EPHA2
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 |
|---|---|---|---|---|
| A0FGR8 | Y824 | Sugiyama | ESYT2 FAM62B KIAA1228 | IVVVHACRNLIAFSEDGsDPyVRMYLLPDKRRSGRRKTHVS |
| A0MZ66 | Y24 | Sugiyama | SHTN1 KIAA1598 | sDEEKQLQLITsLKEQAIGEyEDLRAENQKTKEKCDKIRQE |
| A1X283 | Y855 | Sugiyama | SH3PXD2B FAD49 KIAA1295 TKS4 | NREKAAAASVPNADGLKDSLyVAVADFEGDKDTSSFQEGTV |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y1572 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | RMPEQIRLKVGGVDPKQLAVyEEFARNVPGFLPTNDLSQPT |
| A6NEC2 | Y173 | Sugiyama | NPEPPSL1 | NDKMKGFYRSKYTTPSGEVRyAAVTQFEATDARRAFPCWDE |
| A6NHL2 | Y319 | Sugiyama | TUBAL3 | TTACFESSNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAI |
| A6NMY6 | Y147 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| O00116 | Y645 | Sugiyama | AGPS AAG5 | QWLKESIsDVGFGMLKSVKEyVDPNNIFGNRNLL_______ |
| O00232 | S21 | Sugiyama | PSMD12 | MADGGSERADGRIVKMEVDysATVDQRLPECAKLAKEGRLQ |
| O00232 | Y20 | Sugiyama | PSMD12 | _MADGGSERADGRIVKMEVDysATVDQRLPECAKLAKEGRL |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00264 | Y113 | Sugiyama | PGRMC1 HPR6.6 PGRMC | INGKVFDVTKGRKFyGPEGPyGVFAGRDASRGLATFCLDKE |
| O00264 | Y180 | Sugiyama | PGRMC1 HPR6.6 PGRMC | FTFKYHHVGKLLKEGEEPtVysDEEEPKDEsARKND_____ |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00410 | Y33 | Sugiyama | IPO5 KPNB3 RANBP5 | LLLGNLLsPDNVVRKQAEEtyENIPGQSKITFLLQAIRNTT |
| O00410 | Y820 | Sugiyama | IPO5 KPNB3 RANBP5 | KLEEHFKNQELRQVKRQDEDyDEQVEEsLQDEDDNDVyILT |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00469 | S441 | Sugiyama | PLOD2 | HGKLWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYM |
| O00469 | Y444 | Sugiyama | PLOD2 | LWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYMANV |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O14493 | Y208 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CLDN4 CPER CPETR1 WBSCR8 | RtDKPYsAKYSAARsAAAsNyV___________________ |
| O14579 | Y304 | Sugiyama | COPE | HPFIKEYQAKENDFDRLVLQyAPsA________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14602 | Y35 | Sugiyama | EIF1AY | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEALCFDGV |
| O14818 | T147 | Sugiyama | PSMA7 HSPC | FGISALIVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKS |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| O14818 | Y176 | Sugiyama | PSMA7 HSPC | WKANAIGRGAKSVREFLEKNyTDEAIETDDLTIKLVIKALL |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14950 | Y143 | Sugiyama | MYL12B MRLC2 MYLC2B | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14964 | Y216 | Sugiyama | HGS HRS | KYSTIPKFGIEKEVRVCEPCyEQLNRKAEGKAtsttELPPE |
| O14974 | Y911 | Sugiyama | PPP1R12A MBS MYPT1 | ETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDSTD |
| O14979 | Y167 | Sugiyama | HNRNPDL HNRPDL JKTBP | DGKMFIGGLSWDTsKKDLtEyLSRFGEVVDCtIKTDPVTGR |
| O14980 | Y463 | Sugiyama | XPO1 CRM1 | EFMKDTDsINLyKNMRETLVyLTHLDyVDTERIMTEKLHNQ |
| O14980 | Y469 | Sugiyama | XPO1 CRM1 | DsINLyKNMRETLVyLTHLDyVDTERIMTEKLHNQVNGTEW |
| O15013 | Y1307 | Sugiyama | ARHGEF10 KIAA0294 | sLsLsHGsssLEHRSEDsTIyDLLKDPVSLRSKARRAKKAK |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15173 | Y210 | Sugiyama | PGRMC2 DG6 PMBP | FKEKYDYVGRLLKPGEEPsEytDEEDtKDHNKQD_______ |
| O15230 | Y81 | Sugiyama | LAMA5 KIAA0533 KIAA1907 | SATCGEEAPARGSPRPTEDLyCKLVGGPVAGGDPNQTIRGQ |
| O15270 | Y557 | Sugiyama | SPTLC2 KIAA0526 LCB2 | LKYSRHRLVPLLDRPFDETTyEEtED_______________ |
| O15357 | Y886 | Sugiyama | INPPL1 SHIP2 | IRGSMKVRVPTERLGTRERLyEWISIDKDEAGAKSKAPSVS |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15372 | Y350 | Sugiyama | EIF3H EIF3S3 | IKEFTAQNLGKLFMAQALQEyNN__________________ |
| O15397 | Y598 | Sugiyama | IPO8 RANBP8 | AVDMTQHLAEIFGKVLQsDEyEEVEDKTVMAMGILHTIDTI |
| O15460 | Y342 | Sugiyama | P4HA2 UNQ290/PRO330 | LLIAPFKEEDEWDSPHIVRYyDVMsDEEIERIKEIAKPKLA |
| O43164 | Y63 | Sugiyama | PJA2 KIAA0438 RNF131 | VSFKPCMTRHERSLGRAGDDyEVLELDDVPKENssGssPLD |
| O43237 | Y184 | Sugiyama | DYNC1LI2 DNCLI2 LIC2 | KIPPEKMRELERKFVKDFQDyMEPEEGCQGsPQRRGPLtsG |
| O43252 | Y617 | Sugiyama | PAPSS1 ATPSK1 PAPSS | EGQKPPEGFMAPKAWtVLtEyyKSLEKA_____________ |
| O43252 | Y618 | Sugiyama | PAPSS1 ATPSK1 PAPSS | GQKPPEGFMAPKAWtVLtEyyKSLEKA______________ |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y177 | Sugiyama | HNRNPR HNRPR | SGVQPGIGTEVFVGKIPRDLyEDELVPLFEKAGPIWDLRLM |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43390 | Y434 | Sugiyama | HNRNPR HNRPR | KKRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGG |
| O43390 | Y435 | Sugiyama | HNRNPR HNRPR | KRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGGR |
| O43464 | Y147 | Sugiyama | HTRA2 OMI PRSS25 | GPPAVLAAVPSPPPAsPRSQyNFIADVVEKTAPAVVYIEIL |
| O43707 | Y212 | Sugiyama | ACTN4 | WKDGLAFNALIHRHRPELIEyDKLRKDDPVTNLNNAFEVAE |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y298 | Sugiyama | ACTN4 | ANRICKVLAVNQENEHLMEDyEKLASDLLEWIRRTIPWLED |
| O43707 | Y338 | Sugiyama | ACTN4 | DRVPQKTIQEMQQKLEDFRDyRRVHKPPKVQEKCQLEINFN |
| O43707 | Y397 | Sugiyama | ACTN4 | GKMVSDINNGWQHLEQAEKGyEEWLLNEIRRLERLDHLAEK |
| O43707 | Y441 | Sugiyama | ACTN4 | KAsIHEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEs |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43765 | Y195 | Sugiyama | SGTA SGT SGT1 | HVEAVAYYKKALELDPDNEtyKsNLKIAELKLREAPSPTGG |
| O43795 | Y234 | Sugiyama | MYO1B | GASEELLNKLKLERDFSRyNyLSLDSAKVNGVDDAANFRTV |
| O43823 | Y311 | Sugiyama | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| O43837 | Y171 | Sugiyama | IDH3B | YMTRHNNLDLVIIREQtEGEySsLEHESARGVIECLKIVTR |
| O43852 | S219 | Sugiyama | CALU | DIDKNADGFIDLEEyIGDMysHDGNtDEPEWVKTEREQFVE |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y129 | Sugiyama | CALU | VERQWKGHDLNEDGLVsWEEyKNATYGYVLDDPDPDDGFNY |
| O43852 | Y185 | Sugiyama | CALU | KDGDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNAD |
| O43852 | Y187 | Sugiyama | CALU | GDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNADGF |
| O43852 | Y213 | Sugiyama | CALU | VQEtMEDIDKNADGFIDLEEyIGDMysHDGNtDEPEWVKTE |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O43865 | Y291 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDVMFGG |
| O43865 | Y527 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | LTDDQAKYLGLNKNGPFKPNyYRY_________________ |
| O60341 | Y494 | Sugiyama | KDM1A AOF2 KDM1 KIAA0601 LSD1 | ITAEFLVKSKHRDLTALCKEyDELAETQGKLEEKLQELEAN |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60488 | Y582 | Sugiyama | ACSL4 ACS4 FACL4 LACS4 | DGCLQIIDRKKDLVKLQAGEyVsLGKVEAALKNCPLIDNIC |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y293 | Sugiyama | SYNCRIP HNRPQ NSAP1 | VILyHQPDDKKKNRGFCFLEyEDHKTAAQARRRLMSGKVKV |
| O60506 | Y373 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ILEKAFsQFGKLERVKKLKDyAFIHFDERDGAVKAMEEMNG |
| O60506 | Y614 | Sugiyama | SYNCRIP HNRPQ NSAP1 | PLQGGDHSGNYGYKSENQEFyQDTFGQQWK___________ |
| O60568 | Y444 | Sugiyama | PLOD3 | LWSNFWGALSPDEYYARSEDyVELVQRKRVGVWNVPYISQA |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60739 | Y30 | Sugiyama | EIF1B | FDPFADATKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O75116 | Y722 | Sugiyama | ROCK2 KIAA0619 | EQEEAEHKATKARLADKNKIyEsIEEAKSEAMKEMEKKLLE |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75208 | Y93 | Sugiyama | COQ9 C16orf49 HSPC326 PSEC0129 | PEssHsPPRYTDQGGEEEEDyEsEEQLQHRILTAALEFVPA |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75347 | Y94 | Sugiyama | TBCA | AyLDLQRILENEKDLEEAEEyKEARLVLDsVKLEA______ |
| O75369 | Y1576 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYGG |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75369 | Y904 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | FNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLVTY |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75822 | Y254 | Sugiyama | EIF3J EIF3S1 PRO0391 | ATMKDDLADyGGyDGGyVQDyEDFM________________ |
| O75874 | Y391 | Sugiyama | IDH1 PICD | FMTKDLAACIKGLPNVQRsDyLNTFEFMDKLGENLKIKLAQ |
| O75962 | Y621 | Sugiyama | TRIO | HRARALQKRHEDFEEVAQNTyTNADKLLEAAEQLAQTGECD |
| O76003 | Y302 | Sugiyama | GLRX3 PICOT TXNL2 HUSSY-22 | DILEDEEVRQGLKAYSNWPTyPQLyVKGELVGGLDIVKELK |
| O76003 | Y306 | Sugiyama | GLRX3 PICOT TXNL2 HUSSY-22 | DEEVRQGLKAYSNWPTyPQLyVKGELVGGLDIVKELKENGE |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| O94919 | Y134 | Sugiyama | ENDOD1 KIAA0830 | EAEAITSVNSLGSKQALNtDyLDsDyQRGQLYPFSLSSDVQ |
| O94979 | Y489 | Sugiyama | SEC31A KIAA0905 SEC31L1 HSPC275 HSPC334 | FEKNVWSFLKVNFEDDSRGKyLELLGYRKEDLGKKIALALN |
| O95297 | Y263 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | QLDHsGGHHSDKINKSEsVVyADIRKN______________ |
| O95340 | Y182 | Sugiyama | PAPSS2 ATPSK2 | GLYKRARAGEIKGFTGIDsDyEKPEtPERVLKTNLSTVSDC |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95400 | Y340 | Sugiyama | CD2BP2 KIAA1178 | RKLDPPGGQFYNSKRIDFDLyT___________________ |
| O95551 | Y84 | Sugiyama | TDP2 EAP2 TTRAP AD-022 | PPVEESALERRPETISEPKTyVDLtNEEtTDsttsKISPSE |
| O95573 | Y591 | Sugiyama | ACSL3 ACS3 FACL3 LACS3 | DGCLKIIDRKKDLVKLQAGEyVsLGKVEAALKNLPLVDNIC |
| O95757 | Y600 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | IDLPIQssLCRQLGQDLLNsyIENEGKMIMQDKLEKERNDA |
| O95757 | Y627 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MIMQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPED |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O96007 | Y170 | Sugiyama | MOCS2 MCBPE MOCO1 | AVSYAIDTLKAKVPIWKKEIyEESSTWKGNKECFWASNs__ |
| 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 |
| P00491 | Y249 | Sugiyama | PNP NP | RHCGLRVFGFSLITNKVIMDyESLEKANHEEVLAAGKQAAQ |
| P00505 | Y96 | Sugiyama | GOT2 KYAT4 | VLPSVRKAEAQIAAKNLDKEyLPIGGLAEFCKASAELALGE |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00813 | Y290 | Sugiyama | ADA ADA1 | GAWKPDTEHAVIRLKNDQANysLNTDDPLIFKSTLDTDyQM |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P01111 | Y137 | Sugiyama | NRAS HRAS1 | KCDLPTRTVDTKQAHELAKSyGIPFIETSAKTRQGVEDAFy |
| P01116 | Y137 | Sugiyama | KRAS KRAS2 RASK2 | KCDLPSRTVDTKQAQDLARSyGIPFIEtSAKtRQRVEDAFY |
| P01893 | Y147 | Sugiyama | HLA-H HLAH | VGPDGPFLRGYEQHAYDGKDyIALNEDLRSWTAADMAAQIT |
| P02533 | S435 | Sugiyama | KRT14 | yRRLLEGEDAHLSSSQFSSGsQSSRDVTSSSRQIRTKVMDV |
| P02545 | Y211 | Sugiyama | LMNA LMN1 | VDAENRLQtMKEELDFQKNIysEELREtKRRHETRLVEIDN |
| P02786 | Y168 | Sugiyama | TFRC | NENsyVPREAGsQKDENLALyVENQFREFKLSKVWRDQHFV |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P04080 | Y97 | Sugiyama | CSTB CST6 STFB | NKPLtLsNyQTNKAKHDELtyF___________________ |
| P04083 | Y21 | Sugiyama | ANXA1 ANX1 LPC1 | MAMVsEFLKQAWFIENEEQEyVQtVKssKGGPGsAVsPyPt |
| P04181 | Y69 | Sugiyama | OAT | KyGAHNyHPLPVALERGKGIyLWDVEGRKYFDFLSSYSAVN |
| P04406 | Y314 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | tFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsK |
| P04406 | Y320 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsKE_____ |
| P04406 | Y94 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | ItIFQERDPsKIKWGDAGAEyVVEstGVFttMEKAGAHLQG |
| P04632 | Y87 | Sugiyama | CAPNS1 CAPN4 CAPNS | sAISEAAAQYNPEPPPPRtHysNIEANEsEEVRQFRRLFAQ |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P04818 | Y153 | Sugiyama | TYMS TS OK/SW-cl.29 | PVyGFQWRHFGAEyRDMEsDysGQGVDQLQRVIDTIKtNPD |
| P05023 | Y542 | Sugiyama | ATP1A1 | LLHGKEQPLDEELKDAFQNAyLELGGLGERVLGFCHLFLPD |
| P05067 | Y308 | Sugiyama | APP A4 AD1 | REVCSEQAETGPCRAMISRWyFDVTEGKCAPFFyGGCGGNR |
| P05783 | Y363 | Sugiyama | KRT18 CYK18 PIG46 | LHLESELAQTRAEGQRQAQEyEALLNIKVKLEAEIATYRRL |
| P05997 | Y1311 | Sugiyama | COL5A2 | HPARTCDDLKLCHSAKQsGEyWIDPNQGSVEDAIKVYCNME |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06730 | Y34 | Sugiyama | EIF4E EIF4EL1 EIF4F | PPttEEEKtEsNQEVANPEHyIKHPLQNRWALWFFKNDKsK |
| P06733 | S268 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyP |
| P06733 | Y131 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ILGVsLAVCKAGAVEKGVPLyRHIADLAGNsEVILPVPAFN |
| 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 | Y287 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | PsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDDWGAWQKF |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06737 | Y732 | Sugiyama | PYGL | FGMRIDDVAALDKKGYEAKEyyEALPELKLVIDQIDNGFFS |
| P06737 | Y733 | Sugiyama | PYGL | GMRIDDVAALDKKGYEAKEyyEALPELKLVIDQIDNGFFSP |
| P06737 | Y821 | Sugiyama | PYGL | MVLKNIAASGKFSSDRTIKEyAQNIWNVEPsDLKIsLSNES |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07195 | Y84 | Sugiyama | LDHB | MDLQHGsLFLQtPKIVADKDysVtANSKIVVVtAGVRQQEG |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07205 | Y196 | Sugiyama | PGK2 PGKB | MVGVNLPHKASGFLMKKELDyFAKALENPVRPFLAILGGAK |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07237 | Y99 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPKEytAG |
| P07355 | Y147 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07355 | Y199 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RAEDGsVIDyELIDQDARDLyDAGVKRKGTDVPKWIsIMTE |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | T107 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAESC |
| 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_________ |
| P07741 | Y60 | Sugiyama | APRT | RAAIGLLARHLKATHGGRIDyIAGLDsRGFLFGPSLAQELG |
| 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 | T65 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | LRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLIPNKQ |
| P07900 | Y160 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGEPM |
| P07900 | Y197 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | GEPMGRGTKVILHLKEDQtEyLEERRIKEIVKKHSQFIGyP |
| 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 |
| P07947 | Y426 | SIGNOR|PSP | YES1 YES | ENLVCKIADFGLARLIEDNEytARQGAKFPIKWTAPEAALy |
| P07954 | Y54 | Sugiyama | FH | PSFWPPNAARMAsQNSFRIEyDtFGELKVPNDKYYGAQTVR |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | T60 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | LRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDIIPNPQ |
| P08238 | Y155 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | SAYLVAEKVVVITKHNDDEQyAWEssAGGsFtVRADHGEPI |
| P08238 | Y192 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| 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 | Y430 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KKCLELFsELAEDKENyKKFyEAFSKNLKLGIHEDstNRRR |
| 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 |
| P08238 | Y619 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | TANMERIMKAQALRDNstMGyMMAKKHLEINPDHPIVEtLR |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| 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 | Y202 | Sugiyama | RPSA LAMBR LAMR1 | VLRMRGTISREHPWEVMPDLyFyRDPEEIEKEEQAAAEKAV |
| P09104 | T41 | Sugiyama | ENO2 | EVDLyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKG |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09234 | Y12 | Sugiyama | SNRPC | _________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKE |
| P09234 | Y8 | Sugiyama | SNRPC | _____________MPKFyCDyCDtyLtHDsPsVRKTHCSGR |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09874 | Y794 | Sugiyama | PARP1 ADPRT PPOL | AySLLRGGsDDssKDPIDVNyEKLKTDIKVVDRDSEEAEII |
| P09960 | Y233 | Sugiyama | LTA4H LTA4 | RQIGPRTLVWSEKEQVEKSAyEFsETEsMLKIAEDLGGPYV |
| P09972 | Y358 | Sugiyama | ALDOC ALDC | AAQGKYEGSGEDGGAAAQsLyIANHAY______________ |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0DPH7 | T225 | Sugiyama | TUBA3C TUBA2 | DNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRFD |
| P0DPH7 | Y224 | Sugiyama | TUBA3C TUBA2 | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| P10398 | S157 | Sugiyama | ARAF ARAF1 PKS PKS2 | SSKVPTVCVDMSTNRQQFyHsVQDLsGGsRQHEAPsNRPLN |
| P10398 | Y155 | Sugiyama | ARAF ARAF1 PKS PKS2 | HCSSKVPTVCVDMSTNRQQFyHsVQDLsGGsRQHEAPsNRP |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11047 | S348 | Sugiyama | LAMC1 LAMB2 | WRRAtAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCT |
| P11047 | Y352 | Sugiyama | LAMC1 LAMB2 | tAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQD |
| P11142 | S40 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P11142 | T427 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | GGVMTVLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGER |
| P11142 | Y443 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KQtQtFttysDNQPGVLIQVyEGERAMTKDNNLLGKFELTG |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11233 | Y153 | Sugiyama | RALA RAL | DKRQVsVEEAKNRAEQWNVNyVETSAKTRANVDKVFFDLMR |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11413 | Y112 | Sugiyama | G6PD | PEEKLKLEDFFARNsyVAGQyDDAAsyQRLNsHMNALHLGs |
| P11498 | Y834 | Sugiyama | PC | VACTRGTPLDTEVPMERVFDySEyWEGARGLYAAFDCTATM |
| P11498 | Y837 | Sugiyama | PC | TRGTPLDTEVPMERVFDySEyWEGARGLYAAFDCTATMKSG |
| P11940 | Y194 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLFGKF |
| P11940 | Y297 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLRKEFsPF |
| P12004 | Y250 | Sugiyama | PCNA | SADVPLVVEYKIADMGHLKyyLAPKIEDEEGs_________ |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12814 | Y193 | Sugiyama | ACTN1 | WKDGLGFCALIHRHRPELIDyGKLRKDDPLTNLNTAFDVAE |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y319 | Sugiyama | ACTN1 | NRVPENTMHAMQQKLEDFRDyRRLHKPPKVQEKCQLEINFN |
| P12814 | Y378 | Sugiyama | ACTN1 | GRMVSDINNAWGCLEQVEKGyEEWLLNEIRRLERLDHLAEK |
| P12814 | Y422 | Sugiyama | ACTN1 | KAsIHEAWtDGKEAMLRQKDyEtAtLsEIKALLKKHEAFEs |
| P12814 | Y842 | Sugiyama | ACTN1 | DTDTADQVMASFKILAGDKNyITMDELRRELPPDQAEyCIA |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | Y367 | Sugiyama | EEF2 EF2 | GDALLQMITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKs |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13667 | S135 | Sugiyama | PDIA4 ERP70 ERP72 | IPVAKIDAtsAsVLAsRFDVsGyPtIKILKKGQAVDyEGsR |
| P13667 | Y137 | Sugiyama | PDIA4 ERP70 ERP72 | VAKIDAtsAsVLAsRFDVsGyPtIKILKKGQAVDyEGsRtQ |
| P13667 | Y151 | Sugiyama | PDIA4 ERP70 ERP72 | RFDVsGyPtIKILKKGQAVDyEGsRtQEEIVAKVREVSQPD |
| P13667 | Y273 | Sugiyama | PDIA4 ERP70 ERP72 | PTLKIFRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTL |
| P13667 | Y278 | Sugiyama | PDIA4 ERP70 ERP72 | FRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTLKQVQE |
| P13667 | Y448 | Sugiyama | PDIA4 ERP70 ERP72 | RAATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLs |
| P13667 | Y458 | Sugiyama | PDIA4 ERP70 ERP72 | VLEVAKDFPEytFAIADEEDyAGEVKDLGLsEsGEDVNAAI |
| P13667 | Y565 | Sugiyama | PDIA4 ERP70 ERP72 | DVLIEFYAPWCGHCKQLEPVyNsLAKKYKGQKGLVIAKMDA |
| P13674 | Y141 | Sugiyama | P4HA1 P4HA | FPNDEDQVGAAKALLRLQDtyNLDTDtIsKGNLPGVKHKSF |
| P13674 | Y282 | Sugiyama | P4HA1 P4HA | ASDDQSDQKTTPKKKGVAVDyLPERQKyEMLCRGEGIKMTP |
| P13796 | Y462 | Sugiyama | LCP1 PLS2 | VNKPPYPKLGGNMKKLENCNyAVELGKNQAKFsLVGIGGQD |
| P13797 | Y465 | Sugiyama | PLS3 | VNKPPYPKLGANMKKLENCNyAVELGKHPAKFSLVGIGGQD |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13929 | T41 | Sugiyama | ENO3 | EVDLHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKG |
| P13929 | Y131 | Sugiyama | ENO3 | ILGVSLAVCKAGAAEKGVPLyRHIADLAGNPDLILPVPAFN |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14618 | Y148 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | GtAEVELKKGATLKITLDNAyMEKCDENILWLDYKNICKVV |
| P14618 | Y370 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | NAVLDGADCIMLSGEtAKGDyPLEAVRMQHLIAREAEAAIy |
| P14625 | Y258 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | GNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFINFP |
| P14625 | Y401 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | VTFKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDD |
| P14625 | Y429 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | IKLYVRRVFITDDFHDMMPKyLNFVKGVVDsDDLPLNVsRE |
| P14625 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14635 | Y175 | Sugiyama | CCNB1 CCNB | DVDAEDGADPNLCSEYVKDIyAYLRQLEEEQAVRPKYLLGR |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14854 | Y34 | Sugiyama | COX6B1 COX6B | TAPFDSRFPNQNQTRNCWQNyLDFHRCQKAMTAKGGDIsVC |
| P14866 | T282 | Sugiyama | HNRNPL HNRPL P/OKcl.14 | TLKIEYAKPTRLNVFKNDQDtWDyTNPNLsGQGDPGsNPNK |
| P14866 | Y92 | Sugiyama | HNRNPL HNRPL P/OKcl.14 | GGGGGGGGAGAAGGGGGGENyDDPHKtPAsPVVHIRGLIDG |
| P15121 | Y310 | Sugiyama | AKR1B1 ALDR1 ALR2 | LSYNRNWRVCALLSCTSHKDyPFHEEF______________ |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15311 | Y424 | Sugiyama | EZR VIL2 | ERQAVDQIKsQEQLAAELAEytAKIALLEEARRRKEDEVEE |
| P15374 | Y141 | Sugiyama | UCHL3 | KFLEEsVsMsPEERARyLENyDAIRVtHEtsAHEGQTEAPs |
| P15880 | S249 | Sugiyama | RPS2 RPS4 | CtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEF |
| P15880 | S264 | Sugiyama | RPS2 RPS4 | ISKTysyLtPDLWKEtVFtKsPyQEFtDHLVKtHtRVsVQR |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y266 | Sugiyama | RPS2 RPS4 | KTysyLtPDLWKEtVFtKsPyQEFtDHLVKtHtRVsVQRtQ |
| P16278 | Y444 | Sugiyama | GLB1 ELNR1 | QDCSNPAPLssPLNGVHDRAyVAVDGIPQGVLERNNVITLN |
| P17066 | S42 | Sugiyama | HSPA6 HSP70B' | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P17676 | Y137 | Sugiyama | CEBPB TCF5 PP9092 | FLSDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCF |
| P17706 | Y68 | Sugiyama | PTPN2 PTPT | YRDVSPYDHSRVKLQNAENDyINAsLVDIEEAQRSYILTQG |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17812 | Y473 | Sugiyama | CTPS1 CTPS | RRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVWKKCLE |
| P17812 | Y94 | Sugiyama | CTPS1 CTPS | YERFLDIRLTKDNNLTTGKIyQYVINKERKGDYLGKTVQVV |
| P17844 | Y244 | Sugiyama | DDX5 G17P1 HELR HLR1 | tPGRLIDFLECGKTNLRRTTyLVLDEADRMLDMGFEPQIRK |
| P17844 | Y416 | Sugiyama | DDX5 G17P1 HELR HLR1 | IATDVAsRGLDVEDVKFVINyDyPNSsEDyIHRIGRTARST |
| P17844 | Y425 | Sugiyama | DDX5 G17P1 HELR HLR1 | LDVEDVKFVINyDyPNSsEDyIHRIGRTARSTKtGtAytFF |
| P17844 | Y59 | Sugiyama | DDX5 G17P1 HELR HLR1 | EKLVKKKWNLDELPKFEKNFyQEHPDLARRtAQEVETYRRS |
| P17980 | Y185 | Sugiyama | PSMC3 TBP1 | PtEyDsRVKAMEVDERPtEQysDIGGLDKQIQELVEAIVLP |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18124 | Y155 | Sugiyama | RPL7 | IVEPYIAWGYPNLKsVNELIyKRGYGKINKKRIALtDNALI |
| P18124 | Y82 | Sugiyama | RPL7 | RQMYRTEIRMARMARKAGNFyVPAEPKLAFVIRIRGINGVS |
| P18206 | Y822 | Sugiyama | VCL | KAVAGNIsDPGLQKsFLDsGyRILGAVAKVREAFQPQEPDF |
| P18615 | Y133 | Sugiyama | NELFE RD RDBP | sIsADDDLQEsSRRPQRKsLyEsFVsssDRLRELGPDGEEA |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18669 | S134 | Sugiyama | PGAM1 PGAMA CDABP0006 | IWRRsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCE |
| 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 | Y142 | Sugiyama | MYL12A MLCB MRLC3 RLC | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19338 | Y462 | Sugiyama | NCL | AEKTFEEKQGtEIDGRsIsLyytGEKGQNQDYRGGKNSTWs |
| P19387 | Y208 | Sugiyama | POLR2C A-152E5.7 | PDNALRHTVYPKPEEWPKSEySELDEDESQAPYDPNGKPER |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | S157 | Sugiyama | PSMB1 PSC5 | IIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLL |
| P20618 | T217 | Sugiyama | PSMB1 PSC5 | DRAMRLVKDVFISAAERDVytGDALRICIVTKEGIREETVS |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21127 | Y449 | Sugiyama | CDK11B CDC2L1 CDK11 PITSLREA PK58 | LQGCRsVEEFQCLNRIEEGtyGVVYRAKDKKTDEIVALKRL |
| P21333 | Y319 | Sugiyama | FLNA FLN FLN1 | KKRAEFTVETRsAGQGEVLVyVEDPAGHQEEAKVTANNDKN |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P22059 | Y456 | Sugiyama | OSBP OSBP1 | MPVNFNEPLSMLQRLTEDLEyHELLDRAAKCENSLEQLCYV |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22314 | Y60 | Sugiyama | UBA1 A1S9T UBE1 | GMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSVLVSGL |
| P22314 | Y873 | Sugiyama | UBA1 A1S9T UBE1 | DDSNFHMDFIVAASNLRAENyDIPsADRHKSKLIAGKIIPA |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22626 | Y336 | Sugiyama | HNRNPA2B1 HNRPA2B1 | MKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRsRy___ |
| 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 |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | Y140 | Sugiyama | CFL1 CFL | SKDAIKKKLtGIKHELQANCyEEVKDRCTLAEKLGGsAVIs |
| P23528 | Y68 | Sugiyama | CFL1 CFL | ILEEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAt |
| P23528 | Y82 | Sugiyama | CFL1 CFL | QtVDDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFI |
| P23528 | Y85 | Sugiyama | CFL1 CFL | DDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWA |
| P23528 | Y89 | Sugiyama | CFL1 CFL | AtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| P23588 | Y609 | Sugiyama | EIF4B | sASKyAALsVDGEDENEGEDyAE__________________ |
| P23921 | Y232 | Sugiyama | RRM1 RR1 | RPQLSSCFLLSMKDDSIEGIyDTLKQCALISKSAGGIGVAV |
| P23921 | Y556 | Sugiyama | RRM1 RR1 | yyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPT |
| P23921 | Y74 | Sugiyama | RRM1 RR1 | VELDTLAAETAATLTTKHPDyAILAARIAVSNLHKETKKVF |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P25205 | Y19 | Sugiyama | MCM3 | __MAGtVVLDDVELREAQRDyLDFLDDEEDQGIyQsKVREL |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y456 | Sugiyama | MCM3 | AGIHARLNARCsVLAAANPVyGRyDQyKTPMENIGLQDSLL |
| P25208 | Y58 | Sugiyama | NFYB HAP3 | SMNDHEDTNGSKESFREQDIyLPIANVARIMKNAIPQTGKI |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P25787 | Y57 | Sugiyama | PSMA2 HC3 PSC3 | GIKAANGVVLATEKKQKSILyDERSVHKVEPITKHIGLVys |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26599 | Y127 | Sugiyama | PTBP1 PTB | ANTMVNYYTSVTPVLRGQPIyIQFsNHKELKtDSSPNQARA |
| P26640 | Y601 | Sugiyama | VARS1 G7A VARS VARS2 | VDMDFGTGAVKITPAHDQNDyEVGQRHGLEAIsIMDsRGAL |
| P26885 | Y112 | Sugiyama | FKBP2 FKBP13 | GLLGMCEGEKRKLVIPsELGyGERGAPPKIPGGATLVFEVE |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27348 | Y48 | Sugiyama | YWHAQ | AVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSIEQK |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27708 | Y602 | Sugiyama | CAD | FAHTSQVLVDKSLKGWKEIEyEVVRDAYGNCVTVCNMENLD |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P27816 | Y47 | Sugiyama | MAP4 | AtLEAEAFDDVVGETVGKTDyIPLLDVDEKtGNsESKKKPC |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P28062 | Y184 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | GMGLSMGSMICGWDKKGPGLyyVDEHGTRLSGNMFSTGSGN |
| P28062 | Y185 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | MGLSMGSMICGWDKKGPGLyyVDEHGTRLSGNMFSTGSGNT |
| P28062 | Y271 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | MKEDGWVKVEsTDVSDLLHQyREANQ_______________ |
| P28074 | Y172 | Sugiyama | PSMB5 LMPX MB1 X | MGLSMGTMICGWDKRGPGLyyVDsEGNRISGATFSVGSGSV |
| P29144 | Y1042 | Sugiyama | TPP2 | TEALRDLKIQWMTKLDSsDIyNELKEtyPNyLPLyVARLHQ |
| P29144 | Y1052 | Sugiyama | TPP2 | WMTKLDSsDIyNELKEtyPNyLPLyVARLHQLDAEKERMKR |
| P29317 | S570 | iPTMNet|EPSD | EPHA2 ECK | VLAGVGFFIHRRRKNQRARQsPEDVyFsKsEQLKPLKtyVD |
| P29317 | S897 | iPTMNet|EPSD|Sugiyama | EPHA2 ECK | APDSLKTLADFDPRVsIRLPstsGsEGVPFRTVsEWLESIK |
| P29317 | S899 | iPTMNet|EPSD | EPHA2 ECK | DSLKTLADFDPRVsIRLPstsGsEGVPFRTVsEWLESIKMQ |
| P29317 | S901 | iPTMNet|EPSD | EPHA2 ECK | LKTLADFDPRVsIRLPstsGsEGVPFRTVsEWLESIKMQQy |
| P29317 | T587 | Sugiyama | EPHA2 ECK | ARQsPEDVyFsKsEQLKPLKtyVDPHtyEDPNQAVLKFTTE |
| P29317 | T773 | Sugiyama | EPHA2 ECK | CKVSDFGLsRVLEDDPEAtyttsGGKIPIRWTAPEAISyRK |
| P29317 | T898 | iPTMNet|EPSD | EPHA2 ECK | PDSLKTLADFDPRVsIRLPstsGsEGVPFRTVsEWLESIKM |
| P29317 | T931 | Sugiyama | EPHA2 ECK | EWLESIKMQQytEHFMAAGytAIEKVVQMTNDDIKRIGVRL |
| P29317 | Y575 | EPSD|PSP | EPHA2 ECK | GFFIHRRRKNQRARQsPEDVyFsKsEQLKPLKtyVDPHtyE |
| P29317 | Y588 | SIGNOR|EPSD|PSP|Sugiyama | EPHA2 ECK | RQsPEDVyFsKsEQLKPLKtyVDPHtyEDPNQAVLKFTTEI |
| P29317 | Y594 | GPS6|SIGNOR|EPSD|PSP|Sugiyama | EPHA2 ECK | VyFsKsEQLKPLKtyVDPHtyEDPNQAVLKFTTEIHPSCVT |
| P29317 | Y628 | EPSD|PSP|Sugiyama | EPHA2 ECK | IHPSCVTRQKVIGAGEFGEVyKGMLKTSSGKKEVPVAIKTL |
| P29317 | Y694 | EPSD|PSP | EPHA2 ECK | NIIRLEGVISKYKPMMIITEyMENGALDKFLREKDGEFSVL |
| P29317 | Y729 | Sugiyama | EPHA2 ECK | GEFSVLQLVGMLRGIAAGMKyLANMNyVHRDLAARNILVNS |
| P29317 | Y735 | SIGNOR|EPSD|PSP|Sugiyama | EPHA2 ECK | QLVGMLRGIAAGMKyLANMNyVHRDLAARNILVNSNLVCKV |
| P29317 | Y772 | GPS6|SIGNOR|EPSD|PSP|Sugiyama | EPHA2 ECK | VCKVSDFGLsRVLEDDPEAtyttsGGKIPIRWTAPEAISyR |
| P29317 | Y791 | Sugiyama | EPHA2 ECK | tyttsGGKIPIRWTAPEAISyRKFTSASDVWSFGIVMWEVM |
| P29317 | Y921 | EPSD|PSP|Sugiyama | EPHA2 ECK | sEGVPFRTVsEWLESIKMQQytEHFMAAGytAIEKVVQMTN |
| P29317 | Y930 | Sugiyama | EPHA2 ECK | sEWLESIKMQQytEHFMAAGytAIEKVVQMTNDDIKRIGVR |
| P29317 | Y960 | EPSD|PSP | EPHA2 ECK | TNDDIKRIGVRLPGHQKRIAySLLGLKDQVNTVGIPI____ |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30041 | Y89 | Sugiyama | PRDX6 AOP2 KIAA0106 | IALSIDSVEDHLAWSKDINAyNCEEPtEKLPFPIIDDRNRE |
| P30043 | S202 | Sugiyama | BLVRB FLR SCAN | GHFMLRCLttDEyDGHstyPsHQyQ________________ |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| P30086 | Y106 | Sugiyama | PEBP1 PBP PEBP | HFLVVNMKGNDIssGtVLsDyVGsGPPKGtGLHRyVWLVyE |
| P30086 | Y120 | Sugiyama | PEBP1 PBP PEBP | GtVLsDyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsN |
| P30086 | Y125 | Sugiyama | PEBP1 PBP PEBP | DyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsNRsGDH |
| P30086 | Y176 | Sugiyama | PEBP1 PBP PEBP | KKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK_________ |
| P30086 | Y181 | Sugiyama | PEBP1 PBP PEBP | RAPVAGtCyQAEWDDyVPKLyEQLsGK______________ |
| 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 | Y356 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | FVMQEEFsRDGKALERFLQDyFDGNLKRyLKsEPIPESNDG |
| P30101 | Y445 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KDPNIVIAKMDAtANDVPsPyEVRGFPtIyFsPANKKLNPK |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30101 | Y95 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KGIVPLAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAy |
| P30520 | Y428 | Sugiyama | ADSS2 ADSS | WNTDISNARAFKELPVNAQNyVRFIEDELQIPVKWIGVGKs |
| P30876 | Y845 | Sugiyama | POLR2B | QEEVFEKPTRETCQGMRHAIyDKLDDDGLIAPGVRVSGDDV |
| P31150 | Y197 | Sugiyama | GDI1 GDIL OPHN2 RABGDIA XAP4 | LGQDVIDFTGHALALYRTDDyLDQPCLETVNRIKLYsEsLA |
| P31153 | Y235 | Sugiyama | MAT2A AMS2 MATA2 | LDEMRDALKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGP |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1031 | Sugiyama | CPS1 | VVVNCNPETVstDFDECDKLyFEELSLERILDIYHQEACGG |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31327 | Y634 | Sugiyama | CPS1 | FAMTNQILVEKSVTGWKEIEyEVVRDADDNCVTVCNMENVD |
| P31749 | T308 | Sugiyama | AKT1 PKB RAC | IKITDFGLCKEGIKDGAtMKtFCGtPEyLAPEVLEDNDyGR |
| P31751 | T309 | Sugiyama | AKT2 | IKITDFGLCKEGISDGATMKtFCGtPEyLAPEVLEDNDyGR |
| P31939 | Y362 | Sugiyama | ATIC PURH OK/SW-cl.86 | IAPGyEEEALTILSKKKNGNyCVLQMDQsYKPDENEVRTLF |
| P31939 | Y464 | Sugiyama | ATIC PURH OK/SW-cl.86 | IGAGQQsRIHCTRLAGDKANyWWLRHHPQVLSMKFKTGVKR |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31946 | S212 | Sugiyama | YWHAB | SLAKTAFDEAIAELDtLNEEsyKDstLIMQLLRDNLtLWtS |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| 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 |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32780 | Y360 | Sugiyama | GTF2H1 BTF2 | GDADCFQPAVKRAKLQEsIEyEDLGKNNSVKTIALNLKKSD |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33121 | T695 | Sugiyama | ACSL1 FACL1 FACL2 LACS LACS1 LACS2 | KAKRPELRNYFRSQIDDLyStIKV_________________ |
| 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 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33993 | Y102 | Sugiyama | MCM7 CDC47 MCM2 | QELLPQYKEREVVNKDVLDVyIEHRLMMEQRSRDPGMVRsP |
| P34896 | Y180 | Sugiyama | SHMT1 | ISATSIFFESMPYKVNPDtGyINyDQLEENARLFHPKLIIA |
| P34896 | Y183 | Sugiyama | SHMT1 | TSIFFESMPYKVNPDtGyINyDQLEENARLFHPKLIIAGTS |
| P34931 | S42 | Sugiyama | HSPA1L | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P34932 | Y30 | Sugiyama | HSPA4 APG2 HSPH2 | FQSCYVAVARAGGIETIANEysDRCtPACIsFGPKNRSIGA |
| 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 |
| P35080 | Y79 | Sugiyama | PFN2 | FFtNGLtLGAKKCSVIRDSLyVDGDCtMDIRTKsQGGEPTy |
| P35250 | S30 | Sugiyama | RFC2 | AGEVEAQDSDPAPAFSKAPGsAGHyELPWVEKYRPVKLNEI |
| P35579 | Y9 | Sugiyama | MYH9 | ____________MAQQAADKyLyVDKNFINNPLAQADWAAK |
| P35580 | Y13 | Sugiyama | MYH10 | ________MAQRTGLEDPERyLFVDRAVIYNPATQADWTAK |
| P35609 | Y326 | Sugiyama | ACTN2 | NRtPEKTMQAMQKKLEDFRDyRRKHKPPKVQEKCQLEINFN |
| P35609 | Y385 | Sugiyama | ACTN2 | GKMVSDIAGAWQRLEQAEKGyEEWLLNEIRRLERLEHLAEK |
| P35637 | Y468 | Sugiyama | FUS TLS | KAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRGGYRGRG |
| P36871 | T426 | Sugiyama | PGM1 | KQsVEDILKDHWQKYGRNFFtRyDyEEVEAEGANKMMKDLE |
| P36871 | Y157 | Sugiyama | PGM1 | GPAPEAITDKIFQISKTIEEyAVCPDLKVDLGVLGKQQFDL |
| P36871 | Y430 | Sugiyama | PGM1 | EDILKDHWQKYGRNFFtRyDyEEVEAEGANKMMKDLEALMF |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P37837 | Y206 | Sugiyama | TALDO1 TAL TALDO TALDOR | ISPFVGRILDWHVANTDKKSyEPLEDPGVKSVTKIYNYYKK |
| P38646 | Y118 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | ERLVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIK |
| P38646 | Y196 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | EtAENyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNV |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40337 | Y185 | Sugiyama | VHL | VVRsLVKPENyRRLDIVRsLyEDLEDHPNVQKDLERLtQER |
| P40429 | Y149 | Sugiyama | RPL13A | LKPTRKFAYLGRLAHEVGWKyQAVtAtLEEKRKEKAKIHYR |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40926 | Y80 | Sugiyama | MDH2 | HtPGVAADLsHIEtKAAVKGyLGPEQLPDCLKGCDVVVIPA |
| P40939 | Y637 | Sugiyama | HADHA HADH | ELLTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILA |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41091 | Y102 | Sugiyama | EIF2S3 EIF2G | GYANAKIYKLDDPSCPRPECyRSCGsstPDEFPtDIPGtKG |
| P41252 | Y148 | Sugiyama | IARS1 IARS | SAEWKSTVsRLGRWIDFDNDyKTLYPQFMESVWWVFKQLYD |
| P41252 | Y273 | Sugiyama | IARS1 IARS | GRLLILMEARLSALYKLEsDyEILERFPGAYLKGKKYRPLF |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P43034 | Y137 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | HPVFSVMVSASEDATIKVWDyEtGDFERtLKGHtDsVQDIs |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43243 | Y773 | Sugiyama | MATR3 KIAA0723 | DPNKDtsENADGQsDENKDDyTIPDEYRIGPYQPNVPVGID |
| P43246 | Y238 | Sugiyama | MSH2 | QRGGILITERKKADFSTKDIyQDLNRLLKGKKGEQMNSAVL |
| P43490 | Y34 | Sugiyama | NAMPT PBEF PBEF1 | ATDSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKY |
| P43490 | Y36 | Sugiyama | NAMPT PBEF PBEF1 | DSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKYEE |
| P45974 | Y851 | Sugiyama | USP5 ISOT | IYNDQKVCASEKPPKDLGyIyFyQRVAS_____________ |
| P45974 | Y853 | Sugiyama | USP5 ISOT | NDQKVCASEKPPKDLGyIyFyQRVAS_______________ |
| P46063 | Y61 | Sugiyama | RECQL RECQ1 RECQL1 | VLTKKIKQCLEDsDAGAsNEyDssPAAWNKEDFPWSGKVKD |
| P46777 | Y207 | Sugiyama | RPL5 MSTP030 | sKEFNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyI |
| P46777 | Y219 | Sugiyama | RPL5 MSTP030 | IMGQNVADyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEM |
| P46777 | Y226 | Sugiyama | RPL5 MSTP030 | DyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEMyKKAHAA |
| P46777 | Y240 | Sugiyama | RPL5 MSTP030 | KKQFsQyIKNsVtPDMMEEMyKKAHAAIRENPVyEKKPKKE |
| P46777 | Y253 | Sugiyama | RPL5 MSTP030 | PDMMEEMyKKAHAAIRENPVyEKKPKKEVKKKRWNRPKMsL |
| P46778 | Y156 | Sugiyama | RPL21 | REAHFVRTNGKEPELLEPIPyEFMA________________ |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46781 | Y35 | Sugiyama | RPS9 | TPRRPFEKSRLDQELKLIGEyGLRNKREVWRVKFTLAKIRK |
| P46940 | Y41 | Sugiyama | IQGAP1 KIAA0051 | LDNERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGED |
| P46940 | Y43 | Sugiyama | IQGAP1 KIAA0051 | NERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGEDLP |
| P46976 | Y332 | Sugiyama | GYG1 GYG | AQPFVSSEERKERWEQGQADyMGADSFDNIKRKLDTYLQ__ |
| P47756 | Y59 | Sugiyama | CAPZB | LLSSVDQPLKIARDKVVGKDyLLCDyNRDGDSyRsPWSNKy |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47813 | Y35 | Sugiyama | EIF1AX EIF1A EIF4C | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEAMCFDGV |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48147 | Y28 | Sugiyama | PREP PEP | DVYRDETAVQDYHGHKICDPyAWLEDPDSEQTKAFVEAQNK |
| P48637 | Y375 | Sugiyama | GSS | LAAPSRFVLKPQREGGGNNLyGEEMVQALKQLKDSEERAsy |
| P48637 | Y395 | Sugiyama | GSS | yGEEMVQALKQLKDSEERAsyILMEKIEPEPFENCLLRPGs |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | S42 | Sugiyama | HSPA7 HSP70B | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | T2450 | Sugiyama | FASN FAS | AEQYtPKAKyHGNVMLLRAKtGGAyGEDLGADyNLsQVCDG |
| 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 |
| P49458 | Y18 | Sugiyama | SRP9 | ___MPQYQTWEEFSRAAEKLyLADPMKARVVLKYRHsDGNL |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y535 | Sugiyama | AARS1 AARS | FVEEVSTGQECGVVLDKTCFyAEQGGQIyDEGYLVKVDDss |
| P49588 | Y543 | Sugiyama | AARS1 AARS | QECGVVLDKTCFyAEQGGQIyDEGYLVKVDDssEDKTEFTV |
| P49588 | Y690 | Sugiyama | AARS1 AARS | DCPLAAAKAIQGLRAVFDEtyPDPVRVVSIGVPVSELLDDP |
| P49591 | Y248 | Sugiyama | SARS1 SARS SERS | FMRKEVMQEVAQLsQFDEELyKVIGKGSEKSDDNSYDEKYL |
| P49591 | Y294 | Sugiyama | SARS1 SARS SERS | QPIAALHRDEWLRPEDLPIKyAGLsTCFRQEVGSHGRDTRG |
| P49736 | Y137 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | MRQRDREAGRGLGRMRRGLLyDsDEEDEERPARKRRQVERA |
| P49736 | Y234 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | VFKERIsDMCKENREsLVVNyEDLAAREHVLAYFLPEAPAE |
| P49753 | Y351 | Sugiyama | ACOT2 PTE2 PTE2A | GETLPPVGVNRNRIKVTKDGyADIVDVLNsPLEGPDQKSFI |
| P50395 | Y197 | Sugiyama | GDI2 RABGDIB | LGQDVIDFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLA |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50395 | Y404 | Sugiyama | GDI2 RABGDIB | SDLLVPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRM |
| P50454 | Y135 | Sugiyama | SERPINH1 CBP1 CBP2 HSP47 SERPINH2 PIG14 | LRSLSNSTARNVTWKLGsRLyGPssVsFADDFVRssKQHYN |
| P50502 | Y213 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | RLLGHWEEAAHDLALACKLDyDEDAsAMLKEVQPRAQKIAE |
| P50542 | Y163 | Sugiyama | PEX5 PXR1 | EFISEVTDPLSVSPARWAEEyLEQsEEKLWLGEPEGTATDR |
| P50542 | Y312 | Sugiyama | PEX5 PXR1 | QAELEEMAKRDAEAHPWLSDyDDLtsATyDKGYQFEEENPL |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50995 | Y482 | Sugiyama | ANXA11 ANX11 | sEtDLLDIRSEYKRMYGKsLyHDISGDtsGDyRKILLKICG |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51149 | Y183 | Sugiyama | RAB7A RAB7 | EQAFQtIARNALKQETEVELyNEFPEPIKLDKNDRAKASAE |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52298 | Y14 | Sugiyama | NCBP2 CBP20 PIG55 | _______MSGGLLKALRsDsyVELSQYRDQHFRGDNEEQEK |
| P52565 | Y144 | Sugiyama | ARHGDIA GDIA1 | SGMKYIQHTyRKGVKIDKtDyMVGsYGPRAEEyEFLtPVEE |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | S193 | Sugiyama | HNRNPF HNRPF | KERIGHRYIEVFKssQEEVRsysDPPLKFMsVQRPGPYDRP |
| P52597 | Y266 | Sugiyama | HNRNPF HNRPF | ySGLSDGYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQsT |
| P52597 | Y82 | Sugiyama | HNRNPF HNRPF | GsEDDVKMALKKDRESMGHRyIEVFKSHRTEMDWVLKHsGP |
| P52788 | Y336 | Sugiyama | SMS | GNCVNLTEALSLYEEQLGRLyCPVEFSKEIVCVPSYLELWV |
| P52789 | Y112 | Sugiyama | HK2 | VLWVKVTDNGLQKVEMENQIyAIPEDIMRGsGTQLFDHIAE |
| P52888 | Y48 | Sugiyama | THOP1 | LsAQQIEERTRELIEQTKRVyDQVGTQEFEDVSyESTLKAL |
| P52888 | Y576 | Sugiyama | THOP1 | VLAKVDQALHTQTDADPAEEyARLCQEILGVPATPGTNMPA |
| P52888 | Y61 | Sugiyama | THOP1 | IEQTKRVyDQVGTQEFEDVSyESTLKALADVEVTytVQRNI |
| P52907 | Y239 | Sugiyama | CAPZA1 | sNEAQtAKEFIKIIENAENEyQTAIsENyQtMSDTTFKALR |
| P52907 | Y247 | Sugiyama | CAPZA1 | EFIKIIENAENEyQTAIsENyQtMSDTTFKALRRQLPVTRT |
| P52948 | Y1215 | Sugiyama | NUP98 ADAR2 | KVHLEKLSLRQRKPDEDMKLyQTPLELKLKHSTVHVDELCP |
| P52948 | Y848 | Sugiyama | NUP98 ADAR2 | PTDKTSRCLIKsPDRLADINyEGRLEAVSRKQGAQFKEyRP |
| P53611 | Y26 | Sugiyama | RABGGTB GGTB | KDVIIKsDAPDTLLLEKHADyIASYGSKKDDYEYCMSEYLR |
| P53621 | Y391 | Sugiyama | COPA | NPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGK |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P53675 | Y921 | Sugiyama | CLTCL1 CLH22 CLTCL CLTD | DSSVVGRYCEKRDPHLACVAyERGQCDLELIKVCNENSLFK |
| P54105 | Y38 | Sugiyama | CLNS1A CLCI ICLN | RQQPDTEAVLNGKGLGtGtLyIAEsRLSWLDGsGLGFSLEY |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54577 | Y388 | Sugiyama | YARS1 YARS | LDIRVGKIITVEKHPDADsLyVEKIDVGEAEPRTVVSGLVQ |
| P54646 | Y179 | Sugiyama | PRKAA2 AMPK AMPK2 | GLSNMMsDGEFLRtsCGsPNyAAPEVISGRLYAGPEVDIWS |
| P54652 | S41 | Sugiyama | HSPA2 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P55084 | T359 | Sugiyama | HADHB MSTP029 | DFMYVSQDPKDQLLLGPtYAtPKVLEKAGLTMNDIDAFEFH |
| P55084 | Y244 | Sugiyama | HADHB MSTP029 | GHSADRLAAAFAVSRLEQDEyALRsHSLAKKAQDEGLLSDV |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y66 | Sugiyama | NAP1L1 NRP | PQILAALQERLDGLVEtPtGyIEsLPRVVKRRVNALKNLQV |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55786 | Y173 | Sugiyama | NPEPPS PSA | NDKMKGFYRSKYTTPSGEVRyAAVTQFEATDARRAFPCWDE |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55809 | Y43 | Sugiyama | OXCT1 OXCT SCOT | TWYKGCVCSFSTSAHRHTKFyTDPVEAVKDIPDGATVLVGG |
| P55884 | Y222 | Sugiyama | EIF3B EIF3S9 | KLKNVIHKIFSKFGKITNDFyPEEDGKTKGyIFLEyAsPAH |
| P55884 | Y768 | Sugiyama | EIF3B EIF3S9 | ERRRTMMEDFRKYRKMAQELyMEQKNERLELRGGVDTDELD |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60228 | Y62 | Sugiyama | EIF3E EIF3S6 INT6 | LDLLSDTNMVDFAMDVYKNLySDDIPHALREKRTTVVAQLK |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | T297 | Sugiyama | ACTB | TTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQKEI |
| 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 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60900 | Y160 | Sugiyama | PSMA6 PROS27 | LIGIDEEQGPQVYKCDPAGyyCGFKATAAGVKQtEstsFLE |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61106 | Y136 | Sugiyama | RAB14 | NTVIILIGNKADLEAQRDVTyEEAKQFAEENGLLFLEASAK |
| P61158 | Y231 | Sugiyama | ACTR3 ARP3 | REVGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSK |
| P61158 | Y233 | Sugiyama | ACTR3 ARP3 | VGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSKWI |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61221 | Y594 | Sugiyama | ABCE1 RLI RNASEL1 RNASELI RNS4I OK/SW-cl.40 | RPRINKLNsIKDVEQKKsGNyFFLDD_______________ |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61247 | Y31 | Sugiyama | RPS3A FTE1 MFTL | KGGKKGAKKKVVDPFSKKDWyDVKAPAMFNIRNIGKTLVTR |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61353 | Y77 | Sugiyama | RPL27 | MGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVN |
| P61353 | Y85 | Sugiyama | RPL27 | RSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVNKDVFRDPA |
| P61604 | T79 | Sugiyama | HSPE1 | EIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDILGK |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | S215 | Sugiyama | YWHAG | HLAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWts |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y216 | Sugiyama | YWHAG | LAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWtsD |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62195 | Y148 | Sugiyama | PSMC5 SUG1 | PNKVDPLVSLMMVEKVPDSTyEMIGGLDKQIKEIKEVIELP |
| P62241 | S115 | Sugiyama | RPS8 OK/SW-cl.83 | TLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEE |
| 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 | Y214 | Sugiyama | YWHAE | LAKAAFDDAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P62258 | Y49 | Sugiyama | YWHAE | KVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssIEQK |
| P62263 | S70 | Sugiyama | RPS14 PRO2640 | KETICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELGI |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62280 | T54 | Sugiyama | RPS11 | PRYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILs |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62333 | Y328 | Sugiyama | PSMC6 SUG2 | ARLDILKIHAGPITKHGEIDyEAIVKLSDGFNGADLRNVCT |
| P62495 | Y345 | Sugiyama | ETF1 ERF1 RF1 SUP45L1 | NLDIMRYVLHCQGTEEEKILyLTPEQEKDKSHFTDKETGQE |
| P62714 | Y284 | Sugiyama | PPP2CB | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRT |
| P62714 | Y80 | Sugiyama | PPP2CB | GQFHDLMELFRIGGKsPDtNyLFMGDyVDRGYYSVETVTLL |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y144 | Sugiyama | RPL23A | VNtLIRPDGEKKAYVRLAPDyDALDVANKIGII________ |
| P62750 | Y74 | Sugiyama | RPL23A | LRRQPKYPRKSAPRRNKLDHyAIIKFPLTTEsAMKKIEDNN |
| P62753 | Y156 | Sugiyama | RPS6 OK/SW-cl.2 | KRASRIRKLFNLsKEDDVRQyVVRKPLNKEGKKPRTKAPKI |
| 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 | 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 |
| P62847 | Y76 | Sugiyama | RPS24 | FVFGFRTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGL |
| P62847 | Y81 | Sugiyama | RPS24 | RTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGLYEKKK |
| P62888 | Y62 | Sugiyama | RPL30 | KAKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELG |
| P62888 | Y63 | Sugiyama | RPL30 | AKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELGt |
| P62899 | Y103 | Sugiyama | RPL31 | RIRVRLSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVD |
| P62899 | Y108 | Sugiyama | RPL31 | LSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVDEN___ |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63010 | Y524 | Sugiyama | AP2B1 ADTB2 CLAPB1 | QQVLSLATQDSDNPDLRDRGyIyWRLLsTDPVTAKEVVLSE |
| P63010 | Y526 | Sugiyama | AP2B1 ADTB2 CLAPB1 | VLSLATQDSDNPDLRDRGyIyWRLLsTDPVTAKEVVLSEKP |
| P63092 | Y190 | Sugiyama | GNAS GNAS1 GSP | QLIDCAQYFLDKIDVIKQADyVPSDQDLLRCRVLTSGIFET |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63151 | Y71 | Sugiyama | PPP2R2A | RVVIFQQEQENKIQSHSRGEyNVystFQsHEPEFDyLKSLE |
| P63151 | Y74 | Sugiyama | PPP2R2A | IFQQEQENKIQSHSRGEyNVystFQsHEPEFDyLKSLEIEE |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | T297 | Sugiyama | ACTG1 ACTG | TTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQKEI |
| 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 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67775 | Y284 | Sugiyama | PPP2CA | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRt |
| P67775 | Y80 | Sugiyama | PPP2CA | GQFHDLMELFRIGGKsPDtNyLFMGDyVDRGYYSVETVTLL |
| P67809 | Y208 | Sugiyama | YBX1 NSEP1 YB1 | yRRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGE |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68363 | T225 | Sugiyama | TUBA1B | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| P68363 | Y224 | Sugiyama | TUBA1B | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| P68363 | Y312 | Sugiyama | TUBA1B | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68366 | T225 | Sugiyama | TUBA4A TUBA1 | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| P68366 | Y224 | Sugiyama | TUBA4A TUBA1 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| P68366 | Y312 | Sugiyama | TUBA4A TUBA1 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68400 | Y12 | Sugiyama | CSNK2A1 CK2A1 | _________MSGPVPSRARVytDVNTHRPREYWDYESHVVE |
| P68400 | Y125 | Sugiyama | CSNK2A1 CK2A1 | VSRTPALVFEHVNNTDFKQLyQtLTDYDIRFYMYEILKALD |
| P68400 | Y255 | Sugiyama | CSNK2A1 CK2A1 | GHDNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGR |
| P68400 | Y257 | Sugiyama | CSNK2A1 CK2A1 | DNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGRHS |
| P68400 | Y323 | Sugiyama | CSNK2A1 CK2A1 | KLLRYDHQSRLTAREAMEHPyFytVVKDQARMGSSSMPGGS |
| P68400 | Y325 | Sugiyama | CSNK2A1 CK2A1 | LRYDHQSRLTAREAMEHPyFytVVKDQARMGSSSMPGGStP |
| P78527 | Y4077 | Sugiyama | PRKDC HYRC HYRC1 | AVITCDELLLGHEKAPAFRDyVAVARGSKDHNIRAQEPESG |
| P80303 | Y350 | Sugiyama | NUCB2 NEFA | PDsWEtLDQQQFFtEEELKEyENIIALQENELKKKADELQK |
| P84090 | Y22 | Sugiyama | ERH | sHTILLVQPTKRPEGRtyADyEsVNECMEGVCKMYEEHLKR |
| P84095 | Y40 | Sugiyama | RHOG ARHG | LICYTTNAFPKEyIPTVFDNySAQsAVDGRTVNLNLWDTAG |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| P98175 | Y694 | Sugiyama | RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122 | QPISSLRDDERREsAtADAGyAILEKKGALAERQHTsMDLP |
| Q00005 | Y67 | Sugiyama | PPP2R2B | RVVIFQREQESKNQVHRRGEyNVystFQsHEPEFDyLKSLE |
| Q00005 | Y70 | Sugiyama | PPP2R2B | IFQREQESKNQVHRRGEyNVystFQsHEPEFDyLKSLEIEE |
| Q00169 | Y140 | Sugiyama | PITPNA PITPN | GTQENVHKLEPEAWKHVEAVyIDIADRSQVLSKDYKAEEDP |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00610 | Y1477 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | NHNNKsVNEsLNNLFITEEDyQALRTsIDAyDNFDNIsLAQ |
| Q00610 | Y1487 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LNNLFITEEDyQALRTsIDAyDNFDNIsLAQRLEKHELIEF |
| Q00610 | Y377 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LAGAEELFARKFNALFAQGNySEAAKVAANAPKGILRtPDt |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00610 | Y899 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LAKIyIDsNNNPERFLRENPyyDsRVVGKYCEKRDPHLACV |
| Q00610 | Y900 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | AKIyIDsNNNPERFLRENPyyDsRVVGKYCEKRDPHLACVA |
| 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 |
| Q01082 | Y493 | Sugiyama | SPTBN1 SPTB2 | AYEERVQAVVAVARELEAENyHDIKRITARKDNVIRLWEYL |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q02809 | Y434 | Sugiyama | PLOD1 LLH PLOD | LWSNFWGALSADGYYARSEDyVDIVQGRRVGVWNVPYISNI |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04721 | Y129 | Sugiyama | NOTCH2 | CFVSRPCLNGGTCHMLSRDtyECtCQVGFTGKECQWTDACL |
| Q04760 | Y136 | PSP | GLO1 | HNGNsDPRGFGHIGIAVPDVySACKRFEELGVKFVKKPDDG |
| Q04837 | S67 | Sugiyama | SSBP1 SSBP | QVEGKNPVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRI |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | S215 | Sugiyama | YWHAH YWHA1 | LLAKQAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWTS |
| Q04917 | Y154 | Sugiyama | YWHAH YWHA1 | LAEVASGEKKNsVVEAsEAAyKEAFEISKEQMQPTHPIRLG |
| Q04917 | Y20 | Sugiyama | YWHAH YWHA1 | _MGDREQLLQRARLAEQAERyDDMAsAMKAVtELNEPLsNE |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05209 | Y88 | Sugiyama | PTPN12 | LPFDHSRVKLTLKtPsQDSDyINANFIKGVYGPKAYVATQG |
| Q05519 | T422 | Sugiyama | SRSF11 SFRS11 | KDKEKDRERKSEsDKDVKQVtRDyDEEEQGYDsEKEKKEEK |
| Q05519 | Y425 | Sugiyama | SRSF11 SFRS11 | EKDRERKSEsDKDVKQVtRDyDEEEQGYDsEKEKKEEKKPI |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q05655 | Y630 | Sugiyama | PRKCD PKCD | LLEKRRLEPPFRPKVKsPRDysNFDQEFLNEKARLsysDKN |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q06830 | Y34 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | NFKAtAVMPDGQFKDIsLsDyKGKYVVFFFYPLDFTFVCPT |
| Q07157 | Y1066 | Sugiyama | TJP1 ZO1 | VEKQAsRDLEQPtyRyEsssytDQFsRNYEHRLRYEDRVPM |
| Q07666 | Y145 | Sugiyama | KHDRBS1 SAM68 | LtAEIEKIQKGDSKKDDEENyLDLFsHKNMKLKERVLIPVK |
| Q07955 | Y189 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | TYAVRKLDNTKFRsHEGEtAyIRVKVDGPRsPsyGRsRsRs |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08043 | Y333 | Sugiyama | ACTN3 | NRVGEPsMsAMQRKLEDFRDyRRLHKPPRIQEKCQLEINFN |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q08752 | Y323 | Sugiyama | PPID CYP40 CYPD | DPSNTKALYRRAQGWQGLKEyDQALADLKKAQGIAPEDKAI |
| Q08945 | Y441 | Sugiyama | SSRP1 FACT80 | KKLNIKNRGLKEGMNPsyDEyADsDEDQHDAYLERMKEEGK |
| Q08J23 | Y51 | Sugiyama | NSUN2 SAKI TRM4 | EAGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALR |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q09028 | Y154 | Sugiyama | RBBP4 RBAP48 | PQNPCIIATKtPssDVLVFDyTKHPsKPDPsGECNPDLRLR |
| Q10567 | Y524 | Sugiyama | AP1B1 ADTB1 BAM22 CLAPB2 | QQVLSLATQDSDNPDLRDRGyIyWRLLsTDPVAAKEVVLAE |
| Q10567 | Y526 | Sugiyama | AP1B1 ADTB1 BAM22 CLAPB2 | VLSLATQDSDNPDLRDRGyIyWRLLsTDPVAAKEVVLAEKP |
| Q12874 | Y479 | Sugiyama | SF3A3 SAP61 | WAKLKLQKASERWQPDtEEEyEDssGNVVNKKTYEDLKRQG |
| Q12874 | Y50 | Sugiyama | SF3A3 SAP61 | KSTLRDQINSDHRTRAMQDRyMEVSGNLRDLyDDKDGLRKE |
| Q12874 | Y61 | Sugiyama | SF3A3 SAP61 | HRTRAMQDRyMEVSGNLRDLyDDKDGLRKEELNAIsGPNEF |
| Q12931 | Y498 | Sugiyama | TRAP1 HSP75 HSPC5 | GQLtsLsEyASRMRAGtRNIyyLCAPNRHLAEHsPyyEAMK |
| Q12931 | Y499 | Sugiyama | TRAP1 HSP75 HSPC5 | QLtsLsEyASRMRAGtRNIyyLCAPNRHLAEHsPyyEAMKK |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q13017 | Y1109 | Sugiyama | ARHGAP5 RHOGAP5 | DNyAEPIDTIFKQKGYsDEIyVVPDDsQNRIKIRNsFVNNt |
| Q13131 | Y190 | Sugiyama | PRKAA1 AMPK1 | GLsNMMsDGEFLRtsCGsPNyAAPEVISGRLYAGPEVDIWS |
| 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 |
| Q13228 | Y43 | Sugiyama | SELENBP1 SBP | REEIVyLPCIyRNtGtEAPDyLATVDVDPKsPQyCQVIHRL |
| Q13263 | Y133 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TVVDCPVCKQQCFSKDIVENyFMRDsGsKAATDAQDANQCC |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13263 | Y517 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | LtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQPGtA |
| 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 | Y238 | Sugiyama | PABPC4 APP1 PABP4 | LSVKVMRDPNGKSKGFGFVSyEKHEDANKAVEEMNGKEISG |
| 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__________________ |
| Q13405 | Y45 | Sugiyama | MRPL49 C11orf4 NOF1 OK/SW-cl.67 | LLSQTQGPPDYPRFVEsVDEyQFVERLLPATRIPDPPKHEH |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13442 | S19 | Sugiyama | PDAP1 HASPP28 | __MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEEE |
| Q13509 | T107 | Sugiyama | TUBB3 TUBB4 | PDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECENC |
| Q13561 | Y207 | Sugiyama | DCTN2 DCTN50 | SKGGSGGKttGtPPDssLVtyELHsRPEQDKFSQAAKVAEL |
| Q13561 | Y6 | Sugiyama | DCTN2 DCTN50 | _______________MADPKyADLPGIARNEPDVYETSDLP |
| Q13561 | Y81 | Sugiyama | DCTN2 DCTN50 | RVGTKGLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQ |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q13885 | T107 | Sugiyama | TUBB2A TUBB2 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q14204 | Y2881 | Sugiyama | DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325 | IDREKAMSRPILYSNWLSKDyIPVDQEELRDyVKARLKVFY |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | Y421 | Sugiyama | CTTN EMS1 | tPPVsPAPQPtEERLPssPVyEDAAsFKAELsyRGPVsGtE |
| Q14247 | Y545 | Sugiyama | CTTN EMS1 | IDDGWWRGVCKGRyGLFPANyVELRQ_______________ |
| Q14257 | Y303 | Sugiyama | RCN2 ERC55 | LsEEEILENPDLFLtsEAtDyGRQLHDDyFyHDEL______ |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14257 | Y39 | Sugiyama | RCN2 ERC55 | AAGAGKAEELHyPLGERRsDyDREALLGVQEDVDEyVKLGH |
| Q14257 | Y54 | Sugiyama | RCN2 ERC55 | ERRsDyDREALLGVQEDVDEyVKLGHEEQQKRLQAIIKKID |
| Q14258 | Y245 | Sugiyama | TRIM25 EFP RNF147 ZNF147 | NRQQDVRMTANRKVEQLQQEytEMKALLDASETTSTRKIKE |
| Q14318 | Y322 | Sugiyama | FKBP8 FKBP38 | QPDNIKALFRKGKVLAQQGEysEAIPILRAALKLEPSNKTI |
| Q14566 | Y111 | Sugiyama | MCM6 | CRALKTFVKDRKEIPLAKDFyVAFQDLPTRHKIRELTSSRI |
| Q14568 | Y160 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGERM |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14671 | Y83 | Sugiyama | PUM1 KIAA0099 PUMH1 | SPVPGSIGVAGRsQDDAMVDyFFQRQHGEQLGGGGsGGGGy |
| Q14677 | Y114 | Sugiyama | CLINT1 ENTH EPN4 EPNR KIAA0171 | SERVVTSAREHIyDLRSLENyHFVDEHGKDQGINIRQKVKE |
| Q14697 | Y489 | Sugiyama | GANAB G2AN KIAA0088 | PHIKVDSGyRVHEELRNLGLyVKtRDGSDyEGWCWPGSAGY |
| Q14764 | Y389 | Sugiyama | MVP LRP | AKVEVVEERQAIPLDENEGIyVQDVKTGKVRAVIGSTYMLT |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q15019 | Y211 | Sugiyama | SEPTIN2 DIFF6 KIAA0158 NEDD5 SEPT2 | ERERLKKRILDEIEEHNIKIyHLPDAEsDEDEDFKEQtRLL |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15056 | Y86 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | sIRsVRLVRDKDTDKFKGFCyVEFDEVDsLKEALtyDGALL |
| Q15067 | Y232 | Sugiyama | ACOX1 ACOX | IGTHKPLPGITVGDIGPKFGyDEIDNGyLKMDNHRIPRENM |
| Q15067 | Y239 | Sugiyama | ACOX1 ACOX | PGITVGDIGPKFGyDEIDNGyLKMDNHRIPRENMLMKYAQV |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15293 | Y140 | Sugiyama | RCN1 RCN | VAKVWKDYDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssD |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15293 | Y320 | Sugiyama | RCN1 RCN | LTKEEILENWNMFVGsQAtNyGEDLtKNHDEL_________ |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15427 | T14 | Sugiyama | SF3B4 SAP49 | _______MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFL |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15650 | Y289 | Sugiyama | TRIP4 RQT4 | LLEFDRtsIRRtQVIDDESDyFASDSNQWLSKLERETLQKR |
| Q15691 | Y119 | Sugiyama | MAPRE1 | GKFQDNFEFVQWFKKFFDANyDGKDyDPVAARQGQEtAVAP |
| Q15691 | Y124 | Sugiyama | MAPRE1 | NFEFVQWFKKFFDANyDGKDyDPVAARQGQEtAVAPsLVAP |
| Q16181 | Y223 | Sugiyama | SEPTIN7 CDC10 SEPT7 | ECQQFKKQIMKEIQEHKIKIyEFPEtDDEEENKLVKKIKDR |
| Q16204 | Y134 | Sugiyama | CCDC6 D10S170 TST1 | NtLFKKIQALQKEKETLAVNyEKEEEFLTNELSRKLMQLQH |
| Q16576 | Y153 | Sugiyama | RBBP7 RBAP46 | PQNPHIIATKtPssDVLVFDyTKHPAKPDPsGECNPDLRLR |
| Q16658 | Y493 | Sugiyama | FSCN1 FAN1 HSN SNL | DHAGVLKASAEtVDPAsLWEy____________________ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16762 | Y165 | Sugiyama | TST | PSRPEPAVFKATLDRSLLKTyEQVLENLESKRFQLVDSRSQ |
| Q16763 | Y141 | Sugiyama | UBE2S E2EPF OK/SW-cl.73 | IHPNPESALNEEAGRLLLENyEEyAARARLLtEIHGGAGGP |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q16851 | Y89 | Sugiyama | UGP2 UGP1 | KGPSVDWGKIQRPPEDSIQPyEKIKARGLPDNISsVLNKLV |
| Q4J6C6 | Y142 | Sugiyama | PREPL KIAA0436 | YYQEGCCLVRSKDEEADNDNyEVLFNLEELKLDQPFIDCIR |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | Y167 | Sugiyama | HSP90AB4P | GEPIDRDTKVILHLKEDQtEyLEERWVKEVVKKHPQFIGCL |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | T60 | Sugiyama | HSP90AB3P HSP90BC | LQELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPNPQ |
| Q58FF7 | Y171 | Sugiyama | HSP90AB3P HSP90BC | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| Q58FF7 | Y492 | Sugiyama | HSP90AB3P HSP90BC | TANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIMETLR |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | T60 | Sugiyama | HSP90AB2P HSP90BB | LWELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPNTQ |
| 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 |
| Q5JWF2 | Y833 | Sugiyama | GNAS GNAS1 | QLIDCAQYFLDKIDVIKQADyVPSDQDLLRCRVLTSGIFET |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VV41 | Y216 | Sugiyama | ARHGEF16 EPHEXIN4 NBR | KKTLGRKRGHKGsFKDDPQLyQEIQERGLNtsQEsDDDILD |
| Q66LE6 | Y77 | Sugiyama | PPP2R2D KIAA1541 | RVVIFQREQENKSRPHSRGEyNVystFQsHEPEFDyLKSLE |
| Q66LE6 | Y80 | Sugiyama | PPP2R2D KIAA1541 | IFQREQENKSRPHSRGEyNVystFQsHEPEFDyLKSLEIEE |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6PEY2 | T225 | Sugiyama | TUBA3E | DNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRFD |
| Q6PEY2 | Y224 | Sugiyama | TUBA3E | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6WCQ1 | Y945 | Sugiyama | MPRIP KIAA0864 MRIP RHOIP3 | DELQTALRDKKYASDKYKDIyTELSIAKAKADCDISRLKEQ |
| Q709C8 | Y306 | Sugiyama | VPS13C KIAA1421 | GNIPPNYQYIFQPISASAKLyMNPyAESELKTPKLDCNIEI |
| Q71U36 | T225 | Sugiyama | TUBA1A TUBA3 | DNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRFD |
| Q71U36 | Y224 | Sugiyama | TUBA1A TUBA3 | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| 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 |
| Q7RTV0 | Y51 | Sugiyama | PHF5A | VICDSyVRPCTLVRICDECNyGsyQGRCVICGGPGVSDAyy |
| Q7Z2W4 | Y642 | Sugiyama | ZC3HAV1 ZC3HDC2 PRO1677 | GEEKDKRKNsNVDssyLEsLyQSCPRGVVPFQAGSRNYELS |
| Q86SX6 | Y85 | Sugiyama | GLRX5 C14orf87 | PQCGFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSN |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86TX2 | Y289 | Sugiyama | ACOT1 CTE1 | GETLPPVGVNRNRIKVTKDGyADIVDVLNsPLEGPDQKSFI |
| Q86UK7 | Y306 | Sugiyama | ZNF598 | QFSYAPRHSRRNEGVVGGEDyEEVDRysRQGRVARAGTRGA |
| Q86W92 | Y951 | Sugiyama | PPFIBP1 KIAA1230 | GQASGsASKKGFKPGLDMRLyEEDDLDRLEQMEDsEGtVRQ |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q86XP3 | Y573 | Sugiyama | DDX42 | VATDVAARGLDIPSIKTVINyDVARDIDTHTHRIGRTGRAG |
| Q8IZP0 | Y23 | Sugiyama | ABI1 SSH3BP1 | ELQMLLEEEIPSGKRALIEsyQNLTRVADyCENNyIQATDK |
| Q8N0Y7 | S134 | Sugiyama | PGAM4 PGAM3 | IWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYE |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y133 | Sugiyama | PGAM4 PGAM3 | KIWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSY |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N1G4 | Y257 | Sugiyama | LRRC47 KIAA1185 | LRDKRLEKMVSGCQTRSILEyLRVGGRGGGKGKGRAEGSEK |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N3D4 | T1359 | Sugiyama | EHBP1L1 | PSEEPPPSPGEEAGLQRFQDtsQyVCAELQALEQEQRQIDG |
| Q8NBF2 | Y39 | Sugiyama | NHLRC2 | TSLEYALLDAVTQQEKDSLVyQyLQKVDGWEQDLSVPEFPE |
| Q8NBP7 | Y521 | Sugiyama | PCSK9 NARC1 PSEC0052 | EAQGGKLVCRAHNAFGGEGVyAIARCCLLPQANCSVHTAPP |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NBS9 | Y289 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | RDGKKVDQYKGKRDLEsLREyVEsQLQRTETGATETVTPSE |
| Q8ND04 | Y631 | Sugiyama | SMG8 ABC2 C17orf71 | CNCGRKQAPRDDPFDIKAANyDFyQLLEEKCCGKLDHINFP |
| Q8ND04 | Y634 | Sugiyama | SMG8 ABC2 C17orf71 | GRKQAPRDDPFDIKAANyDFyQLLEEKCCGKLDHINFPVFE |
| Q8NDI1 | Y585 | Sugiyama | EHBP1 KIAA0903 NACSIN | TYKVGNYETDTNssVDQEKFyAELSDLKREPELQQPISGAV |
| Q8NFI4 | Y213 | Sugiyama | ST13P5 FAM10A5 | RLLGHWEEAAHDLAFACKLDyDEDAsAMLKEVQPRAQKIAE |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TAT6 | Y426 | Sugiyama | NPLOC4 KIAA1499 NPL4 | APELGYAKESSSEQyVPDVFyKDVDKFGNEITQLARPLPVE |
| Q8WWM7 | Y264 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | ESDMSNGWDPNEMFKFNEENyGVKTtyDssLssytVPLEKD |
| Q8WWM7 | Y270 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | GWDPNEMFKFNEENyGVKTtyDssLssytVPLEKDNsEEFR |
| Q8WWM7 | Y277 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | FKFNEENyGVKTtyDssLssytVPLEKDNsEEFRQRELRAA |
| Q92598 | Y641 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MIMQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQD |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y89 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | RFHGRAFNDPFIQKEKENLsyDLVPLKNGGVGIKVMYMGEE |
| Q92796 | Y673 | Sugiyama | DLG3 KIAA1232 | GSCVPHTTRPRRDNEVDGQDyHFVVsREQMEKDIQDNKFIE |
| Q92882 | Y207 | Sugiyama | OSTF1 | sLLKKKQGTDAVRtLsNAEDyLDDEDsD_____________ |
| Q92905 | Y203 | Sugiyama | COPS5 CSN5 JAB1 | LGAFRTYPKGYKPPDEGPsEyQtIPLNKIEDFGVHCKQYYA |
| Q93009 | Y749 | Sugiyama | USP7 HAUSP | DTSLILYEEVKPNLTERIQDyDVsLDKALDELMDGDIIVFQ |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96A49 | Y327 | Sugiyama | SYAP1 PRO3113 | AVLEEDsADWEKELQQELQEyEVVtESEKRDENWDKEIEKM |
| 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 |
| Q96D15 | T127 | Sugiyama | RCN3 UNQ239/PRO272 | AHTQQRHIRDsVsAAWDtyDtDRDGRVGWEELRNATYGHYA |
| Q96D46 | Y459 | Sugiyama | NMD3 CGI-07 | YQDFLEDLEEDEAIRKNVNIyRDsAIPVEsDtDDEGAPRIS |
| Q96FW1 | Y26 | Sugiyama | OTUB1 OTB1 OTU1 HSPC263 | PQQQKQEPLGsDsEGVNCLAyDEAIMAQQDRIQQEIAVQNP |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96HE7 | Y178 | Sugiyama | ERO1A ERO1L UNQ434/PRO865 | HDDSSDNFCEADDIQsPEAEyVDLLLNPERYTGYKGPDAWK |
| Q96HE7 | Y73 | Sugiyama | ERO1A ERO1L UNQ434/PRO865 | IDRFNNYRLFPRLQKLLEsDyFRyyKVNLKRPCPFWNDISQ |
| Q96HN2 | Y372 | Sugiyama | AHCYL2 KIAA0828 | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDMMFGG |
| Q96HN2 | Y608 | Sugiyama | AHCYL2 KIAA0828 | LTDEQAKYLGLNKNGPFKPNyYRY_________________ |
| Q96I25 | Y214 | Sugiyama | RBM17 SPF45 | yEEDSRPRsQsSKAAIPPPVyEEQDRPRsPtGPsNsFLANM |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96PZ0 | S135 | Sugiyama | PUS7 KIAA1897 | GItKFVSSHQGFSGILKERysDFVVHEIGKDGRISHLNDLs |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q96QK1 | Y791 | Sugiyama | VPS35 MEM3 TCCCTA00141 | HNtLEHLRLRREsPEsEGPIyEGLIL_______________ |
| Q96RT6 | Y307 | Sugiyama | CTAGE1 CTAGE2 | IHAAKLNASLKTLEGERNQIyIQLSEVDKTKEELTEHIKNL |
| Q96T37 | Y608 | Sugiyama | RBM15 OTT OTT1 | PPPPPVRERSTRTAATsVPAyEPLDSLDRRRDGWsLDRDRG |
| Q99426 | Y107 | Sugiyama | TBCB CG22 CKAP1 | VIDHsGARLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKR |
| Q99426 | Y114 | Sugiyama | TBCB CG22 CKAP1 | RLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKRsKLGRyN |
| Q99426 | Y98 | Sugiyama | TBCB CG22 CKAP1 | PVDDGCRIHVIDHsGARLGEyEDVSRVEKytIsQEAyDQRQ |
| Q99459 | T510 | Sugiyama | CDC5L KIAA0432 PCDC5RP | FEIVLPENAEKELEEREIDDtyIEDAADVDARKQAIRDAER |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99460 | Y950 | Sugiyama | PSMD1 | AHGPKIEEEEQEPEPPEPFEyIDD_________________ |
| Q99613 | T880 | Sugiyama | EIF3C EIF3S8 | AEKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMR |
| Q99615 | Y145 | Sugiyama | DNAJC7 TPR2 TTC2 | LDHKNAQAQQEFKNANAVMEyEKIAETDFEKRDFRKVVFCM |
| Q99615 | Y351 | Sugiyama | DNAJC7 TPR2 TTC2 | YLRRAQCYMDtEQyEEAVRDyEKVyQTEKTKEHKQLLKNAQ |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y544 | Sugiyama | ACO2 | LEAPDADELPKGEFDPGQDtyQHPPKDSsGQHVDVsPtsQR |
| Q99798 | Y665 | Sugiyama | ACO2 | DtARYYKKHGIRWVVIGDENyGEGSSREHAALEPRHLGGRA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| Q99848 | Y265 | Sugiyama | EBNA1BP2 EBP2 | NQKFGFGGKKKGSKWNtREsyDDVssFRAKTAHGRGLKRPG |
| Q99877 | Y41 | Sugiyama | H2BC15 H2BFD HIST1H2BN | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99877 | Y43 | Sugiyama | H2BC15 H2BFD HIST1H2BN | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99879 | Y41 | Sugiyama | H2BC14 H2BFE HIST1H2BM | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99879 | Y43 | Sugiyama | H2BC14 H2BFE HIST1H2BM | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99880 | Y41 | Sugiyama | H2BC13 H2BFC HIST1H2BL | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99880 | Y43 | Sugiyama | H2BC13 H2BFC HIST1H2BL | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q9BPW8 | Y148 | Sugiyama | NIPSNAP1 | FSGGYPALMDCMNKLKNNKEyLEFRRERSQMLLSRRNQLLL |
| Q9BPX3 | Y929 | Sugiyama | NCAPG CAPG NYMEL3 | QDATLTTTTFQNEDEKNKEVyMtPLRGVKATQASKSTQLKT |
| Q9BQE3 | T225 | Sugiyama | TUBA1C TUBA6 | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| Q9BQE3 | Y224 | Sugiyama | TUBA1C TUBA6 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| Q9BQE3 | Y312 | Sugiyama | TUBA1C TUBA6 | TNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BQS8 | Y646 | Sugiyama | FYCO1 ZFYVE7 | QNVVGRNQLLEGKLQALQADyQALQQRESAIQGsLASLEAE |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BS26 | T398 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | VASSPPESSFQKLAPsEyRytLLRDRDEL____________ |
| Q9BS26 | Y395 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | AQDVASSPPESSFQKLAPsEyRytLLRDRDEL_________ |
| Q9BS26 | Y397 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | DVASSPPESSFQKLAPsEyRytLLRDRDEL___________ |
| Q9BVA1 | T107 | Sugiyama | TUBB2B | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q9BXJ9 | Y280 | Sugiyama | NAA15 GA19 NARG1 NATH TBDN100 | YYKGLEKALKPANMLERLKIyEEAWTKYPRGLVPRRLPLNF |
| Q9BXP5 | Y864 | Sugiyama | SRRT ARS2 ASR2 | GYPGKPRNRMVRGDPRAIVEyRDLDAPDDVDFF________ |
| Q9BXS5 | Y418 | Sugiyama | AP1M1 CLTNM | IEKSGYQALPWVRYITQNGDyQLRtQ_______________ |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9GZL7 | Y380 | Sugiyama | WDR12 | SGSLDNIVKLWDTRSCKAPLyDLAAHEDKVLSVDWTDTGLL |
| Q9GZT8 | Y175 | Sugiyama | NIF3L1 ALS2CR1 MDS015 My018 | PSKAPNyPTEGNHRVEFNVNytQDLDKVMSAVKGIDGVsVT |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H2H8 | Y75 | Sugiyama | PPIL3 | DPTGTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPN |
| Q9H2H8 | Y78 | Sugiyama | PPIL3 | GTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPNTNG |
| Q9H2J4 | Y48 | Sugiyama | PDCL3 PhLP2A VIAF1 | ELEEEAEEEQRILQQsVVKTyEDMTLEELEDHEDEFNEEDE |
| Q9H4F8 | Y407 | Sugiyama | SMOC1 | FKRYVKKKAKPKKCARRFtDyCDLNKDKVISLPELKGCLGV |
| Q9H6H4 | Y167 | Sugiyama | REEP4 C8orf20 PP432 | RLRsFsMQDLRSISDAPAPAyHDPLyLEDQVSHRRPPIGYR |
| Q9H6H4 | Y172 | Sugiyama | REEP4 C8orf20 PP432 | sMQDLRSISDAPAPAyHDPLyLEDQVSHRRPPIGYRAGGLQ |
| Q9H6T3 | Y88 | Sugiyama | RPAP3 | KAKESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKD |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9H814 | T151 | Sugiyama | PHAX RNUXA | ATELGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDL |
| Q9H814 | Y152 | Sugiyama | PHAX RNUXA | TELGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDLD |
| Q9H814 | Y154 | Sugiyama | PHAX RNUXA | LGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDLDKE |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HB71 | Y165 | Sugiyama | CACYBP S100A6BP SIP PNAS-107 | VKTDTVLILCRKKVENTRWDyLtQVEKECKEKEKPsYDtEt |
| Q9NNW7 | Y70 | Sugiyama | TXNRD2 KIAA1652 TRXR2 | GGLACAKEAAQLGRKVAVVDyVEPSPQGTRWGLGGTCVNVG |
| Q9NP61 | Y408 | Sugiyama | ARFGAP3 ARFGAP1 | ETVLKTTGYSDRPTARRKPDyEPVENTDEAQKKFGNVKAIs |
| Q9NP74 | Y257 | Sugiyama | PALMD C1orf11 PALML | VEVEELLRQASERNsKsPtEyHEPVyANPFyRPttPQREtV |
| Q9NP74 | Y262 | Sugiyama | PALMD C1orf11 PALML | LLRQASERNsKsPtEyHEPVyANPFyRPttPQREtVtPGPN |
| Q9NPI1 | Y190 | Sugiyama | BRD7 BP75 CELTIX1 | MIIKHPMDFSTMKEKIKNNDyQsIEELKDNFKLMCTNAMIY |
| Q9NQE9 | Y44 | Sugiyama | HINT3 | TTVssVGTCEAAGKsPEPKDyDstCVFCRIAGRQDPGTELL |
| Q9NQR4 | Y202 | Sugiyama | NIT2 CUA002 | TTGPAHWELLQRSRAVDNQVyVAtAsPARDDKASYVAWGHS |
| Q9NRX4 | Y116 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AyGPAQHAISTEKIKAKyPDyEVtWANDGy___________ |
| Q9NRX4 | Y52 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | RSGAPAAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCE |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NY33 | Y251 | Sugiyama | DPP3 | TSKLKSYEFRGsPFQVTRGDyAPILQKVVEQLEKAKAYAAN |
| Q9NY65 | T225 | Sugiyama | TUBA8 TUBAL2 | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| Q9NY65 | Y224 | Sugiyama | TUBA8 TUBAL2 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| Q9NYU2 | Y1516 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | PMTKEPKLEAAVRIVPEWQDyDQEIKQLQIRFQKEKETGAL |
| Q9NYU2 | Y449 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | IEGLSLHNVLKLNIQPsEADyAVDIRSPAISWVNNLEVDSR |
| Q9NYU2 | Y966 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | LVMKVDALLsAQPKGDPRIEyQFFEDRHSAIKLRPKEGETY |
| Q9NZB2 | Y9 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | ____________MGVQGFQDyIEKHCPsAVVPVELQKLARG |
| Q9UBQ7 | Y255 | Sugiyama | GRHPR GLXR MSTP035 | KETAVFINISRGDVVNQDDLyQALAsGKIAAAGLDVtsPEP |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y352 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | TEEAREGIKQLLKQGSVQKVyNGLQGY______________ |
| Q9UBS4 | Y74 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | PDRNPDDPQAQEKFQDLGAAyEVLsDSEKRKQyDTyGEEGL |
| Q9UBS4 | Y89 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | DLGAAyEVLsDSEKRKQyDTyGEEGLKDGHQSSHGDIFSHF |
| Q9UHR4 | Y163 | Sugiyama | BAIAP2L1 IRTKS | IRRKSQGSRNALKyEHKEIEyVEtVTSRQSEIQKFIADGCK |
| Q9UHX1 | Y269 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | FGKIKSCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNL |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UJU6 | Y16 | Sugiyama | DBNL CMAP SH3P7 PP5423 | _____MAANLSRNGPALQEAyVRVVtEKsPtDWALFTyEGN |
| Q9UK59 | Y533 | Sugiyama | DBR1 | LsDEHEPEQRKKIKRRNQAIyAAVDDDDDDAA_________ |
| Q9UKF6 | Y677 | Sugiyama | CPSF3 CPSF73 | EGsEDDESLREMVELAAQRLyEALtPVH_____________ |
| Q9UKK9 | Y198 | Sugiyama | NUDT5 NUDIX5 HSPC115 | LLQRLDALVAEEHLTVDARVySyALALKHANAKPFEVPFLK |
| Q9UKS6 | Y206 | Sugiyama | PACSIN3 | RKLQERVERCAKEAEKTKAQyEQtLAELHRYTPRYMEDMEQ |
| Q9UKV3 | Y1086 | Sugiyama | ACIN1 ACINUS KIAA0670 | RTALHGVKWPQSNPKFLCADyAEQDELDyHRGLLVDRPsEt |
| Q9ULF5 | Y596 | Sugiyama | SLC39A10 KIAA1265 ZIP10 | RLNEtELtDLEGQQEsPPKNyLCIEEEKIIDHsHsDGLHtI |
| Q9UMS0 | Y194 | Sugiyama | NFU1 HIRIP5 CGI-33 | KELLDTRIRPTVQEDGGDVIyKGFEDGIVQLKLQGSCTSCP |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UNF0 | Y267 | Sugiyama | PACSIN2 | VLLEVQKHLDLSNVAGYKAIyHDLEQsIRAADAVEDLRWFR |
| Q9UNF1 | Y313 | Sugiyama | MAGED2 BCG1 | KDQTKIPIKRSDMLKDIIKEyTDVyPEIIERAGYSLEKVFG |
| Q9UNM6 | Y60 | Sugiyama | PSMD13 | QVLDFVQDPCFAQGDGLIKLyENFISEFEHRVNPLSLVEII |
| Q9UNZ2 | S205 | Sugiyama | NSFL1C UBXN2C | KLWKsGFsLDNGELRSyQDPsNAQFLEsIRRGEVPAELRRL |
| Q9UPQ0 | Y179 | Sugiyama | LIMCH1 KIAA1102 | QMRKDTDDIEsPKRSIRDsGyIDCWDsERsDsLsPPRHGRD |
| Q9UQ80 | Y343 | Sugiyama | PA2G4 EBP1 | VLLMPNGPMRITsGPFEPDLyKsEMEVQDAELKALLQssAs |
| Q9UQB8 | Y164 | Sugiyama | BAIAP2 | LRKKSQGSKNPQKYSDKELQyIDAISNKQGELENyVSDGYK |
| Q9Y230 | Y172 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | TGTGSKVGKLTLKTTEMETIyDLGTKMIESLTKDKVQAGDV |
| Q9Y230 | Y446 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | IKRVysLFLDEsRSTQYMKEyQDAFLFNELKGEtMDTS___ |
| Q9Y243 | T305 | Sugiyama | AKT3 PKBG | IKITDFGLCKEGITDAATMKtFCGtPEyLAPEVLEDNDyGR |
| Q9Y262 | S416 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | DKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNYH |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y262 | Y45 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | MHTGDPKQDLAyERQyEQQtyQVIPEVIKNFIQYFHKTVSD |
| Q9Y265 | Y220 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | VKRQGRCDTYAtEFDLEAEEyVPLPKGDVHKKKEIIQDVtL |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2S7 | Y133 | Sugiyama | POLDIP2 PDIP38 POLD4 HSPC017 | EKAENPAGHGSKEVKGKTHTyyQVLIDARDCPHISQRSQTE |
| Q9Y2S7 | Y134 | Sugiyama | POLDIP2 PDIP38 POLD4 HSPC017 | KAENPAGHGSKEVKGKTHTyyQVLIDARDCPHISQRSQTEA |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y3C1 | Y118 | Sugiyama | NOP16 CGI-117 HSPC111 | EAEASLPEKKGNTLSRDLIDyVRYMVENHGEDYKAMARDEK |
| Q9Y3D8 | Y31 | Sugiyama | AK6 CINAP AD-004 CGI-137 | TPGVGKTTLGKELASKSGLKyINVGDLAREEQLYDGYDEEY |
| Q9Y3F4 | Y114 | Sugiyama | STRAP MAWD UNRIP | LMTLAHKHIVKtVDFtQDSNyLLtGGQDKLLRIYDLNKPEA |
| Q9Y3F4 | Y252 | Sugiyama | STRAP MAWD UNRIP | HPEKEFLVAGGEDFKLyKyDyNsGEELEsyKGHFGPIHCVR |
| Q9Y3F4 | Y280 | Sugiyama | STRAP MAWD UNRIP | syKGHFGPIHCVRFSPDGELyAsGSEDGTLRLWQTVVGKty |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3P9 | Y472 | Sugiyama | RABGAP1 HSPC094 | FFLKLKQIKQRERKNNTDTLyEVVCLESESERERRKTTAsP |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y490 | Y127 | Sugiyama | TLN1 KIAA1027 TLN | TVTDMLMTICARIGITNHDEysLVRELMEEKKEEItGtLRK |
| Q9Y490 | Y1893 | Sugiyama | TLN1 KIAA1027 TLN | TKsNtsPEELGPLANQLTsDyGRLAsEAKPAAVAAENEEIG |
| Q9Y4H2 | Y919 | Sugiyama | IRS2 | PSLPSMHEYPLPPEPKsPGEyINIDFGEPGARLsPPAPPLL |
| Q9Y4L1 | Y755 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | EREKAANsLEAFIFEtQDKLyQPEyQEVsTEEQREEISGKL |
| Q9Y4L1 | Y759 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | AANsLEAFIFEtQDKLyQPEyQEVsTEEQREEISGKLSAAS |
| Q9Y5Q8 | Y393 | Sugiyama | GTF3C5 CDABP0017 | SGtsGARKPASSKYKLKDSVyIFREGALPPYRQMFYQLCDL |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y5V3 | Y505 | Sugiyama | MAGED1 NRAGE PP2250 PRO2292 | KDYTKVPIKRSEMLRDIIREyTDVyPEIIERACFVLEKKFG |
| Q9Y617 | Y70 | Sugiyama | PSAT1 PSA | AKIINNTENLVRELLAVPDNyKVIFLQGGGCGQFSAVPLNL |
| 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 |
|---|---|---|---|---|---|
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 3.245404e-08 | 7.489 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 2.596841e-08 | 7.586 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.986391e-07 | 6.702 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 4.431783e-06 | 5.353 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 6.240103e-06 | 5.205 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 6.240103e-06 | 5.205 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.546476e-05 | 4.811 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 1.879410e-05 | 4.726 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 3.843342e-05 | 4.415 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 4.626044e-05 | 4.335 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 6.071887e-05 | 4.217 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 8.199238e-05 | 4.086 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition | R-HSA-9926550 | 1.183386e-04 | 3.927 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 1.396063e-04 | 3.855 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.430551e-04 | 3.844 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 2.395278e-04 | 3.621 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 2.595232e-04 | 3.586 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 3.070725e-04 | 3.513 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 5.749513e-04 | 3.240 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 5.789401e-04 | 3.237 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 6.053123e-04 | 3.218 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 6.382707e-04 | 3.195 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 7.063810e-04 | 3.151 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 7.187565e-04 | 3.143 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 8.721420e-04 | 3.059 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 9.414356e-04 | 3.026 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 1.044635e-03 | 2.981 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 1.044635e-03 | 2.981 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 9.968135e-04 | 3.001 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.127704e-03 | 2.948 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.127704e-03 | 2.948 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.226743e-03 | 2.911 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 1.341351e-03 | 2.872 | 1 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 1.694570e-03 | 2.771 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 1.828194e-03 | 2.738 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 1.864590e-03 | 2.729 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 1.935164e-03 | 2.713 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 2.117883e-03 | 2.674 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 2.274331e-03 | 2.643 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.249092e-03 | 2.648 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 2.190713e-03 | 2.659 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.283993e-03 | 2.641 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.399577e-03 | 2.620 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.437495e-03 | 2.613 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 3.128933e-03 | 2.505 | 0 | 0 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | R-HSA-9758919 | 3.392763e-03 | 2.469 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 3.690904e-03 | 2.433 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 4.591867e-03 | 2.338 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 5.081321e-03 | 2.294 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 5.228077e-03 | 2.282 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 6.282253e-03 | 2.202 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 6.282253e-03 | 2.202 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 6.194405e-03 | 2.208 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 5.945612e-03 | 2.226 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 6.913787e-03 | 2.160 | 0 | 0 |
| Drug resistance of KIT mutants | R-HSA-9669937 | 1.056328e-02 | 1.976 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.056328e-02 | 1.976 | 0 | 0 |
| KIT mutants bind TKIs | R-HSA-9669921 | 1.056328e-02 | 1.976 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.056328e-02 | 1.976 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 1.056328e-02 | 1.976 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.056328e-02 | 1.976 | 0 | 0 |
| Imatinib-resistant KIT mutants | R-HSA-9669917 | 1.056328e-02 | 1.976 | 0 | 0 |
| Dasatinib-resistant KIT mutants | R-HSA-9669914 | 1.056328e-02 | 1.976 | 0 | 0 |
| Sunitinib-resistant KIT mutants | R-HSA-9669934 | 1.056328e-02 | 1.976 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.056328e-02 | 1.976 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.056328e-02 | 1.976 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.056328e-02 | 1.976 | 0 | 0 |
| Sorafenib-resistant KIT mutants | R-HSA-9669936 | 1.056328e-02 | 1.976 | 0 | 0 |
| Regorafenib-resistant KIT mutants | R-HSA-9669929 | 1.056328e-02 | 1.976 | 0 | 0 |
| Masitinib-resistant KIT mutants | R-HSA-9669924 | 1.056328e-02 | 1.976 | 0 | 0 |
| Nilotinib-resistant KIT mutants | R-HSA-9669926 | 1.056328e-02 | 1.976 | 0 | 0 |
| Positive Regulation of CDH1 Gene Transcription | R-HSA-9764790 | 8.653675e-03 | 2.063 | 0 | 0 |
| MET activates RAP1 and RAC1 | R-HSA-8875555 | 8.653675e-03 | 2.063 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 9.967028e-03 | 2.001 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 1.136293e-02 | 1.945 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 8.597633e-03 | 2.066 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 8.653675e-03 | 2.063 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.087727e-02 | 1.963 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 9.540274e-03 | 2.020 | 0 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 9.837262e-03 | 2.007 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 1.125910e-02 | 1.948 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 1.019046e-02 | 1.992 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 1.261410e-02 | 1.899 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.270470e-02 | 1.896 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 1.387123e-02 | 1.858 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.496177e-02 | 1.825 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.506097e-02 | 1.822 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 1.598086e-02 | 1.796 | 1 | 0 |
| Regulation of CDH1 mRNA translation by microRNAs | R-HSA-9764562 | 1.602741e-02 | 1.795 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.665477e-02 | 1.778 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.773513e-02 | 1.751 | 0 | 0 |
| Drug-mediated inhibition of MET activation | R-HSA-9734091 | 2.101563e-02 | 1.677 | 0 | 0 |
| SARS-CoV-1 targets PDZ proteins in cell-cell junction | R-HSA-9692912 | 2.101563e-02 | 1.677 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.329239e-02 | 1.633 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.329239e-02 | 1.633 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | R-HSA-2892247 | 2.136933e-02 | 1.670 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | R-HSA-8866910 | 2.136933e-02 | 1.670 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 2.407975e-02 | 1.618 | 1 | 1 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 2.483816e-02 | 1.605 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 2.528387e-02 | 1.597 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 2.688340e-02 | 1.571 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 2.688340e-02 | 1.571 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 2.688340e-02 | 1.571 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 2.752187e-02 | 1.560 | 0 | 0 |
| Signaling by extracellular domain mutants of KIT | R-HSA-9680187 | 3.135819e-02 | 1.504 | 0 | 0 |
| Signaling by juxtamembrane domain KIT mutants | R-HSA-9669935 | 3.135819e-02 | 1.504 | 0 | 0 |
| Signaling by kinase domain mutants of KIT | R-HSA-9669933 | 3.135819e-02 | 1.504 | 0 | 0 |
| Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) | R-HSA-5619050 | 3.135819e-02 | 1.504 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 3.621084e-02 | 1.441 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 3.654287e-02 | 1.437 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 3.654287e-02 | 1.437 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.946550e-02 | 1.531 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 3.140179e-02 | 1.503 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.390142e-02 | 1.470 | 0 | 0 |
| Formation of definitive endoderm | R-HSA-9823730 | 2.946550e-02 | 1.531 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 3.443991e-02 | 1.463 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.394339e-02 | 1.469 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 3.795327e-02 | 1.421 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 3.906489e-02 | 1.408 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.159212e-02 | 1.381 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.159212e-02 | 1.381 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.159212e-02 | 1.381 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.159212e-02 | 1.381 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 4.159212e-02 | 1.381 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.159212e-02 | 1.381 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.171856e-02 | 1.286 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 5.171856e-02 | 1.286 | 0 | 0 |
| MET activates PTPN11 | R-HSA-8865999 | 5.171856e-02 | 1.286 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 4.602328e-02 | 1.337 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.861283e-02 | 1.313 | 1 | 1 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 4.602328e-02 | 1.337 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 5.114969e-02 | 1.291 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 4.100505e-02 | 1.387 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 4.348688e-02 | 1.362 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 5.394583e-02 | 1.268 | 0 | 0 |
| MET activates STAT3 | R-HSA-8875791 | 5.171856e-02 | 1.286 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 5.394583e-02 | 1.268 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 4.412396e-02 | 1.355 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 5.394583e-02 | 1.268 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 4.066459e-02 | 1.391 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 5.274473e-02 | 1.278 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 4.602328e-02 | 1.337 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 4.405208e-02 | 1.356 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 5.600615e-02 | 1.252 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 5.611516e-02 | 1.251 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 5.668656e-02 | 1.247 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 5.668656e-02 | 1.247 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 5.668656e-02 | 1.247 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 6.173862e-02 | 1.209 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 6.173862e-02 | 1.209 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 6.173862e-02 | 1.209 | 0 | 0 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 6.173862e-02 | 1.209 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 6.227700e-02 | 1.206 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 6.518991e-02 | 1.186 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.518991e-02 | 1.186 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 7.165341e-02 | 1.145 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 7.165341e-02 | 1.145 | 0 | 0 |
| IRS activation | R-HSA-74713 | 7.165341e-02 | 1.145 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 7.165341e-02 | 1.145 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.146404e-02 | 1.089 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.146404e-02 | 1.089 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 9.117159e-02 | 1.040 | 0 | 0 |
| MET activates PI3K/AKT signaling | R-HSA-8851907 | 1.007771e-01 | 0.997 | 0 | 0 |
| IFNG signaling activates MAPKs | R-HSA-9732724 | 1.007771e-01 | 0.997 | 0 | 0 |
| SOS-mediated signalling | R-HSA-112412 | 1.007771e-01 | 0.997 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 9.620659e-02 | 1.017 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.815196e-02 | 1.167 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 1.007771e-01 | 0.997 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 9.620659e-02 | 1.017 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 9.563416e-02 | 1.019 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 7.165341e-02 | 1.145 | 0 | 0 |
| Signaling by MST1 | R-HSA-8852405 | 8.146404e-02 | 1.089 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 7.108037e-02 | 1.148 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 7.108037e-02 | 1.148 | 0 | 0 |
| MET Receptor Activation | R-HSA-6806942 | 9.117159e-02 | 1.040 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 7.408835e-02 | 1.130 | 0 | 0 |
| Activated NTRK3 signals through PI3K | R-HSA-9603381 | 1.007771e-01 | 0.997 | 0 | 0 |
| Negative feedback regulation of MAPK pathway | R-HSA-5674499 | 8.146404e-02 | 1.089 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 9.620659e-02 | 1.017 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 7.108037e-02 | 1.148 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 7.165341e-02 | 1.145 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 8.921578e-02 | 1.050 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 7.713658e-02 | 1.113 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.146404e-02 | 1.089 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 8.535585e-02 | 1.069 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 8.022386e-02 | 1.096 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 8.893935e-02 | 1.051 | 0 | 0 |
| Nectin/Necl trans heterodimerization | R-HSA-420597 | 7.165341e-02 | 1.145 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 9.117159e-02 | 1.040 | 0 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 9.117159e-02 | 1.040 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 1.007771e-01 | 0.997 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 8.585618e-02 | 1.066 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 8.651104e-02 | 1.063 | 0 | 0 |
| Immune System | R-HSA-168256 | 8.621215e-02 | 1.064 | 0 | 0 |
| Transcriptional regulation of pluripotent stem cells | R-HSA-452723 | 8.334906e-02 | 1.079 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 8.835660e-02 | 1.054 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 8.459098e-02 | 1.073 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.028342e-01 | 0.988 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 1.030514e-01 | 0.987 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 1.030514e-01 | 0.987 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.061941e-01 | 0.974 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.061941e-01 | 0.974 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 1.085981e-01 | 0.964 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.095834e-01 | 0.960 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 1.102818e-01 | 0.957 | 0 | 0 |
| Type I hemidesmosome assembly | R-HSA-446107 | 1.102818e-01 | 0.957 | 0 | 0 |
| MET receptor recycling | R-HSA-8875656 | 1.102818e-01 | 0.957 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 1.102818e-01 | 0.957 | 0 | 0 |
| PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | R-HSA-8849469 | 1.102818e-01 | 0.957 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 1.289924e-01 | 0.889 | 0 | 0 |
| MET activates RAS signaling | R-HSA-8851805 | 1.563273e-01 | 0.806 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.563273e-01 | 0.806 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 1.652481e-01 | 0.782 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.740751e-01 | 0.759 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 1.740751e-01 | 0.759 | 0 | 0 |
| InlB-mediated entry of Listeria monocytogenes into host cell | R-HSA-8875360 | 1.828093e-01 | 0.738 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.828093e-01 | 0.738 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.828093e-01 | 0.738 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.828093e-01 | 0.738 | 0 | 0 |
| G beta:gamma signalling through BTK | R-HSA-8964315 | 1.828093e-01 | 0.738 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 1.828093e-01 | 0.738 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 1.914516e-01 | 0.718 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.914516e-01 | 0.718 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.130010e-01 | 0.947 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 1.234147e-01 | 0.909 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 1.340499e-01 | 0.873 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 1.412512e-01 | 0.850 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 1.485336e-01 | 0.828 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 1.522032e-01 | 0.818 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.084647e-01 | 0.681 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.084647e-01 | 0.681 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.130010e-01 | 0.947 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.130010e-01 | 0.947 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.828093e-01 | 0.738 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.289924e-01 | 0.889 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.289924e-01 | 0.889 | 0 | 0 |
| Polo-like kinase mediated events | R-HSA-156711 | 2.168373e-01 | 0.664 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.130010e-01 | 0.947 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.652481e-01 | 0.782 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.084647e-01 | 0.681 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.164461e-01 | 0.934 | 1 | 1 |
| Signaling by ERBB2 | R-HSA-1227986 | 1.633157e-01 | 0.787 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.563273e-01 | 0.806 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.563273e-01 | 0.806 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 1.670520e-01 | 0.777 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 1.974157e-01 | 0.705 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 1.289924e-01 | 0.889 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 1.448827e-01 | 0.839 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.740751e-01 | 0.759 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.828093e-01 | 0.738 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.821378e-01 | 0.740 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 1.189926e-01 | 0.924 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 1.783467e-01 | 0.749 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 2.000031e-01 | 0.699 | 0 | 0 |
| mRNA decay by 3' to 5' exoribonuclease | R-HSA-429958 | 2.251218e-01 | 0.648 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 1.130010e-01 | 0.947 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 1.558906e-01 | 0.807 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 1.821378e-01 | 0.740 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.563273e-01 | 0.806 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 2.084647e-01 | 0.681 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.168373e-01 | 0.664 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 2.251218e-01 | 0.648 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.196865e-01 | 0.922 | 0 | 0 |
| Bicarbonate transporters | R-HSA-425381 | 1.382005e-01 | 0.859 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.473118e-01 | 0.832 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 1.563273e-01 | 0.806 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.563273e-01 | 0.806 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 1.670520e-01 | 0.777 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 2.128438e-01 | 0.672 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.196865e-01 | 0.922 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.828093e-01 | 0.738 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.168373e-01 | 0.664 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.501241e-01 | 0.824 | 1 | 0 |
| STAT3 nuclear events downstream of ALK signaling | R-HSA-9701898 | 1.828093e-01 | 0.738 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 1.934951e-01 | 0.713 | 1 | 0 |
| Erythrocytes take up oxygen and release carbon dioxide | R-HSA-1247673 | 1.563273e-01 | 0.806 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.168373e-01 | 0.664 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.251218e-01 | 0.648 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.652481e-01 | 0.782 | 0 | 0 |
| O2/CO2 exchange in erythrocytes | R-HSA-1480926 | 2.251218e-01 | 0.648 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.251218e-01 | 0.648 | 0 | 0 |
| Erythrocytes take up carbon dioxide and release oxygen | R-HSA-1237044 | 2.251218e-01 | 0.648 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 1.198917e-01 | 0.921 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 1.628068e-01 | 0.788 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 1.473118e-01 | 0.832 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 1.563273e-01 | 0.806 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 1.563273e-01 | 0.806 | 0 | 0 |
| Gastrin-CREB signalling pathway via PKC and MAPK | R-HSA-881907 | 2.251218e-01 | 0.648 | 0 | 0 |
| Signaling by Leptin | R-HSA-2586552 | 1.289924e-01 | 0.889 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.382005e-01 | 0.859 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 1.914516e-01 | 0.718 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 1.196865e-01 | 0.922 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.828093e-01 | 0.738 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 2.168373e-01 | 0.664 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 1.340499e-01 | 0.873 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 1.914516e-01 | 0.718 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 1.914516e-01 | 0.718 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 2.206021e-01 | 0.656 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 1.269363e-01 | 0.896 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 1.425348e-01 | 0.846 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.382005e-01 | 0.859 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 1.897554e-01 | 0.722 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.084647e-01 | 0.681 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.821378e-01 | 0.740 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 1.528201e-01 | 0.816 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.130639e-01 | 0.947 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.244902e-01 | 0.649 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 2.281350e-01 | 0.642 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.333192e-01 | 0.632 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.333192e-01 | 0.632 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.333192e-01 | 0.632 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.333192e-01 | 0.632 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 2.333192e-01 | 0.632 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 2.333192e-01 | 0.632 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 2.377891e-01 | 0.624 | 0 | 0 |
| MyD88 deficiency (TLR2/4) | R-HSA-5602498 | 2.414304e-01 | 0.617 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.414304e-01 | 0.617 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.414304e-01 | 0.617 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 2.414304e-01 | 0.617 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 2.469114e-01 | 0.607 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 2.479111e-01 | 0.606 | 0 | 0 |
| IRAK4 deficiency (TLR2/4) | R-HSA-5603041 | 2.494563e-01 | 0.603 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.494563e-01 | 0.603 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 2.494563e-01 | 0.603 | 0 | 0 |
| Signaling by NTRK3 (TRKC) | R-HSA-9034015 | 2.494563e-01 | 0.603 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 2.573977e-01 | 0.589 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 2.573977e-01 | 0.589 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.573977e-01 | 0.589 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 2.573977e-01 | 0.589 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.596579e-01 | 0.586 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 2.619470e-01 | 0.582 | 0 | 0 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | R-HSA-9634638 | 2.652557e-01 | 0.576 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 2.652557e-01 | 0.576 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.652557e-01 | 0.576 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 2.705057e-01 | 0.568 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 2.714116e-01 | 0.566 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 2.730244e-01 | 0.564 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.730309e-01 | 0.564 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 2.730309e-01 | 0.564 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 2.753290e-01 | 0.560 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 2.762293e-01 | 0.559 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.807243e-01 | 0.552 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.807243e-01 | 0.552 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.807243e-01 | 0.552 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 2.807243e-01 | 0.552 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 2.841986e-01 | 0.546 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 2.870737e-01 | 0.542 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 2.870737e-01 | 0.542 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.883368e-01 | 0.540 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 2.883368e-01 | 0.540 | 0 | 0 |
| Metalloprotease DUBs | R-HSA-5689901 | 2.883368e-01 | 0.540 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 2.958692e-01 | 0.529 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 2.958692e-01 | 0.529 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.033223e-01 | 0.518 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 3.065993e-01 | 0.513 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 3.104937e-01 | 0.508 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.106970e-01 | 0.508 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 3.106970e-01 | 0.508 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 3.179941e-01 | 0.498 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.179941e-01 | 0.498 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 3.179941e-01 | 0.498 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.182690e-01 | 0.497 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 3.221492e-01 | 0.492 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 3.252144e-01 | 0.488 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 3.323587e-01 | 0.478 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.323587e-01 | 0.478 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 3.323587e-01 | 0.478 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 3.354393e-01 | 0.474 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.394277e-01 | 0.469 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 3.394277e-01 | 0.469 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.394277e-01 | 0.469 | 0 | 0 |
| Translation | R-HSA-72766 | 3.446940e-01 | 0.463 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.453062e-01 | 0.462 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.533434e-01 | 0.452 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.601916e-01 | 0.443 | 0 | 0 |
| Formation of WDR5-containing histone-modifying complexes | R-HSA-9772755 | 3.601916e-01 | 0.443 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 3.601916e-01 | 0.443 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 3.611505e-01 | 0.442 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 3.637821e-01 | 0.439 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 3.644088e-01 | 0.438 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 3.644088e-01 | 0.438 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 3.669676e-01 | 0.435 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 3.669676e-01 | 0.435 | 0 | 0 |
| Voltage gated Potassium channels | R-HSA-1296072 | 3.736724e-01 | 0.428 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 3.736724e-01 | 0.428 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.803065e-01 | 0.420 | 0 | 0 |
| SLC-mediated transport of inorganic anions | R-HSA-9958790 | 3.803065e-01 | 0.420 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.868707e-01 | 0.412 | 0 | 0 |
| Transcriptional Regulation by E2F6 | R-HSA-8953750 | 3.868707e-01 | 0.412 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 3.868707e-01 | 0.412 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 3.870487e-01 | 0.412 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 3.907887e-01 | 0.408 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 3.922994e-01 | 0.406 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 3.933658e-01 | 0.405 | 0 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 3.933658e-01 | 0.405 | 0 | 0 |
| Diseases of Immune System | R-HSA-5260271 | 3.933658e-01 | 0.405 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 3.933658e-01 | 0.405 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 3.942897e-01 | 0.404 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 3.997925e-01 | 0.398 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 3.997925e-01 | 0.398 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 4.019473e-01 | 0.396 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 4.019473e-01 | 0.396 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 4.019473e-01 | 0.396 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 4.059067e-01 | 0.392 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.124436e-01 | 0.385 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 4.130096e-01 | 0.384 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 4.186693e-01 | 0.378 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.186693e-01 | 0.378 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 4.248295e-01 | 0.372 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 4.254071e-01 | 0.371 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.309248e-01 | 0.366 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 4.369558e-01 | 0.360 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.369558e-01 | 0.360 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.369558e-01 | 0.360 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 4.428943e-01 | 0.354 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.429233e-01 | 0.354 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.488279e-01 | 0.348 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 4.491285e-01 | 0.348 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 4.546703e-01 | 0.342 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 4.604511e-01 | 0.337 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 4.667183e-01 | 0.331 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.718307e-01 | 0.326 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 4.718307e-01 | 0.326 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 4.774306e-01 | 0.321 | 0 | 0 |
| Amino acids regulate mTORC1 | R-HSA-9639288 | 4.774306e-01 | 0.321 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 4.774306e-01 | 0.321 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 4.774306e-01 | 0.321 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 4.829715e-01 | 0.316 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 4.829715e-01 | 0.316 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 4.873841e-01 | 0.312 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 4.911835e-01 | 0.309 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 4.938788e-01 | 0.306 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 4.938788e-01 | 0.306 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 4.978567e-01 | 0.303 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 4.992463e-01 | 0.302 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 4.992463e-01 | 0.302 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.098121e-01 | 0.293 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 5.098121e-01 | 0.293 | 0 | 0 |
| Assembly of collagen fibrils and other multimeric structures | R-HSA-2022090 | 5.098121e-01 | 0.293 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 5.150117e-01 | 0.288 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.201563e-01 | 0.284 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 5.239545e-01 | 0.281 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 5.252468e-01 | 0.280 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 5.252468e-01 | 0.280 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 5.252468e-01 | 0.280 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 5.252468e-01 | 0.280 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 5.271919e-01 | 0.278 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 5.352671e-01 | 0.271 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.352671e-01 | 0.271 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.352671e-01 | 0.271 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 5.399930e-01 | 0.268 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 5.499047e-01 | 0.260 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 5.546813e-01 | 0.256 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 5.546813e-01 | 0.256 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 5.546813e-01 | 0.256 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 5.546813e-01 | 0.256 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.587447e-01 | 0.253 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.640839e-01 | 0.249 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.648741e-01 | 0.248 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 5.687109e-01 | 0.245 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 5.687109e-01 | 0.245 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 5.687109e-01 | 0.245 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 5.732890e-01 | 0.242 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.732890e-01 | 0.242 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.778189e-01 | 0.238 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 5.823009e-01 | 0.235 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 5.870800e-01 | 0.231 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 5.911236e-01 | 0.228 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 5.945839e-01 | 0.226 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 5.997610e-01 | 0.222 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 5.997610e-01 | 0.222 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 6.040114e-01 | 0.219 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 6.082169e-01 | 0.216 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 6.082169e-01 | 0.216 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 6.164953e-01 | 0.210 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 6.205690e-01 | 0.207 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 6.245997e-01 | 0.204 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.285878e-01 | 0.202 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.325338e-01 | 0.199 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.325338e-01 | 0.199 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 6.325338e-01 | 0.199 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.364381e-01 | 0.196 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 6.364381e-01 | 0.196 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 6.403012e-01 | 0.194 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 6.416298e-01 | 0.193 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 6.441235e-01 | 0.191 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 6.468724e-01 | 0.189 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.479053e-01 | 0.188 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 6.553497e-01 | 0.184 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 6.571763e-01 | 0.182 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.590129e-01 | 0.181 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 6.597148e-01 | 0.181 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 6.626375e-01 | 0.179 | 0 | 0 |
| Protein folding | R-HSA-391251 | 6.626375e-01 | 0.179 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 6.662237e-01 | 0.176 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 6.672402e-01 | 0.176 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 6.697721e-01 | 0.174 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 6.704409e-01 | 0.174 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.767567e-01 | 0.170 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 6.770660e-01 | 0.169 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 6.801937e-01 | 0.167 | 0 | 0 |
| Potassium Channels | R-HSA-1296071 | 6.801937e-01 | 0.167 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.818903e-01 | 0.166 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 6.902883e-01 | 0.161 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 6.902883e-01 | 0.161 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 6.935822e-01 | 0.159 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 6.968413e-01 | 0.157 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 6.968413e-01 | 0.157 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 7.000660e-01 | 0.155 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 7.000660e-01 | 0.155 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.032566e-01 | 0.153 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 7.064134e-01 | 0.151 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 7.077534e-01 | 0.150 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 7.095368e-01 | 0.149 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 7.162263e-01 | 0.145 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 7.184017e-01 | 0.144 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.187102e-01 | 0.143 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 7.187102e-01 | 0.143 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 7.187102e-01 | 0.143 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 7.205630e-01 | 0.142 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.217036e-01 | 0.142 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.217036e-01 | 0.142 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 7.223388e-01 | 0.141 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 7.246653e-01 | 0.140 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 7.246653e-01 | 0.140 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 7.333636e-01 | 0.135 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 7.333636e-01 | 0.135 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 7.362019e-01 | 0.133 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 7.445378e-01 | 0.128 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 7.530910e-01 | 0.123 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 7.578530e-01 | 0.120 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 7.578530e-01 | 0.120 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 7.590486e-01 | 0.120 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 7.604321e-01 | 0.119 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 7.629838e-01 | 0.117 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 7.629838e-01 | 0.117 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 7.655085e-01 | 0.116 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 7.655085e-01 | 0.116 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 7.680065e-01 | 0.115 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.704781e-01 | 0.113 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 7.801051e-01 | 0.108 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 7.809377e-01 | 0.107 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 7.826813e-01 | 0.106 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 7.902797e-01 | 0.102 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 7.912188e-01 | 0.102 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 7.928906e-01 | 0.101 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 7.937981e-01 | 0.100 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 7.937981e-01 | 0.100 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 7.959964e-01 | 0.099 | 0 | 0 |
| M Phase | R-HSA-68886 | 8.037124e-01 | 0.095 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 8.045589e-01 | 0.094 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 8.058470e-01 | 0.094 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 8.120528e-01 | 0.090 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 8.263073e-01 | 0.083 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 8.299948e-01 | 0.081 | 0 | 0 |
| S Phase | R-HSA-69242 | 8.299948e-01 | 0.081 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 8.336043e-01 | 0.079 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 8.353805e-01 | 0.078 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 8.371377e-01 | 0.077 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 8.388763e-01 | 0.076 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 8.388763e-01 | 0.076 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 8.388763e-01 | 0.076 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 8.405965e-01 | 0.075 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 8.422984e-01 | 0.075 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 8.456482e-01 | 0.073 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.489273e-01 | 0.071 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 8.495167e-01 | 0.071 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 8.505407e-01 | 0.070 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 8.526596e-01 | 0.069 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 8.568251e-01 | 0.067 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 8.568251e-01 | 0.067 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 8.613653e-01 | 0.065 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 8.671970e-01 | 0.062 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 8.686164e-01 | 0.061 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 8.700207e-01 | 0.060 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 8.741448e-01 | 0.058 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 8.794419e-01 | 0.056 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 8.845172e-01 | 0.053 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 8.881838e-01 | 0.051 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 8.905637e-01 | 0.050 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 8.917347e-01 | 0.050 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 8.940394e-01 | 0.049 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 8.960843e-01 | 0.048 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 9.038216e-01 | 0.044 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 9.068785e-01 | 0.042 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.068785e-01 | 0.042 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 9.088372e-01 | 0.042 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.108046e-01 | 0.041 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 9.157643e-01 | 0.038 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 9.163873e-01 | 0.038 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 9.277088e-01 | 0.033 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.299375e-01 | 0.032 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.326049e-01 | 0.030 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 9.340435e-01 | 0.030 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.381073e-01 | 0.028 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 9.381788e-01 | 0.028 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.426785e-01 | 0.026 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 9.426799e-01 | 0.026 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 9.491004e-01 | 0.023 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 9.505068e-01 | 0.022 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 9.607355e-01 | 0.017 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 9.665073e-01 | 0.015 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 9.669811e-01 | 0.015 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.674160e-01 | 0.014 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 9.831541e-01 | 0.007 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 9.870268e-01 | 0.006 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.884921e-01 | 0.005 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.944163e-01 | 0.002 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 9.949142e-01 | 0.002 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.986445e-01 | 0.001 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.987068e-01 | 0.001 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.990160e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999991e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.999991e-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 |
|---|---|---|---|---|---|
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 1.110223e-16 | 15.955 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 1.110223e-16 | 15.955 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 1.110223e-16 | 15.955 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 1.110223e-16 | 15.955 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 1.110223e-16 | 15.955 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 1.110223e-16 | 15.955 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 1.110223e-16 | 15.955 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 1.110223e-16 | 15.955 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 1.110223e-16 | 15.955 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.110223e-16 | 15.955 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 1.110223e-16 | 15.955 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.110223e-16 | 15.955 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 1.110223e-16 | 15.955 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.110223e-16 | 15.955 | 1 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.110223e-16 | 15.955 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 1.110223e-16 | 15.955 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 1.110223e-16 | 15.955 | 1 | 0 |
| Aggrephagy | R-HSA-9646399 | 6.661338e-16 | 15.176 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 8.881784e-16 | 15.051 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 1.332268e-15 | 14.875 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 1.776357e-15 | 14.750 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 2.664535e-15 | 14.574 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 3.330669e-15 | 14.477 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 3.441691e-15 | 14.463 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 6.106227e-15 | 14.214 | 1 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 7.882583e-15 | 14.103 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 8.659740e-15 | 14.062 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 1.032507e-14 | 13.986 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.221245e-14 | 13.913 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.221245e-14 | 13.913 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 2.242651e-14 | 13.649 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 3.175238e-14 | 13.498 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 6.139533e-14 | 13.212 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 6.594725e-14 | 13.181 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 9.947598e-14 | 13.002 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 1.049161e-13 | 12.979 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 1.101341e-13 | 12.958 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 1.345590e-13 | 12.871 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.671996e-13 | 12.777 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 1.794120e-13 | 12.746 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 2.754463e-13 | 12.560 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 2.754463e-13 | 12.560 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 5.160317e-13 | 12.287 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 5.547784e-13 | 12.256 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 7.018830e-13 | 12.154 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 7.268630e-13 | 12.139 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 7.076562e-13 | 12.150 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 7.095435e-13 | 12.149 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 8.041345e-13 | 12.095 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 1.115885e-12 | 11.952 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 1.238232e-12 | 11.907 | 0 | 0 |
| Protein folding | R-HSA-391251 | 1.431966e-12 | 11.844 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 1.631695e-12 | 11.787 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 1.867950e-12 | 11.729 | 0 | 0 |
| Kinesins | R-HSA-983189 | 1.867950e-12 | 11.729 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 1.958322e-12 | 11.708 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 1.958322e-12 | 11.708 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 2.141398e-12 | 11.669 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 2.443490e-12 | 11.612 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 2.426837e-12 | 11.615 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 2.773670e-12 | 11.557 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 2.773670e-12 | 11.557 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 4.592993e-12 | 11.338 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 4.870104e-12 | 11.312 | 1 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 5.856871e-12 | 11.232 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 5.856871e-12 | 11.232 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 6.687317e-12 | 11.175 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 7.332690e-12 | 11.135 | 0 | 0 |
| Depurination | R-HSA-73927 | 7.426393e-12 | 11.129 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 7.876255e-12 | 11.104 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 9.096945e-12 | 11.041 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 9.096945e-12 | 11.041 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 9.782952e-12 | 11.010 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 1.041467e-11 | 10.982 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 1.174938e-11 | 10.930 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 1.174938e-11 | 10.930 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 1.466716e-11 | 10.834 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 1.466716e-11 | 10.834 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 2.253520e-11 | 10.647 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 2.253520e-11 | 10.647 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 2.583300e-11 | 10.588 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 2.774692e-11 | 10.557 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 4.670730e-11 | 10.331 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 4.670730e-11 | 10.331 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 6.942102e-11 | 10.159 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 7.392065e-11 | 10.131 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 7.430678e-11 | 10.129 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 7.547329e-11 | 10.122 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 1.518331e-10 | 9.819 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 1.803360e-10 | 9.744 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 1.818083e-10 | 9.740 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 1.825705e-10 | 9.739 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 2.135573e-10 | 9.670 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 2.416655e-10 | 9.617 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 2.521758e-10 | 9.598 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 2.604679e-10 | 9.584 | 1 | 1 |
| Centrosome maturation | R-HSA-380287 | 3.175559e-10 | 9.498 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 4.085037e-10 | 9.389 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 4.772955e-10 | 9.321 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 4.620035e-10 | 9.335 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 4.620035e-10 | 9.335 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 5.563071e-10 | 9.255 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 5.866873e-10 | 9.232 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 6.918794e-10 | 9.160 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 7.834389e-10 | 9.106 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 8.685901e-10 | 9.061 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 8.685901e-10 | 9.061 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 8.841953e-10 | 9.053 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 8.853626e-10 | 9.053 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 1.127521e-09 | 8.948 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 1.000088e-09 | 9.000 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 1.122632e-09 | 8.950 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 1.049538e-09 | 8.979 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.025831e-09 | 8.989 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 1.136578e-09 | 8.944 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.329778e-09 | 8.876 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 1.329778e-09 | 8.876 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 1.353686e-09 | 8.868 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 1.526359e-09 | 8.816 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 1.991766e-09 | 8.701 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.251236e-09 | 8.648 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 2.281821e-09 | 8.642 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 2.281821e-09 | 8.642 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 2.505189e-09 | 8.601 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 2.599512e-09 | 8.585 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 2.665665e-09 | 8.574 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 2.956219e-09 | 8.529 | 0 | 0 |
| Immune System | R-HSA-168256 | 3.024591e-09 | 8.519 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 3.481976e-09 | 8.458 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 3.867234e-09 | 8.413 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 4.307549e-09 | 8.366 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 4.862188e-09 | 8.313 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 5.855861e-09 | 8.232 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 6.176600e-09 | 8.209 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 6.607286e-09 | 8.180 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 7.156634e-09 | 8.145 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 7.206771e-09 | 8.142 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 7.799794e-09 | 8.108 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 7.872526e-09 | 8.104 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 7.899832e-09 | 8.102 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 8.746163e-09 | 8.058 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.223082e-08 | 7.913 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.255201e-08 | 7.901 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 1.683727e-08 | 7.774 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.925780e-08 | 7.715 | 1 | 1 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 2.096227e-08 | 7.679 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 2.558923e-08 | 7.592 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 2.830251e-08 | 7.548 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 3.074190e-08 | 7.512 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 3.121601e-08 | 7.506 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 4.160747e-08 | 7.381 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 4.801026e-08 | 7.319 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 5.256654e-08 | 7.279 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 4.853464e-08 | 7.314 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 5.143950e-08 | 7.289 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 5.455711e-08 | 7.263 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 5.812197e-08 | 7.236 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 6.446238e-08 | 7.191 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 7.652267e-08 | 7.116 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 9.561119e-08 | 7.019 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 9.636530e-08 | 7.016 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 9.636530e-08 | 7.016 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 9.636530e-08 | 7.016 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 1.072584e-07 | 6.970 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 1.094050e-07 | 6.961 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 1.238661e-07 | 6.907 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 1.238661e-07 | 6.907 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 1.365050e-07 | 6.865 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 1.432551e-07 | 6.844 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 1.503495e-07 | 6.823 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 1.895187e-07 | 6.722 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 2.580696e-07 | 6.588 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 2.711167e-07 | 6.567 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 2.813777e-07 | 6.551 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 2.813777e-07 | 6.551 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 2.822134e-07 | 6.549 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 5.552756e-07 | 6.255 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 5.565101e-07 | 6.255 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 5.779311e-07 | 6.238 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 6.291072e-07 | 6.201 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 7.843814e-07 | 6.105 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 8.330373e-07 | 6.079 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 1.006208e-06 | 5.997 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 1.590762e-06 | 5.798 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 1.820598e-06 | 5.740 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 3.679735e-06 | 5.434 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 4.991167e-06 | 5.302 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 4.396570e-06 | 5.357 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 5.698086e-06 | 5.244 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 5.982736e-06 | 5.223 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.219292e-05 | 4.914 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 1.611909e-05 | 4.793 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 2.020977e-05 | 4.694 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 3.777548e-05 | 4.423 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.321502e-05 | 4.364 | 1 | 1 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 4.455748e-05 | 4.351 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 4.455748e-05 | 4.351 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 4.644499e-05 | 4.333 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 4.830099e-05 | 4.316 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 5.324287e-05 | 4.274 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 7.404503e-05 | 4.131 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 7.404503e-05 | 4.131 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 1.008013e-04 | 3.997 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.262958e-04 | 3.899 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 1.300926e-04 | 3.886 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 1.410252e-04 | 3.851 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 1.481623e-04 | 3.829 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 1.495129e-04 | 3.825 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 1.861857e-04 | 3.730 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.104923e-04 | 3.677 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 2.262078e-04 | 3.645 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 2.453590e-04 | 3.610 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 2.720997e-04 | 3.565 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 2.921262e-04 | 3.534 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.954830e-04 | 3.529 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 3.530123e-04 | 3.452 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 3.646596e-04 | 3.438 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 3.761117e-04 | 3.425 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 4.096780e-04 | 3.388 | 0 | 0 |
| CASP4 inflammasome assembly | R-HSA-9948001 | 4.742264e-04 | 3.324 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 5.033837e-04 | 3.298 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 6.061460e-04 | 3.217 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 7.219645e-04 | 3.141 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 7.404763e-04 | 3.130 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 8.623327e-04 | 3.064 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 9.572449e-04 | 3.019 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 9.753109e-04 | 3.011 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 9.811998e-04 | 3.008 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 1.002140e-03 | 2.999 | 0 | 0 |
| Microbial factors inhibit CASP4 activity | R-HSA-9956593 | 1.025775e-03 | 2.989 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.207577e-03 | 2.918 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 1.408485e-03 | 2.851 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 1.408485e-03 | 2.851 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 1.528137e-03 | 2.816 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 1.408485e-03 | 2.851 | 0 | 0 |
| Non-canonical inflammasome activation | R-HSA-9686114 | 1.207577e-03 | 2.918 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.572605e-03 | 2.803 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 1.853472e-03 | 2.732 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.870438e-03 | 2.728 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 2.063079e-03 | 2.685 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 2.177142e-03 | 2.662 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.416968e-03 | 2.617 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.416968e-03 | 2.617 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 2.488588e-03 | 2.604 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 2.516039e-03 | 2.599 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.905055e-03 | 2.537 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.986522e-03 | 2.525 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 3.075495e-03 | 2.512 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 3.093455e-03 | 2.510 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 3.402696e-03 | 2.468 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 3.487224e-03 | 2.458 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 3.552514e-03 | 2.449 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 3.552514e-03 | 2.449 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 3.552514e-03 | 2.449 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 3.552514e-03 | 2.449 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 3.565085e-03 | 2.448 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 4.184082e-03 | 2.378 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 5.061966e-03 | 2.296 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 5.061966e-03 | 2.296 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 5.083099e-03 | 2.294 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 5.138606e-03 | 2.289 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 5.960478e-03 | 2.225 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 5.960478e-03 | 2.225 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 6.013739e-03 | 2.221 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 6.424535e-03 | 2.192 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 6.424535e-03 | 2.192 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 6.572886e-03 | 2.182 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 6.635412e-03 | 2.178 | 0 | 0 |
| Interleukin-18 signaling | R-HSA-9012546 | 7.158842e-03 | 2.145 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 7.899871e-03 | 2.102 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 8.325275e-03 | 2.080 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 8.325275e-03 | 2.080 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 8.456666e-03 | 2.073 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 8.714788e-03 | 2.060 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 8.853490e-03 | 2.053 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 9.340498e-03 | 2.030 | 0 | 0 |
| Drug resistance of FLT3 mutants | R-HSA-9702506 | 1.130036e-02 | 1.947 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.130036e-02 | 1.947 | 0 | 0 |
| FLT3 mutants bind TKIs | R-HSA-9702509 | 1.130036e-02 | 1.947 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.130036e-02 | 1.947 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.130036e-02 | 1.947 | 0 | 0 |
| semaxanib-resistant FLT3 mutants | R-HSA-9702577 | 1.130036e-02 | 1.947 | 0 | 0 |
| ponatinib-resistant FLT3 mutants | R-HSA-9702614 | 1.130036e-02 | 1.947 | 0 | 0 |
| gilteritinib-resistant FLT3 mutants | R-HSA-9702590 | 1.130036e-02 | 1.947 | 0 | 0 |
| quizartinib-resistant FLT3 mutants | R-HSA-9702620 | 1.130036e-02 | 1.947 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.130036e-02 | 1.947 | 0 | 0 |
| tamatinib-resistant FLT3 mutants | R-HSA-9703009 | 1.130036e-02 | 1.947 | 0 | 0 |
| midostaurin-resistant FLT3 mutants | R-HSA-9702600 | 1.130036e-02 | 1.947 | 0 | 0 |
| linifanib-resistant FLT3 mutants | R-HSA-9702998 | 1.130036e-02 | 1.947 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.130036e-02 | 1.947 | 0 | 0 |
| crenolanib-resistant FLT3 mutants | R-HSA-9702581 | 1.130036e-02 | 1.947 | 0 | 0 |
| sorafenib-resistant FLT3 mutants | R-HSA-9702624 | 1.130036e-02 | 1.947 | 0 | 0 |
| lestaurtinib-resistant FLT3 mutants | R-HSA-9702596 | 1.130036e-02 | 1.947 | 0 | 0 |
| KW2449-resistant FLT3 mutants | R-HSA-9702569 | 1.130036e-02 | 1.947 | 0 | 0 |
| pexidartinib-resistant FLT3 mutants | R-HSA-9702605 | 1.130036e-02 | 1.947 | 0 | 0 |
| sunitinib-resistant FLT3 mutants | R-HSA-9702632 | 1.130036e-02 | 1.947 | 0 | 0 |
| tandutinib-resistant FLT3 mutants | R-HSA-9702636 | 1.130036e-02 | 1.947 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.130036e-02 | 1.947 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.005729e-02 | 1.998 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.423451e-02 | 1.847 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.365337e-02 | 1.865 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 1.134123e-02 | 1.945 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 1.180350e-02 | 1.928 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 9.851575e-03 | 2.006 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.292334e-02 | 1.889 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 1.258482e-02 | 1.900 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 1.097936e-02 | 1.959 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 1.414802e-02 | 1.849 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 9.851575e-03 | 2.006 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 9.758915e-03 | 2.011 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 1.170701e-02 | 1.932 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.005729e-02 | 1.998 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.443598e-02 | 1.841 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.459565e-02 | 1.836 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.459565e-02 | 1.836 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.481261e-02 | 1.829 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 1.511526e-02 | 1.821 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 1.600118e-02 | 1.796 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.656988e-02 | 1.781 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 1.678885e-02 | 1.775 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 1.692863e-02 | 1.771 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 1.731333e-02 | 1.762 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 1.809792e-02 | 1.742 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.820203e-02 | 1.740 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 1.887220e-02 | 1.724 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 2.013178e-02 | 1.696 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 2.013178e-02 | 1.696 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 2.013178e-02 | 1.696 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 2.013178e-02 | 1.696 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 2.084645e-02 | 1.681 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.200995e-02 | 1.657 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 2.214308e-02 | 1.655 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.214308e-02 | 1.655 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.229181e-02 | 1.652 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH3 | R-HSA-5632927 | 2.247371e-02 | 1.648 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH6 | R-HSA-5632968 | 2.247371e-02 | 1.648 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 2.311527e-02 | 1.636 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 2.385453e-02 | 1.622 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 2.385854e-02 | 1.622 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | R-HSA-2892247 | 2.423387e-02 | 1.616 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 2.613420e-02 | 1.583 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.640211e-02 | 1.578 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 2.660940e-02 | 1.575 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 2.851613e-02 | 1.545 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.864581e-02 | 1.543 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.908697e-02 | 1.536 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 2.985891e-02 | 1.525 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 3.037004e-02 | 1.518 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 3.078245e-02 | 1.512 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 3.096300e-02 | 1.509 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 3.172272e-02 | 1.499 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 3.302441e-02 | 1.481 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 3.335176e-02 | 1.477 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 3.335176e-02 | 1.477 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH2 | R-HSA-5632928 | 3.352148e-02 | 1.475 | 0 | 0 |
| PTEN Loss of Function in Cancer | R-HSA-5674404 | 3.352148e-02 | 1.475 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.352148e-02 | 1.475 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 3.371876e-02 | 1.472 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 3.450702e-02 | 1.462 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 3.450702e-02 | 1.462 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 3.450702e-02 | 1.462 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.581019e-02 | 1.446 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 3.694011e-02 | 1.433 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 3.833643e-02 | 1.416 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.833643e-02 | 1.416 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.833643e-02 | 1.416 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 4.034475e-02 | 1.394 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 4.092865e-02 | 1.388 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 4.092865e-02 | 1.388 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 4.094170e-02 | 1.388 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 4.358506e-02 | 1.361 | 0 | 0 |
| Regulation of PTEN mRNA translation | R-HSA-8943723 | 4.358506e-02 | 1.361 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 4.431845e-02 | 1.353 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.444506e-02 | 1.352 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.444506e-02 | 1.352 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.444506e-02 | 1.352 | 0 | 0 |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.444506e-02 | 1.352 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.444506e-02 | 1.352 | 0 | 0 |
| Neurophilin interactions with VEGF and VEGFR | R-HSA-194306 | 4.444506e-02 | 1.352 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.444506e-02 | 1.352 | 0 | 0 |
| Activation, myristolyation of BID and translocation to mitochondria | R-HSA-75108 | 4.444506e-02 | 1.352 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 4.480253e-02 | 1.349 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 4.640317e-02 | 1.333 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 4.803183e-02 | 1.318 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 4.803183e-02 | 1.318 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 4.905698e-02 | 1.309 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 4.908341e-02 | 1.309 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 4.908341e-02 | 1.309 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 4.908341e-02 | 1.309 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 4.968831e-02 | 1.304 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 5.132196e-02 | 1.290 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 5.152720e-02 | 1.288 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 5.167265e-02 | 1.287 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 5.192191e-02 | 1.285 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 5.481773e-02 | 1.261 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 5.481773e-02 | 1.261 | 0 | 0 |
| Diseases of Mismatch Repair (MMR) | R-HSA-5423599 | 5.524584e-02 | 1.258 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.524584e-02 | 1.258 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 5.575062e-02 | 1.254 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 5.582270e-02 | 1.253 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 6.592520e-02 | 1.181 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.592520e-02 | 1.181 | 0 | 0 |
| IRS activation | R-HSA-74713 | 7.648449e-02 | 1.116 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.648449e-02 | 1.116 | 0 | 0 |
| Loss of phosphorylation of MECP2 at T308 | R-HSA-9022535 | 7.648449e-02 | 1.116 | 0 | 0 |
| FLT3 signaling by CBL mutants | R-HSA-9706377 | 7.648449e-02 | 1.116 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.692507e-02 | 1.061 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 9.724824e-02 | 1.012 | 0 | 0 |
| STAT5 Activation | R-HSA-9645135 | 9.724824e-02 | 1.012 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.724824e-02 | 1.012 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.724824e-02 | 1.012 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 1.074553e-01 | 0.969 | 0 | 0 |
| IFNG signaling activates MAPKs | R-HSA-9732724 | 1.074553e-01 | 0.969 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 1.074553e-01 | 0.969 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 7.655906e-02 | 1.116 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 6.694178e-02 | 1.174 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 7.330638e-02 | 1.135 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 7.330638e-02 | 1.135 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 1.112149e-01 | 0.954 | 0 | 0 |
| NOSTRIN mediated eNOS trafficking | R-HSA-203641 | 1.074553e-01 | 0.969 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.005096e-01 | 0.998 | 0 | 0 |
| PTK6 Down-Regulation | R-HSA-8849472 | 7.648449e-02 | 1.116 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.113340e-01 | 0.953 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.692507e-02 | 1.061 | 0 | 0 |
| Cam-PDE 1 activation | R-HSA-111957 | 8.692507e-02 | 1.061 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.692507e-02 | 1.061 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.074553e-01 | 0.969 | 0 | 0 |
| Insulin receptor recycling | R-HSA-77387 | 5.776923e-02 | 1.238 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 1.125539e-01 | 0.949 | 0 | 0 |
| PTK6 Activates STAT3 | R-HSA-8849474 | 7.648449e-02 | 1.116 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 6.204654e-02 | 1.207 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 6.204654e-02 | 1.207 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 7.673610e-02 | 1.115 | 0 | 0 |
| NADE modulates death signalling | R-HSA-205025 | 6.592520e-02 | 1.181 | 0 | 0 |
| Biosynthesis of DPAn-3-derived 13-series resolvins | R-HSA-9026403 | 7.648449e-02 | 1.116 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 1.005096e-01 | 0.998 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 1.040838e-01 | 0.983 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 1.054274e-01 | 0.977 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 7.568655e-02 | 1.121 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 6.077479e-02 | 1.216 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.724824e-02 | 1.012 | 0 | 0 |
| Signaling by LTK in cancer | R-HSA-9842640 | 9.724824e-02 | 1.012 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 6.077479e-02 | 1.216 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 7.980769e-02 | 1.098 | 0 | 0 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 8.692507e-02 | 1.061 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 9.273726e-02 | 1.033 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 7.330638e-02 | 1.135 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 1.041278e-01 | 0.982 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 5.757687e-02 | 1.240 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 5.757687e-02 | 1.240 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 8.960410e-02 | 1.048 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 1.072146e-01 | 0.970 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 7.330638e-02 | 1.135 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 9.000549e-02 | 1.046 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 9.346913e-02 | 1.029 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 6.383282e-02 | 1.195 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 7.985671e-02 | 1.098 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 6.694178e-02 | 1.174 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.150076e-01 | 0.939 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 7.655906e-02 | 1.116 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 8.658131e-02 | 1.063 | 0 | 0 |
| TBC/RABGAPs | R-HSA-8854214 | 1.150076e-01 | 0.939 | 0 | 0 |
| Transcriptional regulation of pluripotent stem cells | R-HSA-452723 | 9.346913e-02 | 1.029 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 8.658131e-02 | 1.063 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 9.697092e-02 | 1.013 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 7.182077e-02 | 1.144 | 0 | 0 |
| CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | R-HSA-442729 | 1.175476e-01 | 0.930 | 0 | 0 |
| Interleukin-9 signaling | R-HSA-8985947 | 1.175476e-01 | 0.930 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 1.175476e-01 | 0.930 | 0 | 0 |
| Adrenoceptors | R-HSA-390696 | 1.175476e-01 | 0.930 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 1.184821e-01 | 0.926 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.187119e-01 | 0.926 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.224458e-01 | 0.912 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 1.224458e-01 | 0.912 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 1.258895e-01 | 0.900 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 1.262082e-01 | 0.899 | 0 | 0 |
| Inactivation, recovery and regulation of the phototransduction cascade | R-HSA-2514859 | 1.262082e-01 | 0.899 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.275265e-01 | 0.894 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 1.275265e-01 | 0.894 | 0 | 0 |
| Activation of RAC1 downstream of NMDARs | R-HSA-9619229 | 1.275265e-01 | 0.894 | 0 | 0 |
| Calcineurin activates NFAT | R-HSA-2025928 | 1.275265e-01 | 0.894 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.275265e-01 | 0.894 | 0 | 0 |
| MAPK1 (ERK2) activation | R-HSA-112411 | 1.275265e-01 | 0.894 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.275265e-01 | 0.894 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.275265e-01 | 0.894 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 1.275265e-01 | 0.894 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 1.275265e-01 | 0.894 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 1.335243e-01 | 0.874 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 1.338138e-01 | 0.873 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 1.338138e-01 | 0.873 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.373930e-01 | 0.862 | 0 | 0 |
| Activation of Ca-permeable Kainate Receptor | R-HSA-451308 | 1.373930e-01 | 0.862 | 0 | 0 |
| CaMK IV-mediated phosphorylation of CREB | R-HSA-111932 | 1.373930e-01 | 0.862 | 0 | 0 |
| Interleukin-27 signaling | R-HSA-9020956 | 1.373930e-01 | 0.862 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.373930e-01 | 0.862 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.373930e-01 | 0.862 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.373930e-01 | 0.862 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 1.373930e-01 | 0.862 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 1.376550e-01 | 0.861 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.376550e-01 | 0.861 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.376550e-01 | 0.861 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 1.386802e-01 | 0.858 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 1.415203e-01 | 0.849 | 0 | 0 |
| The phototransduction cascade | R-HSA-2514856 | 1.454087e-01 | 0.837 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.471486e-01 | 0.832 | 0 | 0 |
| Ionotropic activity of kainate receptors | R-HSA-451306 | 1.471486e-01 | 0.832 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.471486e-01 | 0.832 | 0 | 0 |
| Biosynthesis of DPAn-3-derived maresins | R-HSA-9026290 | 1.471486e-01 | 0.832 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.471486e-01 | 0.832 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 1.493192e-01 | 0.826 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.493192e-01 | 0.826 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.493192e-01 | 0.826 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 1.519663e-01 | 0.818 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 1.532508e-01 | 0.815 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.545392e-01 | 0.811 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.545392e-01 | 0.811 | 0 | 0 |
| Reduction of cytosolic Ca++ levels | R-HSA-418359 | 1.567945e-01 | 0.805 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.567945e-01 | 0.805 | 0 | 0 |
| Sodium/Calcium exchangers | R-HSA-425561 | 1.567945e-01 | 0.805 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 1.572025e-01 | 0.804 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 1.572025e-01 | 0.804 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 1.572363e-01 | 0.803 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 1.572363e-01 | 0.803 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 1.611735e-01 | 0.793 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 1.651627e-01 | 0.782 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 1.651627e-01 | 0.782 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.651627e-01 | 0.782 | 0 | 0 |
| Interleukin-15 signaling | R-HSA-8983432 | 1.663319e-01 | 0.779 | 0 | 0 |
| Interleukin-35 Signalling | R-HSA-8984722 | 1.663319e-01 | 0.779 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.663319e-01 | 0.779 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.663319e-01 | 0.779 | 0 | 0 |
| Biosynthesis of DPAn-3-derived protectins and resolvins | R-HSA-9026286 | 1.663319e-01 | 0.779 | 0 | 0 |
| Disorders of Nervous System Development | R-HSA-9697154 | 1.663319e-01 | 0.779 | 0 | 0 |
| Pervasive developmental disorders | R-HSA-9005895 | 1.663319e-01 | 0.779 | 0 | 0 |
| Loss of function of MECP2 in Rett syndrome | R-HSA-9005891 | 1.663319e-01 | 0.779 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.663319e-01 | 0.779 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 1.681680e-01 | 0.774 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.691693e-01 | 0.772 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 1.691693e-01 | 0.772 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 1.731923e-01 | 0.761 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.757619e-01 | 0.755 | 0 | 0 |
| IL-6-type cytokine receptor ligand interactions | R-HSA-6788467 | 1.757619e-01 | 0.755 | 0 | 0 |
| Interleukin-6 signaling | R-HSA-1059683 | 1.757619e-01 | 0.755 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.757619e-01 | 0.755 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.757619e-01 | 0.755 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.757619e-01 | 0.755 | 0 | 0 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | R-HSA-442720 | 1.757619e-01 | 0.755 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.757619e-01 | 0.755 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.757619e-01 | 0.755 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 1.793311e-01 | 0.746 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 1.812843e-01 | 0.742 | 0 | 0 |
| RAB geranylgeranylation | R-HSA-8873719 | 1.812843e-01 | 0.742 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 1.821326e-01 | 0.740 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.849625e-01 | 0.733 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.849625e-01 | 0.733 | 0 | 0 |
| CLEC7A (Dectin-1) induces NFAT activation | R-HSA-5607763 | 1.850859e-01 | 0.733 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 1.850859e-01 | 0.733 | 0 | 0 |
| Biosynthesis of E-series 18(R)-resolvins | R-HSA-9023661 | 1.850859e-01 | 0.733 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.850859e-01 | 0.733 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.850859e-01 | 0.733 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 1.853515e-01 | 0.732 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 1.878042e-01 | 0.726 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 1.878042e-01 | 0.726 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 1.890864e-01 | 0.723 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 1.894318e-01 | 0.723 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 1.894318e-01 | 0.723 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.935243e-01 | 0.713 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.943050e-01 | 0.712 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.943050e-01 | 0.712 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 1.976283e-01 | 0.704 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 1.976283e-01 | 0.704 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 2.017429e-01 | 0.695 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 2.034203e-01 | 0.692 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 2.034203e-01 | 0.692 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 2.034203e-01 | 0.692 | 0 | 0 |
| KSRP (KHSRP) binds and destabilizes mRNA | R-HSA-450604 | 2.034203e-01 | 0.692 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 2.034203e-01 | 0.692 | 0 | 0 |
| G beta:gamma signalling through CDC42 | R-HSA-8964616 | 2.124331e-01 | 0.673 | 0 | 0 |
| The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CLOCK) complex | R-HSA-9931521 | 2.124331e-01 | 0.673 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 2.124331e-01 | 0.673 | 0 | 0 |
| STAT5 activation downstream of FLT3 ITD mutants | R-HSA-9702518 | 2.124331e-01 | 0.673 | 0 | 0 |
| Disorders of Developmental Biology | R-HSA-9675151 | 2.124331e-01 | 0.673 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 2.141435e-01 | 0.669 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 2.141435e-01 | 0.669 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 2.182934e-01 | 0.661 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.213444e-01 | 0.655 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.213444e-01 | 0.655 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.213444e-01 | 0.655 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | R-HSA-5358606 | 2.213444e-01 | 0.655 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | R-HSA-5358565 | 2.213444e-01 | 0.655 | 0 | 0 |
| Biosynthesis of aspirin-triggered D-series resolvins | R-HSA-9020265 | 2.213444e-01 | 0.655 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.213444e-01 | 0.655 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 2.224503e-01 | 0.653 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 2.224503e-01 | 0.653 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 2.224503e-01 | 0.653 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 2.227103e-01 | 0.652 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 2.247780e-01 | 0.648 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 2.266136e-01 | 0.645 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 2.266136e-01 | 0.645 | 0 | 0 |
| Mismatch Repair | R-HSA-5358508 | 2.301555e-01 | 0.638 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.301555e-01 | 0.638 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.301555e-01 | 0.638 | 0 | 0 |
| PKA activation | R-HSA-163615 | 2.301555e-01 | 0.638 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 2.301555e-01 | 0.638 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 2.301555e-01 | 0.638 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 2.307826e-01 | 0.637 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 2.307826e-01 | 0.637 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 2.307826e-01 | 0.637 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 2.349566e-01 | 0.629 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.388674e-01 | 0.622 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.388674e-01 | 0.622 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.388674e-01 | 0.622 | 0 | 0 |
| Synthesis of 5-eicosatetraenoic acids | R-HSA-2142688 | 2.388674e-01 | 0.622 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.388674e-01 | 0.622 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.388674e-01 | 0.622 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 2.388674e-01 | 0.622 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 2.433172e-01 | 0.614 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.474812e-01 | 0.606 | 0 | 0 |
| VxPx cargo-targeting to cilium | R-HSA-5620916 | 2.474812e-01 | 0.606 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.474812e-01 | 0.606 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.474812e-01 | 0.606 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.475024e-01 | 0.606 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 2.515244e-01 | 0.599 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 2.558800e-01 | 0.592 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.559981e-01 | 0.592 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.559981e-01 | 0.592 | 0 | 0 |
| Biosynthesis of E-series 18(S)-resolvins | R-HSA-9018896 | 2.559981e-01 | 0.592 | 0 | 0 |
| PKA-mediated phosphorylation of CREB | R-HSA-111931 | 2.559981e-01 | 0.592 | 0 | 0 |
| PD-L1(CD274) glycosylation and translocation to plasma membrane | R-HSA-9931295 | 2.559981e-01 | 0.592 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.559981e-01 | 0.592 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 2.600712e-01 | 0.585 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 2.618185e-01 | 0.582 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 2.642631e-01 | 0.578 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 2.644191e-01 | 0.578 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 2.644191e-01 | 0.578 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 2.644191e-01 | 0.578 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 2.644191e-01 | 0.578 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.644191e-01 | 0.578 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.727453e-01 | 0.564 | 0 | 0 |
| Biosynthesis of D-series resolvins | R-HSA-9018676 | 2.727453e-01 | 0.564 | 0 | 0 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | R-HSA-6804115 | 2.727453e-01 | 0.564 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 2.740363e-01 | 0.562 | 0 | 0 |
| Interleukin-20 family signaling | R-HSA-8854691 | 2.809778e-01 | 0.551 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 2.809778e-01 | 0.551 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.809778e-01 | 0.551 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.809778e-01 | 0.551 | 0 | 0 |
| Biosynthesis of maresins | R-HSA-9018682 | 2.809778e-01 | 0.551 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 2.809778e-01 | 0.551 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 2.852162e-01 | 0.545 | 0 | 0 |
| Interleukin-6 family signaling | R-HSA-6783589 | 2.891176e-01 | 0.539 | 0 | 0 |
| Signaling by FLT3 ITD and TKD mutants | R-HSA-9703648 | 2.891176e-01 | 0.539 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.891176e-01 | 0.539 | 0 | 0 |
| Mitochondrial RNA degradation | R-HSA-9836573 | 2.891176e-01 | 0.539 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 2.924696e-01 | 0.534 | 0 | 0 |
| XBP1(S) activates chaperone genes | R-HSA-381038 | 2.935847e-01 | 0.532 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 2.955512e-01 | 0.529 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 2.971657e-01 | 0.527 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 2.971657e-01 | 0.527 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.971657e-01 | 0.527 | 0 | 0 |
| Glycogen breakdown (glycogenolysis) | R-HSA-70221 | 2.971657e-01 | 0.527 | 0 | 0 |
| Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives | R-HSA-9027604 | 2.971657e-01 | 0.527 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 2.971657e-01 | 0.527 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.971657e-01 | 0.527 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 3.019402e-01 | 0.520 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 3.048079e-01 | 0.516 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 3.051232e-01 | 0.516 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 3.051232e-01 | 0.516 | 0 | 0 |
| Activated NOTCH1 Transmits Signal to the Nucleus | R-HSA-2122948 | 3.051232e-01 | 0.516 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 3.051232e-01 | 0.516 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 3.129911e-01 | 0.504 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 3.129911e-01 | 0.504 | 0 | 0 |
| Biosynthesis of DPAn-3 SPMs | R-HSA-9025094 | 3.129911e-01 | 0.504 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 3.129911e-01 | 0.504 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 3.129911e-01 | 0.504 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 3.129911e-01 | 0.504 | 0 | 0 |
| IRE1alpha activates chaperones | R-HSA-381070 | 3.185978e-01 | 0.497 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 3.202619e-01 | 0.494 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 3.207704e-01 | 0.494 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 3.207704e-01 | 0.494 | 0 | 0 |
| Phase 0 - rapid depolarisation | R-HSA-5576892 | 3.207704e-01 | 0.494 | 0 | 0 |
| Activation of kainate receptors upon glutamate binding | R-HSA-451326 | 3.207704e-01 | 0.494 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.207704e-01 | 0.494 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.207704e-01 | 0.494 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 3.284621e-01 | 0.484 | 0 | 0 |
| Biosynthesis of EPA-derived SPMs | R-HSA-9018679 | 3.284621e-01 | 0.484 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.284621e-01 | 0.484 | 0 | 0 |
| Platelet calcium homeostasis | R-HSA-418360 | 3.284621e-01 | 0.484 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.360672e-01 | 0.474 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.360672e-01 | 0.474 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.360672e-01 | 0.474 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.360672e-01 | 0.474 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 3.392853e-01 | 0.469 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 3.392853e-01 | 0.469 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.434010e-01 | 0.464 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.435866e-01 | 0.464 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 3.435866e-01 | 0.464 | 0 | 0 |
| Biosynthesis of DPA-derived SPMs | R-HSA-9018683 | 3.435866e-01 | 0.464 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 3.435866e-01 | 0.464 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 3.435866e-01 | 0.464 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 3.510213e-01 | 0.455 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.510213e-01 | 0.455 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 3.516079e-01 | 0.454 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 3.556983e-01 | 0.449 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 3.583722e-01 | 0.446 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 3.583722e-01 | 0.446 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.583722e-01 | 0.446 | 0 | 0 |
| Regulation of MECP2 expression and activity | R-HSA-9022692 | 3.583722e-01 | 0.446 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.583722e-01 | 0.446 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 3.597796e-01 | 0.444 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 3.638515e-01 | 0.439 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 3.656403e-01 | 0.437 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.656403e-01 | 0.437 | 0 | 0 |
| Nuclear import of Rev protein | R-HSA-180746 | 3.728266e-01 | 0.428 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.728266e-01 | 0.428 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.728266e-01 | 0.428 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 3.728266e-01 | 0.428 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 3.728266e-01 | 0.428 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.728266e-01 | 0.428 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.728266e-01 | 0.428 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 3.728266e-01 | 0.428 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 3.760078e-01 | 0.425 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.760078e-01 | 0.425 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.799319e-01 | 0.420 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 3.799319e-01 | 0.420 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.799319e-01 | 0.420 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 3.799319e-01 | 0.420 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.799319e-01 | 0.420 | 0 | 0 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | R-HSA-2408508 | 3.799319e-01 | 0.420 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 3.819865e-01 | 0.418 | 0 | 0 |
| FLT3 signaling in disease | R-HSA-9682385 | 3.869571e-01 | 0.412 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.869571e-01 | 0.412 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.869571e-01 | 0.412 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 3.869571e-01 | 0.412 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 3.869571e-01 | 0.412 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 3.869571e-01 | 0.412 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 3.869571e-01 | 0.412 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 3.920665e-01 | 0.407 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 3.939031e-01 | 0.405 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 3.939031e-01 | 0.405 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 3.939031e-01 | 0.405 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 3.939031e-01 | 0.405 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 4.007709e-01 | 0.397 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 4.007709e-01 | 0.397 | 0 | 0 |
| Translation | R-HSA-72766 | 4.042995e-01 | 0.393 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 4.075613e-01 | 0.390 | 0 | 0 |
| RAS processing | R-HSA-9648002 | 4.075613e-01 | 0.390 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 4.075613e-01 | 0.390 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 4.075613e-01 | 0.390 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 4.075613e-01 | 0.390 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 4.075613e-01 | 0.390 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 4.075613e-01 | 0.390 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 4.118760e-01 | 0.385 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 4.142168e-01 | 0.383 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 4.142751e-01 | 0.383 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 4.142751e-01 | 0.383 | 0 | 0 |
| Interactions of Rev with host cellular proteins | R-HSA-177243 | 4.142751e-01 | 0.383 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 4.142751e-01 | 0.383 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 4.142751e-01 | 0.383 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 4.142751e-01 | 0.383 | 0 | 0 |
| Glycogen metabolism | R-HSA-8982491 | 4.142751e-01 | 0.383 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 4.209133e-01 | 0.376 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 4.209133e-01 | 0.376 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 4.209133e-01 | 0.376 | 0 | 0 |
| Purine ribonucleoside monophosphate biosynthesis | R-HSA-73817 | 4.209133e-01 | 0.376 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 4.209133e-01 | 0.376 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 4.209133e-01 | 0.376 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 4.236097e-01 | 0.373 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 4.274766e-01 | 0.369 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 4.274766e-01 | 0.369 | 0 | 0 |
| Intra-Golgi traffic | R-HSA-6811438 | 4.274766e-01 | 0.369 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 4.274766e-01 | 0.369 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 4.274766e-01 | 0.369 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.339660e-01 | 0.363 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.403822e-01 | 0.356 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.403822e-01 | 0.356 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.403822e-01 | 0.356 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 4.420055e-01 | 0.355 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 4.467089e-01 | 0.350 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.467260e-01 | 0.350 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.467260e-01 | 0.350 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 4.467260e-01 | 0.350 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 4.467260e-01 | 0.350 | 0 | 0 |
| Amine ligand-binding receptors | R-HSA-375280 | 4.467260e-01 | 0.350 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.467260e-01 | 0.350 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.467260e-01 | 0.350 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.467260e-01 | 0.350 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.529984e-01 | 0.344 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 4.529984e-01 | 0.344 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.529984e-01 | 0.344 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 4.529984e-01 | 0.344 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 4.529984e-01 | 0.344 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 4.529984e-01 | 0.344 | 0 | 0 |
| Vasopressin regulates renal water homeostasis via Aquaporins | R-HSA-432040 | 4.529984e-01 | 0.344 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 4.592000e-01 | 0.338 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.592000e-01 | 0.338 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.592000e-01 | 0.338 | 0 | 0 |
| Diseases of DNA repair | R-HSA-9675135 | 4.592000e-01 | 0.338 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 4.592000e-01 | 0.338 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 4.629695e-01 | 0.334 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 4.629695e-01 | 0.334 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 4.653317e-01 | 0.332 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.653317e-01 | 0.332 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 4.655608e-01 | 0.332 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 4.713942e-01 | 0.327 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.713942e-01 | 0.327 | 0 | 0 |
| Metal ion SLC transporters | R-HSA-425410 | 4.713942e-01 | 0.327 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 4.816981e-01 | 0.317 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 4.833149e-01 | 0.316 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 4.891746e-01 | 0.311 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 4.891746e-01 | 0.311 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.891746e-01 | 0.311 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 4.949683e-01 | 0.305 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 4.949683e-01 | 0.305 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 5.006965e-01 | 0.300 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 5.006965e-01 | 0.300 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 5.006965e-01 | 0.300 | 0 | 0 |
| Nucleotide biosynthesis | R-HSA-8956320 | 5.006965e-01 | 0.300 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 5.088132e-01 | 0.293 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 5.174965e-01 | 0.286 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 5.174965e-01 | 0.286 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 5.174965e-01 | 0.286 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 5.197681e-01 | 0.284 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 5.267165e-01 | 0.278 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.283829e-01 | 0.277 | 0 | 0 |
| Metabolism of non-coding RNA | R-HSA-194441 | 5.337342e-01 | 0.273 | 0 | 0 |
| snRNP Assembly | R-HSA-191859 | 5.337342e-01 | 0.273 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.337342e-01 | 0.273 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 5.390250e-01 | 0.268 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 5.390250e-01 | 0.268 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.442562e-01 | 0.264 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.442562e-01 | 0.264 | 0 | 0 |
| Aquaporin-mediated transport | R-HSA-445717 | 5.442562e-01 | 0.264 | 0 | 0 |
| Heme signaling | R-HSA-9707616 | 5.494283e-01 | 0.260 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.595980e-01 | 0.252 | 0 | 0 |
| Ion transport by P-type ATPases | R-HSA-936837 | 5.595980e-01 | 0.252 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 5.604338e-01 | 0.251 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 5.604993e-01 | 0.251 | 0 | 0 |
| S Phase | R-HSA-69242 | 5.637105e-01 | 0.249 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 5.645969e-01 | 0.248 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.702115e-01 | 0.244 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 5.734358e-01 | 0.242 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.744261e-01 | 0.241 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.744261e-01 | 0.241 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.766426e-01 | 0.239 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 5.766426e-01 | 0.239 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.792576e-01 | 0.237 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.861579e-01 | 0.232 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 5.887576e-01 | 0.230 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 5.934273e-01 | 0.227 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 5.934273e-01 | 0.227 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.955152e-01 | 0.225 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 5.980442e-01 | 0.223 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 5.985991e-01 | 0.223 | 0 | 0 |
| Ca2+ pathway | R-HSA-4086398 | 6.026090e-01 | 0.220 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 6.071223e-01 | 0.217 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 6.137553e-01 | 0.212 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 6.159964e-01 | 0.210 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 6.246711e-01 | 0.204 | 0 | 0 |
| Interleukin-10 signaling | R-HSA-6783783 | 6.246711e-01 | 0.204 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.246711e-01 | 0.204 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 6.246711e-01 | 0.204 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.289351e-01 | 0.201 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 6.331509e-01 | 0.198 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 6.342374e-01 | 0.198 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 6.370936e-01 | 0.196 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 6.370936e-01 | 0.196 | 0 | 0 |
| Biosynthesis of DHA-derived SPMs | R-HSA-9018677 | 6.373191e-01 | 0.196 | 0 | 0 |
| Transcriptional activation of mitochondrial biogenesis | R-HSA-2151201 | 6.373191e-01 | 0.196 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 6.455146e-01 | 0.190 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 6.455146e-01 | 0.190 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.495431e-01 | 0.187 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.574639e-01 | 0.182 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.574639e-01 | 0.182 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 6.574639e-01 | 0.182 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 6.593188e-01 | 0.181 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 6.613573e-01 | 0.180 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.613573e-01 | 0.180 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.727753e-01 | 0.172 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.801738e-01 | 0.167 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 6.830119e-01 | 0.166 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.838104e-01 | 0.165 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 6.861474e-01 | 0.164 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.979502e-01 | 0.156 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 7.013857e-01 | 0.154 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 7.047824e-01 | 0.152 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 7.081406e-01 | 0.150 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 7.081406e-01 | 0.150 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 7.114609e-01 | 0.148 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 7.179891e-01 | 0.144 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 7.211980e-01 | 0.142 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 7.211980e-01 | 0.142 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.275071e-01 | 0.138 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 7.306082e-01 | 0.136 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.367054e-01 | 0.133 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.397024e-01 | 0.131 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.426655e-01 | 0.129 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.455950e-01 | 0.127 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.455950e-01 | 0.127 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 7.569850e-01 | 0.121 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 7.569850e-01 | 0.121 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 7.705118e-01 | 0.113 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.757104e-01 | 0.110 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 7.819628e-01 | 0.107 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 7.853345e-01 | 0.105 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.857589e-01 | 0.105 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 7.857589e-01 | 0.105 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 7.920786e-01 | 0.101 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 7.999982e-01 | 0.097 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 8.132959e-01 | 0.090 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.410025e-01 | 0.075 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.428173e-01 | 0.074 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 8.498727e-01 | 0.071 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.566130e-01 | 0.067 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 8.582506e-01 | 0.066 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 8.692040e-01 | 0.061 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 8.886488e-01 | 0.051 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 8.886488e-01 | 0.051 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 9.073737e-01 | 0.042 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 9.094823e-01 | 0.041 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.211680e-01 | 0.036 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.339543e-01 | 0.030 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.366771e-01 | 0.028 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 9.422613e-01 | 0.026 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.467440e-01 | 0.024 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.485576e-01 | 0.023 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.530990e-01 | 0.021 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.566535e-01 | 0.019 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.672320e-01 | 0.014 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 9.687152e-01 | 0.014 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.776068e-01 | 0.010 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.862647e-01 | 0.006 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.904362e-01 | 0.004 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.915875e-01 | 0.004 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.918768e-01 | 0.004 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.927717e-01 | 0.003 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.942777e-01 | 0.002 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.970224e-01 | 0.001 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.991472e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.997436e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999020e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999998e-01 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
