EPHA7
Normalized values from positional scanning peptide array
Phospho-serine (pS) is a duplicate of phospho-tyrosine (pT) in PSPA
Position-wise Probabilities
Log-Odds: Probabilities / STY Background
Sites with acceptor types representing >8% and count ≥10 are included
Y Sites Probabilities
Log-Odds: Y Sites / Y Background
Sites with acceptor types representing >8% and count ≥10 are included
Motif clusters with count ≥ 10 are shown
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| substrate_uniprot | site | source | substrate_genes | site_seq |
|---|---|---|---|---|
| A0FGR8 | Y824 | Sugiyama | ESYT2 FAM62B KIAA1228 | IVVVHACRNLIAFSEDGsDPyVRMYLLPDKRRSGRRKTHVS |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y1572 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | RMPEQIRLKVGGVDPKQLAVyEEFARNVPGFLPTNDLSQPT |
| A6NEC2 | Y173 | Sugiyama | NPEPPSL1 | NDKMKGFYRSKYTTPSGEVRyAAVTQFEATDARRAFPCWDE |
| A6NHL2 | Y319 | Sugiyama | TUBAL3 | TTACFESSNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAI |
| A6NMY6 | Y147 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| A6NMY6 | Y235 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sIMTERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENA |
| A6NMY6 | Y238 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | TERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENAFLN |
| O00116 | Y645 | Sugiyama | AGPS AAG5 | QWLKESIsDVGFGMLKSVKEyVDPNNIFGNRNLL_______ |
| O00170 | Y202 | Sugiyama | AIP XAP2 | IHQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPE |
| O00170 | Y203 | Sugiyama | AIP XAP2 | HQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPEW |
| O00232 | S21 | Sugiyama | PSMD12 | MADGGSERADGRIVKMEVDysATVDQRLPECAKLAKEGRLQ |
| O00232 | Y20 | Sugiyama | PSMD12 | _MADGGSERADGRIVKMEVDysATVDQRLPECAKLAKEGRL |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00410 | Y33 | Sugiyama | IPO5 KPNB3 RANBP5 | LLLGNLLsPDNVVRKQAEEtyENIPGQSKITFLLQAIRNTT |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00469 | S441 | Sugiyama | PLOD2 | HGKLWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYM |
| O00469 | Y444 | Sugiyama | PLOD2 | LWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYMANV |
| O00541 | T365 | Sugiyama | PES1 | FIIRSFGGEVSWDKSLCIGAtyDVTDSRITHQIVDRPGQQT |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O14579 | Y304 | Sugiyama | COPE | HPFIKEYQAKENDFDRLVLQyAPsA________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14602 | Y35 | Sugiyama | EIF1AY | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEALCFDGV |
| O14786 | Y546 | Sugiyama | NRP1 NRP VEGF165R | WKMIMDDSKRKAKSFEGNNNyDTPELRTFPALSTRFIRIYP |
| O14818 | Y145 | Sugiyama | PSMA7 HSPC | RPFGISALIVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGA |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| O14818 | Y176 | Sugiyama | PSMA7 HSPC | WKANAIGRGAKSVREFLEKNyTDEAIETDDLTIKLVIKALL |
| O14910 | S130 | Sugiyama | LIN7A MALS1 VELI1 | ELPKTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLK |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14964 | Y216 | Sugiyama | HGS HRS | KYSTIPKFGIEKEVRVCEPCyEQLNRKAEGKAtsttELPPE |
| O14974 | S910 | Sugiyama | PPP1R12A MBS MYPT1 | yETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDST |
| O14979 | Y167 | Sugiyama | HNRNPDL HNRPDL JKTBP | DGKMFIGGLSWDTsKKDLtEyLSRFGEVVDCtIKTDPVTGR |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15173 | T211 | Sugiyama | PGRMC2 DG6 PMBP | KEKYDYVGRLLKPGEEPsEytDEEDtKDHNKQD________ |
| O15173 | Y210 | Sugiyama | PGRMC2 DG6 PMBP | FKEKYDYVGRLLKPGEEPsEytDEEDtKDHNKQD_______ |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15372 | Y350 | Sugiyama | EIF3H EIF3S3 | IKEFTAQNLGKLFMAQALQEyNN__________________ |
| O43164 | Y63 | Sugiyama | PJA2 KIAA0438 RNF131 | VSFKPCMTRHERSLGRAGDDyEVLELDDVPKENssGssPLD |
| O43237 | Y184 | Sugiyama | DYNC1LI2 DNCLI2 LIC2 | KIPPEKMRELERKFVKDFQDyMEPEEGCQGsPQRRGPLtsG |
| O43252 | Y238 | Sugiyama | PAPSS1 ATPSK1 PAPSS | ELLQERDIVPVDAsYEVKELyVPENKLHLAKTDAETLPALK |
| O43324 | Y59 | Sugiyama | EEF1E1 AIMP3 P18 | PSLTGLTTIAAHLVKQANKEyLLGSTAEEKAIVQQWLEYRV |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43390 | Y431 | Sugiyama | HNRNPR HNRPR | PPDKKRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGR |
| O43390 | Y434 | Sugiyama | HNRNPR HNRPR | KKRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGG |
| O43707 | T725 | Sugiyama | ACTN4 | DLLEQQHQLIQEALIFDNKHtNytMEHIRVGWEQLLTTIAR |
| O43707 | Y212 | Sugiyama | ACTN4 | WKDGLAFNALIHRHRPELIEyDKLRKDDPVTNLNNAFEVAE |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y298 | Sugiyama | ACTN4 | ANRICKVLAVNQENEHLMEDyEKLASDLLEWIRRTIPWLED |
| O43707 | Y441 | Sugiyama | ACTN4 | KAsIHEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEs |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43765 | T194 | Sugiyama | SGTA SGT SGT1 | KHVEAVAYYKKALELDPDNEtyKsNLKIAELKLREAPSPTG |
| O43765 | Y141 | Sugiyama | SGTA SGT SGT1 | NPANAVYFCNRAAAYSKLGNyAGAVQDCERAICIDPAySKA |
| O43795 | Y234 | Sugiyama | MYO1B | GASEELLNKLKLERDFSRyNyLSLDSAKVNGVDDAANFRTV |
| O43823 | Y311 | Sugiyama | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| O43837 | Y171 | Sugiyama | IDH3B | YMTRHNNLDLVIIREQtEGEySsLEHESARGVIECLKIVTR |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y129 | Sugiyama | CALU | VERQWKGHDLNEDGLVsWEEyKNATYGYVLDDPDPDDGFNY |
| 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 |
| O60343 | Y879 | Sugiyama | TBC1D4 AS160 KIAA0603 | ENQKLEASRDELQSRKVKLDyEEVGACQKEVLITWDKKLLN |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60488 | Y582 | Sugiyama | ACSL4 ACS4 FACL4 LACS4 | DGCLQIIDRKKDLVKLQAGEyVsLGKVEAALKNCPLIDNIC |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y293 | Sugiyama | SYNCRIP HNRPQ NSAP1 | VILyHQPDDKKKNRGFCFLEyEDHKTAAQARRRLMSGKVKV |
| O60506 | Y373 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ILEKAFsQFGKLERVKKLKDyAFIHFDERDGAVKAMEEMNG |
| O60568 | Y444 | Sugiyama | PLOD3 | LWSNFWGALSPDEYYARSEDyVELVQRKRVGVWNVPYISQA |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60739 | Y30 | Sugiyama | EIF1B | FDPFADATKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| O60814 | Y38 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60884 | Y66 | Sugiyama | DNAJA2 CPR3 HIRIP4 | KFKEISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDD |
| O60884 | Y69 | Sugiyama | DNAJA2 CPR3 HIRIP4 | EISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDDIFS |
| O60934 | Y679 | Sugiyama | NBN NBS NBS1 P95 | FRSLVIKNSTSRNPSGINDDyGQLKNFKKFKKVTYPGAGKL |
| O75116 | Y722 | Sugiyama | ROCK2 KIAA0619 | EQEEAEHKATKARLADKNKIyEsIEEAKSEAMKEMEKKLLE |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75208 | Y93 | Sugiyama | COQ9 C16orf49 HSPC326 PSEC0129 | PEssHsPPRYTDQGGEEEEDyEsEEQLQHRILTAALEFVPA |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75369 | Y1576 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYGG |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75369 | Y904 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | FNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLVTY |
| O75390 | Y80 | Sugiyama | CS | VGQITVDMMYGGMRGMKGLVyEtsVLDPDEGIRFRGFsIPE |
| O75436 | Y40 | Sugiyama | VPS26A VPS26 | DGETRKMAEMKTEDGKVEKHyLFyDGEsVSGKVNLAFKQPG |
| O75817 | Y38 | Sugiyama | POP7 RPP20 | VEytLRKRLPSRLPRRPNDIyVNMKTDFKAQLARCQKLLDG |
| O75874 | Y231 | Sugiyama | IDH1 PICD | TKNTILKKYDGRFKDIFQEIyDKQyKSQFEAQKIWYEHRLI |
| O75874 | Y391 | Sugiyama | IDH1 PICD | FMTKDLAACIKGLPNVQRsDyLNTFEFMDKLGENLKIKLAQ |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| O94925 | Y249 | Sugiyama | GLS GLS1 KIAA0838 | SHIDELYESAKKQSGGKVADyIPQLAKFSPDLWGVSVCTVD |
| O95218 | Y167 | Sugiyama | ZRANB2 ZIS ZNF265 | EVEDKEsEGEEEDEDEDLsKyKLDEDEDEDDADLsKyNLDA |
| O95297 | Y263 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | QLDHsGGHHSDKINKSEsVVyADIRKN______________ |
| O95340 | Y182 | Sugiyama | PAPSS2 ATPSK2 | GLYKRARAGEIKGFTGIDsDyEKPEtPERVLKTNLSTVSDC |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95376 | Y289 | Sugiyama | ARIH2 ARI2 TRIAD1 HT005 | DCATIRKWLTKCADDSETANyISAHTKDCPKCNICIEKNGG |
| O95400 | Y340 | Sugiyama | CD2BP2 KIAA1178 | RKLDPPGGQFYNSKRIDFDLyT___________________ |
| O95456 | Y287 | Sugiyama | PSMG1 C21LRP DSCR2 PAC1 | PQSTEILKKLMTTNEIQsNIyt___________________ |
| O95551 | Y84 | Sugiyama | TDP2 EAP2 TTRAP AD-022 | PPVEESALERRPETISEPKTyVDLtNEEtTDsttsKISPSE |
| O95573 | Y591 | Sugiyama | ACSL3 ACS3 FACL3 LACS3 | DGCLKIIDRKKDLVKLQAGEyVsLGKVEAALKNLPLVDNIC |
| O95757 | Y30 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | FLNCYIAVARsGGIETIANEySDRCtPACIsLGSRTRAIGN |
| O95757 | Y600 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | IDLPIQssLCRQLGQDLLNsyIENEGKMIMQDKLEKERNDA |
| O95757 | Y627 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MIMQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPED |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O95817 | Y240 | Sugiyama | BAG3 BIS | AAQPsFHQAQKTHyPAQQGEyQtHQPVyHKIQGDDWEPRPL |
| O95834 | Y352 | Sugiyama | EML2 EMAP2 EMAPL2 | EVPEDFGPVRTVAEGHGDtLyVGtTRNSILQGSVHTGFSLL |
| O96019 | T67 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | RDDGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsP |
| O96019 | Y69 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | DGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsPLK |
| P00338 | Y10 | Sugiyama | LDHA PIG19 | ___________MAtLKDQLIyNLLKEEQtPQNKITVVGVGA |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00390 | Y371 | Sugiyama | GSR GLUR GRD1 | TDDKGHIIVDEFQNtNVKGIyAVGDVCGKALLtPVAIAAGR |
| P00491 | Y249 | Sugiyama | PNP NP | RHCGLRVFGFSLITNKVIMDyESLEKANHEEVLAAGKQAAQ |
| 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 |
| P00813 | Y290 | Sugiyama | ADA ADA1 | GAWKPDTEHAVIRLKNDQANysLNTDDPLIFKSTLDTDyQM |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P01893 | Y147 | Sugiyama | HLA-H HLAH | VGPDGPFLRGYEQHAYDGKDyIALNEDLRSWTAADMAAQIT |
| P02545 | Y45 | Sugiyama | LMNA LMN1 | RItRLQEKEDLQELNDRLAVyIDRVRsLETENAGLRLRItE |
| P02786 | Y168 | Sugiyama | TFRC | NENsyVPREAGsQKDENLALyVENQFREFKLSKVWRDQHFV |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P04040 | Y447 | Sugiyama | CAT | GEVRRFNtANDDNVtQVRAFyVNVLNEEQRKRLCENIAGHL |
| 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 | Y87 | Sugiyama | CAPNS1 CAPN4 CAPNS | sAISEAAAQYNPEPPPPRtHysNIEANEsEEVRQFRRLFAQ |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P05067 | Y308 | Sugiyama | APP A4 AD1 | REVCSEQAETGPCRAMISRWyFDVTEGKCAPFFyGGCGGNR |
| P05187 | Y182 | Sugiyama | ALPP PLAP | GKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADVPASARQ |
| P05198 | Y150 | Sugiyama | EIF2S1 EIF2A | LFQRTAWVFDDKyKRPGyGAyDAFKHAVsDPsILDsLDLNE |
| P05783 | Y363 | Sugiyama | KRT18 CYK18 PIG46 | LHLESELAQTRAEGQRQAQEyEALLNIKVKLEAEIATYRRL |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06730 | Y197 | Sugiyama | EIF4E EIF4EL1 EIF4F | THIGRVYKERLGLPPKIVIGyQsHADTAtKsGsttKNRFVV |
| P06733 | S268 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyP |
| P06733 | Y131 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ILGVsLAVCKAGAVEKGVPLyRHIADLAGNsEVILPVPAFN |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y257 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | TDKVVIGMDVAASEFFRsGKyDLDFKsPDDPsRyIsPDQLA |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06737 | Y732 | Sugiyama | PYGL | FGMRIDDVAALDKKGYEAKEyyEALPELKLVIDQIDNGFFS |
| P06737 | Y733 | Sugiyama | PYGL | GMRIDDVAALDKKGYEAKEyyEALPELKLVIDQIDNGFFSP |
| P06737 | Y778 | Sugiyama | PYGL | LFKDIINMLFYHDRFKVFADyEAyVKCQDKVSQLyMNPKAW |
| P06737 | Y781 | Sugiyama | PYGL | DIINMLFYHDRFKVFADyEAyVKCQDKVSQLyMNPKAWNTM |
| P06737 | Y821 | Sugiyama | PYGL | MVLKNIAASGKFSSDRTIKEyAQNIWNVEPsDLKIsLSNES |
| P06744 | Y351 | Sugiyama | GPI | FGCETHAMLPYDQYLHRFAAyFQQGDMEsNGKYITKSGtRV |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07195 | Y84 | Sugiyama | LDHB | MDLQHGsLFLQtPKIVADKDysVtANSKIVVVtAGVRQQEG |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| 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 |
| P07355 | Y238 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | TERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENAFLN |
| P07384 | Y37 | Sugiyama | CAPN1 CANPL1 PIG30 | QVQKQRARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFR |
| 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_________ |
| P07741 | Y60 | Sugiyama | APRT | RAAIGLLARHLKATHGGRIDyIAGLDsRGFLFGPSLAQELG |
| P07814 | Y1504 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | KPLCELQPGAKCVCGKNPAKyytLFGRsy____________ |
| P07814 | Y1505 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PLCELQPGAKCVCGKNPAKyytLFGRsy_____________ |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07858 | Y215 | Sugiyama | CTSB CPSB | RPPCTGEGDTPKCSKICEPGysPtyKQDKHYGYNSYSVSNS |
| P07858 | Y219 | Sugiyama | CTSB CPSB | TGEGDTPKCSKICEPGysPtyKQDKHYGYNSYSVSNSEKDI |
| 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 | Y438 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KKCLELFtELAEDKENyKKFyEQFSKNIKLGIHEDsQNRKK |
| P07900 | Y492 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLR |
| P07900 | Y493 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | EMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLRK |
| P07900 | Y61 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KEIFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLI |
| P07954 | Y54 | Sugiyama | FH | PSFWPPNAARMAsQNSFRIEyDtFGELKVPNDKYYGAQTVR |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | Y155 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | SAYLVAEKVVVITKHNDDEQyAWEssAGGsFtVRADHGEPI |
| P08238 | Y192 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| P08238 | Y276 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P08238 | Y301 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | ELNKtKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHF |
| P08238 | Y305 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | tKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P08238 | Y430 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KKCLELFsELAEDKENyKKFyEAFSKNLKLGIHEDstNRRR |
| P08238 | Y472 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | sELLRyHtsQsGDEMtsLsEyVsRMKEtQKsIyyItGEsKE |
| P08238 | Y484 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVR |
| P08238 | Y485 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVRK |
| P08238 | Y56 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KEIFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDII |
| P08238 | Y619 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | TANMERIMKAQALRDNstMGyMMAKKHLEINPDHPIVEtLR |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| P08758 | S136 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | sRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRMLVVL |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P08865 | Y156 | Sugiyama | RPSA LAMBR LAMR1 | EAsyVNLPtIALCNTDSPLRyVDIAIPCNNKGAHSVGLMWW |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09234 | Y8 | Sugiyama | SNRPC | _____________MPKFyCDyCDtyLtHDsPsVRKTHCSGR |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09874 | Y794 | Sugiyama | PARP1 ADPRT PPOL | AySLLRGGsDDssKDPIDVNyEKLKTDIKVVDRDSEEAEII |
| P09923 | Y179 | Sugiyama | ALPI | GKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADMPASARQ |
| P09972 | Y358 | Sugiyama | ALDOC ALDC | AAQGKYEGSGEDGGAAAQsLyIANHAY______________ |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11047 | Y352 | Sugiyama | LAMC1 LAMB2 | tAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQD |
| P11142 | S432 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGERAMTKD |
| P11142 | T427 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | GGVMTVLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGER |
| P11142 | Y41 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P11142 | Y443 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KQtQtFttysDNQPGVLIQVyEGERAMTKDNNLLGKFELTG |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11233 | Y153 | Sugiyama | RALA RAL | DKRQVsVEEAKNRAEQWNVNyVETSAKTRANVDKVFFDLMR |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11413 | Y118 | Sugiyama | G6PD | LEDFFARNsyVAGQyDDAAsyQRLNsHMNALHLGsQANRLF |
| P11586 | Y258 | Sugiyama | MTHFD1 MTHFC MTHFD | INYVPDDKKPNGRKVVGDVAyDEAKERASFITPVPGGVGPM |
| 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_________ |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12814 | T706 | Sugiyama | ACTN1 | DQLEGDHQLIQEALIFDNKHtNytMEHIRVGWEQLLTTIAR |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y422 | Sugiyama | ACTN1 | KAsIHEAWtDGKEAMLRQKDyEtAtLsEIKALLKKHEAFEs |
| P12814 | Y842 | Sugiyama | ACTN1 | DTDTADQVMASFKILAGDKNyITMDELRRELPPDQAEyCIA |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| 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 | Y137 | Sugiyama | PDIA4 ERP70 ERP72 | VAKIDAtsAsVLAsRFDVsGyPtIKILKKGQAVDyEGsRtQ |
| 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 |
| P13796 | Y462 | Sugiyama | LCP1 PLS2 | VNKPPYPKLGGNMKKLENCNyAVELGKNQAKFsLVGIGGQD |
| P13797 | Y465 | Sugiyama | PLS3 | VNKPPYPKLGANMKKLENCNyAVELGKHPAKFSLVGIGGQD |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13929 | Y131 | Sugiyama | ENO3 | ILGVSLAVCKAGAAEKGVPLyRHIADLAGNPDLILPVPAFN |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14618 | Y148 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | GtAEVELKKGATLKITLDNAyMEKCDENILWLDYKNICKVV |
| P14618 | Y370 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | NAVLDGADCIMLSGEtAKGDyPLEAVRMQHLIAREAEAAIy |
| P14625 | S256 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | PRGNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFIN |
| P14625 | Y258 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | GNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFINFP |
| P14625 | Y401 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | VTFKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDD |
| P14625 | Y429 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | IKLYVRRVFITDDFHDMMPKyLNFVKGVVDsDDLPLNVsRE |
| P14625 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14635 | Y175 | Sugiyama | CCNB1 CCNB | DVDAEDGADPNLCSEYVKDIyAYLRQLEEEQAVRPKYLLGR |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14854 | Y34 | Sugiyama | COX6B1 COX6B | TAPFDSRFPNQNQTRNCWQNyLDFHRCQKAMTAKGGDIsVC |
| P14854 | Y57 | Sugiyama | COX6B1 COX6B | FHRCQKAMTAKGGDIsVCEWyQRVYQsLCPtsWVTDWDEQR |
| P14866 | Y285 | Sugiyama | HNRNPL HNRPL P/OKcl.14 | IEYAKPTRLNVFKNDQDtWDyTNPNLsGQGDPGsNPNKRQR |
| P15153 | Y154 | Sugiyama | RAC2 | LAPITYPQGLALAKEIDSVKyLECsALtQRGLKtVFDEAIR |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15311 | Y424 | Sugiyama | EZR VIL2 | ERQAVDQIKsQEQLAAELAEytAKIALLEEARRRKEDEVEE |
| P15328 | Y80 | Sugiyama | FOLR1 FOLR | WRKNACCSTNTSQEAHKDVsyLyRFNWNHCGEMAPACKRHF |
| P15374 | Y141 | Sugiyama | UCHL3 | KFLEEsVsMsPEERARyLENyDAIRVtHEtsAHEGQTEAPs |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y250 | Sugiyama | RPS2 RPS4 | tAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEFt |
| P17066 | Y43 | Sugiyama | HSPA6 HSP70B' | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P17174 | Y264 | Sugiyama | GOT1 | FVSEGFEFFCAQSFSKNFGLyNERVGNLTVVGKEPESILQV |
| P17706 | Y68 | Sugiyama | PTPN2 PTPT | YRDVSPYDHSRVKLQNAENDyINAsLVDIEEAQRSYILTQG |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17812 | Y473 | Sugiyama | CTPS1 CTPS | RRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVWKKCLE |
| P17812 | Y94 | Sugiyama | CTPS1 CTPS | YERFLDIRLTKDNNLTTGKIyQYVINKERKGDYLGKTVQVV |
| P17844 | Y59 | Sugiyama | DDX5 G17P1 HELR HLR1 | EKLVKKKWNLDELPKFEKNFyQEHPDLARRtAQEVETYRRS |
| P17980 | Y185 | Sugiyama | PSMC3 TBP1 | PtEyDsRVKAMEVDERPtEQysDIGGLDKQIQELVEAIVLP |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17980 | Y438 | Sugiyama | PSMC3 TBP1 | EDYMEGILEVQAKKKANLQYyA___________________ |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18077 | Y106 | Sugiyama | RPL35A GIG33 | AKFRsNLPAKAIGHRIRVMLyPSRI________________ |
| 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 |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18621 | Y4 | Sugiyama | RPL17 | _________________MVRysLDPENPtKsCKSRGSNLRV |
| P18669 | S137 | Sugiyama | PGAM1 PGAMA CDABP0006 | RsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLK |
| P18669 | Y119 | Sugiyama | PGAM1 PGAMA CDABP0006 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| P18669 | Y142 | Sugiyama | PGAM1 PGAMA CDABP0006 | PPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLKDtIAR |
| P18669 | Y26 | Sugiyama | PGAM1 PGAMA CDABP0006 | LVLIRHGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALR |
| P18669 | Y92 | Sugiyama | PGAM1 PGAMA CDABP0006 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| P18754 | Y89 | Sugiyama | RCC1 CHC1 | VVQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSE |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21333 | T730 | Sugiyama | FLNA FLN FLN1 | QVQDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWG |
| P21333 | Y319 | Sugiyama | FLNA FLN FLN1 | KKRAEFTVETRsAGQGEVLVyVEDPAGHQEEAKVTANNDKN |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y451 | Sugiyama | UBA1 A1S9T UBE1 | CLPEDKEVLTEDKCLQRQNRyDGQVAVFGsDLQEKLGKQKY |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22314 | Y60 | Sugiyama | UBA1 A1S9T UBE1 | GMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSVLVSGL |
| P22314 | Y873 | Sugiyama | UBA1 A1S9T UBE1 | DDSNFHMDFIVAASNLRAENyDIPsADRHKSKLIAGKIIPA |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22626 | Y336 | Sugiyama | HNRNPA2B1 HNRPA2B1 | MKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRsRy___ |
| P23193 | Y126 | Sugiyama | TCEA1 GTF2S TFIIS | EsTSsGNVsNRKDETNARDTyVsSFPRAPstsDsVRLKCRE |
| P23246 | Y488 | Sugiyama | SFPQ PSF | PMYQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQV |
| P23246 | Y490 | Sugiyama | SFPQ PSF | YQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQVEK |
| P23284 | Y119 | Sugiyama | PPIB CYPB | DFMIQGGDFtRGDGtGGKsIyGERFPDENFKLKHyGPGWVs |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | T70 | Sugiyama | CFL1 CFL | EEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAtyE |
| 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 |
| P23921 | Y556 | Sugiyama | RRM1 RR1 | yyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPT |
| P23921 | Y74 | Sugiyama | RRM1 RR1 | VELDTLAAETAATLTTKHPDyAILAARIAVSNLHKETKKVF |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P25205 | Y19 | Sugiyama | MCM3 | __MAGtVVLDDVELREAQRDyLDFLDDEEDQGIyQsKVREL |
| P25208 | Y58 | Sugiyama | NFYB HAP3 | SMNDHEDTNGSKESFREQDIyLPIANVARIMKNAIPQTGKI |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26599 | Y127 | Sugiyama | PTBP1 PTB | ANTMVNYYTSVTPVLRGQPIyIQFsNHKELKtDSSPNQARA |
| P26639 | T574 | Sugiyama | TARS1 TARS | RYHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAIL |
| P26639 | Y575 | Sugiyama | TARS1 TARS | YHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAILG |
| P26640 | Y601 | Sugiyama | VARS1 G7A VARS VARS2 | VDMDFGTGAVKITPAHDQNDyEVGQRHGLEAIsIMDsRGAL |
| P26885 | Y112 | Sugiyama | FKBP2 FKBP13 | GLLGMCEGEKRKLVIPsELGyGERGAPPKIPGGATLVFEVE |
| P27348 | Y118 | Sugiyama | YWHAQ | LELLDKYLIANATNPESKVFyLKMKGDYFRyLAEVACGDDR |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27348 | Y19 | Sugiyama | YWHAQ | __MEKTELIQKAKLAEQAERyDDMAtCMKAVtEQGAELsNE |
| P27348 | Y48 | Sugiyama | YWHAQ | AVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSIEQK |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27708 | Y602 | Sugiyama | CAD | FAHTSQVLVDKSLKGWKEIEyEVVRDAYGNCVTVCNMENLD |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P27816 | Y47 | Sugiyama | MAP4 | AtLEAEAFDDVVGETVGKTDyIPLLDVDEKtGNsESKKKPC |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P28066 | Y8 | Sugiyama | PSMA5 | _____________MFLTRsEyDRGVNtFsPEGRLFQVEyAI |
| P28074 | Y171 | Sugiyama | PSMB5 LMPX MB1 X | GMGLSMGTMICGWDKRGPGLyyVDsEGNRISGATFSVGSGS |
| P29144 | Y1042 | Sugiyama | TPP2 | TEALRDLKIQWMTKLDSsDIyNELKEtyPNyLPLyVARLHQ |
| P29144 | Y1052 | Sugiyama | TPP2 | WMTKLDSsDIyNELKEtyPNyLPLyVARLHQLDAEKERMKR |
| P29144 | Y1056 | Sugiyama | TPP2 | LDSsDIyNELKEtyPNyLPLyVARLHQLDAEKERMKRLNEI |
| P29323 | Y800 | Sugiyama | EPHB2 DRT EPHT3 EPTH3 ERK HEK5 TYRO5 | ytsALGGKIPIRWTAPEAIQyRKFTSASDVWSYGIVMWEVM |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | Y202 | Sugiyama | TKT | LDINRLGQsDPAPLQHQMDIyQKRCEAFGWHAIIVDGHSVE |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30043 | S202 | Sugiyama | BLVRB FLR SCAN | GHFMLRCLttDEyDGHstyPsHQyQ________________ |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| P30086 | Y106 | Sugiyama | PEBP1 PBP PEBP | HFLVVNMKGNDIssGtVLsDyVGsGPPKGtGLHRyVWLVyE |
| P30086 | Y120 | Sugiyama | PEBP1 PBP PEBP | GtVLsDyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsN |
| P30086 | Y125 | Sugiyama | PEBP1 PBP PEBP | DyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsNRsGDH |
| P30086 | 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 |
| P30520 | Y428 | Sugiyama | ADSS2 ADSS | WNTDISNARAFKELPVNAQNyVRFIEDELQIPVKWIGVGKs |
| P31150 | Y197 | Sugiyama | GDI1 GDIL OPHN2 RABGDIA XAP4 | LGQDVIDFTGHALALYRTDDyLDQPCLETVNRIKLYsEsLA |
| P31153 | Y235 | Sugiyama | MAT2A AMS2 MATA2 | LDEMRDALKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGP |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31327 | Y634 | Sugiyama | CPS1 | FAMTNQILVEKSVTGWKEIEyEVVRDADDNCVTVCNMENVD |
| P31689 | Y52 | Sugiyama | DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4 | KYHPDKNPNEGEKFKQISQAyEVLSDAKKRELYDKGGEQAI |
| P31939 | T143 | Sugiyama | ATIC PURH OK/SW-cl.86 | QIDIGGVTLLRAAAKNHARVtVVCEPEDyVVVSTEMQSSES |
| P31939 | Y362 | Sugiyama | ATIC PURH OK/SW-cl.86 | IAPGyEEEALTILSKKKNGNyCVLQMDQsYKPDENEVRTLF |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31943 | Y82 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | EsEDEVKLALKKDRETMGHRyVEVFKSNNVEMDWVLKHtGP |
| P31946 | Y120 | Sugiyama | YWHAB | LELLDKyLIPNATQPESKVFyLKMKGDYFRyLsEVAsGDNK |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31946 | Y50 | Sugiyama | YWHAB | AVtEQGHELsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P31947 | Y120 | Sugiyama | SFN HME1 | LGLLDSHLIKEAGDAESRVFyLKMKGDYYRyLAEVATGDDK |
| P31947 | Y151 | Sugiyama | SFN HME1 | LAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIRLG |
| P31947 | Y19 | Sugiyama | SFN HME1 | __MERASLIQKAKLAEQAERyEDMAAFMKGAVEKGEELsCE |
| P31947 | Y48 | Sugiyama | SFN HME1 | GAVEKGEELsCEERNLLsVAyKNVVGGQRAAWRVLSsIEQK |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32780 | Y360 | Sugiyama | GTF2H1 BTF2 | GDADCFQPAVKRAKLQEsIEyEDLGKNNSVKTIALNLKKSD |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32969 | S182 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | QQATTVKNKDIRKFLDGIyVsEKGtVQQADE__________ |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33121 | Y693 | Sugiyama | ACSL1 FACL1 FACL2 LACS LACS1 LACS2 | TMKAKRPELRNYFRSQIDDLyStIKV_______________ |
| P33176 | Y516 | Sugiyama | KIF5B KNS KNS1 | EELAVNyDQKSQEVEDKTKEyELLSDELNQKsATLAsIDAE |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33993 | Y102 | Sugiyama | MCM7 CDC47 MCM2 | QELLPQYKEREVVNKDVLDVyIEHRLMMEQRSRDPGMVRsP |
| P33993 | Y333 | Sugiyama | MCM7 CDC47 MCM2 | EsGAGELtREELRQIAEEDFyEKLAASIAPEIYGHEDVKKA |
| P34897 | Y228 | Sugiyama | SHMT2 | QLALTARLFRPRLIIAGTsAyARLIDYARMREVCDEVKAHL |
| P34931 | Y43 | Sugiyama | HSPA1L | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P34931 | Y547 | Sugiyama | HSPA1L | YKAEDEVQREKIAAKNALEsyAFNMKSVVSDEGLKGKISES |
| 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 |
| P35270 | Y259 | Sugiyama | SPR | QKLLSLLEKDEFKSGAHVDFyDK__________________ |
| P35580 | Y13 | Sugiyama | MYH10 | ________MAQRTGLEDPERyLFVDRAVIYNPATQADWTAK |
| P35609 | T713 | Sugiyama | ACTN2 | DKLEGDHQLIQEALVFDNKHtNytMEHIRVGWELLLTTIAR |
| P35637 | Y468 | Sugiyama | FUS TLS | KAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRGGYRGRG |
| P36871 | Y157 | Sugiyama | PGM1 | GPAPEAITDKIFQISKTIEEyAVCPDLKVDLGVLGKQQFDL |
| P36871 | Y430 | Sugiyama | PGM1 | EDILKDHWQKYGRNFFtRyDyEEVEAEGANKMMKDLEALMF |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P36915 | Y599 | Sugiyama | GNL1 HSR1 | EGDEEtPTSAPGSSLAGRNPyALLGEDEC____________ |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P37837 | Y206 | Sugiyama | TALDO1 TAL TALDO TALDOR | ISPFVGRILDWHVANTDKKSyEPLEDPGVKSVTKIYNYYKK |
| P38646 | Y118 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | ERLVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIK |
| P38646 | Y181 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | YSPSQIGAFVLMKMKEtAENyLGHtAKNAVItVPAyFNDsQ |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40429 | Y149 | Sugiyama | RPL13A | LKPTRKFAYLGRLAHEVGWKyQAVtAtLEEKRKEKAKIHYR |
| P40429 | Y192 | Sugiyama | RPL13A | KQLMRLRKQAEKNVEKKIDKyTEVLKTHGLLV_________ |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40926 | Y80 | Sugiyama | MDH2 | HtPGVAADLsHIEtKAAVKGyLGPEQLPDCLKGCDVVVIPA |
| P40939 | Y637 | Sugiyama | HADHA HADH | ELLTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILA |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41252 | Y148 | Sugiyama | IARS1 IARS | SAEWKSTVsRLGRWIDFDNDyKTLYPQFMESVWWVFKQLYD |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42025 | Y33 | Sugiyama | ACTR1B CTRN2 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALE |
| P42025 | Y38 | Sugiyama | ACTR1B CTRN2 | SGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALEGDLFI |
| P42704 | Y1341 | Sugiyama | LRPPRC LRP130 | YNSLMKSYVSEKDVTSAKALyEHLTAKNTKLDDLFLKRYAS |
| P43034 | Y137 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | HPVFSVMVSASEDATIKVWDyEtGDFERtLKGHtDsVQDIs |
| P43034 | Y18 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | ___MVLSQRQRDELNRAIADyLRSNGyEEAySVFKKEAELD |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43246 | Y238 | Sugiyama | MSH2 | QRGGILITERKKADFSTKDIyQDLNRLLKGKKGEQMNSAVL |
| P43490 | Y34 | Sugiyama | NAMPT PBEF PBEF1 | ATDSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKY |
| P43490 | Y36 | Sugiyama | NAMPT PBEF PBEF1 | DSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKYEE |
| P43490 | Y471 | Sugiyama | NAMPT PBEF PBEF1 | EEYGQDLLHTVFKNGKVTKsysFDEIRKNAQLNIELEAAHH |
| P45974 | Y70 | Sugiyama | USP5 ISOT | FLGFGKQYVERHFNKTGQRVyLHLRRTRRPKEEDPATGTGD |
| P46109 | Y15 | Sugiyama | CRKL | ______MSSARFDssDRsAWyMGPVsRQEAQtRLQGQRHGM |
| P46777 | Y207 | Sugiyama | RPL5 MSTP030 | sKEFNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyI |
| P46777 | Y219 | Sugiyama | RPL5 MSTP030 | IMGQNVADyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEM |
| P46777 | Y226 | Sugiyama | RPL5 MSTP030 | DyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEMyKKAHAA |
| P46777 | Y253 | Sugiyama | RPL5 MSTP030 | PDMMEEMyKKAHAAIRENPVyEKKPKKEVKKKRWNRPKMsL |
| P46778 | Y156 | Sugiyama | RPL21 | REAHFVRTNGKEPELLEPIPyEFMA________________ |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P47224 | Y114 | Sugiyama | RABIF MSS4 RASGRF3 | CADCEIGPIGWHCLDDKNSFyVALERVSHE___________ |
| P47712 | Y535 | Sugiyama | PLA2G4A CPLA2 PLA2G4 | sFDDDELDAAVADPDEFERIyEPLDVKSKKIHVVDSGLTFN |
| P47756 | Y232 | Sugiyama | CAPZB | NIGRLVEDMENKIRstLNEIyFGKTKDIVNGLRSVQTFADK |
| P47756 | Y59 | Sugiyama | CAPZB | LLSSVDQPLKIARDKVVGKDyLLCDyNRDGDSyRsPWSNKy |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47813 | Y35 | Sugiyama | EIF1AX EIF1A EIF4C | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEAMCFDGV |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48637 | S394 | Sugiyama | GSS | LyGEEMVQALKQLKDSEERAsyILMEKIEPEPFENCLLRPG |
| P48637 | Y395 | Sugiyama | GSS | yGEEMVQALKQLKDSEERAsyILMEKIEPEPFENCLLRPGs |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | Y43 | Sugiyama | HSPA7 HSP70B | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P49189 | Y360 | Sugiyama | ALDH9A1 ALDH4 ALDH7 ALDH9 | LGFVKVAKEQGAKVLCGGDIyVPEDPKLKDGYYMRPCVLTN |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | Y2034 | Sugiyama | FASN FAS | DYFVVFSSVSCGRGNAGQsNyGFANsAMERICEKRRHEGLP |
| P49327 | Y277 | Sugiyama | FASN FAS | KEQGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGT |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49458 | Y18 | Sugiyama | SRP9 | ___MPQYQTWEEFSRAAEKLyLADPMKARVVLKYRHsDGNL |
| P49588 | Y667 | Sugiyama | AARS1 AARS | QQIKKAEEIANEMIEAAKAVyTQDCPLAAAKAIQGLRAVFD |
| P49588 | Y690 | Sugiyama | AARS1 AARS | DCPLAAAKAIQGLRAVFDEtyPDPVRVVSIGVPVSELLDDP |
| P49736 | Y137 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | MRQRDREAGRGLGRMRRGLLyDsDEEDEERPARKRRQVERA |
| P49736 | Y234 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | VFKERIsDMCKENREsLVVNyEDLAAREHVLAYFLPEAPAE |
| P49756 | Y503 | Sugiyama | RBM25 RNPC7 | EERRREMAKEAKRLKEFLEDyDDDRDDPKYYRGsALQKRLR |
| P49903 | Y12 | Sugiyama | SEPHS1 SELD SPS SPS1 | _________MsTREsFNPESyELDKsFRLTRFTELKGTGCK |
| P50395 | T408 | Sugiyama | GDI2 RABGDIB | VPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRMtGsE |
| P50395 | Y197 | Sugiyama | GDI2 RABGDIB | LGQDVIDFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLA |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50395 | Y404 | Sugiyama | GDI2 RABGDIB | SDLLVPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRM |
| P50502 | Y213 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | RLLGHWEEAAHDLALACKLDyDEDAsAMLKEVQPRAQKIAE |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50995 | Y482 | Sugiyama | ANXA11 ANX11 | sEtDLLDIRSEYKRMYGKsLyHDISGDtsGDyRKILLKICG |
| P50995 | Y493 | Sugiyama | ANXA11 ANX11 | YKRMYGKsLyHDISGDtsGDyRKILLKICGGND________ |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51659 | Y73 | Sugiyama | HSD17B4 EDH17B4 SDR8C1 | LAADKVVEEIRRRGGKAVANyDsVEEGEKVVKTALDAFGRI |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52298 | Y14 | Sugiyama | NCBP2 CBP20 PIG55 | _______MSGGLLKALRsDsyVELSQYRDQHFRGDNEEQEK |
| P52565 | Y144 | Sugiyama | ARHGDIA GDIA1 | SGMKYIQHTyRKGVKIDKtDyMVGsYGPRAEEyEFLtPVEE |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | Y82 | Sugiyama | HNRNPF HNRPF | GsEDDVKMALKKDRESMGHRyIEVFKSHRTEMDWVLKHsGP |
| P52788 | Y336 | Sugiyama | SMS | GNCVNLTEALSLYEEQLGRLyCPVEFSKEIVCVPSYLELWV |
| 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 | T121 | Sugiyama | PPP5C PPP5 | RRAASNMALGKFRAALRDyEtVVKVKPHDKDAKMKYQECNK |
| P53611 | Y26 | Sugiyama | RABGGTB GGTB | KDVIIKsDAPDTLLLEKHADyIASYGSKKDDYEYCMSEYLR |
| P53621 | T390 | Sugiyama | COPA | YNPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEG |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P54105 | Y38 | Sugiyama | CLNS1A CLCI ICLN | RQQPDTEAVLNGKGLGtGtLyIAEsRLSWLDGsGLGFSLEY |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54577 | Y388 | Sugiyama | YARS1 YARS | LDIRVGKIITVEKHPDADsLyVEKIDVGEAEPRTVVSGLVQ |
| P54646 | Y179 | Sugiyama | PRKAA2 AMPK AMPK2 | GLSNMMsDGEFLRtsCGsPNyAAPEVISGRLYAGPEVDIWS |
| P54652 | Y42 | Sugiyama | HSPA2 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P55060 | Y278 | Sugiyama | CSE1L CAS XPO2 | EEEAGLLELLKSQICDNAALyAQKyDEEFQRYLPRFVTAIW |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55084 | T359 | Sugiyama | HADHB MSTP029 | DFMYVSQDPKDQLLLGPtYAtPKVLEKAGLTMNDIDAFEFH |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55786 | Y173 | Sugiyama | NPEPPS PSA | NDKMKGFYRSKYTTPSGEVRyAAVTQFEATDARRAFPCWDE |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55795 | Y82 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | EsEEEVKLALKKDRETMGHRyVEVFKSNsVEMDWVLKHtGP |
| P55809 | Y43 | Sugiyama | OXCT1 OXCT SCOT | TWYKGCVCSFSTSAHRHTKFyTDPVEAVKDIPDGATVLVGG |
| P55884 | Y222 | Sugiyama | EIF3B EIF3S9 | KLKNVIHKIFSKFGKITNDFyPEEDGKTKGyIFLEyAsPAH |
| P55884 | Y306 | Sugiyama | EIF3B EIF3S9 | PFKDLGNLRYWLEEAECRDQysVIFESGDRTSIFWNDVKDP |
| P55884 | Y768 | Sugiyama | EIF3B EIF3S9 | ERRRTMMEDFRKYRKMAQELyMEQKNERLELRGGVDTDELD |
| P57053 | Y38 | Sugiyama | H2BC12L H2BFS H2BS1 | AVTKAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y38 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | S212 | Sugiyama | TPI1 TPI | WLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDGFLV |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60174 | Y48 | Sugiyama | TPI1 TPI | tLNAAKVPADtEVVCAPPtAyIDFARQKLDPKIAVAAQNCy |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | Y198 | Sugiyama | ACTB | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P60709 | Y240 | Sugiyama | ACTB | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P60709 | Y294 | Sugiyama | ACTB | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P60709 | Y362 | Sugiyama | ACTB | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P60763 | Y154 | Sugiyama | RAC3 | LAPITYPQGLAMAREIGSVKyLECsALtQRGLKtVFDEAIR |
| P60842 | Y197 | Sugiyama | EIF4A1 DDX2A EIF4A | KMFVLDEADEMLsRGFKDQIyDIFQKLNsNtQVVLLSATMP |
| P60842 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60900 | Y160 | Sugiyama | PSMA6 PROS27 | LIGIDEEQGPQVYKCDPAGyyCGFKATAAGVKQtEstsFLE |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61081 | T176 | Sugiyama | UBE2M UBC12 | NRRLFEQNVQRSMRGGyIGstyFERCLK_____________ |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61088 | Y147 | Sugiyama | UBE2N BLU | EQWKTNEAQAIETARAWtRLyAMNNI_______________ |
| P61158 | Y231 | Sugiyama | ACTR3 ARP3 | REVGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSK |
| P61158 | Y233 | Sugiyama | ACTR3 ARP3 | VGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSKWI |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61163 | Y33 | Sugiyama | ACTR1A CTRN1 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALE |
| P61163 | Y38 | Sugiyama | ACTR1A CTRN1 | SGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALEGDIFI |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61247 | Y31 | Sugiyama | RPS3A FTE1 MFTL | KGGKKGAKKKVVDPFSKKDWyDVKAPAMFNIRNIGKTLVTR |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61353 | Y75 | Sugiyama | RPL27 | AAMGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtV |
| P61353 | Y77 | Sugiyama | RPL27 | MGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVN |
| P61353 | Y85 | Sugiyama | RPL27 | RSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVNKDVFRDPA |
| P61604 | Y100 | Sugiyama | HSPE1 | KVVLDDKDyFLFRDGDILGKyVD__________________ |
| P61604 | Y88 | Sugiyama | HSPE1 | GDKVLLPEyGGtKVVLDDKDyFLFRDGDILGKyVD______ |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | Y123 | Sugiyama | YWHAG | LLDNYLIKNCsETQyEsKVFyLKMKGDYYRYLAEVATGEKR |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62191 | Y439 | Sugiyama | PSMC1 | FKKSKENVLyKKQEGtPEGLyL___________________ |
| P62195 | Y148 | Sugiyama | PSMC5 SUG1 | PNKVDPLVSLMMVEKVPDSTyEMIGGLDKQIKEIKEVIELP |
| P62241 | Y113 | Sugiyama | RPS8 OK/SW-cl.83 | TKTLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEE |
| P62241 | Y117 | Sugiyama | RPS8 OK/SW-cl.83 | VKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEEIL |
| P62249 | Y115 | Sugiyama | RPS16 | YYQKYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGP |
| P62258 | Y131 | Sugiyama | YWHAE | AANtGEsKVFyyKMKGDYHRyLAEFAtGNDRKEAAENsLVA |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y214 | Sugiyama | YWHAE | LAKAAFDDAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P62258 | Y49 | Sugiyama | YWHAE | KVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssIEQK |
| P62263 | S69 | Sugiyama | RPS14 PRO2640 | GKETICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELG |
| P62269 | S96 | Sugiyama | RPS18 D6S218E | QYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLKK |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62333 | Y328 | Sugiyama | PSMC6 SUG2 | ARLDILKIHAGPITKHGEIDyEAIVKLSDGFNGADLRNVCT |
| P62714 | Y284 | Sugiyama | PPP2CB | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRT |
| P62714 | Y80 | Sugiyama | PPP2CB | GQFHDLMELFRIGGKsPDtNyLFMGDyVDRGYYSVETVTLL |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62745 | Y154 | Sugiyama | RHOB ARH6 ARHB | MKQEPVRTDDGRAMAVRIQAyDyLECSAKTKEGVREVFETA |
| P62745 | Y156 | Sugiyama | RHOB ARH6 ARHB | QEPVRTDDGRAMAVRIQAyDyLECSAKTKEGVREVFETATR |
| 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 | Y38 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | AVTKAQKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssK |
| P62807 | Y41 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | KAQKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P62807 | Y43 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | QKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P62826 | Y146 | Sugiyama | RAN ARA24 OK/SW-cl.81 | IKDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLAR |
| P62826 | Y147 | Sugiyama | RAN ARA24 OK/SW-cl.81 | KDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLARK |
| P62847 | Y76 | Sugiyama | RPS24 | FVFGFRTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGL |
| P62847 | Y81 | Sugiyama | RPS24 | RTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGLYEKKK |
| P62888 | Y62 | Sugiyama | RPL30 | KAKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELG |
| P62888 | Y63 | Sugiyama | RPL30 | AKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELGt |
| P62899 | Y25 | Sugiyama | RPL31 | KKGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRA |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63000 | Y154 | Sugiyama | RAC1 TC25 MIG5 | LTPITYPQGLAMAKEIGAVKyLECsALtQRGLKtVFDEAIR |
| P63092 | Y190 | Sugiyama | GNAS GNAS1 GSP | QLIDCAQYFLDKIDVIKQADyVPSDQDLLRCRVLTSGIFET |
| P63104 | Y118 | Sugiyama | YWHAZ | LsLLEKFLIPNAsQAEsKVFyLKMKGDYYRyLAEVAAGDDK |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | Y198 | Sugiyama | ACTG1 ACTG | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P63261 | Y240 | Sugiyama | ACTG1 ACTG | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P63261 | Y294 | Sugiyama | ACTG1 ACTG | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P63261 | Y362 | Sugiyama | ACTG1 ACTG | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67775 | Y284 | Sugiyama | PPP2CA | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRt |
| P67775 | Y80 | Sugiyama | PPP2CA | GQFHDLMELFRIGGKsPDtNyLFMGDyVDRGYYSVETVTLL |
| P67809 | Y162 | Sugiyama | YBX1 NSEP1 YB1 | RNHYRRYPRRRGPPRNyQQNyQNsEsGEKNEGsEsAPEGQA |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68104 | Y254 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68104 | Y86 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | ERERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGT |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68363 | S439 | Sugiyama | TUBA1B | SEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy________ |
| P68363 | Y312 | Sugiyama | TUBA1B | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68366 | Y312 | Sugiyama | TUBA4A TUBA1 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68400 | T326 | Sugiyama | CSNK2A1 CK2A1 | RYDHQSRLTAREAMEHPyFytVVKDQARMGSSSMPGGStPV |
| P68400 | Y255 | Sugiyama | CSNK2A1 CK2A1 | GHDNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGR |
| P68400 | Y323 | Sugiyama | CSNK2A1 CK2A1 | KLLRYDHQSRLTAREAMEHPyFytVVKDQARMGSSSMPGGS |
| P78356 | Y117 | Sugiyama | PIP4K2B PIP5K2B | EYCPMVFRNLRERFGIDDQDyQNsVTRSAPINSDSQGRCGT |
| P80303 | Y350 | Sugiyama | NUCB2 NEFA | PDsWEtLDQQQFFtEEELKEyENIIALQENELKKKADELQK |
| P84090 | Y22 | Sugiyama | ERH | sHTILLVQPTKRPEGRtyADyEsVNECMEGVCKMYEEHLKR |
| P84095 | Y40 | Sugiyama | RHOG ARHG | LICYTTNAFPKEyIPTVFDNySAQsAVDGRTVNLNLWDTAG |
| P84103 | Y13 | Sugiyama | SRSF3 SFRS3 SRP20 | ________MHRDsCPLDCKVyVGNLGNNGNKtELERAFGyy |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| Q00169 | Y140 | Sugiyama | PITPNA PITPN | GTQENVHKLEPEAWKHVEAVyIDIADRSQVLSKDYKAEEDP |
| Q00341 | Y358 | Sugiyama | HDLBP HBP VGL | SETVILRGEPEKLGQALTEVyAKANsFTVSSVAAPSWLHRF |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00534 | Y13 | Sugiyama | CDK6 CDKN6 | ________MEKDGLCRADQQyECVAEIGEGAyGKVFKARDL |
| Q00610 | Y1487 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LNNLFITEEDyQALRTsIDAyDNFDNIsLAQRLEKHELIEF |
| Q00610 | Y377 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LAGAEELFARKFNALFAQGNySEAAKVAANAPKGILRtPDt |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00653 | Y247 | Sugiyama | NFKB2 LYT10 | NLKISRMDKTAGSVRGGDEVyLLCDKVQKDDIEVRFYEDDE |
| Q00839 | Y260 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | GDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVEEED |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q02543 | Y110 | Sugiyama | RPL18A | tHNMYREyRDLttAGAVtQCyRDMGARHRARAHsIQIMKVE |
| Q02809 | Y434 | Sugiyama | PLOD1 LLH PLOD | LWSNFWGALSADGYYARSEDyVDIVQGRRVGVWNVPYISNI |
| Q02878 | Y115 | Sugiyama | RPL6 TXREB1 | PVGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQ |
| Q04206 | Y100 | Sugiyama | RELA NFKB3 | DPPHRPHPHELVGKDCRDGFyEAELCPDRCIHSFQNLGIQC |
| Q04446 | Y200 | Sugiyama | GBE1 | PEHSYEFKHSRPKKPRSLRIyESHVGISSHEGKVASYKHFT |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04721 | Y129 | Sugiyama | NOTCH2 | CFVSRPCLNGGTCHMLSRDtyECtCQVGFTGKECQWTDACL |
| Q04760 | Y136 | PSP | GLO1 | HNGNsDPRGFGHIGIAVPDVySACKRFEELGVKFVKKPDDG |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y123 | Sugiyama | YWHAH YWHA1 | LLDKFLIKNCNDFQYESKVFyLKMKGDYYRYLAEVASGEKK |
| Q04917 | Y154 | Sugiyama | YWHAH YWHA1 | LAEVASGEKKNsVVEAsEAAyKEAFEISKEQMQPTHPIRLG |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05048 | T364 | Sugiyama | CSTF1 | YTGAGLSGRQVHRTQAVFNHtEDyVLLPDERTIsLCCWDSR |
| Q05048 | Y367 | Sugiyama | CSTF1 | AGLSGRQVHRTQAVFNHtEDyVLLPDERTIsLCCWDSRTAE |
| Q05209 | Y88 | Sugiyama | PTPN12 | LPFDHSRVKLTLKtPsQDSDyINANFIKGVYGPKAYVATQG |
| Q05519 | Y425 | Sugiyama | SRSF11 SFRS11 | EKDRERKSEsDKDVKQVtRDyDEEEQGYDsEKEKKEEKKPI |
| Q05639 | Y254 | Sugiyama | EEF1A2 EEF1AL STN | TILPPTRPTDKPLRLPLQDVyKIGGIGtVPVGRVETGILRP |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q06830 | Y34 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | NFKAtAVMPDGQFKDIsLsDyKGKYVVFFFYPLDFTFVCPT |
| Q07157 | Y1066 | Sugiyama | TJP1 ZO1 | VEKQAsRDLEQPtyRyEsssytDQFsRNYEHRLRYEDRVPM |
| Q07157 | Y669 | Sugiyama | TJP1 ZO1 | IFGPIADVAREKLAREEPDIyQIAKSEPRDAGTDQRSsGII |
| Q07666 | Y145 | Sugiyama | KHDRBS1 SAM68 | LtAEIEKIQKGDSKKDDEENyLDLFsHKNMKLKERVLIPVK |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q08752 | Y323 | Sugiyama | PPID CYP40 CYPD | DPSNTKALYRRAQGWQGLKEyDQALADLKKAQGIAPEDKAI |
| Q08J23 | Y51 | Sugiyama | NSUN2 SAKI TRM4 | EAGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALR |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q08J23 | Y537 | Sugiyama | NSUN2 SAKI TRM4 | EDPFVFIPEDDPLFPPIEKFyALDPSFPRMNLLTRTTEGKK |
| Q12805 | Y369 | Sugiyama | EFEMP1 FBLN3 FBNL | MCWNYHGGFRCYPRNPCQDPyILTPENRCVCPVsNAMCREL |
| Q12874 | Y50 | Sugiyama | SF3A3 SAP61 | KSTLRDQINSDHRTRAMQDRyMEVSGNLRDLyDDKDGLRKE |
| Q12906 | Y579 | Sugiyama | ILF3 DRBF MPHOSPH4 NF90 | VEVDGQKFQGAGSNKKVAKAyAALAALEKLFPDtPLALDAN |
| Q12931 | Y498 | Sugiyama | TRAP1 HSP75 HSPC5 | GQLtsLsEyASRMRAGtRNIyyLCAPNRHLAEHsPyyEAMK |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q13085 | Y2144 | Sugiyama | ACACA ACAC ACC1 ACCA | VEIKFRRKDLVKTMRRVDPVyIHLAERLGTPELSTAERKEL |
| Q13131 | Y190 | Sugiyama | PRKAA1 AMPK1 | GLsNMMsDGEFLRtsCGsPNyAAPEVISGRLYAGPEVDIWS |
| Q13200 | Y110 | Sugiyama | PSMD2 TRAP2 | TSVPKPLKFLRPHyGKLKEIyENMAPGENKRFAADIISVLA |
| Q13242 | Y17 | Sugiyama | SRSF9 SFRS9 SRP30C | ____MsGWADERGGEGDGRIyVGNLPTDVREKDLEDLFyKY |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13263 | Y517 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | LtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQPGtA |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13310 | Y238 | Sugiyama | PABPC4 APP1 PABP4 | LSVKVMRDPNGKSKGFGFVSyEKHEDANKAVEEMNGKEISG |
| Q13310 | Y291 | Sugiyama | PABPC4 APP1 PABP4 | ERQAELKRKFEQLKQERISRyQGVNLyIKNLDDTIDDEKLR |
| Q13310 | Y297 | Sugiyama | PABPC4 APP1 PABP4 | KRKFEQLKQERISRyQGVNLyIKNLDDTIDDEKLRKEFsPF |
| Q13356 | Y212 | Sugiyama | PPIL2 | DPSYYLKNTNAETRETLQELyKEFKGDEILAATMKAPEKKK |
| 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 | T18 | Sugiyama | PDAP1 HASPP28 | ___MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEE |
| Q13510 | Y305 | Sugiyama | ASAH1 ASAH HSD-33 HSD33 | GNQSGEGCVITRDRKESLDVyELDAKQGRWYVVQTNYDRWK |
| Q13561 | Y207 | Sugiyama | DCTN2 DCTN50 | SKGGSGGKttGtPPDssLVtyELHsRPEQDKFSQAAKVAEL |
| Q13561 | Y313 | Sugiyama | DCTN2 DCTN50 | IAKHKASVEDADTQSKVHQLyEtIQRWsPIASTLPELVQRL |
| Q13561 | Y6 | Sugiyama | DCTN2 DCTN50 | _______________MADPKyADLPGIARNEPDVYETSDLP |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13630 | Y316 | Sugiyama | GFUS SDR4E1 TSTA3 | FRFTPFKQAVKETCAWFTDNyEQARK_______________ |
| Q13642 | Y117 | Sugiyama | FHL1 SLIM1 | DsPKCKGCFKAIVAGDQNVEyKGtVWHKDCFTCSNCKQVIG |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q14118 | Y524 | Sugiyama | DAG1 | DRVDAWVGTYFEVKIPSDtFyDHEDTTTDKLKLTLKLREQQ |
| Q14152 | Y697 | Sugiyama | EIF3A EIF3S10 KIAA0139 | LEKEKKELQERLKNQEKKIDyFERAKRLEEIPLIKSAYEEQ |
| Q14192 | Y154 | Sugiyama | FHL2 DRAL SLIM3 | QPIGTKSFIPKDNQNFCVPCyEKQHAMQCVQCKKPITTGGV |
| Q14204 | Y2265 | Sugiyama | DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325 | EGVEGVAHIIDPKAISKDHLyGtLDPNTREWTDGLFTHVLR |
| Q14204 | Y2881 | Sugiyama | DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325 | IDREKAMSRPILYSNWLSKDyIPVDQEELRDyVKARLKVFY |
| Q14204 | Y3379 | Sugiyama | DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325 | ISDAIREKMKKNYMSNPSYNyEIVNRASLACGPMVKWAIAQ |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | Y421 | Sugiyama | CTTN EMS1 | tPPVsPAPQPtEERLPssPVyEDAAsFKAELsyRGPVsGtE |
| Q14247 | Y545 | Sugiyama | CTTN EMS1 | IDDGWWRGVCKGRyGLFPANyVELRQ_______________ |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14258 | Y245 | Sugiyama | TRIM25 EFP RNF147 ZNF147 | NRQQDVRMTANRKVEQLQQEytEMKALLDASETTSTRKIKE |
| Q14432 | Y405 | Sugiyama | PDE3A | LTFQAIHKPRVNPVtsLsENytCsDsEESSEKDKLAIPKRL |
| Q14568 | Y160 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGERM |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14671 | Y1123 | Sugiyama | PUM1 KIAA0099 PUMH1 | TMNDGPHSALYTMMKDQYANyVVQKMIDVAEPGQRKIVMHK |
| Q14677 | Y114 | Sugiyama | CLINT1 ENTH EPN4 EPNR KIAA0171 | SERVVTSAREHIyDLRSLENyHFVDEHGKDQGINIRQKVKE |
| Q14683 | Y516 | Sugiyama | SMC1A DXS423E KIAA0178 SB1.8 SMC1 SMC1L1 | RQQRKAEIMESIKRLYPGsVyGRLIDLCQPTQKKYQIAVTK |
| Q14696 | Y58 | Sugiyama | MESD KIAA0081 MESDC2 MESDM UNQ1911/PRO4369 | PGTPDESTPPPRKKKKDIRDyNDADMARLLEQWEKDDDIEE |
| Q14697 | Y489 | Sugiyama | GANAB G2AN KIAA0088 | PHIKVDSGyRVHEELRNLGLyVKtRDGSDyEGWCWPGSAGY |
| Q14697 | Y60 | Sugiyama | GANAB G2AN KIAA0088 | tCEEssFCKRQRsIRPGLsPyRALLDSLQLGPDSLTVHLIH |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q15008 | Y366 | Sugiyama | PSMD6 KIAA0107 PFAAP4 | KIDKVNEIVETNRPDsKNWQyQETIKKGDLLLNRVQKLSRV |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15056 | Y86 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | sIRsVRLVRDKDTDKFKGFCyVEFDEVDsLKEALtyDGALL |
| Q15067 | Y232 | Sugiyama | ACOX1 ACOX | IGTHKPLPGITVGDIGPKFGyDEIDNGyLKMDNHRIPRENM |
| Q15067 | Y239 | Sugiyama | ACOX1 ACOX | PGITVGDIGPKFGyDEIDNGyLKMDNHRIPRENMLMKYAQV |
| Q15149 | Y3362 | Sugiyama | PLEC PLEC1 | TGLsLLPLSEKAARARQEELySELQAREtFEKTPVEVPVGG |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15375 | T613 | Sugiyama | EPHA7 EHK3 HEK11 | DEELyFHFKFPGTKTyIDPEtyEDPNRAVHQFAKELDASCI |
| Q15375 | T792 | Sugiyama | EPHA7 EHK3 HEK11 | CKVSDFGLsRVIEDDPEAVytttGGKIPVRWTAPEAIQyRK |
| Q15375 | T793 | Sugiyama | EPHA7 EHK3 HEK11 | KVSDFGLsRVIEDDPEAVytttGGKIPVRWTAPEAIQyRKF |
| Q15375 | T794 | Sugiyama | EPHA7 EHK3 HEK11 | VSDFGLsRVIEDDPEAVytttGGKIPVRWTAPEAIQyRKFT |
| Q15375 | T945 | Sugiyama | EPHA7 EHK3 HEK11 | FCSVGEWLQAIKMERyKDNFtAAGyNsLESVARMTIEDVMS |
| Q15375 | Y608 | Sugiyama | EPHA7 EHK3 HEK11 | ADQEGDEELyFHFKFPGTKTyIDPEtyEDPNRAVHQFAKEL |
| Q15375 | Y614 | Sugiyama | EPHA7 EHK3 HEK11 | EELyFHFKFPGTKTyIDPEtyEDPNRAVHQFAKELDASCIK |
| Q15375 | Y748 | Sugiyama | EPHA7 EHK3 HEK11 | GQFTVIQLVGMLRGIAAGMRyLADMGyVHRDLAARNILVNS |
| Q15375 | Y754 | Sugiyama | EPHA7 EHK3 HEK11 | QLVGMLRGIAAGMRyLADMGyVHRDLAARNILVNSNLVCKV |
| Q15375 | Y791 | Sugiyama | EPHA7 EHK3 HEK11 | VCKVSDFGLsRVIEDDPEAVytttGGKIPVRWTAPEAIQyR |
| Q15375 | Y810 | Sugiyama | EPHA7 EHK3 HEK11 | VytttGGKIPVRWTAPEAIQyRKFTSASDVWSYGIVMWEVM |
| Q15375 | Y940 | Sugiyama | EPHA7 EHK3 HEK11 | PDFTTFCSVGEWLQAIKMERyKDNFtAAGyNsLESVARMTI |
| Q15375 | Y949 | Sugiyama | EPHA7 EHK3 HEK11 | GEWLQAIKMERyKDNFtAAGyNsLESVARMTIEDVMSLGIT |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15459 | S451 | Sugiyama | SF3A1 SAP114 | IGLLDPRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAE |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15643 | Y452 | Sugiyama | TRIP11 CEV14 | SLLSQEKEELQMSLLKLNNEyEVIKSTATRDIsLDsELHDL |
| Q15691 | Y119 | Sugiyama | MAPRE1 | GKFQDNFEFVQWFKKFFDANyDGKDyDPVAARQGQEtAVAP |
| Q15691 | Y124 | Sugiyama | MAPRE1 | NFEFVQWFKKFFDANyDGKDyDPVAARQGQEtAVAPsLVAP |
| Q15785 | Y25 | Sugiyama | TOMM34 URCC3 | FPDsVEELRAAGNESFRNGQyAEASALyGRALRVLQAQGss |
| Q15785 | Y54 | Sugiyama | TOMM34 URCC3 | RALRVLQAQGssDPEEEsVLysNRAACHLKDGNCRDCIKDC |
| Q16181 | Y223 | Sugiyama | SEPTIN7 CDC10 SEPT7 | ECQQFKKQIMKEIQEHKIKIyEFPEtDDEEENKLVKKIKDR |
| Q16555 | Y499 | Sugiyama | DPYSL2 CRMP2 ULIP2 | yKRIKARSRLAELRGVPRGLyDGPVCEVsVtPKtVtPAssA |
| Q16658 | Y230 | Sugiyama | FSCN1 FAN1 HSN SNL | TGytLEFRsGKVAFRDCEGRyLAPsGPsGtLKAGKATKVGK |
| Q16658 | Y493 | Sugiyama | FSCN1 FAN1 HSN SNL | DHAGVLKASAEtVDPAsLWEy____________________ |
| Q16719 | S443 | Sugiyama | KYNU | VVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAET |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16719 | Y86 | Sugiyama | KYNU | ENAIYFLGNSLGLQPKMVKtyLEEELDKWAKIAAYGHEVGK |
| Q16762 | Y165 | Sugiyama | TST | PSRPEPAVFKATLDRSLLKTyEQVLENLESKRFQLVDSRSQ |
| Q16763 | Y141 | Sugiyama | UBE2S E2EPF OK/SW-cl.73 | IHPNPESALNEEAGRLLLENyEEyAARARLLtEIHGGAGGP |
| Q16763 | Y144 | Sugiyama | UBE2S E2EPF OK/SW-cl.73 | NPESALNEEAGRLLLENyEEyAARARLLtEIHGGAGGPSGR |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q16851 | Y89 | Sugiyama | UGP2 UGP1 | KGPSVDWGKIQRPPEDSIQPyEKIKARGLPDNISsVLNKLV |
| Q2NKX8 | T1202 | Sugiyama | ERCC6L PICH | GEQLVGsPQDKAAEATNDyEtLVKRGKELKECGKIQEALNC |
| Q3V6T2 | Y1153 | Sugiyama | CCDC88A APE GRDN KIAA1212 | SSLENENESVIKEREDLKSLyDSLIKDHEKLELLHERQAsE |
| Q3V6T2 | Y1174 | Sugiyama | CCDC88A APE GRDN KIAA1212 | DSLIKDHEKLELLHERQAsEyESLISKHGTLKSAHKNLEVE |
| Q4V328 | Y25 | Sugiyama | GRIPAP1 KIAA1167 | LSEEEFQRMQAQLLELRTNNyQLSDELRKNGVELTSLRQKV |
| Q4VXU2 | Y291 | Sugiyama | PABPC1L C20orf119 | ERQNELKRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLR |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q53H82 | Y99 | Sugiyama | LACTB2 CGI-83 | HRDHSGGIGDICKSINNDtTyCIKKLPRNPQREEIIGNGEQ |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | Y167 | Sugiyama | HSP90AB4P | GEPIDRDTKVILHLKEDQtEyLEERWVKEVVKKHPQFIGCL |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | Y171 | Sugiyama | HSP90AB3P HSP90BC | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| Q58FF7 | Y492 | Sugiyama | HSP90AB3P HSP90BC | TANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIMETLR |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | Y198 | Sugiyama | HSP90AB2P HSP90BB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKTKPIWTRNTEDI |
| Q58FF8 | Y260 | Sugiyama | HSP90AB2P HSP90BB | VRYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVW |
| Q58FF8 | Y261 | Sugiyama | HSP90AB2P HSP90BB | RYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVWK |
| Q58FF8 | Y56 | Sugiyama | HSP90AB2P HSP90BB | KEIFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FG0 | Y177 | Sugiyama | HSP90AA5P HSP90AE | GQLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQ |
| Q58FG0 | Y178 | Sugiyama | HSP90AA5P HSP90AE | QLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQK |
| Q5JWF2 | Y833 | Sugiyama | GNAS GNAS1 | QLIDCAQYFLDKIDVIKQADyVPSDQDLLRCRVLTSGIFET |
| Q5QNW6 | Y38 | Sugiyama | H2BC18 HIST2H2BF | AVTKVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5VTE0 | Y254 | Sugiyama | EEF1A1P5 EEF1AL3 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VTE0 | Y86 | Sugiyama | EEF1A1P5 EEF1AL3 | ERERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGT |
| Q5VV41 | Y216 | Sugiyama | ARHGEF16 EPHEXIN4 NBR | KKTLGRKRGHKGsFKDDPQLyQEIQERGLNtsQEsDDDILD |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6NVY1 | Y247 | Sugiyama | HIBCH | EDLLALKsPSKENIAsVLENyHtESKIDRDKSFILEEHMDK |
| Q6PIW4 | Y663 | Sugiyama | FIGNL1 | DFENAFRTVRPSVSPKDLELyENWNKTFGCGK_________ |
| Q6PKG0 | Y633 | Sugiyama | LARP1 KIAA0731 LARP | MEQMDGRKNtFtAWsDEEsDyEIDDRDVNKILIVtQtPHyM |
| Q6PKG0 | Y777 | Sugiyama | LARP1 KIAA0731 LARP | APEPstIARsLPttVPEsPNyRNtRtPRtPRtPQLKDSSQT |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q71U36 | S439 | Sugiyama | TUBA1A TUBA3 | SEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy________ |
| Q71U36 | Y312 | Sugiyama | TUBA1A TUBA3 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q7KZF4 | Y476 | Sugiyama | SND1 TDRD11 | SKGLATVIRYRQDDDQRssHyDELLAAEARAIKNGKGLHSK |
| Q86SX6 | Y85 | Sugiyama | GLRX5 C14orf87 | PQCGFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSN |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86UK7 | Y306 | Sugiyama | ZNF598 | QFSYAPRHSRRNEGVVGGEDyEEVDRysRQGRVARAGTRGA |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86VS8 | Y171 | Sugiyama | HOOK3 | MTAIQELMSKEsPVSAGNDAyVDLDRQLKKTTEELNEALSA |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q8IUD2 | Y987 | Sugiyama | ERC1 ELKS KIAA1081 RAB6IP2 | RLVQQLKQQTQNRMKLMADNyEDDHFKssHsNQtNHKPsPD |
| Q8IWA5 | Y308 | Sugiyama | SLC44A2 CTL2 PSEC0210 | GEAGSDVSLVDLGFQTDFRVyLHLRQTWLAFMIILSILEVI |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N1G4 | Y257 | Sugiyama | LRRC47 KIAA1185 | LRDKRLEKMVSGCQTRSILEyLRVGGRGGGKGKGRAEGSEK |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N5M4 | Y11 | Sugiyama | TTC9C | __________MEKRLQEAQLyKEEGNQRYREGKYRDAVSRY |
| Q8NBF2 | Y39 | Sugiyama | NHLRC2 | TSLEYALLDAVTQQEKDSLVyQyLQKVDGWEQDLSVPEFPE |
| Q8NBP7 | Y521 | Sugiyama | PCSK9 NARC1 PSEC0052 | EAQGGKLVCRAHNAFGGEGVyAIARCCLLPQANCSVHTAPP |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NDI1 | Y585 | Sugiyama | EHBP1 KIAA0903 NACSIN | TYKVGNYETDTNssVDQEKFyAELSDLKREPELQQPISGAV |
| Q8NFI4 | Y213 | Sugiyama | ST13P5 FAM10A5 | RLLGHWEEAAHDLAFACKLDyDEDAsAMLKEVQPRAQKIAE |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TB72 | Y1003 | Sugiyama | PUM2 KIAA0235 PUMH2 | CQNDGPHSALYTMMKDQYANyVVQKMIDMAEPAQRKIIMHK |
| Q8TD19 | Y52 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PSASQGPRAGGGAAEQEELHyIPIRVLGRGAFGEAtLyRRT |
| Q8WUM4 | Y39 | Sugiyama | PDCD6IP AIP1 ALIX KIAA1375 | KPLVKFIQQTYPSGGEEQAQyCRAAEELSKLRRAAVGRPLD |
| Q8WVJ2 | Y145 | Sugiyama | NUDCD2 | ERFQKENPGFDFsGAEIsGNytKGGPDFsNLEK________ |
| Q8WWM7 | Y264 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | ESDMSNGWDPNEMFKFNEENyGVKTtyDssLssytVPLEKD |
| Q8WWM7 | Y277 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | FKFNEENyGVKTtyDssLssytVPLEKDNsEEFRQRELRAA |
| Q92522 | Y48 | Sugiyama | H1-10 H1FX | AALsPsKKRKNSKKKNQPGKySQLVVEtIRRLGERNGSSLA |
| Q92598 | Y614 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | VELPIEANLVWQLGKDLLNMyIETEGKMIMQDKLEKERNDA |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y677 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | ICEQDHQNFLRLLTETEDWLyEEGEDQAKQAyVDKLEELMK |
| Q92598 | Y89 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | RFHGRAFNDPFIQKEKENLsyDLVPLKNGGVGIKVMYMGEE |
| Q92890 | Y261 | Sugiyama | UFD1 UFD1L | GVEPsPsPIKPGDIKRGIPNyEFKLGKITFIRNSRPLVKKV |
| Q92905 | Y203 | Sugiyama | COPS5 CSN5 JAB1 | LGAFRTYPKGYKPPDEGPsEyQtIPLNKIEDFGVHCKQYYA |
| Q93079 | Y38 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96A49 | T331 | Sugiyama | SYAP1 PRO3113 | EDsADWEKELQQELQEyEVVtESEKRDENWDKEIEKMLQEE |
| Q96A49 | Y327 | Sugiyama | SYAP1 PRO3113 | AVLEEDsADWEKELQQELQEyEVVtESEKRDENWDKEIEKM |
| Q96AY3 | Y201 | Sugiyama | FKBP10 FKBP65 PSEC0056 | YNGTLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGM |
| Q96AY3 | Y204 | Sugiyama | FKBP10 FKBP65 PSEC0056 | TLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGMCPG |
| Q96C19 | T84 | Sugiyama | EFHD2 SWS1 | DLNQGIGEPQsPsRRVFNPytEFKEFSRKQIKDMEKMFKQy |
| Q96D46 | Y459 | Sugiyama | NMD3 CGI-07 | YQDFLEDLEEDEAIRKNVNIyRDsAIPVEsDtDDEGAPRIS |
| Q96F86 | Y225 | Sugiyama | EDC3 LSM16 YJDC YJEFN2 PP844 | DFEGNLALFDKAAVFEEIDtyERRSGTRsRGIPNERPTRYR |
| Q96G03 | Y177 | Sugiyama | PGM2 MSTP006 | CAGIMItAsHNPKQDNGYKVyWDNGAQIIsPHDKGISQAIE |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96I25 | Y214 | Sugiyama | RBM17 SPF45 | yEEDSRPRsQsSKAAIPPPVyEEQDRPRsPtGPsNsFLANM |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q96SN8 | Y369 | Sugiyama | CDK5RAP2 CEP215 KIAA1633 | AKAREALQKAQTQEFQGsEDyETALSGKEALSAALRSQNLT |
| Q96T37 | Y608 | Sugiyama | RBM15 OTT OTT1 | PPPPPVRERSTRTAATsVPAyEPLDSLDRRRDGWsLDRDRG |
| Q99426 | Y98 | Sugiyama | TBCB CG22 CKAP1 | PVDDGCRIHVIDHsGARLGEyEDVSRVEKytIsQEAyDQRQ |
| Q99459 | Y511 | Sugiyama | CDC5L KIAA0432 PCDC5RP | EIVLPENAEKELEEREIDDtyIEDAADVDARKQAIRDAERV |
| Q99459 | Y788 | Sugiyama | CDC5L KIAA0432 PCDC5RP | ECLKEDVQRQQEREKELQHRyADLLLEKETLKSKF______ |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99470 | Y187 | Sugiyama | SDF2 | GRPISGQKEVHGMAQPSQNNyWKAMEGIFMKPSELLKAEAH |
| Q99536 | T242 | Sugiyama | VAT1 | SASKHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIVMD |
| Q99536 | Y240 | Sugiyama | VAT1 | TASASKHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIV |
| Q99536 | Y245 | Sugiyama | VAT1 | KHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIVMDPLG |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99614 | Y96 | Sugiyama | TTC1 TPR1 | ADKVENKsNEDVNssELDEEyLIELEKNMSDEEKQKRREES |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y390 | Sugiyama | ACO2 | KEGWPLDIRVGLIGSCTNssyEDMGRSAAVAKQALAHGLKC |
| Q99798 | Y544 | Sugiyama | ACO2 | LEAPDADELPKGEFDPGQDtyQHPPKDSsGQHVDVsPtsQR |
| Q99798 | Y665 | Sugiyama | ACO2 | DtARYYKKHGIRWVVIGDENyGEGSSREHAALEPRHLGGRA |
| Q99832 | Y438 | Sugiyama | CCT7 CCTH NIP7-1 | KYLRDYSRTIPGKQQLLIGAyAKALEIIPRQLCDNAGFDAt |
| Q99848 | Y265 | Sugiyama | EBNA1BP2 EBP2 | NQKFGFGGKKKGSKWNtREsyDDVssFRAKTAHGRGLKRPG |
| Q99877 | Y38 | Sugiyama | H2BC15 H2BFD HIST1H2BN | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q99877 | Y41 | Sugiyama | H2BC15 H2BFD HIST1H2BN | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99877 | Y43 | Sugiyama | H2BC15 H2BFD HIST1H2BN | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99879 | Y38 | Sugiyama | H2BC14 H2BFE HIST1H2BM | AINKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q99879 | Y41 | Sugiyama | H2BC14 H2BFE HIST1H2BM | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99879 | Y43 | Sugiyama | H2BC14 H2BFE HIST1H2BM | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99880 | Y38 | Sugiyama | H2BC13 H2BFC HIST1H2BL | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q99880 | Y41 | Sugiyama | H2BC13 H2BFC HIST1H2BL | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99880 | Y43 | Sugiyama | H2BC13 H2BFC HIST1H2BL | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99961 | Y57 | Sugiyama | SH3GL1 CNSA1 SH3D2B | EKKVDVTSKAVTEVLARTIEyLQPNPAsRAKLTMLNTVSKI |
| Q99962 | Y57 | Sugiyama | SH3GL2 CNSA2 SH3D2A | ERKVDVTSRAVMEIMTKTIEyLQPNPAsRAKLSMINTMsKI |
| Q9BQE3 | Y312 | Sugiyama | TUBA1C TUBA6 | TNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BQS8 | Y646 | Sugiyama | FYCO1 ZFYVE7 | QNVVGRNQLLEGKLQALQADyQALQQRESAIQGsLASLEAE |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BS26 | T398 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | VASSPPESSFQKLAPsEyRytLLRDRDEL____________ |
| Q9BS26 | Y397 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | DVASSPPESSFQKLAPsEyRytLLRDRDEL___________ |
| Q9BS40 | Y20 | Sugiyama | LXN | _MEIPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQA |
| Q9BS40 | Y23 | Sugiyama | LXN | IPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQAsME |
| Q9BU89 | Y290 | Sugiyama | DOHH HLRC1 | RESCEVALDMyEHETGRAFQyADGLEQLRGAPS________ |
| Q9BUP3 | Y62 | Sugiyama | HTATIP2 CC3 TIP30 | GLFSKVTLIGRRKLTFDEEAyKNVNQEVVDFEKLDDYASAF |
| Q9BW91 | Y140 | Sugiyama | NUDT9 NUDT10 PSEC0099 UNQ3012/PRO9771 | FsPKFNEKDGHVERKSKNGLyEIENGRPRNPAGRTGLVGRG |
| Q9BXS5 | Y418 | Sugiyama | AP1M1 CLTNM | IEKSGYQALPWVRYITQNGDyQLRtQ_______________ |
| Q9BXS6 | Y370 | Sugiyama | NUSAP1 ANKT BM-037 PRO0310 | PVsNKKPVFDLKAsLsRPLNyEPHKGKLKPWGQSKENNyLN |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BZI7 | Y167 | Sugiyama | UPF3B RENT3B UPF3X | RDTKVGtIDDDPEyRKFLEsyAtDNEKMTstPEtLLEEIEA |
| Q9BZX2 | Y203 | Sugiyama | UCK2 UMPK | SQYITFVKPAFEEFCLPTKKyADVIIPRGADNLVAINLIVQ |
| Q9GZT8 | Y175 | Sugiyama | NIF3L1 ALS2CR1 MDS015 My018 | PSKAPNyPTEGNHRVEFNVNytQDLDKVMSAVKGIDGVsVT |
| Q9H3G5 | Y199 | Sugiyama | CPVL VLP PSEC0124 UNQ197/PRO223 | LYSALIQFFQIFPEYKNNDFyVTGESyAGKYVPAIAHLIHS |
| Q9H4F8 | Y407 | Sugiyama | SMOC1 | FKRYVKKKAKPKKCARRFtDyCDLNKDKVISLPELKGCLGV |
| Q9H4M9 | Y339 | Sugiyama | EHD1 PAST PAST1 CDABP0131 | PNVFGKESKKKELVNNLGEIyQKIEREHQIsPGDFPsLRKM |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9HA47 | Y205 | Sugiyama | UCK1 URK1 | TQYTTFVKPAFEEFCLPTKKyADVIIPRGVDNMVAINLIVQ |
| Q9HAP6 | S115 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | ELPKTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLK |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HB71 | Y165 | Sugiyama | CACYBP S100A6BP SIP PNAS-107 | VKTDTVLILCRKKVENTRWDyLtQVEKECKEKEKPsYDtEt |
| Q9HC35 | Y226 | Sugiyama | EML4 C2orf2 EMAPL4 | PKVTKTADKHKDVIINQEGEyIKMFMRGRPItMFIPSDVDN |
| Q9HCG8 | Y45 | Sugiyama | CWC22 KIAA1604 NCM | RNssPEDRYEEQERsPRDRDyFDYsRsDYEHSRRGRsYDsS |
| Q9NNW7 | Y70 | Sugiyama | TXNRD2 KIAA1652 TRXR2 | GGLACAKEAAQLGRKVAVVDyVEPSPQGTRWGLGGTCVNVG |
| Q9NPI1 | Y190 | Sugiyama | BRD7 BP75 CELTIX1 | MIIKHPMDFSTMKEKIKNNDyQsIEELKDNFKLMCTNAMIY |
| Q9NQA5 | Y647 | Sugiyama | TRPV5 ECAC1 | DRWFLRVENHNDQNPLRVLRyVEVFKNsDKEDDQEHPSEKQ |
| Q9NQE9 | Y44 | Sugiyama | HINT3 | TTVssVGTCEAAGKsPEPKDyDstCVFCRIAGRQDPGTELL |
| Q9NR46 | Y77 | Sugiyama | SH3GLB2 KIAA1848 PP578 | LRQTEVLLQPNPSARVEEFLyEKLDRKVPSRVTNGELLAQY |
| Q9NRX4 | Y116 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AyGPAQHAISTEKIKAKyPDyEVtWANDGy___________ |
| Q9NRX4 | Y52 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | RSGAPAAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCE |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NUL3 | Y326 | Sugiyama | STAU2 | MNPISRLAQIQQAKKEKEPDyVLLSERGMPRRREFVMQVKV |
| Q9NUP9 | S115 | Sugiyama | LIN7C MALS3 VELI3 | ELPKTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLK |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NWS0 | Y194 | Sugiyama | PIH1D1 NOP17 | IsQQNIRSEQRPRIQELGDLytPAPGRAESGPEKPHLNLWL |
| Q9NYL9 | Y86 | Sugiyama | TMOD3 | REHLLsYLEKEALEHKDREDyVPYTGEKKGKIFIPKQKPVQ |
| Q9NYU2 | Y449 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | IEGLSLHNVLKLNIQPsEADyAVDIRSPAISWVNNLEVDSR |
| Q9NYU2 | Y779 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | RPVTFWIVGDFDSPSGRQLLyDAIKHQKSSNNVRISMINNP |
| Q9NYU2 | Y966 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | LVMKVDALLsAQPKGDPRIEyQFFEDRHSAIKLRPKEGETY |
| Q9NZB2 | Y9 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | ____________MGVQGFQDyIEKHCPsAVVPVELQKLARG |
| Q9UBQ7 | Y255 | Sugiyama | GRHPR GLXR MSTP035 | KETAVFINISRGDVVNQDDLyQALAsGKIAAAGLDVtsPEP |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | 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 |
| Q9UGI8 | Y251 | Sugiyama | TES | RTQYSCYCCKLSMKEGDPAIyAERAGyDKLWHPACFVCSTC |
| Q9UHR4 | Y163 | Sugiyama | BAIAP2L1 IRTKS | IRRKSQGSRNALKyEHKEIEyVEtVTSRQSEIQKFIADGCK |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UIQ6 | Y70 | Sugiyama | LNPEP OTASE | GsRLLVRGLGEHEMEEDEEDyEssAKLLGMsFMNRssGLRN |
| Q9UK59 | Y533 | Sugiyama | DBR1 | LsDEHEPEQRKKIKRRNQAIyAAVDDDDDDAA_________ |
| Q9UKF6 | Y677 | Sugiyama | CPSF3 CPSF73 | EGsEDDESLREMVELAAQRLyEALtPVH_____________ |
| Q9UKK9 | Y198 | Sugiyama | NUDT5 NUDIX5 HSPC115 | LLQRLDALVAEEHLTVDARVySyALALKHANAKPFEVPFLK |
| Q9UKS6 | Y206 | Sugiyama | PACSIN3 | RKLQERVERCAKEAEKTKAQyEQtLAELHRYTPRYMEDMEQ |
| Q9UKS6 | Y372 | Sugiyama | PACSIN3 | EWsDEEsPRKAATGVRVRALyDyAGQEADELsFRAGEELLK |
| Q9UKS6 | Y374 | Sugiyama | PACSIN3 | sDEEsPRKAATGVRVRALyDyAGQEADELsFRAGEELLKMS |
| Q9UKV3 | Y1086 | Sugiyama | ACIN1 ACINUS KIAA0670 | RTALHGVKWPQSNPKFLCADyAEQDELDyHRGLLVDRPsEt |
| Q9ULF5 | Y596 | Sugiyama | SLC39A10 KIAA1265 ZIP10 | RLNEtELtDLEGQQEsPPKNyLCIEEEKIIDHsHsDGLHtI |
| Q9UMS4 | Y108 | Sugiyama | PRPF19 NMP200 PRP19 SNEV | HSFTLRQQLQTTRQELSHALyQHDAACRVIARLTKEVTAAR |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UNF0 | Y267 | Sugiyama | PACSIN2 | VLLEVQKHLDLSNVAGYKAIyHDLEQsIRAADAVEDLRWFR |
| Q9UNF1 | Y313 | Sugiyama | MAGED2 BCG1 | KDQTKIPIKRSDMLKDIIKEyTDVyPEIIERAGYSLEKVFG |
| Q9UNM6 | Y60 | Sugiyama | PSMD13 | QVLDFVQDPCFAQGDGLIKLyENFISEFEHRVNPLSLVEII |
| Q9UPQ0 | Y179 | Sugiyama | LIMCH1 KIAA1102 | QMRKDTDDIEsPKRSIRDsGyIDCWDsERsDsLsPPRHGRD |
| Q9UQ80 | Y98 | Sugiyama | PA2G4 EBP1 | TSISVNNCVCHFsPLKSDQDyILKEGDLVKIDLGVHVDGFI |
| Q9UQB8 | Y164 | Sugiyama | BAIAP2 | LRKKSQGSKNPQKYSDKELQyIDAISNKQGELENyVSDGYK |
| Q9UQB8 | Y178 | Sugiyama | BAIAP2 | SDKELQyIDAISNKQGELENyVSDGYKTALTEERRRFCFLV |
| Q9Y230 | Y172 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | TGTGSKVGKLTLKTTEMETIyDLGTKMIESLTKDKVQAGDV |
| Q9Y230 | Y446 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | IKRVysLFLDEsRSTQYMKEyQDAFLFNELKGEtMDTS___ |
| Q9Y262 | S416 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | DKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNYH |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y262 | Y45 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | MHTGDPKQDLAyERQyEQQtyQVIPEVIKNFIQYFHKTVSD |
| Q9Y265 | 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 |
| Q9Y2S7 | Y133 | Sugiyama | POLDIP2 PDIP38 POLD4 HSPC017 | EKAENPAGHGSKEVKGKTHTyyQVLIDARDCPHISQRSQTE |
| Q9Y2S7 | Y134 | Sugiyama | POLDIP2 PDIP38 POLD4 HSPC017 | KAENPAGHGSKEVKGKTHTyyQVLIDARDCPHISQRSQTEA |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y3D8 | Y31 | Sugiyama | AK6 CINAP AD-004 CGI-137 | TPGVGKTTLGKELASKSGLKyINVGDLAREEQLYDGYDEEY |
| Q9Y3F4 | Y252 | Sugiyama | STRAP MAWD UNRIP | HPEKEFLVAGGEDFKLyKyDyNsGEELEsyKGHFGPIHCVR |
| Q9Y3P9 | Y472 | Sugiyama | RABGAP1 HSPC094 | FFLKLKQIKQRERKNNTDTLyEVVCLESESERERRKTTAsP |
| Q9Y3S2 | Y315 | Sugiyama | ZNF330 NOA36 | ssDLFTNLNLGRTYAsGYAHyEEQEN_______________ |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y490 | Y127 | Sugiyama | TLN1 KIAA1027 TLN | TVTDMLMTICARIGITNHDEysLVRELMEEKKEEItGtLRK |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y5V3 | Y505 | Sugiyama | MAGED1 NRAGE PP2250 PRO2292 | KDYTKVPIKRSEMLRDIIREyTDVyPEIIERACFVLEKKFG |
| Q9Y617 | Y101 | Sugiyama | PSAT1 PSA | GQFSAVPLNLIGLKAGRCADyVVTGAWSAKAAEEAKKFGTI |
| Q9Y617 | Y70 | Sugiyama | PSAT1 PSA | AKIINNTENLVRELLAVPDNyKVIFLQGGGCGQFSAVPLNL |
| Q9Y639 | Y216 | Sugiyama | NPTN SDFR1 SDR1 | KNASNMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKA |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | Y244 | Sugiyama | CLIC4 | AysRDEFtNtCPsDKEVEIAysDVAKRLTK___________ |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 0.000012 | 4.908 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 0.000017 | 4.773 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 0.000023 | 4.632 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 0.000036 | 4.449 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 0.000045 | 4.348 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 0.000096 | 4.018 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 0.000228 | 3.642 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 0.000296 | 3.528 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 0.000588 | 3.231 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 0.000677 | 3.169 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 0.000882 | 3.054 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 0.000960 | 3.018 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 0.001011 | 2.995 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 0.001253 | 2.902 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 0.001275 | 2.894 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 0.001957 | 2.708 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 0.001891 | 2.723 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 0.001891 | 2.723 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 0.001903 | 2.721 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 0.003147 | 2.502 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 0.003767 | 2.424 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 0.005053 | 2.296 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 0.004941 | 2.306 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 0.005251 | 2.280 | 0 | 0 |
| Drug resistance of KIT mutants | R-HSA-9669937 | 0.010625 | 1.974 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 0.010625 | 1.974 | 0 | 0 |
| KIT mutants bind TKIs | R-HSA-9669921 | 0.010625 | 1.974 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 0.010625 | 1.974 | 0 | 0 |
| Regorafenib-resistant KIT mutants | R-HSA-9669929 | 0.010625 | 1.974 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 0.010625 | 1.974 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 0.010625 | 1.974 | 0 | 0 |
| Imatinib-resistant KIT mutants | R-HSA-9669917 | 0.010625 | 1.974 | 0 | 0 |
| Masitinib-resistant KIT mutants | R-HSA-9669924 | 0.010625 | 1.974 | 0 | 0 |
| Nilotinib-resistant KIT mutants | R-HSA-9669926 | 0.010625 | 1.974 | 0 | 0 |
| Sunitinib-resistant KIT mutants | R-HSA-9669934 | 0.010625 | 1.974 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 0.010625 | 1.974 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 0.010625 | 1.974 | 0 | 0 |
| Dasatinib-resistant KIT mutants | R-HSA-9669914 | 0.010625 | 1.974 | 0 | 0 |
| Sorafenib-resistant KIT mutants | R-HSA-9669936 | 0.010625 | 1.974 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 0.010625 | 1.974 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 0.007575 | 2.121 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 0.007031 | 2.153 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 0.010432 | 1.982 | 0 | 0 |
| Interleukin-18 signaling | R-HSA-9012546 | 0.006353 | 2.197 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 0.007406 | 2.130 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 0.007406 | 2.130 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 0.009143 | 2.039 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 0.007604 | 2.119 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 0.010910 | 1.962 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 0.006067 | 2.217 | 0 | 0 |
| Immune System | R-HSA-168256 | 0.011705 | 1.932 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 0.012101 | 1.917 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 0.013001 | 1.886 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 0.014322 | 1.844 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 0.014374 | 1.842 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 0.015194 | 1.818 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 0.016912 | 1.772 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 0.017810 | 1.749 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 0.018734 | 1.727 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 0.019113 | 1.719 | 1 | 0 |
| Activation and oligomerization of BAK protein | R-HSA-111452 | 0.021137 | 1.675 | 0 | 0 |
| SARS-CoV-1 targets PDZ proteins in cell-cell junction | R-HSA-9692912 | 0.021137 | 1.675 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | R-HSA-2892247 | 0.021602 | 1.666 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | R-HSA-8866910 | 0.021602 | 1.666 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 0.020676 | 1.685 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 0.021664 | 1.664 | 1 | 1 |
| Signaling by Interleukins | R-HSA-449147 | 0.021962 | 1.658 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 0.023545 | 1.628 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 0.027637 | 1.559 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 0.024533 | 1.610 | 1 | 1 |
| Nephron development | R-HSA-9831926 | 0.025557 | 1.592 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 0.026416 | 1.578 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition | R-HSA-9926550 | 0.025557 | 1.592 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 0.025560 | 1.592 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 0.029263 | 1.534 | 1 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 0.029381 | 1.532 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 0.029782 | 1.526 | 0 | 0 |
| Signaling by juxtamembrane domain KIT mutants | R-HSA-9669935 | 0.031539 | 1.501 | 0 | 0 |
| Signaling by extracellular domain mutants of KIT | R-HSA-9680187 | 0.031539 | 1.501 | 0 | 0 |
| Signaling by kinase domain mutants of KIT | R-HSA-9669933 | 0.031539 | 1.501 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 0.041830 | 1.379 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 0.041830 | 1.379 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 0.041830 | 1.379 | 0 | 0 |
| Glycogen storage disease type IV (GBE1) | R-HSA-3878781 | 0.041830 | 1.379 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 0.041830 | 1.379 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 0.041830 | 1.379 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 0.041830 | 1.379 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 0.041830 | 1.379 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 0.036595 | 1.437 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 0.036595 | 1.437 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 0.039837 | 1.400 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 0.041437 | 1.383 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 0.038987 | 1.409 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 0.037209 | 1.429 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 0.039837 | 1.400 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 0.041684 | 1.380 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 0.036708 | 1.435 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 0.043624 | 1.360 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 0.043944 | 1.357 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 0.043944 | 1.357 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 0.046505 | 1.333 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 0.049120 | 1.309 | 1 | 1 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 0.049120 | 1.309 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 0.049272 | 1.307 | 0 | 0 |
| Axonal growth stimulation | R-HSA-209563 | 0.052013 | 1.284 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 0.052013 | 1.284 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 0.062088 | 1.207 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 0.049716 | 1.304 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 0.062088 | 1.207 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 0.054504 | 1.264 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 0.057271 | 1.242 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 0.057271 | 1.242 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 0.052013 | 1.284 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 0.062088 | 1.207 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 0.050545 | 1.296 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 0.054275 | 1.265 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 0.056244 | 1.250 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 0.056244 | 1.250 | 0 | 0 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 0.062088 | 1.207 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 0.057271 | 1.242 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 0.065854 | 1.181 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 0.068805 | 1.162 | 0 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 0.071799 | 1.144 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 0.072057 | 1.142 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 0.072057 | 1.142 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 0.072057 | 1.142 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 0.072057 | 1.142 | 0 | 0 |
| Biosynthesis of DPAn-3-derived 13-series resolvins | R-HSA-9026403 | 0.072057 | 1.142 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 0.072057 | 1.142 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 0.072183 | 1.142 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 0.081920 | 1.087 | 0 | 0 |
| Signaling by RNF43 mutants | R-HSA-5340588 | 0.081920 | 1.087 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 0.091680 | 1.038 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 0.101336 | 0.994 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 0.110890 | 0.955 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 0.110890 | 0.955 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 0.110890 | 0.955 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 0.129696 | 0.887 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 0.157166 | 0.804 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 0.166129 | 0.780 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 0.174998 | 0.757 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 0.174998 | 0.757 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 0.183773 | 0.736 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 0.183773 | 0.736 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 0.183773 | 0.736 | 0 | 0 |
| G beta:gamma signalling through BTK | R-HSA-8964315 | 0.183773 | 0.736 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 0.183773 | 0.736 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 0.209546 | 0.679 | 0 | 0 |
| MyD88 deficiency (TLR2/4) | R-HSA-5602498 | 0.242655 | 0.615 | 0 | 0 |
| IRAK4 deficiency (TLR2/4) | R-HSA-5603041 | 0.250715 | 0.601 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 0.142567 | 0.846 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 0.149906 | 0.824 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 0.176137 | 0.754 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 0.176137 | 0.754 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 0.179943 | 0.745 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 0.187591 | 0.727 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 0.214680 | 0.668 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 0.222489 | 0.653 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 0.265729 | 0.576 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 0.265729 | 0.576 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 0.277551 | 0.557 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 0.289361 | 0.539 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 0.242655 | 0.615 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 0.242655 | 0.615 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 0.209546 | 0.679 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 0.209546 | 0.679 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 0.289751 | 0.538 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 0.285426 | 0.545 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 0.101336 | 0.994 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 0.250715 | 0.601 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 0.129696 | 0.887 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 0.138950 | 0.857 | 0 | 0 |
| Polo-like kinase mediated events | R-HSA-156711 | 0.217956 | 0.662 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 0.110890 | 0.955 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 0.257848 | 0.589 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 0.297312 | 0.527 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 0.090595 | 1.043 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 0.166129 | 0.780 | 0 | 0 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | R-HSA-3772470 | 0.148106 | 0.829 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 0.164801 | 0.783 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 0.234510 | 0.630 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 0.250715 | 0.601 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 0.289751 | 0.538 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 0.074835 | 1.126 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 0.107774 | 0.967 | 0 | 0 |
| Release of apoptotic factors from the mitochondria | R-HSA-111457 | 0.081920 | 1.087 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 0.101336 | 0.994 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 0.110890 | 0.955 | 0 | 0 |
| p75NTR regulates axonogenesis | R-HSA-193697 | 0.120343 | 0.920 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 0.157166 | 0.804 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 0.157166 | 0.804 | 0 | 0 |
| Membrane binding and targetting of GAG proteins | R-HSA-174490 | 0.166129 | 0.780 | 0 | 0 |
| Regulation of FZD by ubiquitination | R-HSA-4641263 | 0.209546 | 0.679 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 0.153604 | 0.814 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 0.199147 | 0.701 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 0.147948 | 0.830 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 0.259004 | 0.587 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 0.085719 | 1.067 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 0.075303 | 1.123 | 0 | 0 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | R-HSA-174495 | 0.174998 | 0.757 | 0 | 0 |
| Biosynthesis of aspirin-triggered D-series resolvins | R-HSA-9020265 | 0.209546 | 0.679 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 0.183773 | 0.736 | 0 | 0 |
| Biosynthesis of D-series resolvins | R-HSA-9018676 | 0.258689 | 0.587 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 0.192473 | 0.716 | 0 | 0 |
| Axonal growth inhibition (RHOA activation) | R-HSA-193634 | 0.110890 | 0.955 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 0.148106 | 0.829 | 0 | 0 |
| Biosynthesis of DPAn-3-derived protectins and resolvins | R-HSA-9026286 | 0.157166 | 0.804 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 0.201046 | 0.697 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 0.217956 | 0.662 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 0.093856 | 1.028 | 0 | 0 |
| mRNA decay by 3' to 5' exoribonuclease | R-HSA-429958 | 0.226277 | 0.645 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 0.100476 | 0.998 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 0.114087 | 0.943 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 0.157320 | 0.803 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 0.257848 | 0.589 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 0.177594 | 0.751 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 0.181804 | 0.740 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 0.121061 | 0.917 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 0.250715 | 0.601 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 0.124587 | 0.905 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 0.273351 | 0.563 | 0 | 0 |
| Biosynthesis of E-series 18(R)-resolvins | R-HSA-9023661 | 0.174998 | 0.757 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 0.209546 | 0.679 | 0 | 0 |
| Kinesins | R-HSA-983189 | 0.164801 | 0.783 | 0 | 0 |
| Biosynthesis of DPAn-3 SPMs | R-HSA-9025094 | 0.297312 | 0.527 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 0.217956 | 0.662 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 0.090902 | 1.041 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 0.226277 | 0.645 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 0.088818 | 1.052 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 0.088818 | 1.052 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 0.088818 | 1.052 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 0.101336 | 0.994 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 0.120343 | 0.920 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 0.148106 | 0.829 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 0.157166 | 0.804 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 0.157166 | 0.804 | 0 | 0 |
| Synthesis of 5-eicosatetraenoic acids | R-HSA-2142688 | 0.226277 | 0.645 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 0.090387 | 1.044 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 0.210785 | 0.676 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 0.234510 | 0.630 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 0.187103 | 0.728 | 0 | 0 |
| Biosynthesis of E-series 18(S)-resolvins | R-HSA-9018896 | 0.242655 | 0.615 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 0.297312 | 0.527 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 0.246107 | 0.609 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 0.077911 | 1.108 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 0.248414 | 0.605 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 0.242655 | 0.615 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 0.100103 | 1.000 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 0.081920 | 1.087 | 0 | 0 |
| Biosynthesis of DPAn-3-derived maresins | R-HSA-9026290 | 0.138950 | 0.857 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 0.107223 | 0.970 | 0 | 0 |
| STAT3 nuclear events downstream of ALK signaling | R-HSA-9701898 | 0.183773 | 0.736 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 0.194822 | 0.710 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 0.281489 | 0.551 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 0.168565 | 0.773 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 0.082000 | 1.086 | 0 | 0 |
| Zinc influx into cells by the SLC39 gene family | R-HSA-442380 | 0.120343 | 0.920 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 0.226277 | 0.645 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 0.207730 | 0.683 | 0 | 0 |
| M Phase | R-HSA-68886 | 0.262607 | 0.581 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 0.265729 | 0.576 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 0.138927 | 0.857 | 0 | 0 |
| Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives | R-HSA-9027604 | 0.282109 | 0.550 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 0.291963 | 0.535 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 0.176137 | 0.754 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 0.129696 | 0.887 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 0.153080 | 0.815 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 0.213955 | 0.670 | 0 | 0 |
| Glycogen synthesis | R-HSA-3322077 | 0.234510 | 0.630 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 0.274385 | 0.562 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 0.274385 | 0.562 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 0.091680 | 1.038 | 0 | 0 |
| Assembly Of The HIV Virion | R-HSA-175474 | 0.250715 | 0.601 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 0.297312 | 0.527 | 0 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 0.091680 | 1.038 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 0.101336 | 0.994 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 0.148106 | 0.829 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 0.157166 | 0.804 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 0.157166 | 0.804 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 0.277551 | 0.557 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 0.138950 | 0.857 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 0.220737 | 0.656 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 0.220737 | 0.656 | 0 | 0 |
| Disease | R-HSA-1643685 | 0.209067 | 0.680 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 0.110890 | 0.955 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 0.183773 | 0.736 | 0 | 0 |
| Glycogen storage diseases | R-HSA-3229121 | 0.209546 | 0.679 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 0.234510 | 0.630 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 0.217956 | 0.662 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 0.135308 | 0.869 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 0.170915 | 0.767 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 0.192456 | 0.716 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 0.234510 | 0.630 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 0.297312 | 0.527 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 0.103733 | 0.984 | 1 | 0 |
| Zinc transporters | R-HSA-435354 | 0.174998 | 0.757 | 0 | 0 |
| Biosynthesis of maresins | R-HSA-9018682 | 0.266579 | 0.574 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 0.282109 | 0.550 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 0.163146 | 0.787 | 0 | 0 |
| Apoptotic factor-mediated response | R-HSA-111471 | 0.217956 | 0.662 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 0.258689 | 0.587 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 0.192456 | 0.716 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 0.192456 | 0.716 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 0.133249 | 0.875 | 0 | 0 |
| Transcriptional regulation of pluripotent stem cells | R-HSA-452723 | 0.084179 | 1.075 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 0.195285 | 0.709 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 0.128138 | 0.892 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 0.106803 | 0.971 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 0.297312 | 0.527 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 0.138950 | 0.857 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 0.221077 | 0.655 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 0.107223 | 0.970 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 0.121420 | 0.916 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 0.190323 | 0.721 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 0.191433 | 0.718 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 0.242102 | 0.616 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 0.181435 | 0.741 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 0.209546 | 0.679 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 0.183761 | 0.736 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 0.275043 | 0.561 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 0.226403 | 0.645 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 0.273611 | 0.563 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 0.302270 | 0.520 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 0.304793 | 0.516 | 0 | 0 |
| Pyroptosis | R-HSA-5620971 | 0.304793 | 0.516 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 0.308077 | 0.511 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 0.308990 | 0.510 | 0 | 0 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | R-HSA-917729 | 0.312195 | 0.506 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 0.312195 | 0.506 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 0.312195 | 0.506 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 0.312195 | 0.506 | 0 | 0 |
| Biosynthesis of EPA-derived SPMs | R-HSA-9018679 | 0.312195 | 0.506 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 0.312195 | 0.506 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 0.312905 | 0.505 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 0.316814 | 0.499 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 0.319519 | 0.496 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 0.320719 | 0.494 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 0.324619 | 0.489 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 0.326765 | 0.486 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 0.326765 | 0.486 | 0 | 0 |
| Biosynthesis of DPA-derived SPMs | R-HSA-9018683 | 0.326765 | 0.486 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 0.326765 | 0.486 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 0.332400 | 0.478 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 0.332400 | 0.478 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 0.333934 | 0.476 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 0.333934 | 0.476 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 0.333934 | 0.476 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 0.333934 | 0.476 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 0.333934 | 0.476 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 0.340156 | 0.468 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 0.341018 | 0.467 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 0.341028 | 0.467 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 0.341028 | 0.467 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 0.341028 | 0.467 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 0.341028 | 0.467 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 0.341028 | 0.467 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 0.341028 | 0.467 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 0.342962 | 0.465 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 0.342962 | 0.465 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 0.347885 | 0.459 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 0.348046 | 0.458 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 0.354990 | 0.450 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 0.354990 | 0.450 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 0.354990 | 0.450 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 0.354990 | 0.450 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 0.354990 | 0.450 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 0.354990 | 0.450 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 0.354990 | 0.450 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 0.361860 | 0.441 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 0.361860 | 0.441 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 0.361860 | 0.441 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 0.366164 | 0.436 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 0.367071 | 0.435 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 0.367071 | 0.435 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 0.367071 | 0.435 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 0.367071 | 0.435 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 0.368658 | 0.433 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 0.368658 | 0.433 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 0.368658 | 0.433 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 0.368658 | 0.433 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 0.369983 | 0.432 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 0.369994 | 0.432 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 0.370883 | 0.431 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 0.375384 | 0.426 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 0.375384 | 0.426 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 0.375384 | 0.426 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 0.375384 | 0.426 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 0.375384 | 0.426 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 0.382038 | 0.418 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 0.382038 | 0.418 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 0.388622 | 0.410 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 0.388622 | 0.410 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 0.388622 | 0.410 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 0.388622 | 0.410 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 0.388622 | 0.410 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 0.389803 | 0.409 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 0.393557 | 0.405 | 0 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 0.395136 | 0.403 | 0 | 0 |
| Diseases of Immune System | R-HSA-5260271 | 0.395136 | 0.403 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 0.395136 | 0.403 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 0.395136 | 0.403 | 0 | 0 |
| Glycogen metabolism | R-HSA-8982491 | 0.395136 | 0.403 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 0.397834 | 0.400 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 0.401582 | 0.396 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 0.401582 | 0.396 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 0.401582 | 0.396 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 0.404757 | 0.393 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 0.404757 | 0.393 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 0.407959 | 0.389 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 0.407959 | 0.389 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 0.407959 | 0.389 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 0.407959 | 0.389 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 0.407959 | 0.389 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 0.407959 | 0.389 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 0.407959 | 0.389 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 0.420510 | 0.376 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 0.420510 | 0.376 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 0.420510 | 0.376 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 0.420606 | 0.376 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 0.423201 | 0.373 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 0.423433 | 0.373 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 0.426687 | 0.370 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 0.426687 | 0.370 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 0.426687 | 0.370 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 0.429074 | 0.367 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 0.432798 | 0.364 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 0.432798 | 0.364 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 0.432798 | 0.364 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 0.432798 | 0.364 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 0.432798 | 0.364 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 0.432798 | 0.364 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 0.432798 | 0.364 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 0.433271 | 0.363 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 0.434674 | 0.362 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 0.438844 | 0.358 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 0.438844 | 0.358 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 0.438844 | 0.358 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 0.438844 | 0.358 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 0.438844 | 0.358 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 0.438844 | 0.358 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 0.438844 | 0.358 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 0.438844 | 0.358 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 0.444826 | 0.352 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 0.444826 | 0.352 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 0.444826 | 0.352 | 0 | 0 |
| Metal ion SLC transporters | R-HSA-425410 | 0.450745 | 0.346 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 0.454207 | 0.343 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 0.456601 | 0.340 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 0.456601 | 0.340 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 0.456601 | 0.340 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 0.462395 | 0.335 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 0.468127 | 0.330 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 0.468127 | 0.330 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 0.468127 | 0.330 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 0.469724 | 0.328 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 0.469724 | 0.328 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 0.473799 | 0.324 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 0.473799 | 0.324 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 0.473799 | 0.324 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 0.473799 | 0.324 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 0.479410 | 0.319 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 0.479410 | 0.319 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 0.479410 | 0.319 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 0.484962 | 0.314 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 0.484962 | 0.314 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 0.490437 | 0.309 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 0.490455 | 0.309 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 0.490455 | 0.309 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 0.495037 | 0.305 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 0.495890 | 0.305 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 0.495890 | 0.305 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 0.495890 | 0.305 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 0.495890 | 0.305 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 0.495890 | 0.305 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 0.497229 | 0.303 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 0.497707 | 0.303 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 0.511852 | 0.291 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 0.517060 | 0.286 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 0.517060 | 0.286 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 0.519489 | 0.284 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 0.522212 | 0.282 | 0 | 0 |
| Collagen degradation | R-HSA-1442490 | 0.522212 | 0.282 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 0.523815 | 0.281 | 0 | 0 |
| Translation | R-HSA-72766 | 0.527014 | 0.278 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 0.527311 | 0.278 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 0.527311 | 0.278 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 0.527311 | 0.278 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 0.532355 | 0.274 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 0.536752 | 0.270 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 0.537345 | 0.270 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 0.539949 | 0.268 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 0.542283 | 0.266 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 0.542283 | 0.266 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 0.543130 | 0.265 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 0.555704 | 0.255 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 0.556783 | 0.254 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 0.556783 | 0.254 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 0.556783 | 0.254 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 0.564640 | 0.248 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 0.566195 | 0.247 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 0.566195 | 0.247 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 0.566195 | 0.247 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 0.566195 | 0.247 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 0.566195 | 0.247 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 0.568032 | 0.246 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 0.570827 | 0.243 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 0.570827 | 0.243 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 0.570827 | 0.243 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 0.570827 | 0.243 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 0.570827 | 0.243 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 0.571827 | 0.243 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 0.573268 | 0.242 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 0.575326 | 0.240 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 0.575409 | 0.240 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 0.575409 | 0.240 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 0.579943 | 0.237 | 0 | 0 |
| Diseases of carbohydrate metabolism | R-HSA-5663084 | 0.579943 | 0.237 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 0.584428 | 0.233 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 0.584428 | 0.233 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 0.593256 | 0.227 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 0.601898 | 0.220 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 0.601898 | 0.220 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 0.601898 | 0.220 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 0.606151 | 0.217 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 0.606390 | 0.217 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 0.610358 | 0.214 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 0.610358 | 0.214 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 0.610358 | 0.214 | 0 | 0 |
| Biosynthesis of DHA-derived SPMs | R-HSA-9018677 | 0.614520 | 0.211 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 0.618227 | 0.209 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 0.621119 | 0.207 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 0.622713 | 0.206 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 0.622713 | 0.206 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 0.628691 | 0.202 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 0.630733 | 0.200 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 0.630733 | 0.200 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 0.638583 | 0.195 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 0.638583 | 0.195 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 0.642446 | 0.192 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 0.646267 | 0.190 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 0.646267 | 0.190 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 0.653789 | 0.185 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 0.655180 | 0.184 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 0.657490 | 0.182 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 0.661152 | 0.180 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 0.662301 | 0.179 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 0.664763 | 0.177 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 0.664774 | 0.177 | 0 | 0 |
| Protein folding | R-HSA-391251 | 0.664774 | 0.177 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 0.668359 | 0.175 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 0.678884 | 0.168 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 0.678884 | 0.168 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 0.680150 | 0.167 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 0.682319 | 0.166 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 0.692404 | 0.160 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 0.695694 | 0.158 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 0.698950 | 0.156 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 0.698950 | 0.156 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 0.698950 | 0.156 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 0.705357 | 0.152 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 0.708510 | 0.150 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 0.711629 | 0.148 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 0.720789 | 0.142 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 0.720789 | 0.142 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 0.723535 | 0.141 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 0.725640 | 0.139 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 0.726734 | 0.139 | 0 | 0 |
| Antimicrobial peptides | R-HSA-6803157 | 0.732554 | 0.135 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 0.735417 | 0.133 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 0.735417 | 0.133 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 0.735417 | 0.133 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 0.738250 | 0.132 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 0.742303 | 0.129 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 0.756569 | 0.121 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 0.759853 | 0.119 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 0.759853 | 0.119 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 0.761875 | 0.118 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 0.761875 | 0.118 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 0.764971 | 0.116 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 0.767489 | 0.115 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 0.767489 | 0.115 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 0.767492 | 0.115 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 0.772445 | 0.112 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 0.772445 | 0.112 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 0.777296 | 0.109 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 0.782044 | 0.107 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 0.805073 | 0.094 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 0.806416 | 0.093 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 0.806416 | 0.093 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 0.808194 | 0.092 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 0.808430 | 0.092 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 0.810546 | 0.091 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 0.816579 | 0.088 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 0.817342 | 0.088 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 0.820494 | 0.086 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 0.822420 | 0.085 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 0.824326 | 0.084 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 0.831747 | 0.080 | 0 | 0 |
| S Phase | R-HSA-69242 | 0.831747 | 0.080 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 0.831747 | 0.080 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 0.833553 | 0.079 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 0.834815 | 0.078 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 0.835340 | 0.078 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 0.838857 | 0.076 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 0.840587 | 0.075 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 0.843993 | 0.074 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 0.847326 | 0.072 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 0.847326 | 0.072 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 0.848965 | 0.071 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 0.852193 | 0.069 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 0.854599 | 0.068 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 0.858443 | 0.066 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 0.868756 | 0.061 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 0.870167 | 0.060 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 0.871420 | 0.060 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 0.872943 | 0.059 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 0.880068 | 0.055 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 0.880924 | 0.055 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 0.890866 | 0.050 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 0.891970 | 0.050 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 0.895421 | 0.048 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 0.899074 | 0.046 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 0.908162 | 0.042 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 0.912056 | 0.040 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 0.917380 | 0.037 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 0.917592 | 0.037 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 0.919030 | 0.037 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 0.925252 | 0.034 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 0.933660 | 0.030 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 0.939425 | 0.027 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 0.943629 | 0.025 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 0.945436 | 0.024 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 0.948321 | 0.023 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 0.960835 | 0.017 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 0.975357 | 0.011 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 0.983982 | 0.007 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 0.990279 | 0.004 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 0.992195 | 0.003 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 0.992339 | 0.003 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 0.994264 | 0.002 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 0.994862 | 0.002 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 0.994907 | 0.002 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 0.999320 | 0.000 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 0.999627 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 0.999771 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 0.999999 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.110223e-16 | 15.955 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 7.771561e-16 | 15.109 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 4.107825e-15 | 14.386 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 1.261213e-13 | 12.899 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 3.491651e-13 | 12.457 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 3.491651e-13 | 12.457 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 6.538103e-13 | 12.185 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 1.567635e-12 | 11.805 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 2.065348e-12 | 11.685 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.956324e-12 | 11.709 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.956324e-12 | 11.709 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 3.132161e-12 | 11.504 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 3.509193e-12 | 11.455 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 3.509193e-12 | 11.455 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 5.808243e-12 | 11.236 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 6.464163e-12 | 11.189 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 7.404966e-12 | 11.130 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 7.404966e-12 | 11.130 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 8.621215e-12 | 11.064 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 9.635848e-12 | 11.016 | 0 | 0 |
| Depurination | R-HSA-73927 | 9.387158e-12 | 11.027 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 1.260636e-11 | 10.899 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 1.260636e-11 | 10.899 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 1.334755e-11 | 10.875 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 1.484490e-11 | 10.828 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 1.484490e-11 | 10.828 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 1.852707e-11 | 10.732 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 1.852707e-11 | 10.732 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.903055e-11 | 10.721 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 2.373757e-11 | 10.625 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 2.845291e-11 | 10.546 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 2.845291e-11 | 10.546 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 3.502520e-11 | 10.456 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 4.327660e-11 | 10.364 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 4.156486e-11 | 10.381 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 5.241407e-11 | 10.281 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 5.241407e-11 | 10.281 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 6.006373e-11 | 10.221 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 5.857415e-11 | 10.232 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 6.006373e-11 | 10.221 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 7.316925e-11 | 10.136 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 9.320511e-11 | 10.031 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 1.120708e-10 | 9.951 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.298519e-10 | 9.887 | 1 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 1.912700e-10 | 9.718 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 1.861279e-10 | 9.730 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 2.342971e-10 | 9.630 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 2.689043e-10 | 9.570 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 2.697534e-10 | 9.569 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 3.165264e-10 | 9.500 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 3.174597e-10 | 9.498 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 3.402415e-10 | 9.468 | 1 | 1 |
| Cell junction organization | R-HSA-446728 | 4.514134e-10 | 9.345 | 0 | 0 |
| M Phase | R-HSA-68886 | 4.656651e-10 | 9.332 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 5.139090e-10 | 9.289 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 5.322036e-10 | 9.274 | 1 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 5.511867e-10 | 9.259 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 6.003154e-10 | 9.222 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 6.203255e-10 | 9.207 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 6.995332e-10 | 9.155 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 8.858839e-10 | 9.053 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 9.736887e-10 | 9.012 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 1.002888e-09 | 8.999 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 1.370897e-09 | 8.863 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 1.669873e-09 | 8.777 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 1.916297e-09 | 8.718 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 2.128128e-09 | 8.672 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 2.728715e-09 | 8.564 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 2.745812e-09 | 8.561 | 1 | 0 |
| HSF1 activation | R-HSA-3371511 | 2.853413e-09 | 8.545 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 2.862814e-09 | 8.543 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 2.862814e-09 | 8.543 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 3.260658e-09 | 8.487 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 3.744668e-09 | 8.427 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 3.744668e-09 | 8.427 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 3.744668e-09 | 8.427 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 3.406589e-09 | 8.468 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 6.014604e-09 | 8.221 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 6.091925e-09 | 8.215 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 6.536021e-09 | 8.185 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 7.465499e-09 | 8.127 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 7.735281e-09 | 8.112 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 9.119675e-09 | 8.040 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 9.763682e-09 | 8.010 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 1.094586e-08 | 7.961 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 1.222219e-08 | 7.913 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 1.284235e-08 | 7.891 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 1.529656e-08 | 7.815 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.541878e-08 | 7.812 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 2.316315e-08 | 7.635 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 2.563358e-08 | 7.591 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 3.533292e-08 | 7.452 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 3.195287e-08 | 7.495 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 3.963410e-08 | 7.402 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 3.969107e-08 | 7.401 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 4.746355e-08 | 7.324 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 5.553209e-08 | 7.255 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 6.522242e-08 | 7.186 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 7.145323e-08 | 7.146 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 7.657086e-08 | 7.116 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 8.288185e-08 | 7.082 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 1.219643e-07 | 6.914 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 1.219643e-07 | 6.914 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 1.219643e-07 | 6.914 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.190122e-07 | 6.924 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 1.190122e-07 | 6.924 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 1.439860e-07 | 6.842 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 1.540784e-07 | 6.812 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 1.540784e-07 | 6.812 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 2.695623e-07 | 6.569 | 0 | 0 |
| Disease | R-HSA-1643685 | 2.755612e-07 | 6.560 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 2.781323e-07 | 6.556 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 3.203664e-07 | 6.494 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 3.430798e-07 | 6.465 | 1 | 1 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 3.461884e-07 | 6.461 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 3.661592e-07 | 6.436 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 6.551481e-07 | 6.184 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 7.137933e-07 | 6.146 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 7.862161e-07 | 6.104 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 7.789131e-07 | 6.109 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 8.990206e-07 | 6.046 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 9.858067e-07 | 6.006 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 9.858067e-07 | 6.006 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 1.042535e-06 | 5.982 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 1.046721e-06 | 5.980 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 1.055563e-06 | 5.977 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 1.150023e-06 | 5.939 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 1.256893e-06 | 5.901 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 1.421701e-06 | 5.847 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 1.552255e-06 | 5.809 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 1.560701e-06 | 5.807 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 2.038036e-06 | 5.691 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 2.260613e-06 | 5.646 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 2.260613e-06 | 5.646 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 2.348646e-06 | 5.629 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 2.681022e-06 | 5.572 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 3.056403e-06 | 5.515 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.977058e-06 | 5.526 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 3.392442e-06 | 5.469 | 0 | 0 |
| Immune System | R-HSA-168256 | 3.530913e-06 | 5.452 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 3.169821e-06 | 5.499 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 3.207325e-06 | 5.494 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 4.277763e-06 | 5.369 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 4.491168e-06 | 5.348 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 4.595551e-06 | 5.338 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 5.057465e-06 | 5.296 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 5.648373e-06 | 5.248 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 5.648373e-06 | 5.248 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 5.880004e-06 | 5.231 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 6.181161e-06 | 5.209 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 6.708142e-06 | 5.173 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 6.807323e-06 | 5.167 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 6.892744e-06 | 5.162 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 7.008003e-06 | 5.154 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 7.008003e-06 | 5.154 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 8.622548e-06 | 5.064 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 1.077382e-05 | 4.968 | 0 | 0 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 1.287662e-05 | 4.890 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.461892e-05 | 4.835 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 1.555595e-05 | 4.808 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 1.750740e-05 | 4.757 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 2.082479e-05 | 4.681 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 2.510857e-05 | 4.600 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 2.605127e-05 | 4.584 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 2.716535e-05 | 4.566 | 0 | 0 |
| Protein folding | R-HSA-391251 | 3.025745e-05 | 4.519 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 3.057608e-05 | 4.515 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 3.770561e-05 | 4.424 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 3.955062e-05 | 4.403 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 3.770561e-05 | 4.424 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 3.192444e-05 | 4.496 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 4.534377e-05 | 4.343 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 4.639274e-05 | 4.334 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 4.639274e-05 | 4.334 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 4.639274e-05 | 4.334 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 4.639274e-05 | 4.334 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.788076e-05 | 4.320 | 1 | 1 |
| Chromatin modifying enzymes | R-HSA-3247509 | 4.956961e-05 | 4.305 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 5.507144e-05 | 4.259 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 6.235830e-05 | 4.205 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 8.048924e-05 | 4.094 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 8.494759e-05 | 4.071 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 1.052727e-04 | 3.978 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 1.159298e-04 | 3.936 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 1.270508e-04 | 3.896 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 1.377683e-04 | 3.861 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 1.408155e-04 | 3.851 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 1.489493e-04 | 3.827 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 1.586141e-04 | 3.800 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 1.632026e-04 | 3.787 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.667065e-04 | 3.778 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.667065e-04 | 3.778 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 1.757941e-04 | 3.755 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 1.767981e-04 | 3.753 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.820765e-04 | 3.740 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 1.962956e-04 | 3.707 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 2.121611e-04 | 3.673 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 2.135368e-04 | 3.671 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 2.272530e-04 | 3.643 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.285433e-04 | 3.641 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 2.362291e-04 | 3.627 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 2.462275e-04 | 3.609 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 2.710240e-04 | 3.567 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 2.799998e-04 | 3.553 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 2.884564e-04 | 3.540 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 2.976715e-04 | 3.526 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.410329e-04 | 3.467 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 4.618672e-04 | 3.335 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 4.790999e-04 | 3.320 | 0 | 0 |
| CASP4 inflammasome assembly | R-HSA-9948001 | 5.049712e-04 | 3.297 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 5.437661e-04 | 3.265 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 5.802342e-04 | 3.236 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 6.911517e-04 | 3.160 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 7.247741e-04 | 3.140 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 8.024158e-04 | 3.096 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 8.351279e-04 | 3.078 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 8.555118e-04 | 3.068 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 8.957554e-04 | 3.048 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 9.745485e-04 | 3.011 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 9.842549e-04 | 3.007 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 1.085337e-03 | 2.964 | 0 | 0 |
| Microbial factors inhibit CASP4 activity | R-HSA-9956593 | 1.091477e-03 | 2.962 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 1.126865e-03 | 2.948 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 1.193418e-03 | 2.923 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 1.194633e-03 | 2.923 | 0 | 0 |
| Non-canonical inflammasome activation | R-HSA-9686114 | 1.284689e-03 | 2.891 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 1.329051e-03 | 2.876 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 1.367259e-03 | 2.864 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 1.431797e-03 | 2.844 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 1.480970e-03 | 2.829 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.498154e-03 | 2.824 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.498154e-03 | 2.824 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 1.562612e-03 | 2.806 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 1.939254e-03 | 2.712 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.988791e-03 | 2.701 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 2.169363e-03 | 2.664 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 2.424441e-03 | 2.615 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 2.454871e-03 | 2.610 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 2.454871e-03 | 2.610 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 2.529715e-03 | 2.597 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.568969e-03 | 2.590 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 2.681874e-03 | 2.572 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 2.719165e-03 | 2.566 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.894237e-03 | 2.538 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.921803e-03 | 2.534 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 3.108444e-03 | 2.507 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 3.115284e-03 | 2.507 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 3.176683e-03 | 2.498 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 3.185947e-03 | 2.497 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 3.243751e-03 | 2.489 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 3.780789e-03 | 2.422 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 3.874667e-03 | 2.412 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 4.091118e-03 | 2.388 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 4.232771e-03 | 2.373 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 4.357845e-03 | 2.361 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 4.894976e-03 | 2.310 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 5.254932e-03 | 2.279 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 5.541835e-03 | 2.256 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 5.561451e-03 | 2.255 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 5.561451e-03 | 2.255 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 5.879205e-03 | 2.231 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 6.214420e-03 | 2.207 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 6.214420e-03 | 2.207 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 6.269336e-03 | 2.203 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 6.558781e-03 | 2.183 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 7.301242e-03 | 2.137 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 7.462629e-03 | 2.127 | 0 | 0 |
| Interleukin-18 signaling | R-HSA-9012546 | 7.462629e-03 | 2.127 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.154593e-02 | 1.938 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.154593e-02 | 1.938 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.154593e-02 | 1.938 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.154593e-02 | 1.938 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.154593e-02 | 1.938 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.154593e-02 | 1.938 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 8.814099e-03 | 2.055 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.026630e-02 | 1.989 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 8.326775e-03 | 2.080 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.026630e-02 | 1.989 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 1.075200e-02 | 1.969 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 1.026630e-02 | 1.989 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 8.814099e-03 | 2.055 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 9.504290e-03 | 2.022 | 0 | 0 |
| Kinesins | R-HSA-983189 | 8.515575e-03 | 2.070 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 7.998910e-03 | 2.097 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 1.001529e-02 | 1.999 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.081995e-02 | 1.966 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 9.660272e-03 | 2.015 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 1.171018e-02 | 1.931 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 1.218320e-02 | 1.914 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 1.250534e-02 | 1.903 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 1.250534e-02 | 1.903 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.346305e-02 | 1.871 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 1.362105e-02 | 1.866 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 1.362105e-02 | 1.866 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.418655e-02 | 1.848 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.466954e-02 | 1.834 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.520275e-02 | 1.818 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.520275e-02 | 1.818 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.528141e-02 | 1.816 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 1.598988e-02 | 1.796 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.855321e-02 | 1.732 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.855321e-02 | 1.732 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 1.858121e-02 | 1.731 | 0 | 0 |
| CLEC7A (Dectin-1) induces NFAT activation | R-HSA-5607763 | 1.895305e-02 | 1.722 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.895305e-02 | 1.722 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 1.910316e-02 | 1.719 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 2.108436e-02 | 1.676 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 2.234481e-02 | 1.651 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH3 | R-HSA-5632927 | 2.295926e-02 | 1.639 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH6 | R-HSA-5632968 | 2.295926e-02 | 1.639 | 0 | 0 |
| Inhibition of PKR | R-HSA-169131 | 2.295926e-02 | 1.639 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 2.304935e-02 | 1.637 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.304935e-02 | 1.637 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 2.349856e-02 | 1.629 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | R-HSA-2892247 | 2.522170e-02 | 1.598 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 2.530550e-02 | 1.597 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 2.530550e-02 | 1.597 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 2.556333e-02 | 1.592 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.747396e-02 | 1.561 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.747396e-02 | 1.561 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.747396e-02 | 1.561 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.859952e-02 | 1.544 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 2.891837e-02 | 1.539 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 3.072466e-02 | 1.513 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 3.195158e-02 | 1.496 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 3.220980e-02 | 1.492 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 3.271168e-02 | 1.485 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 3.293386e-02 | 1.482 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH2 | R-HSA-5632928 | 3.424150e-02 | 1.465 | 0 | 0 |
| PTEN Loss of Function in Cancer | R-HSA-5674404 | 3.424150e-02 | 1.465 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.424150e-02 | 1.465 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 3.563679e-02 | 1.448 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 3.703853e-02 | 1.431 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 3.703853e-02 | 1.431 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.724042e-02 | 1.429 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 3.731606e-02 | 1.428 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 3.731606e-02 | 1.428 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 3.731606e-02 | 1.428 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 3.928023e-02 | 1.406 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.986129e-02 | 1.399 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 3.992487e-02 | 1.399 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 4.030190e-02 | 1.395 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 4.081855e-02 | 1.389 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 4.142496e-02 | 1.383 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 4.254995e-02 | 1.371 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 4.254995e-02 | 1.371 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 4.254995e-02 | 1.371 | 0 | 0 |
| Regulation of PTEN mRNA translation | R-HSA-8943723 | 4.530449e-02 | 1.344 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.539415e-02 | 1.343 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.539415e-02 | 1.343 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.539415e-02 | 1.343 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.539415e-02 | 1.343 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.539415e-02 | 1.343 | 0 | 0 |
| Activation, myristolyation of BID and translocation to mitochondria | R-HSA-75108 | 4.539415e-02 | 1.343 | 0 | 0 |
| RAB geranylgeranylation | R-HSA-8873719 | 4.558543e-02 | 1.341 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 4.622841e-02 | 1.335 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 4.812306e-02 | 1.318 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 4.812306e-02 | 1.318 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 4.850119e-02 | 1.314 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.731657e-02 | 1.172 | 0 | 0 |
| Interleukin-36 pathway | R-HSA-9014826 | 7.808926e-02 | 1.107 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.808926e-02 | 1.107 | 0 | 0 |
| Loss of phosphorylation of MECP2 at T308 | R-HSA-9022535 | 7.808926e-02 | 1.107 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.873818e-02 | 1.052 | 0 | 0 |
| Chylomicron clearance | R-HSA-8964026 | 9.926475e-02 | 1.003 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.926475e-02 | 1.003 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.926475e-02 | 1.003 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 8.285338e-02 | 1.082 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 7.608049e-02 | 1.119 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 7.608049e-02 | 1.119 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 8.285338e-02 | 1.082 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 6.463946e-02 | 1.190 | 0 | 0 |
| Diseases of Mismatch Repair (MMR) | R-HSA-5423599 | 5.641868e-02 | 1.249 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.873818e-02 | 1.052 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 5.694481e-02 | 1.245 | 0 | 0 |
| Interleukin-10 signaling | R-HSA-6783783 | 7.956809e-02 | 1.099 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 6.202247e-02 | 1.207 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.641868e-02 | 1.249 | 0 | 0 |
| Cam-PDE 1 activation | R-HSA-111957 | 8.873818e-02 | 1.052 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.873818e-02 | 1.052 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 5.694481e-02 | 1.245 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 5.232509e-02 | 1.281 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 6.627896e-02 | 1.179 | 0 | 0 |
| NADE modulates death signalling | R-HSA-205025 | 6.731657e-02 | 1.172 | 0 | 0 |
| Biosynthesis of DPAn-3-derived 13-series resolvins | R-HSA-9026403 | 7.808926e-02 | 1.107 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 7.956809e-02 | 1.099 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.926475e-02 | 1.003 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 6.311347e-02 | 1.200 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 6.239810e-02 | 1.205 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 6.726400e-02 | 1.172 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 9.510459e-02 | 1.022 | 0 | 0 |
| Interleukin-38 signaling | R-HSA-9007892 | 6.731657e-02 | 1.172 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 6.949635e-02 | 1.158 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 7.329966e-02 | 1.135 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 9.691777e-02 | 1.014 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 5.100382e-02 | 1.292 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 7.608049e-02 | 1.119 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 8.387268e-02 | 1.076 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 9.736420e-02 | 1.012 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 7.126155e-02 | 1.147 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 7.608049e-02 | 1.119 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 9.334045e-02 | 1.030 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 9.691777e-02 | 1.014 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 6.627896e-02 | 1.179 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 5.866496e-02 | 1.232 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 5.962294e-02 | 1.225 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 6.756501e-02 | 1.170 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 8.285338e-02 | 1.082 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 7.944410e-02 | 1.100 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 8.980300e-02 | 1.047 | 0 | 0 |
| Transcriptional regulation of pluripotent stem cells | R-HSA-452723 | 9.691777e-02 | 1.014 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 5.787233e-02 | 1.238 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 7.674579e-02 | 1.115 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 5.145043e-02 | 1.289 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 8.980300e-02 | 1.047 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.005336e-01 | 0.998 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 1.044202e-01 | 0.981 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 1.078753e-01 | 0.967 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 1.096377e-01 | 0.960 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 1.096704e-01 | 0.960 | 0 | 0 |
| IFNG signaling activates MAPKs | R-HSA-9732724 | 1.096704e-01 | 0.960 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 1.096704e-01 | 0.960 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.096704e-01 | 0.960 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 1.116720e-01 | 0.952 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.153551e-01 | 0.938 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.191436e-01 | 0.924 | 0 | 0 |
| TBC/RABGAPs | R-HSA-8854214 | 1.191436e-01 | 0.924 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 1.191436e-01 | 0.924 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 1.199564e-01 | 0.921 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 1.199564e-01 | 0.921 | 0 | 0 |
| CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde | R-HSA-442729 | 1.199564e-01 | 0.921 | 0 | 0 |
| Interleukin-9 signaling | R-HSA-8985947 | 1.199564e-01 | 0.921 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 1.229628e-01 | 0.910 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 1.241706e-01 | 0.906 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 1.251015e-01 | 0.903 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.268116e-01 | 0.897 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 1.268116e-01 | 0.897 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 1.270968e-01 | 0.896 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 1.270968e-01 | 0.896 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.301242e-01 | 0.886 | 0 | 0 |
| Lipophagy | R-HSA-9613354 | 1.301242e-01 | 0.886 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 1.301242e-01 | 0.886 | 0 | 0 |
| Activation of RAC1 downstream of NMDARs | R-HSA-9619229 | 1.301242e-01 | 0.886 | 0 | 0 |
| Calcineurin activates NFAT | R-HSA-2025928 | 1.301242e-01 | 0.886 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.301242e-01 | 0.886 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.301242e-01 | 0.886 | 0 | 0 |
| MAPK1 (ERK2) activation | R-HSA-112411 | 1.301242e-01 | 0.886 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.301242e-01 | 0.886 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.301242e-01 | 0.886 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 1.301242e-01 | 0.886 | 0 | 0 |
| Inactivation, recovery and regulation of the phototransduction cascade | R-HSA-2514859 | 1.306887e-01 | 0.884 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 1.348111e-01 | 0.870 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 1.372717e-01 | 0.862 | 0 | 0 |
| Activation of Ca-permeable Kainate Receptor | R-HSA-451308 | 1.401752e-01 | 0.853 | 0 | 0 |
| CaMK IV-mediated phosphorylation of CREB | R-HSA-111932 | 1.401752e-01 | 0.853 | 0 | 0 |
| Interleukin-27 signaling | R-HSA-9020956 | 1.401752e-01 | 0.853 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.401752e-01 | 0.853 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.401752e-01 | 0.853 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 1.499003e-01 | 0.824 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.501107e-01 | 0.824 | 0 | 0 |
| Ionotropic activity of kainate receptors | R-HSA-451306 | 1.501107e-01 | 0.824 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.501107e-01 | 0.824 | 0 | 0 |
| Biosynthesis of DPAn-3-derived maresins | R-HSA-9026290 | 1.501107e-01 | 0.824 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.501107e-01 | 0.824 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.501107e-01 | 0.824 | 0 | 0 |
| The phototransduction cascade | R-HSA-2514856 | 1.504601e-01 | 0.823 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 1.505704e-01 | 0.822 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.544839e-01 | 0.811 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 1.585284e-01 | 0.800 | 0 | 0 |
| Reduction of cytosolic Ca++ levels | R-HSA-418359 | 1.599319e-01 | 0.796 | 0 | 0 |
| Sodium/Calcium exchangers | R-HSA-425561 | 1.599319e-01 | 0.796 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.599319e-01 | 0.796 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 1.620803e-01 | 0.790 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 1.625926e-01 | 0.789 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.696403e-01 | 0.770 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.696403e-01 | 0.770 | 0 | 0 |
| Interleukin-15 signaling | R-HSA-8983432 | 1.696403e-01 | 0.770 | 0 | 0 |
| Interleukin-35 Signalling | R-HSA-8984722 | 1.696403e-01 | 0.770 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.696403e-01 | 0.770 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.696403e-01 | 0.770 | 0 | 0 |
| Biosynthesis of DPAn-3-derived protectins and resolvins | R-HSA-9026286 | 1.696403e-01 | 0.770 | 0 | 0 |
| Pervasive developmental disorders | R-HSA-9005895 | 1.696403e-01 | 0.770 | 0 | 0 |
| Disorders of Nervous System Development | R-HSA-9697154 | 1.696403e-01 | 0.770 | 0 | 0 |
| Loss of function of MECP2 in Rett syndrome | R-HSA-9005891 | 1.696403e-01 | 0.770 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 1.707762e-01 | 0.768 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.707762e-01 | 0.768 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 1.757103e-01 | 0.755 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.792370e-01 | 0.747 | 0 | 0 |
| IL-6-type cytokine receptor ligand interactions | R-HSA-6788467 | 1.792370e-01 | 0.747 | 0 | 0 |
| Interleukin-6 signaling | R-HSA-1059683 | 1.792370e-01 | 0.747 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.792370e-01 | 0.747 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.792370e-01 | 0.747 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.792370e-01 | 0.747 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.792370e-01 | 0.747 | 0 | 0 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | R-HSA-442720 | 1.792370e-01 | 0.747 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.792370e-01 | 0.747 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.792370e-01 | 0.747 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 1.873379e-01 | 0.727 | 0 | 0 |
| Biosynthesis of E-series 18(R)-resolvins | R-HSA-9023661 | 1.887235e-01 | 0.724 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.887235e-01 | 0.724 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.887235e-01 | 0.724 | 0 | 0 |
| Respiratory syncytial virus genome transcription | R-HSA-9828642 | 1.887235e-01 | 0.724 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 1.915135e-01 | 0.718 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 1.957015e-01 | 0.708 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.981008e-01 | 0.703 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.981008e-01 | 0.703 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.981008e-01 | 0.703 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 1.981008e-01 | 0.703 | 0 | 0 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 1.981008e-01 | 0.703 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.981008e-01 | 0.703 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.981008e-01 | 0.703 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 1.989609e-01 | 0.701 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 1.996285e-01 | 0.700 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 2.031879e-01 | 0.692 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 2.073704e-01 | 0.683 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 2.073704e-01 | 0.683 | 0 | 0 |
| KSRP (KHSRP) binds and destabilizes mRNA | R-HSA-450604 | 2.073704e-01 | 0.683 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 2.073704e-01 | 0.683 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 2.073704e-01 | 0.683 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 2.105262e-01 | 0.677 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 2.165333e-01 | 0.664 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 2.165333e-01 | 0.664 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 2.165333e-01 | 0.664 | 0 | 0 |
| Disorders of Developmental Biology | R-HSA-9675151 | 2.165333e-01 | 0.664 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 2.167983e-01 | 0.664 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 2.210435e-01 | 0.656 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 2.210435e-01 | 0.656 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 2.228980e-01 | 0.652 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 2.231630e-01 | 0.651 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 2.252955e-01 | 0.647 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.255909e-01 | 0.647 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.255909e-01 | 0.647 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.255909e-01 | 0.647 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | R-HSA-5358606 | 2.255909e-01 | 0.647 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | R-HSA-5358565 | 2.255909e-01 | 0.647 | 0 | 0 |
| Biosynthesis of aspirin-triggered D-series resolvins | R-HSA-9020265 | 2.255909e-01 | 0.647 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 2.338174e-01 | 0.631 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 2.338174e-01 | 0.631 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 2.338174e-01 | 0.631 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 2.338174e-01 | 0.631 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 2.338174e-01 | 0.631 | 0 | 0 |
| Mismatch Repair | R-HSA-5358508 | 2.345444e-01 | 0.630 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.345444e-01 | 0.630 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.345444e-01 | 0.630 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.345444e-01 | 0.630 | 0 | 0 |
| PKA activation | R-HSA-163615 | 2.345444e-01 | 0.630 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 2.360261e-01 | 0.627 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 2.381398e-01 | 0.623 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.433948e-01 | 0.614 | 0 | 0 |
| Synthesis of 5-eicosatetraenoic acids | R-HSA-2142688 | 2.433948e-01 | 0.614 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.433948e-01 | 0.614 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.433948e-01 | 0.614 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.433948e-01 | 0.614 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 2.433948e-01 | 0.614 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 2.510148e-01 | 0.600 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.521435e-01 | 0.598 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.521435e-01 | 0.598 | 0 | 0 |
| VxPx cargo-targeting to cilium | R-HSA-5620916 | 2.521435e-01 | 0.598 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 2.560564e-01 | 0.592 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.607916e-01 | 0.584 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.607916e-01 | 0.584 | 0 | 0 |
| Biosynthesis of E-series 18(S)-resolvins | R-HSA-9018896 | 2.607916e-01 | 0.584 | 0 | 0 |
| PD-L1(CD274) glycosylation and translocation to plasma membrane | R-HSA-9931295 | 2.607916e-01 | 0.584 | 0 | 0 |
| PKA-mediated phosphorylation of CREB | R-HSA-111931 | 2.607916e-01 | 0.584 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.607916e-01 | 0.584 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 2.636573e-01 | 0.579 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 2.637592e-01 | 0.579 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 2.637592e-01 | 0.579 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 2.680428e-01 | 0.572 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 2.693401e-01 | 0.570 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 2.693401e-01 | 0.570 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.693401e-01 | 0.570 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 2.693401e-01 | 0.570 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.693401e-01 | 0.570 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 2.693401e-01 | 0.570 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 2.693401e-01 | 0.570 | 0 | 0 |
| Translation | R-HSA-72766 | 2.698212e-01 | 0.569 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 2.766087e-01 | 0.558 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.777904e-01 | 0.556 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 2.777904e-01 | 0.556 | 0 | 0 |
| Biosynthesis of D-series resolvins | R-HSA-9018676 | 2.777904e-01 | 0.556 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.777904e-01 | 0.556 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 2.847720e-01 | 0.546 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 2.861434e-01 | 0.543 | 0 | 0 |
| Interleukin-20 family signaling | R-HSA-8854691 | 2.861434e-01 | 0.543 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.861434e-01 | 0.543 | 0 | 0 |
| Biosynthesis of maresins | R-HSA-9018682 | 2.861434e-01 | 0.543 | 0 | 0 |
| Interleukin-6 family signaling | R-HSA-6783589 | 2.944003e-01 | 0.531 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.944003e-01 | 0.531 | 0 | 0 |
| Mitochondrial RNA degradation | R-HSA-9836573 | 2.944003e-01 | 0.531 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 2.979905e-01 | 0.526 | 0 | 0 |
| XBP1(S) activates chaperone genes | R-HSA-381038 | 3.022571e-01 | 0.520 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 3.025622e-01 | 0.519 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 3.025622e-01 | 0.519 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 3.025622e-01 | 0.519 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 3.025622e-01 | 0.519 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 3.025622e-01 | 0.519 | 0 | 0 |
| Glycogen breakdown (glycogenolysis) | R-HSA-70221 | 3.025622e-01 | 0.519 | 0 | 0 |
| Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives | R-HSA-9027604 | 3.025622e-01 | 0.519 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 3.025622e-01 | 0.519 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 3.099751e-01 | 0.509 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 3.106302e-01 | 0.508 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 3.106302e-01 | 0.508 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 3.106302e-01 | 0.508 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 3.162918e-01 | 0.500 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 3.171789e-01 | 0.499 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 3.186054e-01 | 0.497 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 3.186054e-01 | 0.497 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 3.186054e-01 | 0.497 | 0 | 0 |
| Biosynthesis of DPAn-3 SPMs | R-HSA-9025094 | 3.186054e-01 | 0.497 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 3.186054e-01 | 0.497 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 3.186054e-01 | 0.497 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 3.208890e-01 | 0.494 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 3.235151e-01 | 0.490 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 3.257714e-01 | 0.487 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 3.264888e-01 | 0.486 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 3.264888e-01 | 0.486 | 0 | 0 |
| Phase 0 - rapid depolarisation | R-HSA-5576892 | 3.264888e-01 | 0.486 | 0 | 0 |
| Activation of kainate receptors upon glutamate binding | R-HSA-451326 | 3.264888e-01 | 0.486 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.264888e-01 | 0.486 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.264888e-01 | 0.486 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 3.277486e-01 | 0.484 | 0 | 0 |
| IRE1alpha activates chaperones | R-HSA-381070 | 3.277486e-01 | 0.484 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 3.320917e-01 | 0.479 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 3.342815e-01 | 0.476 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 3.342815e-01 | 0.476 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.342815e-01 | 0.476 | 0 | 0 |
| Biosynthesis of EPA-derived SPMs | R-HSA-9018679 | 3.342815e-01 | 0.476 | 0 | 0 |
| Platelet calcium homeostasis | R-HSA-418360 | 3.342815e-01 | 0.476 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.342815e-01 | 0.476 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 3.404053e-01 | 0.468 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.419845e-01 | 0.466 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.419845e-01 | 0.466 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.419845e-01 | 0.466 | 0 | 0 |
| GABA synthesis, release, reuptake and degradation | R-HSA-888590 | 3.419845e-01 | 0.466 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.419845e-01 | 0.466 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 3.446083e-01 | 0.463 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 3.488028e-01 | 0.457 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.495988e-01 | 0.456 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.495988e-01 | 0.456 | 0 | 0 |
| Biosynthesis of DPA-derived SPMs | R-HSA-9018683 | 3.495988e-01 | 0.456 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.495988e-01 | 0.456 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 3.495988e-01 | 0.456 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.529884e-01 | 0.452 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.571255e-01 | 0.447 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 3.571255e-01 | 0.447 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.571646e-01 | 0.447 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 3.645655e-01 | 0.438 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.645655e-01 | 0.438 | 0 | 0 |
| Regulation of MECP2 expression and activity | R-HSA-9022692 | 3.645655e-01 | 0.438 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.645655e-01 | 0.438 | 0 | 0 |
| Association of TriC/CCT with target proteins during biosynthesis | R-HSA-390471 | 3.719199e-01 | 0.430 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.719199e-01 | 0.430 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 3.737702e-01 | 0.427 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 3.737702e-01 | 0.427 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 3.778951e-01 | 0.423 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 3.791896e-01 | 0.421 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 3.791896e-01 | 0.421 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 3.820088e-01 | 0.418 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 3.861110e-01 | 0.413 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.863757e-01 | 0.413 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 3.863757e-01 | 0.413 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 3.934789e-01 | 0.405 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.934789e-01 | 0.405 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.934789e-01 | 0.405 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 3.934789e-01 | 0.405 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 3.934789e-01 | 0.405 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 4.005004e-01 | 0.397 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 4.023993e-01 | 0.395 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 4.023993e-01 | 0.395 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 4.023993e-01 | 0.395 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 4.064399e-01 | 0.391 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 4.074411e-01 | 0.390 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 4.143018e-01 | 0.383 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 4.143018e-01 | 0.383 | 0 | 0 |
| RAS processing | R-HSA-9648002 | 4.143018e-01 | 0.383 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 4.143018e-01 | 0.383 | 0 | 0 |
| NS1 Mediated Effects on Host Pathways | R-HSA-168276 | 4.143018e-01 | 0.383 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 4.210835e-01 | 0.376 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 4.210835e-01 | 0.376 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 4.210835e-01 | 0.376 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 4.210835e-01 | 0.376 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 4.210835e-01 | 0.376 | 0 | 0 |
| Glycogen metabolism | R-HSA-8982491 | 4.210835e-01 | 0.376 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 4.224694e-01 | 0.374 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 4.224694e-01 | 0.374 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 4.224694e-01 | 0.374 | 0 | 0 |
| Purine ribonucleoside monophosphate biosynthesis | R-HSA-73817 | 4.277871e-01 | 0.369 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 4.344134e-01 | 0.362 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.409635e-01 | 0.356 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.409635e-01 | 0.356 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.474381e-01 | 0.349 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 4.499752e-01 | 0.347 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 4.538381e-01 | 0.343 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.538381e-01 | 0.343 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.538381e-01 | 0.343 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.538381e-01 | 0.343 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 4.583161e-01 | 0.339 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 4.601643e-01 | 0.337 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.601643e-01 | 0.337 | 0 | 0 |
| Vasopressin regulates renal water homeostasis via Aquaporins | R-HSA-432040 | 4.601643e-01 | 0.337 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.664177e-01 | 0.331 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.664177e-01 | 0.331 | 0 | 0 |
| Diseases of DNA repair | R-HSA-9675135 | 4.664177e-01 | 0.331 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 4.664177e-01 | 0.331 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 4.664177e-01 | 0.331 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.725990e-01 | 0.326 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 4.729575e-01 | 0.325 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 4.770528e-01 | 0.321 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.787091e-01 | 0.320 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.787091e-01 | 0.320 | 0 | 0 |
| Metal ion SLC transporters | R-HSA-425410 | 4.787091e-01 | 0.320 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.787091e-01 | 0.320 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 4.847488e-01 | 0.314 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 4.847488e-01 | 0.314 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 4.879566e-01 | 0.312 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 4.953564e-01 | 0.305 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 5.024533e-01 | 0.299 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 5.024533e-01 | 0.299 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 5.024533e-01 | 0.299 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 5.031857e-01 | 0.298 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 5.082193e-01 | 0.294 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 5.082193e-01 | 0.294 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 5.082193e-01 | 0.294 | 0 | 0 |
| Nucleotide biosynthesis | R-HSA-8956320 | 5.082193e-01 | 0.294 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 5.099520e-01 | 0.292 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 5.135578e-01 | 0.289 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 5.139188e-01 | 0.289 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 5.195527e-01 | 0.284 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 5.232505e-01 | 0.281 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 5.251215e-01 | 0.280 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 5.251215e-01 | 0.280 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 5.306262e-01 | 0.275 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.360674e-01 | 0.271 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 5.378486e-01 | 0.269 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 5.383069e-01 | 0.269 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 5.414459e-01 | 0.266 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.414459e-01 | 0.266 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 5.417715e-01 | 0.266 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 5.467623e-01 | 0.262 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 5.482461e-01 | 0.261 | 0 | 0 |
| Aquaporin-mediated transport | R-HSA-445717 | 5.520174e-01 | 0.258 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.572119e-01 | 0.254 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 5.572119e-01 | 0.254 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 5.572119e-01 | 0.254 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 5.623465e-01 | 0.250 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.623465e-01 | 0.250 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.623465e-01 | 0.250 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 5.674219e-01 | 0.246 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.674219e-01 | 0.246 | 0 | 0 |
| Ion transport by P-type ATPases | R-HSA-936837 | 5.674219e-01 | 0.246 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 5.751069e-01 | 0.240 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 5.754235e-01 | 0.240 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.819353e-01 | 0.235 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.822994e-01 | 0.235 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.871445e-01 | 0.231 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.883739e-01 | 0.230 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 5.966678e-01 | 0.224 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 5.966678e-01 | 0.224 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 6.059726e-01 | 0.218 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 6.059726e-01 | 0.218 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 6.059726e-01 | 0.218 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 6.072495e-01 | 0.217 | 0 | 0 |
| Ca2+ pathway | R-HSA-4086398 | 6.105446e-01 | 0.214 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 6.105446e-01 | 0.214 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 6.133946e-01 | 0.212 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 6.150638e-01 | 0.211 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 6.239464e-01 | 0.205 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 6.254650e-01 | 0.204 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 6.368894e-01 | 0.196 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 6.411045e-01 | 0.193 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.411045e-01 | 0.193 | 0 | 0 |
| Biosynthesis of DHA-derived SPMs | R-HSA-9018677 | 6.452709e-01 | 0.190 | 0 | 0 |
| Transcriptional activation of mitochondrial biogenesis | R-HSA-2151201 | 6.452709e-01 | 0.190 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 6.458863e-01 | 0.190 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 6.487311e-01 | 0.188 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 6.538029e-01 | 0.185 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 6.543666e-01 | 0.184 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 6.543666e-01 | 0.184 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.574837e-01 | 0.182 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 6.614609e-01 | 0.179 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.653923e-01 | 0.177 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.653923e-01 | 0.177 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.692782e-01 | 0.174 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 6.731192e-01 | 0.172 | 0 | 0 |
| Neurotransmitter release cycle | R-HSA-112310 | 6.843780e-01 | 0.165 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 6.843780e-01 | 0.165 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 6.943651e-01 | 0.158 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 6.952511e-01 | 0.158 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 6.968916e-01 | 0.157 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 7.022920e-01 | 0.153 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 7.088625e-01 | 0.149 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 7.102163e-01 | 0.149 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 7.191943e-01 | 0.143 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 7.191943e-01 | 0.143 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 7.191943e-01 | 0.143 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 7.256849e-01 | 0.139 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 7.288739e-01 | 0.137 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 7.304849e-01 | 0.136 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 7.382216e-01 | 0.132 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.442746e-01 | 0.128 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.472486e-01 | 0.127 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 7.501883e-01 | 0.125 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 7.586198e-01 | 0.120 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 7.588048e-01 | 0.120 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.725136e-01 | 0.112 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 7.777776e-01 | 0.109 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 7.879447e-01 | 0.104 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 7.919643e-01 | 0.101 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 7.920199e-01 | 0.101 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.928535e-01 | 0.101 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 8.044891e-01 | 0.094 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 8.322439e-01 | 0.080 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 8.322439e-01 | 0.080 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.472665e-01 | 0.072 | 0 | 0 |
| S Phase | R-HSA-69242 | 8.559681e-01 | 0.068 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 8.609504e-01 | 0.065 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.625728e-01 | 0.064 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 8.641763e-01 | 0.063 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.734143e-01 | 0.059 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 8.762256e-01 | 0.057 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.913411e-01 | 0.050 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.999234e-01 | 0.046 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 9.067407e-01 | 0.043 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 9.161102e-01 | 0.038 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.254261e-01 | 0.034 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 9.457505e-01 | 0.024 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.500507e-01 | 0.022 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 9.657730e-01 | 0.015 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.695911e-01 | 0.013 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.926880e-01 | 0.003 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.935100e-01 | 0.003 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.948884e-01 | 0.002 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.955075e-01 | 0.002 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.972185e-01 | 0.001 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.975560e-01 | 0.001 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.983819e-01 | 0.001 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999816e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999858e-01 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
