Motif 36 (n=96)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A5A3E0 | POTEF | S932 | ochoa | POTE ankyrin domain family member F (ANKRD26-like family C member 1B) (Chimeric POTE-actin protein) | None |
A6H8Y1 | BDP1 | S1621 | ochoa | Transcription factor TFIIIB component B'' homolog (Transcription factor IIIB 150) (TFIIIB150) (Transcription factor-like nuclear regulator) | General activator of RNA polymerase III transcription. Requires for transcription from all three types of polymerase III promoters. Requires for transcription of genes with internal promoter elements and with promoter elements upstream of the initiation site. {ECO:0000269|PubMed:11040218}. |
A6NKT7 | RGPD3 | S393 | ochoa | RanBP2-like and GRIP domain-containing protein 3 | None |
A6NKT7 | RGPD3 | S1545 | ochoa | RanBP2-like and GRIP domain-containing protein 3 | None |
O14682 | ENC1 | S406 | ochoa | Ectoderm-neural cortex protein 1 (ENC-1) (Kelch-like protein 37) (Nuclear matrix protein NRP/B) (p53-induced gene 10 protein) | Actin-binding protein involved in the regulation of neuronal process formation and in differentiation of neural crest cells. Down-regulates transcription factor NF2L2/NRF2 by decreasing the rate of protein synthesis and not via a ubiquitin-mediated proteasomal degradation mechanism. {ECO:0000269|PubMed:19424503}. |
O43741 | PRKAB2 | S184 | ochoa | 5'-AMP-activated protein kinase subunit beta-2 (AMPK subunit beta-2) | Non-catalytic subunit of AMP-activated protein kinase (AMPK), an energy sensor protein kinase that plays a key role in regulating cellular energy metabolism. In response to reduction of intracellular ATP levels, AMPK activates energy-producing pathways and inhibits energy-consuming processes: inhibits protein, carbohydrate and lipid biosynthesis, as well as cell growth and proliferation. AMPK acts via direct phosphorylation of metabolic enzymes, and by longer-term effects via phosphorylation of transcription regulators. Also acts as a regulator of cellular polarity by remodeling the actin cytoskeleton; probably by indirectly activating myosin. Beta non-catalytic subunit acts as a scaffold on which the AMPK complex assembles, via its C-terminus that bridges alpha (PRKAA1 or PRKAA2) and gamma subunits (PRKAG1, PRKAG2 or PRKAG3). |
O60508 | CDC40 | S43 | ochoa | Pre-mRNA-processing factor 17 (Cell division cycle 40 homolog) (EH-binding protein 3) (Ehb3) (PRP17 homolog) (hPRP17) | Required for pre-mRNA splicing as component of the activated spliceosome (PubMed:33220177). Plays an important role in embryonic brain development; this function does not require proline isomerization (PubMed:33220177). {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:33220177, ECO:0000269|PubMed:9830021}. |
O75376 | NCOR1 | S172 | ochoa | Nuclear receptor corepressor 1 (N-CoR) (N-CoR1) | Mediates transcriptional repression by certain nuclear receptors (PubMed:20812024). Part of a complex which promotes histone deacetylation and the formation of repressive chromatin structures which may impede the access of basal transcription factors. Participates in the transcriptional repressor activity produced by BCL6. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). Mediates the NR1D1-dependent repression and circadian regulation of TSHB expression (By similarity). The NCOR1-HDAC3 complex regulates the circadian expression of the core clock gene ARTNL/BMAL1 and the genes involved in lipid metabolism in the liver (By similarity). {ECO:0000250|UniProtKB:Q60974, ECO:0000269|PubMed:14527417, ECO:0000269|PubMed:20812024}. |
O94887 | FARP2 | S410 | ochoa | FERM, ARHGEF and pleckstrin domain-containing protein 2 (FERM domain-including RhoGEF) (FIR) (FERM, RhoGEF and pleckstrin domain-containing protein 2) (Pleckstrin homology domain-containing family C member 3) (PH domain-containing family C member 3) | Functions as a guanine nucleotide exchange factor that activates RAC1. May have relatively low activity. Plays a role in the response to class 3 semaphorins and remodeling of the actin cytoskeleton. Plays a role in TNFSF11-mediated osteoclast differentiation, especially in podosome rearrangement and reorganization of the actin cytoskeleton. Regulates the activation of ITGB3, integrin signaling and cell adhesion (By similarity). {ECO:0000250}. |
P04637 | TP53 | S46 | psp | Cellular tumor antigen p53 (Antigen NY-CO-13) (Phosphoprotein p53) (Tumor suppressor p53) | Multifunctional transcription factor that induces cell cycle arrest, DNA repair or apoptosis upon binding to its target DNA sequence (PubMed:11025664, PubMed:12524540, PubMed:12810724, PubMed:15186775, PubMed:15340061, PubMed:17317671, PubMed:17349958, PubMed:19556538, PubMed:20673990, PubMed:20959462, PubMed:22726440, PubMed:24051492, PubMed:24652652, PubMed:35618207, PubMed:36634798, PubMed:38653238, PubMed:9840937). Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type (PubMed:11025664, PubMed:12524540, PubMed:12810724, PubMed:15186775, PubMed:15340061, PubMed:17189187, PubMed:17317671, PubMed:17349958, PubMed:19556538, PubMed:20673990, PubMed:20959462, PubMed:22726440, PubMed:24051492, PubMed:24652652, PubMed:38653238, PubMed:9840937). Negatively regulates cell division by controlling expression of a set of genes required for this process (PubMed:11025664, PubMed:12524540, PubMed:12810724, PubMed:15186775, PubMed:15340061, PubMed:17317671, PubMed:17349958, PubMed:19556538, PubMed:20673990, PubMed:20959462, PubMed:22726440, PubMed:24051492, PubMed:24652652, PubMed:9840937). One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression (PubMed:12524540, PubMed:17189187). Its pro-apoptotic activity is activated via its interaction with PPP1R13B/ASPP1 or TP53BP2/ASPP2 (PubMed:12524540). However, this activity is inhibited when the interaction with PPP1R13B/ASPP1 or TP53BP2/ASPP2 is displaced by PPP1R13L/iASPP (PubMed:12524540). In cooperation with mitochondrial PPIF is involved in activating oxidative stress-induced necrosis; the function is largely independent of transcription. Induces the transcription of long intergenic non-coding RNA p21 (lincRNA-p21) and lincRNA-Mkln1. LincRNA-p21 participates in TP53-dependent transcriptional repression leading to apoptosis and seems to have an effect on cell-cycle regulation. Implicated in Notch signaling cross-over. Prevents CDK7 kinase activity when associated to CAK complex in response to DNA damage, thus stopping cell cycle progression. Isoform 2 enhances the transactivation activity of isoform 1 from some but not all TP53-inducible promoters. Isoform 4 suppresses transactivation activity and impairs growth suppression mediated by isoform 1. Isoform 7 inhibits isoform 1-mediated apoptosis. Regulates the circadian clock by repressing CLOCK-BMAL1-mediated transcriptional activation of PER2 (PubMed:24051492). {ECO:0000269|PubMed:11025664, ECO:0000269|PubMed:12524540, ECO:0000269|PubMed:12810724, ECO:0000269|PubMed:15186775, ECO:0000269|PubMed:15340061, ECO:0000269|PubMed:17189187, ECO:0000269|PubMed:17317671, ECO:0000269|PubMed:17349958, ECO:0000269|PubMed:19556538, ECO:0000269|PubMed:20673990, ECO:0000269|PubMed:20959462, ECO:0000269|PubMed:22726440, ECO:0000269|PubMed:24051492, ECO:0000269|PubMed:24652652, ECO:0000269|PubMed:35618207, ECO:0000269|PubMed:36634798, ECO:0000269|PubMed:38653238, ECO:0000269|PubMed:9840937}. |
P05023 | ATP1A1 | S694 | ochoa | Sodium/potassium-transporting ATPase subunit alpha-1 (Na(+)/K(+) ATPase alpha-1 subunit) (EC 7.2.2.13) (Sodium pump subunit alpha-1) | This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium ions, providing the energy for active transport of various nutrients (PubMed:29499166, PubMed:30388404). Could also be part of an osmosensory signaling pathway that senses body-fluid sodium levels and controls salt intake behavior as well as voluntary water intake to regulate sodium homeostasis (By similarity). {ECO:0000250|UniProtKB:Q8VDN2, ECO:0000269|PubMed:29499166, ECO:0000269|PubMed:30388404}. |
P07900 | HSP90AA1 | S595 | ochoa|psp | Heat shock protein HSP 90-alpha (EC 3.6.4.10) (Heat shock 86 kDa) (HSP 86) (HSP86) (Heat shock protein family C member 1) (Lipopolysaccharide-associated protein 2) (LAP-2) (LPS-associated protein 2) (Renal carcinoma antigen NY-REN-38) | Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle that is linked to its ATPase activity which is essential for its chaperone activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:11274138, PubMed:12526792, PubMed:15577939, PubMed:15937123, PubMed:27353360, PubMed:29127155). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself (PubMed:29127155). Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:26991466, PubMed:27295069). Plays a critical role in mitochondrial import, delivers preproteins to the mitochondrial import receptor TOMM70 (PubMed:12526792). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels (PubMed:25973397). In the first place, they alter the steady-state levels of certain transcription factors in response to various physiological cues (PubMed:25973397). Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment (PubMed:25973397). Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes (PubMed:11276205). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Mediates the association of TOMM70 with IRF3 or TBK1 in mitochondrial outer membrane which promotes host antiviral response (PubMed:20628368, PubMed:25609812). {ECO:0000269|PubMed:11274138, ECO:0000269|PubMed:11276205, ECO:0000269|PubMed:12526792, ECO:0000269|PubMed:15577939, ECO:0000269|PubMed:15937123, ECO:0000269|PubMed:20628368, ECO:0000269|PubMed:24613385, ECO:0000269|PubMed:25609812, ECO:0000269|PubMed:27353360, ECO:0000269|PubMed:29127155, ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466, ECO:0000303|PubMed:27295069}.; FUNCTION: (Microbial infection) Seems to interfere with N.meningitidis NadA-mediated invasion of human cells. Decreasing HSP90 levels increases adhesion and entry of E.coli expressing NadA into human Chang cells; increasing its levels leads to decreased adhesion and invasion. {ECO:0000305|PubMed:22066472}. |
P08238 | HSP90AB1 | S587 | ochoa | Heat shock protein HSP 90-beta (HSP 90) (Heat shock 84 kDa) (HSP 84) (HSP84) (Heat shock protein family C member 3) | Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle linked to its ATPase activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:16478993, PubMed:19696785). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself. Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:26991466, PubMed:27295069). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels. They first alter the steady-state levels of certain transcription factors in response to various physiological cues. Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment. Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Promotes cell differentiation by chaperoning BIRC2 and thereby protecting from auto-ubiquitination and degradation by the proteasomal machinery (PubMed:18239673). Main chaperone involved in the phosphorylation/activation of the STAT1 by chaperoning both JAK2 and PRKCE under heat shock and in turn, activates its own transcription (PubMed:20353823). Involved in the translocation into ERGIC (endoplasmic reticulum-Golgi intermediate compartment) of leaderless cargos (lacking the secretion signal sequence) such as the interleukin 1/IL-1; the translocation process is mediated by the cargo receptor TMED10 (PubMed:32272059). {ECO:0000269|PubMed:16478993, ECO:0000269|PubMed:18239673, ECO:0000269|PubMed:19696785, ECO:0000269|PubMed:20353823, ECO:0000269|PubMed:24613385, ECO:0000269|PubMed:32272059, ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466, ECO:0000303|PubMed:27295069}.; FUNCTION: (Microbial infection) Binding to N.meningitidis NadA stimulates monocytes (PubMed:21949862). Seems to interfere with N.meningitidis NadA-mediated invasion of human cells (Probable). {ECO:0000269|PubMed:21949862, ECO:0000305|PubMed:22066472}. |
P0DJD0 | RGPD1 | S1529 | ochoa | RANBP2-like and GRIP domain-containing protein 1 (Ran-binding protein 2-like 6) (RanBP2-like 6) (RanBP2L6) | None |
P0DJD1 | RGPD2 | S1537 | ochoa | RANBP2-like and GRIP domain-containing protein 2 (Ran-binding protein 2-like 2) (RanBP2-like 2) (RanBP2L2) | None |
P0DMM9 | SULT1A3 | S253 | ochoa | Sulfotransferase 1A3 (ST1A3) (EC 2.8.2.1) (Aryl sulfotransferase 1A3/1A4) (Catecholamine-sulfating phenol sulfotransferase) (HAST3) (M-PST) (Monoamine-sulfating phenol sulfotransferase) (Placental estrogen sulfotransferase) (Sulfotransferase 1A3/1A4) (Sulfotransferase, monoamine-preferring) (Thermolabile phenol sulfotransferase) (TL-PST) | Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of phenolic monoamines (neurotransmitters such as dopamine, (R)-adrenaline/epinephrine, (R)-noradrenaline/norepinephrine and serotonin) and phenolic and catechol drugs (PubMed:8093002, PubMed:29524394, PubMed:14622112, PubMed:15358107). Catalyzes the sulfation of T4 (L-thyroxine/3,5,3',5'-tetraiodothyronine), T3 (3,5,3'-triiodothyronine), rT3 (3,3',5'-triiodothyronine) and 3,3'-T2 (3,3'-diiodothyronine), with a substrate preference of 3,3'-T2 > rT3 > T3 > T4 (PubMed:10199779). {ECO:0000269|PubMed:10199779, ECO:0000269|PubMed:14622112, ECO:0000269|PubMed:15358107, ECO:0000269|PubMed:29524394, ECO:0000269|PubMed:8093002}. |
P0DMN0 | SULT1A4 | S253 | ochoa | Sulfotransferase 1A4 (ST1A4) (EC 2.8.2.1) (Aryl sulfotransferase 1A3/1A4) (Sulfotransferase 1A3/1A4) | Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of phenolic monoamines (neurotransmitters such as dopamine, (R)-adrenaline/epinephrine, (R)-noradrenaline/norepinephrine and serotonin) and phenolic and catechol drugs (PubMed:15358107, PubMed:29524394). Catalyzes the sulfation of T4 (L-thyroxine/3,5,3',5'-tetraiodothyronine), T3 (3,5,3'-triiodothyronine), rT3 (3,3',5'-triiodothyronine) and 3,3'-T2 (3,3'-diiodothyronine), with a substrate preference of 3,3'-T2 > rT3 > T3 > T4 (PubMed:10199779). {ECO:0000269|PubMed:10199779, ECO:0000269|PubMed:15358107, ECO:0000269|PubMed:29524394}. |
P11441 | UBL4A | S90 | ochoa | Ubiquitin-like protein 4A (Ubiquitin-like protein GDX) | As part of a cytosolic protein quality control complex, the BAG6/BAT3 complex, maintains misfolded and hydrophobic patches-containing proteins in a soluble state and participates in their proper delivery to the endoplasmic reticulum or alternatively can promote their sorting to the proteasome where they undergo degradation (PubMed:20676083, PubMed:21636303, PubMed:21743475, PubMed:28104892). The BAG6/BAT3 complex is involved in the post-translational delivery of tail-anchored/type II transmembrane proteins to the endoplasmic reticulum membrane. Recruited to ribosomes, it interacts with the transmembrane region of newly synthesized tail-anchored proteins and together with SGTA and ASNA1 mediates their delivery to the endoplasmic reticulum (PubMed:20676083, PubMed:25535373, PubMed:28104892). Client proteins that cannot be properly delivered to the endoplasmic reticulum are ubiquitinated and sorted to the proteasome (PubMed:28104892). Similarly, the BAG6/BAT3 complex also functions as a sorting platform for proteins of the secretory pathway that are mislocalized to the cytosol either delivering them to the proteasome for degradation or to the endoplasmic reticulum (PubMed:21743475). The BAG6/BAT3 complex also plays a role in the endoplasmic reticulum-associated degradation (ERAD), a quality control mechanism that eliminates unwanted proteins of the endoplasmic reticulum through their retrotranslocation to the cytosol and their targeting to the proteasome. It maintains these retrotranslocated proteins in an unfolded yet soluble state condition in the cytosol to ensure their proper delivery to the proteasome (PubMed:21636303). {ECO:0000269|PubMed:20676083, ECO:0000269|PubMed:21636303, ECO:0000269|PubMed:21743475, ECO:0000269|PubMed:25535373, ECO:0000269|PubMed:28104892}. |
P13798 | APEH | S185 | ochoa | Acylamino-acid-releasing enzyme (AARE) (EC 3.4.19.1) (Acyl-peptide hydrolase) (APH) (Acylaminoacyl-peptidase) (Oxidized protein hydrolase) (OPH) | This enzyme catalyzes the hydrolysis of the N-terminal peptide bond of an N-acetylated peptide to generate an N-acetylated amino acid and a peptide with a free N-terminus (PubMed:10719179, PubMed:1740429, PubMed:2006156). It preferentially cleaves off Ac-Ala, Ac-Met and Ac-Ser (By similarity). Also, involved in the degradation of oxidized and glycated proteins (PubMed:10719179). {ECO:0000250|UniProtKB:P13676, ECO:0000269|PubMed:10719179, ECO:0000269|PubMed:1740429, ECO:0000269|PubMed:2006156}. |
P14618 | PKM | S77 | ochoa | Pyruvate kinase PKM (EC 2.7.1.40) (Cytosolic thyroid hormone-binding protein) (CTHBP) (Opa-interacting protein 3) (OIP-3) (Pyruvate kinase 2/3) (Pyruvate kinase muscle isozyme) (Threonine-protein kinase PKM2) (EC 2.7.11.1) (Thyroid hormone-binding protein 1) (THBP1) (Tumor M2-PK) (Tyrosine-protein kinase PKM2) (EC 2.7.10.2) (p58) | Catalyzes the final rate-limiting step of glycolysis by mediating the transfer of a phosphoryl group from phosphoenolpyruvate (PEP) to ADP, generating ATP (PubMed:15996096, PubMed:1854723, PubMed:20847263). The ratio between the highly active tetrameric form and nearly inactive dimeric form determines whether glucose carbons are channeled to biosynthetic processes or used for glycolytic ATP production (PubMed:15996096, PubMed:1854723, PubMed:20847263). The transition between the 2 forms contributes to the control of glycolysis and is important for tumor cell proliferation and survival (PubMed:15996096, PubMed:1854723, PubMed:20847263). {ECO:0000269|PubMed:15996096, ECO:0000269|PubMed:1854723, ECO:0000269|PubMed:20847263}.; FUNCTION: [Isoform M2]: Isoform specifically expressed during embryogenesis that has low pyruvate kinase activity by itself and requires allosteric activation by D-fructose 1,6-bisphosphate (FBP) for pyruvate kinase activity (PubMed:18337823, PubMed:20847263). In addition to its pyruvate kinase activity in the cytoplasm, also acts as a regulator of transcription in the nucleus by acting as a protein kinase (PubMed:18191611, PubMed:21620138, PubMed:22056988, PubMed:22306293, PubMed:22901803, PubMed:24120661). Translocates into the nucleus in response to various signals, such as EGF receptor activation, and homodimerizes, leading to its conversion into a protein threonine- and tyrosine-protein kinase (PubMed:22056988, PubMed:22306293, PubMed:22901803, PubMed:24120661, PubMed:26787900). Catalyzes phosphorylation of STAT3 at 'Tyr-705' and histone H3 at 'Thr-11' (H3T11ph), leading to activate transcription (PubMed:22306293, PubMed:22901803, PubMed:24120661). Its ability to activate transcription plays a role in cancer cells by promoting cell proliferation and promote tumorigenesis (PubMed:18337823, PubMed:22901803, PubMed:26787900). Promotes the expression of the immune checkpoint protein CD274 in BMAL1-deficient macrophages (By similarity). May also act as a translation regulator for a subset of mRNAs, independently of its pyruvate kinase activity: associates with subpools of endoplasmic reticulum-associated ribosomes, binds directly to the mRNAs translated at the endoplasmic reticulum and promotes translation of these endoplasmic reticulum-destined mRNAs (By similarity). Plays a role in caspase independent cell death of tumor cells (PubMed:17308100). {ECO:0000250|UniProtKB:P52480, ECO:0000269|PubMed:17308100, ECO:0000269|PubMed:18191611, ECO:0000269|PubMed:18337823, ECO:0000269|PubMed:20847263, ECO:0000269|PubMed:21620138, ECO:0000269|PubMed:22056988, ECO:0000269|PubMed:22306293, ECO:0000269|PubMed:22901803, ECO:0000269|PubMed:24120661, ECO:0000269|PubMed:26787900}.; FUNCTION: [Isoform M1]: Pyruvate kinase isoform expressed in adult tissues, which replaces isoform M2 after birth (PubMed:18337823). In contrast to isoform M2, has high pyruvate kinase activity by itself and does not require allosteric activation by D-fructose 1,6-bisphosphate (FBP) for activity (PubMed:20847263). {ECO:0000269|PubMed:18337823, ECO:0000269|PubMed:20847263}. |
P14635 | CCNB1 | S126 | psp | G2/mitotic-specific cyclin-B1 | Essential for the control of the cell cycle at the G2/M (mitosis) transition. {ECO:0000269|PubMed:17495531, ECO:0000269|PubMed:17495533, ECO:0000269|PubMed:27030811}. |
P25054 | APC | S1042 | 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}. |
P30304 | CDC25A | S261 | ochoa | M-phase inducer phosphatase 1 (EC 3.1.3.48) (Dual specificity phosphatase Cdc25A) | Tyrosine protein phosphatase which functions as a dosage-dependent inducer of mitotic progression (PubMed:12676925, PubMed:14559997, PubMed:1836978, PubMed:20360007). Directly dephosphorylates CDK1 and stimulates its kinase activity (PubMed:20360007). Also dephosphorylates CDK2 in complex with cyclin-E, in vitro (PubMed:20360007). {ECO:0000269|PubMed:12676925, ECO:0000269|PubMed:14559997, ECO:0000269|PubMed:1836978, ECO:0000269|PubMed:20360007}. |
P30305 | CDC25B | S160 | ochoa | M-phase inducer phosphatase 2 (EC 3.1.3.48) (Dual specificity phosphatase Cdc25B) | Tyrosine protein phosphatase which functions as a dosage-dependent inducer of mitotic progression (PubMed:1836978, PubMed:20360007). Directly dephosphorylates CDK1 and stimulates its kinase activity (PubMed:20360007). Required for G2/M phases of the cell cycle progression and abscission during cytokinesis in a ECT2-dependent manner (PubMed:17332740). The three isoforms seem to have a different level of activity (PubMed:1836978). {ECO:0000269|PubMed:17332740, ECO:0000269|PubMed:1836978, ECO:0000269|PubMed:20360007}. |
P30307 | CDC25C | S214 | ochoa|psp | M-phase inducer phosphatase 3 (EC 3.1.3.48) (Dual specificity phosphatase Cdc25C) | Functions as a dosage-dependent inducer in mitotic control. Tyrosine protein phosphatase required for progression of the cell cycle (PubMed:8119945). When phosphorylated, highly effective in activating G2 cells into prophase (PubMed:8119945). Directly dephosphorylates CDK1 and activates its kinase activity (PubMed:8119945). {ECO:0000269|PubMed:8119945}. |
P42568 | MLLT3 | S309 | ochoa | Protein AF-9 (ALL1-fused gene from chromosome 9 protein) (Myeloid/lymphoid or mixed-lineage leukemia translocated to chromosome 3 protein) (YEATS domain-containing protein 3) | Chromatin reader component of the super elongation complex (SEC), a complex required to increase the catalytic rate of RNA polymerase II transcription by suppressing transient pausing by the polymerase at multiple sites along the DNA (PubMed:20159561, PubMed:20471948, PubMed:25417107, PubMed:27105114, PubMed:27545619). Specifically recognizes and binds acylated histone H3, with a preference for histone H3 that is crotonylated (PubMed:25417107, PubMed:27105114, PubMed:27545619, PubMed:30374167, PubMed:30385749). Crotonylation marks active promoters and enhancers and confers resistance to transcriptional repressors (PubMed:25417107, PubMed:27105114, PubMed:27545619). Recognizes and binds histone H3 crotonylated at 'Lys-9' (H3K9cr), and with slightly lower affinity histone H3 crotonylated at 'Lys-18' (H3K18cr) (PubMed:27105114). Also recognizes and binds histone H3 acetylated and butyrylated at 'Lys-9' (H3K9ac and H3K9bu, respectively), but with lower affinity than crotonylated histone H3 (PubMed:25417107, PubMed:27105114, PubMed:30385749). In the SEC complex, MLLT3 is required to recruit the complex to crotonylated histones (PubMed:27105114, PubMed:27545619). Recruitment of the SEC complex to crotonylated histones promotes recruitment of DOT1L on active chromatin to deposit histone H3 'Lys-79' methylation (H3K79me) (PubMed:25417107). Plays a key role in hematopoietic stem cell (HSC) maintenance by preserving, rather than conferring, HSC stemness (PubMed:31776511). Acts by binding to the transcription start site of active genes in HSCs and sustaining level of H3K79me2, probably by recruiting DOT1L (PubMed:31776511). {ECO:0000269|PubMed:20159561, ECO:0000269|PubMed:20471948, ECO:0000269|PubMed:25417107, ECO:0000269|PubMed:27105114, ECO:0000269|PubMed:27545619, ECO:0000269|PubMed:30374167, ECO:0000269|PubMed:30385749, ECO:0000269|PubMed:31776511}. |
P42702 | LIFR | S927 | ochoa | Leukemia inhibitory factor receptor (LIF receptor) (LIF-R) (CD antigen CD118) | Signal-transducing molecule. May have a common pathway with IL6ST. The soluble form inhibits the biological activity of LIF by blocking its binding to receptors on target cells. |
P46821 | MAP1B | S25 | ochoa | Microtubule-associated protein 1B (MAP-1B) [Cleaved into: MAP1B heavy chain; MAP1 light chain LC1] | Facilitates tyrosination of alpha-tubulin in neuronal microtubules (By similarity). Phosphorylated MAP1B is required for proper microtubule dynamics and plays a role in the cytoskeletal changes that accompany neuronal differentiation and neurite extension (PubMed:33268592). Possibly MAP1B binds to at least two tubulin subunits in the polymer, and this bridging of subunits might be involved in nucleating microtubule polymerization and in stabilizing microtubules. Acts as a positive cofactor in DAPK1-mediated autophagic vesicle formation and membrane blebbing. {ECO:0000250, ECO:0000269|PubMed:18195017, ECO:0000269|PubMed:33268592}. |
P46821 | MAP1B | S1406 | ochoa | Microtubule-associated protein 1B (MAP-1B) [Cleaved into: MAP1B heavy chain; MAP1 light chain LC1] | Facilitates tyrosination of alpha-tubulin in neuronal microtubules (By similarity). Phosphorylated MAP1B is required for proper microtubule dynamics and plays a role in the cytoskeletal changes that accompany neuronal differentiation and neurite extension (PubMed:33268592). Possibly MAP1B binds to at least two tubulin subunits in the polymer, and this bridging of subunits might be involved in nucleating microtubule polymerization and in stabilizing microtubules. Acts as a positive cofactor in DAPK1-mediated autophagic vesicle formation and membrane blebbing. {ECO:0000250, ECO:0000269|PubMed:18195017, ECO:0000269|PubMed:33268592}. |
P48634 | PRRC2A | S1306 | 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}. |
P49792 | RANBP2 | S392 | ochoa | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
P49792 | RANBP2 | S2520 | ochoa | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
P50225 | SULT1A1 | S253 | ochoa | Sulfotransferase 1A1 (ST1A1) (EC 2.8.2.1) (Aryl sulfotransferase 1) (HAST1/HAST2) (Phenol sulfotransferase 1) (Phenol-sulfating phenol sulfotransferase 1) (P-PST 1) (ST1A3) (Thermostable phenol sulfotransferase) (Ts-PST) | Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of a wide variety of acceptor molecules bearing a hydroxyl or an amine group. Sulfonation increases the water solubility of most compounds, and therefore their renal excretion, but it can also result in bioactivation to form active metabolites. Displays broad substrate specificity for small phenolic compounds. Plays an important role in the sulfonation of endogenous molecules such as steroid hormones (PubMed:12471039, PubMed:16221673, PubMed:21723874, PubMed:22069470, PubMed:7834621). Mediates the sulfate conjugation of a variety of xenobiotics, including the drugs acetaminophen and minoxidil (By similarity). Mediates also the metabolic activation of carcinogenic N-hydroxyarylamines leading to highly reactive intermediates capable of forming DNA adducts, potentially resulting in mutagenesis (PubMed:7834621). May play a role in gut microbiota-host metabolic interaction. O-sulfonates 4-ethylphenol (4-EP), a dietary tyrosine-derived metabolite produced by gut bacteria. The product 4-EPS crosses the blood-brain barrier and may negatively regulate oligodendrocyte maturation and myelination, affecting the functional connectivity of different brain regions associated with the limbic system (PubMed:35165440). Catalyzes the sulfate conjugation of dopamine (PubMed:8093002). Catalyzes the sulfation of T4 (L-thyroxine/3,5,3',5'-tetraiodothyronine), T3 (3,5,3'-triiodothyronine), rT3 (3,3',5'-triiodothyronine) and 3,3'-T2 (3,3'-diiodothyronine), with a substrate preference of 3,3'-T2 > rT3 > T3 > T4 (PubMed:10199779). {ECO:0000250|UniProtKB:P17988, ECO:0000269|PubMed:10199779, ECO:0000269|PubMed:12471039, ECO:0000269|PubMed:16221673, ECO:0000269|PubMed:21723874, ECO:0000269|PubMed:22069470, ECO:0000269|PubMed:35165440, ECO:0000269|PubMed:7834621, ECO:0000269|PubMed:8093002}. |
P60709 | ACTB | S232 | ochoa | Actin, cytoplasmic 1 (EC 3.6.4.-) (Beta-actin) [Cleaved into: Actin, cytoplasmic 1, N-terminally processed] | Actin is a highly conserved protein that polymerizes to produce filaments that form cross-linked networks in the cytoplasm of cells (PubMed:25255767, PubMed:29581253). Actin exists in both monomeric (G-actin) and polymeric (F-actin) forms, both forms playing key functions, such as cell motility and contraction (PubMed:29581253). In addition to their role in the cytoplasmic cytoskeleton, G- and F-actin also localize in the nucleus, and regulate gene transcription and motility and repair of damaged DNA (PubMed:29925947). Plays a role in the assembly of the gamma-tubulin ring complex (gTuRC), which regulates the minus-end nucleation of alpha-beta tubulin heterodimers that grow into microtubule protafilaments (PubMed:39321809, PubMed:38609661). Part of the ACTR1A/ACTB filament around which the dynactin complex is built (By similarity). The dynactin multiprotein complex activates the molecular motor dynein for ultra-processive transport along microtubules (By similarity). {ECO:0000250|UniProtKB:Q6QAQ1, ECO:0000269|PubMed:25255767, ECO:0000269|PubMed:29581253, ECO:0000269|PubMed:29925947, ECO:0000269|PubMed:38609661, ECO:0000269|PubMed:39321809}. |
P62736 | ACTA2 | S234 | ochoa | Actin, aortic smooth muscle (EC 3.6.4.-) (Alpha-actin-2) (Cell growth-inhibiting gene 46 protein) [Cleaved into: Actin, aortic smooth muscle, intermediate form] | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. |
P63261 | ACTG1 | S232 | ochoa | Actin, cytoplasmic 2 (EC 3.6.4.-) (Gamma-actin) [Cleaved into: Actin, cytoplasmic 2, N-terminally processed] | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. May play a role in the repair of noise-induced stereocilia gaps thereby maintains hearing sensitivity following loud noise damage (By similarity). {ECO:0000250|UniProtKB:P63260, ECO:0000305|PubMed:29581253}. |
P63267 | ACTG2 | S233 | ochoa | Actin, gamma-enteric smooth muscle (EC 3.6.4.-) (Alpha-actin-3) (Gamma-2-actin) (Smooth muscle gamma-actin) [Cleaved into: Actin, gamma-enteric smooth muscle, intermediate form] | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. |
P68032 | ACTC1 | S234 | ochoa | Actin, alpha cardiac muscle 1 (EC 3.6.4.-) (Alpha-cardiac actin) [Cleaved into: Actin, alpha cardiac muscle 1, intermediate form] | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. |
P68133 | ACTA1 | S234 | ochoa | Actin, alpha skeletal muscle (EC 3.6.4.-) (Alpha-actin-1) [Cleaved into: Actin, alpha skeletal muscle, intermediate form] | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. |
P82094 | TMF1 | S112 | ochoa | TATA element modulatory factor (TMF) (Androgen receptor coactivator 160 kDa protein) (Androgen receptor-associated protein of 160 kDa) | Potential coactivator of the androgen receptor. Mediates STAT3 degradation. May play critical roles in two RAB6-dependent retrograde transport processes: one from endosomes to the Golgi and the other from the Golgi to the ER. This protein binds the HIV-1 TATA element and inhibits transcriptional activation by the TATA-binding protein (TBP). {ECO:0000269|PubMed:10428808, ECO:0000269|PubMed:1409643, ECO:0000269|PubMed:15467733, ECO:0000269|PubMed:17698061}. |
Q02880 | TOP2B | S1476 | ochoa | DNA topoisomerase 2-beta (EC 5.6.2.2) (DNA topoisomerase II, beta isozyme) | Key decatenating enzyme that alters DNA topology by binding to two double-stranded DNA molecules, generating a double-stranded break in one of the strands, passing the intact strand through the broken strand, and religating the broken strand. Plays a role in B-cell differentiation. {ECO:0000269|PubMed:10684600, ECO:0000269|PubMed:31409799, ECO:0000269|PubMed:32128574}. |
Q03164 | KMT2A | S2098 | ochoa | Histone-lysine N-methyltransferase 2A (Lysine N-methyltransferase 2A) (EC 2.1.1.364) (ALL-1) (CXXC-type zinc finger protein 7) (Cysteine methyltransferase KMT2A) (EC 2.1.1.-) (Myeloid/lymphoid or mixed-lineage leukemia) (Myeloid/lymphoid or mixed-lineage leukemia protein 1) (Trithorax-like protein) (Zinc finger protein HRX) [Cleaved into: MLL cleavage product N320 (N-terminal cleavage product of 320 kDa) (p320); MLL cleavage product C180 (C-terminal cleavage product of 180 kDa) (p180)] | Histone methyltransferase that plays an essential role in early development and hematopoiesis (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:26886794). Catalytic subunit of the MLL1/MLL complex, a multiprotein complex that mediates both methylation of 'Lys-4' of histone H3 (H3K4me) complex and acetylation of 'Lys-16' of histone H4 (H4K16ac) (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:24235145, PubMed:26886794). Catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) via a non-processive mechanism. Part of chromatin remodeling machinery predominantly forms H3K4me1 and H3K4me2 methylation marks at active chromatin sites where transcription and DNA repair take place (PubMed:12453419, PubMed:15960975, PubMed:19187761, PubMed:19556245, PubMed:20677832, PubMed:21220120, PubMed:25561738, PubMed:26886794). Has weak methyltransferase activity by itself, and requires other component of the MLL1/MLL complex to obtain full methyltransferase activity (PubMed:19187761, PubMed:26886794). Has no activity toward histone H3 phosphorylated on 'Thr-3', less activity toward H3 dimethylated on 'Arg-8' or 'Lys-9', while it has higher activity toward H3 acetylated on 'Lys-9' (PubMed:19187761). Binds to unmethylated CpG elements in the promoter of target genes and helps maintain them in the nonmethylated state (PubMed:20010842). Required for transcriptional activation of HOXA9 (PubMed:12453419, PubMed:20010842, PubMed:20677832). Promotes PPP1R15A-induced apoptosis (PubMed:10490642). Plays a critical role in the control of circadian gene expression and is essential for the transcriptional activation mediated by the CLOCK-BMAL1 heterodimer (By similarity). Establishes a permissive chromatin state for circadian transcription by mediating a rhythmic methylation of 'Lys-4' of histone H3 (H3K4me) and this histone modification directs the circadian acetylation at H3K9 and H3K14 allowing the recruitment of CLOCK-BMAL1 to chromatin (By similarity). Also has auto-methylation activity on Cys-3882 in absence of histone H3 substrate (PubMed:24235145). {ECO:0000250|UniProtKB:P55200, ECO:0000269|PubMed:10490642, ECO:0000269|PubMed:12453419, ECO:0000269|PubMed:15960975, ECO:0000269|PubMed:19187761, ECO:0000269|PubMed:19556245, ECO:0000269|PubMed:20010842, ECO:0000269|PubMed:21220120, ECO:0000269|PubMed:24235145, ECO:0000269|PubMed:26886794, ECO:0000305|PubMed:20677832}. |
Q04759 | PRKCQ | S685 | ochoa | Protein kinase C theta type (EC 2.7.11.13) (nPKC-theta) | Calcium-independent, phospholipid- and diacylglycerol (DAG)-dependent serine/threonine-protein kinase that mediates non-redundant functions in T-cell receptor (TCR) signaling, including T-cells activation, proliferation, differentiation and survival, by mediating activation of multiple transcription factors such as NF-kappa-B, JUN, NFATC1 and NFATC2. In TCR-CD3/CD28-co-stimulated T-cells, is required for the activation of NF-kappa-B and JUN, which in turn are essential for IL2 production, and participates in the calcium-dependent NFATC1 and NFATC2 transactivation (PubMed:21964608). Mediates the activation of the canonical NF-kappa-B pathway (NFKB1) by direct phosphorylation of CARD11 on several serine residues, inducing CARD11 association with lipid rafts and recruitment of the BCL10-MALT1 complex, which then activates IKK complex, resulting in nuclear translocation and activation of NFKB1. May also play an indirect role in activation of the non-canonical NF-kappa-B (NFKB2) pathway. In the signaling pathway leading to JUN activation, acts by phosphorylating the mediator STK39/SPAK and may not act through MAP kinases signaling. Plays a critical role in TCR/CD28-induced NFATC1 and NFATC2 transactivation by participating in the regulation of reduced inositol 1,4,5-trisphosphate generation and intracellular calcium mobilization. After costimulation of T-cells through CD28 can phosphorylate CBLB and is required for the ubiquitination and subsequent degradation of CBLB, which is a prerequisite for the activation of TCR. During T-cells differentiation, plays an important role in the development of T-helper 2 (Th2) cells following immune and inflammatory responses, and, in the development of inflammatory autoimmune diseases, is necessary for the activation of IL17-producing Th17 cells. May play a minor role in Th1 response. Upon TCR stimulation, mediates T-cell protective survival signal by phosphorylating BAD, thus protecting T-cells from BAD-induced apoptosis, and by up-regulating BCL-X(L)/BCL2L1 levels through NF-kappa-B and JUN pathways. In platelets, regulates signal transduction downstream of the ITGA2B, CD36/GP4, F2R/PAR1 and F2RL3/PAR4 receptors, playing a positive role in 'outside-in' signaling and granule secretion signal transduction. May relay signals from the activated ITGA2B receptor by regulating the uncoupling of WASP and WIPF1, thereby permitting the regulation of actin filament nucleation and branching activity of the Arp2/3 complex. May mediate inhibitory effects of free fatty acids on insulin signaling by phosphorylating IRS1, which in turn blocks IRS1 tyrosine phosphorylation and downstream activation of the PI3K/AKT pathway. Phosphorylates MSN (moesin) in the presence of phosphatidylglycerol or phosphatidylinositol. Phosphorylates PDPK1 at 'Ser-504' and 'Ser-532' and negatively regulates its ability to phosphorylate PKB/AKT1. Phosphorylates CCDC88A/GIV and inhibits its guanine nucleotide exchange factor activity (PubMed:23509302). Phosphorylates and activates LRRK1, which phosphorylates RAB proteins involved in intracellular trafficking (PubMed:36040231). {ECO:0000269|PubMed:11342610, ECO:0000269|PubMed:14988727, ECO:0000269|PubMed:15364919, ECO:0000269|PubMed:16252004, ECO:0000269|PubMed:16356855, ECO:0000269|PubMed:16709830, ECO:0000269|PubMed:19549985, ECO:0000269|PubMed:21964608, ECO:0000269|PubMed:23509302, ECO:0000269|PubMed:36040231, ECO:0000269|PubMed:8657160}. |
Q12986 | NFX1 | S150 | ochoa | Transcriptional repressor NF-X1 (EC 2.3.2.-) (Nuclear transcription factor, X box-binding protein 1) | Binds to the X-box motif of MHC class II genes and represses their expression. May play an important role in regulating the duration of an inflammatory response by limiting the period in which MHC class II molecules are induced by interferon-gamma. Isoform 3 binds to the X-box motif of TERT promoter and represses its expression. Together with PABPC1 or PABPC4, isoform 1 acts as a coactivator for TERT expression. Mediates E2-dependent ubiquitination. {ECO:0000269|PubMed:10500182, ECO:0000269|PubMed:15371341, ECO:0000269|PubMed:17267499}. |
Q13352 | ITGB3BP | S46 | psp | Centromere protein R (CENP-R) (Beta-3-endonexin) (Integrin beta-3-binding protein) (Nuclear receptor-interacting factor 3) | Transcription coregulator that can have both coactivator and corepressor functions. Isoform 1, but not other isoforms, is involved in the coactivation of nuclear receptors for retinoid X (RXRs) and thyroid hormone (TRs) in a ligand-dependent fashion. In contrast, it does not coactivate nuclear receptors for retinoic acid, vitamin D, progesterone receptor, nor glucocorticoid. Acts as a coactivator for estrogen receptor alpha. Acts as a transcriptional corepressor via its interaction with the NFKB1 NF-kappa-B subunit, possibly by interfering with the transactivation domain of NFKB1. Induces apoptosis in breast cancer cells, but not in other cancer cells, via a caspase-2 mediated pathway that involves mitochondrial membrane permeabilization but does not require other caspases. May also act as an inhibitor of cyclin A-associated kinase. Also acts a component of the CENPA-CAD (nucleosome distal) complex, a complex recruited to centromeres which is involved in assembly of kinetochore proteins, mitotic progression and chromosome segregation. May be involved in incorporation of newly synthesized CENPA into centromeres via its interaction with the CENPA-NAC complex. {ECO:0000269|PubMed:11713274, ECO:0000269|PubMed:12244126, ECO:0000269|PubMed:15082778, ECO:0000269|PubMed:15254226, ECO:0000269|PubMed:16622420}. |
Q13480 | GAB1 | S274 | ochoa | GRB2-associated-binding protein 1 (GRB2-associated binder 1) (Growth factor receptor bound protein 2-associated protein 1) | Adapter protein that plays a role in intracellular signaling cascades triggered by activated receptor-type kinases. Plays a role in FGFR1 signaling. Probably involved in signaling by the epidermal growth factor receptor (EGFR) and the insulin receptor (INSR). Involved in the MET/HGF-signaling pathway (PubMed:29408807). {ECO:0000269|PubMed:29408807}. |
Q13522 | PPP1R1A | S67 | ochoa|psp | Protein phosphatase 1 regulatory subunit 1A (Protein phosphatase inhibitor 1) (I-1) (IPP-1) | Inhibitor of protein-phosphatase 1. This protein may be important in hormonal control of glycogen metabolism. Hormones that elevate intracellular cAMP increase I-1 activity in many tissues. I-1 activation may impose cAMP control over proteins that are not directly phosphorylated by PKA. Following a rise in intracellular calcium, I-1 is inactivated by calcineurin (or PP2B). Does not inhibit type-2 phosphatases. |
Q13829 | TNFAIP1 | S278 | ochoa|psp | BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 (hBACURD2) (BTB/POZ domain-containing protein TNFAIP1) (Protein B12) (Tumor necrosis factor, alpha-induced protein 1, endothelial) | Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex involved in regulation of cytoskeleton structure. The BCR(TNFAIP1) E3 ubiquitin ligase complex mediates the ubiquitination of RHOA, leading to its degradation by the proteasome, thereby regulating the actin cytoskeleton and cell migration. Its interaction with RHOB may regulate apoptosis. May enhance the PCNA-dependent DNA polymerase delta activity. {ECO:0000269|PubMed:19637314, ECO:0000269|PubMed:19782033}. |
Q15120 | PDK3 | S23 | ochoa | [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 3, mitochondrial (EC 2.7.11.2) (Pyruvate dehydrogenase kinase isoform 3) | Inhibits pyruvate dehydrogenase activity by phosphorylation of the E1 subunit PDHA1, and thereby regulates glucose metabolism and aerobic respiration. Can also phosphorylate PDHA2. Decreases glucose utilization and increases fat metabolism in response to prolonged fasting, and as adaptation to a high-fat diet. Plays a role in glucose homeostasis and in maintaining normal blood glucose levels in function of nutrient levels and under starvation. Plays a role in the generation of reactive oxygen species. {ECO:0000269|PubMed:10748134, ECO:0000269|PubMed:11486000, ECO:0000269|PubMed:15861126, ECO:0000269|PubMed:16436377, ECO:0000269|PubMed:17683942, ECO:0000269|PubMed:18718909, ECO:0000269|PubMed:22865452}. |
Q15697 | ZNF174 | S266 | ochoa | Zinc finger protein 174 (AW-1) (Zinc finger and SCAN domain-containing protein 8) | Transcriptional repressor. {ECO:0000269|PubMed:7673192}. |
Q15772 | SPEG | S2343 | 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. |
Q1MSJ5 | CSPP1 | S747 | ochoa | Centrosome and spindle pole-associated protein 1 | May play a role in cell-cycle-dependent microtubule organization. {ECO:0000269|PubMed:16826565}. |
Q2TAZ0 | ATG2A | S775 | ochoa | Autophagy-related protein 2 homolog A | Lipid transfer protein involved in autophagosome assembly (PubMed:28561066, PubMed:30952800, PubMed:31271352). Tethers the edge of the isolation membrane (IM) to the endoplasmic reticulum (ER) and mediates direct lipid transfer from ER to IM for IM expansion (PubMed:30952800, PubMed:31271352). Binds to the ER exit site (ERES), which is the membrane source for autophagosome formation, and extracts phospholipids from the membrane source and transfers them to ATG9 (ATG9A or ATG9B) to the IM for membrane expansion (PubMed:30952800, PubMed:31271352). Lipid transfer activity is enhanced by WIPI1 and WDR45/WIPI4, which promote ATG2A-association with phosphatidylinositol 3-monophosphate (PI3P)-containing membranes (PubMed:31271352). Also regulates lipid droplets morphology and distribution within the cell (PubMed:22219374, PubMed:28561066). {ECO:0000269|PubMed:22219374, ECO:0000269|PubMed:28561066, ECO:0000269|PubMed:30952800, ECO:0000269|PubMed:31271352}. |
Q3T8J9 | GON4L | S1268 | ochoa | GON-4-like protein (GON-4 homolog) | Has transcriptional repressor activity, probably as part of a complex with YY1, SIN3A and HDAC1. Required for B cell lymphopoiesis. {ECO:0000250|UniProtKB:Q9DB00}. |
Q53EZ4 | CEP55 | S425 | ochoa|psp | Centrosomal protein of 55 kDa (Cep55) (Up-regulated in colon cancer 6) | Plays a role in mitotic exit and cytokinesis (PubMed:16198290, PubMed:17853893). Recruits PDCD6IP and TSG101 to midbody during cytokinesis. Required for successful completion of cytokinesis (PubMed:17853893). Not required for microtubule nucleation (PubMed:16198290). Plays a role in the development of the brain and kidney (PubMed:28264986). {ECO:0000269|PubMed:16198290, ECO:0000269|PubMed:17853893, ECO:0000269|PubMed:28264986}. |
Q53HL2 | CDCA8 | S244 | ochoa | Borealin (Cell division cycle-associated protein 8) (Dasra-B) (hDasra-B) (Pluripotent embryonic stem cell-related gene 3 protein) | Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Major effector of the TTK kinase in the control of attachment-error-correction and chromosome alignment. {ECO:0000269|PubMed:15249581, ECO:0000269|PubMed:15260989, ECO:0000269|PubMed:16571674, ECO:0000269|PubMed:18243099}. |
Q5T1M5 | FKBP15 | S1065 | ochoa | FK506-binding protein 15 (FKBP-15) (133 kDa FK506-binding protein) (133 kDa FKBP) (FKBP-133) (WASP- and FKBP-like protein) (WAFL) | May be involved in the cytoskeletal organization of neuronal growth cones. Seems to be inactive as a PPIase (By similarity). Involved in the transport of early endosomes at the level of transition between microfilament-based and microtubule-based movement. {ECO:0000250, ECO:0000269|PubMed:19121306}. |
Q5TAX3 | TUT4 | S841 | ochoa | Terminal uridylyltransferase 4 (TUTase 4) (EC 2.7.7.52) (Zinc finger CCHC domain-containing protein 11) | Uridylyltransferase that mediates the terminal uridylation of mRNAs with short (less than 25 nucleotides) poly(A) tails, hence facilitating global mRNA decay (PubMed:25480299, PubMed:31036859). Essential for both oocyte maturation and fertility. Through 3' terminal uridylation of mRNA, sculpts, with TUT7, the maternal transcriptome by eliminating transcripts during oocyte growth (By similarity). Involved in microRNA (miRNA)-induced gene silencing through uridylation of deadenylated miRNA targets. Also functions as an integral regulator of microRNA biogenesis using 3 different uridylation mechanisms (PubMed:25979828). Acts as a suppressor of miRNA biogenesis by mediating the terminal uridylation of some miRNA precursors, including that of let-7 (pre-let-7), miR107, miR-143 and miR-200c. Uridylated miRNAs are not processed by Dicer and undergo degradation. Degradation of pre-let-7 contributes to the maintenance of embryonic stem (ES) cell pluripotency (By similarity). Also catalyzes the 3' uridylation of miR-26A, a miRNA that targets IL6 transcript. This abrogates the silencing of IL6 transcript, hence promoting cytokine expression (PubMed:19703396). In the absence of LIN28A, TUT7 and TUT4 monouridylate group II pre-miRNAs, which includes most of pre-let7 members, that shapes an optimal 3' end overhang for efficient processing (PubMed:25979828). Adds oligo-U tails to truncated pre-miRNAS with a 5' overhang which may promote rapid degradation of non-functional pre-miRNA species (PubMed:25979828). May also suppress Toll-like receptor-induced NF-kappa-B activation via binding to T2BP (PubMed:16643855). Does not play a role in replication-dependent histone mRNA degradation (PubMed:18172165). Due to functional redundancy between TUT4 and TUT7, the identification of the specific role of each of these proteins is difficult (By similarity) (PubMed:16643855, PubMed:18172165, PubMed:19703396, PubMed:25480299, PubMed:25979828). TUT4 and TUT7 restrict retrotransposition of long interspersed element-1 (LINE-1) in cooperation with MOV10 counteracting the RNA chaperonne activity of L1RE1. TUT7 uridylates LINE-1 mRNAs in the cytoplasm which inhibits initiation of reverse transcription once in the nucleus, whereas uridylation by TUT4 destabilizes mRNAs in cytoplasmic ribonucleoprotein granules (PubMed:30122351). {ECO:0000250|UniProtKB:B2RX14, ECO:0000269|PubMed:16643855, ECO:0000269|PubMed:18172165, ECO:0000269|PubMed:19703396, ECO:0000269|PubMed:25480299, ECO:0000269|PubMed:25979828, ECO:0000269|PubMed:30122351, ECO:0000269|PubMed:31036859}. |
Q6PFW1 | PPIP5K1 | S964 | ochoa | Inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1 (EC 2.7.4.24) (Diphosphoinositol pentakisphosphate kinase 1) (Histidine acid phosphatase domain-containing protein 2A) (IP6 kinase) (Inositol pyrophosphate synthase 1) (InsP6 and PP-IP5 kinase 1) (VIP1 homolog) (hsVIP1) | Bifunctional inositol kinase that acts in concert with the IP6K kinases IP6K1, IP6K2 and IP6K3 to synthesize the diphosphate group-containing inositol pyrophosphates diphosphoinositol pentakisphosphate, PP-InsP5, and bis-diphosphoinositol tetrakisphosphate, (PP)2-InsP4. PP-InsP5 and (PP)2-InsP4, also respectively called InsP7 and InsP8, regulate a variety of cellular processes, including apoptosis, vesicle trafficking, cytoskeletal dynamics, exocytosis, insulin signaling and neutrophil activation. Phosphorylates inositol hexakisphosphate (InsP6) at position 1 to produce PP-InsP5 which is in turn phosphorylated by IP6Ks to produce (PP)2-InsP4. Alternatively, phosphorylates PP-InsP5 at position 1, produced by IP6Ks from InsP6, to produce (PP)2-InsP4. Activated when cells are exposed to hyperosmotic stress. {ECO:0000269|PubMed:17690096, ECO:0000269|PubMed:17702752}. |
Q6S8J3 | POTEE | S932 | ochoa | POTE ankyrin domain family member E (ANKRD26-like family C member 1A) (Prostate, ovary, testis-expressed protein on chromosome 2) (POTE-2) | None |
Q6VY07 | PACS1 | S495 | ochoa | Phosphofurin acidic cluster sorting protein 1 (PACS-1) | Coat protein that is involved in the localization of trans-Golgi network (TGN) membrane proteins that contain acidic cluster sorting motifs. Controls the endosome-to-Golgi trafficking of furin and mannose-6-phosphate receptor by connecting the acidic-cluster-containing cytoplasmic domain of these molecules with the adapter-protein complex-1 (AP-1) of endosomal clathrin-coated membrane pits. Involved in HIV-1 nef-mediated removal of MHC-I from the cell surface to the TGN. Required for normal ER Ca2+ handling in lymphocytes. Together with WDR37, it plays an essential role in lymphocyte development, quiescence and survival. Required for stabilizing peripheral lymphocyte populations (By similarity). {ECO:0000250|UniProtKB:Q8K212, ECO:0000269|PubMed:11331585, ECO:0000269|PubMed:15692563}. |
Q6WCQ1 | MPRIP | S326 | ochoa | Myosin phosphatase Rho-interacting protein (M-RIP) (Rho-interacting protein 3) (RIP3) (p116Rip) | Targets myosin phosphatase to the actin cytoskeleton. Required for the regulation of the actin cytoskeleton by RhoA and ROCK1. Depletion leads to an increased number of stress fibers in smooth muscle cells through stabilization of actin fibers by phosphorylated myosin. Overexpression of MRIP as well as its F-actin-binding region leads to disassembly of stress fibers in neuronal cells. {ECO:0000250|UniProtKB:P97434, ECO:0000269|PubMed:15545284, ECO:0000269|PubMed:16257966}. |
Q6ZQN7 | SLCO4C1 | S26 | ochoa | Solute carrier organic anion transporter family member 4C1 (SLCO4C1) (OATP-H) (Organic anion transporter M1) (OATP-M1) (Organic anion transporting polypeptide 4C1) (OATP4C1) (Solute carrier family 21 member 20) | Mediates the transport of organic anions such as steroids (estrone 3-sulfate, chenodeoxycholate, glycocholate) and thyroid hormones (3,3',5-triiodo-L-thyronine (T3), L-thyroxine (T4)), in the kidney (PubMed:14993604, PubMed:19129463, PubMed:20610891). Capable of transporting cAMP and pharmacological substances such as digoxin, ouabain and methotrexate (PubMed:14993604). Transport is independent of sodium, chloride ion, and ATP (PubMed:14993604). Transport activity is stimulated by an acidic extracellular environment due to increased substrate affinity to the transporter (PubMed:19129463). The driving force for this transport activity is currently not known (By similarity). The role of hydrogencarbonate (HCO3(-), bicarbonate) as the probable counteranion that exchanges for organic anions is still not well defined (PubMed:19129463). Functions as an uptake transporter at the apical membrane, suggesting a role in renal reabsorption (By similarity). Involved in the renal secretion of the uremic toxin ADMA (N(omega),N(omega)-dimethyl-L-arginine or asymmetrical dimethylarginine), which is associated to cardiovascular events and mortality, and the structurally related amino acids L-arginine and L-homoarginine (a cardioprotective biomarker) (PubMed:30865704). Can act bidirectionally, suggesting a dual protective role of this transport protein; exporting L-homoarginine after being synthesized in proximal tubule cells, and mediating uptake of ADMA from the blood into proximal tubule cells where it is degraded by the enzyme dimethylarginine dimethylaminohydrolase 1 (DDAH1) (PubMed:30865704, PubMed:32642843). May be involved in sperm maturation by enabling directed movement of organic anions and compounds within or between cells (By similarity). This ion-transporting process is important to maintain the strict epididymal homeostasis necessary for sperm maturation (By similarity). May have a role in secretory functions since seminal vesicle epithelial cells are assumed to secrete proteins involved in decapacitation by modifying surface proteins to facilitate the acquisition of the ability to fertilize the egg (By similarity). {ECO:0000250|UniProtKB:Q71MB6, ECO:0000250|UniProtKB:Q8BGD4, ECO:0000269|PubMed:14993604, ECO:0000269|PubMed:19129463, ECO:0000269|PubMed:20610891, ECO:0000269|PubMed:30865704, ECO:0000269|PubMed:32642843}. |
Q76FK4 | NOL8 | S660 | ochoa | Nucleolar protein 8 (Nucleolar protein Nop132) | Plays an essential role in the survival of diffuse-type gastric cancer cells. Acts as a nucleolar anchoring protein for DDX47. May be involved in regulation of gene expression at the post-transcriptional level or in ribosome biogenesis in cancer cells. {ECO:0000269|PubMed:14660641, ECO:0000269|PubMed:15132771, ECO:0000269|PubMed:16963496}. |
Q7L9B9 | EEPD1 | S247 | ochoa | Endonuclease/exonuclease/phosphatase family domain-containing protein 1 | None |
Q7Z3J3 | RGPD4 | S393 | ochoa | RanBP2-like and GRIP domain-containing protein 4 | None |
Q7Z3J3 | RGPD4 | S1545 | ochoa | RanBP2-like and GRIP domain-containing protein 4 | None |
Q86WW8 | COA5 | S37 | ochoa | Cytochrome c oxidase assembly factor 5 | Involved in an early step of the mitochondrial complex IV assembly process. {ECO:0000269|PubMed:21457908}. |
Q8IWR0 | ZC3H7A | S316 | ochoa | Zinc finger CCCH domain-containing protein 7A | May be a specific regulator of miRNA biogenesis. Binds to microRNAs MIR7-1, MIR16-2 and MIR29A hairpins recognizing the 3'-ATA(A/T)-5' motif in the apical loop. {ECO:0000269|PubMed:28431233}. |
Q8NHV4 | NEDD1 | S516 | ochoa|psp | Protein NEDD1 (Neural precursor cell expressed developmentally down-regulated protein 1) (NEDD-1) | Required for mitosis progression. Promotes the nucleation of microtubules from the spindle. {ECO:0000269|PubMed:19029337, ECO:0000269|PubMed:19509060}. |
Q8TD26 | CHD6 | S34 | ochoa | Chromodomain-helicase-DNA-binding protein 6 (CHD-6) (EC 3.6.4.-) (ATP-dependent helicase CHD6) (Radiation-induced gene B protein) | ATP-dependent chromatin-remodeling factor (PubMed:17027977, PubMed:28533432). Regulates transcription by disrupting nucleosomes in a largely non-sliding manner which strongly increases the accessibility of chromatin; nucleosome disruption requires ATP (PubMed:28533432). Activates transcription of specific genes in response to oxidative stress through interaction with NFE2L2. {ECO:0000269|PubMed:16314513, ECO:0000269|PubMed:17027977, ECO:0000269|PubMed:28533432}.; FUNCTION: (Microbial infection) Acts as a transcriptional repressor of different viruses including influenza virus or papillomavirus. During influenza virus infection, the viral polymerase complex localizes CHD6 to inactive chromatin where it gets degraded in a proteasome independent-manner. {ECO:0000269|PubMed:20631145, ECO:0000269|PubMed:21899694, ECO:0000269|PubMed:23408615}. |
Q8TDB6 | DTX3L | S221 | ochoa | E3 ubiquitin-protein ligase DTX3L (EC 2.3.2.27) (B-lymphoma- and BAL-associated protein) (Protein deltex-3-like) (RING-type E3 ubiquitin transferase DTX3L) (Rhysin-2) (Rhysin2) | E3 ubiquitin-protein ligase which, in association with ADP-ribosyltransferase PARP9, plays a role in DNA damage repair and in interferon-mediated antiviral responses (PubMed:12670957, PubMed:19818714, PubMed:23230272, PubMed:26479788). Monoubiquitinates several histones, including histone H2A, H2B, H3 and H4 (PubMed:28525742). In response to DNA damage, mediates monoubiquitination of 'Lys-91' of histone H4 (H4K91ub1) (PubMed:19818714). The exact role of H4K91ub1 in DNA damage response is still unclear but it may function as a licensing signal for additional histone H4 post-translational modifications such as H4 'Lys-20' methylation (H4K20me) (PubMed:19818714). PARP1-dependent PARP9-DTX3L-mediated ubiquitination promotes the rapid and specific recruitment of 53BP1/TP53BP1, UIMC1/RAP80, and BRCA1 to DNA damage sites (PubMed:23230272). By monoubiquitinating histone H2B H2BC9/H2BJ and thereby promoting chromatin remodeling, positively regulates STAT1-dependent interferon-stimulated gene transcription and thus STAT1-mediated control of viral replication (PubMed:26479788). Independently of its catalytic activity, promotes the sorting of chemokine receptor CXCR4 from early endosome to lysosome following CXCL12 stimulation by reducing E3 ligase ITCH activity and thus ITCH-mediated ubiquitination of endosomal sorting complex required for transport ESCRT-0 components HGS and STAM (PubMed:24790097). In addition, required for the recruitment of HGS and STAM to early endosomes (PubMed:24790097). In association with PARP9, plays a role in antiviral responses by mediating 'Lys-48'-linked ubiquitination of encephalomyocarditis virus (EMCV) and human rhinovirus (HRV) C3 proteases and thus promoting their proteasomal-mediated degradation (PubMed:26479788). {ECO:0000269|PubMed:12670957, ECO:0000269|PubMed:19818714, ECO:0000269|PubMed:23230272, ECO:0000269|PubMed:24790097, ECO:0000269|PubMed:26479788, ECO:0000269|PubMed:28525742}. |
Q8TEC5 | SH3RF2 | S112 | ochoa | E3 ubiquitin-protein ligase SH3RF2 (EC 2.3.2.27) (Heart protein phosphatase 1-binding protein) (HEPP1) (POSH-eliminating RING protein) (Protein phosphatase 1 regulatory subunit 39) (RING finger protein 158) (RING-type E3 ubiquitin transferase SH3RF2) (SH3 domain-containing RING finger protein 2) | Has E3 ubiquitin-protein ligase activity (PubMed:24130170). Acts as an anti-apoptotic regulator of the JNK pathway by ubiquitinating and promoting the degradation of SH3RF1, a scaffold protein that is required for pro-apoptotic JNK activation (PubMed:22128169). Facilitates TNF-alpha-mediated recruitment of adapter proteins TRADD and RIPK1 to TNFRSF1A and regulates PAK4 protein stability via inhibition of its ubiquitin-mediated proteasomal degradation (PubMed:24130170). Inhibits PPP1CA phosphatase activity (PubMed:19389623, PubMed:19945436). {ECO:0000269|PubMed:19389623, ECO:0000269|PubMed:19945436, ECO:0000269|PubMed:22128169, ECO:0000269|PubMed:24130170}. |
Q8WUU5 | GATAD1 | S235 | ochoa | GATA zinc finger domain-containing protein 1 (Ocular development-associated gene protein) | Component of some chromatin complex recruited to chromatin sites methylated 'Lys-4' of histone H3 (H3K4me), with a preference for trimethylated form (H3K4me3). {ECO:0000269|PubMed:20850016}. |
Q8WUY3 | PRUNE2 | S1803 | ochoa | Protein prune homolog 2 (BNIP2 motif-containing molecule at the C-terminal region 1) | May play an important role in regulating differentiation, survival and aggressiveness of the tumor cells. {ECO:0000269|PubMed:16288218}. |
Q96KB5 | PBK | S59 | ochoa | Lymphokine-activated killer T-cell-originated protein kinase (EC 2.7.12.2) (Cancer/testis antigen 84) (CT84) (MAPKK-like protein kinase) (Nori-3) (PDZ-binding kinase) (Spermatogenesis-related protein kinase) (SPK) (T-LAK cell-originated protein kinase) | Phosphorylates MAP kinase p38. Seems to be active only in mitosis. May also play a role in the activation of lymphoid cells. When phosphorylated, forms a complex with TP53, leading to TP53 destabilization and attenuation of G2/M checkpoint during doxorubicin-induced DNA damage. {ECO:0000269|PubMed:10781613, ECO:0000269|PubMed:17482142}. |
Q9BY77 | POLDIP3 | S368 | ochoa | Polymerase delta-interacting protein 3 (46 kDa DNA polymerase delta interaction protein) (p46) (S6K1 Aly/REF-like target) (SKAR) | Is involved in regulation of translation. Is preferentially associated with CBC-bound spliced mRNA-protein complexes during the pioneer round of mRNA translation. Contributes to enhanced translational efficiency of spliced over nonspliced mRNAs. Recruits activated ribosomal protein S6 kinase beta-1 I/RPS6KB1 to newly synthesized mRNA. Involved in nuclear mRNA export; probably mediated by association with the TREX complex. {ECO:0000269|PubMed:18423201, ECO:0000269|PubMed:22928037}. |
Q9BYW2 | SETD2 | S624 | ochoa | Histone-lysine N-methyltransferase SETD2 (EC 2.1.1.359) (HIF-1) (Huntingtin yeast partner B) (Huntingtin-interacting protein 1) (HIP-1) (Huntingtin-interacting protein B) (Lysine N-methyltransferase 3A) (Protein-lysine N-methyltransferase SETD2) (EC 2.1.1.-) (SET domain-containing protein 2) (hSET2) (p231HBP) | Histone methyltransferase that specifically trimethylates 'Lys-36' of histone H3 (H3K36me3) using dimethylated 'Lys-36' (H3K36me2) as substrate (PubMed:16118227, PubMed:19141475, PubMed:21526191, PubMed:21792193, PubMed:23043551, PubMed:27474439). It is capable of trimethylating unmethylated H3K36 (H3K36me0) in vitro (PubMed:19332550). Represents the main enzyme generating H3K36me3, a specific tag for epigenetic transcriptional activation (By similarity). Plays a role in chromatin structure modulation during elongation by coordinating recruitment of the FACT complex and by interacting with hyperphosphorylated POLR2A (PubMed:23325844). Acts as a key regulator of DNA mismatch repair in G1 and early S phase by generating H3K36me3, a mark required to recruit MSH6 subunit of the MutS alpha complex: early recruitment of the MutS alpha complex to chromatin to be replicated allows a quick identification of mismatch DNA to initiate the mismatch repair reaction (PubMed:23622243). Required for DNA double-strand break repair in response to DNA damage: acts by mediating formation of H3K36me3, promoting recruitment of RAD51 and DNA repair via homologous recombination (HR) (PubMed:24843002). Acts as a tumor suppressor (PubMed:24509477). H3K36me3 also plays an essential role in the maintenance of a heterochromatic state, by recruiting DNA methyltransferase DNMT3A (PubMed:27317772). H3K36me3 is also enhanced in intron-containing genes, suggesting that SETD2 recruitment is enhanced by splicing and that splicing is coupled to recruitment of elongating RNA polymerase (PubMed:21792193). Required during angiogenesis (By similarity). Required for endoderm development by promoting embryonic stem cell differentiation toward endoderm: acts by mediating formation of H3K36me3 in distal promoter regions of FGFR3, leading to regulate transcription initiation of FGFR3 (By similarity). In addition to histones, also mediates methylation of other proteins, such as tubulins and STAT1 (PubMed:27518565, PubMed:28753426). Trimethylates 'Lys-40' of alpha-tubulins such as TUBA1B (alpha-TubK40me3); alpha-TubK40me3 is required for normal mitosis and cytokinesis and may be a specific tag in cytoskeletal remodeling (PubMed:27518565). Involved in interferon-alpha-induced antiviral defense by mediating both monomethylation of STAT1 at 'Lys-525' and catalyzing H3K36me3 on promoters of some interferon-stimulated genes (ISGs) to activate gene transcription (PubMed:28753426). {ECO:0000250|UniProtKB:E9Q5F9, ECO:0000269|PubMed:16118227, ECO:0000269|PubMed:19141475, ECO:0000269|PubMed:21526191, ECO:0000269|PubMed:21792193, ECO:0000269|PubMed:23043551, ECO:0000269|PubMed:23325844, ECO:0000269|PubMed:23622243, ECO:0000269|PubMed:24509477, ECO:0000269|PubMed:24843002, ECO:0000269|PubMed:27317772, ECO:0000269|PubMed:27474439, ECO:0000269|PubMed:27518565, ECO:0000269|PubMed:28753426}.; FUNCTION: (Microbial infection) Recruited to the promoters of adenovirus 12 E1A gene in case of infection, possibly leading to regulate its expression. {ECO:0000269|PubMed:11461154}. |
Q9H2P0 | ADNP | S738 | ochoa | Activity-dependent neuroprotector homeobox protein (Activity-dependent neuroprotective protein) | May be involved in transcriptional regulation. May mediate some of the neuroprotective peptide VIP-associated effects involving normal growth and cancer proliferation. Positively modulates WNT-beta-catenin/CTNN1B signaling, acting by regulating phosphorylation of, and thereby stabilizing, CTNNB1. May be required for neural induction and neuronal differentiation. May be involved in erythroid differentiation (By similarity). {ECO:0000250|UniProtKB:Q9Z103}. |
Q9H5I5 | PIEZO2 | S376 | ochoa | Piezo-type mechanosensitive ion channel component 2 (Protein FAM38B) | Pore-forming subunit of the mechanosensitive non-specific cation Piezo channel required for rapidly adapting mechanically activated (MA) currents and has a key role in sensing touch and tactile pain (PubMed:37590348). Piezo channels are homotrimeric three-blade propeller-shaped structures that utilize a cap-motion and plug-and-latch mechanism to gate their ion-conducting pathways (PubMed:37590348). Expressed in sensory neurons, is essential for diverse physiological processes, including respiratory control, systemic metabolism, urinary function, and proprioception (By similarity). Mediates airway stretch sensing, enabling efficient respiration at birth and maintaining normal breathing in adults (By similarity). It regulates brown and beige adipose tissue morphology and function, preventing systemic hypermetabolism (By similarity). In the lower urinary tract, acts as a sensor in both the bladder urothelium and innervating sensory neurons being required for bladder-stretch sensing and urethral micturition reflexes, ensuring proper urinary function (PubMed:33057202). Additionally, PIEZO2 serves as the principal mechanotransducer in proprioceptors, facilitating proprioception and coordinated body movements (By similarity). In inner ear hair cells, PIEZO1/2 subunits may constitute part of the mechanotransducer (MET) non-selective cation channel complex where they may act as pore-forming ion-conducting component in the complex (By similarity). Required for Merkel-cell mechanotransduction (By similarity). Plays a major role in light-touch mechanosensation (By similarity). {ECO:0000250|UniProtKB:Q8CD54, ECO:0000269|PubMed:33057202, ECO:0000269|PubMed:37590348}. |
Q9H869 | YY1AP1 | S724 | ochoa | YY1-associated protein 1 (Hepatocellular carcinoma susceptibility protein) (Hepatocellular carcinoma-associated protein 2) | Associates with the INO80 chromatin remodeling complex, which is responsible for transcriptional regulation, DNA repair, and replication (PubMed:27939641). Enhances transcription activation by YY1 (PubMed:14744866). Plays a role in cell cycle regulation (PubMed:17541814, PubMed:27939641). {ECO:0000269|PubMed:14744866, ECO:0000269|PubMed:17541814, ECO:0000269|PubMed:27939641}. |
Q9NR48 | ASH1L | S22 | ochoa | Histone-lysine N-methyltransferase ASH1L (EC 2.1.1.359) (EC 2.1.1.367) (ASH1-like protein) (huASH1) (Absent small and homeotic disks protein 1 homolog) (Lysine N-methyltransferase 2H) | Histone methyltransferase specifically trimethylating 'Lys-36' of histone H3 forming H3K36me3 (PubMed:21239497). Also monomethylates 'Lys-9' of histone H3 (H3K9me1) in vitro (By similarity). The physiological significance of the H3K9me1 activity is unclear (By similarity). {ECO:0000250|UniProtKB:Q99MY8, ECO:0000269|PubMed:21239497}. |
Q9NYF8 | BCLAF1 | S658 | ochoa | Bcl-2-associated transcription factor 1 (Btf) (BCLAF1 and THRAP3 family member 1) | Death-promoting transcriptional repressor. May be involved in cyclin-D1/CCND1 mRNA stability through the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA. {ECO:0000269|PubMed:18794151}. |
Q9P2K3 | RCOR3 | S33 | ochoa | REST corepressor 3 | May act as a component of a corepressor complex that represses transcription. {ECO:0000305}. |
Q9UKL0 | RCOR1 | S139 | ochoa | REST corepressor 1 (Protein CoREST) | Essential component of the BHC complex, a corepressor complex that represses transcription of neuron-specific genes in non-neuronal cells. The BHC complex is recruited at RE1/NRSE sites by REST and acts by deacetylating and demethylating specific sites on histones, thereby acting as a chromatin modifier. In the BHC complex, it serves as a molecular beacon for the recruitment of molecular machinery, including MeCP2 and SUV39H1, that imposes silencing across a chromosomal interval. Plays a central role in demethylation of Lys-4 of histone H3 by promoting demethylase activity of KDM1A on core histones and nucleosomal substrates. It also protects KDM1A from the proteasome. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development and controls hematopoietic differentiation. {ECO:0000269|PubMed:11171972, ECO:0000269|PubMed:11516394, ECO:0000269|PubMed:12032298, ECO:0000269|PubMed:12399542, ECO:0000269|PubMed:12493763, ECO:0000269|PubMed:16079794, ECO:0000269|PubMed:16140033}. |
Q9Y2F5 | ICE1 | S516 | ochoa | Little elongation complex subunit 1 (Interactor of little elongator complex ELL subunit 1) | Component of the little elongation complex (LEC), a complex required to regulate small nuclear RNA (snRNA) gene transcription by RNA polymerase II and III (PubMed:22195968, PubMed:23932780). Specifically acts as a scaffold protein that promotes the LEC complex formation and recruitment and RNA polymerase II occupancy at snRNA genes in subnuclear bodies (PubMed:23932780). {ECO:0000269|PubMed:22195968, ECO:0000269|PubMed:23932780}. |
Q9Y2J2 | EPB41L3 | S762 | ochoa | Band 4.1-like protein 3 (4.1B) (Differentially expressed in adenocarcinoma of the lung protein 1) (DAL-1) (Erythrocyte membrane protein band 4.1-like 3) [Cleaved into: Band 4.1-like protein 3, N-terminally processed] | Tumor suppressor that inhibits cell proliferation and promotes apoptosis. Modulates the activity of protein arginine N-methyltransferases, including PRMT3 and PRMT5. {ECO:0000269|PubMed:15334060, ECO:0000269|PubMed:15737618, ECO:0000269|PubMed:16420693, ECO:0000269|PubMed:9892180}. |
Q9Y2W1 | THRAP3 | S682 | ochoa | Thyroid hormone receptor-associated protein 3 (BCLAF1 and THRAP3 family member 2) (Thyroid hormone receptor-associated protein complex 150 kDa component) (Trap150) | Involved in pre-mRNA splicing. Remains associated with spliced mRNA after splicing which probably involves interactions with the exon junction complex (EJC). Can trigger mRNA decay which seems to be independent of nonsense-mediated decay involving premature stop codons (PTC) recognition. May be involved in nuclear mRNA decay. Involved in regulation of signal-induced alternative splicing. During splicing of PTPRC/CD45 is proposed to sequester phosphorylated SFPQ from PTPRC/CD45 pre-mRNA in resting T-cells. Involved in cyclin-D1/CCND1 mRNA stability probably by acting as component of the SNARP complex which associates with both the 3'end of the CCND1 gene and its mRNA. Involved in response to DNA damage. Is excluced from DNA damage sites in a manner that parallels transcription inhibition; the function may involve the SNARP complex. Initially thought to play a role in transcriptional coactivation through its association with the TRAP complex; however, it is not regarded as a stable Mediator complex subunit. Cooperatively with HELZ2, enhances the transcriptional activation mediated by PPARG, maybe through the stabilization of the PPARG binding to DNA in presence of ligand. May play a role in the terminal stage of adipocyte differentiation. Plays a role in the positive regulation of the circadian clock. Acts as a coactivator of the CLOCK-BMAL1 heterodimer and promotes its transcriptional activator activity and binding to circadian target genes (PubMed:24043798). {ECO:0000269|PubMed:20123736, ECO:0000269|PubMed:20932480, ECO:0000269|PubMed:22424773, ECO:0000269|PubMed:23525231, ECO:0000269|PubMed:24043798}. |
Q9Y6X0 | SETBP1 | S611 | ochoa | SET-binding protein (SEB) | None |
Q9Y6X2 | PIAS3 | S431 | ochoa | E3 SUMO-protein ligase PIAS3 (EC 2.3.2.-) (E3 SUMO-protein transferase PIAS3) (Protein inhibitor of activated STAT protein 3) | Functions as an E3-type small ubiquitin-like modifier (SUMO) ligase, stabilizing the interaction between UBE2I and the substrate, and as a SUMO-tethering factor. Plays a crucial role as a transcriptional coregulation in various cellular pathways, including the STAT pathway and the steroid hormone signaling pathway. Involved in regulating STAT3 signaling via inhibiting STAT3 DNA-binding and suppressing cell growth. Enhances the sumoylation of MTA1 and may participate in its paralog-selective sumoylation (PubMed:21965678, PubMed:9388184). Sumoylates CCAR2 which promotes its interaction with SIRT1 (PubMed:25406032). Diminishes the sumoylation of ZFHX3 by preventing the colocalization of ZFHX3 with SUMO1 in the nucleus (PubMed:24651376). {ECO:0000269|PubMed:21965678, ECO:0000269|PubMed:24651376, ECO:0000269|PubMed:25406032, ECO:0000269|PubMed:9388184}. |
P22314 | UBA1 | Y845 | Sugiyama | Ubiquitin-like modifier-activating enzyme 1 (EC 6.2.1.45) (Protein A1S9) (Ubiquitin-activating enzyme E1) | Catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation through the ubiquitin-proteasome system (PubMed:1447181, PubMed:1606621, PubMed:33108101). Activates ubiquitin by first adenylating its C-terminal glycine residue with ATP, and thereafter linking this residue to the side chain of a cysteine residue in E1, yielding a ubiquitin-E1 thioester and free AMP (PubMed:1447181). Essential for the formation of radiation-induced foci, timely DNA repair and for response to replication stress. Promotes the recruitment of TP53BP1 and BRCA1 at DNA damage sites (PubMed:22456334). {ECO:0000269|PubMed:1447181, ECO:0000269|PubMed:1606621, ECO:0000269|PubMed:22456334, ECO:0000269|PubMed:33108101}. |
P49585 | PCYT1A | S174 | Sugiyama | Choline-phosphate cytidylyltransferase A (EC 2.7.7.15) (CCT-alpha) (CTP:phosphocholine cytidylyltransferase A) (CCT A) (CT A) (Phosphorylcholine transferase A) | Catalyzes the key rate-limiting step in the CDP-choline pathway for phosphatidylcholine biosynthesis. {ECO:0000269|PubMed:10480912, ECO:0000269|PubMed:30559292, ECO:0000269|PubMed:7918629}. |
Q13164 | MAPK7 | S210 | Sugiyama | Mitogen-activated protein kinase 7 (MAP kinase 7) (MAPK 7) (EC 2.7.11.24) (Big MAP kinase 1) (BMK-1) (Extracellular signal-regulated kinase 5) (ERK-5) | Plays a role in various cellular processes such as proliferation, differentiation and cell survival. The upstream activator of MAPK7 is the MAPK kinase MAP2K5. Upon activation, it translocates to the nucleus and phosphorylates various downstream targets including MEF2C. EGF activates MAPK7 through a Ras-independent and MAP2K5-dependent pathway. As part of the MAPK/ERK signaling pathway, acts as a negative regulator of apoptosis in cardiomyocytes via interaction with STUB1/CHIP and promotion of STUB1-mediated ubiquitination and degradation of ICER-type isoforms of CREM (By similarity). May have a role in muscle cell differentiation. May be important for endothelial function and maintenance of blood vessel integrity. MAP2K5 and MAPK7 interact specifically with one another and not with MEK1/ERK1 or MEK2/ERK2 pathways. Phosphorylates SGK1 at Ser-78 and this is required for growth factor-induced cell cycle progression. Involved in the regulation of p53/TP53 by disrupting the PML-MDM2 interaction. {ECO:0000250|UniProtKB:P0C865, ECO:0000269|PubMed:11254654, ECO:0000269|PubMed:11278431, ECO:0000269|PubMed:22869143, ECO:0000269|PubMed:9384584, ECO:0000269|PubMed:9790194}. |
Q5S007 | LRRK2 | S1445 | EPSD|PSP|Sugiyama | Leucine-rich repeat serine/threonine-protein kinase 2 (EC 2.7.11.1) (EC 3.6.5.-) (Dardarin) | Serine/threonine-protein kinase which phosphorylates a broad range of proteins involved in multiple processes such as neuronal plasticity, innate immunity, autophagy, and vesicle trafficking (PubMed:17114044, PubMed:20949042, PubMed:21850687, PubMed:22012985, PubMed:23395371, PubMed:24687852, PubMed:25201882, PubMed:26014385, PubMed:26824392, PubMed:27830463, PubMed:28720718, PubMed:29125462, PubMed:29127255, PubMed:29212815, PubMed:30398148, PubMed:30635421). Is a key regulator of RAB GTPases by regulating the GTP/GDP exchange and interaction partners of RABs through phosphorylation (PubMed:26824392, PubMed:28720718, PubMed:29125462, PubMed:29127255, PubMed:29212815, PubMed:30398148, PubMed:30635421). Phosphorylates RAB3A, RAB3B, RAB3C, RAB3D, RAB5A, RAB5B, RAB5C, RAB8A, RAB8B, RAB10, RAB12, RAB29, RAB35, and RAB43 (PubMed:23395371, PubMed:26824392, PubMed:28720718, PubMed:29125462, PubMed:29127255, PubMed:29212815, PubMed:30398148, PubMed:30635421, PubMed:38127736). Regulates the RAB3IP-catalyzed GDP/GTP exchange for RAB8A through the phosphorylation of 'Thr-72' on RAB8A (PubMed:26824392). Inhibits the interaction between RAB8A and GDI1 and/or GDI2 by phosphorylating 'Thr-72' on RAB8A (PubMed:26824392). Regulates primary ciliogenesis through phosphorylation of RAB8A and RAB10, which promotes SHH signaling in the brain (PubMed:29125462, PubMed:30398148). Together with RAB29, plays a role in the retrograde trafficking pathway for recycling proteins, such as mannose-6-phosphate receptor (M6PR), between lysosomes and the Golgi apparatus in a retromer-dependent manner (PubMed:23395371). Regulates neuronal process morphology in the intact central nervous system (CNS) (PubMed:17114044). Plays a role in synaptic vesicle trafficking (PubMed:24687852). Plays an important role in recruiting SEC16A to endoplasmic reticulum exit sites (ERES) and in regulating ER to Golgi vesicle-mediated transport and ERES organization (PubMed:25201882). Positively regulates autophagy through a calcium-dependent activation of the CaMKK/AMPK signaling pathway (PubMed:22012985). The process involves activation of nicotinic acid adenine dinucleotide phosphate (NAADP) receptors, increase in lysosomal pH, and calcium release from lysosomes (PubMed:22012985). Phosphorylates PRDX3 (PubMed:21850687). By phosphorylating APP on 'Thr-743', which promotes the production and the nuclear translocation of the APP intracellular domain (AICD), regulates dopaminergic neuron apoptosis (PubMed:28720718). Acts as a positive regulator of innate immunity by mediating phosphorylation of RIPK2 downstream of NOD1 and NOD2, thereby enhancing RIPK2 activation (PubMed:27830463). Independent of its kinase activity, inhibits the proteasomal degradation of MAPT, thus promoting MAPT oligomerization and secretion (PubMed:26014385). In addition, has GTPase activity via its Roc domain which regulates LRRK2 kinase activity (PubMed:18230735, PubMed:26824392, PubMed:28720718, PubMed:29125462, PubMed:29212815). Recruited by RAB29/RAB7L1 to overloaded lysosomes where it phosphorylates and stabilizes RAB8A and RAB10 which promote lysosomal content release and suppress lysosomal enlargement through the EHBP1 and EHBP1L1 effector proteins (PubMed:30209220, PubMed:38227290). {ECO:0000269|PubMed:17114044, ECO:0000269|PubMed:18230735, ECO:0000269|PubMed:20949042, ECO:0000269|PubMed:21850687, ECO:0000269|PubMed:22012985, ECO:0000269|PubMed:23395371, ECO:0000269|PubMed:24687852, ECO:0000269|PubMed:25201882, ECO:0000269|PubMed:26014385, ECO:0000269|PubMed:26824392, ECO:0000269|PubMed:27830463, ECO:0000269|PubMed:28720718, ECO:0000269|PubMed:29125462, ECO:0000269|PubMed:29127255, ECO:0000269|PubMed:29212815, ECO:0000269|PubMed:30209220, ECO:0000269|PubMed:30398148, ECO:0000269|PubMed:30635421, ECO:0000269|PubMed:38127736, ECO:0000269|PubMed:38227290}. |
Q7KZF4 | SND1 | S720 | Sugiyama | Staphylococcal nuclease domain-containing protein 1 (EC 3.1.31.1) (100 kDa coactivator) (EBNA2 coactivator p100) (Tudor domain-containing protein 11) (p100 co-activator) | Endonuclease that mediates miRNA decay of both protein-free and AGO2-loaded miRNAs (PubMed:18453631, PubMed:28546213). As part of its function in miRNA decay, regulates mRNAs involved in G1-to-S phase transition (PubMed:28546213). Functions as a bridging factor between STAT6 and the basal transcription factor (PubMed:12234934). Plays a role in PIM1 regulation of MYB activity (PubMed:9809063). Functions as a transcriptional coactivator for STAT5 (By similarity). {ECO:0000250|UniProtKB:Q78PY7, ECO:0000269|PubMed:12234934, ECO:0000269|PubMed:18453631, ECO:0000269|PubMed:28546213, ECO:0000269|PubMed:9809063}.; FUNCTION: (Microbial infection) Functions as a transcriptional coactivator for the Epstein-Barr virus nuclear antigen 2 (EBNA2). {ECO:0000269|PubMed:7651391}.; FUNCTION: (Microbial infection) Promotes SARS-CoV-2 RNA synthesis by binding to negative-sense RNA and the viral protein nsp9. {ECO:0000269|PubMed:37794589}. |
Q14524 | SCN5A | S464 | PSP | Sodium channel protein type 5 subunit alpha (Sodium channel protein cardiac muscle subunit alpha) (Sodium channel protein type V subunit alpha) (Voltage-gated sodium channel subunit alpha Nav1.5) (hH1) | Pore-forming subunit of Nav1.5, a voltage-gated sodium (Nav) channel that directly mediates the depolarizing phase of action potentials in excitable membranes. Navs, also called VGSCs (voltage-gated sodium channels) or VDSCs (voltage-dependent sodium channels), operate by switching between closed and open conformations depending on the voltage difference across the membrane. In the open conformation they allow Na(+) ions to selectively pass through the pore, along their electrochemical gradient. The influx of Na(+) ions provokes membrane depolarization, initiating the propagation of electrical signals throughout cells and tissues (PubMed:1309946, PubMed:21447824, PubMed:23085483, PubMed:23420830, PubMed:25370050, PubMed:26279430, PubMed:26392562, PubMed:26776555). Nav1.5 is the predominant sodium channel expressed in myocardial cells and it is responsible for the initial upstroke of the action potential in cardiac myocytes, thereby initiating the heartbeat (PubMed:11234013, PubMed:11804990, PubMed:12569159, PubMed:1309946). Required for normal electrical conduction including formation of the infranodal ventricular conduction system and normal action potential configuration, as a result of its interaction with XIRP2 (By similarity). {ECO:0000250|UniProtKB:Q9JJV9, ECO:0000269|PubMed:11234013, ECO:0000269|PubMed:11804990, ECO:0000269|PubMed:12569159, ECO:0000269|PubMed:1309946, ECO:0000269|PubMed:19074138, ECO:0000269|PubMed:21447824, ECO:0000269|PubMed:23085483, ECO:0000269|PubMed:23420830, ECO:0000269|PubMed:24167619, ECO:0000269|PubMed:25370050, ECO:0000269|PubMed:26279430, ECO:0000269|PubMed:26392562, ECO:0000269|PubMed:26776555}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-9913351 | Formation of the dystrophin-glycoprotein complex (DGC) | 3.173367e-07 | 6.498 |
R-HSA-156711 | Polo-like kinase mediated events | 7.665979e-07 | 6.115 |
R-HSA-69275 | G2/M Transition | 2.282407e-06 | 5.642 |
R-HSA-453274 | Mitotic G2-G2/M phases | 2.485739e-06 | 5.605 |
R-HSA-9764561 | Regulation of CDH1 Function | 7.945708e-06 | 5.100 |
R-HSA-6804114 | TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 1.721140e-05 | 4.764 |
R-HSA-3000171 | Non-integrin membrane-ECM interactions | 3.107558e-05 | 4.508 |
R-HSA-9825892 | Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 4.552138e-05 | 4.342 |
R-HSA-156584 | Cytosolic sulfonation of small molecules | 6.956733e-05 | 4.158 |
R-HSA-9734009 | Defective Intrinsic Pathway for Apoptosis | 9.832260e-05 | 4.007 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 1.856561e-04 | 3.731 |
R-HSA-69278 | Cell Cycle, Mitotic | 2.784710e-04 | 3.555 |
R-HSA-6804754 | Regulation of TP53 Expression | 3.901336e-04 | 3.409 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 4.387170e-04 | 3.358 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 4.638477e-04 | 3.334 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 4.638477e-04 | 3.334 |
R-HSA-9819196 | Zygotic genome activation (ZGA) | 8.853207e-04 | 3.053 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 8.971148e-04 | 3.047 |
R-HSA-6791312 | TP53 Regulates Transcription of Cell Cycle Genes | 1.244485e-03 | 2.905 |
R-HSA-8939247 | RUNX1 regulates transcription of genes involved in interleukin signaling | 1.178327e-03 | 2.929 |
R-HSA-8862803 | Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's dis... | 1.332414e-03 | 2.875 |
R-HSA-8863678 | Neurodegenerative Diseases | 1.332414e-03 | 2.875 |
R-HSA-9753281 | Paracetamol ADME | 1.110168e-03 | 2.955 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 1.629340e-03 | 2.788 |
R-HSA-418990 | Adherens junctions interactions | 1.601093e-03 | 2.796 |
R-HSA-445095 | Interaction between L1 and Ankyrins | 1.746408e-03 | 2.758 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 1.896210e-03 | 2.722 |
R-HSA-1640170 | Cell Cycle | 2.016539e-03 | 2.695 |
R-HSA-5336415 | Uptake and function of diphtheria toxin | 2.371680e-03 | 2.625 |
R-HSA-196025 | Formation of annular gap junctions | 2.856532e-03 | 2.544 |
R-HSA-190873 | Gap junction degradation | 3.383880e-03 | 2.471 |
R-HSA-9834752 | Respiratory syncytial virus genome replication | 3.383880e-03 | 2.471 |
R-HSA-421270 | Cell-cell junction organization | 3.288266e-03 | 2.483 |
R-HSA-8853659 | RET signaling | 3.671271e-03 | 2.435 |
R-HSA-69620 | Cell Cycle Checkpoints | 3.776466e-03 | 2.423 |
R-HSA-68877 | Mitotic Prometaphase | 4.146049e-03 | 2.382 |
R-HSA-9820962 | Assembly and release of respiratory syncytial virus (RSV) virions | 3.953110e-03 | 2.403 |
R-HSA-6802957 | Oncogenic MAPK signaling | 4.485466e-03 | 2.348 |
R-HSA-3214841 | PKMTs methylate histone lysines | 4.978115e-03 | 2.303 |
R-HSA-9645723 | Diseases of programmed cell death | 5.195678e-03 | 2.284 |
R-HSA-446728 | Cell junction organization | 5.477660e-03 | 2.261 |
R-HSA-5467333 | APC truncation mutants are not K63 polyubiquitinated | 7.054644e-03 | 2.152 |
R-HSA-9723907 | Loss of Function of TP53 in Cancer | 7.054644e-03 | 2.152 |
R-HSA-9723905 | Loss of function of TP53 in cancer due to loss of tetramerization ability | 7.054644e-03 | 2.152 |
R-HSA-75035 | Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 6.636821e-03 | 2.178 |
R-HSA-397014 | Muscle contraction | 6.361387e-03 | 2.196 |
R-HSA-422475 | Axon guidance | 7.080547e-03 | 2.150 |
R-HSA-9856651 | MITF-M-dependent gene expression | 7.101843e-03 | 2.149 |
R-HSA-399954 | Sema3A PAK dependent Axon repulsion | 8.214498e-03 | 2.085 |
R-HSA-446353 | Cell-extracellular matrix interactions | 8.214498e-03 | 2.085 |
R-HSA-3247509 | Chromatin modifying enzymes | 9.679558e-03 | 2.014 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 1.046222e-02 | 1.980 |
R-HSA-9700206 | Signaling by ALK in cancer | 1.046222e-02 | 1.980 |
R-HSA-1500931 | Cell-Cell communication | 1.021561e-02 | 1.991 |
R-HSA-5637810 | Constitutive Signaling by EGFRvIII | 1.086288e-02 | 1.964 |
R-HSA-5637812 | Signaling by EGFRvIII in Cancer | 1.086288e-02 | 1.964 |
R-HSA-9613829 | Chaperone Mediated Autophagy | 1.181860e-02 | 1.927 |
R-HSA-9665348 | Signaling by ERBB2 ECD mutants | 1.181860e-02 | 1.927 |
R-HSA-9662361 | Sensory processing of sound by outer hair cells of the cochlea | 1.087873e-02 | 1.963 |
R-HSA-9675108 | Nervous system development | 1.074789e-02 | 1.969 |
R-HSA-9029569 | NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflu... | 1.181055e-02 | 1.928 |
R-HSA-4839726 | Chromatin organization | 1.255401e-02 | 1.901 |
R-HSA-1227986 | Signaling by ERBB2 | 1.278698e-02 | 1.893 |
R-HSA-1236382 | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 1.489689e-02 | 1.827 |
R-HSA-5637815 | Signaling by Ligand-Responsive EGFR Variants in Cancer | 1.489689e-02 | 1.827 |
R-HSA-1362277 | Transcription of E2F targets under negative control by DREAM complex | 1.383614e-02 | 1.859 |
R-HSA-373755 | Semaphorin interactions | 1.433596e-02 | 1.844 |
R-HSA-9013695 | NOTCH4 Intracellular Domain Regulates Transcription | 1.489689e-02 | 1.827 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 1.591288e-02 | 1.798 |
R-HSA-6804115 | TP53 regulates transcription of additional cell cycle genes whose exact role in ... | 1.711972e-02 | 1.767 |
R-HSA-69481 | G2/M Checkpoints | 1.876774e-02 | 1.727 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 1.714448e-02 | 1.766 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 1.714448e-02 | 1.766 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 1.959712e-02 | 1.708 |
R-HSA-1266738 | Developmental Biology | 1.973954e-02 | 1.705 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 2.023899e-02 | 1.694 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 2.023899e-02 | 1.694 |
R-HSA-69473 | G2/M DNA damage checkpoint | 2.089237e-02 | 1.680 |
R-HSA-9665230 | Drug resistance in ERBB2 KD mutants | 2.792394e-02 | 1.554 |
R-HSA-9652282 | Drug-mediated inhibition of ERBB2 signaling | 2.792394e-02 | 1.554 |
R-HSA-198765 | Signalling to ERK5 | 2.792394e-02 | 1.554 |
R-HSA-9665245 | Resistance of ERBB2 KD mutants to tesevatinib | 2.792394e-02 | 1.554 |
R-HSA-9665246 | Resistance of ERBB2 KD mutants to neratinib | 2.792394e-02 | 1.554 |
R-HSA-9665737 | Drug resistance in ERBB2 TMD/JMD mutants | 2.792394e-02 | 1.554 |
R-HSA-9665244 | Resistance of ERBB2 KD mutants to sapitinib | 2.792394e-02 | 1.554 |
R-HSA-9665251 | Resistance of ERBB2 KD mutants to lapatinib | 2.792394e-02 | 1.554 |
R-HSA-9665233 | Resistance of ERBB2 KD mutants to trastuzumab | 2.792394e-02 | 1.554 |
R-HSA-9665247 | Resistance of ERBB2 KD mutants to osimertinib | 2.792394e-02 | 1.554 |
R-HSA-9665250 | Resistance of ERBB2 KD mutants to AEE788 | 2.792394e-02 | 1.554 |
R-HSA-9665249 | Resistance of ERBB2 KD mutants to afatinib | 2.792394e-02 | 1.554 |
R-HSA-9927432 | Developmental Lineage of Mammary Gland Myoepithelial Cells | 2.590966e-02 | 1.587 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 2.653380e-02 | 1.576 |
R-HSA-1643713 | Signaling by EGFR in Cancer | 2.195617e-02 | 1.658 |
R-HSA-1227990 | Signaling by ERBB2 in Cancer | 2.728700e-02 | 1.564 |
R-HSA-9664565 | Signaling by ERBB2 KD Mutants | 2.590966e-02 | 1.587 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 2.642774e-02 | 1.578 |
R-HSA-8863795 | Downregulation of ERBB2 signaling | 2.728700e-02 | 1.564 |
R-HSA-9659379 | Sensory processing of sound | 2.433195e-02 | 1.614 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 2.292158e-02 | 1.640 |
R-HSA-9008059 | Interleukin-37 signaling | 2.728700e-02 | 1.564 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 2.550293e-02 | 1.593 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 2.805915e-02 | 1.552 |
R-HSA-390522 | Striated Muscle Contraction | 3.308131e-02 | 1.480 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 2.963034e-02 | 1.528 |
R-HSA-141424 | Amplification of signal from the kinetochores | 2.963034e-02 | 1.528 |
R-HSA-176187 | Activation of ATR in response to replication stress | 3.159092e-02 | 1.500 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 3.116624e-02 | 1.506 |
R-HSA-70268 | Pyruvate metabolism | 3.124726e-02 | 1.505 |
R-HSA-9679191 | Potential therapeutics for SARS | 3.204223e-02 | 1.494 |
R-HSA-1538133 | G0 and Early G1 | 3.012809e-02 | 1.521 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 3.012809e-02 | 1.521 |
R-HSA-8865999 | MET activates PTPN11 | 3.478328e-02 | 1.459 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 3.614299e-02 | 1.442 |
R-HSA-156580 | Phase II - Conjugation of compounds | 3.756441e-02 | 1.425 |
R-HSA-3371511 | HSF1 activation | 3.771338e-02 | 1.424 |
R-HSA-1474244 | Extracellular matrix organization | 3.920220e-02 | 1.407 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 3.930955e-02 | 1.406 |
R-HSA-5689896 | Ovarian tumor domain proteases | 3.930955e-02 | 1.406 |
R-HSA-69895 | Transcriptional activation of cell cycle inhibitor p21 | 4.159465e-02 | 1.381 |
R-HSA-69560 | Transcriptional activation of p53 responsive genes | 4.159465e-02 | 1.381 |
R-HSA-111448 | Activation of NOXA and translocation to mitochondria | 4.159465e-02 | 1.381 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 4.257750e-02 | 1.371 |
R-HSA-9820965 | Respiratory syncytial virus (RSV) genome replication, transcription and translat... | 4.257750e-02 | 1.371 |
R-HSA-9022537 | Loss of MECP2 binding ability to the NCoR/SMRT complex | 5.507478e-02 | 1.259 |
R-HSA-69478 | G2/M DNA replication checkpoint | 6.174419e-02 | 1.209 |
R-HSA-113507 | E2F-enabled inhibition of pre-replication complex formation | 6.174419e-02 | 1.209 |
R-HSA-8851907 | MET activates PI3K/AKT signaling | 6.836694e-02 | 1.165 |
R-HSA-9028335 | Activated NTRK2 signals through PI3K | 7.494335e-02 | 1.125 |
R-HSA-8875656 | MET receptor recycling | 7.494335e-02 | 1.125 |
R-HSA-8875555 | MET activates RAP1 and RAC1 | 8.795843e-02 | 1.056 |
R-HSA-390450 | Folding of actin by CCT/TriC | 8.795843e-02 | 1.056 |
R-HSA-4839744 | Signaling by APC mutants | 9.439774e-02 | 1.025 |
R-HSA-5467340 | AXIN missense mutants destabilize the destruction complex | 9.439774e-02 | 1.025 |
R-HSA-5467337 | APC truncation mutants have impaired AXIN binding | 9.439774e-02 | 1.025 |
R-HSA-5467348 | Truncations of AMER1 destabilize the destruction complex | 9.439774e-02 | 1.025 |
R-HSA-202670 | ERKs are inactivated | 1.007920e-01 | 0.997 |
R-HSA-9931512 | Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | 1.007920e-01 | 0.997 |
R-HSA-5339716 | Signaling by GSK3beta mutants | 1.007920e-01 | 0.997 |
R-HSA-4839743 | Signaling by CTNNB1 phospho-site mutants | 1.071415e-01 | 0.970 |
R-HSA-3000484 | Scavenging by Class F Receptors | 1.071415e-01 | 0.970 |
R-HSA-5358751 | CTNNB1 S45 mutants aren't phosphorylated | 1.071415e-01 | 0.970 |
R-HSA-5358749 | CTNNB1 S37 mutants aren't phosphorylated | 1.071415e-01 | 0.970 |
R-HSA-5358747 | CTNNB1 S33 mutants aren't phosphorylated | 1.071415e-01 | 0.970 |
R-HSA-5358752 | CTNNB1 T41 mutants aren't phosphorylated | 1.071415e-01 | 0.970 |
R-HSA-205043 | NRIF signals cell death from the nucleus | 1.197074e-01 | 0.922 |
R-HSA-196299 | Beta-catenin phosphorylation cascade | 1.259245e-01 | 0.900 |
R-HSA-180292 | GAB1 signalosome | 1.503606e-01 | 0.823 |
R-HSA-5654710 | PI-3K cascade:FGFR3 | 1.563630e-01 | 0.806 |
R-HSA-174048 | APC/C:Cdc20 mediated degradation of Cyclin B | 1.563630e-01 | 0.806 |
R-HSA-5654720 | PI-3K cascade:FGFR4 | 1.623234e-01 | 0.790 |
R-HSA-9934037 | Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | 1.623234e-01 | 0.790 |
R-HSA-5654689 | PI-3K cascade:FGFR1 | 1.799553e-01 | 0.745 |
R-HSA-389957 | Prefoldin mediated transfer of substrate to CCT/TriC | 1.857505e-01 | 0.731 |
R-HSA-72187 | mRNA 3'-end processing | 6.801376e-02 | 1.167 |
R-HSA-5654695 | PI-3K cascade:FGFR2 | 1.972193e-01 | 0.705 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 9.067004e-02 | 1.043 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 9.067004e-02 | 1.043 |
R-HSA-8854518 | AURKA Activation by TPX2 | 9.718806e-02 | 1.012 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 1.128841e-01 | 0.947 |
R-HSA-380287 | Centrosome maturation | 1.174833e-01 | 0.930 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 1.508676e-01 | 0.821 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 1.016056e-01 | 0.993 |
R-HSA-6804759 | Regulation of TP53 Activity through Association with Co-factors | 1.134465e-01 | 0.945 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 2.028935e-01 | 0.693 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 1.557823e-01 | 0.807 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 1.459854e-01 | 0.836 |
R-HSA-6803211 | TP53 Regulates Transcription of Death Receptors and Ligands | 1.197074e-01 | 0.922 |
R-HSA-6803204 | TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 2.085280e-01 | 0.681 |
R-HSA-164940 | Nef mediated downregulation of MHC class I complex cell surface expression | 7.494335e-02 | 1.125 |
R-HSA-163680 | AMPK inhibits chREBP transcriptional activation activity | 8.147374e-02 | 1.089 |
R-HSA-9931521 | The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CL... | 1.382284e-01 | 0.859 |
R-HSA-76066 | RNA Polymerase III Transcription Initiation From Type 2 Promoter | 1.741193e-01 | 0.759 |
R-HSA-76071 | RNA Polymerase III Transcription Initiation From Type 3 Promoter | 1.799553e-01 | 0.745 |
R-HSA-6803205 | TP53 regulates transcription of several additional cell death genes whose specif... | 1.799553e-01 | 0.745 |
R-HSA-6803207 | TP53 Regulates Transcription of Caspase Activators and Caspases | 1.320980e-01 | 0.879 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 1.757291e-01 | 0.755 |
R-HSA-8857538 | PTK6 promotes HIF1A stabilization | 6.174419e-02 | 1.209 |
R-HSA-6804760 | Regulation of TP53 Activity through Methylation | 1.503606e-01 | 0.823 |
R-HSA-5674135 | MAP2K and MAPK activation | 4.766206e-02 | 1.322 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 1.315353e-01 | 0.881 |
R-HSA-5633007 | Regulation of TP53 Activity | 1.328768e-01 | 0.877 |
R-HSA-8937144 | Aryl hydrocarbon receptor signalling | 5.507478e-02 | 1.259 |
R-HSA-76061 | RNA Polymerase III Transcription Initiation From Type 1 Promoter | 1.799553e-01 | 0.745 |
R-HSA-3214815 | HDACs deacetylate histones | 7.398429e-02 | 1.131 |
R-HSA-69615 | G1/S DNA Damage Checkpoints | 9.067004e-02 | 1.043 |
R-HSA-9027276 | Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 1.071415e-01 | 0.970 |
R-HSA-9656223 | Signaling by RAF1 mutants | 4.766206e-02 | 1.322 |
R-HSA-198753 | ERK/MAPK targets | 1.682421e-01 | 0.774 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 5.659583e-02 | 1.247 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 5.659583e-02 | 1.247 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 5.659583e-02 | 1.247 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 4.481300e-02 | 1.349 |
R-HSA-176417 | Phosphorylation of Emi1 | 5.507478e-02 | 1.259 |
R-HSA-2151209 | Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 8.795843e-02 | 1.056 |
R-HSA-192905 | vRNP Assembly | 9.439774e-02 | 1.025 |
R-HSA-4839735 | Signaling by AXIN mutants | 1.007920e-01 | 0.997 |
R-HSA-4839748 | Signaling by AMER1 mutants | 1.007920e-01 | 0.997 |
R-HSA-9634285 | Constitutive Signaling by Overexpressed ERBB2 | 1.071415e-01 | 0.970 |
R-HSA-9933947 | Formation of the non-canonical BAF (ncBAF) complex | 1.134465e-01 | 0.945 |
R-HSA-2559584 | Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 1.134465e-01 | 0.945 |
R-HSA-399955 | SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 1.320980e-01 | 0.879 |
R-HSA-176412 | Phosphorylation of the APC/C | 1.320980e-01 | 0.879 |
R-HSA-350054 | Notch-HLH transcription pathway | 1.799553e-01 | 0.745 |
R-HSA-8866652 | Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 2.085280e-01 | 0.681 |
R-HSA-6804116 | TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 1.320980e-01 | 0.879 |
R-HSA-6802949 | Signaling by RAS mutants | 5.659583e-02 | 1.247 |
R-HSA-6788467 | IL-6-type cytokine receptor ligand interactions | 1.134465e-01 | 0.945 |
R-HSA-1963642 | PI3K events in ERBB2 signaling | 1.443158e-01 | 0.841 |
R-HSA-9609523 | Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 1.623234e-01 | 0.790 |
R-HSA-139915 | Activation of PUMA and translocation to mitochondria | 6.836694e-02 | 1.165 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 7.805493e-02 | 1.108 |
R-HSA-428359 | Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RN... | 8.795843e-02 | 1.056 |
R-HSA-9623433 | NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | 1.007920e-01 | 0.997 |
R-HSA-4419969 | Depolymerization of the Nuclear Lamina | 1.503606e-01 | 0.823 |
R-HSA-9665686 | Signaling by ERBB2 TMD/JMD mutants | 1.915051e-01 | 0.718 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 1.972193e-01 | 0.705 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 1.972193e-01 | 0.705 |
R-HSA-4641262 | Disassembly of the destruction complex and recruitment of AXIN to the membrane | 2.085280e-01 | 0.681 |
R-HSA-390466 | Chaperonin-mediated protein folding | 1.484223e-01 | 0.829 |
R-HSA-2980767 | Activation of NIMA Kinases NEK9, NEK6, NEK7 | 6.174419e-02 | 1.209 |
R-HSA-2465910 | MASTL Facilitates Mitotic Progression | 8.147374e-02 | 1.089 |
R-HSA-2514853 | Condensation of Prometaphase Chromosomes | 1.007920e-01 | 0.997 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 1.071415e-01 | 0.970 |
R-HSA-6811555 | PI5P Regulates TP53 Acetylation | 1.134465e-01 | 0.945 |
R-HSA-113510 | E2F mediated regulation of DNA replication | 1.563630e-01 | 0.806 |
R-HSA-3371571 | HSF1-dependent transactivation | 6.606111e-02 | 1.180 |
R-HSA-429947 | Deadenylation of mRNA | 1.915051e-01 | 0.718 |
R-HSA-445355 | Smooth Muscle Contraction | 6.998541e-02 | 1.155 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 8.640048e-02 | 1.063 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 1.106027e-01 | 0.956 |
R-HSA-2467813 | Separation of Sister Chromatids | 1.393059e-01 | 0.856 |
R-HSA-68886 | M Phase | 6.735551e-02 | 1.172 |
R-HSA-73857 | RNA Polymerase II Transcription | 1.537014e-01 | 0.813 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 6.432226e-02 | 1.192 |
R-HSA-844456 | The NLRP3 inflammasome | 1.563630e-01 | 0.806 |
R-HSA-74160 | Gene expression (Transcription) | 6.673355e-02 | 1.176 |
R-HSA-437239 | Recycling pathway of L1 | 5.844791e-02 | 1.233 |
R-HSA-194138 | Signaling by VEGF | 7.786935e-02 | 1.109 |
R-HSA-3371556 | Cellular response to heat stress | 7.156544e-02 | 1.145 |
R-HSA-9613354 | Lipophagy | 8.147374e-02 | 1.089 |
R-HSA-9005891 | Loss of function of MECP2 in Rett syndrome | 1.071415e-01 | 0.970 |
R-HSA-9697154 | Disorders of Nervous System Development | 1.071415e-01 | 0.970 |
R-HSA-9005895 | Pervasive developmental disorders | 1.071415e-01 | 0.970 |
R-HSA-5655291 | Signaling by FGFR4 in disease | 1.197074e-01 | 0.922 |
R-HSA-9933937 | Formation of the canonical BAF (cBAF) complex | 1.197074e-01 | 0.922 |
R-HSA-9933946 | Formation of the embryonic stem cell BAF (esBAF) complex | 1.259245e-01 | 0.900 |
R-HSA-164938 | Nef-mediates down modulation of cell surface receptors by recruiting them to cla... | 1.443158e-01 | 0.841 |
R-HSA-3371568 | Attenuation phase | 4.424842e-02 | 1.354 |
R-HSA-190828 | Gap junction trafficking | 5.295582e-02 | 1.276 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 8.428940e-02 | 1.074 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 5.523064e-02 | 1.258 |
R-HSA-9612973 | Autophagy | 1.265565e-01 | 0.898 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 4.893223e-02 | 1.310 |
R-HSA-9758274 | Regulation of NF-kappa B signaling | 1.320980e-01 | 0.879 |
R-HSA-9861718 | Regulation of pyruvate metabolism | 5.659583e-02 | 1.247 |
R-HSA-391251 | Protein folding | 1.632111e-01 | 0.787 |
R-HSA-6783589 | Interleukin-6 family signaling | 1.915051e-01 | 0.718 |
R-HSA-8941855 | RUNX3 regulates CDKN1A transcription | 5.507478e-02 | 1.259 |
R-HSA-162658 | Golgi Cisternae Pericentriolar Stack Reorganization | 1.134465e-01 | 0.945 |
R-HSA-9933939 | Formation of the polybromo-BAF (pBAF) complex | 1.197074e-01 | 0.922 |
R-HSA-975577 | N-Glycan antennae elongation | 1.320980e-01 | 0.879 |
R-HSA-9675151 | Disorders of Developmental Biology | 1.382284e-01 | 0.859 |
R-HSA-157858 | Gap junction trafficking and regulation | 6.221429e-02 | 1.206 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 2.089052e-01 | 0.680 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 4.594341e-02 | 1.338 |
R-HSA-164952 | The role of Nef in HIV-1 replication and disease pathogenesis | 1.857505e-01 | 0.731 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 1.060779e-01 | 0.974 |
R-HSA-2995383 | Initiation of Nuclear Envelope (NE) Reformation | 1.741193e-01 | 0.759 |
R-HSA-5655332 | Signaling by FGFR3 in disease | 2.085280e-01 | 0.681 |
R-HSA-1855167 | Synthesis of pyrophosphates in the cytosol | 1.857505e-01 | 0.731 |
R-HSA-5673001 | RAF/MAP kinase cascade | 1.766484e-01 | 0.753 |
R-HSA-70171 | Glycolysis | 4.481300e-02 | 1.349 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 1.635398e-01 | 0.786 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 1.864697e-01 | 0.729 |
R-HSA-881907 | Gastrin-CREB signalling pathway via PKC and MAPK | 1.563630e-01 | 0.806 |
R-HSA-3928665 | EPH-ephrin mediated repulsion of cells | 5.844791e-02 | 1.233 |
R-HSA-879518 | Organic anion transport by SLCO transporters | 1.857505e-01 | 0.731 |
R-HSA-200425 | Carnitine shuttle | 1.857505e-01 | 0.731 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 1.387271e-01 | 0.858 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 2.089052e-01 | 0.680 |
R-HSA-68882 | Mitotic Anaphase | 8.742186e-02 | 1.058 |
R-HSA-373760 | L1CAM interactions | 6.550461e-02 | 1.184 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 8.845323e-02 | 1.053 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 7.405825e-02 | 1.130 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 1.807791e-01 | 0.743 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 1.807791e-01 | 0.743 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 1.807791e-01 | 0.743 |
R-HSA-69206 | G1/S Transition | 7.786935e-02 | 1.109 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 2.114863e-01 | 0.675 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 2.140706e-01 | 0.669 |
R-HSA-211859 | Biological oxidations | 1.890676e-01 | 0.723 |
R-HSA-5688426 | Deubiquitination | 1.318112e-01 | 0.880 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 2.140706e-01 | 0.669 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 5.542062e-02 | 1.256 |
R-HSA-162582 | Signal Transduction | 8.177717e-02 | 1.087 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 2.011832e-01 | 0.696 |
R-HSA-5218859 | Regulated Necrosis | 1.016056e-01 | 0.993 |
R-HSA-70326 | Glucose metabolism | 6.669697e-02 | 1.176 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 1.591997e-01 | 0.798 |
R-HSA-5601884 | PIWI-interacting RNA (piRNA) biogenesis | 1.972193e-01 | 0.705 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 1.053584e-01 | 0.977 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 1.112618e-01 | 0.954 |
R-HSA-5696398 | Nucleotide Excision Repair | 2.011832e-01 | 0.696 |
R-HSA-9663891 | Selective autophagy | 1.508676e-01 | 0.821 |
R-HSA-9006115 | Signaling by NTRK2 (TRKB) | 2.085280e-01 | 0.681 |
R-HSA-5357801 | Programmed Cell Death | 7.647354e-02 | 1.116 |
R-HSA-9013694 | Signaling by NOTCH4 | 1.151777e-01 | 0.939 |
R-HSA-211000 | Gene Silencing by RNA | 2.063276e-01 | 0.685 |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | 6.361976e-02 | 1.196 |
R-HSA-109581 | Apoptosis | 1.360781e-01 | 0.866 |
R-HSA-3928662 | EPHB-mediated forward signaling | 5.295582e-02 | 1.276 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 1.707027e-01 | 0.768 |
R-HSA-69242 | S Phase | 1.142606e-01 | 0.942 |
R-HSA-2682334 | EPH-Ephrin signaling | 1.632111e-01 | 0.787 |
R-HSA-75153 | Apoptotic execution phase | 5.659583e-02 | 1.247 |
R-HSA-446652 | Interleukin-1 family signaling | 1.203495e-01 | 0.920 |
R-HSA-9725371 | Nuclear events stimulated by ALK signaling in cancer | 6.032086e-02 | 1.220 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 9.674726e-02 | 1.014 |
R-HSA-449147 | Signaling by Interleukins | 8.847687e-02 | 1.053 |
R-HSA-157118 | Signaling by NOTCH | 1.137619e-01 | 0.944 |
R-HSA-381038 | XBP1(S) activates chaperone genes | 1.459854e-01 | 0.836 |
R-HSA-381070 | IRE1alpha activates chaperones | 1.607275e-01 | 0.794 |
R-HSA-5339562 | Uptake and actions of bacterial toxins | 6.801376e-02 | 1.167 |
R-HSA-9748784 | Drug ADME | 8.949053e-02 | 1.048 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 2.141230e-01 | 0.669 |
R-HSA-5576892 | Phase 0 - rapid depolarisation | 2.141230e-01 | 0.669 |
R-HSA-622312 | Inflammasomes | 2.141230e-01 | 0.669 |
R-HSA-5620971 | Pyroptosis | 2.141230e-01 | 0.669 |
R-HSA-1483249 | Inositol phosphate metabolism | 2.192484e-01 | 0.659 |
R-HSA-5654708 | Downstream signaling of activated FGFR3 | 2.196787e-01 | 0.658 |
R-HSA-450282 | MAPK targets/ Nuclear events mediated by MAP kinases | 2.196787e-01 | 0.658 |
R-HSA-204174 | Regulation of pyruvate dehydrogenase (PDH) complex | 2.196787e-01 | 0.658 |
R-HSA-9006335 | Signaling by Erythropoietin | 2.196787e-01 | 0.658 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 2.214011e-01 | 0.655 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 2.218414e-01 | 0.654 |
R-HSA-9679506 | SARS-CoV Infections | 2.244194e-01 | 0.649 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 2.251956e-01 | 0.647 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 2.251956e-01 | 0.647 |
R-HSA-76046 | RNA Polymerase III Transcription Initiation | 2.251956e-01 | 0.647 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 2.251956e-01 | 0.647 |
R-HSA-5654716 | Downstream signaling of activated FGFR4 | 2.251956e-01 | 0.647 |
R-HSA-114452 | Activation of BH3-only proteins | 2.251956e-01 | 0.647 |
R-HSA-1474151 | Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 2.251956e-01 | 0.647 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 2.296353e-01 | 0.639 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 2.296353e-01 | 0.639 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 2.306738e-01 | 0.637 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 2.306738e-01 | 0.637 |
R-HSA-389958 | Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 2.306738e-01 | 0.637 |
R-HSA-4791275 | Signaling by WNT in cancer | 2.361135e-01 | 0.627 |
R-HSA-2173795 | Downregulation of SMAD2/3:SMAD4 transcriptional activity | 2.361135e-01 | 0.627 |
R-HSA-1592230 | Mitochondrial biogenesis | 2.374480e-01 | 0.624 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 2.415152e-01 | 0.617 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 2.415152e-01 | 0.617 |
R-HSA-6804758 | Regulation of TP53 Activity through Acetylation | 2.415152e-01 | 0.617 |
R-HSA-5675482 | Regulation of necroptotic cell death | 2.415152e-01 | 0.617 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 2.415152e-01 | 0.617 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 2.426648e-01 | 0.615 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 2.426648e-01 | 0.615 |
R-HSA-68875 | Mitotic Prophase | 2.452752e-01 | 0.610 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 2.468790e-01 | 0.608 |
R-HSA-390471 | Association of TriC/CCT with target proteins during biosynthesis | 2.468790e-01 | 0.608 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 2.468790e-01 | 0.608 |
R-HSA-5696394 | DNA Damage Recognition in GG-NER | 2.468790e-01 | 0.608 |
R-HSA-114508 | Effects of PIP2 hydrolysis | 2.468790e-01 | 0.608 |
R-HSA-9818027 | NFE2L2 regulating anti-oxidant/detoxification enzymes | 2.468790e-01 | 0.608 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 2.504995e-01 | 0.601 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 2.504995e-01 | 0.601 |
R-HSA-6798695 | Neutrophil degranulation | 2.510943e-01 | 0.600 |
R-HSA-203615 | eNOS activation | 2.522052e-01 | 0.598 |
R-HSA-180746 | Nuclear import of Rev protein | 2.522052e-01 | 0.598 |
R-HSA-349425 | Autodegradation of the E3 ubiquitin ligase COP1 | 2.522052e-01 | 0.598 |
R-HSA-1428517 | Aerobic respiration and respiratory electron transport | 2.532833e-01 | 0.596 |
R-HSA-162909 | Host Interactions of HIV factors | 2.557274e-01 | 0.592 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 2.570341e-01 | 0.590 |
R-HSA-5654696 | Downstream signaling of activated FGFR2 | 2.574940e-01 | 0.589 |
R-HSA-5654687 | Downstream signaling of activated FGFR1 | 2.574940e-01 | 0.589 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 2.574940e-01 | 0.589 |
R-HSA-2559585 | Oncogene Induced Senescence | 2.574940e-01 | 0.589 |
R-HSA-5683057 | MAPK family signaling cascades | 2.625713e-01 | 0.581 |
R-HSA-749476 | RNA Polymerase III Abortive And Retractive Initiation | 2.627458e-01 | 0.580 |
R-HSA-74158 | RNA Polymerase III Transcription | 2.627458e-01 | 0.580 |
R-HSA-6804757 | Regulation of TP53 Degradation | 2.627458e-01 | 0.580 |
R-HSA-69205 | G1/S-Specific Transcription | 2.627458e-01 | 0.580 |
R-HSA-9694516 | SARS-CoV-2 Infection | 2.656824e-01 | 0.576 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 2.679607e-01 | 0.572 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 2.679607e-01 | 0.572 |
R-HSA-8875878 | MET promotes cell motility | 2.731391e-01 | 0.564 |
R-HSA-202131 | Metabolism of nitric oxide: NOS3 activation and regulation | 2.731391e-01 | 0.564 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 2.731391e-01 | 0.564 |
R-HSA-5213460 | RIPK1-mediated regulated necrosis | 2.731391e-01 | 0.564 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 2.782812e-01 | 0.556 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 2.782812e-01 | 0.556 |
R-HSA-69541 | Stabilization of p53 | 2.782812e-01 | 0.556 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 2.782812e-01 | 0.556 |
R-HSA-9648002 | RAS processing | 2.782812e-01 | 0.556 |
R-HSA-9843745 | Adipogenesis | 2.792670e-01 | 0.554 |
R-HSA-5576891 | Cardiac conduction | 2.792670e-01 | 0.554 |
R-HSA-9909396 | Circadian clock | 2.818814e-01 | 0.550 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 2.833872e-01 | 0.548 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 2.833872e-01 | 0.548 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 2.833872e-01 | 0.548 |
R-HSA-1251985 | Nuclear signaling by ERBB4 | 2.833872e-01 | 0.548 |
R-HSA-9646399 | Aggrephagy | 2.833872e-01 | 0.548 |
R-HSA-5696395 | Formation of Incision Complex in GG-NER | 2.833872e-01 | 0.548 |
R-HSA-975576 | N-glycan antennae elongation in the medial/trans-Golgi | 2.833872e-01 | 0.548 |
R-HSA-5218920 | VEGFR2 mediated vascular permeability | 2.884574e-01 | 0.540 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 2.884574e-01 | 0.540 |
R-HSA-9694548 | Maturation of spike protein | 2.884574e-01 | 0.540 |
R-HSA-5655302 | Signaling by FGFR1 in disease | 2.934920e-01 | 0.532 |
R-HSA-9018519 | Estrogen-dependent gene expression | 2.949406e-01 | 0.530 |
R-HSA-165159 | MTOR signalling | 2.984913e-01 | 0.525 |
R-HSA-6807070 | PTEN Regulation | 3.027618e-01 | 0.519 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 3.027618e-01 | 0.519 |
R-HSA-5654743 | Signaling by FGFR4 | 3.034556e-01 | 0.518 |
R-HSA-9664417 | Leishmania phagocytosis | 3.053658e-01 | 0.515 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 3.053658e-01 | 0.515 |
R-HSA-9664407 | Parasite infection | 3.053658e-01 | 0.515 |
R-HSA-1632852 | Macroautophagy | 3.079681e-01 | 0.511 |
R-HSA-373752 | Netrin-1 signaling | 3.083850e-01 | 0.511 |
R-HSA-774815 | Nucleosome assembly | 3.132798e-01 | 0.504 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 3.132798e-01 | 0.504 |
R-HSA-69601 | Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | 3.132798e-01 | 0.504 |
R-HSA-69613 | p53-Independent G1/S DNA Damage Checkpoint | 3.132798e-01 | 0.504 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 3.132798e-01 | 0.504 |
R-HSA-9824585 | Regulation of MITF-M-dependent genes involved in pigmentation | 3.132798e-01 | 0.504 |
R-HSA-5654741 | Signaling by FGFR3 | 3.132798e-01 | 0.504 |
R-HSA-2262752 | Cellular responses to stress | 3.152757e-01 | 0.501 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 3.157638e-01 | 0.501 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 3.181404e-01 | 0.497 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 3.181404e-01 | 0.497 |
R-HSA-9664424 | Cell recruitment (pro-inflammatory response) | 3.181404e-01 | 0.497 |
R-HSA-9660826 | Purinergic signaling in leishmaniasis infection | 3.181404e-01 | 0.497 |
R-HSA-2514859 | Inactivation, recovery and regulation of the phototransduction cascade | 3.181404e-01 | 0.497 |
R-HSA-6811440 | Retrograde transport at the Trans-Golgi-Network | 3.229668e-01 | 0.491 |
R-HSA-445989 | TAK1-dependent IKK and NF-kappa-B activation | 3.229668e-01 | 0.491 |
R-HSA-1483191 | Synthesis of PC | 3.229668e-01 | 0.491 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 3.287131e-01 | 0.483 |
R-HSA-166520 | Signaling by NTRKs | 3.287131e-01 | 0.483 |
R-HSA-69563 | p53-Dependent G1 DNA Damage Response | 3.325182e-01 | 0.478 |
R-HSA-69580 | p53-Dependent G1/S DNA damage checkpoint | 3.325182e-01 | 0.478 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 3.325182e-01 | 0.478 |
R-HSA-109704 | PI3K Cascade | 3.372437e-01 | 0.472 |
R-HSA-5655253 | Signaling by FGFR2 in disease | 3.372437e-01 | 0.472 |
R-HSA-9864848 | Complex IV assembly | 3.419361e-01 | 0.466 |
R-HSA-2514856 | The phototransduction cascade | 3.419361e-01 | 0.466 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 3.441658e-01 | 0.463 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 3.441658e-01 | 0.463 |
R-HSA-112382 | Formation of RNA Pol II elongation complex | 3.465955e-01 | 0.460 |
R-HSA-9931269 | AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | 3.465955e-01 | 0.460 |
R-HSA-6794361 | Neurexins and neuroligins | 3.465955e-01 | 0.460 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 3.467308e-01 | 0.460 |
R-HSA-1989781 | PPARA activates gene expression | 3.467308e-01 | 0.460 |
R-HSA-75955 | RNA Polymerase II Transcription Elongation | 3.512222e-01 | 0.454 |
R-HSA-5250924 | B-WICH complex positively regulates rRNA expression | 3.512222e-01 | 0.454 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 3.518512e-01 | 0.454 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 3.551782e-01 | 0.450 |
R-HSA-9824443 | Parasitic Infection Pathways | 3.590343e-01 | 0.445 |
R-HSA-9658195 | Leishmania infection | 3.590343e-01 | 0.445 |
R-HSA-176409 | APC/C:Cdc20 mediated degradation of mitotic proteins | 3.603784e-01 | 0.443 |
R-HSA-418597 | G alpha (z) signalling events | 3.603784e-01 | 0.443 |
R-HSA-176814 | Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 3.649084e-01 | 0.438 |
R-HSA-177929 | Signaling by EGFR | 3.649084e-01 | 0.438 |
R-HSA-5654736 | Signaling by FGFR1 | 3.649084e-01 | 0.438 |
R-HSA-5578775 | Ion homeostasis | 3.649084e-01 | 0.438 |
R-HSA-109606 | Intrinsic Pathway for Apoptosis | 3.649084e-01 | 0.438 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 3.649084e-01 | 0.438 |
R-HSA-112399 | IRS-mediated signalling | 3.694066e-01 | 0.432 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 3.715809e-01 | 0.430 |
R-HSA-191859 | snRNP Assembly | 3.783084e-01 | 0.422 |
R-HSA-194441 | Metabolism of non-coding RNA | 3.783084e-01 | 0.422 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 3.783084e-01 | 0.422 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 3.783084e-01 | 0.422 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 3.827124e-01 | 0.417 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 3.827124e-01 | 0.417 |
R-HSA-5362517 | Signaling by Retinoic Acid | 3.827124e-01 | 0.417 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 3.827124e-01 | 0.417 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 3.827124e-01 | 0.417 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 3.827124e-01 | 0.417 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 3.827124e-01 | 0.417 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 3.827124e-01 | 0.417 |
R-HSA-1257604 | PIP3 activates AKT signaling | 3.859268e-01 | 0.413 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 3.870856e-01 | 0.412 |
R-HSA-450294 | MAP kinase activation | 3.870856e-01 | 0.412 |
R-HSA-2428928 | IRS-related events triggered by IGF1R | 3.870856e-01 | 0.412 |
R-HSA-9707616 | Heme signaling | 3.914280e-01 | 0.407 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 3.914280e-01 | 0.407 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 3.914280e-01 | 0.407 |
R-HSA-6784531 | tRNA processing in the nucleus | 3.914280e-01 | 0.407 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 3.914280e-01 | 0.407 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 3.922784e-01 | 0.406 |
R-HSA-5689880 | Ub-specific processing proteases | 3.947697e-01 | 0.404 |
R-HSA-8848021 | Signaling by PTK6 | 3.957399e-01 | 0.403 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 3.957399e-01 | 0.403 |
R-HSA-936837 | Ion transport by P-type ATPases | 4.000216e-01 | 0.398 |
R-HSA-168643 | Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signali... | 4.000216e-01 | 0.398 |
R-HSA-2428924 | IGF1R signaling cascade | 4.000216e-01 | 0.398 |
R-HSA-74751 | Insulin receptor signalling cascade | 4.000216e-01 | 0.398 |
R-HSA-2404192 | Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 4.042732e-01 | 0.393 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 4.084949e-01 | 0.389 |
R-HSA-168255 | Influenza Infection | 4.096196e-01 | 0.388 |
R-HSA-2559583 | Cellular Senescence | 4.120778e-01 | 0.385 |
R-HSA-5693606 | DNA Double Strand Break Response | 4.126869e-01 | 0.384 |
R-HSA-195253 | Degradation of beta-catenin by the destruction complex | 4.250872e-01 | 0.372 |
R-HSA-448424 | Interleukin-17 signaling | 4.250872e-01 | 0.372 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 4.250872e-01 | 0.372 |
R-HSA-9824446 | Viral Infection Pathways | 4.258050e-01 | 0.371 |
R-HSA-453276 | Regulation of mitotic cell cycle | 4.291627e-01 | 0.367 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 4.291627e-01 | 0.367 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 4.291627e-01 | 0.367 |
R-HSA-8978934 | Metabolism of cofactors | 4.291627e-01 | 0.367 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 4.332095e-01 | 0.363 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 4.332095e-01 | 0.363 |
R-HSA-5617833 | Cilium Assembly | 4.363787e-01 | 0.360 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 4.372279e-01 | 0.359 |
R-HSA-212436 | Generic Transcription Pathway | 4.377080e-01 | 0.359 |
R-HSA-168898 | Toll-like Receptor Cascades | 4.387796e-01 | 0.358 |
R-HSA-212165 | Epigenetic regulation of gene expression | 4.388486e-01 | 0.358 |
R-HSA-674695 | RNA Polymerase II Pre-transcription Events | 4.412181e-01 | 0.355 |
R-HSA-1226099 | Signaling by FGFR in disease | 4.412181e-01 | 0.355 |
R-HSA-1236394 | Signaling by ERBB4 | 4.412181e-01 | 0.355 |
R-HSA-8953897 | Cellular responses to stimuli | 4.442376e-01 | 0.352 |
R-HSA-5633008 | TP53 Regulates Transcription of Cell Death Genes | 4.451802e-01 | 0.351 |
R-HSA-8852135 | Protein ubiquitination | 4.451802e-01 | 0.351 |
R-HSA-1169408 | ISG15 antiviral mechanism | 4.451802e-01 | 0.351 |
R-HSA-5689603 | UCH proteinases | 4.491145e-01 | 0.348 |
R-HSA-1980143 | Signaling by NOTCH1 | 4.491145e-01 | 0.348 |
R-HSA-9609690 | HCMV Early Events | 4.507013e-01 | 0.346 |
R-HSA-9694635 | Translation of Structural Proteins | 4.530211e-01 | 0.344 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 4.569002e-01 | 0.340 |
R-HSA-383280 | Nuclear Receptor transcription pathway | 4.569002e-01 | 0.340 |
R-HSA-9955298 | SLC-mediated transport of organic anions | 4.569002e-01 | 0.340 |
R-HSA-389948 | Co-inhibition by PD-1 | 4.601366e-01 | 0.337 |
R-HSA-1643685 | Disease | 4.606662e-01 | 0.337 |
R-HSA-6806834 | Signaling by MET | 4.645769e-01 | 0.333 |
R-HSA-5654738 | Signaling by FGFR2 | 4.645769e-01 | 0.333 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 4.645769e-01 | 0.333 |
R-HSA-9833482 | PKR-mediated signaling | 4.645769e-01 | 0.333 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 4.683748e-01 | 0.329 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 4.721460e-01 | 0.326 |
R-HSA-9006925 | Intracellular signaling by second messengers | 4.737985e-01 | 0.324 |
R-HSA-9707564 | Cytoprotection by HMOX1 | 4.758907e-01 | 0.322 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 4.796090e-01 | 0.319 |
R-HSA-6794362 | Protein-protein interactions at synapses | 4.833012e-01 | 0.316 |
R-HSA-9909615 | Regulation of PD-L1(CD274) Post-translational modification | 4.869674e-01 | 0.313 |
R-HSA-168249 | Innate Immune System | 4.887519e-01 | 0.311 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 4.906079e-01 | 0.309 |
R-HSA-438064 | Post NMDA receptor activation events | 4.942227e-01 | 0.306 |
R-HSA-202424 | Downstream TCR signaling | 5.049153e-01 | 0.297 |
R-HSA-73894 | DNA Repair | 5.059916e-01 | 0.296 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 5.084295e-01 | 0.294 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 5.084295e-01 | 0.294 |
R-HSA-74752 | Signaling by Insulin receptor | 5.153839e-01 | 0.288 |
R-HSA-9772573 | Late SARS-CoV-2 Infection Events | 5.153839e-01 | 0.288 |
R-HSA-168256 | Immune System | 5.161116e-01 | 0.287 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 5.222407e-01 | 0.282 |
R-HSA-162906 | HIV Infection | 5.234621e-01 | 0.281 |
R-HSA-72764 | Eukaryotic Translation Termination | 5.290013e-01 | 0.277 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 5.356671e-01 | 0.271 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 5.356671e-01 | 0.271 |
R-HSA-8957275 | Post-translational protein phosphorylation | 5.389648e-01 | 0.268 |
R-HSA-190236 | Signaling by FGFR | 5.389648e-01 | 0.268 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 5.422394e-01 | 0.266 |
R-HSA-3214847 | HATs acetylate histones | 5.422394e-01 | 0.266 |
R-HSA-8939211 | ESR-mediated signaling | 5.448587e-01 | 0.264 |
R-HSA-9020702 | Interleukin-1 signaling | 5.487194e-01 | 0.261 |
R-HSA-9009391 | Extra-nuclear estrogen signaling | 5.487194e-01 | 0.261 |
R-HSA-9842860 | Regulation of endogenous retroelements | 5.519252e-01 | 0.258 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 5.519252e-01 | 0.258 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 5.519252e-01 | 0.258 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 5.519252e-01 | 0.258 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 5.614080e-01 | 0.251 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 5.614080e-01 | 0.251 |
R-HSA-9833110 | RSV-host interactions | 5.614080e-01 | 0.251 |
R-HSA-9609646 | HCMV Infection | 5.716729e-01 | 0.243 |
R-HSA-202403 | TCR signaling | 5.797806e-01 | 0.237 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 5.836619e-01 | 0.234 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 5.886788e-01 | 0.230 |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-l... | 5.945069e-01 | 0.226 |
R-HSA-9734767 | Developmental Cell Lineages | 5.973383e-01 | 0.224 |
R-HSA-416476 | G alpha (q) signalling events | 5.992648e-01 | 0.222 |
R-HSA-9711123 | Cellular response to chemical stress | 6.069020e-01 | 0.217 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 6.087214e-01 | 0.216 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 6.115045e-01 | 0.214 |
R-HSA-73886 | Chromosome Maintenance | 6.170119e-01 | 0.210 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 6.170119e-01 | 0.210 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 6.224419e-01 | 0.206 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 6.304441e-01 | 0.200 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 6.304441e-01 | 0.200 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 6.304441e-01 | 0.200 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 6.327711e-01 | 0.199 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 6.382782e-01 | 0.195 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 6.434092e-01 | 0.192 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 6.584137e-01 | 0.182 |
R-HSA-163685 | Integration of energy metabolism | 6.632218e-01 | 0.178 |
R-HSA-5663205 | Infectious disease | 6.775654e-01 | 0.169 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 6.796602e-01 | 0.168 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 6.842091e-01 | 0.165 |
R-HSA-2187338 | Visual phototransduction | 6.909126e-01 | 0.161 |
R-HSA-2173782 | Binding and Uptake of Ligands by Scavenger Receptors | 6.974750e-01 | 0.156 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 6.996316e-01 | 0.155 |
R-HSA-199991 | Membrane Trafficking | 7.016875e-01 | 0.154 |
R-HSA-9609507 | Protein localization | 7.038992e-01 | 0.152 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 7.038992e-01 | 0.152 |
R-HSA-5653656 | Vesicle-mediated transport | 7.039084e-01 | 0.152 |
R-HSA-73887 | Death Receptor Signaling | 7.060104e-01 | 0.151 |
R-HSA-9610379 | HCMV Late Events | 7.122550e-01 | 0.147 |
R-HSA-162587 | HIV Life Cycle | 7.122550e-01 | 0.147 |
R-HSA-9006936 | Signaling by TGFB family members | 7.183681e-01 | 0.144 |
R-HSA-8953854 | Metabolism of RNA | 7.302696e-01 | 0.137 |
R-HSA-5619102 | SLC transporter disorders | 7.321358e-01 | 0.135 |
R-HSA-72306 | tRNA processing | 7.397013e-01 | 0.131 |
R-HSA-611105 | Respiratory electron transport | 7.542027e-01 | 0.123 |
R-HSA-597592 | Post-translational protein modification | 7.624800e-01 | 0.118 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 7.628564e-01 | 0.118 |
R-HSA-983712 | Ion channel transport | 7.728429e-01 | 0.112 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 7.808458e-01 | 0.107 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 7.828136e-01 | 0.106 |
R-HSA-913531 | Interferon Signaling | 7.828136e-01 | 0.106 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 7.900810e-01 | 0.102 |
R-HSA-9824439 | Bacterial Infection Pathways | 7.908427e-01 | 0.102 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 7.930729e-01 | 0.101 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 7.945529e-01 | 0.100 |
R-HSA-1483206 | Glycerophospholipid biosynthesis | 7.945529e-01 | 0.100 |
R-HSA-72172 | mRNA Splicing | 7.974816e-01 | 0.098 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 8.087881e-01 | 0.092 |
R-HSA-109582 | Hemostasis | 8.269401e-01 | 0.083 |
R-HSA-5619115 | Disorders of transmembrane transporters | 8.513339e-01 | 0.070 |
R-HSA-112316 | Neuronal System | 8.641116e-01 | 0.063 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 8.776153e-01 | 0.057 |
R-HSA-1280218 | Adaptive Immune System | 8.803300e-01 | 0.055 |
R-HSA-211945 | Phase I - Functionalization of compounds | 8.810954e-01 | 0.055 |
R-HSA-1483257 | Phospholipid metabolism | 8.948239e-01 | 0.048 |
R-HSA-195721 | Signaling by WNT | 8.970779e-01 | 0.047 |
R-HSA-112315 | Transmission across Chemical Synapses | 9.140919e-01 | 0.039 |
R-HSA-196854 | Metabolism of vitamins and cofactors | 9.361640e-01 | 0.029 |
R-HSA-425407 | SLC-mediated transmembrane transport | 9.501275e-01 | 0.022 |
R-HSA-8978868 | Fatty acid metabolism | 9.536248e-01 | 0.021 |
R-HSA-446203 | Asparagine N-linked glycosylation | 9.584199e-01 | 0.018 |
R-HSA-72766 | Translation | 9.604861e-01 | 0.018 |
R-HSA-392499 | Metabolism of proteins | 9.666934e-01 | 0.015 |
R-HSA-388396 | GPCR downstream signalling | 9.784492e-01 | 0.009 |
R-HSA-9709957 | Sensory Perception | 9.809102e-01 | 0.008 |
R-HSA-372790 | Signaling by GPCR | 9.873091e-01 | 0.006 |
R-HSA-1430728 | Metabolism | 9.905164e-01 | 0.004 |
R-HSA-382551 | Transport of small molecules | 9.943511e-01 | 0.002 |
R-HSA-556833 | Metabolism of lipids | 9.953289e-01 | 0.002 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
KIS |
0.794 | 0.565 | 1 | 0.828 |
DYRK4 |
0.788 | 0.629 | 1 | 0.870 |
DYRK2 |
0.786 | 0.585 | 1 | 0.812 |
JNK2 |
0.786 | 0.671 | 1 | 0.870 |
P38G |
0.784 | 0.639 | 1 | 0.885 |
CDK19 |
0.783 | 0.578 | 1 | 0.884 |
CDK8 |
0.782 | 0.577 | 1 | 0.870 |
CDK17 |
0.781 | 0.614 | 1 | 0.876 |
CDK18 |
0.781 | 0.595 | 1 | 0.865 |
HIPK2 |
0.781 | 0.553 | 1 | 0.851 |
P38D |
0.780 | 0.633 | 1 | 0.891 |
JNK3 |
0.778 | 0.653 | 1 | 0.861 |
CDK1 |
0.778 | 0.591 | 1 | 0.867 |
P38B |
0.778 | 0.617 | 1 | 0.839 |
DYRK1B |
0.775 | 0.562 | 1 | 0.838 |
ERK1 |
0.775 | 0.593 | 1 | 0.847 |
CDK16 |
0.775 | 0.594 | 1 | 0.868 |
CDK13 |
0.775 | 0.585 | 1 | 0.858 |
CDK7 |
0.774 | 0.563 | 1 | 0.855 |
HIPK1 |
0.772 | 0.518 | 1 | 0.796 |
CDK3 |
0.771 | 0.526 | 1 | 0.876 |
CDK12 |
0.771 | 0.582 | 1 | 0.868 |
NLK |
0.770 | 0.530 | 1 | 0.678 |
CDK10 |
0.770 | 0.568 | 1 | 0.848 |
HIPK4 |
0.769 | 0.342 | 1 | 0.658 |
HIPK3 |
0.769 | 0.510 | 1 | 0.765 |
CDK14 |
0.768 | 0.584 | 1 | 0.839 |
CDK9 |
0.768 | 0.581 | 1 | 0.853 |
P38A |
0.768 | 0.582 | 1 | 0.801 |
CLK3 |
0.767 | 0.365 | 1 | 0.654 |
ERK2 |
0.767 | 0.594 | 1 | 0.825 |
CDK5 |
0.766 | 0.542 | 1 | 0.837 |
DYRK1A |
0.764 | 0.436 | 1 | 0.791 |
DYRK3 |
0.762 | 0.430 | 1 | 0.768 |
CDK2 |
0.761 | 0.450 | 1 | 0.792 |
SRPK1 |
0.760 | 0.234 | -3 | 0.542 |
CLK1 |
0.760 | 0.319 | -3 | 0.517 |
JNK1 |
0.759 | 0.582 | 1 | 0.869 |
CLK2 |
0.758 | 0.348 | -3 | 0.515 |
ERK5 |
0.757 | 0.268 | 1 | 0.580 |
CLK4 |
0.756 | 0.295 | -3 | 0.545 |
SRPK2 |
0.755 | 0.185 | -3 | 0.467 |
CDK6 |
0.754 | 0.555 | 1 | 0.848 |
CDK4 |
0.754 | 0.572 | 1 | 0.868 |
PRP4 |
0.753 | 0.358 | -3 | 0.649 |
MTOR |
0.753 | 0.158 | 1 | 0.490 |
SRPK3 |
0.747 | 0.169 | -3 | 0.526 |
COT |
0.746 | -0.087 | 2 | 0.739 |
CDC7 |
0.744 | -0.092 | 1 | 0.389 |
PRPK |
0.744 | -0.083 | -1 | 0.810 |
DSTYK |
0.744 | -0.023 | 2 | 0.747 |
CDKL5 |
0.743 | 0.078 | -3 | 0.587 |
CDKL1 |
0.743 | 0.063 | -3 | 0.598 |
MOS |
0.743 | -0.027 | 1 | 0.404 |
ICK |
0.742 | 0.202 | -3 | 0.622 |
NUAK2 |
0.742 | 0.032 | -3 | 0.613 |
GCN2 |
0.741 | -0.158 | 2 | 0.676 |
ATR |
0.740 | -0.024 | 1 | 0.414 |
NEK6 |
0.739 | -0.031 | -2 | 0.767 |
CAMK1B |
0.739 | -0.027 | -3 | 0.651 |
RAF1 |
0.739 | -0.098 | 1 | 0.350 |
ULK2 |
0.739 | -0.135 | 2 | 0.675 |
NEK7 |
0.738 | -0.056 | -3 | 0.751 |
HUNK |
0.738 | -0.025 | 2 | 0.731 |
PDHK4 |
0.737 | -0.157 | 1 | 0.411 |
ULK1 |
0.737 | -0.100 | -3 | 0.699 |
TBK1 |
0.737 | -0.169 | 1 | 0.300 |
WNK1 |
0.737 | -0.043 | -2 | 0.810 |
BMPR2 |
0.736 | -0.157 | -2 | 0.806 |
IKKE |
0.735 | -0.156 | 1 | 0.301 |
IKKB |
0.733 | -0.162 | -2 | 0.707 |
CAMLCK |
0.733 | -0.009 | -2 | 0.786 |
PDHK1 |
0.733 | -0.165 | 1 | 0.383 |
BMPR1B |
0.733 | 0.023 | 1 | 0.369 |
MLK1 |
0.733 | -0.123 | 2 | 0.702 |
MARK4 |
0.733 | -0.016 | 4 | 0.887 |
CAMK2G |
0.733 | -0.093 | 2 | 0.676 |
RIPK3 |
0.733 | -0.097 | 3 | 0.669 |
NIK |
0.732 | -0.073 | -3 | 0.675 |
AMPKA1 |
0.731 | -0.045 | -3 | 0.617 |
RSK2 |
0.731 | -0.023 | -3 | 0.543 |
DAPK2 |
0.730 | -0.034 | -3 | 0.665 |
PKN2 |
0.730 | -0.056 | -3 | 0.629 |
PRKD1 |
0.730 | -0.059 | -3 | 0.579 |
TSSK2 |
0.730 | -0.045 | -5 | 0.753 |
MST4 |
0.730 | -0.059 | 2 | 0.709 |
TGFBR2 |
0.730 | -0.109 | -2 | 0.724 |
PIM3 |
0.729 | -0.085 | -3 | 0.600 |
ERK7 |
0.729 | 0.172 | 2 | 0.446 |
MOK |
0.728 | 0.323 | 1 | 0.696 |
SKMLCK |
0.728 | -0.051 | -2 | 0.800 |
P70S6KB |
0.728 | -0.019 | -3 | 0.575 |
PKN3 |
0.728 | -0.089 | -3 | 0.599 |
RSK3 |
0.727 | -0.040 | -3 | 0.536 |
P90RSK |
0.727 | -0.037 | -3 | 0.551 |
GRK1 |
0.727 | -0.039 | -2 | 0.767 |
GRK5 |
0.727 | -0.163 | -3 | 0.704 |
WNK3 |
0.727 | -0.169 | 1 | 0.346 |
PRKD2 |
0.727 | -0.044 | -3 | 0.514 |
NIM1 |
0.726 | -0.087 | 3 | 0.674 |
CHAK2 |
0.726 | -0.092 | -1 | 0.793 |
AMPKA2 |
0.726 | -0.041 | -3 | 0.580 |
MAK |
0.725 | 0.314 | -2 | 0.652 |
NDR1 |
0.725 | -0.085 | -3 | 0.595 |
IRE1 |
0.725 | -0.097 | 1 | 0.322 |
ATM |
0.725 | -0.046 | 1 | 0.379 |
TGFBR1 |
0.725 | -0.025 | -2 | 0.742 |
ANKRD3 |
0.724 | -0.135 | 1 | 0.375 |
QIK |
0.724 | -0.052 | -3 | 0.639 |
ALK4 |
0.724 | -0.041 | -2 | 0.762 |
MAPKAPK3 |
0.724 | -0.087 | -3 | 0.538 |
NEK9 |
0.724 | -0.136 | 2 | 0.701 |
BRSK1 |
0.724 | -0.031 | -3 | 0.554 |
PINK1 |
0.723 | 0.138 | 1 | 0.506 |
NDR2 |
0.723 | -0.112 | -3 | 0.588 |
GRK4 |
0.723 | -0.127 | -2 | 0.766 |
TSSK1 |
0.723 | -0.057 | -3 | 0.627 |
GRK6 |
0.723 | -0.112 | 1 | 0.374 |
MARK3 |
0.722 | 0.027 | 4 | 0.870 |
BRSK2 |
0.722 | -0.046 | -3 | 0.586 |
RIPK1 |
0.722 | -0.145 | 1 | 0.335 |
MASTL |
0.722 | -0.190 | -2 | 0.764 |
PRKD3 |
0.722 | -0.045 | -3 | 0.514 |
MLK3 |
0.721 | -0.090 | 2 | 0.646 |
PKCD |
0.721 | -0.073 | 2 | 0.678 |
DNAPK |
0.721 | -0.007 | 1 | 0.360 |
IRE2 |
0.721 | -0.095 | 2 | 0.661 |
QSK |
0.721 | -0.020 | 4 | 0.891 |
TTBK2 |
0.720 | -0.169 | 2 | 0.599 |
NEK2 |
0.720 | -0.074 | 2 | 0.686 |
ACVR2B |
0.720 | -0.051 | -2 | 0.729 |
NUAK1 |
0.720 | -0.059 | -3 | 0.549 |
PAK3 |
0.720 | -0.073 | -2 | 0.736 |
SMG1 |
0.720 | -0.054 | 1 | 0.385 |
MYLK4 |
0.720 | -0.009 | -2 | 0.723 |
PAK6 |
0.720 | -0.027 | -2 | 0.668 |
MARK2 |
0.720 | 0.010 | 4 | 0.839 |
MLK2 |
0.720 | -0.164 | 2 | 0.688 |
DLK |
0.719 | -0.179 | 1 | 0.392 |
BCKDK |
0.719 | -0.184 | -1 | 0.714 |
ACVR2A |
0.719 | -0.066 | -2 | 0.721 |
PIM1 |
0.719 | -0.041 | -3 | 0.546 |
SNRK |
0.719 | -0.103 | 2 | 0.645 |
PLK1 |
0.719 | -0.103 | -2 | 0.724 |
PKACG |
0.718 | -0.063 | -2 | 0.672 |
PHKG1 |
0.718 | -0.106 | -3 | 0.591 |
CAMK2D |
0.718 | -0.126 | -3 | 0.631 |
MELK |
0.718 | -0.097 | -3 | 0.572 |
AURC |
0.718 | -0.019 | -2 | 0.609 |
SIK |
0.717 | -0.050 | -3 | 0.531 |
IKKA |
0.717 | -0.147 | -2 | 0.690 |
DRAK1 |
0.717 | -0.033 | 1 | 0.352 |
VRK2 |
0.717 | -0.052 | 1 | 0.454 |
PAK1 |
0.717 | -0.066 | -2 | 0.730 |
MSK2 |
0.716 | -0.064 | -3 | 0.528 |
CAMK4 |
0.716 | -0.127 | -3 | 0.589 |
YSK4 |
0.716 | -0.128 | 1 | 0.327 |
CK1E |
0.716 | -0.007 | -3 | 0.488 |
MARK1 |
0.716 | -0.010 | 4 | 0.876 |
MAPKAPK2 |
0.716 | -0.074 | -3 | 0.484 |
MNK2 |
0.716 | -0.065 | -2 | 0.738 |
CAMK1G |
0.715 | -0.040 | -3 | 0.546 |
MEK1 |
0.715 | -0.113 | 2 | 0.712 |
PKR |
0.714 | -0.115 | 1 | 0.355 |
AKT2 |
0.714 | -0.006 | -3 | 0.472 |
SSTK |
0.714 | -0.023 | 4 | 0.881 |
BMPR1A |
0.713 | -0.017 | 1 | 0.362 |
MSK1 |
0.713 | -0.027 | -3 | 0.533 |
CHAK1 |
0.713 | -0.143 | 2 | 0.670 |
PKCB |
0.713 | -0.074 | 2 | 0.643 |
PAK2 |
0.713 | -0.074 | -2 | 0.719 |
GRK2 |
0.712 | -0.062 | -2 | 0.651 |
LATS2 |
0.712 | -0.117 | -5 | 0.640 |
PKG2 |
0.712 | -0.040 | -2 | 0.609 |
PIM2 |
0.712 | -0.007 | -3 | 0.525 |
ALK2 |
0.712 | -0.050 | -2 | 0.740 |
MLK4 |
0.712 | -0.136 | 2 | 0.619 |
CK1D |
0.712 | 0.012 | -3 | 0.458 |
PKCG |
0.712 | -0.080 | 2 | 0.656 |
GRK7 |
0.712 | -0.043 | 1 | 0.371 |
AURB |
0.711 | -0.027 | -2 | 0.605 |
SGK3 |
0.711 | -0.043 | -3 | 0.541 |
PKCA |
0.711 | -0.073 | 2 | 0.639 |
RSK4 |
0.711 | -0.024 | -3 | 0.500 |
PKCH |
0.711 | -0.089 | 2 | 0.645 |
PLK3 |
0.711 | -0.095 | 2 | 0.675 |
MAPKAPK5 |
0.710 | -0.108 | -3 | 0.530 |
FAM20C |
0.710 | -0.066 | 2 | 0.449 |
TLK1 |
0.710 | -0.098 | -2 | 0.761 |
MNK1 |
0.709 | -0.065 | -2 | 0.742 |
CAMK2A |
0.709 | -0.062 | 2 | 0.664 |
GSK3A |
0.709 | 0.111 | 4 | 0.368 |
MST3 |
0.708 | -0.038 | 2 | 0.730 |
TLK2 |
0.708 | -0.145 | 1 | 0.352 |
HRI |
0.708 | -0.144 | -2 | 0.769 |
MEKK3 |
0.708 | -0.113 | 1 | 0.359 |
PKACB |
0.708 | -0.026 | -2 | 0.618 |
SMMLCK |
0.708 | -0.023 | -3 | 0.611 |
CK1A2 |
0.707 | -0.010 | -3 | 0.450 |
PHKG2 |
0.707 | -0.098 | -3 | 0.570 |
PERK |
0.707 | -0.149 | -2 | 0.762 |
PKCZ |
0.707 | -0.107 | 2 | 0.668 |
WNK4 |
0.707 | -0.111 | -2 | 0.792 |
PLK4 |
0.706 | -0.145 | 2 | 0.597 |
MEK5 |
0.706 | -0.149 | 2 | 0.707 |
BRAF |
0.706 | -0.090 | -4 | 0.723 |
MPSK1 |
0.706 | -0.014 | 1 | 0.359 |
AURA |
0.706 | -0.031 | -2 | 0.588 |
CAMK2B |
0.706 | -0.104 | 2 | 0.628 |
IRAK4 |
0.706 | -0.126 | 1 | 0.317 |
ZAK |
0.705 | -0.151 | 1 | 0.361 |
LATS1 |
0.704 | -0.094 | -3 | 0.608 |
CK1G1 |
0.704 | -0.058 | -3 | 0.486 |
TTBK1 |
0.704 | -0.135 | 2 | 0.551 |
MEKK1 |
0.704 | -0.176 | 1 | 0.363 |
NEK11 |
0.703 | -0.071 | 1 | 0.362 |
P70S6K |
0.703 | -0.044 | -3 | 0.503 |
PKCT |
0.703 | -0.083 | 2 | 0.645 |
CHK1 |
0.703 | -0.115 | -3 | 0.566 |
NEK5 |
0.702 | -0.118 | 1 | 0.343 |
GSK3B |
0.702 | 0.011 | 4 | 0.362 |
PKCI |
0.702 | -0.053 | 2 | 0.645 |
MEKK2 |
0.702 | -0.145 | 2 | 0.682 |
GAK |
0.702 | 0.017 | 1 | 0.380 |
AKT1 |
0.701 | -0.031 | -3 | 0.485 |
DCAMKL1 |
0.701 | -0.100 | -3 | 0.531 |
DCAMKL2 |
0.700 | -0.090 | -3 | 0.566 |
PASK |
0.700 | -0.021 | -3 | 0.632 |
MEKK6 |
0.700 | -0.069 | 1 | 0.365 |
PAK5 |
0.699 | -0.059 | -2 | 0.617 |
NEK8 |
0.699 | -0.120 | 2 | 0.716 |
PKN1 |
0.699 | -0.062 | -3 | 0.516 |
LKB1 |
0.699 | -0.041 | -3 | 0.692 |
IRAK1 |
0.698 | -0.168 | -1 | 0.722 |
GRK3 |
0.698 | -0.073 | -2 | 0.614 |
CK2A2 |
0.698 | -0.049 | 1 | 0.314 |
PRKX |
0.698 | -0.027 | -3 | 0.441 |
PKCE |
0.697 | -0.033 | 2 | 0.647 |
PAK4 |
0.696 | -0.053 | -2 | 0.623 |
TAK1 |
0.696 | -0.066 | 1 | 0.351 |
TAO2 |
0.696 | -0.097 | 2 | 0.723 |
PKACA |
0.695 | -0.036 | -2 | 0.571 |
CHK2 |
0.695 | -0.043 | -3 | 0.418 |
NEK4 |
0.695 | -0.089 | 1 | 0.312 |
SBK |
0.694 | 0.043 | -3 | 0.356 |
TAO3 |
0.694 | -0.121 | 1 | 0.371 |
CAMKK1 |
0.694 | -0.150 | -2 | 0.692 |
EEF2K |
0.693 | -0.075 | 3 | 0.729 |
MAP3K15 |
0.693 | -0.110 | 1 | 0.356 |
RIPK2 |
0.692 | -0.140 | 1 | 0.319 |
DAPK3 |
0.692 | -0.047 | -3 | 0.568 |
CK2A1 |
0.692 | -0.046 | 1 | 0.306 |
CAMK1D |
0.692 | -0.074 | -3 | 0.445 |
STK33 |
0.692 | -0.091 | 2 | 0.560 |
PDK1 |
0.692 | -0.109 | 1 | 0.364 |
SGK1 |
0.691 | -0.008 | -3 | 0.401 |
CAMKK2 |
0.691 | -0.129 | -2 | 0.693 |
HPK1 |
0.690 | -0.056 | 1 | 0.335 |
AKT3 |
0.690 | -0.022 | -3 | 0.411 |
DAPK1 |
0.690 | -0.037 | -3 | 0.563 |
BUB1 |
0.690 | -0.024 | -5 | 0.708 |
LRRK2 |
0.690 | -0.065 | 2 | 0.728 |
MRCKB |
0.689 | -0.023 | -3 | 0.515 |
GCK |
0.689 | -0.087 | 1 | 0.348 |
HGK |
0.689 | -0.106 | 3 | 0.778 |
LOK |
0.688 | -0.095 | -2 | 0.735 |
MST2 |
0.688 | -0.136 | 1 | 0.343 |
NEK3 |
0.688 | -0.074 | 1 | 0.344 |
CAMK1A |
0.687 | -0.057 | -3 | 0.423 |
NEK1 |
0.687 | -0.096 | 1 | 0.315 |
MINK |
0.686 | -0.131 | 1 | 0.321 |
MRCKA |
0.686 | -0.030 | -3 | 0.525 |
TNIK |
0.686 | -0.094 | 3 | 0.771 |
VRK1 |
0.684 | -0.167 | 2 | 0.741 |
PBK |
0.684 | -0.055 | 1 | 0.332 |
MST1 |
0.682 | -0.130 | 1 | 0.323 |
PKG1 |
0.682 | -0.059 | -2 | 0.548 |
PDHK3_TYR |
0.681 | 0.080 | 4 | 0.826 |
DMPK1 |
0.681 | 0.008 | -3 | 0.526 |
YSK1 |
0.681 | -0.126 | 2 | 0.682 |
ROCK2 |
0.681 | -0.043 | -3 | 0.555 |
MEK2 |
0.680 | -0.169 | 2 | 0.684 |
PLK2 |
0.680 | -0.093 | -3 | 0.615 |
SLK |
0.679 | -0.096 | -2 | 0.689 |
CRIK |
0.678 | 0.005 | -3 | 0.475 |
KHS2 |
0.678 | -0.066 | 1 | 0.339 |
KHS1 |
0.678 | -0.103 | 1 | 0.323 |
TESK1_TYR |
0.677 | 0.004 | 3 | 0.794 |
HASPIN |
0.677 | -0.041 | -1 | 0.595 |
PKMYT1_TYR |
0.676 | 0.048 | 3 | 0.760 |
BIKE |
0.676 | -0.035 | 1 | 0.320 |
EPHA6 |
0.675 | 0.007 | -1 | 0.848 |
BMPR2_TYR |
0.675 | 0.050 | -1 | 0.822 |
ROCK1 |
0.674 | -0.034 | -3 | 0.525 |
MAP2K7_TYR |
0.673 | -0.065 | 2 | 0.747 |
CK1A |
0.673 | -0.041 | -3 | 0.387 |
MAP2K6_TYR |
0.673 | 0.036 | -1 | 0.818 |
PDHK4_TYR |
0.673 | 0.047 | 2 | 0.759 |
MAP2K4_TYR |
0.672 | -0.024 | -1 | 0.811 |
LIMK2_TYR |
0.672 | 0.034 | -3 | 0.696 |
PDHK1_TYR |
0.672 | -0.008 | -1 | 0.839 |
ASK1 |
0.672 | -0.123 | 1 | 0.352 |
ALPHAK3 |
0.671 | -0.071 | -1 | 0.767 |
TTK |
0.670 | -0.121 | -2 | 0.739 |
OSR1 |
0.670 | -0.132 | 2 | 0.664 |
PINK1_TYR |
0.670 | -0.113 | 1 | 0.401 |
YANK3 |
0.668 | -0.065 | 2 | 0.360 |
RET |
0.667 | -0.109 | 1 | 0.370 |
MYO3B |
0.667 | -0.099 | 2 | 0.693 |
TXK |
0.667 | -0.012 | 1 | 0.380 |
TAO1 |
0.667 | -0.123 | 1 | 0.322 |
EPHB4 |
0.667 | -0.060 | -1 | 0.806 |
MST1R |
0.667 | -0.082 | 3 | 0.726 |
LIMK1_TYR |
0.665 | -0.064 | 2 | 0.727 |
FGFR2 |
0.665 | -0.016 | 3 | 0.725 |
JAK3 |
0.664 | -0.078 | 1 | 0.379 |
MYO3A |
0.663 | -0.124 | 1 | 0.321 |
JAK2 |
0.663 | -0.133 | 1 | 0.380 |
AAK1 |
0.663 | -0.014 | 1 | 0.287 |
CSF1R |
0.663 | -0.086 | 3 | 0.708 |
TYRO3 |
0.663 | -0.134 | 3 | 0.707 |
FGFR1 |
0.661 | -0.038 | 3 | 0.687 |
TEK |
0.661 | 0.008 | 3 | 0.636 |
ABL1 |
0.661 | -0.070 | -1 | 0.814 |
DDR1 |
0.661 | -0.076 | 4 | 0.782 |
ABL2 |
0.661 | -0.079 | -1 | 0.813 |
EPHA4 |
0.661 | -0.024 | 2 | 0.692 |
ITK |
0.660 | -0.047 | -1 | 0.802 |
ROS1 |
0.660 | -0.157 | 3 | 0.678 |
FGR |
0.659 | -0.118 | 1 | 0.354 |
TYK2 |
0.659 | -0.211 | 1 | 0.353 |
EPHB1 |
0.659 | -0.084 | 1 | 0.375 |
SRMS |
0.659 | -0.073 | 1 | 0.366 |
KDR |
0.658 | -0.062 | 3 | 0.688 |
KIT |
0.658 | -0.076 | 3 | 0.705 |
FER |
0.658 | -0.141 | 1 | 0.385 |
HCK |
0.657 | -0.102 | -1 | 0.834 |
NEK10_TYR |
0.657 | -0.096 | 1 | 0.314 |
TNNI3K_TYR |
0.657 | -0.047 | 1 | 0.390 |
EPHB2 |
0.657 | -0.074 | -1 | 0.798 |
YES1 |
0.656 | -0.094 | -1 | 0.829 |
LCK |
0.656 | -0.071 | -1 | 0.844 |
STLK3 |
0.656 | -0.186 | 1 | 0.331 |
FGFR3 |
0.656 | -0.025 | 3 | 0.700 |
BLK |
0.655 | -0.045 | -1 | 0.841 |
EPHB3 |
0.655 | -0.096 | -1 | 0.803 |
FLT3 |
0.655 | -0.127 | 3 | 0.705 |
PTK2B |
0.655 | -0.016 | -1 | 0.786 |
JAK1 |
0.655 | -0.107 | 1 | 0.337 |
TEC |
0.655 | -0.061 | -1 | 0.749 |
INSRR |
0.654 | -0.123 | 3 | 0.666 |
BMX |
0.654 | -0.045 | -1 | 0.730 |
FLT1 |
0.654 | -0.060 | -1 | 0.814 |
MERTK |
0.653 | -0.112 | 3 | 0.700 |
TNK2 |
0.653 | -0.106 | 3 | 0.663 |
PDGFRB |
0.653 | -0.181 | 3 | 0.711 |
MET |
0.653 | -0.083 | 3 | 0.705 |
AXL |
0.652 | -0.132 | 3 | 0.700 |
FRK |
0.651 | -0.082 | -1 | 0.837 |
WEE1_TYR |
0.651 | -0.067 | -1 | 0.718 |
CK1G3 |
0.651 | -0.054 | -3 | 0.352 |
EPHA7 |
0.650 | -0.076 | 2 | 0.688 |
BTK |
0.650 | -0.135 | -1 | 0.766 |
ERBB2 |
0.649 | -0.107 | 1 | 0.348 |
FYN |
0.649 | -0.042 | -1 | 0.821 |
EPHA1 |
0.649 | -0.106 | 3 | 0.693 |
TNK1 |
0.648 | -0.125 | 3 | 0.688 |
FLT4 |
0.648 | -0.101 | 3 | 0.673 |
PDGFRA |
0.647 | -0.199 | 3 | 0.696 |
EPHA3 |
0.646 | -0.093 | 2 | 0.672 |
PTK2 |
0.646 | 0.009 | -1 | 0.785 |
ALK |
0.646 | -0.152 | 3 | 0.626 |
LYN |
0.645 | -0.093 | 3 | 0.614 |
LTK |
0.645 | -0.146 | 3 | 0.655 |
EGFR |
0.645 | -0.082 | 1 | 0.320 |
MATK |
0.644 | -0.077 | -1 | 0.748 |
EPHA8 |
0.643 | -0.078 | -1 | 0.810 |
DDR2 |
0.642 | -0.045 | 3 | 0.658 |
SYK |
0.642 | -0.019 | -1 | 0.781 |
EPHA5 |
0.642 | -0.084 | 2 | 0.685 |
PTK6 |
0.642 | -0.193 | -1 | 0.752 |
INSR |
0.642 | -0.150 | 3 | 0.640 |
SRC |
0.640 | -0.082 | -1 | 0.825 |
NTRK2 |
0.640 | -0.196 | 3 | 0.662 |
MUSK |
0.640 | -0.108 | 1 | 0.285 |
NTRK1 |
0.640 | -0.201 | -1 | 0.774 |
FGFR4 |
0.638 | -0.088 | -1 | 0.771 |
EPHA2 |
0.637 | -0.068 | -1 | 0.774 |
ERBB4 |
0.637 | -0.047 | 1 | 0.327 |
NTRK3 |
0.637 | -0.159 | -1 | 0.736 |
YANK2 |
0.637 | -0.080 | 2 | 0.360 |
CK1G2 |
0.637 | -0.039 | -3 | 0.422 |
CSK |
0.635 | -0.129 | 2 | 0.684 |
ZAP70 |
0.630 | -0.016 | -1 | 0.706 |
FES |
0.627 | -0.093 | -1 | 0.727 |
IGF1R |
0.626 | -0.141 | 3 | 0.576 |