LCK
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 |
|---|---|---|---|---|
| A1L429 | Y10 | Sugiyama | GAGE12B; GAGE12C; GAGE12D; GAGE12E | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| A1L429 | Y9 | Sugiyama | GAGE12B; GAGE12C; GAGE12D; GAGE12E | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A1X283 | Y855 | Sugiyama | SH3PXD2B FAD49 KIAA1295 TKS4 | NREKAAAASVPNADGLKDSLyVAVADFEGDKDTSSFQEGTV |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y791 | Sugiyama | POTEF A26C1B | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPVLLTEATLN |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y1572 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | RMPEQIRLKVGGVDPKQLAVyEEFARNVPGFLPTNDLSQPT |
| A6NDE8 | Y10 | Sugiyama | GAGE12H | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| A6NDE8 | Y9 | Sugiyama | GAGE12H | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A6NER3 | Y10 | Sugiyama | GAGE12J | ___________MSWRGRsTyyWPRPRPYVQPPEMIGPMRPE |
| A6NER3 | Y9 | Sugiyama | GAGE12J | ____________MSWRGRsTyyWPRPRPYVQPPEMIGPMRP |
| A6NHL2 | Y319 | Sugiyama | TUBAL3 | TTACFESSNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAI |
| A6NHL2 | Y326 | Sugiyama | TUBAL3 | SNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAIAATKSRH |
| A6NMY6 | S22 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | stVHEILCKLsLEGDHstPPsAyGsVKAytNFDAERDALNI |
| A6NMY6 | S236 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | IMTERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENAF |
| A6NMY6 | Y147 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| A6NMY6 | Y235 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sIMTERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENA |
| O00116 | Y645 | Sugiyama | AGPS AAG5 | QWLKESIsDVGFGMLKSVKEyVDPNNIFGNRNLL_______ |
| O00151 | Y306 | Sugiyama | PDLIM1 CLIM1 CLP36 | CtDCGtNLKQKGHFFVEDQIyCEKHARERVtPPEGyEVVTV |
| O00170 | Y203 | Sugiyama | AIP XAP2 | HQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPEW |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00233 | Y70 | Sugiyama | PSMD9 | IGMNEPLVDCEGyPRSDVDLyQVRTARHNIICLQNDHKAVM |
| O00264 | Y113 | Sugiyama | PGRMC1 HPR6.6 PGRMC | INGKVFDVTKGRKFyGPEGPyGVFAGRDASRGLATFCLDKE |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00429 | Y266 | Sugiyama | DNM1L DLP1 DRP1 | NRSQLDINNKKSVTDsIRDEyAFLQKKYPSLANRNGTKYLA |
| O00469 | Y586 | Sugiyama | PLOD2 | FWFPIFSEKACDELVEEMEHyGKWSGGKHHDsRIsGGyENV |
| O00566 | Y473 | Sugiyama | MPHOSPH10 MPP10 | EYKKRLTLDHEKSKLSLAEIyEQEyIKLNQQKTAEEENPEH |
| O00566 | Y477 | Sugiyama | MPHOSPH10 MPP10 | RLTLDHEKSKLSLAEIyEQEyIKLNQQKTAEEENPEHVEIQ |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O14543 | Y204 | ELM|iPTMNet|EPSD|PSP | SOCS3 CIS3 SSI3 | SNVATLQHLCRKTVNGHLDSyEKVTQLPGPIREFLDQyDAP |
| O14543 | Y221 | ELM|iPTMNet|EPSD|PSP | SOCS3 CIS3 SSI3 | LDSyEKVTQLPGPIREFLDQyDAPL________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14602 | Y35 | Sugiyama | EIF1AY | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEALCFDGV |
| O14818 | Y145 | Sugiyama | PSMA7 HSPC | RPFGISALIVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGA |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| 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 | S910 | Sugiyama | PPP1R12A MBS MYPT1 | yETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDST |
| O14974 | Y901 | Sugiyama | PPP1R12A MBS MYPT1 | EtQtDsIsRyETssTsAGDRyDsLLGRsGsysYLEERKPYS |
| 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 |
| O15031 | Y485 | Sugiyama | PLXNB2 KIAA0315 | PVQECLSYPTCTQCRDSQDPyCGWCVVEGRCTRKAECPRAE |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15230 | Y81 | Sugiyama | LAMA5 KIAA0533 KIAA1907 | SATCGEEAPARGSPRPTEDLyCKLVGGPVAGGDPNQTIRGQ |
| O15234 | Y240 | Sugiyama | CASC3 MLN51 | HDKFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRK |
| O15234 | Y242 | Sugiyama | CASC3 MLN51 | KFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRKPR |
| O15294 | Y316 | Sugiyama | OGT | YCNLANALKEKGSVAEAEDCyNTALRLCPTHADSLNNLANI |
| O15305 | Y205 | Sugiyama | PMM2 | DGWDKRYCLRHVENDGYKTIyFFGDKTMPGGNDHEIFTDPR |
| O15357 | Y190 | Sugiyama | INPPL1 SHIP2 | AAESAPNGLSTVSHDYLKGsyGLDLEAVRGGASHLPHLTRT |
| O15371 | Y201 | Sugiyama | EIF3D EIF3S7 | KMRyLEVSEPQDIECCGALEyyDKAFDRITTRSEKPLRSIK |
| O15371 | Y202 | Sugiyama | EIF3D EIF3S7 | MRyLEVSEPQDIECCGALEyyDKAFDRITTRSEKPLRSIKR |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O43143 | Y128 | Sugiyama | DHX15 DBP1 DDX15 | HTSLPQCINPFTNLPHTPRyyDILKKRLQLPVWEYKDRFTD |
| O43164 | Y63 | Sugiyama | PJA2 KIAA0438 RNF131 | VSFKPCMTRHERSLGRAGDDyEVLELDDVPKENssGssPLD |
| O43252 | Y617 | Sugiyama | PAPSS1 ATPSK1 PAPSS | EGQKPPEGFMAPKAWtVLtEyyKSLEKA_____________ |
| O43252 | Y618 | Sugiyama | PAPSS1 ATPSK1 PAPSS | GQKPPEGFMAPKAWtVLtEyyKSLEKA______________ |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43561 | Y200 | SIGNOR | LAT | PALStPGIRDSAFSMESIDDyVNVPEsGEsAEAsLDGSREy |
| O43561 | Y220 | SIGNOR | LAT | yVNVPEsGEsAEAsLDGSREyVNVsQELHPGAAKtEPAALs |
| O43615 | T198 | Sugiyama | TIMM44 MIMT44 TIM44 | ALsQGVEsVKKEIDDsVLGQtGPyRRPQRLRKRTEFAGDKF |
| O43615 | Y201 | Sugiyama | TIMM44 MIMT44 TIM44 | QGVEsVKKEIDDsVLGQtGPyRRPQRLRKRTEFAGDKFKEE |
| O43707 | Y212 | Sugiyama | ACTN4 | WKDGLAFNALIHRHRPELIEyDKLRKDDPVTNLNNAFEVAE |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y397 | Sugiyama | ACTN4 | GKMVSDINNGWQHLEQAEKGyEEWLLNEIRRLERLDHLAEK |
| O43707 | Y441 | Sugiyama | ACTN4 | KAsIHEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEs |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43765 | Y195 | Sugiyama | SGTA SGT SGT1 | HVEAVAYYKKALELDPDNEtyKsNLKIAELKLREAPSPTGG |
| O43823 | Y311 | Sugiyama | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y185 | Sugiyama | CALU | KDGDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNAD |
| O43852 | Y187 | Sugiyama | CALU | GDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNADGF |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O43865 | Y28 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | PLPGVGEELKQAKEIEDAEKysFMATVTKAPKKQIQFADDM |
| O43865 | Y291 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDVMFGG |
| 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 | Y47 | Sugiyama | SYNCRIP HNRPQ NSAP1 | FQTLLDAGLPQKVAEKLDEIyVAGLVAHsDLDERAIEALKE |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60716 | S232 | Sugiyama | CTNND1 KIAA0384 | GysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGyRAPs |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60716 | Y257 | Sugiyama | CTNND1 KIAA0384 | IEERyRPsMEGyRAPsRQDVyGPQPQVRVGGssVDLHRFHP |
| O60739 | Y30 | Sugiyama | EIF1B | FDPFADATKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60841 | Y134 | Sugiyama | EIF5B IF2 KIAA0741 | EELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKA |
| O60884 | Y128 | Sugiyama | DNAJA2 CPR3 HIRIP4 | NGRRRGEDMMHPLKVsLEDLyNGKTTKLQLSKNVLCsACsG |
| O60884 | Y66 | Sugiyama | DNAJA2 CPR3 HIRIP4 | KFKEISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDD |
| O60884 | Y69 | Sugiyama | DNAJA2 CPR3 HIRIP4 | EISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDDIFS |
| O60927 | Y64 | Sugiyama | PPP1R11 HCGV TCTE5 | TsDTVDNEHMGRRssKCCCIyEKPRAFGEsstEsDEEEEEG |
| O60934 | Y679 | Sugiyama | NBN NBS NBS1 P95 | FRSLVIKNSTSRNPSGINDDyGQLKNFKKFKKVTYPGAGKL |
| O75116 | Y722 | Sugiyama | ROCK2 KIAA0619 | EQEEAEHKATKARLADKNKIyEsIEEAKSEAMKEMEKKLLE |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75347 | Y48 | Sugiyama | TBCA | KEAKQQEEKIEKMRAEDGENyDIKKQAEILQEsRMMIPDCQ |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75348 | Y47 | Sugiyama | ATP6V1G1 ATP6G ATP6G1 ATP6J | KRKNRRLKQAKEEAQAEIEQyRLQREKEFKAKEAAALGsRG |
| O75369 | Y1576 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYGG |
| O75369 | Y2502 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ANEtssILVEsVTRsstETCysAIPKASSDASKVTSKGAGL |
| O75390 | Y345 | Sugiyama | CS | DEKLRDYIWNtLNSGRVVPGyGHAVLRKTDPRYTCQREFAL |
| O75533 | Y44 | Sugiyama | SF3B1 SAP155 | ALDEAQGVGLDstGYyDQEIyGGSDSRFAGYVtSIAAtELE |
| O75534 | Y461 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | PKTtsPNKGKEKEAEDGIIAyDDCGVKLTIAFQAKDVEGsT |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75688 | Y367 | Sugiyama | PPM1B PP2CB | IPNLPPGGGLAGKRNVIEAVySRLNPHREsDGAsDEAEEsG |
| O75718 | Y372 | Sugiyama | CRTAP CASP | FQPRPEAVQFFNVTTLQKELyDFAKENIMDDDEGEVVEyVD |
| O75817 | Y20 | Sugiyama | POP7 RPP20 | _MAENREPRGAVEAELDPVEytLRKRLPSRLPRRPNDIyVN |
| O75886 | Y371 | Sugiyama | STAM2 HBP | NVKVLEALELYNKLVNEAPVysVysKLHPPAHYPPASSGVP |
| O75976 | Y1376 | Sugiyama | CPD | KKsLLsHEFQDEtDtEEEtLyssKH________________ |
| O76087 | Y10 | Sugiyama | GAGE7 GAGE12I GAGE7B | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| O76087 | Y9 | Sugiyama | GAGE7 GAGE12I GAGE7B | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| O95218 | S120 | Sugiyama | ZRANB2 ZIS ZNF265 | tGYGGGFNERENVEyIEREEsDGEyDEFGRKKKKYRGKAVG |
| O95218 | Y124 | Sugiyama | ZRANB2 ZIS ZNF265 | GGFNERENVEyIEREEsDGEyDEFGRKKKKYRGKAVGPAsI |
| O95218 | Y167 | Sugiyama | ZRANB2 ZIS ZNF265 | EVEDKEsEGEEEDEDEDLsKyKLDEDEDEDDADLsKyNLDA |
| O95297 | Y263 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | QLDHsGGHHSDKINKSEsVVyADIRKN______________ |
| O95347 | Y773 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | EESEETLKNTKEIQRKAEEKyEVLENKMKNAEAERERELKD |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95456 | Y287 | Sugiyama | PSMG1 C21LRP DSCR2 PAC1 | PQSTEILKKLMTTNEIQsNIyt___________________ |
| O95573 | Y591 | Sugiyama | ACSL3 ACS3 FACL3 LACS3 | DGCLKIIDRKKDLVKLQAGEyVsLGKVEAALKNLPLVDNIC |
| O95757 | Y627 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MIMQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPED |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| P00338 | Y10 | Sugiyama | LDHA PIG19 | ___________MAtLKDQLIyNLLKEEQtPQNKITVVGVGA |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00491 | Y166 | Sugiyama | PNP NP | PLRGPNDERFGDRFPAMsDAyDRtMRQRALstWKQMGEQRE |
| P00505 | Y96 | Sugiyama | GOT2 KYAT4 | VLPSVRKAEAQIAAKNLDKEyLPIGGLAEFCKASAELALGE |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00558 | Y196 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | MVGVNLPQKAGGFLMKKELNyFAKALEsPERPFLAILGGAK |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P02545 | Y211 | Sugiyama | LMNA LMN1 | VDAENRLQtMKEELDFQKNIysEELREtKRRHETRLVEIDN |
| P02545 | Y45 | Sugiyama | LMNA LMN1 | RItRLQEKEDLQELNDRLAVyIDRVRsLETENAGLRLRItE |
| P02786 | Y152 | Sugiyama | TFRC | sEKLDstDFTGtIKLLNENsyVPREAGsQKDENLALyVENQ |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P02788 | Y545 | Sugiyama | LTF GIG12 LF | LCIGDEQGENKCVPNSNERYyGYTGAFRCLAENAGDVAFVK |
| P03372 | Y537 | SIGNOR|ELM|iPTMNet|EPSD|PSP | ESR1 ESR NR3A1 | MSNKGMEHLYSMKCKNVVPLyDLLLEMLDAHRLHAPTsRGG |
| P04080 | Y97 | Sugiyama | CSTB CST6 STFB | NKPLtLsNyQTNKAKHDELtyF___________________ |
| 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_____ |
| P04632 | S88 | Sugiyama | CAPNS1 CAPN4 CAPNS | AISEAAAQYNPEPPPPRtHysNIEANEsEEVRQFRRLFAQL |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P04818 | Y135 | Sugiyama | TYMS TS OK/SW-cl.29 | RDFLDsLGFsTREEGDLGPVyGFQWRHFGAEyRDMEsDysG |
| P05067 | Y321 | Sugiyama | APP A4 AD1 | RAMISRWyFDVTEGKCAPFFyGGCGGNRNNFDTEEYCMAVC |
| P05107 | Y735 | EPSD|PSP | ITGB2 CD18 MFI7 | IGILLLVIWKALIHLSDLREyRRFEKEKLKsQWNNDNPLFK |
| P05198 | Y150 | Sugiyama | EIF2S1 EIF2A | LFQRTAWVFDDKyKRPGyGAyDAFKHAVsDPsILDsLDLNE |
| P05362 | Y455 | Sugiyama | ICAM1 | GtFPLPIGEsVtVtRDLEGtyLCRARSTQGEVTRKVTVNVL |
| P05455 | Y104 | Sugiyama | SSB | EDKTKIRRsPsKPLPEVTDEyKNDVKNRsVYIKGFPtDAtL |
| P05787 | S280 | Sugiyama | KRT8 CYK8 | IAEVKAQyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDL |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P05997 | Y1311 | Sugiyama | COL5A2 | HPARTCDDLKLCHSAKQsGEyWIDPNQGSVEDAIKVYCNME |
| P06127 | Y453 | SIGNOR|ELM|iPTMNet|EPSD|PSP | CD5 LEU1 | HtAtVRsHAENPtASHVDNEysQPPRNSHLSAyPALEGALH |
| P06127 | Y487 | SIGNOR|ELM|iPTMNet|EPSD|PSP | CD5 LEU1 | ALEGALHRSSMQPDNssDsDyDLHGAQRL____________ |
| P06239 | T395 | Sugiyama | LCK | TLSCKIADFGLARLIEDNEytAREGAKFPIKWTAPEAINyG |
| P06239 | Y192 | Sugiyama | LCK | QNQGEVVKHYKIRNLDNGGFyIsPRITFPGLHELVRHYtNA |
| P06239 | Y394 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | LCK | DTLSCKIADFGLARLIEDNEytAREGAKFPIKWTAPEAINy |
| P06239 | Y470 | Sugiyama | LCK | IQNLERGYRMVRPDNCPEELyQLMRLCWKERPEDRPTFDyL |
| P06239 | Y505 | ELM|iPTMNet|EPSD|PSP|Sugiyama | LCK | PTFDyLRSVLEDFFtAtEGQyQPQP________________ |
| P06241 | Y420 | Sugiyama | FYN | NGLICKIADFGLARLIEDNEytARQGAKFPIKWTAPEAALy |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06493 | Y270 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ASHVKNLDENGLDLLSKMLIyDPAKRISGKMALNHPyFNDL |
| P06576 | Y418 | Sugiyama | ATP5F1B ATP5B ATPMB ATPSB | VDPLDSTSRIMDPNIVGsEHyDVARGVQKILQDYKSLQDII |
| P06733 | S268 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyP |
| P06733 | S272 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | FRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsI |
| P06733 | Y131 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ILGVsLAVCKAGAVEKGVPLyRHIADLAGNsEVILPVPAFN |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| 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 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07108 | Y29 | Sugiyama | DBI | AAEEVRHLKTKPsDEEMLFIyGHyKQAtVGDINtERPGMLD |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07237 | Y99 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPKEytAG |
| P07355 | S22 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | stVHEILCKLsLEGDHstPPsAyGsVKAytNFDAERDALNI |
| P07355 | S236 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | IMTERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENAF |
| 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 |
| P07355 | Y235 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | sIMTERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENA |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | Y50 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IDPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEP |
| P07437 | Y51 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPG |
| P07686 | Y526 | Sugiyama | HEXB HCC7 | ASAVGERLWSSKDVRDMDDAyDRLTRHRCRMVERGIAAQPL |
| P07686 | Y547 | Sugiyama | HEXB HCC7 | DRLTRHRCRMVERGIAAQPLyAGyCNHENM___________ |
| P07711 | Y112 | Sugiyama | CTSL CTSL1 | MNGFQNRKPRKGKVFQEPLFyEAPRSVDWREKGyVTPVKNQ |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07766 | Y188 | SIGNOR|iPTMNet|EPSD | CD3E T3E | AGGRQRGQNKERPPPVPNPDyEPIRKGQRDLysGLNQRRI_ |
| P07766 | Y199 | SIGNOR|iPTMNet|EPSD | CD3E T3E | RPPPVPNPDyEPIRKGQRDLysGLNQRRI____________ |
| P07814 | Y1504 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | KPLCELQPGAKCVCGKNPAKyytLFGRsy____________ |
| P07814 | Y684 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | LKKGDIIQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPD |
| P07814 | Y690 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | IQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPDGHtKEM |
| P07814 | Y701 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | DQPyEPVsPysCKEAPCVLIyIPDGHtKEMPTSGSKEKTKV |
| P07814 | Y754 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | ERPtPsLNNNCttsEDsLVLyNRVAVQGDVVRELKAKKAPK |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07858 | Y215 | Sugiyama | CTSB CPSB | RPPCTGEGDTPKCSKICEPGysPtyKQDKHYGYNSYSVSNS |
| P07858 | Y219 | Sugiyama | CTSB CPSB | TGEGDTPKCSKICEPGysPtyKQDKHYGYNSYSVSNSEKDI |
| P07858 | Y244 | Sugiyama | CTSB CPSB | HYGYNSYSVSNSEKDIMAEIyKNGPVEGAFSVYSDFLLYKS |
| P07900 | S63 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | IFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLIPN |
| 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 |
| P07900 | Y627 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | TANMERIMKAQALRDNstMGyMAAKKHLEINPDHsIIEtLR |
| P07947 | Y426 | Sugiyama | YES1 YES | ENLVCKIADFGLARLIEDNEytARQGAKFPIKWTAPEAALy |
| P07954 | Y110 | Sugiyama | FH | tPVIKAFGILKRAAAEVNQDyGLDPKIANAIMKAADEVAEG |
| P07954 | Y54 | Sugiyama | FH | PSFWPPNAARMAsQNSFRIEyDtFGELKVPNDKYYGAQTVR |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | S58 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | IFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDIIPN |
| 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 |
| P08621 | Y126 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | FVARVNYDTTEsKLRREFEVyGPIKRIHMVYSKRsGKPRGy |
| P08621 | Y38 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | PIPYLPPLEKLPHEKHHNQPyCGIAPYIREFEDPRDAPPPT |
| P08670 | Y291 | Sugiyama | VIM | DVRQQyEsVAAKNLQEAEEWyKSKFADLsEAANRNNDALRQ |
| P08670 | Y53 | Sugiyama | VIM | tsTRtYsLGsALRPstsRsLyAssPGGVyAtRssAVRLRss |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| P08758 | S135 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | AsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRMLVV |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09211 | Y50 | Sugiyama | GSTP1 FAEES3 GST3 | KEEVVTVETWQEGsLKASCLyGQLPKFQDGDLtLyQsNtIL |
| P09234 | Y12 | Sugiyama | SNRPC | _________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKE |
| P09234 | Y8 | Sugiyama | SNRPC | _____________MPKFyCDyCDtyLtHDsPsVRKTHCSGR |
| P09651 | S338 | Sugiyama | HNRNPA1 HNRPA1 | YNNQSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyG |
| 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_______ |
| P0CG38 | Y791 | Sugiyama | POTEI | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y754 | Sugiyama | POTEJ | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CL80 | Y10 | Sugiyama | GAGE12F | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| P0CL80 | Y9 | Sugiyama | GAGE12F | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P0DSO3 | Y10 | Sugiyama | GAGE4 | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| P0DSO3 | Y9 | Sugiyama | GAGE4 | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P10398 | Y155 | Sugiyama | ARAF ARAF1 PKS PKS2 | HCSSKVPTVCVDMSTNRQQFyHsVQDLsGGsRQHEAPsNRP |
| P10412 | Y71 | Sugiyama | H1-4 H1F4 HIST1H1E | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P10747 | Y191 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CD28 | TVAFIIFWVRSKRSRLLHsDyMNMtPRRPGPTRKHyQPyAP |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11047 | Y352 | Sugiyama | LAMC1 LAMB2 | tAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQD |
| P11047 | Y358 | Sugiyama | LAMC1 LAMB2 | ECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQDNTDGAH |
| P11142 | S432 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGERAMTKD |
| P11142 | Y134 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FYPEEVSSMVLTKMKEIAEAyLGKtVTNAVVtVPAyFNDsQ |
| P11142 | Y149 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | EIAEAyLGKtVTNAVVtVPAyFNDsQRQAtKDAGtIAGLNV |
| P11142 | Y371 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | QDFFNGKELNKsINPDEAVAyGAAVQAAILsGDKSENVQDL |
| P11142 | Y41 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P11142 | Y443 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KQtQtFttysDNQPGVLIQVyEGERAMTKDNNLLGKFELTG |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11498 | Y84 | Sugiyama | PC | VAIYSEQDTGQMHRQKADEAyLIGRGLAPVQAYLHIPDIIK |
| P11940 | Y194 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLFGKF |
| P11940 | Y291 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | ERQTELKRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLR |
| P11940 | Y297 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLRKEFsPF |
| P12004 | Y249 | Sugiyama | PCNA | MSADVPLVVEYKIADMGHLKyyLAPKIEDEEGs________ |
| P12004 | Y250 | Sugiyama | PCNA | SADVPLVVEYKIADMGHLKyyLAPKIEDEEGs_________ |
| P12235 | Y195 | EPSD|PSP | SLC25A4 AAC1 ANT1 | QGFNVSVQGIIIYRAAyFGVyDTAKGMLPDPKNVHIFVSWM |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12270 | Y140 | Sugiyama | TPR | LEAEKRDLIRTNERLsQELEyLTEDVKRLNEKLKESNTTKG |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12814 | Y193 | Sugiyama | ACTN1 | WKDGLGFCALIHRHRPELIDyGKLRKDDPLTNLNTAFDVAE |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y378 | Sugiyama | ACTN1 | GRMVSDINNAWGCLEQVEKGyEEWLLNEIRRLERLDHLAEK |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P12931 | Y419 | Sugiyama | SRC SRC1 | ENLVCKVADFGLARLIEDNEytARQGAKFPIKWTAPEAALy |
| P12956 | Y530 | Sugiyama | XRCC6 G22P1 | KVEAMNKRLGsLVDEFKELVyPPDyNPEGKVtKRKHDNEGS |
| P13010 | Y295 | Sugiyama | XRCC5 G22P2 | TWTVVDAKTLKKEDIQKETVyCLNDDDETEVLKEDIIQGFR |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | S732 | Sugiyama | EEF2 EF2 | DAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQCP |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | T449 | Sugiyama | PDIA4 ERP70 ERP72 | AATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLsE |
| P13667 | Y273 | Sugiyama | PDIA4 ERP70 ERP72 | PTLKIFRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTL |
| P13667 | Y278 | Sugiyama | PDIA4 ERP70 ERP72 | FRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTLKQVQE |
| P13667 | Y392 | Sugiyama | PDIA4 ERP70 ERP72 | HMMDVQGstQDsAIKDFVLKyALPLVGHRKVSNDAKRYTRR |
| 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 |
| P13693 | Y18 | Sugiyama | TPT1 | ___MIIYRDLIsHDEMFsDIyKIREIADGLCLEVEGKMVSR |
| P13798 | S187 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | EKKRPKAEsFFQTKALDVsAsDDEIARLKKPDQAIKGDQFV |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13861 | Y184 | Sugiyama | PRKAR2A PKR2 PRKAR2 | EHVIDQGDDGDNFyVIERGTyDILVTKDNQTRSVGQYDNRG |
| P13929 | Y131 | Sugiyama | ENO3 | ILGVSLAVCKAGAAEKGVPLyRHIADLAGNPDLILPVPAFN |
| P13929 | Y189 | Sugiyama | ENO3 | MILPVGAsSFKEAMRIGAEVyHHLKGVIKAKYGKDATNVGD |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y86 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | KFEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTS |
| P13987 | Y87 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | FEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTSL |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14324 | Y349 | Sugiyama | FDPS FPS KIAA1293 | QDNKCSWLVVQCLQRATPEQyQILKENYGQKEAEKVARVKA |
| P14625 | S403 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | FKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDDFH |
| 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 | S87 | Sugiyama | MYL6B MLC1SA | EEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVLK |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14784 | Y381 | SIGNOR|ELM|iPTMNet|EPSD|PSP | IL2RB IL15RB | NQGyFFFHLPDALEIEACQVyFTyDPySEEDPDEGVAGAPT |
| P14784 | Y384 | SIGNOR|ELM|iPTMNet|EPSD|PSP | IL2RB IL15RB | yFFFHLPDALEIEACQVyFTyDPySEEDPDEGVAGAPTGSS |
| P14784 | Y387 | SIGNOR|ELM|iPTMNet|EPSD|PSP | IL2RB IL15RB | FHLPDALEIEACQVyFTyDPySEEDPDEGVAGAPTGSSPQP |
| P14784 | Y418 | SIGNOR|ELM|iPTMNet|EPSD|PSP | IL2RB IL15RB | GAPTGSSPQPLQPLSGEDDAyCTFPSRDDLLLFSPSLLGGP |
| P14784 | Y536 | SIGNOR|ELM|iPTMNet|EPSD|PSP | IL2RB IL15RB | PPGQGEFRALNARLPLNtDAyLSLQELQGQDPTHLV_____ |
| P14854 | Y34 | Sugiyama | COX6B1 COX6B | TAPFDSRFPNQNQTRNCWQNyLDFHRCQKAMTAKGGDIsVC |
| P14868 | S33 | Sugiyama | DARS1 DARS PIG40 | KPREIMDAAEDyAKERyGIssMIQsQEKPDRVLVRVRDLtI |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15311 | Y146 | SIGNOR|ELM|iPTMNet|EPSD|PSP | EZR VIL2 | GSYAVQAKFGDYNKEVHKsGyLSsERLIPQRVMDQHKLTRD |
| P15311 | Y424 | Sugiyama | EZR VIL2 | ERQAVDQIKsQEQLAAELAEytAKIALLEEARRRKEDEVEE |
| P15374 | Y141 | Sugiyama | UCHL3 | KFLEEsVsMsPEERARyLENyDAIRVtHEtsAHEGQTEAPs |
| P15498 | Y142 | SIGNOR|ELM|iPTMNet|EPSD|PSP | VAV1 VAV | QNRGIMPFPTEEESVGDEDIySGLSDQIDDTVEEDEDLyDC |
| P15498 | Y160 | SIGNOR|ELM|iPTMNet|EPSD|PSP | VAV1 VAV | DIySGLSDQIDDTVEEDEDLyDCVENEEAEGDEIyEDLMRS |
| P15498 | Y174 | SIGNOR|iPTMNet|EPSD|PSP | VAV1 VAV | EEDEDLyDCVENEEAEGDEIyEDLMRSEPVSMPPKMTEYDK |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y250 | Sugiyama | RPS2 RPS4 | tAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEFt |
| P15941 | Y1229 | SIGNOR | MUC1 PUM | yPtyHtHGRyVPPsstDRsPyEKVsAGNGGssLsytNPAVA |
| P16035 | Y62 | Sugiyama | TIMP2 | DVVIRAKAVSEKEVDSGNDIyGNPIKRIQYEIKQIKMFKGP |
| P16284 | Y713 | SIGNOR|EPSD|PSP | PECAM1 | VQVSsAEsHKDLGKKDtEtVysEVRKAVPDAVEsRYsRtEG |
| P16402 | Y72 | Sugiyama | H1-3 H1F3 HIST1H1D | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P16403 | Y71 | Sugiyama | H1-2 H1F2 HIST1H1C | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P16410 | Y201 | SIGNOR|iPTMNet|EPSD | CTLA4 CD152 | LTAVSLSKMLKKRSPLTTGVyVKMPPTEPECEKQFQPyFIP |
| P16410 | Y218 | SIGNOR | CTLA4 CD152 | TGVyVKMPPTEPECEKQFQPyFIPIN_______________ |
| P16885 | Y1197 | ELM|iPTMNet|EPSD|PSP | PLCG2 | LASLLVFCEMRPVLESEEELySSCRQLRRRQEELNNQLFLy |
| P16885 | Y1217 | ELM|iPTMNet|EPSD|PSP | PLCG2 | ySSCRQLRRRQEELNNQLFLyDtHQNLRNANRDALVKEFsV |
| P16885 | Y743 | GPS6|ELM|iPTMNet|EPSD | PLCG2 | HSLYRKMRLRYPVTPELLERyNMERDINSLyDVSRMyVDPS |
| P16885 | Y753 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PLCG2 | YPVTPELLERyNMERDINSLyDVSRMyVDPSEINPSMPQRT |
| P16885 | Y759 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PLCG2 | LLERyNMERDINSLyDVSRMyVDPSEINPSMPQRTVKALYD |
| P17066 | Y43 | Sugiyama | HSPA6 HSP70B' | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P17676 | Y137 | Sugiyama | CEBPB TCF5 PP9092 | FLSDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCF |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17931 | Y221 | Sugiyama | LGALS3 MAC2 | QVLVEPDHFKVAVNDAHLLQyNHRVKKLNEISKLGISGDID |
| 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 |
| P18615 | Y170 | Sugiyama | NELFE RD RDBP | GEEAEGPGAGDGPPRsFDWGyEERSGAHSsAsPPRsRSRDR |
| P18615 | Y372 | Sugiyama | NELFE RD RDBP | NsPKGCHRDKRTQIVysDDVyKENLVDGF____________ |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18621 | Y4 | Sugiyama | RPL17 | _________________MVRysLDPENPtKsCKSRGSNLRV |
| P18669 | S134 | Sugiyama | PGAM1 PGAMA CDABP0006 | IWRRsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCE |
| P18669 | S137 | Sugiyama | PGAM1 PGAMA CDABP0006 | RsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLK |
| P18669 | Y119 | Sugiyama | PGAM1 PGAMA CDABP0006 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| 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____ |
| P19174 | Y771 | GPS6 | PLCG1 PLC1 | KLRYPINEEALEKIGTAEPDyGALyEGRNPGFyVEANPMPT |
| P19174 | Y783 | GPS6 | PLCG1 PLC1 | KIGTAEPDyGALyEGRNPGFyVEANPMPTFKCAVKALFDYK |
| P19838 | Y240 | Sugiyama | NFKB1 | LPDSTGSFTRRLEPVVSDAIyDSKAPNASNLKIVRMDRTAG |
| P20020 | Y57 | Sugiyama | ATP2B1 PMCA1 | LMELRSTDALRKIQEsyGDVyGICTKLKTSPNEGLSGNPAD |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20138 | Y340 | SIGNOR|ELM|iPTMNet|EPSD|PSP | CD33 SIGLEC3 | TETSSCSGAAPTVEMDEELHyASLNFHGMNPSKDTSTEySE |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P20618 | Y216 | Sugiyama | PSMB1 PSC5 | LDRAMRLVKDVFISAAERDVytGDALRICIVTKEGIREETV |
| P20936 | Y460 | EPSD | RASA1 GAP RASA | PVPMQDQEQVLNDTVDGKEIyNtIRRKTKDAFYKNIVKKGY |
| P20963 | Y142 | EPSD|PSP | CD247 CD3Z T3Z TCRZ | AysEIGMKGERRRGKGHDGLyQGLstAtKDtyDALHMQALP |
| P21127 | Y449 | Sugiyama | CDK11B CDC2L1 CDK11 PITSLREA PK58 | LQGCRsVEEFQCLNRIEEGtyGVVYRAKDKKTDEIVALKRL |
| P21333 | S732 | Sugiyama | FLNA FLN FLN1 | QDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWGGV |
| P21333 | Y373 | Sugiyama | FLNA FLN FLN1 | THKVTVLFAGQHIAKsPFEVyVDKsQGDASKVTAQGPGLEP |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P22059 | Y767 | Sugiyama | OSBP OSBP1 | RKKREAEAMKATEDGtPYDPyKALWFERKKDPVTKELTHIy |
| P22087 | Y118 | Sugiyama | FBL FIB1 FLRN | ICRGKEDALVTKNLVPGEsVyGEKRVsIsEGDDKIEyRAWN |
| P22087 | Y134 | Sugiyama | FBL FIB1 FLRN | GEsVyGEKRVsIsEGDDKIEyRAWNPFRSKLAAAILGGVDQ |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y451 | Sugiyama | UBA1 A1S9T UBE1 | CLPEDKEVLTEDKCLQRQNRyDGQVAVFGsDLQEKLGKQKY |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22314 | Y560 | Sugiyama | UBA1 A1S9T UBE1 | NPHIRVTSHQNRVGPDtERIyDDDFFQNLDGVANALDNVDA |
| P22314 | Y60 | Sugiyama | UBA1 A1S9T UBE1 | GMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSVLVSGL |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22492 | Y75 | Sugiyama | H1-6 H1FT H1T HIST1H1T | SQERVGMSLVALKKALAAAGyDVEKNNSRIKLSLKSLVNKG |
| P22626 | Y331 | Sugiyama | HNRNPA2B1 HNRPA2B1 | SNYGPMKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRs |
| P22626 | Y347 | Sugiyama | HNRNPA2B1 HNRPA2B1 | MGGPyGGGNyGPGGsGGsGGyGGRsRy______________ |
| P22681 | Y700 | EPSD|PSP | CBL CBL2 RNF55 | PLPVPKLPPGEQCEGEEDtEyMtPssRPLRPLDTsQSsRAC |
| P22681 | Y731 | EPSD|PSP | CBL CBL2 RNF55 | LDTsQSsRACDCDQQIDSCTyEAMYNIQSQAPSITESSTFG |
| P22681 | Y774 | EPSD|PSP | CBL CBL2 RNF55 | NLAAAHANTGPEESENEDDGyDVPKPPVPAVLARRtLsDIs |
| P23142 | Y175 | Sugiyama | FBLN1 PP213 | VGGLQETDKIIEVEEEQEDPyLNDRCRGGGPCKQQCRDTGD |
| 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 |
| P23396 | Y34 | Sugiyama | RPS3 OK/SW-cl.26 | DGIFKAELNEFLtRELAEDGysGVEVRVtPTRTEIIILATR |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23434 | Y164 | Sugiyama | GCSH | LIKMtLsNPsELDELMsEEAyEKYIKSIEE___________ |
| 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 |
| P23743 | Y335 | EPSD|PSP | DGKA DAGK DAGK1 | VGHECDCGLLRDHILPPSSIyPSVLASGPDRKNSKTSQKTM |
| P23921 | Y232 | Sugiyama | RRM1 RR1 | RPQLSSCFLLSMKDDSIEGIyDTLKQCALISKSAGGIGVAV |
| P23921 | Y556 | Sugiyama | RRM1 RR1 | yyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPT |
| P24666 | Y132 | SIGNOR|iPTMNet|EPSD|PSP | ACP1 | AKIELLGsYDPQKQLIIEDPyyGNDsDFEtVyQQCVRCCRA |
| P24666 | Y133 | SIGNOR|iPTMNet|EPSD|PSP | ACP1 | KIELLGsYDPQKQLIIEDPyyGNDsDFEtVyQQCVRCCRAF |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P25205 | Y188 | Sugiyama | MCM3 | FPSSSVYPTKDEENNPLETEyGLSVyKDHQtITIQEMPEKA |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y45 | Sugiyama | MCM3 | DEEDQGIyQsKVRELIsDNQyRLIVNVNDLRRKNEKRANRL |
| P25205 | Y708 | Sugiyama | MCM3 | KRKRRKTRQPDAKDGDsyDPyDFsDtEEEMPQVHtPKTADs |
| P25208 | Y58 | Sugiyama | NFYB HAP3 | SMNDHEDTNGSKESFREQDIyLPIANVARIMKNAIPQTGKI |
| P25685 | Y176 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | ARKKQDPPVTHDLRVsLEEIysGCtKKMKISHKRLNPDGKS |
| P25685 | Y52 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | HPDKNKEPGAEEKFKEIAEAyDVLSDPRKREIFDRYGEEGL |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P25787 | Y57 | Sugiyama | PSMA2 HC3 PSC3 | GIKAANGVVLATEKKQKSILyDERSVHKVEPITKHIGLVys |
| P25963 | Y42 | SIGNOR|ELM|iPTMNet|EPSD|PSP | NFKBIA IKBA MAD3 NFKBI | KERLLDDRHDsGLDsMKDEEyEQMVKELQEIRLEPQEVPRG |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26639 | T574 | Sugiyama | TARS1 TARS | RYHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAIL |
| P26639 | T629 | Sugiyama | TARS1 TARS | GGKWPFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMAD |
| P26640 | Y601 | Sugiyama | VARS1 G7A VARS VARS2 | VDMDFGTGAVKITPAHDQNDyEVGQRHGLEAIsIMDsRGAL |
| P26885 | Y112 | Sugiyama | FKBP2 FKBP13 | GLLGMCEGEKRKLVIPsELGyGERGAPPKIPGGATLVFEVE |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27348 | Y19 | Sugiyama | YWHAQ | __MEKTELIQKAKLAEQAERyDDMAtCMKAVtEQGAELsNE |
| P27348 | Y48 | Sugiyama | YWHAQ | AVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSIEQK |
| P27361 | Y204 | SIGNOR | MAPK3 ERK1 PRKM3 | DFGLARIADPEHDHtGFLtEyVAtRWyRAPEIMLNSKGYTK |
| P27540 | Y561 | Sugiyama | ARNT BHLHE2 | PLEKSDGLFAQDRDPRFsEIyHNINADQSKGISSSTVPATQ |
| P27695 | Y128 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | LQELPGLSHQYWSAPsDKEGysGVGLLsRQCPLKVsyGIGD |
| P27695 | Y144 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | DKEGysGVGLLsRQCPLKVsyGIGDEEHDQEGRVIVAEFDS |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P27986 | Y688 | GPS6|SIGNOR|EPSD | PIK3R1 GRB1 | KHCVINKTATGyGFAEPYNLySSLKELVLHYQHTSLVQHND |
| P28062 | Y271 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | MKEDGWVKVEsTDVSDLLHQyREANQ_______________ |
| P28066 | Y185 | Sugiyama | PSMA5 | CDARAIGsAsEGAQssLQEVyHKSMTLKEAIKSSLIILKQV |
| P28066 | Y8 | Sugiyama | PSMA5 | _____________MFLTRsEyDRGVNtFsPEGRLFQVEyAI |
| P28074 | Y171 | Sugiyama | PSMB5 LMPX MB1 X | GMGLSMGTMICGWDKRGPGLyyVDsEGNRISGATFSVGSGS |
| P28074 | Y212 | Sugiyama | PSMB5 LMPX MB1 X | VYAYGVMDRGYSYDLEVEQAyDLARRAIyQATYRDAysGGA |
| P29350 | Y536 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PTPN6 HCP PTP1C | IETTKKKLEVLQSQKGQEsEyGNITyPPAMKNAHAKAsRts |
| P29350 | Y564 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PTPN6 HCP PTP1C | AMKNAHAKAsRtssKHKEDVyENLHTKNKREEKVKKQRSAD |
| P29353 | Y427 | SIGNOR|EPSD|Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | S276 | Sugiyama | TKT | sWHGKPLPKNMAEQIIQEIysQIQsKKKILAtPPQEDAPsV |
| P29401 | S308 | Sugiyama | TKT | PPQEDAPsVDIANIRMPsLPsyKVGDKIATRKAYGQALAKL |
| P29401 | Y202 | Sugiyama | TKT | LDINRLGQsDPAPLQHQMDIyQKRCEAFGWHAIIVDGHSVE |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30041 | Y89 | Sugiyama | PRDX6 AOP2 KIAA0106 | IALSIDSVEDHLAWSKDINAyNCEEPtEKLPFPIIDDRNRE |
| P30043 | S198 | Sugiyama | BLVRB FLR SCAN | KHDLGHFMLRCLttDEyDGHstyPsHQyQ____________ |
| P30043 | T199 | Sugiyama | BLVRB FLR SCAN | HDLGHFMLRCLttDEyDGHstyPsHQyQ_____________ |
| P30043 | Y194 | Sugiyama | BLVRB FLR SCAN | RVISKHDLGHFMLRCLttDEyDGHstyPsHQyQ________ |
| P30043 | Y205 | Sugiyama | BLVRB FLR SCAN | MLRCLttDEyDGHstyPsHQyQ___________________ |
| P30084 | Y112 | Sugiyama | ECHS1 | KAFAAGADIKEMQNLsFQDCySSKFLKHWDHLTQVKKPVIA |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| 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 | 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 |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31153 | Y377 | Sugiyama | MAT2A AMS2 MATA2 | PGVIVRDLDLKKPIYQRTAAyGHFGRDsFPWEVPKKLKY__ |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31689 | Y52 | Sugiyama | DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4 | KYHPDKNPNEGEKFKQISQAyEVLSDAKKRELYDKGGEQAI |
| P31939 | Y290 | Sugiyama | ATIC PURH OK/SW-cl.86 | PAGAAVGIPLsEDEAKVCMVyDLyKTLtPIsAAyARARGAD |
| P31939 | Y293 | Sugiyama | ATIC PURH OK/SW-cl.86 | AAVGIPLsEDEAKVCMVyDLyKTLtPIsAAyARARGADRMs |
| 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 |
| P32119 | Y193 | SIGNOR | PRDX2 NKEFB TDPX1 | PAGWKPGSDTIKPNVDDSKEyFSKHN_______________ |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32929 | Y114 | Sugiyama | CTH | TVTITHLLKAGDQIICMDDVyGGTNRYFRQVASEFGLKISF |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33121 | Y693 | Sugiyama | ACSL1 FACL1 FACL2 LACS LACS1 LACS2 | TMKAKRPELRNYFRSQIDDLyStIKV_______________ |
| P33176 | Y62 | Sugiyama | KIF5B KNS KNS1 | ASKPYAFDRVFQSsTsQEQVyNDCAKKIVKDVLEGyNGtIF |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33991 | Y394 | Sugiyama | MCM4 CDC21 | AHNDLVDKVQPGDRVNVTGIyRAVPIRVNPRVSNVKSVYKT |
| P33993 | Y102 | Sugiyama | MCM7 CDC47 MCM2 | QELLPQYKEREVVNKDVLDVyIEHRLMMEQRSRDPGMVRsP |
| P34896 | Y34 | Sugiyama | SHMT1 | LWSsHDKMLAQPLKDSDVEVyNIIKKESNRQRVGLELIASE |
| P34931 | Y43 | Sugiyama | HSPA1L | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| 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 |
| P34932 | Y660 | Sugiyama | HSPA4 APG2 HSPH2 | VSEDDRNsFtLKLEDTENWLyEDGEDQPKQVYVDKLAELKN |
| P35080 | Y99 | Sugiyama | PFN2 | yVDGDCtMDIRTKsQGGEPTyNVAVGRAGRVLVFVMGKEGV |
| P35221 | Y619 | Sugiyama | CTNNA1 | SSDPAQPMDENEFIDASRLVyDGIRDIRKAVLMIRtPEELD |
| P35270 | Y259 | Sugiyama | SPR | QKLLSLLEKDEFKSGAHVDFyDK__________________ |
| P35579 | Y130 | Sugiyama | MYH9 | IYTYSGLFCVVINPYKNLPIysEEIVEMyKGKKRHEMPPHI |
| P35579 | Y138 | Sugiyama | MYH9 | CVVINPYKNLPIysEEIVEMyKGKKRHEMPPHIyAITDtAy |
| P35579 | Y297 | Sugiyama | MYH9 | FYYLLSGAGEHLKTDLLLEPyNKyRFLsNGHVtIPGQQDKD |
| P35606 | Y354 | Sugiyama | COPB2 | EIKDGERLPLAVKDMGsCEIyPQtIQHNPNGRFVVVCGDGE |
| P35609 | Y385 | Sugiyama | ACTN2 | GKMVSDIAGAWQRLEQAEKGyEEWLLNEIRRLERLEHLAEK |
| P35659 | Y357 | Sugiyama | DEK | NLEEVTMKQICKKVyENyPTyDLTERKDFIKTTVKELIS__ |
| P36578 | Y211 | Sugiyama | RPL4 RPL1 | AGKGKMRNRRRIQRRGPCIIyNEDNGIIKAFRNIPGITLLN |
| P36578 | Y264 | Sugiyama | RPL4 RPL1 | GHVGRFCIWtEsAFRKLDELyGtWRKAAsLKsNyNLPMHKM |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P37108 | T29 | Sugiyama | SRP14 | FLtELTRLFQKCRTSGsVyItLKKYDGRTKPIPKKGtVEGF |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P38646 | T120 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | LVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIKNV |
| P38646 | Y118 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | ERLVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIK |
| P38646 | Y196 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | EtAENyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNV |
| P38919 | Y54 | Sugiyama | EIF4A3 DDX48 KIAA0111 | VDVTPTFDTMGLREDLLRGIyAyGFEKPsAIQQRAIKQIIK |
| P38919 | Y56 | Sugiyama | EIF4A3 DDX48 KIAA0111 | VTPTFDTMGLREDLLRGIyAyGFEKPsAIQQRAIKQIIKGR |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P40259 | Y196 | iPTMNet|EPSD | CD79B B29 IGB | PIFLLLDKDDSKAGMEEDHtyEGLDIDQTAtyEDIVTLRTG |
| P40259 | Y207 | iPTMNet|EPSD | CD79B B29 IGB | KAGMEEDHtyEGLDIDQTAtyEDIVTLRTGEVKWsVGEHPG |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40429 | Y149 | Sugiyama | RPL13A | LKPTRKFAYLGRLAHEVGWKyQAVtAtLEEKRKEKAKIHYR |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41219 | Y287 | Sugiyama | PRPH NEF4 PRPH1 | DIRAQYESIAAKNLQEAEEWyKSKYADLSDAANRNHEALRQ |
| P41227 | Y145 | Sugiyama | NAA10 ARD1 ARD1A TE2 | TLNFQISEVEPKyyADGEDAyAMKRDLtQMADELRRHLELK |
| P41252 | Y148 | Sugiyama | IARS1 IARS | SAEWKSTVsRLGRWIDFDNDyKTLYPQFMESVWWVFKQLYD |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42025 | Y33 | Sugiyama | ACTR1B CTRN2 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALE |
| P42025 | Y38 | Sugiyama | ACTR1B CTRN2 | SGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALEGDLFI |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P42224 | Y701 | iPTMNet|EPSD | STAT1 | YSRPKEAPEPMELDGPKGtGyIKtELIsVsEVHPSRLQttD |
| P42229 | Y694 | EPSD|PSP | STAT5A STAT5 | PKDEVFSKYYTPVLAKAVDGyVKPQIKQVVPEFVNASADAG |
| P42768 | Y291 | EPSD|PSP | WAS IMD2 | FSRAGIsEAQLtDAETsKLIyDFIEDQGGLEAVRQEMRRQE |
| P43034 | Y28 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | RDELNRAIADyLRSNGyEEAySVFKKEAELDVNEELDKKYA |
| P43121 | Y222 | Sugiyama | MCAM MUC18 | YTLQSILKAQLVKEDKDAQFyCELNYRLPSGNHMKEsREVT |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43403 | Y12 | EPSD | ZAP70 SRK | _________MPDPAAHLPFFyGSIsRAEAEEHLKLAGMADG |
| P43403 | Y126 | EPSD|PSP | ZAP70 SRK | sGLEPQPGVFDCLRDAMVRDyVRQTWKLEGEALEQAIISQA |
| P43403 | Y178 | SIGNOR|iPTMNet|EPSD|PSP | ZAP70 SRK | HERMPWyHSSLTREEAERKLySGAQTDGKFLLRPRKEQGTy |
| P43403 | Y292 | ELM|iPTMNet|EPSD|PSP | ZAP70 SRK | AHPSTLTHPQRRIDtLNsDGytPEPARItsPDKPRPMPMDt |
| P43403 | Y315 | EPSD|PSP | ZAP70 SRK | EPARItsPDKPRPMPMDtsVyEsPysDPEELKDKKLFLKRD |
| P43403 | Y319 | SIGNOR|iPTMNet|EPSD|PSP | ZAP70 SRK | ItsPDKPRPMPMDtsVyEsPysDPEELKDKKLFLKRDNLLI |
| P43403 | Y474 | SIGNOR|ELM|iPTMNet|EPSD|PSP | ZAP70 SRK | EKNFVHRDLAARNVLLVNRHyAKISDFGLSKALGADDsyyt |
| P43403 | Y492 | SIGNOR|ELM|iPTMNet|EPSD|PSP | ZAP70 SRK | RHyAKISDFGLSKALGADDsyytARSAGKWPLKWyAPECIN |
| P43403 | Y493 | SIGNOR|ELM|iPTMNet|EPSD|PSP | ZAP70 SRK | HyAKISDFGLSKALGADDsyytARSAGKWPLKWyAPECINF |
| P43403 | Y69 | SIGNOR|iPTMNet|EPSD|PSP | ZAP70 SRK | SLVHDVRFHHFPIERQLNGTyAIAGGKAHCGPAELCEFysR |
| P43490 | Y471 | Sugiyama | NAMPT PBEF PBEF1 | EEYGQDLLHTVFKNGKVTKsysFDEIRKNAQLNIELEAAHH |
| P46777 | Y210 | Sugiyama | RPL5 MSTP030 | FNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyIKNs |
| 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 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46940 | Y1095 | Sugiyama | IQGAP1 KIAA0051 | VVKEIMDDKSLNIKTDPVDIyKsWVNQMESQTGEASKLPyD |
| P46940 | Y140 | Sugiyama | IQGAP1 KIAA0051 | LNAMDEIGLPKIFYPETTDIyDRKNMPRCIYCIHALSLYLF |
| P46940 | Y287 | Sugiyama | IQGAP1 KIAA0051 | QDKMTNAKNRTENSERERDVyEELLTQAEIQGNINKVNTFS |
| P47224 | Y114 | Sugiyama | RABIF MSS4 RASGRF3 | CADCEIGPIGWHCLDDKNSFyVALERVSHE___________ |
| P47712 | Y535 | Sugiyama | PLA2G4A CPLA2 PLA2G4 | sFDDDELDAAVADPDEFERIyEPLDVKSKKIHVVDSGLTFN |
| P47756 | Y232 | Sugiyama | CAPZB | NIGRLVEDMENKIRstLNEIyFGKTKDIVNGLRSVQTFADK |
| 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 |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | Y43 | Sugiyama | HSPA7 HSP70B | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P49023 | Y88 | Sugiyama | PXN | QWQPSSSRFIHQQPQsssPVyGssAKtssVsNPQDsVGsPC |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | S279 | Sugiyama | FASN FAS | QGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGTKV |
| P49327 | T2450 | Sugiyama | FASN FAS | AEQYtPKAKyHGNVMLLRAKtGGAyGEDLGADyNLsQVCDG |
| P49327 | Y2034 | Sugiyama | FASN FAS | DYFVVFSSVSCGRGNAGQsNyGFANsAMERICEKRRHEGLP |
| P49327 | Y2462 | Sugiyama | FASN FAS | NVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsVHVIEGDHR |
| P49327 | Y277 | Sugiyama | FASN FAS | KEQGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGT |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49327 | Y959 | Sugiyama | FASN FAS | EASRAFEVSENGNLVVSGKVyQWDDPDPRLFDHPEsPtPNP |
| P49419 | Y55 | Sugiyama | ALDH7A1 ATQ1 | NQPQYAWLKELGLREENEGVyNGSWGGRGEVIttyCPANNE |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y295 | Sugiyama | AARS1 AARS | GARPYTGKVGAEDADGIDMAyRVLADHARTITVALADGGRP |
| P49588 | Y543 | Sugiyama | AARS1 AARS | QECGVVLDKTCFyAEQGGQIyDEGYLVKVDDssEDKTEFTV |
| P49588 | Y667 | Sugiyama | AARS1 AARS | QQIKKAEEIANEMIEAAKAVyTQDCPLAAAKAIQGLRAVFD |
| P49588 | Y690 | Sugiyama | AARS1 AARS | DCPLAAAKAIQGLRAVFDEtyPDPVRVVSIGVPVSELLDDP |
| P49591 | Y248 | Sugiyama | SARS1 SARS SERS | FMRKEVMQEVAQLsQFDEELyKVIGKGSEKSDDNSYDEKYL |
| P49591 | Y294 | Sugiyama | SARS1 SARS SERS | QPIAALHRDEWLRPEDLPIKyAGLsTCFRQEVGSHGRDTRG |
| P49792 | S3137 | Sugiyama | RANBP2 NUP358 | IPDFVCQGGDITKHDGTGGQsIyGDKFEDENFDVKHTGPGL |
| P50238 | Y12 | Sugiyama | CRIP1 CRIP CRP1 | _________MPKCPKCNKEVyFAERVTSLGKDWHRPCLKCE |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50395 | Y404 | Sugiyama | GDI2 RABGDIB | SDLLVPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRM |
| P50402 | Y95 | Sugiyama | EMD EDMD STA | DLPKKEDALLyQsKGyNDDyyEEsyFTTRTyGEPEsAGPSR |
| P50502 | Y185 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | NAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50990 | S425 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | DKRLVPGGGAtEIELAKQItsyGETCPGLEQyAIKKFAEAF |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50990 | Y436 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | EIELAKQItsyGETCPGLEQyAIKKFAEAFEAIPRALAENS |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51511 | Y60 | Sugiyama | MMP15 | LGLGVAAEDAEVHAENWLRLyGYLPQPSRHMSTMRSAQILA |
| P51532 | Y718 | Sugiyama | SMARCA4 BAF190A BRG1 SNF2B SNF2L4 | VsEVDARHIIENAKQDVDDEyGVsQALARGLQSyyAVAHAV |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | Y266 | Sugiyama | HNRNPF HNRPF | ySGLSDGYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQsT |
| P52597 | Y82 | Sugiyama | HNRNPF HNRPF | GsEDDVKMALKKDRESMGHRyIEVFKSHRTEMDWVLKHsGP |
| P52630 | Y690 | EPSD|PSP | STAT2 | RDEAFGCYYQEKVNLQERRKyLKHRLIVVSNRQVDELQQPL |
| P52735 | Y142 | GPS6|ELM|iPTMNet|EPSD | VAV2 | QNKGIRPFPSEETTENDDDVyRSLEELADEHDLGEDIyDCV |
| P52735 | Y159 | GPS6|ELM|iPTMNet|EPSD | VAV2 | DDVyRSLEELADEHDLGEDIyDCVPCEDGGDDIyEDIIKVE |
| P52735 | Y172 | GPS6|ELM|iPTMNet|EPSD | VAV2 | HDLGEDIyDCVPCEDGGDDIyEDIIKVEVQQPMIRYMQKMG |
| P52757 | Y153 | SIGNOR|EPSD|PSP | CHN2 ARHGAP3 BCH | TLYIETKAAEYISKMTTNPIyEHIGYATLLREKVsRRLsRs |
| P52789 | Y417 | Sugiyama | HK2 | IKENKGEERLRstIGVDGsVyKKHPHFAKRLHKTVRRLVPG |
| P52888 | Y576 | Sugiyama | THOP1 | VLAKVDQALHTQTDADPAEEyARLCQEILGVPATPGTNMPA |
| P52907 | Y239 | Sugiyama | CAPZA1 | sNEAQtAKEFIKIIENAENEyQTAIsENyQtMSDTTFKALR |
| P52907 | Y247 | Sugiyama | CAPZA1 | EFIKIIENAENEyQTAIsENyQtMSDTTFKALRRQLPVTRT |
| P52948 | Y1215 | Sugiyama | NUP98 ADAR2 | KVHLEKLSLRQRKPDEDMKLyQTPLELKLKHSTVHVDELCP |
| P52948 | Y848 | Sugiyama | NUP98 ADAR2 | PTDKTSRCLIKsPDRLADINyEGRLEAVSRKQGAQFKEyRP |
| P53041 | Y313 | Sugiyama | PPP5C PPP5 | YPDHFHLLRGNHETDNMNQIyGFEGEVKAKYTAQMYELFSE |
| P53597 | Y78 | Sugiyama | SUCLG1 | IICQGFTGKQGtFHSQQALEyGtKLVGGTTPGKGGQTHLGL |
| P53621 | Y391 | Sugiyama | COPA | NPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGK |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P54105 | Y38 | Sugiyama | CLNS1A CLCI ICLN | RQQPDTEAVLNGKGLGtGtLyIAEsRLSWLDGsGLGFSLEY |
| P54136 | Y323 | Sugiyama | RARS1 RARS | DITKAWKLICDVSRQELNKIyDALDVsLIERGEsFYQDRMN |
| P54136 | Y384 | Sugiyama | RARS1 RARS | VFVPGCSIPLTIVKsDGGytyDtSDLAAIKQRLFEEKADMI |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54652 | Y42 | Sugiyama | HSPA2 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P55060 | Y278 | Sugiyama | CSE1L CAS XPO2 | EEEAGLLELLKSQICDNAALyAQKyDEEFQRYLPRFVTAIW |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55072 | Y203 | Sugiyama | VCP HEL-220 HEL-S-70 | HCEGEPIKREDEEEsLNEVGyDDIGGCRKQLAQIKEMVELP |
| P55081 | Y276 | Sugiyama | MFAP1 | KRsLAALDALNtDDENDEEEyEAWKVRELKRIKRDREDREA |
| P55084 | Y244 | Sugiyama | HADHB MSTP029 | GHSADRLAAAFAVSRLEQDEyALRsHSLAKKAQDEGLLSDV |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55884 | Y222 | Sugiyama | EIF3B EIF3S9 | KLKNVIHKIFSKFGKITNDFyPEEDGKTKGyIFLEyAsPAH |
| P56945 | Y234 | Sugiyama | BCAR1 CAS CASS1 CRKAS | VPtRVGQGyVyEAAQPEQDEyDIPRHLLAPGPQDIyDVPPV |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60228 | Y62 | Sugiyama | EIF3E EIF3S6 INT6 | LDLLSDTNMVDFAMDVYKNLySDDIPHALREKRTTVVAQLK |
| P60484 | Y240 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PTEN MMAC1 TEP1 | LKVKIYSSNsGPtRREDKFMyFEFPQPLPVCGDIKVEFFHK |
| P60484 | Y315 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PTEN MMAC1 TEP1 | LCDQEIDsICSIERADNDKEyLVLtLtKNDLDKANKDKANR |
| P60510 | Y124 | Sugiyama | PPP4C PPP4 PPX | YPDRITLIRGNHESRQITQVyGFyDECLRKYGSVTVWRYCT |
| P60510 | Y127 | Sugiyama | PPP4C PPP4 PPX | RITLIRGNHESRQITQVyGFyDECLRKYGSVTVWRYCTEIF |
| P60660 | S30 | Sugiyama | MYL6 | AEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVLK |
| 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_______ |
| P60709 | Y91 | Sugiyama | ACTB | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P60842 | Y197 | Sugiyama | EIF4A1 DDX2A EIF4A | KMFVLDEADEMLsRGFKDQIyDIFQKLNsNtQVVLLSATMP |
| P60842 | Y48 | Sugiyama | EIF4A1 DDX2A EIF4A | NEIVDSFDDMNLSESLLRGIyAyGFEKPsAIQQRAILPCIK |
| P60842 | Y50 | Sugiyama | EIF4A1 DDX2A EIF4A | IVDSFDDMNLSESLLRGIyAyGFEKPsAIQQRAILPCIKGy |
| P60842 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60900 | Y160 | Sugiyama | PSMA6 PROS27 | LIGIDEEQGPQVYKCDPAGyyCGFKATAAGVKQtEstsFLE |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61163 | Y241 | Sugiyama | ACTR1A CTRN1 | ACYLSINPQKDETLETEKAQyyLPDGstIEIGPSRFRAPEL |
| P61163 | Y242 | Sugiyama | ACTR1A CTRN1 | CYLSINPQKDETLETEKAQyyLPDGstIEIGPSRFRAPELL |
| P61163 | Y33 | Sugiyama | ACTR1A CTRN1 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALE |
| P61163 | Y38 | Sugiyama | ACTR1A CTRN1 | SGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALEGDIFI |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61313 | Y62 | Sugiyama | RPL15 EC45 TCBAP0781 | PTRPDKARRLGYKAKQGyVIyRIRVRRGGRKRPVPKGAtyG |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| P61353 | Y85 | Sugiyama | RPL27 | RSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVNKDVFRDPA |
| P61604 | Y76 | Sugiyama | HSPE1 | KGGEIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDI |
| P61604 | Y88 | Sugiyama | HSPE1 | GDKVLLPEyGGtKVVLDDKDyFLFRDGDILGKyVD______ |
| P61758 | Y180 | Sugiyama | VBP1 PFDN3 | EDLDFLRDQFTtTEVNMARVyNWDVKRRNKDDSTKNKA___ |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | S215 | Sugiyama | YWHAG | HLAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWts |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62140 | Y304 | Sugiyama | PPP1CB | VDETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPP |
| P62140 | Y306 | Sugiyama | PPP1CB | ETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPPKK |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62191 | Y225 | Sugiyama | PSMC1 | LTHPEyyEEMGIKPPKGVILyGPPGtGKTLLAKAVANQTsA |
| 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 |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62277 | Y18 | Sugiyama | RPS13 | ___MGRMHAPGKGLsQsALPyRRsVPtWLKLTsDDVKEQIy |
| P62280 | T54 | Sugiyama | RPS11 | PRYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILs |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62312 | Y72 | Sugiyama | LSM6 | VNGQLKNKyGDAFIRGNNVLyIstQKRRM____________ |
| P62333 | Y328 | Sugiyama | PSMC6 SUG2 | ARLDILKIHAGPITKHGEIDyEAIVKLSDGFNGADLRNVCT |
| P62495 | Y345 | Sugiyama | ETF1 ERF1 RF1 SUP45L1 | NLDIMRYVLHCQGTEEEKILyLTPEQEKDKSHFTDKETGQE |
| P62633 | S121 | Sugiyama | CNBP RNF163 ZNF9 | CGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRCG |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62633 | Y75 | Sugiyama | CNBP RNF163 ZNF9 | YRCGESGHLAKDCDLQEDACyNCGRGGHIAKDCKEPKRERE |
| P62714 | Y127 | Sugiyama | PPP2CB | YPERITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFT |
| P62714 | Y130 | Sugiyama | PPP2CB | RITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFTDLF |
| P62714 | Y284 | Sugiyama | PPP2CB | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRT |
| 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 |
| P62753 | Y28 | Sugiyama | RPS6 OK/SW-cl.2 | PAtGCQKLIEVDDERKLRtFyEKRMAtEVAADALGEEWKGY |
| 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 | 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 |
| P62899 | T26 | Sugiyama | RPL31 | KGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRAL |
| P62899 | Y25 | Sugiyama | RPL31 | KKGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRA |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62979 | T147 | Sugiyama | RPS27A UBA80 UBCEP1 | GAGVFMAsHFDRHyCGKCCLtyCFNKPEDK___________ |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63151 | T76 | Sugiyama | PPP2R2A | QQEQENKIQSHSRGEyNVystFQsHEPEFDyLKSLEIEEKI |
| 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_______ |
| P63261 | Y91 | Sugiyama | ACTG1 ACTG | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67775 | Y127 | Sugiyama | PPP2CA | YRERITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFT |
| P67775 | Y130 | Sugiyama | PPP2CA | RITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFTDLF |
| P67775 | Y284 | Sugiyama | PPP2CA | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRt |
| P67775 | Y307 | EPSD|PSP | PPP2CA | LQFDPAPRRGEPHVTRRtPDyFL__________________ |
| P67809 | Y196 | Sugiyama | YBX1 NSEP1 YB1 | sAPEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGE |
| P67809 | Y197 | Sugiyama | YBX1 NSEP1 YB1 | APEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGEV |
| P67809 | Y208 | Sugiyama | YBX1 NSEP1 YB1 | yRRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGE |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68032 | Y93 | Sugiyama | ACTC1 ACTC | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68104 | Y254 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68133 | Y93 | Sugiyama | ACTA1 ACTA | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68363 | Y312 | Sugiyama | TUBA1B | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68363 | Y319 | Sugiyama | TUBA1B | ANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAIAtIKtKR |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68363 | Y451 | Sugiyama | TUBA1B | DyEEVGVDsVEGEGEEEGEEy____________________ |
| P68366 | Y312 | Sugiyama | TUBA4A TUBA1 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68366 | Y319 | Sugiyama | TUBA4A TUBA1 | ANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAIAAIKTKR |
| P68400 | T127 | Sugiyama | CSNK2A1 CK2A1 | RTPALVFEHVNNTDFKQLyQtLTDYDIRFYMYEILKALDYC |
| P68400 | Y255 | Sugiyama | CSNK2A1 CK2A1 | GHDNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGR |
| P83731 | Y11 | Sugiyama | RPL24 | __________MKVELCsFsGyKIYPGHGRRYARTDGKVFQF |
| P84090 | Y22 | Sugiyama | ERH | sHTILLVQPTKRPEGRtyADyEsVNECMEGVCKMYEEHLKR |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| P98175 | Y694 | Sugiyama | RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122 | QPISSLRDDERREsAtADAGyAILEKKGALAERQHTsMDLP |
| P98179 | Y118 | Sugiyama | RBM3 RNPL | GRGRSYSRGGGDQGYGSGRyyDsRPGGyGyGyGRSRDYNGR |
| P98179 | Y127 | Sugiyama | RBM3 RNPL | GGDQGYGSGRyyDsRPGGyGyGyGRSRDYNGRNQGGYDRys |
| Q00005 | T72 | Sugiyama | PPP2R2B | QREQESKNQVHRRGEyNVystFQsHEPEFDyLKSLEIEEKI |
| Q00005 | Y67 | Sugiyama | PPP2R2B | RVVIFQREQESKNQVHRRGEyNVystFQsHEPEFDyLKSLE |
| Q00005 | Y70 | Sugiyama | PPP2R2B | IFQREQESKNQVHRRGEyNVystFQsHEPEFDyLKSLEIEE |
| Q00169 | Y140 | Sugiyama | PITPNA PITPN | GTQENVHKLEPEAWKHVEAVyIDIADRSQVLSKDYKAEEDP |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00534 | Y24 | Sugiyama | CDK6 CDKN6 | DGLCRADQQyECVAEIGEGAyGKVFKARDLKNGGRFVALKR |
| Q00535 | T17 | Sugiyama | CDK5 CDKN5 PSSALRE | ____MQKYEKLEKIGEGtyGtVFKAKNRETHEIVALKRVRL |
| Q00535 | Y15 | Sugiyama | CDK5 CDKN5 PSSALRE | ______MQKYEKLEKIGEGtyGtVFKAKNRETHEIVALKRV |
| Q00610 | Y1487 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LNNLFITEEDyQALRTsIDAyDNFDNIsLAQRLEKHELIEF |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00653 | Y285 | Sugiyama | NFKB2 LYT10 | DDENGWQAFGDFsPTDVHKQyAIVFRTPPYHKMKIERPVTV |
| Q00839 | Y257 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | QKGGDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVE |
| Q00839 | Y260 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | GDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVEEED |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01814 | Y1152 | Sugiyama | ATP2B2 PMCA2 | RGLNRIQtQIRVVKAFRssLyEGLEKPEsRtsIHNFMAHPE |
| Q01844 | Y278 | Sugiyama | EWSR1 EWS | SSSYGQQSsFRQDHPssMGVyGQESGGFSGPGENRSMSGPD |
| Q02539 | Y74 | Sugiyama | H1-1 H1F1 HIST1H1A | SKERGGVSLAALKKALAAAGyDVEKNNSRIKLGIKsLVsKG |
| Q02878 | Y115 | Sugiyama | RPL6 TXREB1 | PVGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQ |
| Q02878 | Y116 | Sugiyama | RPL6 TXREB1 | VGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQH |
| Q02878 | Y216 | Sugiyama | RPL6 TXREB1 | AtsTKIDISNVKIPKHLtDAyFKKKKLRKPRHQEGEIFDtE |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04759 | Y90 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PRKCQ PRKCT | MQIIVKGKNVDLISETTVELySLAERCRKNNGKTEIWLELK |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05639 | Y254 | Sugiyama | EEF1A2 EEF1AL STN | TILPPTRPTDKPLRLPLQDVyKIGGIGtVPVGRVETGILRP |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q05655 | Y313 | SIGNOR|iPTMNet|EPSD | PRKCD PKCD | QVtQRAsRRsDsAssEPVGIyQGFEKKTGVAGEDMQDNsGt |
| Q05655 | Y334 | SIGNOR|iPTMNet|EPSD | PRKCD PKCD | QGFEKKTGVAGEDMQDNsGtyGKIWEGSsKCNINNFIFHKV |
| Q05655 | Y514 | SIGNOR|iPTMNet|EPSD | PRKCD PKCD | MCKENIFGEsRAstFCGtPDyIAPEILQGLKyTFSVDWWSF |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q06830 | Y194 | SIGNOR|EPSD|PSP | PRDX1 PAGA PAGB TDPX2 | PAGWKPGsDtIKPDVQKSKEyFSKQK_______________ |
| Q07666 | Y145 | Sugiyama | KHDRBS1 SAM68 | LtAEIEKIQKGDSKKDDEENyLDLFsHKNMKLKERVLIPVK |
| Q07866 | Y449 | Sugiyama | KLC1 KLC KNS2 | HAEEREECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKN |
| Q07866 | Y453 | Sugiyama | KLC1 KLC KNS2 | REECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKNLGAL |
| Q07955 | Y189 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | TYAVRKLDNTKFRsHEGEtAyIRVKVDGPRsPsyGRsRsRs |
| Q07955 | Y37 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | RIyVGNLPPDIRtKDIEDVFyKYGAIRDIDLKNRRGGPPFA |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q08378 | Y329 | Sugiyama | GOLGA3 | EVDGNDsDsSSYSSASTRGTyGILSKTVGTQDTPYMVNGQE |
| Q08881 | Y512 | SIGNOR|ELM|iPTMNet|EPSD|PSP | ITK EMT LYK | ENQVIKVSDFGMTRFVLDDQytssTGtKFPVKWAsPEVFSF |
| Q08J23 | Y51 | Sugiyama | NSUN2 SAKI TRM4 | EAGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALR |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q12792 | Y309 | Sugiyama | TWF1 PTK9 | MDVIRKIEIDNGDELtADFLyEEVHPKQHAHKQSFAKPKGP |
| Q12904 | Y288 | Sugiyama | AIMP1 EMAP2 SCYE1 | KKIWEQIQPDLHtNDECVAtyKGVPFEVKGKGVCRAQTMSN |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q12996 | Y708 | Sugiyama | CSTF3 | NEDsDEDEEKGAVVPPVHDIyRARQQKRIR___________ |
| Q13017 | Y1109 | Sugiyama | ARHGAP5 RHOGAP5 | DNyAEPIDTIFKQKGYsDEIyVVPDDsQNRIKIRNsFVNNt |
| Q13069 | Y10 | Sugiyama | GAGE5 | ___________MSWRGRsTyyWPRPRRYVQPPEVIGPMRPE |
| Q13069 | Y9 | Sugiyama | GAGE5 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13070 | Y10 | Sugiyama | GAGE6 | ___________MSWRGRsTyyWPRPRRYVQPPEVIGPMRPE |
| Q13070 | Y9 | Sugiyama | GAGE6 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13094 | Y113 | ELM|iPTMNet|EPSD|PSP | LCP2 | EETESHEEDNGGWSSFEEDDyESPNDDQDGEDDGDyEsPNE |
| Q13094 | Y128 | ELM|iPTMNet|EPSD|PSP | LCP2 | FEEDDyESPNDDQDGEDDGDyEsPNEEEEAPVEDDADyEPP |
| Q13094 | Y145 | EPSD|PSP | LCP2 | DGDyEsPNEEEEAPVEDDADyEPPPSNDEEALQNSILPAKP |
| Q13094 | Y423 | SIGNOR|iPTMNet|EPSD | LCP2 | PNKPRPPsPAEEENsLNEEWyVSyITRPEAEAALRKINQDG |
| Q13094 | Y426 | SIGNOR|iPTMNet|EPSD | LCP2 | PRPPsPAEEENsLNEEWyVSyITRPEAEAALRKINQDGTFL |
| Q13151 | Y180 | Sugiyama | HNRNPA0 HNRPA0 | FHPIQGHRVEVKKAVPKEDIySGGGGGGsRSSRGGRGGRGR |
| Q13162 | Y188 | Sugiyama | PRDX4 | GLGPIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDK |
| Q13162 | Y191 | Sugiyama | PRDX4 | PIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDKGIL |
| Q13162 | Y54 | Sugiyama | PRDX4 | AVQGWETEERPRTREEECHFyAGGQVyPGEAsRVsVADHsL |
| Q13228 | Y28 | Sugiyama | SELENBP1 SBP | CGPGySTPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVD |
| Q13242 | Y17 | Sugiyama | SRSF9 SFRS9 SRP30C | ____MsGWADERGGEGDGRIyVGNLPTDVREKDLEDLFyKY |
| Q13242 | Y70 | Sugiyama | SRSF9 SFRS9 SRP30C | GLVPFAFVRFEDPRDAEDAIyGRNGyDYGQCRLRVEFPRTY |
| Q13263 | T514 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | DLDLtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQP |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13263 | Y517 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | LtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQPGtA |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13283 | Y56 | EPSD|PSP|Sugiyama | G3BP1 G3BP | KNssyVHGGLDsNGKPADAVyGQKEIHRKVMsQNFtNCHTK |
| Q13291 | Y307 | ELM|iPTMNet|EPSD|PSP | SLAMF1 SLAM | PGPLQKKLDSFPAQDPCTTIyVAATEPVPESVQETNSITVy |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13310 | Y238 | Sugiyama | PABPC4 APP1 PABP4 | LSVKVMRDPNGKSKGFGFVSyEKHEDANKAVEEMNGKEISG |
| 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 |
| Q13442 | Y70 | Sugiyama | PDAP1 HASPP28 | DPKKEKKsLDsDEsEDEEDDyQQKRKGVEGLIDIENPNRVA |
| Q13444 | Y715 | GPS6|SIGNOR|EPSD|PSP | ADAM15 MDC15 | TTGLLLSLLVLLVLVMLGASyWYRARLHQRLCQLKGPTCQy |
| Q13444 | Y735 | GPS6|SIGNOR | ADAM15 MDC15 | yWYRARLHQRLCQLKGPTCQyRAAQSGPSERPGPPQRALLA |
| Q13510 | Y305 | Sugiyama | ASAH1 ASAH HSD-33 HSD33 | GNQSGEGCVITRDRKESLDVyELDAKQGRWYVVQTNYDRWK |
| Q13546 | Y387 | Sugiyama | RIPK1 RIP RIP1 | QEENEPSLQSKLQDEANyHLyGsRMDRQTKQQPRQNVAYNR |
| Q13561 | T79 | Sugiyama | DCTN2 DCTN50 | DKRVGTKGLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETP |
| Q13561 | Y313 | Sugiyama | DCTN2 DCTN50 | IAKHKASVEDADTQSKVHQLyEtIQRWsPIASTLPELVQRL |
| Q13561 | Y6 | Sugiyama | DCTN2 DCTN50 | _______________MADPKyADLPGIARNEPDVYETSDLP |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13573 | Y430 | Sugiyama | SNW1 SKIIP SKIP | RLFNQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRP |
| Q13573 | Y433 | Sugiyama | SNW1 SKIIP SKIP | NQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRPSKN |
| Q13596 | Y162 | Sugiyama | SNX1 | QFDLTVGITDPEKIGDGMNAyVAyKVTTQTsLPLFRSKQFA |
| Q13601 | Y287 | Sugiyama | KRR1 HRB2 | tPFPPPQPESQIDKELAsGEyFLKANQKKRQKMEAIKAKQA |
| Q13642 | Y117 | Sugiyama | FHL1 SLIM1 | DsPKCKGCFKAIVAGDQNVEyKGtVWHKDCFTCSNCKQVIG |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q13813 | Y1176 | GPS6|ELM|iPTMNet|EPSD | SPTAN1 NEAS SPTA2 | DLESEGLMAEEVQAVQQQEVyGMMPRDEtDsKTAsPWKSAR |
| Q13907 | Y173 | Sugiyama | IDI1 | LLVRKNVTLNPDPNEIKSYCyVSKEELKELLKKAASGEIKI |
| Q14126 | Y968 | Sugiyama | DSG2 CDHF5 | PTTVILGPSQPQSLIVTERVyAPAstLVDQPyANEGtVVVT |
| Q14157 | Y858 | Sugiyama | UBAP2L KIAA0144 NICE4 | PFPtPttPLtGRDGsLAsNPysGDLtKFGRGDASSPAPATT |
| Q14240 | Y49 | Sugiyama | EIF4A2 DDX2B EIF4F | NEIVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIK |
| Q14240 | Y51 | Sugiyama | EIF4A2 DDX2B EIF4F | IVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIKGy |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | Y141 | Sugiyama | CTTN EMS1 | FGGKFGVQMDRVDQsAVGFEyQGKtEKHAsQKDyssGFGGK |
| Q14247 | Y215 | Sugiyama | CTTN EMS1 | FGGKyGIDKDKVDKsAVGFEyQGKtEKHESQKDyVKGFGGK |
| Q14247 | Y334 | Sugiyama | CTTN EMS1 | KDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRANF |
| Q14247 | Y421 | Sugiyama | CTTN EMS1 | tPPVsPAPQPtEERLPssPVyEDAAsFKAELsyRGPVsGtE |
| Q14247 | Y446 | Sugiyama | CTTN EMS1 | sFKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYAT |
| 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 |
| Q14289 | Y579 | GPS6 | PTK2B FAK2 PYK2 RAFTK | SPECVKLGDFGLsRYIEDEDyyKASVTRLPIKWMSPESINF |
| Q14289 | Y580 | GPS6 | PTK2B FAK2 PYK2 RAFTK | PECVKLGDFGLsRYIEDEDyyKASVTRLPIKWMSPESINFR |
| Q14566 | Y111 | Sugiyama | MCM6 | CRALKTFVKDRKEIPLAKDFyVAFQDLPTRHKIRELTSSRI |
| Q14566 | Y276 | Sugiyama | MCM6 | KLSTPGARAEtNsRVsGVDGyEtEGIRGLRALGVRDLSYRL |
| Q14566 | Y810 | Sugiyama | MCM6 | LTQAGLKGstEGsEsYEEDPyLVVNPNyLLED_________ |
| Q14568 | Y160 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGERM |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14671 | Y83 | Sugiyama | PUM1 KIAA0099 PUMH1 | SPVPGSIGVAGRsQDDAMVDyFFQRQHGEQLGGGGsGGGGy |
| Q14677 | Y106 | Sugiyama | CLINT1 ENTH EPN4 EPNR KIAA0171 | LAYLIRNGSERVVTSAREHIyDLRSLENyHFVDEHGKDQGI |
| Q14692 | Y780 | Sugiyama | BMS1 BMS1L KIAA0187 | TGKWEDDKDAAKVLAEDEELyGDFEDLETGDVHKGKSGPNT |
| Q14697 | Y489 | Sugiyama | GANAB G2AN KIAA0088 | PHIKVDSGyRVHEELRNLGLyVKtRDGSDyEGWCWPGSAGY |
| Q14738 | Y580 | Sugiyama | PPP2R5D | KDIKKEKVLLRRKsELPQDVyTIKALEAHKRAEEFLTAsQE |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q15024 | Y13 | Sugiyama | EXOSC7 KIAA0116 RRP42 | ________MASVTLSEAEKVyIVHGVQEDLRVDGRGCEDYR |
| Q15024 | Y187 | Sugiyama | EXOSC7 KIAA0116 RRP42 | RVRVLEDEEGsKDIELSDDPyDCIRLSVENVPCIVTLCKIG |
| Q15056 | T100 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | KFKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRK |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15056 | Y86 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | sIRsVRLVRDKDTDKFKGFCyVEFDEVDsLKEALtyDGALL |
| Q15149 | Y3362 | Sugiyama | PLEC PLEC1 | TGLsLLPLSEKAARARQEELySELQAREtFEKTPVEVPVGG |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15293 | T144 | Sugiyama | RCN1 RCN | WKDYDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtF |
| Q15293 | Y145 | Sugiyama | RCN1 RCN | KDYDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFK |
| Q15293 | Y147 | Sugiyama | RCN1 RCN | YDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKM |
| Q15293 | Y148 | Sugiyama | RCN1 RCN | DRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKML |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15417 | Y261 | Sugiyama | CNN3 | STISLQMGTNKVAsQKGMsVyGLGRQVYDPKYCAAPTEPVI |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15436 | Y678 | Sugiyama | SEC23A | IYHGETIAQWRKSGYQDMPEyENFRHLLQAPVDDAQEILHS |
| Q15459 | S451 | Sugiyama | SF3A1 SAP114 | IGLLDPRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAE |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15631 | Y210 | Sugiyama | TSN | sLRKRYDGLKYDVKKVEEVVyDLSIRGFNKETAAACVEK__ |
| Q15637 | Y87 | Sugiyama | SF1 ZFM1 ZNF162 | tGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFRTRKKLEE |
| Q15785 | Y32 | Sugiyama | TOMM34 URCC3 | LRAAGNESFRNGQyAEASALyGRALRVLQAQGssDPEEEsV |
| Q15785 | Y54 | Sugiyama | TOMM34 URCC3 | RALRVLQAQGssDPEEEsVLysNRAACHLKDGNCRDCIKDC |
| Q15907 | Y173 | Sugiyama | RAB11B YPT3 | TSALDSTNVEEAFKNILTEIyRIVSQKQIADRAAHDESPGN |
| Q16539 | Y323 | SIGNOR|EPSD|PSP | MAPK14 CSBP CSBP1 CSBP2 CSPB1 MXI2 SAPK2A | LAHAYFAQYHDPDDEPVADPyDQsFESRDLLIDEWKSLTYD |
| Q16595 | T93 | Sugiyama | FXN FRDA X25 | VYLMNLRKsGtLGHPGsLDEttyERLAEETLDSLAEFFEDL |
| Q16658 | Y493 | Sugiyama | FSCN1 FAN1 HSN SNL | DHAGVLKASAEtVDPAsLWEy____________________ |
| Q16719 | S443 | Sugiyama | KYNU | VVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAET |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16740 | Y209 | Sugiyama | CLPP | TDIAIQAEEIMKLKKQLYNIyAKHTKQSLQVIEsAMERDRY |
| Q16762 | Y165 | Sugiyama | TST | PSRPEPAVFKATLDRSLLKTyEQVLENLESKRFQLVDSRSQ |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q16851 | Y89 | Sugiyama | UGP2 UGP1 | KGPSVDWGKIQRPPEDSIQPyEKIKARGLPDNISsVLNKLV |
| Q16881 | Y281 | Sugiyama | TXNRD1 GRIM12 KDRF | SLNWGYRVALREKKVVyENAyGQFIGPHRIKATNNKGKEKI |
| Q1KMD3 | Y610 | Sugiyama | HNRNPUL2 HNRPUL2 | LEMKANFsLPEKCDYMDEVTyGELEKEEAQPIVTKYKEEAR |
| Q32MZ4 | Y597 | Sugiyama | LRRFIP1 GCF2 TRIP | KKKKsPVPVETLKDVKKELtyQNTDLsEIKEEEQVKstDRK |
| Q495A1 | Y225 | PSP | TIGIT VSIG9 VSTM3 | AAPAGLCGEQRGEDCAELHDyFNVLSYRSLGNCSFFTETG_ |
| Q4VXU2 | Y291 | Sugiyama | PABPC1L C20orf119 | ERQNELKRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLR |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q53GQ0 | Y115 | Sugiyama | HSD17B12 SDR12C1 | KEKFKVETRTIAVDFASEDIyDKIKTGLAGLEIGILVNNVG |
| Q53H82 | Y99 | Sugiyama | LACTB2 CGI-83 | HRDHSGGIGDICKSINNDtTyCIKKLPRNPQREEIIGNGEQ |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | S60 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | FKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDDFR |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | S34 | Sugiyama | HSP90AB4P | IFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDIIPN |
| Q58FF6 | Y167 | Sugiyama | HSP90AB4P | GEPIDRDTKVILHLKEDQtEyLEERWVKEVVKKHPQFIGCL |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | S58 | Sugiyama | HSP90AB3P HSP90BC | IFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPN |
| Q58FF7 | Y171 | Sugiyama | HSP90AB3P HSP90BC | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| Q58FF7 | Y492 | Sugiyama | HSP90AB3P HSP90BC | TANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIMETLR |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | S58 | Sugiyama | HSP90AB2P HSP90BB | IFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPN |
| 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 |
| Q5F1R6 | Y5 | Sugiyama | DNAJC21 DNAJA5 | ________________MKCHyEALGVRRDASEEELKKAYRK |
| Q5JTH9 | Y1251 | Sugiyama | RRP12 KIAA0690 | AEYKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQG |
| Q5JTH9 | Y1253 | Sugiyama | RRP12 KIAA0690 | YKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQGQF |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5SW79 | Y364 | Sugiyama | CEP170 FAM68A KAB KIAA0470 | QMLWERTEEDsKsIKsDVPVyLKRLKGNKHDDGtQsDsENA |
| Q5T035 | Y67 | Sugiyama | FAM120A2P C9orf129 | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERSLPIN |
| Q5VTE0 | Y254 | Sugiyama | EEF1A1P5 EEF1AL3 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VUA4 | Y1569 | Sugiyama | ZNF318 HRIHFB2436 | QAKKLEKRNsCLATANAKDLyDIFySSGGKGAPETKGAPET |
| Q5VV41 | Y216 | Sugiyama | ARHGEF16 EPHEXIN4 NBR | KKTLGRKRGHKGsFKDDPQLyQEIQERGLNtsQEsDDDILD |
| Q66LE6 | T82 | Sugiyama | PPP2R2D KIAA1541 | QREQENKSRPHSRGEyNVystFQsHEPEFDyLKSLEIEEKI |
| 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 |
| Q6L8Q7 | Y235 | Sugiyama | PDE12 | sLsPssPsssWtEtDVEERVytPSNADIGLRLKLHCTPGDG |
| Q6P2Q9 | Y871 | Sugiyama | PRPF8 PRPC8 | SVKSRLNQsQREELGLIEQAyDNPHEALSRIKRHLLTQRAF |
| Q6PIW4 | Y663 | Sugiyama | FIGNL1 | DFENAFRTVRPSVSPKDLELyENWNKTFGCGK_________ |
| Q6PKG0 | Y633 | Sugiyama | LARP1 KIAA0731 LARP | MEQMDGRKNtFtAWsDEEsDyEIDDRDVNKILIVtQtPHyM |
| Q6QNY0 | Y40 | Sugiyama | BLOC1S3 BLOS3 | GEAtEtDsERsAsssEEEELyLGPSGPTRGRPTGLRVAGEA |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y791 | Sugiyama | POTEE A26C1A POTE2 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6UN15 | Y454 | Sugiyama | FIP1L1 FIP1 RHE | LPGSAPsWPSLVDTSKQWDyyARREKDRDRERDRDRERDRD |
| Q71U36 | Y312 | Sugiyama | TUBA1A TUBA3 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q71U36 | Y319 | Sugiyama | TUBA1A TUBA3 | ANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAIAtIKtKR |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q71U36 | Y451 | Sugiyama | TUBA1A TUBA3 | DyEEVGVDsVEGEGEEEGEEy____________________ |
| Q7KZF4 | Y109 | Sugiyama | SND1 TDRD11 | KLIGKEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVA |
| Q7KZF4 | Y113 | Sugiyama | SND1 TDRD11 | KEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVAEGLA |
| Q7KZF4 | Y476 | Sugiyama | SND1 TDRD11 | SKGLATVIRYRQDDDQRssHyDELLAAEARAIKNGKGLHSK |
| Q7KZF4 | Y728 | Sugiyama | SND1 TDRD11 | EKLMENMRNDIAsHPPVEGsyAPRRGEFCIAKFVDGEWYRA |
| Q7RTV0 | Y100 | Sugiyama | PHF5A | KDRDGCPKIVNLGSsKTDLFyERKKYGFKKR__________ |
| Q7RTV0 | Y51 | Sugiyama | PHF5A | VICDSyVRPCTLVRICDECNyGsyQGRCVICGGPGVSDAyy |
| Q7Z2W4 | Y642 | Sugiyama | ZC3HAV1 ZC3HDC2 PRO1677 | GEEKDKRKNsNVDssyLEsLyQSCPRGVVPFQAGSRNYELS |
| Q7Z6A9 | Y226 | PSP | BTLA | EQTEASTRQNSQVLLSETGIyDNDPDLCFRMQEGSEVySNP |
| Q7Z6A9 | Y243 | PSP | BTLA | TGIyDNDPDLCFRMQEGSEVySNPCLEENKPGIVyASLNHS |
| Q7Z6A9 | Y257 | PSP | BTLA | QEGSEVySNPCLEENKPGIVyASLNHSVIGPNSRLARNVKE |
| Q7Z6A9 | Y282 | PSP | BTLA | HSVIGPNSRLARNVKEAPTEyASICVRS_____________ |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86UK7 | Y306 | Sugiyama | ZNF598 | QFSYAPRHSRRNEGVVGGEDyEEVDRysRQGRVARAGTRGA |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q8IV50 | T210 | Sugiyama | LYSMD2 | STQAAKKLKEESRDEEsPyAtSLyHs_______________ |
| Q8IVM0 | Y217 | SIGNOR|EPSD|PSP | CCDC50 C3orf6 | AQVAQDEEIARLLMAEEKKAyKKAKEREKSSLDKRKQDPEW |
| Q8IVM0 | Y279 | SIGNOR|EPSD|PSP | CCDC50 C3orf6 | KNERPARPPPPIMtDGEDADytHFTNQQssTRHFSKSESSH |
| Q8IVM0 | Y304 | SIGNOR|EPSD|PSP | CCDC50 C3orf6 | NQQssTRHFSKSESSHKGFHyKH__________________ |
| Q8IWV1 | Y193 | SIGNOR|PSP | LAX1 LAX | CINVRASRDCASISSEDSHDyVNVPTAEEIAETLASTKSPS |
| Q8IWV1 | Y268 | SIGNOR|PSP | LAX1 LAX | GAEDSDSLSNGEGSSQISNDyVNMTGLDLSAIQERQLWVAF |
| Q8IWV1 | Y294 | SIGNOR|PSP | LAX1 LAX | LDLSAIQERQLWVAFQCCRDyENVPAADPSGSQQQAEKDVP |
| Q8IWV1 | Y373 | SIGNOR|PSP | LAX1 LAX | QSEDSQMKHREEMSNEDSSDyENVLTAKLGGRDSEQGPGTQ |
| Q8IWX8 | Y894 | Sugiyama | CHERP DAN26 SCAF6 | GDVRDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDE |
| Q8IWX8 | Y897 | Sugiyama | CHERP DAN26 SCAF6 | RDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDECK_ |
| Q8IZP0 | S22 | Sugiyama | ABI1 SSH3BP1 | AELQMLLEEEIPSGKRALIEsyQNLTRVADyCENNyIQATD |
| Q8N0Y7 | S134 | Sugiyama | PGAM4 PGAM3 | IWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYE |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N1G4 | Y257 | Sugiyama | LRRC47 KIAA1185 | LRDKRLEKMVSGCQTRSILEyLRVGGRGGGKGKGRAEGSEK |
| Q8N1K5 | Y174 | PSP | THEMIS C6orf190 C6orf207 | VARNHQTHSFNLPLSQEGEFyECEDERIYTLKEIVEWKIPK |
| Q8N1K5 | Y353 | PSP | THEMIS C6orf190 C6orf207 | LIPTSYKGKFKRRPREFPTAyDLEIAKSEKEPLHVVATKAF |
| Q8N1K5 | Y429 | PSP | THEMIS C6orf190 C6orf207 | NVLACEKILKKSYEAALLPLyMEGGFVEVIHDKKQYPISEL |
| Q8N1K5 | Y540 | EPSD|PSP | THEMIS C6orf190 C6orf207 | SRDAEPFLVRTLVEEITEEQyyMMRRYESSASHPPPRPPKH |
| Q8N1K5 | Y541 | EPSD|PSP | THEMIS C6orf190 C6orf207 | RDAEPFLVRTLVEEITEEQyyMMRRYESSASHPPPRPPKHP |
| Q8N1K5 | Y95 | PSP | THEMIS C6orf190 C6orf207 | PFELPMNFPGLFKIVADKTPyLTMEEITRTIHIGPSRLGHP |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N5M4 | Y11 | Sugiyama | TTC9C | __________MEKRLQEAQLyKEEGNQRYREGKYRDAVSRY |
| Q8N7H5 | Y169 | Sugiyama | PAF1 PD2 | EKPEVKIGVSVKQQFTEEEIyKDRDSQITAIEKTFEDAQKS |
| Q8NBF2 | Y39 | Sugiyama | NHLRC2 | TSLEYALLDAVTQQEKDSLVyQyLQKVDGWEQDLSVPEFPE |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NBS9 | Y289 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | RDGKKVDQYKGKRDLEsLREyVEsQLQRTETGATETVTPSE |
| Q8NDI1 | Y585 | Sugiyama | EHBP1 KIAA0903 NACSIN | TYKVGNYETDTNssVDQEKFyAELSDLKREPELQQPISGAV |
| Q8NFI4 | Y185 | Sugiyama | ST13P5 FAM10A5 | NAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TD19 | Y52 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PSASQGPRAGGGAAEQEELHyIPIRVLGRGAFGEAtLyRRT |
| Q8TD19 | Y845 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PDsPsPLsAAFsEsEKDTLPyEELQGLKVAsEAPLEHKPQV |
| Q8TDD1 | Y681 | Sugiyama | DDX54 | GPNRGAKRRREEARQRDQEFyIPyRPKDFDSERGLsIsGEG |
| Q8TEW0 | S720 | Sugiyama | PARD3 PAR3 PAR3A | ELPIETALDDRERRIsHsLysGIEGLDEsPsRNAALsRIMG |
| Q8WUF5 | Y132 | Sugiyama | PPP1R13L IASPP NKIP1 PPP1R13BL RAI | LsPKGRPssPRtPLyLQPDAyGsLDRATSPRPRAFDGAGss |
| Q8WVK2 | Y127 | Sugiyama | SNRNP27 | MGFASFDSTKGKKVDGsVNAyAINVsQKRKYRQYMNRKGGF |
| Q8WWM7 | Y264 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | ESDMSNGWDPNEMFKFNEENyGVKTtyDssLssytVPLEKD |
| Q8WXF1 | Y275 | Sugiyama | PSPC1 PSP1 | YHKEREQPPRFAQPGTFEFEyASRWKALDEMEKQQREQVDR |
| Q8WXX5 | Y66 | Sugiyama | DNAJC9 | RVGEGDKEDATRRFQILGKVySVLSDREQRAVYDEQGTVDE |
| Q8WYP5 | Y1790 | Sugiyama | AHCTF1 ELYS TMBS62 MSTP108 | QSVRKKTRKAKEISEASENIySDVRGLsQNQQIPQNsVtPR |
| Q92522 | Y48 | Sugiyama | H1-10 H1FX | AALsPsKKRKNSKKKNQPGKySQLVVEtIRRLGERNGSSLA |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y89 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | RFHGRAFNDPFIQKEKENLsyDLVPLKNGGVGIKVMYMGEE |
| Q92620 | S220 | Sugiyama | DHX38 DDX38 KIAA0224 PRP16 | PRHRPKDAAtPSRSTWEEEDsGyGSSRRSQWEsPsPTPSYR |
| Q92626 | Y916 | Sugiyama | PXDN KIAA0230 MG50 PRG2 PXD01 VPO VPO1 | SVYPREQINQLtsyIDASNVyGsTEHEARSIRDLASHRGLL |
| Q92900 | Y958 | Sugiyama | UPF1 KIAA0221 RENT1 | ARFMTTAMyDAREAIIPGsVyDRSSQGRPSSMYFQTHDQIG |
| Q92905 | Y203 | Sugiyama | COPS5 CSN5 JAB1 | LGAFRTYPKGYKPPDEGPsEyQtIPLNKIEDFGVHCKQYYA |
| Q93052 | Y301 | Sugiyama | LPP | LQPEPGYGYAPNQGRyyEGyyAAGPGyGGRNDsDPtyGQQG |
| Q93052 | Y317 | Sugiyama | LPP | yEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPGA |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96AE4 | Y60 | Sugiyama | FUBP1 | QIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKVAP |
| Q96AY3 | T200 | Sugiyama | FKBP10 FKBP65 PSEC0056 | HYNGTLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLG |
| Q96AY3 | Y204 | Sugiyama | FKBP10 FKBP65 PSEC0056 | TLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGMCPG |
| Q96BY7 | Y2012 | Sugiyama | ATG2B C14orf103 | GVAKAYSVVKEGITDTAQTIyETAAREHESRGVTGAVGEVL |
| Q96CT7 | Y38 | Sugiyama | CCDC124 | RRAEAKAAADAKKQKELEDAyWKDDDKHVMRKEQRKEEKEK |
| Q96D46 | Y459 | Sugiyama | NMD3 CGI-07 | YQDFLEDLEEDEAIRKNVNIyRDsAIPVEsDtDDEGAPRIS |
| Q96EU6 | Y138 | Sugiyama | RRP36 C6orf153 HSPC253 | RDPRFDDLSGEYNPEVFDKtyQFLNDIRAKEKELVKKQLKK |
| Q96F86 | Y225 | Sugiyama | EDC3 LSM16 YJDC YJEFN2 PP844 | DFEGNLALFDKAAVFEEIDtyERRSGTRsRGIPNERPTRYR |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96HE7 | Y178 | Sugiyama | ERO1A ERO1L UNQ434/PRO865 | HDDSSDNFCEADDIQsPEAEyVDLLLNPERYTGYKGPDAWK |
| Q96HN2 | Y372 | Sugiyama | AHCYL2 KIAA0828 | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDMMFGG |
| Q96I99 | Y343 | Sugiyama | SUCLG2 | NGGKPANFLDLGGGVKEAQVyQAFKLLTADPKVEAILVNIF |
| Q96LC7 | Y597 | SIGNOR|ELM|iPTMNet|EPSD|PSP | SIGLEC10 SLG2 UNQ477/PRO940 | RRTQTETPRPRFSRHstILDyINVVPTAGPLAQKRNQKATP |
| Q96LC7 | Y667 | SIGNOR|ELM|iPTMNet|EPSD|PSP | SIGLEC10 SLG2 UNQ477/PRO940 | PEPKSSTQAPESQESQEELHyATLNFPGVRPRPEARMPKGT |
| Q96LC7 | Y691 | SIGNOR|ELM|iPTMNet|EPSD|PSP | SIGLEC10 SLG2 UNQ477/PRO940 | NFPGVRPRPEARMPKGTQADyAEVKFQ______________ |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q96QK1 | Y791 | Sugiyama | VPS35 MEM3 TCCCTA00141 | HNtLEHLRLRREsPEsEGPIyEGLIL_______________ |
| Q96RT6 | Y307 | Sugiyama | CTAGE1 CTAGE2 | IHAAKLNASLKTLEGERNQIyIQLSEVDKTKEELTEHIKNL |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99543 | S275 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | RAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAEK |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99614 | Y96 | Sugiyama | TTC1 TPR1 | ADKVENKsNEDVNssELDEEyLIELEKNMSDEEKQKRREES |
| Q99704 | Y174 | iPTMNet|EPSD | DOK1 | QFWVTVQRTEAAERCGLHGSyVLRVEAERLTLLTVGAQSQI |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y432 | Sugiyama | ACO2 | SQFtITPGSEQIRAtIERDGyAQILRDLGGIVLANACGPCI |
| Q99798 | Y665 | Sugiyama | ACO2 | DtARYYKKHGIRWVVIGDENyGEGSSREHAALEPRHLGGRA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| Q99848 | Y265 | Sugiyama | EBNA1BP2 EBP2 | NQKFGFGGKKKGSKWNtREsyDDVssFRAKTAHGRGLKRPG |
| Q99877 | Y43 | Sugiyama | H2BC15 H2BFD HIST1H2BN | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99879 | Y43 | Sugiyama | H2BC14 H2BFE HIST1H2BM | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99880 | Y43 | Sugiyama | H2BC13 H2BFC HIST1H2BL | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q9BPW8 | Y148 | Sugiyama | NIPSNAP1 | FSGGYPALMDCMNKLKNNKEyLEFRRERSQMLLSRRNQLLL |
| Q9BPX3 | Y929 | Sugiyama | NCAPG CAPG NYMEL3 | QDATLTTTTFQNEDEKNKEVyMtPLRGVKATQASKSTQLKT |
| Q9BQE3 | Y312 | Sugiyama | TUBA1C TUBA6 | TNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q9BQE3 | Y319 | Sugiyama | TUBA1C TUBA6 | ANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAIAtIKtKR |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BSU3 | Y145 | Sugiyama | NAA11 ARD1B ARD2 | TLNFQISEVEPKyyADGEDAyAMKRDLSQMADELRRQMDLK |
| Q9BUJ2 | Y111 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | GYSGPDGHYAMDNITRQNQFyDtQVIKQENESGyERRPLEM |
| Q9BUJ2 | Y510 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | RLIQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIV |
| Q9BW91 | Y140 | Sugiyama | NUDT9 NUDT10 PSEC0099 UNQ3012/PRO9771 | FsPKFNEKDGHVERKSKNGLyEIENGRPRNPAGRTGLVGRG |
| Q9BWF3 | Y194 | Sugiyama | RBM4 RBM4A | ECPIDRSGRVADLTEQYNEQyGAVRTPYTMSYGDSLYYNNA |
| Q9BWW4 | Y23 | SIGNOR|EPSD|PSP | SSBP3 SSDP SSDP1 | AKGKGSAVPSDGQAREKLALyVyEYLLHVGAQKSAQTFLSE |
| Q9BWW4 | Y25 | SIGNOR|EPSD|PSP | SSBP3 SSDP SSDP1 | GKGSAVPSDGQAREKLALyVyEYLLHVGAQKSAQTFLSEIR |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BYX7 | Y91 | Sugiyama | POTEKP ACTBL3 FKSG30 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q9BZS1 | Y342 | SIGNOR|EPSD|PSP | FOXP3 IPEX JM2 | PEFLHNMDYFKFHNMRPPFTyATLIRWAILEAPEKQRTLNE |
| Q9C0C2 | Y202 | Sugiyama | TNKS1BP1 KIAA1741 TAB182 | LWGSRLTFNHDGssRYGPRTyGtTTAPRDEDGstLFRGWsQ |
| Q9GZL7 | Y380 | Sugiyama | WDR12 | SGSLDNIVKLWDTRSCKAPLyDLAAHEDKVLSVDWTDTGLL |
| Q9H0B6 | S436 | Sugiyama | KLC2 | EEREESKDKRRDsAPyGEyGsWYKACKVDsPtVNTTLRSLG |
| Q9H0B6 | Y434 | Sugiyama | KLC2 | HAEEREESKDKRRDsAPyGEyGsWYKACKVDsPtVNTTLRS |
| Q9H0D6 | Y666 | Sugiyama | XRN2 | GVALLPFVDERRLRAALEEVyPDLTPEEtRRNsLGGDVLFV |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H204 | Y64 | SIGNOR|iPTMNet|EPSD|PSP | MED28 EG1 FKSG20 | LVDELESSFEACFASLVSQDyVNGTDQEEIRTGVDQCIQKF |
| Q9H2H8 | Y75 | Sugiyama | PPIL3 | DPTGTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPN |
| Q9H2H8 | Y78 | Sugiyama | PPIL3 | GTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPNTNG |
| Q9H4A3 | Y2102 | Sugiyama | WNK1 HSN2 KDP KIAA0344 PRKWNK1 | KHLKEIQDLQSRQKHEIEsLyTKLGKVPPAVIIPPAAPLsG |
| Q9H4E7 | Y133 | SIGNOR | DEF6 IBP | LSNQDAFRLWCLFNFLSEDKyPLIMVPDEVEyLLKKVLSSM |
| Q9H4E7 | Y144 | SIGNOR | DEF6 IBP | LFNFLSEDKyPLIMVPDEVEyLLKKVLSSMSLEVSLGELEE |
| Q9H4E7 | Y210 | SIGNOR|iPTMNet|EPSD | DEF6 IBP | SGRCLRGVGRDTLSMAIHEVyQELIQDVLKQGyLWKRGHLR |
| Q9H501 | S75 | Sugiyama | ESF1 ABTAP C20orf6 HDCMC28P | KRGRPISHSTTEDLKRFyDLsDsDsNLsGEDSKALSQKKIK |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9H814 | Y152 | Sugiyama | PHAX RNUXA | TELGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDLD |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HC35 | Y552 | Sugiyama | EML4 C2orf2 EMAPL4 | KIILWDHDLNPEREIEVPDQyGtIRAVAEGKADQFLVGTSR |
| Q9HCN8 | Y81 | Sugiyama | SDF2L1 UNQ1941/PRO4424 | GSGSGQQSVtGVEAsDDANSyWRIRGGSEGGCPRGSPVRCG |
| Q9NP31 | Y260 | EPSD|PSP | SH2D2A SCAP TSAD VRAP | SQLLRPKPPIPAKPQLPPEVyTIPVPRHRPAPRPKPSNPIy |
| Q9NP31 | Y280 | SIGNOR|EPSD|PSP | SH2D2A SCAP TSAD VRAP | yTIPVPRHRPAPRPKPSNPIyNEPDEPIAFyAMGRGsPGEA |
| Q9NP31 | Y290 | SIGNOR|EPSD|PSP | SH2D2A SCAP TSAD VRAP | APRPKPSNPIyNEPDEPIAFyAMGRGsPGEAPSNIyVEVED |
| Q9NP31 | Y305 | SIGNOR|EPSD|PSP | SH2D2A SCAP TSAD VRAP | EPIAFyAMGRGsPGEAPSNIyVEVEDEGLPATLGHPVLRKS |
| Q9NPD3 | Y53 | Sugiyama | EXOSC4 RRP41 SKI6 | AQADGSAYIEQGNTKALAVVyGPHEIRGsRARALPDRALVN |
| Q9NRX4 | Y52 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | RSGAPAAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCE |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NSE4 | Y260 | Sugiyama | IARS2 | YKPVFWSPSSRTALAEAELEyNPEHVSRSIYVKFPLLKPSP |
| Q9NSE4 | Y97 | Sugiyama | IARS2 | GRQQPDtELEIQQKCGFSELysWQRERKVKTEFCLHDGPPY |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NX18 | Y105 | Sugiyama | SDHAF2 C11orf79 PGL2 SDH5 | LLSLFAKEHLQHMTEKQLNLyDRLINEPSNDWDIYYWATEA |
| Q9NX40 | Y199 | Sugiyama | OCIAD1 ASRIJ OCIA | HIVQGPDPNLEEsPKRKNITyEELRNKNREsyEVSLTQKTD |
| Q9NYF8 | Y219 | Sugiyama | BCLAF1 BTF KIAA0164 | IDEFNKssAtsGDIWPGLsAyDNsPRsPHsPsPIAtPPSQS |
| Q9NYU2 | Y1516 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | PMTKEPKLEAAVRIVPEWQDyDQEIKQLQIRFQKEKETGAL |
| Q9NZB2 | Y418 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERssPIN |
| Q9P031 | Y97 | Sugiyama | CCDC59 BR22 TAP26 HSPC128 | AQTSLESQFtDRYPDNLKHLyLAEEERHRKQARKVDHPLSE |
| Q9P0U3 | Y270 | PSP | SENP1 | TSSSGSASILTNQEQLSHSVySLSSYTPDVAFGSKDSGTLH |
| Q9P270 | Y293 | Sugiyama | SLAIN2 KIAA1458 | NDVTDVQILARMQEESLRQEyAATTSRRSSGSSCNSTRRGt |
| Q9UBB9 | Y51 | Sugiyama | TFIP11 STIP HSPC006 | LQNEFNPNRQRHWQTKEEAtyGVWAERDsDDERPSFGGKRA |
| Q9UBQ5 | Y42 | Sugiyama | EIF3K EIF3S12 ARG134 HSPC029 MSTP001 PTD001 | NPENLAtLERYVETQAKENAyDLEANLAVLKLYQFNPAFFQ |
| 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 |
| Q9UBT2 | Y159 | Sugiyama | UBA2 SAE2 UBLE1B HRIHFB2115 | SGTAGYLGQVTTIKKGVtECyECHPKPTQRTFPGCtIRNTP |
| Q9UDY4 | Y172 | Sugiyama | DNAJB4 DNAJW HLJ1 | SRLKQDPPVIHELRVsLEEIySGCTKRMKISRKRLNADGRS |
| Q9UGI8 | Y251 | Sugiyama | TES | RTQYSCYCCKLSMKEGDPAIyAERAGyDKLWHPACFVCSTC |
| Q9UGK3 | Y250 | PSP | STAP2 BKS | VNYFVSHTKKALVPFLLDEDyEKVLGYVEADKENGENVWVA |
| Q9UHD2 | Y354 | SIGNOR|EPSD|PSP | TBK1 NAK | IFHELVyKQTKIISsNQELIyEGRRLVLEPGRLAQHFPKTT |
| Q9UHD2 | Y394 | SIGNOR|EPSD|PSP | TBK1 NAK | TEENPIFVVsREPLNtIGLIyEKISLPKVHPRYDLDGDAsM |
| Q9UHF1 | Y49 | Sugiyama | EGFL7 MEGF7 UNQ187/PRO1449 | RVCAVRAHGDPVSEsFVQRVyQPFLTTCDGHRACSTYRTIY |
| Q9UHI6 | Y659 | Sugiyama | DDX20 DP103 GEMIN3 | RVPVLASSsQsGDsEsDSDSySSRTSSQSKGNKsyLEGssD |
| Q9UHR4 | Y380 | Sugiyama | BAIAP2L1 IRTKS | SFAQGDVITLLIPEEKDGWLyGEHDVSKARGWFPssYTKLL |
| Q9UHX1 | Y269 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | FGKIKSCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNL |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UIA9 | Y1078 | Sugiyama | XPO7 KIAA0745 RANBP16 | FTQNLSAFRREVNDSMKNSTyGVNSNDMMS___________ |
| Q9UK59 | Y533 | Sugiyama | DBR1 | LsDEHEPEQRKKIKRRNQAIyAAVDDDDDDAA_________ |
| Q9UKK9 | Y198 | Sugiyama | NUDT5 NUDIX5 HSPC115 | LLQRLDALVAEEHLTVDARVySyALALKHANAKPFEVPFLK |
| Q9UKS6 | Y206 | Sugiyama | PACSIN3 | RKLQERVERCAKEAEKTKAQyEQtLAELHRYTPRYMEDMEQ |
| Q9UKY7 | Y244 | Sugiyama | CDV3 H41 | NRGRDEVSKNQALKLQLDNQyAVLENQKSSHSQYN______ |
| Q9UMS0 | Y194 | Sugiyama | NFU1 HIRIP5 CGI-33 | KELLDTRIRPTVQEDGGDVIyKGFEDGIVQLKLQGSCTSCP |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UN19 | Y139 | SIGNOR|ELM|iPTMNet|EPSD|PSP | DAPP1 BAM32 HSPC066 | tGtLMVLKHPYPRKVEEPsIyEsVRVHTAMQTGRTEDDLVP |
| Q9UN86 | T21 | Sugiyama | G3BP2 KIAA0660 | MVMEKPsPLLVGREFVRQyytLLNKAPEYLHRFYGRNSSYV |
| Q9UN86 | Y20 | Sugiyama | G3BP2 KIAA0660 | _MVMEKPsPLLVGREFVRQyytLLNKAPEYLHRFYGRNSSY |
| Q9UNF0 | Y267 | Sugiyama | PACSIN2 | VLLEVQKHLDLSNVAGYKAIyHDLEQsIRAADAVEDLRWFR |
| Q9UNH7 | Y220 | Sugiyama | SNX6 | VSGVKDVDDFFEHERTFLLEyHNRVKDASAKSDRMTRSHKS |
| Q9UNZ2 | Y167 | Sugiyama | NSFL1C UBXN2C | PRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLKLW |
| Q9UQ35 | Y2693 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | RRSRSPRKPIDsLRDsRsLsysPVERRRPsPQPsPRDQQSS |
| Q9UQ80 | Y343 | Sugiyama | PA2G4 EBP1 | VLLMPNGPMRITsGPFEPDLyKsEMEVQDAELKALLQssAs |
| Q9UQQ2 | Y273 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | SH2B3 LNK | ACSSIQEVRWCTRLEMPDNLyTFVLKVKDRTDIIFEVGDEQ |
| Q9Y230 | Y172 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | TGTGSKVGKLTLKTTEMETIyDLGTKMIESLTKDKVQAGDV |
| Q9Y262 | S416 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | DKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNYH |
| Q9Y262 | Y247 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | VLNVLHSLVDKSNINRQLEVytsGGDPEsVAGEyGRHSLYK |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y262 | Y415 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | GDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNY |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2B0 | Y92 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | ARsEAHLtELLEEICDRMKEyGEQIDPstHRKNYVRVVGRN |
| Q9Y2T3 | Y441 | Sugiyama | GDA KIAA1258 | SEAVIQKFLyLGDDRNIEEVyVGGKQVVPFSSsV_______ |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2U5 | Y250 | Sugiyama | MAP3K2 MAPKKK2 MEKK2 | PKSRMPRAQsyPDNHQEFSDyDNPIFEKFGKGGTYPRRYHV |
| Q9Y2W1 | T230 | Sugiyama | THRAP3 BCLAF2 TRAP150 | tsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERsPA |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y371 | Y80 | Sugiyama | SH3GLB1 KIAA0491 CGI-61 | MKQTEVLLQPNPNARIEEFVyEKLDRKAPSRINNPELLGQY |
| Q9Y3C1 | Y118 | Sugiyama | NOP16 CGI-117 HSPC111 | EAEASLPEKKGNTLSRDLIDyVRYMVENHGEDYKAMARDEK |
| Q9Y3D8 | Y31 | Sugiyama | AK6 CINAP AD-004 CGI-137 | TPGVGKTTLGKELASKSGLKyINVGDLAREEQLYDGYDEEY |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3P9 | Y472 | Sugiyama | RABGAP1 HSPC094 | FFLKLKQIKQRERKNNTDTLyEVVCLESESERERRKTTAsP |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y446 | T178 | Sugiyama | PKP3 | PtRPVsFHERGGVGsRADyDtLsLRsLRLGPGGLDDRysLV |
| Q9Y446 | Y176 | Sugiyama | PKP3 | PMPtRPVsFHERGGVGsRADyDtLsLRsLRLGPGGLDDRys |
| Q9Y490 | Y1893 | Sugiyama | TLN1 KIAA1027 TLN | TKsNtsPEELGPLANQLTsDyGRLAsEAKPAAVAAENEEIG |
| Q9Y4L1 | Y116 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | TLRYFQHLLGKQADNPHVALyQARFPEHELTFDPQRQTVHF |
| Q9Y5Q8 | Y393 | Sugiyama | GTF3C5 CDABP0017 | SGtsGARKPASSKYKLKDSVyIFREGALPPYRQMFYQLCDL |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y608 | Y398 | Sugiyama | LRRFIP2 | KYKKAMVSNAQLDNEKNNLIyQVDTLKDVIEEQEEQMAEFY |
| 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 |
|---|---|---|---|---|---|
| mRNA Splicing - Major Pathway | R-HSA-72163 | 0.000030 | 4.525 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 0.000047 | 4.330 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 0.000114 | 3.942 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 0.000260 | 3.585 | 1 | 0 |
| Immune System | R-HSA-168256 | 0.000255 | 3.593 | 1 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 0.000308 | 3.512 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 0.000435 | 3.362 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 0.000552 | 3.258 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 0.000668 | 3.175 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 0.000944 | 3.025 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 0.001115 | 2.953 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 0.001090 | 2.963 | 1 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 0.000987 | 3.006 | 1 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 0.001195 | 2.923 | 0 | 0 |
| TRKA activation by NGF | R-HSA-187042 | 0.001465 | 2.834 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 0.001421 | 2.847 | 1 | 1 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 0.001385 | 2.859 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 0.001679 | 2.775 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 0.001699 | 2.770 | 1 | 0 |
| TGFBR1 KD Mutants in Cancer | R-HSA-3656532 | 0.002094 | 2.679 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 0.002245 | 2.649 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 0.001961 | 2.708 | 1 | 1 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 0.002245 | 2.649 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 0.002537 | 2.596 | 1 | 0 |
| Loss of Function of TGFBR1 in Cancer | R-HSA-3656534 | 0.002829 | 2.548 | 0 | 0 |
| SMAD2/3 Phosphorylation Motif Mutants in Cancer | R-HSA-3304356 | 0.002829 | 2.548 | 0 | 0 |
| Regulation of MITF-M dependent genes involved in invasion | R-HSA-9854909 | 0.002829 | 2.548 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 0.003054 | 2.515 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 0.003330 | 2.478 | 0 | 0 |
| Loss of Function of SMAD2/3 in Cancer | R-HSA-3304349 | 0.003669 | 2.435 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex in Cancer | R-HSA-3304351 | 0.004610 | 2.336 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 0.004663 | 2.331 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 0.004931 | 2.307 | 0 | 0 |
| Activation of TRKA receptors | R-HSA-187015 | 0.005650 | 2.248 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 0.005650 | 2.248 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 0.005778 | 2.238 | 1 | 0 |
| Developmental Biology | R-HSA-1266738 | 0.005477 | 2.261 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 0.008019 | 2.096 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 0.007676 | 2.115 | 1 | 0 |
| Drug resistance of ALK mutants | R-HSA-9700649 | 0.010993 | 1.959 | 0 | 0 |
| ceritinib-resistant ALK mutants | R-HSA-9717323 | 0.010993 | 1.959 | 0 | 0 |
| crizotinib-resistant ALK mutants | R-HSA-9717326 | 0.010993 | 1.959 | 0 | 0 |
| lorlatinib-resistant ALK mutants | R-HSA-9717329 | 0.010993 | 1.959 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 0.010993 | 1.959 | 0 | 0 |
| NVP-TAE684-resistant ALK mutants | R-HSA-9717301 | 0.010993 | 1.959 | 0 | 0 |
| ASP-3026-resistant ALK mutants | R-HSA-9717264 | 0.010993 | 1.959 | 0 | 0 |
| alectinib-resistant ALK mutants | R-HSA-9717316 | 0.010993 | 1.959 | 0 | 0 |
| brigatinib-resistant ALK mutants | R-HSA-9717319 | 0.010993 | 1.959 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 0.009344 | 2.029 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 0.010959 | 1.960 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 0.010482 | 1.980 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 0.010029 | 1.999 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 0.008937 | 2.049 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 0.009154 | 2.038 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 0.011687 | 1.932 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 0.012972 | 1.887 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 0.013852 | 1.858 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 0.013852 | 1.858 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 0.014063 | 1.852 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 0.014873 | 1.828 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 0.015738 | 1.803 | 1 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 0.014630 | 1.835 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 0.015806 | 1.801 | 0 | 0 |
| RNA Polymerase I Transcription Initiation | R-HSA-73762 | 0.018502 | 1.733 | 0 | 0 |
| SARS-CoV-1 targets PDZ proteins in cell-cell junction | R-HSA-9692912 | 0.021866 | 1.660 | 0 | 0 |
| TGFBR2 MSI Frameshift Mutants in Cancer | R-HSA-3642279 | 0.021866 | 1.660 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 0.019118 | 1.719 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 0.021032 | 1.677 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 0.019746 | 1.705 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 0.021032 | 1.677 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 0.021559 | 1.666 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 0.022580 | 1.646 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 0.021597 | 1.666 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 0.022571 | 1.646 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 0.023331 | 1.632 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 0.023331 | 1.632 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 0.028213 | 1.550 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 0.027224 | 1.565 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 0.027285 | 1.564 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 0.028416 | 1.546 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 0.027224 | 1.565 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 0.029539 | 1.530 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5619101 | 0.032621 | 1.487 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5660686 | 0.032621 | 1.487 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 0.034053 | 1.468 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 0.030796 | 1.512 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 0.030796 | 1.512 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 0.031709 | 1.499 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 0.034347 | 1.464 | 1 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 0.034053 | 1.468 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 0.034278 | 1.465 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 0.034736 | 1.459 | 0 | 0 |
| Loss of Function of TGFBR2 in Cancer | R-HSA-3642278 | 0.043257 | 1.364 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 0.043257 | 1.364 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 0.043257 | 1.364 | 0 | 0 |
| TGFBR1 LBD Mutants in Cancer | R-HSA-3656535 | 0.043257 | 1.364 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 0.043257 | 1.364 | 0 | 0 |
| TGFBR2 Kinase Domain Mutants in Cancer | R-HSA-3645790 | 0.043257 | 1.364 | 0 | 0 |
| PLC-gamma1 signalling | R-HSA-167021 | 0.053778 | 1.269 | 0 | 0 |
| Signalling to STAT3 | R-HSA-198745 | 0.053778 | 1.269 | 0 | 0 |
| Defective ABCC2 causes DJS | R-HSA-5679001 | 0.053778 | 1.269 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 0.053778 | 1.269 | 0 | 0 |
| TLR3-mediated TICAM1-dependent programmed cell death | R-HSA-9013957 | 0.064183 | 1.193 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 0.064183 | 1.193 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 0.074475 | 1.128 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 0.074475 | 1.128 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 0.074475 | 1.128 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 0.084654 | 1.072 | 0 | 0 |
| NGF-independant TRKA activation | R-HSA-187024 | 0.084654 | 1.072 | 0 | 0 |
| Signalling to p38 via RIT and RIN | R-HSA-187706 | 0.084654 | 1.072 | 0 | 0 |
| Defective CSF2RA causes SMDP4 | R-HSA-5688890 | 0.084654 | 1.072 | 0 | 0 |
| Defective CSF2RB causes SMDP5 | R-HSA-5688849 | 0.084654 | 1.072 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 0.094721 | 1.024 | 0 | 0 |
| TRIF-mediated programmed cell death | R-HSA-2562578 | 0.104679 | 0.980 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 0.114527 | 0.941 | 0 | 0 |
| Type I hemidesmosome assembly | R-HSA-446107 | 0.114527 | 0.941 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 0.124268 | 0.906 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 0.124268 | 0.906 | 0 | 0 |
| CASP8 activity is inhibited | R-HSA-5218900 | 0.124268 | 0.906 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 0.124268 | 0.906 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 0.133903 | 0.873 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 0.133903 | 0.873 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 0.038936 | 1.410 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 0.143432 | 0.843 | 1 | 1 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | R-HSA-933543 | 0.143432 | 0.843 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 0.044067 | 1.356 | 1 | 1 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 0.152856 | 0.816 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 0.162178 | 0.790 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 0.171397 | 0.766 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 0.180516 | 0.743 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 0.180516 | 0.743 | 0 | 0 |
| TICAM1, RIP1-mediated IKK complex recruitment | R-HSA-168927 | 0.189535 | 0.722 | 0 | 0 |
| RNA Polymerase III Chain Elongation | R-HSA-73780 | 0.189535 | 0.722 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 0.069886 | 1.156 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 0.198455 | 0.702 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 0.198455 | 0.702 | 0 | 0 |
| Defective GALNT3 causes HFTC | R-HSA-5083625 | 0.198455 | 0.702 | 0 | 0 |
| Defective GALNT12 causes CRCS1 | R-HSA-5083636 | 0.198455 | 0.702 | 0 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 0.076160 | 1.118 | 0 | 0 |
| Antigen processing: Ub, ATP-independent proteasomal degradation | R-HSA-9912633 | 0.207278 | 0.683 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 0.216004 | 0.666 | 0 | 0 |
| Defective C1GALT1C1 causes TNPS | R-HSA-5083632 | 0.216004 | 0.666 | 0 | 0 |
| RNA Polymerase III Transcription Termination | R-HSA-73980 | 0.224634 | 0.649 | 0 | 0 |
| IKK complex recruitment mediated by RIP1 | R-HSA-937041 | 0.233170 | 0.632 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 0.233170 | 0.632 | 0 | 0 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | R-HSA-167242 | 0.233170 | 0.632 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 0.106361 | 0.973 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 0.249963 | 0.602 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 0.061638 | 1.210 | 0 | 0 |
| mRNA Splicing - Minor Pathway | R-HSA-72165 | 0.120661 | 0.918 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 0.120661 | 0.918 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 0.124307 | 0.906 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 0.274468 | 0.562 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE | R-HSA-77075 | 0.274468 | 0.562 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | R-HSA-167160 | 0.274468 | 0.562 | 0 | 0 |
| Termination of O-glycan biosynthesis | R-HSA-977068 | 0.274468 | 0.562 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 0.142914 | 0.845 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 0.146704 | 0.834 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 0.146704 | 0.834 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 0.154344 | 0.812 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 0.158193 | 0.801 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 0.185592 | 0.731 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 0.185592 | 0.731 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 0.197534 | 0.704 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 0.205548 | 0.687 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 0.049433 | 1.306 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 0.056858 | 1.245 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 0.036105 | 1.442 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 0.245934 | 0.609 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 0.104679 | 0.980 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 0.052200 | 1.282 | 1 | 1 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 0.113852 | 0.944 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 0.060820 | 1.216 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 0.189535 | 0.722 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 0.133903 | 0.873 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 0.258221 | 0.588 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 0.142914 | 0.845 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 0.082918 | 1.081 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 0.074475 | 1.128 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 0.114527 | 0.941 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 0.217632 | 0.662 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 0.217632 | 0.662 | 0 | 0 |
| MDK and PTN in ALK signaling | R-HSA-9851151 | 0.064183 | 1.193 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 0.125823 | 0.900 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 0.074475 | 1.128 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 0.114527 | 0.941 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 0.152856 | 0.816 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 0.171397 | 0.766 | 1 | 1 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 0.216004 | 0.666 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 0.099397 | 1.003 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 0.124307 | 0.906 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 0.243248 | 0.614 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 0.106361 | 0.973 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 0.070956 | 1.149 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 0.221675 | 0.654 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 0.143988 | 0.842 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 0.131678 | 0.880 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 0.120661 | 0.918 | 0 | 0 |
| SARS-CoV-1-mediated effects on programmed cell death | R-HSA-9692913 | 0.064183 | 1.193 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 0.180516 | 0.743 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 0.189535 | 0.722 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 0.067157 | 1.173 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 0.044067 | 1.356 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 0.044067 | 1.356 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 0.158193 | 0.801 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 0.109891 | 0.959 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 0.217632 | 0.662 | 0 | 0 |
| Caspase activation via Death Receptors in the presence of ligand | R-HSA-140534 | 0.198455 | 0.702 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 0.113452 | 0.945 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 0.052200 | 1.282 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 0.079362 | 1.100 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 0.173760 | 0.760 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 0.173760 | 0.760 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 0.173760 | 0.760 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 0.173760 | 0.760 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 0.053778 | 1.269 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 0.064183 | 1.193 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 0.064183 | 1.193 | 0 | 0 |
| TGFBR3 regulates TGF-beta signaling | R-HSA-9839389 | 0.104679 | 0.980 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 0.104679 | 0.980 | 0 | 0 |
| Regulation by c-FLIP | R-HSA-3371378 | 0.114527 | 0.941 | 0 | 0 |
| Defective RIPK1-mediated regulated necrosis | R-HSA-9693928 | 0.133903 | 0.873 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 0.038936 | 1.410 | 0 | 0 |
| Conjugation of benzoate with glycine | R-HSA-177135 | 0.143432 | 0.843 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 0.162178 | 0.790 | 0 | 0 |
| Conjugation of salicylate with glycine | R-HSA-177128 | 0.162178 | 0.790 | 0 | 0 |
| RIP-mediated NFkB activation via ZBP1 | R-HSA-1810476 | 0.189535 | 0.722 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 0.207278 | 0.683 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 0.040374 | 1.394 | 0 | 0 |
| Signaling by FGFR2 IIIa TM | R-HSA-8851708 | 0.233170 | 0.632 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 0.117042 | 0.932 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | R-HSA-76066 | 0.258221 | 0.588 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | R-HSA-76071 | 0.266389 | 0.574 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 0.150514 | 0.822 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 0.209568 | 0.679 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 0.060820 | 1.216 | 1 | 1 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 0.207278 | 0.683 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 0.055959 | 1.252 | 0 | 0 |
| Microbial modulation of RIPK1-mediated regulated necrosis | R-HSA-9686347 | 0.104679 | 0.980 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 0.207278 | 0.683 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 0.224634 | 0.649 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 0.046905 | 1.329 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 0.109891 | 0.959 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 0.241612 | 0.617 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 0.058083 | 1.236 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 0.082918 | 1.081 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 0.152856 | 0.816 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 0.207278 | 0.683 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | R-HSA-76061 | 0.266389 | 0.574 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 0.049787 | 1.303 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 0.038936 | 1.410 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 0.171397 | 0.766 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 0.171397 | 0.766 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 0.189535 | 0.722 | 0 | 0 |
| Synaptic adhesion-like molecules | R-HSA-8849932 | 0.224634 | 0.649 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 0.205364 | 0.687 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 0.211182 | 0.675 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 0.181634 | 0.741 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 0.101357 | 0.994 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 0.056344 | 1.249 | 0 | 0 |
| VLDL clearance | R-HSA-8964046 | 0.104679 | 0.980 | 0 | 0 |
| Dimerization of procaspase-8 | R-HSA-69416 | 0.114527 | 0.941 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 0.207278 | 0.683 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 0.207278 | 0.683 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 0.099397 | 1.003 | 0 | 0 |
| Amino Acid conjugation | R-HSA-156587 | 0.233170 | 0.632 | 0 | 0 |
| Conjugation of carboxylic acids | R-HSA-159424 | 0.233170 | 0.632 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 0.039680 | 1.401 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 0.254185 | 0.595 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 0.233170 | 0.632 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 0.065293 | 1.185 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 0.078839 | 1.103 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 0.249963 | 0.602 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 0.225723 | 0.646 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 0.043268 | 1.364 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 0.185592 | 0.731 | 0 | 0 |
| Diseases associated with surfactant metabolism | R-HSA-5687613 | 0.162178 | 0.790 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 0.216004 | 0.666 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 0.052941 | 1.276 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 0.173760 | 0.760 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 0.237900 | 0.624 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 0.087086 | 1.060 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 0.052208 | 1.282 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 0.237900 | 0.624 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 0.139146 | 0.857 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 0.233170 | 0.632 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 0.074475 | 1.128 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 0.124268 | 0.906 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 0.152856 | 0.816 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 0.152856 | 0.816 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 0.162178 | 0.790 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 0.041852 | 1.378 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 0.233170 | 0.632 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 0.258221 | 0.588 | 0 | 0 |
| WNT ligand biogenesis and trafficking | R-HSA-3238698 | 0.266389 | 0.574 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 0.142914 | 0.845 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 0.278519 | 0.555 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 0.113452 | 0.945 | 1 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 0.241612 | 0.617 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 0.057895 | 1.237 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 0.072892 | 1.137 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 0.192215 | 0.716 | 0 | 0 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | R-HSA-2032785 | 0.180516 | 0.743 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 0.035603 | 1.449 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 0.225536 | 0.647 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 0.065293 | 1.185 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 0.070956 | 1.149 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 0.085888 | 1.066 | 0 | 0 |
| Kinesins | R-HSA-983189 | 0.173760 | 0.760 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 0.082605 | 1.083 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 0.249963 | 0.602 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 0.093660 | 1.028 | 0 | 0 |
| Synthesis of PIPs at the ER membrane | R-HSA-1483248 | 0.143432 | 0.843 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 0.099397 | 1.003 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 0.064338 | 1.192 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 0.052200 | 1.282 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 0.251816 | 0.599 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 0.251816 | 0.599 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 0.251816 | 0.599 | 0 | 0 |
| STAT3 nuclear events downstream of ALK signaling | R-HSA-9701898 | 0.189535 | 0.722 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 0.208336 | 0.681 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 0.240074 | 0.620 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 0.116210 | 0.935 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 0.203710 | 0.691 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 0.133903 | 0.873 | 0 | 0 |
| Physiological factors | R-HSA-5578768 | 0.180516 | 0.743 | 0 | 0 |
| Creatine metabolism | R-HSA-71288 | 0.241612 | 0.617 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 0.057241 | 1.242 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 0.254765 | 0.594 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 0.254185 | 0.595 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 0.265258 | 0.576 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 0.086233 | 1.064 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 0.267682 | 0.572 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 0.185355 | 0.732 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 0.105691 | 0.976 | 0 | 0 |
| HuR (ELAVL1) binds and stabilizes mRNA | R-HSA-450520 | 0.124268 | 0.906 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 0.233170 | 0.632 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 0.274468 | 0.562 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 0.228430 | 0.641 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 0.181254 | 0.742 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 0.060820 | 1.216 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 0.099309 | 1.003 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 0.100105 | 1.000 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 0.123393 | 0.909 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 0.191942 | 0.717 | 1 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 0.224794 | 0.648 | 1 | 1 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 0.064183 | 1.193 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 0.094721 | 1.024 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 0.158193 | 0.801 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 0.113452 | 0.945 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 0.101357 | 0.994 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 0.278519 | 0.555 | 0 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 0.094721 | 1.024 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 0.104679 | 0.980 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 0.152856 | 0.816 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 0.162178 | 0.790 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 0.162178 | 0.790 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 0.189535 | 0.722 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 0.128303 | 0.892 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 0.161524 | 0.792 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 0.143432 | 0.843 | 1 | 1 |
| Formation of the nephric duct | R-HSA-9830364 | 0.046721 | 1.330 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 0.041852 | 1.378 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 0.162178 | 0.790 | 0 | 0 |
| Attachment and Entry | R-HSA-9678110 | 0.198455 | 0.702 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 0.241612 | 0.617 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 0.063453 | 1.198 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 0.168833 | 0.773 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 0.224634 | 0.649 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 0.233170 | 0.632 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 0.258221 | 0.588 | 0 | 0 |
| Disease | R-HSA-1643685 | 0.216441 | 0.665 | 1 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 0.124500 | 0.905 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 0.254185 | 0.595 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 0.189535 | 0.722 | 0 | 0 |
| Atorvastatin ADME | R-HSA-9754706 | 0.198455 | 0.702 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 0.039807 | 1.400 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 0.154344 | 0.812 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 0.049433 | 1.306 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 0.241612 | 0.617 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 0.221675 | 0.654 | 0 | 0 |
| Aspirin ADME | R-HSA-9749641 | 0.225723 | 0.646 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 0.225536 | 0.647 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 0.185592 | 0.731 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 0.185592 | 0.731 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 0.056134 | 1.251 | 1 | 0 |
| PTEN Regulation | R-HSA-6807070 | 0.248872 | 0.604 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 0.213311 | 0.671 | 1 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 0.118888 | 0.925 | 0 | 0 |
| Formation of WDR5-containing histone-modifying complexes | R-HSA-9772755 | 0.079362 | 1.100 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 0.142914 | 0.845 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 0.050719 | 1.295 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 0.198455 | 0.702 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 0.198455 | 0.702 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 0.099321 | 1.003 | 1 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 0.183152 | 0.737 | 0 | 0 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | R-HSA-9615017 | 0.102863 | 0.988 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 0.061638 | 1.210 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 0.158193 | 0.801 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 0.101680 | 0.993 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 0.270178 | 0.568 | 1 | 1 |
| Azathioprine ADME | R-HSA-9748787 | 0.135400 | 0.868 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 0.266389 | 0.574 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 0.189417 | 0.723 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 0.143432 | 0.843 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 0.052200 | 1.282 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 0.270111 | 0.568 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 0.246037 | 0.609 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 0.123393 | 0.909 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 0.257661 | 0.589 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 0.272277 | 0.565 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 0.123393 | 0.909 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 0.278648 | 0.555 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 0.278648 | 0.555 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 0.281504 | 0.551 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 0.282459 | 0.549 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 0.282459 | 0.549 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 0.282459 | 0.549 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 0.282723 | 0.549 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 0.282723 | 0.549 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 0.288635 | 0.540 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 0.288678 | 0.540 | 1 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 0.290361 | 0.537 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 0.290361 | 0.537 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 0.290361 | 0.537 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 0.290361 | 0.537 | 0 | 0 |
| MicroRNA (miRNA) biogenesis | R-HSA-203927 | 0.290361 | 0.537 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 0.290361 | 0.537 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 0.290479 | 0.537 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 0.290479 | 0.537 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 0.290867 | 0.536 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 0.296474 | 0.528 | 0 | 0 |
| TRP channels | R-HSA-3295583 | 0.298178 | 0.526 | 0 | 0 |
| Caspase activation via extrinsic apoptotic signalling pathway | R-HSA-5357769 | 0.298178 | 0.526 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 0.298178 | 0.526 | 0 | 0 |
| Metalloprotease DUBs | R-HSA-5689901 | 0.298178 | 0.526 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 0.298178 | 0.526 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 0.299000 | 0.524 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 0.299000 | 0.524 | 1 | 1 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 0.303061 | 0.518 | 0 | 0 |
| TNFR1-induced NF-kappa-B signaling pathway | R-HSA-5357956 | 0.305908 | 0.514 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 0.305908 | 0.514 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 0.305908 | 0.514 | 0 | 0 |
| RNA Polymerase I Transcription Termination | R-HSA-73863 | 0.305908 | 0.514 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 0.305908 | 0.514 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 0.305908 | 0.514 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 0.305908 | 0.514 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 0.305908 | 0.514 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 0.311170 | 0.507 | 0 | 0 |
| Formation of the HIV-1 Early Elongation Complex | R-HSA-167158 | 0.313554 | 0.504 | 0 | 0 |
| Formation of the Early Elongation Complex | R-HSA-113418 | 0.313554 | 0.504 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 0.313554 | 0.504 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 0.313554 | 0.504 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 0.313554 | 0.504 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 0.313554 | 0.504 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 0.315218 | 0.501 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 0.319261 | 0.496 | 1 | 1 |
| mRNA Capping | R-HSA-72086 | 0.321116 | 0.493 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 0.321116 | 0.493 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 0.321116 | 0.493 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 0.321116 | 0.493 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 0.323298 | 0.490 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 0.324329 | 0.489 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 0.327329 | 0.485 | 0 | 0 |
| RNA Polymerase III Transcription Initiation | R-HSA-76046 | 0.328596 | 0.483 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 0.328596 | 0.483 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 0.328596 | 0.483 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 0.328596 | 0.483 | 0 | 0 |
| GABA synthesis, release, reuptake and degradation | R-HSA-888590 | 0.328596 | 0.483 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 0.328596 | 0.483 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 0.331353 | 0.480 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 0.335371 | 0.474 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 0.335993 | 0.474 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 0.335993 | 0.474 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 0.335993 | 0.474 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 0.335993 | 0.474 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 0.339382 | 0.469 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 0.341779 | 0.466 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 0.343309 | 0.464 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 0.343309 | 0.464 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 0.343309 | 0.464 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 0.350546 | 0.455 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 0.350546 | 0.455 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 0.350546 | 0.455 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 0.350546 | 0.455 | 0 | 0 |
| Cardiogenesis | R-HSA-9733709 | 0.350546 | 0.455 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 0.353591 | 0.451 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 0.356592 | 0.448 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 0.356686 | 0.448 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 0.357703 | 0.446 | 0 | 0 |
| Effects of PIP2 hydrolysis | R-HSA-114508 | 0.357703 | 0.446 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 0.357703 | 0.446 | 0 | 0 |
| Miscellaneous transport and binding events | R-HSA-5223345 | 0.357703 | 0.446 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 0.357703 | 0.446 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 0.363283 | 0.440 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 0.364781 | 0.438 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 0.364781 | 0.438 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 0.364781 | 0.438 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 0.364781 | 0.438 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 0.364781 | 0.438 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 0.369248 | 0.433 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 0.371180 | 0.430 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 0.371782 | 0.430 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 0.371782 | 0.430 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 0.371782 | 0.430 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 0.378706 | 0.422 | 0 | 0 |
| RNA Polymerase III Abortive And Retractive Initiation | R-HSA-749476 | 0.378706 | 0.422 | 0 | 0 |
| RNA Polymerase III Transcription | R-HSA-74158 | 0.378706 | 0.422 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 0.378706 | 0.422 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 0.378706 | 0.422 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 0.378706 | 0.422 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 0.378706 | 0.422 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 0.378706 | 0.422 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 0.378706 | 0.422 | 0 | 0 |
| FGFR2 mutant receptor activation | R-HSA-1839126 | 0.378706 | 0.422 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 0.378706 | 0.422 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 0.379038 | 0.421 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 0.382371 | 0.418 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 0.382952 | 0.417 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 0.382952 | 0.417 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 0.382952 | 0.417 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 0.385554 | 0.414 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 0.385554 | 0.414 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 0.385554 | 0.414 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 0.385554 | 0.414 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 0.385554 | 0.414 | 0 | 0 |
| Metabolism of folate and pterines | R-HSA-196757 | 0.385554 | 0.414 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 0.386855 | 0.412 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 0.386855 | 0.412 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 0.390748 | 0.408 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 0.390748 | 0.408 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 0.392327 | 0.406 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 0.398500 | 0.400 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 0.398500 | 0.400 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 0.399026 | 0.399 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 0.399026 | 0.399 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 0.399026 | 0.399 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 0.399026 | 0.399 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 0.399026 | 0.399 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 0.399026 | 0.399 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 0.405652 | 0.392 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 0.405652 | 0.392 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 0.405652 | 0.392 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 0.405652 | 0.392 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 0.405652 | 0.392 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 0.405652 | 0.392 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 0.405652 | 0.392 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 0.405652 | 0.392 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 0.410159 | 0.387 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 0.412205 | 0.385 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 0.412205 | 0.385 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 0.412205 | 0.385 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 0.412205 | 0.385 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 0.416038 | 0.381 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 0.417678 | 0.379 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 0.418686 | 0.378 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 0.418686 | 0.378 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 0.418686 | 0.378 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 0.418686 | 0.378 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 0.418686 | 0.378 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 0.418686 | 0.378 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 0.418686 | 0.378 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 0.418686 | 0.378 | 0 | 0 |
| SLC-mediated transport of neurotransmitters | R-HSA-442660 | 0.418686 | 0.378 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 0.418950 | 0.378 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 0.421476 | 0.375 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 0.421476 | 0.375 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 0.425096 | 0.372 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 0.426342 | 0.370 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 0.426342 | 0.370 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 0.429036 | 0.368 | 1 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 0.431435 | 0.365 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 0.431435 | 0.365 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 0.431435 | 0.365 | 1 | 1 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 0.436463 | 0.360 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 0.437706 | 0.359 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 0.437706 | 0.359 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 0.437706 | 0.359 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 0.437706 | 0.359 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 0.440279 | 0.356 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 0.443907 | 0.353 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 0.443907 | 0.353 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 0.443907 | 0.353 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 0.443907 | 0.353 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 0.443907 | 0.353 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 0.443907 | 0.353 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 0.443907 | 0.353 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 0.443907 | 0.353 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 0.447706 | 0.349 | 1 | 1 |
| MHC class II antigen presentation | R-HSA-2132295 | 0.447706 | 0.349 | 0 | 0 |
| Formation of TC-NER Pre-Incision Complex | R-HSA-6781823 | 0.450040 | 0.347 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 0.450040 | 0.347 | 0 | 0 |
| Signaling by TGFBR3 | R-HSA-9839373 | 0.450040 | 0.347 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 0.451400 | 0.345 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 0.456107 | 0.341 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 0.456107 | 0.341 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 0.458744 | 0.338 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 0.458744 | 0.338 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 0.458744 | 0.338 | 0 | 0 |
| M Phase | R-HSA-68886 | 0.460373 | 0.337 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 0.462106 | 0.335 | 1 | 1 |
| NGF-stimulated transcription | R-HSA-9031628 | 0.462106 | 0.335 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 0.462508 | 0.335 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 0.468040 | 0.330 | 0 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 0.468040 | 0.330 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 0.468040 | 0.330 | 0 | 0 |
| Chemokine receptors bind chemokines | R-HSA-380108 | 0.468040 | 0.330 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 0.468040 | 0.330 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 0.468040 | 0.330 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 0.473909 | 0.324 | 0 | 0 |
| Signaling by FGFR2 in disease | R-HSA-5655253 | 0.473909 | 0.324 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 0.476855 | 0.322 | 1 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 0.479713 | 0.319 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 0.479713 | 0.319 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 0.485453 | 0.314 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 0.485453 | 0.314 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 0.485453 | 0.314 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 0.485453 | 0.314 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 0.491131 | 0.309 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 0.491131 | 0.309 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 0.491131 | 0.309 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 0.496746 | 0.304 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 0.498748 | 0.302 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 0.502300 | 0.299 | 0 | 0 |
| G alpha (z) signalling events | R-HSA-418597 | 0.502300 | 0.299 | 0 | 0 |
| Paracetamol ADME | R-HSA-9753281 | 0.502300 | 0.299 | 0 | 0 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | R-HSA-6782210 | 0.507793 | 0.294 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 0.507793 | 0.294 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 0.507793 | 0.294 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 0.508513 | 0.294 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 0.511953 | 0.291 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 0.513225 | 0.290 | 0 | 0 |
| Dual incision in TC-NER | R-HSA-6782135 | 0.518598 | 0.285 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 0.518598 | 0.285 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 0.518598 | 0.285 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 0.523912 | 0.281 | 0 | 0 |
| Peroxisomal protein import | R-HSA-9033241 | 0.523912 | 0.281 | 0 | 0 |
| Assembly of collagen fibrils and other multimeric structures | R-HSA-2022090 | 0.523912 | 0.281 | 0 | 0 |
| Amino acid transport across the plasma membrane | R-HSA-352230 | 0.523912 | 0.281 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 0.523912 | 0.281 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 0.528335 | 0.277 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 0.529167 | 0.276 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 0.533902 | 0.273 | 0 | 0 |
| Viral Messenger RNA Synthesis | R-HSA-168325 | 0.534365 | 0.272 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 0.534365 | 0.272 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 0.534365 | 0.272 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 0.535591 | 0.271 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 0.539506 | 0.268 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 0.539506 | 0.268 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 0.539506 | 0.268 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 0.539506 | 0.268 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 0.541818 | 0.266 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 0.542200 | 0.266 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 0.544590 | 0.264 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 0.544672 | 0.264 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 0.545481 | 0.263 | 0 | 0 |
| S Phase | R-HSA-69242 | 0.548745 | 0.261 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 0.549619 | 0.260 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 0.554592 | 0.256 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 0.555223 | 0.256 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 0.561636 | 0.251 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 0.564376 | 0.248 | 0 | 0 |
| SLC-mediated transport of amino acids | R-HSA-9958863 | 0.564376 | 0.248 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 0.564376 | 0.248 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 0.564818 | 0.248 | 0 | 0 |
| O-linked glycosylation of mucins | R-HSA-913709 | 0.569187 | 0.245 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 0.569187 | 0.245 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 0.569187 | 0.245 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 0.571132 | 0.243 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 0.572697 | 0.242 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 0.577718 | 0.238 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 0.578651 | 0.238 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 0.578651 | 0.238 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 0.578651 | 0.238 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 0.578651 | 0.238 | 0 | 0 |
| Diseases associated with O-glycosylation of proteins | R-HSA-3906995 | 0.583306 | 0.234 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 0.583306 | 0.234 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 0.583306 | 0.234 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 0.586628 | 0.232 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 0.586628 | 0.232 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 0.587909 | 0.231 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 0.587909 | 0.231 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 0.587909 | 0.231 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 0.587909 | 0.231 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 0.596965 | 0.224 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 0.596965 | 0.224 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 0.596965 | 0.224 | 0 | 0 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | R-HSA-6781827 | 0.601418 | 0.221 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 0.601418 | 0.221 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 0.611486 | 0.214 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 0.614486 | 0.211 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 0.614486 | 0.211 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 0.614486 | 0.211 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 0.627806 | 0.202 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 0.627806 | 0.202 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 0.631250 | 0.200 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 0.635326 | 0.197 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 0.643345 | 0.192 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 0.643345 | 0.192 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 0.643345 | 0.192 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 0.644460 | 0.191 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 0.647289 | 0.189 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 0.651189 | 0.186 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 0.655046 | 0.184 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 0.655046 | 0.184 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 0.655072 | 0.184 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 0.655235 | 0.184 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 0.656237 | 0.183 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 0.658861 | 0.181 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 0.662634 | 0.179 | 0 | 0 |
| Neurotransmitter release cycle | R-HSA-112310 | 0.666365 | 0.176 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 0.670055 | 0.174 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 0.673464 | 0.172 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 0.673705 | 0.172 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 0.677315 | 0.169 | 0 | 0 |
| Protein folding | R-HSA-391251 | 0.677315 | 0.169 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 0.677315 | 0.169 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 0.678528 | 0.168 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 0.684415 | 0.165 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 0.684717 | 0.164 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 0.685461 | 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 | 0.687907 | 0.162 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 0.688465 | 0.162 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 0.691360 | 0.160 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 0.694776 | 0.158 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 0.694776 | 0.158 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 0.698153 | 0.156 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 0.698803 | 0.156 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 0.701494 | 0.154 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 0.702898 | 0.153 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 0.708065 | 0.150 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 0.711297 | 0.148 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 0.711297 | 0.148 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 0.714493 | 0.146 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 0.714493 | 0.146 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 0.714499 | 0.146 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 0.715026 | 0.146 | 1 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 0.717653 | 0.144 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 0.720779 | 0.142 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 0.720779 | 0.142 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 0.723871 | 0.140 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 0.723871 | 0.140 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 0.723871 | 0.140 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 0.726928 | 0.139 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 0.727920 | 0.138 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 0.729952 | 0.137 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 0.730105 | 0.137 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 0.732943 | 0.135 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 0.732943 | 0.135 | 0 | 0 |
| Translation | R-HSA-72766 | 0.735302 | 0.134 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 0.735900 | 0.133 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 0.735900 | 0.133 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 0.740807 | 0.130 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 0.747408 | 0.126 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 0.752974 | 0.123 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 0.755711 | 0.122 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 0.758418 | 0.120 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 0.759162 | 0.120 | 1 | 0 |
| Signaling by GPCR | R-HSA-372790 | 0.759487 | 0.119 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 0.761131 | 0.119 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 0.766360 | 0.116 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 0.768950 | 0.114 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 0.776548 | 0.110 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 0.776548 | 0.110 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 0.776548 | 0.110 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 0.776612 | 0.110 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 0.778235 | 0.109 | 1 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 0.781475 | 0.107 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 0.783265 | 0.106 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 0.783898 | 0.106 | 1 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 0.787739 | 0.104 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 0.788664 | 0.103 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 0.791007 | 0.102 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 0.793287 | 0.101 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 0.793325 | 0.101 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 0.797653 | 0.098 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 0.802343 | 0.096 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 0.804536 | 0.094 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 0.814891 | 0.089 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 0.817177 | 0.088 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 0.817193 | 0.088 | 0 | 0 |
| O-linked glycosylation | R-HSA-5173105 | 0.819222 | 0.087 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 0.830933 | 0.080 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 0.830933 | 0.080 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 0.832810 | 0.079 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 0.850478 | 0.070 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 0.850478 | 0.070 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 0.857014 | 0.067 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 0.857014 | 0.067 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 0.858603 | 0.066 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 0.860175 | 0.065 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 0.864803 | 0.063 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 0.867776 | 0.062 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 0.869981 | 0.060 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 0.872137 | 0.059 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 0.877731 | 0.057 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 0.881766 | 0.055 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 0.881766 | 0.055 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 0.890674 | 0.050 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 0.891582 | 0.050 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 0.894444 | 0.048 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 0.895461 | 0.048 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 0.897776 | 0.047 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 0.900039 | 0.046 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 0.901153 | 0.045 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 0.912188 | 0.040 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 0.915502 | 0.038 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 0.924464 | 0.034 | 0 | 0 |
| Metabolism of water-soluble vitamins and cofactors | R-HSA-196849 | 0.938279 | 0.028 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 0.939650 | 0.027 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 0.942301 | 0.026 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 0.944213 | 0.025 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 0.946786 | 0.024 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 0.950700 | 0.022 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 0.957883 | 0.019 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 0.959846 | 0.018 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 0.972837 | 0.012 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 0.973874 | 0.011 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 0.986378 | 0.006 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 0.990414 | 0.004 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 0.997795 | 0.001 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 0.998966 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 0.999933 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 1.000000 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000 | 0.000 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.000000 | 0.000 | 1 | 1 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 1.000000 | 0.000 | 1 | 0 |
| Nef and signal transduction | R-HSA-164944 | 1.000000 | 0.000 | 1 | 1 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 1.000000 | 0.000 | 1 | 0 |
| Nef Mediated CD4 Down-regulation | R-HSA-167590 | 1.000000 | 0.000 | 1 | 1 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 1.000000 | 0.000 | 1 | 1 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 1.000000 | 0.000 | 1 | 1 |
| FLT3 Signaling | R-HSA-9607240 | 1.000000 | 0.000 | 1 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 1.000000 | 0.000 | 1 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 1.000000 | 0.000 | 1 | 1 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 1.000000 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 3.330669e-16 | 15.477 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 3.330669e-16 | 15.477 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 7.771561e-16 | 15.109 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 3.552714e-15 | 14.449 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 2.720046e-14 | 13.565 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 3.230749e-14 | 13.491 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 5.706546e-14 | 13.244 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 1.583178e-13 | 12.800 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 1.583178e-13 | 12.800 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 2.968736e-13 | 12.527 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 3.501643e-13 | 12.456 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 5.757617e-13 | 12.240 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 7.133183e-13 | 12.147 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 9.404699e-13 | 12.027 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 1.336042e-12 | 11.874 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 1.600386e-12 | 11.796 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 1.600386e-12 | 11.796 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 1.967981e-12 | 11.706 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 2.652767e-12 | 11.576 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 3.384515e-12 | 11.471 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 3.384515e-12 | 11.471 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 3.691047e-12 | 11.433 | 0 | 0 |
| Depurination | R-HSA-73927 | 4.293566e-12 | 11.367 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 5.405343e-12 | 11.267 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 5.955791e-12 | 11.225 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 6.800005e-12 | 11.167 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 6.800005e-12 | 11.167 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 8.492873e-12 | 11.071 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 8.492873e-12 | 11.071 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 9.870771e-12 | 11.006 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 1.306222e-11 | 10.884 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 1.306222e-11 | 10.884 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 1.609124e-11 | 10.793 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 1.865275e-11 | 10.729 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 2.411560e-11 | 10.618 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 2.411560e-11 | 10.618 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 2.592659e-11 | 10.586 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 2.592659e-11 | 10.586 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 3.270340e-11 | 10.485 | 1 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 4.297829e-11 | 10.367 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 4.866507e-11 | 10.313 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 5.503209e-11 | 10.259 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 8.845757e-11 | 10.053 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 9.302004e-11 | 10.031 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 1.018118e-10 | 9.992 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 1.051168e-10 | 9.978 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.087411e-10 | 9.964 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 1.245448e-10 | 9.905 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 1.471417e-10 | 9.832 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 1.566626e-10 | 9.805 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 2.387218e-10 | 9.622 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 2.790647e-10 | 9.554 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 3.254268e-10 | 9.488 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 3.342497e-10 | 9.476 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 3.440339e-10 | 9.463 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 3.794921e-10 | 9.421 | 1 | 1 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 3.878161e-10 | 9.411 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 4.753767e-10 | 9.323 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 5.614381e-10 | 9.251 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 6.333019e-10 | 9.198 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 8.960727e-10 | 9.048 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 1.027052e-09 | 8.988 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 1.011454e-09 | 8.995 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 1.341625e-09 | 8.872 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 1.341625e-09 | 8.872 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 1.417712e-09 | 8.848 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 1.529193e-09 | 8.816 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 1.739916e-09 | 8.759 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 1.764921e-09 | 8.753 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 1.845649e-09 | 8.734 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 1.860459e-09 | 8.730 | 1 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.922212e-09 | 8.716 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 2.867522e-09 | 8.542 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 3.314474e-09 | 8.480 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 3.646416e-09 | 8.438 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 3.670191e-09 | 8.435 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 4.054875e-09 | 8.392 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 4.609368e-09 | 8.336 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 5.446409e-09 | 8.264 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 5.446409e-09 | 8.264 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 5.171262e-09 | 8.286 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 7.409235e-09 | 8.130 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 9.583862e-09 | 8.018 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 1.275617e-08 | 7.894 | 1 | 0 |
| Infectious disease | R-HSA-5663205 | 1.277276e-08 | 7.894 | 1 | 0 |
| Axon guidance | R-HSA-422475 | 1.364121e-08 | 7.865 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 1.520696e-08 | 7.818 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 1.733551e-08 | 7.761 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 1.635710e-08 | 7.786 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 1.783204e-08 | 7.749 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 2.600234e-08 | 7.585 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 2.947489e-08 | 7.531 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 3.308347e-08 | 7.480 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 3.753841e-08 | 7.426 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 4.395971e-08 | 7.357 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 4.442459e-08 | 7.352 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 5.103855e-08 | 7.292 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 4.772605e-08 | 7.321 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 5.544351e-08 | 7.256 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 5.544351e-08 | 7.256 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 5.544351e-08 | 7.256 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 5.722974e-08 | 7.242 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 7.424760e-08 | 7.129 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 7.424760e-08 | 7.129 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 8.676851e-08 | 7.062 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 1.973948e-07 | 6.705 | 0 | 0 |
| Disease | R-HSA-1643685 | 2.223912e-07 | 6.653 | 1 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 2.248367e-07 | 6.648 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 2.787211e-07 | 6.555 | 0 | 0 |
| Immune System | R-HSA-168256 | 2.553830e-07 | 6.593 | 1 | 0 |
| HCMV Infection | R-HSA-9609646 | 3.168256e-07 | 6.499 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 3.982604e-07 | 6.400 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 3.982640e-07 | 6.400 | 1 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 4.584805e-07 | 6.339 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 4.669791e-07 | 6.331 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 4.871684e-07 | 6.312 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 5.200465e-07 | 6.284 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 6.000198e-07 | 6.222 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 8.718620e-07 | 6.060 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 9.993726e-07 | 6.000 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.320876e-06 | 5.879 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 1.693352e-06 | 5.771 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 1.779476e-06 | 5.750 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.939002e-06 | 5.712 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 2.429920e-06 | 5.614 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 2.794677e-06 | 5.554 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 3.644317e-06 | 5.438 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 3.737320e-06 | 5.427 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 4.129622e-06 | 5.384 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 8.729485e-06 | 5.059 | 1 | 1 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 9.095697e-06 | 5.041 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 9.845403e-06 | 5.007 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 1.034787e-05 | 4.985 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 1.117815e-05 | 4.952 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.320457e-05 | 4.879 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 1.959766e-05 | 4.708 | 1 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.997609e-05 | 4.699 | 1 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 2.125977e-05 | 4.672 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 2.458429e-05 | 4.609 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 3.322059e-05 | 4.479 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 3.322059e-05 | 4.479 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 3.870273e-05 | 4.412 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 4.476032e-05 | 4.349 | 1 | 1 |
| PKR-mediated signaling | R-HSA-9833482 | 5.572350e-05 | 4.254 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 6.092671e-05 | 4.215 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 8.256886e-05 | 4.083 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 9.754132e-05 | 4.011 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 1.016077e-04 | 3.993 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 1.021397e-04 | 3.991 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 1.044352e-04 | 3.981 | 0 | 0 |
| Protein folding | R-HSA-391251 | 1.381091e-04 | 3.860 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.601664e-04 | 3.795 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 1.764822e-04 | 3.753 | 1 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 1.908742e-04 | 3.719 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.943750e-04 | 3.711 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 1.986056e-04 | 3.702 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 2.039364e-04 | 3.691 | 1 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 2.459054e-04 | 3.609 | 1 | 0 |
| Gap junction trafficking | R-HSA-190828 | 2.801671e-04 | 3.553 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 2.806709e-04 | 3.552 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 3.455684e-04 | 3.461 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 3.455684e-04 | 3.461 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 3.455684e-04 | 3.461 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 3.613661e-04 | 3.442 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 3.373509e-04 | 3.472 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 4.246211e-04 | 3.372 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 4.304924e-04 | 3.366 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 4.828165e-04 | 3.316 | 1 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 4.930744e-04 | 3.307 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 5.361224e-04 | 3.271 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 5.546042e-04 | 3.256 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 5.666318e-04 | 3.247 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 6.135798e-04 | 3.212 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 6.744304e-04 | 3.171 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 6.761679e-04 | 3.170 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 6.810543e-04 | 3.167 | 1 | 1 |
| Selective autophagy | R-HSA-9663891 | 7.132310e-04 | 3.147 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 7.173681e-04 | 3.144 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 7.455654e-04 | 3.128 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 7.536206e-04 | 3.123 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 7.636584e-04 | 3.117 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 7.959311e-04 | 3.099 | 1 | 1 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 8.872411e-04 | 3.052 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 9.697794e-04 | 3.013 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.044920e-03 | 2.981 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.128417e-03 | 2.948 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.128417e-03 | 2.948 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 1.307644e-03 | 2.884 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.352446e-03 | 2.869 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 1.476935e-03 | 2.831 | 1 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 1.533697e-03 | 2.814 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 1.550778e-03 | 2.809 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 1.604343e-03 | 2.795 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.095701e-03 | 2.679 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.095701e-03 | 2.679 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 2.002379e-03 | 2.698 | 1 | 1 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 1.848564e-03 | 2.733 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 1.805281e-03 | 2.743 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 2.095701e-03 | 2.679 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 2.097557e-03 | 2.678 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 2.117946e-03 | 2.674 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 2.206191e-03 | 2.656 | 1 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.255275e-03 | 2.647 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.327572e-03 | 2.633 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.362440e-03 | 2.627 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 2.392138e-03 | 2.621 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 2.420981e-03 | 2.616 | 1 | 1 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 2.577131e-03 | 2.589 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.594875e-03 | 2.586 | 1 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.649294e-03 | 2.577 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.706227e-03 | 2.568 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 2.956752e-03 | 2.529 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 3.241569e-03 | 2.489 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 3.246429e-03 | 2.489 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.285283e-03 | 2.483 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 3.330532e-03 | 2.477 | 1 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 3.441694e-03 | 2.463 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 3.712506e-03 | 2.430 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 4.007318e-03 | 2.397 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 4.114458e-03 | 2.386 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 4.401649e-03 | 2.356 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 4.410727e-03 | 2.355 | 1 | 1 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 4.410727e-03 | 2.355 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 4.418183e-03 | 2.355 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 4.518517e-03 | 2.345 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 4.529346e-03 | 2.344 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 4.560479e-03 | 2.341 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 4.560479e-03 | 2.341 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 4.677188e-03 | 2.330 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 5.103458e-03 | 2.292 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 5.390509e-03 | 2.268 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 5.470347e-03 | 2.262 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 5.722420e-03 | 2.242 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 5.733441e-03 | 2.242 | 1 | 1 |
| Parasitic Infection Pathways | R-HSA-9824443 | 5.795213e-03 | 2.237 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 5.795213e-03 | 2.237 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 6.496479e-03 | 2.187 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 7.677025e-03 | 2.115 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 7.817173e-03 | 2.107 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 7.357986e-03 | 2.133 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 7.256842e-03 | 2.139 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 7.677025e-03 | 2.115 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 7.341321e-03 | 2.134 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 6.209743e-03 | 2.207 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 8.067279e-03 | 2.093 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 7.677025e-03 | 2.115 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 7.256842e-03 | 2.139 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 6.617348e-03 | 2.179 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 7.805220e-03 | 2.108 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 8.402364e-03 | 2.076 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 8.402364e-03 | 2.076 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 8.946591e-03 | 2.048 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 9.012650e-03 | 2.045 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 9.012650e-03 | 2.045 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 9.264411e-03 | 2.033 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.030315e-02 | 1.987 | 1 | 1 |
| Gap junction assembly | R-HSA-190861 | 1.030936e-02 | 1.987 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 1.062159e-02 | 1.974 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.074760e-02 | 1.969 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.074760e-02 | 1.969 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.074760e-02 | 1.969 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.074760e-02 | 1.969 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.074760e-02 | 1.969 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.074760e-02 | 1.969 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 1.092527e-02 | 1.962 | 1 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 1.097182e-02 | 1.960 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 1.099617e-02 | 1.959 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 1.105825e-02 | 1.956 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 1.105825e-02 | 1.956 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.153363e-02 | 1.938 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 1.170884e-02 | 1.931 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.174471e-02 | 1.930 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 1.174471e-02 | 1.930 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.202198e-02 | 1.920 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.252340e-02 | 1.902 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 1.303802e-02 | 1.885 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.326930e-02 | 1.877 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 1.341052e-02 | 1.873 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.360701e-02 | 1.866 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.380035e-02 | 1.860 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.400357e-02 | 1.854 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 1.400357e-02 | 1.854 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 1.466216e-02 | 1.834 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 1.480092e-02 | 1.830 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 1.482113e-02 | 1.829 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 1.482113e-02 | 1.829 | 1 | 1 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.487501e-02 | 1.828 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.487501e-02 | 1.828 | 1 | 1 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.487501e-02 | 1.828 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.487501e-02 | 1.828 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 1.566520e-02 | 1.805 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.623276e-02 | 1.790 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 1.623276e-02 | 1.790 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.655991e-02 | 1.781 | 1 | 1 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.655991e-02 | 1.781 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 1.669706e-02 | 1.777 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 1.832216e-02 | 1.737 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 1.832216e-02 | 1.737 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 1.832216e-02 | 1.737 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.866307e-02 | 1.729 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 1.894535e-02 | 1.722 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 1.930804e-02 | 1.714 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 1.930804e-02 | 1.714 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 1.963701e-02 | 1.707 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 2.015992e-02 | 1.696 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 2.015992e-02 | 1.696 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.015992e-02 | 1.696 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 2.097619e-02 | 1.678 | 0 | 0 |
| Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 | R-HSA-9630794 | 3.189947e-02 | 1.496 | 0 | 0 |
| PTEN Loss of Function in Cancer | R-HSA-5674404 | 3.189947e-02 | 1.496 | 0 | 0 |
| Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 | R-HSA-9632700 | 3.189947e-02 | 1.496 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.823027e-02 | 1.549 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 3.041902e-02 | 1.517 | 1 | 1 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 2.232147e-02 | 1.651 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 2.788069e-02 | 1.555 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 2.907287e-02 | 1.537 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 3.153719e-02 | 1.501 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 2.545485e-02 | 1.594 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 3.029172e-02 | 1.519 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 2.671524e-02 | 1.573 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 2.337965e-02 | 1.631 | 1 | 1 |
| Inhibition of PKR | R-HSA-169131 | 2.138035e-02 | 1.670 | 0 | 0 |
| Evasion of Oncogene Induced Senescence Due to p16INK4A Defects | R-HSA-9630750 | 3.189947e-02 | 1.496 | 0 | 0 |
| Evasion of Oxidative Stress Induced Senescence Due to p16INK4A Defects | R-HSA-9632693 | 3.189947e-02 | 1.496 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.189947e-02 | 1.496 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.610827e-02 | 1.583 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.823027e-02 | 1.549 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 2.337965e-02 | 1.631 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.823027e-02 | 1.549 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 2.446469e-02 | 1.611 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.610827e-02 | 1.583 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 3.073865e-02 | 1.512 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 2.959489e-02 | 1.529 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.557656e-02 | 1.592 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 2.788069e-02 | 1.555 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 3.225939e-02 | 1.491 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 3.243442e-02 | 1.489 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 3.280920e-02 | 1.484 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 3.317784e-02 | 1.479 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 3.437618e-02 | 1.464 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.499019e-02 | 1.456 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 3.506031e-02 | 1.455 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.700368e-02 | 1.432 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 3.736936e-02 | 1.427 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 3.796498e-02 | 1.421 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 3.799823e-02 | 1.420 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 3.816092e-02 | 1.418 | 0 | 0 |
| Kinesins | R-HSA-983189 | 3.816092e-02 | 1.418 | 0 | 0 |
| Regulation of PTEN mRNA translation | R-HSA-8943723 | 3.980882e-02 | 1.400 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 3.980882e-02 | 1.400 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 3.980882e-02 | 1.400 | 1 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 3.990073e-02 | 1.399 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 4.003312e-02 | 1.398 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 4.099358e-02 | 1.387 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 4.126705e-02 | 1.384 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 4.212911e-02 | 1.375 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.230615e-02 | 1.374 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.230615e-02 | 1.374 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.230615e-02 | 1.374 | 0 | 0 |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.230615e-02 | 1.374 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.230615e-02 | 1.374 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.230615e-02 | 1.374 | 0 | 0 |
| Diseases of Cellular Senescence | R-HSA-9630747 | 4.230615e-02 | 1.374 | 0 | 0 |
| Diseases of cellular response to stress | R-HSA-9675132 | 4.230615e-02 | 1.374 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 4.230699e-02 | 1.374 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 4.244871e-02 | 1.372 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 4.244871e-02 | 1.372 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 4.320001e-02 | 1.365 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 4.392953e-02 | 1.357 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 4.538711e-02 | 1.343 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 4.650428e-02 | 1.333 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 4.878335e-02 | 1.312 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 5.010694e-02 | 1.300 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 5.013869e-02 | 1.300 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 5.013869e-02 | 1.300 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 5.013869e-02 | 1.300 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.260161e-02 | 1.279 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.260161e-02 | 1.279 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 5.500249e-02 | 1.260 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 5.562610e-02 | 1.255 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 5.562610e-02 | 1.255 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.838866e-02 | 1.234 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 5.844540e-02 | 1.233 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 5.844540e-02 | 1.233 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 5.844540e-02 | 1.233 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 6.061338e-02 | 1.217 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 6.239998e-02 | 1.205 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 6.278702e-02 | 1.202 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.278702e-02 | 1.202 | 0 | 0 |
| Drug-mediated inhibition of CDK4/CDK6 activity | R-HSA-9754119 | 6.278702e-02 | 1.202 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 6.911873e-02 | 1.160 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 6.918643e-02 | 1.160 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 7.019471e-02 | 1.154 | 0 | 0 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | R-HSA-9818027 | 7.019471e-02 | 1.154 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 7.019471e-02 | 1.154 | 0 | 0 |
| IRS activation | R-HSA-74713 | 7.286355e-02 | 1.137 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.286355e-02 | 1.137 | 0 | 0 |
| NTRK2 activates RAC1 | R-HSA-9032759 | 7.286355e-02 | 1.137 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 7.286355e-02 | 1.137 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 7.286355e-02 | 1.137 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 7.286355e-02 | 1.137 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 7.324345e-02 | 1.135 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 7.324345e-02 | 1.135 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.283235e-02 | 1.082 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.283235e-02 | 1.082 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.269458e-02 | 1.033 | 0 | 0 |
| Metabolism of ingested MeSeO2H into MeSeH | R-HSA-5263617 | 9.269458e-02 | 1.033 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.269458e-02 | 1.033 | 0 | 0 |
| Branched-chain ketoacid dehydrogenase kinase deficiency | R-HSA-9912481 | 9.269458e-02 | 1.033 | 0 | 0 |
| PP2A-mediated dephosphorylation of key metabolic factors | R-HSA-163767 | 1.024514e-01 | 0.989 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 1.024514e-01 | 0.989 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 1.024514e-01 | 0.989 | 0 | 0 |
| Activated NTRK2 signals through FYN | R-HSA-9032500 | 1.121038e-01 | 0.950 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.311002e-01 | 0.882 | 0 | 0 |
| Truncations of AMER1 destabilize the destruction complex | R-HSA-5467348 | 1.404463e-01 | 0.852 | 0 | 0 |
| AXIN missense mutants destabilize the destruction complex | R-HSA-5467340 | 1.404463e-01 | 0.852 | 0 | 0 |
| APC truncation mutants have impaired AXIN binding | R-HSA-5467337 | 1.404463e-01 | 0.852 | 0 | 0 |
| Signaling by GSK3beta mutants | R-HSA-5339716 | 1.496924e-01 | 0.825 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 1.162681e-01 | 0.935 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 1.197994e-01 | 0.922 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 1.415093e-01 | 0.849 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 1.452061e-01 | 0.838 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 1.415101e-01 | 0.849 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.092890e-01 | 0.961 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.311002e-01 | 0.882 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.404463e-01 | 0.852 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 1.121038e-01 | 0.950 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 1.496924e-01 | 0.825 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 8.263677e-02 | 1.083 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 9.904385e-02 | 1.004 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.024277e-01 | 0.990 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 1.016266e-01 | 0.993 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 1.415101e-01 | 0.849 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.283235e-02 | 1.082 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 1.305481e-01 | 0.884 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 9.904385e-02 | 1.004 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.162681e-01 | 0.935 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.162681e-01 | 0.935 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.162681e-01 | 0.935 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.283235e-02 | 1.082 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.024514e-01 | 0.989 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.404463e-01 | 0.852 | 0 | 0 |
| Signaling by APC mutants | R-HSA-4839744 | 1.404463e-01 | 0.852 | 0 | 0 |
| ERKs are inactivated | R-HSA-202670 | 1.496924e-01 | 0.825 | 0 | 0 |
| Signaling by AMER1 mutants | R-HSA-4839748 | 1.496924e-01 | 0.825 | 0 | 0 |
| Signaling by AXIN mutants | R-HSA-4839735 | 1.496924e-01 | 0.825 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.378335e-01 | 0.861 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.244965e-01 | 0.905 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.162681e-01 | 0.935 | 0 | 0 |
| Translation | R-HSA-72766 | 1.164054e-01 | 0.934 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.496924e-01 | 0.825 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.311002e-01 | 0.882 | 0 | 0 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | R-HSA-113501 | 1.496924e-01 | 0.825 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 8.806504e-02 | 1.055 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.269458e-02 | 1.033 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.216531e-01 | 0.915 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.311002e-01 | 0.882 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.496924e-01 | 0.825 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 1.060553e-01 | 0.974 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 8.267434e-02 | 1.083 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 7.781129e-02 | 1.109 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 7.929897e-02 | 1.101 | 0 | 0 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 8.283235e-02 | 1.082 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.283235e-02 | 1.082 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 1.024514e-01 | 0.989 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 1.404463e-01 | 0.852 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 1.390331e-01 | 0.857 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 1.105586e-01 | 0.956 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 1.216531e-01 | 0.915 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 8.469798e-02 | 1.072 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 7.781129e-02 | 1.109 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 1.428712e-01 | 0.845 | 1 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.311002e-01 | 0.882 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 1.311002e-01 | 0.882 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 8.263677e-02 | 1.083 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.269403e-01 | 0.896 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.269403e-01 | 0.896 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 1.197813e-01 | 0.922 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 9.300113e-02 | 1.032 | 1 | 1 |
| Gluconeogenesis | R-HSA-70263 | 1.233571e-01 | 0.909 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 8.852008e-02 | 1.053 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.404463e-01 | 0.852 | 1 | 1 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.946571e-02 | 1.100 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.378335e-01 | 0.861 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.233571e-01 | 0.909 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 9.377514e-02 | 1.028 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 9.237526e-02 | 1.034 | 1 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 9.298042e-02 | 1.032 | 0 | 0 |
| PPARA activates gene expression | R-HSA-1989781 | 1.190732e-01 | 0.924 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 1.097309e-01 | 0.960 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 9.569268e-02 | 1.019 | 1 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.092890e-01 | 0.961 | 0 | 0 |
| Regulation of lipid metabolism by PPARalpha | R-HSA-400206 | 1.227200e-01 | 0.911 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 1.136940e-01 | 0.944 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 1.526588e-01 | 0.816 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.526588e-01 | 0.816 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 1.526588e-01 | 0.816 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 1.564132e-01 | 0.806 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.564132e-01 | 0.806 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 1.564132e-01 | 0.806 | 0 | 0 |
| Signaling by CTNNB1 phospho-site mutants | R-HSA-4839743 | 1.588397e-01 | 0.799 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.588397e-01 | 0.799 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.588397e-01 | 0.799 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.588397e-01 | 0.799 | 0 | 0 |
| CTNNB1 S45 mutants aren't phosphorylated | R-HSA-5358751 | 1.588397e-01 | 0.799 | 0 | 0 |
| CTNNB1 S33 mutants aren't phosphorylated | R-HSA-5358747 | 1.588397e-01 | 0.799 | 0 | 0 |
| CTNNB1 T41 mutants aren't phosphorylated | R-HSA-5358752 | 1.588397e-01 | 0.799 | 0 | 0 |
| CTNNB1 S37 mutants aren't phosphorylated | R-HSA-5358749 | 1.588397e-01 | 0.799 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 1.588397e-01 | 0.799 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.588397e-01 | 0.799 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.588397e-01 | 0.799 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.588397e-01 | 0.799 | 0 | 0 |
| Advanced glycosylation endproduct receptor signaling | R-HSA-879415 | 1.588397e-01 | 0.799 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 1.601851e-01 | 0.795 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 1.601851e-01 | 0.795 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 1.644400e-01 | 0.784 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.670538e-01 | 0.777 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.670538e-01 | 0.777 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 1.677782e-01 | 0.775 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.678891e-01 | 0.775 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.678891e-01 | 0.775 | 0 | 0 |
| Replication of the SARS-CoV-1 genome | R-HSA-9682706 | 1.678891e-01 | 0.775 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 1.696798e-01 | 0.770 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 1.715980e-01 | 0.765 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 1.754321e-01 | 0.756 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 1.768417e-01 | 0.752 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.768417e-01 | 0.752 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.768417e-01 | 0.752 | 0 | 0 |
| SARS-CoV-1 Genome Replication and Transcription | R-HSA-9679514 | 1.768417e-01 | 0.752 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.792799e-01 | 0.746 | 0 | 0 |
| Activation of gene expression by SREBF (SREBP) | R-HSA-2426168 | 1.792799e-01 | 0.746 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.856985e-01 | 0.731 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.856985e-01 | 0.731 | 0 | 0 |
| Beta-catenin phosphorylation cascade | R-HSA-196299 | 1.856985e-01 | 0.731 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 1.856985e-01 | 0.731 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.856985e-01 | 0.731 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 1.856985e-01 | 0.731 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.856985e-01 | 0.731 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.856985e-01 | 0.731 | 0 | 0 |
| Protein lipoylation | R-HSA-9857492 | 1.856985e-01 | 0.731 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.856985e-01 | 0.731 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.856985e-01 | 0.731 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.856985e-01 | 0.731 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.870136e-01 | 0.728 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 1.876524e-01 | 0.727 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 1.883839e-01 | 0.725 | 1 | 0 |
| Membrane Trafficking | R-HSA-199991 | 1.893498e-01 | 0.723 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.944606e-01 | 0.711 | 0 | 0 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | R-HSA-9634600 | 1.944606e-01 | 0.711 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 1.944606e-01 | 0.711 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.944606e-01 | 0.711 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 1.956227e-01 | 0.709 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 1.965586e-01 | 0.707 | 0 | 0 |
| G beta:gamma signalling through CDC42 | R-HSA-8964616 | 2.031289e-01 | 0.692 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 2.031289e-01 | 0.692 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 2.031289e-01 | 0.692 | 0 | 0 |
| The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CLOCK) complex | R-HSA-9931521 | 2.031289e-01 | 0.692 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 2.031289e-01 | 0.692 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 2.031289e-01 | 0.692 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 2.031289e-01 | 0.692 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 2.031289e-01 | 0.692 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 2.031289e-01 | 0.692 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 2.031289e-01 | 0.692 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 2.031289e-01 | 0.692 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 2.065376e-01 | 0.685 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 2.065376e-01 | 0.685 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 2.104696e-01 | 0.677 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.117045e-01 | 0.674 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.117045e-01 | 0.674 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.117045e-01 | 0.674 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.117045e-01 | 0.674 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 2.117045e-01 | 0.674 | 0 | 0 |
| Metabolism of ingested H2SeO4 and H2SeO3 into H2Se | R-HSA-2408550 | 2.117045e-01 | 0.674 | 0 | 0 |
| Replication of the SARS-CoV-2 genome | R-HSA-9694686 | 2.117045e-01 | 0.674 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 2.133767e-01 | 0.671 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 2.144092e-01 | 0.669 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 2.144092e-01 | 0.669 | 0 | 0 |
| Synaptic adhesion-like molecules | R-HSA-8849932 | 2.201883e-01 | 0.657 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.201883e-01 | 0.657 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.201883e-01 | 0.657 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 2.201883e-01 | 0.657 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 2.269785e-01 | 0.644 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.285813e-01 | 0.641 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.285813e-01 | 0.641 | 0 | 0 |
| SARS-CoV-2 Genome Replication and Transcription | R-HSA-9694682 | 2.285813e-01 | 0.641 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.302311e-01 | 0.638 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.368845e-01 | 0.625 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.368845e-01 | 0.625 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.368845e-01 | 0.625 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.368845e-01 | 0.625 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.368845e-01 | 0.625 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 2.421483e-01 | 0.616 | 0 | 0 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | R-HSA-1655829 | 2.421483e-01 | 0.616 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 2.431186e-01 | 0.614 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.450989e-01 | 0.611 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.450989e-01 | 0.611 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 2.450989e-01 | 0.611 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 2.450989e-01 | 0.611 | 0 | 0 |
| ERK/MAPK targets | R-HSA-198753 | 2.450989e-01 | 0.611 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.450989e-01 | 0.611 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 2.461274e-01 | 0.609 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.529342e-01 | 0.597 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 2.532253e-01 | 0.596 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 2.532253e-01 | 0.596 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.532253e-01 | 0.596 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 2.532253e-01 | 0.596 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.532253e-01 | 0.596 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.532253e-01 | 0.596 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 2.532253e-01 | 0.596 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 2.612647e-01 | 0.583 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 2.612647e-01 | 0.583 | 1 | 1 |
| Signaling by KIT in disease | R-HSA-9669938 | 2.612647e-01 | 0.583 | 1 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 2.612647e-01 | 0.583 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.612647e-01 | 0.583 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.660501e-01 | 0.575 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 2.660501e-01 | 0.575 | 0 | 0 |
| S Phase | R-HSA-69242 | 2.674038e-01 | 0.573 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 2.674038e-01 | 0.573 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 2.692181e-01 | 0.570 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 2.692181e-01 | 0.570 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.692181e-01 | 0.570 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.692181e-01 | 0.570 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.732200e-01 | 0.563 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.770864e-01 | 0.557 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.770864e-01 | 0.557 | 1 | 1 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.770864e-01 | 0.557 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.770864e-01 | 0.557 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 2.770864e-01 | 0.557 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 2.780081e-01 | 0.556 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 2.819693e-01 | 0.550 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 2.819921e-01 | 0.550 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 2.848704e-01 | 0.545 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.848704e-01 | 0.545 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.848704e-01 | 0.545 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.848704e-01 | 0.545 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 2.848704e-01 | 0.545 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.848704e-01 | 0.545 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.848704e-01 | 0.545 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 2.857871e-01 | 0.544 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.925711e-01 | 0.534 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.925711e-01 | 0.534 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.925711e-01 | 0.534 | 0 | 0 |
| Diseases of branched-chain amino acid catabolism | R-HSA-9865118 | 2.925711e-01 | 0.534 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 2.925711e-01 | 0.534 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 2.939319e-01 | 0.532 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 3.001893e-01 | 0.523 | 1 | 1 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 3.001893e-01 | 0.523 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 3.001893e-01 | 0.523 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 3.001893e-01 | 0.523 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 3.001893e-01 | 0.523 | 1 | 1 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 3.001893e-01 | 0.523 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 3.025442e-01 | 0.519 | 1 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 3.077259e-01 | 0.512 | 0 | 0 |
| Insulin receptor recycling | R-HSA-77387 | 3.077259e-01 | 0.512 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 3.077259e-01 | 0.512 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.077259e-01 | 0.512 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.077259e-01 | 0.512 | 0 | 0 |
| Iron assimilation using enterobactin | R-HSA-9638334 | 3.077259e-01 | 0.512 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 3.083481e-01 | 0.511 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 3.098082e-01 | 0.509 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 3.137670e-01 | 0.503 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 3.142269e-01 | 0.503 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 3.151819e-01 | 0.501 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 3.151819e-01 | 0.501 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.151819e-01 | 0.501 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.151819e-01 | 0.501 | 0 | 0 |
| MAPK targets/ Nuclear events mediated by MAP kinases | R-HSA-450282 | 3.151819e-01 | 0.501 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 3.177210e-01 | 0.498 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 3.216697e-01 | 0.493 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.216697e-01 | 0.493 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 3.225580e-01 | 0.491 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.225580e-01 | 0.491 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 3.225580e-01 | 0.491 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.225580e-01 | 0.491 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 3.256128e-01 | 0.487 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.256128e-01 | 0.487 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 3.298551e-01 | 0.482 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 3.298551e-01 | 0.482 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.298551e-01 | 0.482 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 3.298551e-01 | 0.482 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 3.298551e-01 | 0.482 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 3.370740e-01 | 0.472 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 3.370740e-01 | 0.472 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 3.370740e-01 | 0.472 | 0 | 0 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | R-HSA-2173795 | 3.370740e-01 | 0.472 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 3.374057e-01 | 0.472 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 3.374057e-01 | 0.472 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 3.377572e-01 | 0.471 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 3.436367e-01 | 0.464 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 3.436367e-01 | 0.464 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 3.442157e-01 | 0.463 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 3.442157e-01 | 0.463 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 3.442157e-01 | 0.463 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.442157e-01 | 0.463 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.442157e-01 | 0.463 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.442157e-01 | 0.463 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.442157e-01 | 0.463 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 3.442157e-01 | 0.463 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.442157e-01 | 0.463 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 3.452339e-01 | 0.462 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 3.512808e-01 | 0.454 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.512808e-01 | 0.454 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 3.530324e-01 | 0.452 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.530324e-01 | 0.452 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 3.582702e-01 | 0.446 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.582702e-01 | 0.446 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 3.582702e-01 | 0.446 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.582702e-01 | 0.446 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.582702e-01 | 0.446 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 3.582702e-01 | 0.446 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 3.582702e-01 | 0.446 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.582702e-01 | 0.446 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.582702e-01 | 0.446 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 3.607987e-01 | 0.443 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 3.612468e-01 | 0.442 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 3.646691e-01 | 0.438 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.651848e-01 | 0.437 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 3.651848e-01 | 0.437 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.651848e-01 | 0.437 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 3.651848e-01 | 0.437 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.651848e-01 | 0.437 | 0 | 0 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | R-HSA-2408508 | 3.651848e-01 | 0.437 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 3.651848e-01 | 0.437 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 3.685308e-01 | 0.434 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 3.685308e-01 | 0.434 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 3.720253e-01 | 0.429 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 3.720253e-01 | 0.429 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 3.720253e-01 | 0.429 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 3.787925e-01 | 0.422 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 3.787925e-01 | 0.422 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 3.787925e-01 | 0.422 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 3.787925e-01 | 0.422 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 3.800600e-01 | 0.420 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 3.800600e-01 | 0.420 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.854872e-01 | 0.414 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 3.854872e-01 | 0.414 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.854872e-01 | 0.414 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.854872e-01 | 0.414 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 3.876975e-01 | 0.412 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 3.876975e-01 | 0.412 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.921101e-01 | 0.407 | 0 | 0 |
| NS1 Mediated Effects on Host Pathways | R-HSA-168276 | 3.921101e-01 | 0.407 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 3.921101e-01 | 0.407 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 3.921101e-01 | 0.407 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 3.921101e-01 | 0.407 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.921101e-01 | 0.407 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 3.921101e-01 | 0.407 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 3.986621e-01 | 0.399 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 3.986621e-01 | 0.399 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 4.051439e-01 | 0.392 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 4.051439e-01 | 0.392 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 4.051439e-01 | 0.392 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 4.051439e-01 | 0.392 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 4.051439e-01 | 0.392 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 4.066075e-01 | 0.391 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 4.115561e-01 | 0.386 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 4.115561e-01 | 0.386 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 4.115561e-01 | 0.386 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 4.115561e-01 | 0.386 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 4.115561e-01 | 0.386 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 4.120773e-01 | 0.385 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 4.215331e-01 | 0.375 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 4.241753e-01 | 0.372 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.241753e-01 | 0.372 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.241753e-01 | 0.372 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.241753e-01 | 0.372 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.303836e-01 | 0.366 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 4.303836e-01 | 0.366 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 4.303836e-01 | 0.366 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.303836e-01 | 0.366 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 4.365253e-01 | 0.360 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.365253e-01 | 0.360 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 4.365253e-01 | 0.360 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 4.365253e-01 | 0.360 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.365253e-01 | 0.360 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 4.365253e-01 | 0.360 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 4.365253e-01 | 0.360 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 4.365253e-01 | 0.360 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 4.365253e-01 | 0.360 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 4.365253e-01 | 0.360 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 4.426012e-01 | 0.354 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.426012e-01 | 0.354 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.426012e-01 | 0.354 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 4.426012e-01 | 0.354 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 4.426012e-01 | 0.354 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.486119e-01 | 0.348 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.545582e-01 | 0.342 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.545582e-01 | 0.342 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 4.579810e-01 | 0.339 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 4.604408e-01 | 0.337 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 4.720173e-01 | 0.326 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 4.720173e-01 | 0.326 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.720173e-01 | 0.326 | 0 | 0 |
| Branched-chain amino acid catabolism | R-HSA-70895 | 4.720173e-01 | 0.326 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 4.755165e-01 | 0.323 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.777126e-01 | 0.321 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.777126e-01 | 0.321 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 4.777126e-01 | 0.321 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 4.777126e-01 | 0.321 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 4.944346e-01 | 0.306 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 4.998894e-01 | 0.301 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 4.998894e-01 | 0.301 | 0 | 0 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | R-HSA-2173793 | 4.998894e-01 | 0.301 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 4.998894e-01 | 0.301 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 4.999254e-01 | 0.301 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 5.000140e-01 | 0.301 | 1 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 5.087392e-01 | 0.294 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 5.159053e-01 | 0.287 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.159053e-01 | 0.287 | 0 | 0 |
| snRNP Assembly | R-HSA-191859 | 5.159053e-01 | 0.287 | 0 | 0 |
| Metabolism of non-coding RNA | R-HSA-194441 | 5.159053e-01 | 0.287 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.159053e-01 | 0.287 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 5.159053e-01 | 0.287 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 5.211298e-01 | 0.283 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 5.211298e-01 | 0.283 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 5.211298e-01 | 0.283 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 5.211298e-01 | 0.283 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 5.211298e-01 | 0.283 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 5.211298e-01 | 0.283 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 5.233412e-01 | 0.281 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.262982e-01 | 0.279 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.262982e-01 | 0.279 | 0 | 0 |
| MAP kinase activation | R-HSA-450294 | 5.262982e-01 | 0.279 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 5.314112e-01 | 0.275 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 5.314112e-01 | 0.275 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 5.364692e-01 | 0.270 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 5.365140e-01 | 0.270 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 5.397485e-01 | 0.268 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.414730e-01 | 0.266 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.414730e-01 | 0.266 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.429676e-01 | 0.265 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 5.464231e-01 | 0.262 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 5.489510e-01 | 0.260 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.493590e-01 | 0.260 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 5.493590e-01 | 0.260 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.561644e-01 | 0.255 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.588289e-01 | 0.253 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 5.609568e-01 | 0.251 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.681573e-01 | 0.246 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 5.703877e-01 | 0.244 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 5.703877e-01 | 0.244 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.703877e-01 | 0.244 | 0 | 0 |
| Interleukin-17 signaling | R-HSA-448424 | 5.703877e-01 | 0.244 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.742973e-01 | 0.241 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 5.750274e-01 | 0.240 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 5.750274e-01 | 0.240 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.750274e-01 | 0.240 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 5.750274e-01 | 0.240 | 0 | 0 |
| Metal ion assimilation from the host | R-HSA-9638482 | 5.750274e-01 | 0.240 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 5.796172e-01 | 0.237 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.796172e-01 | 0.237 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.841578e-01 | 0.233 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 5.872212e-01 | 0.231 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 5.886495e-01 | 0.230 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 5.909448e-01 | 0.228 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 5.974889e-01 | 0.224 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 6.061394e-01 | 0.217 | 0 | 0 |
| Cholesterol biosynthesis | R-HSA-191273 | 6.061394e-01 | 0.217 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.061394e-01 | 0.217 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 6.061394e-01 | 0.217 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 6.069335e-01 | 0.217 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.103950e-01 | 0.214 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 6.146050e-01 | 0.211 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.146050e-01 | 0.211 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 6.187697e-01 | 0.208 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.228896e-01 | 0.206 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 6.269653e-01 | 0.203 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.309972e-01 | 0.200 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.349858e-01 | 0.197 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 6.375471e-01 | 0.195 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.389315e-01 | 0.195 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.389315e-01 | 0.195 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 6.428348e-01 | 0.192 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.428348e-01 | 0.192 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.542947e-01 | 0.184 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 6.562036e-01 | 0.183 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.617307e-01 | 0.179 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 6.636465e-01 | 0.178 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 6.639216e-01 | 0.178 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.653889e-01 | 0.177 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 6.690078e-01 | 0.175 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.796325e-01 | 0.168 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.830981e-01 | 0.166 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 6.830981e-01 | 0.166 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 6.932730e-01 | 0.159 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 6.932730e-01 | 0.159 | 0 | 0 |
| MyD88 cascade initiated on plasma membrane | R-HSA-975871 | 6.932730e-01 | 0.159 | 0 | 0 |
| Toll Like Receptor 10 (TLR10) Cascade | R-HSA-168142 | 6.932730e-01 | 0.159 | 0 | 0 |
| Toll Like Receptor 5 (TLR5) Cascade | R-HSA-168176 | 6.932730e-01 | 0.159 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 6.934131e-01 | 0.159 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 6.965919e-01 | 0.157 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 7.031230e-01 | 0.153 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 7.031230e-01 | 0.153 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 7.031230e-01 | 0.153 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.095144e-01 | 0.149 | 0 | 0 |
| Mitochondrial ribosome-associated quality control | R-HSA-9937383 | 7.095144e-01 | 0.149 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.188457e-01 | 0.143 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.249004e-01 | 0.140 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.278790e-01 | 0.138 | 0 | 0 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | R-HSA-975138 | 7.278790e-01 | 0.138 | 0 | 0 |
| MyD88 dependent cascade initiated on endosome | R-HSA-975155 | 7.308254e-01 | 0.136 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 7.394759e-01 | 0.131 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 7.422975e-01 | 0.129 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.478500e-01 | 0.126 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 7.505814e-01 | 0.125 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 7.520211e-01 | 0.124 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 7.579036e-01 | 0.120 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.586004e-01 | 0.120 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 7.601186e-01 | 0.119 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 7.638035e-01 | 0.117 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 7.638035e-01 | 0.117 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.688951e-01 | 0.114 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 7.713998e-01 | 0.113 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 7.713998e-01 | 0.113 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 7.769663e-01 | 0.110 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 8.100770e-01 | 0.091 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 8.100770e-01 | 0.091 | 0 | 0 |
| Mitochondrial translation | R-HSA-5368287 | 8.141761e-01 | 0.089 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 8.161926e-01 | 0.088 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 8.236912e-01 | 0.084 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.278426e-01 | 0.082 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 8.333892e-01 | 0.079 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 8.415177e-01 | 0.075 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.538544e-01 | 0.069 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 8.649712e-01 | 0.063 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.732123e-01 | 0.059 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.825567e-01 | 0.054 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 8.879831e-01 | 0.052 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 8.900190e-01 | 0.051 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 9.003375e-01 | 0.046 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 9.106770e-01 | 0.041 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.106770e-01 | 0.041 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.212290e-01 | 0.036 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.274729e-01 | 0.033 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.384814e-01 | 0.028 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.404750e-01 | 0.027 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.454828e-01 | 0.024 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.470245e-01 | 0.024 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.470245e-01 | 0.024 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.612331e-01 | 0.017 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.820820e-01 | 0.008 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.852602e-01 | 0.006 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.995372e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.997257e-01 | 0.000 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.998247e-01 | 0.000 | 0 | 0 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 1.000000e+00 | 0.000 | 1 | 0 |
| Nef Mediated CD4 Down-regulation | R-HSA-167590 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
