. PAN specifically shortens poly(A) tails of RNA and the activity is stimulated by poly(A)-binding protein (PABP). PAN deadenylation is followed by rapid degradation of the shortened mRNA tails by the CCR4-NOT complex. Deadenylated mRNAs are then degraded by two alternative mechanisms, namely exosome-mediated 3'-5' exonucleolytic degradation, or deadenylation-dependent mRNA decapping and subsequent 5'-3' exonucleolytic degradation by XRN1. PAN3 acts as a regulator for PAN activity, recruiting the catalytic subunit PAN2 to mRNA via its interaction with RNA and PABP, and to miRNA targets via its interaction with GW182 family proteins. {ECO:0000255|HAMAP-Rule:MF_03181, ECO:0000269|PubMed:14583602, ECO:0000269|PubMed:23932717}.; FUNCTION: [Isoform 1]: Decreases PAN2-mediated deadenylation, possibly by preventing progression into the second CCR4-NOT mediated stage of biphasic deadenylation. Has a significant effect on mRNA stability, generally stabilizing a subset of the transcriptome. Stabilizes mRNAs degraded by the AU-rich element (ARE)-mediated mRNA decay pathway but promotes degradation of mRNAs by the microRNA-mediated pathway (PubMed:28559491). Its activity influences mRNP remodeling, specifically reducing formation of a subset of P-bodies containing GW220, an isoform of TNRC6A (PubMed:28559491). {ECO:0000269|PubMed:28559491}.; FUNCTION: [Isoform 3]: Enhances PAN2 deadenylase activity and has an extensive effect on mRNA stability, generally enhancing mRNA decay across the transcriptome by multiple pathways, including the AU-rich element (ARE)-mediated pathway, microRNA-mediated pathway and the nonsense-mediated pathway (NMD) (PubMed:28559491). Its activity is required for efficient P-body formation (PubMed:28559491). May be involved in regulating mRNAs of genes involved in cell cycle progression and cell proliferation (PubMed:28559491). {ECO:0000269|PubMed:28559491}. |
Q5M7Z0 | RNFT1 | S58 | ochoa | E3 ubiquitin-protein ligase RNFT1 (EC 2.3.2.27) (Protein PTD016) (RING finger and transmembrane domain-containing protein 1) | E3 ubiquitin-protein ligase that acts in the endoplasmic reticulum (ER)-associated degradation (ERAD) pathway, which targets misfolded proteins that accumulate in the endoplasmic reticulum (ER) for ubiquitination and subsequent proteasome-mediated degradation. Protects cells from ER stress-induced apoptosis. {ECO:0000269|PubMed:27485036}. |
Q5T5P2 | KIAA1217 | S169 | ochoa | Sickle tail protein homolog | Required for normal development of intervertebral disks. {ECO:0000250|UniProtKB:A2AQ25}. |
Q5TCZ1 | SH3PXD2A | S800 | ochoa | SH3 and PX domain-containing protein 2A (Adapter protein TKS5) (Five SH3 domain-containing protein) (SH3 multiple domains protein 1) (Tyrosine kinase substrate with five SH3 domains) | Adapter protein involved in invadopodia and podosome formation, extracellular matrix degradation and invasiveness of some cancer cells (PubMed:27789576). Binds matrix metalloproteinases (ADAMs), NADPH oxidases (NOXs) and phosphoinositides. Acts as an organizer protein that allows NOX1- or NOX3-dependent reactive oxygen species (ROS) generation and ROS localization. In association with ADAM12, mediates the neurotoxic effect of amyloid-beta peptide. {ECO:0000269|PubMed:12615925, ECO:0000269|PubMed:15710328, ECO:0000269|PubMed:15710903, ECO:0000269|PubMed:19755710, ECO:0000269|PubMed:20609497, ECO:0000269|PubMed:27789576}. |
Q5VSL9 | STRIP1 | S788 | ochoa | Striatin-interacting protein 1 (Protein FAM40A) | Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the cortical actin filament dynamics and cell shape. Part of the striatin-interacting phosphatase and kinase (STRIPAK) complexes. STRIPAK complexes have critical roles in protein (de)phosphorylation and are regulators of multiple signaling pathways including Hippo, MAPK, nuclear receptor and cytoskeleton remodeling. Different types of STRIPAK complexes are involved in a variety of biological processes such as cell growth, differentiation, apoptosis, metabolism and immune regulation. {ECO:0000269|PubMed:18782753, ECO:0000269|PubMed:21834987, ECO:0000269|PubMed:30622739, ECO:0000269|PubMed:33633399}. |
Q5VYK3 | ECPAS | S833 | ochoa | Proteasome adapter and scaffold protein ECM29 (Ecm29 proteasome adapter and scaffold) (Proteasome-associated protein ECM29 homolog) | Adapter/scaffolding protein that binds to the 26S proteasome, motor proteins and other compartment specific proteins. May couple the proteasome to different compartments including endosome, endoplasmic reticulum and centrosome. May play a role in ERAD and other enhanced proteolysis (PubMed:15496406). Promotes proteasome dissociation under oxidative stress (By similarity). {ECO:0000250|UniProtKB:Q6PDI5, ECO:0000269|PubMed:15496406, ECO:0000269|PubMed:20682791}. |
Q641Q2 | WASHC2A | S1091 | ochoa | WASH complex subunit 2A | Acts at least in part as component of the WASH core complex whose assembly at the surface of endosomes inhibits WASH nucleation-promoting factor (NPF) activity in recruiting and activating the Arp2/3 complex to induce actin polymerization and is involved in the fission of tubules that serve as transport intermediates during endosome sorting. Mediates the recruitment of the WASH core complex to endosome membranes via binding to phospholipids and VPS35 of the retromer CSC. Mediates the recruitment of the F-actin-capping protein dimer to the WASH core complex probably promoting localized F-actin polymerization needed for vesicle scission. Via its C-terminus binds various phospholipids, most strongly phosphatidylinositol 4-phosphate (PtdIns-(4)P), phosphatidylinositol 5-phosphate (PtdIns-(5)P) and phosphatidylinositol 3,5-bisphosphate (PtdIns-(3,5)P2). Involved in the endosome-to-plasma membrane trafficking and recycling of SNX27-retromer-dependent cargo proteins, such as GLUT1. Required for the association of DNAJC13, ENTR1, ANKRD50 with retromer CSC subunit VPS35. Required for the endosomal recruitment of CCC complex subunits COMMD1 and CCDC93 as well as the retriever complex subunit VPS35L. {ECO:0000269|PubMed:25355947, ECO:0000269|PubMed:28892079}. |
Q6PJ61 | FBXO46 | S67 | psp | F-box only protein 46 (F-box only protein 34-like) | Substrate-recognition component of the SCF(FBXO46) protein ligase complex, which mediates the ubiquitination and degradation of target proteins (PubMed:30171069). In absence of stress, the SCF(FBXO46) complex catalyzes ubiquitination and degradation of MTOR-phosphorylated FBXO31 (PubMed:30171069). {ECO:0000269|PubMed:30171069}. |
Q6PJI9 | WDR59 | S756 | ochoa | GATOR2 complex protein WDR59 (WD repeat-containing protein 59) | As a component of the GATOR2 complex, functions as an activator of the amino acid-sensing branch of the mTORC1 signaling pathway (PubMed:23723238, PubMed:25457612, PubMed:27487210, PubMed:35831510, PubMed:36528027, PubMed:36577058). The GATOR2 complex indirectly activates mTORC1 through the inhibition of the GATOR1 subcomplex (PubMed:23723238, PubMed:27487210, PubMed:35831510, PubMed:36528027). GATOR2 probably acts as an E3 ubiquitin-protein ligase toward GATOR1 (PubMed:36528027). In the presence of abundant amino acids, the GATOR2 complex mediates ubiquitination of the NPRL2 core component of the GATOR1 complex, leading to GATOR1 inactivation (PubMed:36528027). In the absence of amino acids, GATOR2 is inhibited, activating the GATOR1 complex (PubMed:25457612, PubMed:27487210). {ECO:0000269|PubMed:23723238, ECO:0000269|PubMed:25457612, ECO:0000269|PubMed:27487210, ECO:0000269|PubMed:35831510, ECO:0000269|PubMed:36528027, ECO:0000269|PubMed:36577058}. |
Q6PKG0 | LARP1 | S584 | ochoa | La-related protein 1 (La ribonucleoprotein domain family member 1) | RNA-binding protein that regulates the translation of specific target mRNA species downstream of the mTORC1 complex, in function of growth signals and nutrient availability (PubMed:20430826, PubMed:23711370, PubMed:24532714, PubMed:25940091, PubMed:28650797, PubMed:28673543, PubMed:29244122). Interacts on the one hand with the 3' poly-A tails that are present in all mRNA molecules, and on the other hand with the 7-methylguanosine cap structure of mRNAs containing a 5' terminal oligopyrimidine (5'TOP) motif, which is present in mRNAs encoding ribosomal proteins and several components of the translation machinery (PubMed:23711370, PubMed:25940091, PubMed:26206669, PubMed:28379136, PubMed:28650797, PubMed:29244122). The interaction with the 5' end of mRNAs containing a 5'TOP motif leads to translational repression by preventing the binding of EIF4G1 (PubMed:25940091, PubMed:28379136, PubMed:28650797, PubMed:29244122). When mTORC1 is activated, LARP1 is phosphorylated and dissociates from the 5' untranslated region (UTR) of mRNA (PubMed:25940091, PubMed:28650797). Does not prevent binding of EIF4G1 to mRNAs that lack a 5'TOP motif (PubMed:28379136). Interacts with the free 40S ribosome subunit and with ribosomes, both monosomes and polysomes (PubMed:20430826, PubMed:24532714, PubMed:25940091, PubMed:28673543). Under normal nutrient availability, interacts primarily with the 3' untranslated region (UTR) of mRNAs encoding ribosomal proteins and increases protein synthesis (PubMed:23711370, PubMed:28650797). Associates with actively translating ribosomes and stimulates translation of mRNAs containing a 5'TOP motif, thereby regulating protein synthesis, and as a consequence, cell growth and proliferation (PubMed:20430826, PubMed:24532714). Stabilizes mRNAs species with a 5'TOP motif, which is required to prevent apoptosis (PubMed:20430826, PubMed:23711370, PubMed:25940091, PubMed:28673543). {ECO:0000269|PubMed:20430826, ECO:0000269|PubMed:23711370, ECO:0000269|PubMed:24532714, ECO:0000269|PubMed:25940091, ECO:0000269|PubMed:26206669, ECO:0000269|PubMed:28379136, ECO:0000269|PubMed:28650797, ECO:0000269|PubMed:28673543, ECO:0000269|PubMed:29244122}.; FUNCTION: (Microbial infection) Positively regulates the replication of dengue virus (DENV). {ECO:0000269|PubMed:26735137}. |
Q6ZRS2 | SRCAP | S3211 | ochoa | Helicase SRCAP (EC 3.6.4.-) (Domino homolog 2) (Snf2-related CBP activator) | Catalytic component of the SRCAP complex which mediates the ATP-dependent exchange of histone H2AZ/H2B dimers for nucleosomal H2A/H2B, leading to transcriptional regulation of selected genes by chromatin remodeling. Acts as a coactivator for CREB-mediated transcription, steroid receptor-mediated transcription, and Notch-mediated transcription. {ECO:0000269|PubMed:10347196, ECO:0000269|PubMed:11522779, ECO:0000269|PubMed:14500758, ECO:0000269|PubMed:16024792, ECO:0000269|PubMed:16634648, ECO:0000269|PubMed:17617668}. |
Q76N89 | HECW1 | S532 | ochoa | E3 ubiquitin-protein ligase HECW1 (EC 2.3.2.26) (HECT, C2 and WW domain-containing protein 1) (HECT-type E3 ubiquitin transferase HECW1) (NEDD4-like E3 ubiquitin-protein ligase 1) (hNEDL1) | E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent degradation of DVL1. Also targets the mutant SOD1 protein involved in familial amyotrophic lateral sclerosis (FALS). Forms cytotoxic aggregates with DVL1, SSR3 and mutant SOD1 that lead to motor neuron death in FALS. {ECO:0000269|PubMed:14684739}. |
Q7KZ85 | SUPT6H | S1708 | ochoa | Transcription elongation factor SPT6 (hSPT6) (Histone chaperone suppressor of Ty6) (Tat-cotransactivator 2 protein) (Tat-CT2 protein) | Histone H3-H4 chaperone that plays a key role in the regulation of transcription elongation and mRNA processing. Enhances the transcription elongation by RNA polymerase II (RNAPII) and is also required for the efficient activation of transcriptional elongation by the HIV-1 nuclear transcriptional activator, Tat. Besides chaperoning histones in transcription, acts to transport and splice mRNA by forming a complex with IWS1 and the C-terminal domain (CTD) of the RNAPII subunit RPB1 (POLR2A). The SUPT6H:IWS1:CTD complex recruits mRNA export factors (ALYREF/THOC4, EXOSC10) as well as histone modifying enzymes (such as SETD2), to ensure proper mRNA splicing, efficient mRNA export and elongation-coupled H3K36 methylation, a signature chromatin mark of active transcription. SUPT6H via its association with SETD1A, regulates both class-switch recombination and somatic hypermutation through formation of H3K4me3 epigenetic marks on activation-induced cytidine deaminase (AICDA) target loci. Promotes the activation of the myogenic gene program by entailing erasure of the repressive H3K27me3 epigenetic mark through stabilization of the chromatin interaction of the H3K27 demethylase KDM6A. {ECO:0000269|PubMed:15060154, ECO:0000269|PubMed:17234882, ECO:0000269|PubMed:22316138, ECO:0000269|PubMed:23503590, ECO:0000269|PubMed:9514752}. |
Q7Z434 | MAVS | S419 | ochoa | Mitochondrial antiviral-signaling protein (MAVS) (CARD adapter inducing interferon beta) (Cardif) (Interferon beta promoter stimulator protein 1) (IPS-1) (Putative NF-kappa-B-activating protein 031N) (Virus-induced-signaling adapter) (VISA) | Adapter required for innate immune defense against viruses (PubMed:16125763, PubMed:16127453, PubMed:16153868, PubMed:16177806, PubMed:19631370, PubMed:20127681, PubMed:20451243, PubMed:21170385, PubMed:23087404, PubMed:27992402, PubMed:33139700, PubMed:37582970). Acts downstream of DHX33, RIGI and IFIH1/MDA5, which detect intracellular dsRNA produced during viral replication, to coordinate pathways leading to the activation of NF-kappa-B, IRF3 and IRF7, and to the subsequent induction of antiviral cytokines such as IFNB and RANTES (CCL5) (PubMed:16125763, PubMed:16127453, PubMed:16153868, PubMed:16177806, PubMed:19631370, PubMed:20127681, PubMed:20451243, PubMed:20628368, PubMed:21170385, PubMed:23087404, PubMed:25636800, PubMed:27736772, PubMed:33110251). Peroxisomal and mitochondrial MAVS act sequentially to create an antiviral cellular state (PubMed:20451243). Upon viral infection, peroxisomal MAVS induces the rapid interferon-independent expression of defense factors that provide short-term protection, whereas mitochondrial MAVS activates an interferon-dependent signaling pathway with delayed kinetics, which amplifies and stabilizes the antiviral response (PubMed:20451243). May activate the same pathways following detection of extracellular dsRNA by TLR3 (PubMed:16153868). May protect cells from apoptosis (PubMed:16125763). Involved in NLRP3 inflammasome activation by mediating NLRP3 recruitment to mitochondria (PubMed:23582325). {ECO:0000269|PubMed:16125763, ECO:0000269|PubMed:16127453, ECO:0000269|PubMed:16153868, ECO:0000269|PubMed:16177806, ECO:0000269|PubMed:19631370, ECO:0000269|PubMed:20127681, ECO:0000269|PubMed:20451243, ECO:0000269|PubMed:20628368, ECO:0000269|PubMed:21170385, ECO:0000269|PubMed:23087404, ECO:0000269|PubMed:23582325, ECO:0000269|PubMed:25636800, ECO:0000269|PubMed:27736772, ECO:0000269|PubMed:27992402, ECO:0000269|PubMed:33110251, ECO:0000269|PubMed:33139700, ECO:0000269|PubMed:37582970}. |
Q86UY5 | FAM83A | S113 | ochoa | Protein FAM83A (Tumor antigen BJ-TSA-9) (Tumor-specific gene expressed in prostate protein) | Involved in mitochondrial maintenance during adipogenesis. May be acting by playing a role in the maintenance of normal mitochondrial function. {ECO:0000250|UniProtKB:Q8K2P2}. |
Q86V48 | LUZP1 | S839 | ochoa | Leucine zipper protein 1 (Filamin mechanobinding actin cross-linking protein) (Fimbacin) | F-actin cross-linking protein (PubMed:30990684). Stabilizes actin and acts as a negative regulator of primary cilium formation (PubMed:32496561). Positively regulates the phosphorylation of both myosin II and protein phosphatase 1 regulatory subunit PPP1R12A/MYPT1 and promotes the assembly of myosin II stacks within actin stress fibers (PubMed:38832964). Inhibits the phosphorylation of myosin light chain MYL9 by DAPK3 and suppresses the constriction velocity of the contractile ring during cytokinesis (PubMed:38009294). Binds to microtubules and promotes epithelial cell apical constriction by up-regulating levels of diphosphorylated myosin light chain (MLC) through microtubule-dependent inhibition of MLC dephosphorylation by myosin phosphatase (By similarity). Involved in regulation of cell migration, nuclear size and centriole number, probably through regulation of the actin cytoskeleton (By similarity). Component of the CERF-1 and CERF-5 chromatin remodeling complexes in embryonic stem cells where it acts to stabilize the complexes (By similarity). Plays a role in embryonic brain and cardiovascular development (By similarity). {ECO:0000250|UniProtKB:Q8R4U7, ECO:0000269|PubMed:30990684, ECO:0000269|PubMed:32496561, ECO:0000269|PubMed:38009294, ECO:0000269|PubMed:38832964}. |
Q86VQ1 | GLCCI1 | S277 | ochoa | Glucocorticoid-induced transcript 1 protein | None |
Q86YC2 | PALB2 | S376 | ochoa|psp | Partner and localizer of BRCA2 | Plays a critical role in homologous recombination repair (HRR) through its ability to recruit BRCA2 and RAD51 to DNA breaks (PubMed:16793542, PubMed:19369211, PubMed:19423707, PubMed:22941656, PubMed:24141787, PubMed:28319063). Strongly stimulates the DNA strand-invasion activity of RAD51, stabilizes the nucleoprotein filament against a disruptive BRC3-BRC4 polypeptide and helps RAD51 to overcome the suppressive effect of replication protein A (RPA) (PubMed:20871615). Functionally cooperates with RAD51AP1 in promoting of D-loop formation by RAD51 (PubMed:20871616). Serves as the molecular scaffold in the formation of the BRCA1-PALB2-BRCA2 complex which is essential for homologous recombination (PubMed:19369211). Via its WD repeats is proposed to scaffold a HR complex containing RAD51C and BRCA2 which is thought to play a role in HR-mediated DNA repair (PubMed:24141787). Essential partner of BRCA2 that promotes the localization and stability of BRCA2 (PubMed:16793542). Also enables its recombinational repair and checkpoint functions of BRCA2 (PubMed:16793542). May act by promoting stable association of BRCA2 with nuclear structures, allowing BRCA2 to escape the effects of proteasome-mediated degradation (PubMed:16793542). Binds DNA with high affinity for D loop, which comprises single-stranded, double-stranded and branched DNA structures (PubMed:20871616). May play a role in the extension step after strand invasion at replication-dependent DNA double-strand breaks; together with BRCA2 is involved in both POLH localization at collapsed replication forks and DNA polymerization activity (PubMed:24485656). {ECO:0000269|PubMed:16793542, ECO:0000269|PubMed:19369211, ECO:0000269|PubMed:19423707, ECO:0000269|PubMed:20871615, ECO:0000269|PubMed:20871616, ECO:0000269|PubMed:22941656, ECO:0000269|PubMed:24141787, ECO:0000269|PubMed:24485656, ECO:0000269|PubMed:28319063}. |
Q8N5S9 | CAMKK1 | S475 | ochoa|psp | Calcium/calmodulin-dependent protein kinase kinase 1 (CaM-KK 1) (CaM-kinase kinase 1) (CaMKK 1) (EC 2.7.11.17) (CaM-kinase IV kinase) (Calcium/calmodulin-dependent protein kinase kinase alpha) (CaM-KK alpha) (CaM-kinase kinase alpha) (CaMKK alpha) | Calcium/calmodulin-dependent protein kinase that belongs to a proposed calcium-triggered signaling cascade involved in a number of cellular processes. Phosphorylates CAMK1, CAMK1D, CAMK1G and CAMK4. Involved in regulating cell apoptosis. Promotes cell survival by phosphorylating AKT1/PKB that inhibits pro-apoptotic BAD/Bcl2-antagonist of cell death. {ECO:0000269|PubMed:12935886}. |
Q8N612 | FHIP1B | S901 | ochoa | FHF complex subunit HOOK-interacting protein 1B (FHIP1B) (FTS- and Hook-interacting protein) (FHIP) | Component of the FTS/Hook/FHIP complex (FHF complex). The FHF complex may function to promote vesicle trafficking and/or fusion via the homotypic vesicular protein sorting complex (the HOPS complex). FHF complex promotes the distribution of AP-4 complex to the perinuclear area of the cell (PubMed:32073997). {ECO:0000269|PubMed:18799622, ECO:0000269|PubMed:32073997}. |
Q8ND25 | ZNRF1 | S123 | ochoa | E3 ubiquitin-protein ligase ZNRF1 (EC 2.3.2.27) (Nerve injury-induced gene 283 protein) (RING-type E3 ubiquitin transferase ZNRF1) (Zinc/RING finger protein 1) | E3 ubiquitin-protein ligase that plays a role in different processes including cell differentiation, receptor recycling or regulation of inflammation (PubMed:28593998, PubMed:33996800, PubMed:37158982). Mediates the ubiquitination of AKT1 and GLUL, thereby playing a role in neuron cells differentiation. Plays a role in the establishment and maintenance of neuronal transmission and plasticity. Regulates Schwann cells differentiation by mediating ubiquitination of GLUL. Promotes neurodegeneration by mediating 'Lys-48'-linked polyubiquitination and subsequent degradation of AKT1 in axons: degradation of AKT1 prevents AKT1-mediated phosphorylation of GSK3B, leading to GSK3B activation and phosphorylation of DPYSL2/CRMP2 followed by destabilization of microtubule assembly in axons. Ubiquitinates the Na(+)/K(+) ATPase alpha-1 subunit/ATP1A1 and thereby influences its endocytosis and/or degradation (PubMed:22797923). Controls ligand-induced EGFR signaling via mediating receptor ubiquitination and recruitment of the ESCRT machinery (PubMed:33996800). Acts as a negative feedback mechanism controlling TLR3 trafficking by mediating TLR3 'Lys-63'-linked polyubiquitination to reduce type I IFN production (PubMed:37158982). Modulates inflammation by promoting caveolin-1/CAV1 ubiquitination and degradation to regulate TLR4-activated immune response (PubMed:28593998). {ECO:0000269|PubMed:22797923, ECO:0000269|PubMed:28593998, ECO:0000269|PubMed:29626159, ECO:0000269|PubMed:33996800, ECO:0000269|PubMed:37158982, ECO:0000305|PubMed:14561866}. |
Q8NEY1 | NAV1 | S1381 | ochoa | Neuron navigator 1 (Pore membrane and/or filament-interacting-like protein 3) (Steerin-1) (Unc-53 homolog 1) (unc53H1) | May be involved in neuronal migration. {ECO:0000250}. |
Q8TE76 | MORC4 | S620 | ochoa | MORC family CW-type zinc finger protein 4 (Zinc finger CW-type coiled-coil domain protein 2) (Zinc finger CW-type domain protein 4) | Histone methylation reader which binds to non-methylated (H3K4me0), monomethylated (H3K4me1), dimethylated (H3K4me2) and trimethylated (H3K4me3) 'Lys-4' on histone H3 (PubMed:26933034). The order of binding preference is H3K4me3 > H3K4me2 > H3K4me1 > H3K4me0 (PubMed:26933034). {ECO:0000269|PubMed:26933034}. |
Q8WU79 | SMAP2 | S240 | ochoa | Stromal membrane-associated protein 2 (Stromal membrane-associated protein 1-like) | GTPase activating protein that acts on ARF1. Can also activate ARF6 (in vitro). May play a role in clathrin-dependent retrograde transport from early endosomes to the trans-Golgi network (By similarity). {ECO:0000250}. |
Q8WUA7 | TBC1D22A | S150 | ochoa | TBC1 domain family member 22A | May act as a GTPase-activating protein for Rab family protein(s). {ECO:0000250}. |
Q8WVM7 | STAG1 | S1142 | ochoa | Cohesin subunit SA-1 (SCC3 homolog 1) (Stromal antigen 1) | Component of cohesin complex, a complex required for the cohesion of sister chromatids after DNA replication. The cohesin complex apparently forms a large proteinaceous ring within which sister chromatids can be trapped. At anaphase, the complex is cleaved and dissociates from chromatin, allowing sister chromatids to segregate. The cohesin complex may also play a role in spindle pole assembly during mitosis. |
Q92625 | ANKS1A | S579 | ochoa | Ankyrin repeat and SAM domain-containing protein 1A (Odin) | Regulator of different signaling pathways. Regulates EPHA8 receptor tyrosine kinase signaling to control cell migration and neurite retraction (By similarity). {ECO:0000250, ECO:0000269|PubMed:17875921}. |
Q96F15 | GIMAP5 | S220 | ochoa | GTPase IMAP family member 5 (Immune-associated nucleotide-binding protein 5) (Immunity-associated nucleotide 4-like 1 protein) (Immunity-associated nucleotide 5 protein) (IAN-5) (hIAN5) (Immunity-associated protein 3) | Plays a role in T lymphocyte development and the optimal generation of CD4/CD8 double-positive thymocytes (By similarity). Inhibitor of GSK3A, possibly by sequestering GSK3A in cytoplasmic vesicles and impairing its translocation to the nucleus. Consequently, impairs GSK3A-dependent transcriptional program and regulation of the DNA damage response occurring during T cells proliferation (PubMed:29382851). Required for the survival of peripheral T cells, natural killer (NK) and NK T-cell development and the maintenance of normal liver function (By similarity). May promote the survival of mature T lymphocytes upon cytokine withdrawal (By similarity). May regulate Ca(2+) homeostasis by modulating lysosomal Ca(2+) stores, preventing its accumulation in the absence of T cell activation (By similarity). May play a role in mitochondrial DNA segregation in hematopoietic tissues (By similarity). Is a regulator of liver endothelial cell homeostasis (By similarity). {ECO:0000250|UniProtKB:Q8BWF2, ECO:0000250|UniProtKB:Q8K3L6, ECO:0000269|PubMed:29382851}. |
Q96F81 | DISP1 | S64 | ochoa | Protein dispatched homolog 1 | Functions in hedgehog (Hh) signaling. Regulates the release and extracellular accumulation of cholesterol-modified hedgehog proteins and is hence required for effective production of the Hh signal (By similarity). Synergizes with SCUBE2 to cause an increase in SHH secretion (PubMed:22902404). {ECO:0000250|UniProtKB:Q3TDN0, ECO:0000269|PubMed:22902404}. |
Q96HA1 | POM121 | S351 | ochoa | Nuclear envelope pore membrane protein POM 121 (Nuclear envelope pore membrane protein POM 121A) (Nucleoporin Nup121) (Pore membrane protein of 121 kDa) | Essential component of the nuclear pore complex (NPC). The repeat-containing domain may be involved in anchoring components of the pore complex to the pore membrane. When overexpressed in cells induces the formation of cytoplasmic annulate lamellae (AL). {ECO:0000269|PubMed:17900573}. |
Q96JT2 | SLC45A3 | S422 | ochoa | Solute carrier family 45 member 3 (Prostate cancer-associated protein 6) (Prostein) | Proton-associated sucrose transporter. May be able to transport also glucose and fructose. {ECO:0000250|UniProtKB:Q8K0H7}. |
Q96RG2 | PASK | S119 | ochoa | PAS domain-containing serine/threonine-protein kinase (PAS-kinase) (PASKIN) (hPASK) (EC 2.7.11.1) | Serine/threonine-protein kinase involved in energy homeostasis and protein translation. Phosphorylates EEF1A1, GYS1, PDX1 and RPS6. Probably plays a role under changing environmental conditions (oxygen, glucose, nutrition), rather than under standard conditions. Acts as a sensor involved in energy homeostasis: regulates glycogen synthase synthesis by mediating phosphorylation of GYS1, leading to GYS1 inactivation. May be involved in glucose-stimulated insulin production in pancreas and regulation of glucagon secretion by glucose in alpha cells; however such data require additional evidences. May play a role in regulation of protein translation by phosphorylating EEF1A1, leading to increase translation efficiency. May also participate in respiratory regulation. {ECO:0000269|PubMed:16275910, ECO:0000269|PubMed:17052199, ECO:0000269|PubMed:17595531, ECO:0000269|PubMed:20943661, ECO:0000269|PubMed:21181396, ECO:0000269|PubMed:21418524}. |
Q96RG2 | PASK | S956 | ochoa|psp | PAS domain-containing serine/threonine-protein kinase (PAS-kinase) (PASKIN) (hPASK) (EC 2.7.11.1) | Serine/threonine-protein kinase involved in energy homeostasis and protein translation. Phosphorylates EEF1A1, GYS1, PDX1 and RPS6. Probably plays a role under changing environmental conditions (oxygen, glucose, nutrition), rather than under standard conditions. Acts as a sensor involved in energy homeostasis: regulates glycogen synthase synthesis by mediating phosphorylation of GYS1, leading to GYS1 inactivation. May be involved in glucose-stimulated insulin production in pancreas and regulation of glucagon secretion by glucose in alpha cells; however such data require additional evidences. May play a role in regulation of protein translation by phosphorylating EEF1A1, leading to increase translation efficiency. May also participate in respiratory regulation. {ECO:0000269|PubMed:16275910, ECO:0000269|PubMed:17052199, ECO:0000269|PubMed:17595531, ECO:0000269|PubMed:20943661, ECO:0000269|PubMed:21181396, ECO:0000269|PubMed:21418524}. |
Q96T37 | RBM15 | S159 | ochoa | RNA-binding protein 15 (One-twenty two protein 1) (RNA-binding motif protein 15) | RNA-binding protein that acts as a key regulator of N6-methyladenosine (m6A) methylation of RNAs, thereby regulating different processes, such as hematopoietic cell homeostasis, alternative splicing of mRNAs and X chromosome inactivation mediated by Xist RNA (PubMed:27602518). 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 (By similarity). Plays a key role in m6A methylation, possibly by binding target RNAs and recruiting the WMM complex (PubMed:27602518). Involved in random X inactivation mediated by Xist RNA: acts by binding Xist RNA and recruiting the WMM complex, which mediates m6A methylation, leading to target YTHDC1 reader on Xist RNA and promoting transcription repression activity of Xist (PubMed:27602518). Required for the development of multiple tissues, such as the maintenance of the homeostasis of long-term hematopoietic stem cells and for megakaryocyte (MK) and B-cell differentiation (By similarity). Regulates megakaryocyte differentiation by regulating alternative splicing of genes important for megakaryocyte differentiation; probably regulates alternative splicing via m6A regulation (PubMed:26575292). Required for placental vascular branching morphogenesis and embryonic development of the heart and spleen (By similarity). Acts as a regulator of thrombopoietin response in hematopoietic stem cells by regulating alternative splicing of MPL (By similarity). May also function as an mRNA export factor, stimulating export and expression of RTE-containing mRNAs which are present in many retrotransposons that require to be exported prior to splicing (PubMed:17001072, PubMed:19786495). High affinity binding of pre-mRNA to RBM15 may allow targeting of the mRNP to the export helicase DBP5 in a manner that is independent of splicing-mediated NXF1 deposition, resulting in export prior to splicing (PubMed:17001072, PubMed:19786495). May be implicated in HOX gene regulation (PubMed:11344311). {ECO:0000250|UniProtKB:Q0VBL3, ECO:0000269|PubMed:17001072, ECO:0000269|PubMed:19786495, ECO:0000269|PubMed:26575292, ECO:0000269|PubMed:27602518, ECO:0000305|PubMed:11344311}. |
Q99611 | SEPHS2 | S97 | ochoa | Selenide, water dikinase 2 (EC 2.7.9.3) (Selenium donor protein 2) (Selenophosphate synthase 2) | Synthesizes selenophosphate from selenide and ATP. {ECO:0000250|UniProtKB:P49903}. |
Q9BRK4 | LZTS2 | S227 | ochoa | Leucine zipper putative tumor suppressor 2 (hLZTS2) (Protein LAPSER1) | Negative regulator of katanin-mediated microtubule severing and release from the centrosome. Required for central spindle formation and the completion of cytokinesis. May negatively regulate axonal outgrowth by preventing the formation of microtubule bundles that are necessary for transport within the elongating axon. Negative regulator of the Wnt signaling pathway. Represses beta-catenin-mediated transcriptional activation by promoting the nuclear exclusion of beta-catenin. {ECO:0000255|HAMAP-Rule:MF_03026, ECO:0000269|PubMed:17000760, ECO:0000269|PubMed:17351128, ECO:0000269|PubMed:17950943, ECO:0000269|PubMed:18490357}. |
Q9BU19 | ZNF692 | S470 | psp | Zinc finger protein 692 (AICAR responsive element binding protein) | May act as an transcriptional repressor for PCK1 gene expression, in turn may participate in the hepatic gluconeogenesis regulation through the activated AMPK signaling pathway. {ECO:0000269|PubMed:17097062, ECO:0000269|PubMed:21910974}. |
Q9BV38 | WDR18 | S368 | ochoa | WD repeat-containing protein 18 | Functions as a component of the Five Friends of Methylated CHTOP (5FMC) complex; the 5FMC complex is recruited to ZNF148 by methylated CHTOP, leading to desumoylation of ZNF148 and subsequent transactivation of ZNF148 target genes (PubMed:22872859). Component of the PELP1 complex involved in the nucleolar steps of 28S rRNA maturation and the subsequent nucleoplasmic transit of the pre-60S ribosomal subunit (PubMed:21326211). May play a role during development (By similarity). {ECO:0000250|UniProtKB:Q68EI0, ECO:0000269|PubMed:21326211, ECO:0000269|PubMed:22872859}. |
Q9BX66 | SORBS1 | S146 | ochoa | Sorbin and SH3 domain-containing protein 1 (Ponsin) (SH3 domain protein 5) (SH3P12) (c-Cbl-associated protein) (CAP) | Plays a role in tyrosine phosphorylation of CBL by linking CBL to the insulin receptor. Required for insulin-stimulated glucose transport. Involved in formation of actin stress fibers and focal adhesions (By similarity). {ECO:0000250|UniProtKB:Q62417}. |
Q9C0D0 | PHACTR1 | S190 | ochoa | Phosphatase and actin regulator 1 | Binds actin monomers (G actin) and plays a role in multiple processes including the regulation of actin cytoskeleton dynamics, actin stress fibers formation, cell motility and survival, formation of tubules by endothelial cells, and regulation of PPP1CA activity (PubMed:21798305, PubMed:21939755). Involved in the regulation of cortical neuron migration and dendrite arborization (By similarity). {ECO:0000250|UniProtKB:Q2M3X8, ECO:0000269|PubMed:21798305, ECO:0000269|PubMed:21939755}. |
Q9C0K0 | BCL11B | S110 | ochoa | B-cell lymphoma/leukemia 11B (BCL-11B) (B-cell CLL/lymphoma 11B) (COUP-TF-interacting protein 2) (Radiation-induced tumor suppressor gene 1 protein) (hRit1) | Key regulator of both differentiation and survival of T-lymphocytes during thymocyte development in mammals. Essential in controlling the responsiveness of hematopoietic stem cells to chemotactic signals by modulating the expression of the receptors CCR7 and CCR9, which direct the movement of progenitor cells from the bone marrow to the thymus (PubMed:27959755). Is a regulator of IL2 promoter and enhances IL2 expression in activated CD4(+) T-lymphocytes (PubMed:16809611). Tumor-suppressor that represses transcription through direct, TFCOUP2-independent binding to a GC-rich response element (By similarity). May also function in the P53-signaling pathway (By similarity). {ECO:0000250|UniProtKB:Q99PV8, ECO:0000269|PubMed:16809611, ECO:0000269|PubMed:27959755}. |
Q9GZY6 | LAT2 | S55 | ochoa | Linker for activation of T-cells family member 2 (Linker for activation of B-cells) (Membrane-associated adapter molecule) (Non-T-cell activation linker) (Williams-Beuren syndrome chromosomal region 15 protein) (Williams-Beuren syndrome chromosomal region 5 protein) | Involved in FCER1 (high affinity immunoglobulin epsilon receptor)-mediated signaling in mast cells. May also be involved in BCR (B-cell antigen receptor)-mediated signaling in B-cells and FCGR1 (high affinity immunoglobulin gamma Fc receptor I)-mediated signaling in myeloid cells. Couples activation of these receptors and their associated kinases with distal intracellular events through the recruitment of GRB2. {ECO:0000269|PubMed:12486104, ECO:0000269|PubMed:12514734, ECO:0000269|PubMed:15010370}. |
Q9H4B6 | SAV1 | S94 | ochoa | Protein salvador homolog 1 (45 kDa WW domain protein) (hWW45) | Regulator of STK3/MST2 and STK4/MST1 in the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis (PubMed:29063833). 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. Phosphorylation of YAP1 by LATS1/2 inhibits its translocation into the nucleus to regulate cellular genes important for cell proliferation, cell death, and cell migration. SAV1 is required for STK3/MST2 and STK4/MST1 activation and promotes cell-cycle exit and terminal differentiation in developing epithelial tissues. Plays a role in centrosome disjunction by regulating the localization of NEK2 to centrosomes, and its ability to phosphorylate CROCC and CEP250. In conjunction with STK3/MST2, activates the transcriptional activity of ESR1 through the modulation of its phosphorylation. {ECO:0000269|PubMed:16930133, ECO:0000269|PubMed:19212654, ECO:0000269|PubMed:21076410, ECO:0000269|PubMed:21104395, ECO:0000269|PubMed:29063833}. |
Q9H706 | GAREM1 | S625 | ochoa | GRB2-associated and regulator of MAPK protein 1 (GRB2-associated and regulator of MAPK1) | [Isoform 1]: Acts as an adapter protein that plays a role in intracellular signaling cascades triggered either by the cell surface activated epidermal growth factor receptor and/or cytoplasmic protein tyrosine kinases. Promotes activation of the MAPK/ERK signaling pathway. Plays a role in the regulation of cell proliferation. {ECO:0000269|PubMed:19509291}. |
Q9HAU0 | PLEKHA5 | S596 | ochoa | Pleckstrin homology domain-containing family A member 5 (PH domain-containing family A member 5) (Phosphoinositol 3-phosphate-binding protein 2) (PEPP-2) | None |
Q9HCL2 | GPAM | S604 | ochoa | Glycerol-3-phosphate acyltransferase 1, mitochondrial (GPAT-1) (EC 2.3.1.15) | Mitochondrial membrane protein that catalyzes the essential first step of biosynthesis of glycerolipids such as triglycerides, phosphatidic acids and lysophosphatidic acids (PubMed:18238778, PubMed:19075029, PubMed:36522428). Esterifies acyl-group from acyl-coenzyme A (acyl-CoA) to the sn-1 position of glycerol-3-phosphate, to produce lysophosphatidic acid (PubMed:18238778). Has a narrow hydrophobic binding cleft that selects for a linear acyl chain (PubMed:36522428). Catalytic activity is higher for substrates with a 16-carbon acyl chain (PubMed:36522428). {ECO:0000269|PubMed:18238778, ECO:0000269|PubMed:19075029, ECO:0000269|PubMed:36522428}. |
Q9HCM4 | EPB41L5 | S423 | ochoa | Band 4.1-like protein 5 (Erythrocyte membrane protein band 4.1-like 5) | Plays a role in the formation and organization of tight junctions during the establishment of polarity in epithelial cells. {ECO:0000269|PubMed:17920587}. |
Q9P107 | GMIP | S440 | ochoa | GEM-interacting protein (GMIP) | Stimulates, in vitro and in vivo, the GTPase activity of RhoA. {ECO:0000269|PubMed:12093360}. |
Q9UJM3 | ERRFI1 | S126 | ochoa | ERBB receptor feedback inhibitor 1 (Mitogen-inducible gene 6 protein) (MIG-6) | Negative regulator of EGFR signaling in skin morphogenesis. Acts as a negative regulator for several EGFR family members, including ERBB2, ERBB3 and ERBB4. Inhibits EGFR catalytic activity by interfering with its dimerization. Inhibits autophosphorylation of EGFR, ERBB2 and ERBB4. Important for normal keratinocyte proliferation and differentiation. Plays a role in modulating the response to steroid hormones in the uterus. Required for normal response to progesterone in the uterus and for fertility. Mediates epithelial estrogen responses in the uterus by regulating ESR1 levels and activation. Important for regulation of endometrium cell proliferation. Important for normal prenatal and perinatal lung development (By similarity). {ECO:0000250}. |
Q9UQL6 | HDAC5 | S498 | ochoa|psp | Histone deacetylase 5 (HD5) (EC 3.5.1.98) (Antigen NY-CO-9) | 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 by repressing transcription of myocyte enhancer MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Serves as a corepressor of RARA and causes its deacetylation (PubMed:28167758). In association with RARA, plays a role in the repression of microRNA-10a and thereby in the inflammatory response (PubMed:28167758). {ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:28167758}. |
Q9Y3M8 | STARD13 | S182 | ochoa | StAR-related lipid transfer protein 13 (46H23.2) (Deleted in liver cancer 2 protein) (DLC-2) (Rho GTPase-activating protein) (START domain-containing protein 13) (StARD13) | GTPase-activating protein for RhoA, and perhaps for Cdc42. May be involved in regulation of cytoskeletal reorganization, cell proliferation and cell motility. Acts a tumor suppressor in hepatocellular carcinoma cells. {ECO:0000269|PubMed:14697242, ECO:0000269|PubMed:16217026}. |
Q9Y6A5 | TACC3 | S505 | ochoa | Transforming acidic coiled-coil-containing protein 3 (ERIC-1) | Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors (By similarity). Acts as a component of the TACC3/ch-TOG/clathrin complex proposed to contribute to stabilization of kinetochore fibers of the mitotic spindle by acting as inter-microtubule bridge. The TACC3/ch-TOG/clathrin complex is required for the maintenance of kinetochore fiber tension (PubMed:21297582, PubMed:23532825). May be involved in the control of cell growth and differentiation. May contribute to cancer (PubMed:14767476). {ECO:0000250|UniProtKB:Q9JJ11, ECO:0000269|PubMed:14767476, ECO:0000269|PubMed:21297582, ECO:0000269|PubMed:23532825}. |
Q9Y6X9 | MORC2 | S686 | ochoa | ATPase MORC2 (EC 3.6.1.-) (MORC family CW-type zinc finger protein 2) (Zinc finger CW-type coiled-coil domain protein 1) | Essential for epigenetic silencing by the HUSH (human silencing hub) complex. Recruited by HUSH to target site in heterochromatin, the ATPase activity and homodimerization are critical for HUSH-mediated silencing (PubMed:28581500, PubMed:29440755, PubMed:32693025). Represses germ cell-related genes and L1 retrotransposons in collaboration with SETDB1 and the HUSH complex, the silencing is dependent of repressive epigenetic modifications, such as H3K9me3 mark. Silencing events often occur within introns of transcriptionally active genes, and lead to the down-regulation of host gene expression (PubMed:29211708). During DNA damage response, regulates chromatin remodeling through ATP hydrolysis. Upon DNA damage, is phosphorylated by PAK1, both colocalize to chromatin and induce H2AX expression. ATPase activity is required and dependent of phosphorylation by PAK1 and presence of DNA (PubMed:23260667). Recruits histone deacetylases, such as HDAC4, to promoter regions, causing local histone H3 deacetylation and transcriptional repression of genes such as CA9 (PubMed:20110259, PubMed:20225202). Exhibits a cytosolic function in lipogenesis, adipogenic differentiation, and lipid homeostasis by increasing the activity of ACLY, possibly preventing its dephosphorylation (PubMed:24286864). {ECO:0000269|PubMed:20110259, ECO:0000269|PubMed:20225202, ECO:0000269|PubMed:23260667, ECO:0000269|PubMed:24286864, ECO:0000269|PubMed:28581500, ECO:0000269|PubMed:29211708, ECO:0000269|PubMed:29440755, ECO:0000269|PubMed:32693025}. |
Q9NRR5 | UBQLN4 | S274 | Sugiyama | Ubiquilin-4 (Ataxin-1 interacting ubiquitin-like protein) (A1Up) (Ataxin-1 ubiquitin-like-interacting protein A1U) (Connexin43-interacting protein of 75 kDa) (CIP75) | Regulator of protein degradation that mediates the proteasomal targeting of misfolded, mislocalized or accumulated proteins (PubMed:15280365, PubMed:27113755, PubMed:29666234, PubMed:30612738). Acts by binding polyubiquitin chains of target proteins via its UBA domain and by interacting with subunits of the proteasome via its ubiquitin-like domain (PubMed:15280365, PubMed:27113755, PubMed:30612738). Key regulator of DNA repair that represses homologous recombination repair: in response to DNA damage, recruited to sites of DNA damage following phosphorylation by ATM and acts by binding and removing ubiquitinated MRE11 from damaged chromatin, leading to MRE11 degradation by the proteasome (PubMed:30612738). MRE11 degradation prevents homologous recombination repair, redirecting double-strand break repair toward non-homologous end joining (NHEJ) (PubMed:30612738). Specifically recognizes and binds mislocalized transmembrane-containing proteins and targets them to proteasomal degradation (PubMed:27113755). Collaborates with DESI1/POST in the export of ubiquitinated proteins from the nucleus to the cytoplasm (PubMed:29666234). Also plays a role in the regulation of the proteasomal degradation of non-ubiquitinated GJA1 (By similarity). Acts as an adapter protein that recruits UBQLN1 to the autophagy machinery (PubMed:23459205). Mediates the association of UBQLN1 with autophagosomes and the autophagy-related protein LC3 (MAP1LC3A/B/C) and may assist in the maturation of autophagosomes to autolysosomes by mediating autophagosome-lysosome fusion (PubMed:23459205). {ECO:0000250|UniProtKB:Q99NB8, ECO:0000269|PubMed:15280365, ECO:0000269|PubMed:23459205, ECO:0000269|PubMed:27113755, ECO:0000269|PubMed:29666234, ECO:0000269|PubMed:30612738}. |
Q9UMX0 | UBQLN1 | S264 | Sugiyama | Ubiquilin-1 (Protein linking IAP with cytoskeleton 1) (PLIC-1) (hPLIC-1) | Plays an important role in the regulation of different protein degradation mechanisms and pathways including ubiquitin-proteasome system (UPS), autophagy and endoplasmic reticulum-associated protein degradation (ERAD) pathway. Mediates the proteasomal targeting of misfolded or accumulated proteins for degradation by binding (via UBA domain) to their polyubiquitin chains and by interacting (via ubiquitin-like domain) with the subunits of the proteasome (PubMed:15147878). Plays a role in the ERAD pathway via its interaction with ER-localized proteins UBXN4, VCP and HERPUD1 and may form a link between the polyubiquitinated ERAD substrates and the proteasome (PubMed:18307982, PubMed:19822669). Involved in the regulation of macroautophagy and autophagosome formation; required for maturation of autophagy-related protein LC3 from the cytosolic form LC3-I to the membrane-bound form LC3-II and may assist in the maturation of autophagosomes to autolysosomes by mediating autophagosome-lysosome fusion (PubMed:19148225, PubMed:20529957, PubMed:23459205). Negatively regulates the TICAM1/TRIF-dependent toll-like receptor signaling pathway by decreasing the abundance of TICAM1 via the autophagic pathway (PubMed:21695056). Promotes the ubiquitination and lysosomal degradation of ORAI1, consequently down-regulating the ORAI1-mediated Ca2+ mobilization (PubMed:23307288). Suppresses the maturation and proteasomal degradation of amyloid beta A4 protein (A4) by stimulating the lysine 63 (K63)-linked polyubiquitination. Delays the maturation of A4 by sequestering it in the Golgi apparatus and preventing its transport to the cell surface for subsequent processing (By similarity). Ubiquitinates BCL2L10 and thereby stabilizes protein abundance (PubMed:22233804). {ECO:0000250|UniProtKB:Q9JJP9, ECO:0000269|PubMed:18307982, ECO:0000269|PubMed:19148225, ECO:0000269|PubMed:19822669, ECO:0000269|PubMed:20529957, ECO:0000269|PubMed:21695056, ECO:0000269|PubMed:22233804, ECO:0000269|PubMed:23307288, ECO:0000269|PubMed:23459205, ECO:0000303|PubMed:15147878}.; FUNCTION: [Isoform 1]: Plays a role in unfolded protein response (UPR) by attenuating the induction of UPR-inducible genes, DDTI3/CHOP, HSPA5 and PDIA2 during ER stress (PubMed:18953672). Plays a key role in the regulation of the levels of PSEN1 by targeting its accumulation to aggresomes which may then be removed from cells by autophagocytosis (PubMed:21143716). {ECO:0000269|PubMed:18953672, ECO:0000269|PubMed:21143716}.; FUNCTION: [Isoform 2]: Plays a role in unfolded protein response (UPR) by attenuating the induction of UPR-inducible genes, DDTI3/CHOP, HSPA5 and PDIA2 during ER stress. {ECO:0000269|PubMed:18953672}.; FUNCTION: [Isoform 3]: Plays a role in unfolded protein response (UPR) by attenuating the induction of UPR-inducible genes, DDTI3/CHOP, HSPA5 and PDIA2 during ER stress (PubMed:18953672). Plays a key role in the regulation of the levels of PSEN1 by targeting its accumulation to aggresomes which may then be removed from cells by autophagocytosis (PubMed:21143716). {ECO:0000269|PubMed:18953672, ECO:0000269|PubMed:21143716}. |
Q9Y262 | EIF3L | S416 | Sugiyama | Eukaryotic translation initiation factor 3 subunit L (eIF3l) (Eukaryotic translation initiation factor 3 subunit 6-interacting protein) (Eukaryotic translation initiation factor 3 subunit E-interacting protein) | Component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis (PubMed:17581632, PubMed:25849773, PubMed:27462815). The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation (PubMed:17581632). The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression (PubMed:25849773). {ECO:0000255|HAMAP-Rule:MF_03011, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815}.; FUNCTION: (Microbial infection) In case of FCV infection, plays a role in the ribosomal termination-reinitiation event leading to the translation of VP2 (PubMed:18056426). {ECO:0000269|PubMed:18056426}. |
O60941 | DTNB | S465 | Sugiyama | Dystrobrevin beta (DTN-B) (Beta-dystrobrevin) | Scaffolding protein that assembles DMD and SNTA1 molecules to the basal membrane of kidney cells and liver sinusoids (By similarity). May function as a repressor of the SYN1 promoter through the binding of repressor element-1 (RE-1), in turn regulates SYN1 expression and may be involved in cell proliferation regulation during the early phase of neural differentiation (PubMed:27223470). May be required for proper maturation and function of a subset of inhibitory synapses (By similarity). {ECO:0000250|UniProtKB:O70585, ECO:0000269|PubMed:27223470}. |
Q9Y4J8 | DTNA | S501 | Sugiyama | Dystrobrevin alpha (DTN-A) (Alpha-dystrobrevin) (Dystrophin-related protein 3) | May be involved in the formation and stability of synapses as well as being involved in the clustering of nicotinic acetylcholine receptors. |
O15037 | KHNYN | S299 | Sugiyama | Protein KHNYN (KH and NYN domain-containing protein) | None |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-9764790 | Positive Regulation of CDH1 Gene Transcription | 0.000148 | 3.829 |
R-HSA-2559585 | Oncogene Induced Senescence | 0.000328 | 3.484 |
R-HSA-9944997 | Loss of Function of KMT2D in MLL4 Complex Formation in Kabuki Syndrome | 0.037477 | 1.426 |
R-HSA-9944971 | Loss of Function of KMT2D in Kabuki Syndrome | 0.037477 | 1.426 |
R-HSA-8941237 | Invadopodia formation | 0.037477 | 1.426 |
R-HSA-9706377 | FLT3 signaling by CBL mutants | 0.052075 | 1.283 |
R-HSA-176417 | Phosphorylation of Emi1 | 0.059291 | 1.227 |
R-HSA-5603029 | IkBA variant leads to EDA-ID | 0.059291 | 1.227 |
R-HSA-8985586 | SLIT2:ROBO1 increases RHOA activity | 0.059291 | 1.227 |
R-HSA-9912481 | Branched-chain ketoacid dehydrogenase kinase deficiency | 0.066453 | 1.177 |
R-HSA-2892245 | POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | 0.073561 | 1.133 |
R-HSA-418886 | Netrin mediated repulsion signals | 0.073561 | 1.133 |
R-HSA-2470946 | Cohesin Loading onto Chromatin | 0.073561 | 1.133 |
R-HSA-9726840 | SHOC2 M1731 mutant abolishes MRAS complex function | 0.073561 | 1.133 |
R-HSA-446107 | Type I hemidesmosome assembly | 0.080615 | 1.094 |
R-HSA-9660537 | Signaling by MRAS-complex mutants | 0.080615 | 1.094 |
R-HSA-8875656 | MET receptor recycling | 0.080615 | 1.094 |
R-HSA-9726842 | Gain-of-function MRAS complexes activate RAF signaling | 0.080615 | 1.094 |
R-HSA-912631 | Regulation of signaling by CBL | 0.014791 | 1.830 |
R-HSA-8875555 | MET activates RAP1 and RAC1 | 0.094564 | 1.024 |
R-HSA-2468052 | Establishment of Sister Chromatid Cohesion | 0.094564 | 1.024 |
R-HSA-9938206 | Developmental Lineage of Mammary Stem Cells | 0.019739 | 1.705 |
R-HSA-8876493 | InlA-mediated entry of Listeria monocytogenes into host cells | 0.101459 | 0.994 |
R-HSA-933543 | NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 0.101459 | 0.994 |
R-HSA-933542 | TRAF6 mediated NF-kB activation | 0.022437 | 1.649 |
R-HSA-9931512 | Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | 0.108302 | 0.965 |
R-HSA-9931530 | Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | 0.115094 | 0.939 |
R-HSA-445095 | Interaction between L1 and Ankyrins | 0.026752 | 1.573 |
R-HSA-9709570 | Impaired BRCA2 binding to RAD51 | 0.029799 | 1.526 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 0.031372 | 1.503 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 0.032977 | 1.482 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 0.032977 | 1.482 |
R-HSA-418885 | DCC mediated attractive signaling | 0.135163 | 0.869 |
R-HSA-9027284 | Erythropoietin activates RAS | 0.135163 | 0.869 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 0.036281 | 1.440 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 0.036281 | 1.440 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 0.037979 | 1.420 |
R-HSA-9687136 | Aberrant regulation of mitotic exit in cancer due to RB1 defects | 0.141751 | 0.848 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 0.041465 | 1.382 |
R-HSA-2892247 | POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | 0.148290 | 0.829 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 0.048778 | 1.312 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 0.050674 | 1.295 |
R-HSA-9709603 | Impaired BRCA2 binding to PALB2 | 0.167612 | 0.776 |
R-HSA-9927418 | Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 0.056519 | 1.248 |
R-HSA-9934037 | Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | 0.173955 | 0.760 |
R-HSA-9701193 | Defective homologous recombination repair (HRR) due to PALB2 loss of function | 0.173955 | 0.760 |
R-HSA-9704646 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.173955 | 0.760 |
R-HSA-9704331 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.173955 | 0.760 |
R-HSA-9701192 | Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 0.173955 | 0.760 |
R-HSA-5693554 | Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SD... | 0.211022 | 0.676 |
R-HSA-73863 | RNA Polymerase I Transcription Termination | 0.223007 | 0.652 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 0.022368 | 1.650 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 0.060398 | 1.219 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 0.060398 | 1.219 |
R-HSA-452723 | Transcriptional regulation of pluripotent stem cells | 0.005145 | 2.289 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 0.095830 | 1.018 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 0.151150 | 0.821 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 0.092692 | 1.033 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 0.092692 | 1.033 |
R-HSA-5684264 | MAP3K8 (TPL2)-dependent MAPK1/3 activation | 0.128524 | 0.891 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 0.092692 | 1.033 |
R-HSA-8876384 | Listeria monocytogenes entry into host cells | 0.018445 | 1.734 |
R-HSA-191650 | Regulation of gap junction activity | 0.044804 | 1.349 |
R-HSA-9931521 | The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CL... | 0.011494 | 1.940 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 0.125236 | 0.902 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 0.127776 | 0.894 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 0.083434 | 1.079 |
R-HSA-170968 | Frs2-mediated activation | 0.007683 | 2.114 |
R-HSA-9764562 | Regulation of CDH1 mRNA translation by microRNAs | 0.008571 | 2.067 |
R-HSA-5685938 | HDR through Single Strand Annealing (SSA) | 0.036281 | 1.440 |
R-HSA-176407 | Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 0.154780 | 0.810 |
R-HSA-418990 | Adherens junctions interactions | 0.110167 | 0.958 |
R-HSA-421270 | Cell-cell junction organization | 0.154238 | 0.812 |
R-HSA-8875360 | InlB-mediated entry of Listeria monocytogenes into host cell | 0.135163 | 0.869 |
R-HSA-9703465 | Signaling by FLT3 fusion proteins | 0.217037 | 0.663 |
R-HSA-446728 | Cell junction organization | 0.079141 | 1.102 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 0.191701 | 0.717 |
R-HSA-140342 | Apoptosis induced DNA fragmentation | 0.094564 | 1.024 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 0.064935 | 1.188 |
R-HSA-169893 | Prolonged ERK activation events | 0.010477 | 1.980 |
R-HSA-9675136 | Diseases of DNA Double-Strand Break Repair | 0.003978 | 2.400 |
R-HSA-918233 | TRAF3-dependent IRF activation pathway | 0.148290 | 0.829 |
R-HSA-1500931 | Cell-Cell communication | 0.044786 | 1.349 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 0.145215 | 0.838 |
R-HSA-9705677 | SARS-CoV-2 targets PDZ proteins in cell-cell junction | 0.044804 | 1.349 |
R-HSA-9619229 | Activation of RAC1 downstream of NMDARs | 0.087616 | 1.057 |
R-HSA-9701190 | Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 0.003978 | 2.400 |
R-HSA-350054 | Notch-HLH transcription pathway | 0.019739 | 1.705 |
R-HSA-68884 | Mitotic Telophase/Cytokinesis | 0.108302 | 0.965 |
R-HSA-209560 | NF-kB is activated and signals survival | 0.108302 | 0.965 |
R-HSA-418890 | Role of second messengers in netrin-1 signaling | 0.115094 | 0.939 |
R-HSA-5654732 | Negative regulation of FGFR3 signaling | 0.028259 | 1.549 |
R-HSA-5654733 | Negative regulation of FGFR4 signaling | 0.029799 | 1.526 |
R-HSA-9927432 | Developmental Lineage of Mammary Gland Myoepithelial Cells | 0.029799 | 1.526 |
R-HSA-1810476 | RIP-mediated NFkB activation via ZBP1 | 0.135163 | 0.869 |
R-HSA-5654727 | Negative regulation of FGFR2 signaling | 0.039707 | 1.401 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 0.045066 | 1.346 |
R-HSA-181429 | Serotonin Neurotransmitter Release Cycle | 0.161220 | 0.793 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 0.020212 | 1.694 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 0.062586 | 1.204 |
R-HSA-6807878 | COPI-mediated anterograde transport | 0.197218 | 0.705 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 0.017526 | 1.756 |
R-HSA-5654726 | Negative regulation of FGFR1 signaling | 0.036281 | 1.440 |
R-HSA-177929 | Signaling by EGFR | 0.086536 | 1.063 |
R-HSA-1295596 | Spry regulation of FGF signaling | 0.009502 | 2.022 |
R-HSA-9754189 | Germ layer formation at gastrulation | 0.014791 | 1.830 |
R-HSA-2028269 | Signaling by Hippo | 0.012552 | 1.901 |
R-HSA-447043 | Neurofascin interactions | 0.066453 | 1.177 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 0.072799 | 1.138 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 0.004646 | 2.333 |
R-HSA-6807004 | Negative regulation of MET activity | 0.173955 | 0.760 |
R-HSA-139915 | Activation of PUMA and translocation to mitochondria | 0.073561 | 1.133 |
R-HSA-428542 | Regulation of commissural axon pathfinding by SLIT and ROBO | 0.087616 | 1.057 |
R-HSA-450341 | Activation of the AP-1 family of transcription factors | 0.087616 | 1.057 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 0.037979 | 1.420 |
R-HSA-212676 | Dopamine Neurotransmitter Release Cycle | 0.192700 | 0.715 |
R-HSA-187687 | Signalling to ERKs | 0.041465 | 1.382 |
R-HSA-212165 | Epigenetic regulation of gene expression | 0.123275 | 0.909 |
R-HSA-9913351 | Formation of the dystrophin-glycoprotein complex (DGC) | 0.002989 | 2.524 |
R-HSA-5693538 | Homology Directed Repair | 0.081067 | 1.091 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 0.151150 | 0.821 |
R-HSA-8935964 | RUNX1 regulates expression of components of tight junctions | 0.001779 | 2.750 |
R-HSA-376172 | DSCAM interactions | 0.030095 | 1.522 |
R-HSA-5674499 | Negative feedback regulation of MAPK pathway | 0.059291 | 1.227 |
R-HSA-187706 | Signalling to p38 via RIT and RIN | 0.059291 | 1.227 |
R-HSA-170984 | ARMS-mediated activation | 0.087616 | 1.057 |
R-HSA-191859 | snRNP Assembly | 0.093480 | 1.029 |
R-HSA-194441 | Metabolism of non-coding RNA | 0.093480 | 1.029 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 0.098196 | 1.008 |
R-HSA-9006335 | Signaling by Erythropoietin | 0.234811 | 0.629 |
R-HSA-442729 | CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | 0.080615 | 1.094 |
R-HSA-5693579 | Homologous DNA Pairing and Strand Exchange | 0.005145 | 2.289 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 0.217037 | 0.663 |
R-HSA-9818749 | Regulation of NFE2L2 gene expression | 0.066453 | 1.177 |
R-HSA-6803211 | TP53 Regulates Transcription of Death Receptors and Ligands | 0.128524 | 0.891 |
R-HSA-180746 | Nuclear import of Rev protein | 0.039707 | 1.401 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 0.115203 | 0.939 |
R-HSA-450294 | MAP kinase activation | 0.098196 | 1.008 |
R-HSA-5621575 | CD209 (DC-SIGN) signaling | 0.204961 | 0.688 |
R-HSA-9834899 | Specification of the neural plate border | 0.167612 | 0.776 |
R-HSA-448424 | Interleukin-17 signaling | 0.120193 | 0.920 |
R-HSA-8931987 | RUNX1 regulates estrogen receptor mediated transcription | 0.002753 | 2.560 |
R-HSA-447038 | NrCAM interactions | 0.052075 | 1.283 |
R-HSA-8941284 | RUNX2 regulates chondrocyte maturation | 0.052075 | 1.283 |
R-HSA-5660668 | CLEC7A/inflammasome pathway | 0.059291 | 1.227 |
R-HSA-8849469 | PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | 0.080615 | 1.094 |
R-HSA-8951936 | RUNX3 regulates p14-ARF | 0.115094 | 0.939 |
R-HSA-9706369 | Negative regulation of FLT3 | 0.141751 | 0.848 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 0.050674 | 1.295 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 0.050674 | 1.295 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 0.052597 | 1.279 |
R-HSA-429947 | Deadenylation of mRNA | 0.204961 | 0.688 |
R-HSA-9839394 | TGFBR3 expression | 0.211022 | 0.676 |
R-HSA-9609690 | HCMV Early Events | 0.226979 | 0.644 |
R-HSA-6806834 | Signaling by MET | 0.145882 | 0.836 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 0.148511 | 0.828 |
R-HSA-111932 | CaMK IV-mediated phosphorylation of CREB | 0.094564 | 1.024 |
R-HSA-9682385 | FLT3 signaling in disease | 0.043251 | 1.364 |
R-HSA-9659379 | Sensory processing of sound | 0.143263 | 0.844 |
R-HSA-176187 | Activation of ATR in response to replication stress | 0.036281 | 1.440 |
R-HSA-9762293 | Regulation of CDH11 gene transcription | 0.087616 | 1.057 |
R-HSA-351906 | Apoptotic cleavage of cell adhesion proteins | 0.003314 | 2.480 |
R-HSA-3134963 | DEx/H-box helicases activate type I IFN and inflammatory cytokines production | 0.052075 | 1.283 |
R-HSA-9758919 | Epithelial-Mesenchymal Transition (EMT) during gastrulation | 0.059291 | 1.227 |
R-HSA-447041 | CHL1 interactions | 0.073561 | 1.133 |
R-HSA-448706 | Interleukin-1 processing | 0.087616 | 1.057 |
R-HSA-193692 | Regulated proteolysis of p75NTR | 0.087616 | 1.057 |
R-HSA-9933946 | Formation of the embryonic stem cell BAF (esBAF) complex | 0.135163 | 0.869 |
R-HSA-1483148 | Synthesis of PG | 0.148290 | 0.829 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 0.046908 | 1.329 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 0.064656 | 1.189 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 0.095830 | 1.018 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 0.125236 | 0.902 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 0.233480 | 0.632 |
R-HSA-9909396 | Circadian clock | 0.104964 | 0.979 |
R-HSA-512988 | Interleukin-3, Interleukin-5 and GM-CSF signaling | 0.056519 | 1.248 |
R-HSA-1606322 | ZBP1(DAI) mediated induction of type I IFNs | 0.161220 | 0.793 |
R-HSA-3214841 | PKMTs methylate histone lysines | 0.052597 | 1.279 |
R-HSA-1474165 | Reproduction | 0.101838 | 0.992 |
R-HSA-2559583 | Cellular Senescence | 0.004431 | 2.353 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 0.143446 | 0.843 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 0.202755 | 0.693 |
R-HSA-5654743 | Signaling by FGFR4 | 0.058517 | 1.233 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 0.034926 | 1.457 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 0.202755 | 0.693 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 0.202755 | 0.693 |
R-HSA-9818030 | NFE2L2 regulating tumorigenic genes | 0.121834 | 0.914 |
R-HSA-9675151 | Disorders of Developmental Biology | 0.148290 | 0.829 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 0.048778 | 1.312 |
R-HSA-5654741 | Signaling by FGFR3 | 0.062586 | 1.204 |
R-HSA-6803204 | TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 0.223007 | 0.652 |
R-HSA-75153 | Apoptotic execution phase | 0.008462 | 2.073 |
R-HSA-193639 | p75NTR signals via NF-kB | 0.135163 | 0.869 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 0.052597 | 1.279 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 0.088833 | 1.051 |
R-HSA-5654738 | Signaling by FGFR2 | 0.145882 | 0.836 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 0.225064 | 0.648 |
R-HSA-3000171 | Non-integrin membrane-ECM interactions | 0.003939 | 2.405 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 0.211022 | 0.676 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 0.211022 | 0.676 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 0.042303 | 1.374 |
R-HSA-9675135 | Diseases of DNA repair | 0.008462 | 2.073 |
R-HSA-5654736 | Signaling by FGFR1 | 0.086536 | 1.063 |
R-HSA-9735871 | SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 0.135163 | 0.869 |
R-HSA-5693616 | Presynaptic phase of homologous DNA pairing and strand exchange | 0.041465 | 1.382 |
R-HSA-75109 | Triglyceride biosynthesis | 0.223007 | 0.652 |
R-HSA-6784531 | tRNA processing in the nucleus | 0.100580 | 0.997 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 0.097221 | 1.012 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 0.077539 | 1.110 |
R-HSA-3214847 | HATs acetylate histones | 0.205530 | 0.687 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 0.219466 | 0.659 |
R-HSA-1236382 | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 0.180251 | 0.744 |
R-HSA-5637815 | Signaling by Ligand-Responsive EGFR Variants in Cancer | 0.180251 | 0.744 |
R-HSA-1433559 | Regulation of KIT signaling | 0.128524 | 0.891 |
R-HSA-450282 | MAPK targets/ Nuclear events mediated by MAP kinases | 0.234811 | 0.629 |
R-HSA-9018519 | Estrogen-dependent gene expression | 0.006637 | 2.178 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 0.041105 | 1.386 |
R-HSA-9758941 | Gastrulation | 0.039831 | 1.400 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 0.025279 | 1.597 |
R-HSA-9748787 | Azathioprine ADME | 0.073159 | 1.136 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 0.234811 | 0.629 |
R-HSA-9827857 | Specification of primordial germ cells | 0.012552 | 1.901 |
R-HSA-6803205 | TP53 regulates transcription of several additional cell death genes whose specif... | 0.192700 | 0.715 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 0.062407 | 1.205 |
R-HSA-6804759 | Regulation of TP53 Activity through Association with Co-factors | 0.121834 | 0.914 |
R-HSA-210991 | Basigin interactions | 0.180251 | 0.744 |
R-HSA-74160 | Gene expression (Transcription) | 0.121385 | 0.916 |
R-HSA-1643713 | Signaling by EGFR in Cancer | 0.217037 | 0.663 |
R-HSA-190236 | Signaling by FGFR | 0.202755 | 0.693 |
R-HSA-9926550 | Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adh... | 0.013651 | 1.865 |
R-HSA-2173789 | TGF-beta receptor signaling activates SMADs | 0.058517 | 1.233 |
R-HSA-499943 | Interconversion of nucleotide di- and triphosphates | 0.023872 | 1.622 |
R-HSA-9865118 | Diseases of branched-chain amino acid catabolism | 0.217037 | 0.663 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 0.050485 | 1.297 |
R-HSA-68875 | Mitotic Prophase | 0.083910 | 1.076 |
R-HSA-70171 | Glycolysis | 0.208310 | 0.681 |
R-HSA-4839726 | Chromatin organization | 0.056164 | 1.251 |
R-HSA-166520 | Signaling by NTRKs | 0.134712 | 0.871 |
R-HSA-9755088 | Ribavirin ADME | 0.018445 | 1.734 |
R-HSA-69473 | G2/M DNA damage checkpoint | 0.130329 | 0.885 |
R-HSA-9856649 | Transcriptional and post-translational regulation of MITF-M expression and activ... | 0.122708 | 0.911 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 0.205530 | 0.687 |
R-HSA-109581 | Apoptosis | 0.049934 | 1.302 |
R-HSA-9823730 | Formation of definitive endoderm | 0.015970 | 1.797 |
R-HSA-373753 | Nephrin family interactions | 0.173955 | 0.760 |
R-HSA-9006936 | Signaling by TGFB family members | 0.155981 | 0.807 |
R-HSA-2173788 | Downregulation of TGF-beta receptor signaling | 0.192700 | 0.715 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 0.213881 | 0.670 |
R-HSA-3247509 | Chromatin modifying enzymes | 0.130756 | 0.884 |
R-HSA-8939211 | ESR-mediated signaling | 0.047958 | 1.319 |
R-HSA-9823739 | Formation of the anterior neural plate | 0.135163 | 0.869 |
R-HSA-9013507 | NOTCH3 Activation and Transmission of Signal to the Nucleus | 0.192700 | 0.715 |
R-HSA-3000170 | Syndecan interactions | 0.198853 | 0.701 |
R-HSA-3000157 | Laminin interactions | 0.211022 | 0.676 |
R-HSA-1169408 | ISG15 antiviral mechanism | 0.132893 | 0.876 |
R-HSA-5357801 | Programmed Cell Death | 0.094622 | 1.024 |
R-HSA-2262752 | Cellular responses to stress | 0.171007 | 0.767 |
R-HSA-5637812 | Signaling by EGFRvIII in Cancer | 0.154780 | 0.810 |
R-HSA-5637810 | Constitutive Signaling by EGFRvIII | 0.154780 | 0.810 |
R-HSA-844456 | The NLRP3 inflammasome | 0.167612 | 0.776 |
R-HSA-189200 | Cellular hexose transport | 0.192700 | 0.715 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 0.071001 | 1.149 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 0.034613 | 1.461 |
R-HSA-1059683 | Interleukin-6 signaling | 0.121834 | 0.914 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 0.095830 | 1.018 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 0.095830 | 1.018 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 0.095830 | 1.018 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 0.095830 | 1.018 |
R-HSA-9694516 | SARS-CoV-2 Infection | 0.153056 | 0.815 |
R-HSA-212436 | Generic Transcription Pathway | 0.219823 | 0.658 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 0.139930 | 0.854 |
R-HSA-1474244 | Extracellular matrix organization | 0.053203 | 1.274 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 0.145215 | 0.838 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 0.170237 | 0.769 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 0.164478 | 0.784 |
R-HSA-9679506 | SARS-CoV Infections | 0.152673 | 0.816 |
R-HSA-622312 | Inflammasomes | 0.228931 | 0.640 |
R-HSA-9678108 | SARS-CoV-1 Infection | 0.185818 | 0.731 |
R-HSA-6783589 | Interleukin-6 family signaling | 0.204961 | 0.688 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 0.095830 | 1.018 |
R-HSA-1980143 | Signaling by NOTCH1 | 0.135469 | 0.868 |
R-HSA-211000 | Gene Silencing by RNA | 0.230672 | 0.637 |
R-HSA-5633007 | Regulation of TP53 Activity | 0.155981 | 0.807 |
R-HSA-73857 | RNA Polymerase II Transcription | 0.235357 | 0.628 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 0.236291 | 0.627 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 0.239103 | 0.621 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 0.239103 | 0.621 |
R-HSA-9687139 | Aberrant regulation of mitotic cell cycle due to RB1 defects | 0.240646 | 0.619 |
R-HSA-114452 | Activation of BH3-only proteins | 0.240646 | 0.619 |
R-HSA-1483249 | Inositol phosphate metabolism | 0.244732 | 0.611 |
R-HSA-182971 | EGFR downregulation | 0.246438 | 0.608 |
R-HSA-936440 | Negative regulators of DDX58/IFIH1 signaling | 0.246438 | 0.608 |
R-HSA-9833109 | Evasion by RSV of host interferon responses | 0.246438 | 0.608 |
R-HSA-186763 | Downstream signal transduction | 0.246438 | 0.608 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 0.247549 | 0.606 |
R-HSA-9675126 | Diseases of mitotic cell cycle | 0.252185 | 0.598 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 0.256006 | 0.592 |
R-HSA-5693568 | Resolution of D-loop Structures through Holliday Junction Intermediates | 0.257889 | 0.589 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 0.257889 | 0.589 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 0.257889 | 0.589 |
R-HSA-373760 | L1CAM interactions | 0.261647 | 0.582 |
R-HSA-9768727 | Regulation of CDH1 posttranslational processing and trafficking to plasma membra... | 0.263549 | 0.579 |
R-HSA-5693537 | Resolution of D-Loop Structures | 0.263549 | 0.579 |
R-HSA-9619665 | EGR2 and SOX10-mediated initiation of Schwann cell myelination | 0.263549 | 0.579 |
R-HSA-70326 | Glucose metabolism | 0.264468 | 0.578 |
R-HSA-8957322 | Metabolism of steroids | 0.269120 | 0.570 |
R-HSA-5673000 | RAF activation | 0.269167 | 0.570 |
R-HSA-9680350 | Signaling by CSF1 (M-CSF) in myeloid cells | 0.269167 | 0.570 |
R-HSA-9843970 | Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | 0.269167 | 0.570 |
R-HSA-9927426 | Developmental Lineage of Mammary Gland Alveolar Cells | 0.269167 | 0.570 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 0.270112 | 0.568 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 0.270112 | 0.568 |
R-HSA-174113 | SCF-beta-TrCP mediated degradation of Emi1 | 0.274743 | 0.561 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 0.274743 | 0.561 |
R-HSA-9860927 | Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZ... | 0.274743 | 0.561 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 0.275754 | 0.559 |
R-HSA-3371556 | Cellular response to heat stress | 0.275754 | 0.559 |
R-HSA-8953897 | Cellular responses to stimuli | 0.277993 | 0.556 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 0.278574 | 0.555 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 0.278574 | 0.555 |
R-HSA-111933 | Calmodulin induced events | 0.280276 | 0.552 |
R-HSA-111997 | CaM pathway | 0.280276 | 0.552 |
R-HSA-8941326 | RUNX2 regulates bone development | 0.280276 | 0.552 |
R-HSA-162909 | Host Interactions of HIV factors | 0.284214 | 0.546 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 0.285767 | 0.544 |
R-HSA-933541 | TRAF6 mediated IRF7 activation | 0.285767 | 0.544 |
R-HSA-4641258 | Degradation of DVL | 0.285767 | 0.544 |
R-HSA-2173796 | SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 0.285767 | 0.544 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 0.285767 | 0.544 |
R-HSA-5689896 | Ovarian tumor domain proteases | 0.285767 | 0.544 |
R-HSA-8875878 | MET promotes cell motility | 0.291217 | 0.536 |
R-HSA-69481 | G2/M Checkpoints | 0.295479 | 0.529 |
R-HSA-9725554 | Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | 0.296626 | 0.528 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 0.296626 | 0.528 |
R-HSA-162582 | Signal Transduction | 0.299364 | 0.524 |
R-HSA-427389 | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 0.301993 | 0.520 |
R-HSA-9604323 | Negative regulation of NOTCH4 signaling | 0.301993 | 0.520 |
R-HSA-5602358 | Diseases associated with the TLR signaling cascade | 0.301993 | 0.520 |
R-HSA-5260271 | Diseases of Immune System | 0.301993 | 0.520 |
R-HSA-9607240 | FLT3 Signaling | 0.307320 | 0.512 |
R-HSA-15869 | Metabolism of nucleotides | 0.311154 | 0.507 |
R-HSA-9656223 | Signaling by RAF1 mutants | 0.312607 | 0.505 |
R-HSA-5674135 | MAP2K and MAPK activation | 0.312607 | 0.505 |
R-HSA-9932298 | Degradation of CRY and PER proteins | 0.312607 | 0.505 |
R-HSA-5675221 | Negative regulation of MAPK pathway | 0.312607 | 0.505 |
R-HSA-73762 | RNA Polymerase I Transcription Initiation | 0.317853 | 0.498 |
R-HSA-111996 | Ca-dependent events | 0.317853 | 0.498 |
R-HSA-157118 | Signaling by NOTCH | 0.319488 | 0.496 |
R-HSA-1433557 | Signaling by SCF-KIT | 0.323060 | 0.491 |
R-HSA-1640170 | Cell Cycle | 0.323105 | 0.491 |
R-HSA-373752 | Netrin-1 signaling | 0.328228 | 0.484 |
R-HSA-5683826 | Surfactant metabolism | 0.328228 | 0.484 |
R-HSA-1489509 | DAG and IP3 signaling | 0.333356 | 0.477 |
R-HSA-6807070 | PTEN Regulation | 0.334663 | 0.475 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 0.338445 | 0.471 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 0.338445 | 0.471 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 0.338445 | 0.471 |
R-HSA-174084 | Autodegradation of Cdh1 by Cdh1:APC/C | 0.338445 | 0.471 |
R-HSA-6802949 | Signaling by RAS mutants | 0.338445 | 0.471 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 0.338445 | 0.471 |
R-HSA-9839373 | Signaling by TGFBR3 | 0.338445 | 0.471 |
R-HSA-9660826 | Purinergic signaling in leishmaniasis infection | 0.338445 | 0.471 |
R-HSA-9664424 | Cell recruitment (pro-inflammatory response) | 0.338445 | 0.471 |
R-HSA-9609646 | HCMV Infection | 0.340331 | 0.468 |
R-HSA-445989 | TAK1-dependent IKK and NF-kappa-B activation | 0.343496 | 0.464 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 0.345755 | 0.461 |
R-HSA-9031628 | NGF-stimulated transcription | 0.348509 | 0.458 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 0.348519 | 0.458 |
R-HSA-9766229 | Degradation of CDH1 | 0.353484 | 0.452 |
R-HSA-157858 | Gap junction trafficking and regulation | 0.353484 | 0.452 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 0.359535 | 0.444 |
R-HSA-69242 | S Phase | 0.362279 | 0.441 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 0.362279 | 0.441 |
R-HSA-1169091 | Activation of NF-kappaB in B cells | 0.363321 | 0.440 |
R-HSA-70895 | Branched-chain amino acid catabolism | 0.363321 | 0.440 |
R-HSA-9734767 | Developmental Cell Lineages | 0.367366 | 0.435 |
R-HSA-9856651 | MITF-M-dependent gene expression | 0.367754 | 0.434 |
R-HSA-112382 | Formation of RNA Pol II elongation complex | 0.368183 | 0.434 |
R-HSA-8866654 | E3 ubiquitin ligases ubiquitinate target proteins | 0.368183 | 0.434 |
R-HSA-6794361 | Neurexins and neuroligins | 0.368183 | 0.434 |
R-HSA-68886 | M Phase | 0.370504 | 0.431 |
R-HSA-174178 | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins ... | 0.373009 | 0.428 |
R-HSA-1221632 | Meiotic synapsis | 0.373009 | 0.428 |
R-HSA-75955 | RNA Polymerase II Transcription Elongation | 0.373009 | 0.428 |
R-HSA-9639288 | Amino acids regulate mTORC1 | 0.373009 | 0.428 |
R-HSA-445355 | Smooth Muscle Contraction | 0.373009 | 0.428 |
R-HSA-9711123 | Cellular response to chemical stress | 0.377722 | 0.423 |
R-HSA-72649 | Translation initiation complex formation | 0.377798 | 0.423 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 0.377798 | 0.423 |
R-HSA-73887 | Death Receptor Signaling | 0.378649 | 0.422 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 0.381361 | 0.419 |
R-HSA-9012852 | Signaling by NOTCH3 | 0.382551 | 0.417 |
R-HSA-9610379 | HCMV Late Events | 0.386770 | 0.413 |
R-HSA-162587 | HIV Life Cycle | 0.386770 | 0.413 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 0.387268 | 0.412 |
R-HSA-193648 | NRAGE signals death through JNK | 0.387268 | 0.412 |
R-HSA-9662361 | Sensory processing of sound by outer hair cells of the cochlea | 0.387268 | 0.412 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 0.387268 | 0.412 |
R-HSA-109606 | Intrinsic Pathway for Apoptosis | 0.387268 | 0.412 |
R-HSA-9711097 | Cellular response to starvation | 0.389467 | 0.410 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 0.389844 | 0.409 |
R-HSA-9764561 | Regulation of CDH1 Function | 0.391949 | 0.407 |
R-HSA-1483166 | Synthesis of PA | 0.391949 | 0.407 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 0.396594 | 0.402 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 0.396594 | 0.402 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 0.401205 | 0.397 |
R-HSA-8979227 | Triglyceride metabolism | 0.401205 | 0.397 |
R-HSA-2022090 | Assembly of collagen fibrils and other multimeric structures | 0.401205 | 0.397 |
R-HSA-352230 | Amino acid transport across the plasma membrane | 0.401205 | 0.397 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 0.406523 | 0.391 |
R-HSA-112043 | PLC beta mediated events | 0.410321 | 0.387 |
R-HSA-5619102 | SLC transporter disorders | 0.413498 | 0.384 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 0.414827 | 0.382 |
R-HSA-375165 | NCAM signaling for neurite out-growth | 0.414827 | 0.382 |
R-HSA-186797 | Signaling by PDGF | 0.414827 | 0.382 |
R-HSA-9707616 | Heme signaling | 0.414827 | 0.382 |
R-HSA-1660499 | Synthesis of PIPs at the plasma membrane | 0.414827 | 0.382 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 0.419300 | 0.377 |
R-HSA-8848021 | Signaling by PTK6 | 0.419300 | 0.377 |
R-HSA-168643 | Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signali... | 0.423738 | 0.373 |
R-HSA-72306 | tRNA processing | 0.424031 | 0.373 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 0.428143 | 0.368 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 0.432514 | 0.364 |
R-HSA-1483257 | Phospholipid metabolism | 0.432922 | 0.364 |
R-HSA-112040 | G-protein mediated events | 0.436852 | 0.360 |
R-HSA-9958863 | SLC-mediated transport of amino acids | 0.436852 | 0.360 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 0.441157 | 0.355 |
R-HSA-168255 | Influenza Infection | 0.447369 | 0.349 |
R-HSA-1168372 | Downstream signaling events of B Cell Receptor (BCR) | 0.449670 | 0.347 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 0.449670 | 0.347 |
R-HSA-75105 | Fatty acyl-CoA biosynthesis | 0.449670 | 0.347 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 0.453878 | 0.343 |
R-HSA-453276 | Regulation of mitotic cell cycle | 0.453878 | 0.343 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 0.453878 | 0.343 |
R-HSA-427413 | NoRC negatively regulates rRNA expression | 0.453878 | 0.343 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 0.457573 | 0.340 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 0.458054 | 0.339 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 0.458054 | 0.339 |
R-HSA-69052 | Switching of origins to a post-replicative state | 0.462199 | 0.335 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 0.462199 | 0.335 |
R-HSA-674695 | RNA Polymerase II Pre-transcription Events | 0.466312 | 0.331 |
R-HSA-9013694 | Signaling by NOTCH4 | 0.466312 | 0.331 |
R-HSA-69278 | Cell Cycle, Mitotic | 0.466502 | 0.331 |
R-HSA-5633008 | TP53 Regulates Transcription of Cell Death Genes | 0.470393 | 0.328 |
R-HSA-8852135 | Protein ubiquitination | 0.470393 | 0.328 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 0.474444 | 0.324 |
R-HSA-168898 | Toll-like Receptor Cascades | 0.477655 | 0.321 |
R-HSA-73864 | RNA Polymerase I Transcription | 0.482454 | 0.317 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 0.482454 | 0.317 |
R-HSA-416482 | G alpha (12/13) signalling events | 0.482454 | 0.317 |
R-HSA-216083 | Integrin cell surface interactions | 0.482454 | 0.317 |
R-HSA-68877 | Mitotic Prometaphase | 0.482605 | 0.316 |
R-HSA-9675108 | Nervous system development | 0.490039 | 0.310 |
R-HSA-5250941 | Negative epigenetic regulation of rRNA expression | 0.490342 | 0.310 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 0.490342 | 0.310 |
R-HSA-9833482 | PKR-mediated signaling | 0.490342 | 0.310 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 0.494242 | 0.306 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 0.504524 | 0.297 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 0.506923 | 0.295 |
R-HSA-376176 | Signaling by ROBO receptors | 0.506923 | 0.295 |
R-HSA-1483206 | Glycerophospholipid biosynthesis | 0.506923 | 0.295 |
R-HSA-6802957 | Oncogenic MAPK signaling | 0.509546 | 0.293 |
R-HSA-1500620 | Meiosis | 0.509546 | 0.293 |
R-HSA-6794362 | Protein-protein interactions at synapses | 0.509546 | 0.293 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 0.510669 | 0.292 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 0.517025 | 0.286 |
R-HSA-438064 | Post NMDA receptor activation events | 0.520722 | 0.283 |
R-HSA-9006925 | Intracellular signaling by second messengers | 0.524274 | 0.280 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 0.524391 | 0.280 |
R-HSA-202424 | Downstream TCR signaling | 0.531645 | 0.274 |
R-HSA-112310 | Neurotransmitter release cycle | 0.531645 | 0.274 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 0.532811 | 0.273 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 0.534549 | 0.272 |
R-HSA-68882 | Mitotic Anaphase | 0.539711 | 0.268 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 0.541995 | 0.266 |
R-HSA-9748784 | Drug ADME | 0.544272 | 0.264 |
R-HSA-68867 | Assembly of the pre-replicative complex | 0.545826 | 0.263 |
R-HSA-1474290 | Collagen formation | 0.549304 | 0.260 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 0.556181 | 0.255 |
R-HSA-73894 | DNA Repair | 0.557123 | 0.254 |
R-HSA-2730905 | Role of LAT2/NTAL/LAB on calcium mobilization | 0.559581 | 0.252 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 0.559581 | 0.252 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 0.559581 | 0.252 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 0.562955 | 0.250 |
R-HSA-162906 | HIV Infection | 0.564410 | 0.248 |
R-HSA-9020702 | Interleukin-1 signaling | 0.576195 | 0.239 |
R-HSA-2408557 | Selenocysteine synthesis | 0.576195 | 0.239 |
R-HSA-9842860 | Regulation of endogenous retroelements | 0.579442 | 0.237 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 0.579442 | 0.237 |
R-HSA-1483255 | PI Metabolism | 0.579442 | 0.237 |
R-HSA-199991 | Membrane Trafficking | 0.582646 | 0.235 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 0.585863 | 0.232 |
R-HSA-111885 | Opioid Signalling | 0.585863 | 0.232 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 0.585863 | 0.232 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 0.589037 | 0.230 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 0.589037 | 0.230 |
R-HSA-9833110 | RSV-host interactions | 0.589037 | 0.230 |
R-HSA-69239 | Synthesis of DNA | 0.598415 | 0.223 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 0.598777 | 0.223 |
R-HSA-913531 | Interferon Signaling | 0.598777 | 0.223 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 0.601494 | 0.221 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 0.601494 | 0.221 |
R-HSA-69002 | DNA Replication Pre-Initiation | 0.604549 | 0.219 |
R-HSA-5619115 | Disorders of transmembrane transporters | 0.606868 | 0.217 |
R-HSA-202403 | TCR signaling | 0.607581 | 0.216 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 0.619479 | 0.208 |
R-HSA-69620 | Cell Cycle Checkpoints | 0.628864 | 0.201 |
R-HSA-72737 | Cap-dependent Translation Initiation | 0.631020 | 0.200 |
R-HSA-72613 | Eukaryotic Translation Initiation | 0.631020 | 0.200 |
R-HSA-422475 | Axon guidance | 0.631252 | 0.200 |
R-HSA-1592230 | Mitochondrial biogenesis | 0.633850 | 0.198 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 0.639447 | 0.194 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 0.644959 | 0.190 |
R-HSA-1266738 | Developmental Biology | 0.652630 | 0.185 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 0.668205 | 0.175 |
R-HSA-9658195 | Leishmania infection | 0.671772 | 0.173 |
R-HSA-9824443 | Parasitic Infection Pathways | 0.671772 | 0.173 |
R-HSA-9843745 | Adipogenesis | 0.676317 | 0.170 |
R-HSA-1474228 | Degradation of the extracellular matrix | 0.678803 | 0.168 |
R-HSA-5673001 | RAF/MAP kinase cascade | 0.685736 | 0.164 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 0.693324 | 0.159 |
R-HSA-1257604 | PIP3 activates AKT signaling | 0.695889 | 0.157 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 0.697555 | 0.156 |
R-HSA-1643685 | Disease | 0.700058 | 0.155 |
R-HSA-9664417 | Leishmania phagocytosis | 0.700339 | 0.155 |
R-HSA-9664407 | Parasite infection | 0.700339 | 0.155 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 0.700339 | 0.155 |
R-HSA-195721 | Signaling by WNT | 0.700864 | 0.154 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 0.702641 | 0.153 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 0.711677 | 0.148 |
R-HSA-112316 | Neuronal System | 0.724915 | 0.140 |
R-HSA-446652 | Interleukin-1 family signaling | 0.728941 | 0.137 |
R-HSA-69306 | DNA Replication | 0.731026 | 0.136 |
R-HSA-449147 | Signaling by Interleukins | 0.731338 | 0.136 |
R-HSA-1989781 | PPARA activates gene expression | 0.735147 | 0.134 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 0.738265 | 0.132 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 0.739206 | 0.131 |
R-HSA-112315 | Transmission across Chemical Synapses | 0.739763 | 0.131 |
R-HSA-983705 | Signaling by the B Cell Receptor (BCR) | 0.741212 | 0.130 |
R-HSA-2467813 | Separation of Sister Chromatids | 0.752932 | 0.123 |
R-HSA-2408522 | Selenoamino acid metabolism | 0.752932 | 0.123 |
R-HSA-5653656 | Vesicle-mediated transport | 0.764276 | 0.117 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 0.765941 | 0.116 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 0.767743 | 0.115 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 0.769532 | 0.114 |
R-HSA-5683057 | MAPK family signaling cascades | 0.772999 | 0.112 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 0.773068 | 0.112 |
R-HSA-9824446 | Viral Infection Pathways | 0.781366 | 0.107 |
R-HSA-69275 | G2/M Transition | 0.793181 | 0.101 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 0.796357 | 0.099 |
R-HSA-453274 | Mitotic G2-G2/M phases | 0.796357 | 0.099 |
R-HSA-389948 | Co-inhibition by PD-1 | 0.814421 | 0.089 |
R-HSA-9824439 | Bacterial Infection Pathways | 0.824462 | 0.084 |
R-HSA-425407 | SLC-mediated transmembrane transport | 0.831619 | 0.080 |
R-HSA-397014 | Muscle contraction | 0.832200 | 0.080 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 0.832200 | 0.080 |
R-HSA-8951664 | Neddylation | 0.843508 | 0.074 |
R-HSA-198933 | Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 0.852923 | 0.069 |
R-HSA-5663205 | Infectious disease | 0.853766 | 0.069 |
R-HSA-446203 | Asparagine N-linked glycosylation | 0.855096 | 0.068 |
R-HSA-72312 | rRNA processing | 0.856307 | 0.067 |
R-HSA-202733 | Cell surface interactions at the vascular wall | 0.861777 | 0.065 |
R-HSA-5688426 | Deubiquitination | 0.879810 | 0.056 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 0.880741 | 0.055 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 0.881547 | 0.055 |
R-HSA-6798695 | Neutrophil degranulation | 0.882998 | 0.054 |
R-HSA-8953854 | Metabolism of RNA | 0.897174 | 0.047 |
R-HSA-597592 | Post-translational protein modification | 0.904924 | 0.043 |
R-HSA-1280218 | Adaptive Immune System | 0.916018 | 0.038 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 0.927549 | 0.033 |
R-HSA-556833 | Metabolism of lipids | 0.948914 | 0.023 |
R-HSA-168249 | Innate Immune System | 0.951014 | 0.022 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 0.958204 | 0.019 |
R-HSA-418594 | G alpha (i) signalling events | 0.963609 | 0.016 |
R-HSA-8978868 | Fatty acid metabolism | 0.963609 | 0.016 |
R-HSA-5668914 | Diseases of metabolism | 0.968898 | 0.014 |
R-HSA-72766 | Translation | 0.969383 | 0.014 |
R-HSA-168256 | Immune System | 0.974167 | 0.011 |
R-HSA-392499 | Metabolism of proteins | 0.984198 | 0.007 |
R-HSA-388396 | GPCR downstream signalling | 0.985413 | 0.006 |
R-HSA-372790 | Signaling by GPCR | 0.991813 | 0.004 |
R-HSA-382551 | Transport of small molecules | 0.996611 | 0.001 |
R-HSA-109582 | Hemostasis | 0.998178 | 0.001 |
R-HSA-9709957 | Sensory Perception | 0.999484 | 0.000 |
R-HSA-1430728 | Metabolism | 0.999770 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
COT |
0.780 | 0.063 | 2 | 0.275 |
CDC7 |
0.779 | 0.193 | 1 | 0.774 |
FAM20C |
0.776 | 0.056 | 2 | 0.322 |
CLK3 |
0.775 | 0.134 | 1 | 0.741 |
HIPK4 |
0.774 | 0.181 | 1 | 0.746 |
CHAK2 |
0.772 | 0.243 | -1 | 0.809 |
PRKD1 |
0.771 | 0.158 | -3 | 0.697 |
MOS |
0.771 | 0.142 | 1 | 0.781 |
KIS |
0.770 | 0.123 | 1 | 0.587 |
SKMLCK |
0.769 | 0.104 | -2 | 0.841 |
ATR |
0.767 | 0.135 | 1 | 0.835 |
PIM3 |
0.767 | 0.068 | -3 | 0.741 |
IKKB |
0.766 | 0.042 | -2 | 0.691 |
GRK1 |
0.766 | 0.093 | -2 | 0.731 |
BMPR1B |
0.766 | 0.179 | 1 | 0.765 |
PRKD2 |
0.765 | 0.132 | -3 | 0.667 |
CK1E |
0.763 | 0.193 | -3 | 0.730 |
RAF1 |
0.761 | 0.033 | 1 | 0.772 |
NDR2 |
0.761 | -0.003 | -3 | 0.733 |
PRPK |
0.761 | -0.031 | -1 | 0.805 |
DSTYK |
0.760 | -0.028 | 2 | 0.315 |
IKKA |
0.759 | 0.048 | -2 | 0.680 |
CAMK1B |
0.759 | 0.017 | -3 | 0.759 |
AURC |
0.759 | 0.112 | -2 | 0.671 |
CDKL5 |
0.759 | 0.075 | -3 | 0.709 |
ATM |
0.758 | 0.095 | 1 | 0.800 |
GCN2 |
0.758 | -0.115 | 2 | 0.263 |
MTOR |
0.758 | -0.000 | 1 | 0.692 |
ERK5 |
0.757 | 0.069 | 1 | 0.790 |
CAMK2G |
0.757 | -0.066 | 2 | 0.335 |
CDKL1 |
0.757 | 0.038 | -3 | 0.722 |
GRK5 |
0.756 | 0.034 | -3 | 0.792 |
MAPKAPK2 |
0.756 | 0.067 | -3 | 0.643 |
SRPK1 |
0.756 | 0.062 | -3 | 0.681 |
CK1D |
0.756 | 0.216 | -3 | 0.694 |
NEK6 |
0.755 | 0.008 | -2 | 0.773 |
GRK6 |
0.755 | 0.043 | 1 | 0.774 |
PIM1 |
0.755 | 0.064 | -3 | 0.720 |
CAMK2B |
0.755 | 0.013 | 2 | 0.335 |
RSK2 |
0.755 | 0.028 | -3 | 0.683 |
TBK1 |
0.754 | -0.053 | 1 | 0.648 |
BMPR2 |
0.754 | 0.003 | -2 | 0.817 |
GRK7 |
0.754 | 0.117 | 1 | 0.707 |
CK1A2 |
0.753 | 0.199 | -3 | 0.699 |
ULK2 |
0.753 | -0.115 | 2 | 0.240 |
CLK2 |
0.753 | 0.089 | -3 | 0.682 |
GRK4 |
0.752 | 0.009 | -2 | 0.750 |
ICK |
0.752 | 0.061 | -3 | 0.739 |
TGFBR1 |
0.751 | 0.090 | -2 | 0.781 |
PDHK4 |
0.751 | -0.158 | 1 | 0.768 |
TLK2 |
0.751 | 0.104 | 1 | 0.804 |
MLK1 |
0.751 | -0.051 | 2 | 0.237 |
PAK1 |
0.751 | 0.031 | -2 | 0.789 |
CAMK2D |
0.751 | -0.026 | -3 | 0.714 |
IKKE |
0.751 | -0.051 | 1 | 0.643 |
CK1G1 |
0.751 | 0.155 | -3 | 0.708 |
DAPK2 |
0.751 | 0.057 | -3 | 0.752 |
AMPKA1 |
0.751 | 0.056 | -3 | 0.742 |
PKACB |
0.751 | 0.092 | -2 | 0.670 |
CAMK2A |
0.750 | 0.012 | 2 | 0.343 |
MAPKAPK3 |
0.750 | 0.038 | -3 | 0.663 |
CAMLCK |
0.750 | 0.031 | -2 | 0.825 |
PKACG |
0.750 | 0.037 | -2 | 0.714 |
NLK |
0.750 | -0.036 | 1 | 0.727 |
RIPK3 |
0.750 | -0.035 | 3 | 0.735 |
MARK4 |
0.750 | -0.007 | 4 | 0.787 |
TGFBR2 |
0.750 | 0.001 | -2 | 0.747 |
P90RSK |
0.750 | 0.007 | -3 | 0.689 |
WNK1 |
0.750 | -0.056 | -2 | 0.843 |
HIPK2 |
0.749 | 0.081 | 1 | 0.539 |
PRKX |
0.749 | 0.107 | -3 | 0.618 |
NDR1 |
0.749 | -0.034 | -3 | 0.728 |
DYRK2 |
0.749 | 0.024 | 1 | 0.638 |
NEK7 |
0.749 | -0.075 | -3 | 0.721 |
MST4 |
0.748 | -0.007 | 2 | 0.308 |
ALK4 |
0.748 | 0.090 | -2 | 0.803 |
SMG1 |
0.748 | 0.102 | 1 | 0.808 |
RSK3 |
0.747 | 0.008 | -3 | 0.672 |
NIK |
0.747 | -0.027 | -3 | 0.764 |
TSSK2 |
0.747 | -0.003 | -5 | 0.787 |
BMPR1A |
0.747 | 0.135 | 1 | 0.731 |
CLK4 |
0.747 | 0.066 | -3 | 0.702 |
SRPK2 |
0.747 | 0.043 | -3 | 0.626 |
MLK3 |
0.747 | -0.028 | 2 | 0.212 |
MNK2 |
0.746 | 0.016 | -2 | 0.770 |
PRKD3 |
0.745 | 0.064 | -3 | 0.650 |
LATS2 |
0.745 | -0.026 | -5 | 0.630 |
ACVR2B |
0.745 | 0.112 | -2 | 0.745 |
AMPKA2 |
0.745 | 0.050 | -3 | 0.715 |
ULK1 |
0.745 | -0.143 | -3 | 0.706 |
PAK3 |
0.745 | 0.004 | -2 | 0.780 |
MSK1 |
0.745 | 0.036 | -3 | 0.664 |
DNAPK |
0.745 | 0.084 | 1 | 0.721 |
PDHK1 |
0.744 | -0.138 | 1 | 0.754 |
MLK2 |
0.744 | -0.019 | 2 | 0.274 |
RSK4 |
0.744 | 0.024 | -3 | 0.670 |
ACVR2A |
0.744 | 0.084 | -2 | 0.738 |
PKN3 |
0.743 | -0.067 | -3 | 0.728 |
DLK |
0.743 | -0.048 | 1 | 0.774 |
P70S6KB |
0.743 | -0.001 | -3 | 0.705 |
TTBK2 |
0.743 | -0.095 | 2 | 0.198 |
NUAK2 |
0.743 | -0.032 | -3 | 0.743 |
NIM1 |
0.743 | -0.047 | 3 | 0.757 |
TSSK1 |
0.743 | 0.004 | -3 | 0.747 |
PKCD |
0.742 | -0.023 | 2 | 0.236 |
HUNK |
0.742 | -0.132 | 2 | 0.250 |
ALK2 |
0.742 | 0.073 | -2 | 0.778 |
PKN2 |
0.742 | -0.056 | -3 | 0.734 |
RIPK1 |
0.741 | -0.081 | 1 | 0.775 |
PAK6 |
0.741 | 0.029 | -2 | 0.721 |
MSK2 |
0.741 | -0.002 | -3 | 0.671 |
CK1A |
0.741 | 0.200 | -3 | 0.633 |
IRE1 |
0.740 | -0.059 | 1 | 0.782 |
AURA |
0.740 | 0.049 | -2 | 0.648 |
CDK8 |
0.740 | -0.014 | 1 | 0.558 |
BCKDK |
0.740 | -0.125 | -1 | 0.720 |
MASTL |
0.739 | -0.153 | -2 | 0.743 |
HIPK1 |
0.739 | 0.055 | 1 | 0.642 |
PAK2 |
0.739 | 0.004 | -2 | 0.770 |
MYLK4 |
0.739 | 0.030 | -2 | 0.766 |
PKCB |
0.739 | -0.033 | 2 | 0.192 |
MLK4 |
0.739 | -0.040 | 2 | 0.182 |
AURB |
0.739 | 0.059 | -2 | 0.665 |
CLK1 |
0.739 | 0.047 | -3 | 0.666 |
QSK |
0.739 | 0.032 | 4 | 0.761 |
SRPK3 |
0.739 | 0.017 | -3 | 0.673 |
CHAK1 |
0.739 | 0.033 | 2 | 0.325 |
NEK9 |
0.739 | -0.110 | 2 | 0.257 |
CDK19 |
0.738 | -0.002 | 1 | 0.522 |
GRK2 |
0.738 | 0.026 | -2 | 0.671 |
BRSK1 |
0.737 | -0.041 | -3 | 0.687 |
CDK7 |
0.737 | 0.014 | 1 | 0.565 |
SIK |
0.737 | 0.021 | -3 | 0.674 |
ANKRD3 |
0.736 | -0.090 | 1 | 0.792 |
LATS1 |
0.736 | -0.007 | -3 | 0.720 |
TLK1 |
0.736 | 0.028 | -2 | 0.767 |
PKCA |
0.735 | -0.034 | 2 | 0.202 |
AKT2 |
0.735 | 0.046 | -3 | 0.630 |
PKCG |
0.735 | -0.054 | 2 | 0.202 |
WNK3 |
0.735 | -0.205 | 1 | 0.763 |
CAMK4 |
0.734 | -0.061 | -3 | 0.722 |
PKG2 |
0.734 | 0.028 | -2 | 0.666 |
MNK1 |
0.734 | -0.014 | -2 | 0.767 |
PLK1 |
0.734 | -0.081 | -2 | 0.705 |
DYRK4 |
0.734 | -0.000 | 1 | 0.538 |
PKCZ |
0.734 | -0.028 | 2 | 0.230 |
PKR |
0.733 | -0.040 | 1 | 0.802 |
PHKG1 |
0.733 | -0.044 | -3 | 0.720 |
CDK1 |
0.733 | 0.010 | 1 | 0.532 |
P38B |
0.733 | 0.026 | 1 | 0.558 |
CDK18 |
0.733 | 0.010 | 1 | 0.498 |
GRK3 |
0.732 | 0.045 | -2 | 0.633 |
MARK3 |
0.732 | -0.005 | 4 | 0.718 |
MEK1 |
0.732 | -0.057 | 2 | 0.313 |
P38A |
0.731 | 0.008 | 1 | 0.629 |
JNK2 |
0.731 | 0.001 | 1 | 0.509 |
DYRK1A |
0.731 | 0.021 | 1 | 0.633 |
PKACA |
0.731 | 0.057 | -2 | 0.633 |
NEK2 |
0.731 | -0.067 | 2 | 0.274 |
MELK |
0.731 | -0.043 | -3 | 0.692 |
PLK4 |
0.730 | -0.102 | 2 | 0.192 |
QIK |
0.730 | -0.070 | -3 | 0.716 |
BRSK2 |
0.730 | -0.072 | -3 | 0.697 |
DCAMKL1 |
0.729 | -0.019 | -3 | 0.685 |
PLK3 |
0.729 | -0.097 | 2 | 0.294 |
ERK1 |
0.729 | 0.001 | 1 | 0.539 |
MAPKAPK5 |
0.729 | -0.035 | -3 | 0.633 |
VRK2 |
0.729 | -0.116 | 1 | 0.804 |
DYRK3 |
0.729 | 0.029 | 1 | 0.655 |
SGK3 |
0.729 | -0.002 | -3 | 0.665 |
IRE2 |
0.728 | -0.093 | 2 | 0.195 |
PKCH |
0.728 | -0.080 | 2 | 0.180 |
MARK2 |
0.728 | -0.032 | 4 | 0.690 |
PRP4 |
0.728 | 0.005 | -3 | 0.674 |
PASK |
0.727 | 0.002 | -3 | 0.755 |
MEKK3 |
0.727 | -0.062 | 1 | 0.752 |
HIPK3 |
0.727 | 0.023 | 1 | 0.637 |
YSK4 |
0.727 | -0.099 | 1 | 0.706 |
JNK3 |
0.727 | -0.021 | 1 | 0.535 |
SNRK |
0.727 | -0.126 | 2 | 0.228 |
MEKK2 |
0.726 | -0.025 | 2 | 0.239 |
PIM2 |
0.726 | 0.021 | -3 | 0.668 |
NUAK1 |
0.726 | -0.048 | -3 | 0.691 |
CHK1 |
0.725 | -0.027 | -3 | 0.690 |
P38G |
0.725 | -0.010 | 1 | 0.445 |
P38D |
0.725 | 0.023 | 1 | 0.467 |
YANK3 |
0.725 | 0.017 | 2 | 0.134 |
PAK4 |
0.724 | 0.021 | -2 | 0.671 |
LKB1 |
0.724 | 0.131 | -3 | 0.701 |
MPSK1 |
0.724 | 0.051 | 1 | 0.734 |
MST3 |
0.724 | 0.000 | 2 | 0.280 |
SSTK |
0.724 | -0.036 | 4 | 0.761 |
PAK5 |
0.724 | 0.019 | -2 | 0.659 |
CDK13 |
0.724 | -0.038 | 1 | 0.533 |
CAMK1G |
0.724 | -0.043 | -3 | 0.682 |
NEK5 |
0.724 | -0.023 | 1 | 0.801 |
PINK1 |
0.724 | -0.031 | 1 | 0.750 |
PERK |
0.724 | -0.070 | -2 | 0.766 |
DYRK1B |
0.724 | 0.005 | 1 | 0.558 |
MAK |
0.723 | 0.091 | -2 | 0.793 |
BRAF |
0.723 | -0.067 | -4 | 0.758 |
CDK5 |
0.723 | -0.033 | 1 | 0.593 |
GSK3A |
0.723 | 0.033 | 4 | 0.502 |
DRAK1 |
0.722 | -0.091 | 1 | 0.710 |
MARK1 |
0.722 | -0.055 | 4 | 0.734 |
DAPK3 |
0.722 | 0.052 | -3 | 0.711 |
DCAMKL2 |
0.721 | -0.058 | -3 | 0.698 |
TAO3 |
0.721 | 0.013 | 1 | 0.727 |
CK2A2 |
0.721 | 0.021 | 1 | 0.625 |
MEK5 |
0.721 | -0.121 | 2 | 0.277 |
GSK3B |
0.721 | 0.019 | 4 | 0.496 |
ERK7 |
0.721 | -0.040 | 2 | 0.138 |
CDK17 |
0.720 | -0.021 | 1 | 0.444 |
CAMK1D |
0.720 | 0.003 | -3 | 0.609 |
WNK4 |
0.720 | -0.115 | -2 | 0.828 |
SMMLCK |
0.719 | -0.017 | -3 | 0.719 |
AKT1 |
0.719 | 0.025 | -3 | 0.632 |
PLK2 |
0.719 | -0.028 | -3 | 0.707 |
ERK2 |
0.719 | -0.049 | 1 | 0.580 |
ZAK |
0.718 | -0.116 | 1 | 0.714 |
DAPK1 |
0.718 | 0.039 | -3 | 0.709 |
CDK12 |
0.717 | -0.040 | 1 | 0.507 |
MEKK1 |
0.717 | -0.120 | 1 | 0.749 |
TTBK1 |
0.716 | -0.128 | 2 | 0.170 |
BUB1 |
0.716 | 0.142 | -5 | 0.747 |
PKCT |
0.716 | -0.064 | 2 | 0.185 |
IRAK4 |
0.716 | -0.101 | 1 | 0.783 |
MOK |
0.715 | 0.071 | 1 | 0.716 |
GAK |
0.715 | -0.001 | 1 | 0.764 |
CDK14 |
0.714 | -0.025 | 1 | 0.536 |
CK2A1 |
0.714 | 0.017 | 1 | 0.605 |
NEK11 |
0.714 | -0.070 | 1 | 0.711 |
HRI |
0.714 | -0.149 | -2 | 0.782 |
CAMKK1 |
0.713 | -0.059 | -2 | 0.689 |
CDK3 |
0.713 | -0.009 | 1 | 0.464 |
NEK8 |
0.713 | -0.090 | 2 | 0.256 |
PKCE |
0.713 | -0.032 | 2 | 0.196 |
CAMKK2 |
0.713 | -0.004 | -2 | 0.698 |
GCK |
0.712 | 0.024 | 1 | 0.750 |
P70S6K |
0.712 | -0.034 | -3 | 0.630 |
PKCI |
0.712 | -0.059 | 2 | 0.201 |
AKT3 |
0.712 | 0.038 | -3 | 0.577 |
CDK9 |
0.711 | -0.070 | 1 | 0.541 |
SGK1 |
0.710 | 0.032 | -3 | 0.566 |
CDK2 |
0.710 | -0.075 | 1 | 0.612 |
EEF2K |
0.709 | -0.044 | 3 | 0.798 |
STK33 |
0.709 | -0.092 | 2 | 0.193 |
TAK1 |
0.709 | -0.021 | 1 | 0.783 |
CDK16 |
0.709 | -0.027 | 1 | 0.460 |
ROCK2 |
0.709 | 0.044 | -3 | 0.693 |
CHK2 |
0.708 | 0.010 | -3 | 0.578 |
JNK1 |
0.708 | -0.030 | 1 | 0.482 |
TNIK |
0.708 | 0.013 | 3 | 0.842 |
CDK10 |
0.708 | -0.027 | 1 | 0.522 |
HPK1 |
0.708 | 0.014 | 1 | 0.728 |
MEKK6 |
0.708 | -0.083 | 1 | 0.776 |
CK1G3 |
0.707 | 0.164 | -3 | 0.595 |
PHKG2 |
0.707 | -0.117 | -3 | 0.693 |
PDK1 |
0.707 | -0.056 | 1 | 0.692 |
NEK4 |
0.707 | -0.048 | 1 | 0.757 |
MRCKB |
0.707 | 0.023 | -3 | 0.656 |
MINK |
0.705 | -0.005 | 1 | 0.744 |
MAP3K15 |
0.705 | -0.065 | 1 | 0.696 |
MRCKA |
0.705 | 0.018 | -3 | 0.666 |
MST2 |
0.704 | -0.072 | 1 | 0.757 |
HGK |
0.704 | -0.029 | 3 | 0.833 |
TAO2 |
0.704 | -0.105 | 2 | 0.293 |
SBK |
0.703 | 0.020 | -3 | 0.527 |
CAMK1A |
0.703 | -0.002 | -3 | 0.589 |
KHS2 |
0.702 | 0.029 | 1 | 0.739 |
IRAK1 |
0.702 | -0.208 | -1 | 0.703 |
NEK1 |
0.701 | -0.046 | 1 | 0.765 |
PKN1 |
0.700 | -0.058 | -3 | 0.637 |
PBK |
0.700 | 0.026 | 1 | 0.698 |
KHS1 |
0.700 | 0.006 | 1 | 0.726 |
LOK |
0.700 | -0.035 | -2 | 0.700 |
LRRK2 |
0.699 | -0.114 | 2 | 0.297 |
TTK |
0.699 | 0.031 | -2 | 0.739 |
SLK |
0.698 | -0.032 | -2 | 0.643 |
OSR1 |
0.698 | -0.004 | 2 | 0.253 |
VRK1 |
0.696 | -0.144 | 2 | 0.247 |
CRIK |
0.696 | 0.042 | -3 | 0.630 |
PKG1 |
0.696 | -0.005 | -2 | 0.592 |
ALPHAK3 |
0.696 | 0.031 | -1 | 0.745 |
DMPK1 |
0.695 | 0.026 | -3 | 0.679 |
YANK2 |
0.695 | 0.013 | 2 | 0.138 |
PDHK3_TYR |
0.694 | 0.125 | 4 | 0.859 |
MAP2K6_TYR |
0.693 | 0.113 | -1 | 0.832 |
ROCK1 |
0.693 | 0.013 | -3 | 0.669 |
MST1 |
0.692 | -0.094 | 1 | 0.739 |
PDHK4_TYR |
0.691 | 0.102 | 2 | 0.363 |
YSK1 |
0.691 | -0.103 | 2 | 0.248 |
MAP2K4_TYR |
0.691 | 0.154 | -1 | 0.822 |
PDHK1_TYR |
0.689 | 0.100 | -1 | 0.836 |
MEK2 |
0.689 | -0.172 | 2 | 0.285 |
CK1G2 |
0.688 | 0.125 | -3 | 0.658 |
CDK6 |
0.688 | -0.066 | 1 | 0.511 |
CDK4 |
0.687 | -0.064 | 1 | 0.495 |
MYO3B |
0.687 | -0.022 | 2 | 0.295 |
HASPIN |
0.686 | -0.032 | -1 | 0.672 |
ABL2 |
0.685 | 0.110 | -1 | 0.772 |
BMPR2_TYR |
0.685 | 0.014 | -1 | 0.826 |
TESK1_TYR |
0.684 | 0.013 | 3 | 0.861 |
RIPK2 |
0.684 | -0.223 | 1 | 0.658 |
NEK3 |
0.683 | -0.119 | 1 | 0.706 |
MAP2K7_TYR |
0.682 | -0.094 | 2 | 0.335 |
EPHB4 |
0.681 | 0.024 | -1 | 0.757 |
EPHA6 |
0.681 | -0.011 | -1 | 0.798 |
LIMK2_TYR |
0.681 | 0.060 | -3 | 0.743 |
ABL1 |
0.681 | 0.083 | -1 | 0.763 |
TXK |
0.679 | 0.070 | 1 | 0.790 |
PKMYT1_TYR |
0.679 | -0.026 | 3 | 0.830 |
ASK1 |
0.678 | -0.134 | 1 | 0.669 |
MYO3A |
0.678 | -0.063 | 1 | 0.739 |
RET |
0.677 | -0.024 | 1 | 0.750 |
TNK2 |
0.676 | 0.071 | 3 | 0.745 |
FGR |
0.675 | 0.025 | 1 | 0.825 |
PINK1_TYR |
0.675 | -0.136 | 1 | 0.764 |
BIKE |
0.675 | -0.042 | 1 | 0.637 |
EPHA4 |
0.674 | -0.039 | 2 | 0.316 |
FER |
0.674 | -0.002 | 1 | 0.830 |
BLK |
0.674 | 0.083 | -1 | 0.777 |
SRMS |
0.673 | -0.025 | 1 | 0.813 |
ROS1 |
0.672 | -0.022 | 3 | 0.754 |
CSF1R |
0.672 | -0.025 | 3 | 0.779 |
TAO1 |
0.672 | -0.112 | 1 | 0.657 |
STLK3 |
0.671 | -0.116 | 1 | 0.692 |
TYRO3 |
0.671 | -0.066 | 3 | 0.776 |
MERTK |
0.671 | -0.003 | 3 | 0.772 |
LCK |
0.671 | 0.072 | -1 | 0.772 |
INSRR |
0.670 | -0.022 | 3 | 0.729 |
JAK2 |
0.670 | -0.027 | 1 | 0.735 |
EPHB1 |
0.670 | -0.019 | 1 | 0.813 |
EPHB3 |
0.669 | -0.022 | -1 | 0.738 |
MST1R |
0.669 | -0.072 | 3 | 0.794 |
TYK2 |
0.669 | -0.066 | 1 | 0.745 |
JAK3 |
0.668 | -0.038 | 1 | 0.718 |
YES1 |
0.668 | -0.043 | -1 | 0.768 |
BMX |
0.668 | 0.004 | -1 | 0.676 |
MET |
0.668 | 0.012 | 3 | 0.771 |
EPHB2 |
0.668 | -0.028 | -1 | 0.737 |
LIMK1_TYR |
0.668 | -0.137 | 2 | 0.320 |
HCK |
0.668 | -0.007 | -1 | 0.767 |
ITK |
0.667 | -0.043 | -1 | 0.740 |
PTK2 |
0.667 | 0.027 | -1 | 0.740 |
DDR1 |
0.666 | -0.123 | 4 | 0.814 |
KIT |
0.666 | -0.030 | 3 | 0.773 |
FGFR2 |
0.665 | -0.101 | 3 | 0.780 |
FYN |
0.665 | 0.010 | -1 | 0.737 |
KDR |
0.664 | -0.048 | 3 | 0.755 |
EPHA7 |
0.663 | -0.048 | 2 | 0.299 |
AXL |
0.662 | -0.057 | 3 | 0.764 |
SYK |
0.661 | 0.044 | -1 | 0.735 |
PDGFRB |
0.661 | -0.104 | 3 | 0.782 |
TNK1 |
0.661 | -0.043 | 3 | 0.762 |
PTK6 |
0.661 | -0.046 | -1 | 0.670 |
FLT1 |
0.660 | -0.042 | -1 | 0.786 |
EPHA3 |
0.660 | -0.088 | 2 | 0.295 |
NEK10_TYR |
0.660 | -0.007 | 1 | 0.605 |
TNNI3K_TYR |
0.660 | -0.026 | 1 | 0.781 |
JAK1 |
0.659 | 0.021 | 1 | 0.673 |
EPHA5 |
0.659 | -0.056 | 2 | 0.305 |
LTK |
0.659 | -0.061 | 3 | 0.726 |
FLT3 |
0.659 | -0.102 | 3 | 0.774 |
MATK |
0.658 | -0.032 | -1 | 0.710 |
AAK1 |
0.657 | -0.019 | 1 | 0.542 |
FGFR3 |
0.657 | -0.090 | 3 | 0.754 |
EPHA8 |
0.657 | -0.039 | -1 | 0.735 |
TEC |
0.657 | -0.062 | -1 | 0.664 |
PTK2B |
0.657 | -0.042 | -1 | 0.698 |
ERBB2 |
0.656 | -0.079 | 1 | 0.687 |
FGFR1 |
0.656 | -0.117 | 3 | 0.752 |
FRK |
0.656 | -0.062 | -1 | 0.784 |
ALK |
0.656 | -0.058 | 3 | 0.694 |
EPHA1 |
0.655 | -0.080 | 3 | 0.757 |
CSK |
0.655 | -0.071 | 2 | 0.295 |
FGFR4 |
0.655 | -0.035 | -1 | 0.720 |
NTRK1 |
0.654 | -0.110 | -1 | 0.741 |
TEK |
0.654 | -0.141 | 3 | 0.712 |
EGFR |
0.653 | -0.052 | 1 | 0.599 |
LYN |
0.653 | -0.039 | 3 | 0.688 |
BTK |
0.653 | -0.135 | -1 | 0.704 |
NTRK3 |
0.652 | -0.044 | -1 | 0.699 |
INSR |
0.652 | -0.085 | 3 | 0.704 |
DDR2 |
0.652 | -0.056 | 3 | 0.716 |
SRC |
0.651 | -0.044 | -1 | 0.732 |
EPHA2 |
0.651 | -0.051 | -1 | 0.716 |
PDGFRA |
0.651 | -0.143 | 3 | 0.777 |
ZAP70 |
0.650 | 0.059 | -1 | 0.677 |
WEE1_TYR |
0.649 | -0.092 | -1 | 0.684 |
ERBB4 |
0.648 | -0.015 | 1 | 0.629 |
FLT4 |
0.648 | -0.141 | 3 | 0.743 |
NTRK2 |
0.645 | -0.135 | 3 | 0.729 |
IGF1R |
0.642 | -0.080 | 3 | 0.637 |
FES |
0.631 | -0.071 | -1 | 0.642 |
MUSK |
0.625 | -0.134 | 1 | 0.604 |