Motif 697 (n=61)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
O00512 | BCL9 | T172 | psp | B-cell CLL/lymphoma 9 protein (B-cell lymphoma 9 protein) (Bcl-9) (Protein legless homolog) | Involved in signal transduction through the Wnt pathway. Promotes beta-catenin's transcriptional activity (By similarity). {ECO:0000250, ECO:0000269|PubMed:11955446}. |
O15234 | CASC3 | S373 | ochoa | Protein CASC3 (Cancer susceptibility candidate gene 3 protein) (Metastatic lymph node gene 51 protein) (MLN 51) (Protein barentsz) (Btz) | Required for pre-mRNA splicing as component of the spliceosome (PubMed:28502770, PubMed:29301961). Core component of the splicing-dependent multiprotein exon junction complex (EJC) deposited at splice junctions on mRNAs. The EJC is a dynamic structure consisting of core proteins and several peripheral nuclear and cytoplasmic associated factors that join the complex only transiently either during EJC assembly or during subsequent mRNA metabolism. The EJC marks the position of the exon-exon junction in the mature mRNA for the gene expression machinery and the core components remain bound to spliced mRNAs throughout all stages of mRNA metabolism thereby influencing downstream processes including nuclear mRNA export, subcellular mRNA localization, translation efficiency and nonsense-mediated mRNA decay (NMD). Stimulates the ATPase and RNA-helicase activities of EIF4A3. Plays a role in the stress response by participating in cytoplasmic stress granules assembly and by favoring cell recovery following stress. Component of the dendritic ribonucleoprotein particles (RNPs) in hippocampal neurons. May play a role in mRNA transport. Binds spliced mRNA in sequence-independent manner, 20-24 nucleotides upstream of mRNA exon-exon junctions. Binds poly(G) and poly(U) RNA homomer. {ECO:0000269|PubMed:17375189, ECO:0000269|PubMed:17652158, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961}. |
O75962 | TRIO | S2417 | ochoa | Triple functional domain protein (EC 2.7.11.1) (PTPRF-interacting protein) | Guanine nucleotide exchange factor (GEF) for RHOA and RAC1 GTPases (PubMed:22155786, PubMed:27418539, PubMed:8643598). Involved in coordinating actin remodeling, which is necessary for cell migration and growth (PubMed:10341202, PubMed:22155786). Plays a key role in the regulation of neurite outgrowth and lamellipodia formation (PubMed:32109419). In developing hippocampal neurons, limits dendrite formation, without affecting the establishment of axon polarity. Once dendrites are formed, involved in the control of synaptic function by regulating the endocytosis of AMPA-selective glutamate receptors (AMPARs) at CA1 excitatory synapses (By similarity). May act as a regulator of adipogenesis (By similarity). {ECO:0000250|UniProtKB:F1M0Z1, ECO:0000269|PubMed:10341202, ECO:0000269|PubMed:22155786, ECO:0000269|PubMed:27418539, ECO:0000269|PubMed:32109419, ECO:0000269|PubMed:8643598}. |
O76021 | RSL1D1 | S392 | ochoa | Ribosomal L1 domain-containing protein 1 (CATX-11) (Cellular senescence-inhibited gene protein) (Protein PBK1) | Regulates cellular senescence through inhibition of PTEN translation. Acts as a pro-apoptotic regulator in response to DNA damage. {ECO:0000269|PubMed:18678645, ECO:0000269|PubMed:22419112}. |
O76021 | RSL1D1 | S443 | ochoa | Ribosomal L1 domain-containing protein 1 (CATX-11) (Cellular senescence-inhibited gene protein) (Protein PBK1) | Regulates cellular senescence through inhibition of PTEN translation. Acts as a pro-apoptotic regulator in response to DNA damage. {ECO:0000269|PubMed:18678645, ECO:0000269|PubMed:22419112}. |
P07197 | NEFM | S620 | ochoa | Neurofilament medium polypeptide (NF-M) (160 kDa neurofilament protein) (Neurofilament 3) (Neurofilament triplet M protein) | Neurofilaments usually contain three intermediate filament proteins: NEFL, NEFM, and NEFH which are involved in the maintenance of neuronal caliber. May additionally cooperate with the neuronal intermediate filament proteins PRPH and INA to form neuronal filamentous networks (By similarity). {ECO:0000250|UniProtKB:P08553}. |
P07197 | NEFM | S633 | ochoa | Neurofilament medium polypeptide (NF-M) (160 kDa neurofilament protein) (Neurofilament 3) (Neurofilament triplet M protein) | Neurofilaments usually contain three intermediate filament proteins: NEFL, NEFM, and NEFH which are involved in the maintenance of neuronal caliber. May additionally cooperate with the neuronal intermediate filament proteins PRPH and INA to form neuronal filamentous networks (By similarity). {ECO:0000250|UniProtKB:P08553}. |
P07197 | NEFM | S672 | ochoa | Neurofilament medium polypeptide (NF-M) (160 kDa neurofilament protein) (Neurofilament 3) (Neurofilament triplet M protein) | Neurofilaments usually contain three intermediate filament proteins: NEFL, NEFM, and NEFH which are involved in the maintenance of neuronal caliber. May additionally cooperate with the neuronal intermediate filament proteins PRPH and INA to form neuronal filamentous networks (By similarity). {ECO:0000250|UniProtKB:P08553}. |
P07197 | NEFM | S736 | ochoa | Neurofilament medium polypeptide (NF-M) (160 kDa neurofilament protein) (Neurofilament 3) (Neurofilament triplet M protein) | Neurofilaments usually contain three intermediate filament proteins: NEFL, NEFM, and NEFH which are involved in the maintenance of neuronal caliber. May additionally cooperate with the neuronal intermediate filament proteins PRPH and INA to form neuronal filamentous networks (By similarity). {ECO:0000250|UniProtKB:P08553}. |
P10412 | H1-4 | T18 | ochoa|psp | Histone H1.4 (Histone H1b) (Histone H1s-4) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P10412 | H1-4 | T146 | ochoa|psp | Histone H1.4 (Histone H1b) (Histone H1s-4) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P10412 | H1-4 | S172 | psp | Histone H1.4 (Histone H1b) (Histone H1s-4) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P10412 | H1-4 | S187 | ochoa|psp | Histone H1.4 (Histone H1b) (Histone H1s-4) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P12272 | PTHLH | T121 | psp | Parathyroid hormone-related protein (PTH-rP) (PTHrP) (Parathyroid hormone-like protein) (PLP) [Cleaved into: PTHrP[1-36]; PTHrP[38-94]; Osteostatin (PTHrP[107-139])] | Neuroendocrine peptide which is a critical regulator of cellular and organ growth, development, migration, differentiation and survival and of epithelial calcium ion transport (PubMed:12538599, PubMed:35932760, PubMed:3616618). Acts by binding to its receptor, PTH1R, activating G protein-coupled receptor signaling (PubMed:19674967, PubMed:35932760). Regulates endochondral bone development and epithelial-mesenchymal interactions during the formation of the mammary glands and teeth (By similarity). Required for skeletal homeostasis (PubMed:12538599). Promotes mammary mesenchyme differentiation and bud outgrowth by modulating mesenchymal cell responsiveness to BMPs (PubMed:12538599). Up-regulates BMPR1A expression in the mammary mesenchyme and this increases the sensitivity of these cells to BMPs and allows them to respond to BMP4 in a paracrine and/or autocrine fashion (By similarity). BMP4 signaling in the mesenchyme, in turn, triggers epithelial outgrowth and augments MSX2 expression, which causes the mammary mesenchyme to inhibit hair follicle formation within the nipple sheath (By similarity). Promotes colon cancer cell migration and invasion in an integrin alpha-6/beta-1-dependent manner through activation of Rac1 (PubMed:20637541). {ECO:0000250|UniProtKB:P22858, ECO:0000269|PubMed:19674967, ECO:0000269|PubMed:20637541, ECO:0000269|PubMed:35932760, ECO:0000269|PubMed:3616618, ECO:0000303|PubMed:12538599}.; FUNCTION: [Osteostatin]: Potent inhibitor of osteoclastic bone resorption. {ECO:0000269|PubMed:1915066, ECO:0000269|PubMed:1954916, ECO:0000269|PubMed:20637541, ECO:0000269|PubMed:9048639, ECO:0000269|PubMed:9144344}. |
P16401 | H1-5 | S18 | ochoa|psp | Histone H1.5 (Histone H1a) (Histone H1b) (Histone H1s-3) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16401 | H1-5 | T138 | ochoa|psp | Histone H1.5 (Histone H1a) (Histone H1b) (Histone H1s-3) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16401 | H1-5 | T155 | psp | Histone H1.5 (Histone H1a) (Histone H1b) (Histone H1s-3) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16401 | H1-5 | S173 | psp | Histone H1.5 (Histone H1a) (Histone H1b) (Histone H1s-3) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16401 | H1-5 | S189 | ochoa|psp | Histone H1.5 (Histone H1a) (Histone H1b) (Histone H1s-3) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16402 | H1-3 | T18 | ochoa | Histone H1.3 (Histone H1c) (Histone H1s-2) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16402 | H1-3 | T147 | ochoa | Histone H1.3 (Histone H1c) (Histone H1s-2) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16402 | H1-3 | S189 | psp | Histone H1.3 (Histone H1c) (Histone H1s-2) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16403 | H1-2 | T31 | ochoa | Histone H1.2 (Histone H1c) (Histone H1d) (Histone H1s-1) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16403 | H1-2 | T146 | ochoa|psp | Histone H1.2 (Histone H1c) (Histone H1d) (Histone H1s-1) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16403 | H1-2 | T165 | ochoa|psp | Histone H1.2 (Histone H1c) (Histone H1d) (Histone H1s-1) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P16403 | H1-2 | S173 | psp | Histone H1.2 (Histone H1c) (Histone H1d) (Histone H1s-1) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
P17677 | GAP43 | T107 | ochoa | Neuromodulin (Axonal membrane protein GAP-43) (Growth-associated protein 43) (Neural phosphoprotein B-50) (pp46) | This protein is associated with nerve growth. It is a major component of the motile 'growth cones' that form the tips of elongating axons. Plays a role in axonal and dendritic filopodia induction. {ECO:0000269|PubMed:14978216, ECO:0000269|PubMed:21152083}. |
P17677 | GAP43 | T181 | ochoa | Neuromodulin (Axonal membrane protein GAP-43) (Growth-associated protein 43) (Neural phosphoprotein B-50) (pp46) | This protein is associated with nerve growth. It is a major component of the motile 'growth cones' that form the tips of elongating axons. Plays a role in axonal and dendritic filopodia induction. {ECO:0000269|PubMed:14978216, ECO:0000269|PubMed:21152083}. |
P19338 | NCL | S67 | ochoa | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T76 | ochoa|psp | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T84 | psp | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T92 | ochoa | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T99 | ochoa | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T106 | ochoa | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T113 | ochoa | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P19338 | NCL | T121 | ochoa|psp | Nucleolin (Protein C23) | Nucleolin is the major nucleolar protein of growing eukaryotic cells. It is found associated with intranucleolar chromatin and pre-ribosomal particles. It induces chromatin decondensation by binding to histone H1. It is thought to play a role in pre-rRNA transcription and ribosome assembly. May play a role in the process of transcriptional elongation. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'-TTAGGG-3' repeats. {ECO:0000269|PubMed:10393184}. |
P35251 | RFC1 | S360 | ochoa | Replication factor C subunit 1 (Activator 1 140 kDa subunit) (A1 140 kDa subunit) (Activator 1 large subunit) (Activator 1 subunit 1) (DNA-binding protein PO-GA) (Replication factor C 140 kDa subunit) (RF-C 140 kDa subunit) (RFC140) (Replication factor C large subunit) | Subunit of the replication factor C (RFC) complex which acts during elongation of primed DNA templates by DNA polymerases delta and epsilon, and is necessary for ATP-dependent loading of proliferating cell nuclear antigen (PCNA) onto primed DNA (PubMed:9488738). This subunit binds to the primer-template junction. Binds the PO-B transcription element as well as other GA rich DNA sequences. Can bind single- or double-stranded DNA. {ECO:0000269|PubMed:8999859, ECO:0000269|PubMed:9488738}. |
P38432 | COIL | S184 | psp | Coilin (p80-coilin) | Component of nuclear coiled bodies, also known as Cajal bodies or CBs, which are involved in the modification and assembly of nucleoplasmic snRNPs. {ECO:0000269|PubMed:7679389}. |
P46821 | MAP1B | T704 | ochoa | Microtubule-associated protein 1B (MAP-1B) [Cleaved into: MAP1B heavy chain; MAP1 light chain LC1] | Facilitates tyrosination of alpha-tubulin in neuronal microtubules (By similarity). Phosphorylated MAP1B is required for proper microtubule dynamics and plays a role in the cytoskeletal changes that accompany neuronal differentiation and neurite extension (PubMed:33268592). Possibly MAP1B binds to at least two tubulin subunits in the polymer, and this bridging of subunits might be involved in nucleating microtubule polymerization and in stabilizing microtubules. Acts as a positive cofactor in DAPK1-mediated autophagic vesicle formation and membrane blebbing. {ECO:0000250, ECO:0000269|PubMed:18195017, ECO:0000269|PubMed:33268592}. |
P50914 | RPL14 | S139 | ochoa | Large ribosomal subunit protein eL14 (60S ribosomal protein L14) (CAG-ISL 7) | Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:12962325, PubMed:23636399, PubMed:32669547). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547, ECO:0000305|PubMed:12962325}. |
P61353 | RPL27 | Y49 | ochoa | Large ribosomal subunit protein eL27 (60S ribosomal protein L27) | Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:25901680, PubMed:25957688, PubMed:32669547). Required for proper rRNA processing and maturation of 28S and 5.8S rRNAs (PubMed:25424902). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:25424902, ECO:0000269|PubMed:25901680, ECO:0000269|PubMed:25957688, ECO:0000269|PubMed:32669547, ECO:0000305|PubMed:12962325}. |
Q02539 | H1-1 | T152 | psp | Histone H1.1 (Histone H1a) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
Q02539 | H1-1 | S183 | psp | Histone H1.1 (Histone H1a) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
Q13428 | TCOF1 | T310 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q13428 | TCOF1 | S381 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q13428 | TCOF1 | S446 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q13428 | TCOF1 | S583 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q13428 | TCOF1 | S906 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q13428 | TCOF1 | S1378 | ochoa | Treacle protein (Treacher Collins syndrome protein) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:12777385, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with NOLC1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). {ECO:0000269|PubMed:12777385, ECO:0000269|PubMed:26399832}. |
Q14839 | CHD4 | S277 | ochoa | Chromodomain-helicase-DNA-binding protein 4 (CHD-4) (EC 3.6.4.-) (ATP-dependent helicase CHD4) (Mi-2 autoantigen 218 kDa protein) (Mi2-beta) | ATP-dependent chromatin-remodeling factor that binds and distorts nucleosomal DNA (PubMed:28977666, PubMed:32543371). Acts as a component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin (PubMed:16428440, PubMed:17626165, PubMed:28977666, PubMed:9804427). Localizes to acetylated damaged chromatin in a ZMYND8-dependent manner, to promote transcriptional repression and double-strand break repair by homologous recombination (PubMed:25593309). Involved in neurogenesis (By similarity). {ECO:0000250|UniProtKB:Q6PDQ2, ECO:0000269|PubMed:16428440, ECO:0000269|PubMed:17626165, ECO:0000269|PubMed:25593309, ECO:0000269|PubMed:28977666, ECO:0000269|PubMed:32543371, ECO:0000269|PubMed:9804427}. |
Q14978 | NOLC1 | S397 | ochoa | Nucleolar and coiled-body phosphoprotein 1 (140 kDa nucleolar phosphoprotein) (Nopp140) (Hepatitis C virus NS5A-transactivated protein 13) (HCV NS5A-transactivated protein 13) (Nucleolar 130 kDa protein) (Nucleolar phosphoprotein p130) | Nucleolar protein that acts as a regulator of RNA polymerase I by connecting RNA polymerase I with enzymes responsible for ribosomal processing and modification (PubMed:10567578, PubMed:26399832). Required for neural crest specification: following monoubiquitination by the BCR(KBTBD8) complex, associates with TCOF1 and acts as a platform to connect RNA polymerase I with enzymes responsible for ribosomal processing and modification, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). Involved in nucleologenesis, possibly by playing a role in the maintenance of the fundamental structure of the fibrillar center and dense fibrillar component in the nucleolus (PubMed:9016786). It has intrinsic GTPase and ATPase activities (PubMed:9016786). {ECO:0000269|PubMed:10567578, ECO:0000269|PubMed:26399832, ECO:0000269|PubMed:9016786}. |
Q86YV5 | PRAG1 | T417 | ochoa | Inactive tyrosine-protein kinase PRAG1 (PEAK1-related kinase-activating pseudokinase 1) (Pragmin) (Sugen kinase 223) (SgK223) | Catalytically inactive protein kinase that acts as a scaffold protein. Functions as an effector of the small GTPase RND2, which stimulates RhoA activity and inhibits NGF-induced neurite outgrowth (By similarity). Promotes Src family kinase (SFK) signaling by regulating the subcellular localization of CSK, a negative regulator of these kinases, leading to the regulation of cell morphology and motility by a CSK-dependent mechanism (By similarity). Acts as a critical coactivator of Notch signaling (By similarity). {ECO:0000250|UniProtKB:D3ZMK9, ECO:0000250|UniProtKB:Q571I4}. |
Q8IYB3 | SRRM1 | T846 | ochoa | Serine/arginine repetitive matrix protein 1 (SR-related nuclear matrix protein of 160 kDa) (SRm160) (Ser/Arg-related nuclear matrix protein) | Part of pre- and post-splicing multiprotein mRNP complexes. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). Involved in numerous pre-mRNA processing events. Promotes constitutive and exonic splicing enhancer (ESE)-dependent splicing activation by bridging together sequence-specific (SR family proteins, SFRS4, SFRS5 and TRA2B/SFRS10) and basal snRNP (SNRP70 and SNRPA1) factors of the spliceosome. Stimulates mRNA 3'-end cleavage independently of the formation of an exon junction complex. Binds both pre-mRNA and spliced mRNA 20-25 nt upstream of exon-exon junctions. Binds RNA and DNA with low sequence specificity and has similar preference for either double- or single-stranded nucleic acid substrates. {ECO:0000269|PubMed:10339552, ECO:0000269|PubMed:10668804, ECO:0000269|PubMed:11739730, ECO:0000269|PubMed:12600940, ECO:0000269|PubMed:12944400, ECO:0000269|PubMed:9531537, ECO:0000305|PubMed:33509932}. |
Q8N0X7 | SPART | S470 | ochoa | Spartin (Spastic paraplegia 20 protein) (Trans-activated by hepatitis C virus core protein 1) | Lipophagy receptor that plays an important role in lipid droplet (LD) turnover in motor neurons (PubMed:37443287). Localizes to LDs and interacts with components of the autophagy machinery, such as MAP1LC3A/C proteins to deliver LDs to autophagosomes for degradation via lipophagy (PubMed:37443287). Lipid transfer protein required for lipid droplet degradation, including by lipophagy (PubMed:38190532). Can bind and transfer all lipid species found in lipid droplets, from phospholipids to triglycerides and sterol esters but the direction of lipid transfer by spartin and its cargos are unknown (PubMed:38190532). May be implicated in endosomal trafficking, or microtubule dynamics, or both. Participates in cytokinesis (PubMed:20719964). {ECO:0000269|PubMed:20719964, ECO:0000269|PubMed:37443287, ECO:0000269|PubMed:38190532}. |
Q9H1E3 | NUCKS1 | S181 | ochoa|psp | Nuclear ubiquitous casein and cyclin-dependent kinase substrate 1 (P1) | Chromatin-associated protein involved in DNA repair by promoting homologous recombination (HR) (PubMed:26323318). Binds double-stranded DNA (dsDNA) and secondary DNA structures, such as D-loop structures, but with less affinity than RAD51AP1 (PubMed:26323318). {ECO:0000269|PubMed:26323318}. |
Q9P2E9 | RRBP1 | T225 | ochoa | Ribosome-binding protein 1 (180 kDa ribosome receptor homolog) (RRp) (ES/130-related protein) (Ribosome receptor protein) | Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane. {ECO:0000250}. |
Q9P2E9 | RRBP1 | T275 | ochoa | Ribosome-binding protein 1 (180 kDa ribosome receptor homolog) (RRp) (ES/130-related protein) (Ribosome receptor protein) | Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane. {ECO:0000250}. |
Q9P2E9 | RRBP1 | S533 | ochoa | Ribosome-binding protein 1 (180 kDa ribosome receptor homolog) (RRp) (ES/130-related protein) (Ribosome receptor protein) | Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane. {ECO:0000250}. |
Q9P2E9 | RRBP1 | S573 | ochoa | Ribosome-binding protein 1 (180 kDa ribosome receptor homolog) (RRp) (ES/130-related protein) (Ribosome receptor protein) | Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane. {ECO:0000250}. |
Q9P2E9 | RRBP1 | S583 | ochoa | Ribosome-binding protein 1 (180 kDa ribosome receptor homolog) (RRp) (ES/130-related protein) (Ribosome receptor protein) | Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane. {ECO:0000250}. |
P16403 | H1-2 | T167 | EPSD|PSP | Histone H1.2 (Histone H1c) (Histone H1d) (Histone H1s-1) | Histone H1 protein binds to linker DNA between nucleosomes forming the macromolecular structure known as the chromatin fiber. Histones H1 are necessary for the condensation of nucleosome chains into higher-order structured fibers. Also acts as a regulator of individual gene transcription through chromatin remodeling, nucleosome spacing and DNA methylation (By similarity). {ECO:0000250}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-140342 | Apoptosis induced DNA fragmentation | 4.805190e-11 | 10.318 |
R-HSA-2559584 | Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 1.828061e-10 | 9.738 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 3.663494e-09 | 8.436 |
R-HSA-75153 | Apoptotic execution phase | 5.635259e-08 | 7.249 |
R-HSA-2559583 | Cellular Senescence | 1.639059e-06 | 5.785 |
R-HSA-109581 | Apoptosis | 1.969631e-05 | 4.706 |
R-HSA-5357801 | Programmed Cell Death | 5.669897e-05 | 4.246 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 2.572966e-04 | 3.590 |
R-HSA-2262752 | Cellular responses to stress | 4.849258e-04 | 3.314 |
R-HSA-422475 | Axon guidance | 5.404363e-04 | 3.267 |
R-HSA-9675108 | Nervous system development | 7.532198e-04 | 3.123 |
R-HSA-8953897 | Cellular responses to stimuli | 1.038603e-03 | 2.984 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 1.586718e-03 | 2.800 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 1.586718e-03 | 2.800 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 3.086585e-03 | 2.511 |
R-HSA-427389 | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 3.509660e-03 | 2.455 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 3.860079e-03 | 2.413 |
R-HSA-72187 | mRNA 3'-end processing | 5.634589e-03 | 2.249 |
R-HSA-3214815 | HDACs deacetylate histones | 6.190701e-03 | 2.208 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 7.170937e-03 | 2.144 |
R-HSA-9843940 | Regulation of endogenous retroelements by KRAB-ZFP proteins | 9.327170e-03 | 2.030 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 1.002380e-02 | 1.999 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 9.556864e-03 | 2.020 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 5.179986e-03 | 2.286 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 7.374903e-03 | 2.132 |
R-HSA-193648 | NRAGE signals death through JNK | 6.381436e-03 | 2.195 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 6.654231e-03 | 2.177 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 6.222291e-03 | 2.206 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 1.002380e-02 | 1.999 |
R-HSA-376176 | Signaling by ROBO receptors | 8.056034e-03 | 2.094 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 1.224773e-02 | 1.912 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 1.074294e-02 | 1.969 |
R-HSA-73864 | RNA Polymerase I Transcription | 1.123475e-02 | 1.949 |
R-HSA-72312 | rRNA processing | 1.135092e-02 | 1.945 |
R-HSA-416482 | G alpha (12/13) signalling events | 1.123475e-02 | 1.949 |
R-HSA-9954714 | PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | 1.494806e-02 | 1.825 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 1.523103e-02 | 1.817 |
R-HSA-9954716 | ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ri... | 1.638598e-02 | 1.786 |
R-HSA-192823 | Viral mRNA Translation | 1.911714e-02 | 1.719 |
R-HSA-9842860 | Regulation of endogenous retroelements | 1.880476e-02 | 1.726 |
R-HSA-156902 | Peptide chain elongation | 1.411313e-02 | 1.850 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 1.668044e-02 | 1.778 |
R-HSA-72764 | Eukaryotic Translation Termination | 1.668044e-02 | 1.778 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 1.668044e-02 | 1.778 |
R-HSA-156842 | Eukaryotic Translation Elongation | 1.551631e-02 | 1.809 |
R-HSA-2408557 | Selenocysteine synthesis | 1.849458e-02 | 1.733 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 1.943173e-02 | 1.711 |
R-HSA-157579 | Telomere Maintenance | 1.727616e-02 | 1.763 |
R-HSA-73884 | Base Excision Repair | 1.466741e-02 | 1.834 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 1.788090e-02 | 1.748 |
R-HSA-9824446 | Viral Infection Pathways | 1.762655e-02 | 1.754 |
R-HSA-8953854 | Metabolism of RNA | 1.987489e-02 | 1.702 |
R-HSA-1799339 | SRP-dependent cotranslational protein targeting to membrane | 2.071190e-02 | 1.684 |
R-HSA-195721 | Signaling by WNT | 2.101242e-02 | 1.678 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 2.103736e-02 | 1.677 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 2.103736e-02 | 1.677 |
R-HSA-69091 | Polymerase switching | 2.938261e-02 | 1.532 |
R-HSA-69109 | Leading Strand Synthesis | 2.938261e-02 | 1.532 |
R-HSA-73886 | Chromosome Maintenance | 2.617237e-02 | 1.582 |
R-HSA-72613 | Eukaryotic Translation Initiation | 2.440874e-02 | 1.612 |
R-HSA-72737 | Cap-dependent Translation Initiation | 2.440874e-02 | 1.612 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 2.303494e-02 | 1.638 |
R-HSA-1266738 | Developmental Biology | 2.436393e-02 | 1.613 |
R-HSA-5693538 | Homology Directed Repair | 2.510806e-02 | 1.600 |
R-HSA-5656121 | Translesion synthesis by POLI | 3.659683e-02 | 1.437 |
R-HSA-5655862 | Translesion synthesis by POLK | 3.839227e-02 | 1.416 |
R-HSA-5651801 | PCNA-Dependent Long Patch Base Excision Repair | 4.197345e-02 | 1.377 |
R-HSA-5696397 | Gap-filling DNA repair synthesis and ligation in GG-NER | 4.909717e-02 | 1.309 |
R-HSA-171306 | Packaging Of Telomere Ends | 5.968684e-02 | 1.224 |
R-HSA-5334118 | DNA methylation | 6.319132e-02 | 1.199 |
R-HSA-212300 | PRC2 methylates histones and DNA | 7.708344e-02 | 1.113 |
R-HSA-5656169 | Termination of translesion DNA synthesis | 6.319132e-02 | 1.199 |
R-HSA-110313 | Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA templa... | 8.566465e-02 | 1.067 |
R-HSA-110314 | Recognition of DNA damage by PCNA-containing replication complex | 5.440634e-02 | 1.264 |
R-HSA-110312 | Translesion synthesis by REV1 | 3.479815e-02 | 1.458 |
R-HSA-9948299 | Ribosome-associated quality control | 3.372254e-02 | 1.472 |
R-HSA-110320 | Translesion Synthesis by POLH | 4.375920e-02 | 1.359 |
R-HSA-9670095 | Inhibition of DNA recombination at telomere | 8.395460e-02 | 1.076 |
R-HSA-5625886 | Activated PKN1 stimulates transcription of AR (androgen receptor) regulated gene... | 8.566465e-02 | 1.067 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 5.961776e-02 | 1.225 |
R-HSA-5696400 | Dual Incision in GG-NER | 7.362920e-02 | 1.133 |
R-HSA-9843970 | Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | 7.362920e-02 | 1.133 |
R-HSA-427359 | SIRT1 negatively regulates rRNA expression | 7.880588e-02 | 1.103 |
R-HSA-9820960 | Respiratory syncytial virus (RSV) attachment and entry | 6.668318e-02 | 1.176 |
R-HSA-174411 | Polymerase switching on the C-strand of the telomere | 5.616968e-02 | 1.250 |
R-HSA-73728 | RNA Polymerase I Promoter Opening | 5.968684e-02 | 1.224 |
R-HSA-9821002 | Chromatin modifications during the maternal to zygotic transition (MZT) | 8.566465e-02 | 1.067 |
R-HSA-72172 | mRNA Splicing | 6.511811e-02 | 1.186 |
R-HSA-418885 | DCC mediated attractive signaling | 3.479815e-02 | 1.458 |
R-HSA-9844594 | Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | 8.395460e-02 | 1.076 |
R-HSA-9843743 | Transcriptional regulation of brown and beige adipocyte differentiation | 8.395460e-02 | 1.076 |
R-HSA-9710421 | Defective pyroptosis | 9.077631e-02 | 1.042 |
R-HSA-110373 | Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 5.792985e-02 | 1.237 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 4.030230e-02 | 1.395 |
R-HSA-69186 | Lagging Strand Synthesis | 4.732106e-02 | 1.325 |
R-HSA-110331 | Cleavage of the damaged purine | 7.880588e-02 | 1.103 |
R-HSA-73927 | Depurination | 8.052522e-02 | 1.094 |
R-HSA-69190 | DNA strand elongation | 6.842439e-02 | 1.165 |
R-HSA-110330 | Recognition and association of DNA glycosylase with site containing an affected ... | 6.842439e-02 | 1.165 |
R-HSA-68616 | Assembly of the ORC complex at the origin of replication | 7.016246e-02 | 1.154 |
R-HSA-9821993 | Replacement of protamines by nucleosomes in the male pronucleus | 5.440634e-02 | 1.264 |
R-HSA-174417 | Telomere C-strand (Lagging Strand) Synthesis | 8.737162e-02 | 1.059 |
R-HSA-73762 | RNA Polymerase I Transcription Initiation | 8.907550e-02 | 1.050 |
R-HSA-373752 | Netrin-1 signaling | 9.247405e-02 | 1.034 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 4.115673e-02 | 1.386 |
R-HSA-9711097 | Cellular response to starvation | 4.245130e-02 | 1.372 |
R-HSA-73933 | Resolution of Abasic Sites (AP sites) | 8.566465e-02 | 1.067 |
R-HSA-3247509 | Chromatin modifying enzymes | 8.093782e-02 | 1.092 |
R-HSA-3928662 | EPHB-mediated forward signaling | 9.247405e-02 | 1.034 |
R-HSA-4839726 | Chromatin organization | 8.925799e-02 | 1.049 |
R-HSA-6804758 | Regulation of TP53 Activity through Acetylation | 7.016246e-02 | 1.154 |
R-HSA-69306 | DNA Replication | 4.030230e-02 | 1.395 |
R-HSA-2408522 | Selenoamino acid metabolism | 4.508623e-02 | 1.346 |
R-HSA-110329 | Cleavage of the damaged pyrimidine | 8.907550e-02 | 1.050 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 3.332681e-02 | 1.477 |
R-HSA-73928 | Depyrimidination | 8.907550e-02 | 1.050 |
R-HSA-110328 | Recognition and association of DNA glycosylase with site containing an affected ... | 7.362920e-02 | 1.133 |
R-HSA-168255 | Influenza Infection | 5.240057e-02 | 1.281 |
R-HSA-196757 | Metabolism of folate and pterines | 7.880588e-02 | 1.103 |
R-HSA-5663205 | Infectious disease | 9.245923e-02 | 1.034 |
R-HSA-73887 | Death Receptor Signaling | 4.072865e-02 | 1.390 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 9.416872e-02 | 1.026 |
R-HSA-774815 | Nucleosome assembly | 9.416872e-02 | 1.026 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 9.586033e-02 | 1.018 |
R-HSA-416476 | G alpha (q) signalling events | 9.782519e-02 | 1.010 |
R-HSA-162582 | Signal Transduction | 9.864361e-02 | 1.006 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 9.923440e-02 | 1.003 |
R-HSA-9031628 | NGF-stimulated transcription | 9.923440e-02 | 1.003 |
R-HSA-73893 | DNA Damage Bypass | 1.009169e-01 | 0.996 |
R-HSA-912446 | Meiotic recombination | 1.042727e-01 | 0.982 |
R-HSA-73772 | RNA Polymerase I Promoter Escape | 1.059461e-01 | 0.975 |
R-HSA-8866654 | E3 ubiquitin ligases ubiquitinate target proteins | 1.059461e-01 | 0.975 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 1.066206e-01 | 0.972 |
R-HSA-1221632 | Meiotic synapsis | 1.076164e-01 | 0.968 |
R-HSA-5250924 | B-WICH complex positively regulates rRNA expression | 1.076164e-01 | 0.968 |
R-HSA-73929 | Base-Excision Repair, AP Site Formation | 1.092837e-01 | 0.961 |
R-HSA-6782210 | Gap-filling DNA repair synthesis and ligation in TC-NER | 1.126094e-01 | 0.948 |
R-HSA-6782135 | Dual incision in TC-NER | 1.159230e-01 | 0.936 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 1.175753e-01 | 0.930 |
R-HSA-180786 | Extension of Telomeres | 1.175753e-01 | 0.930 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 1.192247e-01 | 0.924 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 1.192247e-01 | 0.924 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 1.225144e-01 | 0.912 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 1.290583e-01 | 0.889 |
R-HSA-5693606 | DNA Double Strand Break Response | 1.306869e-01 | 0.884 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 1.306869e-01 | 0.884 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 1.323125e-01 | 0.878 |
R-HSA-212165 | Epigenetic regulation of gene expression | 1.335687e-01 | 0.874 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 1.355550e-01 | 0.868 |
R-HSA-427413 | NoRC negatively regulates rRNA expression | 1.371719e-01 | 0.863 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 1.387858e-01 | 0.858 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 1.387858e-01 | 0.858 |
R-HSA-69473 | G2/M DNA damage checkpoint | 1.420049e-01 | 0.848 |
R-HSA-6781827 | Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 1.436100e-01 | 0.843 |
R-HSA-8852135 | Protein ubiquitination | 1.436100e-01 | 0.843 |
R-HSA-5250941 | Negative epigenetic regulation of rRNA expression | 1.515925e-01 | 0.819 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 1.531803e-01 | 0.815 |
R-HSA-977225 | Amyloid fiber formation | 1.531803e-01 | 0.815 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 1.547653e-01 | 0.810 |
R-HSA-73894 | DNA Repair | 1.573234e-01 | 0.803 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 1.579266e-01 | 0.802 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 1.579266e-01 | 0.802 |
R-HSA-1500620 | Meiosis | 1.595030e-01 | 0.797 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 1.595030e-01 | 0.797 |
R-HSA-9645723 | Diseases of programmed cell death | 1.657800e-01 | 0.780 |
R-HSA-373080 | Class B/2 (Secretin family receptors) | 1.689015e-01 | 0.772 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 1.704580e-01 | 0.768 |
R-HSA-2682334 | EPH-Ephrin signaling | 1.735626e-01 | 0.761 |
R-HSA-68867 | Assembly of the pre-replicative complex | 1.751107e-01 | 0.757 |
R-HSA-388396 | GPCR downstream signalling | 1.830340e-01 | 0.737 |
R-HSA-3214847 | HATs acetylate histones | 1.858689e-01 | 0.731 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 1.904380e-01 | 0.720 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 1.949822e-01 | 0.710 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 1.949822e-01 | 0.710 |
R-HSA-9833110 | RSV-host interactions | 1.949822e-01 | 0.710 |
R-HSA-5696398 | Nucleotide Excision Repair | 1.964915e-01 | 0.707 |
R-HSA-69239 | Synthesis of DNA | 1.995018e-01 | 0.700 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 1.995018e-01 | 0.700 |
R-HSA-9700206 | Signaling by ALK in cancer | 1.995018e-01 | 0.700 |
R-HSA-211000 | Gene Silencing by RNA | 1.995018e-01 | 0.700 |
R-HSA-69002 | DNA Replication Pre-Initiation | 2.025013e-01 | 0.694 |
R-HSA-72766 | Translation | 2.041899e-01 | 0.690 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 2.084676e-01 | 0.681 |
R-HSA-373760 | L1CAM interactions | 2.158648e-01 | 0.666 |
R-HSA-68875 | Mitotic Prophase | 2.217344e-01 | 0.654 |
R-HSA-372790 | Signaling by GPCR | 2.231297e-01 | 0.651 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 2.261087e-01 | 0.646 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 2.304593e-01 | 0.637 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 2.304593e-01 | 0.637 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 2.304593e-01 | 0.637 |
R-HSA-69481 | G2/M Checkpoints | 2.333465e-01 | 0.632 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 2.347861e-01 | 0.629 |
R-HSA-1474165 | Reproduction | 2.390895e-01 | 0.621 |
R-HSA-9843745 | Adipogenesis | 2.405188e-01 | 0.619 |
R-HSA-9018519 | Estrogen-dependent gene expression | 2.490399e-01 | 0.604 |
R-HSA-6807070 | PTEN Regulation | 2.532658e-01 | 0.596 |
R-HSA-69242 | S Phase | 2.671866e-01 | 0.573 |
R-HSA-166520 | Signaling by NTRKs | 2.671866e-01 | 0.573 |
R-HSA-9679191 | Potential therapeutics for SARS | 2.699405e-01 | 0.569 |
R-HSA-1643685 | Disease | 2.741784e-01 | 0.562 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 2.754183e-01 | 0.560 |
R-HSA-5633007 | Regulation of TP53 Activity | 2.835606e-01 | 0.547 |
R-HSA-69278 | Cell Cycle, Mitotic | 2.992251e-01 | 0.524 |
R-HSA-418555 | G alpha (s) signalling events | 2.995807e-01 | 0.523 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 3.009000e-01 | 0.522 |
R-HSA-5689880 | Ub-specific processing proteases | 3.022168e-01 | 0.520 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 3.022168e-01 | 0.520 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 3.022168e-01 | 0.520 |
R-HSA-9609690 | HCMV Early Events | 3.318513e-01 | 0.479 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 3.318513e-01 | 0.479 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 3.352899e-01 | 0.475 |
R-HSA-389948 | Co-inhibition by PD-1 | 3.368793e-01 | 0.473 |
R-HSA-418990 | Adherens junctions interactions | 3.602674e-01 | 0.443 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 3.698746e-01 | 0.432 |
R-HSA-196849 | Metabolism of water-soluble vitamins and cofactors | 3.746257e-01 | 0.426 |
R-HSA-8939211 | ESR-mediated signaling | 3.828571e-01 | 0.417 |
R-HSA-157118 | Signaling by NOTCH | 3.863526e-01 | 0.413 |
R-HSA-1640170 | Cell Cycle | 3.965074e-01 | 0.402 |
R-HSA-9609646 | HCMV Infection | 3.978668e-01 | 0.400 |
R-HSA-73857 | RNA Polymerase II Transcription | 3.986730e-01 | 0.399 |
R-HSA-421270 | Cell-cell junction organization | 3.990067e-01 | 0.399 |
R-HSA-5688426 | Deubiquitination | 4.035453e-01 | 0.394 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 4.046748e-01 | 0.393 |
R-HSA-69620 | Cell Cycle Checkpoints | 4.069275e-01 | 0.390 |
R-HSA-446728 | Cell junction organization | 4.290064e-01 | 0.368 |
R-HSA-1257604 | PIP3 activates AKT signaling | 4.471469e-01 | 0.350 |
R-HSA-1500931 | Cell-Cell communication | 4.687876e-01 | 0.329 |
R-HSA-9006925 | Intracellular signaling by second messengers | 4.944481e-01 | 0.306 |
R-HSA-5683057 | MAPK family signaling cascades | 4.992435e-01 | 0.302 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 5.142951e-01 | 0.289 |
R-HSA-196854 | Metabolism of vitamins and cofactors | 5.152212e-01 | 0.288 |
R-HSA-74160 | Gene expression (Transcription) | 5.171300e-01 | 0.286 |
R-HSA-68886 | M Phase | 5.324955e-01 | 0.274 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 6.012281e-01 | 0.221 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 6.378037e-01 | 0.195 |
R-HSA-9679506 | SARS-CoV Infections | 6.647083e-01 | 0.177 |
R-HSA-500792 | GPCR ligand binding | 6.860490e-01 | 0.164 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 7.003161e-01 | 0.155 |
R-HSA-212436 | Generic Transcription Pathway | 8.054976e-01 | 0.094 |
R-HSA-392499 | Metabolism of proteins | 8.516506e-01 | 0.070 |
R-HSA-1280218 | Adaptive Immune System | 8.721309e-01 | 0.059 |
R-HSA-597592 | Post-translational protein modification | 9.633170e-01 | 0.016 |
R-HSA-1430728 | Metabolism | 9.827969e-01 | 0.008 |
R-HSA-168256 | Immune System | 9.967029e-01 | 0.001 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
CDK3 |
0.663 | 0.751 | 1 | 0.836 |
CDK5 |
0.631 | 0.661 | 1 | 0.738 |
CDK1 |
0.625 | 0.671 | 1 | 0.793 |
CDK16 |
0.624 | 0.604 | 1 | 0.830 |
CDK18 |
0.619 | 0.596 | 1 | 0.815 |
CDK10 |
0.616 | 0.583 | 1 | 0.791 |
P38G |
0.613 | 0.583 | 1 | 0.852 |
CDK17 |
0.613 | 0.592 | 1 | 0.845 |
CDK6 |
0.612 | 0.609 | 1 | 0.793 |
CDK2 |
0.611 | 0.695 | 1 | 0.667 |
JNK2 |
0.605 | 0.573 | 1 | 0.807 |
CDK4 |
0.601 | 0.572 | 1 | 0.819 |
CLK3 |
0.601 | 0.499 | 1 | 0.481 |
HIPK2 |
0.601 | 0.501 | 1 | 0.800 |
CDK14 |
0.599 | 0.559 | 1 | 0.774 |
P38D |
0.596 | 0.534 | 1 | 0.851 |
ERK1 |
0.595 | 0.541 | 1 | 0.790 |
CDK7 |
0.595 | 0.556 | 1 | 0.765 |
HIPK1 |
0.594 | 0.465 | 1 | 0.698 |
CDK9 |
0.594 | 0.558 | 1 | 0.782 |
JNK3 |
0.592 | 0.547 | 1 | 0.782 |
P38B |
0.591 | 0.525 | 1 | 0.775 |
CLK1 |
0.591 | 0.394 | -3 | 0.420 |
CDK12 |
0.590 | 0.541 | 1 | 0.809 |
CDK13 |
0.589 | 0.544 | 1 | 0.788 |
P38A |
0.588 | 0.521 | 1 | 0.706 |
MAK |
0.583 | 0.339 | -2 | 0.581 |
CLK2 |
0.579 | 0.317 | -3 | 0.388 |
SRPK1 |
0.579 | 0.276 | -3 | 0.396 |
CDK8 |
0.578 | 0.519 | 1 | 0.769 |
CDK19 |
0.578 | 0.515 | 1 | 0.805 |
JNK1 |
0.577 | 0.480 | 1 | 0.807 |
HIPK3 |
0.577 | 0.436 | 1 | 0.661 |
ERK2 |
0.577 | 0.530 | 1 | 0.746 |
NLK |
0.575 | 0.534 | 1 | 0.499 |
CLK4 |
0.575 | 0.320 | -3 | 0.406 |
DYRK1B |
0.574 | 0.457 | 1 | 0.768 |
MOK |
0.572 | 0.315 | 1 | 0.582 |
DYRK2 |
0.571 | 0.450 | 1 | 0.713 |
ERK7 |
0.570 | 0.257 | 2 | 0.529 |
MST4 |
0.569 | 0.240 | 2 | 0.713 |
PKCB |
0.565 | 0.204 | 2 | 0.667 |
DYRK1A |
0.565 | 0.370 | 1 | 0.676 |
KIS |
0.563 | 0.462 | 1 | 0.744 |
SRPK2 |
0.563 | 0.218 | -3 | 0.320 |
PKCE |
0.563 | 0.204 | 2 | 0.650 |
DYRK4 |
0.562 | 0.450 | 1 | 0.808 |
HIPK4 |
0.561 | 0.297 | 1 | 0.504 |
PKCD |
0.559 | 0.180 | 2 | 0.638 |
MST3 |
0.559 | 0.200 | 2 | 0.701 |
WNK1 |
0.559 | 0.161 | -2 | 0.691 |
PRP4 |
0.558 | 0.301 | -3 | 0.477 |
PKCA |
0.557 | 0.161 | 2 | 0.653 |
CDKL5 |
0.557 | 0.156 | -3 | 0.419 |
ICK |
0.557 | 0.255 | -3 | 0.451 |
ERK5 |
0.553 | 0.246 | 1 | 0.406 |
DYRK3 |
0.553 | 0.320 | 1 | 0.662 |
PKCZ |
0.551 | 0.164 | 2 | 0.638 |
TNIK |
0.551 | 0.230 | 3 | 0.470 |
PKCG |
0.551 | 0.163 | 2 | 0.634 |
CDKL1 |
0.551 | 0.126 | -3 | 0.410 |
PKR |
0.551 | 0.137 | 1 | 0.141 |
MPSK1 |
0.550 | 0.109 | 1 | 0.184 |
PKCH |
0.550 | 0.150 | 2 | 0.623 |
PKN2 |
0.549 | 0.119 | -3 | 0.473 |
PKCI |
0.549 | 0.161 | 2 | 0.635 |
CHAK2 |
0.549 | 0.169 | -1 | 0.657 |
SRPK3 |
0.547 | 0.148 | -3 | 0.338 |
NIK |
0.545 | 0.114 | -3 | 0.485 |
EEF2K |
0.545 | 0.173 | 3 | 0.486 |
HASPIN |
0.545 | 0.092 | -1 | 0.503 |
MLK3 |
0.545 | 0.133 | 2 | 0.648 |
MNK2 |
0.544 | 0.129 | -2 | 0.605 |
SGK3 |
0.544 | 0.065 | -3 | 0.434 |
IRE1 |
0.544 | 0.094 | 1 | 0.126 |
PKCT |
0.544 | 0.124 | 2 | 0.625 |
MNK1 |
0.543 | 0.145 | -2 | 0.620 |
IRAK4 |
0.542 | 0.103 | 1 | 0.108 |
PIM1 |
0.542 | 0.085 | -3 | 0.393 |
PKN3 |
0.542 | 0.045 | -3 | 0.437 |
TAO3 |
0.541 | 0.124 | 1 | 0.140 |
KHS2 |
0.541 | 0.137 | 1 | 0.122 |
HGK |
0.540 | 0.146 | 3 | 0.430 |
TAO2 |
0.540 | 0.142 | 2 | 0.670 |
COT |
0.539 | 0.040 | 2 | 0.603 |
NEK2 |
0.539 | 0.056 | 2 | 0.654 |
AKT2 |
0.539 | 0.066 | -3 | 0.368 |
NUAK2 |
0.539 | 0.069 | -3 | 0.468 |
MTOR |
0.539 | 0.170 | 1 | 0.289 |
KHS1 |
0.538 | 0.112 | 1 | 0.112 |
BUB1 |
0.538 | 0.083 | -5 | 0.343 |
LOK |
0.537 | 0.138 | -2 | 0.560 |
YSK1 |
0.537 | 0.106 | 2 | 0.686 |
ROCK2 |
0.537 | 0.086 | -3 | 0.433 |
PRPK |
0.537 | -0.014 | -1 | 0.543 |
DCAMKL1 |
0.536 | 0.065 | -3 | 0.451 |
NEK6 |
0.536 | 0.057 | -2 | 0.680 |
MEKK6 |
0.536 | 0.075 | 1 | 0.116 |
MLK2 |
0.535 | 0.022 | 2 | 0.626 |
WNK4 |
0.535 | 0.028 | -2 | 0.683 |
P70S6KB |
0.535 | 0.047 | -3 | 0.423 |
CHAK1 |
0.534 | 0.118 | 2 | 0.562 |
AMPKA1 |
0.534 | 0.043 | -3 | 0.488 |
IRE2 |
0.534 | 0.052 | 2 | 0.565 |
GSK3A |
0.534 | 0.111 | 4 | 0.259 |
CAMLCK |
0.533 | -0.003 | -2 | 0.642 |
AURC |
0.533 | 0.075 | -2 | 0.512 |
ULK2 |
0.533 | 0.034 | 2 | 0.544 |
RSK2 |
0.532 | 0.030 | -3 | 0.420 |
PKG2 |
0.532 | 0.066 | -2 | 0.553 |
MINK |
0.532 | 0.102 | 1 | 0.097 |
LATS1 |
0.532 | 0.024 | -3 | 0.449 |
NEK9 |
0.532 | -0.005 | 2 | 0.662 |
CAMK1B |
0.532 | -0.001 | -3 | 0.475 |
VRK2 |
0.531 | 0.032 | 1 | 0.217 |
PIM2 |
0.531 | 0.056 | -3 | 0.403 |
MOS |
0.531 | -0.046 | 1 | 0.156 |
GRK7 |
0.531 | 0.008 | 1 | 0.127 |
MLK1 |
0.531 | 0.013 | 2 | 0.656 |
PHKG1 |
0.531 | 0.065 | -3 | 0.452 |
BMPR2 |
0.530 | -0.098 | -2 | 0.692 |
LRRK2 |
0.530 | 0.134 | 2 | 0.622 |
NEK5 |
0.530 | 0.007 | 1 | 0.108 |
PIM3 |
0.530 | 0.017 | -3 | 0.430 |
MRCKB |
0.530 | 0.066 | -3 | 0.402 |
AKT3 |
0.530 | 0.064 | -3 | 0.329 |
MAP3K15 |
0.530 | 0.029 | 1 | 0.118 |
RSK3 |
0.530 | 0.033 | -3 | 0.409 |
NDR1 |
0.529 | 0.061 | -3 | 0.443 |
HPK1 |
0.529 | 0.065 | 1 | 0.114 |
PBK |
0.529 | 0.039 | 1 | 0.141 |
MEKK2 |
0.528 | -0.016 | 2 | 0.591 |
SGK1 |
0.528 | 0.046 | -3 | 0.300 |
PRKD3 |
0.528 | 0.045 | -3 | 0.438 |
DMPK1 |
0.527 | 0.067 | -3 | 0.423 |
NEK1 |
0.527 | 0.020 | 1 | 0.095 |
AKT1 |
0.527 | 0.041 | -3 | 0.391 |
AMPKA2 |
0.527 | 0.028 | -3 | 0.462 |
SKMLCK |
0.527 | -0.039 | -2 | 0.674 |
MYO3B |
0.527 | 0.115 | 2 | 0.673 |
RSK4 |
0.527 | 0.035 | -3 | 0.370 |
TSSK1 |
0.526 | 0.021 | -3 | 0.514 |
DSTYK |
0.526 | -0.043 | 2 | 0.656 |
PAK6 |
0.525 | 0.068 | -2 | 0.480 |
ZAK |
0.525 | -0.007 | 1 | 0.110 |
TAO1 |
0.525 | 0.097 | 1 | 0.116 |
MYO3A |
0.525 | 0.134 | 1 | 0.128 |
GCK |
0.525 | 0.053 | 1 | 0.112 |
NEK4 |
0.525 | -0.005 | 1 | 0.099 |
PKACG |
0.525 | 0.047 | -2 | 0.587 |
AAK1 |
0.524 | 0.048 | 1 | 0.163 |
NEK11 |
0.524 | -0.003 | 1 | 0.131 |
ATR |
0.524 | -0.067 | 1 | 0.157 |
SSTK |
0.524 | 0.063 | 4 | 0.423 |
PKN1 |
0.524 | 0.044 | -3 | 0.409 |
NEK7 |
0.524 | -0.036 | -3 | 0.449 |
PRKD2 |
0.524 | 0.051 | -3 | 0.455 |
DAPK2 |
0.523 | -0.060 | -3 | 0.484 |
GAK |
0.523 | 0.007 | 1 | 0.160 |
TGFBR2 |
0.523 | 0.004 | -2 | 0.671 |
PHKG2 |
0.523 | 0.075 | -3 | 0.473 |
MELK |
0.523 | 0.015 | -3 | 0.466 |
DCAMKL2 |
0.523 | 0.031 | -3 | 0.469 |
MARK4 |
0.523 | -0.019 | 4 | 0.462 |
BMPR1B |
0.523 | -0.026 | 1 | 0.085 |
SLK |
0.523 | 0.091 | -2 | 0.507 |
ALK4 |
0.522 | -0.032 | -2 | 0.720 |
PDK1 |
0.522 | -0.025 | 1 | 0.148 |
ROCK1 |
0.522 | 0.052 | -3 | 0.406 |
YSK4 |
0.522 | -0.049 | 1 | 0.091 |
HRI |
0.522 | -0.004 | -2 | 0.672 |
ANKRD3 |
0.521 | -0.094 | 1 | 0.122 |
TSSK2 |
0.521 | -0.006 | -5 | 0.431 |
MEK5 |
0.521 | -0.054 | 2 | 0.567 |
PAK1 |
0.521 | 0.003 | -2 | 0.577 |
PERK |
0.520 | -0.035 | -2 | 0.659 |
MRCKA |
0.520 | 0.073 | -3 | 0.395 |
NIM1 |
0.520 | 0.002 | 3 | 0.270 |
MLK4 |
0.520 | -0.005 | 2 | 0.581 |
LKB1 |
0.520 | -0.005 | -3 | 0.478 |
RIPK3 |
0.519 | -0.083 | 3 | 0.231 |
P90RSK |
0.519 | -0.008 | -3 | 0.410 |
MEKK1 |
0.519 | -0.080 | 1 | 0.122 |
WNK3 |
0.518 | -0.070 | 1 | 0.110 |
ULK1 |
0.518 | -0.015 | -3 | 0.438 |
NEK3 |
0.518 | -0.002 | 1 | 0.125 |
PKACB |
0.517 | 0.031 | -2 | 0.529 |
TGFBR1 |
0.517 | -0.044 | -2 | 0.708 |
PAK3 |
0.517 | -0.012 | -2 | 0.567 |
BIKE |
0.517 | 0.019 | 1 | 0.153 |
PRKD1 |
0.517 | -0.002 | -3 | 0.498 |
QIK |
0.516 | -0.016 | -3 | 0.479 |
CRIK |
0.516 | 0.029 | -3 | 0.384 |
PINK1 |
0.516 | 0.095 | 1 | 0.333 |
NDR2 |
0.516 | 0.023 | -3 | 0.443 |
PRKX |
0.516 | 0.066 | -3 | 0.361 |
GSK3B |
0.516 | 0.018 | 4 | 0.250 |
CDC7 |
0.516 | -0.099 | 1 | 0.111 |
RAF1 |
0.515 | -0.166 | 1 | 0.101 |
NUAK1 |
0.515 | 0.010 | -3 | 0.418 |
HUNK |
0.515 | -0.097 | 2 | 0.545 |
NEK8 |
0.514 | -0.041 | 2 | 0.627 |
AURB |
0.513 | 0.006 | -2 | 0.493 |
MST1 |
0.513 | 0.016 | 1 | 0.094 |
MEK1 |
0.513 | -0.137 | 2 | 0.526 |
GRK5 |
0.512 | -0.138 | -3 | 0.455 |
MEKK3 |
0.512 | -0.106 | 1 | 0.112 |
PLK4 |
0.512 | -0.040 | 2 | 0.317 |
CAMK2G |
0.512 | -0.111 | 2 | 0.463 |
OSR1 |
0.511 | 0.028 | 2 | 0.586 |
DLK |
0.511 | -0.164 | 1 | 0.121 |
TTBK2 |
0.511 | -0.105 | 2 | 0.513 |
PDHK4 |
0.511 | -0.216 | 1 | 0.171 |
BRAF |
0.511 | -0.117 | -4 | 0.459 |
SMMLCK |
0.511 | -0.037 | -3 | 0.442 |
MAPKAPK3 |
0.510 | -0.047 | -3 | 0.440 |
CAMKK2 |
0.510 | -0.068 | -2 | 0.515 |
PASK |
0.510 | -0.059 | -3 | 0.442 |
RIPK1 |
0.510 | -0.161 | 1 | 0.107 |
MST2 |
0.510 | -0.048 | 1 | 0.097 |
QSK |
0.510 | -0.026 | 4 | 0.438 |
TBK1 |
0.510 | -0.143 | 1 | 0.082 |
DNAPK |
0.509 | -0.059 | 1 | 0.139 |
VRK1 |
0.509 | -0.105 | 2 | 0.577 |
PDHK1 |
0.509 | -0.194 | 1 | 0.152 |
DRAK1 |
0.509 | -0.073 | 1 | 0.070 |
LATS2 |
0.509 | -0.013 | -5 | 0.409 |
CAMKK1 |
0.508 | -0.084 | -2 | 0.509 |
ASK1 |
0.508 | -0.026 | 1 | 0.119 |
MARK3 |
0.508 | -0.019 | 4 | 0.388 |
SIK |
0.508 | -0.017 | -3 | 0.407 |
MYLK4 |
0.507 | -0.033 | -2 | 0.573 |
ALK2 |
0.507 | -0.083 | -2 | 0.695 |
CAMK2D |
0.506 | -0.103 | -3 | 0.480 |
PKACA |
0.506 | 0.013 | -2 | 0.509 |
CAMK1G |
0.506 | -0.013 | -3 | 0.395 |
P70S6K |
0.506 | -0.010 | -3 | 0.366 |
STK33 |
0.506 | -0.001 | 2 | 0.364 |
GRK1 |
0.506 | -0.070 | -2 | 0.575 |
TAK1 |
0.505 | -0.095 | 1 | 0.087 |
TLK2 |
0.504 | -0.134 | 1 | 0.100 |
ACVR2A |
0.504 | -0.092 | -2 | 0.662 |
MASTL |
0.503 | -0.199 | -2 | 0.585 |
GCN2 |
0.503 | -0.116 | 2 | 0.544 |
DAPK3 |
0.502 | -0.054 | -3 | 0.428 |
TTK |
0.502 | -0.042 | -2 | 0.640 |
ACVR2B |
0.501 | -0.112 | -2 | 0.671 |
IKKE |
0.500 | -0.173 | 1 | 0.082 |
CAMK2A |
0.500 | -0.062 | 2 | 0.455 |
PLK1 |
0.500 | -0.147 | -2 | 0.603 |
BRSK2 |
0.500 | -0.035 | -3 | 0.469 |
CHK2 |
0.499 | -0.031 | -3 | 0.351 |
PAK2 |
0.499 | -0.070 | -2 | 0.544 |
BMPR1A |
0.499 | -0.071 | 1 | 0.079 |
GRK6 |
0.499 | -0.176 | 1 | 0.100 |
MARK2 |
0.498 | -0.073 | 4 | 0.374 |
CK1E |
0.498 | -0.038 | -3 | 0.221 |
CHK1 |
0.497 | -0.098 | -3 | 0.443 |
TLK1 |
0.497 | -0.134 | -2 | 0.684 |
MAPKAPK2 |
0.496 | -0.059 | -3 | 0.378 |
CAMK4 |
0.496 | -0.098 | -3 | 0.445 |
MEK2 |
0.496 | -0.135 | 2 | 0.527 |
SBK |
0.496 | 0.024 | -3 | 0.297 |
SMG1 |
0.496 | -0.101 | 1 | 0.145 |
PAK5 |
0.495 | -0.006 | -2 | 0.417 |
BRSK1 |
0.494 | -0.045 | -3 | 0.435 |
MARK1 |
0.492 | -0.080 | 4 | 0.397 |
MSK2 |
0.492 | -0.065 | -3 | 0.370 |
BCKDK |
0.492 | -0.155 | -1 | 0.432 |
DAPK1 |
0.491 | -0.071 | -3 | 0.410 |
CAMK1D |
0.491 | -0.045 | -3 | 0.362 |
IKKB |
0.491 | -0.191 | -2 | 0.514 |
GRK2 |
0.490 | -0.105 | -2 | 0.549 |
ATM |
0.489 | -0.124 | 1 | 0.121 |
PAK4 |
0.489 | -0.003 | -2 | 0.422 |
CAMK1A |
0.489 | -0.032 | -3 | 0.353 |
CK1A2 |
0.489 | -0.060 | -3 | 0.191 |
CK1D |
0.489 | -0.053 | -3 | 0.195 |
MSK1 |
0.489 | -0.062 | -3 | 0.383 |
IKKA |
0.488 | -0.145 | -2 | 0.521 |
IRAK1 |
0.487 | -0.172 | -1 | 0.443 |
CAMK2B |
0.486 | -0.126 | 2 | 0.422 |
PKG1 |
0.486 | -0.013 | -2 | 0.509 |
TTBK1 |
0.483 | -0.131 | 2 | 0.424 |
CK2A2 |
0.483 | -0.087 | 1 | 0.065 |
SNRK |
0.483 | -0.127 | 2 | 0.370 |
GRK4 |
0.481 | -0.214 | -2 | 0.626 |
AURA |
0.480 | -0.064 | -2 | 0.452 |
ALPHAK3 |
0.480 | -0.120 | -1 | 0.479 |
PLK3 |
0.480 | -0.169 | 2 | 0.408 |
MAPKAPK5 |
0.479 | -0.113 | -3 | 0.355 |
FAM20C |
0.479 | -0.064 | 2 | 0.324 |
CK1G1 |
0.475 | -0.071 | -3 | 0.196 |
RIPK2 |
0.474 | -0.198 | 1 | 0.089 |
CK2A1 |
0.473 | -0.096 | 1 | 0.057 |
STLK3 |
0.473 | -0.166 | 1 | 0.092 |
GRK3 |
0.472 | -0.118 | -2 | 0.523 |
LIMK2_TYR |
0.469 | 0.274 | -3 | 0.525 |
YANK3 |
0.464 | -0.076 | 2 | 0.191 |
PKMYT1_TYR |
0.458 | 0.176 | 3 | 0.311 |
TNNI3K_TYR |
0.456 | 0.114 | 1 | 0.166 |
PLK2 |
0.455 | -0.161 | -3 | 0.319 |
PDHK3_TYR |
0.453 | 0.094 | 4 | 0.566 |
TESK1_TYR |
0.452 | 0.145 | 3 | 0.362 |
LIMK1_TYR |
0.450 | 0.149 | 2 | 0.598 |
YANK2 |
0.449 | -0.082 | 2 | 0.205 |
CK1G3 |
0.442 | -0.099 | -3 | 0.098 |
PINK1_TYR |
0.440 | -0.007 | 1 | 0.164 |
TNK1 |
0.439 | 0.017 | 3 | 0.288 |
JAK1 |
0.439 | -0.033 | 1 | 0.112 |
CK1A |
0.439 | -0.091 | -3 | 0.131 |
MAP2K7_TYR |
0.438 | -0.072 | 2 | 0.546 |
EPHA6 |
0.435 | -0.049 | -1 | 0.499 |
ROS1 |
0.434 | -0.070 | 3 | 0.303 |
MAP2K4_TYR |
0.434 | -0.102 | -1 | 0.535 |
WEE1_TYR |
0.433 | 0.029 | -1 | 0.419 |
JAK2 |
0.433 | -0.116 | 1 | 0.143 |
NEK10_TYR |
0.432 | -0.030 | 1 | 0.110 |
TYK2 |
0.431 | -0.133 | 1 | 0.120 |
TNK2 |
0.430 | -0.075 | 3 | 0.264 |
MAP2K6_TYR |
0.430 | -0.092 | -1 | 0.541 |
BMPR2_TYR |
0.430 | -0.077 | -1 | 0.535 |
RET |
0.429 | -0.130 | 1 | 0.134 |
MST1R |
0.429 | -0.113 | 3 | 0.288 |
CK1G2 |
0.428 | -0.100 | -3 | 0.146 |
PDHK4_TYR |
0.428 | -0.120 | 2 | 0.520 |
TYRO3 |
0.428 | -0.089 | 3 | 0.327 |
KDR |
0.426 | -0.081 | 3 | 0.263 |
PDHK1_TYR |
0.426 | -0.153 | -1 | 0.562 |
DDR1 |
0.426 | -0.085 | 4 | 0.461 |
CSF1R |
0.424 | -0.122 | 3 | 0.283 |
JAK3 |
0.420 | -0.125 | 1 | 0.126 |
ABL2 |
0.420 | -0.135 | -1 | 0.461 |
ABL1 |
0.417 | -0.136 | -1 | 0.459 |
LCK |
0.417 | -0.115 | -1 | 0.492 |
FGFR1 |
0.416 | -0.105 | 3 | 0.265 |
BLK |
0.416 | -0.112 | -1 | 0.504 |
DDR2 |
0.416 | -0.061 | 3 | 0.254 |
TEK |
0.416 | -0.074 | 3 | 0.288 |
YES1 |
0.415 | -0.140 | -1 | 0.510 |
EPHB4 |
0.415 | -0.177 | -1 | 0.444 |
FGFR2 |
0.414 | -0.125 | 3 | 0.260 |
PDGFRB |
0.414 | -0.166 | 3 | 0.306 |
FGR |
0.413 | -0.182 | 1 | 0.088 |
FLT3 |
0.413 | -0.160 | 3 | 0.315 |
HCK |
0.413 | -0.166 | -1 | 0.474 |
TXK |
0.412 | -0.131 | 1 | 0.075 |
PDGFRA |
0.410 | -0.160 | 3 | 0.322 |
KIT |
0.410 | -0.165 | 3 | 0.283 |
ITK |
0.410 | -0.156 | -1 | 0.423 |
MET |
0.408 | -0.156 | 3 | 0.270 |
AXL |
0.408 | -0.179 | 3 | 0.257 |
INSRR |
0.408 | -0.182 | 3 | 0.264 |
ALK |
0.407 | -0.162 | 3 | 0.255 |
MATK |
0.407 | -0.087 | -1 | 0.441 |
MUSK |
0.404 | -0.087 | 1 | 0.061 |
MERTK |
0.403 | -0.193 | 3 | 0.252 |
EPHA4 |
0.402 | -0.164 | 2 | 0.412 |
LTK |
0.401 | -0.173 | 3 | 0.252 |
TEC |
0.401 | -0.154 | -1 | 0.373 |
BMX |
0.401 | -0.145 | -1 | 0.369 |
FLT1 |
0.401 | -0.166 | -1 | 0.467 |
EPHB1 |
0.401 | -0.233 | 1 | 0.078 |
FER |
0.400 | -0.259 | 1 | 0.095 |
FGFR3 |
0.400 | -0.150 | 3 | 0.255 |
FRK |
0.399 | -0.179 | -1 | 0.482 |
EPHA1 |
0.399 | -0.183 | 3 | 0.264 |
FYN |
0.399 | -0.157 | -1 | 0.478 |
SRMS |
0.398 | -0.248 | 1 | 0.071 |
EPHB3 |
0.398 | -0.231 | -1 | 0.420 |
INSR |
0.397 | -0.184 | 3 | 0.252 |
FLT4 |
0.397 | -0.189 | 3 | 0.246 |
EPHA7 |
0.396 | -0.181 | 2 | 0.429 |
BTK |
0.396 | -0.213 | -1 | 0.383 |
ERBB2 |
0.396 | -0.197 | 1 | 0.102 |
EPHB2 |
0.395 | -0.228 | -1 | 0.425 |
PTK2B |
0.394 | -0.154 | -1 | 0.439 |
EGFR |
0.393 | -0.146 | 1 | 0.081 |
SRC |
0.393 | -0.171 | -1 | 0.481 |
CSK |
0.393 | -0.173 | 2 | 0.439 |
NTRK2 |
0.393 | -0.231 | 3 | 0.244 |
LYN |
0.392 | -0.202 | 3 | 0.237 |
PTK6 |
0.392 | -0.220 | -1 | 0.369 |
NTRK3 |
0.391 | -0.198 | -1 | 0.378 |
EPHA3 |
0.388 | -0.205 | 2 | 0.391 |
FGFR4 |
0.385 | -0.170 | -1 | 0.420 |
ZAP70 |
0.384 | -0.106 | -1 | 0.396 |
NTRK1 |
0.384 | -0.289 | -1 | 0.414 |
ERBB4 |
0.384 | -0.138 | 1 | 0.076 |
EPHA8 |
0.384 | -0.192 | -1 | 0.427 |
PTK2 |
0.381 | -0.138 | -1 | 0.443 |
IGF1R |
0.379 | -0.191 | 3 | 0.218 |
SYK |
0.378 | -0.165 | -1 | 0.429 |
EPHA5 |
0.375 | -0.237 | 2 | 0.377 |
EPHA2 |
0.373 | -0.205 | -1 | 0.382 |
FES |
0.369 | -0.188 | -1 | 0.359 |