Motif 539 (n=44)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
O75526 | RBMXL2 | S58 | ochoa | RNA-binding motif protein, X-linked-like-2 (Testis-specific heterogeneous nuclear ribonucleoprotein G-T) (hnRNP G-T) | None |
P05455 | SSB | S160 | ochoa | Lupus La protein (La autoantigen) (La ribonucleoprotein) (Sjoegren syndrome type B antigen) (SS-B) | Binds to the 3' poly(U) terminus of nascent RNA polymerase III transcripts, protecting them from exonuclease digestion and facilitating their folding and maturation (PubMed:2470590, PubMed:3192525). In case of Coxsackievirus B3 infection, binds to the viral internal ribosome entry site (IRES) and stimulates the IRES-mediated translation (PubMed:12384597). {ECO:0000269|PubMed:12384597, ECO:0000269|PubMed:2470590, ECO:0000269|PubMed:3192525}. |
P11055 | MYH3 | Y554 | ochoa | Myosin-3 (Muscle embryonic myosin heavy chain) (Myosin heavy chain 3) (Myosin heavy chain, fast skeletal muscle, embryonic) (SMHCE) | Muscle contraction. |
P11940 | PABPC1 | S342 | ochoa | Polyadenylate-binding protein 1 (PABP-1) (Poly(A)-binding protein 1) | Binds the poly(A) tail of mRNA, including that of its own transcript, and regulates processes of mRNA metabolism such as pre-mRNA splicing and mRNA stability (PubMed:11051545, PubMed:17212783, PubMed:25480299). Its function in translational initiation regulation can either be enhanced by PAIP1 or repressed by PAIP2 (PubMed:11051545, PubMed:20573744). Can probably bind to cytoplasmic RNA sequences other than poly(A) in vivo. Binds to N6-methyladenosine (m6A)-containing mRNAs and contributes to MYC stability by binding to m6A-containing MYC mRNAs (PubMed:32245947). Involved in translationally coupled mRNA turnover (PubMed:11051545). Implicated with other RNA-binding proteins in the cytoplasmic deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of instability (mCRD) domain (PubMed:11051545). Involved in regulation of nonsense-mediated decay (NMD) of mRNAs containing premature stop codons; for the recognition of premature termination codons (PTC) and initiation of NMD a competitive interaction between UPF1 and PABPC1 with the ribosome-bound release factors is proposed (PubMed:18447585). By binding to long poly(A) tails, may protect them from uridylation by ZCCHC6/ZCCHC11 and hence contribute to mRNA stability (PubMed:25480299). {ECO:0000269|PubMed:11051545, ECO:0000269|PubMed:17212783, ECO:0000269|PubMed:18447585, ECO:0000269|PubMed:20573744, ECO:0000269|PubMed:25480299, ECO:0000269|PubMed:32245947}.; FUNCTION: (Microbial infection) Positively regulates the replication of dengue virus (DENV). {ECO:0000269|PubMed:26735137}. |
P13535 | MYH8 | Y556 | ochoa | Myosin-8 (Myosin heavy chain 8) (Myosin heavy chain, skeletal muscle, perinatal) (MyHC-perinatal) | Muscle contraction. |
P19338 | NCL | S356 | 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 | S619 | 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}. |
P22626 | HNRNPA2B1 | S71 | ochoa | Heterogeneous nuclear ribonucleoproteins A2/B1 (hnRNP A2/B1) | Heterogeneous nuclear ribonucleoprotein (hnRNP) that associates with nascent pre-mRNAs, packaging them into hnRNP particles. The hnRNP particle arrangement on nascent hnRNA is non-random and sequence-dependent and serves to condense and stabilize the transcripts and minimize tangling and knotting. Packaging plays a role in various processes such as transcription, pre-mRNA processing, RNA nuclear export, subcellular location, mRNA translation and stability of mature mRNAs (PubMed:19099192). Forms hnRNP particles with at least 20 other different hnRNP and heterogeneous nuclear RNA in the nucleus. Involved in transport of specific mRNAs to the cytoplasm in oligodendrocytes and neurons: acts by specifically recognizing and binding the A2RE (21 nucleotide hnRNP A2 response element) or the A2RE11 (derivative 11 nucleotide oligonucleotide) sequence motifs present on some mRNAs, and promotes their transport to the cytoplasm (PubMed:10567417). Specifically binds single-stranded telomeric DNA sequences, protecting telomeric DNA repeat against endonuclease digestion (By similarity). Also binds other RNA molecules, such as primary miRNA (pri-miRNAs): acts as a nuclear 'reader' of the N6-methyladenosine (m6A) mark by specifically recognizing and binding a subset of nuclear m6A-containing pri-miRNAs. Binding to m6A-containing pri-miRNAs promotes pri-miRNA processing by enhancing binding of DGCR8 to pri-miRNA transcripts (PubMed:26321680). Involved in miRNA sorting into exosomes following sumoylation, possibly by binding (m6A)-containing pre-miRNAs (PubMed:24356509). Acts as a regulator of efficiency of mRNA splicing, possibly by binding to m6A-containing pre-mRNAs (PubMed:26321680). Plays a role in the splicing of pyruvate kinase PKM by binding repressively to sequences flanking PKM exon 9, inhibiting exon 9 inclusion and resulting in exon 10 inclusion and production of the PKM M2 isoform (PubMed:20010808). Also plays a role in the activation of the innate immune response (PubMed:31320558). Mechanistically, senses the presence of viral DNA in the nucleus, homodimerizes and is demethylated by JMJD6 (PubMed:31320558). In turn, translocates to the cytoplasm where it activates the TBK1-IRF3 pathway, leading to interferon alpha/beta production (PubMed:31320558). {ECO:0000250|UniProtKB:A7VJC2, ECO:0000269|PubMed:10567417, ECO:0000269|PubMed:20010808, ECO:0000269|PubMed:24356509, ECO:0000269|PubMed:26321680, ECO:0000303|PubMed:19099192}.; FUNCTION: (Microbial infection) Involved in the transport of HIV-1 genomic RNA out of the nucleus, to the microtubule organizing center (MTOC), and then from the MTOC to the cytoplasm: acts by specifically recognizing and binding the A2RE (21 nucleotide hnRNP A2 response element) sequence motifs present on HIV-1 genomic RNA, and promotes its transport. {ECO:0000269|PubMed:15294897, ECO:0000269|PubMed:17004321}. |
P29558 | RBMS1 | S112 | ochoa | RNA-binding motif, single-stranded-interacting protein 1 (Single-stranded DNA-binding protein MSSP-1) (Suppressor of CDC2 with RNA-binding motif 2) | Single-stranded DNA binding protein that interacts with the region upstream of the MYC gene. Binds specifically to the DNA sequence motif 5'-[AT]CT[AT][AT]T-3'. Probably has a role in DNA replication. |
P31943 | HNRNPH1 | S63 | ochoa | Heterogeneous nuclear ribonucleoprotein H (hnRNP H) [Cleaved into: Heterogeneous nuclear ribonucleoprotein H, N-terminally processed] | This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Mediates pre-mRNA alternative splicing regulation. Inhibits, together with CUGBP1, insulin receptor (IR) pre-mRNA exon 11 inclusion in myoblast. Binds to the IR RNA. Binds poly(RG). {ECO:0000269|PubMed:11003644, ECO:0000269|PubMed:16946708}. |
P31943 | HNRNPH1 | S161 | ochoa | Heterogeneous nuclear ribonucleoprotein H (hnRNP H) [Cleaved into: Heterogeneous nuclear ribonucleoprotein H, N-terminally processed] | This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Mediates pre-mRNA alternative splicing regulation. Inhibits, together with CUGBP1, insulin receptor (IR) pre-mRNA exon 11 inclusion in myoblast. Binds to the IR RNA. Binds poly(RG). {ECO:0000269|PubMed:11003644, ECO:0000269|PubMed:16946708}. |
P38159 | RBMX | S58 | ochoa | RNA-binding motif protein, X chromosome (Glycoprotein p43) (Heterogeneous nuclear ribonucleoprotein G) (hnRNP G) [Cleaved into: RNA-binding motif protein, X chromosome, N-terminally processed] | RNA-binding protein that plays several role in the regulation of pre- and post-transcriptional processes. Implicated in tissue-specific regulation of gene transcription and alternative splicing of several pre-mRNAs. Binds to and stimulates transcription from the tumor suppressor TXNIP gene promoter; may thus be involved in tumor suppression. When associated with SAFB, binds to and stimulates transcription from the SREBF1 promoter. Associates with nascent mRNAs transcribed by RNA polymerase II. Component of the supraspliceosome complex that regulates pre-mRNA alternative splice site selection. Can either activate or suppress exon inclusion; acts additively with TRA2B to promote exon 7 inclusion of the survival motor neuron SMN2. Represses the splicing of MAPT/Tau exon 10. Binds preferentially to single-stranded 5'-CC[A/C]-rich RNA sequence motifs localized in a single-stranded conformation; probably binds RNA as a homodimer. Binds non-specifically to pre-mRNAs. Also plays a role in the cytoplasmic TNFR1 trafficking pathways; promotes both the IL-1-beta-mediated inducible proteolytic cleavage of TNFR1 ectodomains and the release of TNFR1 exosome-like vesicles to the extracellular compartment. {ECO:0000269|PubMed:12165565, ECO:0000269|PubMed:12761049, ECO:0000269|PubMed:16707624, ECO:0000269|PubMed:18445477, ECO:0000269|PubMed:18541147, ECO:0000269|PubMed:19282290, ECO:0000269|PubMed:21327109}. |
P52272 | HNRNPM | S701 | ochoa | Heterogeneous nuclear ribonucleoprotein M (hnRNP M) | Pre-mRNA binding protein in vivo, binds avidly to poly(G) and poly(U) RNA homopolymers in vitro. Involved in splicing. Acts as a receptor for carcinoembryonic antigen in Kupffer cells, may initiate a series of signaling events leading to tyrosine phosphorylation of proteins and induction of IL-1 alpha, IL-6, IL-10 and tumor necrosis factor alpha cytokines. |
P52597 | HNRNPF | S161 | ochoa | Heterogeneous nuclear ribonucleoprotein F (hnRNP F) (Nucleolin-like protein mcs94-1) [Cleaved into: Heterogeneous nuclear ribonucleoprotein F, N-terminally processed] | Component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Plays a role in the regulation of alternative splicing events. Binds G-rich sequences in pre-mRNAs and keeps target RNA in an unfolded state. {ECO:0000269|PubMed:20526337}. |
P55795 | HNRNPH2 | S63 | ochoa | Heterogeneous nuclear ribonucleoprotein H2 (hnRNP H2) (FTP-3) (Heterogeneous nuclear ribonucleoprotein H') (hnRNP H') [Cleaved into: Heterogeneous nuclear ribonucleoprotein H2, N-terminally processed] | This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Binds poly(RG). |
P55795 | HNRNPH2 | S161 | ochoa | Heterogeneous nuclear ribonucleoprotein H2 (hnRNP H2) (FTP-3) (Heterogeneous nuclear ribonucleoprotein H') (hnRNP H') [Cleaved into: Heterogeneous nuclear ribonucleoprotein H2, N-terminally processed] | This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Binds poly(RG). |
P55884 | EIF3B | S239 | ochoa | Eukaryotic translation initiation factor 3 subunit B (eIF3b) (Eukaryotic translation initiation factor 3 subunit 9) (Prt1 homolog) (hPrt1) (eIF-3-eta) (eIF3 p110) (eIF3 p116) | RNA-binding component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis (PubMed:17581632, PubMed:25849773, PubMed:27462815, PubMed:9388245). The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation (PubMed:17581632, PubMed:9388245). The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression (PubMed:25849773). {ECO:0000255|HAMAP-Rule:MF_03001, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815, ECO:0000269|PubMed:9388245}.; FUNCTION: (Microbial infection) In case of FCV infection, plays a role in the ribosomal termination-reinitiation event leading to the translation of VP2 (PubMed:18056426). {ECO:0000269|PubMed:18056426}. |
Q13243 | SRSF5 | S153 | ochoa | Serine/arginine-rich splicing factor 5 (Delayed-early protein HRS) (Pre-mRNA-splicing factor SRP40) (Splicing factor, arginine/serine-rich 5) | Plays a role in constitutive splicing and can modulate the selection of alternative splice sites. |
Q13310 | PABPC4 | S342 | ochoa | Polyadenylate-binding protein 4 (PABP-4) (Poly(A)-binding protein 4) (Activated-platelet protein 1) (APP-1) (Inducible poly(A)-binding protein) (iPABP) | Binds the poly(A) tail of mRNA (PubMed:8524242). Binds to SMIM26 mRNA and plays a role in its post-transcriptional regulation (PubMed:37009826). May be involved in cytoplasmic regulatory processes of mRNA metabolism. Can probably bind to cytoplasmic RNA sequences other than poly(A) in vivo (By similarity). {ECO:0000250|UniProtKB:P11940, ECO:0000269|PubMed:37009826, ECO:0000269|PubMed:8524242}. |
Q15434 | RBMS2 | S106 | ochoa | RNA-binding motif, single-stranded-interacting protein 2 (Suppressor of CDC2 with RNA-binding motif 3) | None |
Q4VXU2 | PABPC1L | S342 | ochoa | Polyadenylate-binding protein 1-like (Embryonic poly(A)-binding protein) (Poly(A) binding protein cytoplasmic 1 like) | Poly(A)-binding protein involved in oocyte maturation and early embryo development (PubMed:37723834, PubMed:37052235). It is required for cytosolic mRNA polyadenylation and translational activation of maternally stored mRNA in oocytes (By similarity). {ECO:0000250|UniProtKB:A2A5N3, ECO:0000269|PubMed:37052235, ECO:0000269|PubMed:37723834}. |
Q6XE24 | RBMS3 | S111 | ochoa | RNA-binding motif, single-stranded-interacting protein 3 | Binds poly(A) and poly(U) oligoribonucleotides. {ECO:0000269|PubMed:10675610}. |
Q8N7X1 | RBMXL3 | S58 | ochoa | RNA-binding motif protein, X-linked-like-3 | None |
Q96E39 | RBMXL1 | S58 | ochoa | RNA binding motif protein, X-linked-like-1 (Heterogeneous nuclear ribonucleoprotein G-like 1) | RNA-binding protein which may be involved in pre-mRNA splicing. {ECO:0000250}. |
Q9GZT3 | SLIRP | S69 | ochoa | SRA stem-loop-interacting RNA-binding protein, mitochondrial | RNA-binding protein that acts as a nuclear receptor corepressor. Probably acts by binding the SRA RNA, and repressing the SRA-mediated nuclear receptor coactivation. Binds the STR7 loop of SRA RNA. Also able to repress glucocorticoid (GR), androgen (AR), thyroid (TR) and VDR-mediated transactivation. {ECO:0000269|PubMed:16762838}. |
Q9H361 | PABPC3 | S342 | ochoa | Polyadenylate-binding protein 3 (PABP-3) (Poly(A)-binding protein 3) (Testis-specific poly(A)-binding protein) | Binds the poly(A) tail of mRNA. May be involved in cytoplasmic regulatory processes of mRNA metabolism. Binds poly(A) with a slightly lower affinity as compared to PABPC1. |
Q9NTZ6 | RBM12 | S352 | ochoa | RNA-binding protein 12 (RNA-binding motif protein 12) (SH3/WW domain anchor protein in the nucleus) (SWAN) | None |
Q9P2K5 | MYEF2 | S571 | ochoa | Myelin expression factor 2 (MEF-2) (MyEF-2) (MST156) | Transcriptional repressor of the myelin basic protein gene (MBP). Binds to the proximal MB1 element 5'-TTGTCC-3' of the MBP promoter. Its binding to MB1 and function are inhibited by PURA (By similarity). {ECO:0000250}. |
Q9UKX2 | MYH2 | Y556 | 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 | Y555 | 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}. |
Q9Y490 | TLN1 | S52 | ochoa | Talin-1 | High molecular weight cytoskeletal protein concentrated at regions of cell-matrix and cell-cell contacts. Involved in connections of major cytoskeletal structures to the plasma membrane. With KANK1 co-organize the assembly of cortical microtubule stabilizing complexes (CMSCs) positioned to control microtubule-actin crosstalk at focal adhesions (FAs) rims. {ECO:0000250|UniProtKB:P26039}. |
P19338 | NCL | S532 | Sugiyama | 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}. |
A6NKT7 | RGPD3 | T1210 | Sugiyama | RanBP2-like and GRIP domain-containing protein 3 | None |
O14715 | RGPD8 | T1209 | Sugiyama | RANBP2-like and GRIP domain-containing protein 8 (Ran-binding protein 2-like 3) (RanBP2-like 3) (RanBP2L3) | None |
P0DJD0 | RGPD1 | T1194 | Sugiyama | RANBP2-like and GRIP domain-containing protein 1 (Ran-binding protein 2-like 6) (RanBP2-like 6) (RanBP2L6) | None |
P49792 | RANBP2 | T2185 | Sugiyama | E3 SUMO-protein ligase RanBP2 (EC 2.3.2.-) (358 kDa nucleoporin) (Nuclear pore complex protein Nup358) (Nucleoporin Nup358) (Ran-binding protein 2) (RanBP2) (p270) | E3 SUMO-protein ligase which facilitates SUMO1 and SUMO2 conjugation by UBE2I (PubMed:11792325, PubMed:12032081, PubMed:15378033, PubMed:15931224, PubMed:22194619). Involved in transport factor (Ran-GTP, karyopherin)-mediated protein import via the F-G repeat-containing domain which acts as a docking site for substrates (PubMed:7775481). Binds single-stranded RNA (in vitro) (PubMed:7775481). May bind DNA (PubMed:7775481). Component of the nuclear export pathway (PubMed:10078529). Specific docking site for the nuclear export factor exportin-1 (PubMed:10078529). Inhibits EIF4E-dependent mRNA export (PubMed:22902403). Sumoylates PML at 'Lys-490' which is essential for the proper assembly of PML-NB (PubMed:22155184). Recruits BICD2 to the nuclear envelope and cytoplasmic stacks of nuclear pore complex known as annulate lamellae during G2 phase of cell cycle (PubMed:20386726). Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity (PubMed:20676357, PubMed:23353830). {ECO:0000269|PubMed:11792325, ECO:0000269|PubMed:12032081, ECO:0000269|PubMed:15378033, ECO:0000269|PubMed:15931224, ECO:0000269|PubMed:20386726, ECO:0000269|PubMed:20676357, ECO:0000269|PubMed:22155184, ECO:0000269|PubMed:22194619, ECO:0000269|PubMed:22902403, ECO:0000269|PubMed:23353830, ECO:0000269|PubMed:7775481, ECO:0000303|PubMed:10078529}. |
Q7Z3J3 | RGPD4 | T1210 | Sugiyama | RanBP2-like and GRIP domain-containing protein 4 | None |
Q99666 | RGPD5 | T1209 | Sugiyama | RANBP2-like and GRIP domain-containing protein 5/6 (Ran-binding protein 2-like 1/2) (RanBP2-like 1/2) (RanBP2L1) (RanBP2L2) (Sperm membrane protein BS-63) | None |
P52597 | HNRNPF | S63 | Sugiyama | Heterogeneous nuclear ribonucleoprotein F (hnRNP F) (Nucleolin-like protein mcs94-1) [Cleaved into: Heterogeneous nuclear ribonucleoprotein F, N-terminally processed] | Component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Plays a role in the regulation of alternative splicing events. Binds G-rich sequences in pre-mRNAs and keeps target RNA in an unfolded state. {ECO:0000269|PubMed:20526337}. |
Q16836 | HADH | S196 | Sugiyama | Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial (HCDH) (EC 1.1.1.35) (Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase) (Short-chain 3-hydroxyacyl-CoA dehydrogenase) | Mitochondrial fatty acid beta-oxidation enzyme that catalyzes the third step of the beta-oxidation cycle for medium and short-chain 3-hydroxy fatty acyl-CoAs (C4 to C10) (PubMed:10231530, PubMed:11489939, PubMed:16725361). Plays a role in the control of insulin secretion by inhibiting the activation of glutamate dehydrogenase 1 (GLUD1), an enzyme that has an important role in regulating amino acid-induced insulin secretion (By similarity). Plays a role in the maintenance of normal spermatogenesis through the reduction of fatty acid accumulation in the testes (By similarity). {ECO:0000250|UniProtKB:Q61425, ECO:0000269|PubMed:10231530, ECO:0000269|PubMed:11489939, ECO:0000269|PubMed:16725361}. |
Q12849 | GRSF1 | S202 | Sugiyama | G-rich sequence factor 1 (GRSF-1) | Regulator of post-transcriptional mitochondrial gene expression, required for assembly of the mitochondrial ribosome and for recruitment of mRNA and lncRNA. Binds RNAs containing the 14 base G-rich element. Preferentially binds RNAs transcribed from three contiguous genes on the light strand of mtDNA, the ND6 mRNA, and the long non-coding RNAs for MT-CYB and MT-ND5, each of which contains multiple consensus binding sequences (PubMed:23473033, PubMed:23473034, PubMed:29967381). Involved in the degradosome-mediated decay of non-coding mitochondrial transcripts (MT-ncRNA) and tRNA-like molecules (PubMed:29967381). Acts by unwinding G-quadruplex RNA structures in MT-ncRNA, thus facilitating their degradation by the degradosome (PubMed:29967381). G-quadruplexes (G4) are non-canonical 4 stranded structures formed by transcripts from the light strand of mtDNA (PubMed:29967381). {ECO:0000269|PubMed:23473033, ECO:0000269|PubMed:23473034, ECO:0000269|PubMed:29967381}. |
H0YHG0 | None | S428 | ochoa | DnaJ homolog subfamily C member 14 (Nuclear protein Hcc-1) (SAP domain-containing ribonucleoprotein) | Binds both single-stranded and double-stranded DNA with higher affinity for the single-stranded form. Specifically binds to scaffold/matrix attachment region DNA. Also binds single-stranded RNA. Enhances RNA unwinding activity of DDX39A. May participate in important transcriptional or translational control of cell growth, metabolism and carcinogenesis. Component of the TREX complex which is thought to couple mRNA transcription, processing and nuclear export, and specifically associates with spliced mRNA and not with unspliced pre-mRNA. The TREX complex is recruited to spliced mRNAs by a transcription-independent mechanism, binds to mRNA upstream of the exon-junction complex (EJC) and is recruited in a splicing- and cap-dependent manner to a region near the 5' end of the mRNA where it functions in mRNA export to the cytoplasm via the TAP/NXF1 pathway. Associates with DDX39B, which facilitates RNA binding of DDX39B and likely plays a role in mRNA export. {ECO:0000256|ARBA:ARBA00054093}.; FUNCTION: Regulates the export of target proteins, such as DRD1, from the endoplasmic reticulum to the cell surface. {ECO:0000256|ARBA:ARBA00055510}. |
P82979 | SARNP | S115 | ochoa | SAP domain-containing ribonucleoprotein (Cytokine-induced protein of 29 kDa) (Nuclear protein Hcc-1) (Proliferation-associated cytokine-inducible protein CIP29) | Binds both single-stranded and double-stranded DNA with higher affinity for the single-stranded form. Specifically binds to scaffold/matrix attachment region DNA. Also binds single-stranded RNA. Enhances RNA unwinding activity of DDX39A. May participate in important transcriptional or translational control of cell growth, metabolism and carcinogenesis. Component of the TREX complex which is thought to couple mRNA transcription, processing and nuclear export, and specifically associates with spliced mRNA and not with unspliced pre-mRNA (PubMed:15338056, PubMed:17196963, PubMed:20844015). The TREX complex is recruited to spliced mRNAs by a transcription-independent mechanism, binds to mRNA upstream of the exon-junction complex (EJC) and is recruited in a splicing- and cap-dependent manner to a region near the 5' end of the mRNA where it functions in mRNA export to the cytoplasm via the TAP/NXF1 pathway (PubMed:15338056, PubMed:17196963, PubMed:20844015). Associates with DDX39B, which facilitates RNA binding of DDX39B and likely plays a role in mRNA export (PubMed:37578863). {ECO:0000269|PubMed:15338056, ECO:0000269|PubMed:17196963, ECO:0000269|PubMed:20844015, ECO:0000269|PubMed:37578863}. |
O14490 | DLGAP1 | S169 | ochoa | Disks large-associated protein 1 (DAP-1) (Guanylate kinase-associated protein) (hGKAP) (PSD-95/SAP90-binding protein 1) (SAP90/PSD-95-associated protein 1) (SAPAP1) | Part of the postsynaptic scaffold in neuronal cells. |
Download
reactome_id | name | p | -log10_p |
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R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 6.718499e-08 | 7.173 |
R-HSA-8953854 | Metabolism of RNA | 1.600518e-07 | 6.796 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 1.273346e-06 | 5.895 |
R-HSA-72172 | mRNA Splicing | 1.773753e-06 | 5.751 |
R-HSA-8950505 | Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulati... | 4.119275e-05 | 4.385 |
R-HSA-6803529 | FGFR2 alternative splicing | 5.736271e-05 | 4.241 |
R-HSA-9020591 | Interleukin-12 signaling | 7.073724e-05 | 4.150 |
R-HSA-447115 | Interleukin-12 family signaling | 1.179786e-04 | 3.928 |
R-HSA-77348 | Beta oxidation of octanoyl-CoA to hexanoyl-CoA | 1.044258e-03 | 2.981 |
R-HSA-77310 | Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA | 1.044258e-03 | 2.981 |
R-HSA-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA | 1.044258e-03 | 2.981 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 1.261736e-03 | 2.899 |
R-HSA-77346 | Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA | 1.414330e-03 | 2.849 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 1.702889e-03 | 2.769 |
R-HSA-5654738 | Signaling by FGFR2 | 1.597622e-03 | 2.797 |
R-HSA-9836573 | Mitochondrial RNA degradation | 2.843862e-03 | 2.546 |
R-HSA-190236 | Signaling by FGFR | 2.923223e-03 | 2.534 |
R-HSA-390522 | Striated Muscle Contraction | 4.973189e-03 | 2.303 |
R-HSA-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids | 8.546494e-03 | 2.068 |
R-HSA-72187 | mRNA 3'-end processing | 1.082807e-02 | 1.965 |
R-HSA-72649 | Translation initiation complex formation | 1.152412e-02 | 1.938 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 1.297376e-02 | 1.887 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 1.411050e-02 | 1.850 |
R-HSA-397014 | Muscle contraction | 2.261041e-02 | 1.646 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 4.089249e-02 | 1.388 |
R-HSA-354194 | GRB2:SOS provides linkage to MAPK signaling for Integrins | 5.085777e-02 | 1.294 |
R-HSA-372708 | p130Cas linkage to MAPK signaling for integrins | 5.580243e-02 | 1.253 |
R-HSA-429947 | Deadenylation of mRNA | 7.533084e-02 | 1.123 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 8.971784e-02 | 1.047 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 9.209433e-02 | 1.036 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 9.209433e-02 | 1.036 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 9.682916e-02 | 1.014 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 9.682916e-02 | 1.014 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 9.918753e-02 | 1.004 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 1.038862e-01 | 0.983 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 1.132120e-01 | 0.946 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 1.155286e-01 | 0.937 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 1.540187e-01 | 0.812 |
R-HSA-354192 | Integrin signaling | 9.682916e-02 | 1.014 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 1.737288e-01 | 0.760 |
R-HSA-77285 | Beta oxidation of myristoyl-CoA to lauroyl-CoA | 4.089249e-02 | 1.388 |
R-HSA-77305 | Beta oxidation of palmitoyl-CoA to myristoyl-CoA | 4.089249e-02 | 1.388 |
R-HSA-76009 | Platelet Aggregation (Plug Formation) | 1.293046e-01 | 0.888 |
R-HSA-6802948 | Signaling by high-kinase activity BRAF mutants | 1.085610e-01 | 0.964 |
R-HSA-5674135 | MAP2K and MAPK activation | 1.201441e-01 | 0.920 |
R-HSA-9820960 | Respiratory syncytial virus (RSV) attachment and entry | 9.209433e-02 | 1.036 |
R-HSA-9656223 | Signaling by RAF1 mutants | 1.201441e-01 | 0.920 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 1.315802e-01 | 0.881 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 1.315802e-01 | 0.881 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 1.315802e-01 | 0.881 |
R-HSA-73980 | RNA Polymerase III Transcription Termination | 5.826532e-02 | 1.235 |
R-HSA-450408 | AUF1 (hnRNP D0) binds and destabilizes mRNA | 1.062266e-01 | 0.974 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 1.085610e-01 | 0.964 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 1.293046e-01 | 0.888 |
R-HSA-6802949 | Signaling by RAS mutants | 1.315802e-01 | 0.881 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 9.918753e-02 | 1.004 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 1.606392e-01 | 0.794 |
R-HSA-72737 | Cap-dependent Translation Initiation | 4.535079e-02 | 1.343 |
R-HSA-72613 | Eukaryotic Translation Initiation | 4.535079e-02 | 1.343 |
R-HSA-77289 | Mitochondrial Fatty Acid Beta-Oxidation | 3.081087e-02 | 1.511 |
R-HSA-77288 | mitochondrial fatty acid beta-oxidation of unsaturated fatty acids | 5.333325e-02 | 1.273 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 1.315802e-01 | 0.881 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 3.927373e-02 | 1.406 |
R-HSA-191859 | snRNP Assembly | 1.606392e-01 | 0.794 |
R-HSA-194441 | Metabolism of non-coding RNA | 1.606392e-01 | 0.794 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 1.650247e-01 | 0.782 |
R-HSA-180746 | Nuclear import of Rev protein | 1.015399e-01 | 0.993 |
R-HSA-9820841 | M-decay: degradation of maternal mRNAs by maternally stored factors | 1.178393e-01 | 0.929 |
R-HSA-77352 | Beta oxidation of butanoyl-CoA to acetyl-CoA | 4.837596e-02 | 1.315 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 1.155286e-01 | 0.937 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 1.155286e-01 | 0.937 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 1.178393e-01 | 0.929 |
R-HSA-445355 | Smooth Muscle Contraction | 1.473472e-01 | 0.832 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 7.492998e-02 | 1.125 |
R-HSA-6794361 | Neurexins and neuroligins | 1.451120e-01 | 0.838 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 1.108895e-01 | 0.955 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 1.315802e-01 | 0.881 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 1.887482e-01 | 0.724 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 1.132120e-01 | 0.946 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 1.562312e-01 | 0.806 |
R-HSA-6784531 | tRNA processing in the nucleus | 1.672091e-01 | 0.777 |
R-HSA-399955 | SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 5.085777e-02 | 1.294 |
R-HSA-9937008 | Mitochondrial mRNA modification | 7.291152e-02 | 1.137 |
R-HSA-168255 | Influenza Infection | 9.429372e-02 | 1.026 |
R-HSA-1482798 | Acyl chain remodeling of CL | 4.588783e-02 | 1.338 |
R-HSA-749476 | RNA Polymerase III Abortive And Retractive Initiation | 1.062266e-01 | 0.974 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 1.887482e-01 | 0.724 |
R-HSA-74158 | RNA Polymerase III Transcription | 1.062266e-01 | 0.974 |
R-HSA-373755 | Semaphorin interactions | 1.693879e-01 | 0.771 |
R-HSA-381038 | XBP1(S) activates chaperone genes | 2.563570e-02 | 1.591 |
R-HSA-381070 | IRE1alpha activates chaperones | 2.869431e-02 | 1.542 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 6.261786e-02 | 1.203 |
R-HSA-449147 | Signaling by Interleukins | 8.691801e-02 | 1.061 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 1.545577e-01 | 0.811 |
R-HSA-1169408 | ISG15 antiviral mechanism | 1.951032e-01 | 0.710 |
R-HSA-9856530 | High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR... | 2.055871e-01 | 0.687 |
R-HSA-6802957 | Oncogenic MAPK signaling | 2.159376e-01 | 0.666 |
R-HSA-6794362 | Protein-protein interactions at synapses | 2.159376e-01 | 0.666 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 2.179918e-01 | 0.662 |
R-HSA-141424 | Amplification of signal from the kinetochores | 2.179918e-01 | 0.662 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 2.287014e-01 | 0.641 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 2.322252e-01 | 0.634 |
R-HSA-9837999 | Mitochondrial protein degradation | 2.382475e-01 | 0.623 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 2.422367e-01 | 0.616 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 2.521207e-01 | 0.598 |
R-HSA-70171 | Glycolysis | 2.521207e-01 | 0.598 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 2.560390e-01 | 0.592 |
R-HSA-192823 | Viral mRNA Translation | 2.579906e-01 | 0.588 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 2.599372e-01 | 0.585 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 2.676740e-01 | 0.572 |
R-HSA-9700206 | Signaling by ALK in cancer | 2.676740e-01 | 0.572 |
R-HSA-211000 | Gene Silencing by RNA | 2.676740e-01 | 0.572 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 2.695958e-01 | 0.569 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 2.715127e-01 | 0.566 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 2.772339e-01 | 0.557 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 2.772339e-01 | 0.557 |
R-HSA-1483249 | Inositol phosphate metabolism | 2.772339e-01 | 0.557 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 2.810237e-01 | 0.551 |
R-HSA-70326 | Glucose metabolism | 2.904135e-01 | 0.537 |
R-HSA-68875 | Mitotic Prophase | 2.959898e-01 | 0.529 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 2.978390e-01 | 0.526 |
R-HSA-3371556 | Cellular response to heat stress | 2.978390e-01 | 0.526 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 3.015233e-01 | 0.521 |
R-HSA-162909 | Host Interactions of HIV factors | 3.033583e-01 | 0.518 |
R-HSA-8978868 | Fatty acid metabolism | 3.074961e-01 | 0.512 |
R-HSA-114608 | Platelet degranulation | 3.106516e-01 | 0.508 |
R-HSA-76005 | Response to elevated platelet cytosolic Ca2+ | 3.232358e-01 | 0.490 |
R-HSA-72766 | Translation | 3.287235e-01 | 0.483 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 3.320869e-01 | 0.479 |
R-HSA-9664407 | Parasite infection | 3.373433e-01 | 0.472 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 3.373433e-01 | 0.472 |
R-HSA-9664417 | Leishmania phagocytosis | 3.373433e-01 | 0.472 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 3.390864e-01 | 0.470 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 3.425592e-01 | 0.465 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 3.425592e-01 | 0.465 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 3.596579e-01 | 0.444 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 3.630252e-01 | 0.440 |
R-HSA-9610379 | HCMV Late Events | 3.680437e-01 | 0.434 |
R-HSA-162587 | HIV Life Cycle | 3.680437e-01 | 0.434 |
R-HSA-2467813 | Separation of Sister Chromatids | 3.796039e-01 | 0.421 |
R-HSA-5619102 | SLC transporter disorders | 3.844948e-01 | 0.415 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 3.909576e-01 | 0.408 |
R-HSA-72306 | tRNA processing | 3.909576e-01 | 0.408 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 3.973541e-01 | 0.401 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 4.097960e-01 | 0.387 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 4.192295e-01 | 0.378 |
R-HSA-68877 | Mitotic Prometaphase | 4.268527e-01 | 0.370 |
R-HSA-9609690 | HCMV Early Events | 4.313796e-01 | 0.365 |
R-HSA-422475 | Axon guidance | 4.370621e-01 | 0.359 |
R-HSA-376176 | Signaling by ROBO receptors | 4.418072e-01 | 0.355 |
R-HSA-1483206 | Glycerophospholipid biosynthesis | 4.418072e-01 | 0.355 |
R-HSA-68882 | Mitotic Anaphase | 4.621054e-01 | 0.335 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 4.635273e-01 | 0.334 |
R-HSA-9675108 | Nervous system development | 4.697860e-01 | 0.328 |
R-HSA-162906 | HIV Infection | 4.775467e-01 | 0.321 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 4.789288e-01 | 0.320 |
R-HSA-72312 | rRNA processing | 4.844217e-01 | 0.315 |
R-HSA-5619115 | Disorders of transmembrane transporters | 5.045208e-01 | 0.297 |
R-HSA-9609646 | HCMV Infection | 5.084479e-01 | 0.294 |
R-HSA-2262752 | Cellular responses to stress | 5.145936e-01 | 0.289 |
R-HSA-69620 | Cell Cycle Checkpoints | 5.187720e-01 | 0.285 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 5.387892e-01 | 0.269 |
R-HSA-9824443 | Parasitic Infection Pathways | 5.472889e-01 | 0.262 |
R-HSA-9658195 | Leishmania infection | 5.472889e-01 | 0.262 |
R-HSA-5673001 | RAF/MAP kinase cascade | 5.568158e-01 | 0.254 |
R-HSA-1483257 | Phospholipid metabolism | 5.638322e-01 | 0.249 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 5.649910e-01 | 0.248 |
R-HSA-9824446 | Viral Infection Pathways | 5.837854e-01 | 0.234 |
R-HSA-8953897 | Cellular responses to stimuli | 5.946343e-01 | 0.226 |
R-HSA-5683057 | MAPK family signaling cascades | 6.202679e-01 | 0.207 |
R-HSA-9694516 | SARS-CoV-2 Infection | 6.222897e-01 | 0.206 |
R-HSA-68886 | M Phase | 6.550945e-01 | 0.184 |
R-HSA-913531 | Interferon Signaling | 6.560160e-01 | 0.183 |
R-HSA-5663205 | Infectious disease | 6.659020e-01 | 0.177 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 7.164103e-01 | 0.145 |
R-HSA-112316 | Neuronal System | 7.261517e-01 | 0.139 |
R-HSA-168256 | Immune System | 7.596289e-01 | 0.119 |
R-HSA-74160 | Gene expression (Transcription) | 7.792720e-01 | 0.108 |
R-HSA-9679506 | SARS-CoV Infections | 7.834332e-01 | 0.106 |
R-HSA-69278 | Cell Cycle, Mitotic | 7.897843e-01 | 0.102 |
R-HSA-162582 | Signal Transduction | 8.326400e-01 | 0.080 |
R-HSA-1640170 | Cell Cycle | 8.571226e-01 | 0.067 |
R-HSA-109582 | Hemostasis | 8.839700e-01 | 0.054 |
R-HSA-1643685 | Disease | 8.878313e-01 | 0.052 |
R-HSA-392499 | Metabolism of proteins | 8.960954e-01 | 0.048 |
R-HSA-556833 | Metabolism of lipids | 9.142959e-01 | 0.039 |
R-HSA-73857 | RNA Polymerase II Transcription | 9.469682e-01 | 0.024 |
R-HSA-1266738 | Developmental Biology | 9.713003e-01 | 0.013 |
R-HSA-168249 | Innate Immune System | 9.747135e-01 | 0.011 |
R-HSA-597592 | Post-translational protein modification | 9.902220e-01 | 0.004 |
R-HSA-1430728 | Metabolism | 9.986924e-01 | 0.001 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
FAM20C |
0.544 | 0.220 | 2 | 0.704 |
CHK1 |
0.521 | 0.135 | -3 | 0.568 |
CAMK2G |
0.518 | 0.076 | 2 | 0.528 |
JNK2 |
0.515 | 0.185 | 1 | 0.699 |
CDK8 |
0.515 | 0.168 | 1 | 0.705 |
ATM |
0.514 | 0.054 | 1 | 0.549 |
CAMK2B |
0.514 | 0.066 | 2 | 0.612 |
DNAPK |
0.514 | 0.081 | 1 | 0.550 |
CDC7 |
0.513 | 0.022 | 1 | 0.603 |
P38B |
0.513 | 0.175 | 1 | 0.678 |
CK2A2 |
0.513 | 0.112 | 1 | 0.498 |
JNK3 |
0.512 | 0.177 | 1 | 0.718 |
CAMK2D |
0.511 | 0.062 | -3 | 0.535 |
P38D |
0.511 | 0.176 | 1 | 0.707 |
ATR |
0.510 | 0.025 | 1 | 0.566 |
MOS |
0.510 | -0.016 | 1 | 0.622 |
NLK |
0.509 | 0.090 | 1 | 0.673 |
CAMK2A |
0.509 | 0.055 | 2 | 0.559 |
MARK4 |
0.509 | 0.028 | 4 | 0.497 |
MARK2 |
0.508 | 0.057 | 4 | 0.484 |
SBK |
0.508 | 0.082 | -3 | 0.363 |
HIPK4 |
0.508 | 0.065 | 1 | 0.659 |
PDHK4 |
0.507 | -0.012 | 1 | 0.554 |
CAMK1B |
0.507 | -0.008 | -3 | 0.571 |
PRPK |
0.507 | -0.065 | -1 | 0.506 |
TSSK2 |
0.506 | 0.000 | -5 | 0.387 |
SMG1 |
0.506 | 0.072 | 1 | 0.540 |
P38A |
0.506 | 0.147 | 1 | 0.681 |
PDHK1 |
0.506 | -0.006 | 1 | 0.538 |
MAPKAPK3 |
0.506 | 0.045 | -3 | 0.493 |
CDK19 |
0.506 | 0.159 | 1 | 0.690 |
MAPKAPK2 |
0.506 | 0.025 | -3 | 0.483 |
IKKB |
0.505 | 0.018 | -2 | 0.392 |
ERK5 |
0.505 | 0.039 | 1 | 0.594 |
GRK6 |
0.505 | 0.018 | 1 | 0.501 |
CDK7 |
0.504 | 0.139 | 1 | 0.724 |
IKKE |
0.503 | -0.012 | 1 | 0.451 |
JNK1 |
0.502 | 0.155 | 1 | 0.696 |
MARK1 |
0.502 | 0.057 | 4 | 0.474 |
PRKD1 |
0.501 | -0.040 | -3 | 0.533 |
MARK3 |
0.501 | 0.041 | 4 | 0.486 |
CK2A1 |
0.501 | 0.082 | 1 | 0.472 |
CLK3 |
0.501 | 0.031 | 1 | 0.687 |
BMPR2 |
0.500 | -0.095 | -2 | 0.310 |
BCKDK |
0.500 | -0.008 | -1 | 0.451 |
IKKA |
0.500 | -0.018 | -2 | 0.369 |
CDK5 |
0.500 | 0.136 | 1 | 0.714 |
TBK1 |
0.500 | -0.053 | 1 | 0.449 |
DYRK2 |
0.500 | 0.117 | 1 | 0.673 |
TGFBR1 |
0.499 | -0.011 | -2 | 0.210 |
P38G |
0.498 | 0.158 | 1 | 0.655 |
GRK5 |
0.498 | -0.025 | -3 | 0.556 |
KIS |
0.498 | 0.106 | 1 | 0.715 |
CDKL1 |
0.498 | -0.008 | -3 | 0.517 |
CDK9 |
0.497 | 0.156 | 1 | 0.702 |
MEK1 |
0.497 | 0.122 | 2 | 0.387 |
TSSK1 |
0.497 | -0.021 | -3 | 0.556 |
ALK2 |
0.497 | 0.012 | -2 | 0.228 |
GRK1 |
0.496 | 0.001 | -2 | 0.361 |
ICK |
0.496 | 0.015 | -3 | 0.538 |
RAF1 |
0.496 | -0.125 | 1 | 0.519 |
DYRK4 |
0.496 | 0.133 | 1 | 0.682 |
ERK1 |
0.495 | 0.142 | 1 | 0.679 |
AMPKA2 |
0.495 | -0.013 | -3 | 0.522 |
AMPKA1 |
0.495 | -0.032 | -3 | 0.540 |
PLK3 |
0.494 | -0.002 | 2 | 0.423 |
CDK2 |
0.494 | 0.102 | 1 | 0.662 |
CDKL5 |
0.494 | -0.007 | -3 | 0.508 |
DSTYK |
0.494 | -0.082 | 2 | 0.481 |
CDK13 |
0.494 | 0.140 | 1 | 0.713 |
MTOR |
0.494 | -0.057 | 1 | 0.570 |
QSK |
0.494 | -0.002 | 4 | 0.498 |
SIK |
0.493 | -0.001 | -3 | 0.485 |
PRKD2 |
0.493 | -0.035 | -3 | 0.495 |
COT |
0.493 | -0.139 | 2 | 0.440 |
QIK |
0.493 | 0.002 | -3 | 0.512 |
CDK18 |
0.492 | 0.135 | 1 | 0.674 |
CDK1 |
0.492 | 0.129 | 1 | 0.683 |
BRSK1 |
0.492 | -0.001 | -3 | 0.505 |
CDK17 |
0.491 | 0.143 | 1 | 0.659 |
CAMLCK |
0.491 | -0.063 | -2 | 0.317 |
MASTL |
0.490 | -0.064 | -2 | 0.372 |
BMPR1B |
0.490 | -0.028 | 1 | 0.480 |
ERK2 |
0.490 | 0.125 | 1 | 0.678 |
DAPK2 |
0.490 | -0.080 | -3 | 0.558 |
NDR2 |
0.490 | -0.081 | -3 | 0.543 |
PIM3 |
0.490 | -0.077 | -3 | 0.545 |
DYRK1A |
0.489 | 0.079 | 1 | 0.709 |
PRP4 |
0.489 | 0.059 | -3 | 0.479 |
NIK |
0.489 | -0.112 | -3 | 0.586 |
BMPR1A |
0.489 | -0.008 | 1 | 0.487 |
CDK16 |
0.489 | 0.125 | 1 | 0.671 |
NUAK2 |
0.488 | -0.048 | -3 | 0.522 |
ALK4 |
0.488 | -0.050 | -2 | 0.235 |
WNK1 |
0.488 | -0.068 | -2 | 0.328 |
TLK1 |
0.488 | -0.030 | -2 | 0.216 |
ACVR2B |
0.488 | -0.042 | -2 | 0.224 |
PKN3 |
0.488 | -0.077 | -3 | 0.534 |
CDK3 |
0.488 | 0.128 | 1 | 0.672 |
GCN2 |
0.488 | -0.110 | 2 | 0.357 |
LATS2 |
0.488 | -0.053 | -5 | 0.296 |
PIM1 |
0.488 | -0.041 | -3 | 0.499 |
SRPK1 |
0.487 | 0.018 | -3 | 0.474 |
SSTK |
0.487 | -0.035 | 4 | 0.483 |
CDK12 |
0.487 | 0.133 | 1 | 0.703 |
CAMK4 |
0.486 | -0.035 | -3 | 0.525 |
RSK2 |
0.486 | -0.053 | -3 | 0.504 |
WNK3 |
0.486 | -0.124 | 1 | 0.489 |
PLK2 |
0.485 | 0.013 | -3 | 0.651 |
PRKD3 |
0.485 | -0.045 | -3 | 0.470 |
P70S6KB |
0.485 | -0.072 | -3 | 0.518 |
GRK4 |
0.485 | -0.099 | -2 | 0.272 |
NIM1 |
0.484 | -0.055 | 3 | 0.518 |
CAMK1D |
0.484 | -0.007 | -3 | 0.438 |
P90RSK |
0.484 | -0.061 | -3 | 0.504 |
HIPK3 |
0.483 | 0.093 | 1 | 0.660 |
ACVR2A |
0.483 | -0.060 | -2 | 0.214 |
LATS1 |
0.483 | -0.052 | -3 | 0.563 |
HIPK2 |
0.483 | 0.102 | 1 | 0.663 |
SRPK2 |
0.483 | 0.010 | -3 | 0.432 |
BRSK2 |
0.483 | -0.032 | -3 | 0.520 |
PAK6 |
0.482 | -0.019 | -2 | 0.290 |
PINK1 |
0.482 | -0.016 | 1 | 0.608 |
DYRK1B |
0.482 | 0.096 | 1 | 0.664 |
SRPK3 |
0.481 | 0.000 | -3 | 0.456 |
NDR1 |
0.481 | -0.105 | -3 | 0.548 |
MLK2 |
0.481 | -0.098 | 2 | 0.351 |
TGFBR2 |
0.480 | -0.123 | -2 | 0.205 |
CLK4 |
0.480 | 0.021 | -3 | 0.490 |
BRAF |
0.480 | -0.088 | -4 | 0.296 |
MELK |
0.480 | -0.049 | -3 | 0.520 |
CLK1 |
0.480 | 0.043 | -3 | 0.485 |
HIPK1 |
0.479 | 0.070 | 1 | 0.663 |
NUAK1 |
0.479 | -0.064 | -3 | 0.518 |
ERK7 |
0.479 | 0.015 | 2 | 0.176 |
CDK14 |
0.479 | 0.110 | 1 | 0.676 |
GSK3A |
0.479 | -0.015 | 4 | 0.108 |
YSK4 |
0.479 | -0.057 | 1 | 0.452 |
MAPKAPK5 |
0.479 | -0.033 | -3 | 0.438 |
HUNK |
0.479 | -0.138 | 2 | 0.348 |
PKACG |
0.479 | -0.071 | -2 | 0.343 |
MST4 |
0.478 | -0.106 | 2 | 0.350 |
ULK2 |
0.478 | -0.188 | 2 | 0.304 |
CDK10 |
0.478 | 0.111 | 1 | 0.675 |
RSK3 |
0.478 | -0.067 | -3 | 0.504 |
SKMLCK |
0.477 | -0.116 | -2 | 0.286 |
MSK1 |
0.477 | -0.054 | -3 | 0.462 |
AURA |
0.477 | -0.062 | -2 | 0.209 |
TLK2 |
0.477 | -0.118 | 1 | 0.527 |
VRK2 |
0.477 | -0.154 | 1 | 0.547 |
CAMK1A |
0.476 | -0.012 | -3 | 0.429 |
CDK4 |
0.476 | 0.130 | 1 | 0.700 |
DYRK3 |
0.476 | 0.053 | 1 | 0.646 |
GRK7 |
0.476 | -0.069 | 1 | 0.469 |
MYLK4 |
0.476 | -0.053 | -2 | 0.272 |
DLK |
0.475 | -0.195 | 1 | 0.475 |
NEK6 |
0.475 | -0.159 | -2 | 0.279 |
TTBK2 |
0.475 | -0.140 | 2 | 0.278 |
GRK2 |
0.475 | -0.068 | -2 | 0.262 |
MLK1 |
0.474 | -0.146 | 2 | 0.325 |
MSK2 |
0.474 | -0.065 | -3 | 0.454 |
CDK6 |
0.474 | 0.120 | 1 | 0.679 |
PIM2 |
0.474 | -0.051 | -3 | 0.477 |
NEK7 |
0.474 | -0.195 | -3 | 0.505 |
CAMKK2 |
0.473 | -0.013 | -2 | 0.448 |
PLK1 |
0.473 | -0.131 | -2 | 0.239 |
ANKRD3 |
0.473 | -0.193 | 1 | 0.491 |
NEK9 |
0.473 | -0.164 | 2 | 0.340 |
CAMKK1 |
0.472 | -0.039 | -2 | 0.407 |
PKN2 |
0.472 | -0.126 | -3 | 0.528 |
AURB |
0.472 | -0.074 | -2 | 0.252 |
PKR |
0.472 | -0.136 | 1 | 0.484 |
ULK1 |
0.472 | -0.166 | -3 | 0.529 |
RSK4 |
0.472 | -0.066 | -3 | 0.480 |
NEK2 |
0.472 | -0.085 | 2 | 0.300 |
SNRK |
0.471 | -0.077 | 2 | 0.214 |
CHAK2 |
0.471 | -0.131 | -1 | 0.430 |
SMMLCK |
0.471 | -0.058 | -3 | 0.528 |
PKG2 |
0.471 | -0.064 | -2 | 0.308 |
CLK2 |
0.471 | 0.018 | -3 | 0.492 |
TTBK1 |
0.471 | -0.053 | 2 | 0.221 |
AURC |
0.471 | -0.077 | -2 | 0.255 |
MNK2 |
0.471 | -0.099 | -2 | 0.293 |
MEK5 |
0.471 | -0.086 | 2 | 0.339 |
RIPK3 |
0.470 | -0.173 | 3 | 0.422 |
GSK3B |
0.470 | -0.048 | 4 | 0.108 |
PKACB |
0.470 | -0.066 | -2 | 0.263 |
PKACA |
0.469 | -0.046 | -2 | 0.266 |
MAK |
0.469 | 0.051 | -2 | 0.285 |
HRI |
0.469 | -0.127 | -2 | 0.280 |
AKT2 |
0.468 | -0.058 | -3 | 0.424 |
PERK |
0.468 | -0.103 | -2 | 0.311 |
SGK3 |
0.468 | -0.068 | -3 | 0.463 |
RIPK1 |
0.467 | -0.185 | 1 | 0.429 |
P70S6K |
0.467 | -0.060 | -3 | 0.443 |
CAMK1G |
0.467 | -0.076 | -3 | 0.488 |
PRKX |
0.467 | -0.042 | -3 | 0.410 |
WNK4 |
0.467 | -0.109 | -2 | 0.325 |
DCAMKL2 |
0.467 | -0.058 | -3 | 0.531 |
PAK3 |
0.466 | -0.123 | -2 | 0.280 |
GRK3 |
0.465 | -0.071 | -2 | 0.227 |
MOK |
0.465 | 0.036 | 1 | 0.600 |
MST2 |
0.465 | -0.053 | 1 | 0.471 |
PKCD |
0.465 | -0.139 | 2 | 0.301 |
MEK2 |
0.464 | -0.023 | 2 | 0.345 |
DCAMKL1 |
0.463 | -0.096 | -3 | 0.503 |
PAK1 |
0.463 | -0.125 | -2 | 0.266 |
IRE2 |
0.463 | -0.152 | 2 | 0.243 |
MPSK1 |
0.463 | -0.071 | 1 | 0.478 |
IRAK1 |
0.463 | -0.119 | -1 | 0.379 |
PLK4 |
0.462 | -0.135 | 2 | 0.202 |
MEKK2 |
0.462 | -0.153 | 2 | 0.332 |
MEKK3 |
0.462 | -0.164 | 1 | 0.438 |
PAK5 |
0.461 | -0.072 | -2 | 0.253 |
PHKG1 |
0.461 | -0.111 | -3 | 0.530 |
LKB1 |
0.461 | -0.109 | -3 | 0.499 |
DRAK1 |
0.461 | -0.135 | 1 | 0.408 |
IRE1 |
0.461 | -0.160 | 1 | 0.431 |
PASK |
0.461 | -0.104 | -3 | 0.526 |
PHKG2 |
0.461 | -0.095 | -3 | 0.517 |
PAK2 |
0.461 | -0.133 | -2 | 0.272 |
TAO2 |
0.460 | -0.103 | 2 | 0.352 |
PAK4 |
0.460 | -0.065 | -2 | 0.240 |
LRRK2 |
0.459 | -0.043 | 2 | 0.338 |
PDK1 |
0.459 | -0.089 | 1 | 0.495 |
TAK1 |
0.458 | -0.100 | 1 | 0.547 |
LOK |
0.458 | -0.033 | -2 | 0.453 |
MRCKA |
0.458 | -0.067 | -3 | 0.490 |
MLK3 |
0.458 | -0.158 | 2 | 0.270 |
MEKK1 |
0.458 | -0.196 | 1 | 0.473 |
AKT1 |
0.458 | -0.070 | -3 | 0.428 |
CHK2 |
0.458 | -0.043 | -3 | 0.399 |
DAPK3 |
0.458 | -0.091 | -3 | 0.509 |
CHAK1 |
0.458 | -0.171 | 2 | 0.280 |
PKCA |
0.457 | -0.116 | 2 | 0.237 |
GAK |
0.457 | -0.107 | 1 | 0.477 |
MNK1 |
0.457 | -0.128 | -2 | 0.302 |
PKCH |
0.457 | -0.122 | 2 | 0.227 |
PKG1 |
0.456 | -0.053 | -2 | 0.272 |
ZAK |
0.456 | -0.180 | 1 | 0.435 |
PKN1 |
0.456 | -0.060 | -3 | 0.445 |
MRCKB |
0.456 | -0.065 | -3 | 0.467 |
PKCG |
0.456 | -0.128 | 2 | 0.245 |
PKCZ |
0.455 | -0.134 | 2 | 0.279 |
PKCB |
0.454 | -0.134 | 2 | 0.253 |
NEK11 |
0.454 | -0.143 | 1 | 0.477 |
MLK4 |
0.454 | -0.175 | 2 | 0.272 |
DMPK1 |
0.454 | -0.051 | -3 | 0.493 |
TAO3 |
0.454 | -0.149 | 1 | 0.472 |
SGK1 |
0.453 | -0.053 | -3 | 0.373 |
EEF2K |
0.453 | -0.106 | 3 | 0.481 |
SLK |
0.453 | -0.040 | -2 | 0.455 |
HGK |
0.452 | -0.088 | 3 | 0.478 |
MST1 |
0.452 | -0.084 | 1 | 0.444 |
DAPK1 |
0.452 | -0.090 | -3 | 0.481 |
NEK4 |
0.452 | -0.127 | 1 | 0.439 |
MINK |
0.452 | -0.091 | 1 | 0.448 |
IRAK4 |
0.452 | -0.176 | 1 | 0.419 |
PKCI |
0.451 | -0.086 | 2 | 0.237 |
MST3 |
0.451 | -0.144 | 2 | 0.317 |
NEK5 |
0.450 | -0.219 | 1 | 0.472 |
HPK1 |
0.450 | -0.084 | 1 | 0.452 |
GCK |
0.450 | -0.116 | 1 | 0.469 |
TNIK |
0.449 | -0.093 | 3 | 0.477 |
RIPK2 |
0.449 | -0.113 | 1 | 0.421 |
PBK |
0.449 | -0.063 | 1 | 0.432 |
CRIK |
0.449 | -0.055 | -3 | 0.436 |
CK1D |
0.449 | -0.085 | -3 | 0.205 |
CK1E |
0.449 | -0.099 | -3 | 0.251 |
NEK8 |
0.448 | -0.206 | 2 | 0.299 |
PDHK3_TYR |
0.448 | 0.034 | 4 | 0.415 |
ALPHAK3 |
0.448 | -0.053 | -1 | 0.479 |
AKT3 |
0.447 | -0.073 | -3 | 0.378 |
MAP3K15 |
0.447 | -0.173 | 1 | 0.442 |
VRK1 |
0.447 | -0.168 | 2 | 0.355 |
PKCT |
0.446 | -0.133 | 2 | 0.239 |
NEK3 |
0.445 | -0.111 | 1 | 0.435 |
MEKK6 |
0.445 | -0.193 | 1 | 0.458 |
ROCK2 |
0.445 | -0.094 | -3 | 0.495 |
BIKE |
0.444 | -0.047 | 1 | 0.386 |
CK1A2 |
0.444 | -0.090 | -3 | 0.205 |
KHS1 |
0.444 | -0.101 | 1 | 0.462 |
PKCE |
0.443 | -0.091 | 2 | 0.224 |
NEK1 |
0.442 | -0.150 | 1 | 0.429 |
BMPR2_TYR |
0.442 | 0.009 | -1 | 0.557 |
MAP2K4_TYR |
0.441 | -0.005 | -1 | 0.539 |
MAP2K7_TYR |
0.441 | 0.001 | 2 | 0.411 |
YSK1 |
0.440 | -0.132 | 2 | 0.302 |
EPHA6 |
0.440 | -0.016 | -1 | 0.601 |
EPHA4 |
0.440 | 0.011 | 2 | 0.425 |
KHS2 |
0.439 | -0.102 | 1 | 0.471 |
BUB1 |
0.438 | -0.110 | -5 | 0.330 |
PDHK1_TYR |
0.438 | -0.055 | -1 | 0.571 |
MAP2K6_TYR |
0.438 | -0.033 | -1 | 0.542 |
ROCK1 |
0.437 | -0.094 | -3 | 0.484 |
TESK1_TYR |
0.437 | -0.089 | 3 | 0.564 |
PDHK4_TYR |
0.436 | -0.069 | 2 | 0.450 |
ASK1 |
0.435 | -0.127 | 1 | 0.446 |
TAO1 |
0.433 | -0.102 | 1 | 0.427 |
AAK1 |
0.432 | -0.041 | 1 | 0.321 |
YANK3 |
0.432 | -0.082 | 2 | 0.150 |
STK33 |
0.431 | -0.126 | 2 | 0.198 |
LIMK2_TYR |
0.431 | -0.050 | -3 | 0.602 |
STLK3 |
0.431 | -0.122 | 1 | 0.416 |
DDR1 |
0.430 | -0.055 | 4 | 0.394 |
EPHB2 |
0.430 | -0.046 | -1 | 0.600 |
MYO3A |
0.430 | -0.114 | 1 | 0.441 |
LIMK1_TYR |
0.430 | -0.065 | 2 | 0.375 |
PKMYT1_TYR |
0.429 | -0.072 | 3 | 0.528 |
CK1G1 |
0.429 | -0.134 | -3 | 0.281 |
EPHB4 |
0.428 | -0.086 | -1 | 0.588 |
EPHB1 |
0.428 | -0.063 | 1 | 0.496 |
MYO3B |
0.428 | -0.113 | 2 | 0.305 |
PINK1_TYR |
0.427 | -0.144 | 1 | 0.521 |
EPHB3 |
0.426 | -0.057 | -1 | 0.590 |
FER |
0.426 | -0.090 | 1 | 0.536 |
OSR1 |
0.425 | -0.187 | 2 | 0.305 |
TTK |
0.425 | -0.186 | -2 | 0.207 |
EPHA3 |
0.425 | -0.047 | 2 | 0.391 |
JAK3 |
0.424 | -0.090 | 1 | 0.474 |
HASPIN |
0.424 | -0.100 | -1 | 0.278 |
EPHA5 |
0.424 | -0.033 | 2 | 0.430 |
INSRR |
0.424 | -0.092 | 3 | 0.467 |
TEK |
0.424 | -0.046 | 3 | 0.446 |
SRMS |
0.424 | -0.063 | 1 | 0.500 |
FGFR2 |
0.424 | -0.085 | 3 | 0.515 |
RET |
0.423 | -0.158 | 1 | 0.474 |
JAK2 |
0.423 | -0.121 | 1 | 0.489 |
TYK2 |
0.422 | -0.161 | 1 | 0.482 |
MST1R |
0.422 | -0.126 | 3 | 0.480 |
EPHA7 |
0.421 | -0.051 | 2 | 0.390 |
NEK10_TYR |
0.421 | -0.061 | 1 | 0.443 |
FGFR1 |
0.421 | -0.102 | 3 | 0.492 |
TXK |
0.419 | -0.074 | 1 | 0.477 |
HCK |
0.418 | -0.100 | -1 | 0.555 |
TNNI3K_TYR |
0.418 | -0.073 | 1 | 0.464 |
YES1 |
0.417 | -0.105 | -1 | 0.522 |
EGFR |
0.417 | -0.047 | 1 | 0.369 |
ROS1 |
0.417 | -0.170 | 3 | 0.456 |
LCK |
0.416 | -0.096 | -1 | 0.559 |
FGFR3 |
0.416 | -0.096 | 3 | 0.494 |
CSF1R |
0.415 | -0.144 | 3 | 0.446 |
TYRO3 |
0.415 | -0.177 | 3 | 0.472 |
ERBB2 |
0.414 | -0.090 | 1 | 0.438 |
EPHA8 |
0.413 | -0.067 | -1 | 0.574 |
ITK |
0.413 | -0.113 | -1 | 0.507 |
BLK |
0.413 | -0.095 | -1 | 0.571 |
BTK |
0.412 | -0.091 | -1 | 0.476 |
YANK2 |
0.411 | -0.088 | 2 | 0.177 |
LYN |
0.411 | -0.082 | 3 | 0.398 |
EPHA2 |
0.411 | -0.059 | -1 | 0.579 |
BMX |
0.410 | -0.090 | -1 | 0.479 |
FGR |
0.410 | -0.153 | 1 | 0.444 |
LTK |
0.409 | -0.119 | 3 | 0.441 |
SYK |
0.409 | -0.056 | -1 | 0.581 |
ABL2 |
0.409 | -0.138 | -1 | 0.517 |
MERTK |
0.409 | -0.108 | 3 | 0.472 |
EPHA1 |
0.409 | -0.109 | 3 | 0.445 |
PTK2 |
0.409 | -0.049 | -1 | 0.559 |
FYN |
0.408 | -0.084 | -1 | 0.533 |
PDGFRA |
0.408 | -0.156 | 3 | 0.447 |
KIT |
0.408 | -0.152 | 3 | 0.461 |
FLT3 |
0.408 | -0.164 | 3 | 0.445 |
ALK |
0.407 | -0.136 | 3 | 0.427 |
FRK |
0.407 | -0.099 | -1 | 0.604 |
CK1A |
0.407 | -0.120 | -3 | 0.152 |
FLT1 |
0.407 | -0.110 | -1 | 0.577 |
NTRK1 |
0.406 | -0.149 | -1 | 0.516 |
JAK1 |
0.406 | -0.132 | 1 | 0.446 |
ABL1 |
0.406 | -0.142 | -1 | 0.505 |
CSK |
0.406 | -0.087 | 2 | 0.387 |
AXL |
0.405 | -0.140 | 3 | 0.489 |
FLT4 |
0.405 | -0.128 | 3 | 0.436 |
INSR |
0.405 | -0.140 | 3 | 0.447 |
TEC |
0.404 | -0.121 | -1 | 0.472 |
NTRK2 |
0.404 | -0.138 | 3 | 0.442 |
PDGFRB |
0.403 | -0.198 | 3 | 0.466 |
KDR |
0.403 | -0.175 | 3 | 0.421 |
FGFR4 |
0.403 | -0.100 | -1 | 0.522 |
TNK2 |
0.402 | -0.145 | 3 | 0.443 |
PTK2B |
0.401 | -0.100 | -1 | 0.488 |
MET |
0.401 | -0.166 | 3 | 0.459 |
PTK6 |
0.401 | -0.157 | -1 | 0.423 |
ERBB4 |
0.401 | -0.064 | 1 | 0.386 |
CK1G3 |
0.400 | -0.114 | -3 | 0.120 |
NTRK3 |
0.400 | -0.126 | -1 | 0.501 |
SRC |
0.400 | -0.107 | -1 | 0.519 |
IGF1R |
0.399 | -0.108 | 3 | 0.423 |
DDR2 |
0.398 | -0.138 | 3 | 0.457 |
TNK1 |
0.396 | -0.183 | 3 | 0.452 |
CK1G2 |
0.392 | -0.113 | -3 | 0.203 |
WEE1_TYR |
0.392 | -0.143 | -1 | 0.408 |
MATK |
0.390 | -0.137 | -1 | 0.447 |
FES |
0.388 | -0.101 | -1 | 0.438 |
MUSK |
0.387 | -0.106 | 1 | 0.342 |
ZAP70 |
0.369 | -0.117 | -1 | 0.470 |