Motif 1112 (n=50)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A0B4J1V8 | PPAN-P2RY11 | T233 | ochoa | HCG2039996 (PPAN-P2RY11 readthrough) | None |
M0QZ24 | None | T35 | ochoa | Glycosyl hydrolases family 38 C-terminal beta sandwich domain-containing protein | None |
O00754 | MAN2B1 | T848 | ochoa | Lysosomal alpha-mannosidase (Laman) (EC 3.2.1.24) (Lysosomal acid alpha-mannosidase) (Mannosidase alpha class 2B member 1) (Mannosidase alpha-B) [Cleaved into: Lysosomal alpha-mannosidase A peptide; Lysosomal alpha-mannosidase B peptide; Lysosomal alpha-mannosidase C peptide; Lysosomal alpha-mannosidase D peptide; Lysosomal alpha-mannosidase E peptide] | Necessary for the catabolism of N-linked carbohydrates released during glycoprotein turnover. Cleaves all known types of alpha-mannosidic linkages. |
O75381 | PEX14 | T48 | ochoa | Peroxisomal membrane protein PEX14 (PTS1 receptor-docking protein) (Peroxin-14) (Peroxisomal membrane anchor protein PEX14) | Component of the PEX13-PEX14 docking complex, a translocon channel that specifically mediates the import of peroxisomal cargo proteins bound to PEX5 receptor (PubMed:24235149, PubMed:28765278, PubMed:9653144). The PEX13-PEX14 docking complex forms a large import pore which can be opened to a diameter of about 9 nm (By similarity). Mechanistically, PEX5 receptor along with cargo proteins associates with the PEX14 subunit of the PEX13-PEX14 docking complex in the cytosol, leading to the insertion of the receptor into the organelle membrane with the concomitant translocation of the cargo into the peroxisome matrix (PubMed:24235149, PubMed:28765278). Plays a key role for peroxisome movement through a direct interaction with tubulin (PubMed:21525035). {ECO:0000250|UniProtKB:P53112, ECO:0000269|PubMed:21525035, ECO:0000269|PubMed:24235149, ECO:0000269|PubMed:28765278, ECO:0000269|PubMed:9653144}. |
P04626 | ERBB2 | T1236 | ochoa | Receptor tyrosine-protein kinase erbB-2 (EC 2.7.10.1) (Metastatic lymph node gene 19 protein) (MLN 19) (Proto-oncogene Neu) (Proto-oncogene c-ErbB-2) (Tyrosine kinase-type cell surface receptor HER2) (p185erbB2) (CD antigen CD340) | Protein tyrosine kinase that is part of several cell surface receptor complexes, but that apparently needs a coreceptor for ligand binding. Essential component of a neuregulin-receptor complex, although neuregulins do not interact with it alone. GP30 is a potential ligand for this receptor. Regulates outgrowth and stabilization of peripheral microtubules (MTs). Upon ERBB2 activation, the MEMO1-RHOA-DIAPH1 signaling pathway elicits the phosphorylation and thus the inhibition of GSK3B at cell membrane. This prevents the phosphorylation of APC and CLASP2, allowing its association with the cell membrane. In turn, membrane-bound APC allows the localization of MACF1 to the cell membrane, which is required for microtubule capture and stabilization. {ECO:0000305}.; FUNCTION: In the nucleus is involved in transcriptional regulation. Associates with the 5'-TCAAATTC-3' sequence in the PTGS2/COX-2 promoter and activates its transcription. Implicated in transcriptional activation of CDKN1A; the function involves STAT3 and SRC. Involved in the transcription of rRNA genes by RNA Pol I and enhances protein synthesis and cell growth. {ECO:0000269|PubMed:10358079, ECO:0000269|PubMed:15380516, ECO:0000269|PubMed:21555369}. |
P0DPH7 | TUBA3C | T271 | ochoa | Tubulin alpha-3C chain (EC 3.6.5.-) (Alpha-tubulin 2) (Alpha-tubulin 3C) (Tubulin alpha-2 chain) [Cleaved into: Detyrosinated tubulin alpha-3C chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
P0DPH8 | TUBA3D | T271 | ochoa | Tubulin alpha-3D chain (EC 3.6.5.-) (Alpha-tubulin 3D) [Cleaved into: Detyrosinated tubulin alpha-3D chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
P12882 | MYH1 | T682 | ochoa | Myosin-1 (Myosin heavy chain 1) (Myosin heavy chain 2x) (MyHC-2x) (Myosin heavy chain IIx/d) (MyHC-IIx/d) (Myosin heavy chain, skeletal muscle, adult 1) | Required for normal hearing. It plays a role in cochlear amplification of auditory stimuli, likely through the positive regulation of prestin (SLC26A5) activity and outer hair cell (OHC) electromotility. {ECO:0000250|UniProtKB:Q5SX40}. |
P12883 | MYH7 | T678 | ochoa | Myosin-7 (Myosin heavy chain 7) (Myosin heavy chain slow isoform) (MyHC-slow) (Myosin heavy chain, cardiac muscle beta isoform) (MyHC-beta) | Myosins are actin-based motor molecules with ATPase activity essential for muscle contraction. Forms regular bipolar thick filaments that, together with actin thin filaments, constitute the fundamental contractile unit of skeletal and cardiac muscle. {ECO:0000305|PubMed:26150528, ECO:0000305|PubMed:26246073}. |
P13535 | MYH8 | T681 | ochoa | Myosin-8 (Myosin heavy chain 8) (Myosin heavy chain, skeletal muscle, perinatal) (MyHC-perinatal) | Muscle contraction. |
P46013 | MKI67 | T1176 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P46013 | MKI67 | T1298 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P46013 | MKI67 | T1540 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P46013 | MKI67 | T1784 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P46013 | MKI67 | T2268 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P46013 | MKI67 | T2389 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P49959 | MRE11 | T329 | psp | Double-strand break repair protein MRE11 (EC 3.1.-.-) (Meiotic recombination 11 homolog 1) (MRE11 homolog 1) (Meiotic recombination 11 homolog A) (MRE11 homolog A) | Core component of the MRN complex, which plays a central role in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity and meiosis (PubMed:11741547, PubMed:14657032, PubMed:22078559, PubMed:23080121, PubMed:24316220, PubMed:26240375, PubMed:27889449, PubMed:28867292, PubMed:29670289, PubMed:30464262, PubMed:30612738, PubMed:31353207, PubMed:37696958, PubMed:38128537, PubMed:9590181, PubMed:9651580, PubMed:9705271). The MRN complex is involved in the repair of DNA double-strand breaks (DSBs) via homologous recombination (HR), an error-free mechanism which primarily occurs during S and G2 phases (PubMed:24316220, PubMed:28867292, PubMed:31353207, PubMed:38128537). The complex (1) mediates the end resection of damaged DNA, which generates proper single-stranded DNA, a key initial steps in HR, and is (2) required for the recruitment of other repair factors and efficient activation of ATM and ATR upon DNA damage (PubMed:24316220, PubMed:27889449, PubMed:28867292, PubMed:36050397, PubMed:38128537). Within the MRN complex, MRE11 possesses both single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity (PubMed:11741547, PubMed:22078559, PubMed:24316220, PubMed:26240375, PubMed:27889449, PubMed:29670289, PubMed:31353207, PubMed:36563124, PubMed:9590181, PubMed:9651580, PubMed:9705271). After DSBs, MRE11 is loaded onto DSBs sites and cleaves DNA by cooperating with RBBP8/CtIP to initiate end resection (PubMed:27814491, PubMed:27889449, PubMed:30787182). MRE11 first endonucleolytically cleaves the 5' strand at DNA DSB ends to prevent non-homologous end joining (NHEJ) and licence HR (PubMed:24316220). It then generates a single-stranded DNA gap via 3' to 5' exonucleolytic degradation to create entry sites for EXO1- and DNA2-mediated 5' to 3' long-range resection, which is required for single-strand invasion and recombination (PubMed:24316220, PubMed:28867292). RBBP8/CtIP specifically promotes the endonuclease activity of MRE11 to clear protein-DNA adducts and generate clean double-strand break ends (PubMed:27814491, PubMed:27889449, PubMed:30787182). MRE11 endonuclease activity is also enhanced by AGER/RAGE (By similarity). The MRN complex is also required for DNA damage signaling via activation of the ATM and ATR kinases: the nuclease activity of MRE11 is not required to activate ATM and ATR (PubMed:14657032, PubMed:15064416, PubMed:15790808, PubMed:16622404). The MRN complex is also required for the processing of R-loops (PubMed:31537797). The MRN complex is involved in the activation of the cGAS-STING pathway induced by DNA damage during tumorigenesis: the MRN complex acts by displacing CGAS from nucleosome sequestration, thereby activating it (By similarity). In telomeres the MRN complex may modulate t-loop formation (PubMed:10888888). {ECO:0000250|UniProtKB:Q61216, ECO:0000269|PubMed:10888888, ECO:0000269|PubMed:11741547, ECO:0000269|PubMed:14657032, ECO:0000269|PubMed:15064416, ECO:0000269|PubMed:15790808, ECO:0000269|PubMed:16622404, ECO:0000269|PubMed:22078559, ECO:0000269|PubMed:23080121, ECO:0000269|PubMed:24316220, ECO:0000269|PubMed:26240375, ECO:0000269|PubMed:27814491, ECO:0000269|PubMed:27889449, ECO:0000269|PubMed:28867292, ECO:0000269|PubMed:29670289, ECO:0000269|PubMed:30464262, ECO:0000269|PubMed:30612738, ECO:0000269|PubMed:30787182, ECO:0000269|PubMed:31353207, ECO:0000269|PubMed:31537797, ECO:0000269|PubMed:36050397, ECO:0000269|PubMed:36563124, ECO:0000269|PubMed:37696958, ECO:0000269|PubMed:38128537, ECO:0000269|PubMed:9590181, ECO:0000269|PubMed:9651580, ECO:0000269|PubMed:9705271}.; FUNCTION: MRE11 contains two DNA-binding domains (DBDs), enabling it to bind both single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA). {ECO:0000305}. |
P60709 | ACTB | T106 | 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}. |
P63261 | ACTG1 | T106 | 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}. |
P68363 | TUBA1B | T271 | ochoa | Tubulin alpha-1B chain (EC 3.6.5.-) (Alpha-tubulin ubiquitous) (Tubulin K-alpha-1) (Tubulin alpha-ubiquitous chain) [Cleaved into: Detyrosinated tubulin alpha-1B chain] | Tubulin is the major constituent of microtubules, protein filaments consisting of alpha- and beta-tubulin heterodimers (PubMed:38305685, PubMed:34996871, PubMed:38609661). Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms (PubMed:38305685, PubMed:34996871, PubMed:38609661). Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin (PubMed:34996871, PubMed:38609661). {ECO:0000269|PubMed:34996871, ECO:0000269|PubMed:38305685, ECO:0000269|PubMed:38609661}. |
P68366 | TUBA4A | T271 | ochoa | Tubulin alpha-4A chain (EC 3.6.5.-) (Alpha-tubulin 1) (Testis-specific alpha-tubulin) (Tubulin H2-alpha) (Tubulin alpha-1 chain) | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q02952 | AKAP12 | T401 | ochoa | A-kinase anchor protein 12 (AKAP-12) (A-kinase anchor protein 250 kDa) (AKAP 250) (Gravin) (Myasthenia gravis autoantigen) | Anchoring protein that mediates the subcellular compartmentation of protein kinase A (PKA) and protein kinase C (PKC). |
Q13164 | MAPK7 | T28 | psp | 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}. |
Q13976 | PRKG1 | T59 | ochoa|psp | cGMP-dependent protein kinase 1 (cGK 1) (cGK1) (EC 2.7.11.12) (cGMP-dependent protein kinase I) (cGKI) | Serine/threonine protein kinase that acts as a key mediator of the nitric oxide (NO)/cGMP signaling pathway. GMP binding activates PRKG1, which phosphorylates serines and threonines on many cellular proteins. Numerous protein targets for PRKG1 phosphorylation are implicated in modulating cellular calcium, but the contribution of each of these targets may vary substantially among cell types. Proteins that are phosphorylated by PRKG1 regulate platelet activation and adhesion, smooth muscle contraction, cardiac function, gene expression, feedback of the NO-signaling pathway, and other processes involved in several aspects of the CNS like axon guidance, hippocampal and cerebellar learning, circadian rhythm and nociception. Smooth muscle relaxation is mediated through lowering of intracellular free calcium, by desensitization of contractile proteins to calcium, and by decrease in the contractile state of smooth muscle or in platelet activation. Regulates intracellular calcium levels via several pathways: phosphorylates IRAG1 and inhibits IP3-induced Ca(2+) release from intracellular stores, phosphorylation of KCNMA1 (BKCa) channels decreases intracellular Ca(2+) levels, which leads to increased opening of this channel. PRKG1 phosphorylates the canonical transient receptor potential channel (TRPC) family which inactivates the associated inward calcium current. Another mode of action of NO/cGMP/PKGI signaling involves PKGI-mediated inactivation of the Ras homolog gene family member A (RhoA). Phosphorylation of RHOA by PRKG1 blocks the action of this protein in myriad processes: regulation of RHOA translocation; decreasing contraction; controlling vesicle trafficking, reduction of myosin light chain phosphorylation resulting in vasorelaxation. Activation of PRKG1 by NO signaling also alters gene expression in a number of tissues. In smooth muscle cells, increased cGMP and PRKG1 activity influence expression of smooth muscle-specific contractile proteins, levels of proteins in the NO/cGMP signaling pathway, down-regulation of the matrix proteins osteopontin and thrombospondin-1 to limit smooth muscle cell migration and phenotype. Regulates vasodilator-stimulated phosphoprotein (VASP) functions in platelets and smooth muscle. {ECO:0000269|PubMed:10567269, ECO:0000269|PubMed:11162591, ECO:0000269|PubMed:11723116, ECO:0000269|PubMed:12082086, ECO:0000269|PubMed:14608379, ECO:0000269|PubMed:15194681, ECO:0000269|PubMed:16990611, ECO:0000269|PubMed:8182057}. |
Q6PEY2 | TUBA3E | T271 | ochoa | Tubulin alpha-3E chain (EC 3.6.5.-) (Alpha-tubulin 3E) [Cleaved into: Detyrosinated tubulin alpha-3E chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q71U36 | TUBA1A | T271 | ochoa | Tubulin alpha-1A chain (EC 3.6.5.-) (Alpha-tubulin 3) (Tubulin B-alpha-1) (Tubulin alpha-3 chain) [Cleaved into: Detyrosinated tubulin alpha-1A chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q8IYK8 | REM2 | T31 | ochoa | GTP-binding protein REM 2 (Rad and Gem-like GTP-binding protein 2) | Binds GTP saturably and exhibits a low intrinsic rate of GTP hydrolysis. {ECO:0000250|UniProtKB:Q9WTY2}. |
Q8N5A5 | ZGPAT | T271 | ochoa | Zinc finger CCCH-type with G patch domain-containing protein (G patch domain-containing protein 6) (Zinc finger CCCH domain-containing protein 9) (Zinc finger and G patch domain-containing protein) | Transcription repressor that specifically binds the 5'-GGAG[GA]A[GA]A-3' consensus sequence. Represses transcription by recruiting the chromatin multiprotein complex NuRD to target promoters. Negatively regulates expression of EGFR, a gene involved in cell proliferation, survival and migration. Its ability to repress genes of the EGFR pathway suggest it may act as a tumor suppressor. Able to suppress breast carcinogenesis. {ECO:0000269|PubMed:19644445}.; FUNCTION: [Isoform 4]: Antagonizes the transcription repression by isoform 1 by competing for the binding of the NuRD complex. Does not bind DNA. {ECO:0000269|PubMed:19644445}. |
Q8TEH3 | DENND1A | T532 | ochoa | DENN domain-containing protein 1A (Connecdenn 1) (Connecdenn) (Protein FAM31A) | Guanine nucleotide exchange factor (GEF) regulating clathrin-mediated endocytosis through RAB35 activation. Promotes the exchange of GDP to GTP, converting inactive GDP-bound RAB35 into its active GTP-bound form. Regulates clathrin-mediated endocytosis of synaptic vesicles and mediates exit from early endosomes (PubMed:20154091, PubMed:20937701). Binds phosphatidylinositol-phosphates (PtdInsPs), with some preference for PtdIns(3)P (By similarity). {ECO:0000250|UniProtKB:Q8K382, ECO:0000269|PubMed:20154091, ECO:0000269|PubMed:20937701}. |
Q92766 | RREB1 | T1318 | ochoa | Ras-responsive element-binding protein 1 (RREB-1) (Finger protein in nuclear bodies) (Raf-responsive zinc finger protein LZ321) (Zinc finger motif enhancer-binding protein 1) (Zep-1) | Transcription factor that binds specifically to the RAS-responsive elements (RRE) of gene promoters (PubMed:10390538, PubMed:15067362, PubMed:17550981, PubMed:8816445, PubMed:9305772). Represses the angiotensinogen gene (PubMed:15067362). Negatively regulates the transcriptional activity of AR (PubMed:17550981). Potentiates the transcriptional activity of NEUROD1 (PubMed:12482979). Promotes brown adipocyte differentiation (By similarity). May be involved in Ras/Raf-mediated cell differentiation by enhancing calcitonin expression (PubMed:8816445). {ECO:0000250|UniProtKB:Q3UH06, ECO:0000269|PubMed:10390538, ECO:0000269|PubMed:12482979, ECO:0000269|PubMed:15067362, ECO:0000269|PubMed:17550981, ECO:0000269|PubMed:8816445, ECO:0000269|PubMed:9305772}. |
Q9BQE3 | TUBA1C | T271 | ochoa | Tubulin alpha-1C chain (EC 3.6.5.-) (Alpha-tubulin 6) (Tubulin alpha-6 chain) [Cleaved into: Detyrosinated tubulin alpha-1C chain] | Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin. |
Q9BY77 | POLDIP3 | T138 | 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}. |
Q9BYI3 | HYCC1 | T445 | ochoa | Hyccin (Down-regulated by CTNNB1 protein A) | Component of a complex required to localize phosphatidylinositol 4-kinase (PI4K) to the plasma membrane (PubMed:26571211). The complex acts as a regulator of phosphatidylinositol 4-phosphate (PtdIns(4)P) synthesis (PubMed:26571211). HYCC1 plays a key role in oligodendrocytes formation, a cell type with expanded plasma membrane that requires generation of PtdIns(4)P (PubMed:26571211). Its role in oligodendrocytes formation probably explains its importance in myelination of the central and peripheral nervous system (PubMed:16951682, PubMed:26571211). May also have a role in the beta-catenin/Lef signaling pathway (Probable). {ECO:0000269|PubMed:16951682, ECO:0000269|PubMed:26571211, ECO:0000305|PubMed:10910037}. |
Q9NQ55 | PPAN | T233 | ochoa | Suppressor of SWI4 1 homolog (Ssf-1) (Brix domain-containing protein 3) (Peter Pan homolog) | May have a role in cell growth. |
Q9P227 | ARHGAP23 | T538 | ochoa | Rho GTPase-activating protein 23 (Rho-type GTPase-activating protein 23) | GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state. {ECO:0000250}. |
Q9UKX2 | MYH2 | T684 | ochoa | Myosin-2 (Myosin heavy chain 2) (Myosin heavy chain 2a) (MyHC-2a) (Myosin heavy chain IIa) (MyHC-IIa) (Myosin heavy chain, skeletal muscle, adult 2) | Myosins are actin-based motor molecules with ATPase activity essential for muscle contraction. {ECO:0000250|UniProtKB:P12883}. |
Q9ULV3 | CIZ1 | T293 | ochoa | Cip1-interacting zinc finger protein (CDKN1A-interacting zinc finger protein 1) (Nuclear protein NP94) (Zinc finger protein 356) | May regulate the subcellular localization of CIP/WAF1. |
Q9Y2J2 | EPB41L3 | T848 | 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}. |
Q9Y2W2 | WBP11 | T593 | ochoa | WW domain-binding protein 11 (WBP-11) (Npw38-binding protein) (NpwBP) (SH3 domain-binding protein SNP70) (Splicing factor that interacts with PQBP-1 and PP1) | Activates pre-mRNA splicing. May inhibit PP1 phosphatase activity. {ECO:0000269|PubMed:10593949, ECO:0000269|PubMed:11375989, ECO:0000269|PubMed:14640981}. |
Q9Y520 | PRRC2C | T887 | ochoa | Protein PRRC2C (BAT2 domain-containing protein 1) (HBV X-transactivated gene 2 protein) (HBV XAg-transactivated protein 2) (HLA-B-associated transcript 2-like 2) (Proline-rich and coiled-coil-containing protein 2C) | Required for efficient formation of stress granules. {ECO:0000269|PubMed:29395067}. |
Q9Y623 | MYH4 | T682 | ochoa | Myosin-4 (Myosin heavy chain 2b) (MyHC-2b) (Myosin heavy chain 4) (Myosin heavy chain IIb) (MyHC-IIb) (Myosin heavy chain, skeletal muscle, fetal) | Muscle contraction. |
V9GY48 | None | T177 | ochoa | Zinc finger CCCH-type with G patch domain-containing protein | None |
P33992 | MCM5 | T633 | EPSD|PSP | DNA replication licensing factor MCM5 (EC 3.6.4.12) (CDC46 homolog) (P1-CDC46) | Acts as a component of the MCM2-7 complex (MCM complex) which is the replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. Core component of CDC45-MCM-GINS (CMG) helicase, the molecular machine that unwinds template DNA during replication, and around which the replisome is built (PubMed:16899510, PubMed:32453425, PubMed:34694004, PubMed:34700328, PubMed:35585232). The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity (PubMed:32453425). {ECO:0000269|PubMed:16899510, ECO:0000269|PubMed:32453425, ECO:0000269|PubMed:34694004, ECO:0000269|PubMed:34700328, ECO:0000269|PubMed:35585232}. |
P62899 | RPL31 | T107 | Sugiyama | Large ribosomal subunit protein eL31 (60S ribosomal protein L31) | Component of the large ribosomal subunit (PubMed:23636399, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:23636399, PubMed:32669547). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547}. |
Q562R1 | ACTBL2 | T107 | Sugiyama | Beta-actin-like protein 2 (Kappa-actin) | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. {ECO:0000250}. |
Q13228 | SELENBP1 | T38 | Sugiyama | Methanethiol oxidase (MTO) (EC 1.8.3.4) (56 kDa selenium-binding protein) (SBP56) (SP56) (Selenium-binding protein 1) | Catalyzes the oxidation of methanethiol, an organosulfur compound known to be produced in substantial amounts by gut bacteria (PubMed:29255262). Selenium-binding protein which may be involved in the sensing of reactive xenobiotics in the cytoplasm. May be involved in intra-Golgi protein transport (By similarity). {ECO:0000250|UniProtKB:Q8VIF7, ECO:0000269|PubMed:29255262}. |
Q99759 | MAP3K3 | T307 | Sugiyama | Mitogen-activated protein kinase kinase kinase 3 (EC 2.7.11.25) (MAPK/ERK kinase kinase 3) (MEK kinase 3) (MEKK 3) | Component of a protein kinase signal transduction cascade. Mediates activation of the NF-kappa-B, AP1 and DDIT3 transcriptional regulators. {ECO:0000269|PubMed:12912994, ECO:0000269|PubMed:14661019, ECO:0000269|PubMed:14743216, ECO:0000269|PubMed:33729480, ECO:0000269|PubMed:33891857, ECO:0000269|PubMed:9006902}. |
Q02952 | AKAP12 | T951 | Sugiyama | A-kinase anchor protein 12 (AKAP-12) (A-kinase anchor protein 250 kDa) (AKAP 250) (Gravin) (Myasthenia gravis autoantigen) | Anchoring protein that mediates the subcellular compartmentation of protein kinase A (PKA) and protein kinase C (PKC). |
P61163 | ACTR1A | T111 | Sugiyama | Alpha-centractin (Centractin) (ARP1) (Actin-RPV) (Centrosome-associated actin homolog) | Part of the ACTR1A/ACTB filament around which the dynactin complex is built. The dynactin multiprotein complex activates the molecular motor dynein for ultra-processive transport along microtubules. {ECO:0000250|UniProtKB:F2Z5G5}. |
P22314 | UBA1 | T633 | 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}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-190828 | Gap junction trafficking | 5.717649e-14 | 13.243 |
R-HSA-437239 | Recycling pathway of L1 | 9.403589e-14 | 13.027 |
R-HSA-157858 | Gap junction trafficking and regulation | 1.292300e-13 | 12.889 |
R-HSA-389958 | Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 2.701173e-13 | 12.568 |
R-HSA-190840 | Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 6.228351e-13 | 12.206 |
R-HSA-190872 | Transport of connexons to the plasma membrane | 8.483214e-13 | 12.071 |
R-HSA-389977 | Post-chaperonin tubulin folding pathway | 1.513900e-12 | 11.820 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 2.897238e-12 | 11.538 |
R-HSA-389960 | Formation of tubulin folding intermediates by CCT/TriC | 5.364376e-12 | 11.270 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 1.276868e-11 | 10.894 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 1.801970e-11 | 10.744 |
R-HSA-9668328 | Sealing of the nuclear envelope (NE) by ESCRT-III | 3.299172e-11 | 10.482 |
R-HSA-190861 | Gap junction assembly | 4.661260e-11 | 10.331 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 7.853107e-11 | 10.105 |
R-HSA-9646399 | Aggrephagy | 1.196442e-10 | 9.922 |
R-HSA-9609736 | Assembly and cell surface presentation of NMDA receptors | 1.594564e-10 | 9.797 |
R-HSA-373760 | L1CAM interactions | 1.838881e-10 | 9.735 |
R-HSA-8955332 | Carboxyterminal post-translational modifications of tubulin | 3.531809e-10 | 9.452 |
R-HSA-389957 | Prefoldin mediated transfer of substrate to CCT/TriC | 3.923609e-10 | 9.406 |
R-HSA-390466 | Chaperonin-mediated protein folding | 4.869435e-10 | 9.313 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 5.278628e-10 | 9.277 |
R-HSA-391251 | Protein folding | 7.804422e-10 | 9.108 |
R-HSA-6807878 | COPI-mediated anterograde transport | 1.131882e-09 | 8.946 |
R-HSA-983189 | Kinesins | 1.515053e-09 | 8.820 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 1.847626e-09 | 8.733 |
R-HSA-5620920 | Cargo trafficking to the periciliary membrane | 4.222768e-09 | 8.374 |
R-HSA-2132295 | MHC class II antigen presentation | 7.649464e-09 | 8.116 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 8.807741e-09 | 8.055 |
R-HSA-9833482 | PKR-mediated signaling | 8.807741e-09 | 8.055 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 1.384748e-08 | 7.859 |
R-HSA-438064 | Post NMDA receptor activation events | 1.590855e-08 | 7.798 |
R-HSA-9663891 | Selective autophagy | 1.706730e-08 | 7.768 |
R-HSA-5620924 | Intraflagellar transport | 1.915152e-08 | 7.718 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 3.182564e-08 | 7.497 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 3.317073e-08 | 7.479 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 4.795131e-08 | 7.319 |
R-HSA-422475 | Axon guidance | 7.589201e-08 | 7.120 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 7.603116e-08 | 7.119 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 1.089871e-07 | 6.963 |
R-HSA-9675108 | Nervous system development | 1.500281e-07 | 6.824 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 1.585815e-07 | 6.800 |
R-HSA-69275 | G2/M Transition | 1.653434e-07 | 6.782 |
R-HSA-5617833 | Cilium Assembly | 1.912798e-07 | 6.718 |
R-HSA-453274 | Mitotic G2-G2/M phases | 1.779059e-07 | 6.750 |
R-HSA-68877 | Mitotic Prometaphase | 2.129574e-07 | 6.672 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 2.718988e-07 | 6.566 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 2.911142e-07 | 6.536 |
R-HSA-1632852 | Macroautophagy | 4.531083e-07 | 6.344 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 7.956373e-07 | 6.099 |
R-HSA-9612973 | Autophagy | 8.588544e-07 | 6.066 |
R-HSA-5610787 | Hedgehog 'off' state | 1.027031e-06 | 5.988 |
R-HSA-2467813 | Separation of Sister Chromatids | 1.155604e-06 | 5.937 |
R-HSA-199991 | Membrane Trafficking | 3.445009e-06 | 5.463 |
R-HSA-9609690 | HCMV Early Events | 3.446165e-06 | 5.463 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 5.651573e-06 | 5.248 |
R-HSA-68882 | Mitotic Anaphase | 6.313227e-06 | 5.200 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 6.488349e-06 | 5.188 |
R-HSA-5358351 | Signaling by Hedgehog | 6.900526e-06 | 5.161 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 7.011284e-06 | 5.154 |
R-HSA-9609646 | HCMV Infection | 1.500972e-05 | 4.824 |
R-HSA-68886 | M Phase | 2.373638e-05 | 4.625 |
R-HSA-5653656 | Vesicle-mediated transport | 2.574628e-05 | 4.589 |
R-HSA-69278 | Cell Cycle, Mitotic | 5.237550e-05 | 4.281 |
R-HSA-1640170 | Cell Cycle | 4.845108e-05 | 4.315 |
R-HSA-446203 | Asparagine N-linked glycosylation | 4.628434e-05 | 4.335 |
R-HSA-112315 | Transmission across Chemical Synapses | 6.805969e-05 | 4.167 |
R-HSA-112316 | Neuronal System | 9.205519e-05 | 4.036 |
R-HSA-913531 | Interferon Signaling | 1.866918e-04 | 3.729 |
R-HSA-2262752 | Cellular responses to stress | 1.949669e-04 | 3.710 |
R-HSA-1266738 | Developmental Biology | 4.158282e-04 | 3.381 |
R-HSA-196025 | Formation of annular gap junctions | 5.154573e-04 | 3.288 |
R-HSA-9825895 | Regulation of MITF-M-dependent genes involved in DNA replication, damage repair ... | 5.154573e-04 | 3.288 |
R-HSA-8953897 | Cellular responses to stimuli | 5.242423e-04 | 3.280 |
R-HSA-109582 | Hemostasis | 5.529916e-04 | 3.257 |
R-HSA-190873 | Gap junction degradation | 6.122722e-04 | 3.213 |
R-HSA-9662361 | Sensory processing of sound by outer hair cells of the cochlea | 9.499093e-04 | 3.022 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 1.278162e-03 | 2.893 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 1.278162e-03 | 2.893 |
R-HSA-1280218 | Adaptive Immune System | 1.034082e-03 | 2.985 |
R-HSA-8854518 | AURKA Activation by TPX2 | 1.438115e-03 | 2.842 |
R-HSA-446353 | Cell-extracellular matrix interactions | 1.514667e-03 | 2.820 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 1.551428e-03 | 2.809 |
R-HSA-8866910 | TFAP2 (AP-2) family regulates transcription of growth factors and their receptor... | 1.843320e-03 | 2.734 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 1.858781e-03 | 2.731 |
R-HSA-380287 | Centrosome maturation | 1.991595e-03 | 2.701 |
R-HSA-168256 | Immune System | 2.060842e-03 | 2.686 |
R-HSA-9659379 | Sensory processing of sound | 2.274640e-03 | 2.643 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 2.661986e-03 | 2.575 |
R-HSA-9938206 | Developmental Lineage of Mammary Stem Cells | 3.233821e-03 | 2.490 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 3.269142e-03 | 2.486 |
R-HSA-445095 | Interaction between L1 and Ankyrins | 4.449558e-03 | 2.352 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 4.603494e-03 | 2.337 |
R-HSA-9927432 | Developmental Lineage of Mammary Gland Myoepithelial Cells | 4.986340e-03 | 2.302 |
R-HSA-9913351 | Formation of the dystrophin-glycoprotein complex (DGC) | 5.551452e-03 | 2.256 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 7.747553e-03 | 2.111 |
R-HSA-5674135 | MAP2K and MAPK activation | 9.518170e-03 | 2.021 |
R-HSA-9656223 | Signaling by RAF1 mutants | 9.518170e-03 | 2.021 |
R-HSA-597592 | Post-translational protein modification | 9.287451e-03 | 2.032 |
R-HSA-9927418 | Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 9.891956e-03 | 2.005 |
R-HSA-5663205 | Infectious disease | 1.063843e-02 | 1.973 |
R-HSA-8864260 | Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 1.065887e-02 | 1.972 |
R-HSA-3928662 | EPHB-mediated forward signaling | 1.065887e-02 | 1.972 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 1.145130e-02 | 1.941 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 1.145130e-02 | 1.941 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 1.145130e-02 | 1.941 |
R-HSA-6802949 | Signaling by RAS mutants | 1.145130e-02 | 1.941 |
R-HSA-9664407 | Parasite infection | 1.156338e-02 | 1.937 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 1.156338e-02 | 1.937 |
R-HSA-9664417 | Leishmania phagocytosis | 1.156338e-02 | 1.937 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 1.176145e-02 | 1.930 |
R-HSA-9665230 | Drug resistance in ERBB2 KD mutants | 1.185391e-02 | 1.926 |
R-HSA-9652282 | Drug-mediated inhibition of ERBB2 signaling | 1.185391e-02 | 1.926 |
R-HSA-198765 | Signalling to ERK5 | 1.185391e-02 | 1.926 |
R-HSA-9665249 | Resistance of ERBB2 KD mutants to afatinib | 1.185391e-02 | 1.926 |
R-HSA-9665245 | Resistance of ERBB2 KD mutants to tesevatinib | 1.185391e-02 | 1.926 |
R-HSA-9665251 | Resistance of ERBB2 KD mutants to lapatinib | 1.185391e-02 | 1.926 |
R-HSA-9665233 | Resistance of ERBB2 KD mutants to trastuzumab | 1.185391e-02 | 1.926 |
R-HSA-9665250 | Resistance of ERBB2 KD mutants to AEE788 | 1.185391e-02 | 1.926 |
R-HSA-9665246 | Resistance of ERBB2 KD mutants to neratinib | 1.185391e-02 | 1.926 |
R-HSA-9665247 | Resistance of ERBB2 KD mutants to osimertinib | 1.185391e-02 | 1.926 |
R-HSA-9665244 | Resistance of ERBB2 KD mutants to sapitinib | 1.185391e-02 | 1.926 |
R-HSA-9665737 | Drug resistance in ERBB2 TMD/JMD mutants | 1.185391e-02 | 1.926 |
R-HSA-3928665 | EPH-ephrin mediated repulsion of cells | 1.185699e-02 | 1.926 |
R-HSA-9856651 | MITF-M-dependent gene expression | 1.385033e-02 | 1.859 |
R-HSA-9764561 | Regulation of CDH1 Function | 1.625183e-02 | 1.789 |
R-HSA-1251932 | PLCG1 events in ERBB2 signaling | 1.772915e-02 | 1.751 |
R-HSA-1306955 | GRB7 events in ERBB2 signaling | 1.772915e-02 | 1.751 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 2.019269e-02 | 1.695 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 2.393460e-02 | 1.621 |
R-HSA-8852135 | Protein ubiquitination | 2.561893e-02 | 1.591 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 1.994593e-02 | 1.700 |
R-HSA-3000171 | Non-integrin membrane-ECM interactions | 2.561893e-02 | 1.591 |
R-HSA-162582 | Signal Transduction | 2.821319e-02 | 1.550 |
R-HSA-9824446 | Viral Infection Pathways | 1.932084e-02 | 1.714 |
R-HSA-6802957 | Oncogenic MAPK signaling | 3.156776e-02 | 1.501 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 3.233104e-02 | 1.490 |
R-HSA-176974 | Unwinding of DNA | 3.515042e-02 | 1.454 |
R-HSA-8853383 | Lysosomal oligosaccharide catabolism | 3.515042e-02 | 1.454 |
R-HSA-2682334 | EPH-Ephrin signaling | 3.734035e-02 | 1.428 |
R-HSA-390450 | Folding of actin by CCT/TriC | 3.802440e-02 | 1.420 |
R-HSA-428359 | Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RN... | 3.802440e-02 | 1.420 |
R-HSA-202670 | ERKs are inactivated | 4.374724e-02 | 1.359 |
R-HSA-5693548 | Sensing of DNA Double Strand Breaks | 4.374724e-02 | 1.359 |
R-HSA-9634285 | Constitutive Signaling by Overexpressed ERBB2 | 4.659614e-02 | 1.332 |
R-HSA-5685939 | HDR through MMEJ (alt-NHEJ) | 4.943673e-02 | 1.306 |
R-HSA-8847993 | ERBB2 Activates PTK6 Signaling | 5.226903e-02 | 1.282 |
R-HSA-6785631 | ERBB2 Regulates Cell Motility | 5.509307e-02 | 1.259 |
R-HSA-1963640 | GRB2 events in ERBB2 signaling | 6.071646e-02 | 1.217 |
R-HSA-1963642 | PI3K events in ERBB2 signaling | 6.351585e-02 | 1.197 |
R-HSA-9665348 | Signaling by ERBB2 ECD mutants | 6.630707e-02 | 1.178 |
R-HSA-9709603 | Impaired BRCA2 binding to PALB2 | 6.909014e-02 | 1.161 |
R-HSA-9701193 | Defective homologous recombination repair (HRR) due to PALB2 loss of function | 7.186509e-02 | 1.143 |
R-HSA-9934037 | Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | 7.186509e-02 | 1.143 |
R-HSA-9704331 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 7.186509e-02 | 1.143 |
R-HSA-9701192 | Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 7.186509e-02 | 1.143 |
R-HSA-9704646 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 7.186509e-02 | 1.143 |
R-HSA-9665686 | Signaling by ERBB2 TMD/JMD mutants | 8.561881e-02 | 1.067 |
R-HSA-5693554 | Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SD... | 8.834550e-02 | 1.054 |
R-HSA-418457 | cGMP effects | 5.226903e-02 | 1.282 |
R-HSA-198753 | ERK/MAPK targets | 7.463194e-02 | 1.127 |
R-HSA-9933947 | Formation of the non-canonical BAF (ncBAF) complex | 4.943673e-02 | 1.306 |
R-HSA-9603798 | Class I peroxisomal membrane protein import | 5.790887e-02 | 1.237 |
R-HSA-416572 | Sema4D induced cell migration and growth-cone collapse | 7.186509e-02 | 1.143 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 4.997840e-02 | 1.301 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 8.339120e-02 | 1.079 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 8.834550e-02 | 1.054 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 8.834550e-02 | 1.054 |
R-HSA-1358803 | Downregulation of ERBB2:ERBB3 signaling | 4.659614e-02 | 1.332 |
R-HSA-400685 | Sema4D in semaphorin signaling | 8.834550e-02 | 1.054 |
R-HSA-69481 | G2/M Checkpoints | 6.718602e-02 | 1.173 |
R-HSA-9933937 | Formation of the canonical BAF (cBAF) complex | 5.226903e-02 | 1.282 |
R-HSA-3270619 | IRF3-mediated induction of type I IFN | 5.509307e-02 | 1.259 |
R-HSA-9933946 | Formation of the embryonic stem cell BAF (esBAF) complex | 5.509307e-02 | 1.259 |
R-HSA-9933939 | Formation of the polybromo-BAF (pBAF) complex | 5.226903e-02 | 1.282 |
R-HSA-392517 | Rap1 signalling | 6.909014e-02 | 1.161 |
R-HSA-5673001 | RAF/MAP kinase cascade | 6.459332e-02 | 1.190 |
R-HSA-881907 | Gastrin-CREB signalling pathway via PKC and MAPK | 6.909014e-02 | 1.161 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 6.811011e-02 | 1.167 |
R-HSA-392499 | Metabolism of proteins | 4.968704e-02 | 1.304 |
R-HSA-9824443 | Parasitic Infection Pathways | 6.068206e-02 | 1.217 |
R-HSA-9658195 | Leishmania infection | 6.068206e-02 | 1.217 |
R-HSA-1834941 | STING mediated induction of host immune responses | 6.909014e-02 | 1.161 |
R-HSA-1643685 | Disease | 7.086449e-02 | 1.150 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 5.679904e-02 | 1.246 |
R-HSA-194138 | Signaling by VEGF | 6.554891e-02 | 1.183 |
R-HSA-8866652 | Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 9.377503e-02 | 1.028 |
R-HSA-5683057 | MAPK family signaling cascades | 9.625443e-02 | 1.017 |
R-HSA-9664565 | Signaling by ERBB2 KD Mutants | 9.917289e-02 | 1.004 |
R-HSA-9709570 | Impaired BRCA2 binding to RAD51 | 9.917289e-02 | 1.004 |
R-HSA-392154 | Nitric oxide stimulates guanylate cyclase | 9.917289e-02 | 1.004 |
R-HSA-450282 | MAPK targets/ Nuclear events mediated by MAP kinases | 9.917289e-02 | 1.004 |
R-HSA-1227990 | Signaling by ERBB2 in Cancer | 1.018600e-01 | 0.992 |
R-HSA-68962 | Activation of the pre-replicative complex | 1.018600e-01 | 0.992 |
R-HSA-1250196 | SHC1 events in ERBB2 signaling | 1.018600e-01 | 0.992 |
R-HSA-8863795 | Downregulation of ERBB2 signaling | 1.018600e-01 | 0.992 |
R-HSA-69190 | DNA strand elongation | 1.072107e-01 | 0.970 |
R-HSA-5685938 | HDR through Single Strand Annealing (SSA) | 1.098743e-01 | 0.959 |
R-HSA-5693568 | Resolution of D-loop Structures through Holliday Junction Intermediates | 1.098743e-01 | 0.959 |
R-HSA-176187 | Activation of ATR in response to replication stress | 1.098743e-01 | 0.959 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 1.120348e-01 | 0.951 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 1.120348e-01 | 0.951 |
R-HSA-390522 | Striated Muscle Contraction | 1.125302e-01 | 0.949 |
R-HSA-5693537 | Resolution of D-Loop Structures | 1.125302e-01 | 0.949 |
R-HSA-5696394 | DNA Damage Recognition in GG-NER | 1.125302e-01 | 0.949 |
R-HSA-9675136 | Diseases of DNA Double-Strand Break Repair | 1.151783e-01 | 0.939 |
R-HSA-9701190 | Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 1.151783e-01 | 0.939 |
R-HSA-5693616 | Presynaptic phase of homologous DNA pairing and strand exchange | 1.178186e-01 | 0.929 |
R-HSA-2559583 | Cellular Senescence | 1.188226e-01 | 0.925 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 1.197182e-01 | 0.922 |
R-HSA-8853659 | RET signaling | 1.204513e-01 | 0.919 |
R-HSA-5693579 | Homologous DNA Pairing and Strand Exchange | 1.256935e-01 | 0.901 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 1.347100e-01 | 0.871 |
R-HSA-9824585 | Regulation of MITF-M-dependent genes involved in pigmentation | 1.463581e-01 | 0.835 |
R-HSA-9675135 | Diseases of DNA repair | 1.489074e-01 | 0.827 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 1.539834e-01 | 0.813 |
R-HSA-418990 | Adherens junctions interactions | 1.583236e-01 | 0.800 |
R-HSA-912446 | Meiotic recombination | 1.615420e-01 | 0.792 |
R-HSA-72187 | mRNA 3'-end processing | 1.640468e-01 | 0.785 |
R-HSA-68949 | Orc1 removal from chromatin | 1.640468e-01 | 0.785 |
R-HSA-8866654 | E3 ubiquitin ligases ubiquitinate target proteins | 1.640468e-01 | 0.785 |
R-HSA-6794361 | Neurexins and neuroligins | 1.640468e-01 | 0.785 |
R-HSA-5250924 | B-WICH complex positively regulates rRNA expression | 1.665443e-01 | 0.778 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 1.813765e-01 | 0.741 |
R-HSA-9033241 | Peroxisomal protein import | 1.813765e-01 | 0.741 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 1.838232e-01 | 0.736 |
R-HSA-1227986 | Signaling by ERBB2 | 1.838232e-01 | 0.736 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 1.862628e-01 | 0.730 |
R-HSA-450294 | MAP kinase activation | 1.862628e-01 | 0.730 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 1.886953e-01 | 0.724 |
R-HSA-373755 | Semaphorin interactions | 1.911207e-01 | 0.719 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 1.911207e-01 | 0.719 |
R-HSA-8848021 | Signaling by PTK6 | 1.911207e-01 | 0.719 |
R-HSA-421270 | Cell-cell junction organization | 1.934136e-01 | 0.714 |
R-HSA-5693606 | DNA Double Strand Break Response | 2.007513e-01 | 0.697 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 2.007513e-01 | 0.697 |
R-HSA-69620 | Cell Cycle Checkpoints | 2.009936e-01 | 0.697 |
R-HSA-9734767 | Developmental Cell Lineages | 2.064307e-01 | 0.685 |
R-HSA-448424 | Interleukin-17 signaling | 2.079004e-01 | 0.682 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 2.079004e-01 | 0.682 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 2.102696e-01 | 0.677 |
R-HSA-168249 | Innate Immune System | 2.116793e-01 | 0.674 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 2.126317e-01 | 0.672 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 2.142468e-01 | 0.669 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 2.149870e-01 | 0.668 |
R-HSA-69052 | Switching of origins to a post-replicative state | 2.149870e-01 | 0.668 |
R-HSA-4086398 | Ca2+ pathway | 2.149870e-01 | 0.668 |
R-HSA-69473 | G2/M DNA damage checkpoint | 2.173353e-01 | 0.663 |
R-HSA-5689603 | UCH proteinases | 2.220114e-01 | 0.654 |
R-HSA-446728 | Cell junction organization | 2.228376e-01 | 0.652 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 2.239358e-01 | 0.650 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 2.335823e-01 | 0.632 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 2.358762e-01 | 0.627 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 2.358762e-01 | 0.627 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 2.404438e-01 | 0.619 |
R-HSA-1500620 | Meiosis | 2.427176e-01 | 0.615 |
R-HSA-6794362 | Protein-protein interactions at synapses | 2.427176e-01 | 0.615 |
R-HSA-8876198 | RAB GEFs exchange GTP for GDP on RABs | 2.449847e-01 | 0.611 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 2.472451e-01 | 0.607 |
R-HSA-8953854 | Metabolism of RNA | 2.507608e-01 | 0.601 |
R-HSA-156902 | Peptide chain elongation | 2.517462e-01 | 0.599 |
R-HSA-9954714 | PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | 2.584484e-01 | 0.588 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 2.606694e-01 | 0.584 |
R-HSA-156842 | Eukaryotic Translation Elongation | 2.628838e-01 | 0.580 |
R-HSA-1500931 | Cell-Cell communication | 2.648047e-01 | 0.577 |
R-HSA-68867 | Assembly of the pre-replicative complex | 2.650918e-01 | 0.577 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 2.672933e-01 | 0.573 |
R-HSA-9954716 | ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ri... | 2.694883e-01 | 0.569 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 2.716769e-01 | 0.566 |
R-HSA-72764 | Eukaryotic Translation Termination | 2.716769e-01 | 0.566 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 2.716769e-01 | 0.566 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 2.782042e-01 | 0.556 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 2.782042e-01 | 0.556 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 2.782042e-01 | 0.556 |
R-HSA-3214847 | HATs acetylate histones | 2.803672e-01 | 0.552 |
R-HSA-1474244 | Extracellular matrix organization | 2.814292e-01 | 0.551 |
R-HSA-2408557 | Selenocysteine synthesis | 2.846743e-01 | 0.546 |
R-HSA-9020702 | Interleukin-1 signaling | 2.846743e-01 | 0.546 |
R-HSA-9842860 | Regulation of endogenous retroelements | 2.868183e-01 | 0.542 |
R-HSA-192823 | Viral mRNA Translation | 2.889560e-01 | 0.539 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 2.910875e-01 | 0.536 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 2.953317e-01 | 0.530 |
R-HSA-5696398 | Nucleotide Excision Repair | 2.953317e-01 | 0.530 |
R-HSA-418346 | Platelet homeostasis | 2.974444e-01 | 0.527 |
R-HSA-1799339 | SRP-dependent cotranslational protein targeting to membrane | 2.995510e-01 | 0.524 |
R-HSA-69239 | Synthesis of DNA | 2.995510e-01 | 0.524 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 3.016513e-01 | 0.520 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 3.016513e-01 | 0.520 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 3.016513e-01 | 0.520 |
R-HSA-69002 | DNA Replication Pre-Initiation | 3.037455e-01 | 0.517 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 3.037455e-01 | 0.517 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 3.058336e-01 | 0.515 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 3.058336e-01 | 0.515 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 3.099913e-01 | 0.509 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 3.099913e-01 | 0.509 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 3.120610e-01 | 0.506 |
R-HSA-73894 | DNA Repair | 3.134938e-01 | 0.504 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 3.141246e-01 | 0.503 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 3.182337e-01 | 0.497 |
R-HSA-72613 | Eukaryotic Translation Initiation | 3.223186e-01 | 0.492 |
R-HSA-72737 | Cap-dependent Translation Initiation | 3.223186e-01 | 0.492 |
R-HSA-9007101 | Rab regulation of trafficking | 3.243521e-01 | 0.489 |
R-HSA-5693538 | Homology Directed Repair | 3.263796e-01 | 0.486 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 3.263796e-01 | 0.486 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 3.284012e-01 | 0.484 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 3.284012e-01 | 0.484 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 3.344303e-01 | 0.476 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 3.344303e-01 | 0.476 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 3.364282e-01 | 0.473 |
R-HSA-69206 | G1/S Transition | 3.423867e-01 | 0.465 |
R-HSA-114608 | Platelet degranulation | 3.463299e-01 | 0.461 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 3.482928e-01 | 0.458 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 3.522013e-01 | 0.453 |
R-HSA-1474165 | Reproduction | 3.541470e-01 | 0.451 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 3.599496e-01 | 0.444 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 3.676072e-01 | 0.435 |
R-HSA-9948299 | Ribosome-associated quality control | 3.714022e-01 | 0.430 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 3.882058e-01 | 0.411 |
R-HSA-69242 | S Phase | 3.918798e-01 | 0.407 |
R-HSA-166520 | Signaling by NTRKs | 3.918798e-01 | 0.407 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 3.918798e-01 | 0.407 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 3.991630e-01 | 0.399 |
R-HSA-446652 | Interleukin-1 family signaling | 3.991630e-01 | 0.399 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 4.009705e-01 | 0.397 |
R-HSA-9609507 | Protein localization | 4.009705e-01 | 0.397 |
R-HSA-69306 | DNA Replication | 4.009705e-01 | 0.397 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 4.045694e-01 | 0.393 |
R-HSA-9711097 | Cellular response to starvation | 4.099280e-01 | 0.387 |
R-HSA-5633007 | Regulation of TP53 Activity | 4.134742e-01 | 0.384 |
R-HSA-2408522 | Selenoamino acid metabolism | 4.205041e-01 | 0.376 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 4.326084e-01 | 0.364 |
R-HSA-168255 | Influenza Infection | 4.478078e-01 | 0.349 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 4.626083e-01 | 0.335 |
R-HSA-168898 | Toll-like Receptor Cascades | 4.674550e-01 | 0.330 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 4.722588e-01 | 0.326 |
R-HSA-376176 | Signaling by ROBO receptors | 4.864171e-01 | 0.313 |
R-HSA-72172 | mRNA Splicing | 4.895125e-01 | 0.310 |
R-HSA-397014 | Muscle contraction | 5.017126e-01 | 0.300 |
R-HSA-72312 | rRNA processing | 5.309773e-01 | 0.275 |
R-HSA-3247509 | Chromatin modifying enzymes | 5.338094e-01 | 0.273 |
R-HSA-4839726 | Chromatin organization | 5.545236e-01 | 0.256 |
R-HSA-5688426 | Deubiquitination | 5.625545e-01 | 0.250 |
R-HSA-416476 | G alpha (q) signalling events | 5.743357e-01 | 0.241 |
R-HSA-449147 | Signaling by Interleukins | 5.788036e-01 | 0.237 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 5.870617e-01 | 0.231 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 5.969736e-01 | 0.224 |
R-HSA-1257604 | PIP3 activates AKT signaling | 6.125858e-01 | 0.213 |
R-HSA-195721 | Signaling by WNT | 6.161036e-01 | 0.210 |
R-HSA-212165 | Epigenetic regulation of gene expression | 6.442277e-01 | 0.191 |
R-HSA-9006925 | Intracellular signaling by second messengers | 6.642429e-01 | 0.178 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 7.046551e-01 | 0.152 |
R-HSA-74160 | Gene expression (Transcription) | 7.231640e-01 | 0.141 |
R-HSA-9709957 | Sensory Perception | 7.346331e-01 | 0.134 |
R-HSA-72766 | Translation | 7.434583e-01 | 0.129 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 7.631337e-01 | 0.117 |
R-HSA-6798695 | Neutrophil degranulation | 7.645844e-01 | 0.117 |
R-HSA-73857 | RNA Polymerase II Transcription | 7.662112e-01 | 0.116 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 7.703009e-01 | 0.113 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 8.568068e-01 | 0.067 |
R-HSA-212436 | Generic Transcription Pathway | 8.602360e-01 | 0.065 |
R-HSA-388396 | GPCR downstream signalling | 9.119844e-01 | 0.040 |
R-HSA-372790 | Signaling by GPCR | 9.322008e-01 | 0.030 |
R-HSA-1430728 | Metabolism | 9.999559e-01 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
BUB1 |
0.642 | 0.324 | -5 | 0.655 |
CAMKK2 |
0.641 | 0.219 | -2 | 0.697 |
P38B |
0.640 | 0.177 | 1 | 0.633 |
NEK1 |
0.636 | 0.118 | 1 | 0.542 |
CAMKK1 |
0.634 | 0.148 | -2 | 0.706 |
P38D |
0.633 | 0.182 | 1 | 0.556 |
LKB1 |
0.632 | 0.147 | -3 | 0.421 |
P38A |
0.631 | 0.151 | 1 | 0.644 |
MPSK1 |
0.631 | 0.161 | 1 | 0.559 |
ERK5 |
0.628 | 0.249 | 1 | 0.699 |
JNK2 |
0.628 | 0.127 | 1 | 0.567 |
VRK2 |
0.627 | -0.017 | 1 | 0.648 |
AAK1 |
0.626 | 0.057 | 1 | 0.457 |
GAK |
0.626 | -0.056 | 1 | 0.601 |
VRK1 |
0.625 | -0.071 | 2 | 0.512 |
BIKE |
0.624 | 0.018 | 1 | 0.520 |
LRRK2 |
0.624 | -0.052 | 2 | 0.493 |
NEK4 |
0.621 | 0.039 | 1 | 0.512 |
JNK3 |
0.620 | 0.101 | 1 | 0.616 |
TNIK |
0.620 | 0.000 | 3 | 0.509 |
NEK5 |
0.620 | 0.031 | 1 | 0.565 |
PBK |
0.620 | 0.041 | 1 | 0.542 |
PKR |
0.620 | -0.014 | 1 | 0.611 |
MYO3B |
0.618 | -0.005 | 2 | 0.518 |
TAK1 |
0.618 | -0.092 | 1 | 0.507 |
ASK1 |
0.617 | -0.052 | 1 | 0.478 |
EEF2K |
0.617 | -0.043 | 3 | 0.422 |
MAK |
0.615 | 0.106 | -2 | 0.507 |
NLK |
0.613 | 0.114 | 1 | 0.665 |
PRP4 |
0.613 | 0.065 | -3 | 0.328 |
HGK |
0.612 | -0.036 | 3 | 0.497 |
MST2 |
0.612 | -0.057 | 1 | 0.512 |
MAP3K15 |
0.612 | -0.018 | 1 | 0.477 |
PDK1 |
0.612 | -0.069 | 1 | 0.552 |
KHS1 |
0.612 | -0.026 | 1 | 0.495 |
ERK1 |
0.611 | 0.140 | 1 | 0.602 |
DYRK2 |
0.611 | 0.147 | 1 | 0.656 |
HIPK1 |
0.611 | 0.118 | 1 | 0.658 |
PASK |
0.611 | 0.035 | -3 | 0.439 |
HIPK4 |
0.610 | 0.230 | 1 | 0.671 |
P38G |
0.610 | 0.117 | 1 | 0.542 |
NIK |
0.610 | -0.070 | -3 | 0.402 |
LATS1 |
0.609 | 0.106 | -3 | 0.463 |
MST1 |
0.609 | -0.069 | 1 | 0.503 |
ERK7 |
0.609 | 0.046 | 2 | 0.366 |
MEK1 |
0.609 | -0.130 | 2 | 0.473 |
MINK |
0.609 | -0.089 | 1 | 0.485 |
MEKK6 |
0.608 | -0.052 | 1 | 0.510 |
CAMLCK |
0.608 | -0.040 | -2 | 0.563 |
MOK |
0.608 | 0.074 | 1 | 0.686 |
GCK |
0.608 | -0.054 | 1 | 0.482 |
MYO3A |
0.608 | -0.073 | 1 | 0.521 |
BRAF |
0.607 | -0.104 | -4 | 0.638 |
MLK2 |
0.607 | 0.050 | 2 | 0.511 |
TAO2 |
0.607 | -0.092 | 2 | 0.535 |
JNK1 |
0.607 | 0.092 | 1 | 0.592 |
HPK1 |
0.607 | -0.063 | 1 | 0.473 |
DAPK2 |
0.606 | -0.061 | -3 | 0.406 |
MOS |
0.606 | 0.057 | 1 | 0.676 |
ERK2 |
0.606 | 0.103 | 1 | 0.633 |
KHS2 |
0.606 | -0.042 | 1 | 0.490 |
LOK |
0.606 | -0.007 | -2 | 0.564 |
ALPHAK3 |
0.606 | -0.065 | -1 | 0.582 |
BMPR2 |
0.605 | -0.117 | -2 | 0.554 |
MEK2 |
0.605 | -0.113 | 2 | 0.440 |
MST3 |
0.604 | -0.058 | 2 | 0.584 |
YSK1 |
0.604 | -0.068 | 2 | 0.513 |
CDK18 |
0.604 | 0.169 | 1 | 0.587 |
HIPK3 |
0.604 | 0.110 | 1 | 0.632 |
CDK16 |
0.603 | 0.140 | 1 | 0.582 |
CAMK1B |
0.603 | -0.052 | -3 | 0.385 |
PRPK |
0.603 | -0.049 | -1 | 0.651 |
MEKK1 |
0.602 | -0.069 | 1 | 0.519 |
ALK4 |
0.602 | -0.028 | -2 | 0.467 |
ICK |
0.602 | 0.014 | -3 | 0.405 |
CDK14 |
0.602 | 0.105 | 1 | 0.602 |
CDKL1 |
0.602 | -0.016 | -3 | 0.356 |
MEK5 |
0.602 | -0.179 | 2 | 0.473 |
NEK11 |
0.601 | -0.113 | 1 | 0.490 |
DYRK4 |
0.601 | 0.136 | 1 | 0.605 |
MEKK2 |
0.601 | -0.153 | 2 | 0.478 |
ATR |
0.600 | -0.013 | 1 | 0.597 |
CDK5 |
0.600 | 0.109 | 1 | 0.625 |
ALK2 |
0.600 | -0.012 | -2 | 0.469 |
ROCK2 |
0.600 | -0.027 | -3 | 0.346 |
DMPK1 |
0.599 | -0.055 | -3 | 0.313 |
OSR1 |
0.599 | -0.075 | 2 | 0.454 |
CHAK2 |
0.599 | 0.054 | -1 | 0.638 |
NEK2 |
0.599 | 0.005 | 2 | 0.500 |
NEK8 |
0.598 | -0.112 | 2 | 0.500 |
TAO3 |
0.598 | -0.076 | 1 | 0.521 |
TGFBR1 |
0.598 | -0.006 | -2 | 0.440 |
CDK17 |
0.598 | 0.134 | 1 | 0.559 |
NEK9 |
0.597 | 0.005 | 2 | 0.510 |
YSK4 |
0.596 | -0.072 | 1 | 0.478 |
CDKL5 |
0.596 | 0.035 | -3 | 0.364 |
CDK4 |
0.595 | 0.078 | 1 | 0.587 |
SKMLCK |
0.595 | -0.020 | -2 | 0.551 |
DLK |
0.595 | -0.127 | 1 | 0.553 |
NEK3 |
0.594 | -0.040 | 1 | 0.487 |
TTK |
0.594 | -0.141 | -2 | 0.457 |
DYRK1A |
0.594 | 0.061 | 1 | 0.651 |
HASPIN |
0.594 | 0.002 | -1 | 0.541 |
HIPK2 |
0.594 | 0.147 | 1 | 0.595 |
ANKRD3 |
0.593 | -0.160 | 1 | 0.563 |
TSSK2 |
0.593 | -0.012 | -5 | 0.696 |
CDK6 |
0.592 | 0.067 | 1 | 0.582 |
CLK3 |
0.592 | 0.122 | 1 | 0.754 |
CHK1 |
0.592 | 0.026 | -3 | 0.398 |
PERK |
0.592 | -0.050 | -2 | 0.509 |
SMMLCK |
0.591 | -0.107 | -3 | 0.355 |
STLK3 |
0.591 | -0.166 | 1 | 0.453 |
DAPK3 |
0.591 | -0.077 | -3 | 0.340 |
BMPR1B |
0.591 | 0.004 | 1 | 0.577 |
GRK6 |
0.590 | -0.016 | 1 | 0.636 |
GRK5 |
0.590 | -0.036 | -3 | 0.403 |
CDK1 |
0.590 | 0.087 | 1 | 0.600 |
GRK7 |
0.590 | 0.039 | 1 | 0.665 |
IRAK4 |
0.590 | -0.062 | 1 | 0.570 |
CDK3 |
0.589 | 0.094 | 1 | 0.571 |
DYRK1B |
0.589 | 0.090 | 1 | 0.620 |
ZAK |
0.589 | -0.124 | 1 | 0.482 |
CDK9 |
0.588 | 0.096 | 1 | 0.609 |
CDK7 |
0.588 | 0.130 | 1 | 0.604 |
PINK1 |
0.588 | -0.055 | 1 | 0.639 |
TAO1 |
0.588 | -0.075 | 1 | 0.445 |
SLK |
0.587 | -0.043 | -2 | 0.501 |
CDK13 |
0.587 | 0.100 | 1 | 0.603 |
CRIK |
0.587 | -0.032 | -3 | 0.321 |
DNAPK |
0.586 | -0.018 | 1 | 0.477 |
CDK8 |
0.586 | 0.122 | 1 | 0.584 |
CDK2 |
0.586 | 0.039 | 1 | 0.665 |
PDHK1 |
0.585 | -0.067 | 1 | 0.586 |
PDHK4 |
0.585 | -0.127 | 1 | 0.606 |
DYRK3 |
0.585 | 0.042 | 1 | 0.652 |
RAF1 |
0.585 | -0.120 | 1 | 0.560 |
CDC7 |
0.585 | 0.087 | 1 | 0.637 |
WNK4 |
0.584 | -0.107 | -2 | 0.584 |
SMG1 |
0.584 | -0.012 | 1 | 0.560 |
ROCK1 |
0.584 | -0.062 | -3 | 0.297 |
MASTL |
0.584 | -0.146 | -2 | 0.559 |
AMPKA1 |
0.584 | -0.029 | -3 | 0.407 |
MLK3 |
0.583 | -0.007 | 2 | 0.522 |
ACVR2B |
0.583 | -0.058 | -2 | 0.437 |
WNK1 |
0.583 | -0.061 | -2 | 0.582 |
GSK3B |
0.582 | -0.005 | 4 | 0.356 |
TSSK1 |
0.582 | -0.009 | -3 | 0.433 |
HRI |
0.582 | -0.142 | -2 | 0.500 |
TLK2 |
0.582 | -0.057 | 1 | 0.525 |
DSTYK |
0.582 | -0.028 | 2 | 0.581 |
CAMK2G |
0.582 | -0.115 | 2 | 0.413 |
CDK19 |
0.581 | 0.146 | 1 | 0.562 |
NUAK2 |
0.581 | -0.032 | -3 | 0.385 |
CDK12 |
0.581 | 0.081 | 1 | 0.584 |
MLK1 |
0.581 | -0.105 | 2 | 0.534 |
GSK3A |
0.581 | 0.014 | 4 | 0.364 |
HUNK |
0.581 | -0.058 | 2 | 0.508 |
PIM1 |
0.580 | -0.047 | -3 | 0.331 |
MEKK3 |
0.580 | -0.246 | 1 | 0.505 |
CLK4 |
0.579 | 0.020 | -3 | 0.308 |
MARK4 |
0.579 | -0.025 | 4 | 0.671 |
PIM2 |
0.579 | -0.051 | -3 | 0.311 |
MRCKB |
0.579 | -0.058 | -3 | 0.296 |
PRKD1 |
0.579 | 0.111 | -3 | 0.436 |
PKN3 |
0.579 | -0.064 | -3 | 0.367 |
CDK10 |
0.579 | 0.073 | 1 | 0.590 |
MAPKAPK3 |
0.579 | 0.038 | -3 | 0.358 |
GRK1 |
0.578 | 0.065 | -2 | 0.511 |
ACVR2A |
0.578 | -0.076 | -2 | 0.410 |
PIM3 |
0.578 | -0.016 | -3 | 0.391 |
CHAK1 |
0.578 | -0.068 | 2 | 0.465 |
RIPK1 |
0.578 | -0.162 | 1 | 0.550 |
NEK6 |
0.578 | 0.051 | -2 | 0.541 |
SRPK1 |
0.578 | 0.030 | -3 | 0.324 |
DAPK1 |
0.577 | -0.098 | -3 | 0.323 |
PKCD |
0.577 | -0.042 | 2 | 0.506 |
DCAMKL1 |
0.577 | -0.073 | -3 | 0.346 |
SBK |
0.577 | -0.016 | -3 | 0.205 |
AMPKA2 |
0.576 | -0.020 | -3 | 0.385 |
TLK1 |
0.576 | -0.112 | -2 | 0.460 |
BMPR1A |
0.576 | -0.036 | 1 | 0.569 |
P70S6KB |
0.576 | -0.048 | -3 | 0.336 |
COT |
0.576 | -0.050 | 2 | 0.539 |
SGK3 |
0.576 | -0.046 | -3 | 0.337 |
RIPK3 |
0.575 | -0.108 | 3 | 0.413 |
PKN2 |
0.575 | -0.079 | -3 | 0.375 |
MTOR |
0.574 | -0.061 | 1 | 0.605 |
CAMK2D |
0.574 | -0.058 | -3 | 0.398 |
PRKD3 |
0.574 | 0.005 | -3 | 0.325 |
PRKD2 |
0.574 | 0.076 | -3 | 0.372 |
MRCKA |
0.573 | -0.077 | -3 | 0.302 |
NEK7 |
0.573 | -0.063 | -3 | 0.465 |
DCAMKL2 |
0.572 | -0.096 | -3 | 0.358 |
PKCZ |
0.572 | -0.043 | 2 | 0.497 |
PAK6 |
0.572 | 0.108 | -2 | 0.503 |
MELK |
0.572 | -0.062 | -3 | 0.364 |
MYLK4 |
0.571 | -0.083 | -2 | 0.505 |
PKCA |
0.571 | -0.015 | 2 | 0.502 |
CLK1 |
0.571 | 0.021 | -3 | 0.305 |
RSK2 |
0.570 | -0.008 | -3 | 0.348 |
AKT2 |
0.570 | -0.042 | -3 | 0.274 |
PLK1 |
0.570 | -0.169 | -2 | 0.504 |
PKCB |
0.569 | -0.015 | 2 | 0.528 |
IRE1 |
0.569 | -0.069 | 1 | 0.577 |
ULK2 |
0.569 | -0.108 | 2 | 0.427 |
SSTK |
0.569 | -0.045 | 4 | 0.633 |
MST4 |
0.569 | -0.082 | 2 | 0.542 |
CHK2 |
0.568 | -0.068 | -3 | 0.233 |
SRPK3 |
0.568 | -0.022 | -3 | 0.281 |
NIM1 |
0.568 | -0.045 | 3 | 0.454 |
PAK1 |
0.568 | -0.054 | -2 | 0.504 |
IRAK1 |
0.567 | -0.164 | -1 | 0.581 |
CAMK1D |
0.567 | -0.074 | -3 | 0.259 |
CLK2 |
0.566 | 0.048 | -3 | 0.293 |
P90RSK |
0.566 | -0.034 | -3 | 0.340 |
MAPKAPK2 |
0.566 | 0.038 | -3 | 0.323 |
ATM |
0.566 | -0.078 | 1 | 0.553 |
MNK2 |
0.566 | 0.004 | -2 | 0.528 |
MLK4 |
0.565 | -0.130 | 2 | 0.464 |
IKKE |
0.565 | -0.022 | 1 | 0.444 |
TTBK2 |
0.565 | -0.092 | 2 | 0.432 |
KIS |
0.565 | 0.201 | 1 | 0.634 |
DRAK1 |
0.565 | -0.140 | 1 | 0.456 |
CAMK2A |
0.565 | -0.046 | 2 | 0.427 |
TBK1 |
0.564 | -0.059 | 1 | 0.454 |
PKCH |
0.564 | -0.076 | 2 | 0.488 |
PAK3 |
0.564 | -0.066 | -2 | 0.523 |
SGK1 |
0.563 | -0.063 | -3 | 0.224 |
MARK2 |
0.563 | -0.054 | 4 | 0.623 |
PKCI |
0.563 | -0.064 | 2 | 0.481 |
QIK |
0.563 | -0.096 | -3 | 0.390 |
PLK3 |
0.563 | -0.143 | 2 | 0.395 |
CAMK1A |
0.563 | -0.060 | -3 | 0.251 |
IRE2 |
0.563 | -0.100 | 2 | 0.433 |
PAK2 |
0.562 | -0.098 | -2 | 0.502 |
STK33 |
0.562 | -0.111 | 2 | 0.324 |
PKCE |
0.562 | -0.047 | 2 | 0.523 |
CAMK2B |
0.562 | -0.068 | 2 | 0.387 |
QSK |
0.562 | -0.038 | 4 | 0.641 |
PKG2 |
0.562 | -0.012 | -2 | 0.453 |
NDR1 |
0.561 | -0.008 | -3 | 0.390 |
IKKB |
0.561 | -0.052 | -2 | 0.570 |
WNK3 |
0.561 | -0.197 | 1 | 0.547 |
PLK2 |
0.561 | -0.091 | -3 | 0.298 |
AURC |
0.560 | 0.029 | -2 | 0.417 |
MARK3 |
0.560 | -0.038 | 4 | 0.629 |
AKT1 |
0.560 | -0.054 | -3 | 0.296 |
RSK3 |
0.560 | -0.020 | -3 | 0.322 |
GRK2 |
0.559 | -0.112 | -2 | 0.418 |
LATS2 |
0.559 | 0.075 | -5 | 0.729 |
PKCG |
0.559 | -0.048 | 2 | 0.522 |
IKKA |
0.559 | 0.021 | -2 | 0.555 |
SRPK2 |
0.559 | 0.014 | -3 | 0.254 |
NDR2 |
0.558 | 0.096 | -3 | 0.437 |
CAMK4 |
0.558 | -0.126 | -3 | 0.356 |
GRK4 |
0.558 | -0.092 | -2 | 0.480 |
CAMK1G |
0.557 | -0.101 | -3 | 0.301 |
PDHK3_TYR |
0.557 | 0.184 | 4 | 0.669 |
MARK1 |
0.557 | -0.085 | 4 | 0.629 |
AURB |
0.557 | -0.043 | -2 | 0.415 |
MNK1 |
0.556 | -0.041 | -2 | 0.535 |
P70S6K |
0.556 | -0.058 | -3 | 0.279 |
PKACG |
0.555 | -0.041 | -2 | 0.499 |
PKACB |
0.554 | -0.012 | -2 | 0.438 |
RIPK2 |
0.554 | -0.210 | 1 | 0.431 |
PKCT |
0.554 | -0.079 | 2 | 0.480 |
ULK1 |
0.554 | -0.116 | -3 | 0.412 |
CK1D |
0.554 | -0.060 | -3 | 0.218 |
PLK4 |
0.554 | -0.088 | 2 | 0.280 |
MSK1 |
0.554 | -0.063 | -3 | 0.313 |
TGFBR2 |
0.553 | -0.098 | -2 | 0.424 |
RSK4 |
0.552 | -0.036 | -3 | 0.341 |
NUAK1 |
0.552 | -0.060 | -3 | 0.336 |
BCKDK |
0.551 | -0.101 | -1 | 0.614 |
MSK2 |
0.550 | -0.076 | -3 | 0.315 |
SIK |
0.549 | -0.068 | -3 | 0.314 |
ABL2 |
0.549 | 0.163 | -1 | 0.640 |
TTBK1 |
0.549 | -0.094 | 2 | 0.366 |
LIMK2_TYR |
0.548 | 0.106 | -3 | 0.461 |
YANK3 |
0.548 | -0.075 | 2 | 0.200 |
PKN1 |
0.548 | -0.076 | -3 | 0.297 |
MAPKAPK5 |
0.547 | -0.055 | -3 | 0.274 |
FAM20C |
0.547 | -0.028 | 2 | 0.315 |
ABL1 |
0.547 | 0.158 | -1 | 0.637 |
PKACA |
0.546 | -0.029 | -2 | 0.401 |
GCN2 |
0.546 | -0.079 | 2 | 0.430 |
CK1A2 |
0.546 | -0.072 | -3 | 0.209 |
PKMYT1_TYR |
0.545 | 0.019 | 3 | 0.538 |
AKT3 |
0.544 | -0.050 | -3 | 0.251 |
PHKG1 |
0.544 | -0.064 | -3 | 0.369 |
EPHA6 |
0.544 | 0.042 | -1 | 0.646 |
MAP2K4_TYR |
0.543 | -0.010 | -1 | 0.672 |
TESK1_TYR |
0.542 | 0.011 | 3 | 0.551 |
CK2A2 |
0.542 | -0.051 | 1 | 0.482 |
CK1E |
0.541 | -0.068 | -3 | 0.239 |
PDHK4_TYR |
0.541 | 0.010 | 2 | 0.471 |
EPHB4 |
0.540 | 0.049 | -1 | 0.620 |
JAK2 |
0.540 | 0.047 | 1 | 0.566 |
PAK5 |
0.539 | -0.002 | -2 | 0.435 |
YANK2 |
0.539 | -0.088 | 2 | 0.213 |
SNRK |
0.538 | -0.176 | 2 | 0.315 |
MAP2K6_TYR |
0.538 | -0.092 | -1 | 0.674 |
MAP2K7_TYR |
0.537 | -0.145 | 2 | 0.476 |
AURA |
0.537 | -0.061 | -2 | 0.366 |
TNK2 |
0.537 | 0.018 | 3 | 0.478 |
GRK3 |
0.537 | -0.104 | -2 | 0.368 |
EPHA4 |
0.536 | 0.027 | 2 | 0.419 |
TYK2 |
0.535 | -0.042 | 1 | 0.579 |
LIMK1_TYR |
0.535 | -0.050 | 2 | 0.484 |
PAK4 |
0.534 | 0.019 | -2 | 0.420 |
BMPR2_TYR |
0.534 | -0.081 | -1 | 0.646 |
CK2A1 |
0.533 | -0.064 | 1 | 0.451 |
TNNI3K_TYR |
0.533 | 0.025 | 1 | 0.585 |
RET |
0.533 | -0.054 | 1 | 0.580 |
MST1R |
0.532 | -0.034 | 3 | 0.517 |
PINK1_TYR |
0.532 | -0.149 | 1 | 0.622 |
EPHB3 |
0.531 | 0.018 | -1 | 0.606 |
PRKX |
0.531 | -0.025 | -3 | 0.290 |
EPHB1 |
0.531 | -0.007 | 1 | 0.614 |
PDHK1_TYR |
0.531 | -0.142 | -1 | 0.677 |
CSF1R |
0.530 | -0.023 | 3 | 0.498 |
TNK1 |
0.530 | -0.009 | 3 | 0.483 |
PHKG2 |
0.530 | -0.100 | -3 | 0.336 |
BRSK2 |
0.530 | -0.121 | -3 | 0.360 |
DDR1 |
0.530 | -0.099 | 4 | 0.613 |
TYRO3 |
0.530 | -0.050 | 3 | 0.474 |
FER |
0.529 | -0.041 | 1 | 0.673 |
EPHB2 |
0.528 | 0.003 | -1 | 0.606 |
JAK1 |
0.528 | 0.010 | 1 | 0.488 |
SRMS |
0.527 | -0.033 | 1 | 0.639 |
ROS1 |
0.527 | -0.077 | 3 | 0.431 |
BRSK1 |
0.527 | -0.119 | -3 | 0.335 |
MERTK |
0.526 | -0.008 | 3 | 0.502 |
FGR |
0.524 | -0.061 | 1 | 0.611 |
AXL |
0.523 | -0.045 | 3 | 0.482 |
HCK |
0.523 | -0.056 | -1 | 0.616 |
PTK2B |
0.523 | 0.038 | -1 | 0.589 |
TEK |
0.522 | -0.078 | 3 | 0.412 |
EPHA3 |
0.522 | -0.031 | 2 | 0.387 |
FRK |
0.522 | -0.006 | -1 | 0.645 |
EPHA7 |
0.521 | -0.030 | 2 | 0.412 |
KIT |
0.520 | -0.076 | 3 | 0.499 |
FGFR1 |
0.520 | -0.100 | 3 | 0.453 |
KDR |
0.520 | -0.094 | 3 | 0.453 |
FGFR2 |
0.520 | -0.118 | 3 | 0.470 |
YES1 |
0.520 | -0.096 | -1 | 0.625 |
LCK |
0.519 | -0.048 | -1 | 0.617 |
ITK |
0.519 | -0.042 | -1 | 0.593 |
JAK3 |
0.518 | -0.113 | 1 | 0.542 |
BLK |
0.518 | -0.052 | -1 | 0.623 |
NEK10_TYR |
0.518 | -0.067 | 1 | 0.425 |
PDGFRA |
0.517 | -0.092 | 3 | 0.482 |
EPHA5 |
0.517 | -0.015 | 2 | 0.395 |
FLT3 |
0.517 | -0.121 | 3 | 0.475 |
TXK |
0.517 | -0.051 | 1 | 0.559 |
MET |
0.516 | -0.041 | 3 | 0.518 |
LTK |
0.516 | -0.084 | 3 | 0.446 |
MUSK |
0.516 | 0.028 | 1 | 0.579 |
PKG1 |
0.516 | -0.072 | -2 | 0.379 |
PDGFRB |
0.515 | -0.124 | 3 | 0.484 |
EPHA1 |
0.515 | -0.047 | 3 | 0.495 |
BTK |
0.514 | -0.101 | -1 | 0.573 |
ALK |
0.513 | -0.094 | 3 | 0.406 |
NTRK1 |
0.513 | -0.120 | -1 | 0.613 |
ERBB2 |
0.512 | -0.089 | 1 | 0.616 |
FYN |
0.512 | -0.065 | -1 | 0.569 |
EPHA8 |
0.512 | -0.038 | -1 | 0.578 |
CK1G3 |
0.511 | -0.097 | -3 | 0.138 |
DDR2 |
0.511 | -0.083 | 3 | 0.399 |
CSK |
0.510 | -0.078 | 2 | 0.417 |
BMX |
0.510 | -0.078 | -1 | 0.515 |
EGFR |
0.510 | -0.024 | 1 | 0.582 |
MATK |
0.510 | -0.068 | -1 | 0.574 |
SYK |
0.510 | -0.000 | -1 | 0.565 |
FGFR3 |
0.510 | -0.128 | 3 | 0.446 |
TEC |
0.510 | -0.084 | -1 | 0.539 |
LYN |
0.510 | -0.074 | 3 | 0.423 |
WEE1_TYR |
0.509 | -0.111 | -1 | 0.542 |
CK1G1 |
0.509 | -0.087 | -3 | 0.212 |
EPHA2 |
0.509 | -0.022 | -1 | 0.568 |
PTK6 |
0.509 | -0.125 | -1 | 0.548 |
NTRK3 |
0.508 | -0.084 | -1 | 0.572 |
INSRR |
0.508 | -0.189 | 3 | 0.411 |
PTK2 |
0.508 | -0.043 | -1 | 0.564 |
FLT4 |
0.507 | -0.148 | 3 | 0.441 |
FLT1 |
0.505 | -0.131 | -1 | 0.640 |
NTRK2 |
0.504 | -0.140 | 3 | 0.447 |
SRC |
0.504 | -0.089 | -1 | 0.578 |
ZAP70 |
0.503 | 0.045 | -1 | 0.496 |
ERBB4 |
0.503 | -0.019 | 1 | 0.618 |
FGFR4 |
0.500 | -0.099 | -1 | 0.587 |
INSR |
0.500 | -0.151 | 3 | 0.404 |
CK1G2 |
0.495 | -0.095 | -3 | 0.173 |
FES |
0.488 | -0.102 | -1 | 0.493 |
IGF1R |
0.485 | -0.157 | 3 | 0.363 |
CK1A |
0.484 | -0.089 | -3 | 0.165 |