Motif 319 (n=179)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A0A0MRY4 | None | S579 | ochoa | Spermatogenesis-associated protein 13 | None |
A0A0C4DFX4 | None | S3033 | ochoa | Snf2 related CREBBP activator protein | None |
A8MVW0 | FAM171A2 | S422 | ochoa | Protein FAM171A2 | None |
H3BQZ7 | HNRNPUL2-BSCL2 | S655 | ochoa | Heterogeneous nuclear ribonucleoprotein U-like protein 2 | None |
O00471 | EXOC5 | S378 | ochoa | Exocyst complex component 5 (Exocyst complex component Sec10) (hSec10) | Component of the exocyst complex involved in the docking of exocytic vesicles with fusion sites on the plasma membrane. |
O00515 | LAD1 | S38 | ochoa|psp | Ladinin-1 (Lad-1) (Linear IgA disease antigen) (LADA) | Anchoring filament protein which is a component of the basement membrane zone. {ECO:0000250}. |
O14646 | CHD1 | S1096 | ochoa | Chromodomain-helicase-DNA-binding protein 1 (CHD-1) (EC 3.6.4.-) (ATP-dependent helicase CHD1) | ATP-dependent chromatin-remodeling factor which functions as substrate recognition component of the transcription regulatory histone acetylation (HAT) complex SAGA. Regulates polymerase II transcription. Also required for efficient transcription by RNA polymerase I, and more specifically the polymerase I transcription termination step. Regulates negatively DNA replication. Not only involved in transcription-related chromatin-remodeling, but also required to maintain a specific chromatin configuration across the genome. Is also associated with histone deacetylase (HDAC) activity (By similarity). Required for the bridging of SNF2, the FACT complex, the PAF complex as well as the U2 snRNP complex to H3K4me3. Functions to modulate the efficiency of pre-mRNA splicing in part through physical bridging of spliceosomal components to H3K4me3 (PubMed:18042460, PubMed:28866611). Required for maintaining open chromatin and pluripotency in embryonic stem cells (By similarity). {ECO:0000250|UniProtKB:P40201, ECO:0000269|PubMed:18042460, ECO:0000269|PubMed:28866611}. |
O14646 | CHD1 | S1098 | ochoa | Chromodomain-helicase-DNA-binding protein 1 (CHD-1) (EC 3.6.4.-) (ATP-dependent helicase CHD1) | ATP-dependent chromatin-remodeling factor which functions as substrate recognition component of the transcription regulatory histone acetylation (HAT) complex SAGA. Regulates polymerase II transcription. Also required for efficient transcription by RNA polymerase I, and more specifically the polymerase I transcription termination step. Regulates negatively DNA replication. Not only involved in transcription-related chromatin-remodeling, but also required to maintain a specific chromatin configuration across the genome. Is also associated with histone deacetylase (HDAC) activity (By similarity). Required for the bridging of SNF2, the FACT complex, the PAF complex as well as the U2 snRNP complex to H3K4me3. Functions to modulate the efficiency of pre-mRNA splicing in part through physical bridging of spliceosomal components to H3K4me3 (PubMed:18042460, PubMed:28866611). Required for maintaining open chromatin and pluripotency in embryonic stem cells (By similarity). {ECO:0000250|UniProtKB:P40201, ECO:0000269|PubMed:18042460, ECO:0000269|PubMed:28866611}. |
O14646 | CHD1 | S1100 | ochoa | Chromodomain-helicase-DNA-binding protein 1 (CHD-1) (EC 3.6.4.-) (ATP-dependent helicase CHD1) | ATP-dependent chromatin-remodeling factor which functions as substrate recognition component of the transcription regulatory histone acetylation (HAT) complex SAGA. Regulates polymerase II transcription. Also required for efficient transcription by RNA polymerase I, and more specifically the polymerase I transcription termination step. Regulates negatively DNA replication. Not only involved in transcription-related chromatin-remodeling, but also required to maintain a specific chromatin configuration across the genome. Is also associated with histone deacetylase (HDAC) activity (By similarity). Required for the bridging of SNF2, the FACT complex, the PAF complex as well as the U2 snRNP complex to H3K4me3. Functions to modulate the efficiency of pre-mRNA splicing in part through physical bridging of spliceosomal components to H3K4me3 (PubMed:18042460, PubMed:28866611). Required for maintaining open chromatin and pluripotency in embryonic stem cells (By similarity). {ECO:0000250|UniProtKB:P40201, ECO:0000269|PubMed:18042460, ECO:0000269|PubMed:28866611}. |
O15085 | ARHGEF11 | S633 | ochoa | Rho guanine nucleotide exchange factor 11 (PDZ-RhoGEF) | May play a role in the regulation of RhoA GTPase by guanine nucleotide-binding alpha-12 (GNA12) and alpha-13 (GNA13). Acts as guanine nucleotide exchange factor (GEF) for RhoA GTPase and may act as GTPase-activating protein (GAP) for GNA12 and GNA13. Involved in neurotrophin-induced neurite outgrowth. {ECO:0000269|PubMed:21670212}. |
O15234 | CASC3 | Y263 | ochoa | Protein CASC3 (Cancer susceptibility candidate gene 3 protein) (Metastatic lymph node gene 51 protein) (MLN 51) (Protein barentsz) (Btz) | Required for pre-mRNA splicing as component of the spliceosome (PubMed:28502770, PubMed:29301961). Core component of the splicing-dependent multiprotein exon junction complex (EJC) deposited at splice junctions on mRNAs. The EJC is a dynamic structure consisting of core proteins and several peripheral nuclear and cytoplasmic associated factors that join the complex only transiently either during EJC assembly or during subsequent mRNA metabolism. The EJC marks the position of the exon-exon junction in the mature mRNA for the gene expression machinery and the core components remain bound to spliced mRNAs throughout all stages of mRNA metabolism thereby influencing downstream processes including nuclear mRNA export, subcellular mRNA localization, translation efficiency and nonsense-mediated mRNA decay (NMD). Stimulates the ATPase and RNA-helicase activities of EIF4A3. Plays a role in the stress response by participating in cytoplasmic stress granules assembly and by favoring cell recovery following stress. Component of the dendritic ribonucleoprotein particles (RNPs) in hippocampal neurons. May play a role in mRNA transport. Binds spliced mRNA in sequence-independent manner, 20-24 nucleotides upstream of mRNA exon-exon junctions. Binds poly(G) and poly(U) RNA homomer. {ECO:0000269|PubMed:17375189, ECO:0000269|PubMed:17652158, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961}. |
O43166 | SIPA1L1 | S174 | ochoa | Signal-induced proliferation-associated 1-like protein 1 (SIPA1-like protein 1) (High-risk human papilloma viruses E6 oncoproteins targeted protein 1) (E6-targeted protein 1) | Stimulates the GTPase activity of RAP2A. Promotes reorganization of the actin cytoskeleton and recruits DLG4 to F-actin. Contributes to the regulation of dendritic spine morphogenesis (By similarity). {ECO:0000250}. |
O60307 | MAST3 | S153 | ochoa | Microtubule-associated serine/threonine-protein kinase 3 (EC 2.7.11.1) | None |
O60307 | MAST3 | S155 | ochoa | Microtubule-associated serine/threonine-protein kinase 3 (EC 2.7.11.1) | None |
O60825 | PFKFB2 | S471 | ochoa | 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 2 (6PF-2-K/Fru-2,6-P2ase 2) (PFK/FBPase 2) (6PF-2-K/Fru-2,6-P2ase heart-type isozyme) [Includes: 6-phosphofructo-2-kinase (EC 2.7.1.105); Fructose-2,6-bisphosphatase (EC 3.1.3.46)] | Synthesis and degradation of fructose 2,6-bisphosphate. {ECO:0000269|PubMed:11069105}. |
O75420 | GIGYF1 | S155 | ochoa | GRB10-interacting GYF protein 1 (PERQ amino acid-rich with GYF domain-containing protein 1) | May act cooperatively with GRB10 to regulate tyrosine kinase receptor signaling. May increase IGF1 receptor phosphorylation under IGF1 stimulation as well as phosphorylation of IRS1 and SHC1 (By similarity). {ECO:0000250, ECO:0000269|PubMed:12771153}. |
O75494 | SRSF10 | S106 | ochoa | Serine/arginine-rich splicing factor 10 (40 kDa SR-repressor protein) (SRrp40) (FUS-interacting serine-arginine-rich protein 1) (Splicing factor SRp38) (Splicing factor, arginine/serine-rich 13A) (TLS-associated protein with Ser-Arg repeats) (TASR) (TLS-associated protein with SR repeats) (TLS-associated serine-arginine protein) (TLS-associated SR protein) | Splicing factor that in its dephosphorylated form acts as a general repressor of pre-mRNA splicing (PubMed:11684676, PubMed:12419250, PubMed:14765198). Seems to interfere with the U1 snRNP 5'-splice recognition of SNRNP70 (PubMed:14765198). Required for splicing repression in M-phase cells and after heat shock (PubMed:14765198). Also acts as a splicing factor that specifically promotes exon skipping during alternative splicing (PubMed:26876937). Interaction with YTHDC1, a RNA-binding protein that recognizes and binds N6-methyladenosine (m6A)-containing RNAs, prevents SRSF10 from binding to its mRNA-binding sites close to m6A-containing regions, leading to inhibit exon skipping during alternative splicing (PubMed:26876937). May be involved in regulation of alternative splicing in neurons, with isoform 1 acting as a positive and isoform 3 as a negative regulator (PubMed:12419250). {ECO:0000269|PubMed:11684676, ECO:0000269|PubMed:12419250, ECO:0000269|PubMed:14765198, ECO:0000269|PubMed:26876937}. |
O75494 | SRSF10 | S108 | ochoa | Serine/arginine-rich splicing factor 10 (40 kDa SR-repressor protein) (SRrp40) (FUS-interacting serine-arginine-rich protein 1) (Splicing factor SRp38) (Splicing factor, arginine/serine-rich 13A) (TLS-associated protein with Ser-Arg repeats) (TASR) (TLS-associated protein with SR repeats) (TLS-associated serine-arginine protein) (TLS-associated SR protein) | Splicing factor that in its dephosphorylated form acts as a general repressor of pre-mRNA splicing (PubMed:11684676, PubMed:12419250, PubMed:14765198). Seems to interfere with the U1 snRNP 5'-splice recognition of SNRNP70 (PubMed:14765198). Required for splicing repression in M-phase cells and after heat shock (PubMed:14765198). Also acts as a splicing factor that specifically promotes exon skipping during alternative splicing (PubMed:26876937). Interaction with YTHDC1, a RNA-binding protein that recognizes and binds N6-methyladenosine (m6A)-containing RNAs, prevents SRSF10 from binding to its mRNA-binding sites close to m6A-containing regions, leading to inhibit exon skipping during alternative splicing (PubMed:26876937). May be involved in regulation of alternative splicing in neurons, with isoform 1 acting as a positive and isoform 3 as a negative regulator (PubMed:12419250). {ECO:0000269|PubMed:11684676, ECO:0000269|PubMed:12419250, ECO:0000269|PubMed:14765198, ECO:0000269|PubMed:26876937}. |
O75494 | SRSF10 | S156 | ochoa | Serine/arginine-rich splicing factor 10 (40 kDa SR-repressor protein) (SRrp40) (FUS-interacting serine-arginine-rich protein 1) (Splicing factor SRp38) (Splicing factor, arginine/serine-rich 13A) (TLS-associated protein with Ser-Arg repeats) (TASR) (TLS-associated protein with SR repeats) (TLS-associated serine-arginine protein) (TLS-associated SR protein) | Splicing factor that in its dephosphorylated form acts as a general repressor of pre-mRNA splicing (PubMed:11684676, PubMed:12419250, PubMed:14765198). Seems to interfere with the U1 snRNP 5'-splice recognition of SNRNP70 (PubMed:14765198). Required for splicing repression in M-phase cells and after heat shock (PubMed:14765198). Also acts as a splicing factor that specifically promotes exon skipping during alternative splicing (PubMed:26876937). Interaction with YTHDC1, a RNA-binding protein that recognizes and binds N6-methyladenosine (m6A)-containing RNAs, prevents SRSF10 from binding to its mRNA-binding sites close to m6A-containing regions, leading to inhibit exon skipping during alternative splicing (PubMed:26876937). May be involved in regulation of alternative splicing in neurons, with isoform 1 acting as a positive and isoform 3 as a negative regulator (PubMed:12419250). {ECO:0000269|PubMed:11684676, ECO:0000269|PubMed:12419250, ECO:0000269|PubMed:14765198, ECO:0000269|PubMed:26876937}. |
O75494 | SRSF10 | S158 | ochoa | Serine/arginine-rich splicing factor 10 (40 kDa SR-repressor protein) (SRrp40) (FUS-interacting serine-arginine-rich protein 1) (Splicing factor SRp38) (Splicing factor, arginine/serine-rich 13A) (TLS-associated protein with Ser-Arg repeats) (TASR) (TLS-associated protein with SR repeats) (TLS-associated serine-arginine protein) (TLS-associated SR protein) | Splicing factor that in its dephosphorylated form acts as a general repressor of pre-mRNA splicing (PubMed:11684676, PubMed:12419250, PubMed:14765198). Seems to interfere with the U1 snRNP 5'-splice recognition of SNRNP70 (PubMed:14765198). Required for splicing repression in M-phase cells and after heat shock (PubMed:14765198). Also acts as a splicing factor that specifically promotes exon skipping during alternative splicing (PubMed:26876937). Interaction with YTHDC1, a RNA-binding protein that recognizes and binds N6-methyladenosine (m6A)-containing RNAs, prevents SRSF10 from binding to its mRNA-binding sites close to m6A-containing regions, leading to inhibit exon skipping during alternative splicing (PubMed:26876937). May be involved in regulation of alternative splicing in neurons, with isoform 1 acting as a positive and isoform 3 as a negative regulator (PubMed:12419250). {ECO:0000269|PubMed:11684676, ECO:0000269|PubMed:12419250, ECO:0000269|PubMed:14765198, ECO:0000269|PubMed:26876937}. |
O75494 | SRSF10 | S160 | ochoa | Serine/arginine-rich splicing factor 10 (40 kDa SR-repressor protein) (SRrp40) (FUS-interacting serine-arginine-rich protein 1) (Splicing factor SRp38) (Splicing factor, arginine/serine-rich 13A) (TLS-associated protein with Ser-Arg repeats) (TASR) (TLS-associated protein with SR repeats) (TLS-associated serine-arginine protein) (TLS-associated SR protein) | Splicing factor that in its dephosphorylated form acts as a general repressor of pre-mRNA splicing (PubMed:11684676, PubMed:12419250, PubMed:14765198). Seems to interfere with the U1 snRNP 5'-splice recognition of SNRNP70 (PubMed:14765198). Required for splicing repression in M-phase cells and after heat shock (PubMed:14765198). Also acts as a splicing factor that specifically promotes exon skipping during alternative splicing (PubMed:26876937). Interaction with YTHDC1, a RNA-binding protein that recognizes and binds N6-methyladenosine (m6A)-containing RNAs, prevents SRSF10 from binding to its mRNA-binding sites close to m6A-containing regions, leading to inhibit exon skipping during alternative splicing (PubMed:26876937). May be involved in regulation of alternative splicing in neurons, with isoform 1 acting as a positive and isoform 3 as a negative regulator (PubMed:12419250). {ECO:0000269|PubMed:11684676, ECO:0000269|PubMed:12419250, ECO:0000269|PubMed:14765198, ECO:0000269|PubMed:26876937}. |
O94875 | SORBS2 | S841 | ochoa | Sorbin and SH3 domain-containing protein 2 (Arg-binding protein 2) (ArgBP2) (Arg/Abl-interacting protein 2) (Sorbin) | Adapter protein that plays a role in the assembling of signaling complexes, being a link between ABL kinases and actin cytoskeleton. Can form complex with ABL1 and CBL, thus promoting ubiquitination and degradation of ABL1. May play a role in the regulation of pancreatic cell adhesion, possibly by acting on WASF1 phosphorylation, enhancing phosphorylation by ABL1, as well as dephosphorylation by PTPN12 (PubMed:18559503). Isoform 6 increases water and sodium absorption in the intestine and gall-bladder. {ECO:0000269|PubMed:12475393, ECO:0000269|PubMed:18559503, ECO:0000269|PubMed:9211900}. |
O94880 | PHF14 | S835 | ochoa | PHD finger protein 14 | Histone-binding protein (PubMed:23688586). Binds preferentially to unmodified histone H3 but can also bind to a lesser extent to histone H3 trimethylated at 'Lys-9' (H3K9me3) as well as to histone H3 monomethylated at 'Lys-27' (H3K27ac) and trimethylated at 'Lys-27' (H3K27me3) (By similarity). Represses PDGFRA expression, thus playing a role in regulation of mesenchymal cell proliferation (By similarity). Suppresses the expression of CDKN1A/p21 by reducing the level of trimethylation of histone H3 'Lys-4', leading to enhanced proliferation of germinal center B cells (By similarity). {ECO:0000250|UniProtKB:A0A286Y9D1, ECO:0000250|UniProtKB:Q9D4H9, ECO:0000269|PubMed:23688586}. |
O94913 | PCF11 | S487 | ochoa | Pre-mRNA cleavage complex 2 protein Pcf11 (Pre-mRNA cleavage complex II protein Pcf11) | Component of pre-mRNA cleavage complex II, which promotes transcription termination by RNA polymerase II. {ECO:0000269|PubMed:11060040, ECO:0000269|PubMed:29196535}. |
O94913 | PCF11 | S489 | ochoa | Pre-mRNA cleavage complex 2 protein Pcf11 (Pre-mRNA cleavage complex II protein Pcf11) | Component of pre-mRNA cleavage complex II, which promotes transcription termination by RNA polymerase II. {ECO:0000269|PubMed:11060040, ECO:0000269|PubMed:29196535}. |
P08621 | SNRNP70 | S217 | ochoa | U1 small nuclear ribonucleoprotein 70 kDa (U1 snRNP 70 kDa) (U1-70K) (snRNP70) | Component of the spliceosomal U1 snRNP, which is essential for recognition of the pre-mRNA 5' splice-site and the subsequent assembly of the spliceosome (PubMed:19325628, PubMed:25555158). SNRNP70 binds to the loop I region of U1-snRNA (PubMed:19325628, PubMed:2467746, PubMed:25555158). {ECO:0000269|PubMed:19325628, ECO:0000269|PubMed:2467746, ECO:0000269|PubMed:25555158}.; FUNCTION: [Isoform 3]: Truncated isoforms that lack the RRM domain cannot bind U1-snRNA. {ECO:0000269|PubMed:2467746}.; FUNCTION: [Isoform 4]: Truncated isoforms that lack the RRM domain cannot bind U1-snRNA. {ECO:0000269|PubMed:2467746}. |
P08621 | SNRNP70 | Y219 | ochoa | U1 small nuclear ribonucleoprotein 70 kDa (U1 snRNP 70 kDa) (U1-70K) (snRNP70) | Component of the spliceosomal U1 snRNP, which is essential for recognition of the pre-mRNA 5' splice-site and the subsequent assembly of the spliceosome (PubMed:19325628, PubMed:25555158). SNRNP70 binds to the loop I region of U1-snRNA (PubMed:19325628, PubMed:2467746, PubMed:25555158). {ECO:0000269|PubMed:19325628, ECO:0000269|PubMed:2467746, ECO:0000269|PubMed:25555158}.; FUNCTION: [Isoform 3]: Truncated isoforms that lack the RRM domain cannot bind U1-snRNA. {ECO:0000269|PubMed:2467746}.; FUNCTION: [Isoform 4]: Truncated isoforms that lack the RRM domain cannot bind U1-snRNA. {ECO:0000269|PubMed:2467746}. |
P09629 | HOXB7 | S132 | psp | Homeobox protein Hox-B7 (Homeobox protein HHO.C1) (Homeobox protein Hox-2C) | Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. |
P14416 | DRD2 | S228 | psp | D(2) dopamine receptor (Dopamine D2 receptor) | Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase (PubMed:21645528). Positively regulates postnatal regression of retinal hyaloid vessels via suppression of VEGFR2/KDR activity, downstream of OPN5 (By similarity). {ECO:0000250|UniProtKB:P61168, ECO:0000269|PubMed:21645528}. |
P18583 | SON | S2029 | ochoa | Protein SON (Bax antagonist selected in saccharomyces 1) (BASS1) (Negative regulatory element-binding protein) (NRE-binding protein) (Protein DBP-5) (SON3) | RNA-binding protein that acts as a mRNA splicing cofactor by promoting efficient splicing of transcripts that possess weak splice sites. Specifically promotes splicing of many cell-cycle and DNA-repair transcripts that possess weak splice sites, such as TUBG1, KATNB1, TUBGCP2, AURKB, PCNT, AKT1, RAD23A, and FANCG. Probably acts by facilitating the interaction between Serine/arginine-rich proteins such as SRSF2 and the RNA polymerase II. Also binds to DNA; binds to the consensus DNA sequence: 5'-GA[GT]AN[CG][AG]CC-3'. May indirectly repress hepatitis B virus (HBV) core promoter activity and transcription of HBV genes and production of HBV virions. Essential for correct RNA splicing of multiple genes critical for brain development, neuronal migration and metabolism, including TUBG1, FLNA, PNKP, WDR62, PSMD3, PCK2, PFKL, IDH2, and ACY1 (PubMed:27545680). {ECO:0000269|PubMed:20581448, ECO:0000269|PubMed:21504830, ECO:0000269|PubMed:27545680}. |
P18583 | SON | S2031 | ochoa | Protein SON (Bax antagonist selected in saccharomyces 1) (BASS1) (Negative regulatory element-binding protein) (NRE-binding protein) (Protein DBP-5) (SON3) | RNA-binding protein that acts as a mRNA splicing cofactor by promoting efficient splicing of transcripts that possess weak splice sites. Specifically promotes splicing of many cell-cycle and DNA-repair transcripts that possess weak splice sites, such as TUBG1, KATNB1, TUBGCP2, AURKB, PCNT, AKT1, RAD23A, and FANCG. Probably acts by facilitating the interaction between Serine/arginine-rich proteins such as SRSF2 and the RNA polymerase II. Also binds to DNA; binds to the consensus DNA sequence: 5'-GA[GT]AN[CG][AG]CC-3'. May indirectly repress hepatitis B virus (HBV) core promoter activity and transcription of HBV genes and production of HBV virions. Essential for correct RNA splicing of multiple genes critical for brain development, neuronal migration and metabolism, including TUBG1, FLNA, PNKP, WDR62, PSMD3, PCK2, PFKL, IDH2, and ACY1 (PubMed:27545680). {ECO:0000269|PubMed:20581448, ECO:0000269|PubMed:21504830, ECO:0000269|PubMed:27545680}. |
P18615 | NELFE | S113 | ochoa | Negative elongation factor E (NELF-E) (RNA-binding protein RD) | Essential component of the NELF complex, a complex that negatively regulates the elongation of transcription by RNA polymerase II (PubMed:10199401, PubMed:27256882). The NELF complex, which acts via an association with the DSIF complex and causes transcriptional pausing, is counteracted by the P-TEFb kinase complex (PubMed:11940650, PubMed:12612062, PubMed:27256882). Provides the strongest RNA binding activity of the NELF complex and may initially recruit the NELF complex to RNA (PubMed:18303858, PubMed:27256882, PubMed:27282391). {ECO:0000269|PubMed:10199401, ECO:0000269|PubMed:11940650, ECO:0000269|PubMed:12612062, ECO:0000269|PubMed:18303858, ECO:0000269|PubMed:27256882, ECO:0000269|PubMed:27282391}.; FUNCTION: (Microbial infection) The NELF complex is involved in HIV-1 latency possibly involving recruitment of PCF11 to paused RNA polymerase II. {ECO:0000269|PubMed:23884411}. |
P18825 | ADRA2C | S352 | ochoa | Alpha-2C adrenergic receptor (Alpha-2 adrenergic receptor subtype C4) (Alpha-2C adrenoreceptor) (Alpha-2C adrenoceptor) (Alpha-2CAR) | Alpha-2 adrenergic receptors mediate the catecholamine-induced inhibition of adenylate cyclase through the action of G proteins. |
P21127 | CDK11B | S113 | ochoa | Cyclin-dependent kinase 11B (EC 2.7.11.22) (Cell division cycle 2-like protein kinase 1) (CLK-1) (Cell division protein kinase 11B) (Galactosyltransferase-associated protein kinase p58/GTA) (PITSLRE serine/threonine-protein kinase CDC2L1) (p58 CLK-1) | Plays multiple roles in cell cycle progression, cytokinesis and apoptosis. Involved in pre-mRNA splicing in a kinase activity-dependent manner. Isoform 7 may act as a negative regulator of normal cell cycle progression. {ECO:0000269|PubMed:12501247, ECO:0000269|PubMed:12624090, ECO:0000269|PubMed:18216018, ECO:0000269|PubMed:2217177}. |
P23588 | EIF4B | S71 | ochoa | Eukaryotic translation initiation factor 4B (eIF-4B) | Required for the binding of mRNA to ribosomes. Functions in close association with EIF4-F and EIF4-A. Binds near the 5'-terminal cap of mRNA in presence of EIF-4F and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both EIF4-A and EIF4-F. |
P23588 | EIF4B | S263 | ochoa | Eukaryotic translation initiation factor 4B (eIF-4B) | Required for the binding of mRNA to ribosomes. Functions in close association with EIF4-F and EIF4-A. Binds near the 5'-terminal cap of mRNA in presence of EIF-4F and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both EIF4-A and EIF4-F. |
P23588 | EIF4B | S309 | ochoa | Eukaryotic translation initiation factor 4B (eIF-4B) | Required for the binding of mRNA to ribosomes. Functions in close association with EIF4-F and EIF4-A. Binds near the 5'-terminal cap of mRNA in presence of EIF-4F and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both EIF4-A and EIF4-F. |
P23588 | EIF4B | S312 | ochoa | Eukaryotic translation initiation factor 4B (eIF-4B) | Required for the binding of mRNA to ribosomes. Functions in close association with EIF4-F and EIF4-A. Binds near the 5'-terminal cap of mRNA in presence of EIF-4F and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both EIF4-A and EIF4-F. |
P25054 | APC | S2531 | ochoa | Adenomatous polyposis coli protein (Protein APC) (Deleted in polyposis 2.5) | Tumor suppressor. Promotes rapid degradation of CTNNB1 and participates in Wnt signaling as a negative regulator. APC activity is correlated with its phosphorylation state. Activates the GEF activity of SPATA13 and ARHGEF4. Plays a role in hepatocyte growth factor (HGF)-induced cell migration. Required for MMP9 up-regulation via the JNK signaling pathway in colorectal tumor cells. Associates with both microtubules and actin filaments, components of the cytoskeleton (PubMed:17293347). Plays a role in mediating the organization of F-actin into ordered bundles (PubMed:17293347). Functions downstream of Rho GTPases and DIAPH1 to selectively stabilize microtubules (By similarity). Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. It is required for the localization of MACF1 to the cell membrane and this localization of MACF1 is critical for its function in microtubule stabilization. {ECO:0000250|UniProtKB:Q61315, ECO:0000269|PubMed:10947987, ECO:0000269|PubMed:17293347, ECO:0000269|PubMed:17599059, ECO:0000269|PubMed:19151759, ECO:0000269|PubMed:19893577, ECO:0000269|PubMed:20937854}. |
P25054 | APC | S2533 | ochoa | Adenomatous polyposis coli protein (Protein APC) (Deleted in polyposis 2.5) | Tumor suppressor. Promotes rapid degradation of CTNNB1 and participates in Wnt signaling as a negative regulator. APC activity is correlated with its phosphorylation state. Activates the GEF activity of SPATA13 and ARHGEF4. Plays a role in hepatocyte growth factor (HGF)-induced cell migration. Required for MMP9 up-regulation via the JNK signaling pathway in colorectal tumor cells. Associates with both microtubules and actin filaments, components of the cytoskeleton (PubMed:17293347). Plays a role in mediating the organization of F-actin into ordered bundles (PubMed:17293347). Functions downstream of Rho GTPases and DIAPH1 to selectively stabilize microtubules (By similarity). Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. It is required for the localization of MACF1 to the cell membrane and this localization of MACF1 is critical for its function in microtubule stabilization. {ECO:0000250|UniProtKB:Q61315, ECO:0000269|PubMed:10947987, ECO:0000269|PubMed:17293347, ECO:0000269|PubMed:17599059, ECO:0000269|PubMed:19151759, ECO:0000269|PubMed:19893577, ECO:0000269|PubMed:20937854}. |
P30414 | NKTR | S406 | ochoa | NK-tumor recognition protein (NK-TR protein) (Natural-killer cells cyclophilin-related protein) (Peptidyl-prolyl cis-trans isomerase NKTR) (PPIase) (EC 5.2.1.8) (Rotamase) | PPIase that catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and may therefore assist protein folding (PubMed:20676357). Component of a putative tumor-recognition complex involved in the function of NK cells (PubMed:8421688). {ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:8421688}. |
P36915 | GNL1 | S32 | ochoa | Guanine nucleotide-binding protein-like 1 (GTP-binding protein HSR1) | Possible regulatory or functional link with the histocompatibility cluster. |
P38159 | RBMX | S249 | ochoa | RNA-binding motif protein, X chromosome (Glycoprotein p43) (Heterogeneous nuclear ribonucleoprotein G) (hnRNP G) [Cleaved into: RNA-binding motif protein, X chromosome, N-terminally processed] | RNA-binding protein that plays several role in the regulation of pre- and post-transcriptional processes. Implicated in tissue-specific regulation of gene transcription and alternative splicing of several pre-mRNAs. Binds to and stimulates transcription from the tumor suppressor TXNIP gene promoter; may thus be involved in tumor suppression. When associated with SAFB, binds to and stimulates transcription from the SREBF1 promoter. Associates with nascent mRNAs transcribed by RNA polymerase II. Component of the supraspliceosome complex that regulates pre-mRNA alternative splice site selection. Can either activate or suppress exon inclusion; acts additively with TRA2B to promote exon 7 inclusion of the survival motor neuron SMN2. Represses the splicing of MAPT/Tau exon 10. Binds preferentially to single-stranded 5'-CC[A/C]-rich RNA sequence motifs localized in a single-stranded conformation; probably binds RNA as a homodimer. Binds non-specifically to pre-mRNAs. Also plays a role in the cytoplasmic TNFR1 trafficking pathways; promotes both the IL-1-beta-mediated inducible proteolytic cleavage of TNFR1 ectodomains and the release of TNFR1 exosome-like vesicles to the extracellular compartment. {ECO:0000269|PubMed:12165565, ECO:0000269|PubMed:12761049, ECO:0000269|PubMed:16707624, ECO:0000269|PubMed:18445477, ECO:0000269|PubMed:18541147, ECO:0000269|PubMed:19282290, ECO:0000269|PubMed:21327109}. |
P40818 | USP8 | S716 | ochoa | Ubiquitin carboxyl-terminal hydrolase 8 (EC 3.4.19.12) (Deubiquitinating enzyme 8) (Ubiquitin isopeptidase Y) (hUBPy) (Ubiquitin thioesterase 8) (Ubiquitin-specific-processing protease 8) | Hydrolase that can remove conjugated ubiquitin from proteins and therefore plays an important regulatory role at the level of protein turnover by preventing degradation. Converts both 'Lys-48' an 'Lys-63'-linked ubiquitin chains. Catalytic activity is enhanced in the M phase. Involved in cell proliferation. Required to enter into S phase in response to serum stimulation. May regulate T-cell anergy mediated by RNF128 via the formation of a complex containing RNF128 and OTUB1. Probably regulates the stability of STAM2 and RASGRF1. Regulates endosomal ubiquitin dynamics, cargo sorting, membrane traffic at early endosomes, and maintenance of ESCRT-0 stability. The level of protein ubiquitination on endosomes is essential for maintaining the morphology of the organelle. Deubiquitinates EPS15 and controls tyrosine kinase stability. Removes conjugated ubiquitin from EGFR thus regulating EGFR degradation and downstream MAPK signaling. Involved in acrosome biogenesis through interaction with the spermatid ESCRT-0 complex and microtubules. Deubiquitinates BIRC6/bruce and KIF23/MKLP1. Deubiquitinates BACE1 which inhibits BACE1 lysosomal degradation and modulates BACE-mediated APP cleavage and amyloid-beta formation (PubMed:27302062). {ECO:0000269|PubMed:16520378, ECO:0000269|PubMed:17711858, ECO:0000269|PubMed:18329369, ECO:0000269|PubMed:27302062, ECO:0000269|PubMed:9628861}. |
P41587 | VIPR2 | S409 | ochoa | Vasoactive intestinal polypeptide receptor 2 (VIP-R-2) (Helodermin-preferring VIP receptor) (Pituitary adenylate cyclase-activating polypeptide type III receptor) (PACAP type III receptor) (PACAP-R-3) (PACAP-R3) (VPAC2 receptor) (VPAC2R) | G protein-coupled receptor activated by the neuropeptides vasoactive intestinal peptide (VIP) and pituitary adenylate cyclase-activating polypeptide (ADCYAP1/PACAP) (PubMed:7811244, PubMed:35477937, PubMed:8933357). Binds VIP and both PACAP27 and PACAP38 bioactive peptides with the following order of potency PACAP38 = VIP > PACAP27 (PubMed:35477937, PubMed:8933357). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of downstream effectors. Activates cAMP-dependent pathway (PubMed:7811244, PubMed:35477937, PubMed:8933357). May be coupled to phospholipase C. {ECO:0000269|PubMed:35477937, ECO:0000269|PubMed:7811244, ECO:0000269|PubMed:8933357}. |
P48634 | PRRC2A | S456 | ochoa | Protein PRRC2A (HLA-B-associated transcript 2) (Large proline-rich protein BAT2) (Proline-rich and coiled-coil-containing protein 2A) (Protein G2) | May play a role in the regulation of pre-mRNA splicing. {ECO:0000269|PubMed:14667819}. |
P48634 | PRRC2A | S1384 | ochoa | Protein PRRC2A (HLA-B-associated transcript 2) (Large proline-rich protein BAT2) (Proline-rich and coiled-coil-containing protein 2A) (Protein G2) | May play a role in the regulation of pre-mRNA splicing. {ECO:0000269|PubMed:14667819}. |
P49815 | TSC2 | S937 | ochoa | Tuberin (Tuberous sclerosis 2 protein) | Catalytic component of the TSC-TBC complex, a multiprotein complex that acts as a negative regulator of the canonical mTORC1 complex, an evolutionarily conserved central nutrient sensor that stimulates anabolic reactions and macromolecule biosynthesis to promote cellular biomass generation and growth (PubMed:12172553, PubMed:12271141, PubMed:12842888, PubMed:12906785, PubMed:15340059, PubMed:22819219, PubMed:24529379, PubMed:28215400, PubMed:33436626, PubMed:35772404). Within the TSC-TBC complex, TSC2 acts as a GTPase-activating protein (GAP) for the small GTPase RHEB, a direct activator of the protein kinase activity of mTORC1 (PubMed:12172553, PubMed:12820960, PubMed:12842888, PubMed:12906785, PubMed:15340059, PubMed:22819219, PubMed:24529379, PubMed:33436626). In absence of nutrients, the TSC-TBC complex inhibits mTORC1, thereby preventing phosphorylation of ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1) by the mTORC1 signaling (PubMed:12172553, PubMed:12271141, PubMed:12842888, PubMed:12906785, PubMed:22819219, PubMed:24529379, PubMed:28215400, PubMed:35772404). The TSC-TBC complex is inactivated in response to nutrients, relieving inhibition of mTORC1 (PubMed:12172553, PubMed:24529379). Involved in microtubule-mediated protein transport via its ability to regulate mTORC1 signaling (By similarity). Also stimulates the intrinsic GTPase activity of the Ras-related proteins RAP1A and RAB5 (By similarity). {ECO:0000250|UniProtKB:P49816, ECO:0000269|PubMed:12172553, ECO:0000269|PubMed:12271141, ECO:0000269|PubMed:12820960, ECO:0000269|PubMed:12842888, ECO:0000269|PubMed:12906785, ECO:0000269|PubMed:15340059, ECO:0000269|PubMed:22819219, ECO:0000269|PubMed:24529379, ECO:0000269|PubMed:28215400, ECO:0000269|PubMed:33436626, ECO:0000269|PubMed:35772404}. |
P51114 | FXR1 | S494 | ochoa | RNA-binding protein FXR1 (FMR1 autosomal homolog 1) (hFXR1p) | mRNA-binding protein that acts as a regulator of mRNAs translation and/or stability, and which is required for various processes, such as neurogenesis, muscle development and spermatogenesis (PubMed:17382880, PubMed:20417602, PubMed:30067974, PubMed:34731628, PubMed:35989368, PubMed:36306353). Specifically binds to AU-rich elements (AREs) in the 3'-UTR of target mRNAs (PubMed:17382880, PubMed:34731628). Promotes formation of some phase-separated membraneless compartment by undergoing liquid-liquid phase separation upon binding to AREs-containing mRNAs, leading to assemble mRNAs into cytoplasmic ribonucleoprotein granules that concentrate mRNAs with associated regulatory factors (By similarity). Required to activate translation of stored mRNAs during late spermatogenesis: acts by undergoing liquid-liquid phase separation to assemble target mRNAs into cytoplasmic ribonucleoprotein granules that recruit translation initiation factor EIF4G3 to activate translation of stored mRNAs in late spermatids (By similarity). Promotes translation of MYC transcripts by recruiting the eIF4F complex to the translation start site (PubMed:34731628). Acts as a negative regulator of inflammation in response to IL19 by promoting destabilization of pro-inflammatory transcripts (PubMed:30067974). Also acts as an inhibitor of inflammation by binding to TNF mRNA, decreasing TNF protein production (By similarity). Acts as a negative regulator of AMPA receptor GRIA2/GluA2 synthesis during long-lasting synaptic potentiation of hippocampal neurons by binding to GRIA2/GluA2 mRNA, thereby inhibiting its translation (By similarity). Regulates proliferation of adult neural stem cells by binding to CDKN1A mRNA and promoting its expression (By similarity). Acts as a regulator of sleep and synaptic homeostasis by regulating translation of transcripts in neurons (By similarity). Required for embryonic and postnatal development of muscle tissue by undergoing liquid-liquid phase separation to assemble target mRNAs into cytoplasmic ribonucleoprotein granules (PubMed:30770808). Involved in the nuclear pore complex localization to the nuclear envelope by preventing cytoplasmic aggregation of nucleoporins: acts by preventing ectopic phase separation of nucleoporins in the cytoplasm via a microtubule-dependent mechanism (PubMed:32706158). Plays a role in the stabilization of PKP2 mRNA and therefore protein abundance, via its interaction with PKP3 (PubMed:25225333). May also do the same for PKP2, PKP3 and DSP via its interaction with PKP1 (PubMed:25225333). Forms a cytoplasmic messenger ribonucleoprotein (mRNP) network by packaging long mRNAs, serving as a scaffold that recruits proteins and signaling molecules. This network facilitates signaling reactions by maintaining proximity between kinases and substrates, crucial for processes like actomyosin reorganization (PubMed:39106863). {ECO:0000250|UniProtKB:Q61584, ECO:0000269|PubMed:17382880, ECO:0000269|PubMed:20417602, ECO:0000269|PubMed:25225333, ECO:0000269|PubMed:30067974, ECO:0000269|PubMed:30770808, ECO:0000269|PubMed:32706158, ECO:0000269|PubMed:34731628, ECO:0000269|PubMed:35989368, ECO:0000269|PubMed:36306353, ECO:0000269|PubMed:39106863}. |
P52756 | RBM5 | Y51 | ochoa | RNA-binding protein 5 (Protein G15) (Putative tumor suppressor LUCA15) (RNA-binding motif protein 5) (Renal carcinoma antigen NY-REN-9) | Component of the spliceosome A complex. Binds to ssRNA containing the consensus sequence 5'-AGGUAA-3' (PubMed:21256132). Regulates alternative splicing of a number of mRNAs. May modulate splice site pairing after recruitment of the U1 and U2 snRNPs to the 5' and 3' splice sites of the intron. May both positively and negatively regulate apoptosis by regulating the alternative splicing of several genes involved in this process, including FAS and CASP2/caspase-2. In the case of FAS, promotes exclusion of exon 6 thereby producing a soluble form of FAS that inhibits apoptosis. In the case of CASP2/caspase-2, promotes exclusion of exon 9 thereby producing a catalytically active form of CASP2/Caspase-2 that induces apoptosis. {ECO:0000269|PubMed:10949932, ECO:0000269|PubMed:12207175, ECO:0000269|PubMed:12581154, ECO:0000269|PubMed:15192330, ECO:0000269|PubMed:16585163, ECO:0000269|PubMed:18840686, ECO:0000269|PubMed:18851835, ECO:0000269|PubMed:21256132}. |
P53804 | TTC3 | S376 | ochoa | E3 ubiquitin-protein ligase TTC3 (EC 2.3.2.27) (Protein DCRR1) (RING finger protein 105) (RING-type E3 ubiquitin transferase TTC3) (TPR repeat protein D) (Tetratricopeptide repeat protein 3) (TPR repeat protein 3) | E3 ubiquitin-protein ligase which catalyzes the formation of 'Lys-48'-polyubiquitin chains (PubMed:20059950, PubMed:30696809). Mediates the ubiquitination and subsequent degradation of phosphorylated Akt (AKT1, AKT2 and AKT3) in the nucleus (PubMed:20059950). Acts as a terminal regulator of Akt signaling after activation; its phosphorylation by Akt, which is a prerequisite for ubiquitin ligase activity, suggests the existence of a regulation mechanism required to control Akt levels after activation (PubMed:20059950). Positively regulates TGFB1-induced epithelial-mesenchymal transition and myofibroblast differentiation by mediating the ubiquitination and subsequent degradation of SMURF2 (PubMed:30696809). Regulates neuronal differentiation by regulating actin remodeling and Golgi organization via a signaling cascade involving RHOA, CIT and ROCK (PubMed:17488780, PubMed:24695496). Inhibits cell proliferation (PubMed:30203323). {ECO:0000269|PubMed:17488780, ECO:0000269|PubMed:20059950, ECO:0000269|PubMed:24695496, ECO:0000269|PubMed:30203323, ECO:0000269|PubMed:30696809}. |
P58340 | MLF1 | S32 | ochoa | Myeloid leukemia factor 1 (Myelodysplasia-myeloid leukemia factor 1) | Involved in lineage commitment of primary hemopoietic progenitors by restricting erythroid formation and enhancing myeloid formation. Interferes with erythropoietin-induced erythroid terminal differentiation by preventing cells from exiting the cell cycle through suppression of CDKN1B/p27Kip1 levels. Suppresses COP1 activity via CSN3 which activates p53 and induces cell cycle arrest. Binds DNA and affects the expression of a number of genes so may function as a transcription factor in the nucleus. {ECO:0000269|PubMed:15861129}. |
P83369 | LSM11 | S278 | ochoa | U7 snRNA-associated Sm-like protein LSm11 | Component of the U7 snRNP complex that is involved in the histone 3'-end pre-mRNA processing (PubMed:11574479, PubMed:16914750, PubMed:33230297). Increases U7 snRNA levels but not histone 3'-end pre-mRNA processing activity, when overexpressed (PubMed:11574479, PubMed:16914750). Required for cell cycle progression from G1 to S phases (By similarity). Binds specifically to the Sm-binding site of U7 snRNA (PubMed:11574479, PubMed:16914750). {ECO:0000250|UniProtKB:Q8BUV6, ECO:0000269|PubMed:11574479, ECO:0000269|PubMed:16914750, ECO:0000269|PubMed:33230297}. |
Q02040 | AKAP17A | S638 | ochoa | A-kinase anchor protein 17A (AKAP-17A) (721P) (B-lymphocyte antigen) (Protein XE7) (Protein kinase A-anchoring protein 17A) (PRKA17A) (Splicing factor, arginine/serine-rich 17A) | Splice factor regulating alternative splice site selection for certain mRNA precursors. Mediates regulation of pre-mRNA splicing in a PKA-dependent manner. {ECO:0000269|PubMed:16982639, ECO:0000269|PubMed:19840947}. |
Q02241 | KIF23 | S812 | psp | Kinesin-like protein KIF23 (Kinesin-like protein 5) (Mitotic kinesin-like protein 1) | Component of the centralspindlin complex that serves as a microtubule-dependent and Rho-mediated signaling required for the myosin contractile ring formation during the cell cycle cytokinesis. Essential for cytokinesis in Rho-mediated signaling. Required for the localization of ECT2 to the central spindle. Plus-end-directed motor enzyme that moves antiparallel microtubules in vitro. {ECO:0000269|PubMed:16103226, ECO:0000269|PubMed:16236794, ECO:0000269|PubMed:22522702, ECO:0000269|PubMed:23570799}. |
Q03113 | GNA12 | S40 | ochoa | Guanine nucleotide-binding protein subunit alpha-12 (G alpha-12) (G-protein subunit alpha-12) | Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems (PubMed:12515866, PubMed:15240885, PubMed:15525651, PubMed:16705036, PubMed:16787920, PubMed:17565996, PubMed:22609986, PubMed:23762476, PubMed:27084452). Activates effector molecule RhoA by binding and activating RhoGEFs (ARHGEF12/LARG) (PubMed:12515866, PubMed:15240885, PubMed:16202387). GNA12-dependent Rho signaling subsequently regulates transcription factor AP-1 (activating protein-1) (By similarity). GNA12-dependent Rho signaling also regulates protein phosphatese 2A activation causing dephosphorylation of its target proteins (PubMed:15525651, PubMed:17565996). Promotes tumor cell invasion and metastasis by activating RhoA/ROCK signaling pathway and up-regulating pro-inflammatory cytokine production (PubMed:16705036, PubMed:16787920, PubMed:23762476, PubMed:27084452). Inhibits CDH1-mediated cell adhesion in process independent from Rho activation (PubMed:11976333, PubMed:16787920). Together with NAPA promotes CDH5 localization to plasma membrane (PubMed:15980433). May play a role in the control of cell migration through the TOR signaling cascade (PubMed:22609986). {ECO:0000250|UniProtKB:P27600, ECO:0000269|PubMed:11976333, ECO:0000269|PubMed:12515866, ECO:0000269|PubMed:15240885, ECO:0000269|PubMed:15525651, ECO:0000269|PubMed:15980433, ECO:0000269|PubMed:16705036, ECO:0000269|PubMed:16787920, ECO:0000269|PubMed:17565996, ECO:0000269|PubMed:22609986, ECO:0000269|PubMed:23762476, ECO:0000269|PubMed:27084452}. |
Q04637 | EIF4G1 | S1185 | ochoa|psp | Eukaryotic translation initiation factor 4 gamma 1 (eIF-4-gamma 1) (eIF-4G 1) (eIF-4G1) (p220) | Component of the protein complex eIF4F, which is involved in the recognition of the mRNA cap, ATP-dependent unwinding of 5'-terminal secondary structure and recruitment of mRNA to the ribosome (PubMed:29987188). Exists in two complexes, either with EIF1 or with EIF4E (mutually exclusive) (PubMed:29987188). Together with EIF1, is required for leaky scanning, in particular for avoiding cap-proximal start codon (PubMed:29987188). Together with EIF4E, antagonizes the scanning promoted by EIF1-EIF4G1 and locates the start codon (through a TISU element) without scanning (PubMed:29987188). As a member of the eIF4F complex, required for endoplasmic reticulum stress-induced ATF4 mRNA translation (PubMed:29062139). {ECO:0000269|PubMed:29062139, ECO:0000269|PubMed:29987188}. |
Q08043 | ACTN3 | S319 | ochoa | Alpha-actinin-3 (Alpha-actinin skeletal muscle isoform 3) (F-actin cross-linking protein) | F-actin cross-linking protein which is thought to anchor actin to a variety of intracellular structures. This is a bundling protein. |
Q12873 | CHD3 | S88 | ochoa | Chromodomain-helicase-DNA-binding protein 3 (CHD-3) (EC 3.6.4.-) (ATP-dependent helicase CHD3) (Mi-2 autoantigen 240 kDa protein) (Mi2-alpha) (Zinc finger helicase) (hZFH) | ATP-dependent chromatin-remodeling factor that binds and distorts nucleosomal DNA (PubMed:28977666). Acts as a component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin (PubMed:16428440, PubMed:28977666, PubMed:30397230, PubMed:9804427). Involved in transcriptional repression as part of the NuRD complex (PubMed:27068747). Required for anchoring centrosomal pericentrin in both interphase and mitosis, for spindle organization and centrosome integrity (PubMed:17626165). {ECO:0000269|PubMed:16428440, ECO:0000269|PubMed:17626165, ECO:0000269|PubMed:27068747, ECO:0000269|PubMed:28977666, ECO:0000269|PubMed:30397230, ECO:0000269|PubMed:9804427}. |
Q13243 | SRSF5 | S250 | ochoa | Serine/arginine-rich splicing factor 5 (Delayed-early protein HRS) (Pre-mRNA-splicing factor SRP40) (Splicing factor, arginine/serine-rich 5) | Plays a role in constitutive splicing and can modulate the selection of alternative splice sites. |
Q13415 | ORC1 | S476 | ochoa | Origin recognition complex subunit 1 (Replication control protein 1) | Component of the origin recognition complex (ORC) that binds origins of replication. DNA-binding is ATP-dependent. The DNA sequences that define origins of replication have not been identified yet. ORC is required to assemble the pre-replication complex necessary to initiate DNA replication. |
Q13427 | PPIG | S356 | ochoa | Peptidyl-prolyl cis-trans isomerase G (PPIase G) (Peptidyl-prolyl isomerase G) (EC 5.2.1.8) (CASP10) (Clk-associating RS-cyclophilin) (CARS-Cyp) (CARS-cyclophilin) (SR-cyclophilin) (SR-cyp) (SRcyp) (Cyclophilin G) (Rotamase G) | PPIase that catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and may therefore assist protein folding (PubMed:20676357). May be implicated in the folding, transport, and assembly of proteins. May play an important role in the regulation of pre-mRNA splicing. {ECO:0000269|PubMed:20676357}. |
Q13523 | PRP4K | S292 | ochoa | Serine/threonine-protein kinase PRP4 homolog (EC 2.7.11.1) (PRP4 kinase) (PRP4 pre-mRNA-processing factor 4 homolog) | Serine/threonine kinase involved in spliceosomal assembly as well as mitosis and signaling regulation (PubMed:10799319, PubMed:12077342, PubMed:17513757, PubMed:17998396). Connects chromatin mediated regulation of transcription and pre-mRNA splicing (PubMed:12077342). During spliceosomal assembly, interacts with and phosphorylates PRPF6 and PRPF31, components of the U4/U6-U5 tri-small nuclear ribonucleoprotein (snRNP), to facilitate the formation of the spliceosome B complex. Plays a role in regulating transcription and the spindle assembly checkpoint (SAC) (PubMed:20118938). Associates with U5 snRNP and NCOR1 deacetylase complexes which may allow a coordination of pre-mRNA splicing with chromatin remodeling events involved in transcriptional regulation (PubMed:12077342). Associates and probably phosphorylates SMARCA4 and NCOR1 (PubMed:12077342). Phosphorylates SRSF1 (PubMed:11418604). Associates with kinetochores during mitosis and is necessary for recruitment and maintenance of the checkpoint proteins such as MAD1L1 and MAD12L1 at the kinetochores (PubMed:17998396). Phosphorylates and regulates the activity of the transcription factors such as ELK1 and KLF13 (PubMed:10799319, PubMed:17513757). Phosphorylates nuclear YAP1 and WWTR1/TAZ which induces nuclear exclusion and regulates Hippo signaling pathway, involved in tissue growth control (PubMed:29695716). {ECO:0000269|PubMed:10799319, ECO:0000269|PubMed:11418604, ECO:0000269|PubMed:12077342, ECO:0000269|PubMed:17513757, ECO:0000269|PubMed:17998396, ECO:0000269|PubMed:20118938, ECO:0000269|PubMed:29695716}. |
Q13523 | PRP4K | S294 | ochoa | Serine/threonine-protein kinase PRP4 homolog (EC 2.7.11.1) (PRP4 kinase) (PRP4 pre-mRNA-processing factor 4 homolog) | Serine/threonine kinase involved in spliceosomal assembly as well as mitosis and signaling regulation (PubMed:10799319, PubMed:12077342, PubMed:17513757, PubMed:17998396). Connects chromatin mediated regulation of transcription and pre-mRNA splicing (PubMed:12077342). During spliceosomal assembly, interacts with and phosphorylates PRPF6 and PRPF31, components of the U4/U6-U5 tri-small nuclear ribonucleoprotein (snRNP), to facilitate the formation of the spliceosome B complex. Plays a role in regulating transcription and the spindle assembly checkpoint (SAC) (PubMed:20118938). Associates with U5 snRNP and NCOR1 deacetylase complexes which may allow a coordination of pre-mRNA splicing with chromatin remodeling events involved in transcriptional regulation (PubMed:12077342). Associates and probably phosphorylates SMARCA4 and NCOR1 (PubMed:12077342). Phosphorylates SRSF1 (PubMed:11418604). Associates with kinetochores during mitosis and is necessary for recruitment and maintenance of the checkpoint proteins such as MAD1L1 and MAD12L1 at the kinetochores (PubMed:17998396). Phosphorylates and regulates the activity of the transcription factors such as ELK1 and KLF13 (PubMed:10799319, PubMed:17513757). Phosphorylates nuclear YAP1 and WWTR1/TAZ which induces nuclear exclusion and regulates Hippo signaling pathway, involved in tissue growth control (PubMed:29695716). {ECO:0000269|PubMed:10799319, ECO:0000269|PubMed:11418604, ECO:0000269|PubMed:12077342, ECO:0000269|PubMed:17513757, ECO:0000269|PubMed:17998396, ECO:0000269|PubMed:20118938, ECO:0000269|PubMed:29695716}. |
Q13523 | PRP4K | S368 | ochoa | Serine/threonine-protein kinase PRP4 homolog (EC 2.7.11.1) (PRP4 kinase) (PRP4 pre-mRNA-processing factor 4 homolog) | Serine/threonine kinase involved in spliceosomal assembly as well as mitosis and signaling regulation (PubMed:10799319, PubMed:12077342, PubMed:17513757, PubMed:17998396). Connects chromatin mediated regulation of transcription and pre-mRNA splicing (PubMed:12077342). During spliceosomal assembly, interacts with and phosphorylates PRPF6 and PRPF31, components of the U4/U6-U5 tri-small nuclear ribonucleoprotein (snRNP), to facilitate the formation of the spliceosome B complex. Plays a role in regulating transcription and the spindle assembly checkpoint (SAC) (PubMed:20118938). Associates with U5 snRNP and NCOR1 deacetylase complexes which may allow a coordination of pre-mRNA splicing with chromatin remodeling events involved in transcriptional regulation (PubMed:12077342). Associates and probably phosphorylates SMARCA4 and NCOR1 (PubMed:12077342). Phosphorylates SRSF1 (PubMed:11418604). Associates with kinetochores during mitosis and is necessary for recruitment and maintenance of the checkpoint proteins such as MAD1L1 and MAD12L1 at the kinetochores (PubMed:17998396). Phosphorylates and regulates the activity of the transcription factors such as ELK1 and KLF13 (PubMed:10799319, PubMed:17513757). Phosphorylates nuclear YAP1 and WWTR1/TAZ which induces nuclear exclusion and regulates Hippo signaling pathway, involved in tissue growth control (PubMed:29695716). {ECO:0000269|PubMed:10799319, ECO:0000269|PubMed:11418604, ECO:0000269|PubMed:12077342, ECO:0000269|PubMed:17513757, ECO:0000269|PubMed:17998396, ECO:0000269|PubMed:20118938, ECO:0000269|PubMed:29695716}. |
Q13523 | PRP4K | S381 | ochoa | Serine/threonine-protein kinase PRP4 homolog (EC 2.7.11.1) (PRP4 kinase) (PRP4 pre-mRNA-processing factor 4 homolog) | Serine/threonine kinase involved in spliceosomal assembly as well as mitosis and signaling regulation (PubMed:10799319, PubMed:12077342, PubMed:17513757, PubMed:17998396). Connects chromatin mediated regulation of transcription and pre-mRNA splicing (PubMed:12077342). During spliceosomal assembly, interacts with and phosphorylates PRPF6 and PRPF31, components of the U4/U6-U5 tri-small nuclear ribonucleoprotein (snRNP), to facilitate the formation of the spliceosome B complex. Plays a role in regulating transcription and the spindle assembly checkpoint (SAC) (PubMed:20118938). Associates with U5 snRNP and NCOR1 deacetylase complexes which may allow a coordination of pre-mRNA splicing with chromatin remodeling events involved in transcriptional regulation (PubMed:12077342). Associates and probably phosphorylates SMARCA4 and NCOR1 (PubMed:12077342). Phosphorylates SRSF1 (PubMed:11418604). Associates with kinetochores during mitosis and is necessary for recruitment and maintenance of the checkpoint proteins such as MAD1L1 and MAD12L1 at the kinetochores (PubMed:17998396). Phosphorylates and regulates the activity of the transcription factors such as ELK1 and KLF13 (PubMed:10799319, PubMed:17513757). Phosphorylates nuclear YAP1 and WWTR1/TAZ which induces nuclear exclusion and regulates Hippo signaling pathway, involved in tissue growth control (PubMed:29695716). {ECO:0000269|PubMed:10799319, ECO:0000269|PubMed:11418604, ECO:0000269|PubMed:12077342, ECO:0000269|PubMed:17513757, ECO:0000269|PubMed:17998396, ECO:0000269|PubMed:20118938, ECO:0000269|PubMed:29695716}. |
Q14152 | EIF3A | S1263 | ochoa | Eukaryotic translation initiation factor 3 subunit A (eIF3a) (Eukaryotic translation initiation factor 3 subunit 10) (eIF-3-theta) (eIF3 p167) (eIF3 p180) (eIF3 p185) | RNA-binding 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). 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:11169732, 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, PubMed:27462815). {ECO:0000255|HAMAP-Rule:MF_03000, ECO:0000269|PubMed:11169732, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815}.; FUNCTION: (Microbial infection) Essential for the initiation of translation on type-1 viral ribosomal entry sites (IRESs), like for HCV, PV, EV71 or BEV translation (PubMed:23766293, PubMed:24357634). {ECO:0000269|PubMed:23766293, ECO:0000269|PubMed:24357634}.; 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}. |
Q14153 | FAM53B | S266 | ochoa | Protein FAM53B (Protein simplet) | Acts as a regulator of Wnt signaling pathway by regulating beta-catenin (CTNNB1) nuclear localization. {ECO:0000269|PubMed:25183871}. |
Q14315 | FLNC | S2181 | ochoa | Filamin-C (FLN-C) (FLNc) (ABP-280-like protein) (ABP-L) (Actin-binding-like protein) (Filamin-2) (Gamma-filamin) | Muscle-specific filamin, which plays a central role in sarcomere assembly and organization (PubMed:34405687). Critical for normal myogenesis, it probably functions as a large actin-cross-linking protein with structural functions at the Z lines in muscle cells. May be involved in reorganizing the actin cytoskeleton in response to signaling events (By similarity). {ECO:0000250|UniProtKB:Q8VHX6, ECO:0000269|PubMed:34405687}. |
Q14493 | SLBP | S59 | ochoa | Histone RNA hairpin-binding protein (Histone stem-loop-binding protein) | RNA-binding protein involved in the histone pre-mRNA processing (PubMed:12588979, PubMed:19155325, PubMed:8957003, PubMed:9049306). Binds the stem-loop structure of replication-dependent histone pre-mRNAs and contributes to efficient 3'-end processing by stabilizing the complex between histone pre-mRNA and U7 small nuclear ribonucleoprotein (snRNP), via the histone downstream element (HDE) (PubMed:12588979, PubMed:19155325, PubMed:8957003, PubMed:9049306). Plays an important role in targeting mature histone mRNA from the nucleus to the cytoplasm and to the translation machinery (PubMed:12588979, PubMed:19155325, PubMed:8957003, PubMed:9049306). Stabilizes mature histone mRNA and could be involved in cell-cycle regulation of histone gene expression (PubMed:12588979, PubMed:19155325, PubMed:8957003, PubMed:9049306). Involved in the mechanism by which growing oocytes accumulate histone proteins that support early embryogenesis (By similarity). Binds to the 5' side of the stem-loop structure of histone pre-mRNAs (By similarity). {ECO:0000250|UniProtKB:P97440, ECO:0000269|PubMed:12588979, ECO:0000269|PubMed:19155325, ECO:0000269|PubMed:8957003, ECO:0000269|PubMed:9049306}. |
Q14498 | RBM39 | Y95 | ochoa|psp | RNA-binding protein 39 (CAPER alpha) (CAPERalpha) (Hepatocellular carcinoma protein 1) (RNA-binding motif protein 39) (RNA-binding region-containing protein 2) (Splicing factor HCC1) | RNA-binding protein that acts as a pre-mRNA splicing factor (PubMed:15694343, PubMed:24795046, PubMed:28302793, PubMed:28437394, PubMed:31271494). Acts by promoting exon inclusion via regulation of exon cassette splicing (PubMed:31271494). Also acts as a transcriptional coactivator for steroid nuclear receptors ESR1/ER-alpha and ESR2/ER-beta, and JUN/AP-1, independently of the pre-mRNA splicing factor activity (By similarity). {ECO:0000250|UniProtKB:Q8VH51, ECO:0000269|PubMed:15694343, ECO:0000269|PubMed:24795046, ECO:0000269|PubMed:28302793, ECO:0000269|PubMed:28437394, ECO:0000269|PubMed:31271494}. |
Q14669 | TRIP12 | S159 | ochoa | E3 ubiquitin-protein ligase TRIP12 (EC 2.3.2.26) (E3 ubiquitin-protein ligase for Arf) (ULF) (HECT-type E3 ubiquitin transferase TRIP12) (Thyroid receptor-interacting protein 12) (TR-interacting protein 12) (TRIP-12) | E3 ubiquitin-protein ligase involved in ubiquitin fusion degradation (UFD) pathway and regulation of DNA repair (PubMed:19028681, PubMed:22884692). Part of the ubiquitin fusion degradation (UFD) pathway, a process that mediates ubiquitination of protein at their N-terminus, regardless of the presence of lysine residues in target proteins (PubMed:19028681). Acts as a key regulator of DNA damage response by acting as a suppressor of RNF168, an E3 ubiquitin-protein ligase that promotes accumulation of 'Lys-63'-linked histone H2A and H2AX at DNA damage sites, thereby acting as a guard against excessive spreading of ubiquitinated chromatin at damaged chromosomes (PubMed:22884692). In normal cells, mediates ubiquitination and degradation of isoform p19ARF/ARF of CDKN2A, a lysine-less tumor suppressor required for p53/TP53 activation under oncogenic stress (PubMed:20208519). In cancer cells, however, isoform p19ARF/ARF and TRIP12 are located in different cell compartments, preventing isoform p19ARF/ARF ubiquitination and degradation (PubMed:20208519). Does not mediate ubiquitination of isoform p16-INK4a of CDKN2A (PubMed:20208519). Also catalyzes ubiquitination of NAE1 and SMARCE1, leading to their degradation (PubMed:18627766). Ubiquitination and degradation of target proteins is regulated by interaction with proteins such as MYC, TRADD or SMARCC1, which disrupt the interaction between TRIP12 and target proteins (PubMed:20829358). Mediates ubiquitination of ASXL1: following binding to N(6)-methyladenosine methylated DNA, ASXL1 is ubiquitinated by TRIP12, leading to its degradation and subsequent inactivation of the PR-DUB complex (PubMed:30982744). {ECO:0000269|PubMed:18627766, ECO:0000269|PubMed:19028681, ECO:0000269|PubMed:20208519, ECO:0000269|PubMed:20829358, ECO:0000269|PubMed:22884692, ECO:0000269|PubMed:30982744}. |
Q14676 | MDC1 | S1797 | ochoa | Mediator of DNA damage checkpoint protein 1 (Nuclear factor with BRCT domains 1) | Histone reader protein required for checkpoint-mediated cell cycle arrest in response to DNA damage within both the S phase and G2/M phases of the cell cycle (PubMed:12475977, PubMed:12499369, PubMed:12551934, PubMed:12607003, PubMed:12607004, PubMed:12607005, PubMed:12611903, PubMed:14695167, PubMed:15201865, PubMed:15377652, PubMed:16049003, PubMed:16377563, PubMed:30898438). Specifically recognizes and binds histone H2AX phosphorylated at 'Ser-139', a marker of DNA damage, serving as a scaffold for the recruitment of DNA repair and signal transduction proteins to discrete foci of DNA damage sites (PubMed:12607005, PubMed:15201865, PubMed:16049003, PubMed:16377563, PubMed:30898438). Also required for downstream events subsequent to the recruitment of these proteins (PubMed:12607005, PubMed:15201865, PubMed:16049003, PubMed:16377563, PubMed:18582474). These include phosphorylation and activation of the ATM, CHEK1 and CHEK2 kinases, and stabilization of TP53/p53 and apoptosis (PubMed:12499369, PubMed:12551934, PubMed:12607004). ATM and CHEK2 may also be activated independently by a parallel pathway mediated by TP53BP1 (PubMed:12499369, PubMed:12551934, PubMed:12607004). Required for chromosomal stability during mitosis by promoting recruitment of TOPBP1 to DNA double strand breaks (DSBs): TOPBP1 forms filamentous assemblies that bridge MDC1 and tether broken chromosomes during mitosis (PubMed:30898438). Required for the repair of DSBs via homologous recombination by promoting recruitment of NBN component of the MRN complex to DSBs (PubMed:18411307, PubMed:18582474, PubMed:18583988, PubMed:18678890). {ECO:0000269|PubMed:12475977, ECO:0000269|PubMed:12499369, ECO:0000269|PubMed:12551934, ECO:0000269|PubMed:12607003, ECO:0000269|PubMed:12607004, ECO:0000269|PubMed:12607005, ECO:0000269|PubMed:12611903, ECO:0000269|PubMed:14695167, ECO:0000269|PubMed:15201865, ECO:0000269|PubMed:15377652, ECO:0000269|PubMed:16049003, ECO:0000269|PubMed:16377563, ECO:0000269|PubMed:18411307, ECO:0000269|PubMed:18582474, ECO:0000269|PubMed:18583988, ECO:0000269|PubMed:18678890, ECO:0000269|PubMed:30898438}. |
Q14678 | KANK1 | S323 | ochoa | KN motif and ankyrin repeat domain-containing protein 1 (Ankyrin repeat domain-containing protein 15) (Kidney ankyrin repeat-containing protein) | Adapter protein that links structural and signaling protein complexes positioned to guide microtubule and actin cytoskeleton dynamics during cell morphogenesis (PubMed:22084092, PubMed:24120883). At focal adhesions (FAs) rims, organizes cortical microtubule stabilizing complexes (CMSCs) and directly interacts with major FA component TLN1, forming macromolecular assemblies positioned to control microtubule-actin crosstalk at the cell edge (PubMed:24120883, PubMed:27410476). Recruits KIF21A in CMSCs at axonal growth cones and regulates axon guidance by suppressing microtubule growth without inducing microtubule disassembly once it reaches the cell cortex (PubMed:24120883). Interacts with ARFGEF1 and participates in establishing microtubule-organizing center (MTOC) orientation and directed cell movement in wound healing (PubMed:22084092). Regulates actin stress fiber formation and cell migration by inhibiting RHOA activation in response to growth factors; this function involves phosphorylation through PI3K/Akt signaling and may depend on the competitive interaction with 14-3-3 adapter proteins to sequester them from active complexes (PubMed:18458160, PubMed:25961457). Inhibits the formation of lamellipodia but not of filopodia; this function may depend on the competitive interaction with BAIAP2 to block its association with activated RAC1. Inhibits fibronectin-mediated cell spreading; this function is partially mediated by BAIAP2 (PubMed:19171758). In the nucleus, is involved in beta-catenin-dependent activation of transcription (PubMed:16968744). During cell division, may regulate DAAM1-dependent RHOA activation that signals centrosome maturation and chromosomal segregation. May also be involved in contractile ring formation during cytokinesis (By similarity). Potential tumor suppressor for renal cell carcinoma (Probable). {ECO:0000250|UniProtKB:E9Q238, ECO:0000269|PubMed:16968744, ECO:0000269|PubMed:18458160, ECO:0000269|PubMed:19171758, ECO:0000269|PubMed:22084092, ECO:0000269|PubMed:24120883, ECO:0000269|PubMed:25961457, ECO:0000269|PubMed:27410476, ECO:0000305|PubMed:12133830}. |
Q14687 | GSE1 | S826 | ochoa | Genetic suppressor element 1 | None |
Q14739 | LBR | S67 | ochoa | Delta(14)-sterol reductase LBR (Delta-14-SR) (EC 1.3.1.70) (3-beta-hydroxysterol Delta (14)-reductase) (C-14 sterol reductase) (C14SR) (Integral nuclear envelope inner membrane protein) (LMN2R) (Lamin-B receptor) (Sterol C14-reductase) | Catalyzes the reduction of the C14-unsaturated bond of lanosterol, as part of the metabolic pathway leading to cholesterol biosynthesis (PubMed:12618959, PubMed:16784888, PubMed:21327084, PubMed:27336722, PubMed:9630650). Plays a critical role in myeloid cell cholesterol biosynthesis which is essential to both myeloid cell growth and functional maturation (By similarity). Mediates the activation of NADPH oxidases, perhaps by maintaining critical levels of cholesterol required for membrane lipid raft formation during neutrophil differentiation (By similarity). Anchors the lamina and the heterochromatin to the inner nuclear membrane (PubMed:10828963). {ECO:0000250|UniProtKB:Q3U9G9, ECO:0000269|PubMed:10828963, ECO:0000269|PubMed:12618959, ECO:0000269|PubMed:16784888, ECO:0000269|PubMed:21327084, ECO:0000269|PubMed:27336722, ECO:0000269|PubMed:9630650}. |
Q14739 | LBR | S69 | ochoa | Delta(14)-sterol reductase LBR (Delta-14-SR) (EC 1.3.1.70) (3-beta-hydroxysterol Delta (14)-reductase) (C-14 sterol reductase) (C14SR) (Integral nuclear envelope inner membrane protein) (LMN2R) (Lamin-B receptor) (Sterol C14-reductase) | Catalyzes the reduction of the C14-unsaturated bond of lanosterol, as part of the metabolic pathway leading to cholesterol biosynthesis (PubMed:12618959, PubMed:16784888, PubMed:21327084, PubMed:27336722, PubMed:9630650). Plays a critical role in myeloid cell cholesterol biosynthesis which is essential to both myeloid cell growth and functional maturation (By similarity). Mediates the activation of NADPH oxidases, perhaps by maintaining critical levels of cholesterol required for membrane lipid raft formation during neutrophil differentiation (By similarity). Anchors the lamina and the heterochromatin to the inner nuclear membrane (PubMed:10828963). {ECO:0000250|UniProtKB:Q3U9G9, ECO:0000269|PubMed:10828963, ECO:0000269|PubMed:12618959, ECO:0000269|PubMed:16784888, ECO:0000269|PubMed:21327084, ECO:0000269|PubMed:27336722, ECO:0000269|PubMed:9630650}. |
Q14739 | LBR | S84 | ochoa | Delta(14)-sterol reductase LBR (Delta-14-SR) (EC 1.3.1.70) (3-beta-hydroxysterol Delta (14)-reductase) (C-14 sterol reductase) (C14SR) (Integral nuclear envelope inner membrane protein) (LMN2R) (Lamin-B receptor) (Sterol C14-reductase) | Catalyzes the reduction of the C14-unsaturated bond of lanosterol, as part of the metabolic pathway leading to cholesterol biosynthesis (PubMed:12618959, PubMed:16784888, PubMed:21327084, PubMed:27336722, PubMed:9630650). Plays a critical role in myeloid cell cholesterol biosynthesis which is essential to both myeloid cell growth and functional maturation (By similarity). Mediates the activation of NADPH oxidases, perhaps by maintaining critical levels of cholesterol required for membrane lipid raft formation during neutrophil differentiation (By similarity). Anchors the lamina and the heterochromatin to the inner nuclear membrane (PubMed:10828963). {ECO:0000250|UniProtKB:Q3U9G9, ECO:0000269|PubMed:10828963, ECO:0000269|PubMed:12618959, ECO:0000269|PubMed:16784888, ECO:0000269|PubMed:21327084, ECO:0000269|PubMed:27336722, ECO:0000269|PubMed:9630650}. |
Q14966 | ZNF638 | S558 | ochoa | Zinc finger protein 638 (Cutaneous T-cell lymphoma-associated antigen se33-1) (CTCL-associated antigen se33-1) (Nuclear protein 220) (Zinc finger matrin-like protein) | Transcription factor that binds to cytidine clusters in double-stranded DNA (PubMed:30487602, PubMed:8647861). Plays a key role in the silencing of unintegrated retroviral DNA: some part of the retroviral DNA formed immediately after infection remains unintegrated in the host genome and is transcriptionally repressed (PubMed:30487602). Mediates transcriptional repression of unintegrated viral DNA by specifically binding to the cytidine clusters of retroviral DNA and mediating the recruitment of chromatin silencers, such as the HUSH complex, SETDB1 and the histone deacetylases HDAC1 and HDAC4 (PubMed:30487602). Acts as an early regulator of adipogenesis by acting as a transcription cofactor of CEBPs (CEBPA, CEBPD and/or CEBPG), controlling the expression of PPARG and probably of other proadipogenic genes, such as SREBF1 (By similarity). May also regulate alternative splicing of target genes during adipogenesis (By similarity). {ECO:0000250|UniProtKB:Q61464, ECO:0000269|PubMed:30487602, ECO:0000269|PubMed:8647861}. |
Q15032 | R3HDM1 | S280 | ochoa | R3H domain-containing protein 1 | None |
Q15772 | SPEG | S417 | 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. |
Q16629 | SRSF7 | S123 | ochoa | Serine/arginine-rich splicing factor 7 (Splicing factor 9G8) (Splicing factor, arginine/serine-rich 7) | Required for pre-mRNA splicing. Can also modulate alternative splicing in vitro. Represses the splicing of MAPT/Tau exon 10. May function as export adapter involved in mRNA nuclear export such as of histone H2A. Binds mRNA which is thought to be transferred to the NXF1-NXT1 heterodimer for export (TAP/NXF1 pathway); enhances NXF1-NXT1 RNA-binding activity. RNA-binding is semi-sequence specific. {ECO:0000269|PubMed:11336712, ECO:0000269|PubMed:12667464, ECO:0000269|PubMed:15009664, ECO:0000269|PubMed:18364396}. |
Q16629 | SRSF7 | S198 | ochoa | Serine/arginine-rich splicing factor 7 (Splicing factor 9G8) (Splicing factor, arginine/serine-rich 7) | Required for pre-mRNA splicing. Can also modulate alternative splicing in vitro. Represses the splicing of MAPT/Tau exon 10. May function as export adapter involved in mRNA nuclear export such as of histone H2A. Binds mRNA which is thought to be transferred to the NXF1-NXT1 heterodimer for export (TAP/NXF1 pathway); enhances NXF1-NXT1 RNA-binding activity. RNA-binding is semi-sequence specific. {ECO:0000269|PubMed:11336712, ECO:0000269|PubMed:12667464, ECO:0000269|PubMed:15009664, ECO:0000269|PubMed:18364396}. |
Q1KMD3 | HNRNPUL2 | S655 | ochoa | Heterogeneous nuclear ribonucleoprotein U-like protein 2 (Scaffold-attachment factor A2) (SAF-A2) | None |
Q32MZ4 | LRRFIP1 | S66 | ochoa | Leucine-rich repeat flightless-interacting protein 1 (LRR FLII-interacting protein 1) (GC-binding factor 2) (TAR RNA-interacting protein) | Transcriptional repressor which preferentially binds to the GC-rich consensus sequence (5'-AGCCCCCGGCG-3') and may regulate expression of TNF, EGFR and PDGFA. May control smooth muscle cells proliferation following artery injury through PDGFA repression. May also bind double-stranded RNA. Positively regulates Toll-like receptor (TLR) signaling in response to agonist probably by competing with the negative FLII regulator for MYD88-binding. {ECO:0000269|PubMed:10364563, ECO:0000269|PubMed:14522076, ECO:0000269|PubMed:16199883, ECO:0000269|PubMed:19265123, ECO:0000269|PubMed:9705290}. |
Q5T200 | ZC3H13 | S108 | ochoa | Zinc finger CCCH domain-containing protein 13 | Associated component of the WMM complex, a complex that mediates N6-methyladenosine (m6A) methylation of RNAs, a modification that plays a role in the efficiency of mRNA splicing and RNA processing (PubMed:29507755). Acts as a key regulator of m6A methylation by promoting m6A methylation of mRNAs at the 3'-UTR (By similarity). Controls embryonic stem cells (ESCs) pluripotency via its role in m6A methylation (By similarity). In the WMM complex, anchors component of the MACOM subcomplex in the nucleus (By similarity). Also required for bridging WTAP to the RNA-binding component RBM15 (RBM15 or RBM15B) (By similarity). {ECO:0000250|UniProtKB:E9Q784}. |
Q5T200 | ZC3H13 | S316 | ochoa | Zinc finger CCCH domain-containing protein 13 | Associated component of the WMM complex, a complex that mediates N6-methyladenosine (m6A) methylation of RNAs, a modification that plays a role in the efficiency of mRNA splicing and RNA processing (PubMed:29507755). Acts as a key regulator of m6A methylation by promoting m6A methylation of mRNAs at the 3'-UTR (By similarity). Controls embryonic stem cells (ESCs) pluripotency via its role in m6A methylation (By similarity). In the WMM complex, anchors component of the MACOM subcomplex in the nucleus (By similarity). Also required for bridging WTAP to the RNA-binding component RBM15 (RBM15 or RBM15B) (By similarity). {ECO:0000250|UniProtKB:E9Q784}. |
Q6JBY9 | RCSD1 | S177 | ochoa | CapZ-interacting protein (Protein kinase substrate CapZIP) (RCSD domain-containing protein 1) | Stress-induced phosphorylation of CAPZIP may regulate the ability of F-actin-capping protein to remodel actin filament assembly. {ECO:0000269|PubMed:15850461}. |
Q6PJF5 | RHBDF2 | S113 | ochoa | Inactive rhomboid protein 2 (iRhom2) (Rhomboid 5 homolog 2) (Rhomboid family member 2) (Rhomboid veinlet-like protein 5) (Rhomboid veinlet-like protein 6) | Regulates ADAM17 protease, a sheddase of the epidermal growth factor (EGF) receptor ligands and TNF, thereby plays a role in sleep, cell survival, proliferation, migration and inflammation. Does not exhibit any protease activity on its own. {ECO:0000250|UniProtKB:Q80WQ6}. |
Q6PJF5 | RHBDF2 | S385 | ochoa | Inactive rhomboid protein 2 (iRhom2) (Rhomboid 5 homolog 2) (Rhomboid family member 2) (Rhomboid veinlet-like protein 5) (Rhomboid veinlet-like protein 6) | Regulates ADAM17 protease, a sheddase of the epidermal growth factor (EGF) receptor ligands and TNF, thereby plays a role in sleep, cell survival, proliferation, migration and inflammation. Does not exhibit any protease activity on its own. {ECO:0000250|UniProtKB:Q80WQ6}. |
Q6VMQ6 | ATF7IP | S557 | ochoa | Activating transcription factor 7-interacting protein 1 (ATF-interacting protein) (ATF-IP) (ATF7-interacting protein) (ATFa-associated modulator) (hAM) (MBD1-containing chromatin-associated factor 1) (P621) | Recruiter that couples transcriptional factors to general transcription apparatus and thereby modulates transcription regulation and chromatin formation. Can both act as an activator or a repressor depending on the context. Required for HUSH-mediated heterochromatin formation and gene silencing (PubMed:27732843). Mediates MBD1-dependent transcriptional repression, probably by recruiting complexes containing SETDB1 (PubMed:12665582). Stabilizes SETDB1, is required to stimulate histone methyltransferase activity of SETDB1 and facilitates the conversion of dimethylated to trimethylated H3 'Lys-9' (H3K9me3). The complex formed with MBD1 and SETDB1 represses transcription and couples DNA methylation and histone H3 'Lys-9' trimethylation (H3K9me3) (PubMed:14536086, PubMed:27732843). Facilitates telomerase TERT and TERC gene expression by SP1 in cancer cells (PubMed:19106100). {ECO:0000269|PubMed:12665582, ECO:0000269|PubMed:14536086, ECO:0000269|PubMed:19106100, ECO:0000269|PubMed:27732843}. |
Q6Y7W6 | GIGYF2 | S158 | ochoa | GRB10-interacting GYF protein 2 (PERQ amino acid-rich with GYF domain-containing protein 2) (Trinucleotide repeat-containing gene 15 protein) | Key component of the 4EHP-GYF2 complex, a multiprotein complex that acts as a repressor of translation initiation (PubMed:22751931, PubMed:31439631, PubMed:35878012). In the 4EHP-GYF2 complex, acts as a factor that bridges EIF4E2 to ZFP36/TTP, linking translation repression with mRNA decay (PubMed:31439631). Also recruits and bridges the association of the 4EHP complex with the decapping effector protein DDX6, which is required for the ZFP36/TTP-mediated down-regulation of AU-rich mRNA (PubMed:31439631). May act cooperatively with GRB10 to regulate tyrosine kinase receptor signaling, including IGF1 and insulin receptors (PubMed:12771153). In association with EIF4E2, assists ribosome-associated quality control (RQC) by sequestering the mRNA cap, blocking ribosome initiation and decreasing the translational load on problematic messages. Part of a pathway that works in parallel to RQC-mediated degradation of the stalled nascent polypeptide (PubMed:32726578). GIGYF2 and EIF4E2 work downstream and independently of ZNF598, which seems to work as a scaffold that can recruit them to faulty mRNA even if alternative recruitment mechanisms may exist (PubMed:32726578). {ECO:0000269|PubMed:12771153, ECO:0000269|PubMed:22751931, ECO:0000269|PubMed:31439631, ECO:0000269|PubMed:32726578, ECO:0000269|PubMed:35878012}.; FUNCTION: (Microbial infection) Upon SARS coronavirus-2/SARS-CoV-2 infection, the interaction with non-structural protein 2 (nsp2) enhances GIGYF2 binding to EIF4E2 and increases repression of translation initiation of genes involved in antiviral innate immune response such as IFNB1. {ECO:0000269|PubMed:35878012}. |
Q6Y7W6 | GIGYF2 | S273 | ochoa | GRB10-interacting GYF protein 2 (PERQ amino acid-rich with GYF domain-containing protein 2) (Trinucleotide repeat-containing gene 15 protein) | Key component of the 4EHP-GYF2 complex, a multiprotein complex that acts as a repressor of translation initiation (PubMed:22751931, PubMed:31439631, PubMed:35878012). In the 4EHP-GYF2 complex, acts as a factor that bridges EIF4E2 to ZFP36/TTP, linking translation repression with mRNA decay (PubMed:31439631). Also recruits and bridges the association of the 4EHP complex with the decapping effector protein DDX6, which is required for the ZFP36/TTP-mediated down-regulation of AU-rich mRNA (PubMed:31439631). May act cooperatively with GRB10 to regulate tyrosine kinase receptor signaling, including IGF1 and insulin receptors (PubMed:12771153). In association with EIF4E2, assists ribosome-associated quality control (RQC) by sequestering the mRNA cap, blocking ribosome initiation and decreasing the translational load on problematic messages. Part of a pathway that works in parallel to RQC-mediated degradation of the stalled nascent polypeptide (PubMed:32726578). GIGYF2 and EIF4E2 work downstream and independently of ZNF598, which seems to work as a scaffold that can recruit them to faulty mRNA even if alternative recruitment mechanisms may exist (PubMed:32726578). {ECO:0000269|PubMed:12771153, ECO:0000269|PubMed:22751931, ECO:0000269|PubMed:31439631, ECO:0000269|PubMed:32726578, ECO:0000269|PubMed:35878012}.; FUNCTION: (Microbial infection) Upon SARS coronavirus-2/SARS-CoV-2 infection, the interaction with non-structural protein 2 (nsp2) enhances GIGYF2 binding to EIF4E2 and increases repression of translation initiation of genes involved in antiviral innate immune response such as IFNB1. {ECO:0000269|PubMed:35878012}. |
Q6ZRS2 | SRCAP | S3210 | 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}. |
Q6ZSZ5 | ARHGEF18 | S83 | ochoa | Rho guanine nucleotide exchange factor 18 (114 kDa Rho-specific guanine nucleotide exchange factor) (p114-Rho-GEF) (p114RhoGEF) (Septin-associated RhoGEF) (SA-RhoGEF) | Acts as a guanine nucleotide exchange factor (GEF) for RhoA GTPases. Its activation induces formation of actin stress fibers. Also acts as a GEF for RAC1, inducing production of reactive oxygen species (ROS). Does not act as a GEF for CDC42. The G protein beta-gamma (Gbetagamma) subunits of heterotrimeric G proteins act as activators, explaining the integrated effects of LPA and other G-protein coupled receptor agonists on actin stress fiber formation, cell shape change and ROS production. Required for EPB41L4B-mediated regulation of the circumferential actomyosin belt in epithelial cells (PubMed:22006950). {ECO:0000269|PubMed:11085924, ECO:0000269|PubMed:14512443, ECO:0000269|PubMed:15558029, ECO:0000269|PubMed:22006950, ECO:0000269|PubMed:28132693}. |
Q7L4I2 | RSRC2 | S30 | ochoa | Arginine/serine-rich coiled-coil protein 2 | None |
Q7L4I2 | RSRC2 | S32 | ochoa | Arginine/serine-rich coiled-coil protein 2 | None |
Q7Z3G6 | PRICKLE2 | S693 | ochoa | Prickle-like protein 2 | None |
Q7Z403 | TMC6 | S112 | ochoa | Transmembrane channel-like protein 6 (Epidermodysplasia verruciformis protein 1) (Protein LAK-4) | Acts as a regulatory protein involved in the regulation of numerous cellular processes (PubMed:18158319, PubMed:30068544, PubMed:32917726). Together with its homolog TMC8/EVER2, forms a complex with CIB1 in lymphocytes and keratynocytes where TMC6 and TMC8 stabilize CIB1 and reciprocally (PubMed:30068544, PubMed:32917726). Together with TMC8, also forms a complex with and activates zinc transporter ZNT1 at the ER membrane of keratynocytes, thereby facilitating zinc uptake into the ER (PubMed:18158319). Down-regulates the activity of transcription factors induced by zinc and cytokines (PubMed:18158319). Also plays a role in thermal sensation by inhibiting the M-channel (KCNQ2-KCNQ3 channel) current in primary sensory neurons (By similarity). {ECO:0000250|UniProtKB:Q7TN60, ECO:0000269|PubMed:18158319, ECO:0000269|PubMed:30068544, ECO:0000269|PubMed:32917726}. |
Q86SG6 | NEK8 | S280 | ochoa | Serine/threonine-protein kinase Nek8 (EC 2.7.11.1) (Never in mitosis A-related kinase 8) (NimA-related protein kinase 8) (Nima-related protein kinase 12a) | Required for renal tubular integrity. May regulate local cytoskeletal structure in kidney tubule epithelial cells. May regulate ciliary biogenesis through targeting of proteins to the cilia (PubMed:37598857). Plays a role in organogenesis, and is involved in the regulation of the Hippo signaling pathway (PubMed:26967905). {ECO:0000269|PubMed:23418306, ECO:0000269|PubMed:26967905, ECO:0000269|PubMed:37598857}. |
Q86SU0 | ILDR1 | S467 | ochoa | Immunoglobulin-like domain-containing receptor 1 (Angulin-2) | Maintains epithelial barrier function by recruiting MARVELD2/tricellulin to tricellular tight junctions (tTJs) (PubMed:23239027). Crucial for normal hearing by maintaining the structural and functional integrity of tTJs, which are critical for the survival of auditory neurosensory HCs. Mediates fatty acids and lipoproteins-stimulated CCK/cholecystokinin secretion in the small intestine. In the inner ear, may regulate alternative pre-mRNA splicing via binding to TRA2A, TRA2B and SRSF1 (By similarity). {ECO:0000250|UniProtKB:Q8CBR1, ECO:0000269|PubMed:23239027}.; FUNCTION: (Microbial infection) Promotes influenza virus infection by inhibiting viral nucleoprotein NP binding to PLSCR1 and thereby PLSCR1-mediated antiviral activity. {ECO:0000269|PubMed:35595813}. |
Q86U06 | RBM23 | Y126 | ochoa | Probable RNA-binding protein 23 (CAPER beta) (CAPERbeta) (RNA-binding motif protein 23) (RNA-binding region-containing protein 4) (Splicing factor SF2) | RNA-binding protein that acts both as a transcription coactivator and pre-mRNA splicing factor (PubMed:15694343). Regulates steroid hormone receptor-mediated transcription, independently of the pre-mRNA splicing factor activity (PubMed:15694343). {ECO:0000269|PubMed:15694343}. |
Q86X51 | EZHIP | S336 | ochoa | EZH inhibitory protein | Inhibits PRC2/EED-EZH1 and PRC2/EED-EZH2 complex function by inhibiting EZH1/EZH2 methyltransferase activity, thereby causing down-regulation of histone H3 trimethylation on 'Lys-27' (H3K27me3) (PubMed:29909548, PubMed:30923826, PubMed:31086175, PubMed:31451685). Probably inhibits methyltransferase activity by limiting the stimulatory effect of cofactors such as AEBP2 and JARID2 (PubMed:30923826). Inhibits H3K27me3 deposition during spermatogenesis and oogenesis (By similarity). {ECO:0000250|UniProtKB:B1B0V2, ECO:0000269|PubMed:29909548, ECO:0000269|PubMed:30923826, ECO:0000269|PubMed:31086175, ECO:0000269|PubMed:31451685}. |
Q86YR5 | GPSM1 | S469 | ochoa | G-protein-signaling modulator 1 (Activator of G-protein signaling 3) | Guanine nucleotide dissociation inhibitor (GDI) which functions as a receptor-independent activator of heterotrimeric G-protein signaling. Keeps G(i/o) alpha subunit in its GDP-bound form thus uncoupling heterotrimeric G-proteins signaling from G protein-coupled receptors. Controls spindle orientation and asymmetric cell fate of cerebral cortical progenitors. May also be involved in macroautophagy in intestinal cells. May play a role in drug addiction. {ECO:0000269|PubMed:11024022, ECO:0000269|PubMed:12642577}. |
Q8N3D4 | EHBP1L1 | S1273 | ochoa | EH domain-binding protein 1-like protein 1 | May act as Rab effector protein and play a role in vesicle trafficking. {ECO:0000305|PubMed:27552051}. |
Q8N4S9 | MARVELD2 | S387 | ochoa | MARVEL domain-containing protein 2 (Tricellulin) | Plays a role in the formation of tricellular tight junctions and of epithelial barriers (By similarity). Required for normal hearing via its role in the separation of the endolymphatic and perilymphatic spaces of the organ of Corti in the inner ear, and for normal survival of hair cells in the organ of Corti (PubMed:17186462). {ECO:0000250|UniProtKB:Q3UZP0, ECO:0000269|PubMed:17186462}. |
Q8NCN4 | RNF169 | S290 | ochoa | E3 ubiquitin-protein ligase RNF169 (EC 2.3.2.27) (RING finger protein 169) (RING-type E3 ubiquitin transferase RNF169) | Probable E3 ubiquitin-protein ligase that acts as a regulator of double-strand breaks (DSBs) repair following DNA damage. Functions in a non-canonical fashion to harness RNF168-mediated protein recruitment to DSB-containing chromatin, thereby contributing to regulation of DSB repair pathway utilization (PubMed:22492721, PubMed:30773093). Once recruited to DSB repair sites by recognizing and binding ubiquitin catalyzed by RNF168, competes with TP53BP1 and BRCA1 for association with RNF168-modified chromatin, thereby favouring homologous recombination repair (HRR) and single-strand annealing (SSA) instead of non-homologous end joining (NHEJ) mediated by TP53BP1 (PubMed:30104380, PubMed:30773093). E3 ubiquitin-protein ligase activity is not required for regulation of DSBs repair. {ECO:0000269|PubMed:22492721, ECO:0000269|PubMed:22733822, ECO:0000269|PubMed:22742833, ECO:0000269|PubMed:30104380, ECO:0000269|PubMed:30773093}. |
Q8NEV8 | EXPH5 | S1851 | ochoa | Exophilin-5 (Synaptotagmin-like protein homolog lacking C2 domains b) (SlaC2-b) (Slp homolog lacking C2 domains b) | May act as Rab effector protein and play a role in vesicle trafficking. |
Q8NFC6 | BOD1L1 | S2954 | ochoa | Biorientation of chromosomes in cell division protein 1-like 1 | Component of the fork protection machinery required to protect stalled/damaged replication forks from uncontrolled DNA2-dependent resection. Acts by stabilizing RAD51 at stalled replication forks and protecting RAD51 nucleofilaments from the antirecombinogenic activities of FBH1 and BLM (PubMed:26166705, PubMed:29937342). Does not regulate spindle orientation (PubMed:26166705). {ECO:0000269|PubMed:26166705, ECO:0000269|PubMed:29937342}. |
Q8TEA8 | DTD1 | S179 | psp | D-aminoacyl-tRNA deacylase 1 (DTD) (EC 3.1.1.96) (DNA-unwinding element-binding protein B) (DUE-B) (Gly-tRNA(Ala) deacylase) (Histidyl-tRNA synthase-related) | Possible ATPase (PubMed:15653697) involved in DNA replication, may facilitate loading of CDC45 onto pre-replication complexes (PubMed:20065034). {ECO:0000269|PubMed:15653697, ECO:0000269|PubMed:20065034}.; FUNCTION: An aminoacyl-tRNA editing enzyme that deacylates mischarged D-aminoacyl-tRNAs. Also deacylates mischarged glycyl-tRNA(Ala), protecting cells against glycine mischarging by AlaRS. Acts via tRNA-based rather than protein-based catalysis; rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality. {ECO:0000250|UniProtKB:Q8IIS0}. |
Q8WUQ7 | CACTIN | S71 | ochoa | Splicing factor Cactin (Renal carcinoma antigen NY-REN-24) | Plays a role in pre-mRNA splicing by facilitating excision of a subset of introns (PubMed:28062851). Required for the splicing of CDCA5/Sororin, a regulator of sister chromatid cohesion (PubMed:28062851). Involved in the regulation of innate immune response (PubMed:20829348). Acts as a negative regulator of Toll-like receptor, interferon-regulatory factor (IRF) and canonical NF-kappa-B signaling pathways (PubMed:20829348, PubMed:26363554). Contributes to the regulation of transcriptional activation of NF-kappa-B target genes in response to endogenous pro-inflammatory stimuli (PubMed:20829348, PubMed:26363554). {ECO:0000269|PubMed:20829348, ECO:0000269|PubMed:26363554, ECO:0000269|PubMed:28062851}. |
Q8WX93 | PALLD | S1101 | ochoa | Palladin (SIH002) (Sarcoma antigen NY-SAR-77) | Cytoskeletal protein required for organization of normal actin cytoskeleton. Roles in establishing cell morphology, motility, cell adhesion and cell-extracellular matrix interactions in a variety of cell types. May function as a scaffolding molecule with the potential to influence both actin polymerization and the assembly of existing actin filaments into higher-order arrays. Binds to proteins that bind to either monomeric or filamentous actin. Localizes at sites where active actin remodeling takes place, such as lamellipodia and membrane ruffles. Different isoforms may have functional differences. Involved in the control of morphological and cytoskeletal changes associated with dendritic cell maturation. Involved in targeting ACTN to specific subcellular foci. {ECO:0000269|PubMed:11598191, ECO:0000269|PubMed:15147863, ECO:0000269|PubMed:17537434}. |
Q8WX93 | PALLD | S1118 | ochoa|psp | Palladin (SIH002) (Sarcoma antigen NY-SAR-77) | Cytoskeletal protein required for organization of normal actin cytoskeleton. Roles in establishing cell morphology, motility, cell adhesion and cell-extracellular matrix interactions in a variety of cell types. May function as a scaffolding molecule with the potential to influence both actin polymerization and the assembly of existing actin filaments into higher-order arrays. Binds to proteins that bind to either monomeric or filamentous actin. Localizes at sites where active actin remodeling takes place, such as lamellipodia and membrane ruffles. Different isoforms may have functional differences. Involved in the control of morphological and cytoskeletal changes associated with dendritic cell maturation. Involved in targeting ACTN to specific subcellular foci. {ECO:0000269|PubMed:11598191, ECO:0000269|PubMed:15147863, ECO:0000269|PubMed:17537434}. |
Q92576 | PHF3 | S1952 | ochoa | PHD finger protein 3 | None |
Q92620 | DHX38 | S119 | ochoa | Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 (EC 3.6.4.13) (ATP-dependent RNA helicase DHX38) (DEAH box protein 38) | Probable ATP-binding RNA helicase (Probable). Involved in pre-mRNA splicing as component of the spliceosome (PubMed:29301961, PubMed:9524131). {ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:9524131, ECO:0000305}. |
Q92997 | DVL3 | S232 | psp | Segment polarity protein dishevelled homolog DVL-3 (Dishevelled-3) (DSH homolog 3) | Involved in the signal transduction pathway mediated by multiple Wnt genes. {ECO:0000250|UniProtKB:Q61062}. |
Q93100 | PHKB | S25 | ochoa | Phosphorylase b kinase regulatory subunit beta (Phosphorylase kinase subunit beta) | Phosphorylase b kinase catalyzes the phosphorylation of serine in certain substrates, including troponin I. The beta chain acts as a regulatory unit and modulates the activity of the holoenzyme in response to phosphorylation. |
Q96E39 | RBMXL1 | S249 | ochoa | RNA binding motif protein, X-linked-like-1 (Heterogeneous nuclear ribonucleoprotein G-like 1) | RNA-binding protein which may be involved in pre-mRNA splicing. {ECO:0000250}. |
Q96F86 | EDC3 | S233 | ochoa | Enhancer of mRNA-decapping protein 3 (LSM16 homolog) (YjeF N-terminal domain-containing protein 2) (YjeF_N2) (hYjeF_N2) (YjeF domain-containing protein 1) | Binds single-stranded RNA. Involved in the process of mRNA degradation and in the positive regulation of mRNA decapping. May play a role in spermiogenesis and oogenesis. {ECO:0000269|PubMed:16364915, ECO:0000269|PubMed:17533573, ECO:0000269|PubMed:18678652, ECO:0000269|PubMed:25701870}. |
Q96G01 | BICD1 | S546 | ochoa | Protein bicaudal D homolog 1 (Bic-D 1) | Regulates coat complex coatomer protein I (COPI)-independent Golgi-endoplasmic reticulum transport by recruiting the dynein-dynactin motor complex. |
Q96GE4 | CEP95 | S451 | ochoa | Centrosomal protein of 95 kDa (Cep95) (Coiled-coil domain-containing protein 45) | None |
Q96I25 | RBM17 | S169 | ochoa | Splicing factor 45 (45 kDa-splicing factor) (RNA-binding motif protein 17) | Splice factor that binds to the single-stranded 3'AG at the exon/intron border and promotes its utilization in the second catalytic step. Involved in the regulation of alternative splicing and the utilization of cryptic splice sites. Promotes the utilization of a cryptic splice site created by the beta-110 mutation in the HBB gene. The resulting frameshift leads to sickle cell anemia. {ECO:0000269|PubMed:12015979, ECO:0000269|PubMed:17589525}. |
Q96N96 | SPATA13 | S76 | ochoa | Spermatogenesis-associated protein 13 (APC-stimulated guanine nucleotide exchange factor 2) (Asef2) | Acts as a guanine nucleotide exchange factor (GEF) for RHOA, RAC1 and CDC42 GTPases. Regulates cell migration and adhesion assembly and disassembly through a RAC1, PI3K, RHOA and AKT1-dependent mechanism. Increases both RAC1 and CDC42 activity, but decreases the amount of active RHOA. Required for MMP9 up-regulation via the JNK signaling pathway in colorectal tumor cells. Involved in tumor angiogenesis and may play a role in intestinal adenoma formation and tumor progression. {ECO:0000269|PubMed:17145773, ECO:0000269|PubMed:17599059, ECO:0000269|PubMed:19151759, ECO:0000269|PubMed:19893577, ECO:0000269|PubMed:19934221}. |
Q96QT4 | TRPM7 | S552 | ochoa | Transient receptor potential cation channel subfamily M member 7 (EC 2.7.11.1) (Channel-kinase 1) (Long transient receptor potential channel 7) (LTrpC-7) (LTrpC7) [Cleaved into: TRPM7 kinase, cleaved form (M7CK); TRPM7 channel, cleaved form] | Bifunctional protein that combines an ion channel with an intrinsic kinase domain, enabling it to modulate cellular functions either by conducting ions through the pore or by phosphorylating downstream proteins via its kinase domain. The channel is highly permeable to divalent cations, specifically calcium (Ca2+), magnesium (Mg2+) and zinc (Zn2+) and mediates their influx (PubMed:11385574, PubMed:12887921, PubMed:15485879, PubMed:24316671, PubMed:35561741, PubMed:36027648). Controls a wide range of biological processes such as Ca2(+), Mg(2+) and Zn(2+) homeostasis, vesicular Zn(2+) release channel and intracellular Ca(2+) signaling, embryonic development, immune responses, cell motility, proliferation and differentiation (By similarity). The C-terminal alpha-kinase domain autophosphorylates cytoplasmic residues of TRPM7 (PubMed:18365021). In vivo, TRPM7 phosphorylates SMAD2, suggesting that TRPM7 kinase may play a role in activating SMAD signaling pathways. In vitro, TRPM7 kinase phosphorylates ANXA1 (annexin A1), myosin II isoforms and a variety of proteins with diverse cellular functions (PubMed:15485879, PubMed:18394644). {ECO:0000250|UniProtKB:Q923J1, ECO:0000269|PubMed:11385574, ECO:0000269|PubMed:12887921, ECO:0000269|PubMed:15485879, ECO:0000269|PubMed:18365021, ECO:0000269|PubMed:18394644, ECO:0000269|PubMed:24316671, ECO:0000269|PubMed:35561741, ECO:0000269|PubMed:36027648}.; FUNCTION: [TRPM7 channel, cleaved form]: The cleaved channel exhibits substantially higher current and potentiates Fas receptor signaling. {ECO:0000250|UniProtKB:Q923J1}.; FUNCTION: [TRPM7 kinase, cleaved form]: The C-terminal kinase domain can be cleaved from the channel segment in a cell-type-specific fashion. In immune cells, the TRPM7 kinase domain is clipped from the channel domain by caspases in response to Fas-receptor stimulation. The cleaved kinase fragments can translocate to the nucleus, and bind chromatin-remodeling complex proteins in a Zn(2+)-dependent manner to ultimately phosphorylate specific Ser/Thr residues of histones known to be functionally important for cell differentiation and embryonic development. {ECO:0000250|UniProtKB:Q923J1}. |
Q96T23 | RSF1 | S1221 | ochoa | Remodeling and spacing factor 1 (Rsf-1) (HBV pX-associated protein 8) (Hepatitis B virus X-associated protein) (p325 subunit of RSF chromatin-remodeling complex) | Regulatory subunit of the ATP-dependent RSF-1 and RSF-5 ISWI chromatin-remodeling complexes, which form ordered nucleosome arrays on chromatin and facilitate access to DNA during DNA-templated processes such as DNA replication, transcription, and repair (PubMed:12972596, PubMed:28801535). Binds to core histones together with SMARCA5, and is required for the assembly of regular nucleosome arrays by the RSF-5 ISWI chromatin-remodeling complex (PubMed:12972596). Directly stimulates the ATPase activity of SMARCA1 and SMARCA5 in the RSF-1 and RSF-5 ISWI chromatin-remodeling complexes, respectively (PubMed:28801535). The RSF-1 ISWI chromatin remodeling complex has a lower ATP hydrolysis rate than the RSF-5 ISWI chromatin-remodeling complex (PubMed:28801535). The complexes do not have the ability to slide mononucleosomes to the center of a DNA template (PubMed:28801535). Facilitates transcription of hepatitis B virus (HBV) genes by the pX transcription activator. In case of infection by HBV, together with pX, it represses TNF-alpha induced NF-kappa-B transcription activation. Represses transcription when artificially recruited to chromatin by fusion to a heterogeneous DNA binding domain (PubMed:11788598, PubMed:11944984). {ECO:0000269|PubMed:11788598, ECO:0000269|PubMed:11944984, ECO:0000269|PubMed:12972596, ECO:0000269|PubMed:28801535}. |
Q96T58 | SPEN | S188 | ochoa | Msx2-interacting protein (SMART/HDAC1-associated repressor protein) (SPEN homolog) | May serve as a nuclear matrix platform that organizes and integrates transcriptional responses. In osteoblasts, supports transcription activation: synergizes with RUNX2 to enhance FGFR2-mediated activation of the osteocalcin FGF-responsive element (OCFRE) (By similarity). Has also been shown to be an essential corepressor protein, which probably regulates different key pathways such as the Notch pathway. Negative regulator of the Notch pathway via its interaction with RBPSUH, which prevents the association between NOTCH1 and RBPSUH, and therefore suppresses the transactivation activity of Notch signaling. Blocks the differentiation of precursor B-cells into marginal zone B-cells. Probably represses transcription via the recruitment of large complexes containing histone deacetylase proteins. May bind both to DNA and RNA. {ECO:0000250|UniProtKB:Q62504, ECO:0000269|PubMed:11331609, ECO:0000269|PubMed:12374742}. |
Q99590 | SCAF11 | S848 | ochoa | Protein SCAF11 (CTD-associated SR protein 11) (Renal carcinoma antigen NY-REN-40) (SC35-interacting protein 1) (SR-related and CTD-associated factor 11) (SRSF2-interacting protein) (Serine/arginine-rich splicing factor 2-interacting protein) (Splicing factor, arginine/serine-rich 2-interacting protein) (Splicing regulatory protein 129) (SRrp129) | Plays a role in pre-mRNA alternative splicing by regulating spliceosome assembly. {ECO:0000269|PubMed:9447963}. |
Q9BRD0 | BUD13 | S402 | ochoa | BUD13 homolog | Involved in pre-mRNA splicing as component of the activated spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000305|PubMed:33509932}. |
Q9BU76 | MMTAG2 | S233 | ochoa | Multiple myeloma tumor-associated protein 2 (hMMTAG2) | None |
Q9BUQ8 | DDX23 | S107 | ochoa | Probable ATP-dependent RNA helicase DDX23 (EC 3.6.4.13) (100 kDa U5 snRNP-specific protein) (DEAD box protein 23) (PRP28 homolog) (U5-100kD) | Involved in pre-mRNA splicing and its phosphorylated form (by SRPK2) is required for spliceosomal B complex formation (PubMed:18425142). Independently of its spliceosome formation function, required for the suppression of incorrect R-loops formed during transcription; R-loops are composed of a DNA:RNA hybrid and the associated non-template single-stranded DNA (PubMed:28076779). {ECO:0000269|PubMed:18425142, ECO:0000269|PubMed:28076779}. |
Q9BXP5 | SRRT | S51 | ochoa | Serrate RNA effector molecule homolog (Arsenite-resistance protein 2) | Acts as a mediator between the cap-binding complex (CBC) and the primary microRNAs (miRNAs) processing machinery during cell proliferation. Contributes to the stability and delivery of capped primary miRNA transcripts to the primary miRNA processing complex containing DGCR8 and DROSHA, thereby playing a role in RNA-mediated gene silencing (RNAi) by miRNAs. Binds capped RNAs (m7GpppG-capped RNA); however interaction is probably mediated via its interaction with NCBP1/CBP80 component of the CBC complex. Involved in cell cycle progression at S phase. Does not directly confer arsenite resistance but rather modulates arsenic sensitivity. Independently of its activity on miRNAs, necessary and sufficient to promote neural stem cell self-renewal. Does so by directly binding SOX2 promoter and positively regulating its transcription (By similarity). {ECO:0000250, ECO:0000269|PubMed:19632182}. |
Q9GZY8 | MFF | S155 | ochoa|psp | Mitochondrial fission factor | Plays a role in mitochondrial and peroxisomal fission (PubMed:18353969, PubMed:23530241, PubMed:24196833). Promotes the recruitment and association of the fission mediator dynamin-related protein 1 (DNM1L) to the mitochondrial surface (PubMed:23530241). May be involved in regulation of synaptic vesicle membrane dynamics by recruitment of DNM1L to clathrin-containing vesicles (By similarity). {ECO:0000250|UniProtKB:Q4KM98, ECO:0000269|PubMed:18353969, ECO:0000269|PubMed:23530241, ECO:0000269|PubMed:24196833}. |
Q9H425 | C1orf198 | S35 | ochoa | Uncharacterized protein C1orf198 | None |
Q9H4L4 | SENP3 | S139 | psp | Sentrin-specific protease 3 (EC 3.4.22.-) (SUMO-1-specific protease 3) (Sentrin/SUMO-specific protease SENP3) | Protease that releases SUMO2 and SUMO3 monomers from sumoylated substrates, but has only weak activity against SUMO1 conjugates (PubMed:16608850, PubMed:32832608, PubMed:36050397). Deconjugates SUMO2 from MEF2D, which increases its transcriptional activation capability (PubMed:15743823). Deconjugates SUMO2 and SUMO3 from CDCA8 (PubMed:18946085). Redox sensor that, when redistributed into nucleoplasm, can act as an effector to enhance HIF1A transcriptional activity by desumoylating EP300 (PubMed:19680224). Required for rRNA processing through deconjugation of SUMO2 and SUMO3 from nucleophosmin, NPM1 (PubMed:19015314). Plays a role in the regulation of sumoylation status of ZNF148 (PubMed:18259216). 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). Deconjugates SUMO2 from KAT5 (PubMed:32832608). Catalyzes desumoylation of MRE11 (PubMed:36050397). {ECO:0000269|PubMed:15743823, ECO:0000269|PubMed:16608850, ECO:0000269|PubMed:18259216, ECO:0000269|PubMed:18946085, ECO:0000269|PubMed:19015314, ECO:0000269|PubMed:19680224, ECO:0000269|PubMed:22872859, ECO:0000269|PubMed:32832608, ECO:0000269|PubMed:36050397}. |
Q9H4L4 | SENP3 | S141 | psp | Sentrin-specific protease 3 (EC 3.4.22.-) (SUMO-1-specific protease 3) (Sentrin/SUMO-specific protease SENP3) | Protease that releases SUMO2 and SUMO3 monomers from sumoylated substrates, but has only weak activity against SUMO1 conjugates (PubMed:16608850, PubMed:32832608, PubMed:36050397). Deconjugates SUMO2 from MEF2D, which increases its transcriptional activation capability (PubMed:15743823). Deconjugates SUMO2 and SUMO3 from CDCA8 (PubMed:18946085). Redox sensor that, when redistributed into nucleoplasm, can act as an effector to enhance HIF1A transcriptional activity by desumoylating EP300 (PubMed:19680224). Required for rRNA processing through deconjugation of SUMO2 and SUMO3 from nucleophosmin, NPM1 (PubMed:19015314). Plays a role in the regulation of sumoylation status of ZNF148 (PubMed:18259216). 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). Deconjugates SUMO2 from KAT5 (PubMed:32832608). Catalyzes desumoylation of MRE11 (PubMed:36050397). {ECO:0000269|PubMed:15743823, ECO:0000269|PubMed:16608850, ECO:0000269|PubMed:18259216, ECO:0000269|PubMed:18946085, ECO:0000269|PubMed:19015314, ECO:0000269|PubMed:19680224, ECO:0000269|PubMed:22872859, ECO:0000269|PubMed:32832608, ECO:0000269|PubMed:36050397}. |
Q9H9J4 | USP42 | S1170 | ochoa | Ubiquitin carboxyl-terminal hydrolase 42 (EC 3.4.19.12) (Deubiquitinating enzyme 42) (Ubiquitin thioesterase 42) (Ubiquitin-specific-processing protease 42) | Deubiquitinating enzyme which may play an important role during spermatogenesis. {ECO:0000250}. |
Q9HCB6 | SPON1 | S740 | ochoa | Spondin-1 (F-spondin) (Vascular smooth muscle cell growth-promoting factor) | Cell adhesion protein that promotes the attachment of spinal cord and sensory neuron cells and the outgrowth of neurites in vitro. May contribute to the growth and guidance of axons in both the spinal cord and the PNS (By similarity). Major factor for vascular smooth muscle cell. {ECO:0000250}. |
Q9HCG8 | CWC22 | S61 | ochoa | Pre-mRNA-splicing factor CWC22 homolog (Nucampholin homolog) (fSAPb) | Required for pre-mRNA splicing as component of the spliceosome (PubMed:11991638, PubMed:12226669, PubMed:22961380, PubMed:28076346, PubMed:28502770, PubMed:29301961, PubMed:29360106). As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). Promotes exon-junction complex (EJC) assembly (PubMed:22959432, PubMed:22961380). Hinders EIF4A3 from non-specifically binding RNA and escorts it to the splicing machinery to promote EJC assembly on mature mRNAs. Through its role in EJC assembly, required for nonsense-mediated mRNA decay. {ECO:0000269|PubMed:11991638, ECO:0000269|PubMed:12226669, ECO:0000269|PubMed:22959432, ECO:0000269|PubMed:22961380, ECO:0000269|PubMed:23236153, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000305|PubMed:33509932}. |
Q9HCG8 | CWC22 | S91 | ochoa | Pre-mRNA-splicing factor CWC22 homolog (Nucampholin homolog) (fSAPb) | Required for pre-mRNA splicing as component of the spliceosome (PubMed:11991638, PubMed:12226669, PubMed:22961380, PubMed:28076346, PubMed:28502770, PubMed:29301961, PubMed:29360106). As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). Promotes exon-junction complex (EJC) assembly (PubMed:22959432, PubMed:22961380). Hinders EIF4A3 from non-specifically binding RNA and escorts it to the splicing machinery to promote EJC assembly on mature mRNAs. Through its role in EJC assembly, required for nonsense-mediated mRNA decay. {ECO:0000269|PubMed:11991638, ECO:0000269|PubMed:12226669, ECO:0000269|PubMed:22959432, ECO:0000269|PubMed:22961380, ECO:0000269|PubMed:23236153, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000305|PubMed:33509932}. |
Q9HCS5 | EPB41L4A | S541 | ochoa | Band 4.1-like protein 4A (Erythrocyte membrane protein band 4.1-like 4A) (Protein NBL4) | None |
Q9NVW2 | RLIM | S228 | ochoa | E3 ubiquitin-protein ligase RLIM (EC 2.3.2.27) (LIM domain-interacting RING finger protein) (RING finger LIM domain-binding protein) (R-LIM) (RING finger protein 12) (RING-type E3 ubiquitin transferase RLIM) (Renal carcinoma antigen NY-REN-43) | E3 ubiquitin-protein ligase. Acts as a negative coregulator for LIM homeodomain transcription factors by mediating the ubiquitination and subsequent degradation of LIM cofactors LDB1 and LDB2 and by mediating the recruitment the SIN3a/histone deacetylase corepressor complex. Ubiquitination and degradation of LIM cofactors LDB1 and LDB2 allows DNA-bound LIM homeodomain transcription factors to interact with other protein partners such as RLIM. Plays a role in telomere length-mediated growth suppression by mediating the ubiquitination and degradation of TERF1. By targeting ZFP42 for degradation, acts as an activator of random inactivation of X chromosome in the embryo, a stochastic process in which one X chromosome is inactivated to minimize sex-related dosage differences of X-encoded genes in somatic cells of female placental mammals. {ECO:0000269|PubMed:19164295, ECO:0000269|PubMed:19945382}. |
Q9NVW2 | RLIM | S230 | ochoa|psp | E3 ubiquitin-protein ligase RLIM (EC 2.3.2.27) (LIM domain-interacting RING finger protein) (RING finger LIM domain-binding protein) (R-LIM) (RING finger protein 12) (RING-type E3 ubiquitin transferase RLIM) (Renal carcinoma antigen NY-REN-43) | E3 ubiquitin-protein ligase. Acts as a negative coregulator for LIM homeodomain transcription factors by mediating the ubiquitination and subsequent degradation of LIM cofactors LDB1 and LDB2 and by mediating the recruitment the SIN3a/histone deacetylase corepressor complex. Ubiquitination and degradation of LIM cofactors LDB1 and LDB2 allows DNA-bound LIM homeodomain transcription factors to interact with other protein partners such as RLIM. Plays a role in telomere length-mediated growth suppression by mediating the ubiquitination and degradation of TERF1. By targeting ZFP42 for degradation, acts as an activator of random inactivation of X chromosome in the embryo, a stochastic process in which one X chromosome is inactivated to minimize sex-related dosage differences of X-encoded genes in somatic cells of female placental mammals. {ECO:0000269|PubMed:19164295, ECO:0000269|PubMed:19945382}. |
Q9NW75 | GPATCH2 | S54 | ochoa | G patch domain-containing protein 2 | Enhances the ATPase activity of DHX15 in vitro. {ECO:0000269|PubMed:19432882}. |
Q9NW75 | GPATCH2 | S56 | ochoa | G patch domain-containing protein 2 | Enhances the ATPase activity of DHX15 in vitro. {ECO:0000269|PubMed:19432882}. |
Q9NW75 | GPATCH2 | S146 | ochoa | G patch domain-containing protein 2 | Enhances the ATPase activity of DHX15 in vitro. {ECO:0000269|PubMed:19432882}. |
Q9NWB6 | ARGLU1 | S56 | ochoa | Arginine and glutamate-rich protein 1 | Dual function regulator of gene expression; regulator of transcription and modulator of alternative splicing (PubMed:30698747). General coactivator of nuclear receptor-induced gene expression, including genes activated by the glucocorticoid receptor NR3C1 (PubMed:30698747). Binds to a subset of pre-mRNAs and to components of the spliceosome machinery to directly modulate basal alternative splicing; involved in simple and complex cassette exon splicing events (PubMed:30698747). Binds its own pre-mRNA and regulates its alternative splicing and degradation; one of the alternatively spliced products is a stable intronic sequence RNA (sisRNA) that binds the protein to regulate its ability to affect splicing (PubMed:27899669, PubMed:36533631). Binding of the sisRNA stimulates phase separation and localization to nuclear speckles, which may contribute to activation of nuclear receptor-induced gene expression (PubMed:36533631). May also indirectly modulate alternative splicing (PubMed:30698747). Regulates transcription of genes involved in heart development, neuronal cell function, protein localization and chromatin localization (By similarity). Regulates splicing of genes involved in neurogenesis and chromatin organization (By similarity). Essential for central nervous system development (By similarity). Required for the estrogen-dependent expression of ESR1 target genes (PubMed:21454576). Can act in cooperation with MED1 (PubMed:21454576). {ECO:0000250|UniProtKB:Q3UL36, ECO:0000269|PubMed:21454576, ECO:0000269|PubMed:27899669, ECO:0000269|PubMed:30698747, ECO:0000269|PubMed:36533631}. |
Q9NWB6 | ARGLU1 | S58 | ochoa | Arginine and glutamate-rich protein 1 | Dual function regulator of gene expression; regulator of transcription and modulator of alternative splicing (PubMed:30698747). General coactivator of nuclear receptor-induced gene expression, including genes activated by the glucocorticoid receptor NR3C1 (PubMed:30698747). Binds to a subset of pre-mRNAs and to components of the spliceosome machinery to directly modulate basal alternative splicing; involved in simple and complex cassette exon splicing events (PubMed:30698747). Binds its own pre-mRNA and regulates its alternative splicing and degradation; one of the alternatively spliced products is a stable intronic sequence RNA (sisRNA) that binds the protein to regulate its ability to affect splicing (PubMed:27899669, PubMed:36533631). Binding of the sisRNA stimulates phase separation and localization to nuclear speckles, which may contribute to activation of nuclear receptor-induced gene expression (PubMed:36533631). May also indirectly modulate alternative splicing (PubMed:30698747). Regulates transcription of genes involved in heart development, neuronal cell function, protein localization and chromatin localization (By similarity). Regulates splicing of genes involved in neurogenesis and chromatin organization (By similarity). Essential for central nervous system development (By similarity). Required for the estrogen-dependent expression of ESR1 target genes (PubMed:21454576). Can act in cooperation with MED1 (PubMed:21454576). {ECO:0000250|UniProtKB:Q3UL36, ECO:0000269|PubMed:21454576, ECO:0000269|PubMed:27899669, ECO:0000269|PubMed:30698747, ECO:0000269|PubMed:36533631}. |
Q9NWB6 | ARGLU1 | S60 | ochoa | Arginine and glutamate-rich protein 1 | Dual function regulator of gene expression; regulator of transcription and modulator of alternative splicing (PubMed:30698747). General coactivator of nuclear receptor-induced gene expression, including genes activated by the glucocorticoid receptor NR3C1 (PubMed:30698747). Binds to a subset of pre-mRNAs and to components of the spliceosome machinery to directly modulate basal alternative splicing; involved in simple and complex cassette exon splicing events (PubMed:30698747). Binds its own pre-mRNA and regulates its alternative splicing and degradation; one of the alternatively spliced products is a stable intronic sequence RNA (sisRNA) that binds the protein to regulate its ability to affect splicing (PubMed:27899669, PubMed:36533631). Binding of the sisRNA stimulates phase separation and localization to nuclear speckles, which may contribute to activation of nuclear receptor-induced gene expression (PubMed:36533631). May also indirectly modulate alternative splicing (PubMed:30698747). Regulates transcription of genes involved in heart development, neuronal cell function, protein localization and chromatin localization (By similarity). Regulates splicing of genes involved in neurogenesis and chromatin organization (By similarity). Essential for central nervous system development (By similarity). Required for the estrogen-dependent expression of ESR1 target genes (PubMed:21454576). Can act in cooperation with MED1 (PubMed:21454576). {ECO:0000250|UniProtKB:Q3UL36, ECO:0000269|PubMed:21454576, ECO:0000269|PubMed:27899669, ECO:0000269|PubMed:30698747, ECO:0000269|PubMed:36533631}. |
Q9NYF3 | FAM53C | S271 | ochoa | Protein FAM53C | None |
Q9NYJ8 | TAB2 | S580 | ochoa | TGF-beta-activated kinase 1 and MAP3K7-binding protein 2 (Mitogen-activated protein kinase kinase kinase 7-interacting protein 2) (TAK1-binding protein 2) (TAB-2) (TGF-beta-activated kinase 1-binding protein 2) | Adapter required to activate the JNK and NF-kappa-B signaling pathways through the specific recognition of 'Lys-63'-linked polyubiquitin chains by its RanBP2-type zinc finger (NZF) (PubMed:10882101, PubMed:11460167, PubMed:15327770, PubMed:22158122, PubMed:27746020, PubMed:33184450, PubMed:36681779). Acts as an adapter linking MAP3K7/TAK1 and TRAF6 to 'Lys-63'-linked polyubiquitin chains (PubMed:10882101, PubMed:11460167, PubMed:15327770, PubMed:22158122, PubMed:27746020). The RanBP2-type zinc finger (NZF) specifically recognizes Lys-63'-linked polyubiquitin chains unanchored or anchored to the substrate proteins such as RIPK1/RIP1 and RIPK2: this acts as a scaffold to organize a large signaling complex to promote autophosphorylation of MAP3K7/TAK1, and subsequent activation of I-kappa-B-kinase (IKK) core complex by MAP3K7/TAK1 (PubMed:15327770, PubMed:18079694, PubMed:22158122). Also recognizes and binds Lys-63'-linked polyubiquitin chains of heterotypic 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains (PubMed:27746020). Regulates the IL1-mediated translocation of NCOR1 out of the nucleus (By similarity). Involved in heart development (PubMed:20493459). {ECO:0000250|UniProtKB:Q99K90, ECO:0000269|PubMed:10882101, ECO:0000269|PubMed:11460167, ECO:0000269|PubMed:15327770, ECO:0000269|PubMed:18079694, ECO:0000269|PubMed:20493459, ECO:0000269|PubMed:22158122, ECO:0000269|PubMed:27746020, ECO:0000269|PubMed:33184450, ECO:0000269|PubMed:36681779}. |
Q9NZM1 | MYOF | S727 | ochoa | Myoferlin (Fer-1-like protein 3) | Calcium/phospholipid-binding protein that plays a role in the plasmalemma repair mechanism of endothelial cells that permits rapid resealing of membranes disrupted by mechanical stress. Involved in endocytic recycling. Implicated in VEGF signal transduction by regulating the levels of the receptor KDR (By similarity). {ECO:0000250}. |
Q9P1Y6 | PHRF1 | S1032 | ochoa | PHD and RING finger domain-containing protein 1 | None |
Q9P1Y6 | PHRF1 | S1091 | ochoa | PHD and RING finger domain-containing protein 1 | None |
Q9P1Y6 | PHRF1 | S1093 | ochoa | PHD and RING finger domain-containing protein 1 | None |
Q9P1Y6 | PHRF1 | S1127 | ochoa | PHD and RING finger domain-containing protein 1 | None |
Q9P1Y6 | PHRF1 | S1165 | ochoa | PHD and RING finger domain-containing protein 1 | None |
Q9UBK2 | PPARGC1A | S571 | psp | Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1-alpha) (PPAR-gamma coactivator 1-alpha) (PPARGC-1-alpha) (Ligand effect modulator 6) | Transcriptional coactivator for steroid receptors and nuclear receptors (PubMed:10713165, PubMed:20005308, PubMed:21376232, PubMed:28363985, PubMed:32433991). Greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter (PubMed:10713165, PubMed:20005308, PubMed:21376232). Can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis (PubMed:10713165, PubMed:20005308, PubMed:21376232). Plays an essential role in metabolic reprogramming in response to dietary availability through coordination of the expression of a wide array of genes involved in glucose and fatty acid metabolism (PubMed:10713165, PubMed:20005308, PubMed:21376232). Acts as a key regulator of gluconeogenesis: stimulates hepatic gluconeogenesis by increasing the expression of gluconeogenic enzymes, and acting together with FOXO1 to promote the fasting gluconeogenic program (PubMed:16753578, PubMed:23142079). Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner (PubMed:23836911). Also involved in the integration of the circadian rhythms and energy metabolism (By similarity). Required for oscillatory expression of clock genes, such as BMAL1 and NR1D1, through the coactivation of RORA and RORC, and metabolic genes, such as PDK4 and PEPCK (By similarity). {ECO:0000250|UniProtKB:O70343, ECO:0000269|PubMed:10713165, ECO:0000269|PubMed:16753578, ECO:0000269|PubMed:20005308, ECO:0000269|PubMed:21376232, ECO:0000269|PubMed:23142079, ECO:0000269|PubMed:23836911, ECO:0000269|PubMed:28363985, ECO:0000269|PubMed:32433991}. |
Q9UBL0 | ARPP21 | S278 | ochoa | cAMP-regulated phosphoprotein 21 (ARPP-21) (Thymocyte cAMP-regulated phosphoprotein) | Isoform 2 may act as a competitive inhibitor of calmodulin-dependent enzymes such as calcineurin in neurons. {ECO:0000250}. |
Q9UKJ3 | GPATCH8 | S1028 | ochoa | G patch domain-containing protein 8 | None |
Q9UKJ3 | GPATCH8 | S1033 | ochoa | G patch domain-containing protein 8 | None |
Q9UKV3 | ACIN1 | S1161 | ochoa | Apoptotic chromatin condensation inducer in the nucleus (Acinus) | Auxiliary component of the splicing-dependent multiprotein exon junction complex (EJC) deposited at splice junction on mRNAs. The EJC is a dynamic structure consisting of core proteins and several peripheral nuclear and cytoplasmic associated factors that join the complex only transiently either during EJC assembly or during subsequent mRNA metabolism. Component of the ASAP complexes which bind RNA in a sequence-independent manner and are proposed to be recruited to the EJC prior to or during the splicing process and to regulate specific excision of introns in specific transcription subsets; ACIN1 confers RNA-binding to the complex. The ASAP complex can inhibit RNA processing during in vitro splicing reactions. The ASAP complex promotes apoptosis and is disassembled after induction of apoptosis. Involved in the splicing modulation of BCL2L1/Bcl-X (and probably other apoptotic genes); specifically inhibits formation of proapoptotic isoforms such as Bcl-X(S); the activity is different from the established EJC assembly and function. Induces apoptotic chromatin condensation after activation by CASP3. Regulates cyclin A1, but not cyclin A2, expression in leukemia cells. {ECO:0000269|PubMed:10490026, ECO:0000269|PubMed:12665594, ECO:0000269|PubMed:18559500, ECO:0000269|PubMed:22203037, ECO:0000269|PubMed:22388736}. |
Q9UPA5 | BSN | S1090 | ochoa | Protein bassoon (Zinc finger protein 231) | Scaffold protein of the presynaptic cytomatrix at the active zone (CAZ) which is the place in the synapse where neurotransmitter is released (PubMed:12812759). After synthesis, participates in the formation of Golgi-derived membranous organelles termed Piccolo-Bassoon transport vesicles (PTVs) that are transported along axons to sites of nascent synaptic contacts (PubMed:19380881). At the presynaptic active zone, regulates the spatial organization of synaptic vesicle cluster, the protein complexes that execute membrane fusion and compensatory endocytosis (By similarity). Also functions in processes other than assembly such as the regulation of specific presynaptic protein ubiquitination by interacting with SIAH1 or the regulation of presynaptic autophagy by associating with ATG5 (By similarity). Also mediates synapse to nucleus communication leading to reconfiguration of gene expression by associating with the transcriptional corepressor CTBP1 and by subsequently reducing the size of its pool available for nuclear import (By similarity). Inhibits the activity of the proportion of DAO enzyme that localizes to the presynaptic active zone, which may modulate synaptic transmission (By similarity). {ECO:0000250|UniProtKB:O35078, ECO:0000250|UniProtKB:O88778, ECO:0000269|PubMed:12812759, ECO:0000269|PubMed:19380881}. |
Q9UQ35 | SRRM2 | S142 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S248 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S484 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S486 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9UQ35 | SRRM2 | S534 | ochoa | Serine/arginine repetitive matrix protein 2 (300 kDa nuclear matrix antigen) (Serine/arginine-rich splicing factor-related nuclear matrix protein of 300 kDa) (SR-related nuclear matrix protein of 300 kDa) (Ser/Arg-related nuclear matrix protein of 300 kDa) (Splicing coactivator subunit SRm300) (Tax-responsive enhancer element-binding protein 803) (TaxREB803) | Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:19854871, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q9Y2H9 | MAST1 | S161 | ochoa | Microtubule-associated serine/threonine-protein kinase 1 (EC 2.7.11.1) (Syntrophin-associated serine/threonine-protein kinase) | Microtubule-associated protein essential for correct brain development (PubMed:30449657). Appears to link the dystrophin/utrophin network with microtubule filaments via the syntrophins. Phosphorylation of DMD or UTRN may modulate their affinities for associated proteins (By similarity). {ECO:0000250|UniProtKB:Q9R1L5, ECO:0000269|PubMed:30449657}. |
Q9Y2L6 | FRMD4B | S675 | ochoa | FERM domain-containing protein 4B (GRP1-binding protein GRSP1) | Member of GRP1 signaling complexes that are acutely recruited to plasma membrane ruffles in response to insulin receptor signaling. May function as a scaffolding protein that regulates epithelial cell polarity by connecting ARF6 activation with the PAR3 complex. Plays a redundant role with FRMD4A in epithelial polarization. {ECO:0000250|UniProtKB:Q920B0}. |
Q9Y383 | LUC7L2 | S370 | ochoa | Putative RNA-binding protein Luc7-like 2 | May bind to RNA via its Arg/Ser-rich domain. |
Q9Y3X0 | CCDC9 | S202 | ochoa | Coiled-coil domain-containing protein 9 | Probable component of the exon junction complex (EJC), a multiprotein complex that associates immediately upstream of the exon-exon junction on mRNAs and serves as a positional landmark for the intron exon structure of genes and directs post-transcriptional processes in the cytoplasm such as mRNA export, nonsense-mediated mRNA decay (NMD) or translation. {ECO:0000305|PubMed:33973408}. |
Q9Y520 | PRRC2C | S1542 | ochoa | Protein PRRC2C (BAT2 domain-containing protein 1) (HBV X-transactivated gene 2 protein) (HBV XAg-transactivated protein 2) (HLA-B-associated transcript 2-like 2) (Proline-rich and coiled-coil-containing protein 2C) | Required for efficient formation of stress granules. {ECO:0000269|PubMed:29395067}. |
Q9Y5Y4 | PTGDR2 | S350 | ochoa | Prostaglandin D2 receptor 2 (Chemoattractant receptor-homologous molecule expressed on Th2 cells) (G-protein coupled receptor 44) (CD antigen CD294) | Receptor for prostaglandin D2 (PGD2). Coupled to the G(i)-protein. Receptor activation may result in pertussis toxin-sensitive decreases in cAMP levels and Ca(2+) mobilization. PI3K signaling is also implicated in mediating PTGDR2 effects. PGD2 induced receptor internalization. CRTH2 internalization can be regulated by diverse kinases such as, PKC, PKA, GRK2, GPRK5/GRK5 and GRK6. Receptor activation is responsible, at least in part, in immune regulation and allergic/inflammation responses. {ECO:0000269|PubMed:11208866, ECO:0000269|PubMed:11535533, ECO:0000269|PubMed:17196174}. |
Q14152 | EIF3A | S1256 | Sugiyama | Eukaryotic translation initiation factor 3 subunit A (eIF3a) (Eukaryotic translation initiation factor 3 subunit 10) (eIF-3-theta) (eIF3 p167) (eIF3 p180) (eIF3 p185) | RNA-binding 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). 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:11169732, 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, PubMed:27462815). {ECO:0000255|HAMAP-Rule:MF_03000, ECO:0000269|PubMed:11169732, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815}.; FUNCTION: (Microbial infection) Essential for the initiation of translation on type-1 viral ribosomal entry sites (IRESs), like for HCV, PV, EV71 or BEV translation (PubMed:23766293, PubMed:24357634). {ECO:0000269|PubMed:23766293, ECO:0000269|PubMed:24357634}.; 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}. |
Q14152 | EIF3A | S1258 | Sugiyama | Eukaryotic translation initiation factor 3 subunit A (eIF3a) (Eukaryotic translation initiation factor 3 subunit 10) (eIF-3-theta) (eIF3 p167) (eIF3 p180) (eIF3 p185) | RNA-binding 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). 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:11169732, 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, PubMed:27462815). {ECO:0000255|HAMAP-Rule:MF_03000, ECO:0000269|PubMed:11169732, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815}.; FUNCTION: (Microbial infection) Essential for the initiation of translation on type-1 viral ribosomal entry sites (IRESs), like for HCV, PV, EV71 or BEV translation (PubMed:23766293, PubMed:24357634). {ECO:0000269|PubMed:23766293, ECO:0000269|PubMed:24357634}.; 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}. |
Q92785 | DPF2 | S68 | Sugiyama | Zinc finger protein ubi-d4 (Apoptosis response zinc finger protein) (BRG1-associated factor 45D) (BAF45D) (D4, zinc and double PHD fingers family 2) (Protein requiem) | Plays an active role in transcriptional regulation by binding modified histones H3 and H4 (PubMed:27775714, PubMed:28533407). Is a negative regulator of myeloid differentiation of hematopoietic progenitor cells (PubMed:28533407). Might also have a role in the development and maturation of lymphoid cells (By similarity). Involved in the regulation of non-canonical NF-kappa-B pathway (PubMed:20460684). {ECO:0000250|UniProtKB:Q61103, ECO:0000269|PubMed:20460684, ECO:0000269|PubMed:27775714, ECO:0000269|PubMed:28533407}. |
P51957 | NEK4 | S531 | Sugiyama | Serine/threonine-protein kinase Nek4 (EC 2.7.11.1) (Never in mitosis A-related kinase 4) (NimA-related protein kinase 4) (Serine/threonine-protein kinase 2) (Serine/threonine-protein kinase NRK2) | Protein kinase that seems to act exclusively upon threonine residues (By similarity). Required for normal entry into proliferative arrest after a limited number of cell divisions, also called replicative senescence. Required for normal cell cycle arrest in response to double-stranded DNA damage. {ECO:0000250|UniProtKB:Q9Z1J2, ECO:0000269|PubMed:22851694}. |
Q14C86 | GAPVD1 | S900 | Sugiyama | GTPase-activating protein and VPS9 domain-containing protein 1 (GAPex-5) (Rab5-activating protein 6) | Acts both as a GTPase-activating protein (GAP) and a guanine nucleotide exchange factor (GEF), and participates in various processes such as endocytosis, insulin receptor internalization or LC2A4/GLUT4 trafficking. Acts as a GEF for the Ras-related protein RAB31 by exchanging bound GDP for free GTP, leading to regulate LC2A4/GLUT4 trafficking. In the absence of insulin, it maintains RAB31 in an active state and promotes a futile cycle between LC2A4/GLUT4 storage vesicles and early endosomes, retaining LC2A4/GLUT4 inside the cells. Upon insulin stimulation, it is translocated to the plasma membrane, releasing LC2A4/GLUT4 from intracellular storage vesicles. Also involved in EGFR trafficking and degradation, possibly by promoting EGFR ubiquitination and subsequent degradation by the proteasome. Has GEF activity for Rab5 and GAP activity for Ras. {ECO:0000269|PubMed:16410077}. |
Q00975 | CACNA1B | S2120 | SIGNOR | Voltage-dependent N-type calcium channel subunit alpha-1B (Brain calcium channel III) (BIII) (Calcium channel, L type, alpha-1 polypeptide isoform 5) (Voltage-gated calcium channel subunit alpha Cav2.2) | Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. This alpha-1B subunit gives rise to N-type calcium currents. N-type calcium channels belong to the 'high-voltage activated' (HVA) group. They are involved in pain signaling (PubMed:25296916). Calcium channels containing alpha-1B subunit may play a role in directed migration of immature neurons. Mediates Ca(2+) release probability at hippocampal neuronal soma and synaptic terminals (By similarity). {ECO:0000250|UniProtKB:Q02294, ECO:0000269|PubMed:25296916}.; FUNCTION: [Isoform Alpha-1B-1]: Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. This alpha-1B subunit gives rise to N-type calcium currents. {ECO:0000269|PubMed:1321501}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-72163 | mRNA Splicing - Major Pathway | 6.883383e-14 | 13.162 |
R-HSA-72172 | mRNA Splicing | 1.655343e-13 | 12.781 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 2.876588e-13 | 12.541 |
R-HSA-8953854 | Metabolism of RNA | 2.884913e-08 | 7.540 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 3.035937e-06 | 5.518 |
R-HSA-72187 | mRNA 3'-end processing | 2.039197e-04 | 3.691 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 1.256971e-03 | 2.901 |
R-HSA-75067 | Processing of Capped Intronless Pre-mRNA | 2.441168e-03 | 2.612 |
R-HSA-77588 | SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 4.324143e-03 | 2.364 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 4.715749e-03 | 2.326 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 5.851853e-03 | 2.233 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 7.192494e-03 | 2.143 |
R-HSA-5467333 | APC truncation mutants are not K63 polyubiquitinated | 8.718179e-03 | 2.060 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 8.891463e-03 | 2.051 |
R-HSA-165159 | MTOR signalling | 9.958528e-03 | 2.002 |
R-HSA-75153 | Apoptotic execution phase | 1.223296e-02 | 1.912 |
R-HSA-5368598 | Negative regulation of TCF-dependent signaling by DVL-interacting proteins | 4.284263e-02 | 1.368 |
R-HSA-392023 | Adrenaline signalling through Alpha-2 adrenergic receptor | 4.284263e-02 | 1.368 |
R-HSA-165181 | Inhibition of TSC complex formation by PKB | 5.118988e-02 | 1.291 |
R-HSA-9673768 | Signaling by membrane-tethered fusions of PDGFRA or PDGFRB | 5.946485e-02 | 1.226 |
R-HSA-2980767 | Activation of NIMA Kinases NEK9, NEK6, NEK7 | 7.580041e-02 | 1.120 |
R-HSA-113507 | E2F-enabled inhibition of pre-replication complex formation | 7.580041e-02 | 1.120 |
R-HSA-111367 | SLBP independent Processing of Histone Pre-mRNAs | 8.386223e-02 | 1.076 |
R-HSA-201688 | WNT mediated activation of DVL | 9.977699e-02 | 1.001 |
R-HSA-2151209 | Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 1.076311e-01 | 0.968 |
R-HSA-4839744 | Signaling by APC mutants | 1.154172e-01 | 0.938 |
R-HSA-5467340 | AXIN missense mutants destabilize the destruction complex | 1.154172e-01 | 0.938 |
R-HSA-5467348 | Truncations of AMER1 destabilize the destruction complex | 1.154172e-01 | 0.938 |
R-HSA-5467337 | APC truncation mutants have impaired AXIN binding | 1.154172e-01 | 0.938 |
R-HSA-112308 | Presynaptic depolarization and calcium channel opening | 1.154172e-01 | 0.938 |
R-HSA-429947 | Deadenylation of mRNA | 2.887604e-02 | 1.539 |
R-HSA-5339716 | Signaling by GSK3beta mutants | 1.231358e-01 | 0.910 |
R-HSA-4839743 | Signaling by CTNNB1 phospho-site mutants | 1.307876e-01 | 0.883 |
R-HSA-5358752 | CTNNB1 T41 mutants aren't phosphorylated | 1.307876e-01 | 0.883 |
R-HSA-5358747 | CTNNB1 S33 mutants aren't phosphorylated | 1.307876e-01 | 0.883 |
R-HSA-5358751 | CTNNB1 S45 mutants aren't phosphorylated | 1.307876e-01 | 0.883 |
R-HSA-5358749 | CTNNB1 S37 mutants aren't phosphorylated | 1.307876e-01 | 0.883 |
R-HSA-2173791 | TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 1.533473e-01 | 0.814 |
R-HSA-196299 | Beta-catenin phosphorylation cascade | 1.533473e-01 | 0.814 |
R-HSA-390522 | Striated Muscle Contraction | 4.853180e-02 | 1.314 |
R-HSA-72649 | Translation initiation complex formation | 1.760809e-02 | 1.754 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 1.912650e-02 | 1.718 |
R-HSA-167242 | Abortive elongation of HIV-1 transcript in the absence of Tat | 1.896621e-01 | 0.722 |
R-HSA-9934037 | Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | 1.967373e-01 | 0.706 |
R-HSA-72165 | mRNA Splicing - Minor Pathway | 8.181797e-02 | 1.087 |
R-HSA-167243 | Tat-mediated HIV elongation arrest and recovery | 2.511742e-01 | 0.600 |
R-HSA-167238 | Pausing and recovery of Tat-mediated HIV elongation | 2.511742e-01 | 0.600 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 1.201125e-01 | 0.920 |
R-HSA-167287 | HIV elongation arrest and recovery | 2.577159e-01 | 0.589 |
R-HSA-167290 | Pausing and recovery of HIV elongation | 2.577159e-01 | 0.589 |
R-HSA-5083635 | Defective B3GALTL causes PpS | 2.895831e-01 | 0.538 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 2.957917e-01 | 0.529 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 1.587683e-01 | 0.799 |
R-HSA-380287 | Centrosome maturation | 1.649085e-01 | 0.783 |
R-HSA-5173214 | O-glycosylation of TSR domain-containing proteins | 3.200916e-01 | 0.495 |
R-HSA-167152 | Formation of HIV elongation complex in the absence of HIV Tat | 3.377684e-01 | 0.471 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 2.958736e-01 | 0.529 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 2.958736e-01 | 0.529 |
R-HSA-167246 | Tat-mediated elongation of the HIV-1 transcript | 3.377684e-01 | 0.471 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 2.071527e-02 | 1.684 |
R-HSA-167200 | Formation of HIV-1 elongation complex containing HIV-1 Tat | 3.319274e-01 | 0.479 |
R-HSA-68962 | Activation of the pre-replicative complex | 2.706296e-01 | 0.568 |
R-HSA-416482 | G alpha (12/13) signalling events | 4.046232e-02 | 1.393 |
R-HSA-167169 | HIV Transcription Elongation | 3.377684e-01 | 0.471 |
R-HSA-4641262 | Disassembly of the destruction complex and recruitment of AXIN to the membrane | 3.435483e-02 | 1.464 |
R-HSA-9664420 | Killing mechanisms | 1.607373e-01 | 0.794 |
R-HSA-9673324 | WNT5:FZD7-mediated leishmania damping | 1.607373e-01 | 0.794 |
R-HSA-9843970 | Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | 3.019463e-01 | 0.520 |
R-HSA-3134973 | LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 5.946485e-02 | 1.226 |
R-HSA-77595 | Processing of Intronless Pre-mRNAs | 1.680632e-01 | 0.775 |
R-HSA-9930044 | Nuclear RNA decay | 2.895831e-01 | 0.538 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 2.861954e-01 | 0.543 |
R-HSA-9842860 | Regulation of endogenous retroelements | 7.772041e-02 | 1.109 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 2.409673e-01 | 0.618 |
R-HSA-9843745 | Adipogenesis | 1.391876e-01 | 0.856 |
R-HSA-9844594 | Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | 6.443705e-02 | 1.191 |
R-HSA-9843743 | Transcriptional regulation of brown and beige adipocyte differentiation | 6.443705e-02 | 1.191 |
R-HSA-4791275 | Signaling by WNT in cancer | 2.833203e-01 | 0.548 |
R-HSA-72737 | Cap-dependent Translation Initiation | 1.066875e-01 | 0.972 |
R-HSA-72613 | Eukaryotic Translation Initiation | 1.066875e-01 | 0.972 |
R-HSA-390651 | Dopamine receptors | 5.118988e-02 | 1.291 |
R-HSA-68689 | CDC6 association with the ORC:origin complex | 6.766815e-02 | 1.170 |
R-HSA-9014325 | TICAM1,TRAF6-dependent induction of TAK1 complex | 1.076311e-01 | 0.968 |
R-HSA-4839748 | Signaling by AMER1 mutants | 1.231358e-01 | 0.910 |
R-HSA-4839735 | Signaling by AXIN mutants | 1.231358e-01 | 0.910 |
R-HSA-937072 | TRAF6-mediated induction of TAK1 complex within TLR4 complex | 1.533473e-01 | 0.814 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 2.153608e-02 | 1.667 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 3.080475e-01 | 0.511 |
R-HSA-450408 | AUF1 (hnRNP D0) binds and destabilizes mRNA | 3.140958e-01 | 0.503 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 3.319274e-01 | 0.479 |
R-HSA-427389 | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 3.377684e-01 | 0.471 |
R-HSA-68616 | Assembly of the ORC complex at the origin of replication | 2.895831e-01 | 0.538 |
R-HSA-1839117 | Signaling by cytosolic FGFR1 fusion mutants | 1.825250e-01 | 0.739 |
R-HSA-9843940 | Regulation of endogenous retroelements by KRAB-ZFP proteins | 1.496434e-01 | 0.825 |
R-HSA-4641258 | Degradation of DVL | 3.200916e-01 | 0.495 |
R-HSA-937042 | IRAK2 mediated activation of TAK1 complex | 9.977699e-02 | 1.001 |
R-HSA-975163 | IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 1.458928e-01 | 0.836 |
R-HSA-9933937 | Formation of the canonical BAF (cBAF) complex | 1.458928e-01 | 0.836 |
R-HSA-9933946 | Formation of the embryonic stem cell BAF (esBAF) complex | 1.533473e-01 | 0.814 |
R-HSA-167158 | Formation of the HIV-1 Early Elongation Complex | 2.577159e-01 | 0.589 |
R-HSA-1358803 | Downregulation of ERBB2:ERBB3 signaling | 1.307876e-01 | 0.883 |
R-HSA-212165 | Epigenetic regulation of gene expression | 1.834795e-01 | 0.736 |
R-HSA-430039 | mRNA decay by 5' to 3' exoribonuclease | 1.680632e-01 | 0.775 |
R-HSA-450321 | JNK (c-Jun kinases) phosphorylation and activation mediated by activated human ... | 2.037511e-01 | 0.691 |
R-HSA-400042 | Adrenaline,noradrenaline inhibits insulin secretion | 2.445752e-01 | 0.612 |
R-HSA-113418 | Formation of the Early Elongation Complex | 2.577159e-01 | 0.589 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 8.917885e-02 | 1.050 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 8.917885e-02 | 1.050 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 3.377684e-01 | 0.471 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 3.772597e-01 | 0.423 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 2.379185e-01 | 0.624 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 2.379185e-01 | 0.624 |
R-HSA-9820841 | M-decay: degradation of maternal mRNAs by maternally stored factors | 6.683528e-02 | 1.175 |
R-HSA-416572 | Sema4D induced cell migration and growth-cone collapse | 1.967373e-01 | 0.706 |
R-HSA-2995383 | Initiation of Nuclear Envelope (NE) Reformation | 2.107041e-01 | 0.676 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 2.706296e-01 | 0.568 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 3.722098e-01 | 0.429 |
R-HSA-5655302 | Signaling by FGFR1 in disease | 3.492987e-01 | 0.457 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 2.606284e-01 | 0.584 |
R-HSA-9854907 | Regulation of MITF-M dependent genes involved in metabolism | 4.284263e-02 | 1.368 |
R-HSA-428890 | Role of ABL in ROBO-SLIT signaling | 8.386223e-02 | 1.076 |
R-HSA-166208 | mTORC1-mediated signalling | 2.543958e-02 | 1.594 |
R-HSA-68884 | Mitotic Telophase/Cytokinesis | 1.231358e-01 | 0.910 |
R-HSA-9634600 | Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 1.607373e-01 | 0.794 |
R-HSA-113510 | E2F mediated regulation of DNA replication | 1.896621e-01 | 0.722 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 3.717646e-01 | 0.430 |
R-HSA-774815 | Nucleosome assembly | 3.717646e-01 | 0.430 |
R-HSA-1839124 | FGFR1 mutant receptor activation | 2.895831e-01 | 0.538 |
R-HSA-9662834 | CD163 mediating an anti-inflammatory response | 1.154172e-01 | 0.938 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 2.706296e-01 | 0.568 |
R-HSA-176187 | Activation of ATR in response to replication stress | 2.895831e-01 | 0.538 |
R-HSA-168638 | NOD1/2 Signaling Pathway | 3.019463e-01 | 0.520 |
R-HSA-8863795 | Downregulation of ERBB2 signaling | 2.706296e-01 | 0.568 |
R-HSA-9645460 | Alpha-protein kinase 1 signaling pathway | 1.154172e-01 | 0.938 |
R-HSA-5620916 | VxPx cargo-targeting to cilium | 1.967373e-01 | 0.706 |
R-HSA-450302 | activated TAK1 mediates p38 MAPK activation | 2.107041e-01 | 0.676 |
R-HSA-5357956 | TNFR1-induced NF-kappa-B signaling pathway | 2.511742e-01 | 0.600 |
R-HSA-70221 | Glycogen breakdown (glycogenolysis) | 2.379185e-01 | 0.624 |
R-HSA-456926 | Thrombin signalling through proteinase activated receptors (PARs) | 2.706296e-01 | 0.568 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 2.025115e-01 | 0.694 |
R-HSA-1251985 | Nuclear signaling by ERBB4 | 3.377684e-01 | 0.471 |
R-HSA-9824585 | Regulation of MITF-M-dependent genes involved in pigmentation | 3.717646e-01 | 0.430 |
R-HSA-390696 | Adrenoceptors | 9.185423e-02 | 1.037 |
R-HSA-4641263 | Regulation of FZD by ubiquitination | 1.753256e-01 | 0.756 |
R-HSA-73762 | RNA Polymerase I Transcription Initiation | 3.549889e-01 | 0.450 |
R-HSA-69481 | G2/M Checkpoints | 3.533739e-01 | 0.452 |
R-HSA-69206 | G1/S Transition | 3.470517e-01 | 0.460 |
R-HSA-6794361 | Neurexins and neuroligins | 9.771623e-02 | 1.010 |
R-HSA-400685 | Sema4D in semaphorin signaling | 2.379185e-01 | 0.624 |
R-HSA-9615017 | FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 3.492987e-01 | 0.457 |
R-HSA-193648 | NRAGE signals death through JNK | 1.087583e-01 | 0.964 |
R-HSA-3295583 | TRP channels | 2.445752e-01 | 0.612 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 3.200916e-01 | 0.495 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 3.375316e-01 | 0.472 |
R-HSA-69278 | Cell Cycle, Mitotic | 2.561019e-01 | 0.592 |
R-HSA-70635 | Urea cycle | 2.445752e-01 | 0.612 |
R-HSA-420092 | Glucagon-type ligand receptors | 2.642009e-01 | 0.578 |
R-HSA-5689880 | Ub-specific processing proteases | 2.373082e-01 | 0.625 |
R-HSA-445989 | TAK1-dependent IKK and NF-kappa-B activation | 3.827071e-01 | 0.417 |
R-HSA-1640170 | Cell Cycle | 1.903576e-01 | 0.720 |
R-HSA-391908 | Prostanoid ligand receptors | 1.154172e-01 | 0.938 |
R-HSA-198323 | AKT phosphorylates targets in the cytosol | 1.307876e-01 | 0.883 |
R-HSA-375280 | Amine ligand-binding receptors | 7.671519e-02 | 1.115 |
R-HSA-264870 | Caspase-mediated cleavage of cytoskeletal proteins | 9.977699e-02 | 1.001 |
R-HSA-446353 | Cell-extracellular matrix interactions | 1.533473e-01 | 0.814 |
R-HSA-6807062 | Cholesterol biosynthesis via lathosterol | 2.175968e-01 | 0.662 |
R-HSA-6794362 | Protein-protein interactions at synapses | 1.961690e-01 | 0.707 |
R-HSA-3214841 | PKMTs methylate histone lysines | 3.435587e-01 | 0.464 |
R-HSA-9007101 | Rab regulation of trafficking | 3.183752e-01 | 0.497 |
R-HSA-6807004 | Negative regulation of MET activity | 1.967373e-01 | 0.706 |
R-HSA-9671555 | Signaling by PDGFR in disease | 2.107041e-01 | 0.676 |
R-HSA-8982491 | Glycogen metabolism | 3.377684e-01 | 0.471 |
R-HSA-5688426 | Deubiquitination | 2.218589e-01 | 0.654 |
R-HSA-373753 | Nephrin family interactions | 1.967373e-01 | 0.706 |
R-HSA-69205 | G1/S-Specific Transcription | 5.515200e-02 | 1.258 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 2.895831e-01 | 0.538 |
R-HSA-6804758 | Regulation of TP53 Activity through Acetylation | 2.895831e-01 | 0.538 |
R-HSA-5689896 | Ovarian tumor domain proteases | 3.200916e-01 | 0.495 |
R-HSA-8854214 | TBC/RABGAPs | 3.606296e-01 | 0.443 |
R-HSA-74160 | Gene expression (Transcription) | 3.803011e-01 | 0.420 |
R-HSA-391903 | Eicosanoid ligand-binding receptors | 1.967373e-01 | 0.706 |
R-HSA-191273 | Cholesterol biosynthesis | 1.741956e-01 | 0.759 |
R-HSA-1169408 | ISG15 antiviral mechanism | 1.649085e-01 | 0.783 |
R-HSA-9018519 | Estrogen-dependent gene expression | 4.632636e-02 | 1.334 |
R-HSA-264876 | Insulin processing | 2.511742e-01 | 0.600 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 1.587683e-01 | 0.799 |
R-HSA-5674400 | Constitutive Signaling by AKT1 E17K in Cancer | 2.244298e-01 | 0.649 |
R-HSA-376176 | Signaling by ROBO receptors | 3.080223e-01 | 0.511 |
R-HSA-76009 | Platelet Aggregation (Plug Formation) | 3.717646e-01 | 0.430 |
R-HSA-8939211 | ESR-mediated signaling | 1.894154e-01 | 0.723 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 2.540539e-01 | 0.595 |
R-HSA-5683826 | Surfactant metabolism | 3.662214e-01 | 0.436 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 3.080475e-01 | 0.511 |
R-HSA-109581 | Apoptosis | 2.098679e-01 | 0.678 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 2.506489e-01 | 0.601 |
R-HSA-73887 | Death Receptor Signaling | 1.920026e-01 | 0.717 |
R-HSA-5357801 | Programmed Cell Death | 3.151776e-01 | 0.501 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 3.881071e-01 | 0.411 |
R-HSA-68949 | Orc1 removal from chromatin | 4.092422e-01 | 0.388 |
R-HSA-112382 | Formation of RNA Pol II elongation complex | 4.092422e-01 | 0.388 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 4.092422e-01 | 0.388 |
R-HSA-75955 | RNA Polymerase II Transcription Elongation | 4.144117e-01 | 0.383 |
R-HSA-4839726 | Chromatin organization | 4.193819e-01 | 0.377 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 4.212944e-01 | 0.375 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 4.246164e-01 | 0.372 |
R-HSA-3214815 | HDACs deacetylate histones | 4.246164e-01 | 0.372 |
R-HSA-418597 | G alpha (z) signalling events | 4.246164e-01 | 0.372 |
R-HSA-75893 | TNF signaling | 4.296523e-01 | 0.367 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 4.324030e-01 | 0.364 |
R-HSA-9856651 | MITF-M-dependent gene expression | 4.332663e-01 | 0.363 |
R-HSA-73857 | RNA Polymerase II Transcription | 4.336193e-01 | 0.363 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 4.346444e-01 | 0.362 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 4.392031e-01 | 0.357 |
R-HSA-69620 | Cell Cycle Checkpoints | 4.401821e-01 | 0.356 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 4.444989e-01 | 0.352 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 4.451063e-01 | 0.352 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 4.451063e-01 | 0.352 |
R-HSA-983189 | Kinesins | 4.493620e-01 | 0.347 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 4.493620e-01 | 0.347 |
R-HSA-1227986 | Signaling by ERBB2 | 4.493620e-01 | 0.347 |
R-HSA-8939902 | Regulation of RUNX2 expression and activity | 4.541829e-01 | 0.343 |
R-HSA-450294 | MAP kinase activation | 4.541829e-01 | 0.343 |
R-HSA-9707616 | Heme signaling | 4.589618e-01 | 0.338 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 4.636991e-01 | 0.334 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 4.636991e-01 | 0.334 |
R-HSA-373755 | Semaphorin interactions | 4.636991e-01 | 0.334 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 4.636991e-01 | 0.334 |
R-HSA-168643 | Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signali... | 4.683953e-01 | 0.329 |
R-HSA-68886 | M Phase | 4.709900e-01 | 0.327 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 4.730507e-01 | 0.325 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 4.764358e-01 | 0.322 |
R-HSA-8854518 | AURKA Activation by TPX2 | 4.776655e-01 | 0.321 |
R-HSA-5693606 | DNA Double Strand Break Response | 4.822403e-01 | 0.317 |
R-HSA-167172 | Transcription of the HIV genome | 4.867752e-01 | 0.313 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 4.867752e-01 | 0.313 |
R-HSA-195253 | Degradation of beta-catenin by the destruction complex | 4.957272e-01 | 0.305 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 4.957272e-01 | 0.305 |
R-HSA-448424 | Interleukin-17 signaling | 4.957272e-01 | 0.305 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 5.001448e-01 | 0.301 |
R-HSA-3906995 | Diseases associated with O-glycosylation of proteins | 5.001448e-01 | 0.301 |
R-HSA-5620920 | Cargo trafficking to the periciliary membrane | 5.001448e-01 | 0.301 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 5.045240e-01 | 0.297 |
R-HSA-372790 | Signaling by GPCR | 5.054771e-01 | 0.296 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 5.063220e-01 | 0.296 |
R-HSA-69052 | Switching of origins to a post-replicative state | 5.088651e-01 | 0.293 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 5.088651e-01 | 0.293 |
R-HSA-674695 | RNA Polymerase II Pre-transcription Events | 5.131685e-01 | 0.290 |
R-HSA-69473 | G2/M DNA damage checkpoint | 5.131685e-01 | 0.290 |
R-HSA-1236394 | Signaling by ERBB4 | 5.131685e-01 | 0.290 |
R-HSA-1226099 | Signaling by FGFR in disease | 5.131685e-01 | 0.290 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 5.216632e-01 | 0.283 |
R-HSA-195721 | Signaling by WNT | 5.287052e-01 | 0.277 |
R-HSA-4086400 | PCP/CE pathway | 5.300107e-01 | 0.276 |
R-HSA-73864 | RNA Polymerase I Transcription | 5.300107e-01 | 0.276 |
R-HSA-9659379 | Sensory processing of sound | 5.341301e-01 | 0.272 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 5.341301e-01 | 0.272 |
R-HSA-69275 | G2/M Transition | 5.371948e-01 | 0.270 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 5.382136e-01 | 0.269 |
R-HSA-6806834 | Signaling by MET | 5.382136e-01 | 0.269 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 5.422615e-01 | 0.266 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 5.422615e-01 | 0.266 |
R-HSA-453274 | Mitotic G2-G2/M phases | 5.424331e-01 | 0.266 |
R-HSA-5617833 | Cilium Assembly | 5.476306e-01 | 0.262 |
R-HSA-388396 | GPCR downstream signalling | 5.481364e-01 | 0.261 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 5.541952e-01 | 0.256 |
R-HSA-68877 | Mitotic Prometaphase | 5.553500e-01 | 0.255 |
R-HSA-6802957 | Oncogenic MAPK signaling | 5.581041e-01 | 0.253 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 5.619789e-01 | 0.250 |
R-HSA-141424 | Amplification of signal from the kinetochores | 5.619789e-01 | 0.250 |
R-HSA-8876198 | RAB GEFs exchange GTP for GDP on RABs | 5.619789e-01 | 0.250 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 5.730003e-01 | 0.242 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 5.734020e-01 | 0.242 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 5.740114e-01 | 0.241 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 5.808527e-01 | 0.236 |
R-HSA-202424 | Downstream TCR signaling | 5.808527e-01 | 0.236 |
R-HSA-373080 | Class B/2 (Secretin family receptors) | 5.808527e-01 | 0.236 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 5.845294e-01 | 0.233 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 5.881740e-01 | 0.230 |
R-HSA-68867 | Assembly of the pre-replicative complex | 5.953684e-01 | 0.225 |
R-HSA-397014 | Muscle contraction | 6.044263e-01 | 0.219 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 6.059267e-01 | 0.218 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 6.067706e-01 | 0.217 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 6.093850e-01 | 0.215 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 6.093850e-01 | 0.215 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 6.128131e-01 | 0.213 |
R-HSA-68882 | Mitotic Anaphase | 6.137407e-01 | 0.212 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 6.160432e-01 | 0.210 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 6.162114e-01 | 0.210 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 6.162114e-01 | 0.210 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 6.162114e-01 | 0.210 |
R-HSA-422356 | Regulation of insulin secretion | 6.162114e-01 | 0.210 |
R-HSA-9614085 | FOXO-mediated transcription | 6.195800e-01 | 0.208 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 6.229193e-01 | 0.206 |
R-HSA-70171 | Glycolysis | 6.229193e-01 | 0.206 |
R-HSA-9020702 | Interleukin-1 signaling | 6.262295e-01 | 0.203 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 6.423525e-01 | 0.192 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 6.454932e-01 | 0.190 |
R-HSA-69239 | Synthesis of DNA | 6.486066e-01 | 0.188 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 6.516928e-01 | 0.186 |
R-HSA-2672351 | Stimuli-sensing channels | 6.516928e-01 | 0.186 |
R-HSA-3247509 | Chromatin modifying enzymes | 6.535959e-01 | 0.185 |
R-HSA-69002 | DNA Replication Pre-Initiation | 6.547521e-01 | 0.184 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 6.547521e-01 | 0.184 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 6.577848e-01 | 0.182 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 6.577848e-01 | 0.182 |
R-HSA-202403 | TCR signaling | 6.577848e-01 | 0.182 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 6.667248e-01 | 0.176 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 6.696530e-01 | 0.174 |
R-HSA-162582 | Signal Transduction | 6.753008e-01 | 0.171 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 6.754330e-01 | 0.170 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 6.754330e-01 | 0.170 |
R-HSA-1592230 | Mitochondrial biogenesis | 6.839151e-01 | 0.165 |
R-HSA-70326 | Glucose metabolism | 6.839151e-01 | 0.165 |
R-HSA-2980736 | Peptide hormone metabolism | 6.839151e-01 | 0.165 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 6.866933e-01 | 0.163 |
R-HSA-5693538 | Homology Directed Repair | 6.866933e-01 | 0.163 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 6.894473e-01 | 0.161 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 6.894473e-01 | 0.161 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 6.894473e-01 | 0.161 |
R-HSA-68875 | Mitotic Prophase | 6.921772e-01 | 0.160 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 6.948832e-01 | 0.158 |
R-HSA-73886 | Chromosome Maintenance | 6.948832e-01 | 0.158 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 6.975657e-01 | 0.156 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 6.975657e-01 | 0.156 |
R-HSA-2132295 | MHC class II antigen presentation | 7.002247e-01 | 0.155 |
R-HSA-199991 | Membrane Trafficking | 7.009952e-01 | 0.154 |
R-HSA-373076 | Class A/1 (Rhodopsin-like receptors) | 7.069090e-01 | 0.151 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 7.080633e-01 | 0.150 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 7.080633e-01 | 0.150 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 7.080633e-01 | 0.150 |
R-HSA-114608 | Platelet degranulation | 7.131757e-01 | 0.147 |
R-HSA-418594 | G alpha (i) signalling events | 7.264306e-01 | 0.139 |
R-HSA-9909396 | Circadian clock | 7.279854e-01 | 0.138 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 7.303788e-01 | 0.136 |
R-HSA-422475 | Axon guidance | 7.337328e-01 | 0.134 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 7.397450e-01 | 0.131 |
R-HSA-163685 | Integration of energy metabolism | 7.397450e-01 | 0.131 |
R-HSA-5173105 | O-linked glycosylation | 7.420356e-01 | 0.130 |
R-HSA-9658195 | Leishmania infection | 7.423240e-01 | 0.129 |
R-HSA-9824443 | Parasitic Infection Pathways | 7.423240e-01 | 0.129 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 7.439830e-01 | 0.128 |
R-HSA-6807070 | PTEN Regulation | 7.465570e-01 | 0.127 |
R-HSA-1632852 | Macroautophagy | 7.509996e-01 | 0.124 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 7.553649e-01 | 0.122 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 7.553649e-01 | 0.122 |
R-HSA-72766 | Translation | 7.571532e-01 | 0.121 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 7.575190e-01 | 0.121 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 7.596543e-01 | 0.119 |
R-HSA-1257604 | PIP3 activates AKT signaling | 7.647353e-01 | 0.116 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 7.680102e-01 | 0.115 |
R-HSA-69242 | S Phase | 7.680102e-01 | 0.115 |
R-HSA-9679191 | Potential therapeutics for SARS | 7.720793e-01 | 0.112 |
R-HSA-446652 | Interleukin-1 family signaling | 7.760776e-01 | 0.110 |
R-HSA-9675108 | Nervous system development | 7.775161e-01 | 0.109 |
R-HSA-69306 | DNA Replication | 7.780505e-01 | 0.109 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 7.780505e-01 | 0.109 |
R-HSA-1989781 | PPARA activates gene expression | 7.819447e-01 | 0.107 |
R-HSA-9612973 | Autophagy | 7.838663e-01 | 0.106 |
R-HSA-500792 | GPCR ligand binding | 7.851339e-01 | 0.105 |
R-HSA-162587 | HIV Life Cycle | 7.857711e-01 | 0.105 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 7.857711e-01 | 0.105 |
R-HSA-9006936 | Signaling by TGFB family members | 7.913860e-01 | 0.102 |
R-HSA-5633007 | Regulation of TP53 Activity | 7.913860e-01 | 0.102 |
R-HSA-6798695 | Neutrophil degranulation | 7.922007e-01 | 0.101 |
R-HSA-1500931 | Cell-Cell communication | 7.951967e-01 | 0.100 |
R-HSA-2467813 | Separation of Sister Chromatids | 7.986459e-01 | 0.098 |
R-HSA-112316 | Neuronal System | 8.047827e-01 | 0.094 |
R-HSA-8957322 | Metabolism of steroids | 8.058600e-01 | 0.094 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 8.107521e-01 | 0.091 |
R-HSA-418555 | G alpha (s) signalling events | 8.124215e-01 | 0.090 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 8.124215e-01 | 0.090 |
R-HSA-9662851 | Anti-inflammatory response favouring Leishmania parasite infection | 8.157166e-01 | 0.088 |
R-HSA-9664433 | Leishmania parasite growth and survival | 8.157166e-01 | 0.088 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 8.189542e-01 | 0.087 |
R-HSA-9678108 | SARS-CoV-1 Infection | 8.189542e-01 | 0.087 |
R-HSA-9006925 | Intracellular signaling by second messengers | 8.280775e-01 | 0.082 |
R-HSA-3781865 | Diseases of glycosylation | 8.328383e-01 | 0.079 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 8.386646e-01 | 0.076 |
R-HSA-983712 | Ion channel transport | 8.400894e-01 | 0.076 |
R-HSA-168898 | Toll-like Receptor Cascades | 8.429016e-01 | 0.074 |
R-HSA-5653656 | Vesicle-mediated transport | 8.562832e-01 | 0.067 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 8.587728e-01 | 0.066 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 8.713132e-01 | 0.060 |
R-HSA-913531 | Interferon Signaling | 8.713132e-01 | 0.060 |
R-HSA-9679506 | SARS-CoV Infections | 8.834680e-01 | 0.054 |
R-HSA-162906 | HIV Infection | 8.869046e-01 | 0.052 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 8.879059e-01 | 0.052 |
R-HSA-72312 | rRNA processing | 8.918237e-01 | 0.050 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 9.230056e-01 | 0.035 |
R-HSA-109582 | Hemostasis | 9.258932e-01 | 0.033 |
R-HSA-446728 | Cell junction organization | 9.281930e-01 | 0.032 |
R-HSA-112315 | Transmission across Chemical Synapses | 9.519638e-01 | 0.021 |
R-HSA-9694516 | SARS-CoV-2 Infection | 9.619406e-01 | 0.017 |
R-HSA-73894 | DNA Repair | 9.655146e-01 | 0.015 |
R-HSA-212436 | Generic Transcription Pathway | 9.705463e-01 | 0.013 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 9.764778e-01 | 0.010 |
R-HSA-5668914 | Diseases of metabolism | 9.812835e-01 | 0.008 |
R-HSA-597592 | Post-translational protein modification | 9.834380e-01 | 0.007 |
R-HSA-392499 | Metabolism of proteins | 9.853400e-01 | 0.006 |
R-HSA-1280218 | Adaptive Immune System | 9.857997e-01 | 0.006 |
R-HSA-9824446 | Viral Infection Pathways | 9.918104e-01 | 0.004 |
R-HSA-1266738 | Developmental Biology | 9.922899e-01 | 0.003 |
R-HSA-168249 | Innate Immune System | 9.932471e-01 | 0.003 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 9.966847e-01 | 0.001 |
R-HSA-449147 | Signaling by Interleukins | 9.968897e-01 | 0.001 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 9.968906e-01 | 0.001 |
R-HSA-5663205 | Infectious disease | 9.981165e-01 | 0.001 |
R-HSA-1643685 | Disease | 9.993882e-01 | 0.000 |
R-HSA-382551 | Transport of small molecules | 9.998836e-01 | 0.000 |
R-HSA-168256 | Immune System | 9.998848e-01 | 0.000 |
R-HSA-556833 | Metabolism of lipids | 9.998857e-01 | 0.000 |
R-HSA-2262752 | Cellular responses to stress | 9.999176e-01 | 0.000 |
R-HSA-8953897 | Cellular responses to stimuli | 9.999750e-01 | 0.000 |
R-HSA-9709957 | Sensory Perception | 9.999896e-01 | 0.000 |
R-HSA-1430728 | Metabolism | 1.000000e+00 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
CLK2 |
0.830 | 0.444 | -3 | 0.943 |
CLK3 |
0.826 | 0.390 | 1 | 0.804 |
RSK2 |
0.825 | 0.376 | -3 | 0.962 |
SRPK1 |
0.824 | 0.368 | -3 | 0.952 |
RSK4 |
0.819 | 0.375 | -3 | 0.936 |
PRKX |
0.819 | 0.352 | -3 | 0.888 |
RSK3 |
0.818 | 0.354 | -3 | 0.962 |
SRPK2 |
0.817 | 0.337 | -3 | 0.923 |
AURC |
0.816 | 0.312 | -2 | 0.736 |
P90RSK |
0.814 | 0.337 | -3 | 0.965 |
PKACB |
0.814 | 0.328 | -2 | 0.753 |
CLK4 |
0.813 | 0.380 | -3 | 0.958 |
PKACG |
0.812 | 0.322 | -2 | 0.812 |
NDR1 |
0.811 | 0.315 | -3 | 0.947 |
P70S6KB |
0.811 | 0.355 | -3 | 0.968 |
CLK1 |
0.811 | 0.382 | -3 | 0.948 |
PIM1 |
0.810 | 0.340 | -3 | 0.947 |
PIM3 |
0.810 | 0.294 | -3 | 0.949 |
NDR2 |
0.810 | 0.214 | -3 | 0.925 |
HIPK4 |
0.809 | 0.315 | 1 | 0.877 |
PRKD2 |
0.808 | 0.318 | -3 | 0.941 |
MSK1 |
0.808 | 0.325 | -3 | 0.951 |
SRPK3 |
0.803 | 0.307 | -3 | 0.936 |
MSK2 |
0.803 | 0.295 | -3 | 0.950 |
CDKL1 |
0.803 | 0.313 | -3 | 0.968 |
PAK1 |
0.802 | 0.275 | -2 | 0.810 |
AURB |
0.802 | 0.275 | -2 | 0.733 |
AKT2 |
0.801 | 0.336 | -3 | 0.930 |
DYRK3 |
0.801 | 0.357 | 1 | 0.808 |
DYRK2 |
0.801 | 0.279 | 1 | 0.768 |
PIM2 |
0.801 | 0.362 | -3 | 0.956 |
LATS2 |
0.800 | 0.184 | -5 | 0.677 |
CAMK1B |
0.800 | 0.321 | -3 | 0.965 |
COT |
0.800 | 0.150 | 2 | 0.591 |
DYRK4 |
0.798 | 0.285 | 1 | 0.670 |
SGK3 |
0.798 | 0.343 | -3 | 0.946 |
WNK1 |
0.798 | 0.317 | -2 | 0.849 |
PKACA |
0.798 | 0.290 | -2 | 0.714 |
CDKL5 |
0.797 | 0.252 | -3 | 0.970 |
PKN2 |
0.796 | 0.277 | -3 | 0.944 |
MNK1 |
0.796 | 0.296 | -2 | 0.830 |
CAMK1G |
0.796 | 0.341 | -3 | 0.963 |
HIPK1 |
0.796 | 0.316 | 1 | 0.783 |
PKCD |
0.795 | 0.238 | 2 | 0.489 |
HIPK2 |
0.795 | 0.257 | 1 | 0.691 |
PKCG |
0.795 | 0.274 | 2 | 0.474 |
PKN3 |
0.795 | 0.204 | -3 | 0.955 |
SKMLCK |
0.795 | 0.252 | -2 | 0.859 |
PAK3 |
0.794 | 0.248 | -2 | 0.802 |
MAPKAPK2 |
0.794 | 0.239 | -3 | 0.924 |
CAMK2A |
0.794 | 0.218 | 2 | 0.584 |
MAPKAPK3 |
0.794 | 0.258 | -3 | 0.946 |
PRKD3 |
0.794 | 0.298 | -3 | 0.951 |
MYLK4 |
0.793 | 0.298 | -2 | 0.804 |
P70S6K |
0.793 | 0.330 | -3 | 0.947 |
ICK |
0.793 | 0.259 | -3 | 0.967 |
PKG2 |
0.792 | 0.251 | -2 | 0.761 |
PAK6 |
0.792 | 0.209 | -2 | 0.737 |
NUAK2 |
0.792 | 0.271 | -3 | 0.958 |
CAMLCK |
0.792 | 0.278 | -2 | 0.860 |
PKCB |
0.791 | 0.229 | 2 | 0.462 |
SGK1 |
0.790 | 0.344 | -3 | 0.882 |
MNK2 |
0.789 | 0.244 | -2 | 0.819 |
CDC7 |
0.789 | 0.050 | 1 | 0.801 |
PKCA |
0.788 | 0.207 | 2 | 0.451 |
MTOR |
0.788 | 0.085 | 1 | 0.796 |
AKT1 |
0.787 | 0.303 | -3 | 0.933 |
AKT3 |
0.787 | 0.318 | -3 | 0.889 |
PRKD1 |
0.787 | 0.147 | -3 | 0.947 |
PAK2 |
0.787 | 0.224 | -2 | 0.797 |
NIK |
0.787 | 0.312 | -3 | 0.933 |
MST4 |
0.787 | 0.163 | 2 | 0.540 |
CAMK4 |
0.786 | 0.214 | -3 | 0.944 |
DCAMKL1 |
0.786 | 0.304 | -3 | 0.937 |
DAPK2 |
0.786 | 0.268 | -3 | 0.960 |
CAMK2B |
0.786 | 0.150 | 2 | 0.550 |
DYRK1B |
0.785 | 0.249 | 1 | 0.701 |
AMPKA1 |
0.785 | 0.223 | -3 | 0.948 |
PKCH |
0.785 | 0.227 | 2 | 0.449 |
RAF1 |
0.785 | 0.145 | 1 | 0.812 |
PKCZ |
0.785 | 0.233 | 2 | 0.481 |
AMPKA2 |
0.784 | 0.233 | -3 | 0.948 |
GCN2 |
0.784 | -0.007 | 2 | 0.529 |
HUNK |
0.784 | 0.201 | 2 | 0.579 |
MELK |
0.784 | 0.241 | -3 | 0.955 |
AURA |
0.783 | 0.163 | -2 | 0.703 |
MOS |
0.783 | 0.074 | 1 | 0.853 |
CAMK2D |
0.782 | 0.120 | -3 | 0.954 |
NLK |
0.782 | 0.102 | 1 | 0.840 |
CAMK2G |
0.782 | 0.021 | 2 | 0.553 |
CAMK1D |
0.782 | 0.298 | -3 | 0.922 |
DYRK1A |
0.782 | 0.238 | 1 | 0.768 |
RIPK1 |
0.782 | 0.241 | 1 | 0.866 |
PKCE |
0.782 | 0.278 | 2 | 0.460 |
CDK10 |
0.782 | 0.213 | 1 | 0.665 |
LATS1 |
0.781 | 0.175 | -3 | 0.920 |
RIPK3 |
0.781 | 0.144 | 3 | 0.701 |
PAK4 |
0.781 | 0.210 | -2 | 0.695 |
HIPK3 |
0.780 | 0.261 | 1 | 0.772 |
MRCKB |
0.780 | 0.347 | -3 | 0.946 |
BRSK1 |
0.779 | 0.183 | -3 | 0.956 |
PRPK |
0.779 | -0.059 | -1 | 0.577 |
PKCT |
0.779 | 0.246 | 2 | 0.440 |
PAK5 |
0.779 | 0.211 | -2 | 0.686 |
TSSK1 |
0.779 | 0.197 | -3 | 0.948 |
CHAK2 |
0.779 | 0.108 | -1 | 0.710 |
CRIK |
0.778 | 0.399 | -3 | 0.927 |
MOK |
0.777 | 0.345 | 1 | 0.815 |
MRCKA |
0.777 | 0.324 | -3 | 0.946 |
ROCK2 |
0.777 | 0.373 | -3 | 0.946 |
PKCI |
0.777 | 0.253 | 2 | 0.463 |
PDHK4 |
0.777 | -0.072 | 1 | 0.844 |
WNK3 |
0.777 | 0.091 | 1 | 0.815 |
DCAMKL2 |
0.777 | 0.230 | -3 | 0.950 |
PHKG1 |
0.777 | 0.163 | -3 | 0.949 |
SMMLCK |
0.776 | 0.303 | -3 | 0.970 |
IKKB |
0.776 | -0.005 | -2 | 0.693 |
DRAK1 |
0.776 | 0.210 | 1 | 0.758 |
ATR |
0.775 | 0.017 | 1 | 0.812 |
DSTYK |
0.775 | 0.008 | 2 | 0.609 |
ULK2 |
0.775 | -0.039 | 2 | 0.482 |
IRE1 |
0.775 | 0.138 | 1 | 0.854 |
PASK |
0.774 | 0.280 | -3 | 0.936 |
TGFBR2 |
0.774 | 0.029 | -2 | 0.809 |
NIM1 |
0.774 | 0.086 | 3 | 0.747 |
SIK |
0.774 | 0.176 | -3 | 0.944 |
MARK4 |
0.774 | 0.078 | 4 | 0.811 |
NUAK1 |
0.773 | 0.167 | -3 | 0.953 |
MAPKAPK5 |
0.772 | 0.191 | -3 | 0.949 |
NEK6 |
0.772 | -0.022 | -2 | 0.825 |
BMPR2 |
0.772 | -0.052 | -2 | 0.852 |
QIK |
0.772 | 0.164 | -3 | 0.946 |
QSK |
0.772 | 0.146 | 4 | 0.782 |
DMPK1 |
0.772 | 0.374 | -3 | 0.939 |
TBK1 |
0.772 | -0.051 | 1 | 0.712 |
TSSK2 |
0.771 | 0.137 | -5 | 0.660 |
HASPIN |
0.771 | 0.478 | -1 | 0.931 |
DAPK3 |
0.771 | 0.296 | -3 | 0.958 |
GRK5 |
0.771 | -0.022 | -3 | 0.814 |
PKR |
0.770 | 0.233 | 1 | 0.869 |
ROCK1 |
0.770 | 0.366 | -3 | 0.946 |
WNK4 |
0.770 | 0.265 | -2 | 0.837 |
DAPK1 |
0.769 | 0.288 | -3 | 0.959 |
BRSK2 |
0.769 | 0.121 | -3 | 0.952 |
GRK6 |
0.768 | 0.029 | 1 | 0.806 |
MLK1 |
0.768 | -0.014 | 2 | 0.529 |
CHK2 |
0.768 | 0.294 | -3 | 0.898 |
GRK1 |
0.768 | 0.013 | -2 | 0.770 |
CAMK1A |
0.768 | 0.276 | -3 | 0.898 |
CDK7 |
0.768 | 0.071 | 1 | 0.686 |
NEK7 |
0.767 | -0.069 | -3 | 0.817 |
DLK |
0.767 | 0.111 | 1 | 0.805 |
SNRK |
0.767 | 0.103 | 2 | 0.435 |
IKKE |
0.767 | -0.065 | 1 | 0.701 |
MAK |
0.767 | 0.258 | -2 | 0.741 |
IRE2 |
0.767 | 0.065 | 2 | 0.438 |
MARK3 |
0.767 | 0.135 | 4 | 0.735 |
MLK3 |
0.766 | 0.030 | 2 | 0.472 |
ULK1 |
0.766 | -0.054 | -3 | 0.785 |
PDHK1 |
0.766 | -0.158 | 1 | 0.815 |
ERK5 |
0.766 | -0.017 | 1 | 0.753 |
PKN1 |
0.765 | 0.223 | -3 | 0.952 |
PLK1 |
0.765 | 0.038 | -2 | 0.787 |
TTBK2 |
0.765 | -0.011 | 2 | 0.444 |
KIS |
0.765 | 0.047 | 1 | 0.703 |
PHKG2 |
0.764 | 0.171 | -3 | 0.944 |
CDK14 |
0.764 | 0.129 | 1 | 0.676 |
BCKDK |
0.764 | -0.108 | -1 | 0.530 |
CDK12 |
0.764 | 0.090 | 1 | 0.647 |
CDK9 |
0.763 | 0.077 | 1 | 0.676 |
MASTL |
0.763 | -0.077 | -2 | 0.779 |
NEK2 |
0.763 | 0.068 | 2 | 0.501 |
FAM20C |
0.763 | -0.026 | 2 | 0.413 |
ANKRD3 |
0.763 | 0.019 | 1 | 0.841 |
CDK13 |
0.762 | 0.054 | 1 | 0.671 |
ATM |
0.762 | -0.004 | 1 | 0.751 |
CHAK1 |
0.762 | 0.076 | 2 | 0.462 |
CDK18 |
0.762 | 0.082 | 1 | 0.627 |
NEK9 |
0.762 | -0.050 | 2 | 0.518 |
PKG1 |
0.762 | 0.228 | -2 | 0.694 |
BUB1 |
0.761 | 0.275 | -5 | 0.669 |
SBK |
0.761 | 0.263 | -3 | 0.857 |
DNAPK |
0.761 | 0.045 | 1 | 0.690 |
BMPR1B |
0.761 | 0.089 | 1 | 0.741 |
ALK4 |
0.760 | 0.036 | -2 | 0.834 |
JNK2 |
0.760 | 0.097 | 1 | 0.637 |
PLK3 |
0.760 | 0.022 | 2 | 0.566 |
CDK8 |
0.760 | 0.021 | 1 | 0.670 |
CHK1 |
0.760 | 0.091 | -3 | 0.910 |
CDK19 |
0.760 | 0.043 | 1 | 0.633 |
MARK1 |
0.760 | 0.113 | 4 | 0.758 |
MLK2 |
0.759 | -0.039 | 2 | 0.507 |
GRK7 |
0.759 | 0.042 | 1 | 0.753 |
SSTK |
0.759 | 0.179 | 4 | 0.769 |
CDK1 |
0.759 | 0.065 | 1 | 0.655 |
STK33 |
0.759 | 0.153 | 2 | 0.423 |
GRK4 |
0.758 | -0.084 | -2 | 0.802 |
MLK4 |
0.758 | 0.001 | 2 | 0.460 |
IRAK4 |
0.758 | 0.169 | 1 | 0.839 |
TGFBR1 |
0.758 | 0.027 | -2 | 0.808 |
IKKA |
0.756 | -0.091 | -2 | 0.676 |
JNK3 |
0.756 | 0.067 | 1 | 0.674 |
PERK |
0.755 | 0.037 | -2 | 0.814 |
MST3 |
0.755 | 0.139 | 2 | 0.564 |
ALK2 |
0.753 | 0.041 | -2 | 0.818 |
MEK1 |
0.753 | -0.026 | 2 | 0.561 |
MARK2 |
0.753 | 0.050 | 4 | 0.700 |
P38A |
0.753 | 0.068 | 1 | 0.703 |
VRK2 |
0.753 | -0.024 | 1 | 0.876 |
PLK4 |
0.752 | -0.004 | 2 | 0.402 |
CDK5 |
0.752 | 0.039 | 1 | 0.702 |
TLK2 |
0.752 | -0.028 | 1 | 0.795 |
ERK2 |
0.752 | 0.057 | 1 | 0.697 |
YSK4 |
0.751 | -0.035 | 1 | 0.749 |
CDK17 |
0.750 | 0.051 | 1 | 0.577 |
P38G |
0.750 | 0.061 | 1 | 0.568 |
PRP4 |
0.749 | 0.064 | -3 | 0.741 |
LOK |
0.749 | 0.177 | -2 | 0.763 |
ERK1 |
0.749 | 0.054 | 1 | 0.627 |
NEK5 |
0.748 | 0.068 | 1 | 0.826 |
ACVR2B |
0.747 | -0.010 | -2 | 0.792 |
HRI |
0.747 | -0.034 | -2 | 0.826 |
SMG1 |
0.747 | -0.061 | 1 | 0.771 |
ERK7 |
0.747 | 0.025 | 2 | 0.375 |
MEK5 |
0.746 | 0.028 | 2 | 0.530 |
LKB1 |
0.746 | 0.129 | -3 | 0.847 |
SLK |
0.746 | 0.116 | -2 | 0.702 |
PINK1 |
0.746 | -0.000 | 1 | 0.867 |
ACVR2A |
0.745 | -0.026 | -2 | 0.784 |
TLK1 |
0.745 | 0.022 | -2 | 0.803 |
CDK4 |
0.745 | 0.098 | 1 | 0.638 |
TAO3 |
0.745 | 0.039 | 1 | 0.779 |
BRAF |
0.745 | -0.019 | -4 | 0.762 |
CDK2 |
0.745 | 0.004 | 1 | 0.729 |
MPSK1 |
0.744 | 0.061 | 1 | 0.815 |
P38B |
0.744 | 0.042 | 1 | 0.628 |
CDK3 |
0.744 | 0.045 | 1 | 0.592 |
PDK1 |
0.744 | 0.129 | 1 | 0.811 |
GAK |
0.744 | 0.139 | 1 | 0.816 |
LRRK2 |
0.744 | 0.204 | 2 | 0.545 |
MEKK3 |
0.744 | 0.018 | 1 | 0.784 |
GRK2 |
0.744 | -0.018 | -2 | 0.701 |
GSK3A |
0.743 | 0.066 | 4 | 0.538 |
NEK8 |
0.743 | 0.060 | 2 | 0.519 |
BMPR1A |
0.743 | 0.049 | 1 | 0.715 |
GSK3B |
0.743 | 0.049 | 4 | 0.530 |
CDK16 |
0.742 | 0.055 | 1 | 0.599 |
MEKK1 |
0.741 | -0.061 | 1 | 0.790 |
HPK1 |
0.741 | 0.146 | 1 | 0.763 |
GCK |
0.740 | 0.121 | 1 | 0.770 |
ZAK |
0.739 | -0.073 | 1 | 0.757 |
TTBK1 |
0.738 | -0.077 | 2 | 0.399 |
PBK |
0.738 | 0.127 | 1 | 0.718 |
CAMKK2 |
0.738 | 0.064 | -2 | 0.699 |
TAO2 |
0.738 | 0.024 | 2 | 0.526 |
NEK11 |
0.738 | 0.033 | 1 | 0.779 |
CAMKK1 |
0.738 | 0.033 | -2 | 0.695 |
CDK6 |
0.737 | 0.063 | 1 | 0.653 |
TNIK |
0.736 | 0.083 | 3 | 0.813 |
KHS2 |
0.736 | 0.137 | 1 | 0.769 |
IRAK1 |
0.736 | -0.047 | -1 | 0.609 |
MEKK2 |
0.735 | -0.058 | 2 | 0.499 |
P38D |
0.735 | 0.043 | 1 | 0.578 |
NEK4 |
0.734 | 0.039 | 1 | 0.787 |
YANK3 |
0.733 | 0.027 | 2 | 0.312 |
JNK1 |
0.732 | 0.043 | 1 | 0.630 |
KHS1 |
0.732 | 0.093 | 1 | 0.758 |
NEK1 |
0.732 | 0.063 | 1 | 0.813 |
MEKK6 |
0.732 | 0.055 | 1 | 0.757 |
CK1E |
0.731 | -0.035 | -3 | 0.463 |
CK2A2 |
0.730 | 0.001 | 1 | 0.665 |
PLK2 |
0.730 | -0.024 | -3 | 0.699 |
TAK1 |
0.729 | 0.035 | 1 | 0.790 |
HGK |
0.729 | 0.009 | 3 | 0.808 |
PDHK3_TYR |
0.728 | 0.184 | 4 | 0.913 |
LIMK2_TYR |
0.728 | 0.263 | -3 | 0.903 |
GRK3 |
0.728 | -0.036 | -2 | 0.668 |
VRK1 |
0.727 | 0.022 | 2 | 0.528 |
MAP3K15 |
0.725 | -0.003 | 1 | 0.747 |
YSK1 |
0.725 | 0.036 | 2 | 0.497 |
EEF2K |
0.725 | -0.024 | 3 | 0.762 |
MINK |
0.724 | -0.010 | 1 | 0.763 |
CK1A2 |
0.724 | -0.027 | -3 | 0.422 |
MST1 |
0.724 | 0.003 | 1 | 0.758 |
CK2A1 |
0.724 | 0.010 | 1 | 0.648 |
TESK1_TYR |
0.723 | 0.166 | 3 | 0.845 |
PDHK4_TYR |
0.722 | 0.161 | 2 | 0.617 |
CK1D |
0.721 | -0.041 | -3 | 0.413 |
NEK3 |
0.721 | 0.030 | 1 | 0.750 |
CK1G1 |
0.720 | -0.069 | -3 | 0.451 |
MEK2 |
0.719 | -0.085 | 2 | 0.500 |
MST2 |
0.719 | -0.094 | 1 | 0.765 |
MAP2K6_TYR |
0.718 | 0.096 | -1 | 0.580 |
RIPK2 |
0.718 | -0.101 | 1 | 0.719 |
PINK1_TYR |
0.718 | 0.129 | 1 | 0.847 |
MAP2K4_TYR |
0.717 | 0.041 | -1 | 0.577 |
MYO3B |
0.717 | 0.073 | 2 | 0.500 |
MAP2K7_TYR |
0.717 | 0.065 | 2 | 0.569 |
PKMYT1_TYR |
0.716 | 0.058 | 3 | 0.821 |
BMPR2_TYR |
0.714 | 0.044 | -1 | 0.571 |
OSR1 |
0.713 | -0.013 | 2 | 0.506 |
LIMK1_TYR |
0.713 | 0.097 | 2 | 0.522 |
TNK2 |
0.712 | 0.144 | 3 | 0.734 |
TNK1 |
0.711 | 0.196 | 3 | 0.744 |
BIKE |
0.710 | 0.032 | 1 | 0.697 |
PDHK1_TYR |
0.710 | -0.016 | -1 | 0.578 |
TAO1 |
0.710 | 0.002 | 1 | 0.719 |
TTK |
0.709 | -0.010 | -2 | 0.809 |
RET |
0.709 | 0.021 | 1 | 0.799 |
EPHA6 |
0.709 | 0.029 | -1 | 0.532 |
DDR1 |
0.708 | 0.045 | 4 | 0.822 |
ALPHAK3 |
0.705 | -0.019 | -1 | 0.514 |
ASK1 |
0.705 | -0.039 | 1 | 0.740 |
MYO3A |
0.703 | -0.023 | 1 | 0.814 |
MST1R |
0.703 | -0.038 | 3 | 0.785 |
EPHA4 |
0.701 | 0.018 | 2 | 0.593 |
EPHB4 |
0.701 | -0.025 | -1 | 0.503 |
NEK10_TYR |
0.701 | 0.009 | 1 | 0.705 |
WEE1_TYR |
0.700 | 0.046 | -1 | 0.529 |
DDR2 |
0.700 | 0.104 | 3 | 0.698 |
FGFR2 |
0.698 | -0.037 | 3 | 0.768 |
TYRO3 |
0.696 | -0.099 | 3 | 0.754 |
ABL2 |
0.696 | -0.023 | -1 | 0.506 |
JAK3 |
0.695 | -0.072 | 1 | 0.778 |
KDR |
0.694 | -0.013 | 3 | 0.710 |
AAK1 |
0.694 | 0.043 | 1 | 0.591 |
TXK |
0.693 | -0.001 | 1 | 0.755 |
SRMS |
0.693 | -0.026 | 1 | 0.776 |
ITK |
0.693 | -0.000 | -1 | 0.492 |
YANK2 |
0.691 | -0.016 | 2 | 0.316 |
AXL |
0.691 | -0.066 | 3 | 0.747 |
CSF1R |
0.691 | -0.115 | 3 | 0.751 |
ABL1 |
0.690 | -0.056 | -1 | 0.501 |
TYK2 |
0.690 | -0.236 | 1 | 0.786 |
TEK |
0.690 | -0.050 | 3 | 0.694 |
YES1 |
0.689 | -0.092 | -1 | 0.518 |
FLT1 |
0.689 | -0.025 | -1 | 0.519 |
INSRR |
0.689 | -0.111 | 3 | 0.706 |
KIT |
0.688 | -0.067 | 3 | 0.758 |
ROS1 |
0.688 | -0.197 | 3 | 0.715 |
EPHB1 |
0.688 | -0.081 | 1 | 0.760 |
EPHB3 |
0.687 | -0.077 | -1 | 0.478 |
FGR |
0.687 | -0.132 | 1 | 0.786 |
PDGFRB |
0.687 | -0.138 | 3 | 0.756 |
JAK2 |
0.687 | -0.217 | 1 | 0.773 |
FLT3 |
0.687 | -0.084 | 3 | 0.753 |
MERTK |
0.686 | -0.081 | 3 | 0.752 |
PTK2B |
0.686 | 0.000 | -1 | 0.477 |
EPHA7 |
0.686 | -0.041 | 2 | 0.566 |
FGFR3 |
0.686 | -0.058 | 3 | 0.739 |
TNNI3K_TYR |
0.686 | -0.076 | 1 | 0.780 |
EPHB2 |
0.685 | -0.075 | -1 | 0.469 |
MET |
0.685 | -0.054 | 3 | 0.767 |
EPHA3 |
0.685 | -0.065 | 2 | 0.551 |
STLK3 |
0.685 | -0.141 | 1 | 0.725 |
BMX |
0.685 | -0.023 | -1 | 0.433 |
FGFR1 |
0.685 | -0.130 | 3 | 0.730 |
FER |
0.684 | -0.179 | 1 | 0.790 |
TEC |
0.684 | -0.067 | -1 | 0.446 |
EPHA1 |
0.683 | -0.059 | 3 | 0.742 |
CK1A |
0.681 | -0.076 | -3 | 0.314 |
PTK2 |
0.681 | 0.013 | -1 | 0.478 |
EPHA5 |
0.681 | -0.031 | 2 | 0.577 |
FLT4 |
0.681 | -0.092 | 3 | 0.704 |
BLK |
0.680 | -0.066 | -1 | 0.490 |
MATK |
0.680 | -0.051 | -1 | 0.483 |
LCK |
0.680 | -0.105 | -1 | 0.487 |
PTK6 |
0.680 | -0.189 | -1 | 0.468 |
PDGFRA |
0.677 | -0.189 | 3 | 0.752 |
LTK |
0.677 | -0.133 | 3 | 0.699 |
BTK |
0.676 | -0.161 | -1 | 0.476 |
HCK |
0.676 | -0.192 | -1 | 0.487 |
NTRK1 |
0.675 | -0.181 | -1 | 0.498 |
FYN |
0.675 | -0.069 | -1 | 0.466 |
EPHA8 |
0.674 | -0.069 | -1 | 0.470 |
ERBB2 |
0.674 | -0.128 | 1 | 0.736 |
JAK1 |
0.674 | -0.183 | 1 | 0.726 |
ALK |
0.673 | -0.176 | 3 | 0.676 |
CSK |
0.671 | -0.106 | 2 | 0.561 |
EPHA2 |
0.670 | -0.045 | -1 | 0.445 |
FRK |
0.669 | -0.126 | -1 | 0.493 |
FGFR4 |
0.668 | -0.092 | -1 | 0.465 |
CK1G3 |
0.668 | -0.059 | -3 | 0.268 |
NTRK2 |
0.667 | -0.227 | 3 | 0.721 |
EGFR |
0.667 | -0.101 | 1 | 0.648 |
INSR |
0.667 | -0.193 | 3 | 0.694 |
NTRK3 |
0.666 | -0.178 | -1 | 0.458 |
SYK |
0.665 | -0.043 | -1 | 0.447 |
SRC |
0.663 | -0.122 | -1 | 0.467 |
LYN |
0.663 | -0.156 | 3 | 0.685 |
IGF1R |
0.655 | -0.156 | 3 | 0.645 |
MUSK |
0.655 | -0.148 | 1 | 0.647 |
ERBB4 |
0.654 | -0.072 | 1 | 0.654 |
CK1G2 |
0.653 | -0.053 | -3 | 0.367 |
ZAP70 |
0.652 | -0.021 | -1 | 0.427 |
FES |
0.641 | -0.150 | -1 | 0.422 |