PTK2B
Normalized values from positional scanning peptide array
Phospho-serine (pS) is a duplicate of phospho-tyrosine (pT) in PSPA
Position-wise Probabilities
Log-Odds: Probabilities / STY Background
Sites with acceptor types representing >8% and count ≥10 are included
Y Sites Probabilities
Log-Odds: Y Sites / Y Background
Sites with acceptor types representing >8% and count ≥10 are included
Motif clusters with count ≥ 10 are shown
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| substrate_uniprot | site | source | substrate_genes | site_seq |
|---|---|---|---|---|
| A0MZ66 | Y24 | Sugiyama | SHTN1 KIAA1598 | sDEEKQLQLITsLKEQAIGEyEDLRAENQKTKEKCDKIRQE |
| A1L429 | Y9 | Sugiyama | GAGE12B; GAGE12C; GAGE12D; GAGE12E | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A1X283 | Y855 | Sugiyama | SH3PXD2B FAD49 KIAA1295 TKS4 | NREKAAAASVPNADGLKDSLyVAVADFEGDKDTSSFQEGTV |
| A5A3E0 | S939 | Sugiyama | POTEF A26C1B | VALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPE |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y1572 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | RMPEQIRLKVGGVDPKQLAVyEEFARNVPGFLPTNDLSQPT |
| A6NDE8 | Y9 | Sugiyama | GAGE12H | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A6NER3 | Y9 | Sugiyama | GAGE12J | ____________MSWRGRsTyyWPRPRPYVQPPEMIGPMRP |
| A6NHL2 | Y319 | Sugiyama | TUBAL3 | TTACFESSNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAI |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00429 | S261 | Sugiyama | DNM1L DLP1 DRP1 | IIGVVNRSQLDINNKKSVTDsIRDEyAFLQKKYPSLANRNG |
| O00469 | Y444 | Sugiyama | PLOD2 | LWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYMANV |
| O00488 | Y97 | Sugiyama | ZNF593 ZT86 | KTHFRSKDHKKRLKQLsVEPysQEEAERAAGMGSYVPPRRL |
| O14579 | Y304 | Sugiyama | COPE | HPFIKEYQAKENDFDRLVLQyAPsA________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14818 | Y176 | Sugiyama | PSMA7 HSPC | WKANAIGRGAKSVREFLEKNyTDEAIETDDLTIKLVIKALL |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14974 | Y901 | Sugiyama | PPP1R12A MBS MYPT1 | EtQtDsIsRyETssTsAGDRyDsLLGRsGsysYLEERKPYS |
| O14974 | Y911 | Sugiyama | PPP1R12A MBS MYPT1 | ETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDSTD |
| O14974 | Y936 | Sugiyama | PPP1R12A MBS MYPT1 | ERKPYSSRLEKDDSTDFKKLyEQILAENEKLKAQLHDTNME |
| O15013 | Y1307 | Sugiyama | ARHGEF10 KIAA0294 | sLsLsHGsssLEHRSEDsTIyDLLKDPVSLRSKARRAKKAK |
| O15259 | Y349 | EPSD|PSP | NPHP1 NPH1 | GFRPSTLSQLLEEGNQFRANyFLQPELMPSQLAFRDLMWDA |
| O15259 | Y46 | EPSD|PSP | NPHP1 NPH1 | SLLSESQLKEALEPNKRQHIyQRCIQLKQAIDENKNALQKL |
| O15357 | Y190 | Sugiyama | INPPL1 SHIP2 | AAESAPNGLSTVSHDYLKGsyGLDLEAVRGGASHLPHLTRT |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15372 | Y350 | Sugiyama | EIF3H EIF3S3 | IKEFTAQNLGKLFMAQALQEyNN__________________ |
| O15397 | Y995 | Sugiyama | IPO8 RANBP8 | WYQLLMAPLSEDQRTALQEVyTLAEHRRTVAEAKKKIEQQG |
| O43164 | Y63 | Sugiyama | PJA2 KIAA0438 RNF131 | VSFKPCMTRHERSLGRAGDDyEVLELDDVPKENssGssPLD |
| O43294 | Y60 | SIGNOR|EPSD|PSP | TGFB1I1 ARA55 | HQPQTGsGESSGASGDKDHLySTVCKPRsPKPAAPAAPPFs |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43464 | Y147 | Sugiyama | HTRA2 OMI PRSS25 | GPPAVLAAVPSPPPAsPRSQyNFIADVVEKTAPAVVYIEIL |
| O43707 | Y212 | Sugiyama | ACTN4 | WKDGLAFNALIHRHRPELIEyDKLRKDDPVTNLNNAFEVAE |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y397 | Sugiyama | ACTN4 | GKMVSDINNGWQHLEQAEKGyEEWLLNEIRRLERLDHLAEK |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43823 | Y311 | Sugiyama | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y185 | Sugiyama | CALU | KDGDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNAD |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O43865 | Y28 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | PLPGVGEELKQAKEIEDAEKysFMATVTKAPKKQIQFADDM |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y373 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ILEKAFsQFGKLERVKKLKDyAFIHFDERDGAVKAMEEMNG |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60716 | Y257 | Sugiyama | CTNND1 KIAA0384 | IEERyRPsMEGyRAPsRQDVyGPQPQVRVGGssVDLHRFHP |
| O60739 | Y30 | Sugiyama | EIF1B | FDPFADATKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| O60814 | Y38 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60841 | Y134 | Sugiyama | EIF5B IF2 KIAA0741 | EELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKA |
| O60884 | Y128 | Sugiyama | DNAJA2 CPR3 HIRIP4 | NGRRRGEDMMHPLKVsLEDLyNGKTTKLQLSKNVLCsACsG |
| O60884 | Y66 | Sugiyama | DNAJA2 CPR3 HIRIP4 | KFKEISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDD |
| O60884 | Y69 | Sugiyama | DNAJA2 CPR3 HIRIP4 | EISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDDIFS |
| O60927 | Y64 | Sugiyama | PPP1R11 HCGV TCTE5 | TsDTVDNEHMGRRssKCCCIyEKPRAFGEsstEsDEEEEEG |
| O75116 | Y722 | Sugiyama | ROCK2 KIAA0619 | EQEEAEHKATKARLADKNKIyEsIEEAKSEAMKEMEKKLLE |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75190 | Y53 | Sugiyama | DNAJB6 HSJ2 MRJ MSJ1 | DKNPENKEEAERKFKQVAEAyEVLSDAKKRDIYDKYGKEGL |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75369 | Y315 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | DPEGNKEEAQVTPDSDKNKTySVEyLPKVTGLHKVTVLFAG |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75369 | Y904 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | FNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLVTY |
| O75688 | Y367 | Sugiyama | PPM1B PP2CB | IPNLPPGGGLAGKRNVIEAVySRLNPHREsDGAsDEAEEsG |
| O75718 | Y372 | Sugiyama | CRTAP CASP | FQPRPEAVQFFNVTTLQKELyDFAKENIMDDDEGEVVEyVD |
| O76087 | Y9 | Sugiyama | GAGE7 GAGE12I GAGE7B | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| O95218 | Y124 | Sugiyama | ZRANB2 ZIS ZNF265 | GGFNERENVEyIEREEsDGEyDEFGRKKKKYRGKAVGPAsI |
| O95297 | Y263 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | QLDHsGGHHSDKINKSEsVVyADIRKN______________ |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95425 | Y120 | Sugiyama | SVIL | SKAERIARYKAERRRQLAEKyGLTLDPEADsEyLsRYTKSR |
| O95456 | Y287 | Sugiyama | PSMG1 C21LRP DSCR2 PAC1 | PQSTEILKKLMTTNEIQsNIyt___________________ |
| O95757 | Y627 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MIMQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPED |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O95817 | Y247 | Sugiyama | BAG3 BIS | QAQKTHyPAQQGEyQtHQPVyHKIQGDDWEPRPLRAAsPFR |
| O96019 | Y68 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | DDGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsPL |
| O96019 | Y69 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | DGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsPLK |
| P00338 | Y10 | Sugiyama | LDHA PIG19 | ___________MAtLKDQLIyNLLKEEQtPQNKITVVGVGA |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00491 | Y166 | Sugiyama | PNP NP | PLRGPNDERFGDRFPAMsDAyDRtMRQRALstWKQMGEQRE |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00558 | Y76 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KSVVLMSHLGRPDGVPMPDKysLEPVAVELKSLLGKDVLFL |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P04040 | Y447 | Sugiyama | CAT | GEVRRFNtANDDNVtQVRAFyVNVLNEEQRKRLCENIAGHL |
| P04075 | S346 | Sugiyama | ALDOA ALDA | EEYVKRALANsLACQGKytPsGQAGAAAsEsLFVsNHAy__ |
| P04075 | Y364 | Sugiyama | ALDOA ALDA | tPsGQAGAAAsEsLFVsNHAy____________________ |
| P04080 | Y97 | Sugiyama | CSTB CST6 STFB | NKPLtLsNyQTNKAKHDELtyF___________________ |
| P04406 | Y314 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | tFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsK |
| P04406 | Y320 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsKE_____ |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P04818 | Y135 | Sugiyama | TYMS TS OK/SW-cl.29 | RDFLDsLGFsTREEGDLGPVyGFQWRHFGAEyRDMEsDysG |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P05997 | Y1311 | Sugiyama | COL5A2 | HPARTCDDLKLCHSAKQsGEyWIDPNQGSVEDAIKVYCNME |
| P06493 | T14 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | _______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKK |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06733 | S268 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyP |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y257 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | TDKVVIGMDVAASEFFRsGKyDLDFKsPDDPsRyIsPDQLA |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06748 | Y271 | Sugiyama | NPM1 NPM | MQAsIEKGGsLPKVEAKFINyVKNCFRMtDQEAIQDLWQWR |
| P06899 | Y38 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSK |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | Y50 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IDPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEP |
| P07437 | Y51 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPG |
| P07686 | Y547 | Sugiyama | HEXB HCC7 | DRLTRHRCRMVERGIAAQPLyAGyCNHENM___________ |
| P07711 | Y112 | Sugiyama | CTSL CTSL1 | MNGFQNRKPRKGKVFQEPLFyEAPRSVDWREKGyVTPVKNQ |
| P07711 | Y330 | Sugiyama | CTSL CTSL1 | GyVKMAKDRRNHCGIAsAAsyPtV_________________ |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07814 | Y1504 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | KPLCELQPGAKCVCGKNPAKyytLFGRsy____________ |
| P07814 | Y1505 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PLCELQPGAKCVCGKNPAKyytLFGRsy_____________ |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07900 | Y160 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGEPM |
| P07900 | Y284 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEEEEKKDGDKKKKKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P07900 | Y309 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | ELNKtKPIWtRNPDDItNEEyGEFyKsLtNDWEDHLAVKHF |
| P07900 | Y313 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | tKPIWtRNPDDItNEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P07900 | Y492 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLR |
| P07900 | Y493 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | EMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLRK |
| P07900 | Y61 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KEIFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLI |
| P07954 | Y110 | Sugiyama | FH | tPVIKAFGILKRAAAEVNQDyGLDPKIANAIMKAADEVAEG |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | Y155 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | SAYLVAEKVVVITKHNDDEQyAWEssAGGsFtVRADHGEPI |
| P08238 | Y276 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P08238 | Y301 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | ELNKtKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHF |
| P08238 | Y305 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | tKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P08238 | Y472 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | sELLRyHtsQsGDEMtsLsEyVsRMKEtQKsIyyItGEsKE |
| P08238 | Y484 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVR |
| P08238 | Y485 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVRK |
| P08238 | Y56 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KEIFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDII |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| P08758 | Y129 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | VLtEIIAsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYY |
| P08758 | Y133 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | IIAsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRML |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P08865 | Y156 | Sugiyama | RPSA LAMBR LAMR1 | EAsyVNLPtIALCNTDSPLRyVDIAIPCNNKGAHSVGLMWW |
| P09104 | T41 | Sugiyama | ENO2 | EVDLyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKG |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09234 | T11 | Sugiyama | SNRPC | __________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHK |
| P09234 | Y8 | Sugiyama | SNRPC | _____________MPKFyCDyCDtyLtHDsPsVRKTHCSGR |
| P09496 | Y147 | Sugiyama | CLTA | NSRKQEAEWKEKAIKELEEWyARQDEQLQKTKANNRVADEA |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09923 | Y188 | Sugiyama | ALPI | TRVQHAsPAGtyAHtVNRNWysDADMPASARQEGCQDIATQ |
| P09960 | Y233 | Sugiyama | LTA4H LTA4 | RQIGPRTLVWSEKEQVEKSAyEFsETEsMLKIAEDLGGPYV |
| P09972 | Y358 | Sugiyama | ALDOC ALDC | AAQGKYEGSGEDGGAAAQsLyIANHAY______________ |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CL80 | Y9 | Sugiyama | GAGE12F | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P0DSO3 | Y9 | Sugiyama | GAGE4 | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P10412 | Y71 | Sugiyama | H1-4 H1F4 HIST1H1E | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11142 | S432 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGERAMTKD |
| P11142 | T427 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | GGVMTVLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGER |
| P11142 | Y41 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P11142 | Y443 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KQtQtFttysDNQPGVLIQVyEGERAMTKDNNLLGKFELTG |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11940 | Y194 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLFGKF |
| P11940 | Y291 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | ERQTELKRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLR |
| P11940 | Y297 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLRKEFsPF |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y378 | Sugiyama | ACTN1 | GRMVSDINNAWGCLEQVEKGyEEWLLNEIRRLERLDHLAEK |
| P12814 | Y422 | Sugiyama | ACTN1 | KAsIHEAWtDGKEAMLRQKDyEtAtLsEIKALLKKHEAFEs |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P13639 | S732 | Sugiyama | EEF2 EF2 | DAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQCP |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y634 | Sugiyama | EEF2 EF2 | AEDIDKGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGP |
| P13639 | Y639 | Sugiyama | EEF2 EF2 | KGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGPDGTGP |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | T449 | Sugiyama | PDIA4 ERP70 ERP72 | AATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLsE |
| P13667 | Y458 | Sugiyama | PDIA4 ERP70 ERP72 | VLEVAKDFPEytFAIADEEDyAGEVKDLGLsEsGEDVNAAI |
| P13674 | Y141 | Sugiyama | P4HA1 P4HA | FPNDEDQVGAAKALLRLQDtyNLDTDtIsKGNLPGVKHKSF |
| P13674 | Y282 | Sugiyama | P4HA1 P4HA | ASDDQSDQKTTPKKKGVAVDyLPERQKyEMLCRGEGIKMTP |
| P13796 | Y462 | Sugiyama | LCP1 PLS2 | VNKPPYPKLGGNMKKLENCNyAVELGKNQAKFsLVGIGGQD |
| P13797 | Y465 | Sugiyama | PLS3 | VNKPPYPKLGANMKKLENCNyAVELGKHPAKFSLVGIGGQD |
| P13929 | T41 | Sugiyama | ENO3 | EVDLHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKG |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y86 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | KFEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTS |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14616 | Y1260 | Sugiyama | INSRR IRR | THILDSIQEELRPSFRLLSFyySPECRGARGsLPTTDAEPD |
| P14616 | Y1261 | Sugiyama | INSRR IRR | HILDSIQEELRPSFRLLSFyySPECRGARGsLPTTDAEPDs |
| P14625 | Y429 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | IKLYVRRVFITDDFHDMMPKyLNFVKGVVDsDDLPLNVsRE |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14635 | Y175 | Sugiyama | CCNB1 CCNB | DVDAEDGADPNLCSEYVKDIyAYLRQLEEEQAVRPKYLLGR |
| P14649 | S87 | Sugiyama | MYL6B MLC1SA | EEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVLK |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y250 | Sugiyama | RPS2 RPS4 | tAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEFt |
| P16402 | Y72 | Sugiyama | H1-3 H1F3 HIST1H1D | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P16403 | Y71 | Sugiyama | H1-2 H1F2 HIST1H1C | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P17066 | Y43 | Sugiyama | HSPA6 HSP70B' | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P17302 | Y247 | GPS6 | GJA1 GJAL | ELFYVFFKGVKDRVKGKSDPyHATsGALsPAKDCGsQKyAy |
| P17302 | Y265 | GPS6 | GJA1 GJAL | DPyHATsGALsPAKDCGsQKyAyFNGCssPtAPLsPMsPPG |
| P17302 | Y267 | GPS6 | GJA1 GJAL | yHATsGALsPAKDCGsQKyAyFNGCssPtAPLsPMsPPGyK |
| P17302 | Y313 | GPS6 | GJA1 GJAL | RNNssCRNYNKQAsEQNWANysAEQNRMGQAGstIsNsHAQ |
| P17676 | Y137 | Sugiyama | CEBPB TCF5 PP9092 | FLSDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCF |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17812 | Y473 | Sugiyama | CTPS1 CTPS | RRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVWKKCLE |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18124 | Y155 | Sugiyama | RPL7 | IVEPYIAWGYPNLKsVNELIyKRGYGKINKKRIALtDNALI |
| P18615 | S368 | Sugiyama | NELFE RD RDBP | LAVQNsPKGCHRDKRTQIVysDDVyKENLVDGF________ |
| P18615 | Y133 | Sugiyama | NELFE RD RDBP | sIsADDDLQEsSRRPQRKsLyEsFVsssDRLRELGPDGEEA |
| P18615 | Y170 | Sugiyama | NELFE RD RDBP | GEEAEGPGAGDGPPRsFDWGyEERSGAHSsAsPPRsRSRDR |
| P18615 | Y367 | Sugiyama | NELFE RD RDBP | SLAVQNsPKGCHRDKRTQIVysDDVyKENLVDGF_______ |
| P18615 | Y372 | Sugiyama | NELFE RD RDBP | NsPKGCHRDKRTQIVysDDVyKENLVDGF____________ |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18621 | Y4 | Sugiyama | RPL17 | _________________MVRysLDPENPtKsCKSRGSNLRV |
| P18669 | S137 | Sugiyama | PGAM1 PGAMA CDABP0006 | RsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLK |
| P18669 | Y119 | Sugiyama | PGAM1 PGAMA CDABP0006 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| P18669 | Y133 | Sugiyama | PGAM1 PGAMA CDABP0006 | KIWRRsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsC |
| P18669 | Y142 | Sugiyama | PGAM1 PGAMA CDABP0006 | PPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLKDtIAR |
| P18669 | Y26 | Sugiyama | PGAM1 PGAMA CDABP0006 | LVLIRHGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALR |
| P18669 | Y92 | Sugiyama | PGAM1 PGAMA CDABP0006 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| P18754 | Y89 | Sugiyama | RCC1 CHC1 | VVQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSE |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19338 | Y462 | Sugiyama | NCL | AEKTFEEKQGtEIDGRsIsLyytGEKGQNQDYRGGKNSTWs |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21333 | S732 | Sugiyama | FLNA FLN FLN1 | QDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWGGV |
| P21333 | Y1519 | Sugiyama | FLNA FLN FLN1 | VVDNADGTQTVNyVPSREGPysIsVLyGDEEVPRsPFKVKV |
| P21333 | Y1525 | Sugiyama | FLNA FLN FLN1 | GTQTVNyVPSREGPysIsVLyGDEEVPRsPFKVKVLPTHDA |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P22087 | Y118 | Sugiyama | FBL FIB1 FLRN | ICRGKEDALVTKNLVPGEsVyGEKRVsIsEGDDKIEyRAWN |
| P22234 | T18 | Sugiyama | PAICS ADE2 AIRC PAIS | ___MAtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQ |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y451 | Sugiyama | UBA1 A1S9T UBE1 | CLPEDKEVLTEDKCLQRQNRyDGQVAVFGsDLQEKLGKQKY |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22314 | Y873 | Sugiyama | UBA1 A1S9T UBE1 | DDSNFHMDFIVAASNLRAENyDIPsADRHKSKLIAGKIIPA |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22492 | Y75 | Sugiyama | H1-6 H1FT H1T HIST1H1T | SQERVGMSLVALKKALAAAGyDVEKNNSRIKLSLKSLVNKG |
| P22626 | Y331 | Sugiyama | HNRNPA2B1 HNRPA2B1 | SNYGPMKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRs |
| P22626 | Y336 | Sugiyama | HNRNPA2B1 HNRPA2B1 | MKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRsRy___ |
| P22692 | Y197 | Sugiyama | IGFBP4 IBP4 | ELHRALERLAASQSRTHEDLyIIPIPNCDRNGNFHPKQCHP |
| P23193 | Y126 | Sugiyama | TCEA1 GTF2S TFIIS | EsTSsGNVsNRKDETNARDTyVsSFPRAPstsDsVRLKCRE |
| P23246 | Y488 | Sugiyama | SFPQ PSF | PMYQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQV |
| P23246 | Y490 | Sugiyama | SFPQ PSF | YQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQVEK |
| P23284 | Y119 | Sugiyama | PPIB CYPB | DFMIQGGDFtRGDGtGGKsIyGERFPDENFKLKHyGPGWVs |
| P23381 | Y212 | Sugiyama | WARS1 IFI53 WARS WRS | VIQMTDDEKYLWKDLtLDQAysyAVENAKDIIACGFDINKT |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23434 | Y164 | Sugiyama | GCSH | LIKMtLsNPsELDELMsEEAyEKYIKSIEE___________ |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y38 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSK |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23528 | T70 | Sugiyama | CFL1 CFL | EEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAtyE |
| P23528 | Y140 | Sugiyama | CFL1 CFL | SKDAIKKKLtGIKHELQANCyEEVKDRCTLAEKLGGsAVIs |
| P23528 | Y82 | Sugiyama | CFL1 CFL | QtVDDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFI |
| P23528 | Y85 | Sugiyama | CFL1 CFL | DDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWA |
| P23528 | Y89 | Sugiyama | CFL1 CFL | AtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| P23588 | Y593 | Sugiyama | EIF4B | APEPKKPEENPASKFssASKyAALsVDGEDENEGEDyAE__ |
| P23588 | Y609 | Sugiyama | EIF4B | sASKyAALsVDGEDENEGEDyAE__________________ |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24752 | Y90 | Sugiyama | ACAT1 ACAT MAT | IAIQGAIEKAGIPKEEVKEAyMGNVLQGGEGQAPTRQAVLG |
| P24941 | T14 | Sugiyama | CDK2 CDKN2 | _______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKK |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P25205 | Y19 | Sugiyama | MCM3 | __MAGtVVLDDVELREAQRDyLDFLDDEEDQGIyQsKVREL |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y708 | Sugiyama | MCM3 | KRKRRKTRQPDAKDGDsyDPyDFsDtEEEMPQVHtPKTADs |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25685 | Y52 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | HPDKNKEPGAEEKFKEIAEAyDVLSDPRKREIFDRYGEEGL |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26599 | Y127 | Sugiyama | PTBP1 PTB | ANTMVNYYTSVTPVLRGQPIyIQFsNHKELKtDSSPNQARA |
| P26639 | T574 | Sugiyama | TARS1 TARS | RYHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAIL |
| P26885 | Y112 | Sugiyama | FKBP2 FKBP13 | GLLGMCEGEKRKLVIPsELGyGERGAPPKIPGGATLVFEVE |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27348 | Y19 | Sugiyama | YWHAQ | __MEKTELIQKAKLAEQAERyDDMAtCMKAVtEQGAELsNE |
| P27348 | Y48 | Sugiyama | YWHAQ | AVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSIEQK |
| P27695 | Y128 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | LQELPGLSHQYWSAPsDKEGysGVGLLsRQCPLKVsyGIGD |
| P27695 | Y144 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | DKEGysGVGLLsRQCPLKVsyGIGDEEHDQEGRVIVAEFDS |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P28062 | Y184 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | GMGLSMGSMICGWDKKGPGLyyVDEHGTRLSGNMFSTGSGN |
| P28062 | Y185 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | MGLSMGSMICGWDKKGPGLyyVDEHGTRLSGNMFSTGSGNT |
| P28074 | S229 | Sugiyama | PSMB5 LMPX MB1 X | EQAyDLARRAIyQATYRDAysGGAVNLyHVREDGWIRVSsD |
| P29144 | Y1042 | Sugiyama | TPP2 | TEALRDLKIQWMTKLDSsDIyNELKEtyPNyLPLyVARLHQ |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29474 | Y657 | SIGNOR|EPSD|PSP | NOS3 | DSAGALGTLRFCVFGLGSRAyPHFCAFARAVDTRLEELGGE |
| P29692 | S162 | Sugiyama | EEF1D EF1D | AKKPAtPAEDDEDDDIDLFGsDNEEEDKEAAQLREERLRQY |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30041 | Y89 | Sugiyama | PRDX6 AOP2 KIAA0106 | IALSIDSVEDHLAWSKDINAyNCEEPtEKLPFPIIDDRNRE |
| P30043 | T199 | Sugiyama | BLVRB FLR SCAN | HDLGHFMLRCLttDEyDGHstyPsHQyQ_____________ |
| P30043 | Y205 | Sugiyama | BLVRB FLR SCAN | MLRCLttDEyDGHstyPsHQyQ___________________ |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| P30086 | Y120 | Sugiyama | PEBP1 PBP PEBP | GtVLsDyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsN |
| P30086 | Y125 | Sugiyama | PEBP1 PBP PEBP | DyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsNRsGDH |
| P30086 | Y169 | Sugiyama | PEBP1 PBP PEBP | FKVAsFRKKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK__ |
| P30086 | Y176 | Sugiyama | PEBP1 PBP PEBP | KKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK_________ |
| P30086 | Y64 | Sugiyama | PEBP1 PBP PEBP | tQVKNRPtsIsWDGLDsGKLytLVLtDPDAPsRKDPKYREW |
| P30101 | Y100 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAyDGPRt |
| P30101 | Y115 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | yGVsGyPtLKIFRDGEEAGAyDGPRtADGIVsHLKKQAGPA |
| P30101 | Y264 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | CPHMTEDNKDLIQGKDLLIAyyDVDyEKNAKGSNYWRNRVM |
| P30101 | Y265 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | PHMTEDNKDLIQGKDLLIAyyDVDyEKNAKGSNYWRNRVMM |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30101 | Y95 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KGIVPLAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAy |
| P31153 | Y235 | Sugiyama | MAT2A AMS2 MATA2 | LDEMRDALKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGP |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31689 | Y52 | Sugiyama | DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4 | KYHPDKNPNEGEKFKQISQAyEVLSDAKKRELYDKGGEQAI |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31946 | Y50 | Sugiyama | YWHAB | AVtEQGHELsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P31947 | Y151 | Sugiyama | SFN HME1 | LAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIRLG |
| P31947 | Y19 | Sugiyama | SFN HME1 | __MERASLIQKAKLAEQAERyEDMAAFMKGAVEKGEELsCE |
| P31947 | Y48 | Sugiyama | SFN HME1 | GAVEKGEELsCEERNLLsVAyKNVVGGQRAAWRVLSsIEQK |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33176 | Y516 | Sugiyama | KIF5B KNS KNS1 | EELAVNyDQKSQEVEDKTKEyELLSDELNQKsATLAsIDAE |
| P33176 | Y62 | Sugiyama | KIF5B KNS KNS1 | ASKPYAFDRVFQSsTsQEQVyNDCAKKIVKDVLEGyNGtIF |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33316 | Y227 | Sugiyama | DUT | EKFEVKKGDRIAQLICERIFyPEIEEVQALDDtERGsGGFG |
| P33778 | Y38 | Sugiyama | H2BC3 H2BFF HIST1H2BB | AITKAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSK |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P34931 | Y43 | Sugiyama | HSPA1L | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P34931 | Y547 | Sugiyama | HSPA1L | YKAEDEVQREKIAAKNALEsyAFNMKSVVSDEGLKGKISES |
| P34932 | S31 | Sugiyama | HSPA4 APG2 HSPH2 | QSCYVAVARAGGIETIANEysDRCtPACIsFGPKNRSIGAA |
| P34932 | Y336 | Sugiyama | HSPA4 APG2 HSPH2 | RVEPPLRSVLEQTKLKKEDIyAVEIVGGATRIPAVKEKISK |
| P34932 | Y597 | Sugiyama | HSPA4 APG2 HSPH2 | VDLPIENQLLWQIDREMLNLyIENEGKMIMQDKLEKERNDA |
| P34932 | Y624 | Sugiyama | HSPA4 APG2 HSPH2 | MIMQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDD |
| P34932 | Y626 | Sugiyama | HSPA4 APG2 HSPH2 | MQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDDRN |
| P34932 | Y660 | Sugiyama | HSPA4 APG2 HSPH2 | VSEDDRNsFtLKLEDTENWLyEDGEDQPKQVYVDKLAELKN |
| P35268 | Y114 | Sugiyama | RPL22 | NNLRDWLRVVANSKESYELRyFQINQDEEEEEDED______ |
| P35269 | Y57 | Sugiyama | GTF2F1 RAP74 | VNFAtWNQARLERDLSNKKIyQEEEMPEsGAGSEFNRKLRE |
| P35556 | Y200 | Sugiyama | FBN2 | CENGCQNGGRCIGPNRCACVyGFTGPQCERDYRTGPCFTQV |
| P35609 | Y385 | Sugiyama | ACTN2 | GKMVSDIAGAWQRLEQAEKGyEEWLLNEIRRLERLEHLAEK |
| P36578 | Y211 | Sugiyama | RPL4 RPL1 | AGKGKMRNRRRIQRRGPCIIyNEDNGIIKAFRNIPGITLLN |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P36915 | Y599 | Sugiyama | GNL1 HSR1 | EGDEEtPTSAPGSSLAGRNPyALLGEDEC____________ |
| P37108 | Y27 | Sugiyama | SRP14 | EQFLtELTRLFQKCRTSGsVyItLKKYDGRTKPIPKKGtVE |
| P37802 | T190 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | GKNVIGLQMGtNRGAsQAGMtGyGMPRQIL___________ |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P37837 | Y206 | Sugiyama | TALDO1 TAL TALDO TALDOR | ISPFVGRILDWHVANTDKKSyEPLEDPGVKSVTKIYNYYKK |
| P37840 | Y125 | SIGNOR|iPTMNet|EPSD|PSP | SNCA NACP PARK1 | EGAPQEGILEDMPVDPDNEAyEMPsEEGyQDyEPEA_____ |
| P38646 | Y196 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | EtAENyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNV |
| P38919 | Y54 | Sugiyama | EIF4A3 DDX48 KIAA0111 | VDVTPTFDTMGLREDLLRGIyAyGFEKPsAIQQRAIKQIIK |
| P38919 | Y56 | Sugiyama | EIF4A3 DDX48 KIAA0111 | VTPTFDTMGLREDLLRGIyAyGFEKPsAIQQRAIKQIIKGR |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40429 | Y149 | Sugiyama | RPL13A | LKPTRKFAYLGRLAHEVGWKyQAVtAtLEEKRKEKAKIHYR |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40939 | Y637 | Sugiyama | HADHA HADH | ELLTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILA |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P42224 | Y666 | Sugiyama | STAT1 | DIIRNYKVMAAENIPENPLKyLyPNIDKDHAFGKYYSRPKE |
| P42224 | Y668 | Sugiyama | STAT1 | IRNYKVMAAENIPENPLKyLyPNIDKDHAFGKYYSRPKEAP |
| P43034 | Y28 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | RDELNRAIADyLRSNGyEEAySVFKKEAELDVNEELDKKYA |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43490 | Y34 | Sugiyama | NAMPT PBEF PBEF1 | ATDSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKY |
| P43490 | Y36 | Sugiyama | NAMPT PBEF PBEF1 | DSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKYEE |
| P43490 | Y471 | Sugiyama | NAMPT PBEF PBEF1 | EEYGQDLLHTVFKNGKVTKsysFDEIRKNAQLNIELEAAHH |
| P46777 | Y226 | Sugiyama | RPL5 MSTP030 | DyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEMyKKAHAA |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46937 | Y407 | Sugiyama | YAP1 YAP65 | NsGtyHsRDEstDsGLsMssysVPRtPDDFLNsVDEMDTGD |
| P46940 | Y1478 | Sugiyama | IQGAP1 KIAA0051 | KIQTGLKKLTELGtVDPKNKyQELINDIARDIRNQRRYRQR |
| P46940 | Y41 | Sugiyama | IQGAP1 KIAA0051 | LDNERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGED |
| P47756 | Y232 | Sugiyama | CAPZB | NIGRLVEDMENKIRstLNEIyFGKTKDIVNGLRSVQTFADK |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48147 | Y28 | Sugiyama | PREP PEP | DVYRDETAVQDYHGHKICDPyAWLEDPDSEQTKAFVEAQNK |
| P48741 | Y43 | Sugiyama | HSPA7 HSP70B | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P49023 | Y118 | Sugiyama | PXN | sNPQDsVGsPCsRVGEEEHVysFPNKQKsAEPsPtVMstsL |
| P49023 | Y468 | Sugiyama | PXN | AFFGPEGFHEKDGKAYCRKDyFDMFAPKCGGCARAILENYI |
| P49023 | Y88 | Sugiyama | PXN | QWQPSSSRFIHQQPQsssPVyGssAKtssVsNPQDsVGsPC |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | Y2034 | Sugiyama | FASN FAS | DYFVVFSSVSCGRGNAGQsNyGFANsAMERICEKRRHEGLP |
| P49327 | Y2454 | Sugiyama | FASN FAS | tPKAKyHGNVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsV |
| P49327 | Y2462 | Sugiyama | FASN FAS | NVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsVHVIEGDHR |
| P49327 | Y277 | Sugiyama | FASN FAS | KEQGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGT |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y690 | Sugiyama | AARS1 AARS | DCPLAAAKAIQGLRAVFDEtyPDPVRVVSIGVPVSELLDDP |
| P49736 | Y137 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | MRQRDREAGRGLGRMRRGLLyDsDEEDEERPARKRRQVERA |
| P49736 | Y234 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | VFKERIsDMCKENREsLVVNyEDLAAREHVLAYFLPEAPAE |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50402 | Y95 | Sugiyama | EMD EDMD STA | DLPKKEDALLyQsKGyNDDyyEEsyFTTRTyGEPEsAGPSR |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50990 | Y426 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | KRLVPGGGAtEIELAKQItsyGETCPGLEQyAIKKFAEAFE |
| P50990 | Y436 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | EIELAKQItsyGETCPGLEQyAIKKFAEAFEAIPRALAENS |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50995 | Y365 | Sugiyama | ANXA11 ANX11 | NRDESTNVDMSLAQRDAQELyAAGENRLGTDESKFNAVLCS |
| P50995 | Y482 | Sugiyama | ANXA11 ANX11 | sEtDLLDIRSEYKRMYGKsLyHDISGDtsGDyRKILLKICG |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | Y266 | Sugiyama | HNRNPF HNRPF | ySGLSDGYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQsT |
| P52756 | Y712 | Sugiyama | RBM5 H37 LUCA15 | LELREREMKYRDRAAERREKyGIPEPPEPKRKKQFDAGTVN |
| P53621 | Y391 | Sugiyama | COPA | NPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGK |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P53675 | Y921 | Sugiyama | CLTCL1 CLH22 CLTCL CLTD | DSSVVGRYCEKRDPHLACVAyERGQCDLELIKVCNENSLFK |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54652 | Y42 | Sugiyama | HSPA2 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55884 | Y222 | Sugiyama | EIF3B EIF3S9 | KLKNVIHKIFSKFGKITNDFyPEEDGKTKGyIFLEyAsPAH |
| P56945 | Y234 | Sugiyama | BCAR1 CAS CASS1 CRKAS | VPtRVGQGyVyEAAQPEQDEyDIPRHLLAPGPQDIyDVPPV |
| P57053 | Y38 | Sugiyama | H2BC12L H2BFS H2BS1 | AVTKAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y38 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | S212 | Sugiyama | TPI1 TPI | WLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDGFLV |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60660 | S30 | Sugiyama | MYL6 | AEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVLK |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | S239 | Sugiyama | ACTB | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P60709 | T303 | Sugiyama | ACTB | MKCDVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPs |
| P60709 | Y198 | Sugiyama | ACTB | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P60709 | Y240 | Sugiyama | ACTB | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P60709 | Y294 | Sugiyama | ACTB | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P60709 | Y306 | Sugiyama | ACTB | DVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPstMK |
| P60709 | Y362 | Sugiyama | ACTB | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P60842 | Y197 | Sugiyama | EIF4A1 DDX2A EIF4A | KMFVLDEADEMLsRGFKDQIyDIFQKLNsNtQVVLLSATMP |
| P60842 | Y48 | Sugiyama | EIF4A1 DDX2A EIF4A | NEIVDSFDDMNLSESLLRGIyAyGFEKPsAIQQRAILPCIK |
| P60842 | Y50 | Sugiyama | EIF4A1 DDX2A EIF4A | IVDSFDDMNLSESLLRGIyAyGFEKPsAIQQRAILPCIKGy |
| P60842 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60981 | Y82 | Sugiyama | DSTN ACTDP DSN | VTITDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFF |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61024 | Y8 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | _____________MSHKQIyysDKyDDEEFEyRHVMLPKDI |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61158 | Y231 | Sugiyama | ACTR3 ARP3 | REVGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSK |
| P61158 | Y233 | Sugiyama | ACTR3 ARP3 | VGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSKWI |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61247 | Y31 | Sugiyama | RPS3A FTE1 MFTL | KGGKKGAKKKVVDPFSKKDWyDVKAPAMFNIRNIGKTLVTR |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| P61353 | Y75 | Sugiyama | RPL27 | AAMGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtV |
| P61353 | Y77 | Sugiyama | RPL27 | MGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVN |
| P61353 | Y85 | Sugiyama | RPL27 | RSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVNKDVFRDPA |
| P61604 | T79 | Sugiyama | HSPE1 | EIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDILGK |
| P61604 | Y100 | Sugiyama | HSPE1 | KVVLDDKDyFLFRDGDILGKyVD__________________ |
| P61604 | Y76 | Sugiyama | HSPE1 | KGGEIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDI |
| P61604 | Y88 | Sugiyama | HSPE1 | GDKVLLPEyGGtKVVLDDKDyFLFRDGDILGKyVD______ |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62140 | Y304 | Sugiyama | PPP1CB | VDETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPP |
| P62140 | Y306 | Sugiyama | PPP1CB | ETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPPKK |
| P62191 | Y439 | Sugiyama | PSMC1 | FKKSKENVLyKKQEGtPEGLyL___________________ |
| P62241 | Y113 | Sugiyama | RPS8 OK/SW-cl.83 | TKTLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEE |
| P62241 | Y117 | Sugiyama | RPS8 OK/SW-cl.83 | VKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEEIL |
| P62249 | Y115 | Sugiyama | RPS16 | YYQKYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGP |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y49 | Sugiyama | YWHAE | KVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssIEQK |
| P62269 | S96 | Sugiyama | RPS18 D6S218E | QYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLKK |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62633 | S121 | Sugiyama | CNBP RNF163 ZNF9 | CGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRCG |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62736 | S241 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y117 | Sugiyama | RPL23A | VFIVDVKANKHQIKQAVKKLyDIDVAKVNtLIRPDGEKKAY |
| P62750 | Y144 | Sugiyama | RPL23A | VNtLIRPDGEKKAYVRLAPDyDALDVANKIGII________ |
| P62750 | Y74 | Sugiyama | RPL23A | LRRQPKYPRKSAPRRNKLDHyAIIKFPLTTEsAMKKIEDNN |
| P62805 | Y52 | Sugiyama | H4C1 H4/A H4FA HIST1H4A; H4C2 H4/I H4FI HIST1H4B; H4C3 H4/G H4FG HIST1H4C; H4C4 H4/B H4FB HIST1H4D; H4C5 H4/J H4FJ HIST1H4E; H4C6 H4/C H4FC HIST1H4F; H4C8 H4/H H4FH HIST1H4H; H4C9 H4/M H4FM HIST1H4I; H4C11 H4/E H4FE HIST1H4J; H4C12 H4/D H4FD HIST1H4K; H4C13 H4/K H4FK HIST1H4L; H4C14 H4/N H4F2 H4FN HIST2H4 HIST2H4A; H4C15 H4/O H4FO HIST2H4B; H4C16 H4-16 HIST4H4 | KPAIRRLARRGGVKRIsGLIyEETRGVLKVFLENVIRDAVt |
| P62807 | Y38 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | AVTKAQKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssK |
| P62807 | Y41 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | KAQKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P62807 | Y43 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | QKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P62826 | Y146 | Sugiyama | RAN ARA24 OK/SW-cl.81 | IKDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLAR |
| P62826 | Y147 | Sugiyama | RAN ARA24 OK/SW-cl.81 | KDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLARK |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62979 | T147 | Sugiyama | RPS27A UBA80 UBCEP1 | GAGVFMAsHFDRHyCGKCCLtyCFNKPEDK___________ |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63173 | T44 | Sugiyama | RPL38 | KIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLPPGL |
| P63173 | Y41 | Sugiyama | RPL38 | KSVKIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLP |
| P63173 | Y43 | Sugiyama | RPL38 | VKIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLPPG |
| P63220 | T52 | Sugiyama | RPS21 | IQMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRL |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | S239 | Sugiyama | ACTG1 ACTG | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P63261 | T303 | Sugiyama | ACTG1 ACTG | MKCDVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPs |
| P63261 | Y198 | Sugiyama | ACTG1 ACTG | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P63261 | Y240 | Sugiyama | ACTG1 ACTG | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P63261 | Y294 | Sugiyama | ACTG1 ACTG | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P63261 | Y306 | Sugiyama | ACTG1 ACTG | DVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPstMK |
| P63261 | Y362 | Sugiyama | ACTG1 ACTG | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P63267 | S240 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67809 | S209 | Sugiyama | YBX1 NSEP1 YB1 | RRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGEQ |
| P67809 | Y196 | Sugiyama | YBX1 NSEP1 YB1 | sAPEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGE |
| P67809 | Y208 | Sugiyama | YBX1 NSEP1 YB1 | yRRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGE |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | S241 | Sugiyama | ACTC1 ACTC | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | S241 | Sugiyama | ACTA1 ACTA | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68363 | S439 | Sugiyama | TUBA1B | SEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy________ |
| P68363 | Y312 | Sugiyama | TUBA1B | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68366 | Y312 | Sugiyama | TUBA4A TUBA1 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P78316 | Y119 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | EKMMKRFALEQQRHHEKKSIyNLNEDEELTHyGQsLADIEK |
| P78316 | Y130 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | QRHHEKKSIyNLNEDEELTHyGQsLADIEKHNDIVDsDsDA |
| P78318 | Y277 | Sugiyama | IGBP1 IBP1 | AGYPSLPTMTVSDWYEQHRKyGALPDQGIAKAAPEEFRKAA |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| P98175 | Y694 | Sugiyama | RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122 | QPISSLRDDERREsAtADAGyAILEKKGALAERQHTsMDLP |
| P98175 | Y825 | Sugiyama | RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122 | EKNDMEQMKYRDRAAERREKyGIPEPPEPKRRKYGGIstAs |
| Q00059 | Y165 | Sugiyama | TFAM TCF6 TCF6L2 | KKKELTLLGKPKRPRsAYNVyVAERFQEAKGDsPQEKLKTV |
| Q00169 | Y140 | Sugiyama | PITPNA PITPN | GTQENVHKLEPEAWKHVEAVyIDIADRSQVLSKDYKAEEDP |
| Q00341 | Y358 | Sugiyama | HDLBP HBP VGL | SETVILRGEPEKLGQALTEVyAKANsFTVSSVAAPSWLHRF |
| Q00526 | T14 | Sugiyama | CDK3 CDKN3 | _______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKK |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00610 | Y921 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | DsRVVGKYCEKRDPHLACVAyERGQCDLELINVCNENSLFK |
| Q00839 | Y257 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | QKGGDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVE |
| Q00839 | Y260 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | GDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVEEED |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01844 | Y278 | Sugiyama | EWSR1 EWS | SSSYGQQSsFRQDHPssMGVyGQESGGFSGPGENRSMSGPD |
| Q01844 | Y417 | Sugiyama | EWSR1 EWS | MIHIYLDKETGKPKGDATVSyEDPPtAKAAVEWFDGKDFQG |
| Q02535 | S18 | PSP | ID3 1R21 BHLHB25 HEIR1 | ___MKALsPVRGCyEAVCCLsERSLAIARGRGKGPAAEEPL |
| Q02535 | S5 | PSP | ID3 1R21 BHLHB25 HEIR1 | ________________MKALsPVRGCyEAVCCLsERSLAIA |
| Q02535 | Y11 | PSP | ID3 1R21 BHLHB25 HEIR1 | __________MKALsPVRGCyEAVCCLsERSLAIARGRGKG |
| Q02535 | Y48 | PSP | ID3 1R21 BHLHB25 HEIR1 | RGKGPAAEEPLSLLDDMNHCySRLRELVPGVPRGTQLsQVE |
| Q02539 | Y74 | Sugiyama | H1-1 H1F1 HIST1H1A | SKERGGVSLAALKKALAAAGyDVEKNNSRIKLGIKsLVsKG |
| Q02878 | Y115 | Sugiyama | RPL6 TXREB1 | PVGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQ |
| Q04206 | Y100 | Sugiyama | RELA NFKB3 | DPPHRPHPHELVGKDCRDGFyEAELCPDRCIHSFQNLGIQC |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04721 | Y129 | Sugiyama | NOTCH2 | CFVSRPCLNGGTCHMLSRDtyECtCQVGFTGKECQWTDACL |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05397 | Y407 | SIGNOR|iPTMNet|EPSD|PSP | PTK2 FAK FAK1 | HAVsVsEtDDyAEIIDEEDtytMPSTRDYEIQRERIELGRC |
| Q05397 | Y925 | Sugiyama | PTK2 FAK FAK1 | QPQEIsPPPtANLDRSNDKVyENVTGLVKAVIEMSSKIQPA |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q07955 | Y189 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | TYAVRKLDNTKFRsHEGEtAyIRVKVDGPRsPsyGRsRsRs |
| Q07960 | Y64 | Sugiyama | ARHGAP1 CDC42GAP RHOGAP1 | sDDsKsssPELVtHLKWDDPyyDIARHQIVEVAGDDKYGRK |
| Q07960 | Y65 | Sugiyama | ARHGAP1 CDC42GAP RHOGAP1 | DDsKsssPELVtHLKWDDPyyDIARHQIVEVAGDDKYGRKI |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08J23 | Y51 | Sugiyama | NSUN2 SAKI TRM4 | EAGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALR |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q12931 | Y498 | Sugiyama | TRAP1 HSP75 HSPC5 | GQLtsLsEyASRMRAGtRNIyyLCAPNRHLAEHsPyyEAMK |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q13017 | Y1109 | Sugiyama | ARHGAP5 RHOGAP5 | DNyAEPIDTIFKQKGYsDEIyVVPDDsQNRIKIRNsFVNNt |
| Q13069 | Y9 | Sugiyama | GAGE5 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13070 | Y9 | Sugiyama | GAGE6 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13162 | Y188 | Sugiyama | PRDX4 | GLGPIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDK |
| Q13162 | Y191 | Sugiyama | PRDX4 | PIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDKGIL |
| Q13200 | Y110 | Sugiyama | PSMD2 TRAP2 | TSVPKPLKFLRPHyGKLKEIyENMAPGENKRFAADIISVLA |
| Q13228 | Y28 | Sugiyama | SELENBP1 SBP | CGPGySTPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVD |
| Q13228 | Y33 | Sugiyama | SELENBP1 SBP | STPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVDVDPKs |
| Q13242 | Y17 | Sugiyama | SRSF9 SFRS9 SRP30C | ____MsGWADERGGEGDGRIyVGNLPTDVREKDLEDLFyKY |
| Q13242 | Y70 | Sugiyama | SRSF9 SFRS9 SRP30C | GLVPFAFVRFEDPRDAEDAIyGRNGyDYGQCRLRVEFPRTY |
| Q13263 | Y133 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TVVDCPVCKQQCFSKDIVENyFMRDsGsKAATDAQDANQCC |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13283 | T21 | Sugiyama | G3BP1 G3BP | MVMEKPsPLLVGREFVRQyytLLNQAPDMLHRFYGKNssyV |
| Q13283 | Y20 | Sugiyama | G3BP1 G3BP | _MVMEKPsPLLVGREFVRQyytLLNQAPDMLHRFYGKNssy |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13310 | Y291 | Sugiyama | PABPC4 APP1 PABP4 | ERQAELKRKFEQLKQERISRyQGVNLyIKNLDDTIDDEKLR |
| Q13310 | Y297 | Sugiyama | PABPC4 APP1 PABP4 | KRKFEQLKQERISRyQGVNLyIKNLDDTIDDEKLRKEFsPF |
| Q13404 | Y145 | Sugiyama | UBE2V1 CROC1 UBE2V UEV1 P/OKcl.19 | RRLMMSKENMKLPQPPEGQCysN__________________ |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13442 | S19 | Sugiyama | PDAP1 HASPP28 | __MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEEE |
| Q13442 | T18 | Sugiyama | PDAP1 HASPP28 | ___MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEE |
| Q13442 | Y17 | Sugiyama | PDAP1 HASPP28 | ____MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREE |
| Q13561 | Y207 | Sugiyama | DCTN2 DCTN50 | SKGGSGGKttGtPPDssLVtyELHsRPEQDKFSQAAKVAEL |
| Q13561 | Y313 | Sugiyama | DCTN2 DCTN50 | IAKHKASVEDADTQSKVHQLyEtIQRWsPIASTLPELVQRL |
| Q13561 | Y6 | Sugiyama | DCTN2 DCTN50 | _______________MADPKyADLPGIARNEPDVYETSDLP |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13573 | Y260 | Sugiyama | SNW1 SKIIP SKIP | KEQQEWKIPPCISNWKNAKGytIPLDKRLAADGRGLQTVHI |
| Q13573 | Y459 | Sugiyama | SNW1 SKIIP SKIP | GGKDMAQsIyRPSKNLDKDMyGDDLEARIKTNRFVPDKEFS |
| Q13586 | Y361 | PSP | STIM1 GOK | WYAPEALQKWLQLTHEVEVQyYNIKKQNAEKQLLVAKEGAE |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q14004 | Y399 | Sugiyama | CDK13 CDC2L CDC2L5 CHED KIAA1791 | GGDVsPsPyssSsWRRsRsPysPVLRRSGKSRSRSPYSSRH |
| Q14157 | Y858 | Sugiyama | UBAP2L KIAA0144 NICE4 | PFPtPttPLtGRDGsLAsNPysGDLtKFGRGDASSPAPATT |
| Q14192 | Y93 | Sugiyama | FHL2 DRAL SLIM3 | NsLVDKPFAAKEDQLLCTDCySNEySSKCQECKKTIMPGTR |
| Q14240 | Y49 | Sugiyama | EIF4A2 DDX2B EIF4F | NEIVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIK |
| Q14240 | Y51 | Sugiyama | EIF4A2 DDX2B EIF4F | IVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIKGy |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | Y334 | Sugiyama | CTTN EMS1 | KDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRANF |
| Q14247 | Y421 | EPSD|PSP|Sugiyama | CTTN EMS1 | tPPVsPAPQPtEERLPssPVyEDAAsFKAELsyRGPVsGtE |
| Q14247 | Y446 | Sugiyama | CTTN EMS1 | sFKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYAT |
| Q14247 | Y470 | EPSD|PSP | CTTN EMS1 | AADyREASSQQGLAYATEAVyESAEAPGHYPAEDSTyDEYE |
| Q14247 | Y486 | EPSD|PSP | CTTN EMS1 | TEAVyESAEAPGHYPAEDSTyDEYENDLGITAVALYDYQAA |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14257 | Y39 | Sugiyama | RCN2 ERC55 | AAGAGKAEELHyPLGERRsDyDREALLGVQEDVDEyVKLGH |
| Q14257 | Y54 | Sugiyama | RCN2 ERC55 | ERRsDyDREALLGVQEDVDEyVKLGHEEQQKRLQAIIKKID |
| Q14289 | S361 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | AENMADLIDGyCRLQGEHQGsLIIHPRKDGEKRNsLPQIPM |
| Q14289 | S375 | iPTMNet|EPSD | PTK2B FAK2 PYK2 RAFTK | QGEHQGsLIIHPRKDGEKRNsLPQIPMLNLEARRsHLsEsC |
| Q14289 | S399 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | IPMLNLEARRsHLsEsCsIEsDIyAEIPDETLRRPGGPQyG |
| Q14289 | S778 | iPTMNet|EPSD | PTK2B FAK2 PYK2 RAFTK | sPVNsLHtPPLHRHNVFKRHsMREEDFIQPSSREEAQQLWE |
| Q14289 | S839 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | yQWLRQEEKSLDPMVyMNDKsPLtPEKEVGyLEFtGPPQKP |
| Q14289 | S866 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | EVGyLEFtGPPQKPPRLGAQsIQPTANLDRTDDLVyLNVME |
| Q14289 | S967 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | NKDLAELINKMRLAQQNAVTsLSEECKRQMLTASHTLAVDA |
| Q14289 | T149 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | YDLQIRYLPEDFMESLKEDRtTLLyFyQQLRNDYMQRYASK |
| Q14289 | T728 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | TAFQEPPPKPSRPKyRPPPQtNLLAPKLQFQVPEGLCAssP |
| Q14289 | T842 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | LRQEEKSLDPMVyMNDKsPLtPEKEVGyLEFtGPPQKPPRL |
| Q14289 | T853 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | VyMNDKsPLtPEKEVGyLEFtGPPQKPPRLGAQsIQPTANL |
| Q14289 | Y153 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | IRYLPEDFMESLKEDRtTLLyFyQQLRNDYMQRYASKVSEG |
| Q14289 | Y155 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | YLPEDFMESLKEDRtTLLyFyQQLRNDYMQRYASKVSEGMA |
| Q14289 | Y351 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | LSIKTSSLAEAENMADLIDGyCRLQGEHQGsLIIHPRKDGE |
| Q14289 | Y402 | SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | PTK2B FAK2 PYK2 RAFTK | LNLEARRsHLsEsCsIEsDIyAEIPDETLRRPGGPQyGIAR |
| Q14289 | Y418 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | EsDIyAEIPDETLRRPGGPQyGIAREDVVLNRILGEGFFGE |
| Q14289 | Y46 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | MVVVPVDVEKEDVRILKVCFySNSFNPGKNFKLVKCTVQTE |
| Q14289 | Y579 | iPTMNet|EPSD|Sugiyama | PTK2B FAK2 PYK2 RAFTK | SPECVKLGDFGLsRYIEDEDyyKASVTRLPIKWMSPESINF |
| Q14289 | Y580 | iPTMNet|EPSD|Sugiyama | PTK2B FAK2 PYK2 RAFTK | PECVKLGDFGLsRYIEDEDyyKASVTRLPIKWMSPESINFR |
| Q14289 | Y722 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | PKILEPTAFQEPPPKPSRPKyRPPPQtNLLAPKLQFQVPEG |
| Q14289 | Y819 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | AEKVKMRQILDKQQKQMVEDyQWLRQEEKSLDPMVyMNDKs |
| Q14289 | Y834 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | QMVEDyQWLRQEEKSLDPMVyMNDKsPLtPEKEVGyLEFtG |
| Q14289 | Y849 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | LDPMVyMNDKsPLtPEKEVGyLEFtGPPQKPPRLGAQsIQP |
| Q14289 | Y881 | iPTMNet|EPSD | PTK2B FAK2 PYK2 RAFTK | RLGAQsIQPTANLDRTDDLVyLNVMELVRAVLELKNELCQL |
| Q14289 | Y90 | Sugiyama | PTK2B FAK2 PYK2 RAFTK | IITSILLSGRIGPNIRLAECyGLRLKHMKSDEIHWLHPQMT |
| Q14568 | Y160 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGERM |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14697 | Y489 | Sugiyama | GANAB G2AN KIAA0088 | PHIKVDSGyRVHEELRNLGLyVKtRDGSDyEGWCWPGSAGY |
| Q14966 | Y217 | Sugiyama | ZNF638 NP220 ZFML | ETLGSEAVSSNVIDYGHASKyGYTEDPLEVRIYDPEIPTDE |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15149 | Y3362 | Sugiyama | PLEC PLEC1 | TGLsLLPLSEKAARARQEELySELQAREtFEKTPVEVPVGG |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15293 | Y148 | Sugiyama | RCN1 RCN | DRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKML |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15417 | Y261 | Sugiyama | CNN3 | STISLQMGTNKVAsQKGMsVyGLGRQVYDPKYCAAPTEPVI |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15459 | S451 | Sugiyama | SF3A1 SAP114 | IGLLDPRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAE |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15631 | Y210 | Sugiyama | TSN | sLRKRYDGLKYDVKKVEEVVyDLSIRGFNKETAAACVEK__ |
| Q16595 | Y95 | Sugiyama | FXN FRDA X25 | LMNLRKsGtLGHPGsLDEttyERLAEETLDSLAEFFEDLAD |
| Q16658 | Y493 | Sugiyama | FSCN1 FAN1 HSN SNL | DHAGVLKASAEtVDPAsLWEy____________________ |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16719 | Y86 | Sugiyama | KYNU | ENAIYFLGNSLGLQPKMVKtyLEEELDKWAKIAAYGHEVGK |
| Q16762 | Y165 | Sugiyama | TST | PSRPEPAVFKATLDRSLLKTyEQVLENLESKRFQLVDSRSQ |
| Q16778 | Y38 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssK |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16881 | Y277 | Sugiyama | TXNRD1 GRIM12 KDRF | NHIGSLNWGYRVALREKKVVyENAyGQFIGPHRIKATNNKG |
| Q16881 | Y281 | Sugiyama | TXNRD1 GRIM12 KDRF | SLNWGYRVALREKKVVyENAyGQFIGPHRIKATNNKGKEKI |
| Q4VXU2 | Y291 | Sugiyama | PABPC1L C20orf119 | ERQNELKRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLR |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q562R1 | S240 | Sugiyama | ACTBL2 | VALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPE |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q56P03 | Y106 | Sugiyama | EAPP C14orf11 BM-036 | GsssGNGKVATAPTRyYDDIyFDsDsEDEDRAVQVtKKKKK |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | Y198 | Sugiyama | HSP90AB2P HSP90BB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKTKPIWTRNTEDI |
| Q58FF8 | Y260 | Sugiyama | HSP90AB2P HSP90BB | VRYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVW |
| Q58FF8 | Y261 | Sugiyama | HSP90AB2P HSP90BB | RYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVWK |
| Q58FF8 | Y56 | Sugiyama | HSP90AB2P HSP90BB | KEIFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FG0 | Y177 | Sugiyama | HSP90AA5P HSP90AE | GQLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQ |
| Q58FG0 | Y178 | Sugiyama | HSP90AA5P HSP90AE | QLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQK |
| Q5JTH9 | Y1251 | Sugiyama | RRP12 KIAA0690 | AEYKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQG |
| Q5JTH9 | Y1253 | Sugiyama | RRP12 KIAA0690 | YKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQGQF |
| Q5QNW6 | Y38 | Sugiyama | H2BC18 HIST2H2BF | AVTKVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VUA4 | Y1569 | Sugiyama | ZNF318 HRIHFB2436 | QAKKLEKRNsCLATANAKDLyDIFySSGGKGAPETKGAPET |
| Q6DN03 | Y38 | Sugiyama | H2BC20P HIST2H2BC | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCK |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y38 | Sugiyama | H2BC19P HIST2H2BD | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCK |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6NW29 | Y18 | Sugiyama | RWDD4 FAM28A RWDD4A | ___MsANEDQEMELEALRSIyEGDEsFRELsPVSFQyRIGE |
| Q6S8J3 | S939 | Sugiyama | POTEE A26C1A POTE2 | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6UVK1 | Y1511 | Sugiyama | CSPG4 MCSP | PIPAEALRSTDGDSGSEDLVyTIEQPSNGRVVLRGAPGTEV |
| Q71U36 | S439 | Sugiyama | TUBA1A TUBA3 | SEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy________ |
| Q71U36 | Y312 | Sugiyama | TUBA1A TUBA3 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q7KZF4 | Y109 | Sugiyama | SND1 TDRD11 | KLIGKEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVA |
| Q7KZF4 | Y113 | Sugiyama | SND1 TDRD11 | KEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVAEGLA |
| Q7KZF4 | Y476 | Sugiyama | SND1 TDRD11 | SKGLATVIRYRQDDDQRssHyDELLAAEARAIKNGKGLHSK |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86UK7 | Y306 | Sugiyama | ZNF598 | QFSYAPRHSRRNEGVVGGEDyEEVDRysRQGRVARAGTRGA |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86VM9 | T393 | Sugiyama | ZC3H18 NHN1 | DYEIERFWRGGQyENFRVQYtEtEPyHNYRERERERERENR |
| Q86X29 | Y535 | Sugiyama | LSR ILDR3 LISCH | sNGGRSRAYMPPRsRsRDDLyDQDDsRDFPRSRDPHyDDFR |
| Q86XP3 | Y573 | Sugiyama | DDX42 | VATDVAARGLDIPSIKTVINyDVARDIDTHTHRIGRTGRAG |
| Q8IWX8 | Y903 | Sugiyama | CHERP DAN26 SCAF6 | YKGVGVALDDPyENyRRNKsysFIARMKARDECK_______ |
| Q8IZ21 | Y647 | Sugiyama | PHACTR4 PRO2963 | LsQRPtVAELLARKILRFNEyVEVTDAQDYDRRADKPWTKL |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y133 | Sugiyama | PGAM4 PGAM3 | KIWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSY |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N257 | Y38 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | AVTKAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssK |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N6H7 | Y278 | Sugiyama | ARFGAP2 ZNF289 Nbla10535 | QAADAKKQAEESMVASMRLAyQELQIDRKKEEKKLQNLEGK |
| Q8NBP7 | Y521 | Sugiyama | PCSK9 NARC1 PSEC0052 | EAQGGKLVCRAHNAFGGEGVyAIARCCLLPQANCSVHTAPP |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TD19 | Y845 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PDsPsPLsAAFsEsEKDTLPyEELQGLKVAsEAPLEHKPQV |
| Q8WU90 | Y137 | Sugiyama | ZC3H15 DFRP1 LEREPO4 HSPC303 HT010 MSTP012 PP730 | DKCKFSHDLTLERKCEKRsVyIDARDEELEKDTMDNWDEKK |
| Q8WUA2 | Y363 | Sugiyama | PPIL4 | QDKPPNLVLKDKVKPKQDtKyDLILDEQAEDsKSSHSHTSK |
| Q8WWF6 | Y53 | Sugiyama | DNAJB3 HCG3 | DKNPENKEEAERRFKQVAEAyEVLSDAKKRDIYDRYGEAGA |
| Q8WWM7 | S276 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | MFKFNEENyGVKTtyDssLssytVPLEKDNsEEFRQRELRA |
| Q8WWM7 | Y270 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | GWDPNEMFKFNEENyGVKTtyDssLssytVPLEKDNsEEFR |
| Q8WWM7 | Y349 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | AVQRQGsGREsPsLASREGKyIPLPQRVREGPRGGVRCSSS |
| Q8WXX5 | Y66 | Sugiyama | DNAJC9 | RVGEGDKEDATRRFQILGKVySVLSDREQRAVYDEQGTVDE |
| Q8WYP5 | Y1790 | Sugiyama | AHCTF1 ELYS TMBS62 MSTP108 | QSVRKKTRKAKEISEASENIySDVRGLsQNQQIPQNsVtPR |
| Q92598 | Y641 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MIMQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQD |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y677 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | ICEQDHQNFLRLLTETEDWLyEEGEDQAKQAyVDKLEELMK |
| Q92598 | Y846 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | EDLEDKNNFGAEPPHQNGECyPNEKNsVNMDLD________ |
| Q92598 | Y89 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | RFHGRAFNDPFIQKEKENLsyDLVPLKNGGVGIKVMYMGEE |
| Q92882 | Y207 | Sugiyama | OSTF1 | sLLKKKQGTDAVRtLsNAEDyLDDEDsD_____________ |
| Q93079 | Y38 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96AE4 | Y58 | Sugiyama | FUBP1 | ARQIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKV |
| Q96AY3 | Y201 | Sugiyama | FKBP10 FKBP65 PSEC0056 | YNGTLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGM |
| Q96AY3 | Y204 | Sugiyama | FKBP10 FKBP65 PSEC0056 | TLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGMCPG |
| Q96C19 | T84 | Sugiyama | EFHD2 SWS1 | DLNQGIGEPQsPsRRVFNPytEFKEFSRKQIKDMEKMFKQy |
| Q96CT7 | Y38 | Sugiyama | CCDC124 | RRAEAKAAADAKKQKELEDAyWKDDDKHVMRKEQRKEEKEK |
| Q96D15 | T127 | Sugiyama | RCN3 UNQ239/PRO272 | AHTQQRHIRDsVsAAWDtyDtDRDGRVGWEELRNATYGHYA |
| Q96D46 | Y459 | Sugiyama | NMD3 CGI-07 | YQDFLEDLEEDEAIRKNVNIyRDsAIPVEsDtDDEGAPRIS |
| Q96EU6 | Y138 | Sugiyama | RRP36 C6orf153 HSPC253 | RDPRFDDLSGEYNPEVFDKtyQFLNDIRAKEKELVKKQLKK |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q99426 | Y107 | Sugiyama | TBCB CG22 CKAP1 | VIDHsGARLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKR |
| Q99426 | Y114 | Sugiyama | TBCB CG22 CKAP1 | RLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKRsKLGRyN |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| Q99848 | Y265 | Sugiyama | EBNA1BP2 EBP2 | NQKFGFGGKKKGSKWNtREsyDDVssFRAKTAHGRGLKRPG |
| Q99877 | Y38 | Sugiyama | H2BC15 H2BFD HIST1H2BN | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q99877 | Y41 | Sugiyama | H2BC15 H2BFD HIST1H2BN | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99877 | Y43 | Sugiyama | H2BC15 H2BFD HIST1H2BN | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99879 | Y38 | Sugiyama | H2BC14 H2BFE HIST1H2BM | AINKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q99879 | Y41 | Sugiyama | H2BC14 H2BFE HIST1H2BM | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99879 | Y43 | Sugiyama | H2BC14 H2BFE HIST1H2BM | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99880 | Y38 | Sugiyama | H2BC13 H2BFC HIST1H2BL | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q99880 | Y41 | Sugiyama | H2BC13 H2BFC HIST1H2BL | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99880 | Y43 | Sugiyama | H2BC13 H2BFC HIST1H2BL | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q9BQ04 | Y340 | Sugiyama | RBM4B RBM30 | YGYGPESELSQASAATRNsLyDMARYEREQYVDRARYSAF_ |
| Q9BQ04 | Y37 | Sugiyama | RBM4B RBM30 | EIRSLFEQYGKVLECDIIKNyGFVHIEDKTAAEDAIRNLHH |
| Q9BQE3 | Y312 | Sugiyama | TUBA1C TUBA6 | TNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BRL6 | Y44 | Sugiyama | SRSF8 SFRS2B SRP46 | RtsPDsLRRVFEKYGRVGDVyIPREPHTKAPRGFAFVRFHD |
| Q9BU89 | Y290 | Sugiyama | DOHH HLRC1 | RESCEVALDMyEHETGRAFQyADGLEQLRGAPS________ |
| Q9BUJ2 | Y111 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | GYSGPDGHYAMDNITRQNQFyDtQVIKQENESGyERRPLEM |
| Q9BUJ2 | Y510 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | RLIQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIV |
| Q9BWF3 | Y194 | Sugiyama | RBM4 RBM4A | ECPIDRSGRVADLTEQYNEQyGAVRTPYTMSYGDSLYYNNA |
| Q9BWF3 | Y345 | Sugiyama | RBM4 RBM4A | YGYGHEsELsQAsAAARNsLyDMARYEREQYADRARYSAF_ |
| Q9BWF3 | Y37 | Sugiyama | RBM4 RBM4A | EIRSLFEQYGKVLECDIIKNyGFVHIEDKTAAEDAIRNLHH |
| Q9BYX7 | S239 | Sugiyama | POTEKP ACTBL3 FKSG30 | VALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPE |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9GZL7 | Y380 | Sugiyama | WDR12 | SGSLDNIVKLWDTRSCKAPLyDLAAHEDKVLSVDWTDTGLL |
| Q9H3G5 | Y199 | Sugiyama | CPVL VLP PSEC0124 UNQ197/PRO223 | LYSALIQFFQIFPEYKNNDFyVTGESyAGKYVPAIAHLIHS |
| Q9H4F8 | Y407 | Sugiyama | SMOC1 | FKRYVKKKAKPKKCARRFtDyCDLNKDKVISLPELKGCLGV |
| Q9H501 | Y72 | Sugiyama | ESF1 ABTAP C20orf6 HDCMC28P | AVDKRGRPISHSTTEDLKRFyDLsDsDsNLsGEDSKALSQK |
| Q9H6T3 | Y88 | Sugiyama | RPAP3 | KAKESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKD |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H7N4 | Y732 | Sugiyama | SCAF1 SFRS19 SRA1 | KSDPRGPsPAPAssPKREVLyDsEGLsGEERGGKSSQKDRR |
| Q9H814 | Y154 | Sugiyama | PHAX RNUXA | LGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDLDKE |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9NP61 | Y408 | Sugiyama | ARFGAP3 ARFGAP1 | ETVLKTTGYSDRPTARRKPDyEPVENTDEAQKKFGNVKAIs |
| Q9NRX4 | Y113 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | ysMAyGPAQHAISTEKIKAKyPDyEVtWANDGy________ |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NX18 | Y105 | Sugiyama | SDHAF2 C11orf79 PGL2 SDH5 | LLSLFAKEHLQHMTEKQLNLyDRLINEPSNDWDIYYWATEA |
| Q9NX40 | Y199 | Sugiyama | OCIAD1 ASRIJ OCIA | HIVQGPDPNLEEsPKRKNITyEELRNKNREsyEVSLTQKTD |
| Q9NYB9 | Y23 | Sugiyama | ABI2 ARGBPIA | ELQMLLEEEIPGGRRALFDsytNLERVADyCENNyIQSADK |
| Q9NYF8 | Y219 | Sugiyama | BCLAF1 BTF KIAA0164 | IDEFNKssAtsGDIWPGLsAyDNsPRsPHsPsPIAtPPSQS |
| Q9P031 | Y97 | Sugiyama | CCDC59 BR22 TAP26 HSPC128 | AQTSLESQFtDRYPDNLKHLyLAEEERHRKQARKVDHPLSE |
| Q9P0P0 | Y152 | Sugiyama | RNF181 HSPC238 | RDKARKQQQQHRLENLHGAMyt___________________ |
| Q9UBB9 | Y51 | Sugiyama | TFIP11 STIP HSPC006 | LQNEFNPNRQRHWQTKEEAtyGVWAERDsDDERPSFGGKRA |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y352 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | TEEAREGIKQLLKQGSVQKVyNGLQGY______________ |
| Q9UBS4 | Y89 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | DLGAAyEVLsDSEKRKQyDTyGEEGLKDGHQSSHGDIFSHF |
| Q9UHD2 | Y591 | SIGNOR | TBK1 NAK | AERRLAyNEEQIHKFDKQKLyyHATKAMTHFTDECVKKYEA |
| Q9UHR5 | Y46 | Sugiyama | SAP30BP HCNGP HTRG HTRP | AGIEAVGSAAEEKGGLVsDAyGEDDFsRLGGDEDGYEEEED |
| Q9UHX1 | Y269 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | FGKIKSCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNL |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | T190 | Sugiyama | TAGLN3 NP25 | GQNVIGLQMGSNKGAsQAGMtGyGMPRQIM___________ |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UK59 | Y533 | Sugiyama | DBR1 | LsDEHEPEQRKKIKRRNQAIyAAVDDDDDDAA_________ |
| Q9UKK9 | Y198 | Sugiyama | NUDT5 NUDIX5 HSPC115 | LLQRLDALVAEEHLTVDARVySyALALKHANAKPFEVPFLK |
| Q9UKS6 | Y206 | Sugiyama | PACSIN3 | RKLQERVERCAKEAEKTKAQyEQtLAELHRYTPRYMEDMEQ |
| Q9UKS6 | Y372 | Sugiyama | PACSIN3 | EWsDEEsPRKAATGVRVRALyDyAGQEADELsFRAGEELLK |
| Q9UKS6 | Y374 | Sugiyama | PACSIN3 | sDEEsPRKAATGVRVRALyDyAGQEADELsFRAGEELLKMS |
| Q9UKY7 | Y244 | Sugiyama | CDV3 H41 | NRGRDEVSKNQALKLQLDNQyAVLENQKSSHSQYN______ |
| Q9ULH1 | Y323 | SIGNOR | ASAP1 DDEF1 KIAA1249 PAG2 | EDsQSRQGGySMHQLQGNKEyGSEKKGYLLKKSDGIRKVWQ |
| Q9ULH1 | Y767 | SIGNOR | ASAP1 DDEF1 KIAA1249 PAG2 | PQDKLALPGFstPRDKQRLSyGAFTNQIFVststDsPtsPt |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UN86 | Y19 | Sugiyama | G3BP2 KIAA0660 | __MVMEKPsPLLVGREFVRQyytLLNKAPEYLHRFYGRNSS |
| Q9UN86 | Y20 | Sugiyama | G3BP2 KIAA0660 | _MVMEKPsPLLVGREFVRQyytLLNKAPEYLHRFYGRNSSY |
| Q9UNF0 | Y435 | Sugiyama | PACSIN2 | DSNPFDDDATSGTEVRVRALyDyEGQEHDELsFKAGDELTK |
| Q9UNF0 | Y437 | Sugiyama | PACSIN2 | NPFDDDATSGTEVRVRALyDyEGQEHDELsFKAGDELTKME |
| Q9UNZ2 | S165 | Sugiyama | NSFL1C UBXN2C | SKPRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLK |
| Q9UQ35 | Y2693 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | RRSRSPRKPIDsLRDsRsLsysPVERRRPsPQPsPRDQQSS |
| Q9Y262 | S249 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | NVLHSLVDKSNINRQLEVytsGGDPEsVAGEyGRHSLYKML |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2B0 | Y71 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | IQMGsFRINPDGsQsVVEVPyARsEAHLtELLEEICDRMKE |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y3D8 | Y31 | Sugiyama | AK6 CINAP AD-004 CGI-137 | TPGVGKTTLGKELASKSGLKyINVGDLAREEQLYDGYDEEY |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3P9 | Y472 | Sugiyama | RABGAP1 HSPC094 | FFLKLKQIKQRERKNNTDTLyEVVCLESESERERRKTTAsP |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y5Q8 | Y393 | Sugiyama | GTF3C5 CDABP0017 | SGtsGARKPASSKYKLKDSVyIFREGALPPYRQMFYQLCDL |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y5V0 | Y39 | Sugiyama | ZNF706 HSPC038 PNAS-113 | AGQKKKQGHDQKAAAKAALIyTCTVCRTQMPDPKTFKQHFE |
| Q9Y639 | Y216 | Sugiyama | NPTN SDFR1 SDR1 | KNASNMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKA |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | Y244 | Sugiyama | CLIC4 | AysRDEFtNtCPsDKEVEIAysDVAKRLTK___________ |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.979360e-07 | 6.703 | 1 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 5.856924e-07 | 6.232 | 1 | 1 |
| Signaling by VEGF | R-HSA-194138 | 1.214248e-06 | 5.916 | 1 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.161399e-06 | 5.665 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 3.338712e-06 | 5.476 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 9.153224e-06 | 5.038 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 9.346793e-06 | 5.029 | 1 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.517333e-05 | 4.819 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.949848e-05 | 4.710 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 2.117216e-05 | 4.674 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 4.003735e-05 | 4.398 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 6.596141e-05 | 4.181 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.056810e-04 | 3.976 | 1 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.027122e-04 | 3.988 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.172568e-04 | 3.663 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 4.878607e-04 | 3.312 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 5.396850e-04 | 3.268 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 6.537788e-04 | 3.185 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 6.537788e-04 | 3.185 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 6.858334e-04 | 3.164 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 7.349091e-04 | 3.134 | 1 | 1 |
| RET signaling | R-HSA-8853659 | 8.331114e-04 | 3.079 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 9.941388e-04 | 3.003 | 0 | 0 |
| TRKA activation by NGF | R-HSA-187042 | 1.100701e-03 | 2.958 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.246846e-03 | 2.904 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 1.304882e-03 | 2.884 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 1.304882e-03 | 2.884 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.439299e-03 | 2.842 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 1.480683e-03 | 2.830 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 1.670662e-03 | 2.777 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 1.815639e-03 | 2.741 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.094749e-03 | 2.679 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.094749e-03 | 2.679 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 2.183244e-03 | 2.661 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 2.183244e-03 | 2.661 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 2.231247e-03 | 2.651 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.329613e-03 | 2.633 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 2.884848e-03 | 2.540 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 3.131774e-03 | 2.504 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 3.504160e-03 | 2.455 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 3.429360e-03 | 2.465 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 3.745978e-03 | 2.426 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 3.905565e-03 | 2.408 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 4.117474e-03 | 2.385 | 0 | 0 |
| Activation of TRKA receptors | R-HSA-187015 | 4.267179e-03 | 2.370 | 0 | 0 |
| PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | R-HSA-8849469 | 5.131150e-03 | 2.290 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 5.131150e-03 | 2.290 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 5.187828e-03 | 2.285 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 5.593419e-03 | 2.252 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 6.011648e-03 | 2.221 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 6.011648e-03 | 2.221 | 0 | 0 |
| Drug resistance of KIT mutants | R-HSA-9669937 | 9.518145e-03 | 2.021 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 9.518145e-03 | 2.021 | 0 | 0 |
| KIT mutants bind TKIs | R-HSA-9669921 | 9.518145e-03 | 2.021 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 9.518145e-03 | 2.021 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 9.518145e-03 | 2.021 | 0 | 0 |
| Masitinib-resistant KIT mutants | R-HSA-9669924 | 9.518145e-03 | 2.021 | 0 | 0 |
| Dasatinib-resistant KIT mutants | R-HSA-9669914 | 9.518145e-03 | 2.021 | 0 | 0 |
| Imatinib-resistant KIT mutants | R-HSA-9669917 | 9.518145e-03 | 2.021 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 9.518145e-03 | 2.021 | 0 | 0 |
| Regorafenib-resistant KIT mutants | R-HSA-9669929 | 9.518145e-03 | 2.021 | 0 | 0 |
| Defective translocation of RB1 mutants to the nucleus | R-HSA-9661070 | 9.518145e-03 | 2.021 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 9.518145e-03 | 2.021 | 0 | 0 |
| Sorafenib-resistant KIT mutants | R-HSA-9669936 | 9.518145e-03 | 2.021 | 0 | 0 |
| Nilotinib-resistant KIT mutants | R-HSA-9669926 | 9.518145e-03 | 2.021 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 9.518145e-03 | 2.021 | 0 | 0 |
| Sunitinib-resistant KIT mutants | R-HSA-9669934 | 9.518145e-03 | 2.021 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 7.903353e-03 | 2.102 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 9.306498e-03 | 2.031 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 8.423088e-03 | 2.075 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 8.157614e-03 | 2.088 | 1 | 1 |
| Cell junction organization | R-HSA-446728 | 8.307971e-03 | 2.081 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 6.526048e-03 | 2.185 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 1.131938e-02 | 1.946 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.180596e-02 | 1.928 | 0 | 0 |
| Replication of the SARS-CoV-1 genome | R-HSA-9682706 | 1.180596e-02 | 1.928 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.261921e-02 | 1.899 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.315380e-02 | 1.881 | 0 | 0 |
| Signaling by FGFR4 in disease | R-HSA-5655291 | 1.315380e-02 | 1.881 | 0 | 0 |
| SARS-CoV-1 Genome Replication and Transcription | R-HSA-9679514 | 1.315380e-02 | 1.881 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.329983e-02 | 1.876 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 1.329983e-02 | 1.876 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 1.400106e-02 | 1.854 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.622903e-02 | 1.790 | 0 | 0 |
| InlB-mediated entry of Listeria monocytogenes into host cell | R-HSA-8875360 | 1.456527e-02 | 1.837 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 1.472295e-02 | 1.832 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.456527e-02 | 1.837 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.701333e-02 | 1.769 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | R-HSA-8866910 | 1.757382e-02 | 1.755 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 1.806992e-02 | 1.743 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 1.806992e-02 | 1.743 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 1.806992e-02 | 1.743 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 1.851401e-02 | 1.732 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 1.864468e-02 | 1.729 | 0 | 0 |
| SARS-CoV-1 targets PDZ proteins in cell-cell junction | R-HSA-9692912 | 1.894628e-02 | 1.722 | 0 | 0 |
| Replication of the SARS-CoV-2 genome | R-HSA-9694686 | 1.916833e-02 | 1.717 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.082131e-02 | 1.681 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition | R-HSA-9926550 | 2.082131e-02 | 1.681 | 0 | 0 |
| PI-3K cascade:FGFR3 | R-HSA-5654710 | 2.253151e-02 | 1.647 | 0 | 0 |
| SARS-CoV-2 Genome Replication and Transcription | R-HSA-9694682 | 2.253151e-02 | 1.647 | 0 | 0 |
| Signaling by extracellular domain mutants of KIT | R-HSA-9680187 | 2.828524e-02 | 1.548 | 0 | 0 |
| Signaling by juxtamembrane domain KIT mutants | R-HSA-9669935 | 2.828524e-02 | 1.548 | 0 | 0 |
| Signaling by kinase domain mutants of KIT | R-HSA-9669933 | 2.828524e-02 | 1.548 | 0 | 0 |
| PI-3K cascade:FGFR4 | R-HSA-5654720 | 2.429771e-02 | 1.614 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.429771e-02 | 1.614 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.429771e-02 | 1.614 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 2.404266e-02 | 1.619 | 0 | 0 |
| Inhibition of membrane repair | R-HSA-9635644 | 2.828524e-02 | 1.548 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.429771e-02 | 1.614 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 2.286021e-02 | 1.641 | 0 | 0 |
| Zygotic genome activation (ZGA) | R-HSA-9819196 | 2.611870e-02 | 1.583 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 2.884942e-02 | 1.540 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 2.884942e-02 | 1.540 | 0 | 0 |
| PI-3K cascade:FGFR1 | R-HSA-5654689 | 2.992035e-02 | 1.524 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 2.992035e-02 | 1.524 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 3.019677e-02 | 1.520 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 3.753588e-02 | 1.426 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 3.753588e-02 | 1.426 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 3.753588e-02 | 1.426 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 3.753588e-02 | 1.426 | 0 | 0 |
| PI-3K cascade:FGFR2 | R-HSA-5654695 | 3.600462e-02 | 1.444 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.030226e-02 | 1.395 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 3.698458e-02 | 1.432 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 3.600462e-02 | 1.444 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 3.698458e-02 | 1.432 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 3.753588e-02 | 1.426 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 3.611750e-02 | 1.442 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 3.881633e-02 | 1.411 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 3.196097e-02 | 1.495 | 0 | 0 |
| Signaling by FGFR3 in disease | R-HSA-5655332 | 4.030226e-02 | 1.395 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 3.129563e-02 | 1.505 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 4.030226e-02 | 1.395 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 3.953879e-02 | 1.403 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 3.264453e-02 | 1.486 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 4.252026e-02 | 1.371 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 4.252026e-02 | 1.371 | 0 | 0 |
| Downstream signaling of activated FGFR3 | R-HSA-5654708 | 4.478297e-02 | 1.349 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 4.478297e-02 | 1.349 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 4.478297e-02 | 1.349 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 4.478297e-02 | 1.349 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 4.608577e-02 | 1.336 | 0 | 0 |
| PLC-gamma1 signalling | R-HSA-167021 | 4.669902e-02 | 1.331 | 0 | 0 |
| MET activates PTPN11 | R-HSA-8865999 | 4.669902e-02 | 1.331 | 0 | 0 |
| Signalling to STAT3 | R-HSA-198745 | 4.669902e-02 | 1.331 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 4.693964e-02 | 1.328 | 0 | 0 |
| Downstream signaling of activated FGFR4 | R-HSA-5654716 | 4.708934e-02 | 1.327 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 4.708934e-02 | 1.327 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 4.943835e-02 | 1.306 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 5.182900e-02 | 1.285 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 5.310114e-02 | 1.275 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 5.310114e-02 | 1.275 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 5.426028e-02 | 1.266 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 5.426028e-02 | 1.266 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 5.483101e-02 | 1.261 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 5.577548e-02 | 1.254 | 0 | 0 |
| FLT3 signaling by CBL mutants | R-HSA-9706377 | 6.476608e-02 | 1.189 | 0 | 0 |
| NGF-independant TRKA activation | R-HSA-187024 | 7.367163e-02 | 1.133 | 0 | 0 |
| Signalling to p38 via RIT and RIN | R-HSA-187706 | 7.367163e-02 | 1.133 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 7.367163e-02 | 1.133 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 6.476608e-02 | 1.189 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 6.505249e-02 | 1.187 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 7.525985e-02 | 1.123 | 0 | 0 |
| Downstream signaling of activated FGFR2 | R-HSA-5654696 | 6.178826e-02 | 1.209 | 0 | 0 |
| Downstream signaling of activated FGFR1 | R-HSA-5654687 | 6.178826e-02 | 1.209 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 6.178826e-02 | 1.209 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 7.697773e-02 | 1.114 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 5.577548e-02 | 1.254 | 0 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 5.924087e-02 | 1.227 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 5.924087e-02 | 1.227 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 5.924087e-02 | 1.227 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 8.341694e-02 | 1.079 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 7.505915e-02 | 1.125 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 7.610421e-02 | 1.119 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 5.577548e-02 | 1.254 | 0 | 0 |
| RUNX2 regulates chondrocyte maturation | R-HSA-8941284 | 6.476608e-02 | 1.189 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 6.476608e-02 | 1.189 | 0 | 0 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 7.367163e-02 | 1.133 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 7.367163e-02 | 1.133 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 8.060008e-02 | 1.094 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 6.022172e-02 | 1.220 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 7.781387e-02 | 1.109 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 5.673123e-02 | 1.246 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 7.505915e-02 | 1.125 | 1 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 6.023345e-02 | 1.220 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 8.764134e-02 | 1.057 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 8.913932e-02 | 1.050 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 8.913932e-02 | 1.050 | 0 | 0 |
| MET activates PI3K/AKT signaling | R-HSA-8851907 | 9.123074e-02 | 1.040 | 0 | 0 |
| Insulin effects increased synthesis of Xylulose-5-Phosphate | R-HSA-163754 | 9.123074e-02 | 1.040 | 0 | 0 |
| Activation of PUMA and translocation to mitochondria | R-HSA-139915 | 9.123074e-02 | 1.040 | 0 | 0 |
| Displacement of DNA glycosylase by APEX1 | R-HSA-110357 | 9.123074e-02 | 1.040 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 9.204322e-02 | 1.036 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 9.497455e-02 | 1.022 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 9.497455e-02 | 1.022 | 0 | 0 |
| MET receptor recycling | R-HSA-8875656 | 9.988589e-02 | 1.000 | 0 | 0 |
| Activated NTRK2 signals through PI3K | R-HSA-9028335 | 9.988589e-02 | 1.000 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.084591e-01 | 0.965 | 0 | 0 |
| MET activates RAP1 and RAC1 | R-HSA-8875555 | 1.169513e-01 | 0.932 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.253630e-01 | 0.902 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.501235e-01 | 0.824 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.501235e-01 | 0.824 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 1.582213e-01 | 0.801 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.662424e-01 | 0.779 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.662424e-01 | 0.779 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.662424e-01 | 0.779 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.741875e-01 | 0.759 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 1.898529e-01 | 0.722 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 1.167838e-01 | 0.933 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.169513e-01 | 0.932 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.169513e-01 | 0.932 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.253630e-01 | 0.902 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 1.167838e-01 | 0.933 | 0 | 0 |
| Activated NTRK2 signals through FRS2 and FRS3 | R-HSA-9028731 | 1.419484e-01 | 0.848 | 0 | 0 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | R-HSA-113501 | 1.336951e-01 | 0.874 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.501235e-01 | 0.824 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 1.753453e-01 | 0.756 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.419484e-01 | 0.848 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 1.599835e-01 | 0.796 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.419484e-01 | 0.848 | 0 | 0 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | R-HSA-2559584 | 1.501235e-01 | 0.824 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 1.683221e-01 | 0.774 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 1.898529e-01 | 0.722 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.662424e-01 | 0.779 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 1.466779e-01 | 0.834 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 9.889070e-02 | 1.005 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 1.580455e-01 | 0.801 | 0 | 0 |
| Activation of RAC1 downstream of NMDARs | R-HSA-9619229 | 1.084591e-01 | 0.965 | 0 | 0 |
| RHOBTB3 ATPase cycle | R-HSA-9706019 | 1.253630e-01 | 0.902 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 1.336951e-01 | 0.874 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 1.161979e-01 | 0.935 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 1.209153e-01 | 0.918 | 0 | 0 |
| TP53 Regulates Transcription of Death Receptors and Ligands | R-HSA-6803211 | 1.582213e-01 | 0.801 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 1.853421e-01 | 0.732 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 1.662424e-01 | 0.779 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 1.645723e-01 | 0.784 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.084591e-01 | 0.965 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.336951e-01 | 0.874 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 1.419484e-01 | 0.848 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.419484e-01 | 0.848 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 1.741875e-01 | 0.759 | 0 | 0 |
| Signaling by FGFR2 in disease | R-HSA-5655253 | 1.069587e-01 | 0.971 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.785028e-01 | 0.748 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 1.384787e-01 | 0.859 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 1.127071e-01 | 0.948 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 1.016350e-01 | 0.993 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 1.557703e-01 | 0.808 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 1.630523e-01 | 0.788 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 1.630523e-01 | 0.788 | 0 | 0 |
| Zinc influx into cells by the SLC39 gene family | R-HSA-442380 | 1.084591e-01 | 0.965 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 1.069587e-01 | 0.971 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 1.193216e-01 | 0.923 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 1.519633e-01 | 0.818 | 0 | 0 |
| Positive Regulation of CDH1 Gene Transcription | R-HSA-9764790 | 1.169513e-01 | 0.932 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.169513e-01 | 0.932 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 1.649516e-01 | 0.783 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 1.719075e-01 | 0.765 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.256310e-01 | 0.901 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 1.288152e-01 | 0.890 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 1.357868e-01 | 0.867 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.134379e-01 | 0.945 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.134379e-01 | 0.945 | 0 | 0 |
| Regulation of TP53 Activity through Association with Co-factors | R-HSA-6804759 | 1.501235e-01 | 0.824 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 1.898529e-01 | 0.722 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 1.417347e-01 | 0.849 | 0 | 0 |
| Zinc transporters | R-HSA-435354 | 1.582213e-01 | 0.801 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.293371e-01 | 0.888 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 1.515983e-01 | 0.819 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 1.039253e-01 | 0.983 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 1.549162e-01 | 0.810 | 0 | 0 |
| Interleukin-6 signaling | R-HSA-1059683 | 1.501235e-01 | 0.824 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.253630e-01 | 0.902 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 1.384787e-01 | 0.859 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 1.384787e-01 | 0.859 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 1.384787e-01 | 0.859 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 1.384787e-01 | 0.859 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 1.047238e-01 | 0.980 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 1.515983e-01 | 0.819 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 1.700893e-01 | 0.769 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.549162e-01 | 0.810 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 1.881706e-01 | 0.725 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 1.320184e-01 | 0.879 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 1.384787e-01 | 0.859 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 1.922186e-01 | 0.716 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 1.922186e-01 | 0.716 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.947152e-01 | 0.711 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 1.975745e-01 | 0.704 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.975745e-01 | 0.704 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 1.975745e-01 | 0.704 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 1.975745e-01 | 0.704 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 1.991284e-01 | 0.701 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.005939e-01 | 0.698 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 2.025946e-01 | 0.693 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.052230e-01 | 0.688 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 2.060678e-01 | 0.686 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.127990e-01 | 0.672 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.127990e-01 | 0.672 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 2.178251e-01 | 0.662 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 2.203033e-01 | 0.657 | 0 | 0 |
| Prevention of phagosomal-lysosomal fusion | R-HSA-9636383 | 2.203033e-01 | 0.657 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 2.203121e-01 | 0.657 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 2.228050e-01 | 0.652 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 2.270287e-01 | 0.644 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.277365e-01 | 0.643 | 0 | 0 |
| FRS-mediated FGFR3 signaling | R-HSA-5654706 | 2.277365e-01 | 0.643 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 2.277365e-01 | 0.643 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 2.278078e-01 | 0.642 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 2.325097e-01 | 0.634 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 2.340520e-01 | 0.631 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 2.350993e-01 | 0.629 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 2.350993e-01 | 0.629 | 0 | 0 |
| FRS-mediated FGFR4 signaling | R-HSA-5654712 | 2.350993e-01 | 0.629 | 0 | 0 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | R-HSA-6803205 | 2.350993e-01 | 0.629 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 2.375688e-01 | 0.624 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 2.375688e-01 | 0.624 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 2.375688e-01 | 0.624 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 2.378768e-01 | 0.624 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 2.464935e-01 | 0.608 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 2.480219e-01 | 0.606 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 2.481347e-01 | 0.605 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.496163e-01 | 0.603 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.496163e-01 | 0.603 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.496163e-01 | 0.603 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.496163e-01 | 0.603 | 0 | 0 |
| Interleukin-6 family signaling | R-HSA-6783589 | 2.496163e-01 | 0.603 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 2.516607e-01 | 0.599 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 2.551881e-01 | 0.593 | 0 | 0 |
| FRS-mediated FGFR1 signaling | R-HSA-5654693 | 2.567719e-01 | 0.590 | 0 | 0 |
| Suppression of phagosomal maturation | R-HSA-9637687 | 2.638596e-01 | 0.579 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 2.657755e-01 | 0.575 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 2.693052e-01 | 0.570 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 2.693052e-01 | 0.570 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 2.708802e-01 | 0.567 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 2.708802e-01 | 0.567 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | R-HSA-6803204 | 2.708802e-01 | 0.567 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 2.708802e-01 | 0.567 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 2.708802e-01 | 0.567 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 2.763636e-01 | 0.559 | 0 | 0 |
| FRS-mediated FGFR2 signaling | R-HSA-5654700 | 2.778342e-01 | 0.556 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 2.789736e-01 | 0.554 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 2.847224e-01 | 0.546 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 2.847224e-01 | 0.546 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 2.847224e-01 | 0.546 | 0 | 0 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | R-HSA-917729 | 2.847224e-01 | 0.546 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 2.867477e-01 | 0.543 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 2.904677e-01 | 0.537 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 2.915453e-01 | 0.535 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 2.915453e-01 | 0.535 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 2.915453e-01 | 0.535 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 2.975087e-01 | 0.527 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 3.010254e-01 | 0.521 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 3.010254e-01 | 0.521 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 3.038565e-01 | 0.517 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.049976e-01 | 0.516 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 3.049976e-01 | 0.516 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.116283e-01 | 0.506 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.116283e-01 | 0.506 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.116283e-01 | 0.506 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 3.150614e-01 | 0.502 | 0 | 0 |
| Acyl chain remodelling of PC | R-HSA-1482788 | 3.181962e-01 | 0.497 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 3.185613e-01 | 0.497 | 0 | 0 |
| Dual Incision in GG-NER | R-HSA-5696400 | 3.247018e-01 | 0.489 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.247018e-01 | 0.489 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 3.247018e-01 | 0.489 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.247018e-01 | 0.489 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 3.247018e-01 | 0.489 | 0 | 0 |
| Acyl chain remodelling of PE | R-HSA-1482839 | 3.311457e-01 | 0.480 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 3.311457e-01 | 0.480 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 3.375285e-01 | 0.472 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 3.375285e-01 | 0.472 | 0 | 0 |
| FLT3 signaling in disease | R-HSA-9682385 | 3.375285e-01 | 0.472 | 0 | 0 |
| M Phase | R-HSA-68886 | 3.423044e-01 | 0.466 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 3.426051e-01 | 0.465 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.501132e-01 | 0.456 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.501132e-01 | 0.456 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.563161e-01 | 0.448 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 3.563161e-01 | 0.448 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 3.563161e-01 | 0.448 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 3.567389e-01 | 0.448 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 3.568248e-01 | 0.448 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 3.577490e-01 | 0.446 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 3.624603e-01 | 0.441 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 3.624603e-01 | 0.441 | 0 | 0 |
| Formation of Incision Complex in GG-NER | R-HSA-5696395 | 3.624603e-01 | 0.441 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 3.670264e-01 | 0.435 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 3.685462e-01 | 0.434 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 3.685462e-01 | 0.434 | 0 | 0 |
| Resolution of Abasic Sites (AP sites) | R-HSA-73933 | 3.685462e-01 | 0.434 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 3.704417e-01 | 0.431 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 3.745743e-01 | 0.426 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 3.745743e-01 | 0.426 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 3.745743e-01 | 0.426 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 3.805453e-01 | 0.420 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 3.805453e-01 | 0.420 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 3.853015e-01 | 0.414 | 0 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 3.864596e-01 | 0.413 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 3.864596e-01 | 0.413 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 3.864596e-01 | 0.413 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 3.923179e-01 | 0.406 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 3.923179e-01 | 0.406 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 3.981205e-01 | 0.400 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 3.981205e-01 | 0.400 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 3.981205e-01 | 0.400 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 3.981573e-01 | 0.400 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 4.038681e-01 | 0.394 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 4.095612e-01 | 0.388 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.095612e-01 | 0.388 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 4.141267e-01 | 0.383 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.152002e-01 | 0.382 | 0 | 0 |
| Metal ion SLC transporters | R-HSA-425410 | 4.152002e-01 | 0.382 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 4.207858e-01 | 0.376 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 4.236440e-01 | 0.373 | 0 | 0 |
| Translation | R-HSA-72766 | 4.310721e-01 | 0.365 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 4.370290e-01 | 0.359 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.372264e-01 | 0.359 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.372264e-01 | 0.359 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 4.426029e-01 | 0.354 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 4.426029e-01 | 0.354 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 4.466969e-01 | 0.350 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 4.479283e-01 | 0.349 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 4.532032e-01 | 0.344 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 4.584281e-01 | 0.339 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 4.586746e-01 | 0.338 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 4.636033e-01 | 0.334 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 4.636033e-01 | 0.334 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 4.657529e-01 | 0.332 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 4.667409e-01 | 0.331 | 0 | 0 |
| Dual incision in TC-NER | R-HSA-6782135 | 4.687294e-01 | 0.329 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 4.688915e-01 | 0.329 | 0 | 0 |
| Disease | R-HSA-1643685 | 4.736131e-01 | 0.325 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 4.782418e-01 | 0.320 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 4.838175e-01 | 0.315 | 0 | 0 |
| Collagen degradation | R-HSA-1442490 | 4.838175e-01 | 0.315 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 4.844199e-01 | 0.315 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 4.887516e-01 | 0.311 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 4.887516e-01 | 0.311 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 4.887516e-01 | 0.311 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 4.923984e-01 | 0.308 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 4.926011e-01 | 0.308 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 4.936024e-01 | 0.307 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 4.936389e-01 | 0.307 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 4.936389e-01 | 0.307 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 4.966404e-01 | 0.304 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 4.997310e-01 | 0.301 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.026819e-01 | 0.299 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 5.080240e-01 | 0.294 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.086769e-01 | 0.294 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 5.086769e-01 | 0.294 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.173877e-01 | 0.286 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 5.173877e-01 | 0.286 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 5.173877e-01 | 0.286 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 5.205258e-01 | 0.284 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 5.212185e-01 | 0.283 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.265744e-01 | 0.279 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 5.265744e-01 | 0.279 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 5.265744e-01 | 0.279 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 5.311023e-01 | 0.275 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 5.311023e-01 | 0.275 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 5.311023e-01 | 0.275 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 5.311023e-01 | 0.275 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 5.355873e-01 | 0.271 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.355873e-01 | 0.271 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.400296e-01 | 0.268 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 5.400296e-01 | 0.268 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 5.408015e-01 | 0.267 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.444297e-01 | 0.264 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 5.487879e-01 | 0.261 | 0 | 0 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | R-HSA-6781827 | 5.487879e-01 | 0.261 | 0 | 0 |
| TP53 Regulates Transcription of Cell Death Genes | R-HSA-5633008 | 5.487879e-01 | 0.261 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 5.487879e-01 | 0.261 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 5.631254e-01 | 0.249 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 5.659939e-01 | 0.247 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 5.724212e-01 | 0.242 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 5.772846e-01 | 0.239 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 5.781576e-01 | 0.238 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 5.818331e-01 | 0.235 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 5.861944e-01 | 0.232 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 5.861944e-01 | 0.232 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 5.862300e-01 | 0.232 | 1 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 5.901556e-01 | 0.229 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 5.901856e-01 | 0.229 | 0 | 0 |
| Immune System | R-HSA-168256 | 5.931500e-01 | 0.227 | 1 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 5.940791e-01 | 0.226 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 5.940791e-01 | 0.226 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 5.940791e-01 | 0.226 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 5.954248e-01 | 0.225 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 5.979653e-01 | 0.223 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 5.979653e-01 | 0.223 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 6.018145e-01 | 0.221 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 6.018145e-01 | 0.221 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 6.056271e-01 | 0.218 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 6.060940e-01 | 0.217 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 6.131439e-01 | 0.212 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 6.131439e-01 | 0.212 | 0 | 0 |
| Protein folding | R-HSA-391251 | 6.241529e-01 | 0.205 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.258136e-01 | 0.204 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 6.277530e-01 | 0.202 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 6.282652e-01 | 0.202 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 6.313188e-01 | 0.200 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 6.334882e-01 | 0.198 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.418138e-01 | 0.193 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 6.418138e-01 | 0.193 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 6.418138e-01 | 0.193 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 6.452458e-01 | 0.190 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 6.463786e-01 | 0.190 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 6.521021e-01 | 0.186 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 6.553469e-01 | 0.184 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 6.619217e-01 | 0.179 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 6.619217e-01 | 0.179 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 6.652040e-01 | 0.177 | 0 | 0 |
| Post-translational modification: synthesis of GPI-anchored proteins | R-HSA-163125 | 6.715509e-01 | 0.173 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 6.746997e-01 | 0.171 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 6.778185e-01 | 0.169 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 6.841140e-01 | 0.165 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 6.869978e-01 | 0.163 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 6.898314e-01 | 0.161 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 6.961317e-01 | 0.157 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 7.015557e-01 | 0.154 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 7.102252e-01 | 0.149 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 7.124197e-01 | 0.147 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.157593e-01 | 0.145 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 7.265143e-01 | 0.139 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 7.265143e-01 | 0.139 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 7.265143e-01 | 0.139 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.265143e-01 | 0.139 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 7.266089e-01 | 0.139 | 1 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 7.317393e-01 | 0.136 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.343144e-01 | 0.134 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 7.393913e-01 | 0.131 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 7.393913e-01 | 0.131 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 7.393913e-01 | 0.131 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 7.393913e-01 | 0.131 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 7.418934e-01 | 0.130 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 7.428187e-01 | 0.129 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 7.449297e-01 | 0.128 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 7.553239e-01 | 0.122 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 7.587527e-01 | 0.120 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 7.587527e-01 | 0.120 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 7.701208e-01 | 0.113 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 7.723297e-01 | 0.112 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 7.766844e-01 | 0.110 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 7.829653e-01 | 0.106 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 7.851472e-01 | 0.105 | 0 | 0 |
| S Phase | R-HSA-69242 | 7.972476e-01 | 0.098 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 8.068122e-01 | 0.093 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 8.086706e-01 | 0.092 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 8.141400e-01 | 0.089 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 8.263053e-01 | 0.083 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 8.392424e-01 | 0.076 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 8.407907e-01 | 0.075 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 8.423242e-01 | 0.075 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 8.423242e-01 | 0.075 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 8.423242e-01 | 0.075 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 8.526553e-01 | 0.069 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 8.568744e-01 | 0.067 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 8.609734e-01 | 0.065 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 8.636411e-01 | 0.064 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 8.786122e-01 | 0.056 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 8.786122e-01 | 0.056 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 8.806210e-01 | 0.055 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 8.865788e-01 | 0.052 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 8.929924e-01 | 0.049 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 8.970666e-01 | 0.047 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 8.980608e-01 | 0.047 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 9.065903e-01 | 0.043 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 9.074931e-01 | 0.042 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 9.270271e-01 | 0.033 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 9.295365e-01 | 0.032 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 9.315637e-01 | 0.031 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 9.483287e-01 | 0.023 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.495708e-01 | 0.022 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 9.536532e-01 | 0.021 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 9.636913e-01 | 0.016 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 9.636913e-01 | 0.016 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 9.695505e-01 | 0.013 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.825831e-01 | 0.008 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.855787e-01 | 0.006 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 9.865547e-01 | 0.006 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 9.901554e-01 | 0.004 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 9.945180e-01 | 0.002 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 9.951169e-01 | 0.002 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 9.976015e-01 | 0.001 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.991551e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.999490e-01 | 0.000 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.999495e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999625e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000e+00 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.110223e-16 | 15.955 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.110223e-16 | 15.955 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.110223e-16 | 15.955 | 1 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.110223e-16 | 15.955 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 1.110223e-16 | 15.955 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 9.992007e-16 | 15.000 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 2.964295e-14 | 13.528 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 8.248957e-14 | 13.084 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 8.248957e-14 | 13.084 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 1.547651e-13 | 12.810 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 3.725908e-13 | 12.429 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 4.595213e-13 | 12.338 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 4.914957e-13 | 12.308 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 6.611378e-13 | 12.180 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 8.372192e-13 | 12.077 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 8.372192e-13 | 12.077 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 1.389333e-12 | 11.857 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.490141e-12 | 11.827 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 1.773581e-12 | 11.751 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 1.831646e-12 | 11.737 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 1.773581e-12 | 11.751 | 0 | 0 |
| Depurination | R-HSA-73927 | 2.251310e-12 | 11.648 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 2.350009e-12 | 11.629 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 2.506217e-12 | 11.601 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 2.685296e-12 | 11.571 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 2.944756e-12 | 11.531 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 3.569589e-12 | 11.447 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 3.569589e-12 | 11.447 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 3.987921e-12 | 11.399 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 4.460765e-12 | 11.351 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 4.460765e-12 | 11.351 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 4.473755e-12 | 11.349 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 6.868506e-12 | 11.163 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 6.868506e-12 | 11.163 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 7.707168e-12 | 11.113 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 8.466006e-12 | 11.072 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 9.303558e-12 | 11.031 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 1.270228e-11 | 10.896 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 1.270228e-11 | 10.896 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 1.294642e-11 | 10.888 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.294642e-11 | 10.888 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 1.450517e-11 | 10.838 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.454503e-11 | 10.837 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 2.011746e-11 | 10.696 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 2.267619e-11 | 10.644 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 4.677803e-11 | 10.330 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 5.110135e-11 | 10.292 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 5.561918e-11 | 10.255 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 6.593626e-11 | 10.181 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 7.794365e-11 | 10.108 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 1.266703e-10 | 9.897 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 1.481609e-10 | 9.829 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 1.957661e-10 | 9.708 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 3.204149e-10 | 9.494 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 3.491610e-10 | 9.457 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 4.159053e-10 | 9.381 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 4.779019e-10 | 9.321 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 5.190695e-10 | 9.285 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 5.256385e-10 | 9.279 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 5.480673e-10 | 9.261 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 7.167438e-10 | 9.145 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 8.174117e-10 | 9.088 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 9.707637e-10 | 9.013 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 9.305769e-10 | 9.031 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 1.000263e-09 | 9.000 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.239676e-09 | 8.907 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 1.505580e-09 | 8.822 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 1.505580e-09 | 8.822 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 1.505580e-09 | 8.822 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 1.691329e-09 | 8.772 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 1.537140e-09 | 8.813 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 1.549490e-09 | 8.810 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 1.746454e-09 | 8.758 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 1.956878e-09 | 8.708 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 2.071503e-09 | 8.684 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 2.476453e-09 | 8.606 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 2.779910e-09 | 8.556 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 2.787148e-09 | 8.555 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 2.787148e-09 | 8.555 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 3.900020e-09 | 8.409 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 4.921225e-09 | 8.308 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 8.221097e-09 | 8.085 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 8.295434e-09 | 8.081 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 9.102551e-09 | 8.041 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 9.193118e-09 | 8.037 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 1.524738e-08 | 7.817 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 1.886705e-08 | 7.724 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 1.945179e-08 | 7.711 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 2.260356e-08 | 7.646 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 2.280510e-08 | 7.642 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 2.301790e-08 | 7.638 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 2.881164e-08 | 7.540 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 2.881164e-08 | 7.540 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 2.881164e-08 | 7.540 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 3.010489e-08 | 7.521 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 3.066117e-08 | 7.513 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 4.052612e-08 | 7.392 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 4.052612e-08 | 7.392 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 4.524380e-08 | 7.344 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 7.256200e-08 | 7.139 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 8.525131e-08 | 7.069 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 1.138703e-07 | 6.944 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 1.142106e-07 | 6.942 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 1.935482e-07 | 6.713 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 2.577976e-07 | 6.589 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 2.424793e-07 | 6.615 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 2.420277e-07 | 6.616 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 4.115786e-07 | 6.386 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 5.608040e-07 | 6.251 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 7.681588e-07 | 6.115 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 8.107410e-07 | 6.091 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 8.536497e-07 | 6.069 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 1.078978e-06 | 5.967 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 1.282618e-06 | 5.892 | 1 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 1.366639e-06 | 5.864 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 1.589042e-06 | 5.799 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 1.754558e-06 | 5.756 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 1.931761e-06 | 5.714 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 1.936273e-06 | 5.713 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.964333e-06 | 5.707 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 2.012621e-06 | 5.696 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 2.657645e-06 | 5.576 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 2.664544e-06 | 5.574 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 2.838769e-06 | 5.547 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 3.863098e-06 | 5.413 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 4.155210e-06 | 5.381 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 5.053093e-06 | 5.296 | 0 | 0 |
| Immune System | R-HSA-168256 | 5.411624e-06 | 5.267 | 1 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 6.152879e-06 | 5.211 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 6.227219e-06 | 5.206 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 6.701933e-06 | 5.174 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 7.926953e-06 | 5.101 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 8.992603e-06 | 5.046 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 9.847495e-06 | 5.007 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 9.847495e-06 | 5.007 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 9.847495e-06 | 5.007 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 1.177984e-05 | 4.929 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.205105e-05 | 4.919 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.282615e-05 | 4.892 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 1.357669e-05 | 4.867 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 1.475597e-05 | 4.831 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 1.806475e-05 | 4.743 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 1.942969e-05 | 4.712 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 2.174064e-05 | 4.663 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 2.275698e-05 | 4.643 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 2.372016e-05 | 4.625 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 2.466645e-05 | 4.608 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 2.654062e-05 | 4.576 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 3.005577e-05 | 4.522 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 3.361428e-05 | 4.473 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 4.395668e-05 | 4.357 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 4.249606e-05 | 4.372 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 4.921302e-05 | 4.308 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 4.927736e-05 | 4.307 | 1 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 5.055915e-05 | 4.296 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 5.109133e-05 | 4.292 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 5.717926e-05 | 4.243 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 6.120837e-05 | 4.213 | 1 | 1 |
| L1CAM interactions | R-HSA-373760 | 6.455518e-05 | 4.190 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 7.962039e-05 | 4.099 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 8.501884e-05 | 4.070 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.007641e-04 | 3.997 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.072349e-04 | 3.970 | 1 | 0 |
| Signaling by WNT | R-HSA-195721 | 1.153727e-04 | 3.938 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.160584e-04 | 3.935 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 1.182100e-04 | 3.927 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 1.339856e-04 | 3.873 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 1.339856e-04 | 3.873 | 0 | 0 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 1.384516e-04 | 3.859 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 1.564529e-04 | 3.806 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 1.568945e-04 | 3.804 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 1.693001e-04 | 3.771 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 1.896021e-04 | 3.722 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.896589e-04 | 3.722 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 2.127614e-04 | 3.672 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 2.132499e-04 | 3.671 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 2.429008e-04 | 3.615 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.458443e-04 | 3.609 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 2.671437e-04 | 3.573 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 2.759937e-04 | 3.559 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 3.143696e-04 | 3.503 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 3.143696e-04 | 3.503 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 3.258633e-04 | 3.487 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 3.518091e-04 | 3.454 | 1 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 3.610493e-04 | 3.442 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 3.787808e-04 | 3.422 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 4.412142e-04 | 3.355 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 3.946464e-04 | 3.404 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 4.237520e-04 | 3.373 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 4.958137e-04 | 3.305 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 5.089880e-04 | 3.293 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 5.469134e-04 | 3.262 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 5.695189e-04 | 3.244 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 5.975690e-04 | 3.224 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 6.671208e-04 | 3.176 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 7.343705e-04 | 3.134 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 8.812803e-04 | 3.055 | 1 | 1 |
| Gap junction assembly | R-HSA-190861 | 8.830163e-04 | 3.054 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 8.830163e-04 | 3.054 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 1.026730e-03 | 2.989 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.028794e-03 | 2.988 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.028794e-03 | 2.988 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 1.051690e-03 | 2.978 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.051690e-03 | 2.978 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 1.103910e-03 | 2.957 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.145431e-03 | 2.941 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 1.232095e-03 | 2.909 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 1.232095e-03 | 2.909 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 1.232095e-03 | 2.909 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.345317e-03 | 2.871 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.368586e-03 | 2.864 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 1.428373e-03 | 2.845 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 1.550377e-03 | 2.810 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.570181e-03 | 2.804 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 1.665777e-03 | 2.778 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 1.691868e-03 | 2.772 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.771539e-03 | 2.752 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 1.804788e-03 | 2.744 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.819954e-03 | 2.740 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.819954e-03 | 2.740 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 2.102127e-03 | 2.677 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 2.194143e-03 | 2.659 | 0 | 0 |
| Nectin/Necl trans heterodimerization | R-HSA-420597 | 2.410191e-03 | 2.618 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 2.562356e-03 | 2.591 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 2.562356e-03 | 2.591 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 2.647472e-03 | 2.577 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 2.725717e-03 | 2.565 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 2.732410e-03 | 2.563 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 3.127088e-03 | 2.505 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 3.201232e-03 | 2.495 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 3.344389e-03 | 2.476 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 3.396695e-03 | 2.469 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 3.397339e-03 | 2.469 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 3.490032e-03 | 2.457 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 3.699595e-03 | 2.432 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 3.732625e-03 | 2.428 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 3.732625e-03 | 2.428 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 3.931444e-03 | 2.405 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 3.975143e-03 | 2.401 | 0 | 0 |
| Protein folding | R-HSA-391251 | 4.130061e-03 | 2.384 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 4.623182e-03 | 2.335 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 4.821436e-03 | 2.317 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.859211e-03 | 2.313 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 4.859211e-03 | 2.313 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 5.039561e-03 | 2.298 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 5.795268e-03 | 2.237 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 6.851169e-03 | 2.164 | 0 | 0 |
| Positive Regulation of CDH1 Gene Transcription | R-HSA-9764790 | 7.987397e-03 | 2.098 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 7.673739e-03 | 2.115 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 7.987397e-03 | 2.098 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 6.851169e-03 | 2.164 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 7.020198e-03 | 2.154 | 0 | 0 |
| Kinesins | R-HSA-983189 | 5.409717e-03 | 2.267 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 5.648826e-03 | 2.248 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 8.839666e-03 | 2.054 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 9.047370e-03 | 2.043 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 9.202236e-03 | 2.036 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 9.202236e-03 | 2.036 | 1 | 1 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.013306e-02 | 1.994 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.013306e-02 | 1.994 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.013306e-02 | 1.994 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.013306e-02 | 1.994 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.013306e-02 | 1.994 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.013306e-02 | 1.994 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 1.024871e-02 | 1.989 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 1.049400e-02 | 1.979 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.062199e-02 | 1.974 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.186101e-02 | 1.926 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.186101e-02 | 1.926 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.186101e-02 | 1.926 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 1.252245e-02 | 1.902 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 1.252245e-02 | 1.902 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.266431e-02 | 1.897 | 1 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.287175e-02 | 1.890 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.341878e-02 | 1.872 | 1 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 1.363431e-02 | 1.865 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 1.414200e-02 | 1.849 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 1.414200e-02 | 1.849 | 0 | 0 |
| Regulation of CDH1 mRNA translation by microRNAs | R-HSA-9764562 | 1.481429e-02 | 1.829 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 1.671698e-02 | 1.777 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 1.729812e-02 | 1.762 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.804926e-02 | 1.744 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.824817e-02 | 1.739 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.824817e-02 | 1.739 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.824817e-02 | 1.739 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.824817e-02 | 1.739 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 1.837560e-02 | 1.736 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 1.976848e-02 | 1.704 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 1.976848e-02 | 1.704 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 2.099671e-02 | 1.678 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 2.104957e-02 | 1.677 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.155350e-02 | 1.666 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.155350e-02 | 1.666 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.196057e-02 | 1.658 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.340282e-02 | 1.631 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition | R-HSA-9926550 | 2.340282e-02 | 1.631 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 2.353317e-02 | 1.628 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 2.395984e-02 | 1.621 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 2.452927e-02 | 1.610 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 2.466598e-02 | 1.608 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.531498e-02 | 1.597 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.531498e-02 | 1.597 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 2.605449e-02 | 1.584 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 2.677436e-02 | 1.572 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.728852e-02 | 1.564 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.728852e-02 | 1.564 | 0 | 0 |
| Formation of definitive endoderm | R-HSA-9823730 | 2.728852e-02 | 1.564 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 2.754920e-02 | 1.560 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 2.764990e-02 | 1.558 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 2.824434e-02 | 1.549 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 2.824434e-02 | 1.549 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 2.913883e-02 | 1.536 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 2.932202e-02 | 1.533 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.954588e-02 | 1.530 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.009404e-02 | 1.522 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 3.052909e-02 | 1.515 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 3.141409e-02 | 1.503 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 3.141409e-02 | 1.503 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.141409e-02 | 1.503 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.141409e-02 | 1.503 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 3.237610e-02 | 1.490 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 3.356333e-02 | 1.474 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 3.473101e-02 | 1.459 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 3.533659e-02 | 1.452 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 3.538161e-02 | 1.451 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 3.603411e-02 | 1.443 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 3.992398e-02 | 1.399 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 3.992398e-02 | 1.399 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 3.992398e-02 | 1.399 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 3.992398e-02 | 1.399 | 0 | 0 |
| Axonal growth stimulation | R-HSA-209563 | 4.965490e-02 | 1.304 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 5.928778e-02 | 1.227 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 6.882362e-02 | 1.162 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 7.826337e-02 | 1.106 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 7.826337e-02 | 1.106 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 6.334074e-02 | 1.198 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 7.178910e-02 | 1.144 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 6.611722e-02 | 1.180 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 3.926637e-02 | 1.406 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 7.031038e-02 | 1.153 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 5.265721e-02 | 1.279 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 4.765589e-02 | 1.322 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 4.765589e-02 | 1.322 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 5.265721e-02 | 1.279 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 6.611722e-02 | 1.180 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 7.826337e-02 | 1.106 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 3.992398e-02 | 1.399 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 4.965490e-02 | 1.304 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 4.512047e-02 | 1.346 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 6.893370e-02 | 1.162 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 5.791223e-02 | 1.237 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 5.791223e-02 | 1.237 | 0 | 0 |
| NADE modulates death signalling | R-HSA-205025 | 5.928778e-02 | 1.227 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 4.034068e-02 | 1.394 | 0 | 0 |
| Histamine receptors | R-HSA-390650 | 4.965490e-02 | 1.304 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 5.825363e-02 | 1.235 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 5.928778e-02 | 1.227 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 6.882362e-02 | 1.162 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 6.882362e-02 | 1.162 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 6.697418e-02 | 1.174 | 0 | 0 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | R-HSA-9758919 | 7.826337e-02 | 1.106 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 7.826337e-02 | 1.106 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 5.845959e-02 | 1.233 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 6.008971e-02 | 1.221 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 5.215448e-02 | 1.283 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 5.526246e-02 | 1.258 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 6.060537e-02 | 1.217 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 4.335876e-02 | 1.363 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 7.761243e-02 | 1.110 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 5.063278e-02 | 1.296 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 7.447876e-02 | 1.128 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 5.265721e-02 | 1.279 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.178910e-02 | 1.144 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 7.673590e-02 | 1.115 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 7.495839e-02 | 1.125 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 8.057827e-02 | 1.094 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 8.340197e-02 | 1.079 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 8.357886e-02 | 1.078 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 8.760801e-02 | 1.057 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 8.760801e-02 | 1.057 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 8.760801e-02 | 1.057 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 8.760801e-02 | 1.057 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 8.779225e-02 | 1.057 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 8.894132e-02 | 1.051 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 8.980352e-02 | 1.047 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 9.229260e-02 | 1.035 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 9.590910e-02 | 1.018 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 9.685848e-02 | 1.014 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 9.685848e-02 | 1.014 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 9.685848e-02 | 1.014 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 9.685848e-02 | 1.014 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 9.859199e-02 | 1.006 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 9.906883e-02 | 1.004 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 9.906883e-02 | 1.004 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.000328e-01 | 1.000 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 1.022576e-01 | 0.990 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 1.022576e-01 | 0.990 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 1.054744e-01 | 0.977 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 1.060157e-01 | 0.975 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 1.060157e-01 | 0.975 | 0 | 0 |
| Axonal growth inhibition (RHOA activation) | R-HSA-193634 | 1.060157e-01 | 0.975 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.060157e-01 | 0.975 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 1.119889e-01 | 0.951 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.119889e-01 | 0.951 | 0 | 0 |
| p75NTR regulates axonogenesis | R-HSA-193697 | 1.150807e-01 | 0.939 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.150807e-01 | 0.939 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.150807e-01 | 0.939 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.150807e-01 | 0.939 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 1.150807e-01 | 0.939 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 1.150807e-01 | 0.939 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.152848e-01 | 0.938 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.152848e-01 | 0.938 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 1.163789e-01 | 0.934 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.224729e-01 | 0.912 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.224729e-01 | 0.912 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.240543e-01 | 0.906 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.240543e-01 | 0.906 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.240543e-01 | 0.906 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.240543e-01 | 0.906 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 1.247050e-01 | 0.904 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 1.247050e-01 | 0.904 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 1.321175e-01 | 0.879 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.329374e-01 | 0.876 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.329374e-01 | 0.876 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.329374e-01 | 0.876 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 1.337788e-01 | 0.874 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 1.390005e-01 | 0.857 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.417310e-01 | 0.849 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.424711e-01 | 0.846 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.454323e-01 | 0.837 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 1.459600e-01 | 0.836 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.478024e-01 | 0.830 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.478024e-01 | 0.830 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 1.494667e-01 | 0.825 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.504360e-01 | 0.823 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.504360e-01 | 0.823 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.504360e-01 | 0.823 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.504360e-01 | 0.823 | 0 | 0 |
| AKT phosphorylates targets in the cytosol | R-HSA-198323 | 1.504360e-01 | 0.823 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 1.525800e-01 | 0.817 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 1.565301e-01 | 0.805 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.590532e-01 | 0.798 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.590532e-01 | 0.798 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.590532e-01 | 0.798 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.590532e-01 | 0.798 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.590532e-01 | 0.798 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.590532e-01 | 0.798 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.590532e-01 | 0.798 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 1.600855e-01 | 0.796 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.636558e-01 | 0.786 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.675835e-01 | 0.776 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.675835e-01 | 0.776 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.675835e-01 | 0.776 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.675835e-01 | 0.776 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 1.696087e-01 | 0.771 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.721606e-01 | 0.764 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 1.732086e-01 | 0.761 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.760279e-01 | 0.754 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.760279e-01 | 0.754 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.760279e-01 | 0.754 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 1.760279e-01 | 0.754 | 0 | 0 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 1.760279e-01 | 0.754 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.760279e-01 | 0.754 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.760279e-01 | 0.754 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.760279e-01 | 0.754 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 1.817081e-01 | 0.741 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.843870e-01 | 0.734 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.843870e-01 | 0.734 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 1.843870e-01 | 0.734 | 0 | 0 |
| KSRP (KHSRP) binds and destabilizes mRNA | R-HSA-450604 | 1.843870e-01 | 0.734 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.843870e-01 | 0.734 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 1.853543e-01 | 0.732 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.907133e-01 | 0.720 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 1.926619e-01 | 0.715 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 1.926777e-01 | 0.715 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 1.963537e-01 | 0.707 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 1.963537e-01 | 0.707 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 2.000385e-01 | 0.699 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.008534e-01 | 0.697 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.008534e-01 | 0.697 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.008534e-01 | 0.697 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.008534e-01 | 0.697 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 2.040832e-01 | 0.690 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 2.074324e-01 | 0.683 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.089622e-01 | 0.680 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.089622e-01 | 0.680 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 2.089622e-01 | 0.680 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.169892e-01 | 0.664 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.169892e-01 | 0.664 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.169892e-01 | 0.664 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.169892e-01 | 0.664 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 2.169892e-01 | 0.664 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 2.185756e-01 | 0.660 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 2.212516e-01 | 0.655 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.249353e-01 | 0.648 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.249353e-01 | 0.648 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.249353e-01 | 0.648 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 2.297696e-01 | 0.639 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.328012e-01 | 0.633 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.328012e-01 | 0.633 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.328012e-01 | 0.633 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.405878e-01 | 0.619 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 2.405878e-01 | 0.619 | 0 | 0 |
| Ribavirin ADME | R-HSA-9755088 | 2.405878e-01 | 0.619 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 2.428066e-01 | 0.615 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 2.447516e-01 | 0.611 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.482959e-01 | 0.605 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.482959e-01 | 0.605 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 2.493437e-01 | 0.603 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 2.506935e-01 | 0.601 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 2.534097e-01 | 0.596 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 2.559261e-01 | 0.592 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 2.559261e-01 | 0.592 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.559261e-01 | 0.592 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.559261e-01 | 0.592 | 0 | 0 |
| Constitutive Signaling by AKT1 E17K in Cancer | R-HSA-5674400 | 2.559261e-01 | 0.592 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 2.559261e-01 | 0.592 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 2.597718e-01 | 0.585 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.634794e-01 | 0.579 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.634794e-01 | 0.579 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.634794e-01 | 0.579 | 0 | 0 |
| Mitochondrial RNA degradation | R-HSA-9836573 | 2.634794e-01 | 0.579 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 2.670520e-01 | 0.573 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 2.671097e-01 | 0.573 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.709565e-01 | 0.567 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.709565e-01 | 0.567 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.709565e-01 | 0.567 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.709565e-01 | 0.567 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 2.722407e-01 | 0.565 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.783581e-01 | 0.555 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 2.783581e-01 | 0.555 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.783581e-01 | 0.555 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 2.823158e-01 | 0.549 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 2.856850e-01 | 0.544 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 2.856850e-01 | 0.544 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 2.856850e-01 | 0.544 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 2.856850e-01 | 0.544 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 2.856850e-01 | 0.544 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 2.860698e-01 | 0.544 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 2.860698e-01 | 0.544 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 2.898218e-01 | 0.538 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 2.929380e-01 | 0.533 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 2.929380e-01 | 0.533 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 2.929380e-01 | 0.533 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 2.929380e-01 | 0.533 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 3.001178e-01 | 0.523 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.001178e-01 | 0.523 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.001178e-01 | 0.523 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.001178e-01 | 0.523 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.001178e-01 | 0.523 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.072251e-01 | 0.513 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.072251e-01 | 0.513 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.072251e-01 | 0.513 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.072251e-01 | 0.513 | 0 | 0 |
| Translation | R-HSA-72766 | 3.102714e-01 | 0.508 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 3.122754e-01 | 0.505 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.142607e-01 | 0.503 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.142607e-01 | 0.503 | 0 | 0 |
| Trafficking of AMPA receptors | R-HSA-399719 | 3.142607e-01 | 0.503 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 3.142607e-01 | 0.503 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 3.142607e-01 | 0.503 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 3.212253e-01 | 0.493 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 3.271650e-01 | 0.485 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.271650e-01 | 0.485 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.281195e-01 | 0.484 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.281195e-01 | 0.484 | 0 | 0 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | R-HSA-399721 | 3.281195e-01 | 0.484 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 3.281195e-01 | 0.484 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 3.349442e-01 | 0.475 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.349442e-01 | 0.475 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.416999e-01 | 0.466 | 0 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 3.416999e-01 | 0.466 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.416999e-01 | 0.466 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 3.419694e-01 | 0.466 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.483875e-01 | 0.458 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.483875e-01 | 0.458 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 3.483875e-01 | 0.458 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.483875e-01 | 0.458 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 3.483875e-01 | 0.458 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 3.530066e-01 | 0.452 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 3.603296e-01 | 0.443 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 3.603296e-01 | 0.443 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 3.605553e-01 | 0.443 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 3.615606e-01 | 0.442 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 3.615606e-01 | 0.442 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 3.676222e-01 | 0.435 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.680476e-01 | 0.434 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 3.680476e-01 | 0.434 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.680476e-01 | 0.434 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 3.693396e-01 | 0.433 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 3.744691e-01 | 0.427 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.744691e-01 | 0.427 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 3.744691e-01 | 0.427 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.744691e-01 | 0.427 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 3.744691e-01 | 0.427 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 3.785005e-01 | 0.422 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 3.785005e-01 | 0.422 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 3.808257e-01 | 0.419 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 3.808257e-01 | 0.419 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 3.808257e-01 | 0.419 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 3.808257e-01 | 0.419 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 3.808257e-01 | 0.419 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 3.857099e-01 | 0.414 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 3.859745e-01 | 0.413 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 3.871181e-01 | 0.412 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 3.871181e-01 | 0.412 | 0 | 0 |
| Purine ribonucleoside monophosphate biosynthesis | R-HSA-73817 | 3.871181e-01 | 0.412 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 3.871181e-01 | 0.412 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 3.871181e-01 | 0.412 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 3.933470e-01 | 0.405 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 3.940594e-01 | 0.404 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 3.995129e-01 | 0.398 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 3.995216e-01 | 0.398 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 4.000190e-01 | 0.398 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.056165e-01 | 0.392 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.056165e-01 | 0.392 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 4.071158e-01 | 0.390 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 4.116585e-01 | 0.385 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.116585e-01 | 0.385 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.116585e-01 | 0.385 | 0 | 0 |
| Amine ligand-binding receptors | R-HSA-375280 | 4.116585e-01 | 0.385 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.176394e-01 | 0.379 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 4.176394e-01 | 0.379 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 4.211872e-01 | 0.376 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 4.235599e-01 | 0.373 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.235599e-01 | 0.373 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.235599e-01 | 0.373 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 4.235599e-01 | 0.373 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 4.235599e-01 | 0.373 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 4.281594e-01 | 0.368 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 4.350877e-01 | 0.361 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.352220e-01 | 0.361 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.352220e-01 | 0.361 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.352220e-01 | 0.361 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 4.373418e-01 | 0.359 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.578473e-01 | 0.339 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 4.578473e-01 | 0.339 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 4.578473e-01 | 0.339 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 4.578473e-01 | 0.339 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 4.611891e-01 | 0.336 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 4.633614e-01 | 0.334 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 4.633614e-01 | 0.334 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 4.633614e-01 | 0.334 | 0 | 0 |
| Nucleotide biosynthesis | R-HSA-8956320 | 4.633614e-01 | 0.334 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 4.688197e-01 | 0.329 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 4.714674e-01 | 0.327 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 4.742229e-01 | 0.324 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 4.795715e-01 | 0.319 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 4.795715e-01 | 0.319 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 4.848659e-01 | 0.314 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 4.855526e-01 | 0.314 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 4.952948e-01 | 0.305 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 4.952948e-01 | 0.305 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 5.004303e-01 | 0.301 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 5.017500e-01 | 0.300 | 0 | 0 |
| S Phase | R-HSA-69242 | 5.049503e-01 | 0.297 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 5.049503e-01 | 0.297 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.055138e-01 | 0.296 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 5.092955e-01 | 0.293 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.105459e-01 | 0.292 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.113111e-01 | 0.291 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 5.122668e-01 | 0.291 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 5.144715e-01 | 0.289 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.155271e-01 | 0.288 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.155271e-01 | 0.288 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.176185e-01 | 0.286 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 5.176185e-01 | 0.286 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 5.204580e-01 | 0.284 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.204580e-01 | 0.284 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.269786e-01 | 0.278 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 5.331508e-01 | 0.273 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 5.347047e-01 | 0.272 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.349532e-01 | 0.272 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.362163e-01 | 0.271 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.396875e-01 | 0.268 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 5.490128e-01 | 0.260 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 5.536048e-01 | 0.257 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.536048e-01 | 0.257 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.581503e-01 | 0.253 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.581503e-01 | 0.253 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 5.586903e-01 | 0.253 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.626499e-01 | 0.250 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 5.635888e-01 | 0.249 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.671039e-01 | 0.246 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 5.758770e-01 | 0.240 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 5.833766e-01 | 0.234 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 5.833766e-01 | 0.234 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 5.844735e-01 | 0.233 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 5.887065e-01 | 0.230 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 5.890104e-01 | 0.230 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 5.928967e-01 | 0.227 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 6.001348e-01 | 0.222 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.011502e-01 | 0.221 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.092374e-01 | 0.215 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 6.137116e-01 | 0.212 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 6.171616e-01 | 0.210 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 6.171616e-01 | 0.210 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 6.242676e-01 | 0.205 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 6.249260e-01 | 0.204 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 6.362802e-01 | 0.196 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 6.372623e-01 | 0.196 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.399885e-01 | 0.194 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.436592e-01 | 0.191 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.579737e-01 | 0.182 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 6.579737e-01 | 0.182 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 6.614621e-01 | 0.179 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.614621e-01 | 0.179 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 6.621024e-01 | 0.179 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.649151e-01 | 0.177 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 6.649151e-01 | 0.177 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 6.683332e-01 | 0.175 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 6.683332e-01 | 0.175 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 6.717165e-01 | 0.173 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 6.783807e-01 | 0.169 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 6.816622e-01 | 0.166 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 6.816622e-01 | 0.166 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 6.881257e-01 | 0.162 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 6.913084e-01 | 0.160 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 6.975772e-01 | 0.156 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.006640e-01 | 0.154 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.037194e-01 | 0.153 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 7.155828e-01 | 0.145 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.270730e-01 | 0.138 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 7.364779e-01 | 0.133 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 7.380542e-01 | 0.132 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.380542e-01 | 0.132 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 7.433790e-01 | 0.129 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.485962e-01 | 0.126 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 7.520619e-01 | 0.124 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.562249e-01 | 0.121 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 7.562249e-01 | 0.121 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 7.800305e-01 | 0.108 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 7.800305e-01 | 0.108 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 7.953050e-01 | 0.099 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 7.973993e-01 | 0.098 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 8.243388e-01 | 0.084 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.367750e-01 | 0.077 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 8.384473e-01 | 0.077 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 8.449677e-01 | 0.073 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 8.557553e-01 | 0.068 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 8.572342e-01 | 0.067 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.572342e-01 | 0.067 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 8.801897e-01 | 0.055 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 8.844422e-01 | 0.053 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 8.875273e-01 | 0.052 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.015284e-01 | 0.045 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.247374e-01 | 0.034 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.443140e-01 | 0.025 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.459686e-01 | 0.024 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.532713e-01 | 0.021 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 9.551713e-01 | 0.020 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.845014e-01 | 0.007 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.861844e-01 | 0.006 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.879406e-01 | 0.005 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.879406e-01 | 0.005 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.964332e-01 | 0.002 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.967052e-01 | 0.001 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.982237e-01 | 0.001 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.986936e-01 | 0.001 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.999734e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999999e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000e+00 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
