Motif 698 (n=59)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A8K0Z3 | WASHC1 | S217 | ochoa | WASH complex subunit 1 (CXYorf1-like protein on chromosome 9) (Protein FAM39E) (WAS protein family homolog 1) | Acts as a component of the WASH core complex that functions as a nucleation-promoting factor (NPF) at the surface of endosomes, where it recruits and activates the Arp2/3 complex to induce actin polymerization, playing a key role in the fission of tubules that serve as transport intermediates during endosome sorting (PubMed:19922874, PubMed:19922875, PubMed:20498093, PubMed:23452853). Involved in endocytic trafficking of EGF (By similarity). Involved in transferrin receptor recycling. Regulates the trafficking of endosomal alpha5beta1 integrin to the plasma membrane and involved in invasive cell migration (PubMed:22114305). In T-cells involved in endosome-to-membrane recycling of receptors including T-cell receptor (TCR), CD28 and ITGAL; proposed to be implicated in T cell proliferation and effector function. In dendritic cells involved in endosome-to-membrane recycling of major histocompatibility complex (MHC) class II probably involving retromer and subsequently allowing antigen sampling, loading and presentation during T-cell activation (By similarity). Involved in Arp2/3 complex-dependent actin assembly driving Salmonella typhimurium invasion independent of ruffling. Involved in the exocytosis of MMP14 leading to matrix remodeling during invasive migration and implicating late endosome-to-plasma membrane tubular connections and cooperation with the exocyst complex (PubMed:24344185). Involved in negative regulation of autophagy independently from its role in endosomal sorting by inhibiting BECN1 ubiquitination to inactivate PIK3C3/Vps34 activity (By similarity). {ECO:0000250|UniProtKB:C4AMC7, ECO:0000250|UniProtKB:Q8VDD8, ECO:0000269|PubMed:19922874, ECO:0000269|PubMed:19922875, ECO:0000269|PubMed:20498093, ECO:0000269|PubMed:22114305, ECO:0000269|PubMed:23452853, ECO:0000305|PubMed:20498093}. |
A8MWX3 | WASH4P | S230 | ochoa | Putative WAS protein family homolog 4 (Protein FAM39CP) | May act as a nucleation-promoting factor at the surface of endosomes, where it recruits and activates the Arp2/3 complex to induce actin polymerization, playing a key role in the fission of tubules that serve as transport intermediates during endosome sorting. {ECO:0000250|UniProtKB:A8K0Z3, ECO:0000250|UniProtKB:C4AMC7}. |
C4AMC7 | WASH3P | S215 | ochoa | Putative WAS protein family homolog 3 (Protein FAM39DP) | Acts as a nucleation-promoting factor at the surface of endosomes, where it recruits and activates the Arp2/3 complex to induce actin polymerization, playing a key role in the fission of tubules that serve as transport intermediates during endosome sorting (PubMed:18159949, PubMed:20175130). Involved in endocytic trafficking of EGF (PubMed:20175130). Involved in transferrin receptor recycling. Regulates the trafficking of endosomal alpha5beta1 integrin to the plasma membrane and involved in invasive cell migration (By similarity). In T-cells involved in endosome-to-membrane recycling of receptors including T-cell receptor (TCR), CD28 and ITGAL; proposed to be implicated in T cell proliferation and effector function. In dendritic cells involved in endosome-to-membrane recycling of major histocompatibility complex (MHC) class II probably involving retromer and subsequently allowing antigen sampling, loading and presentation during T-cell activation. Involved in Arp2/3 complex-dependent actin assembly driving Salmonella typhimurium invasion independent of ruffling (By similarity). Involved in the exocytosis of MMP14 leading to matrix remodeling during invasive migration and implicating late endosome-to-plasma membrane tubular connections and cooperation with the exocyst complex (By similarity). Involved in negative regulation of autophagy independently from its role in endosomal sorting by inhibiting BECN1 ubiquitination to inactivate PIK3C3/Vps34 activity (By similarity). {ECO:0000250|UniProtKB:A8K0Z3, ECO:0000250|UniProtKB:Q8VDD8, ECO:0000269|PubMed:18159949, ECO:0000269|PubMed:20175130}. |
P0C0S8 | H2AC11 | S20 | ochoa | Histone H2A type 1 (H2A.1) (Histone H2A/ptl) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
P0DPH7 | TUBA3C | Y262 | 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 | Y262 | 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. |
P11055 | MYH3 | S1336 | ochoa | Myosin-3 (Muscle embryonic myosin heavy chain) (Myosin heavy chain 3) (Myosin heavy chain, fast skeletal muscle, embryonic) (SMHCE) | Muscle contraction. |
P12882 | MYH1 | S668 | 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}. |
P12882 | MYH1 | S1339 | 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 | S664 | 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}. |
P12883 | MYH7 | S1335 | 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}. |
P13533 | MYH6 | S1337 | ochoa | Myosin-6 (Myosin heavy chain 6) (Myosin heavy chain, cardiac muscle alpha isoform) (MyHC-alpha) | Muscle contraction. |
P13535 | MYH8 | S667 | ochoa | Myosin-8 (Myosin heavy chain 8) (Myosin heavy chain, skeletal muscle, perinatal) (MyHC-perinatal) | Muscle contraction. |
P13535 | MYH8 | S1338 | ochoa | Myosin-8 (Myosin heavy chain 8) (Myosin heavy chain, skeletal muscle, perinatal) (MyHC-perinatal) | Muscle contraction. |
P20671 | H2AC7 | S20 | ochoa | Histone H2A type 1-D (Histone H2A.3) (Histone H2A/g) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
P41229 | KDM5C | S897 | ochoa | Lysine-specific demethylase 5C (EC 1.14.11.67) (Histone demethylase JARID1C) (Jumonji/ARID domain-containing protein 1C) (Protein SmcX) (Protein Xe169) ([histone H3]-trimethyl-L-lysine(4) demethylase 5C) | Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code (PubMed:28262558). Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4'. Participates in transcriptional repression of neuronal genes by recruiting histone deacetylases and REST at neuron-restrictive silencer elements. Represses the CLOCK-BMAL1 heterodimer-mediated transcriptional activation of the core clock component PER2 (By similarity). {ECO:0000250|UniProtKB:P41230, ECO:0000269|PubMed:17320160, ECO:0000269|PubMed:17320161, ECO:0000269|PubMed:17468742, ECO:0000269|PubMed:26645689, ECO:0000269|PubMed:28262558}. |
P46940 | IQGAP1 | S330 | ochoa | Ras GTPase-activating-like protein IQGAP1 (p195) | Plays a crucial role in regulating the dynamics and assembly of the actin cytoskeleton. Recruited to the cell cortex by interaction with ILK which allows it to cooperate with its effector DIAPH1 to locally stabilize microtubules and allow stable insertion of caveolae into the plasma membrane (By similarity). Binds to activated CDC42 but does not stimulate its GTPase activity. Associates with calmodulin. May promote neurite outgrowth (PubMed:15695813). May play a possible role in cell cycle regulation by contributing to cell cycle progression after DNA replication arrest (PubMed:20883816). {ECO:0000250|UniProtKB:Q9JKF1, ECO:0000269|PubMed:15695813, ECO:0000269|PubMed:20883816}. |
P68363 | TUBA1B | Y262 | 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 | Y262 | 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. |
Q6PEY2 | TUBA3E | Y262 | 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. |
Q6VEQ5 | WASH2P | S217 | ochoa | WAS protein family homolog 2 (CXYorf1-like protein on chromosome 2) (Protein FAM39B) | Acts as a nucleation-promoting factor at the surface of endosomes, where it recruits and activates the Arp2/3 complex to induce actin polymerization, playing a key role in the fission of tubules that serve as transport intermediates during endosome sorting. Involved in endocytic trafficking of EGF. Involved in transferrin receptor recycling. Regulates the trafficking of endosomal alpha5beta1 integrin to the plasma membrane and involved in invasive cell migration. In T-cells involved in endosome-to-membrane recycling of receptors including T-cell receptor (TCR), CD28 and ITGAL; proposed to be implicated in T-cell proliferation and effector function. In dendritic cells involved in endosome-to-membrane recycling of major histocompatibility complex (MHC) class II probably involving retromer and subsequently allowing antigen sampling, loading and presentation during T-cell activation. Involved in Arp2/3 complex-dependent actin assembly driving Salmonella typhimurium invasion independent of ruffling. Involved in the exocytosis of MMP14 leading to matrix remodeling during invasive migration and implicating late endosome-to-plasma membrane tubular connections and cooperation with the exocyst complex. Involved in negative regulation of autophagy independently from its role in endosomal sorting by inhibiting BECN1 ubiquitination to inactivate PIK3C3/Vps34 activity (By similarity). {ECO:0000250|UniProtKB:A8K0Z3, ECO:0000250|UniProtKB:C4AMC7, ECO:0000250|UniProtKB:Q8VDD8}. |
Q71U36 | TUBA1A | Y262 | 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. |
Q96KK5 | H2AC12 | S20 | ochoa | Histone H2A type 1-H (H2A-clustered histone 12) (Histone H2A/s) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q99878 | H2AC14 | S20 | ochoa | Histone H2A type 1-J (Histone H2A/e) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q9BQE3 | TUBA1C | Y262 | 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. |
Q9BY66 | KDM5D | S884 | ochoa | Lysine-specific demethylase 5D (EC 1.14.11.67) (Histocompatibility Y antigen) (H-Y) (Histone demethylase JARID1D) (Jumonji/ARID domain-containing protein 1D) (Protein SmcY) ([histone H3]-trimethyl-L-lysine(4) demethylase 5D) | Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4'. May play a role in spermatogenesis. Involved in transcriptional repression of diverse metastasis-associated genes; in this function seems to cooperate with ZMYND8. Suppresses prostate cancer cell invasion. Regulates androgen receptor (AR) transcriptional activity by demethylating H3K4me3 active transcription marks. {ECO:0000269|PubMed:17320160, ECO:0000269|PubMed:17320162, ECO:0000269|PubMed:17351630, ECO:0000269|PubMed:26747897, ECO:0000269|PubMed:27185910, ECO:0000269|PubMed:27427228, ECO:0000269|PubMed:27477906}. |
Q9NQA3 | WASH6P | S199 | ochoa | WAS protein family homolog 6 (Protein FAM39A) | May act as a nucleation-promoting factor at the surface of endosomes, where it recruits and activates the Arp2/3 complex to induce actin polymerization, playing a key role in the fission of tubules that serve as transport intermediates during endosome sorting. {ECO:0000250|UniProtKB:A8K0Z3, ECO:0000250|UniProtKB:C4AMC7}. |
Q9NY65 | TUBA8 | Y262 | ochoa | Tubulin alpha-8 chain (EC 3.6.5.-) (Alpha-tubulin 8) (Tubulin alpha chain-like 2) [Cleaved into: Dephenylalaninated tubulin alpha-8 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. |
Q9UKX2 | MYH2 | S670 | 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}. |
Q9UKX2 | MYH2 | S1341 | 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}. |
Q9UKX3 | MYH13 | S668 | ochoa | Myosin-13 (Myosin heavy chain 13) (Myosin heavy chain, skeletal muscle, extraocular) (MyHC-EO) (Myosin heavy chain, skeletal muscle, laryngeal) (MyHC-IIL) (Superfast myosin) | Fast twitching myosin mediating the high-velocity and low-tension contractions of specific striated muscles. {ECO:0000269|PubMed:23908353}. |
Q9Y623 | MYH4 | S668 | 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. |
O95678 | KRT75 | S162 | Sugiyama | Keratin, type II cytoskeletal 75 (Cytokeratin-75) (CK-75) (Keratin-6 hair follicle) (hK6hf) (Keratin-75) (K75) (Type II keratin-K6hf) (Type-II keratin Kb18) | Plays a central role in hair and nail formation. Essential component of keratin intermediate filaments in the companion layer of the hair follicle. |
P02538 | KRT6A | S176 | Sugiyama | Keratin, type II cytoskeletal 6A (Cytokeratin-6A) (CK-6A) (Cytokeratin-6D) (CK-6D) (Keratin-6A) (K6A) (Type-II keratin Kb6) (allergen Hom s 5) | Epidermis-specific type I keratin involved in wound healing. Involved in the activation of follicular keratinocytes after wounding, while it does not play a major role in keratinocyte proliferation or migration. Participates in the regulation of epithelial migration by inhibiting the activity of SRC during wound repair. {ECO:0000250|UniProtKB:P50446}. |
P04259 | KRT6B | S176 | Sugiyama | Keratin, type II cytoskeletal 6B (Cytokeratin-6B) (CK-6B) (Keratin-6B) (K6B) (Type-II keratin Kb10) | None |
P05787 | KRT8 | S104 | Sugiyama | Keratin, type II cytoskeletal 8 (Cytokeratin-8) (CK-8) (Keratin-8) (K8) (Type-II keratin Kb8) | Together with KRT19, helps to link the contractile apparatus to dystrophin at the costameres of striated muscle. {ECO:0000269|PubMed:16000376}. |
P08729 | KRT7 | S104 | Sugiyama | Keratin, type II cytoskeletal 7 (Cytokeratin-7) (CK-7) (Keratin-7) (K7) (Sarcolectin) (Type-II keratin Kb7) | Blocks interferon-dependent interphase and stimulates DNA synthesis in cells. Involved in the translational regulation of the human papillomavirus type 16 E7 mRNA (HPV16 E7). {ECO:0000269|PubMed:10492017, ECO:0000269|PubMed:12072504}. |
P12035 | KRT3 | S211 | Sugiyama | Keratin, type II cytoskeletal 3 (65 kDa cytokeratin) (Cytokeratin-3) (CK-3) (Keratin-3) (K3) (Type-II keratin Kb3) | None |
P13647 | KRT5 | S181 | Sugiyama | Keratin, type II cytoskeletal 5 (58 kDa cytokeratin) (Cytokeratin-5) (CK-5) (Keratin-5) (K5) (Type-II keratin Kb5) | Required for the formation of keratin intermediate filaments in the basal epidermis and maintenance of the skin barrier in response to mechanical stress (By similarity). Regulates the recruitment of Langerhans cells to the epidermis, potentially by modulation of the abundance of macrophage chemotactic cytokines, macrophage inflammatory cytokines and CTNND1 localization in keratinocytes (By similarity). {ECO:0000250|UniProtKB:Q922U2}. |
P35908 | KRT2 | S191 | Sugiyama | Keratin, type II cytoskeletal 2 epidermal (Cytokeratin-2e) (CK-2e) (Epithelial keratin-2e) (Keratin-2 epidermis) (Keratin-2e) (K2e) (Type-II keratin Kb2) | Probably contributes to terminal cornification (PubMed:1380918). Associated with keratinocyte activation, proliferation and keratinization (PubMed:12598329). Required for maintenance of corneocytes and keratin filaments in suprabasal keratinocytes in the epidermis of the ear, potentially via moderation of expression and localization of keratins and their partner proteins (By similarity). Plays a role in the establishment of the epidermal barrier on plantar skin (By similarity). {ECO:0000250|UniProtKB:Q3TTY5, ECO:0000269|PubMed:12598329, ECO:0000269|PubMed:1380918}. |
P48668 | KRT6C | S176 | Sugiyama | Keratin, type II cytoskeletal 6C (Cytokeratin-6C) (CK-6C) (Cytokeratin-6E) (CK-6E) (Keratin K6h) (Keratin-6C) (K6C) (Type-II keratin Kb12) | None |
Q01546 | KRT76 | S196 | Sugiyama | Keratin, type II cytoskeletal 2 oral (Cytokeratin-2P) (CK-2P) (K2P) (Keratin-76) (K76) (Type-II keratin Kb9) | Probably contributes to terminal cornification. {ECO:0000269|PubMed:1282112}. |
Q14CN4 | KRT72 | S138 | Sugiyama | Keratin, type II cytoskeletal 72 (Cytokeratin-72) (CK-72) (Keratin-72) (K72) (Type II inner root sheath-specific keratin-K6irs2) (Type-II keratin Kb35) | Has a role in hair formation. Specific component of keratin intermediate filaments in the inner root sheath (IRS) of the hair follicle (Probable). {ECO:0000305}. |
Q3SY84 | KRT71 | S143 | Sugiyama | Keratin, type II cytoskeletal 71 (Cytokeratin-71) (CK-71) (Keratin-71) (K71) (Type II inner root sheath-specific keratin-K6irs1) (Keratin 6 irs) (hK6irs) (hK6irs1) (Type-II keratin Kb34) | Plays a central role in hair formation. Essential component of keratin intermediate filaments in the inner root sheath (IRS) of the hair follicle. {ECO:0000269|PubMed:22592156}. |
Q5XKE5 | KRT79 | S155 | Sugiyama | Keratin, type II cytoskeletal 79 (Cytokeratin-79) (CK-79) (Keratin-6-like) (Keratin-6L) (Keratin-79) (K79) (Type-II keratin Kb38) | None |
Q7RTS7 | KRT74 | S153 | Sugiyama | Keratin, type II cytoskeletal 74 (Cytokeratin-74) (CK-74) (Keratin-5c) (K5C) (Keratin-74) (K74) (Type II inner root sheath-specific keratin-K6irs4) (Type-II keratin Kb37) | Has a role in hair formation. Specific component of keratin intermediate filaments in the inner root sheath (IRS) of the hair follicle (Probable). {ECO:0000305}. |
Q7Z794 | KRT77 | S177 | Sugiyama | Keratin, type II cytoskeletal 1b (Cytokeratin-1B) (CK-1B) (Keratin-77) (K77) (Type-II keratin Kb39) | None |
Q86Y46 | KRT73 | S145 | Sugiyama | Keratin, type II cytoskeletal 73 (Cytokeratin-73) (CK-73) (Keratin-73) (K73) (Type II inner root sheath-specific keratin-K6irs3) (Type-II keratin Kb36) | Has a role in hair formation. Specific component of keratin intermediate filaments in the inner root sheath (IRS) of the hair follicle (Probable). {ECO:0000305}. |
Q9NSB2 | KRT84 | S178 | Sugiyama | Keratin, type II cuticular Hb4 (Keratin-84) (K84) (Type II hair keratin Hb4) (Type-II keratin Kb24) | None |
P05783 | KRT18 | S93 | Sugiyama | Keratin, type I cytoskeletal 18 (Cell proliferation-inducing gene 46 protein) (Cytokeratin-18) (CK-18) (Keratin-18) (K18) | Involved in the uptake of thrombin-antithrombin complexes by hepatic cells (By similarity). When phosphorylated, plays a role in filament reorganization. Involved in the delivery of mutated CFTR to the plasma membrane. Together with KRT8, is involved in interleukin-6 (IL-6)-mediated barrier protection. {ECO:0000250, ECO:0000269|PubMed:15529338, ECO:0000269|PubMed:16424149, ECO:0000269|PubMed:17213200, ECO:0000269|PubMed:7523419, ECO:0000269|PubMed:8522591, ECO:0000269|PubMed:9298992, ECO:0000269|PubMed:9524113}. |
P04908 | H2AC4 | S20 | Sugiyama | Histone H2A type 1-B/E (Histone H2A.2) (Histone H2A/a) (Histone H2A/m) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
P16104 | H2AX | S20 | Sugiyama | Histone H2AX (H2a/x) (Histone H2A.X) | Variant histone H2A which replaces conventional H2A in a subset of nucleosomes. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. Required for checkpoint-mediated arrest of cell cycle progression in response to low doses of ionizing radiation and for efficient repair of DNA double strand breaks (DSBs) specifically when modified by C-terminal phosphorylation. {ECO:0000269|PubMed:10959836, ECO:0000269|PubMed:12419185, ECO:0000269|PubMed:12607005, ECO:0000269|PubMed:15201865, ECO:0000269|PubMed:17709392, ECO:0000269|PubMed:26438602}. |
Q16777 | H2AC20 | S20 | Sugiyama | Histone H2A type 2-C (H2A-clustered histone 20) (Histone H2A-GL101) (Histone H2A/q) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q6FI13 | H2AC18 | S20 | Sugiyama | Histone H2A type 2-A (H2A-clustered histone 18) (H2A-clustered histone 19) (Histone H2A.2) (Histone H2A/o) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q7L7L0 | H2AC25 | S20 | Sugiyama | Histone H2A type 3 (H2A-clustered histone 25) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q8IUE6 | H2AC21 | S20 | Sugiyama | Histone H2A type 2-B (H2A-clustered histone 21) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q93077 | H2AC6 | S20 | Sugiyama | Histone H2A type 1-C (H2A-clustered histone 6) (Histone H2A/l) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q96QV6 | H2AC1 | S20 | Sugiyama | Histone H2A type 1-A (H2A-clustered histone 1) (Histone H2A/r) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Q9BTM1 | H2AJ | S20 | Sugiyama | Histone H2A.J (H2a/j) | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-9609690 | HCMV Early Events | 1.110223e-16 | 15.955 |
R-HSA-6805567 | Keratinization | 1.110223e-16 | 15.955 |
R-HSA-5689901 | Metalloprotease DUBs | 1.110223e-16 | 15.955 |
R-HSA-6809371 | Formation of the cornified envelope | 1.110223e-16 | 15.955 |
R-HSA-9609646 | HCMV Infection | 1.110223e-16 | 15.955 |
R-HSA-3214858 | RMTs methylate histone arginines | 1.110223e-16 | 15.955 |
R-HSA-1266738 | Developmental Biology | 1.110223e-16 | 15.955 |
R-HSA-3214815 | HDACs deacetylate histones | 9.992007e-16 | 15.000 |
R-HSA-5689603 | UCH proteinases | 2.109424e-14 | 13.676 |
R-HSA-3247509 | Chromatin modifying enzymes | 2.531308e-14 | 13.597 |
R-HSA-190840 | Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 2.919887e-14 | 13.535 |
R-HSA-190872 | Transport of connexons to the plasma membrane | 4.152234e-14 | 13.382 |
R-HSA-4839726 | Chromatin organization | 5.762057e-14 | 13.239 |
R-HSA-389977 | Post-chaperonin tubulin folding pathway | 8.038015e-14 | 13.095 |
R-HSA-389960 | Formation of tubulin folding intermediates by CCT/TriC | 3.406164e-13 | 12.468 |
R-HSA-3214847 | HATs acetylate histones | 3.808065e-13 | 12.419 |
R-HSA-171306 | Packaging Of Telomere Ends | 7.239764e-13 | 12.140 |
R-HSA-73728 | RNA Polymerase I Promoter Opening | 7.239764e-13 | 12.140 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 9.166001e-13 | 12.038 |
R-HSA-5334118 | DNA methylation | 1.152523e-12 | 11.938 |
R-HSA-68886 | M Phase | 1.243672e-12 | 11.905 |
R-HSA-389958 | Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 1.787459e-12 | 11.748 |
R-HSA-110330 | Recognition and association of DNA glycosylase with site containing an affected ... | 2.206124e-12 | 11.656 |
R-HSA-68616 | Assembly of the ORC complex at the origin of replication | 2.707945e-12 | 11.567 |
R-HSA-9668328 | Sealing of the nuclear envelope (NE) by ESCRT-III | 2.707945e-12 | 11.567 |
R-HSA-9843970 | Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | 4.016898e-12 | 11.396 |
R-HSA-190861 | Gap junction assembly | 4.016898e-12 | 11.396 |
R-HSA-110328 | Recognition and association of DNA glycosylase with site containing an affected ... | 4.016898e-12 | 11.396 |
R-HSA-212300 | PRC2 methylates histones and DNA | 5.846212e-12 | 11.233 |
R-HSA-427359 | SIRT1 negatively regulates rRNA expression | 7.006506e-12 | 11.154 |
R-HSA-110331 | Cleavage of the damaged purine | 7.006506e-12 | 11.154 |
R-HSA-5689880 | Ub-specific processing proteases | 6.797118e-12 | 11.168 |
R-HSA-73927 | Depurination | 8.362422e-12 | 11.078 |
R-HSA-9670095 | Inhibition of DNA recombination at telomere | 1.177380e-11 | 10.929 |
R-HSA-427389 | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 1.177380e-11 | 10.929 |
R-HSA-9646399 | Aggrephagy | 1.177380e-11 | 10.929 |
R-HSA-5625886 | Activated PKN1 stimulates transcription of AR (androgen receptor) regulated gene... | 1.389366e-11 | 10.857 |
R-HSA-9821002 | Chromatin modifications during the maternal to zygotic transition (MZT) | 1.389366e-11 | 10.857 |
R-HSA-9609736 | Assembly and cell surface presentation of NMDA receptors | 1.633826e-11 | 10.787 |
R-HSA-110329 | Cleavage of the damaged pyrimidine | 1.914924e-11 | 10.718 |
R-HSA-73928 | Depyrimidination | 1.914924e-11 | 10.718 |
R-HSA-9710421 | Defective pyroptosis | 2.237199e-11 | 10.650 |
R-HSA-190828 | Gap junction trafficking | 2.605682e-11 | 10.584 |
R-HSA-774815 | Nucleosome assembly | 3.025902e-11 | 10.519 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 3.025902e-11 | 10.519 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 3.503886e-11 | 10.455 |
R-HSA-8955332 | Carboxyterminal post-translational modifications of tubulin | 4.046252e-11 | 10.393 |
R-HSA-437239 | Recycling pathway of L1 | 4.046252e-11 | 10.393 |
R-HSA-9610379 | HCMV Late Events | 5.244094e-11 | 10.280 |
R-HSA-157858 | Gap junction trafficking and regulation | 5.353706e-11 | 10.271 |
R-HSA-912446 | Meiotic recombination | 7.014156e-11 | 10.154 |
R-HSA-73772 | RNA Polymerase I Promoter Escape | 8.000578e-11 | 10.097 |
R-HSA-1221632 | Meiotic synapsis | 9.105461e-11 | 10.041 |
R-HSA-5250924 | B-WICH complex positively regulates rRNA expression | 9.105461e-11 | 10.041 |
R-HSA-73929 | Base-Excision Repair, AP Site Formation | 1.034067e-10 | 9.985 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 1.171903e-10 | 9.931 |
R-HSA-201722 | Formation of the beta-catenin:TCF transactivating complex | 1.685676e-10 | 9.773 |
R-HSA-9845323 | Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | 2.128128e-10 | 9.672 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 2.668173e-10 | 9.574 |
R-HSA-983189 | Kinesins | 2.128128e-10 | 9.672 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 2.128128e-10 | 9.672 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 2.668173e-10 | 9.574 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 2.668173e-10 | 9.574 |
R-HSA-69278 | Cell Cycle, Mitotic | 3.143683e-10 | 9.503 |
R-HSA-5688426 | Deubiquitination | 4.023248e-10 | 9.395 |
R-HSA-9909649 | Regulation of PD-L1(CD274) transcription | 4.114246e-10 | 9.386 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 5.063472e-10 | 9.296 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 5.063472e-10 | 9.296 |
R-HSA-9843940 | Regulation of endogenous retroelements by KRAB-ZFP proteins | 6.197258e-10 | 9.208 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 6.197258e-10 | 9.208 |
R-HSA-427413 | NoRC negatively regulates rRNA expression | 6.842440e-10 | 9.165 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 6.842440e-10 | 9.165 |
R-HSA-5620920 | Cargo trafficking to the periciliary membrane | 6.842440e-10 | 9.165 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 7.545111e-10 | 9.122 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 8.309547e-10 | 9.080 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 1.102011e-09 | 8.958 |
R-HSA-73864 | RNA Polymerase I Transcription | 1.322641e-09 | 8.879 |
R-HSA-5250941 | Negative epigenetic regulation of rRNA expression | 1.580587e-09 | 8.801 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 1.580587e-09 | 8.801 |
R-HSA-9833482 | PKR-mediated signaling | 1.580587e-09 | 8.801 |
R-HSA-1500620 | Meiosis | 2.424246e-09 | 8.615 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 2.229793e-09 | 8.652 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 1.881047e-09 | 8.726 |
R-HSA-390466 | Chaperonin-mediated protein folding | 3.098393e-09 | 8.509 |
R-HSA-438064 | Post NMDA receptor activation events | 3.098393e-09 | 8.509 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 3.356539e-09 | 8.474 |
R-HSA-9663891 | Selective autophagy | 3.356539e-09 | 8.474 |
R-HSA-9645723 | Diseases of programmed cell death | 3.356539e-09 | 8.474 |
R-HSA-73884 | Base Excision Repair | 3.929176e-09 | 8.406 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 4.245912e-09 | 8.372 |
R-HSA-391251 | Protein folding | 4.946231e-09 | 8.306 |
R-HSA-68867 | Assembly of the pre-replicative complex | 5.332389e-09 | 8.273 |
R-HSA-1640170 | Cell Cycle | 6.903136e-09 | 8.161 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 7.149866e-09 | 8.146 |
R-HSA-6807878 | COPI-mediated anterograde transport | 7.149866e-09 | 8.146 |
R-HSA-157579 | Telomere Maintenance | 7.680131e-09 | 8.115 |
R-HSA-9842860 | Regulation of endogenous retroelements | 1.087327e-08 | 7.964 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 1.087327e-08 | 7.964 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 1.087327e-08 | 7.964 |
R-HSA-5619507 | Activation of HOX genes during differentiation | 1.329379e-08 | 7.876 |
R-HSA-5617472 | Activation of anterior HOX genes in hindbrain development during early embryogen... | 1.329379e-08 | 7.876 |
R-HSA-211000 | Gene Silencing by RNA | 1.616637e-08 | 7.791 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 1.836627e-08 | 7.736 |
R-HSA-69002 | DNA Replication Pre-Initiation | 1.836627e-08 | 7.736 |
R-HSA-9824446 | Viral Infection Pathways | 1.882427e-08 | 7.725 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 2.355159e-08 | 7.628 |
R-HSA-373760 | L1CAM interactions | 3.177160e-08 | 7.498 |
R-HSA-9927418 | Developmental Lineage of Mammary Gland Luminal Epithelial Cells | 3.885953e-08 | 7.411 |
R-HSA-68875 | Mitotic Prophase | 4.002506e-08 | 7.398 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 4.235591e-08 | 7.373 |
R-HSA-73886 | Chromosome Maintenance | 4.235591e-08 | 7.373 |
R-HSA-977225 | Amyloid fiber formation | 4.708099e-08 | 7.327 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 4.737061e-08 | 7.324 |
R-HSA-2132295 | MHC class II antigen presentation | 4.737061e-08 | 7.324 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 5.584950e-08 | 7.253 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 5.584950e-08 | 7.253 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 5.584950e-08 | 7.253 |
R-HSA-5620924 | Intraflagellar transport | 7.539083e-08 | 7.123 |
R-HSA-1474165 | Reproduction | 7.679245e-08 | 7.115 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 8.513134e-08 | 7.070 |
R-HSA-389957 | Prefoldin mediated transfer of substrate to CCT/TriC | 9.526569e-08 | 7.021 |
R-HSA-9018519 | Estrogen-dependent gene expression | 1.094654e-07 | 6.961 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 1.934703e-07 | 6.713 |
R-HSA-1632852 | Macroautophagy | 1.395569e-07 | 6.855 |
R-HSA-69306 | DNA Replication | 2.530517e-07 | 6.597 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 2.643733e-07 | 6.578 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 2.643733e-07 | 6.578 |
R-HSA-9612973 | Autophagy | 2.883254e-07 | 6.540 |
R-HSA-2467813 | Separation of Sister Chromatids | 4.036967e-07 | 6.394 |
R-HSA-1500931 | Cell-Cell communication | 4.544999e-07 | 6.342 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 5.787541e-07 | 6.238 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 5.981155e-07 | 6.223 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 6.017084e-07 | 6.221 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 6.017084e-07 | 6.221 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 6.499625e-07 | 6.187 |
R-HSA-2559583 | Cellular Senescence | 7.853157e-07 | 6.105 |
R-HSA-2262752 | Cellular responses to stress | 8.703280e-07 | 6.060 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 8.775613e-07 | 6.057 |
R-HSA-69275 | G2/M Transition | 9.789130e-07 | 6.009 |
R-HSA-453274 | Mitotic G2-G2/M phases | 1.051898e-06 | 5.978 |
R-HSA-5617833 | Cilium Assembly | 1.129481e-06 | 5.947 |
R-HSA-1280218 | Adaptive Immune System | 1.234645e-06 | 5.908 |
R-HSA-68877 | Mitotic Prometaphase | 1.254994e-06 | 5.901 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 1.392222e-06 | 5.856 |
R-HSA-597592 | Post-translational protein modification | 1.524307e-06 | 5.817 |
R-HSA-389948 | Co-inhibition by PD-1 | 1.594955e-06 | 5.797 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 1.594955e-06 | 5.797 |
R-HSA-446728 | Cell junction organization | 1.604057e-06 | 5.795 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 1.705418e-06 | 5.768 |
R-HSA-5663205 | Infectious disease | 2.045982e-06 | 5.689 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 2.436855e-06 | 5.613 |
R-HSA-68882 | Mitotic Anaphase | 2.761946e-06 | 5.559 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 2.848749e-06 | 5.545 |
R-HSA-418990 | Adherens junctions interactions | 2.937862e-06 | 5.532 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 3.740091e-06 | 5.427 |
R-HSA-8953897 | Cellular responses to stimuli | 3.902410e-06 | 5.409 |
R-HSA-5610787 | Hedgehog 'off' state | 3.904034e-06 | 5.408 |
R-HSA-8939211 | ESR-mediated signaling | 5.141555e-06 | 5.289 |
R-HSA-157118 | Signaling by NOTCH | 5.593195e-06 | 5.252 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 6.073499e-06 | 5.217 |
R-HSA-421270 | Cell-cell junction organization | 7.548368e-06 | 5.122 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 8.612111e-06 | 5.065 |
R-HSA-9734767 | Developmental Cell Lineages | 1.031243e-05 | 4.987 |
R-HSA-9927426 | Developmental Lineage of Mammary Gland Alveolar Cells | 1.828654e-05 | 4.738 |
R-HSA-195721 | Signaling by WNT | 2.369402e-05 | 4.625 |
R-HSA-5358351 | Signaling by Hedgehog | 2.550954e-05 | 4.593 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 3.797362e-05 | 4.421 |
R-HSA-212165 | Epigenetic regulation of gene expression | 4.038716e-05 | 4.394 |
R-HSA-112315 | Transmission across Chemical Synapses | 4.038716e-05 | 4.394 |
R-HSA-73894 | DNA Repair | 8.237061e-05 | 4.084 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 8.696246e-05 | 4.061 |
R-HSA-392499 | Metabolism of proteins | 1.104177e-04 | 3.957 |
R-HSA-913531 | Interferon Signaling | 1.254458e-04 | 3.902 |
R-HSA-1643685 | Disease | 1.317557e-04 | 3.880 |
R-HSA-446203 | Asparagine N-linked glycosylation | 2.342666e-04 | 3.630 |
R-HSA-112316 | Neuronal System | 4.520899e-04 | 3.345 |
R-HSA-390522 | Striated Muscle Contraction | 4.717810e-04 | 3.326 |
R-HSA-422475 | Axon guidance | 1.165780e-03 | 2.933 |
R-HSA-9675108 | Nervous system development | 1.738439e-03 | 2.760 |
R-HSA-199991 | Membrane Trafficking | 3.297129e-03 | 2.482 |
R-HSA-9938206 | Developmental Lineage of Mammary Stem Cells | 5.004733e-03 | 2.301 |
R-HSA-3214842 | HDMs demethylate histones | 6.090927e-03 | 2.215 |
R-HSA-9927432 | Developmental Lineage of Mammary Gland Myoepithelial Cells | 7.690599e-03 | 2.114 |
R-HSA-109582 | Hemostasis | 9.778809e-03 | 2.010 |
R-HSA-168256 | Immune System | 1.119000e-02 | 1.951 |
R-HSA-5653656 | Vesicle-mediated transport | 1.154038e-02 | 1.938 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 2.906127e-02 | 1.537 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 2.906127e-02 | 1.537 |
R-HSA-8854518 | AURKA Activation by TPX2 | 3.134672e-02 | 1.504 |
R-HSA-9925563 | Developmental Lineage of Pancreatic Ductal Cells | 3.370104e-02 | 1.472 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 3.694424e-02 | 1.432 |
R-HSA-380287 | Centrosome maturation | 3.860931e-02 | 1.413 |
R-HSA-446107 | Type I hemidesmosome assembly | 4.017102e-02 | 1.396 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 4.644528e-02 | 1.333 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 4.960837e-02 | 1.304 |
R-HSA-162582 | Signal Transduction | 5.017410e-02 | 1.300 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 5.290785e-02 | 1.276 |
R-HSA-397014 | Muscle contraction | 5.582621e-02 | 1.253 |
R-HSA-373753 | Nephrin family interactions | 8.900943e-02 | 1.051 |
R-HSA-9821993 | Replacement of protamines by nucleosomes in the male pronucleus | 1.058526e-01 | 0.975 |
R-HSA-9820448 | Developmental Cell Lineages of the Exocrine Pancreas | 1.323641e-01 | 0.878 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 1.514014e-01 | 0.820 |
R-HSA-9725554 | Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | 1.577193e-01 | 0.802 |
R-HSA-5674135 | MAP2K and MAPK activation | 1.671094e-01 | 0.777 |
R-HSA-9656223 | Signaling by RAF1 mutants | 1.671094e-01 | 0.777 |
R-HSA-381676 | Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 1.702166e-01 | 0.769 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 1.825315e-01 | 0.739 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 1.825315e-01 | 0.739 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 1.825315e-01 | 0.739 |
R-HSA-6802949 | Signaling by RAS mutants | 1.825315e-01 | 0.739 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 1.886213e-01 | 0.724 |
R-HSA-8866654 | E3 ubiquitin ligases ubiquitinate target proteins | 2.006676e-01 | 0.698 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 2.213267e-01 | 0.655 |
R-HSA-212436 | Generic Transcription Pathway | 2.289448e-01 | 0.640 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 2.386160e-01 | 0.622 |
R-HSA-5693606 | DNA Double Strand Break Response | 2.442947e-01 | 0.612 |
R-HSA-69473 | G2/M DNA damage checkpoint | 2.638444e-01 | 0.579 |
R-HSA-8852135 | Protein ubiquitination | 2.665962e-01 | 0.574 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 2.828964e-01 | 0.548 |
R-HSA-6802957 | Oncogenic MAPK signaling | 2.935648e-01 | 0.532 |
R-HSA-73857 | RNA Polymerase II Transcription | 3.059648e-01 | 0.514 |
R-HSA-422356 | Regulation of insulin secretion | 3.346994e-01 | 0.475 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 3.758248e-01 | 0.425 |
R-HSA-5693538 | Homology Directed Repair | 3.897342e-01 | 0.409 |
R-HSA-114608 | Platelet degranulation | 4.122424e-01 | 0.385 |
R-HSA-69481 | G2/M Checkpoints | 4.122424e-01 | 0.385 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 4.275103e-01 | 0.369 |
R-HSA-163685 | Integration of energy metabolism | 4.360590e-01 | 0.360 |
R-HSA-9664417 | Leishmania phagocytosis | 4.444822e-01 | 0.352 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 4.444822e-01 | 0.352 |
R-HSA-9664407 | Parasite infection | 4.444822e-01 | 0.352 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 4.465685e-01 | 0.350 |
R-HSA-74160 | Gene expression (Transcription) | 4.667999e-01 | 0.331 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 4.730004e-01 | 0.325 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 5.149314e-01 | 0.288 |
R-HSA-69620 | Cell Cycle Checkpoints | 6.482650e-01 | 0.188 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 6.689784e-01 | 0.175 |
R-HSA-9824443 | Parasitic Infection Pathways | 6.776588e-01 | 0.169 |
R-HSA-9658195 | Leishmania infection | 6.776588e-01 | 0.169 |
R-HSA-5673001 | RAF/MAP kinase cascade | 6.873054e-01 | 0.163 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 6.955129e-01 | 0.158 |
R-HSA-5683057 | MAPK family signaling cascades | 7.492429e-01 | 0.125 |
R-HSA-6798695 | Neutrophil degranulation | 8.360188e-01 | 0.078 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 8.688139e-01 | 0.061 |
R-HSA-168249 | Innate Immune System | 9.660621e-01 | 0.015 |
R-HSA-1430728 | Metabolism | 9.999999e-01 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
PAK6 |
0.530 | 0.251 | -2 | 0.555 |
MNK1 |
0.518 | 0.214 | -2 | 0.464 |
CDK10 |
0.518 | 0.186 | 1 | 0.548 |
PKCI |
0.517 | 0.237 | 2 | 0.546 |
PHKG2 |
0.516 | 0.206 | -3 | 0.559 |
AURC |
0.515 | 0.174 | -2 | 0.470 |
CDK14 |
0.515 | 0.194 | 1 | 0.547 |
NLK |
0.514 | 0.231 | 1 | 0.592 |
PKCZ |
0.514 | 0.233 | 2 | 0.535 |
CDK16 |
0.514 | 0.195 | 1 | 0.511 |
PKCH |
0.513 | 0.216 | 2 | 0.514 |
PKCG |
0.512 | 0.186 | 2 | 0.504 |
PKN2 |
0.512 | 0.208 | -3 | 0.531 |
HIPK2 |
0.512 | 0.160 | 1 | 0.599 |
PKCE |
0.512 | 0.207 | 2 | 0.512 |
WNK1 |
0.511 | 0.217 | -2 | 0.441 |
PAK4 |
0.511 | 0.190 | -2 | 0.521 |
PHKG1 |
0.510 | 0.184 | -3 | 0.527 |
PKCT |
0.510 | 0.199 | 2 | 0.502 |
CLK1 |
0.510 | 0.145 | -3 | 0.495 |
MNK2 |
0.509 | 0.178 | -2 | 0.471 |
MELK |
0.509 | 0.180 | -3 | 0.548 |
PKCD |
0.509 | 0.188 | 2 | 0.492 |
PKN3 |
0.509 | 0.205 | -3 | 0.471 |
PAK5 |
0.509 | 0.183 | -2 | 0.518 |
PKN1 |
0.508 | 0.178 | -3 | 0.474 |
AMPKA2 |
0.508 | 0.171 | -3 | 0.535 |
PKCB |
0.508 | 0.171 | 2 | 0.521 |
HIPK4 |
0.507 | 0.130 | 1 | 0.623 |
CDK18 |
0.507 | 0.154 | 1 | 0.522 |
AKT1 |
0.507 | 0.157 | -3 | 0.460 |
PKCA |
0.507 | 0.179 | 2 | 0.512 |
HIPK3 |
0.506 | 0.157 | 1 | 0.642 |
DYRK3 |
0.506 | 0.163 | 1 | 0.648 |
CDKL5 |
0.505 | 0.094 | -3 | 0.435 |
AMPKA1 |
0.505 | 0.182 | -3 | 0.543 |
CDK5 |
0.505 | 0.165 | 1 | 0.531 |
HIPK1 |
0.505 | 0.158 | 1 | 0.625 |
AURB |
0.504 | 0.160 | -2 | 0.473 |
DYRK2 |
0.504 | 0.145 | 1 | 0.628 |
PAK3 |
0.503 | 0.151 | -2 | 0.505 |
ERK7 |
0.503 | 0.210 | 2 | 0.551 |
PKG2 |
0.503 | 0.142 | -2 | 0.449 |
CDK7 |
0.503 | 0.134 | 1 | 0.535 |
MST4 |
0.503 | 0.132 | 2 | 0.494 |
CDK9 |
0.502 | 0.141 | 1 | 0.553 |
CDK6 |
0.502 | 0.174 | 1 | 0.540 |
IRE1 |
0.502 | 0.164 | 1 | 0.489 |
RSK3 |
0.502 | 0.085 | -3 | 0.446 |
AKT2 |
0.502 | 0.116 | -3 | 0.431 |
ERK5 |
0.501 | 0.124 | 1 | 0.514 |
TSSK1 |
0.501 | 0.150 | -3 | 0.555 |
PKACG |
0.501 | 0.118 | -2 | 0.442 |
CLK4 |
0.501 | 0.135 | -3 | 0.475 |
NUAK2 |
0.501 | 0.118 | -3 | 0.523 |
SRPK1 |
0.501 | 0.074 | -3 | 0.417 |
CDK4 |
0.500 | 0.170 | 1 | 0.534 |
MAPKAPK3 |
0.500 | 0.074 | -3 | 0.512 |
DYRK1A |
0.500 | 0.128 | 1 | 0.594 |
CDK19 |
0.500 | 0.124 | 1 | 0.516 |
ERK1 |
0.500 | 0.148 | 1 | 0.556 |
CDK17 |
0.499 | 0.143 | 1 | 0.509 |
PAK1 |
0.499 | 0.142 | -2 | 0.508 |
SGK3 |
0.499 | 0.146 | -3 | 0.472 |
SIK |
0.499 | 0.116 | -3 | 0.498 |
ERK2 |
0.499 | 0.151 | 1 | 0.575 |
QIK |
0.498 | 0.134 | -3 | 0.526 |
SSTK |
0.498 | 0.187 | 4 | 0.455 |
ICK |
0.498 | 0.118 | -3 | 0.467 |
RSK2 |
0.497 | 0.075 | -3 | 0.460 |
MOK |
0.497 | 0.155 | 1 | 0.634 |
AKT3 |
0.497 | 0.113 | -3 | 0.383 |
ULK2 |
0.497 | 0.106 | 2 | 0.473 |
DYRK1B |
0.497 | 0.130 | 1 | 0.568 |
CAMK4 |
0.497 | 0.145 | -3 | 0.532 |
NIM1 |
0.497 | 0.102 | 3 | 0.436 |
P38A |
0.497 | 0.157 | 1 | 0.568 |
CLK3 |
0.497 | 0.102 | 1 | 0.487 |
NUAK1 |
0.497 | 0.090 | -3 | 0.515 |
CDK3 |
0.496 | 0.143 | 1 | 0.509 |
RIPK3 |
0.496 | 0.111 | 3 | 0.401 |
CDK8 |
0.495 | 0.115 | 1 | 0.530 |
PRKD2 |
0.495 | 0.058 | -3 | 0.518 |
CDKL1 |
0.495 | 0.074 | -3 | 0.430 |
PKACB |
0.495 | 0.122 | -2 | 0.437 |
QSK |
0.495 | 0.113 | 4 | 0.493 |
PRKX |
0.494 | 0.109 | -3 | 0.448 |
TSSK2 |
0.494 | 0.126 | -5 | 0.392 |
WNK3 |
0.494 | 0.095 | 1 | 0.472 |
GCN2 |
0.493 | 0.037 | 2 | 0.494 |
P38B |
0.493 | 0.152 | 1 | 0.549 |
P38G |
0.493 | 0.145 | 1 | 0.514 |
BRSK2 |
0.493 | 0.089 | -3 | 0.545 |
NDR1 |
0.493 | 0.057 | -3 | 0.505 |
JNK2 |
0.493 | 0.152 | 1 | 0.552 |
NEK2 |
0.493 | 0.171 | 2 | 0.552 |
P90RSK |
0.492 | 0.047 | -3 | 0.448 |
MLK3 |
0.492 | 0.137 | 2 | 0.511 |
CDK13 |
0.491 | 0.108 | 1 | 0.543 |
CDK12 |
0.491 | 0.114 | 1 | 0.546 |
MARK3 |
0.491 | 0.129 | 4 | 0.495 |
PRKD3 |
0.490 | 0.054 | -3 | 0.498 |
IRE2 |
0.490 | 0.122 | 2 | 0.459 |
MLK1 |
0.490 | 0.107 | 2 | 0.536 |
CAMK1G |
0.490 | 0.092 | -3 | 0.480 |
PKACA |
0.490 | 0.113 | -2 | 0.439 |
MLK2 |
0.490 | 0.148 | 2 | 0.502 |
IRAK4 |
0.490 | 0.181 | 1 | 0.493 |
CHAK1 |
0.490 | 0.109 | 2 | 0.472 |
SNRK |
0.489 | 0.065 | 2 | 0.378 |
PAK2 |
0.489 | 0.116 | -2 | 0.511 |
WNK4 |
0.489 | 0.151 | -2 | 0.435 |
RAF1 |
0.489 | 0.070 | 1 | 0.451 |
MTOR |
0.489 | 0.016 | 1 | 0.534 |
NEK9 |
0.489 | 0.120 | 2 | 0.543 |
ULK1 |
0.489 | 0.037 | -3 | 0.462 |
MARK4 |
0.489 | 0.097 | 4 | 0.472 |
DYRK4 |
0.488 | 0.115 | 1 | 0.575 |
PKG1 |
0.488 | 0.108 | -2 | 0.447 |
NIK |
0.488 | 0.181 | -3 | 0.529 |
CDK1 |
0.488 | 0.120 | 1 | 0.536 |
HUNK |
0.488 | 0.092 | 2 | 0.505 |
P70S6KB |
0.487 | 0.061 | -3 | 0.493 |
CDK2 |
0.487 | 0.109 | 1 | 0.560 |
SRPK2 |
0.487 | 0.030 | -3 | 0.369 |
NEK6 |
0.487 | 0.057 | -2 | 0.287 |
AURA |
0.486 | 0.124 | -2 | 0.470 |
CAMK1B |
0.486 | 0.079 | -3 | 0.517 |
NDR2 |
0.486 | 0.003 | -3 | 0.492 |
P38D |
0.486 | 0.145 | 1 | 0.485 |
MAK |
0.486 | 0.123 | -2 | 0.521 |
RSK4 |
0.486 | 0.055 | -3 | 0.429 |
TBK1 |
0.486 | 0.025 | 1 | 0.443 |
COT |
0.486 | -0.002 | 2 | 0.464 |
CLK2 |
0.485 | 0.086 | -3 | 0.461 |
BRSK1 |
0.485 | 0.065 | -3 | 0.510 |
MSK2 |
0.484 | 0.049 | -3 | 0.411 |
PIM2 |
0.483 | 0.067 | -3 | 0.464 |
MARK1 |
0.483 | 0.113 | 4 | 0.483 |
CDC7 |
0.483 | -0.007 | 1 | 0.369 |
CAMLCK |
0.483 | 0.107 | -2 | 0.482 |
MYLK4 |
0.482 | 0.094 | -2 | 0.464 |
P70S6K |
0.482 | 0.045 | -3 | 0.434 |
NEK7 |
0.482 | 0.038 | -3 | 0.476 |
PRKD1 |
0.482 | 0.007 | -3 | 0.520 |
MRCKB |
0.482 | 0.128 | -3 | 0.485 |
IKKE |
0.481 | -0.004 | 1 | 0.427 |
PIM3 |
0.481 | 0.009 | -3 | 0.469 |
JNK3 |
0.481 | 0.126 | 1 | 0.562 |
SKMLCK |
0.481 | 0.078 | -2 | 0.444 |
PIM1 |
0.480 | 0.042 | -3 | 0.462 |
LATS2 |
0.480 | -0.000 | -5 | 0.323 |
KIS |
0.480 | 0.059 | 1 | 0.567 |
MAPKAPK2 |
0.480 | 0.007 | -3 | 0.459 |
MARK2 |
0.479 | 0.101 | 4 | 0.447 |
IKKB |
0.479 | -0.037 | -2 | 0.384 |
MLK4 |
0.479 | 0.083 | 2 | 0.519 |
CAMK1A |
0.479 | 0.085 | -3 | 0.443 |
MST3 |
0.479 | 0.163 | 2 | 0.544 |
CHAK2 |
0.478 | -0.001 | -1 | 0.489 |
PRPK |
0.478 | -0.038 | -1 | 0.477 |
MASTL |
0.478 | 0.037 | -2 | 0.383 |
LOK |
0.477 | 0.180 | -2 | 0.449 |
SGK1 |
0.477 | 0.077 | -3 | 0.363 |
DCAMKL2 |
0.477 | 0.093 | -3 | 0.560 |
CHK1 |
0.477 | 0.050 | -3 | 0.517 |
SRPK3 |
0.477 | 0.008 | -3 | 0.374 |
DAPK2 |
0.477 | 0.073 | -3 | 0.511 |
PDHK1 |
0.477 | -0.036 | 1 | 0.482 |
DCAMKL1 |
0.477 | 0.091 | -3 | 0.534 |
MSK1 |
0.476 | 0.053 | -3 | 0.431 |
PDHK4 |
0.475 | -0.099 | 1 | 0.498 |
PKR |
0.475 | 0.147 | 1 | 0.493 |
ATR |
0.474 | -0.023 | 1 | 0.431 |
RIPK1 |
0.474 | 0.009 | 1 | 0.557 |
BUB1 |
0.474 | 0.105 | -5 | 0.300 |
TGFBR2 |
0.474 | -0.041 | -2 | 0.248 |
ROCK2 |
0.472 | 0.140 | -3 | 0.503 |
TTBK2 |
0.472 | -0.045 | 2 | 0.480 |
PLK4 |
0.472 | 0.039 | 2 | 0.376 |
ROCK1 |
0.472 | 0.144 | -3 | 0.495 |
DRAK1 |
0.472 | 0.049 | 1 | 0.492 |
MRCKA |
0.472 | 0.099 | -3 | 0.486 |
PINK1 |
0.471 | 0.041 | 1 | 0.530 |
CAMK1D |
0.471 | 0.059 | -3 | 0.470 |
IRAK1 |
0.470 | 0.059 | -1 | 0.395 |
CAMK2G |
0.470 | -0.041 | 2 | 0.354 |
CHK2 |
0.470 | 0.044 | -3 | 0.429 |
ANKRD3 |
0.470 | 0.045 | 1 | 0.527 |
CAMK2D |
0.469 | -0.030 | -3 | 0.522 |
SMMLCK |
0.469 | 0.082 | -3 | 0.489 |
PERK |
0.469 | 0.046 | -2 | 0.331 |
BCKDK |
0.468 | -0.067 | -1 | 0.366 |
MOS |
0.468 | -0.067 | 1 | 0.433 |
DSTYK |
0.468 | -0.068 | 2 | 0.499 |
DMPK1 |
0.468 | 0.149 | -3 | 0.501 |
SLK |
0.467 | 0.101 | -2 | 0.407 |
DLK |
0.467 | -0.034 | 1 | 0.474 |
PRP4 |
0.467 | 0.043 | -3 | 0.358 |
MEK1 |
0.466 | 0.045 | 2 | 0.491 |
YSK4 |
0.466 | 0.038 | 1 | 0.422 |
STK33 |
0.465 | 0.027 | 2 | 0.350 |
MAPKAPK5 |
0.464 | -0.061 | -3 | 0.419 |
ZAK |
0.464 | 0.055 | 1 | 0.473 |
MPSK1 |
0.464 | 0.062 | 1 | 0.459 |
NEK8 |
0.464 | 0.122 | 2 | 0.510 |
MEK5 |
0.464 | 0.067 | 2 | 0.488 |
LATS1 |
0.464 | 0.009 | -3 | 0.480 |
NEK5 |
0.463 | 0.088 | 1 | 0.475 |
TAO2 |
0.463 | 0.132 | 2 | 0.500 |
SBK |
0.463 | 0.022 | -3 | 0.377 |
TAO3 |
0.463 | 0.097 | 1 | 0.461 |
GRK5 |
0.463 | -0.095 | -3 | 0.420 |
HRI |
0.463 | 0.005 | -2 | 0.306 |
YSK1 |
0.463 | 0.156 | 2 | 0.539 |
IKKA |
0.463 | -0.054 | -2 | 0.343 |
LIMK2_TYR |
0.463 | 0.203 | -3 | 0.548 |
NEK4 |
0.462 | 0.116 | 1 | 0.454 |
BMPR2 |
0.462 | -0.197 | -2 | 0.355 |
TTBK1 |
0.462 | -0.044 | 2 | 0.387 |
NEK3 |
0.462 | 0.098 | 1 | 0.480 |
HASPIN |
0.462 | 0.084 | -1 | 0.476 |
JNK1 |
0.462 | 0.090 | 1 | 0.534 |
MEKK1 |
0.460 | 0.028 | 1 | 0.472 |
NEK11 |
0.460 | 0.079 | 1 | 0.514 |
LKB1 |
0.460 | 0.091 | -3 | 0.491 |
CAMKK2 |
0.460 | 0.106 | -2 | 0.491 |
PDK1 |
0.460 | 0.136 | 1 | 0.608 |
NEK1 |
0.459 | 0.160 | 1 | 0.485 |
CAMK2A |
0.458 | -0.042 | 2 | 0.339 |
CAMKK1 |
0.458 | 0.088 | -2 | 0.452 |
VRK2 |
0.458 | 0.009 | 1 | 0.534 |
MEKK6 |
0.458 | 0.080 | 1 | 0.416 |
RIPK2 |
0.458 | 0.021 | 1 | 0.478 |
PLK1 |
0.458 | -0.037 | -2 | 0.261 |
GRK1 |
0.458 | -0.066 | -2 | 0.380 |
GRK6 |
0.457 | -0.072 | 1 | 0.441 |
LRRK2 |
0.455 | 0.137 | 2 | 0.518 |
HGK |
0.455 | 0.084 | 3 | 0.458 |
BRAF |
0.454 | 0.014 | -4 | 0.430 |
CRIK |
0.453 | 0.045 | -3 | 0.427 |
TAO1 |
0.453 | 0.112 | 1 | 0.447 |
TNIK |
0.453 | 0.095 | 3 | 0.477 |
SMG1 |
0.453 | -0.067 | 1 | 0.391 |
KHS1 |
0.452 | 0.084 | 1 | 0.447 |
MAP3K15 |
0.452 | 0.067 | 1 | 0.478 |
DAPK3 |
0.452 | 0.065 | -3 | 0.501 |
MEKK2 |
0.452 | 0.001 | 2 | 0.497 |
MYO3B |
0.451 | 0.151 | 2 | 0.521 |
HPK1 |
0.451 | 0.058 | 1 | 0.453 |
TNK1 |
0.451 | 0.099 | 3 | 0.453 |
MINK |
0.451 | 0.084 | 1 | 0.439 |
PLK3 |
0.450 | -0.044 | 2 | 0.362 |
KHS2 |
0.449 | 0.073 | 1 | 0.450 |
EEF2K |
0.449 | 0.052 | 3 | 0.419 |
MEKK3 |
0.449 | -0.067 | 1 | 0.475 |
PBK |
0.449 | 0.033 | 1 | 0.344 |
TNNI3K_TYR |
0.448 | 0.101 | 1 | 0.496 |
CAMK2B |
0.448 | -0.073 | 2 | 0.311 |
DAPK1 |
0.447 | 0.048 | -3 | 0.473 |
DNAPK |
0.447 | -0.070 | 1 | 0.393 |
MEK2 |
0.446 | 0.040 | 2 | 0.495 |
ALK4 |
0.446 | -0.097 | -2 | 0.280 |
LIMK1_TYR |
0.445 | 0.074 | 2 | 0.463 |
GSK3B |
0.445 | -0.050 | 4 | 0.104 |
MYO3A |
0.444 | 0.112 | 1 | 0.474 |
TESK1_TYR |
0.444 | 0.046 | 3 | 0.481 |
PKMYT1_TYR |
0.443 | 0.032 | 3 | 0.481 |
GCK |
0.443 | 0.007 | 1 | 0.437 |
CK1A2 |
0.442 | -0.063 | -3 | 0.188 |
PINK1_TYR |
0.442 | 0.038 | 1 | 0.506 |
CK1E |
0.441 | -0.085 | -3 | 0.207 |
GRK4 |
0.441 | -0.171 | -2 | 0.287 |
PDHK3_TYR |
0.441 | 0.009 | 4 | 0.417 |
GRK2 |
0.439 | -0.099 | -2 | 0.250 |
CK1G1 |
0.439 | -0.095 | -3 | 0.191 |
GSK3A |
0.439 | -0.049 | 4 | 0.110 |
ATM |
0.438 | -0.125 | 1 | 0.381 |
VRK1 |
0.438 | 0.033 | 2 | 0.482 |
GRK7 |
0.438 | -0.098 | 1 | 0.431 |
TAK1 |
0.438 | 0.019 | 1 | 0.442 |
DDR1 |
0.437 | 0.010 | 4 | 0.374 |
TYK2 |
0.437 | 0.020 | 1 | 0.485 |
MST1R |
0.437 | -0.016 | 3 | 0.497 |
TGFBR1 |
0.436 | -0.102 | -2 | 0.237 |
MAP2K7_TYR |
0.436 | -0.048 | 2 | 0.430 |
ROS1 |
0.436 | -0.012 | 3 | 0.450 |
JAK2 |
0.435 | -0.005 | 1 | 0.501 |
NEK10_TYR |
0.435 | 0.035 | 1 | 0.432 |
RET |
0.435 | -0.019 | 1 | 0.498 |
JAK1 |
0.435 | 0.038 | 1 | 0.483 |
GAK |
0.435 | -0.034 | 1 | 0.424 |
CSF1R |
0.434 | -0.019 | 3 | 0.469 |
FAM20C |
0.433 | -0.090 | 2 | 0.202 |
CK1D |
0.433 | -0.085 | -3 | 0.182 |
PASK |
0.433 | -0.085 | -3 | 0.452 |
BMPR1B |
0.432 | -0.106 | 1 | 0.345 |
MST2 |
0.431 | -0.056 | 1 | 0.422 |
WEE1_TYR |
0.431 | 0.035 | -1 | 0.368 |
TLK2 |
0.431 | -0.157 | 1 | 0.416 |
MST1 |
0.431 | -0.033 | 1 | 0.426 |
PDGFRA |
0.431 | -0.017 | 3 | 0.479 |
ACVR2A |
0.431 | -0.145 | -2 | 0.244 |
TYRO3 |
0.431 | -0.060 | 3 | 0.471 |
DDR2 |
0.430 | 0.011 | 3 | 0.410 |
ASK1 |
0.430 | 0.033 | 1 | 0.474 |
PDHK4_TYR |
0.429 | -0.090 | 2 | 0.395 |
BMPR2_TYR |
0.429 | -0.058 | -1 | 0.470 |
OSR1 |
0.429 | 0.001 | 2 | 0.516 |
GRK3 |
0.429 | -0.103 | -2 | 0.214 |
PDGFRB |
0.429 | -0.035 | 3 | 0.464 |
MAP2K4_TYR |
0.428 | -0.158 | -1 | 0.469 |
TNK2 |
0.428 | -0.033 | 3 | 0.449 |
ACVR2B |
0.427 | -0.153 | -2 | 0.247 |
JAK3 |
0.427 | -0.040 | 1 | 0.491 |
YANK3 |
0.427 | -0.053 | 2 | 0.176 |
FLT3 |
0.425 | -0.037 | 3 | 0.445 |
KDR |
0.424 | -0.040 | 3 | 0.411 |
EPHA6 |
0.424 | -0.055 | -1 | 0.431 |
ALK2 |
0.423 | -0.162 | -2 | 0.254 |
TEK |
0.423 | -0.083 | 3 | 0.423 |
TLK1 |
0.423 | -0.191 | -2 | 0.218 |
ABL2 |
0.422 | -0.059 | -1 | 0.387 |
MAP2K6_TYR |
0.422 | -0.174 | -1 | 0.483 |
FGFR1 |
0.422 | -0.058 | 3 | 0.441 |
ABL1 |
0.419 | -0.067 | -1 | 0.377 |
TTK |
0.419 | -0.035 | -2 | 0.246 |
AXL |
0.419 | -0.087 | 3 | 0.460 |
FGFR2 |
0.419 | -0.100 | 3 | 0.433 |
PLK2 |
0.418 | -0.081 | -3 | 0.340 |
BMPR1A |
0.418 | -0.122 | 1 | 0.320 |
ALK |
0.418 | -0.066 | 3 | 0.420 |
KIT |
0.417 | -0.097 | 3 | 0.467 |
PDHK1_TYR |
0.417 | -0.200 | -1 | 0.468 |
FLT4 |
0.415 | -0.081 | 3 | 0.404 |
MUSK |
0.414 | -0.029 | 1 | 0.381 |
INSRR |
0.414 | -0.113 | 3 | 0.418 |
BIKE |
0.414 | -0.041 | 1 | 0.347 |
LCK |
0.413 | -0.078 | -1 | 0.437 |
ITK |
0.413 | -0.109 | -1 | 0.399 |
MET |
0.412 | -0.113 | 3 | 0.471 |
EPHA1 |
0.411 | -0.100 | 3 | 0.453 |
LTK |
0.411 | -0.091 | 3 | 0.429 |
YES1 |
0.411 | -0.131 | -1 | 0.438 |
NTRK2 |
0.410 | -0.111 | 3 | 0.452 |
INSR |
0.410 | -0.105 | 3 | 0.429 |
FLT1 |
0.410 | -0.093 | -1 | 0.389 |
TEC |
0.409 | -0.103 | -1 | 0.349 |
HCK |
0.409 | -0.135 | -1 | 0.430 |
EPHB4 |
0.409 | -0.165 | -1 | 0.396 |
FGR |
0.408 | -0.164 | 1 | 0.410 |
STLK3 |
0.408 | -0.061 | 1 | 0.434 |
CK2A2 |
0.408 | -0.116 | 1 | 0.267 |
CK1A |
0.408 | -0.112 | -3 | 0.126 |
PTK6 |
0.407 | -0.123 | -1 | 0.338 |
MERTK |
0.407 | -0.137 | 3 | 0.439 |
FGFR3 |
0.406 | -0.124 | 3 | 0.421 |
BTK |
0.406 | -0.146 | -1 | 0.372 |
AAK1 |
0.406 | -0.030 | 1 | 0.289 |
BLK |
0.406 | -0.102 | -1 | 0.435 |
FRK |
0.405 | -0.113 | -1 | 0.424 |
YANK2 |
0.404 | -0.065 | 2 | 0.184 |
TXK |
0.404 | -0.128 | 1 | 0.371 |
FER |
0.403 | -0.199 | 1 | 0.392 |
PTK2B |
0.403 | -0.109 | -1 | 0.381 |
EPHA4 |
0.403 | -0.144 | 2 | 0.340 |
CK2A1 |
0.403 | -0.122 | 1 | 0.259 |
NTRK1 |
0.402 | -0.166 | -1 | 0.390 |
BMX |
0.402 | -0.122 | -1 | 0.368 |
EPHB1 |
0.402 | -0.176 | 1 | 0.400 |
ERBB2 |
0.401 | -0.143 | 1 | 0.437 |
SRMS |
0.400 | -0.193 | 1 | 0.394 |
MATK |
0.400 | -0.117 | -1 | 0.323 |
EPHB3 |
0.400 | -0.179 | -1 | 0.380 |
NTRK3 |
0.398 | -0.141 | -1 | 0.366 |
EPHA7 |
0.398 | -0.144 | 2 | 0.366 |
CSK |
0.394 | -0.151 | 2 | 0.371 |
LYN |
0.393 | -0.154 | 3 | 0.413 |
ALPHAK3 |
0.392 | -0.131 | -1 | 0.388 |
EPHA3 |
0.391 | -0.180 | 2 | 0.331 |
CK1G3 |
0.391 | -0.103 | -3 | 0.100 |
EPHB2 |
0.390 | -0.208 | -1 | 0.371 |
IGF1R |
0.389 | -0.143 | 3 | 0.391 |
EGFR |
0.389 | -0.120 | 1 | 0.409 |
FYN |
0.388 | -0.153 | -1 | 0.444 |
FGFR4 |
0.387 | -0.142 | -1 | 0.334 |
PTK2 |
0.386 | -0.098 | -1 | 0.419 |
SRC |
0.385 | -0.170 | -1 | 0.412 |
EPHA8 |
0.384 | -0.162 | -1 | 0.373 |
EPHA5 |
0.378 | -0.206 | 2 | 0.322 |
SYK |
0.375 | -0.148 | -1 | 0.398 |
EPHA2 |
0.375 | -0.170 | -1 | 0.344 |
ERBB4 |
0.374 | -0.133 | 1 | 0.374 |
FES |
0.370 | -0.167 | -1 | 0.328 |
ZAP70 |
0.370 | -0.111 | -1 | 0.368 |
CK1G2 |
0.367 | -0.131 | -3 | 0.148 |