Motif 538 (n=42)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A6NKT7 | RGPD3 | S789 | ochoa | RanBP2-like and GRIP domain-containing protein 3 | None |
K7ERJ3 | None | S30 | ochoa | KS6B1 kinase | None |
O14715 | RGPD8 | S788 | ochoa | RANBP2-like and GRIP domain-containing protein 8 (Ran-binding protein 2-like 3) (RanBP2-like 3) (RanBP2L3) | None |
O43299 | AP5Z1 | S776 | ochoa | AP-5 complex subunit zeta-1 (Adaptor-related protein complex 5 zeta subunit) (Zeta5) | As part of AP-5, a probable fifth adaptor protein complex it may be involved in endosomal transport. According to PubMed:20613862 it is a putative helicase required for efficient homologous recombination DNA double-strand break repair. {ECO:0000269|PubMed:20613862, ECO:0000269|PubMed:22022230}. |
O94763 | URI1 | S488 | ochoa | Unconventional prefoldin RPB5 interactor 1 (Protein NNX3) (Protein phosphatase 1 regulatory subunit 19) (RNA polymerase II subunit 5-mediating protein) (RPB5-mediating protein) | Involved in gene transcription regulation. Acts as a transcriptional repressor in concert with the corepressor UXT to regulate androgen receptor (AR) transcription. May act as a tumor suppressor to repress AR-mediated gene transcription and to inhibit anchorage-independent growth in prostate cancer cells. Required for cell survival in ovarian cancer cells. Together with UXT, associates with chromatin to the NKX3-1 promoter region. Antagonizes transcriptional modulation via hepatitis B virus X protein.; FUNCTION: Plays a central role in maintaining S6K1 signaling and BAD phosphorylation under normal growth conditions thereby protecting cells from potential deleterious effects of sustained S6K1 signaling. The URI1-PPP1CC complex acts as a central component of a negative feedback mechanism that counteracts excessive S6K1 survival signaling to BAD in response to growth factors. Mediates inhibition of PPP1CC phosphatase activity in mitochondria. Coordinates the regulation of nutrient-sensitive gene expression availability in a mTOR-dependent manner. Seems to be a scaffolding protein able to assemble a prefoldin-like complex that contains PFDs and proteins with roles in transcription and ubiquitination. |
O94875 | SORBS2 | Y72 | ochoa | Sorbin and SH3 domain-containing protein 2 (Arg-binding protein 2) (ArgBP2) (Arg/Abl-interacting protein 2) (Sorbin) | Adapter protein that plays a role in the assembling of signaling complexes, being a link between ABL kinases and actin cytoskeleton. Can form complex with ABL1 and CBL, thus promoting ubiquitination and degradation of ABL1. May play a role in the regulation of pancreatic cell adhesion, possibly by acting on WASF1 phosphorylation, enhancing phosphorylation by ABL1, as well as dephosphorylation by PTPN12 (PubMed:18559503). Isoform 6 increases water and sodium absorption in the intestine and gall-bladder. {ECO:0000269|PubMed:12475393, ECO:0000269|PubMed:18559503, ECO:0000269|PubMed:9211900}. |
P0DJD0 | RGPD1 | S779 | ochoa | RANBP2-like and GRIP domain-containing protein 1 (Ran-binding protein 2-like 6) (RanBP2-like 6) (RanBP2L6) | None |
P0DJD1 | RGPD2 | S787 | ochoa | RANBP2-like and GRIP domain-containing protein 2 (Ran-binding protein 2-like 2) (RanBP2-like 2) (RanBP2L2) | None |
P15036 | ETS2 | S88 | ochoa | Protein C-ets-2 | Transcription factor activating transcription. Binds specifically the DNA GGAA/T core motif (Ets-binding site or EBS) in gene promoters and stimulates transcription. {ECO:0000269|PubMed:11909962}. |
P23443 | RPS6KB1 | S427 | ochoa|psp | Ribosomal protein S6 kinase beta-1 (S6K-beta-1) (S6K1) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 1) (P70S6K1) (p70-S6K 1) (Ribosomal protein S6 kinase I) (Serine/threonine-protein kinase 14A) (p70 ribosomal S6 kinase alpha) (p70 S6 kinase alpha) (p70 S6K-alpha) (p70 S6KA) | Serine/threonine-protein kinase that acts downstream of mTOR signaling in response to growth factors and nutrients to promote cell proliferation, cell growth and cell cycle progression (PubMed:11500364, PubMed:12801526, PubMed:14673156, PubMed:15071500, PubMed:15341740, PubMed:16286006, PubMed:17052453, PubMed:17053147, PubMed:17936702, PubMed:18952604, PubMed:19085255, PubMed:19720745, PubMed:19935711, PubMed:19995915, PubMed:22017876, PubMed:23429703, PubMed:28178239). Regulates protein synthesis through phosphorylation of EIF4B, RPS6 and EEF2K, and contributes to cell survival by repressing the pro-apoptotic function of BAD (PubMed:11500364, PubMed:12801526, PubMed:14673156, PubMed:15071500, PubMed:15341740, PubMed:16286006, PubMed:17052453, PubMed:17053147, PubMed:17936702, PubMed:18952604, PubMed:19085255, PubMed:19720745, PubMed:19935711, PubMed:19995915, PubMed:22017876, PubMed:23429703, PubMed:28178239). Under conditions of nutrient depletion, the inactive form associates with the EIF3 translation initiation complex (PubMed:16286006). Upon mitogenic stimulation, phosphorylation by the mechanistic target of rapamycin complex 1 (mTORC1) leads to dissociation from the EIF3 complex and activation (PubMed:16286006). The active form then phosphorylates and activates several substrates in the pre-initiation complex, including the EIF2B complex and the cap-binding complex component EIF4B (PubMed:16286006). Also controls translation initiation by phosphorylating a negative regulator of EIF4A, PDCD4, targeting it for ubiquitination and subsequent proteolysis (PubMed:17053147). Promotes initiation of the pioneer round of protein synthesis by phosphorylating POLDIP3/SKAR (PubMed:15341740). In response to IGF1, activates translation elongation by phosphorylating EEF2 kinase (EEF2K), which leads to its inhibition and thus activation of EEF2 (PubMed:11500364). Also plays a role in feedback regulation of mTORC2 by mTORC1 by phosphorylating MAPKAP1/SIN1, MTOR and RICTOR, resulting in the inhibition of mTORC2 and AKT1 signaling (PubMed:15899889, PubMed:19720745, PubMed:19935711, PubMed:19995915). Also involved in feedback regulation of mTORC1 and mTORC2 by phosphorylating DEPTOR (PubMed:22017876). Mediates cell survival by phosphorylating the pro-apoptotic protein BAD and suppressing its pro-apoptotic function (By similarity). Phosphorylates mitochondrial URI1 leading to dissociation of a URI1-PPP1CC complex (PubMed:17936702). The free mitochondrial PPP1CC can then dephosphorylate RPS6KB1 at Thr-412, which is proposed to be a negative feedback mechanism for the RPS6KB1 anti-apoptotic function (PubMed:17936702). Mediates TNF-alpha-induced insulin resistance by phosphorylating IRS1 at multiple serine residues, resulting in accelerated degradation of IRS1 (PubMed:18952604). In cells lacking functional TSC1-2 complex, constitutively phosphorylates and inhibits GSK3B (PubMed:17052453). May be involved in cytoskeletal rearrangement through binding to neurabin (By similarity). Phosphorylates and activates the pyrimidine biosynthesis enzyme CAD, downstream of MTOR (PubMed:23429703). Following activation by mTORC1, phosphorylates EPRS and thereby plays a key role in fatty acid uptake by adipocytes and also most probably in interferon-gamma-induced translation inhibition (PubMed:28178239). {ECO:0000250|UniProtKB:P67999, ECO:0000250|UniProtKB:Q8BSK8, ECO:0000269|PubMed:11500364, ECO:0000269|PubMed:12801526, ECO:0000269|PubMed:14673156, ECO:0000269|PubMed:15071500, ECO:0000269|PubMed:15341740, ECO:0000269|PubMed:15899889, ECO:0000269|PubMed:16286006, ECO:0000269|PubMed:17052453, ECO:0000269|PubMed:17053147, ECO:0000269|PubMed:17936702, ECO:0000269|PubMed:18952604, ECO:0000269|PubMed:19085255, ECO:0000269|PubMed:19720745, ECO:0000269|PubMed:19935711, ECO:0000269|PubMed:19995915, ECO:0000269|PubMed:22017876, ECO:0000269|PubMed:23429703, ECO:0000269|PubMed:28178239}. |
P30050 | RPL12 | S76 | ochoa | Large ribosomal subunit protein uL11 (60S ribosomal protein L12) | Component of the large ribosomal subunit (PubMed:25901680). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:25901680). Binds directly to 26S ribosomal RNA (PubMed:25901680). {ECO:0000269|PubMed:25901680}. |
P35498 | SCN1A | S551 | ochoa | Sodium channel protein type 1 subunit alpha (Sodium channel protein brain I subunit alpha) (Sodium channel protein type I subunit alpha) (Voltage-gated sodium channel subunit alpha Nav1.1) | Pore-forming subunit of Nav1.1, 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:14672992). By regulating the excitability of neurons, ensures that they respond appropriately to synaptic inputs, maintaining the balance between excitation and inhibition in brain neural circuits (By similarity). Nav1.1 plays a role in controlling the excitability and action potential propagation from somatosensory neurons, thereby contributing to the sensory perception of mechanically-induced pain (By similarity). {ECO:0000250|UniProtKB:A2APX8, ECO:0000269|PubMed:14672992}. |
P46092 | CCR10 | S329 | ochoa | C-C chemokine receptor type 10 (C-C CKR-10) (CC-CKR-10) (CCR-10) (G-protein coupled receptor 2) | Receptor for chemokines SCYA27 and SCYA28. Subsequently transduces a signal by increasing the intracellular calcium ions level and stimulates chemotaxis in a pre-B cell line. |
P49792 | RANBP2 | S788 | 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}. |
P55317 | FOXA1 | S223 | ochoa | Hepatocyte nuclear factor 3-alpha (HNF-3-alpha) (HNF-3A) (Forkhead box protein A1) (Transcription factor 3A) (TCF-3A) | Transcription factor that is involved in embryonic development, establishment of tissue-specific gene expression and regulation of gene expression in differentiated tissues. Is thought to act as a 'pioneer' factor opening the compacted chromatin for other proteins through interactions with nucleosomal core histones and thereby replacing linker histones at target enhancer and/or promoter sites. Binds DNA with the consensus sequence 5'-[AC]A[AT]T[AG]TT[GT][AG][CT]T[CT]-3' (By similarity). Proposed to play a role in translating the epigenetic signatures into cell type-specific enhancer-driven transcriptional programs. Its differential recruitment to chromatin is dependent on distribution of histone H3 methylated at 'Lys-5' (H3K4me2) in estrogen-regulated genes. Involved in the development of multiple endoderm-derived organ systems such as liver, pancreas, lung and prostate; FOXA1 and FOXA2 seem to have at least in part redundant roles (By similarity). Modulates the transcriptional activity of nuclear hormone receptors. Is involved in ESR1-mediated transcription; required for ESR1 binding to the NKX2-1 promoter in breast cancer cells; binds to the RPRM promoter and is required for the estrogen-induced repression of RPRM. Involved in regulation of apoptosis by inhibiting the expression of BCL2. Involved in cell cycle regulation by activating expression of CDKN1B, alone or in conjunction with BRCA1. Originally described as a transcription activator for a number of liver genes such as AFP, albumin, tyrosine aminotransferase, PEPCK, etc. Interacts with the cis-acting regulatory regions of these genes. Involved in glucose homeostasis. {ECO:0000250, ECO:0000269|PubMed:16087863, ECO:0000269|PubMed:16331276, ECO:0000269|PubMed:18358809, ECO:0000269|PubMed:19127412, ECO:0000269|PubMed:19917725}. |
P55318 | FOXA3 | S170 | ochoa | Hepatocyte nuclear factor 3-gamma (HNF-3-gamma) (HNF-3G) (Fork head-related protein FKH H3) (Forkhead box protein A3) (Transcription factor 3G) (TCF-3G) | Transcription factor that is thought to act as a 'pioneer' factor opening the compacted chromatin for other proteins through interactions with nucleosomal core histones and thereby replacing linker histones at target enhancer and/or promoter sites (By similarity). Originally described as a transcription activator for a number of liver genes such as AFP, albumin, tyrosine aminotransferase, PEPCK, etc. Interacts with the cis-acting regulatory regions of these genes. Involved in glucose homeostasis; binds to and activates transcription from the G6PC1 promoter. Binds to the CYP3A4 promoter and activates its transcription in cooperation with CEBPA. Binds to the CYP3A7 promoter together with members of the CTF/NF-I family. Involved in regulation of neuronal-specific transcription. May be involved in regulation of spermatogenesis. {ECO:0000250, ECO:0000269|PubMed:12695546}. |
P85037 | FOXK1 | T202 | ochoa | Forkhead box protein K1 (Myocyte nuclear factor) (MNF) | Transcriptional regulator involved in different processes such as glucose metabolism, aerobic glycolysis, muscle cell differentiation and autophagy (By similarity). Recognizes and binds the forkhead DNA sequence motif (5'-GTAAACA-3') and can both act as a transcription activator or repressor, depending on the context (PubMed:17670796). Together with FOXK2, acts as a key regulator of metabolic reprogramming towards aerobic glycolysis, a process in which glucose is converted to lactate in the presence of oxygen (By similarity). Acts by promoting expression of enzymes for glycolysis (such as hexokinase-2 (HK2), phosphofructokinase, pyruvate kinase (PKLR) and lactate dehydrogenase), while suppressing further oxidation of pyruvate in the mitochondria by up-regulating pyruvate dehydrogenase kinases PDK1 and PDK4 (By similarity). Probably plays a role in gluconeogenesis during overnight fasting, when lactate from white adipose tissue and muscle is the main substrate (By similarity). Involved in mTORC1-mediated metabolic reprogramming: in response to mTORC1 signaling, translocates into the nucleus and regulates the expression of genes associated with glycolysis and downstream anabolic pathways, such as HIF1A, thereby regulating glucose metabolism (By similarity). Together with FOXK2, acts as a negative regulator of autophagy in skeletal muscle: in response to starvation, enters the nucleus, binds the promoters of autophagy genes and represses their expression, preventing proteolysis of skeletal muscle proteins (By similarity). Acts as a transcriptional regulator of the myogenic progenitor cell population in skeletal muscle (By similarity). Binds to the upstream enhancer region (CCAC box) of myoglobin (MB) gene, regulating the myogenic progenitor cell population (By similarity). Promotes muscle progenitor cell proliferation by repressing the transcriptional activity of FOXO4, thereby inhibiting myogenic differentiation (By similarity). Involved in remodeling processes of adult muscles that occur in response to physiological stimuli (By similarity). Required to correct temporal orchestration of molecular and cellular events necessary for muscle repair (By similarity). Represses myogenic differentiation by inhibiting MEFC activity (By similarity). Positively regulates Wnt/beta-catenin signaling by translocating DVL into the nucleus (PubMed:25805136). Reduces virus replication, probably by binding the interferon stimulated response element (ISRE) to promote antiviral gene expression (PubMed:25852164). Accessory component of the polycomb repressive deubiquitinase (PR-DUB) complex; recruits the PR-DUB complex to specific FOXK1-bound genes (PubMed:24634419, PubMed:30664650). {ECO:0000250|UniProtKB:P42128, ECO:0000269|PubMed:17670796, ECO:0000269|PubMed:24634419, ECO:0000269|PubMed:25805136, ECO:0000269|PubMed:25852164, ECO:0000269|PubMed:30664650}. |
Q3T8J9 | GON4L | S1009 | 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}. |
Q5SYE7 | NHSL1 | S723 | ochoa | NHS-like protein 1 | None |
Q6W2J9 | BCOR | S1439 | ochoa | BCL-6 corepressor (BCoR) | Transcriptional corepressor. May specifically inhibit gene expression when recruited to promoter regions by sequence-specific DNA-binding proteins such as BCL6 and MLLT3. This repression may be mediated at least in part by histone deacetylase activities which can associate with this corepressor. Involved in the repression of TFAP2A; impairs binding of BCL6 and KDM2B to TFAP2A promoter regions. Via repression of TFAP2A acts as a negative regulator of osteo-dentiogenic capacity in adult stem cells; the function implies inhibition of methylation on histone H3 'Lys-4' (H3K4me3) and 'Lys-36' (H3K36me2). {ECO:0000269|PubMed:10898795, ECO:0000269|PubMed:15004558, ECO:0000269|PubMed:18280243, ECO:0000269|PubMed:19578371, ECO:0000269|PubMed:23911289}. |
Q7L590 | MCM10 | S593 | ochoa | Protein MCM10 homolog (HsMCM10) | Acts as a replication initiation factor that brings together the MCM2-7 helicase and the DNA polymerase alpha/primase complex in order to initiate DNA replication. Additionally, plays a role in preventing DNA damage during replication. Key effector of the RBBP6 and ZBTB38-mediated regulation of DNA-replication and common fragile sites stability; acts as a direct target of transcriptional repression by ZBTB38 (PubMed:24726359). {ECO:0000269|PubMed:11095689, ECO:0000269|PubMed:15136575, ECO:0000269|PubMed:17699597, ECO:0000269|PubMed:19608746, ECO:0000269|PubMed:24726359, ECO:0000269|PubMed:32865517}. |
Q7RTN6 | STRADA | S387 | ochoa | STE20-related kinase adapter protein alpha (STRAD alpha) (STE20-related adapter protein) (Serologically defined breast cancer antigen NY-BR-96) | Pseudokinase which, in complex with CAB39/MO25 (CAB39/MO25alpha or CAB39L/MO25beta), binds to and activates STK11/LKB1. Adopts a closed conformation typical of active protein kinases and binds STK11/LKB1 as a pseudosubstrate, promoting conformational change of STK11/LKB1 in an active conformation. {ECO:0000269|PubMed:12805220, ECO:0000269|PubMed:14517248, ECO:0000269|PubMed:19892943}. |
Q7Z3J3 | RGPD4 | S789 | ochoa | RanBP2-like and GRIP domain-containing protein 4 | None |
Q8IXZ2 | ZC3H3 | S918 | ochoa | Zinc finger CCCH domain-containing protein 3 (Smad-interacting CPSF-like factor) | Required for the export of polyadenylated mRNAs from the nucleus (PubMed:19364924). Enhances ACVR1B-induced SMAD-dependent transcription. Binds to single-stranded DNA but not to double-stranded DNA in vitro. Involved in RNA cleavage (By similarity). {ECO:0000250|UniProtKB:Q8CHP0, ECO:0000269|PubMed:19364924}. |
Q8IZD2 | KMT2E | S795 | ochoa | Inactive histone-lysine N-methyltransferase 2E (Inactive lysine N-methyltransferase 2E) (Myeloid/lymphoid or mixed-lineage leukemia protein 5) | Associates with chromatin regions downstream of transcriptional start sites of active genes and thus regulates gene transcription (PubMed:23629655, PubMed:23798402, PubMed:24130829). Chromatin interaction is mediated via the binding to tri-methylated histone H3 at 'Lys-4' (H3K4me3) (PubMed:23798402, PubMed:24130829). Key regulator of hematopoiesis involved in terminal myeloid differentiation and in the regulation of hematopoietic stem cell (HSCs) self-renewal by a mechanism that involves DNA methylation (By similarity). Also acts as an important cell cycle regulator, participating in cell cycle regulatory network machinery at multiple cell cycle stages including G1/S transition, S phase progression and mitotic entry (PubMed:14718661, PubMed:18573682, PubMed:19264965, PubMed:23629655). Recruited to E2F1 responsive promoters by HCFC1 where it stimulates tri-methylation of histone H3 at 'Lys-4' and transcriptional activation and thereby facilitates G1 to S phase transition (PubMed:23629655). During myoblast differentiation, required to suppress inappropriate expression of S-phase-promoting genes and maintain expression of determination genes in quiescent cells (By similarity). {ECO:0000250|UniProtKB:Q3UG20, ECO:0000269|PubMed:14718661, ECO:0000269|PubMed:18573682, ECO:0000269|PubMed:23629655, ECO:0000269|PubMed:23798402, ECO:0000269|PubMed:24130829}.; FUNCTION: [Isoform NKp44L]: Cellular ligand for NCR2/NKp44, may play a role as a danger signal in cytotoxicity and NK-cell-mediated innate immunity. {ECO:0000269|PubMed:23958951}. |
Q8ND30 | PPFIBP2 | S476 | ochoa | Liprin-beta-2 (Protein tyrosine phosphatase receptor type f polypeptide-interacting protein-binding protein 2) (PTPRF-interacting protein-binding protein 2) | May regulate the disassembly of focal adhesions. Did not bind receptor-like tyrosine phosphatases type 2A. {ECO:0000269|PubMed:9624153}. |
Q8NHM5 | KDM2B | S820 | ochoa | Lysine-specific demethylase 2B (EC 1.14.11.27) (CXXC-type zinc finger protein 2) (F-box and leucine-rich repeat protein 10) (F-box protein FBL10) (F-box/LRR-repeat protein 10) (JmjC domain-containing histone demethylation protein 1B) (Jumonji domain-containing EMSY-interactor methyltransferase motif protein) (Protein JEMMA) (Protein-containing CXXC domain 2) ([Histone-H3]-lysine-36 demethylase 1B) | Histone demethylase that demethylates 'Lys-4' and 'Lys-36' of histone H3, thereby playing a central role in histone code (PubMed:16362057, PubMed:17994099, PubMed:26237645). Preferentially demethylates trimethylated H3 'Lys-4' and dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys-36' (PubMed:16362057, PubMed:17994099, PubMed:26237645). Preferentially binds the transcribed region of ribosomal RNA and represses the transcription of ribosomal RNA genes which inhibits cell growth and proliferation (PubMed:16362057, PubMed:17994099). May also serve as a substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex (Probable). {ECO:0000269|PubMed:16362057, ECO:0000269|PubMed:17994099, ECO:0000269|PubMed:26237645, ECO:0000305}. |
Q92615 | LARP4B | S572 | ochoa | La-related protein 4B (La ribonucleoprotein domain family member 4B) (La ribonucleoprotein domain family member 5) (La-related protein 5) | Stimulates mRNA translation. {ECO:0000269|PubMed:20573744}. |
Q96A73 | KIAA1191 | T175 | ochoa | Putative monooxygenase p33MONOX (EC 1.-.-.-) (Brain-derived rescue factor p60MONOX) (Flavin monooxygenase motif-containing protein of 33 kDa) | Potential NADPH-dependent oxidoreductase. May be involved in the regulation of neuronal survival, differentiation and axonal outgrowth. |
Q99250 | SCN2A | S554 | ochoa | Sodium channel protein type 2 subunit alpha (HBSC II) (Sodium channel protein brain II subunit alpha) (Sodium channel protein type II subunit alpha) (Voltage-gated sodium channel subunit alpha Nav1.2) | Mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a sodium-selective channel through which Na(+) ions may pass in accordance with their electrochemical gradient (PubMed:1325650, PubMed:17021166, PubMed:28256214, PubMed:29844171). Implicated in the regulation of hippocampal replay occurring within sharp wave ripples (SPW-R) important for memory (By similarity). {ECO:0000250|UniProtKB:B1AWN6, ECO:0000269|PubMed:1325650, ECO:0000269|PubMed:17021166, ECO:0000269|PubMed:28256214, ECO:0000269|PubMed:29844171}. |
Q99666 | RGPD5 | S788 | ochoa | RANBP2-like and GRIP domain-containing protein 5/6 (Ran-binding protein 2-like 1/2) (RanBP2-like 1/2) (RanBP2L1) (RanBP2L2) (Sperm membrane protein BS-63) | None |
Q9C0H5 | ARHGAP39 | S407 | ochoa | Rho GTPase-activating protein 39 | None |
Q9H869 | YY1AP1 | S466 | 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}. |
Q9NRL3 | STRN4 | S635 | ochoa | Striatin-4 (Zinedin) | Calmodulin-binding scaffolding protein which is the center of the striatin-interacting phosphatase and kinase (STRIPAK) complexes (PubMed:18782753, PubMed:32640226). STRIPAK complexes have critical roles in protein (de)phosphorylation and are regulators of multiple signaling pathways including Hippo, MAPK, nuclear receptor and cytoskeleton remodeling (PubMed:32640226). Different types of STRIPAK complexes are involved in a variety of biological processes such as cell growth, differentiation, apoptosis, metabolism and immune regulation (Probable). Key regulator of the expanded Hippo signaling pathway by interacting and allowing the inhibition of MAP4K kinases by the STRIPAK complex (PubMed:32640226). {ECO:0000269|PubMed:18782753, ECO:0000269|PubMed:32640226, ECO:0000305|PubMed:26876214}. |
Q9NZJ5 | EIF2AK3 | S845 | ochoa | Eukaryotic translation initiation factor 2-alpha kinase 3 (EC 2.7.11.1) (PRKR-like endoplasmic reticulum kinase) (Pancreatic eIF2-alpha kinase) (HsPEK) (Protein tyrosine kinase EIF2AK3) (EC 2.7.10.2) | Metabolic-stress sensing protein kinase that phosphorylates the alpha subunit of eukaryotic translation initiation factor 2 (EIF2S1/eIF-2-alpha) in response to various stress, such as unfolded protein response (UPR) (PubMed:10026192, PubMed:10677345, PubMed:11907036, PubMed:12086964, PubMed:25925385, PubMed:31023583). Key effector of the integrated stress response (ISR) to unfolded proteins: EIF2AK3/PERK specifically recognizes and binds misfolded proteins, leading to its activation and EIF2S1/eIF-2-alpha phosphorylation (PubMed:10677345, PubMed:27917829, PubMed:31023583). EIF2S1/eIF-2-alpha phosphorylation in response to stress converts EIF2S1/eIF-2-alpha in a global protein synthesis inhibitor, leading to a global attenuation of cap-dependent translation, while concomitantly initiating the preferential translation of ISR-specific mRNAs, such as the transcriptional activators ATF4 and QRICH1, and hence allowing ATF4- and QRICH1-mediated reprogramming (PubMed:10026192, PubMed:10677345, PubMed:31023583, PubMed:33384352). The EIF2AK3/PERK-mediated unfolded protein response increases mitochondrial oxidative phosphorylation by promoting ATF4-mediated expression of COX7A2L/SCAF1, thereby increasing formation of respiratory chain supercomplexes (PubMed:31023583). In contrast to most subcellular compartments, mitochondria are protected from the EIF2AK3/PERK-mediated unfolded protein response due to EIF2AK3/PERK inhibition by ATAD3A at mitochondria-endoplasmic reticulum contact sites (PubMed:39116259). In addition to EIF2S1/eIF-2-alpha, also phosphorylates NFE2L2/NRF2 in response to stress, promoting release of NFE2L2/NRF2 from the BCR(KEAP1) complex, leading to nuclear accumulation and activation of NFE2L2/NRF2 (By similarity). Serves as a critical effector of unfolded protein response (UPR)-induced G1 growth arrest due to the loss of cyclin-D1 (CCND1) (By similarity). Involved in control of mitochondrial morphology and function (By similarity). {ECO:0000250|UniProtKB:Q9Z2B5, ECO:0000269|PubMed:10026192, ECO:0000269|PubMed:10677345, ECO:0000269|PubMed:11907036, ECO:0000269|PubMed:12086964, ECO:0000269|PubMed:25925385, ECO:0000269|PubMed:27917829, ECO:0000269|PubMed:31023583, ECO:0000269|PubMed:33384352, ECO:0000269|PubMed:39116259}. |
Q9UPU9 | SAMD4A | S420 | ochoa | Protein Smaug homolog 1 (Smaug 1) (hSmaug1) (Sterile alpha motif domain-containing protein 4A) (SAM domain-containing protein 4A) | Acts as a translational repressor of SRE-containing messengers. {ECO:0000269|PubMed:16221671}. |
Q9Y4H4 | GPSM3 | Y85 | ochoa | G-protein-signaling modulator 3 (Activator of G-protein signaling 4) (G18.1b) (Protein G18) | Interacts with subunit of G(i) alpha proteins and regulates the activation of G(i) alpha proteins. {ECO:0000269|PubMed:14656218, ECO:0000269|PubMed:15096500}. |
Q13554 | CAMK2B | Y231 | Sugiyama | Calcium/calmodulin-dependent protein kinase type II subunit beta (CaM kinase II subunit beta) (CaMK-II subunit beta) (EC 2.7.11.17) | Calcium/calmodulin-dependent protein kinase that functions autonomously after Ca(2+)/calmodulin-binding and autophosphorylation, and is involved in dendritic spine and synapse formation, neuronal plasticity and regulation of sarcoplasmic reticulum Ca(2+) transport in skeletal muscle (PubMed:16690701). In neurons, plays an essential structural role in the reorganization of the actin cytoskeleton during plasticity by binding and bundling actin filaments in a kinase-independent manner. This structural function is required for correct targeting of CaMK2A, which acts downstream of NMDAR to promote dendritic spine and synapse formation and maintain synaptic plasticity which enables long-term potentiation (LTP) and hippocampus-dependent learning. In developing hippocampal neurons, promotes arborization of the dendritic tree and in mature neurons, promotes dendritic remodeling. Also regulates the migration of developing neurons (PubMed:29100089). Participates in the modulation of skeletal muscle function in response to exercise (PubMed:16690701). In slow-twitch muscles, is involved in regulation of sarcoplasmic reticulum (SR) Ca(2+) transport and in fast-twitch muscle participates in the control of Ca(2+) release from the SR through phosphorylation of triadin, a ryanodine receptor-coupling factor, and phospholamban (PLN/PLB), an endogenous inhibitor of SERCA2A/ATP2A2. In response to interferon-gamma (IFN-gamma) stimulation, catalyzes phosphorylation of STAT1, stimulating the JAK-STAT signaling pathway (By similarity). Phosphorylates reticulophagy regulator RETREG1 at 'Ser-151' under endoplasmic reticulum stress conditions which enhances RETREG1 oligomerization and its membrane scission and reticulophagy activity (PubMed:31930741). {ECO:0000250|UniProtKB:P08413, ECO:0000269|PubMed:16690701, ECO:0000269|PubMed:29100089, ECO:0000269|PubMed:31930741}. |
Q13555 | CAMK2G | Y231 | Sugiyama | Calcium/calmodulin-dependent protein kinase type II subunit gamma (CaM kinase II subunit gamma) (CaMK-II subunit gamma) (EC 2.7.11.17) | Calcium/calmodulin-dependent protein kinase that functions autonomously after Ca(2+)/calmodulin-binding and autophosphorylation, and is involved in sarcoplasmic reticulum Ca(2+) transport in skeletal muscle and may function in dendritic spine and synapse formation and neuronal plasticity (PubMed:16690701). In slow-twitch muscles, is involved in regulation of sarcoplasmic reticulum (SR) Ca(2+) transport and in fast-twitch muscle participates in the control of Ca(2+) release from the SR through phosphorylation of the ryanodine receptor-coupling factor triadin (PubMed:16690701). In the central nervous system, it is involved in the regulation of neurite formation and arborization (PubMed:30184290). It may participate in the promotion of dendritic spine and synapse formation and maintenance of synaptic plasticity which enables long-term potentiation (LTP) and hippocampus-dependent learning. In response to interferon-gamma (IFN-gamma) stimulation, catalyzes phosphorylation of STAT1, stimulating the JAK-STAT signaling pathway (By similarity). {ECO:0000250|UniProtKB:Q923T9, ECO:0000269|PubMed:16690701, ECO:0000269|PubMed:30184290}. |
Q13557 | CAMK2D | Y231 | Sugiyama | Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17) | Calcium/calmodulin-dependent protein kinase involved in the regulation of Ca(2+) homeostatis and excitation-contraction coupling (ECC) in heart by targeting ion channels, transporters and accessory proteins involved in Ca(2+) influx into the myocyte, Ca(2+) release from the sarcoplasmic reticulum (SR), SR Ca(2+) uptake and Na(+) and K(+) channel transport. Targets also transcription factors and signaling molecules to regulate heart function. In its activated form, is involved in the pathogenesis of dilated cardiomyopathy and heart failure. Contributes to cardiac decompensation and heart failure by regulating SR Ca(2+) release via direct phosphorylation of RYR2 Ca(2+) channel on 'Ser-2808'. In the nucleus, phosphorylates the MEF2 repressor HDAC4, promoting its nuclear export and binding to 14-3-3 protein, and expression of MEF2 and genes involved in the hypertrophic program (PubMed:17179159). Is essential for left ventricular remodeling responses to myocardial infarction. In pathological myocardial remodeling acts downstream of the beta adrenergic receptor signaling cascade to regulate key proteins involved in ECC. Regulates Ca(2+) influx to myocytes by binding and phosphorylating the L-type Ca(2+) channel subunit beta-2 CACNB2. In addition to Ca(2+) channels, can target and regulate the cardiac sarcolemmal Na(+) channel Nav1.5/SCN5A and the K+ channel Kv4.3/KCND3, which contribute to arrhythmogenesis in heart failure. Phosphorylates phospholamban (PLN/PLB), an endogenous inhibitor of SERCA2A/ATP2A2, contributing to the enhancement of SR Ca(2+) uptake that may be important in frequency-dependent acceleration of relaxation (FDAR) and maintenance of contractile function during acidosis (PubMed:16690701). May participate in the modulation of skeletal muscle function in response to exercise, by regulating SR Ca(2+) transport through phosphorylation of PLN/PLB and triadin, a ryanodine receptor-coupling factor. In response to interferon-gamma (IFN-gamma) stimulation, catalyzes phosphorylation of STAT1, stimulating the JAK-STAT signaling pathway (By similarity). {ECO:0000250|UniProtKB:Q6PHZ2, ECO:0000269|PubMed:16690701, ECO:0000269|PubMed:17179159}. |
Q9UQM7 | CAMK2A | Y230 | Sugiyama | Calcium/calmodulin-dependent protein kinase type II subunit alpha (CaM kinase II subunit alpha) (CaMK-II subunit alpha) (EC 2.7.11.17) | Calcium/calmodulin-dependent protein kinase that functions autonomously after Ca(2+)/calmodulin-binding and autophosphorylation, and is involved in various processes, such as synaptic plasticity, neurotransmitter release and long-term potentiation (PubMed:14722083). Member of the NMDAR signaling complex in excitatory synapses, it regulates NMDAR-dependent potentiation of the AMPAR and therefore excitatory synaptic transmission (By similarity). Regulates dendritic spine development (PubMed:28130356). Also regulates the migration of developing neurons (PubMed:29100089). Phosphorylates the transcription factor FOXO3 to activate its transcriptional activity (PubMed:23805378). Phosphorylates the transcription factor ETS1 in response to calcium signaling, thereby decreasing ETS1 affinity for DNA (By similarity). In response to interferon-gamma (IFN-gamma) stimulation, catalyzes phosphorylation of STAT1, stimulating the JAK-STAT signaling pathway (PubMed:11972023). In response to interferon-beta (IFN-beta) stimulation, stimulates the JAK-STAT signaling pathway (PubMed:35568036). Acts as a negative regulator of 2-arachidonoylglycerol (2-AG)-mediated synaptic signaling via modulation of DAGLA activity (By similarity). {ECO:0000250|UniProtKB:P11275, ECO:0000250|UniProtKB:P11798, ECO:0000269|PubMed:11972023, ECO:0000269|PubMed:23805378, ECO:0000269|PubMed:28130356, ECO:0000269|PubMed:29100089}. |
Q9UBS0 | RPS6KB2 | S403 | Sugiyama | Ribosomal protein S6 kinase beta-2 (S6K-beta-2) (S6K2) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 2) (P70S6K2) (p70-S6K 2) (S6 kinase-related kinase) (SRK) (Serine/threonine-protein kinase 14B) (p70 ribosomal S6 kinase beta) (S6K-beta) (p70 S6 kinase beta) (p70 S6K-beta) (p70 S6KB) (p70-beta) | Phosphorylates specifically ribosomal protein S6 (PubMed:29750193). Seems to act downstream of mTOR signaling in response to growth factors and nutrients to promote cell proliferation, cell growth and cell cycle progression in an alternative pathway regulated by MEAK7 (PubMed:29750193). {ECO:0000269|PubMed:29750193}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-5576892 | Phase 0 - rapid depolarisation | 8.833019e-10 | 9.054 |
R-HSA-111932 | CaMK IV-mediated phosphorylation of CREB | 7.368820e-08 | 7.133 |
R-HSA-438066 | Unblocking of NMDA receptors, glutamate binding and activation | 1.330763e-06 | 5.876 |
R-HSA-442982 | Ras activation upon Ca2+ influx through NMDA receptor | 1.330763e-06 | 5.876 |
R-HSA-9617324 | Negative regulation of NMDA receptor-mediated neuronal transmission | 1.330763e-06 | 5.876 |
R-HSA-9620244 | Long-term potentiation | 2.292902e-06 | 5.640 |
R-HSA-442742 | CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 5.646574e-06 | 5.248 |
R-HSA-399719 | Trafficking of AMPA receptors | 4.593951e-06 | 5.338 |
R-HSA-399721 | Glutamate binding, activation of AMPA receptors and synaptic plasticity | 5.646574e-06 | 5.248 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 5.646574e-06 | 5.248 |
R-HSA-5576891 | Cardiac conduction | 4.507812e-06 | 5.346 |
R-HSA-111933 | Calmodulin induced events | 8.273614e-06 | 5.082 |
R-HSA-111997 | CaM pathway | 8.273614e-06 | 5.082 |
R-HSA-5673000 | RAF activation | 6.867670e-06 | 5.163 |
R-HSA-111996 | Ca-dependent events | 1.490112e-05 | 4.827 |
R-HSA-9656223 | Signaling by RAF1 mutants | 1.377365e-05 | 4.861 |
R-HSA-9609736 | Assembly and cell surface presentation of NMDA receptors | 1.377365e-05 | 4.861 |
R-HSA-1489509 | DAG and IP3 signaling | 1.869238e-05 | 4.728 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 2.010066e-05 | 4.697 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 2.010066e-05 | 4.697 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 2.010066e-05 | 4.697 |
R-HSA-6802949 | Signaling by RAS mutants | 2.010066e-05 | 4.697 |
R-HSA-3371571 | HSF1-dependent transactivation | 2.834097e-05 | 4.548 |
R-HSA-5578775 | Ion homeostasis | 3.882388e-05 | 4.411 |
R-HSA-112043 | PLC beta mediated events | 5.189777e-05 | 4.285 |
R-HSA-3371556 | Cellular response to heat stress | 4.738079e-05 | 4.324 |
R-HSA-397014 | Muscle contraction | 5.785370e-05 | 4.238 |
R-HSA-936837 | Ion transport by P-type ATPases | 6.113737e-05 | 4.214 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 6.446783e-05 | 4.191 |
R-HSA-112040 | G-protein mediated events | 7.152314e-05 | 4.146 |
R-HSA-6802957 | Oncogenic MAPK signaling | 1.627382e-04 | 3.789 |
R-HSA-438064 | Post NMDA receptor activation events | 1.835988e-04 | 3.736 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 2.143327e-04 | 3.669 |
R-HSA-2559585 | Oncogene Induced Senescence | 2.640180e-04 | 3.578 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 3.399330e-04 | 3.469 |
R-HSA-111885 | Opioid Signalling | 3.630981e-04 | 3.440 |
R-HSA-442729 | CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | 4.942044e-04 | 3.306 |
R-HSA-2262752 | Cellular responses to stress | 7.084531e-04 | 3.150 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 8.832787e-04 | 3.054 |
R-HSA-913531 | Interferon Signaling | 1.107760e-03 | 2.956 |
R-HSA-418594 | G alpha (i) signalling events | 1.486090e-03 | 2.828 |
R-HSA-8953897 | Cellular responses to stimuli | 1.703573e-03 | 2.769 |
R-HSA-877300 | Interferon gamma signaling | 1.786304e-03 | 2.748 |
R-HSA-112316 | Neuronal System | 2.893076e-03 | 2.539 |
R-HSA-983712 | Ion channel transport | 3.190024e-03 | 2.496 |
R-HSA-445095 | Interaction between L1 and Ankyrins | 4.269948e-03 | 2.370 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 4.692907e-03 | 2.329 |
R-HSA-210745 | Regulation of gene expression in beta cells | 4.785453e-03 | 2.320 |
R-HSA-9006925 | Intracellular signaling by second messengers | 4.017584e-03 | 2.396 |
R-HSA-165159 | MTOR signalling | 9.499224e-03 | 2.022 |
R-HSA-380108 | Chemokine receptors bind chemokines | 1.218686e-02 | 1.914 |
R-HSA-5673001 | RAF/MAP kinase cascade | 1.255365e-02 | 1.901 |
R-HSA-372790 | Signaling by GPCR | 1.319977e-02 | 1.879 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 1.352962e-02 | 1.869 |
R-HSA-186712 | Regulation of beta-cell development | 1.653089e-02 | 1.782 |
R-HSA-112315 | Transmission across Chemical Synapses | 1.774422e-02 | 1.751 |
R-HSA-2559583 | Cellular Senescence | 2.043081e-02 | 1.690 |
R-HSA-5683057 | MAPK family signaling cascades | 2.211371e-02 | 1.655 |
R-HSA-9700645 | ALK mutants bind TKIs | 3.443088e-02 | 1.463 |
R-HSA-428543 | Inactivation of CDC42 and RAC1 | 3.443088e-02 | 1.463 |
R-HSA-198693 | AKT phosphorylates targets in the nucleus | 3.443088e-02 | 1.463 |
R-HSA-264870 | Caspase-mediated cleavage of cytoskeletal proteins | 3.443088e-02 | 1.463 |
R-HSA-6794362 | Protein-protein interactions at synapses | 3.036677e-02 | 1.518 |
R-HSA-388396 | GPCR downstream signalling | 2.740798e-02 | 1.562 |
R-HSA-9700206 | Signaling by ALK in cancer | 4.741562e-02 | 1.324 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 4.741562e-02 | 1.324 |
R-HSA-9796292 | Formation of axial mesoderm | 4.843216e-02 | 1.315 |
R-HSA-373760 | L1CAM interactions | 5.546638e-02 | 1.256 |
R-HSA-388844 | Receptor-type tyrosine-protein phosphatases | 5.673734e-02 | 1.246 |
R-HSA-9909505 | Modulation of host responses by IFN-stimulated genes | 6.223467e-02 | 1.206 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 9.984762e-02 | 1.001 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 1.024770e-01 | 0.989 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 1.024770e-01 | 0.989 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 1.077133e-01 | 0.968 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 1.077133e-01 | 0.968 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 1.103202e-01 | 0.957 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 1.155117e-01 | 0.937 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 1.258059e-01 | 0.900 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 1.283611e-01 | 0.892 |
R-HSA-68962 | Activation of the pre-replicative complex | 9.984762e-02 | 1.001 |
R-HSA-9927418 | Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 1.359828e-01 | 0.867 |
R-HSA-166208 | mTORC1-mediated signalling | 7.853919e-02 | 1.105 |
R-HSA-9927426 | Developmental Lineage of Mammary Gland Alveolar Cells | 1.129197e-01 | 0.947 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 1.206735e-01 | 0.918 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 1.435393e-01 | 0.843 |
R-HSA-9937080 | Developmental Lineage of Multipotent Pancreatic Progenitor Cells | 1.050989e-01 | 0.978 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 1.103202e-01 | 0.957 |
R-HSA-191859 | snRNP Assembly | 1.779562e-01 | 0.750 |
R-HSA-194441 | Metabolism of non-coding RNA | 1.779562e-01 | 0.750 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 1.827610e-01 | 0.738 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 9.984762e-02 | 1.001 |
R-HSA-180746 | Nuclear import of Rev protein | 1.129197e-01 | 0.947 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 9.088234e-02 | 1.042 |
R-HSA-381042 | PERK regulates gene expression | 1.155117e-01 | 0.937 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 1.283611e-01 | 0.892 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 1.283611e-01 | 0.892 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 1.309089e-01 | 0.883 |
R-HSA-176187 | Activation of ATR in response to replication stress | 1.077133e-01 | 0.968 |
R-HSA-9930044 | Nuclear RNA decay | 1.077133e-01 | 0.968 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 1.232434e-01 | 0.909 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 1.460437e-01 | 0.836 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 1.258059e-01 | 0.900 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 1.731237e-01 | 0.762 |
R-HSA-6784531 | tRNA processing in the nucleus | 1.851532e-01 | 0.732 |
R-HSA-168255 | Influenza Infection | 1.138244e-01 | 0.944 |
R-HSA-3214842 | HDMs demethylate histones | 8.658708e-02 | 1.063 |
R-HSA-69620 | Cell Cycle Checkpoints | 1.947062e-01 | 0.711 |
R-HSA-376176 | Signaling by ROBO receptors | 1.370910e-01 | 0.863 |
R-HSA-5674400 | Constitutive Signaling by AKT1 E17K in Cancer | 8.122951e-02 | 1.090 |
R-HSA-6794361 | Neurexins and neuroligins | 1.609204e-01 | 0.793 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 1.050989e-01 | 0.978 |
R-HSA-375276 | Peptide ligand-binding receptors | 1.204972e-01 | 0.919 |
R-HSA-162582 | Signal Transduction | 9.386341e-02 | 1.028 |
R-HSA-75153 | Apoptotic execution phase | 1.460437e-01 | 0.836 |
R-HSA-422475 | Axon guidance | 8.263478e-02 | 1.083 |
R-HSA-9675108 | Nervous system development | 9.862155e-02 | 1.006 |
R-HSA-1266738 | Developmental Biology | 1.133779e-01 | 0.945 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 9.763638e-02 | 1.010 |
R-HSA-9734767 | Developmental Cell Lineages | 2.000091e-01 | 0.699 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 2.087005e-01 | 0.680 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 2.087005e-01 | 0.680 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 2.110183e-01 | 0.676 |
R-HSA-4086398 | Ca2+ pathway | 2.110183e-01 | 0.676 |
R-HSA-1169408 | ISG15 antiviral mechanism | 2.156340e-01 | 0.666 |
R-HSA-5689603 | UCH proteinases | 2.179319e-01 | 0.662 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 2.315815e-01 | 0.635 |
R-HSA-141424 | Amplification of signal from the kinetochores | 2.405515e-01 | 0.619 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 2.405515e-01 | 0.619 |
R-HSA-156902 | Peptide chain elongation | 2.472116e-01 | 0.607 |
R-HSA-9954714 | PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | 2.538145e-01 | 0.595 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 2.560029e-01 | 0.592 |
R-HSA-156842 | Eukaryotic Translation Elongation | 2.581850e-01 | 0.588 |
R-HSA-9954716 | ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ri... | 2.646937e-01 | 0.577 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 2.668508e-01 | 0.574 |
R-HSA-72764 | Eukaryotic Translation Termination | 2.668508e-01 | 0.574 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 2.668508e-01 | 0.574 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 2.775439e-01 | 0.557 |
R-HSA-70171 | Glycolysis | 2.775439e-01 | 0.557 |
R-HSA-2408557 | Selenocysteine synthesis | 2.796642e-01 | 0.553 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 2.817783e-01 | 0.550 |
R-HSA-192823 | Viral mRNA Translation | 2.838864e-01 | 0.547 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 2.859884e-01 | 0.544 |
R-HSA-1799339 | SRP-dependent cotranslational protein targeting to membrane | 2.943362e-01 | 0.531 |
R-HSA-211000 | Gene Silencing by RNA | 2.943362e-01 | 0.531 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 2.964081e-01 | 0.528 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 2.964081e-01 | 0.528 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 2.964081e-01 | 0.528 |
R-HSA-69002 | DNA Replication Pre-Initiation | 2.984742e-01 | 0.525 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 2.984742e-01 | 0.525 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 3.046367e-01 | 0.516 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 3.046367e-01 | 0.516 |
R-HSA-1483249 | Inositol phosphate metabolism | 3.046367e-01 | 0.516 |
R-HSA-72613 | Eukaryotic Translation Initiation | 3.168032e-01 | 0.499 |
R-HSA-72737 | Cap-dependent Translation Initiation | 3.168032e-01 | 0.499 |
R-HSA-70326 | Glucose metabolism | 3.188106e-01 | 0.496 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 3.208122e-01 | 0.494 |
R-HSA-68875 | Mitotic Prophase | 3.247982e-01 | 0.488 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 3.267826e-01 | 0.486 |
R-HSA-9717207 | Sensory perception of sweet, bitter, and umami (glutamate) taste | 3.307342e-01 | 0.481 |
R-HSA-162909 | Host Interactions of HIV factors | 3.327016e-01 | 0.478 |
R-HSA-382551 | Transport of small molecules | 3.352388e-01 | 0.475 |
R-HSA-69206 | G1/S Transition | 3.366192e-01 | 0.473 |
R-HSA-69481 | G2/M Checkpoints | 3.405144e-01 | 0.468 |
R-HSA-373076 | Class A/1 (Rhodopsin-like receptors) | 3.424243e-01 | 0.465 |
R-HSA-9717189 | Sensory perception of taste | 3.501546e-01 | 0.456 |
R-HSA-9018519 | Estrogen-dependent gene expression | 3.615410e-01 | 0.442 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 3.615410e-01 | 0.442 |
R-HSA-9948299 | Ribosome-associated quality control | 3.652928e-01 | 0.437 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 3.671607e-01 | 0.435 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 3.745784e-01 | 0.426 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 3.745784e-01 | 0.426 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 3.819109e-01 | 0.418 |
R-HSA-9758941 | Gastrulation | 3.873551e-01 | 0.412 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 3.909584e-01 | 0.408 |
R-HSA-9820448 | Developmental Cell Lineages of the Exocrine Pancreas | 3.927523e-01 | 0.406 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 3.927523e-01 | 0.406 |
R-HSA-69306 | DNA Replication | 3.945410e-01 | 0.404 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 3.963246e-01 | 0.402 |
R-HSA-9610379 | HCMV Late Events | 4.016444e-01 | 0.396 |
R-HSA-162587 | HIV Life Cycle | 4.016444e-01 | 0.396 |
R-HSA-9711097 | Cellular response to starvation | 4.034075e-01 | 0.394 |
R-HSA-109581 | Apoptosis | 4.104091e-01 | 0.387 |
R-HSA-2467813 | Separation of Sister Chromatids | 4.138796e-01 | 0.383 |
R-HSA-2408522 | Selenoamino acid metabolism | 4.138796e-01 | 0.383 |
R-HSA-5619102 | SLC transporter disorders | 4.190480e-01 | 0.378 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 4.258698e-01 | 0.371 |
R-HSA-72306 | tRNA processing | 4.258698e-01 | 0.371 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 4.556103e-01 | 0.341 |
R-HSA-8953854 | Metabolism of RNA | 4.592628e-01 | 0.338 |
R-HSA-68877 | Mitotic Prometaphase | 4.636004e-01 | 0.334 |
R-HSA-9609690 | HCMV Early Events | 4.683393e-01 | 0.329 |
R-HSA-5357801 | Programmed Cell Death | 4.838413e-01 | 0.315 |
R-HSA-68882 | Mitotic Anaphase | 5.003828e-01 | 0.301 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 5.018606e-01 | 0.299 |
R-HSA-69278 | Cell Cycle, Mitotic | 5.149597e-01 | 0.288 |
R-HSA-162906 | HIV Infection | 5.164051e-01 | 0.287 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 5.178365e-01 | 0.286 |
R-HSA-72312 | rRNA processing | 5.235207e-01 | 0.281 |
R-HSA-3247509 | Chromatin modifying enzymes | 5.263382e-01 | 0.279 |
R-HSA-8939211 | ESR-mediated signaling | 5.305338e-01 | 0.275 |
R-HSA-500792 | GPCR ligand binding | 5.358341e-01 | 0.271 |
R-HSA-5619115 | Disorders of transmembrane transporters | 5.442582e-01 | 0.264 |
R-HSA-4839726 | Chromatin organization | 5.469555e-01 | 0.262 |
R-HSA-9609646 | HCMV Infection | 5.482983e-01 | 0.261 |
R-HSA-5688426 | Deubiquitination | 5.549542e-01 | 0.256 |
R-HSA-9711123 | Cellular response to chemical stress | 5.718135e-01 | 0.243 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 5.855895e-01 | 0.232 |
R-HSA-1257604 | PIP3 activates AKT signaling | 6.048561e-01 | 0.218 |
R-HSA-195721 | Signaling by WNT | 6.083697e-01 | 0.216 |
R-HSA-1643685 | Disease | 6.096306e-01 | 0.215 |
R-HSA-1640170 | Cell Cycle | 6.340830e-01 | 0.198 |
R-HSA-9694516 | SARS-CoV-2 Infection | 6.636274e-01 | 0.178 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 6.774105e-01 | 0.169 |
R-HSA-212436 | Generic Transcription Pathway | 6.862397e-01 | 0.164 |
R-HSA-68886 | M Phase | 6.961464e-01 | 0.157 |
R-HSA-74160 | Gene expression (Transcription) | 7.054759e-01 | 0.152 |
R-HSA-168256 | Immune System | 7.290173e-01 | 0.137 |
R-HSA-72766 | Translation | 7.360831e-01 | 0.133 |
R-HSA-73857 | RNA Polymerase II Transcription | 7.515062e-01 | 0.124 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 7.559187e-01 | 0.122 |
R-HSA-6798695 | Neutrophil degranulation | 7.573826e-01 | 0.121 |
R-HSA-9679506 | SARS-CoV Infections | 8.194923e-01 | 0.086 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 8.508898e-01 | 0.070 |
R-HSA-9824446 | Viral Infection Pathways | 8.574903e-01 | 0.067 |
R-HSA-597592 | Post-translational protein modification | 9.635073e-01 | 0.016 |
R-HSA-5663205 | Infectious disease | 9.665323e-01 | 0.015 |
R-HSA-9709957 | Sensory Perception | 9.781400e-01 | 0.010 |
R-HSA-392499 | Metabolism of proteins | 9.800733e-01 | 0.009 |
R-HSA-168249 | Innate Immune System | 9.836786e-01 | 0.007 |
R-HSA-1430728 | Metabolism | 9.999436e-01 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
CLK1 |
0.668 | 0.325 | -3 | 0.615 |
CDK18 |
0.667 | 0.412 | 1 | 0.847 |
CDK14 |
0.666 | 0.430 | 1 | 0.839 |
CDK10 |
0.666 | 0.415 | 1 | 0.845 |
DYRK4 |
0.665 | 0.428 | 1 | 0.839 |
DYRK2 |
0.664 | 0.400 | 1 | 0.798 |
CDK3 |
0.664 | 0.415 | 1 | 0.849 |
CLK3 |
0.663 | 0.303 | 1 | 0.722 |
CDK7 |
0.662 | 0.385 | 1 | 0.853 |
SRPK1 |
0.662 | 0.252 | -3 | 0.634 |
CDK1 |
0.662 | 0.410 | 1 | 0.843 |
CDK13 |
0.661 | 0.391 | 1 | 0.853 |
CLK4 |
0.661 | 0.296 | -3 | 0.619 |
HIPK2 |
0.661 | 0.397 | 1 | 0.816 |
CDK17 |
0.661 | 0.410 | 1 | 0.841 |
CDK16 |
0.660 | 0.418 | 1 | 0.838 |
CDK9 |
0.659 | 0.393 | 1 | 0.856 |
KIS |
0.658 | 0.368 | 1 | 0.841 |
CLK2 |
0.658 | 0.315 | -3 | 0.594 |
CDK2 |
0.658 | 0.370 | 1 | 0.802 |
HIPK1 |
0.658 | 0.381 | 1 | 0.799 |
JNK2 |
0.657 | 0.421 | 1 | 0.856 |
CDK19 |
0.657 | 0.372 | 1 | 0.834 |
NLK |
0.657 | 0.362 | 1 | 0.750 |
CDK12 |
0.657 | 0.386 | 1 | 0.852 |
DYRK1A |
0.657 | 0.354 | 1 | 0.817 |
HIPK4 |
0.656 | 0.260 | 1 | 0.689 |
CDK8 |
0.655 | 0.368 | 1 | 0.830 |
CDKL5 |
0.655 | 0.166 | -3 | 0.656 |
HIPK3 |
0.654 | 0.371 | 1 | 0.789 |
DYRK1B |
0.653 | 0.390 | 1 | 0.824 |
PRKD2 |
0.653 | 0.142 | -3 | 0.602 |
P38B |
0.653 | 0.389 | 1 | 0.844 |
CDKL1 |
0.652 | 0.164 | -3 | 0.655 |
P38A |
0.652 | 0.381 | 1 | 0.832 |
MAPKAPK3 |
0.652 | 0.146 | -3 | 0.609 |
ICK |
0.652 | 0.234 | -3 | 0.654 |
SRPK2 |
0.651 | 0.208 | -3 | 0.598 |
ERK1 |
0.651 | 0.375 | 1 | 0.852 |
PRKD3 |
0.650 | 0.152 | -3 | 0.636 |
P38G |
0.649 | 0.403 | 1 | 0.844 |
PRKD1 |
0.649 | 0.100 | -3 | 0.650 |
DYRK3 |
0.649 | 0.319 | 1 | 0.770 |
JNK3 |
0.648 | 0.395 | 1 | 0.860 |
GSK3B |
0.647 | 0.238 | 4 | 0.680 |
CAMK1B |
0.647 | 0.134 | -3 | 0.650 |
SBK |
0.647 | 0.214 | -3 | 0.536 |
MTOR |
0.647 | 0.089 | 1 | 0.609 |
P90RSK |
0.646 | 0.119 | -3 | 0.633 |
MAPKAPK2 |
0.646 | 0.128 | -3 | 0.586 |
SRPK3 |
0.646 | 0.175 | -3 | 0.621 |
PKN3 |
0.646 | 0.108 | -3 | 0.616 |
CDK5 |
0.646 | 0.358 | 1 | 0.837 |
RSK2 |
0.646 | 0.114 | -3 | 0.640 |
ERK2 |
0.645 | 0.377 | 1 | 0.829 |
ERK5 |
0.645 | 0.168 | 1 | 0.691 |
PIM1 |
0.644 | 0.129 | -3 | 0.606 |
NUAK2 |
0.644 | 0.118 | -3 | 0.622 |
CDK6 |
0.643 | 0.376 | 1 | 0.848 |
P38D |
0.643 | 0.391 | 1 | 0.846 |
GSK3A |
0.642 | 0.263 | 4 | 0.679 |
CAMK2D |
0.642 | 0.068 | -3 | 0.623 |
CDK4 |
0.642 | 0.385 | 1 | 0.845 |
CDC7 |
0.640 | -0.048 | 1 | 0.533 |
PKN2 |
0.639 | 0.082 | -3 | 0.620 |
CAMK2A |
0.639 | 0.109 | 2 | 0.562 |
PRPK |
0.639 | -0.027 | -1 | 0.583 |
MOS |
0.638 | 0.020 | 1 | 0.580 |
PIM3 |
0.637 | 0.034 | -3 | 0.616 |
RSK3 |
0.636 | 0.069 | -3 | 0.647 |
CAMK4 |
0.636 | 0.064 | -3 | 0.603 |
PDHK4 |
0.636 | -0.087 | 1 | 0.543 |
MOK |
0.636 | 0.277 | 1 | 0.726 |
CAMK2B |
0.635 | 0.086 | 2 | 0.550 |
CHK1 |
0.635 | 0.101 | -3 | 0.608 |
CAMLCK |
0.634 | 0.068 | -2 | 0.650 |
TSSK2 |
0.634 | 0.092 | -5 | 0.700 |
NIK |
0.634 | 0.056 | -3 | 0.620 |
P70S6KB |
0.633 | 0.077 | -3 | 0.626 |
CAMK1G |
0.633 | 0.126 | -3 | 0.606 |
CAMK2G |
0.632 | -0.015 | 2 | 0.562 |
AKT2 |
0.632 | 0.112 | -3 | 0.595 |
WNK1 |
0.632 | 0.043 | -2 | 0.733 |
DAPK2 |
0.632 | 0.038 | -3 | 0.649 |
ATR |
0.632 | -0.048 | 1 | 0.481 |
COT |
0.632 | -0.084 | 2 | 0.650 |
MSK1 |
0.632 | 0.082 | -3 | 0.631 |
MSK2 |
0.631 | 0.063 | -3 | 0.637 |
MAK |
0.631 | 0.264 | -2 | 0.534 |
AMPKA2 |
0.631 | 0.078 | -3 | 0.609 |
MAPKAPK5 |
0.631 | 0.078 | -3 | 0.623 |
PHKG1 |
0.631 | 0.051 | -3 | 0.603 |
NDR1 |
0.630 | 0.038 | -3 | 0.618 |
JNK1 |
0.630 | 0.352 | 1 | 0.859 |
PKN1 |
0.630 | 0.113 | -3 | 0.619 |
NDR2 |
0.630 | 0.008 | -3 | 0.603 |
MELK |
0.630 | 0.074 | -3 | 0.610 |
AMPKA1 |
0.629 | 0.052 | -3 | 0.618 |
PDHK1 |
0.629 | -0.130 | 1 | 0.513 |
MASTL |
0.628 | -0.055 | -2 | 0.683 |
TSSK1 |
0.628 | 0.068 | -3 | 0.626 |
BMPR2 |
0.628 | -0.149 | -2 | 0.683 |
CHK2 |
0.627 | 0.128 | -3 | 0.571 |
PIM2 |
0.627 | 0.088 | -3 | 0.617 |
CAMK1D |
0.627 | 0.134 | -3 | 0.563 |
RSK4 |
0.627 | 0.082 | -3 | 0.595 |
MST4 |
0.626 | -0.005 | 2 | 0.619 |
PKACG |
0.626 | 0.033 | -2 | 0.577 |
MYLK4 |
0.626 | 0.069 | -2 | 0.568 |
NUAK1 |
0.625 | 0.041 | -3 | 0.604 |
PKCD |
0.625 | 0.014 | 2 | 0.581 |
TBK1 |
0.625 | -0.116 | 1 | 0.436 |
P70S6K |
0.625 | 0.083 | -3 | 0.620 |
IKKB |
0.624 | -0.131 | -2 | 0.588 |
CAMK1A |
0.624 | 0.141 | -3 | 0.569 |
RAF1 |
0.623 | -0.154 | 1 | 0.490 |
SMG1 |
0.623 | -0.007 | 1 | 0.434 |
PHKG2 |
0.623 | 0.050 | -3 | 0.608 |
PRP4 |
0.623 | 0.168 | -3 | 0.465 |
SGK3 |
0.622 | 0.060 | -3 | 0.625 |
AURC |
0.622 | 0.022 | -2 | 0.491 |
LATS2 |
0.622 | -0.017 | -5 | 0.459 |
LATS1 |
0.622 | 0.032 | -3 | 0.620 |
IKKE |
0.621 | -0.129 | 1 | 0.427 |
GCN2 |
0.621 | -0.143 | 2 | 0.582 |
DRAK1 |
0.621 | 0.017 | 1 | 0.495 |
DNAPK |
0.621 | -0.007 | 1 | 0.415 |
MLK1 |
0.621 | -0.105 | 2 | 0.617 |
PRKX |
0.621 | 0.090 | -3 | 0.544 |
DCAMKL1 |
0.621 | 0.087 | -3 | 0.598 |
DCAMKL2 |
0.620 | 0.073 | -3 | 0.610 |
BRSK2 |
0.620 | 0.021 | -3 | 0.607 |
RIPK3 |
0.620 | -0.063 | 3 | 0.578 |
BRSK1 |
0.620 | 0.033 | -3 | 0.614 |
GRK6 |
0.620 | -0.046 | 1 | 0.487 |
PAK6 |
0.620 | 0.010 | -2 | 0.542 |
GRK5 |
0.619 | -0.127 | -3 | 0.561 |
SMMLCK |
0.619 | 0.066 | -3 | 0.646 |
MNK1 |
0.619 | 0.028 | -2 | 0.633 |
QIK |
0.619 | -0.025 | -3 | 0.616 |
PKACA |
0.618 | 0.065 | -2 | 0.467 |
PKCH |
0.618 | 0.009 | 2 | 0.545 |
ERK7 |
0.618 | 0.106 | 2 | 0.395 |
MNK2 |
0.618 | -0.001 | -2 | 0.629 |
AURB |
0.618 | 0.014 | -2 | 0.488 |
SKMLCK |
0.617 | -0.039 | -2 | 0.659 |
WNK3 |
0.617 | -0.118 | 1 | 0.467 |
MEK1 |
0.617 | -0.066 | 2 | 0.644 |
BUB1 |
0.617 | 0.107 | -5 | 0.645 |
PKG2 |
0.617 | 0.026 | -2 | 0.513 |
DSTYK |
0.616 | -0.168 | 2 | 0.670 |
SGK1 |
0.616 | 0.110 | -3 | 0.565 |
PASK |
0.616 | 0.073 | -3 | 0.631 |
NIM1 |
0.616 | -0.039 | 3 | 0.574 |
AKT1 |
0.616 | 0.070 | -3 | 0.590 |
PKACB |
0.616 | 0.048 | -2 | 0.499 |
ATM |
0.616 | -0.061 | 1 | 0.422 |
DLK |
0.615 | -0.127 | 1 | 0.484 |
PKCE |
0.615 | 0.068 | 2 | 0.531 |
PKCB |
0.615 | -0.002 | 2 | 0.557 |
CHAK2 |
0.615 | -0.093 | -1 | 0.502 |
GRK1 |
0.615 | -0.036 | -2 | 0.628 |
IRE1 |
0.614 | -0.074 | 1 | 0.433 |
MARK4 |
0.614 | -0.072 | 4 | 0.547 |
MLK2 |
0.614 | -0.124 | 2 | 0.642 |
SNRK |
0.614 | -0.021 | 2 | 0.576 |
RIPK1 |
0.614 | -0.105 | 1 | 0.466 |
PKCA |
0.614 | -0.025 | 2 | 0.549 |
TGFBR2 |
0.614 | -0.114 | -2 | 0.533 |
SIK |
0.613 | 0.002 | -3 | 0.594 |
BCKDK |
0.613 | -0.148 | -1 | 0.495 |
ULK2 |
0.613 | -0.205 | 2 | 0.597 |
PKCI |
0.613 | 0.020 | 2 | 0.553 |
PKCZ |
0.612 | -0.041 | 2 | 0.596 |
PKCG |
0.611 | -0.033 | 2 | 0.547 |
NEK7 |
0.611 | -0.185 | -3 | 0.560 |
PAK3 |
0.611 | -0.055 | -2 | 0.601 |
VRK2 |
0.611 | -0.052 | 1 | 0.556 |
ANKRD3 |
0.611 | -0.143 | 1 | 0.512 |
AKT3 |
0.611 | 0.089 | -3 | 0.570 |
AURA |
0.611 | -0.003 | -2 | 0.459 |
YSK4 |
0.611 | -0.109 | 1 | 0.446 |
PAK1 |
0.610 | -0.027 | -2 | 0.594 |
PKCT |
0.610 | 0.000 | 2 | 0.555 |
PAK2 |
0.610 | -0.035 | -2 | 0.586 |
CHAK1 |
0.609 | -0.088 | 2 | 0.647 |
NEK9 |
0.609 | -0.165 | 2 | 0.626 |
NEK6 |
0.608 | -0.150 | -2 | 0.644 |
PKR |
0.608 | -0.083 | 1 | 0.483 |
HUNK |
0.608 | -0.153 | 2 | 0.597 |
WNK4 |
0.608 | -0.014 | -2 | 0.739 |
PINK1 |
0.608 | -0.023 | 1 | 0.607 |
CRIK |
0.607 | 0.127 | -3 | 0.596 |
ALK4 |
0.607 | -0.085 | -2 | 0.578 |
QSK |
0.607 | -0.042 | 4 | 0.530 |
GRK7 |
0.607 | -0.034 | 1 | 0.482 |
MEK5 |
0.607 | -0.098 | 2 | 0.646 |
MST3 |
0.607 | -0.013 | 2 | 0.629 |
ULK1 |
0.607 | -0.179 | -3 | 0.514 |
MRCKA |
0.607 | 0.080 | -3 | 0.594 |
SSTK |
0.606 | 0.037 | 4 | 0.519 |
MLK3 |
0.606 | -0.101 | 2 | 0.556 |
IRE2 |
0.606 | -0.088 | 2 | 0.532 |
ACVR2A |
0.606 | -0.090 | -2 | 0.538 |
PLK3 |
0.606 | -0.054 | 2 | 0.565 |
NEK2 |
0.605 | -0.125 | 2 | 0.623 |
TGFBR1 |
0.604 | -0.078 | -2 | 0.547 |
BMPR1B |
0.604 | -0.071 | 1 | 0.474 |
GAK |
0.604 | 0.030 | 1 | 0.546 |
HRI |
0.604 | -0.104 | -2 | 0.624 |
DAPK1 |
0.604 | 0.053 | -3 | 0.615 |
PDK1 |
0.604 | 0.018 | 1 | 0.557 |
NEK11 |
0.603 | -0.061 | 1 | 0.495 |
PLK1 |
0.603 | -0.101 | -2 | 0.567 |
FAM20C |
0.602 | -0.034 | 2 | 0.440 |
GRK2 |
0.602 | -0.068 | -2 | 0.506 |
GRK4 |
0.602 | -0.159 | -2 | 0.617 |
MARK3 |
0.602 | -0.037 | 4 | 0.496 |
CK2A1 |
0.601 | 0.022 | 1 | 0.488 |
MARK1 |
0.601 | -0.060 | 4 | 0.512 |
IKKA |
0.600 | -0.167 | -2 | 0.573 |
MPSK1 |
0.600 | -0.042 | 1 | 0.500 |
CK2A2 |
0.600 | -0.005 | 1 | 0.500 |
MRCKB |
0.600 | 0.068 | -3 | 0.596 |
ALK2 |
0.600 | -0.090 | -2 | 0.551 |
ACVR2B |
0.599 | -0.102 | -2 | 0.539 |
TTBK2 |
0.599 | -0.185 | 2 | 0.511 |
DMPK1 |
0.599 | 0.097 | -3 | 0.596 |
MARK2 |
0.599 | -0.064 | 4 | 0.443 |
MEKK3 |
0.599 | -0.116 | 1 | 0.467 |
PAK5 |
0.599 | -0.026 | -2 | 0.509 |
TAO2 |
0.598 | -0.035 | 2 | 0.631 |
ZAK |
0.598 | -0.132 | 1 | 0.449 |
IRAK4 |
0.597 | -0.099 | 1 | 0.431 |
LOK |
0.596 | -0.016 | -2 | 0.681 |
MLK4 |
0.596 | -0.148 | 2 | 0.545 |
DAPK3 |
0.596 | 0.022 | -3 | 0.607 |
PERK |
0.596 | -0.152 | -2 | 0.609 |
TAO3 |
0.596 | -0.078 | 1 | 0.490 |
HPK1 |
0.595 | -0.027 | 1 | 0.457 |
LRRK2 |
0.595 | -0.021 | 2 | 0.641 |
CK1D |
0.595 | -0.054 | -3 | 0.269 |
CK1E |
0.594 | -0.074 | -3 | 0.321 |
BIKE |
0.594 | 0.051 | 1 | 0.489 |
IRAK1 |
0.594 | -0.143 | -1 | 0.518 |
PBK |
0.594 | -0.002 | 1 | 0.508 |
PKG1 |
0.593 | 0.015 | -2 | 0.467 |
PDHK3_TYR |
0.593 | 0.045 | 4 | 0.669 |
RIPK2 |
0.592 | -0.101 | 1 | 0.445 |
PAK4 |
0.592 | -0.026 | -2 | 0.505 |
EEF2K |
0.592 | -0.044 | 3 | 0.654 |
TTBK1 |
0.592 | -0.119 | 2 | 0.448 |
MEKK1 |
0.592 | -0.186 | 1 | 0.460 |
MEKK2 |
0.591 | -0.163 | 2 | 0.617 |
HGK |
0.591 | -0.064 | 3 | 0.688 |
CK1A2 |
0.591 | -0.061 | -3 | 0.282 |
MEKK6 |
0.591 | -0.082 | 1 | 0.440 |
GCK |
0.591 | -0.074 | 1 | 0.462 |
ROCK2 |
0.590 | 0.043 | -3 | 0.606 |
BMPR1A |
0.590 | -0.083 | 1 | 0.466 |
TESK1_TYR |
0.590 | 0.014 | 3 | 0.694 |
PKMYT1_TYR |
0.590 | 0.038 | 3 | 0.663 |
TNIK |
0.590 | -0.041 | 3 | 0.713 |
LIMK2_TYR |
0.590 | 0.073 | -3 | 0.599 |
GRK3 |
0.589 | -0.072 | -2 | 0.461 |
BRAF |
0.589 | -0.187 | -4 | 0.448 |
AAK1 |
0.589 | 0.074 | 1 | 0.450 |
MAP2K4_TYR |
0.589 | -0.030 | -1 | 0.581 |
TAK1 |
0.589 | -0.095 | 1 | 0.457 |
MAP3K15 |
0.589 | -0.099 | 1 | 0.462 |
PLK4 |
0.588 | -0.137 | 2 | 0.474 |
HASPIN |
0.588 | 0.007 | -1 | 0.378 |
MINK |
0.588 | -0.091 | 1 | 0.439 |
MST2 |
0.588 | -0.122 | 1 | 0.452 |
SLK |
0.587 | -0.057 | -2 | 0.641 |
CAMKK2 |
0.587 | -0.142 | -2 | 0.628 |
NEK5 |
0.587 | -0.180 | 1 | 0.464 |
NEK8 |
0.587 | -0.160 | 2 | 0.627 |
MAP2K7_TYR |
0.587 | -0.060 | 2 | 0.659 |
PINK1_TYR |
0.586 | -0.048 | 1 | 0.538 |
BMPR2_TYR |
0.586 | 0.024 | -1 | 0.583 |
MEK2 |
0.586 | -0.136 | 2 | 0.623 |
TLK2 |
0.586 | -0.187 | 1 | 0.392 |
PDHK4_TYR |
0.585 | -0.011 | 2 | 0.685 |
NEK4 |
0.585 | -0.136 | 1 | 0.428 |
KHS2 |
0.585 | -0.035 | 1 | 0.455 |
MAP2K6_TYR |
0.585 | -0.027 | -1 | 0.579 |
PLK2 |
0.584 | -0.027 | -3 | 0.585 |
CAMKK1 |
0.584 | -0.194 | -2 | 0.620 |
KHS1 |
0.584 | -0.063 | 1 | 0.442 |
NEK1 |
0.582 | -0.115 | 1 | 0.445 |
NEK3 |
0.581 | -0.096 | 1 | 0.451 |
TLK1 |
0.581 | -0.186 | -2 | 0.569 |
ROCK1 |
0.581 | 0.032 | -3 | 0.595 |
NEK10_TYR |
0.581 | 0.001 | 1 | 0.425 |
MST1 |
0.580 | -0.120 | 1 | 0.438 |
LIMK1_TYR |
0.580 | -0.033 | 2 | 0.648 |
YSK1 |
0.580 | -0.092 | 2 | 0.610 |
CK1G1 |
0.579 | -0.110 | -3 | 0.307 |
LKB1 |
0.579 | -0.166 | -3 | 0.539 |
STK33 |
0.578 | -0.102 | 2 | 0.475 |
PDHK1_TYR |
0.578 | -0.104 | -1 | 0.581 |
TAO1 |
0.576 | -0.047 | 1 | 0.429 |
RET |
0.576 | -0.084 | 1 | 0.474 |
EPHB4 |
0.576 | -0.057 | -1 | 0.569 |
TXK |
0.575 | -0.016 | 1 | 0.507 |
ALPHAK3 |
0.575 | -0.036 | -1 | 0.489 |
MST1R |
0.574 | -0.074 | 3 | 0.642 |
EPHA6 |
0.573 | -0.067 | -1 | 0.578 |
DDR1 |
0.573 | -0.062 | 4 | 0.561 |
MYO3B |
0.573 | -0.068 | 2 | 0.620 |
TNK2 |
0.573 | -0.044 | 3 | 0.619 |
VRK1 |
0.572 | -0.177 | 2 | 0.593 |
TYRO3 |
0.572 | -0.109 | 3 | 0.616 |
JAK2 |
0.571 | -0.128 | 1 | 0.483 |
JAK1 |
0.571 | -0.060 | 1 | 0.447 |
TYK2 |
0.570 | -0.183 | 1 | 0.462 |
JAK3 |
0.570 | -0.083 | 1 | 0.483 |
AXL |
0.570 | -0.060 | 3 | 0.624 |
WEE1_TYR |
0.570 | -0.041 | -1 | 0.527 |
TEK |
0.569 | -0.016 | 3 | 0.566 |
EPHA4 |
0.569 | -0.052 | 2 | 0.566 |
TNNI3K_TYR |
0.569 | -0.055 | 1 | 0.469 |
SRMS |
0.569 | -0.086 | 1 | 0.472 |
OSR1 |
0.569 | -0.096 | 2 | 0.628 |
HCK |
0.568 | -0.091 | -1 | 0.643 |
LCK |
0.568 | -0.055 | -1 | 0.645 |
YES1 |
0.567 | -0.090 | -1 | 0.605 |
EPHB1 |
0.567 | -0.082 | 1 | 0.468 |
FGR |
0.567 | -0.139 | 1 | 0.487 |
ASK1 |
0.567 | -0.118 | 1 | 0.461 |
CSF1R |
0.567 | -0.110 | 3 | 0.626 |
ROS1 |
0.567 | -0.150 | 3 | 0.578 |
MERTK |
0.566 | -0.069 | 3 | 0.620 |
EPHB3 |
0.566 | -0.079 | -1 | 0.573 |
ABL2 |
0.566 | -0.092 | -1 | 0.545 |
ITK |
0.566 | -0.072 | -1 | 0.617 |
BLK |
0.566 | -0.043 | -1 | 0.622 |
MYO3A |
0.565 | -0.094 | 1 | 0.423 |
YANK3 |
0.565 | -0.066 | 2 | 0.271 |
ABL1 |
0.565 | -0.095 | -1 | 0.544 |
FGFR2 |
0.564 | -0.077 | 3 | 0.625 |
EPHA1 |
0.563 | -0.054 | 3 | 0.613 |
PTK2B |
0.563 | -0.045 | -1 | 0.566 |
DDR2 |
0.563 | 0.007 | 3 | 0.570 |
BTK |
0.563 | -0.114 | -1 | 0.610 |
TEC |
0.562 | -0.080 | -1 | 0.563 |
EPHA7 |
0.562 | -0.064 | 2 | 0.573 |
EPHA3 |
0.562 | -0.074 | 2 | 0.547 |
FER |
0.562 | -0.180 | 1 | 0.500 |
INSRR |
0.562 | -0.122 | 3 | 0.561 |
FGFR1 |
0.561 | -0.088 | 3 | 0.592 |
FYN |
0.561 | -0.045 | -1 | 0.636 |
EPHB2 |
0.561 | -0.098 | -1 | 0.560 |
TNK1 |
0.561 | -0.098 | 3 | 0.587 |
KDR |
0.561 | -0.086 | 3 | 0.606 |
BMX |
0.560 | -0.066 | -1 | 0.550 |
PDGFRA |
0.560 | -0.137 | 3 | 0.624 |
FLT1 |
0.560 | -0.081 | -1 | 0.538 |
TTK |
0.559 | -0.138 | -2 | 0.570 |
PDGFRB |
0.559 | -0.167 | 3 | 0.624 |
KIT |
0.559 | -0.126 | 3 | 0.631 |
STLK3 |
0.558 | -0.129 | 1 | 0.410 |
EPHA5 |
0.557 | -0.066 | 2 | 0.564 |
LYN |
0.557 | -0.095 | 3 | 0.536 |
PTK6 |
0.556 | -0.165 | -1 | 0.553 |
ERBB2 |
0.556 | -0.124 | 1 | 0.451 |
CK1A |
0.555 | -0.088 | -3 | 0.206 |
PTK2 |
0.554 | -0.010 | -1 | 0.555 |
FLT3 |
0.554 | -0.166 | 3 | 0.610 |
FRK |
0.554 | -0.101 | -1 | 0.625 |
EPHA8 |
0.553 | -0.073 | -1 | 0.561 |
FGFR3 |
0.553 | -0.100 | 3 | 0.610 |
LTK |
0.552 | -0.142 | 3 | 0.560 |
CSK |
0.552 | -0.105 | 2 | 0.580 |
FLT4 |
0.552 | -0.126 | 3 | 0.589 |
NTRK2 |
0.551 | -0.176 | 3 | 0.597 |
MET |
0.551 | -0.129 | 3 | 0.633 |
NTRK1 |
0.551 | -0.190 | -1 | 0.536 |
NTRK3 |
0.550 | -0.146 | -1 | 0.512 |
SRC |
0.550 | -0.102 | -1 | 0.605 |
ALK |
0.548 | -0.177 | 3 | 0.522 |
EPHA2 |
0.547 | -0.068 | -1 | 0.540 |
SYK |
0.546 | -0.053 | -1 | 0.550 |
MUSK |
0.544 | -0.113 | 1 | 0.373 |
MATK |
0.543 | -0.120 | -1 | 0.434 |
EGFR |
0.543 | -0.109 | 1 | 0.394 |
INSR |
0.542 | -0.184 | 3 | 0.544 |
CK1G3 |
0.540 | -0.096 | -3 | 0.171 |
FGFR4 |
0.539 | -0.126 | -1 | 0.495 |
YANK2 |
0.538 | -0.087 | 2 | 0.286 |
IGF1R |
0.532 | -0.154 | 3 | 0.492 |
ERBB4 |
0.531 | -0.091 | 1 | 0.384 |
FES |
0.529 | -0.134 | -1 | 0.514 |
ZAP70 |
0.526 | -0.071 | -1 | 0.480 |
CK1G2 |
0.526 | -0.072 | -3 | 0.236 |