IGF1R
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 |
|---|---|---|---|---|
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y791 | Sugiyama | POTEF A26C1B | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPVLLTEATLN |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y851 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | QVWPEANQHFSKEIDDEANSyFQRIYNHPPHPTMSVDEVLE |
| A6NDG6 | Y248 | Sugiyama | PGP | RQADIIGKPSRFIFDCVSQEyGINPERTVMVGDRLDTDILL |
| A8K0Z3 | Y103 | Sugiyama | WASHC1 FAM39E WASH1 | KKAIKVFSSAKYPAPGRLQEyGsIFTGAQDPGLQRRPRHRI |
| C4AMC7 | Y103 | Sugiyama | WASH3P FAM39DP | KKAIKVFSSAKYPAPERLQEyGsIFTGAQDPGLQRRPRHRI |
| O00115 | Y53 | Sugiyama | DNASE2 DNASE2A DNL2 | YKLPALRGSGEAAQRGLQYKyLDEssGGWRDGRALINsPEG |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00264 | Y113 | Sugiyama | PGRMC1 HPR6.6 PGRMC | INGKVFDVTKGRKFyGPEGPyGVFAGRDASRGLATFCLDKE |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00429 | Y266 | Sugiyama | DNM1L DLP1 DRP1 | NRSQLDINNKKSVTDsIRDEyAFLQKKYPSLANRNGTKYLA |
| O00469 | Y586 | Sugiyama | PLOD2 | FWFPIFSEKACDELVEEMEHyGKWSGGKHHDsRIsGGyENV |
| O00488 | Y97 | Sugiyama | ZNF593 ZT86 | KTHFRSKDHKKRLKQLsVEPysQEEAERAAGMGSYVPPRRL |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O14579 | Y304 | Sugiyama | COPE | HPFIKEYQAKENDFDRLVLQyAPsA________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14602 | Y35 | Sugiyama | EIF1AY | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEALCFDGV |
| O14654 | Y656 | PSP | IRS4 | PPPPAGGTGGKGKSGGRFRLyFCVDRGATKECKEAKEVKDA |
| O14654 | Y828 | PSP | IRS4 | YFSLPNPFRssPLGQNDNsEyVPMLPGKFLGRGLDKEVSyN |
| O14654 | Y847 | PSP | IRS4 | EyVPMLPGKFLGRGLDKEVSyNWDPKDAASKPsGEGsFSKP |
| O14654 | Y921 | PSP | IRS4 | IKPKPQKPTHEQREADssSDyVNMDFTKREsNtPAPsTQGL |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| O14818 | Y176 | Sugiyama | PSMA7 HSPC | WKANAIGRGAKSVREFLEKNyTDEAIETDDLTIKLVIKALL |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14974 | S910 | Sugiyama | PPP1R12A MBS MYPT1 | yETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDST |
| O14974 | Y901 | Sugiyama | PPP1R12A MBS MYPT1 | EtQtDsIsRyETssTsAGDRyDsLLGRsGsysYLEERKPYS |
| O14974 | Y911 | Sugiyama | PPP1R12A MBS MYPT1 | ETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDSTD |
| O15234 | Y240 | Sugiyama | CASC3 MLN51 | HDKFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRK |
| O15234 | Y242 | Sugiyama | CASC3 MLN51 | KFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRKPR |
| O15357 | Y1135 | Sugiyama | INPPL1 SHIP2 | SGDDRSCSVLQMAKTLSEVDyAPAGPARSALLPGPLELQPP |
| O15371 | T46 | Sugiyama | EIF3D EIF3S7 | RDMPyQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGG |
| O15371 | Y201 | Sugiyama | EIF3D EIF3S7 | KMRyLEVSEPQDIECCGALEyyDKAFDRITTRSEKPLRSIK |
| O15371 | Y202 | Sugiyama | EIF3D EIF3S7 | MRyLEVSEPQDIECCGALEyyDKAFDRITTRSEKPLRSIKR |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15530 | Y373 | SIGNOR|EPSD|PSP | PDPK1 PDK1 | QtPPKLTAYLPAMSEDDEDCyGNyDNLLSQFGCMQVSSSSs |
| O15530 | Y376 | SIGNOR|EPSD|PSP | PDPK1 PDK1 | PKLTAYLPAMSEDDEDCyGNyDNLLSQFGCMQVSSSSssHs |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43390 | Y434 | Sugiyama | HNRNPR HNRPR | KKRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGG |
| O43390 | Y435 | Sugiyama | HNRNPR HNRPR | KRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGGR |
| O43390 | Y436 | Sugiyama | HNRNPR HNRPR | RKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGGRG |
| O43432 | Y952 | Sugiyama | EIF4G3 | LLTTIGKDLDFEKAKPRMDQyFNQMEKIVKERKTSSRIRFM |
| O43448 | Y311 | Sugiyama | KCNAB3 KCNA3B | LITSKYDGRVPDTCRASIKGyQWLKDKVQSEDGKKQQAKVM |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y397 | Sugiyama | ACTN4 | GKMVSDINNGWQHLEQAEKGyEEWLLNEIRRLERLDHLAEK |
| O43707 | Y441 | Sugiyama | ACTN4 | KAsIHEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEs |
| O43707 | Y533 | Sugiyama | ACTN4 | REALEKTEKQLEAIDQLHLEyAKRAAPFNNWMESAMEDLQD |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43765 | Y141 | Sugiyama | SGTA SGT SGT1 | NPANAVYFCNRAAAYSKLGNyAGAVQDCERAICIDPAySKA |
| O43823 | Y311 | Sugiyama | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| 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 | Y294 | Sugiyama | CALU | VyEsDQNKDGKLTKEEIVDKyDLFVGsQAtDFGEALVRHDE |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O60282 | Y498 | Sugiyama | KIF5C KIAA0531 NKHC2 | EAAKDEVKEVLQALEELAVNyDQKSQEVEDKTRANEQLTDE |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y276 | Sugiyama | SYNCRIP HNRPQ NSAP1 | KEQILEEFSKVTEGLTDVILyHQPDDKKKNRGFCFLEyEDH |
| O60506 | Y293 | Sugiyama | SYNCRIP HNRPQ NSAP1 | VILyHQPDDKKKNRGFCFLEyEDHKTAAQARRRLMSGKVKV |
| O60506 | Y373 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ILEKAFsQFGKLERVKKLKDyAFIHFDERDGAVKAMEEMNG |
| O60506 | Y47 | Sugiyama | SYNCRIP HNRPQ NSAP1 | FQTLLDAGLPQKVAEKLDEIyVAGLVAHsDLDERAIEALKE |
| O60664 | Y235 | Sugiyama | PLIN3 M6PRBP1 TIP47 | AtsLDGFDVAsVQQQRQEQSyFVRLGsLSERLRQHAyEHsL |
| 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 |
| O60841 | Y134 | Sugiyama | EIF5B IF2 KIAA0741 | EELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKA |
| O60869 | Y109 | Sugiyama | EDF1 | GLtQKDLATKINEKPQVIADyESGRAIPNNQVLGKIERAIG |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75208 | S95 | Sugiyama | COQ9 C16orf49 HSPC326 PSEC0129 | ssHsPPRYTDQGGEEEEDyEsEEQLQHRILTAALEFVPAHG |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75347 | Y48 | Sugiyama | TBCA | KEAKQQEEKIEKMRAEDGENyDIKKQAEILQEsRMMIPDCQ |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75348 | Y47 | Sugiyama | ATP6V1G1 ATP6G ATP6G1 ATP6J | KRKNRRLKQAKEEAQAEIEQyRLQREKEFKAKEAAALGsRG |
| O75369 | T1575 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | QITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYG |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75369 | Y904 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | FNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLVTY |
| O75390 | Y345 | Sugiyama | CS | DEKLRDYIWNtLNSGRVVPGyGHAVLRKTDPRYTCQREFAL |
| O75475 | Y18 | Sugiyama | PSIP1 DFS70 LEDGF PSIP2 | ___MTRDFKPGDLIFAKMKGyPHWPARVDEVPDGAVKPPTN |
| O75533 | Y152 | Sugiyama | SF3B1 SAP155 | RLDPFADGGKtPDPKMNARTyMDVMREQHLTKEEREIRQQL |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75794 | Y304 | Sugiyama | CDC123 C10orf7 D123 | SPAFRCTNSEVtVQPsPyLsyRLPKDFVDLsTGEDAHKLID |
| O75874 | Y391 | Sugiyama | IDH1 PICD | FMTKDLAACIKGLPNVQRsDyLNTFEFMDKLGENLKIKLAQ |
| O94919 | Y134 | Sugiyama | ENDOD1 KIAA0830 | EAEAITSVNSLGSKQALNtDyLDsDyQRGQLYPFSLSSDVQ |
| O95218 | S120 | Sugiyama | ZRANB2 ZIS ZNF265 | tGYGGGFNERENVEyIEREEsDGEyDEFGRKKKKYRGKAVG |
| O95218 | Y114 | Sugiyama | ZRANB2 ZIS ZNF265 | AKLEERtGYGGGFNERENVEyIEREEsDGEyDEFGRKKKKY |
| O95218 | Y124 | Sugiyama | ZRANB2 ZIS ZNF265 | GGFNERENVEyIEREEsDGEyDEFGRKKKKYRGKAVGPAsI |
| O95218 | Y167 | Sugiyama | ZRANB2 ZIS ZNF265 | EVEDKEsEGEEEDEDEDLsKyKLDEDEDEDDADLsKyNLDA |
| O95297 | Y263 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | QLDHsGGHHSDKINKSEsVVyADIRKN______________ |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95425 | Y132 | Sugiyama | SVIL | RRRQLAEKyGLTLDPEADsEyLsRYTKSRKEPDAVEKRGGK |
| O95757 | S599 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | sIDLPIQssLCRQLGQDLLNsyIENEGKMIMQDKLEKERND |
| O95757 | Y600 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | IDLPIQssLCRQLGQDLLNsyIENEGKMIMQDKLEKERNDA |
| O95757 | Y627 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MIMQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPED |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O95881 | Y137 | Sugiyama | TXNDC12 TLP19 UNQ713/PRO1376 | FLDPSGKVHPEIINENGNPsyKyFyVsAEQVVQGMKEAQER |
| O95926 | Y210 | Sugiyama | SYF2 CBPIN GCIPIP | IEKRDKYSRRRPYNDDADIDyINERNAKFNKKAERFYGKYT |
| P00338 | S161 | Sugiyama | LDHA PIG19 | DILTYVAWKISGFPKNRVIGsGCNLDsARFRyLMGERLGVH |
| P00338 | Y10 | Sugiyama | LDHA PIG19 | ___________MAtLKDQLIyNLLKEEQtPQNKITVVGVGA |
| P00338 | Y172 | Sugiyama | LDHA PIG19 | GFPKNRVIGsGCNLDsARFRyLMGERLGVHPLSCHGWVLGE |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00558 | T168 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | EAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNLPQKAGGF |
| 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 |
| P01111 | Y137 | Sugiyama | NRAS HRAS1 | KCDLPTRTVDTKQAHELAKSyGIPFIETSAKTRQGVEDAFy |
| P01116 | Y137 | Sugiyama | KRAS KRAS2 RASK2 | KCDLPSRTVDTKQAQDLARSyGIPFIEtSAKtRQRVEDAFY |
| P02786 | Y168 | Sugiyama | TFRC | NENsyVPREAGsQKDENLALyVENQFREFKLSKVWRDQHFV |
| P03372 | Y219 | PSP | ESR1 ESR NR3A1 | VWSCEGCKAFFKRsIQGHNDyMCPATNQCTIDKNRRKsCQA |
| P04075 | S39 | Sugiyama | ALDOA ALDA | IAHRIVAPGKGILAADEstGsIAKRLQsIGtENtEENRRFy |
| P04075 | T119 | Sugiyama | ALDOA ALDA | KsKGGVVGIKVDKGVVPLAGtNGEtttQGLDGLsERCAQYK |
| P04075 | T124 | Sugiyama | ALDOA ALDA | VVGIKVDKGVVPLAGtNGEtttQGLDGLsERCAQYKKDGAD |
| P04075 | T37 | Sugiyama | ALDOA ALDA | sDIAHRIVAPGKGILAADEstGsIAKRLQsIGtENtEENRR |
| P04080 | Y97 | Sugiyama | CSTB CST6 STFB | NKPLtLsNyQTNKAKHDELtyF___________________ |
| P04181 | Y69 | Sugiyama | OAT | KyGAHNyHPLPVALERGKGIyLWDVEGRKYFDFLSSYSAVN |
| P04406 | S210 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GPsGKLWRDGRGALQNIIPAstGAAKAVGKVIPELNGKLtG |
| P04406 | T211 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | PsGKLWRDGRGALQNIIPAstGAAKAVGKVIPELNGKLtGM |
| P04406 | Y314 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | tFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsK |
| P04406 | Y320 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsKE_____ |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P05387 | Y7 | Sugiyama | RPLP2 D11S2243E RPP2 | ______________MRyVAsyLLAALGGNssPsAKDIKKIL |
| P05388 | Y24 | Sugiyama | RPLP0 | EDRATWKSNyFLKIIQLLDDyPKCFIVGADNVGsKQMQQIR |
| P05455 | Y104 | Sugiyama | SSB | EDKTKIRRsPsKPLPEVTDEyKNDVKNRsVYIKGFPtDAtL |
| P05455 | Y23 | Sugiyama | SSB | ENGDNEKMAALEAKICHQIEyyFGDFNLPRDKFLKEQIKLD |
| P05455 | Y24 | Sugiyama | SSB | NGDNEKMAALEAKICHQIEyyFGDFNLPRDKFLKEQIKLDE |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05997 | S1308 | Sugiyama | COL5A2 | SKKHPARTCDDLKLCHSAKQsGEyWIDPNQGSVEDAIKVYC |
| P05997 | Y1311 | Sugiyama | COL5A2 | HPARTCDDLKLCHSAKQsGEyWIDPNQGSVEDAIKVYCNME |
| P06213 | Y1185 | Sugiyama | INSR | CMVAHDFTVKIGDFGMTRDIyEtDyyRKGGKGLLPVRWMAP |
| P06213 | Y1189 | Sugiyama | INSR | HDFTVKIGDFGMTRDIyEtDyyRKGGKGLLPVRWMAPESLK |
| P06733 | S37 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | NPtVEVDLFtsKGLFRAAVPsGAstGIyEALELRDNDKtRY |
| P06733 | S40 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | VEVDLFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGK |
| P06733 | S419 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | CRSERLAKyNQLLRIEEELGsKAKFAGRNFRNPLAK_____ |
| P06733 | T205 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GAEVyHNLKNVIKEKyGKDAtNVGDEGGFAPNILENKEGLE |
| P06733 | Y131 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ILGVsLAVCKAGAVEKGVPLyRHIADLAGNsEVILPVPAFN |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y200 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EAMRIGAEVyHNLKNVIKEKyGKDAtNVGDEGGFAPNILEN |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y287 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | PsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDDWGAWQKF |
| P06733 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06737 | Y821 | Sugiyama | PYGL | MVLKNIAASGKFSSDRTIKEyAQNIWNVEPsDLKIsLSNES |
| P06748 | Y271 | Sugiyama | NPM1 NPM | MQAsIEKGGsLPKVEAKFINyVKNCFRMtDQEAIQDLWQWR |
| P06899 | Y38 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSK |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07195 | S162 | Sugiyama | LDHB | DILTYVTWKLSGLPKHRVIGsGCNLDsARFRyLMAEKLGIH |
| P07195 | S320 | Sugiyama | LDHB | GLtsVINQKLKDDEVAQLKKsADtLWDIQKDLKDL______ |
| P07195 | T18 | Sugiyama | LDHB | ___MATLKEKLIAPVAEEEAtVPNNKITVVGVGQVGMACAI |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07205 | T168 | Sugiyama | PGK2 PGKB | EAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNLPHKASGF |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07237 | Y99 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPKEytAG |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07355 | Y199 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RAEDGsVIDyELIDQDARDLyDAGVKRKGTDVPKWIsIMTE |
| P07355 | Y24 | EPSD|PSP | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | VHEILCKLsLEGDHstPPsAyGsVKAytNFDAERDALNIEt |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | T107 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAESC |
| P07437 | Y106 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAES |
| P07437 | Y36 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IGAKFWEVISDEHGIDPTGtyHGDsDLQLDRIsVyyNEAtG |
| P07437 | Y50 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IDPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEP |
| P07437 | Y51 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPG |
| P07550 | Y132 | GPS6|ELM|iPTMNet|EPSD | ADRB2 ADRB2R B2AR | IDVLCVTASIETLCVIAVDRyFAITSPFKyQSLLTKNKARV |
| P07550 | Y141 | GPS6|ELM|iPTMNet|EPSD | ADRB2 ADRB2R B2AR | IETLCVIAVDRyFAITSPFKyQSLLTKNKARVIILMVWIVS |
| P07686 | Y547 | Sugiyama | HEXB HCC7 | DRLTRHRCRMVERGIAAQPLyAGyCNHENM___________ |
| P07686 | Y550 | Sugiyama | HEXB HCC7 | TRHRCRMVERGIAAQPLyAGyCNHENM______________ |
| P07737 | T65 | Sugiyama | PFN1 | PAEVGVLVGKDRssFyVNGLtLGGQKCsVIRDsLLQDGEFs |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07737 | Y60 | Sugiyama | PFN1 | FVNITPAEVGVLVGKDRssFyVNGLtLGGQKCsVIRDsLLQ |
| P07814 | T707 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | VsPysCKEAPCVLIyIPDGHtKEMPTSGSKEKTKVEATKNE |
| P07814 | Y701 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | DQPyEPVsPysCKEAPCVLIyIPDGHtKEMPTSGSKEKTKV |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07814 | Y872 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EAVECLLSLKAQYKEKTGKEyIPGQPPLsQssDssPtRNsE |
| P07864 | S161 | Sugiyama | LDHC LDH3 LDHX | DILTYIVWKISGLPVTRVIGsGCNLDsARFRYLIGEKLGVH |
| 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 | Y434 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KNLVKKCLELFtELAEDKENyKKFyEQFSKNIKLGIHEDsQ |
| P07900 | Y492 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLR |
| P07900 | Y493 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | EMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLRK |
| P07900 | Y61 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KEIFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLI |
| P07900 | Y627 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | TANMERIMKAQALRDNstMGyMAAKKHLEINPDHsIIEtLR |
| P08069 | S1009 | Sugiyama | IGF1R | PDEWEVAREKITMSRELGQGsFGMVyEGVAKGVVKDEPETR |
| P08069 | S1365 | Sugiyama | IGF1R | PyAHMNGGRKNERALPLPQSstC__________________ |
| P08069 | S982 | EPSD|PSP | IGF1R | RNNSRLGNGVLyAsVNPEyFsAADVYVPDEWEVAREKITMS |
| P08069 | T1366 | Sugiyama | IGF1R | yAHMNGGRKNERALPLPQSstC___________________ |
| P08069 | Y1014 | Sugiyama | IGF1R | VAREKITMSRELGQGsFGMVyEGVAKGVVKDEPETRVAIKT |
| P08069 | Y1161 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | IGF1R | CMVAEDFTVKIGDFGMTRDIyEtDyyRKGGKGLLPVRWMSP |
| P08069 | Y1165 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | IGF1R | EDFTVKIGDFGMTRDIyEtDyyRKGGKGLLPVRWMSPESLK |
| P08069 | Y1166 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | IGF1R | DFTVKIGDFGMTRDIyEtDyyRKGGKGLLPVRWMSPESLKD |
| P08069 | Y1280 | GPS6|ELM|iPTMNet|EPSD|PSP | IGF1R | LEIISSIKEEMEPGFREVsFyySEENKLPEPEELDLEPENM |
| P08069 | Y1281 | GPS6|ELM|iPTMNet|EPSD|PSP | IGF1R | EIISSIKEEMEPGFREVsFyySEENKLPEPEELDLEPENME |
| P08069 | Y1346 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|Sugiyama | IGF1R | ENGPGPGVLVLRAsFDERQPyAHMNGGRKNERALPLPQSst |
| P08069 | Y973 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | IGF1R | IMLYVFHRKRNNSRLGNGVLyAsVNPEyFsAADVYVPDEWE |
| P08069 | Y980 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | IGF1R | RKRNNSRLGNGVLyAsVNPEyFsAADVYVPDEWEVAREKIT |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | T616 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | yGWTANMERIMKAQALRDNstMGyMMAKKHLEINPDHPIVE |
| P08238 | Y155 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | SAYLVAEKVVVITKHNDDEQyAWEssAGGsFtVRADHGEPI |
| P08238 | Y192 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| P08238 | Y211 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EyLEERRVKEVVKKHsQFIGyPItLyLEKEREKEIsDDEAE |
| P08238 | Y216 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | RRVKEVVKKHsQFIGyPItLyLEKEREKEIsDDEAEEEKGE |
| 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 | Y426 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KNIVKKCLELFsELAEDKENyKKFyEAFSKNLKLGIHEDst |
| P08238 | Y472 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | sELLRyHtsQsGDEMtsLsEyVsRMKEtQKsIyyItGEsKE |
| P08238 | Y484 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVR |
| P08238 | Y485 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVRK |
| P08238 | Y56 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KEIFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDII |
| P08238 | Y619 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | TANMERIMKAQALRDNstMGyMMAKKHLEINPDHPIVEtLR |
| P08621 | Y146 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | yGPIKRIHMVYSKRsGKPRGyAFIEyEHERDMHSAYKHADG |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P09104 | S37 | Sugiyama | ENO2 | NPtVEVDLyTAKGLFRAAVPsGAstGIyEALELRDGDKQRY |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09211 | Y199 | Sugiyama | GSTP1 FAEES3 GST3 | AYVGRLsARPKLKAFLASPEyVNLPINGNGKQ_________ |
| P09234 | T14 | Sugiyama | SNRPC | _______MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKENV |
| P09234 | Y12 | Sugiyama | SNRPC | _________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKE |
| P09234 | Y8 | Sugiyama | SNRPC | _____________MPKFyCDyCDtyLtHDsPsVRKTHCSGR |
| P09382 | S63 | Sugiyama | LGALS1 | CLHFNPRFNAHGDANtIVCNsKDGGAWGTEQREAVFPFQPG |
| P09382 | Y120 | Sugiyama | LGALS1 | KLPDGyEFKFPNRLNLEAINyMAADGDFKIKCVAFD_____ |
| P09651 | S338 | Sugiyama | HNRNPA1 HNRPA1 | YNNQSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyG |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09874 | Y639 | Sugiyama | PARP1 ADPRT PPOL | EEKTGNAWHSKNFTKYPKKFyPLEIDyGQDEEAVKKLTVNP |
| P09874 | Y645 | Sugiyama | PARP1 ADPRT PPOL | AWHSKNFTKYPKKFyPLEIDyGQDEEAVKKLTVNPGTKSKL |
| P09960 | Y131 | Sugiyama | LTA4H LTA4 | PKSSALQWLTPEQTSGKEHPyLFSQCQAIHCRAILPCQDTP |
| P09972 | Y358 | Sugiyama | ALDOC ALDC | AAQGKYEGSGEDGGAAAQsLyIANHAY______________ |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG38 | Y791 | Sugiyama | POTEI | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y754 | Sugiyama | POTEJ | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0DPH7 | Y103 | Sugiyama | TUBA3C TUBA2 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIVDLVLDRIR |
| P10109 | Y142 | Sugiyama | FDX1 ADX | HIYEKLDAITDEENDMLDLAyGLTDRsRLGCQICLTKsMDN |
| P10412 | Y71 | Sugiyama | H1-4 H1F4 HIST1H1E | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11047 | Y352 | Sugiyama | LAMC1 LAMB2 | tAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQD |
| P11142 | S153 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | AyLGKtVTNAVVtVPAyFNDsQRQAtKDAGtIAGLNVLRII |
| P11142 | S40 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P11142 | T163 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VVtVPAyFNDsQRQAtKDAGtIAGLNVLRIINEPtAAAIAy |
| P11142 | Y134 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FYPEEVSSMVLTKMKEIAEAyLGKtVTNAVVtVPAyFNDsQ |
| P11142 | Y149 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | EIAEAyLGKtVTNAVVtVPAyFNDsQRQAtKDAGtIAGLNV |
| P11142 | Y183 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | tIAGLNVLRIINEPtAAAIAyGLDKKVGAERNVLIFDLGGG |
| P11142 | Y371 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | QDFFNGKELNKsINPDEAVAyGAAVQAAILsGDKSENVQDL |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11233 | Y153 | Sugiyama | RALA RAL | DKRQVsVEEAKNRAEQWNVNyVETSAKTRANVDKVFFDLMR |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11413 | Y503 | Sugiyama | G6PD | IYGsRGPTEADELMKRVGFQyEGtyKWVNPHKL________ |
| P11413 | Y507 | Sugiyama | G6PD | RGPTEADELMKRVGFQyEGtyKWVNPHKL____________ |
| P11441 | S60 | Sugiyama | UBL4A DXS254E GDX UBL4 | QQRLLFKGKALADGKRLSDYsIGPNSKLNLVVKPLEKVLLE |
| P11586 | Y258 | Sugiyama | MTHFD1 MTHFC MTHFD | INYVPDDKKPNGRKVVGDVAyDEAKERASFITPVPGGVGPM |
| P11940 | T191 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | GRFKSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLF |
| 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 |
| P11940 | Y54 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | AGPILsIRVCRDMITRRsLGyAyVNFQQPADAERALDtMNF |
| P11940 | Y56 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | PILsIRVCRDMITRRsLGyAyVNFQQPADAERALDtMNFDV |
| P12004 | Y133 | SIGNOR|EPSD|PSP | PCNA | DYEMKLMDLDVEQLGIPEQEySCVVKMPSGEFARICRDLsH |
| P12004 | Y250 | SIGNOR|EPSD|PSP | PCNA | SADVPLVVEYKIADMGHLKyyLAPKIEDEEGs_________ |
| P12004 | Y60 | SIGNOR|EPSD|PSP | PCNA | MDSSHVSLVQLTLRSEGFDTyRCDRNLAMGVNLTSMSKILK |
| P12268 | S508 | Sugiyama | IMPDH2 IMPD2 | LKFEKRtssAQVEGGVHsLHsyEKRLF______________ |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12814 | Y193 | Sugiyama | ACTN1 | WKDGLGFCALIHRHRPELIDyGKLRKDDPLTNLNTAFDVAE |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y378 | Sugiyama | ACTN1 | GRMVSDINNAWGCLEQVEKGyEEWLLNEIRRLERLDHLAEK |
| P12814 | Y422 | Sugiyama | ACTN1 | KAsIHEAWtDGKEAMLRQKDyEtAtLsEIKALLKKHEAFEs |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | T5 | Sugiyama | EEF2 EF2 | ________________MVNFtVDQIRAIMDKKANIRNMsVI |
| P13639 | T582 | Sugiyama | EEF2 EF2 | EEDHACIPIKKSDPVVsyREtVsEEsNVLCLsKsPNKHNRL |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y411 | Sugiyama | EEF2 EF2 | KGPLMMYISKMVPTSDKGRFyAFGRVFsGLVsTGLKVRIMG |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y634 | Sugiyama | EEF2 EF2 | AEDIDKGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGP |
| P13639 | Y639 | Sugiyama | EEF2 EF2 | KGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGPDGTGP |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | S379 | Sugiyama | PDIA4 ERP70 ERP72 | QPEKFQSKYEPRSHMMDVQGstQDsAIKDFVLKyALPLVGH |
| 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 | Y448 | Sugiyama | PDIA4 ERP70 ERP72 | RAATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLs |
| P13667 | Y458 | Sugiyama | PDIA4 ERP70 ERP72 | VLEVAKDFPEytFAIADEEDyAGEVKDLGLsEsGEDVNAAI |
| P13667 | Y565 | Sugiyama | PDIA4 ERP70 ERP72 | DVLIEFYAPWCGHCKQLEPVyNsLAKKYKGQKGLVIAKMDA |
| P13674 | Y141 | Sugiyama | P4HA1 P4HA | FPNDEDQVGAAKALLRLQDtyNLDTDtIsKGNLPGVKHKSF |
| P13674 | Y282 | Sugiyama | P4HA1 P4HA | ASDDQSDQKTTPKKKGVAVDyLPERQKyEMLCRGEGIKMTP |
| P13796 | Y462 | Sugiyama | LCP1 PLS2 | VNKPPYPKLGGNMKKLENCNyAVELGKNQAKFsLVGIGGQD |
| P13797 | Y465 | Sugiyama | PLS3 | VNKPPYPKLGANMKKLENCNyAVELGKHPAKFSLVGIGGQD |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13929 | S37 | Sugiyama | ENO3 | NPtVEVDLHtAKGRFRAAVPsGAstGIyEALELRDGDKGRY |
| P13929 | Y131 | Sugiyama | ENO3 | ILGVSLAVCKAGAAEKGVPLyRHIADLAGNPDLILPVPAFN |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y86 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | KFEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTS |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14618 | S202 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | SLQVKQKGADFLVtEVENGGsLGsKKGVNLPGAAVDLPAVs |
| P14618 | Y148 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | GtAEVELKKGATLKITLDNAyMEKCDENILWLDYKNICKVV |
| P14618 | Y370 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | NAVLDGADCIMLSGEtAKGDyPLEAVRMQHLIAREAEAAIy |
| P14625 | Y258 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | GNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFINFP |
| P14625 | Y401 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | VTFKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDD |
| P14625 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14649 | Y146 | Sugiyama | MYL6B MLC1SA | TFLPMLQAVAKNRGQGTyEDyLEGFRVFDKEGNGKVMGAEL |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14854 | Y34 | Sugiyama | COX6B1 COX6B | TAPFDSRFPNQNQTRNCWQNyLDFHRCQKAMTAKGGDIsVC |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15311 | Y191 | Sugiyama | EZR VIL2 | RIQVWHAEHRGMLKDNAMLEyLKIAQDLEMYGINYFEIKNK |
| P15311 | Y424 | Sugiyama | EZR VIL2 | ERQAVDQIKsQEQLAAELAEytAKIALLEEARRRKEDEVEE |
| P15374 | Y141 | Sugiyama | UCHL3 | KFLEEsVsMsPEERARyLENyDAIRVtHEtsAHEGQTEAPs |
| P15531 | Y151 | Sugiyama | NME1 NDPKA NM23 | GLWFHPEELVDyTsCAQNWIyE___________________ |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y250 | Sugiyama | RPS2 RPS4 | tAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEFt |
| P16402 | Y72 | Sugiyama | H1-3 H1F3 HIST1H1D | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P16403 | Y71 | Sugiyama | H1-2 H1F2 HIST1H1C | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P17066 | S42 | Sugiyama | HSPA6 HSP70B' | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P17812 | Y473 | Sugiyama | CTPS1 CTPS | RRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVWKKCLE |
| P17980 | Y185 | Sugiyama | PSMC3 TBP1 | PtEyDsRVKAMEVDERPtEQysDIGGLDKQIQELVEAIVLP |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18077 | Y14 | Sugiyama | RPL35A GIG33 | _______MSGRLWSKAIFAGyKRGLRNQREHTALLKIEGVy |
| P18124 | Y155 | Sugiyama | RPL7 | IVEPYIAWGYPNLKsVNELIyKRGYGKINKKRIALtDNALI |
| P18124 | Y82 | Sugiyama | RPL7 | RQMYRTEIRMARMARKAGNFyVPAEPKLAFVIRIRGINGVS |
| 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 | S134 | Sugiyama | PGAM1 PGAMA CDABP0006 | IWRRsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCE |
| 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 | S90 | Sugiyama | RCC1 CHC1 | VQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSEM |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19338 | Y351 | Sugiyama | NCL | FAKNDLAVVDVRIGMTRKFGyVDFEsAEDLEKALELtGLKV |
| P19338 | Y462 | Sugiyama | NCL | AEKTFEEKQGtEIDGRsIsLyytGEKGQNQDYRGGKNSTWs |
| P19338 | Y525 | Sugiyama | NCL | VFEKATFIKVPQNQNGKSKGyAFIEFAsFEDAKEALNSCNK |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21333 | Y643 | Sugiyama | FLNA FLN FLN1 | CDDKGDGsCDVRyWPQEAGEyAVHVLCNsEDIRLsPFMADI |
| P22059 | Y767 | Sugiyama | OSBP OSBP1 | RKKREAEAMKATEDGtPYDPyKALWFERKKDPVTKELTHIy |
| P22087 | Y118 | Sugiyama | FBL FIB1 FLRN | ICRGKEDALVTKNLVPGEsVyGEKRVsIsEGDDKIEyRAWN |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22392 | Y142 | Sugiyama | NME2 NM23B | sVKsAEKEISLWFKPEELVDyKSCAHDWVyE__________ |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22492 | Y75 | Sugiyama | H1-6 H1FT H1T HIST1H1T | SQERVGMSLVALKKALAAAGyDVEKNNSRIKLSLKSLVNKG |
| 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 |
| P23284 | Y133 | Sugiyama | PPIB CYPB | tGGKsIyGERFPDENFKLKHyGPGWVsMANAGKDTNGsQFF |
| P23381 | Y212 | Sugiyama | WARS1 IFI53 WARS WRS | VIQMTDDEKYLWKDLtLDQAysyAVENAKDIIACGFDINKT |
| P23396 | S83 | Sugiyama | RPS3 OK/SW-cl.26 | GRRIRELtAVVQKRFGFPEGsVELyAEKVAtRGLCAIAQAE |
| P23396 | Y166 | Sugiyama | RPS3 OK/SW-cl.26 | RAKSMKFVDGLMIHSGDPVNyyVDTAVRHVLLRQGVLGIKV |
| P23396 | Y167 | Sugiyama | RPS3 OK/SW-cl.26 | AKSMKFVDGLMIHSGDPVNyyVDTAVRHVLLRQGVLGIKVK |
| P23396 | Y87 | Sugiyama | RPS3 OK/SW-cl.26 | RELtAVVQKRFGFPEGsVELyAEKVAtRGLCAIAQAEsLRy |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y38 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSK |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | T63 | Sugiyama | CFL1 CFL | DKKNIILEEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyA |
| 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 |
| P23588 | Y211 | Sugiyama | EIF4B | DsDKtDTDWRARPAtDsFDDyPPRRGDDsFGDKYRDRYDsD |
| P23588 | Y609 | Sugiyama | EIF4B | sASKyAALsVDGEDENEGEDyAE__________________ |
| P24534 | Y18 | Sugiyama | EEF1B2 EEF1B EF1B | ___MGFGDLKsPAGLQVLNDyLADKSYIEGYVPsQADVAVF |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24752 | Y256 | Sugiyama | ACAT1 ACAT MAT | IPVtVtVKGQPDVVVKEDEEyKRVDFSKVPKLKTVFQKENG |
| P24752 | Y90 | Sugiyama | ACAT1 ACAT MAT | IAIQGAIEKAGIPKEEVKEAyMGNVLQGGEGQAPTRQAVLG |
| P25205 | Y19 | Sugiyama | MCM3 | __MAGtVVLDDVELREAQRDyLDFLDDEEDQGIyQsKVREL |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25685 | Y5 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | ________________MGKDyyQTLGLARGAsDEEIKRAYR |
| P25685 | Y52 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | HPDKNKEPGAEEKFKEIAEAyDVLSDPRKREIFDRYGEEGL |
| P25685 | Y6 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | _______________MGKDyyQTLGLARGAsDEEIKRAYRR |
| P25789 | Y156 | Sugiyama | PSMA4 HC9 PSC9 | YIGWDKHYGFQLYQSDPSGNyGGWKATCIGNNSAAAVsMLK |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26373 | S77 | Sugiyama | RPL13 BBC1 OK/SW-cl.46 | PIVRCPTVRYHTKVRAGRGFsLEELRVAGIHKKVARTIGIs |
| P26639 | Y633 | Sugiyama | TARS1 TARS | PFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMADIDLD |
| P26640 | Y601 | Sugiyama | VARS1 G7A VARS VARS2 | VDMDFGTGAVKITPAHDQNDyEVGQRHGLEAIsIMDsRGAL |
| P26885 | Y112 | Sugiyama | FKBP2 FKBP13 | GLLGMCEGEKRKLVIPsELGyGERGAPPKIPGGATLVFEVE |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27540 | Y561 | Sugiyama | ARNT BHLHE2 | PLEKSDGLFAQDRDPRFsEIyHNINADQSKGISSSTVPATQ |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P27816 | Y47 | Sugiyama | MAP4 | AtLEAEAFDDVVGETVGKTDyIPLLDVDEKtGNsESKKKPC |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P28066 | Y185 | Sugiyama | PSMA5 | CDARAIGsAsEGAQssLQEVyHKSMTLKEAIKSSLIILKQV |
| P28066 | Y8 | Sugiyama | PSMA5 | _____________MFLTRsEyDRGVNtFsPEGRLFQVEyAI |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | S308 | Sugiyama | TKT | PPQEDAPsVDIANIRMPsLPsyKVGDKIATRKAYGQALAKL |
| P29401 | Y202 | Sugiyama | TKT | LDINRLGQsDPAPLQHQMDIyQKRCEAFGWHAIIVDGHSVE |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29558 | Y105 | Sugiyama | RBMS1 C2orf12 MSSP MSSP1 SCR2 | YGKIVSTKAILDKTTNKCKGyGFVDFDsPAAAQKAVSALKA |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30040 | Y115 | Sugiyama | ERP29 C12orf8 ERP28 | DyGDKLNMELSEKYKLDKESyPVFyLFRDGDFENPVPyTGA |
| P30040 | Y119 | Sugiyama | ERP29 C12orf8 ERP28 | KLNMELSEKYKLDKESyPVFyLFRDGDFENPVPyTGAVKVG |
| P30041 | Y89 | Sugiyama | PRDX6 AOP2 KIAA0106 | IALSIDSVEDHLAWSKDINAyNCEEPtEKLPFPIIDDRNRE |
| P30050 | S157 | Sugiyama | RPL12 | QsVGCNVDGRHPHDIIDDINsGAVECPAs____________ |
| 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 | Y169 | Sugiyama | PEBP1 PBP PEBP | FKVAsFRKKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK__ |
| P30086 | Y176 | Sugiyama | PEBP1 PBP PEBP | KKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK_________ |
| P30086 | Y64 | Sugiyama | PEBP1 PBP PEBP | tQVKNRPtsIsWDGLDsGKLytLVLtDPDAPsRKDPKYREW |
| P30101 | Y100 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAyDGPRt |
| P30101 | Y115 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | yGVsGyPtLKIFRDGEEAGAyDGPRtADGIVsHLKKQAGPA |
| P30101 | Y264 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | CPHMTEDNKDLIQGKDLLIAyyDVDyEKNAKGSNYWRNRVM |
| P30101 | Y356 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | FVMQEEFsRDGKALERFLQDyFDGNLKRyLKsEPIPESNDG |
| P30101 | Y445 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KDPNIVIAKMDAtANDVPsPyEVRGFPtIyFsPANKKLNPK |
| P30101 | Y467 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | VRGFPtIyFsPANKKLNPKKyEGGRELsDFIsyLQREAtNP |
| P30101 | Y479 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | NKKLNPKKyEGGRELsDFIsyLQREAtNPPVIQEEKPKKKK |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30101 | Y95 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KGIVPLAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAy |
| P30622 | Y108 | Sugiyama | CLIP1 CYLN1 RSN | AGIVLDEPIGKNDGSVAGVRyFQCEPLKGIFTRPSKLTRKV |
| P31153 | Y188 | Sugiyama | MAT2A AMS2 MATA2 | RRNGTLPWLRPDSKTQVTVQyMQDRGAVLPIRVHTIVISVQ |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31689 | Y52 | Sugiyama | DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4 | KYHPDKNPNEGEKFKQISQAyEVLSDAKKRELYDKGGEQAI |
| P31939 | T182 | Sugiyama | ATIC PURH OK/SW-cl.86 | ESKDTSLETRRQLALKAFTHtAQyDEAISDyFRKQYSKGVs |
| P31939 | Y185 | Sugiyama | ATIC PURH OK/SW-cl.86 | DTSLETRRQLALKAFTHtAQyDEAISDyFRKQYSKGVsQMP |
| P31939 | Y192 | Sugiyama | ATIC PURH OK/SW-cl.86 | RQLALKAFTHtAQyDEAISDyFRKQYSKGVsQMPLRyGMNP |
| P31939 | Y362 | Sugiyama | ATIC PURH OK/SW-cl.86 | IAPGyEEEALTILSKKKNGNyCVLQMDQsYKPDENEVRTLF |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31946 | Y213 | Sugiyama | YWHAB | LAKTAFDEAIAELDtLNEEsyKDstLIMQLLRDNLtLWtSE |
| P31947 | S212 | Sugiyama | SFN HME1 | SLAKTtFDEAMADLHtLsEDsyKDstLIMQLLRDNLtLWTA |
| P31948 | Y27 | Sugiyama | STIP1 | LKEKGNKALsVGNIDDALQCysEAIKLDPHNHVLysNRsAA |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P31948 | Y476 | Sugiyama | STIP1 | DLDssCKEAADGYQRCMMAQyNRHDsPEDVKRRAMADPEVQ |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33176 | Y502 | Sugiyama | KIF5B KNS KNS1 | DASKEEVKEVLQALEELAVNyDQKSQEVEDKTKEyELLSDE |
| P33176 | Y516 | Sugiyama | KIF5B KNS KNS1 | EELAVNyDQKSQEVEDKTKEyELLSDELNQKsATLAsIDAE |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33316 | Y227 | Sugiyama | DUT | EKFEVKKGDRIAQLICERIFyPEIEEVQALDDtERGsGGFG |
| P33778 | Y38 | Sugiyama | H2BC3 H2BFF HIST1H2BB | AITKAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSK |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P34931 | S42 | Sugiyama | HSPA1L | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P34931 | Y185 | Sugiyama | HSPA1L | VIAGLNVLRIINEPtAAAIAyGLDKGGQGERHVLIFDLGGG |
| P34931 | Y547 | Sugiyama | HSPA1L | YKAEDEVQREKIAAKNALEsyAFNMKSVVSDEGLKGKISES |
| 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 |
| P35568 | Y1179 | SIGNOR|EPSD|PSP | IRS1 | APKEPAKLCGAAGGLENGLNyIDLDLVKDFKQCPQECtPEP |
| P35568 | Y1229 | SIGNOR | IRS1 | QPLGSGESSSTRRssEDLSAyASISFQKQPEDRQ_______ |
| P35568 | Y465 | SIGNOR | IRS1 | VtPDsLGHtPPARGEEELsNyICMGGKGPSTLTAPNGHYIL |
| P35568 | Y612 | SIGNOR | IRS1 | LERRGGHHRPDsstLHtDDGyMPMsPGVAPVPSGRKGsGDy |
| P35568 | Y632 | SIGNOR|EPSD|PSP | IRS1 | yMPMsPGVAPVPSGRKGsGDyMPMsPKsVSAPQQIINPIRR |
| P35568 | Y662 | EPSD|PSP | IRS1 | APQQIINPIRRHPQRVDPNGyMMMSPSGGCSPDIGGGPSSS |
| P35568 | Y732 | EPSD|PSP | IRS1 | PHPKPPVESSGGKLLPCTGDyMNMSPVGDSNTSSPSDCYYG |
| P35568 | Y896 | SIGNOR|iPTMNet|EPSD|PSP | IRS1 | EQQQQQQPLLHPPEPKsPGEyVNIEFGSDQSGYLSGPVAFH |
| P35568 | Y941 | SIGNOR|EPSD|PSP | IRS1 | VRCPSQLQPAPREEETGTEEyMKMDLGPGRRAAWQESTGVE |
| P35568 | Y989 | SIGNOR|EPSD|PSP | IRS1 | PPGAASICRPTRAVPSSRGDyMTMQMSCPRQSYVDTsPAAP |
| P35579 | Y9 | Sugiyama | MYH9 | ____________MAQQAADKyLyVDKNFINNPLAQADWAAK |
| P35580 | Y13 | Sugiyama | MYH10 | ________MAQRTGLEDPERyLFVDRAVIYNPATQADWTAK |
| P35609 | Y385 | Sugiyama | ACTN2 | GKMVSDIAGAWQRLEQAEKGyEEWLLNEIRRLERLEHLAEK |
| P35637 | S462 | Sugiyama | FUS TLS | NECNQCKAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRG |
| P35637 | Y325 | Sugiyama | FUS TLS | FKQIGIIKTNKKTGQPMINLyTDRETGKLKGEAtVsFDDPP |
| P35637 | Y468 | Sugiyama | FUS TLS | KAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRGGYRGRG |
| P36578 | S55 | Sugiyama | RPL4 RPL1 | DIVNFVHTNLRKNNRQPyAVsELAGHQtsAEsWGtGRAVAR |
| P36578 | S63 | Sugiyama | RPL4 RPL1 | NLRKNNRQPyAVsELAGHQtsAEsWGtGRAVARIPRVRGGG |
| P36578 | T62 | Sugiyama | RPL4 RPL1 | TNLRKNNRQPyAVsELAGHQtsAEsWGtGRAVARIPRVRGG |
| P36578 | T69 | Sugiyama | RPL4 RPL1 | RQPyAVsELAGHQtsAEsWGtGRAVARIPRVRGGGtHRsGQ |
| P36578 | Y211 | Sugiyama | RPL4 RPL1 | AGKGKMRNRRRIQRRGPCIIyNEDNGIIKAFRNIPGITLLN |
| P36578 | Y264 | Sugiyama | RPL4 RPL1 | GHVGRFCIWtEsAFRKLDELyGtWRKAAsLKsNyNLPMHKM |
| P36578 | Y52 | Sugiyama | RPL4 RPL1 | IRPDIVNFVHTNLRKNNRQPyAVsELAGHQtsAEsWGtGRA |
| P36871 | T426 | Sugiyama | PGM1 | KQsVEDILKDHWQKYGRNFFtRyDyEEVEAEGANKMMKDLE |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P37108 | Y27 | Sugiyama | SRP14 | EQFLtELTRLFQKCRTSGsVyItLKKYDGRTKPIPKKGtVE |
| 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 |
| P38646 | Y196 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | EtAENyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNV |
| P39019 | T55 | Sugiyama | RPS19 | DtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGsM |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P39023 | S13 | Sugiyama | RPL3 OK/SW-cl.32 | ________MSHRKFSAPRHGsLGFLPRKRSSRHRGKVKSFP |
| P39023 | Y291 | Sugiyama | RPL3 OK/SW-cl.32 | QKGYHHRTEINKKIYKIGQGyLIKDGKLIKNNAstDyDLSD |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40261 | Y86 | Sugiyama | NNMT | PTIYQLLSACESFKEIVVTDySDQNLQELEKWLKKEPEAFD |
| P40429 | Y149 | Sugiyama | RPL13A | LKPTRKFAYLGRLAHEVGWKyQAVtAtLEEKRKEKAKIHYR |
| P40939 | Y637 | Sugiyama | HADHA HADH | ELLTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILA |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41091 | Y102 | Sugiyama | EIF2S3 EIF2G | GYANAKIYKLDDPSCPRPECyRSCGsstPDEFPtDIPGtKG |
| P41227 | Y145 | Sugiyama | NAA10 ARD1 ARD1A TE2 | TLNFQISEVEPKyyADGEDAyAMKRDLtQMADELRRHLELK |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42677 | Y31 | Sugiyama | RPS27 MPS1 | sPEEEKRKHKKKRLVQsPNsyFMDVKCPGCYKITTVFSHAQ |
| P42766 | Y114 | Sugiyama | RPL35 | RLNKHEENLKTKKQQRKERLyPLRKYAVKA___________ |
| P43034 | Y18 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | ___MVLSQRQRDELNRAIADyLRSNGyEEAySVFKKEAELD |
| P43243 | Y158 | Sugiyama | MATR3 KIAA0723 | LPQILLQLKRRRtEEGPtLsyGRDGRsAtREPPyRVPRDDW |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43243 | Y213 | Sugiyama | MATR3 KIAA0723 | GPsLNPVLDyDHGsRsQEsGyyDRMDyEDDRLRDGERCRDD |
| P43243 | Y214 | Sugiyama | MATR3 KIAA0723 | PsLNPVLDyDHGsRsQEsGyyDRMDyEDDRLRDGERCRDDs |
| P43490 | Y188 | Sugiyama | NAMPT PBEF PBEF1 | QKKILAKyLLEtsGNLDGLEyKLHDFGyRGVSSQETAGIGA |
| P43490 | Y34 | Sugiyama | NAMPT PBEF PBEF1 | ATDSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKY |
| P43490 | Y471 | Sugiyama | NAMPT PBEF PBEF1 | EEYGQDLLHTVFKNGKVTKsysFDEIRKNAQLNIELEAAHH |
| P45974 | Y849 | Sugiyama | USP5 ISOT | WVIYNDQKVCASEKPPKDLGyIyFyQRVAS___________ |
| P45974 | Y851 | Sugiyama | USP5 ISOT | IYNDQKVCASEKPPKDLGyIyFyQRVAS_____________ |
| P46108 | Y221 | SIGNOR|iPTMNet|EPSD | CRK | IGGNQEGSHPQPLGGPEPGPyAQPSVNTPLPNLQNGPIyAR |
| P46776 | S106 | Sugiyama | RPL27A | tRVNAAKNKtGAAPIIDVVRsGyyKVLGKGKLPKQPVIVKA |
| P46776 | Y108 | Sugiyama | RPL27A | VNAAKNKtGAAPIIDVVRsGyyKVLGKGKLPKQPVIVKAKF |
| P46776 | Y109 | Sugiyama | RPL27A | NAAKNKtGAAPIIDVVRsGyyKVLGKGKLPKQPVIVKAKFF |
| P46776 | Y48 | Sugiyama | RPL27A | HPGGRGNAGGLHHHRINFDKyHPGyFGKVGMKHYHLKRNQs |
| P46776 | Y52 | Sugiyama | RPL27A | RGNAGGLHHHRINFDKyHPGyFGKVGMKHYHLKRNQsFCPt |
| P46777 | Y207 | Sugiyama | RPL5 MSTP030 | sKEFNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyI |
| P46777 | Y210 | Sugiyama | RPL5 MSTP030 | FNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyIKNs |
| P46777 | Y219 | Sugiyama | RPL5 MSTP030 | IMGQNVADyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEM |
| P46777 | Y240 | Sugiyama | RPL5 MSTP030 | KKQFsQyIKNsVtPDMMEEMyKKAHAAIRENPVyEKKPKKE |
| P46778 | T29 | Sugiyama | RPL21 | RGTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQ |
| P46778 | Y156 | Sugiyama | RPL21 | REAHFVRTNGKEPELLEPIPyEFMA________________ |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46940 | Y1095 | Sugiyama | IQGAP1 KIAA0051 | VVKEIMDDKSLNIKTDPVDIyKsWVNQMESQTGEASKLPyD |
| P46940 | Y41 | Sugiyama | IQGAP1 KIAA0051 | LDNERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGED |
| P46940 | Y43 | Sugiyama | IQGAP1 KIAA0051 | NERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGEDLP |
| P46976 | Y332 | Sugiyama | GYG1 GYG | AQPFVSSEERKERWEQGQADyMGADSFDNIKRKLDTYLQ__ |
| P47224 | Y114 | Sugiyama | RABIF MSS4 RASGRF3 | CADCEIGPIGWHCLDDKNSFyVALERVSHE___________ |
| P47756 | Y232 | Sugiyama | CAPZB | NIGRLVEDMENKIRstLNEIyFGKTKDIVNGLRSVQTFADK |
| P47756 | Y59 | Sugiyama | CAPZB | LLSSVDQPLKIARDKVVGKDyLLCDyNRDGDSyRsPWSNKy |
| P47756 | Y64 | Sugiyama | CAPZB | DQPLKIARDKVVGKDyLLCDyNRDGDSyRsPWSNKyDPPLE |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47813 | Y35 | Sugiyama | EIF1AX EIF1A EIF4C | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEAMCFDGV |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48147 | Y28 | Sugiyama | PREP PEP | DVYRDETAVQDYHGHKICDPyAWLEDPDSEQTKAFVEAQNK |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | S42 | Sugiyama | HSPA7 HSP70B | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | Y2034 | Sugiyama | FASN FAS | DYFVVFSSVSCGRGNAGQsNyGFANsAMERICEKRRHEGLP |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49368 | S244 | Sugiyama | CCT3 CCTG TRIC5 | VTHPRMRRYIKNPRIVLLDssLEyKKGEsQtDIEITREEDF |
| P49368 | Y247 | Sugiyama | CCT3 CCTG TRIC5 | PRMRRYIKNPRIVLLDssLEyKKGEsQtDIEITREEDFTRI |
| P49591 | Y248 | Sugiyama | SARS1 SARS SERS | FMRKEVMQEVAQLsQFDEELyKVIGKGSEKSDDNSYDEKYL |
| P49736 | Y234 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | VFKERIsDMCKENREsLVVNyEDLAAREHVLAYFLPEAPAE |
| P49773 | Y109 | Sugiyama | HINT1 HINT PKCI1 PRKCNH1 | GLNKGYRMVVNEGsDGGQsVyHVHLHVLGGRQMHWPPG___ |
| P50454 | Y135 | Sugiyama | SERPINH1 CBP1 CBP2 HSP47 SERPINH2 PIG14 | LRSLSNSTARNVTWKLGsRLyGPssVsFADDFVRssKQHYN |
| P50502 | Y185 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | NAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50914 | Y14 | Sugiyama | RPL14 | _______MVFRRFVEVGRVAyVsFGPHAGKLVAIVDVIDQN |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50991 | Y449 | Sugiyama | CCT4 CCTD SRB | EIELALRLTEYSRTLsGMEsyCVRAFADAMEVIPSTLAENA |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51858 | S69 | Sugiyama | HDGF HMG1L2 | FFGTHETAFLGPKDLFPyEEsKEKFGKPNKRKGFsEGLWEI |
| P51858 | Y23 | Sugiyama | HDGF HMG1L2 | RSNRQKEYKCGDLVFAKMKGyPHWPARIDEMPEAAVKstAN |
| P51858 | Y66 | Sugiyama | HDGF HMG1L2 | QVFFFGTHETAFLGPKDLFPyEEsKEKFGKPNKRKGFsEGL |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52298 | Y14 | Sugiyama | NCBP2 CBP20 PIG55 | _______MSGGLLKALRsDsyVELSQYRDQHFRGDNEEQEK |
| P52565 | Y144 | Sugiyama | ARHGDIA GDIA1 | SGMKYIQHTyRKGVKIDKtDyMVGsYGPRAEEyEFLtPVEE |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | S265 | Sugiyama | HNRNPF HNRPF | EySGLSDGYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQs |
| P52948 | Y848 | Sugiyama | NUP98 ADAR2 | PTDKTSRCLIKsPDRLADINyEGRLEAVSRKQGAQFKEyRP |
| P53041 | Y422 | Sugiyama | PPP5C PPP5 | VsCQFGPDVTKAFLEENNLDyIIRSHEVKAEGYEVAHGGRC |
| P53396 | Y659 | Sugiyama | ACLY | TGGMLDNILASKLyRPGsVAyVSRsGGMsNELNNIISRTTD |
| P53634 | Y438 | Sugiyama | CTSC CPPI | SGMDYWIVKNsWGtGWGENGyFRIRRGtDECAIEsIAVAAt |
| P53999 | S12 | Sugiyama | SUB1 PC4 RPO2TC1 | _________MPKSKELVsssssGsDsDsEVDKKLKRKKQVA |
| P54105 | Y38 | Sugiyama | CLNS1A CLCI ICLN | RQQPDTEAVLNGKGLGtGtLyIAEsRLSWLDGsGLGFSLEY |
| P54652 | S41 | Sugiyama | HSPA2 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P54652 | Y184 | Sugiyama | HSPA2 | tITGLNVLRIINEPtAAAIAyGLDKKGCAGGEKNVLIFDLG |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55084 | Y244 | Sugiyama | HADHB MSTP029 | GHSADRLAAAFAVSRLEQDEyALRsHSLAKKAQDEGLLSDV |
| P55209 | S69 | Sugiyama | NAP1L1 NRP | LAALQERLDGLVEtPtGyIEsLPRVVKRRVNALKNLQVKCA |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y66 | Sugiyama | NAP1L1 NRP | PQILAALQERLDGLVEtPtGyIEsLPRVVKRRVNALKNLQV |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55769 | Y11 | Sugiyama | SNU13 NHP2L1 | __________MTEADVNPKAyPLADAHLTKKLLDLVQQsCN |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| 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 |
| P60174 | Y68 | Sugiyama | TPI1 TPI | yIDFARQKLDPKIAVAAQNCyKVTNGAFtGEIsPGMIKDCG |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | T203 | Sugiyama | ACTB | RDLTDyLMKILtERGysFtttAEREIVRDIKEKLCyVALDF |
| P60709 | T303 | Sugiyama | ACTB | MKCDVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPs |
| P60709 | Y198 | Sugiyama | ACTB | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P60709 | Y240 | Sugiyama | ACTB | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P60709 | Y294 | Sugiyama | ACTB | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P60709 | Y362 | Sugiyama | ACTB | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P60709 | Y91 | Sugiyama | ACTB | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P60842 | Y197 | Sugiyama | EIF4A1 DDX2A EIF4A | KMFVLDEADEMLsRGFKDQIyDIFQKLNsNtQVVLLSATMP |
| P60842 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60900 | Y160 | Sugiyama | PSMA6 PROS27 | LIGIDEEQGPQVYKCDPAGyyCGFKATAAGVKQtEstsFLE |
| P61081 | T176 | Sugiyama | UBE2M UBC12 | NRRLFEQNVQRSMRGGyIGstyFERCLK_____________ |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61221 | Y594 | Sugiyama | ABCE1 RLI RNASEL1 RNASELI RNS4I OK/SW-cl.40 | RPRINKLNsIKDVEQKKsGNyFFLDD_______________ |
| P61247 | S236 | Sugiyama | RPS3A FTE1 MFTL | KMLKKPKFELGKLMELHGEGsssGKAtGDEtGAKVERADGy |
| P61247 | S263 | Sugiyama | RPS3A FTE1 MFTL | GDEtGAKVERADGyEPPVQEsV___________________ |
| P61247 | Y205 | Sugiyama | RPS3A FTE1 MFTL | VNKLIPDsIGKDIEKACQsIyPLHDVFVRKVKMLKKPKFEL |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| P61353 | Y49 | Sugiyama | RPL27 | IDDGtsDRPysHALVAGIDRyPRKVTAAMGKKKIAKRSKIK |
| P61353 | Y75 | Sugiyama | RPL27 | AAMGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtV |
| P61353 | Y77 | Sugiyama | RPL27 | MGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVN |
| P61353 | Y85 | Sugiyama | RPL27 | RSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVNKDVFRDPA |
| P61586 | Y156 | Sugiyama | RHOA ARH12 ARHA RHO12 | QEPVKPEEGRDMANRIGAFGyMECsAKTKDGVREVFEMAtR |
| P61604 | T79 | Sugiyama | HSPE1 | EIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDILGK |
| P61604 | Y88 | Sugiyama | HSPE1 | GDKVLLPEyGGtKVVLDDKDyFLFRDGDILGKyVD______ |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | S215 | Sugiyama | YWHAG | HLAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWts |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P62081 | S174 | Sugiyama | RPS7 | IKVHLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62241 | Y113 | Sugiyama | RPS8 OK/SW-cl.83 | TKTLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEE |
| P62241 | Y117 | Sugiyama | RPS8 OK/SW-cl.83 | VKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEEIL |
| P62241 | Y198 | Sugiyama | RPS8 OK/SW-cl.83 | RPGQCGRADGyVLEGKELEFyLRKIKARKGK__________ |
| P62249 | S9 | Sugiyama | RPS16 | ____________MPsKGPLQsVQVFGRKKTATAVAHCKRGN |
| P62249 | T118 | Sugiyama | RPS16 | KYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGPGAR |
| P62249 | Y115 | Sugiyama | RPS16 | YYQKYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGP |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y214 | Sugiyama | YWHAE | LAKAAFDDAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P62263 | S139 | Sugiyama | RPS14 PRO2640 | LARSGMKIGRIEDVtPIPsDstRRKGGRRGRRL________ |
| P62263 | S69 | Sugiyama | RPS14 PRO2640 | GKETICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELG |
| P62263 | S70 | Sugiyama | RPS14 PRO2640 | KETICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELGI |
| P62263 | Y72 | Sugiyama | RPS14 PRO2640 | TICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELGITA |
| P62269 | S96 | Sugiyama | RPS18 D6S218E | QYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLKK |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | S9 | Sugiyama | RPS29 | ____________MGHQQLyWsHPRKFGQGSRSCRVCSNRHG |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62277 | Y18 | Sugiyama | RPS13 | ___MGRMHAPGKGLsQsALPyRRsVPtWLKLTsDDVKEQIy |
| P62277 | Y89 | Sugiyama | RPS13 | NKILRILKSKGLAPDLPEDLyHLIKKAVAVRKHLERNRKDK |
| P62280 | T54 | Sugiyama | RPS11 | PRYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILs |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62312 | Y72 | Sugiyama | LSM6 | VNGQLKNKyGDAFIRGNNVLyIstQKRRM____________ |
| P62333 | Y328 | Sugiyama | PSMC6 SUG2 | ARLDILKIHAGPITKHGEIDyEAIVKLSDGFNGADLRNVCT |
| P62424 | Y230 | Sugiyama | RPL7A SURF-3 SURF3 | EDKGALAKLVEAIRTNyNDRyDEIRRHWGGNVLGPKSVARI |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62714 | Y284 | Sugiyama | PPP2CB | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRT |
| P62714 | Y80 | Sugiyama | PPP2CB | GQFHDLMELFRIGGKsPDtNyLFMGDyVDRGYYSVETVTLL |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y117 | Sugiyama | RPL23A | VFIVDVKANKHQIKQAVKKLyDIDVAKVNtLIRPDGEKKAY |
| 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 |
| 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 |
| P62851 | T113 | Sugiyama | RPS25 | sKGLIKLVSKHRAQVIytRNtKGGDAPAAGEDA________ |
| P62851 | T54 | Sugiyama | RPS25 | KWSKGKVRDKLNNLVLFDKAtyDKLCKEVPNYKLItPAVVs |
| P62851 | Y109 | Sugiyama | RPS25 | QELLsKGLIKLVSKHRAQVIytRNtKGGDAPAAGEDA____ |
| P62851 | Y55 | Sugiyama | RPS25 | WSKGKVRDKLNNLVLFDKAtyDKLCKEVPNYKLItPAVVsE |
| P62888 | Y62 | Sugiyama | RPL30 | KAKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELG |
| P62888 | Y63 | Sugiyama | RPL30 | AKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELGt |
| P62899 | T107 | Sugiyama | RPL31 | RLSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVDEN__ |
| P62899 | Y103 | Sugiyama | RPL31 | RIRVRLSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVD |
| P62899 | Y108 | Sugiyama | RPL31 | LSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVDEN___ |
| P62899 | Y25 | Sugiyama | RPL31 | KKGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRA |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62910 | Y95 | Sugiyama | RPL32 PP9932 | RKFLVHNVKELEVLLMCNKsyCAEIAHNVSsKNRKAIVERA |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | T135 | Sugiyama | RPL8 | CLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSGSK |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62942 | Y27 | Sugiyama | FKBP1A FKBP1 FKBP12 | tIsPGDGRtFPKRGQtCVVHytGMLEDGKKFDSSRDRNKPF |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63104 | T30 | Sugiyama | YWHAZ | AKLAEQAERyDDMAACMKsVtEQGAELsNEERNLLsVAyKN |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63173 | Y41 | Sugiyama | RPL38 | KSVKIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLP |
| P63173 | Y43 | Sugiyama | RPL38 | VKIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLPPG |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | T203 | Sugiyama | ACTG1 ACTG | RDLTDyLMKILtERGysFtttAEREIVRDIKEKLCyVALDF |
| P63261 | T303 | Sugiyama | ACTG1 ACTG | MKCDVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPs |
| P63261 | Y198 | Sugiyama | ACTG1 ACTG | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P63261 | Y240 | Sugiyama | ACTG1 ACTG | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P63261 | Y294 | Sugiyama | ACTG1 ACTG | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P63261 | Y362 | Sugiyama | ACTG1 ACTG | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P63261 | Y91 | Sugiyama | ACTG1 ACTG | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67775 | Y284 | Sugiyama | PPP2CA | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRt |
| P67775 | Y80 | Sugiyama | PPP2CA | GQFHDLMELFRIGGKsPDtNyLFMGDyVDRGYYSVETVTLL |
| P67809 | Y196 | Sugiyama | YBX1 NSEP1 YB1 | sAPEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGE |
| P67809 | Y197 | Sugiyama | YBX1 NSEP1 YB1 | APEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGEV |
| P67809 | Y208 | Sugiyama | YBX1 NSEP1 YB1 | yRRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGE |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68032 | Y93 | Sugiyama | ACTC1 ACTC | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68036 | Y75 | Sugiyama | UBE2L3 UBCE7 UBCH7 | INFPAEYPFKPPKITFKTKIyHPNIDEKGQVCLPVISAENW |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68133 | Y93 | Sugiyama | ACTA1 ACTA | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68363 | Y103 | Sugiyama | TUBA1B | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68366 | Y103 | Sugiyama | TUBA4A TUBA1 | YRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDPVLDRIR |
| P78324 | Y470 | EPSD|PSP | SIRPA BIT MFR MYD1 PTPNS1 SHPS1 SIRP | HTEyASIQTSPQPASEDTLTyADLDMVHLNRTPKQPAPKPE |
| P78324 | Y496 | EPSD|PSP | SIRPA BIT MFR MYD1 PTPNS1 SHPS1 SIRP | VHLNRTPKQPAPKPEPSFSEyASVQVPRK____________ |
| P78371 | T474 | Sugiyama | CCT2 99D8.1 CCTB | AGYDSADLVAQLRAAHsEGNttAGLDMREGTIGDMAILGIT |
| P80303 | Y350 | Sugiyama | NUCB2 NEFA | PDsWEtLDQQQFFtEEELKEyENIIALQENELKKKADELQK |
| P83731 | Y11 | Sugiyama | RPL24 | __________MKVELCsFsGyKIYPGHGRRYARTDGKVFQF |
| P84103 | Y13 | Sugiyama | SRSF3 SFRS3 SRP20 | ________MHRDsCPLDCKVyVGNLGNNGNKtELERAFGyy |
| P84103 | Y32 | Sugiyama | SRSF3 SFRS3 SRP20 | VyVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVE |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| P98175 | Y694 | Sugiyama | RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122 | QPISSLRDDERREsAtADAGyAILEKKGALAERQHTsMDLP |
| Q00653 | Y247 | Sugiyama | NFKB2 LYT10 | NLKISRMDKTAGSVRGGDEVyLLCDKVQKDDIEVRFYEDDE |
| Q00839 | Y257 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | QKGGDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVE |
| Q00839 | Y260 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | GDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVEEED |
| Q00839 | Y654 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | LKMKGNFTLPEVAECFDEITyVELQKEEAQKLLEQYKEESK |
| Q01105 | S166 | Sugiyama | SET | yFENKVLSKEFHLNEsGDPssKstEIKWKSGKDLTKRssQT |
| Q01105 | Y140 | Sugiyama | SET | LTRVEVtEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNE |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01518 | Y43 | Sugiyama | CAP1 CAP | HtsDMHRGyADsPsKAGAAPyVQAFDSLLAGPVAEyLKISK |
| Q01518 | Y58 | Sugiyama | CAP1 CAP | AGAAPyVQAFDSLLAGPVAEyLKISKEIGGDVQKHAEMVHT |
| Q02539 | Y74 | Sugiyama | H1-1 H1F1 HIST1H1A | SKERGGVSLAALKKALAAAGyDVEKNNSRIKLGIKsLVsKG |
| Q02878 | T118 | Sugiyama | RPL6 TXREB1 | GDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQHVR |
| Q02878 | Y115 | Sugiyama | RPL6 TXREB1 | PVGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQ |
| Q02878 | Y116 | Sugiyama | RPL6 TXREB1 | VGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQH |
| Q02878 | Y216 | Sugiyama | RPL6 TXREB1 | AtsTKIDISNVKIPKHLtDAyFKKKKLRKPRHQEGEIFDtE |
| Q03431 | Y494 | EPSD|PSP | PTH1R PTHR PTHR1 | WSRWTLALDFKRKARsGsssySYGPMVSHtsVTNVGPRVGL |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04637 | Y958 | Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | LLTTIGKDLDFEKAKPRMDQyFNQMEKIIKEKKTSSRIRFM |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y154 | Sugiyama | YWHAH YWHA1 | LAEVASGEKKNsVVEAsEAAyKEAFEISKEQMQPTHPIRLG |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q06830 | Y34 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | NFKAtAVMPDGQFKDIsLsDyKGKYVVFFFYPLDFTFVCPT |
| Q07020 | T85 | Sugiyama | RPL18 | RMIRKMKLPGRENKtAVVVGtItDDVRVQEVPKLKVCALRV |
| Q07666 | Y145 | Sugiyama | KHDRBS1 SAM68 | LtAEIEKIQKGDSKKDDEENyLDLFsHKNMKLKERVLIPVK |
| Q07955 | Y37 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | RIyVGNLPPDIRtKDIEDVFyKYGAIRDIDLKNRRGGPPFA |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08211 | Y616 | Sugiyama | DHX9 DDX9 LKP NDH2 | KDDDGGEDDDANCNLICGDEyGPETRLsMsQLNEKETPFEL |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q09028 | Y154 | Sugiyama | RBBP4 RBAP48 | PQNPCIIATKtPssDVLVFDyTKHPsKPDPsGECNPDLRLR |
| Q12840 | Y498 | Sugiyama | KIF5A NKHC1 | DAAKDEVKEVLQALEELAVNyDQKSQEVEEKSQQNQLLVDE |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q13098 | Y172 | Sugiyama | GPS1 COPS1 CSN1 | YKGNSIKESIRRGHDDLGDHyLDCGDLSNALKCYSRARDYC |
| Q13162 | Y188 | Sugiyama | PRDX4 | GLGPIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDK |
| Q13162 | Y191 | Sugiyama | PRDX4 | PIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDKGIL |
| Q13242 | S178 | Sugiyama | SRSF9 SFRS9 SRP30C | MEYALRKLDDTKFRsHEGEtsYIRVYPERstsYGYsRsRSG |
| Q13242 | Y17 | Sugiyama | SRSF9 SFRS9 SRP30C | ____MsGWADERGGEGDGRIyVGNLPTDVREKDLEDLFyKY |
| Q13263 | Y133 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TVVDCPVCKQQCFSKDIVENyFMRDsGsKAATDAQDANQCC |
| Q13263 | Y517 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | LtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQPGtA |
| Q13263 | Y755 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | GGTLDLTLIRARLQEKLsPPyssPQEFAQDVGRMFKQFNKL |
| Q13283 | T21 | Sugiyama | G3BP1 G3BP | MVMEKPsPLLVGREFVRQyytLLNQAPDMLHRFYGKNssyV |
| Q13283 | Y20 | Sugiyama | G3BP1 G3BP | _MVMEKPsPLLVGREFVRQyytLLNQAPDMLHRFYGKNssy |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13303 | Y270 | Sugiyama | KCNAB2 KCNA2B KCNK2 | IVSGKYDSGIPPYSRAsLKGyQWLKDKILSEEGRRQQAKLK |
| Q13310 | T191 | Sugiyama | PABPC4 APP1 PABP4 | GRFKSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELF |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13310 | Y54 | Sugiyama | PABPC4 APP1 PABP4 | AGPVLsIRVCRDMITRRsLGyAyVNFQQPADAERALDtMNF |
| Q13310 | Y56 | Sugiyama | PABPC4 APP1 PABP4 | PVLsIRVCRDMITRRsLGyAyVNFQQPADAERALDtMNFDV |
| Q13404 | Y145 | Sugiyama | UBE2V1 CROC1 UBE2V UEV1 P/OKcl.19 | RRLMMSKENMKLPQPPEGQCysN__________________ |
| Q13435 | Y371 | Sugiyama | SF3B2 SAP145 | EKDSTRsRGsDsPAADVEIEyVtEEPEIyEPNFIFFKRIFE |
| Q13435 | Y379 | Sugiyama | SF3B2 SAP145 | GsDsPAADVEIEyVtEEPEIyEPNFIFFKRIFEAFKLTDDV |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13442 | S19 | Sugiyama | PDAP1 HASPP28 | __MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEEE |
| Q13442 | Y70 | Sugiyama | PDAP1 HASPP28 | DPKKEKKsLDsDEsEDEEDDyQQKRKGVEGLIDIENPNRVA |
| Q13480 | Y627 | Sugiyama | GAB1 | NSLDGGSSPMIKPKGDKQVEyLDLDLDsGKstPPRKQKssG |
| Q13509 | T107 | Sugiyama | TUBB3 TUBB4 | PDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECENC |
| Q13509 | Y106 | Sugiyama | TUBB3 TUBB4 | RPDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECEN |
| Q13546 | Y384 | Sugiyama | RIPK1 RIP RIP1 | EHPQEENEPSLQSKLQDEANyHLyGsRMDRQTKQQPRQNVA |
| Q13561 | S83 | Sugiyama | DCTN2 DCTN50 | GTKGLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKY |
| Q13561 | Y207 | Sugiyama | DCTN2 DCTN50 | SKGGSGGKttGtPPDssLVtyELHsRPEQDKFSQAAKVAEL |
| Q13561 | Y81 | Sugiyama | DCTN2 DCTN50 | RVGTKGLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQ |
| Q13573 | Y260 | Sugiyama | SNW1 SKIIP SKIP | KEQQEWKIPPCISNWKNAKGytIPLDKRLAADGRGLQTVHI |
| Q13601 | Y287 | Sugiyama | KRR1 HRB2 | tPFPPPQPESQIDKELAsGEyFLKANQKKRQKMEAIKAKQA |
| Q13642 | Y117 | Sugiyama | FHL1 SLIM1 | DsPKCKGCFKAIVAGDQNVEyKGtVWHKDCFTCSNCKQVIG |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13765 | S132 | Sugiyama | NACA HSD48 | YKSPAsDtyIVFGEAKIEDLsQQAQLAAAEKFKVQGEAVsN |
| Q13765 | T119 | Sugiyama | NACA HSD48 | SKNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAA |
| Q13885 | T107 | Sugiyama | TUBB2A TUBB2 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q13885 | Y106 | Sugiyama | TUBB2A TUBB2 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q14157 | Y858 | Sugiyama | UBAP2L KIAA0144 NICE4 | PFPtPttPLtGRDGsLAsNPysGDLtKFGRGDASSPAPATT |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | Y334 | Sugiyama | CTTN EMS1 | KDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRANF |
| Q14247 | Y446 | Sugiyama | CTTN EMS1 | sFKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYAT |
| Q14247 | Y538 | Sugiyama | CTTN EMS1 | IITNIEMIDDGWWRGVCKGRyGLFPANyVELRQ________ |
| Q14247 | Y545 | Sugiyama | CTTN EMS1 | IDDGWWRGVCKGRyGLFPANyVELRQ_______________ |
| Q14257 | Y30 | Sugiyama | RCN2 ERC55 | LGLLLLCAAAAGAGKAEELHyPLGERRsDyDREALLGVQED |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14257 | Y39 | Sugiyama | RCN2 ERC55 | AAGAGKAEELHyPLGERRsDyDREALLGVQEDVDEyVKLGH |
| Q14257 | Y54 | Sugiyama | RCN2 ERC55 | ERRsDyDREALLGVQEDVDEyVKLGHEEQQKRLQAIIKKID |
| Q14568 | Y160 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGERM |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14671 | Y83 | Sugiyama | PUM1 KIAA0099 PUMH1 | SPVPGSIGVAGRsQDDAMVDyFFQRQHGEQLGGGGsGGGGy |
| Q14677 | Y114 | Sugiyama | CLINT1 ENTH EPN4 EPNR KIAA0171 | SERVVTSAREHIyDLRSLENyHFVDEHGKDQGINIRQKVKE |
| Q14696 | Y58 | Sugiyama | MESD KIAA0081 MESDC2 MESDM UNQ1911/PRO4369 | PGTPDESTPPPRKKKKDIRDyNDADMARLLEQWEKDDDIEE |
| Q14CX7 | Y19 | Sugiyama | NAA25 C12orf30 MDM20 NAP1 | __MATRGHVQDPNDRRLRPIyDyLDNGNNKMAIQQADKLLK |
| Q14CX7 | Y21 | Sugiyama | NAA25 C12orf30 MDM20 NAP1 | MATRGHVQDPNDRRLRPIyDyLDNGNNKMAIQQADKLLKKH |
| Q15024 | Y13 | Sugiyama | EXOSC7 KIAA0116 RRP42 | ________MASVTLSEAEKVyIVHGVQEDLRVDGRGCEDYR |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15056 | Y86 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | sIRsVRLVRDKDTDKFKGFCyVEFDEVDsLKEALtyDGALL |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15181 | Y38 | Sugiyama | PPA1 IOPPP PP | RVFLKNEKGQyIsPFHDIPIyADKDVFHMVVEVPRWSNAKM |
| Q15181 | Y90 | Sugiyama | PPA1 IOPPP PP | KQDVKKGKLRyVANLFPyKGyIWNyGAIPQtWEDPGHNDKH |
| Q15181 | Y94 | Sugiyama | PPA1 IOPPP PP | KKGKLRyVANLFPyKGyIWNyGAIPQtWEDPGHNDKHTGCC |
| Q15185 | S82 | Sugiyama | PTGES3 P23 TEBP | NDsKHKRtDRsILCCLRKGEsGQsWPRLTKERAKLNWLsVD |
| Q15293 | S159 | Sugiyama | RCN1 RCN | EyKQAtyGyyLGNPAEFHDssDHHtFKKMLPRDERRFKAAD |
| Q15293 | S80 | Sugiyama | RCN1 RCN | HEAFLGKEDsKtFDQLtPDEsKERLGKIVDRIDNDGDGFVt |
| Q15293 | T144 | Sugiyama | RCN1 RCN | WKDYDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtF |
| Q15293 | Y115 | Sugiyama | RCN1 RCN | GDGFVttEELKtWIKRVQKRyIFDNVAKVWKDYDRDKDDKI |
| Q15293 | Y140 | Sugiyama | RCN1 RCN | VAKVWKDYDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssD |
| Q15293 | Y145 | Sugiyama | RCN1 RCN | KDYDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFK |
| Q15293 | Y147 | Sugiyama | RCN1 RCN | YDRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKM |
| Q15293 | Y148 | Sugiyama | RCN1 RCN | DRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKML |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15555 | Y268 | Sugiyama | MAPRE2 RP1 | NEQVHsLKLALEGVEKERDFyFGKLREIELLCQEHGQENDD |
| Q15631 | Y210 | Sugiyama | TSN | sLRKRYDGLKYDVKKVEEVVyDLSIRGFNKETAAACVEK__ |
| Q15637 | Y87 | Sugiyama | SF1 ZFM1 ZNF162 | tGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFRTRKKLEE |
| Q15642 | Y590 | Sugiyama | TRIP10 CIP4 STOT STP | MEEDKGDGWTRVRRKEGGEGyVPtsyLRVTLN_________ |
| Q15642 | Y595 | Sugiyama | TRIP10 CIP4 STOT STP | GDGWTRVRRKEGGEGyVPtsyLRVTLN______________ |
| Q15691 | Y217 | Sugiyama | MAPRE1 | MQQVNVLKLtVEDLEKERDFyFGKLRNIELICQENEGENDP |
| Q15785 | Y25 | Sugiyama | TOMM34 URCC3 | FPDsVEELRAAGNESFRNGQyAEASALyGRALRVLQAQGss |
| Q15785 | Y54 | Sugiyama | TOMM34 URCC3 | RALRVLQAQGssDPEEEsVLysNRAACHLKDGNCRDCIKDC |
| Q16543 | Y248 | Sugiyama | CDC37 CDC37A | VDPRACFRQFFTKIKtADRQyMEGFNDELEAFKERVRGRAK |
| Q16576 | Y153 | Sugiyama | RBBP7 RBAP46 | PQNPHIIATKtPssDVLVFDyTKHPAKPDPsGECNPDLRLR |
| Q16595 | T93 | Sugiyama | FXN FRDA X25 | VYLMNLRKsGtLGHPGsLDEttyERLAEETLDSLAEFFEDL |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16778 | Y38 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssK |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q16881 | Y161 | Sugiyama | TXNRD1 GRIM12 KDRF | QEGRLQKLLKMNGPEDLPKsyDyDLIIIGGGSGGLAAAKEA |
| Q32MZ4 | Y597 | Sugiyama | LRRFIP1 GCF2 TRIP | KKKKsPVPVETLKDVKKELtyQNTDLsEIKEEEQVKstDRK |
| Q4VXU2 | Y291 | Sugiyama | PABPC1L C20orf119 | ERQNELKRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLR |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | Y167 | Sugiyama | HSP90AB4P | GEPIDRDTKVILHLKEDQtEyLEERWVKEVVKKHPQFIGCL |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | T489 | Sugiyama | HSP90AB3P HSP90BC | YGWTANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIME |
| Q58FF7 | Y171 | Sugiyama | HSP90AB3P HSP90BC | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| Q58FF7 | Y190 | Sugiyama | HSP90AB3P HSP90BC | EyLEERRVKEVVKKHsQFIGyPItLyLEKEQDKEIsDDEAE |
| Q58FF7 | Y195 | Sugiyama | HSP90AB3P HSP90BC | RRVKEVVKKHsQFIGyPItLyLEKEQDKEIsDDEAEEEKGE |
| 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 |
| Q5QNW6 | Y38 | Sugiyama | H2BC18 HIST2H2BF | AVTKVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5T035 | Y67 | Sugiyama | FAM120A2P C9orf129 | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERSLPIN |
| Q5U5X0 | Y96 | Sugiyama | LYRM7 C5orf31 MZM1L | TDHNTLKLVPRKDLLVENVPyCDAPTQKQ____________ |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VV41 | Y216 | Sugiyama | ARHGEF16 EPHEXIN4 NBR | KKTLGRKRGHKGsFKDDPQLyQEIQERGLNtsQEsDDDILD |
| Q6DN03 | Y38 | Sugiyama | H2BC20P HIST2H2BC | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCK |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y38 | Sugiyama | H2BC19P HIST2H2BD | AVTKAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCK |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6FI81 | Y278 | Sugiyama | CIAPIN1 CUA001 PRO0915 | EKEKSREQMSSQPKsACGNCyLGDAFRCAsCPyLGMPAFKP |
| Q6PKG0 | Y633 | Sugiyama | LARP1 KIAA0731 LARP | MEQMDGRKNtFtAWsDEEsDyEIDDRDVNKILIVtQtPHyM |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y791 | Sugiyama | POTEE A26C1A POTE2 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6VEQ5 | Y103 | Sugiyama | WASH2P FAM39B | KKAIKVFSSAKYPAPERLQEyGsIFTGAQDPGLQRRPRHRI |
| Q6WKZ4 | Y1254 | Sugiyama | RAB11FIP1 RCP | VLKQKETISKKEFQVRELEDyIDNLLVRVMEETPNILRIPT |
| Q6XE24 | Y104 | Sugiyama | RBMS3 | YGKIVSTKAILDKNTNQCKGyGFVDFDsPAAAQKAVASLKA |
| Q6ZMR3 | S161 | Sugiyama | LDHAL6A LDHL2 | DILTYVAWKLSGFPKNRVIGsGCNLDsARFRYFIGQRLGIH |
| Q6ZSR9 | Y28 | Sugiyama | None | LYPDPSRVPGTKTQNNLESDyLARDGPSSNSSFHSSEEEGT |
| Q71RC2 | Y425 | Sugiyama | LARP4 PP13296 | SRNFPAERHNPTVTGHQEQtyLQKETSTLQVEQNGDYGRGR |
| Q71U36 | Y103 | Sugiyama | TUBA1A TUBA3 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q71UM5 | Y31 | Sugiyama | RPS27L | sLEEEKKKHKKKRLVQsPNsyFMDVKCPGCYKITTVFSHAQ |
| Q7KZF4 | Y109 | Sugiyama | SND1 TDRD11 | KLIGKEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVA |
| Q7L804 | Y480 | Sugiyama | RAB11FIP2 KIAA0941 | LVKHKELLRRKDTHIRELEDyIDNLLVRVMEETPSILRVPY |
| Q7RTV0 | Y100 | Sugiyama | PHF5A | KDRDGCPKIVNLGSsKTDLFyERKKYGFKKR__________ |
| Q7RTV0 | Y70 | Sugiyama | PHF5A | NyGsyQGRCVICGGPGVSDAyyCKECTIQEKDRDGCPKIVN |
| Q7Z417 | Y265 | Sugiyama | NUFIP2 KIAA1321 PIG1 | MQQETsVPTLKQGLEtFKPDysEQKGNRVDGSKPIWKYETG |
| Q7Z4V5 | Y18 | Sugiyama | HDGFL2 HDGF2 HDGFRP2 HRP2 UNQ785/PRO1604 | ___MPHAFKPGDLVFAKMKGyPHWPARIDDIADGAVKPPPN |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86UK7 | Y306 | Sugiyama | ZNF598 | QFSYAPRHSRRNEGVVGGEDyEEVDRysRQGRVARAGTRGA |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86VM9 | Y251 | Sugiyama | ZC3H18 NHN1 | NCTWGMNCRFIHPGVNDKGNySLITKADPFPPNGAPPLGPH |
| Q8IV50 | T210 | Sugiyama | LYSMD2 | STQAAKKLKEESRDEEsPyAtSLyHs_______________ |
| Q8IWX8 | Y894 | Sugiyama | CHERP DAN26 SCAF6 | GDVRDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDE |
| Q8IWX8 | Y897 | Sugiyama | CHERP DAN26 SCAF6 | RDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDECK_ |
| Q8IWX8 | Y903 | Sugiyama | CHERP DAN26 SCAF6 | YKGVGVALDDPyENyRRNKsysFIARMKARDECK_______ |
| Q8IZP0 | Y32 | Sugiyama | ABI1 SSH3BP1 | IPSGKRALIEsyQNLTRVADyCENNyIQATDKRKALEETKA |
| Q8N0Y7 | S134 | Sugiyama | PGAM4 PGAM3 | IWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYE |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N257 | Y38 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | AVTKAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssK |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N6H7 | Y278 | Sugiyama | ARFGAP2 ZNF289 Nbla10535 | QAADAKKQAEESMVASMRLAyQELQIDRKKEEKKLQNLEGK |
| Q8N6T3 | Y175 | Sugiyama | ARFGAP1 ARF1GAP | sVtAssDKAFEDWLNDDLGsyQGAQGNRyVGFGNtPPPQKK |
| Q8N7H5 | Y311 | Sugiyama | PAF1 PD2 | IAREYNWNVKNKASKGyEENyFFIFREGDGVyyNELETRVR |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NBS9 | Y289 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | RDGKKVDQYKGKRDLEsLREyVEsQLQRTETGATETVTPSE |
| Q8NFI4 | Y185 | Sugiyama | ST13P5 FAM10A5 | NAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| Q8NHW5 | Y24 | Sugiyama | RPLP0P6 | EDRATWKSNyFLKIIQLLDDyPKCFIVGADNVGsKQMQQIR |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8WUA2 | Y401 | Sugiyama | PPIL4 | TSKKHKKKTHHCsEEKEDEDyMPIKNTNQDIYREMGFGHYE |
| Q92522 | Y48 | Sugiyama | H1-10 H1FX | AALsPsKKRKNSKKKNQPGKySQLVVEtIRRLGERNGSSLA |
| Q92598 | Y641 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MIMQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQD |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y677 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | ICEQDHQNFLRLLTETEDWLyEEGEDQAKQAyVDKLEELMK |
| Q92598 | Y89 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | RFHGRAFNDPFIQKEKENLsyDLVPLKNGGVGIKVMYMGEE |
| Q93079 | Y38 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969E8 | Y53 | Sugiyama | TSR2 | GFGGVHSQEKAKWLGGAVEDyFMRNADLELDEVEDFLGELL |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96AE4 | Y58 | Sugiyama | FUBP1 | ARQIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKV |
| Q96AE4 | Y625 | Sugiyama | FUBP1 | PGGQPDYSAAWAEYYRQQAAyyAQtsPQGMPQHPPAPQGQ_ |
| Q96AE4 | Y626 | Sugiyama | FUBP1 | GGQPDYSAAWAEYYRQQAAyyAQtsPQGMPQHPPAPQGQ__ |
| Q96B18 | S422 | Sugiyama | DACT3 RRR1 | RRGRMAEASGRRGSPRARKAsRsQsETSLLGRASAVPSGPP |
| Q96B18 | S424 | Sugiyama | DACT3 RRR1 | GRMAEASGRRGSPRARKAsRsQsETSLLGRASAVPSGPPKY |
| Q96CT7 | Y38 | Sugiyama | CCDC124 | RRAEAKAAADAKKQKELEDAyWKDDDKHVMRKEQRKEEKEK |
| Q96GA3 | Y66 | Sugiyama | LTV1 C6orf93 | IDNEERRAEQRKyGVFFDDDyDyLQHLKEPSGPSELIPSST |
| Q96GA3 | Y68 | Sugiyama | LTV1 C6orf93 | NEERRAEQRKyGVFFDDDyDyLQHLKEPSGPSELIPSSTFS |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q99426 | Y98 | Sugiyama | TBCB CG22 CKAP1 | PVDDGCRIHVIDHsGARLGEyEDVSRVEKytIsQEAyDQRQ |
| Q99470 | Y187 | Sugiyama | SDF2 | GRPISGQKEVHGMAQPSQNNyWKAMEGIFMKPSELLKAEAH |
| Q99497 | Y67 | Sugiyama | PARK7 | sRDVVICPDAsLEDAKKEGPyDVVVLPGGNLGAQNLSESAA |
| Q99536 | T243 | Sugiyama | VAT1 | ASKHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIVMDP |
| Q99536 | Y240 | Sugiyama | VAT1 | TASASKHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIV |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99543 | Y90 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | LEEFPMLKTLDPKDWKNQDHyAVLGLGHVRYKATQRQIKAA |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99614 | S281 | Sugiyama | TTC1 TPR1 | PFGLstENFQIKQDsstGsysINFVQNPNNNR_________ |
| Q99614 | Y96 | Sugiyama | TTC1 TPR1 | ADKVENKsNEDVNssELDEEyLIELEKNMSDEEKQKRREES |
| Q99733 | T58 | Sugiyama | NAP1L4 NAP2 | LAALQERLDNVPHtPssyIEtLPKAVKRRINALKQLQVRCA |
| Q99733 | Y55 | Sugiyama | NAP1L4 NAP2 | PRVLAALQERLDNVPHtPssyIEtLPKAVKRRINALKQLQV |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y432 | Sugiyama | ACO2 | SQFtITPGSEQIRAtIERDGyAQILRDLGGIVLANACGPCI |
| 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 | Y103 | Sugiyama | TUBA1C TUBA6 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BRL6 | Y44 | Sugiyama | SRSF8 SFRS2B SRP46 | RtsPDsLRRVFEKYGRVGDVyIPREPHTKAPRGFAFVRFHD |
| Q9BRT6 | Y93 | Sugiyama | LLPH C12orf31 cPERP-G | MKMETDIKRNKKTLLDQHGQyPIWMNQRQRKRLKAKREKRK |
| Q9BS40 | Y20 | Sugiyama | LXN | _MEIPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQA |
| Q9BS40 | Y23 | Sugiyama | LXN | IPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQAsME |
| Q9BSU3 | Y145 | Sugiyama | NAA11 ARD1B ARD2 | TLNFQISEVEPKyyADGEDAyAMKRDLSQMADELRRQMDLK |
| Q9BTD8 | Y424 | Sugiyama | RBM42 | FPsFLKAKVIRDKRTGKTKGyGFVSFKDPsDyVRAMREMNG |
| Q9BTD8 | Y435 | Sugiyama | RBM42 | DKRTGKTKGyGFVSFKDPsDyVRAMREMNGKYVGSRPIKLR |
| Q9BTT0 | Y235 | Sugiyama | ANP32E | EVGLSYLMKEEIQDEEDDDDyVEEGEEEEEEEEGGLRGEKR |
| Q9BU89 | Y290 | Sugiyama | DOHH HLRC1 | RESCEVALDMyEHETGRAFQyADGLEQLRGAPS________ |
| Q9BVA1 | T107 | Sugiyama | TUBB2B | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q9BVA1 | Y106 | Sugiyama | TUBB2B | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q9BW91 | Y140 | Sugiyama | NUDT9 NUDT10 PSEC0099 UNQ3012/PRO9771 | FsPKFNEKDGHVERKSKNGLyEIENGRPRNPAGRTGLVGRG |
| Q9BWF3 | Y194 | Sugiyama | RBM4 RBM4A | ECPIDRSGRVADLTEQYNEQyGAVRTPYTMSYGDSLYYNNA |
| Q9BX40 | Y311 | Sugiyama | LSM14B C20orf40 FAM61B RAP55B | AVVTQSAEAPAEEDLLGPNCyyDKSKSFFDNIssELKTSSR |
| Q9BX40 | Y312 | Sugiyama | LSM14B C20orf40 FAM61B RAP55B | VVTQSAEAPAEEDLLGPNCyyDKSKSFFDNIssELKTSSRR |
| Q9BXS5 | Y418 | Sugiyama | AP1M1 CLTNM | IEKSGYQALPWVRYITQNGDyQLRtQ_______________ |
| Q9BY32 | Y45 | Sugiyama | ITPA C20orf37 My049 OK/SW-cl.9 | QILGDKFPCTLVAQKIDLPEyQGEPDEIsIQKCQEAVRQVQ |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BYX7 | Y91 | Sugiyama | POTEKP ACTBL3 FKSG30 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q9BZI7 | Y167 | Sugiyama | UPF3B RENT3B UPF3X | RDTKVGtIDDDPEyRKFLEsyAtDNEKMTstPEtLLEEIEA |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H2H8 | Y75 | Sugiyama | PPIL3 | DPTGTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPN |
| Q9H2H8 | Y78 | Sugiyama | PPIL3 | GTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPNTNG |
| Q9H4F8 | Y407 | Sugiyama | SMOC1 | FKRYVKKKAKPKKCARRFtDyCDLNKDKVISLPELKGCLGV |
| Q9H5H4 | Y359 | Sugiyama | ZNF768 | HSGQKPYKCPHCGKAFGDSSyLLRHQRTHSHERPYSCTECG |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H788 | Y131 | Sugiyama | SH2D4A PPP1R38 SH2A | EEPRKTHsEEFTNsLKTKsQyHDLQAPDNQQtKDIWKKVAE |
| Q9H788 | Y449 | Sugiyama | SH2D4A PPP1R38 SH2A | TSLGKELLLYPCGQQDQLPDyLELFE_______________ |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HB71 | Y165 | Sugiyama | CACYBP S100A6BP SIP PNAS-107 | VKTDTVLILCRKKVENTRWDyLtQVEKECKEKEKPsYDtEt |
| Q9HDC5 | Y316 | Sugiyama | JPH1 JP1 | SERSNGMKYEGEWANNKRHGyGCTVFPDGSKEEGKYKNNIL |
| Q9NP61 | Y378 | Sugiyama | ARFGAP3 ARFGAP1 | DEPVELRsssFssWDDssDSyWKKETSKDTETVLKTTGYSD |
| Q9NP61 | Y408 | Sugiyama | ARFGAP3 ARFGAP1 | ETVLKTTGYSDRPTARRKPDyEPVENTDEAQKKFGNVKAIs |
| Q9NQ50 | Y199 | Sugiyama | MRPL40 NLVCF URIM | TPPIPNYQPPEGRYNDITKVyTQVEFKR_____________ |
| Q9NQA3 | Y85 | Sugiyama | WASH6P CXYorf1 FAM39A | KKAIKVFSSAKYPAPERLQEyGsIFTGAQDPGLQRRPRHRI |
| Q9NQW7 | Y588 | Sugiyama | XPNPEP1 XPNPEPL XPNPEPL1 | QTKMIDVDSLTDKECDWLNNyHLtCRDVIGKELQKQGRQEA |
| Q9NRX4 | Y113 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | ysMAyGPAQHAISTEKIKAKyPDyEVtWANDGy________ |
| Q9NRX4 | Y52 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | RSGAPAAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCE |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NX18 | Y105 | Sugiyama | SDHAF2 C11orf79 PGL2 SDH5 | LLSLFAKEHLQHMTEKQLNLyDRLINEPSNDWDIYYWATEA |
| Q9NY12 | Y103 | Sugiyama | GAR1 NOLA1 | DIVCKCTTDENKVPyFNAPVyLENKEQIGKVDEIFGQLRDF |
| Q9NY12 | Y97 | Sugiyama | GAR1 NOLA1 | LHPCEDDIVCKCTTDENKVPyFNAPVyLENKEQIGKVDEIF |
| Q9NY65 | Y103 | Sugiyama | TUBA8 TUBAL2 | YRQLFHPEQLItGKEDAANNyARGHYTVGKESIDLVLDRIR |
| Q9NYB0 | Y359 | Sugiyama | TERF2IP DRIP5 RAP1 PP8000 | NSGELEATSAFLASGQRADGyPIWSRQDDIDLQKDDEDTRE |
| Q9NYF8 | S209 | Sugiyama | BCLAF1 BTF KIAA0164 | DtFEHDPsEsIDEFNKssAtsGDIWPGLsAyDNsPRsPHsP |
| Q9NYF8 | Y219 | Sugiyama | BCLAF1 BTF KIAA0164 | IDEFNKssAtsGDIWPGLsAyDNsPRsPHsPsPIAtPPSQS |
| Q9NYF8 | Y383 | Sugiyama | BCLAF1 BTF KIAA0164 | EKGSEKGRAEGEWEDQEALDyFsDKEsGKQKFNDsEGDDtE |
| Q9NZB2 | Y418 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERssPIN |
| Q9NZB2 | Y9 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | ____________MGVQGFQDyIEKHCPsAVVPVELQKLARG |
| Q9P031 | Y97 | Sugiyama | CCDC59 BR22 TAP26 HSPC128 | AQTSLESQFtDRYPDNLKHLyLAEEERHRKQARKVDHPLSE |
| Q9P0P0 | Y152 | Sugiyama | RNF181 HSPC238 | RDKARKQQQQHRLENLHGAMyt___________________ |
| Q9UBB9 | Y51 | Sugiyama | TFIP11 STIP HSPC006 | LQNEFNPNRQRHWQTKEEAtyGVWAERDsDDERPSFGGKRA |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y74 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | PDRNPDDPQAQEKFQDLGAAyEVLsDSEKRKQyDTyGEEGL |
| Q9UHI6 | Y673 | Sugiyama | DDX20 DP103 GEMIN3 | EsDSDSySSRTSSQSKGNKsyLEGssDNQLKDsEstPVDDR |
| Q9UHR4 | Y380 | Sugiyama | BAIAP2L1 IRTKS | SFAQGDVITLLIPEEKDGWLyGEHDVSKARGWFPssYTKLL |
| Q9UHX1 | Y269 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | FGKIKSCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNL |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UII2 | Y58 | Sugiyama | ATP5IF1 ATPI ATPIF1 | GsIREAGGAFGKREQAEEERyFRAQsREQLAALKKHHEEEI |
| Q9UIQ6 | Y70 | Sugiyama | LNPEP OTASE | GsRLLVRGLGEHEMEEDEEDyEssAKLLGMsFMNRssGLRN |
| Q9UJU6 | Y16 | Sugiyama | DBNL CMAP SH3P7 PP5423 | _____MAANLSRNGPALQEAyVRVVtEKsPtDWALFTyEGN |
| 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 |
| Q9UKV3 | Y1094 | Sugiyama | ACIN1 ACINUS KIAA0670 | WPQSNPKFLCADyAEQDELDyHRGLLVDRPsEtKTEEQGIP |
| Q9ULD2 | Y205 | Sugiyama | MTUS1 ATBP ATIP GK1 KIAA1288 MTSG1 | HtAGSLPPTGRRsGstsSLSySTWTSSHSDKTHARETTYDR |
| Q9UMS0 | Y194 | Sugiyama | NFU1 HIRIP5 CGI-33 | KELLDTRIRPTVQEDGGDVIyKGFEDGIVQLKLQGSCTSCP |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UNF0 | Y267 | Sugiyama | PACSIN2 | VLLEVQKHLDLSNVAGYKAIyHDLEQsIRAADAVEDLRWFR |
| Q9UNH7 | Y220 | Sugiyama | SNX6 | VSGVKDVDDFFEHERTFLLEyHNRVKDASAKSDRMTRSHKS |
| Q9UNZ2 | Y167 | Sugiyama | NSFL1C UBXN2C | PRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLKLW |
| Q9UPY6 | S155 | Sugiyama | WASF3 KIAA0900 SCAR3 WAVE3 | NILTPYRDDKKDGLKFyTDPsyFFDLWKEKMLQDTEDKRKE |
| Q9UPY6 | Y151 | Sugiyama | WASF3 KIAA0900 SCAR3 WAVE3 | PPPLNILTPYRDDKKDGLKFyTDPsyFFDLWKEKMLQDTED |
| Q9UPY6 | Y156 | Sugiyama | WASF3 KIAA0900 SCAR3 WAVE3 | ILTPYRDDKKDGLKFyTDPsyFFDLWKEKMLQDTEDKRKEK |
| Q9UQ80 | Y98 | Sugiyama | PA2G4 EBP1 | TSISVNNCVCHFsPLKSDQDyILKEGDLVKIDLGVHVDGFI |
| Q9Y237 | S72 | Sugiyama | PIN4 | MEAMEKLKSGMRFNEVAAQysEDKARQGGDLGWMTRGSMVG |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y262 | Y415 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | GDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNY |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2B0 | S115 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | QIDPstHRKNYVRVVGRNGEssELDLQGIRIDsDISGtLKF |
| Q9Y2B0 | S63 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | AQVDPKKTIQMGsFRINPDGsQsVVEVPyARsEAHLtELLE |
| Q9Y2B0 | Y71 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | IQMGsFRINPDGsQsVVEVPyARsEAHLtELLEEICDRMKE |
| Q9Y2B0 | Y92 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | ARsEAHLtELLEEICDRMKEyGEQIDPstHRKNYVRVVGRN |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2W1 | T230 | Sugiyama | THRAP3 BCLAF2 TRAP150 | tsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERsPA |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y2W2 | Y236 | Sugiyama | WBP11 NPWBP SIPP1 SNP70 | GRKVGFALDLPPRRRDEDMLysPELAQRGHDDDVSSTSEDD |
| Q9Y3E1 | Y22 | Sugiyama | HDGFL3 HDGF2 HDGFRP3 CGI-142 | ARPRPREYKAGDLVFAKMKGyPHWPARIDELPEGAVKPPAN |
| Q9Y3F4 | Y114 | Sugiyama | STRAP MAWD UNRIP | LMTLAHKHIVKtVDFtQDSNyLLtGGQDKLLRIYDLNKPEA |
| Q9Y3P9 | Y472 | Sugiyama | RABGAP1 HSPC094 | FFLKLKQIKQRERKNNTDTLyEVVCLESESERERRKTTAsP |
| Q9Y3U8 | Y5 | Sugiyama | RPL36 | ________________MALRyPMAVGLNKGHKVTKNVSKPR |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y450 | Y58 | Sugiyama | HBS1L HBS1 KIAA1038 | AQFIYSRRDKPsVEPVEEyDyEDLKEssNsVsNHQLSGFDQ |
| Q9Y490 | Y1893 | Sugiyama | TLN1 KIAA1027 TLN | TKsNtsPEELGPLANQLTsDyGRLAsEAKPAAVAAENEEIG |
| Q9Y4H2 | S915 | Sugiyama | IRS2 | LEGLPSLPSMHEYPLPPEPKsPGEyINIDFGEPGARLsPPA |
| Q9Y5L4 | Y73 | Sugiyama | TIMM13 TIM13B TIMM13A TIMM13B | KPGGsLDNSEQKCIAMCMDRyMDAWNtVsRAYNSRLQRERA |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y639 | Y216 | Sugiyama | NPTN SDFR1 SDR1 | KNASNMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKA |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | Y244 | Sugiyama | CLIC4 | AysRDEFtNtCPsDKEVEIAysDVAKRLTK___________ |
| Q9Y6W5 | S154 | Sugiyama | WASF2 WAVE2 | NNLTPYRDDGKEALKFyTDPsyFFDLWKEKMLQDTKDIMKE |
| Q9Y6W5 | Y150 | Sugiyama | WASF2 WAVE2 | PPPLNNLTPYRDDGKEALKFyTDPsyFFDLWKEKMLQDTKD |
| Q9Y6W5 | Y155 | Sugiyama | WASF2 WAVE2 | NLTPYRDDGKEALKFyTDPsyFFDLWKEKMLQDTKDIMKEK |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 9.787393e-11 | 10.009 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 9.856127e-11 | 10.006 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 1.451187e-10 | 9.838 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 2.448566e-10 | 9.611 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 5.050099e-10 | 9.297 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 4.756170e-10 | 9.323 | 1 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 1.852020e-09 | 8.732 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 1.695475e-09 | 8.771 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 3.762522e-08 | 7.425 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 4.324036e-08 | 7.364 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 2.643950e-07 | 6.578 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 1.728959e-05 | 4.762 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 4.122141e-05 | 4.385 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.585416e-05 | 4.445 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 4.093720e-05 | 4.388 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 4.093720e-05 | 4.388 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 5.076573e-05 | 4.294 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 8.639850e-05 | 4.063 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 8.449863e-05 | 4.073 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 1.067466e-04 | 3.972 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 1.067466e-04 | 3.972 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 1.363341e-04 | 3.865 | 0 | 0 |
| Downregulation of ERBB4 signaling | R-HSA-1253288 | 2.195667e-04 | 3.658 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 3.501280e-04 | 3.456 | 1 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 5.144535e-04 | 3.289 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 5.712489e-04 | 3.243 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 8.224180e-04 | 3.085 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 8.066427e-04 | 3.093 | 1 | 1 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 9.235787e-04 | 3.035 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 9.736372e-04 | 3.012 | 1 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 1.034626e-03 | 2.985 | 1 | 1 |
| SHC1 events in ERBB4 signaling | R-HSA-1250347 | 1.416840e-03 | 2.849 | 0 | 0 |
| GRB2 events in ERBB2 signaling | R-HSA-1963640 | 1.416840e-03 | 2.849 | 0 | 0 |
| Nuclear signaling by ERBB4 | R-HSA-1251985 | 1.520665e-03 | 2.818 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 1.616840e-03 | 2.791 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 1.718643e-03 | 2.765 | 0 | 0 |
| MTF1 activates gene expression | R-HSA-5660489 | 1.825583e-03 | 2.739 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.901905e-03 | 2.721 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 2.335776e-03 | 2.632 | 0 | 0 |
| IRS activation | R-HSA-74713 | 2.468095e-03 | 2.608 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 3.232321e-03 | 2.490 | 0 | 0 |
| Drug resistance of FLT3 mutants | R-HSA-9702506 | 1.025600e-02 | 1.989 | 0 | 0 |
| Drug resistance of KIT mutants | R-HSA-9669937 | 1.025600e-02 | 1.989 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.025600e-02 | 1.989 | 0 | 0 |
| KIT mutants bind TKIs | R-HSA-9669921 | 1.025600e-02 | 1.989 | 0 | 0 |
| FLT3 mutants bind TKIs | R-HSA-9702509 | 1.025600e-02 | 1.989 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.025600e-02 | 1.989 | 0 | 0 |
| midostaurin-resistant FLT3 mutants | R-HSA-9702600 | 1.025600e-02 | 1.989 | 0 | 0 |
| Masitinib-resistant KIT mutants | R-HSA-9669924 | 1.025600e-02 | 1.989 | 0 | 0 |
| tamatinib-resistant FLT3 mutants | R-HSA-9703009 | 1.025600e-02 | 1.989 | 0 | 0 |
| gilteritinib-resistant FLT3 mutants | R-HSA-9702590 | 1.025600e-02 | 1.989 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.025600e-02 | 1.989 | 0 | 0 |
| sorafenib-resistant FLT3 mutants | R-HSA-9702624 | 1.025600e-02 | 1.989 | 0 | 0 |
| ponatinib-resistant FLT3 mutants | R-HSA-9702614 | 1.025600e-02 | 1.989 | 0 | 0 |
| Sorafenib-resistant KIT mutants | R-HSA-9669936 | 1.025600e-02 | 1.989 | 0 | 0 |
| linifanib-resistant FLT3 mutants | R-HSA-9702998 | 1.025600e-02 | 1.989 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.025600e-02 | 1.989 | 0 | 0 |
| KW2449-resistant FLT3 mutants | R-HSA-9702569 | 1.025600e-02 | 1.989 | 0 | 0 |
| tandutinib-resistant FLT3 mutants | R-HSA-9702636 | 1.025600e-02 | 1.989 | 0 | 0 |
| lestaurtinib-resistant FLT3 mutants | R-HSA-9702596 | 1.025600e-02 | 1.989 | 0 | 0 |
| Nilotinib-resistant KIT mutants | R-HSA-9669926 | 1.025600e-02 | 1.989 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 1.025600e-02 | 1.989 | 0 | 0 |
| semaxanib-resistant FLT3 mutants | R-HSA-9702577 | 1.025600e-02 | 1.989 | 0 | 0 |
| Regorafenib-resistant KIT mutants | R-HSA-9669929 | 1.025600e-02 | 1.989 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.025600e-02 | 1.989 | 0 | 0 |
| Dasatinib-resistant KIT mutants | R-HSA-9669914 | 1.025600e-02 | 1.989 | 0 | 0 |
| sunitinib-resistant FLT3 mutants | R-HSA-9702632 | 1.025600e-02 | 1.989 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.025600e-02 | 1.989 | 0 | 0 |
| quizartinib-resistant FLT3 mutants | R-HSA-9702620 | 1.025600e-02 | 1.989 | 0 | 0 |
| Sunitinib-resistant KIT mutants | R-HSA-9669934 | 1.025600e-02 | 1.989 | 0 | 0 |
| Imatinib-resistant KIT mutants | R-HSA-9669917 | 1.025600e-02 | 1.989 | 0 | 0 |
| TLR3 deficiency - HSE | R-HSA-5602410 | 1.025600e-02 | 1.989 | 0 | 0 |
| crenolanib-resistant FLT3 mutants | R-HSA-9702581 | 1.025600e-02 | 1.989 | 0 | 0 |
| pexidartinib-resistant FLT3 mutants | R-HSA-9702605 | 1.025600e-02 | 1.989 | 0 | 0 |
| STAT5 Activation | R-HSA-9645135 | 4.025237e-03 | 2.395 | 0 | 0 |
| Activated NTRK3 signals through PI3K | R-HSA-9603381 | 4.936060e-03 | 2.307 | 0 | 0 |
| SOS-mediated signalling | R-HSA-112412 | 4.936060e-03 | 2.307 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 4.936060e-03 | 2.307 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 5.932560e-03 | 2.227 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 5.932560e-03 | 2.227 | 0 | 0 |
| TICAM1,TRAF6-dependent induction of TAK1 complex | R-HSA-9014325 | 8.175294e-03 | 2.087 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 1.073912e-02 | 1.969 | 0 | 0 |
| PI3K events in ERBB4 signaling | R-HSA-1250342 | 1.073912e-02 | 1.969 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 9.079009e-03 | 2.042 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 1.031883e-02 | 1.986 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 8.175294e-03 | 2.087 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 9.079009e-03 | 2.042 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 9.417949e-03 | 2.026 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 9.837774e-03 | 2.007 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 4.346372e-03 | 2.362 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 4.824443e-03 | 2.317 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 8.175294e-03 | 2.087 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 6.873394e-03 | 2.163 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 4.228435e-03 | 2.374 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 4.090986e-03 | 2.388 | 0 | 0 |
| Cation-coupled Chloride cotransporters | R-HSA-426117 | 4.936060e-03 | 2.307 | 0 | 0 |
| Interleukin-18 signaling | R-HSA-9012546 | 5.932560e-03 | 2.227 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 9.370859e-03 | 2.028 | 0 | 0 |
| Disease | R-HSA-1643685 | 9.044818e-03 | 2.044 | 1 | 0 |
| Immune System | R-HSA-168256 | 1.039908e-02 | 1.983 | 0 | 0 |
| ChREBP activates metabolic gene expression | R-HSA-163765 | 9.417949e-03 | 2.026 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 5.988678e-03 | 2.223 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.069001e-02 | 1.971 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 4.228435e-03 | 2.374 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 7.903844e-03 | 2.102 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 5.508247e-03 | 2.259 | 0 | 0 |
| Signaling by Leptin | R-HSA-2586552 | 8.175294e-03 | 2.087 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 5.360973e-03 | 2.271 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 1.193595e-02 | 1.923 | 0 | 0 |
| Interleukin-15 signaling | R-HSA-8983432 | 1.213709e-02 | 1.916 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.308020e-02 | 1.883 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 1.460383e-02 | 1.836 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.515667e-02 | 1.819 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.515667e-02 | 1.819 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.540174e-02 | 1.812 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.555379e-02 | 1.808 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.622383e-02 | 1.790 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.975513e-02 | 1.704 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 1.799874e-02 | 1.745 | 0 | 0 |
| STAT5 activation downstream of FLT3 ITD mutants | R-HSA-9702518 | 2.022050e-02 | 1.694 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | R-HSA-8866910 | 2.022050e-02 | 1.694 | 0 | 0 |
| Response to metal ions | R-HSA-5660526 | 2.022050e-02 | 1.694 | 0 | 0 |
| Drug-mediated inhibition of MET activation | R-HSA-9734091 | 2.040745e-02 | 1.690 | 0 | 0 |
| TICAM1 deficiency - HSE | R-HSA-5602566 | 2.040745e-02 | 1.690 | 0 | 0 |
| UNC93B1 deficiency - HSE | R-HSA-5602415 | 2.040745e-02 | 1.690 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 2.069891e-02 | 1.684 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 2.183419e-02 | 1.661 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 2.189001e-02 | 1.660 | 0 | 0 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 2.204458e-02 | 1.657 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 2.393413e-02 | 1.621 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 2.588763e-02 | 1.587 | 0 | 0 |
| NTRK3 as a dependence receptor | R-HSA-9603505 | 3.045539e-02 | 1.516 | 0 | 0 |
| Nef mediated downregulation of CD28 cell surface expression | R-HSA-164939 | 3.045539e-02 | 1.516 | 0 | 0 |
| Signaling by extracellular domain mutants of KIT | R-HSA-9680187 | 3.045539e-02 | 1.516 | 0 | 0 |
| Signaling by juxtamembrane domain KIT mutants | R-HSA-9669935 | 3.045539e-02 | 1.516 | 0 | 0 |
| TRAF3 deficiency - HSE | R-HSA-5602571 | 3.045539e-02 | 1.516 | 0 | 0 |
| Signaling by kinase domain mutants of KIT | R-HSA-9669933 | 3.045539e-02 | 1.516 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 2.790361e-02 | 1.554 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 2.998057e-02 | 1.523 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 2.957095e-02 | 1.529 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 3.027170e-02 | 1.519 | 0 | 0 |
| Signaling by NTRK3 (TRKC) | R-HSA-9034015 | 3.211708e-02 | 1.493 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.211708e-02 | 1.493 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.211708e-02 | 1.493 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 3.225873e-02 | 1.491 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.040089e-02 | 1.394 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.040089e-02 | 1.394 | 0 | 0 |
| NTF3 activates NTRK3 signaling | R-HSA-9034013 | 4.040089e-02 | 1.394 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.040089e-02 | 1.394 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.040089e-02 | 1.394 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 4.040089e-02 | 1.394 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.040089e-02 | 1.394 | 0 | 0 |
| Glycogen storage disease type IV (GBE1) | R-HSA-3878781 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.040089e-02 | 1.394 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.040089e-02 | 1.394 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 3.431171e-02 | 1.465 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 3.431171e-02 | 1.465 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 3.656307e-02 | 1.437 | 0 | 0 |
| Signaling by FLT3 ITD and TKD mutants | R-HSA-9703648 | 3.886976e-02 | 1.410 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 3.656307e-02 | 1.437 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 3.646739e-02 | 1.438 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 3.656307e-02 | 1.437 | 0 | 0 |
| Activated NTRK3 signals through PLCG1 | R-HSA-9034793 | 5.024497e-02 | 1.299 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.024497e-02 | 1.299 | 0 | 0 |
| MET activates PTPN11 | R-HSA-8865999 | 5.024497e-02 | 1.299 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 5.024497e-02 | 1.299 | 0 | 0 |
| Defective ABCC2 causes DJS | R-HSA-5679001 | 5.024497e-02 | 1.299 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 5.998867e-02 | 1.222 | 0 | 0 |
| HCN channels | R-HSA-1296061 | 5.998867e-02 | 1.222 | 0 | 0 |
| TLR3-mediated TICAM1-dependent programmed cell death | R-HSA-9013957 | 5.998867e-02 | 1.222 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 5.998867e-02 | 1.222 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 6.963301e-02 | 1.157 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 6.963301e-02 | 1.157 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 6.963301e-02 | 1.157 | 0 | 0 |
| FLT3 signaling by CBL mutants | R-HSA-9706377 | 6.963301e-02 | 1.157 | 0 | 0 |
| Nef Mediated CD8 Down-regulation | R-HSA-182218 | 7.917898e-02 | 1.101 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 8.862760e-02 | 1.052 | 0 | 0 |
| Erythropoietin activates STAT5 | R-HSA-9027283 | 8.862760e-02 | 1.052 | 0 | 0 |
| MET activates PI3K/AKT signaling | R-HSA-8851907 | 9.797983e-02 | 1.009 | 0 | 0 |
| PP2A-mediated dephosphorylation of key metabolic factors | R-HSA-163767 | 9.797983e-02 | 1.009 | 0 | 0 |
| IFNG signaling activates MAPKs | R-HSA-9732724 | 9.797983e-02 | 1.009 | 0 | 0 |
| Cohesin Loading onto Chromatin | R-HSA-2470946 | 9.797983e-02 | 1.009 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 1.072367e-01 | 0.970 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 1.072367e-01 | 0.970 | 0 | 0 |
| MET receptor recycling | R-HSA-8875656 | 1.072367e-01 | 0.970 | 0 | 0 |
| MET activates RAP1 and RAC1 | R-HSA-8875555 | 1.254680e-01 | 0.901 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 1.254680e-01 | 0.901 | 0 | 0 |
| Establishment of Sister Chromatid Cohesion | R-HSA-2468052 | 1.254680e-01 | 0.901 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 1.254680e-01 | 0.901 | 0 | 0 |
| Activated NTRK3 signals through RAS | R-HSA-9034864 | 1.344444e-01 | 0.871 | 0 | 0 |
| APC truncation mutants have impaired AXIN binding | R-HSA-5467337 | 1.344444e-01 | 0.871 | 0 | 0 |
| Truncations of AMER1 destabilize the destruction complex | R-HSA-5467348 | 1.344444e-01 | 0.871 | 0 | 0 |
| AXIN missense mutants destabilize the destruction complex | R-HSA-5467340 | 1.344444e-01 | 0.871 | 0 | 0 |
| Signaling by GSK3beta mutants | R-HSA-5339716 | 1.433293e-01 | 0.844 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 4.364377e-02 | 1.360 | 0 | 0 |
| MET activates RAS signaling | R-HSA-8851805 | 1.521234e-01 | 0.818 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.521234e-01 | 0.818 | 0 | 0 |
| Signaling by CTNNB1 phospho-site mutants | R-HSA-4839743 | 1.521234e-01 | 0.818 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.521234e-01 | 0.818 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.521234e-01 | 0.818 | 0 | 0 |
| CTNNB1 S37 mutants aren't phosphorylated | R-HSA-5358749 | 1.521234e-01 | 0.818 | 0 | 0 |
| CTNNB1 T41 mutants aren't phosphorylated | R-HSA-5358752 | 1.521234e-01 | 0.818 | 0 | 0 |
| CTNNB1 S33 mutants aren't phosphorylated | R-HSA-5358747 | 1.521234e-01 | 0.818 | 0 | 0 |
| CTNNB1 S45 mutants aren't phosphorylated | R-HSA-5358751 | 1.521234e-01 | 0.818 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 1.608279e-01 | 0.794 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 1.694435e-01 | 0.771 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 5.645492e-02 | 1.248 | 0 | 0 |
| InlB-mediated entry of Listeria monocytogenes into host cell | R-HSA-8875360 | 1.779711e-01 | 0.750 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.779711e-01 | 0.750 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.779711e-01 | 0.750 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.779711e-01 | 0.750 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.779711e-01 | 0.750 | 0 | 0 |
| Beta-catenin phosphorylation cascade | R-HSA-196299 | 1.779711e-01 | 0.750 | 0 | 0 |
| RNA Polymerase III Chain Elongation | R-HSA-73780 | 1.779711e-01 | 0.750 | 0 | 0 |
| TICAM1, RIP1-mediated IKK complex recruitment | R-HSA-168927 | 1.779711e-01 | 0.750 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 1.864118e-01 | 0.730 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 1.864118e-01 | 0.730 | 0 | 0 |
| Defective GALNT3 causes HFTC | R-HSA-5083625 | 1.864118e-01 | 0.730 | 0 | 0 |
| Defective GALNT12 causes CRCS1 | R-HSA-5083636 | 1.864118e-01 | 0.730 | 0 | 0 |
| Antigen processing: Ub, ATP-independent proteasomal degradation | R-HSA-9912633 | 1.947663e-01 | 0.710 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 1.947663e-01 | 0.710 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 1.947663e-01 | 0.710 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.030355e-01 | 0.692 | 0 | 0 |
| Defective C1GALT1C1 causes TNPS | R-HSA-5083632 | 2.030355e-01 | 0.692 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.030355e-01 | 0.692 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 7.923834e-02 | 1.101 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 9.153122e-02 | 1.038 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.076107e-01 | 0.968 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 4.364377e-02 | 1.360 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.030355e-01 | 0.692 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.030355e-01 | 0.692 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 4.315421e-02 | 1.365 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 8.840749e-02 | 1.054 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 9.797983e-02 | 1.009 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.433293e-01 | 0.844 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.254680e-01 | 0.901 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.076107e-01 | 0.968 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.076107e-01 | 0.968 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.608279e-01 | 0.794 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.779711e-01 | 0.750 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 9.153122e-02 | 1.038 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.163991e-01 | 0.934 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.076107e-01 | 0.968 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 1.631350e-01 | 0.787 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 5.998867e-02 | 1.222 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 6.963301e-02 | 1.157 | 0 | 0 |
| Signaling by MST1 | R-HSA-8852405 | 7.917898e-02 | 1.101 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 1.072367e-01 | 0.970 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.610844e-02 | 1.336 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 7.053224e-02 | 1.152 | 0 | 0 |
| FLT3 signaling in disease | R-HSA-9682385 | 7.330425e-02 | 1.135 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 1.779711e-01 | 0.750 | 0 | 0 |
| Interleukin-9 signaling | R-HSA-8985947 | 1.072367e-01 | 0.970 | 0 | 0 |
| MET Receptor Activation | R-HSA-6806942 | 8.862760e-02 | 1.052 | 0 | 0 |
| Nef Mediated CD4 Down-regulation | R-HSA-167590 | 9.797983e-02 | 1.009 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 1.010905e-01 | 0.995 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 4.758955e-02 | 1.322 | 0 | 0 |
| MET activates STAT3 | R-HSA-8875791 | 5.024497e-02 | 1.299 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 5.998867e-02 | 1.222 | 0 | 0 |
| Inhibition of TSC complex formation by PKB | R-HSA-165181 | 5.998867e-02 | 1.222 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 5.998867e-02 | 1.222 | 0 | 0 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | R-HSA-5140745 | 1.254680e-01 | 0.901 | 0 | 0 |
| Signaling by APC mutants | R-HSA-4839744 | 1.344444e-01 | 0.871 | 0 | 0 |
| Mitotic Telophase/Cytokinesis | R-HSA-68884 | 1.433293e-01 | 0.844 | 0 | 0 |
| ERKs are inactivated | R-HSA-202670 | 1.433293e-01 | 0.844 | 0 | 0 |
| Signaling by AXIN mutants | R-HSA-4839735 | 1.433293e-01 | 0.844 | 0 | 0 |
| Signaling by AMER1 mutants | R-HSA-4839748 | 1.433293e-01 | 0.844 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.521234e-01 | 0.818 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.521234e-01 | 0.818 | 0 | 0 |
| VLDLR internalisation and degradation | R-HSA-8866427 | 1.521234e-01 | 0.818 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 5.645492e-02 | 1.248 | 0 | 0 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | R-HSA-937072 | 1.779711e-01 | 0.750 | 0 | 0 |
| Class I peroxisomal membrane protein import | R-HSA-9603798 | 1.864118e-01 | 0.730 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 1.076107e-01 | 0.968 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 1.201706e-01 | 0.920 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 4.123044e-02 | 1.385 | 0 | 0 |
| Trafficking and processing of endosomal TLR | R-HSA-1679131 | 1.521234e-01 | 0.818 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 1.212081e-01 | 0.916 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 8.042763e-02 | 1.095 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 8.042763e-02 | 1.095 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 8.042763e-02 | 1.095 | 0 | 0 |
| IRAK2 mediated activation of TAK1 complex | R-HSA-937042 | 1.163991e-01 | 0.934 | 0 | 0 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | R-HSA-975163 | 1.694435e-01 | 0.771 | 0 | 0 |
| WNT5A-dependent internalization of FZD4 | R-HSA-5099900 | 1.864118e-01 | 0.730 | 0 | 0 |
| Biosynthesis of aspirin-triggered D-series resolvins | R-HSA-9020265 | 2.030355e-01 | 0.692 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.740550e-01 | 0.759 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 1.135352e-01 | 0.945 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.010905e-01 | 0.995 | 0 | 0 |
| Biosynthesis of DPAn-3-derived 13-series resolvins | R-HSA-9026403 | 6.963301e-02 | 1.157 | 0 | 0 |
| Negative feedback regulation of MAPK pathway | R-HSA-5674499 | 7.917898e-02 | 1.101 | 0 | 0 |
| VEGF binds to VEGFR leading to receptor dimerization | R-HSA-195399 | 7.917898e-02 | 1.101 | 0 | 0 |
| Ca2+ activated K+ channels | R-HSA-1296052 | 9.797983e-02 | 1.009 | 0 | 0 |
| Activation of RAC1 downstream of NMDARs | R-HSA-9619229 | 1.163991e-01 | 0.934 | 0 | 0 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | R-HSA-113501 | 1.433293e-01 | 0.844 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 4.123044e-02 | 1.385 | 0 | 0 |
| Biosynthesis of DPAn-3-derived protectins and resolvins | R-HSA-9026286 | 1.521234e-01 | 0.818 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 5.915728e-02 | 1.228 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 7.039398e-02 | 1.152 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 7.039398e-02 | 1.152 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 1.947663e-01 | 0.710 | 0 | 0 |
| mRNA decay by 5' to 3' exoribonuclease | R-HSA-430039 | 1.947663e-01 | 0.710 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 9.153122e-02 | 1.038 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 9.153122e-02 | 1.038 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 1.109121e-01 | 0.955 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 1.277979e-01 | 0.893 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 1.312449e-01 | 0.882 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 5.551983e-02 | 1.256 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 1.010905e-01 | 0.995 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 1.694672e-01 | 0.771 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 7.039398e-02 | 1.152 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.521234e-01 | 0.818 | 0 | 0 |
| Biosynthesis of E-series 18(R)-resolvins | R-HSA-9023661 | 1.694435e-01 | 0.771 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 7.625273e-02 | 1.118 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 8.226004e-02 | 1.085 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 6.743770e-02 | 1.171 | 0 | 0 |
| VEGF ligand-receptor interactions | R-HSA-194313 | 7.917898e-02 | 1.101 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.163991e-01 | 0.934 | 0 | 0 |
| Cholesterol biosynthesis via desmosterol | R-HSA-6807047 | 1.344444e-01 | 0.871 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 1.521234e-01 | 0.818 | 0 | 0 |
| Role of second messengers in netrin-1 signaling | R-HSA-418890 | 1.521234e-01 | 0.818 | 0 | 0 |
| RIP-mediated NFkB activation via ZBP1 | R-HSA-1810476 | 1.779711e-01 | 0.750 | 0 | 0 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | R-HSA-9634600 | 1.864118e-01 | 0.730 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 7.330425e-02 | 1.135 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 7.330425e-02 | 1.135 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 7.625273e-02 | 1.118 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 7.625273e-02 | 1.118 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.277979e-01 | 0.893 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 1.347131e-01 | 0.871 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 4.543196e-02 | 1.343 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 1.399000e-01 | 0.854 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.163991e-01 | 0.934 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.779711e-01 | 0.750 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 9.854441e-02 | 1.006 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 1.167532e-01 | 0.933 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 7.330425e-02 | 1.135 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 6.855646e-02 | 1.164 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 9.986323e-02 | 1.001 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 5.551983e-02 | 1.256 | 0 | 0 |
| Alpha-protein kinase 1 signaling pathway | R-HSA-9645460 | 1.344444e-01 | 0.871 | 0 | 0 |
| Biosynthesis of DPAn-3-derived maresins | R-HSA-9026290 | 1.344444e-01 | 0.871 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.779711e-01 | 0.750 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 6.469250e-02 | 1.189 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 6.752303e-02 | 1.171 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 6.752303e-02 | 1.171 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 7.039398e-02 | 1.152 | 0 | 0 |
| Elevation of cytosolic Ca2+ levels | R-HSA-139853 | 2.030355e-01 | 0.692 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 9.153122e-02 | 1.038 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 9.153122e-02 | 1.038 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 1.209713e-01 | 0.917 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 1.277979e-01 | 0.893 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 5.129434e-02 | 1.290 | 1 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 1.631350e-01 | 0.787 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 1.419950e-01 | 0.848 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 1.326365e-01 | 0.877 | 0 | 0 |
| Receptor-type tyrosine-protein phosphatases | R-HSA-388844 | 1.864118e-01 | 0.730 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 7.625273e-02 | 1.118 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 8.531676e-02 | 1.069 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 8.840749e-02 | 1.054 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 8.840749e-02 | 1.054 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 6.017570e-02 | 1.221 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 1.312449e-01 | 0.882 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 7.415178e-02 | 1.130 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 8.840749e-02 | 1.054 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 1.382019e-01 | 0.859 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 1.704015e-01 | 0.769 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 1.962211e-01 | 0.707 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 1.962211e-01 | 0.707 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 1.189728e-01 | 0.925 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 2.008326e-01 | 0.697 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 2.008326e-01 | 0.697 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 4.795120e-02 | 1.319 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.667612e-01 | 0.778 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.344444e-01 | 0.871 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 8.226004e-02 | 1.085 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 9.787371e-02 | 1.009 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.010905e-01 | 0.995 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 1.043365e-01 | 0.982 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 1.850894e-01 | 0.733 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 1.417105e-01 | 0.849 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 9.958798e-02 | 1.002 | 0 | 0 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 5.998867e-02 | 1.222 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 8.862760e-02 | 1.052 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 1.043365e-01 | 0.982 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.417105e-01 | 0.849 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 1.973148e-01 | 0.705 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 4.758955e-02 | 1.322 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 8.226004e-02 | 1.085 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 1.356492e-01 | 0.868 | 1 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 8.862760e-02 | 1.052 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 9.797983e-02 | 1.009 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 1.433293e-01 | 0.844 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 1.521234e-01 | 0.818 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 1.521234e-01 | 0.818 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 1.947663e-01 | 0.710 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 8.531676e-02 | 1.069 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 8.840749e-02 | 1.054 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 1.043365e-01 | 0.982 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 9.698962e-02 | 1.013 | 0 | 0 |
| Formation of the nephric duct | R-HSA-9830364 | 4.123044e-02 | 1.385 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 1.595235e-01 | 0.797 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 1.652279e-01 | 0.782 | 1 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 1.101908e-01 | 0.958 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.072367e-01 | 0.970 | 0 | 0 |
| Glycogen storage diseases | R-HSA-3229121 | 2.030355e-01 | 0.692 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 1.175933e-01 | 0.930 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 1.243732e-01 | 0.905 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.631350e-01 | 0.787 | 0 | 0 |
| MAP kinase activation | R-HSA-450294 | 1.595235e-01 | 0.797 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 1.043365e-01 | 0.982 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 1.043365e-01 | 0.982 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.017570e-02 | 1.221 | 0 | 0 |
| Interleukin-17 signaling | R-HSA-448424 | 1.925007e-01 | 0.716 | 0 | 0 |
| Atorvastatin ADME | R-HSA-9754706 | 1.864118e-01 | 0.730 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 1.243732e-01 | 0.905 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 1.627865e-01 | 0.788 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 6.160509e-02 | 1.210 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 1.667277e-01 | 0.778 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 4.364377e-02 | 1.360 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 1.312449e-01 | 0.882 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 4.977728e-02 | 1.303 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 1.080362e-01 | 0.966 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 1.631350e-01 | 0.787 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 8.226004e-02 | 1.085 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 1.243732e-01 | 0.905 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 1.925007e-01 | 0.716 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 1.864118e-01 | 0.730 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 1.864118e-01 | 0.730 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 1.452381e-01 | 0.838 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.667612e-01 | 0.778 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 1.559273e-01 | 0.807 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 6.752303e-02 | 1.171 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 1.962211e-01 | 0.707 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 5.915728e-02 | 1.228 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 1.043365e-01 | 0.982 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 1.999505e-01 | 0.699 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 1.740550e-01 | 0.759 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 1.925007e-01 | 0.716 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 9.079264e-02 | 1.042 | 0 | 0 |
| SLC-mediated transport of inorganic anions | R-HSA-9958790 | 7.923834e-02 | 1.101 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.010905e-01 | 0.995 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.175933e-01 | 0.930 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.175933e-01 | 0.930 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.277979e-01 | 0.893 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 6.051949e-02 | 1.218 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 1.497354e-01 | 0.825 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 1.344540e-01 | 0.871 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 1.999505e-01 | 0.699 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 1.425789e-01 | 0.846 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 1.954699e-01 | 0.709 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 9.335886e-02 | 1.030 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 1.076107e-01 | 0.968 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 1.595235e-01 | 0.797 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.030355e-01 | 0.692 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.764372e-01 | 0.753 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 1.325751e-01 | 0.878 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.740550e-01 | 0.759 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 8.463455e-02 | 1.072 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 1.167222e-01 | 0.933 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 2.036884e-01 | 0.691 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 2.048570e-01 | 0.689 | 1 | 0 |
| Keratinization | R-HSA-6805567 | 2.057498e-01 | 0.687 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 2.074341e-01 | 0.683 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 2.100957e-01 | 0.678 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 2.102499e-01 | 0.677 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 2.102499e-01 | 0.677 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 2.111872e-01 | 0.675 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 2.112203e-01 | 0.675 | 0 | 0 |
| RNA Polymerase III Transcription Termination | R-HSA-73980 | 2.112203e-01 | 0.675 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.112203e-01 | 0.675 | 0 | 0 |
| Signaling by cytosolic FGFR1 fusion mutants | R-HSA-1839117 | 2.112203e-01 | 0.675 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.112203e-01 | 0.675 | 0 | 0 |
| Trafficking of GluR2-containing AMPA receptors | R-HSA-416993 | 2.112203e-01 | 0.675 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.112203e-01 | 0.675 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.112203e-01 | 0.675 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.112203e-01 | 0.675 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.112203e-01 | 0.675 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.112203e-01 | 0.675 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 2.129098e-01 | 0.672 | 1 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.149471e-01 | 0.668 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.149471e-01 | 0.668 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.182516e-01 | 0.661 | 0 | 0 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | R-HSA-167242 | 2.193215e-01 | 0.659 | 0 | 0 |
| Signaling by FGFR2 IIIa TM | R-HSA-8851708 | 2.193215e-01 | 0.659 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.193215e-01 | 0.659 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 2.193215e-01 | 0.659 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.193215e-01 | 0.659 | 0 | 0 |
| Synthesis of 5-eicosatetraenoic acids | R-HSA-2142688 | 2.193215e-01 | 0.659 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.193215e-01 | 0.659 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.193215e-01 | 0.659 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.193215e-01 | 0.659 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 2.236211e-01 | 0.650 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 2.249430e-01 | 0.648 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 2.262624e-01 | 0.645 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.273400e-01 | 0.643 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.273400e-01 | 0.643 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 2.273400e-01 | 0.643 | 0 | 0 |
| Glycogen synthesis | R-HSA-3322077 | 2.273400e-01 | 0.643 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 2.273400e-01 | 0.643 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 2.300444e-01 | 0.638 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 2.300444e-01 | 0.638 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 2.300444e-01 | 0.638 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 2.338347e-01 | 0.631 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 2.344373e-01 | 0.630 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.352767e-01 | 0.628 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.352767e-01 | 0.628 | 0 | 0 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | R-HSA-450321 | 2.352767e-01 | 0.628 | 0 | 0 |
| Biosynthesis of E-series 18(S)-resolvins | R-HSA-9018896 | 2.352767e-01 | 0.628 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 2.352767e-01 | 0.628 | 0 | 0 |
| ERK/MAPK targets | R-HSA-198753 | 2.352767e-01 | 0.628 | 0 | 0 |
| PD-L1(CD274) glycosylation and translocation to plasma membrane | R-HSA-9931295 | 2.352767e-01 | 0.628 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 2.414137e-01 | 0.617 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.431323e-01 | 0.614 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.431323e-01 | 0.614 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | R-HSA-76066 | 2.431323e-01 | 0.614 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.431323e-01 | 0.614 | 0 | 0 |
| activated TAK1 mediates p38 MAPK activation | R-HSA-450302 | 2.431323e-01 | 0.614 | 0 | 0 |
| S Phase | R-HSA-69242 | 2.453457e-01 | 0.610 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.490082e-01 | 0.604 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 2.490082e-01 | 0.604 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.509077e-01 | 0.600 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | R-HSA-76071 | 2.509077e-01 | 0.600 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | R-HSA-76061 | 2.509077e-01 | 0.600 | 0 | 0 |
| Biosynthesis of D-series resolvins | R-HSA-9018676 | 2.509077e-01 | 0.600 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 2.509077e-01 | 0.600 | 0 | 0 |
| Cholesterol biosynthesis via lathosterol | R-HSA-6807062 | 2.509077e-01 | 0.600 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 2.560667e-01 | 0.592 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | R-HSA-167160 | 2.586037e-01 | 0.587 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE | R-HSA-77075 | 2.586037e-01 | 0.587 | 0 | 0 |
| Termination of O-glycan biosynthesis | R-HSA-977068 | 2.586037e-01 | 0.587 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 2.586037e-01 | 0.587 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.586037e-01 | 0.587 | 0 | 0 |
| Interleukin-20 family signaling | R-HSA-8854691 | 2.586037e-01 | 0.587 | 0 | 0 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | R-HSA-9634638 | 2.586037e-01 | 0.587 | 0 | 0 |
| Biosynthesis of maresins | R-HSA-9018682 | 2.586037e-01 | 0.587 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 2.590919e-01 | 0.587 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 2.604135e-01 | 0.584 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 2.662211e-01 | 0.575 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 2.673896e-01 | 0.573 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 2.680209e-01 | 0.572 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 2.718246e-01 | 0.566 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 2.729393e-01 | 0.564 | 0 | 0 |
| Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives | R-HSA-9027604 | 2.737608e-01 | 0.563 | 0 | 0 |
| MicroRNA (miRNA) biogenesis | R-HSA-203927 | 2.737608e-01 | 0.563 | 0 | 0 |
| HDMs demethylate histones | R-HSA-3214842 | 2.737608e-01 | 0.563 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.737608e-01 | 0.563 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 2.741420e-01 | 0.562 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 2.756278e-01 | 0.560 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 2.803819e-01 | 0.552 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.812234e-01 | 0.551 | 0 | 0 |
| Signaling by FLT3 fusion proteins | R-HSA-9703465 | 2.812234e-01 | 0.551 | 0 | 0 |
| TRP channels | R-HSA-3295583 | 2.812234e-01 | 0.551 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 2.832308e-01 | 0.548 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 2.870300e-01 | 0.542 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 2.886097e-01 | 0.540 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 2.886097e-01 | 0.540 | 0 | 0 |
| RNA Polymerase I Transcription Termination | R-HSA-73863 | 2.886097e-01 | 0.540 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 2.886097e-01 | 0.540 | 0 | 0 |
| Biosynthesis of DPAn-3 SPMs | R-HSA-9025094 | 2.886097e-01 | 0.540 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 2.886097e-01 | 0.540 | 0 | 0 |
| TNFR1-induced NF-kappa-B signaling pathway | R-HSA-5357956 | 2.886097e-01 | 0.540 | 0 | 0 |
| Formation of the HIV-1 Early Elongation Complex | R-HSA-167158 | 2.959207e-01 | 0.529 | 0 | 0 |
| Formation of the Early Elongation Complex | R-HSA-113418 | 2.959207e-01 | 0.529 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 2.959207e-01 | 0.529 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 2.959207e-01 | 0.529 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 2.959207e-01 | 0.529 | 0 | 0 |
| Phase 0 - rapid depolarisation | R-HSA-5576892 | 2.959207e-01 | 0.529 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 2.959207e-01 | 0.529 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 2.959207e-01 | 0.529 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 2.984138e-01 | 0.525 | 0 | 0 |
| Potassium Channels | R-HSA-1296071 | 3.022026e-01 | 0.520 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.031569e-01 | 0.518 | 0 | 0 |
| mRNA Capping | R-HSA-72086 | 3.031569e-01 | 0.518 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 3.031569e-01 | 0.518 | 0 | 0 |
| Biosynthesis of EPA-derived SPMs | R-HSA-9018679 | 3.031569e-01 | 0.518 | 0 | 0 |
| Platelet calcium homeostasis | R-HSA-418360 | 3.031569e-01 | 0.518 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 3.031569e-01 | 0.518 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.031569e-01 | 0.518 | 0 | 0 |
| MAPK targets/ Nuclear events mediated by MAP kinases | R-HSA-450282 | 3.031569e-01 | 0.518 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 3.073673e-01 | 0.512 | 0 | 0 |
| MyD88 cascade initiated on plasma membrane | R-HSA-975871 | 3.097697e-01 | 0.509 | 0 | 0 |
| Toll Like Receptor 5 (TLR5) Cascade | R-HSA-168176 | 3.097697e-01 | 0.509 | 0 | 0 |
| Toll Like Receptor 10 (TLR10) Cascade | R-HSA-168142 | 3.097697e-01 | 0.509 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 3.097697e-01 | 0.509 | 0 | 0 |
| RNA Polymerase III Transcription Initiation | R-HSA-76046 | 3.103192e-01 | 0.508 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 3.103192e-01 | 0.508 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 3.148664e-01 | 0.502 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 3.173205e-01 | 0.499 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 3.173205e-01 | 0.499 | 0 | 0 |
| Trafficking of AMPA receptors | R-HSA-399719 | 3.174084e-01 | 0.498 | 0 | 0 |
| Biosynthesis of DPA-derived SPMs | R-HSA-9018683 | 3.174084e-01 | 0.498 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 3.174084e-01 | 0.498 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.174084e-01 | 0.498 | 1 | 1 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 3.176726e-01 | 0.498 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 3.176726e-01 | 0.498 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 3.244251e-01 | 0.489 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 3.244251e-01 | 0.489 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 3.244251e-01 | 0.489 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 3.244251e-01 | 0.489 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 3.248524e-01 | 0.488 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.313701e-01 | 0.480 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 3.313701e-01 | 0.480 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 3.313701e-01 | 0.480 | 0 | 0 |
| FGFR1 mutant receptor activation | R-HSA-1839124 | 3.313701e-01 | 0.480 | 0 | 0 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | R-HSA-399721 | 3.313701e-01 | 0.480 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.313701e-01 | 0.480 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 3.313701e-01 | 0.480 | 0 | 0 |
| Effects of PIP2 hydrolysis | R-HSA-114508 | 3.382441e-01 | 0.471 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 3.382441e-01 | 0.471 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 3.385051e-01 | 0.470 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 3.435849e-01 | 0.464 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 3.435849e-01 | 0.464 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 3.450479e-01 | 0.462 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 3.450479e-01 | 0.462 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.450479e-01 | 0.462 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 3.450479e-01 | 0.462 | 0 | 0 |
| NOD1/2 Signaling Pathway | R-HSA-168638 | 3.450479e-01 | 0.462 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 3.457287e-01 | 0.461 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 3.457370e-01 | 0.461 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 3.473125e-01 | 0.459 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 3.510331e-01 | 0.455 | 0 | 0 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | R-HSA-975138 | 3.510331e-01 | 0.455 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 3.510331e-01 | 0.455 | 0 | 0 |
| MyD88 dependent cascade initiated on endosome | R-HSA-975155 | 3.547466e-01 | 0.450 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 3.547466e-01 | 0.450 | 0 | 0 |
| RNA Polymerase III Abortive And Retractive Initiation | R-HSA-749476 | 3.584475e-01 | 0.446 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 3.584475e-01 | 0.446 | 0 | 0 |
| RNA Polymerase III Transcription | R-HSA-74158 | 3.584475e-01 | 0.446 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 3.584475e-01 | 0.446 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 3.584475e-01 | 0.446 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 3.584475e-01 | 0.446 | 0 | 0 |
| FGFR2 mutant receptor activation | R-HSA-1839126 | 3.584475e-01 | 0.446 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 3.584527e-01 | 0.446 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 3.584527e-01 | 0.446 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 3.584527e-01 | 0.446 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 3.597122e-01 | 0.444 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 3.650448e-01 | 0.438 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 3.681253e-01 | 0.434 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 3.695242e-01 | 0.432 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.715747e-01 | 0.430 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 3.764908e-01 | 0.424 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 3.780378e-01 | 0.422 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 3.780378e-01 | 0.422 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 3.780378e-01 | 0.422 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 3.805207e-01 | 0.420 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 3.820559e-01 | 0.418 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 3.844348e-01 | 0.415 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 3.844348e-01 | 0.415 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 3.844348e-01 | 0.415 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 3.844348e-01 | 0.415 | 0 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 3.844348e-01 | 0.415 | 0 | 0 |
| Diseases of Immune System | R-HSA-5260271 | 3.844348e-01 | 0.415 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 3.844348e-01 | 0.415 | 0 | 0 |
| Glycogen metabolism | R-HSA-8982491 | 3.844348e-01 | 0.415 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 3.907664e-01 | 0.408 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 3.914367e-01 | 0.407 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 3.931532e-01 | 0.405 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 3.970333e-01 | 0.401 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 3.970333e-01 | 0.401 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 3.970333e-01 | 0.401 | 0 | 0 |
| Intra-Golgi traffic | R-HSA-6811438 | 3.970333e-01 | 0.401 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 3.970333e-01 | 0.401 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 3.986665e-01 | 0.399 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 3.986665e-01 | 0.399 | 0 | 0 |
| M Phase | R-HSA-68886 | 4.016681e-01 | 0.396 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 4.020515e-01 | 0.396 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 4.022667e-01 | 0.395 | 0 | 0 |
| RNA Polymerase I Transcription Initiation | R-HSA-73762 | 4.032361e-01 | 0.394 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.032361e-01 | 0.394 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 4.058568e-01 | 0.392 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 4.058568e-01 | 0.392 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 4.058568e-01 | 0.392 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 4.069537e-01 | 0.390 | 0 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 4.093755e-01 | 0.388 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 4.093755e-01 | 0.388 | 0 | 0 |
| TBC/RABGAPs | R-HSA-8854214 | 4.093755e-01 | 0.388 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 4.094366e-01 | 0.388 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 4.094366e-01 | 0.388 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 4.154397e-01 | 0.381 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.154521e-01 | 0.381 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.154521e-01 | 0.381 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.154521e-01 | 0.381 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 4.154521e-01 | 0.381 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 4.214666e-01 | 0.375 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 4.214666e-01 | 0.375 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 4.214666e-01 | 0.375 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 4.214666e-01 | 0.375 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 4.214666e-01 | 0.375 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 4.214666e-01 | 0.375 | 0 | 0 |
| Formation of TC-NER Pre-Incision Complex | R-HSA-6781823 | 4.274195e-01 | 0.369 | 0 | 0 |
| mRNA Splicing - Minor Pathway | R-HSA-72165 | 4.274195e-01 | 0.369 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.274195e-01 | 0.369 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.274195e-01 | 0.369 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 4.306907e-01 | 0.366 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 4.315545e-01 | 0.365 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 4.333115e-01 | 0.363 | 0 | 0 |
| TAK1-dependent IKK and NF-kappa-B activation | R-HSA-445989 | 4.333115e-01 | 0.363 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 4.391433e-01 | 0.357 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 4.391433e-01 | 0.357 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 4.449154e-01 | 0.352 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 4.450659e-01 | 0.352 | 0 | 0 |
| Signaling by FGFR2 in disease | R-HSA-5655253 | 4.506285e-01 | 0.346 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 4.515370e-01 | 0.345 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 4.618799e-01 | 0.335 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 4.618799e-01 | 0.335 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 4.618799e-01 | 0.335 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 4.618799e-01 | 0.335 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 4.674194e-01 | 0.330 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 4.674194e-01 | 0.330 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 4.753053e-01 | 0.323 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 4.753053e-01 | 0.323 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 4.783289e-01 | 0.320 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 4.783289e-01 | 0.320 | 0 | 0 |
| Paracetamol ADME | R-HSA-9753281 | 4.783289e-01 | 0.320 | 0 | 0 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | R-HSA-6782210 | 4.837001e-01 | 0.315 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 4.837001e-01 | 0.315 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 4.837001e-01 | 0.315 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 4.837001e-01 | 0.315 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 4.853011e-01 | 0.314 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 4.890162e-01 | 0.311 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 4.890162e-01 | 0.311 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 4.894537e-01 | 0.310 | 0 | 0 |
| Dual incision in TC-NER | R-HSA-6782135 | 4.942780e-01 | 0.306 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 4.942780e-01 | 0.306 | 0 | 0 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | R-HSA-9029569 | 4.942780e-01 | 0.306 | 0 | 0 |
| Translation | R-HSA-72766 | 4.957283e-01 | 0.305 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 4.994860e-01 | 0.301 | 0 | 0 |
| Peroxisomal protein import | R-HSA-9033241 | 4.994860e-01 | 0.301 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 4.994860e-01 | 0.301 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 5.046406e-01 | 0.297 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 5.046406e-01 | 0.297 | 0 | 0 |
| Viral Messenger RNA Synthesis | R-HSA-168325 | 5.097424e-01 | 0.293 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 5.113744e-01 | 0.291 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 5.145727e-01 | 0.289 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 5.147920e-01 | 0.288 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 5.147920e-01 | 0.288 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 5.147920e-01 | 0.288 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 5.177573e-01 | 0.286 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 5.197899e-01 | 0.284 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 5.206447e-01 | 0.283 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 5.209281e-01 | 0.283 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.240850e-01 | 0.281 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 5.247367e-01 | 0.280 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 5.272281e-01 | 0.278 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 5.440222e-01 | 0.264 | 0 | 0 |
| O-linked glycosylation of mucins | R-HSA-913709 | 5.440222e-01 | 0.264 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.440222e-01 | 0.264 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 5.440222e-01 | 0.264 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 5.478458e-01 | 0.261 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.533712e-01 | 0.257 | 0 | 0 |
| Fatty acyl-CoA biosynthesis | R-HSA-75105 | 5.533712e-01 | 0.257 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 5.533712e-01 | 0.257 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 5.579740e-01 | 0.253 | 0 | 0 |
| Diseases associated with O-glycosylation of proteins | R-HSA-3906995 | 5.579740e-01 | 0.253 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 5.579740e-01 | 0.253 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 5.579740e-01 | 0.253 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 5.579740e-01 | 0.253 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 5.579740e-01 | 0.253 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 5.625297e-01 | 0.250 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.625297e-01 | 0.250 | 0 | 0 |
| Aspirin ADME | R-HSA-9749641 | 5.670387e-01 | 0.246 | 0 | 0 |
| Diseases of carbohydrate metabolism | R-HSA-5663084 | 5.670387e-01 | 0.246 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.715014e-01 | 0.243 | 0 | 0 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | R-HSA-6781827 | 5.759185e-01 | 0.240 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 5.759185e-01 | 0.240 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 5.802903e-01 | 0.236 | 0 | 0 |
| NR1H2 and NR1H3-mediated signaling | R-HSA-9024446 | 5.846173e-01 | 0.233 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 5.889000e-01 | 0.230 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 5.889000e-01 | 0.230 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 5.889000e-01 | 0.230 | 0 | 0 |
| Cholesterol biosynthesis | R-HSA-191273 | 5.889000e-01 | 0.230 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 5.899571e-01 | 0.229 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 5.956008e-01 | 0.225 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 5.972000e-01 | 0.224 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 5.973340e-01 | 0.224 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 5.973340e-01 | 0.224 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 5.973340e-01 | 0.224 | 0 | 0 |
| Biosynthesis of DHA-derived SPMs | R-HSA-9018677 | 6.014864e-01 | 0.221 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 6.014864e-01 | 0.221 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 6.039607e-01 | 0.219 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 6.096637e-01 | 0.215 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 6.136897e-01 | 0.212 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.176743e-01 | 0.209 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 6.202812e-01 | 0.207 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.216181e-01 | 0.206 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.216181e-01 | 0.206 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 6.255215e-01 | 0.204 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.255215e-01 | 0.204 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 6.332085e-01 | 0.198 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 6.332085e-01 | 0.198 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 6.334874e-01 | 0.198 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 6.437939e-01 | 0.191 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 6.444459e-01 | 0.191 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 6.517468e-01 | 0.186 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 6.553411e-01 | 0.184 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 6.553411e-01 | 0.184 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 6.612816e-01 | 0.180 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 6.685642e-01 | 0.175 | 0 | 0 |
| Mitochondrial translation elongation | R-HSA-5389840 | 6.693534e-01 | 0.174 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.693534e-01 | 0.174 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 6.727671e-01 | 0.172 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 6.727671e-01 | 0.172 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 6.761458e-01 | 0.170 | 0 | 0 |
| Mitochondrial translation initiation | R-HSA-5368286 | 6.761458e-01 | 0.170 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 6.794897e-01 | 0.168 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 6.827994e-01 | 0.166 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 6.860750e-01 | 0.164 | 1 | 1 |
| Membrane Trafficking | R-HSA-199991 | 6.911728e-01 | 0.160 | 0 | 0 |
| Mitochondrial ribosome-associated quality control | R-HSA-9937383 | 6.925259e-01 | 0.160 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 6.957017e-01 | 0.158 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 6.957017e-01 | 0.158 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 6.988449e-01 | 0.156 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 6.988449e-01 | 0.156 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.019558e-01 | 0.154 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 7.080822e-01 | 0.150 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 7.080822e-01 | 0.150 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 7.080822e-01 | 0.150 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 7.108859e-01 | 0.148 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 7.117983e-01 | 0.148 | 0 | 0 |
| Mitochondrial translation termination | R-HSA-5419276 | 7.140834e-01 | 0.146 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 7.140834e-01 | 0.146 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 7.228560e-01 | 0.141 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 7.228560e-01 | 0.141 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 7.257204e-01 | 0.139 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 7.258263e-01 | 0.139 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 7.265027e-01 | 0.139 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.313610e-01 | 0.136 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 7.341380e-01 | 0.134 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 7.350974e-01 | 0.134 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 7.396066e-01 | 0.131 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 7.422988e-01 | 0.129 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 7.527938e-01 | 0.123 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 7.578809e-01 | 0.120 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 7.677449e-01 | 0.115 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 7.692018e-01 | 0.114 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 7.701478e-01 | 0.113 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 7.774186e-01 | 0.109 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 7.817969e-01 | 0.107 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 7.840553e-01 | 0.106 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 7.841558e-01 | 0.106 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 7.862904e-01 | 0.104 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 7.887428e-01 | 0.103 | 0 | 0 |
| O-linked glycosylation | R-HSA-5173105 | 7.971260e-01 | 0.098 | 0 | 0 |
| Mitochondrial translation | R-HSA-5368287 | 7.992267e-01 | 0.097 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 8.075497e-01 | 0.093 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 8.094100e-01 | 0.092 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 8.094100e-01 | 0.092 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 8.113842e-01 | 0.091 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.113842e-01 | 0.091 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 8.190799e-01 | 0.087 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 8.190799e-01 | 0.087 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 8.282619e-01 | 0.082 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.282619e-01 | 0.082 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 8.300419e-01 | 0.081 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 8.318036e-01 | 0.080 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 8.318036e-01 | 0.080 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 8.335472e-01 | 0.079 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 8.369806e-01 | 0.077 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 8.369806e-01 | 0.077 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 8.376495e-01 | 0.077 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.403436e-01 | 0.076 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 8.419991e-01 | 0.075 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 8.419991e-01 | 0.075 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 8.431605e-01 | 0.074 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 8.606709e-01 | 0.065 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 8.634621e-01 | 0.064 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 8.634621e-01 | 0.064 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 8.662817e-01 | 0.062 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.704031e-01 | 0.060 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 8.717486e-01 | 0.060 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 8.788842e-01 | 0.056 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 8.800162e-01 | 0.056 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 8.891907e-01 | 0.051 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 8.926098e-01 | 0.049 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 8.991365e-01 | 0.046 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 9.048610e-01 | 0.043 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 9.100948e-01 | 0.041 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 9.155645e-01 | 0.038 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 9.223419e-01 | 0.035 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 9.285862e-01 | 0.032 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.367803e-01 | 0.028 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 9.389735e-01 | 0.027 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 9.396099e-01 | 0.027 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.478576e-01 | 0.023 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 9.719583e-01 | 0.012 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 9.722522e-01 | 0.012 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 9.768038e-01 | 0.010 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.818027e-01 | 0.008 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 9.842436e-01 | 0.007 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 9.863205e-01 | 0.006 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.885732e-01 | 0.005 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 9.902523e-01 | 0.004 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.905313e-01 | 0.004 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 9.978464e-01 | 0.001 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.989238e-01 | 0.000 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 9.990402e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.996389e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.998450e-01 | 0.000 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 9.999735e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999999e-01 | 0.000 | 0 | 0 |
| SHC-related events triggered by IGF1R | R-HSA-2428933 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
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| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Cell-Cell communication | R-HSA-1500931 | 2.264855e-14 | 13.645 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 2.531308e-14 | 13.597 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 2.531308e-14 | 13.597 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 3.874678e-14 | 13.412 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 1.075806e-13 | 12.968 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 1.075806e-13 | 12.968 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 2.018385e-13 | 12.695 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 1.989520e-13 | 12.701 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 2.212674e-13 | 12.655 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 4.855005e-13 | 12.314 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 6.402656e-13 | 12.194 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 8.807399e-13 | 12.055 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 1.090239e-12 | 11.962 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 1.079026e-12 | 11.967 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 1.090239e-12 | 11.962 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.239564e-12 | 11.907 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 1.627587e-12 | 11.788 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 1.808442e-12 | 11.743 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 2.308154e-12 | 11.637 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 2.437273e-12 | 11.613 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 2.308154e-12 | 11.637 | 0 | 0 |
| Depurination | R-HSA-73927 | 2.929101e-12 | 11.533 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 3.571698e-12 | 11.447 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 4.642065e-12 | 11.333 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 4.642065e-12 | 11.333 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 5.799805e-12 | 11.237 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 5.799805e-12 | 11.237 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 8.926193e-12 | 11.049 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 8.926193e-12 | 11.049 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 1.043554e-11 | 10.981 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 1.099987e-11 | 10.959 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 1.235489e-11 | 10.908 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 1.242983e-11 | 10.906 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 1.649647e-11 | 10.783 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 1.649647e-11 | 10.783 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 1.718459e-11 | 10.765 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.718459e-11 | 10.765 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 1.870137e-11 | 10.728 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 2.221423e-11 | 10.653 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 2.942968e-11 | 10.531 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 3.760781e-11 | 10.425 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 4.112410e-11 | 10.386 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 4.139367e-11 | 10.383 | 0 | 0 |
| M Phase | R-HSA-68886 | 5.295631e-11 | 10.276 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 6.065437e-11 | 10.217 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 5.819611e-11 | 10.235 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 6.769107e-11 | 10.169 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 7.210188e-11 | 10.142 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 8.545697e-11 | 10.068 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 1.009963e-10 | 9.996 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 1.011528e-10 | 9.995 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.030671e-10 | 9.987 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 1.640230e-10 | 9.785 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 2.162089e-10 | 9.665 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 2.237490e-10 | 9.650 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 2.587290e-10 | 9.587 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 3.023313e-10 | 9.520 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 2.932183e-10 | 9.533 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 4.230817e-10 | 9.374 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 5.375729e-10 | 9.270 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 6.920304e-10 | 9.160 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 6.766336e-10 | 9.170 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 7.080764e-10 | 9.150 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 9.255792e-10 | 9.034 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 9.255792e-10 | 9.034 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 1.055339e-09 | 8.977 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 9.744284e-10 | 9.011 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 1.131207e-09 | 8.946 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 1.201172e-09 | 8.920 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.404056e-09 | 8.853 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 1.792268e-09 | 8.747 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 1.962777e-09 | 8.707 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 1.982318e-09 | 8.703 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 2.225639e-09 | 8.653 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 2.522477e-09 | 8.598 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 2.724672e-09 | 8.565 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 2.797800e-09 | 8.553 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 3.190782e-09 | 8.496 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 3.926328e-09 | 8.406 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 3.926328e-09 | 8.406 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 3.926328e-09 | 8.406 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 3.663464e-09 | 8.436 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 3.580960e-09 | 8.446 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 4.716327e-09 | 8.326 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 4.944109e-09 | 8.306 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 6.459691e-09 | 8.190 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 9.170525e-09 | 8.038 | 0 | 0 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 1.153676e-08 | 7.938 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 1.108642e-08 | 7.955 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 1.169640e-08 | 7.932 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 1.056616e-08 | 7.976 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.691411e-08 | 7.772 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 1.855249e-08 | 7.732 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 1.978180e-08 | 7.704 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 2.544000e-08 | 7.594 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 2.981207e-08 | 7.526 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 3.774363e-08 | 7.423 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 3.994946e-08 | 7.398 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 4.006822e-08 | 7.397 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 4.152463e-08 | 7.382 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 4.283848e-08 | 7.368 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 5.188665e-08 | 7.285 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 5.188665e-08 | 7.285 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 5.902431e-08 | 7.229 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 9.178040e-08 | 7.037 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 9.673497e-08 | 7.014 | 1 | 0 |
| Gap junction trafficking | R-HSA-190828 | 9.933103e-08 | 7.003 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 1.006776e-07 | 6.997 | 1 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 1.076924e-07 | 6.968 | 1 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 1.089282e-07 | 6.963 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 1.247755e-07 | 6.904 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 1.535108e-07 | 6.814 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 1.616021e-07 | 6.792 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 1.981257e-07 | 6.703 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.987174e-07 | 6.702 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 2.373629e-07 | 6.625 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 2.898923e-07 | 6.538 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 2.485790e-07 | 6.605 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 2.648151e-07 | 6.577 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 2.908609e-07 | 6.536 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 3.919478e-07 | 6.407 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 7.583382e-07 | 6.120 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 7.904389e-07 | 6.102 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 9.214504e-07 | 6.036 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 1.039896e-06 | 5.983 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 1.511047e-06 | 5.821 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 1.674432e-06 | 5.776 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 2.045509e-06 | 5.689 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 2.194872e-06 | 5.659 | 1 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 2.257551e-06 | 5.646 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 3.053903e-06 | 5.515 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 3.186150e-06 | 5.497 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 3.186150e-06 | 5.497 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 4.116993e-06 | 5.385 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 4.868859e-06 | 5.313 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 5.463177e-06 | 5.263 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 6.220206e-06 | 5.206 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 9.804400e-06 | 5.009 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 9.103933e-06 | 5.041 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 9.804400e-06 | 5.009 | 0 | 0 |
| Disease | R-HSA-1643685 | 9.868907e-06 | 5.006 | 1 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 1.384221e-05 | 4.859 | 1 | 0 |
| Protein folding | R-HSA-391251 | 1.402789e-05 | 4.853 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 1.476430e-05 | 4.831 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 1.726193e-05 | 4.763 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 1.728478e-05 | 4.762 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 1.731975e-05 | 4.761 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 1.817920e-05 | 4.740 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 2.549718e-05 | 4.594 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 2.823743e-05 | 4.549 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 2.890153e-05 | 4.539 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 3.009709e-05 | 4.521 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 3.119323e-05 | 4.506 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 3.421640e-05 | 4.466 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 3.777995e-05 | 4.423 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 4.305243e-05 | 4.366 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 4.464375e-05 | 4.350 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 5.200980e-05 | 4.284 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 5.318021e-05 | 4.274 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 5.956242e-05 | 4.225 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 7.246579e-05 | 4.140 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 7.452996e-05 | 4.128 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 7.658661e-05 | 4.116 | 0 | 0 |
| Kinesins | R-HSA-983189 | 9.024547e-05 | 4.045 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.105379e-04 | 3.956 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.139710e-04 | 3.943 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 9.322363e-05 | 4.030 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.260621e-04 | 3.899 | 1 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.266578e-04 | 3.897 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.323628e-04 | 3.878 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 1.366519e-04 | 3.864 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 1.815853e-04 | 3.741 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 2.020032e-04 | 3.695 | 0 | 0 |
| Immune System | R-HSA-168256 | 2.172985e-04 | 3.663 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 2.184958e-04 | 3.661 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 2.507921e-04 | 3.601 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 2.655796e-04 | 3.576 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.797433e-04 | 3.553 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 2.831006e-04 | 3.548 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 2.831006e-04 | 3.548 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 2.831006e-04 | 3.548 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 2.831006e-04 | 3.548 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 2.847977e-04 | 3.545 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 2.847977e-04 | 3.545 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 2.930002e-04 | 3.533 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 4.321511e-04 | 3.364 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 4.457307e-04 | 3.351 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 4.632601e-04 | 3.334 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 5.221707e-04 | 3.282 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 5.223671e-04 | 3.282 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 5.380805e-04 | 3.269 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 5.627855e-04 | 3.250 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 5.944406e-04 | 3.226 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 8.421374e-04 | 3.075 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 8.421374e-04 | 3.075 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 8.421374e-04 | 3.075 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 8.421374e-04 | 3.075 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 7.972065e-04 | 3.098 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 7.160077e-04 | 3.145 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 8.992873e-04 | 3.046 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 7.298111e-04 | 3.137 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 9.151244e-04 | 3.039 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 9.423142e-04 | 3.026 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 9.827045e-04 | 3.008 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 9.827045e-04 | 3.008 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 1.051138e-03 | 2.978 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 1.054606e-03 | 2.977 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.091140e-03 | 2.962 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.102536e-03 | 2.958 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 1.135535e-03 | 2.945 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 1.149407e-03 | 2.940 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 1.286913e-03 | 2.890 | 0 | 0 |
| Signaling by FGFR1 amplification mutants | R-HSA-1839120 | 1.306861e-03 | 2.884 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 1.711850e-03 | 2.767 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 1.808031e-03 | 2.743 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 1.825046e-03 | 2.739 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 1.846930e-03 | 2.734 | 0 | 0 |
| MTF1 activates gene expression | R-HSA-5660489 | 1.869048e-03 | 2.728 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 1.869220e-03 | 2.728 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.897135e-03 | 2.722 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 2.286798e-03 | 2.641 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.399582e-03 | 2.620 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 2.410398e-03 | 2.618 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 2.802737e-03 | 2.552 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 3.102267e-03 | 2.508 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 3.127020e-03 | 2.505 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 3.232130e-03 | 2.491 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 3.358259e-03 | 2.474 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 3.358259e-03 | 2.474 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 4.029405e-03 | 2.395 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 4.120064e-03 | 2.385 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 4.265963e-03 | 2.370 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 4.570628e-03 | 2.340 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 4.570628e-03 | 2.340 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 4.766850e-03 | 2.322 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 4.864678e-03 | 2.313 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 4.954227e-03 | 2.305 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 5.051932e-03 | 2.297 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 5.051932e-03 | 2.297 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 5.305828e-03 | 2.275 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 6.071331e-03 | 2.217 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 6.232972e-03 | 2.205 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 6.503028e-03 | 2.187 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 6.828045e-03 | 2.166 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 6.828045e-03 | 2.166 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 6.915003e-03 | 2.160 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.037893e-02 | 1.984 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.037893e-02 | 1.984 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.037893e-02 | 1.984 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.037893e-02 | 1.984 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.037893e-02 | 1.984 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.037893e-02 | 1.984 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 7.176366e-03 | 2.144 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 7.867115e-03 | 2.104 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 8.882132e-03 | 2.051 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 8.882132e-03 | 2.051 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.024548e-02 | 1.989 | 0 | 0 |
| FGFR1 mutant receptor activation | R-HSA-1839124 | 8.194084e-03 | 2.086 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.065679e-02 | 1.972 | 0 | 0 |
| Translation | R-HSA-72766 | 7.998740e-03 | 2.097 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 9.820429e-03 | 2.008 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 9.820429e-03 | 2.008 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 9.490228e-03 | 2.023 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 9.635906e-03 | 2.016 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 8.365169e-03 | 2.078 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 7.176366e-03 | 2.144 | 0 | 0 |
| ChREBP activates metabolic gene expression | R-HSA-163765 | 9.635906e-03 | 2.016 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 8.194084e-03 | 2.086 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 8.547725e-03 | 2.068 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 8.614553e-03 | 2.065 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 1.036479e-02 | 1.984 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 8.095754e-03 | 2.092 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 1.068228e-02 | 1.971 | 0 | 0 |
| Signaling by activated point mutants of FGFR1 | R-HSA-1839122 | 1.098677e-02 | 1.959 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 1.098677e-02 | 1.959 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.113095e-02 | 1.953 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 1.145644e-02 | 1.941 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 1.159159e-02 | 1.936 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 1.203167e-02 | 1.920 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.220948e-02 | 1.913 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.220948e-02 | 1.913 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.241597e-02 | 1.906 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.241597e-02 | 1.906 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 1.350380e-02 | 1.870 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 1.415367e-02 | 1.849 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.427663e-02 | 1.845 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 1.507411e-02 | 1.822 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.550244e-02 | 1.810 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.589632e-02 | 1.799 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.629385e-02 | 1.788 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.629610e-02 | 1.788 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.674333e-02 | 1.776 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.761521e-02 | 1.754 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 1.809130e-02 | 1.743 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.888163e-02 | 1.724 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 1.943377e-02 | 1.711 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 1.988407e-02 | 1.701 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.067305e-02 | 1.685 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 2.067305e-02 | 1.685 | 0 | 0 |
| Response to metal ions | R-HSA-5660526 | 2.067683e-02 | 1.685 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 2.234912e-02 | 1.651 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 2.234912e-02 | 1.651 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 2.234912e-02 | 1.651 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.254027e-02 | 1.647 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.254027e-02 | 1.647 | 0 | 0 |
| Phospholipase C-mediated cascade: FGFR1 | R-HSA-5654219 | 2.254027e-02 | 1.647 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 2.341296e-02 | 1.631 | 1 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 2.441784e-02 | 1.612 | 0 | 0 |
| FGFR1 ligand binding and activation | R-HSA-190242 | 2.447036e-02 | 1.611 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.447036e-02 | 1.611 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.457010e-02 | 1.610 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 2.516224e-02 | 1.599 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 2.516224e-02 | 1.599 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 2.516224e-02 | 1.599 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 2.548973e-02 | 1.594 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 2.548973e-02 | 1.594 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 2.548973e-02 | 1.594 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 2.548973e-02 | 1.594 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.646553e-02 | 1.577 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.646553e-02 | 1.577 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 2.658661e-02 | 1.575 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 2.658661e-02 | 1.575 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 2.683111e-02 | 1.571 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 2.770846e-02 | 1.557 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 2.836364e-02 | 1.547 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 2.885523e-02 | 1.540 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 2.927748e-02 | 1.533 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 2.983264e-02 | 1.525 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 3.002687e-02 | 1.522 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 3.002687e-02 | 1.522 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 3.064497e-02 | 1.514 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 3.064497e-02 | 1.514 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.064497e-02 | 1.514 | 0 | 0 |
| PTEN Loss of Function in Cancer | R-HSA-5674404 | 3.081661e-02 | 1.511 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.081661e-02 | 1.511 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.153954e-02 | 1.501 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 3.185519e-02 | 1.497 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 3.217089e-02 | 1.493 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.282624e-02 | 1.484 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 3.298890e-02 | 1.482 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.319045e-02 | 1.479 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 3.506656e-02 | 1.455 | 0 | 0 |
| PI-3K cascade:FGFR1 | R-HSA-5654689 | 3.506656e-02 | 1.455 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 3.625604e-02 | 1.441 | 1 | 1 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 3.625604e-02 | 1.441 | 0 | 0 |
| Regulation of PTEN mRNA translation | R-HSA-8943723 | 3.736450e-02 | 1.428 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 3.736450e-02 | 1.428 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 3.736450e-02 | 1.428 | 0 | 0 |
| Axonal growth stimulation | R-HSA-209563 | 5.083468e-02 | 1.294 | 0 | 0 |
| Signaling by plasma membrane FGFR1 fusions | R-HSA-8853336 | 5.083468e-02 | 1.294 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.068904e-02 | 1.217 | 0 | 0 |
| IRS activation | R-HSA-74713 | 7.044170e-02 | 1.152 | 0 | 0 |
| FGFR1c and Klotho ligand binding and activation | R-HSA-190374 | 7.044170e-02 | 1.152 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.044170e-02 | 1.152 | 0 | 0 |
| SHC-mediated cascade:FGFR1 | R-HSA-5654688 | 3.971863e-02 | 1.401 | 0 | 0 |
| FRS-mediated FGFR1 signaling | R-HSA-5654693 | 4.212756e-02 | 1.375 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 6.605390e-02 | 1.180 | 0 | 0 |
| Downstream signaling of activated FGFR1 | R-HSA-5654687 | 7.186431e-02 | 1.143 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 4.458991e-02 | 1.351 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.321112e-02 | 1.199 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.209050e-02 | 1.283 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 4.899846e-02 | 1.310 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 6.893869e-02 | 1.162 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.087756e-02 | 1.389 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.083468e-02 | 1.294 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 4.710433e-02 | 1.327 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 5.765633e-02 | 1.239 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 3.783899e-02 | 1.422 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 4.167965e-02 | 1.380 | 1 | 1 |
| IGF1R signaling cascade | R-HSA-2428924 | 4.028744e-02 | 1.395 | 1 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 5.494676e-02 | 1.260 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.367120e-02 | 1.270 | 0 | 0 |
| SMAC(DIABLO)-mediated dissociation of IAP:caspase complexes | R-HSA-111464 | 7.044170e-02 | 1.152 | 0 | 0 |
| Pyrophosphate hydrolysis | R-HSA-71737 | 7.044170e-02 | 1.152 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 6.041153e-02 | 1.219 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 7.186431e-02 | 1.143 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 7.186431e-02 | 1.143 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 4.028744e-02 | 1.395 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 3.818390e-02 | 1.418 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 3.971863e-02 | 1.401 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 4.388659e-02 | 1.358 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 5.855015e-02 | 1.232 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 6.321112e-02 | 1.199 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 3.953497e-02 | 1.403 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 3.953497e-02 | 1.403 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 7.044170e-02 | 1.152 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 7.044170e-02 | 1.152 | 0 | 0 |
| SMAC (DIABLO) binds to IAPs | R-HSA-111463 | 7.044170e-02 | 1.152 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 7.482963e-02 | 1.126 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 7.482963e-02 | 1.126 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 5.228405e-02 | 1.282 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 5.527481e-02 | 1.257 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 5.765633e-02 | 1.239 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 6.605390e-02 | 1.180 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 6.893869e-02 | 1.162 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 6.893869e-02 | 1.162 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 7.186431e-02 | 1.143 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 4.866037e-02 | 1.313 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 6.363092e-02 | 1.196 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 5.494676e-02 | 1.260 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 4.599989e-02 | 1.337 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 5.267300e-02 | 1.278 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 4.931750e-02 | 1.307 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 3.937592e-02 | 1.405 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 3.891937e-02 | 1.410 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 6.893869e-02 | 1.162 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 5.494676e-02 | 1.260 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.482963e-02 | 1.126 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 3.975509e-02 | 1.401 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 5.158915e-02 | 1.287 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 7.437889e-02 | 1.129 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 7.482963e-02 | 1.126 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 7.624405e-02 | 1.118 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 7.737137e-02 | 1.111 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 7.742979e-02 | 1.111 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 7.783351e-02 | 1.109 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 7.783351e-02 | 1.109 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 7.783351e-02 | 1.109 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 7.783351e-02 | 1.109 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.009369e-02 | 1.096 | 0 | 0 |
| Activation of caspases through apoptosome-mediated cleavage | R-HSA-111459 | 8.009369e-02 | 1.096 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.009369e-02 | 1.096 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.009369e-02 | 1.096 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.009369e-02 | 1.096 | 0 | 0 |
| Release of apoptotic factors from the mitochondria | R-HSA-111457 | 8.009369e-02 | 1.096 | 0 | 0 |
| SMAC, XIAP-regulated apoptotic response | R-HSA-111469 | 8.009369e-02 | 1.096 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.009369e-02 | 1.096 | 0 | 0 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 8.009369e-02 | 1.096 | 0 | 0 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | R-HSA-9758919 | 8.009369e-02 | 1.096 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 8.024878e-02 | 1.096 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 8.087484e-02 | 1.092 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 8.196216e-02 | 1.086 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 8.256376e-02 | 1.083 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 8.395254e-02 | 1.076 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 8.395254e-02 | 1.076 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 8.395254e-02 | 1.076 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 8.395254e-02 | 1.076 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 8.395254e-02 | 1.076 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 8.706553e-02 | 1.060 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 8.706553e-02 | 1.060 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 8.706553e-02 | 1.060 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 8.706553e-02 | 1.060 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 8.767165e-02 | 1.057 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 8.964605e-02 | 1.047 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 8.964605e-02 | 1.047 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 8.964605e-02 | 1.047 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 8.964605e-02 | 1.047 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.021277e-02 | 1.045 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 9.021277e-02 | 1.045 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 9.021277e-02 | 1.045 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 9.188877e-02 | 1.037 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 9.339320e-02 | 1.030 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 9.339320e-02 | 1.030 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 9.339320e-02 | 1.030 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 9.339320e-02 | 1.030 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 9.339320e-02 | 1.030 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 9.393166e-02 | 1.027 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 9.660582e-02 | 1.015 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 9.909980e-02 | 1.004 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 9.909980e-02 | 1.004 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 9.909980e-02 | 1.004 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 9.909980e-02 | 1.004 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 9.909980e-02 | 1.004 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 9.984963e-02 | 1.001 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 9.984963e-02 | 1.001 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 1.001716e-01 | 0.999 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 1.001716e-01 | 0.999 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 1.002119e-01 | 0.999 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 1.022879e-01 | 0.990 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 1.031236e-01 | 0.987 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 1.031236e-01 | 0.987 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 1.031236e-01 | 0.987 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.031236e-01 | 0.987 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 1.034709e-01 | 0.985 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 1.034709e-01 | 0.985 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 1.064269e-01 | 0.973 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 1.064269e-01 | 0.973 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 1.064269e-01 | 0.973 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 1.064269e-01 | 0.973 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 1.064269e-01 | 0.973 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 1.064269e-01 | 0.973 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 1.065737e-01 | 0.972 | 0 | 0 |
| FGFR1b ligand binding and activation | R-HSA-190370 | 1.084560e-01 | 0.965 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 1.084560e-01 | 0.965 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 1.084560e-01 | 0.965 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 1.084560e-01 | 0.965 | 0 | 0 |
| Axonal growth inhibition (RHOA activation) | R-HSA-193634 | 1.084560e-01 | 0.965 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.087427e-01 | 0.964 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 1.097584e-01 | 0.960 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 1.109289e-01 | 0.955 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 1.131173e-01 | 0.946 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.131173e-01 | 0.946 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 1.131320e-01 | 0.946 | 1 | 1 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.153517e-01 | 0.938 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 1.153517e-01 | 0.938 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 1.165026e-01 | 0.934 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 1.165026e-01 | 0.934 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.165026e-01 | 0.934 | 0 | 0 |
| AMPK inhibits chREBP transcriptional activation activity | R-HSA-163680 | 1.177155e-01 | 0.929 | 0 | 0 |
| Lipophagy | R-HSA-9613354 | 1.177155e-01 | 0.929 | 0 | 0 |
| p75NTR regulates axonogenesis | R-HSA-193697 | 1.177155e-01 | 0.929 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 1.177155e-01 | 0.929 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 1.177890e-01 | 0.929 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 1.192462e-01 | 0.924 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 1.198403e-01 | 0.921 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 1.233489e-01 | 0.909 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 1.233489e-01 | 0.909 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 1.268082e-01 | 0.897 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 1.268082e-01 | 0.897 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 1.268082e-01 | 0.897 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.268795e-01 | 0.897 | 0 | 0 |
| Formation of apoptosome | R-HSA-111458 | 1.268795e-01 | 0.897 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.268795e-01 | 0.897 | 0 | 0 |
| Regulation of the apoptosome activity | R-HSA-9627069 | 1.268795e-01 | 0.897 | 0 | 0 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | R-HSA-2151209 | 1.268795e-01 | 0.897 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.268795e-01 | 0.897 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.268795e-01 | 0.897 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 1.268795e-01 | 0.897 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 1.290075e-01 | 0.889 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.302904e-01 | 0.885 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 1.337946e-01 | 0.874 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.359488e-01 | 0.867 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.359488e-01 | 0.867 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.359488e-01 | 0.867 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 1.410016e-01 | 0.851 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 1.444317e-01 | 0.840 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 1.444317e-01 | 0.840 | 0 | 0 |
| Cytochrome c-mediated apoptotic response | R-HSA-111461 | 1.449245e-01 | 0.839 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.449245e-01 | 0.839 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 1.480161e-01 | 0.830 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 1.480161e-01 | 0.830 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 1.480497e-01 | 0.830 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.538075e-01 | 0.813 | 0 | 0 |
| SHC-related events triggered by IGF1R | R-HSA-2428933 | 1.538075e-01 | 0.813 | 1 | 1 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.538075e-01 | 0.813 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.538075e-01 | 0.813 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 1.588750e-01 | 0.799 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 1.588750e-01 | 0.799 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 1.588750e-01 | 0.799 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 1.625274e-01 | 0.789 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.625988e-01 | 0.789 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.625988e-01 | 0.789 | 0 | 0 |
| FGFR1c ligand binding and activation | R-HSA-190373 | 1.625988e-01 | 0.789 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.625988e-01 | 0.789 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.625988e-01 | 0.789 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.625988e-01 | 0.789 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.625988e-01 | 0.789 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.625988e-01 | 0.789 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 1.661948e-01 | 0.779 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 1.661948e-01 | 0.779 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.712992e-01 | 0.766 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.712992e-01 | 0.766 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.712992e-01 | 0.766 | 0 | 0 |
| CLEC7A (Dectin-1) induces NFAT activation | R-HSA-5607763 | 1.712992e-01 | 0.766 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.712992e-01 | 0.766 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 1.755882e-01 | 0.756 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 1.772813e-01 | 0.751 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 1.798660e-01 | 0.745 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.799098e-01 | 0.745 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.799098e-01 | 0.745 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.799098e-01 | 0.745 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.799098e-01 | 0.745 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.799098e-01 | 0.745 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.799098e-01 | 0.745 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 1.839961e-01 | 0.735 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 1.884315e-01 | 0.725 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.884315e-01 | 0.725 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.884315e-01 | 0.725 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 1.884315e-01 | 0.725 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 1.922342e-01 | 0.716 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 1.959987e-01 | 0.708 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 1.959987e-01 | 0.708 | 0 | 0 |
| G beta:gamma signalling through CDC42 | R-HSA-8964616 | 1.968651e-01 | 0.706 | 0 | 0 |
| Antigen processing: Ub, ATP-independent proteasomal degradation | R-HSA-9912633 | 1.968651e-01 | 0.706 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 1.968651e-01 | 0.706 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.968651e-01 | 0.706 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 1.997725e-01 | 0.699 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 1.997725e-01 | 0.699 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 2.017524e-01 | 0.695 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 2.029551e-01 | 0.693 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 2.035550e-01 | 0.691 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 2.035550e-01 | 0.691 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.052116e-01 | 0.688 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.052116e-01 | 0.688 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 2.072460e-01 | 0.684 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 2.073455e-01 | 0.683 | 0 | 0 |
| Apoptotic factor-mediated response | R-HSA-111471 | 2.134719e-01 | 0.671 | 0 | 0 |
| Synaptic adhesion-like molecules | R-HSA-8849932 | 2.134719e-01 | 0.671 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.134719e-01 | 0.671 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.134719e-01 | 0.671 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.216468e-01 | 0.654 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.216468e-01 | 0.654 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.216468e-01 | 0.654 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 2.264003e-01 | 0.645 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.264003e-01 | 0.645 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 2.264003e-01 | 0.645 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 2.264003e-01 | 0.645 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.297373e-01 | 0.639 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.297373e-01 | 0.639 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.297373e-01 | 0.639 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.297373e-01 | 0.639 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.369975e-01 | 0.625 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.377442e-01 | 0.624 | 0 | 0 |
| Transcriptional activation of mitochondrial biogenesis | R-HSA-2151201 | 2.378955e-01 | 0.624 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 2.455765e-01 | 0.610 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 2.456683e-01 | 0.610 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 2.456683e-01 | 0.610 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.456683e-01 | 0.610 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.456683e-01 | 0.610 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 2.456683e-01 | 0.610 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 2.456683e-01 | 0.610 | 0 | 0 |
| S Phase | R-HSA-69242 | 2.508351e-01 | 0.601 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 2.535105e-01 | 0.596 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 2.535105e-01 | 0.596 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.535105e-01 | 0.596 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 2.535105e-01 | 0.596 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 2.536175e-01 | 0.596 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 2.547777e-01 | 0.594 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.564045e-01 | 0.591 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 2.612717e-01 | 0.583 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.612717e-01 | 0.583 | 0 | 0 |
| Carnitine shuttle | R-HSA-200425 | 2.612717e-01 | 0.583 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.612717e-01 | 0.583 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 2.612717e-01 | 0.583 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 2.675937e-01 | 0.573 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.689527e-01 | 0.570 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.689527e-01 | 0.570 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.689527e-01 | 0.570 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.689527e-01 | 0.570 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 2.704003e-01 | 0.568 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 2.725117e-01 | 0.565 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 2.765542e-01 | 0.558 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.765542e-01 | 0.558 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.765542e-01 | 0.558 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.765542e-01 | 0.558 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 2.765542e-01 | 0.558 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 2.765542e-01 | 0.558 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.765542e-01 | 0.558 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.765542e-01 | 0.558 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 2.788399e-01 | 0.555 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 2.802080e-01 | 0.553 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 2.802080e-01 | 0.553 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 2.812045e-01 | 0.551 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 2.840542e-01 | 0.547 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 2.840772e-01 | 0.547 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.840772e-01 | 0.547 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.840772e-01 | 0.547 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 2.901314e-01 | 0.537 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 2.915225e-01 | 0.535 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 2.915225e-01 | 0.535 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 2.915225e-01 | 0.535 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 2.915225e-01 | 0.535 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 2.915225e-01 | 0.535 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 2.915225e-01 | 0.535 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 2.915225e-01 | 0.535 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 2.915225e-01 | 0.535 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 2.955803e-01 | 0.529 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 2.988907e-01 | 0.524 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 2.988907e-01 | 0.524 | 0 | 0 |
| Insulin receptor recycling | R-HSA-77387 | 2.988907e-01 | 0.524 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 2.988907e-01 | 0.524 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 2.988907e-01 | 0.524 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 2.988907e-01 | 0.524 | 0 | 0 |
| Pyroptosis | R-HSA-5620971 | 2.988907e-01 | 0.524 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 2.994170e-01 | 0.524 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 2.994170e-01 | 0.524 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 3.032504e-01 | 0.518 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.061828e-01 | 0.514 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.061828e-01 | 0.514 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.061828e-01 | 0.514 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 3.109061e-01 | 0.507 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.109061e-01 | 0.507 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 3.133995e-01 | 0.504 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.133995e-01 | 0.504 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.133995e-01 | 0.504 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.133995e-01 | 0.504 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 3.147277e-01 | 0.502 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 3.170656e-01 | 0.499 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 3.184846e-01 | 0.497 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.205415e-01 | 0.494 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.205415e-01 | 0.494 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.205415e-01 | 0.494 | 1 | 1 |
| Selenocysteine synthesis | R-HSA-2408557 | 3.261636e-01 | 0.487 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 3.261636e-01 | 0.487 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.276097e-01 | 0.485 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 3.337604e-01 | 0.477 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 3.346049e-01 | 0.475 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 3.346049e-01 | 0.475 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 3.346049e-01 | 0.475 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.346049e-01 | 0.475 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.346049e-01 | 0.475 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 3.346049e-01 | 0.475 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.346049e-01 | 0.475 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.375498e-01 | 0.472 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 3.412078e-01 | 0.467 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 3.413328e-01 | 0.467 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 3.414806e-01 | 0.467 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.415276e-01 | 0.467 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.483788e-01 | 0.458 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.483788e-01 | 0.458 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 3.488786e-01 | 0.457 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 3.526408e-01 | 0.453 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 3.526408e-01 | 0.453 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 3.526408e-01 | 0.453 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.551591e-01 | 0.450 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.551591e-01 | 0.450 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 3.563956e-01 | 0.448 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 3.618693e-01 | 0.441 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 3.618693e-01 | 0.441 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 3.713353e-01 | 0.430 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 3.713353e-01 | 0.430 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.750821e-01 | 0.426 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.750821e-01 | 0.426 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 3.797471e-01 | 0.421 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.815861e-01 | 0.418 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 3.815861e-01 | 0.418 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.815861e-01 | 0.418 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 3.815861e-01 | 0.418 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 3.816920e-01 | 0.418 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 3.880229e-01 | 0.411 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 3.880229e-01 | 0.411 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 3.880229e-01 | 0.411 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 3.898141e-01 | 0.409 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 3.898141e-01 | 0.409 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 3.943930e-01 | 0.404 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 3.943930e-01 | 0.404 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 3.971391e-01 | 0.401 | 0 | 0 |
| Intra-Golgi traffic | R-HSA-6811438 | 4.006973e-01 | 0.397 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 4.031504e-01 | 0.395 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.069363e-01 | 0.390 | 0 | 0 |
| Cytosolic tRNA aminoacylation | R-HSA-379716 | 4.069363e-01 | 0.390 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.131107e-01 | 0.384 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 4.192213e-01 | 0.378 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.192213e-01 | 0.378 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 4.252686e-01 | 0.371 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.252686e-01 | 0.371 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.252686e-01 | 0.371 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 4.279359e-01 | 0.369 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.312532e-01 | 0.365 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.312532e-01 | 0.365 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 4.331317e-01 | 0.363 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 4.388334e-01 | 0.358 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 4.391454e-01 | 0.357 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.430374e-01 | 0.354 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.430374e-01 | 0.354 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 4.545788e-01 | 0.342 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 4.658825e-01 | 0.332 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.658825e-01 | 0.332 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 4.714467e-01 | 0.327 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 4.714467e-01 | 0.327 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 4.747691e-01 | 0.324 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 4.769532e-01 | 0.322 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 4.877959e-01 | 0.312 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 4.877959e-01 | 0.312 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 4.877959e-01 | 0.312 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 4.931331e-01 | 0.307 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 4.981966e-01 | 0.303 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.036423e-01 | 0.298 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.036423e-01 | 0.298 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 5.047678e-01 | 0.297 | 0 | 0 |
| tRNA Aminoacylation | R-HSA-379724 | 5.088154e-01 | 0.293 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.139348e-01 | 0.289 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.190013e-01 | 0.285 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 5.190013e-01 | 0.285 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.240152e-01 | 0.281 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.240152e-01 | 0.281 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.241464e-01 | 0.281 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 5.289772e-01 | 0.277 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.289772e-01 | 0.277 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 5.304927e-01 | 0.275 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 5.336444e-01 | 0.273 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.435567e-01 | 0.265 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.435567e-01 | 0.265 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 5.461069e-01 | 0.263 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.483161e-01 | 0.261 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.553013e-01 | 0.255 | 0 | 0 |
| Fatty acyl-CoA biosynthesis | R-HSA-75105 | 5.576875e-01 | 0.254 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.623005e-01 | 0.250 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 5.668656e-01 | 0.247 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.668656e-01 | 0.247 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 5.673558e-01 | 0.246 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.758543e-01 | 0.240 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 5.802789e-01 | 0.236 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 5.878839e-01 | 0.231 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 5.932793e-01 | 0.227 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 5.964598e-01 | 0.224 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 5.964598e-01 | 0.224 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.017230e-01 | 0.221 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 6.021029e-01 | 0.220 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 6.140630e-01 | 0.212 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.180912e-01 | 0.209 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.220777e-01 | 0.206 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 6.373410e-01 | 0.196 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 6.403898e-01 | 0.194 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 6.597361e-01 | 0.181 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 6.668076e-01 | 0.176 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 6.805152e-01 | 0.167 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 6.871573e-01 | 0.163 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.062711e-01 | 0.151 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.093419e-01 | 0.149 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 7.179477e-01 | 0.144 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 7.271079e-01 | 0.138 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 7.271079e-01 | 0.138 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 7.345897e-01 | 0.134 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 7.406131e-01 | 0.130 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 7.410851e-01 | 0.130 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 7.484636e-01 | 0.126 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.569214e-01 | 0.121 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 7.690130e-01 | 0.114 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 7.765482e-01 | 0.110 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 7.857625e-01 | 0.105 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 8.051368e-01 | 0.094 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 8.246269e-01 | 0.084 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 8.249969e-01 | 0.084 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 8.262662e-01 | 0.083 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 8.410142e-01 | 0.075 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.438341e-01 | 0.074 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.638539e-01 | 0.064 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.735546e-01 | 0.059 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 8.762519e-01 | 0.057 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 8.924278e-01 | 0.049 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 9.001730e-01 | 0.046 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.037156e-01 | 0.044 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 9.180419e-01 | 0.037 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.254691e-01 | 0.034 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.343929e-01 | 0.029 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.395050e-01 | 0.027 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.496806e-01 | 0.022 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.566355e-01 | 0.019 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.786310e-01 | 0.009 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.826602e-01 | 0.008 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.984818e-01 | 0.001 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.988678e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.993862e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.998653e-01 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
