BLK
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 | S939 | Sugiyama | POTEF A26C1B | VALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPE |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y791 | Sugiyama | POTEF A26C1B | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPVLLTEATLN |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y1572 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | RMPEQIRLKVGGVDPKQLAVyEEFARNVPGFLPTNDLSQPT |
| A5YKK6 | Y1612 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | TGFLAQPMKQAWATDDVAQIyDKCITELEQHLHAIPPTLAM |
| A5YKK6 | Y851 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | QVWPEANQHFSKEIDDEANSyFQRIYNHPPHPTMSVDEVLE |
| A6NEC2 | Y173 | Sugiyama | NPEPPSL1 | NDKMKGFYRSKYTTPSGEVRyAAVTQFEATDARRAFPCWDE |
| A6NHL2 | Y319 | Sugiyama | TUBAL3 | TTACFESSNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAI |
| A6NMY6 | Y147 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| O00116 | Y645 | Sugiyama | AGPS AAG5 | QWLKESIsDVGFGMLKSVKEyVDPNNIFGNRNLL_______ |
| O00170 | Y203 | Sugiyama | AIP XAP2 | HQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPEW |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00233 | Y70 | Sugiyama | PSMD9 | IGMNEPLVDCEGyPRSDVDLyQVRTARHNIICLQNDHKAVM |
| O00264 | Y113 | Sugiyama | PGRMC1 HPR6.6 PGRMC | INGKVFDVTKGRKFyGPEGPyGVFAGRDASRGLATFCLDKE |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00410 | Y33 | Sugiyama | IPO5 KPNB3 RANBP5 | LLLGNLLsPDNVVRKQAEEtyENIPGQSKITFLLQAIRNTT |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00429 | Y266 | Sugiyama | DNM1L DLP1 DRP1 | NRSQLDINNKKSVTDsIRDEyAFLQKKYPSLANRNGTKYLA |
| O00469 | Y444 | Sugiyama | PLOD2 | LWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYMANV |
| O00469 | Y586 | Sugiyama | PLOD2 | FWFPIFSEKACDELVEEMEHyGKWSGGKHHDsRIsGGyENV |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14602 | Y35 | Sugiyama | EIF1AY | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEALCFDGV |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14950 | Y143 | Sugiyama | MYL12B MRLC2 MYLC2B | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14964 | Y216 | Sugiyama | HGS HRS | KYSTIPKFGIEKEVRVCEPCyEQLNRKAEGKAtsttELPPE |
| O14974 | Y901 | Sugiyama | PPP1R12A MBS MYPT1 | EtQtDsIsRyETssTsAGDRyDsLLGRsGsysYLEERKPYS |
| O14974 | Y911 | Sugiyama | PPP1R12A MBS MYPT1 | ETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDSTD |
| O14979 | Y167 | Sugiyama | HNRNPDL HNRPDL JKTBP | DGKMFIGGLSWDTsKKDLtEyLSRFGEVVDCtIKTDPVTGR |
| O15013 | Y1307 | Sugiyama | ARHGEF10 KIAA0294 | sLsLsHGsssLEHRSEDsTIyDLLKDPVSLRSKARRAKKAK |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15234 | Y240 | Sugiyama | CASC3 MLN51 | HDKFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRK |
| O15234 | Y242 | Sugiyama | CASC3 MLN51 | KFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRKPR |
| O15294 | Y316 | Sugiyama | OGT | YCNLANALKEKGSVAEAEDCyNTALRLCPTHADSLNNLANI |
| O15357 | Y1135 | Sugiyama | INPPL1 SHIP2 | SGDDRSCSVLQMAKTLSEVDyAPAGPARSALLPGPLELQPP |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15372 | Y350 | Sugiyama | EIF3H EIF3S3 | IKEFTAQNLGKLFMAQALQEyNN__________________ |
| O15524 | Y80 | SIGNOR|PSP | SOCS1 SSI1 TIP3 | SHADYRRITRASALLDACGFyWGPLSVHGAHERLRAEPVGT |
| O43252 | S231 | Sugiyama | PAPSS1 ATPSK1 PAPSS | DCVQQVVELLQERDIVPVDAsYEVKELyVPENKLHLAKTDA |
| O43390 | T137 | Sugiyama | HNRNPR HNRPR | ESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVYS |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43464 | Y147 | Sugiyama | HTRA2 OMI PRSS25 | GPPAVLAAVPSPPPAsPRSQyNFIADVVEKTAPAVVYIEIL |
| O43615 | Y435 | Sugiyama | TIMM44 MIMT44 TIM44 | KVLRMLYVWALCRDQDELNPyAAWRLLDISASSTEQIL___ |
| O43684 | Y141 | Sugiyama | BUB3 | KLWDPRtPCNAGTFsQPEKVytLSVSGDRLIVGTAGRRVLV |
| O43707 | Y212 | Sugiyama | ACTN4 | WKDGLAFNALIHRHRPELIEyDKLRKDDPVTNLNNAFEVAE |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y397 | Sugiyama | ACTN4 | GKMVSDINNGWQHLEQAEKGyEEWLLNEIRRLERLDHLAEK |
| O43707 | Y441 | Sugiyama | ACTN4 | KAsIHEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEs |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43765 | Y195 | Sugiyama | SGTA SGT SGT1 | HVEAVAYYKKALELDPDNEtyKsNLKIAELKLREAPSPTGG |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y185 | Sugiyama | CALU | KDGDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNAD |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O43865 | Y28 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | PLPGVGEELKQAKEIEDAEKysFMATVTKAPKKQIQFADDM |
| O43865 | Y291 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDVMFGG |
| O60264 | Y80 | Sugiyama | SMARCA5 SNF2H WCRF135 | EIFDDAsPGKQKEIQEPDPtyEEKMQTDRANRFEYLLKQTE |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60506 | T134 | Sugiyama | SYNCRIP HNRPQ NSAP1 | DSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVYS |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y293 | Sugiyama | SYNCRIP HNRPQ NSAP1 | VILyHQPDDKKKNRGFCFLEyEDHKTAAQARRRLMSGKVKV |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60716 | Y257 | Sugiyama | CTNND1 KIAA0384 | IEERyRPsMEGyRAPsRQDVyGPQPQVRVGGssVDLHRFHP |
| O60716 | Y280 | Sugiyama | CTNND1 KIAA0384 | QPQVRVGGssVDLHRFHPEPyGLEDDQRsMGyDDLDyGMMs |
| O60739 | Y30 | Sugiyama | EIF1B | FDPFADATKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| O60814 | Y38 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60884 | Y128 | Sugiyama | DNAJA2 CPR3 HIRIP4 | NGRRRGEDMMHPLKVsLEDLyNGKTTKLQLSKNVLCsACsG |
| O60884 | Y66 | Sugiyama | DNAJA2 CPR3 HIRIP4 | KFKEISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDD |
| O60884 | Y69 | Sugiyama | DNAJA2 CPR3 HIRIP4 | EISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDDIFS |
| O75116 | Y722 | Sugiyama | ROCK2 KIAA0619 | EQEEAEHKATKARLADKNKIyEsIEEAKSEAMKEMEKKLLE |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75190 | Y53 | Sugiyama | DNAJB6 HSJ2 MRJ MSJ1 | DKNPENKEEAERKFKQVAEAyEVLSDAKKRDIYDKYGKEGL |
| O75208 | Y93 | Sugiyama | COQ9 C16orf49 HSPC326 PSEC0129 | PEssHsPPRYTDQGGEEEEDyEsEEQLQHRILTAALEFVPA |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75347 | Y94 | Sugiyama | TBCA | AyLDLQRILENEKDLEEAEEyKEARLVLDsVKLEA______ |
| O75348 | Y47 | Sugiyama | ATP6V1G1 ATP6G ATP6G1 ATP6J | KRKNRRLKQAKEEAQAEIEQyRLQREKEFKAKEAAALGsRG |
| O75369 | Y1576 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYGG |
| O75369 | Y1580 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | EGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYGGDDIP |
| O75369 | Y2502 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ANEtssILVEsVTRsstETCysAIPKASSDASKVTSKGAGL |
| O75369 | Y315 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | DPEGNKEEAQVTPDSDKNKTySVEyLPKVTGLHKVTVLFAG |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75369 | Y904 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | FNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLVTY |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75688 | Y367 | Sugiyama | PPM1B PP2CB | IPNLPPGGGLAGKRNVIEAVySRLNPHREsDGAsDEAEEsG |
| O75794 | Y301 | Sugiyama | CDC123 C10orf7 D123 | EQDSPAFRCTNSEVtVQPsPyLsyRLPKDFVDLsTGEDAHK |
| O75874 | Y231 | Sugiyama | IDH1 PICD | TKNTILKKYDGRFKDIFQEIyDKQyKSQFEAQKIWYEHRLI |
| O75886 | Y371 | Sugiyama | STAM2 HBP | NVKVLEALELYNKLVNEAPVysVysKLHPPAHYPPASSGVP |
| O94826 | Y156 | Sugiyama | TOMM70 KIAA0719 TOM70 TOMM70A | CYTEAISLCPTEKNVDLSTFyQNRAAAFEQLQKWKEVAQDC |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| 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 |
| O95456 | Y287 | Sugiyama | PSMG1 C21LRP DSCR2 PAC1 | PQSTEILKKLMTTNEIQsNIyt___________________ |
| O95602 | Y839 | Sugiyama | POLR1A | STHCGPQAVRAALNLPEAASyDEVRGKWQDAHLGKDQRDFN |
| O95757 | Y30 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | FLNCYIAVARsGGIETIANEySDRCtPACIsLGSRTRAIGN |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O95834 | Y352 | Sugiyama | EML2 EMAP2 EMAPL2 | EVPEDFGPVRTVAEGHGDtLyVGtTRNSILQGSVHTGFSLL |
| O95861 | Y294 | Sugiyama | BPNT1 | KDVKHMNSAGVLAtLRNyDyyASRVPESIKNALVP______ |
| O96019 | Y68 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | DDGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsPL |
| O96019 | Y69 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | DGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsPLK |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00491 | Y166 | Sugiyama | PNP NP | PLRGPNDERFGDRFPAMsDAyDRtMRQRALstWKQMGEQRE |
| P00491 | Y249 | Sugiyama | PNP NP | RHCGLRVFGFSLITNKVIMDyESLEKANHEEVLAAGKQAAQ |
| P00505 | Y96 | Sugiyama | GOT2 KYAT4 | VLPSVRKAEAQIAAKNLDKEyLPIGGLAEFCKASAELALGE |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00558 | Y76 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KSVVLMSHLGRPDGVPMPDKysLEPVAVELKSLLGKDVLFL |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P02545 | Y211 | Sugiyama | LMNA LMN1 | VDAENRLQtMKEELDFQKNIysEELREtKRRHETRLVEIDN |
| P02545 | Y45 | Sugiyama | LMNA LMN1 | RItRLQEKEDLQELNDRLAVyIDRVRsLETENAGLRLRItE |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P04075 | Y343 | Sugiyama | ALDOA ALDA | AAQEEYVKRALANsLACQGKytPsGQAGAAAsEsLFVsNHA |
| P04075 | Y364 | Sugiyama | ALDOA ALDA | tPsGQAGAAAsEsLFVsNHAy____________________ |
| P04181 | Y50 | Sugiyama | OAT | TKKtVQGPPtSDDIFEREyKyGAHNyHPLPVALERGKGIyL |
| P04181 | Y55 | Sugiyama | OAT | QGPPtSDDIFEREyKyGAHNyHPLPVALERGKGIyLWDVEG |
| P04406 | Y314 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | tFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsK |
| P04818 | Y135 | Sugiyama | TYMS TS OK/SW-cl.29 | RDFLDsLGFsTREEGDLGPVyGFQWRHFGAEyRDMEsDysG |
| P05198 | Y150 | Sugiyama | EIF2S1 EIF2A | LFQRTAWVFDDKyKRPGyGAyDAFKHAVsDPsILDsLDLNE |
| P05362 | Y455 | Sugiyama | ICAM1 | GtFPLPIGEsVtVtRDLEGtyLCRARSTQGEVTRKVTVNVL |
| P05455 | Y104 | Sugiyama | SSB | EDKTKIRRsPsKPLPEVTDEyKNDVKNRsVYIKGFPtDAtL |
| P05783 | Y363 | Sugiyama | KRT18 CYK18 PIG46 | LHLESELAQTRAEGQRQAQEyEALLNIKVKLEAEIATYRRL |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P06493 | T14 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | _______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKK |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06493 | Y19 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | __MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKIRLEs |
| P06493 | Y270 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ASHVKNLDENGLDLLSKMLIyDPAKRISGKMALNHPyFNDL |
| P06576 | Y418 | Sugiyama | ATP5F1B ATP5B ATPMB ATPSB | VDPLDSTSRIMDPNIVGsEHyDVARGVQKILQDYKSLQDII |
| P06733 | S268 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyP |
| P06733 | S272 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | FRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsI |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y257 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | TDKVVIGMDVAASEFFRsGKyDLDFKsPDDPsRyIsPDQLA |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06737 | Y733 | Sugiyama | PYGL | GMRIDDVAALDKKGYEAKEyyEALPELKLVIDQIDNGFFSP |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07205 | Y196 | Sugiyama | PGK2 PGKB | MVGVNLPHKASGFLMKKELDyFAKALENPVRPFLAILGGAK |
| P07237 | S331 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | ECPAVRLITLEEEMTKyKPEsEELtAERItEFCHRFLEGKI |
| P07237 | Y327 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LKKEECPAVRLITLEEEMTKyKPEsEELtAERItEFCHRFL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07237 | Y99 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPKEytAG |
| P07355 | Y147 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07355 | Y199 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RAEDGsVIDyELIDQDARDLyDAGVKRKGTDVPKWIsIMTE |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | Y50 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IDPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEP |
| P07437 | Y51 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPG |
| P07686 | Y526 | Sugiyama | HEXB HCC7 | ASAVGERLWSSKDVRDMDDAyDRLTRHRCRMVERGIAAQPL |
| P07686 | Y547 | Sugiyama | HEXB HCC7 | DRLTRHRCRMVERGIAAQPLyAGyCNHENM___________ |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07814 | Y1504 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | KPLCELQPGAKCVCGKNPAKyytLFGRsy____________ |
| P07814 | Y1505 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PLCELQPGAKCVCGKNPAKyytLFGRsy_____________ |
| P07814 | Y754 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | ERPtPsLNNNCttsEDsLVLyNRVAVQGDVVRELKAKKAPK |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07858 | Y244 | Sugiyama | CTSB CPSB | HYGYNSYSVSNSEKDIMAEIyKNGPVEGAFSVYSDFLLYKS |
| P07900 | Y160 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGEPM |
| P07900 | Y197 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | GEPMGRGTKVILHLKEDQtEyLEERRIKEIVKKHSQFIGyP |
| P07900 | Y284 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEEEEKKDGDKKKKKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P07900 | Y309 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | ELNKtKPIWtRNPDDItNEEyGEFyKsLtNDWEDHLAVKHF |
| P07900 | Y313 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | tKPIWtRNPDDItNEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P07900 | Y438 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KKCLELFtELAEDKENyKKFyEQFSKNIKLGIHEDsQNRKK |
| P07900 | Y492 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLR |
| P07900 | Y493 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | EMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLRK |
| P07900 | Y61 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KEIFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLI |
| P07942 | Y1017 | Sugiyama | LAMB1 | CLKCLyHtEGEHCQFCRFGyyGDALQQDCRKCVCNYLGTVQ |
| P07954 | Y54 | Sugiyama | FH | PSFWPPNAARMAsQNSFRIEyDtFGELKVPNDKYYGAQTVR |
| P08174 | Y224 | Sugiyama | CD55 CR DAF | CLISGSSVQWSDPLPECREIyCPAPPQIDNGIIQGERDHyG |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | Y155 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | SAYLVAEKVVVITKHNDDEQyAWEssAGGsFtVRADHGEPI |
| P08238 | Y192 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| P08238 | Y276 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P08238 | Y301 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | ELNKtKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHF |
| P08238 | Y305 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | tKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P08238 | Y430 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KKCLELFsELAEDKENyKKFyEAFSKNLKLGIHEDstNRRR |
| P08238 | Y472 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | sELLRyHtsQsGDEMtsLsEyVsRMKEtQKsIyyItGEsKE |
| P08238 | Y484 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVR |
| P08238 | Y485 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVRK |
| P08238 | Y56 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KEIFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDII |
| P08238 | Y619 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | TANMERIMKAQALRDNstMGyMMAKKHLEINPDHPIVEtLR |
| P08621 | Y126 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | FVARVNYDTTEsKLRREFEVyGPIKRIHMVYSKRsGKPRGy |
| P08621 | Y38 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | PIPYLPPLEKLPHEKHHNQPyCGIAPYIREFEDPRDAPPPT |
| P08670 | Y291 | Sugiyama | VIM | DVRQQyEsVAAKNLQEAEEWyKSKFADLsEAANRNNDALRQ |
| P08670 | Y53 | Sugiyama | VIM | tsTRtYsLGsALRPstsRsLyAssPGGVyAtRssAVRLRss |
| P08758 | S135 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | AsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRMLVV |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09234 | Y12 | Sugiyama | SNRPC | _________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKE |
| P09496 | Y147 | Sugiyama | CLTA | NSRKQEAEWKEKAIKELEEWyARQDEQLQKTKANNRVADEA |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09874 | Y794 | Sugiyama | PARP1 ADPRT PPOL | AySLLRGGsDDssKDPIDVNyEKLKTDIKVVDRDSEEAEII |
| P09884 | Y414 | Sugiyama | POLA1 POLA | MKIDLNTGKEtGtPISMKDVyEEFDEKIATKYKIMKFKSKP |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG38 | Y791 | Sugiyama | POTEI | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y754 | Sugiyama | POTEJ | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P10398 | Y155 | Sugiyama | ARAF ARAF1 PKS PKS2 | HCSSKVPTVCVDMSTNRQQFyHsVQDLsGGsRQHEAPsNRP |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11047 | Y352 | Sugiyama | LAMC1 LAMB2 | tAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQD |
| P11047 | Y854 | Sugiyama | LAMC1 LAMB2 | IDPNAVGNCNRLTGECLKCIyNtAGFyCDRCKDGFFGNPLA |
| P11142 | Y41 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11413 | Y118 | Sugiyama | G6PD | LEDFFARNsyVAGQyDDAAsyQRLNsHMNALHLGsQANRLF |
| P11413 | Y503 | Sugiyama | G6PD | IYGsRGPTEADELMKRVGFQyEGtyKWVNPHKL________ |
| P11413 | Y507 | Sugiyama | G6PD | RGPTEADELMKRVGFQyEGtyKWVNPHKL____________ |
| 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 | Y382 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | PLyVALAQRKEERQAHLtNQyMQRMASVRAVPNPVINPYQP |
| P12004 | Y249 | Sugiyama | PCNA | MSADVPLVVEYKIADMGHLKyyLAPKIEDEEGs________ |
| P12004 | Y250 | Sugiyama | PCNA | SADVPLVVEYKIADMGHLKyyLAPKIEDEEGs_________ |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12318 | Y281 | GPS6|ELM|iPTMNet|EPSD | FCGR2A CD32 FCG2 FCGR2A1 IGFR2 | PPGRQMIAIRKRQLEETNNDyEtADGGyMtLNPRAPTDDDK |
| P12318 | Y288 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FCGR2A CD32 FCG2 FCGR2A1 IGFR2 | AIRKRQLEETNNDyEtADGGyMtLNPRAPTDDDKNIyLTLP |
| P12318 | Y304 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FCGR2A CD32 FCG2 FCGR2A1 IGFR2 | ADGGyMtLNPRAPTDDDKNIyLTLPPNDHVNSNN_______ |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y378 | Sugiyama | ACTN1 | GRMVSDINNAWGCLEQVEKGyEEWLLNEIRRLERLDHLAEK |
| P12814 | Y422 | Sugiyama | ACTN1 | KAsIHEAWtDGKEAMLRQKDyEtAtLsEIKALLKKHEAFEs |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P13010 | Y295 | Sugiyama | XRCC5 G22P2 | TWTVVDAKTLKKEDIQKETVyCLNDDDETEVLKEDIIQGFR |
| P13010 | Y316 | Sugiyama | XRCC5 G22P2 | CLNDDDETEVLKEDIIQGFRyGsDIVPFSKVDEEQMKYKSE |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y634 | Sugiyama | EEF2 EF2 | AEDIDKGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGP |
| P13639 | Y639 | Sugiyama | EEF2 EF2 | KGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGPDGTGP |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | T449 | Sugiyama | PDIA4 ERP70 ERP72 | AATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLsE |
| P13667 | Y101 | Sugiyama | PDIA4 ERP70 ERP72 | TVLLEFYAPWCGHCKQFAPEyEKIANILKDKDPPIPVAKID |
| 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 |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13861 | Y184 | Sugiyama | PRKAR2A PKR2 PRKAR2 | EHVIDQGDDGDNFyVIERGTyDILVTKDNQTRSVGQYDNRG |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y87 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | FEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTSL |
| P14314 | S108 | Sugiyama | PRKCSH G19P1 | PSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREsLQ |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14324 | Y117 | Sugiyama | FDPS FPS KIAA1293 | DEMGHPEIGDAIARLKEVLEyNAIGGKYNRGLTVVVAFREL |
| P14324 | Y349 | Sugiyama | FDPS FPS KIAA1293 | QDNKCSWLVVQCLQRATPEQyQILKENYGQKEAEKVARVKA |
| P14618 | Y148 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | GtAEVELKKGATLKITLDNAyMEKCDENILWLDYKNICKVV |
| P14625 | Y258 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | GNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFINFP |
| P14625 | Y401 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | VTFKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDD |
| P14625 | Y429 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | IKLYVRRVFITDDFHDMMPKyLNFVKGVVDsDDLPLNVsRE |
| P14625 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14625 | Y678 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | MERIMKAQAYQtGKDIstNyyAsQKKTFEINPRHPLIRDML |
| P14635 | Y175 | Sugiyama | CCNB1 CCNB | DVDAEDGADPNLCSEYVKDIyAYLRQLEEEQAVRPKYLLGR |
| P14649 | S87 | Sugiyama | MYL6B MLC1SA | EEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVLK |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14854 | Y57 | Sugiyama | COX6B1 COX6B | FHRCQKAMTAKGGDIsVCEWyQRVYQsLCPtsWVTDWDEQR |
| P15170 | Y234 | Sugiyama | GSPT1 ERF3A | HLIVLINKMDDPTVNWsNERyEECKEKLVPFLKKVGFNPKK |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15374 | Y141 | Sugiyama | UCHL3 | KFLEEsVsMsPEERARyLENyDAIRVtHEtsAHEGQTEAPs |
| P15880 | S249 | Sugiyama | RPS2 RPS4 | CtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEF |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P17066 | Y43 | Sugiyama | HSPA6 HSP70B' | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P17676 | Y137 | Sugiyama | CEBPB TCF5 PP9092 | FLSDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCF |
| P17676 | Y139 | Sugiyama | CEBPB TCF5 PP9092 | SDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCFAP |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17812 | Y473 | Sugiyama | CTPS1 CTPS | RRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVWKKCLE |
| P17812 | Y567 | Sugiyama | CTPS1 CTPS | SVGRLSHYLQKGCRLsPRDtysDRsGsssPDsEItELKFPs |
| P17844 | Y59 | Sugiyama | DDX5 G17P1 HELR HLR1 | EKLVKKKWNLDELPKFEKNFyQEHPDLARRtAQEVETYRRS |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18124 | Y155 | Sugiyama | RPL7 | IVEPYIAWGYPNLKsVNELIyKRGYGKINKKRIALtDNALI |
| P18124 | Y82 | Sugiyama | RPL7 | RQMYRTEIRMARMARKAGNFyVPAEPKLAFVIRIRGINGVS |
| P18206 | Y822 | Sugiyama | VCL | KAVAGNIsDPGLQKsFLDsGyRILGAVAKVREAFQPQEPDF |
| P18615 | Y133 | Sugiyama | NELFE RD RDBP | sIsADDDLQEsSRRPQRKsLyEsFVsssDRLRELGPDGEEA |
| P18615 | Y170 | Sugiyama | NELFE RD RDBP | GEEAEGPGAGDGPPRsFDWGyEERSGAHSsAsPPRsRSRDR |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18621 | Y4 | Sugiyama | RPL17 | _________________MVRysLDPENPtKsCKSRGSNLRV |
| P18669 | S134 | Sugiyama | PGAM1 PGAMA CDABP0006 | IWRRsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCE |
| P18669 | S137 | Sugiyama | PGAM1 PGAMA CDABP0006 | RsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLK |
| P18669 | Y119 | Sugiyama | PGAM1 PGAMA CDABP0006 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| P18669 | Y142 | Sugiyama | PGAM1 PGAMA CDABP0006 | PPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLKDtIAR |
| P18669 | Y26 | Sugiyama | PGAM1 PGAMA CDABP0006 | LVLIRHGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALR |
| P18669 | Y92 | Sugiyama | PGAM1 PGAMA CDABP0006 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| P18754 | Y89 | Sugiyama | RCC1 CHC1 | VVQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSE |
| P19105 | Y142 | Sugiyama | MYL12A MLCB MRLC3 RLC | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19838 | Y240 | Sugiyama | NFKB1 | LPDSTGSFTRRLEPVVSDAIyDSKAPNASNLKIVRMDRTAG |
| P20042 | T175 | Sugiyama | EIF2S2 EIF2B | DGIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMV |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21127 | Y449 | Sugiyama | CDK11B CDC2L1 CDK11 PITSLREA PK58 | LQGCRsVEEFQCLNRIEEGtyGVVYRAKDKKTDEIVALKRL |
| P21333 | Y1604 | Sugiyama | FLNA FLN FLN1 | ITDPEGKPKKTHIQDNHDGtyTVAYVPDVTGRYTILIKYGG |
| P21333 | Y1632 | Sugiyama | FLNA FLN FLN1 | VTGRYTILIKYGGDEIPFsPyRVRAVPTGDASKCTVTVSIG |
| P21333 | Y731 | Sugiyama | FLNA FLN FLN1 | VQDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWGG |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| 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 |
| P22314 | Y60 | Sugiyama | UBA1 A1S9T UBE1 | GMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSVLVSGL |
| P22314 | Y873 | Sugiyama | UBA1 A1S9T UBE1 | DDSNFHMDFIVAASNLRAENyDIPsADRHKSKLIAGKIIPA |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22626 | Y331 | Sugiyama | HNRNPA2B1 HNRPA2B1 | SNYGPMKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRs |
| P22626 | Y347 | Sugiyama | HNRNPA2B1 HNRPA2B1 | MGGPyGGGNyGPGGsGGsGGyGGRsRy______________ |
| P23142 | Y175 | Sugiyama | FBLN1 PP213 | VGGLQETDKIIEVEEEQEDPyLNDRCRGGGPCKQQCRDTGD |
| P23246 | Y488 | Sugiyama | SFPQ PSF | PMYQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQV |
| P23246 | Y490 | Sugiyama | SFPQ PSF | YQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQVEK |
| P23284 | Y119 | Sugiyama | PPIB CYPB | DFMIQGGDFtRGDGtGGKsIyGERFPDENFKLKHyGPGWVs |
| P23396 | Y34 | Sugiyama | RPS3 OK/SW-cl.26 | DGIFKAELNEFLtRELAEDGysGVEVRVtPTRTEIIILATR |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23434 | Y164 | Sugiyama | GCSH | LIKMtLsNPsELDELMsEEAyEKYIKSIEE___________ |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | Y140 | Sugiyama | CFL1 CFL | SKDAIKKKLtGIKHELQANCyEEVKDRCTLAEKLGGsAVIs |
| P23528 | Y68 | Sugiyama | CFL1 CFL | ILEEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAt |
| P23528 | Y82 | Sugiyama | CFL1 CFL | QtVDDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFI |
| P23528 | Y85 | Sugiyama | CFL1 CFL | DDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWA |
| P23528 | Y89 | Sugiyama | CFL1 CFL | AtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| P23588 | Y609 | Sugiyama | EIF4B | sASKyAALsVDGEDENEGEDyAE__________________ |
| P23921 | T555 | Sugiyama | RRM1 RR1 | IyyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTP |
| P23921 | Y232 | Sugiyama | RRM1 RR1 | RPQLSSCFLLSMKDDSIEGIyDTLKQCALISKSAGGIGVAV |
| P23921 | Y553 | Sugiyama | RRM1 RR1 | EtIyyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNV |
| P23921 | Y556 | Sugiyama | RRM1 RR1 | yyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPT |
| P24752 | Y188 | Sugiyama | ACAT1 ACAT MAT | TPYGGVKLEDLIVKDGLtDVyNKIHMGsCAENTAKKLNIAR |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24752 | Y256 | Sugiyama | ACAT1 ACAT MAT | IPVtVtVKGQPDVVVKEDEEyKRVDFSKVPKLKTVFQKENG |
| P24941 | T14 | Sugiyama | CDK2 CDKN2 | _______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKK |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P24941 | Y19 | Sugiyama | CDK2 CDKN2 | __MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKIRLDt |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y456 | Sugiyama | MCM3 | AGIHARLNARCsVLAAANPVyGRyDQyKTPMENIGLQDSLL |
| P25205 | Y708 | Sugiyama | MCM3 | KRKRRKTRQPDAKDGDsyDPyDFsDtEEEMPQVHtPKTADs |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25685 | Y52 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | HPDKNKEPGAEEKFKEIAEAyDVLSDPRKREIFDRYGEEGL |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P25787 | Y57 | Sugiyama | PSMA2 HC3 PSC3 | GIKAANGVVLATEKKQKSILyDERSVHKVEPITKHIGLVys |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26599 | Y127 | Sugiyama | PTBP1 PTB | ANTMVNYYTSVTPVLRGQPIyIQFsNHKELKtDSSPNQARA |
| P26639 | T574 | Sugiyama | TARS1 TARS | RYHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAIL |
| P26639 | T629 | Sugiyama | TARS1 TARS | GGKWPFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMAD |
| P26639 | Y575 | Sugiyama | TARS1 TARS | YHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAILG |
| 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 |
| P27348 | Y48 | Sugiyama | YWHAQ | AVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSIEQK |
| P27540 | Y561 | Sugiyama | ARNT BHLHE2 | PLEKSDGLFAQDRDPRFsEIyHNINADQSKGISSSTVPATQ |
| P27635 | Y199 | Sugiyama | RPL10 DXS648E QM | DEFEDMVAEKRLIPDGCGVKyIPSRGPLDKWRALHS_____ |
| P27695 | Y128 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | LQELPGLSHQYWSAPsDKEGysGVGLLsRQCPLKVsyGIGD |
| P27695 | Y144 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | DKEGysGVGLLsRQCPLKVsyGIGDEEHDQEGRVIVAEFDS |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27708 | Y602 | Sugiyama | CAD | FAHTSQVLVDKSLKGWKEIEyEVVRDAYGNCVTVCNMENLD |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P27816 | Y47 | Sugiyama | MAP4 | AtLEAEAFDDVVGETVGKTDyIPLLDVDEKtGNsESKKKPC |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P28066 | Y8 | Sugiyama | PSMA5 | _____________MFLTRsEyDRGVNtFsPEGRLFQVEyAI |
| P28074 | Y171 | Sugiyama | PSMB5 LMPX MB1 X | GMGLSMGTMICGWDKRGPGLyyVDsEGNRISGATFSVGSGS |
| P28074 | Y236 | Sugiyama | PSMB5 LMPX MB1 X | RRAIyQATYRDAysGGAVNLyHVREDGWIRVSsDNVADLHE |
| P29144 | Y1042 | Sugiyama | TPP2 | TEALRDLKIQWMTKLDSsDIyNELKEtyPNyLPLyVARLHQ |
| P29144 | Y1052 | Sugiyama | TPP2 | WMTKLDSsDIyNELKEtyPNyLPLyVARLHQLDAEKERMKR |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | Y202 | Sugiyama | TKT | LDINRLGQsDPAPLQHQMDIyQKRCEAFGWHAIIVDGHSVE |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30041 | Y89 | Sugiyama | PRDX6 AOP2 KIAA0106 | IALSIDSVEDHLAWSKDINAyNCEEPtEKLPFPIIDDRNRE |
| P30043 | S202 | Sugiyama | BLVRB FLR SCAN | GHFMLRCLttDEyDGHstyPsHQyQ________________ |
| P30043 | T199 | Sugiyama | BLVRB FLR SCAN | HDLGHFMLRCLttDEyDGHstyPsHQyQ_____________ |
| P30084 | Y112 | Sugiyama | ECHS1 | KAFAAGADIKEMQNLsFQDCySSKFLKHWDHLTQVKKPVIA |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| 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 | Y356 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | FVMQEEFsRDGKALERFLQDyFDGNLKRyLKsEPIPESNDG |
| P30101 | Y445 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KDPNIVIAKMDAtANDVPsPyEVRGFPtIyFsPANKKLNPK |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30101 | Y95 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KGIVPLAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAy |
| P30740 | Y112 | Sugiyama | SERPINB1 ELANH2 MNEI PI2 | LYGEKTYNFLPEFLVSTQKtyGADLAsVDFQHASEDARKTI |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31327 | Y162 | Sugiyama | CPS1 | HWLATKsLGQWLQEEKVPAIyGVDtRMLTKIIRDKGTMLGK |
| P31327 | Y582 | Sugiyama | CPS1 | APsFAVEsIEDALKAADTIGyPVMIRSAyALGGLGsGICPN |
| P31327 | Y634 | Sugiyama | CPS1 | FAMTNQILVEKSVTGWKEIEyEVVRDADDNCVTVCNMENVD |
| P31327 | Y852 | Sugiyama | CPS1 | EWPsNLDLRKELSEPSsTRIyAIAKAIDDNMsLDEIEKLTY |
| P31939 | Y290 | Sugiyama | ATIC PURH OK/SW-cl.86 | PAGAAVGIPLsEDEAKVCMVyDLyKTLtPIsAAyARARGAD |
| P31939 | Y293 | Sugiyama | ATIC PURH OK/SW-cl.86 | AAVGIPLsEDEAKVCMVyDLyKTLtPIsAAyARARGADRMs |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31946 | Y50 | Sugiyama | YWHAB | AVtEQGHELsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P31947 | Y151 | Sugiyama | SFN HME1 | LAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIRLG |
| P31947 | Y19 | Sugiyama | SFN HME1 | __MERASLIQKAKLAEQAERyEDMAAFMKGAVEKGEELsCE |
| P31947 | Y48 | Sugiyama | SFN HME1 | GAVEKGEELsCEERNLLsVAyKNVVGGQRAAWRVLSsIEQK |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P31994 | Y292 | GPS6|ELM|iPTMNet|EPSD|PSP | FCGR2B CD32 FCG2 IGFR2 | PANPTNPDEADKVGAENTITySLLMHPDALEEPDDQNRI__ |
| P31995 | Y294 | SIGNOR | FCGR2C CD32 FCG2 IGFR2 | AIRKRQPEETNNDyETADGGyMTLNPRAPTDDDKNIyLTLP |
| P31995 | Y310 | SIGNOR|EPSD|PSP | FCGR2C CD32 FCG2 IGFR2 | ADGGyMTLNPRAPTDDDKNIyLTLPPNDHVNSNN_______ |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32322 | Y135 | Sugiyama | PYCR1 | PRVIRCMTNTPVVVREGATVyAtGTHAQVEDGRLMEQLLSS |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32929 | Y114 | Sugiyama | CTH | TVTITHLLKAGDQIICMDDVyGGTNRYFRQVASEFGLKISF |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33121 | Y693 | Sugiyama | ACSL1 FACL1 FACL2 LACS LACS1 LACS2 | TMKAKRPELRNYFRSQIDDLyStIKV_______________ |
| P33176 | Y516 | Sugiyama | KIF5B KNS KNS1 | EELAVNyDQKSQEVEDKTKEyELLSDELNQKsATLAsIDAE |
| P33176 | Y62 | Sugiyama | KIF5B KNS KNS1 | ASKPYAFDRVFQSsTsQEQVyNDCAKKIVKDVLEGyNGtIF |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33993 | Y102 | Sugiyama | MCM7 CDC47 MCM2 | QELLPQYKEREVVNKDVLDVyIEHRLMMEQRSRDPGMVRsP |
| P33993 | Y333 | Sugiyama | MCM7 CDC47 MCM2 | EsGAGELtREELRQIAEEDFyEKLAASIAPEIYGHEDVKKA |
| P34896 | Y34 | Sugiyama | SHMT1 | LWSsHDKMLAQPLKDSDVEVyNIIKKESNRQRVGLELIASE |
| P34931 | Y43 | Sugiyama | HSPA1L | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P34932 | Y30 | Sugiyama | HSPA4 APG2 HSPH2 | FQSCYVAVARAGGIETIANEysDRCtPACIsFGPKNRSIGA |
| P34932 | Y336 | Sugiyama | HSPA4 APG2 HSPH2 | RVEPPLRSVLEQTKLKKEDIyAVEIVGGATRIPAVKEKISK |
| P34932 | Y597 | Sugiyama | HSPA4 APG2 HSPH2 | VDLPIENQLLWQIDREMLNLyIENEGKMIMQDKLEKERNDA |
| P34932 | Y626 | Sugiyama | HSPA4 APG2 HSPH2 | MQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDDRN |
| P34932 | Y660 | Sugiyama | HSPA4 APG2 HSPH2 | VSEDDRNsFtLKLEDTENWLyEDGEDQPKQVYVDKLAELKN |
| P35221 | Y619 | Sugiyama | CTNNA1 | SSDPAQPMDENEFIDASRLVyDGIRDIRKAVLMIRtPEELD |
| P35270 | Y259 | Sugiyama | SPR | QKLLSLLEKDEFKSGAHVDFyDK__________________ |
| P35579 | Y11 | Sugiyama | MYH9 | __________MAQQAADKyLyVDKNFINNPLAQADWAAKKL |
| P35579 | Y297 | Sugiyama | MYH9 | FYYLLSGAGEHLKTDLLLEPyNKyRFLsNGHVtIPGQQDKD |
| P35609 | Y385 | Sugiyama | ACTN2 | GKMVSDIAGAWQRLEQAEKGyEEWLLNEIRRLERLEHLAEK |
| P35637 | Y325 | Sugiyama | FUS TLS | FKQIGIIKTNKKTGQPMINLyTDRETGKLKGEAtVsFDDPP |
| P35813 | Y362 | Sugiyama | PPM1A PPPM1A | IPSLPPGGELASKRNVIEAVyNRLNPYKNDDTDsTsTDDMW |
| P36578 | Y211 | Sugiyama | RPL4 RPL1 | AGKGKMRNRRRIQRRGPCIIyNEDNGIIKAFRNIPGITLLN |
| P36578 | Y264 | Sugiyama | RPL4 RPL1 | GHVGRFCIWtEsAFRKLDELyGtWRKAAsLKsNyNLPMHKM |
| P36871 | Y157 | Sugiyama | PGM1 | GPAPEAITDKIFQISKTIEEyAVCPDLKVDLGVLGKQQFDL |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P37198 | Y422 | Sugiyama | NUP62 | ELEDLLsPLEELVKEQsGtIyLQHADEEREKTYKLAENIDA |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P37837 | Y206 | Sugiyama | TALDO1 TAL TALDO TALDOR | ISPFVGRILDWHVANTDKKSyEPLEDPGVKSVTKIYNYYKK |
| P38646 | S200 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | NyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNVLRVI |
| P38646 | T120 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | LVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIKNV |
| P38646 | Y118 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | ERLVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIK |
| P38919 | Y202 | Sugiyama | EIF4A3 DDX48 KIAA0111 | KMLVLDEADEMLNKGFKEQIyDVYRYLPPATQVVLISATLP |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40429 | Y149 | Sugiyama | RPL13A | LKPTRKFAYLGRLAHEVGWKyQAVtAtLEEKRKEKAKIHYR |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41219 | Y287 | Sugiyama | PRPH NEF4 PRPH1 | DIRAQYESIAAKNLQEAEEWyKSKYADLSDAANRNHEALRQ |
| P41227 | Y145 | Sugiyama | NAA10 ARD1 ARD1A TE2 | TLNFQISEVEPKyyADGEDAyAMKRDLtQMADELRRHLELK |
| P41252 | Y273 | Sugiyama | IARS1 IARS | GRLLILMEARLSALYKLEsDyEILERFPGAYLKGKKYRPLF |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42025 | Y33 | Sugiyama | ACTR1B CTRN2 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALE |
| P42025 | Y38 | Sugiyama | ACTR1B CTRN2 | SGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALEGDLFI |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P43243 | S211 | Sugiyama | MATR3 KIAA0723 | DRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDDRLRDGERCR |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43243 | Y214 | Sugiyama | MATR3 KIAA0723 | PsLNPVLDyDHGsRsQEsGyyDRMDyEDDRLRDGERCRDDs |
| P45974 | Y70 | Sugiyama | USP5 ISOT | FLGFGKQYVERHFNKTGQRVyLHLRRTRRPKEEDPATGTGD |
| 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 |
| P46777 | Y253 | Sugiyama | RPL5 MSTP030 | PDMMEEMyKKAHAAIRENPVyEKKPKKEVKKKRWNRPKMsL |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46781 | Y35 | Sugiyama | RPS9 | TPRRPFEKSRLDQELKLIGEyGLRNKREVWRVKFTLAKIRK |
| P46940 | Y1095 | Sugiyama | IQGAP1 KIAA0051 | VVKEIMDDKSLNIKTDPVDIyKsWVNQMESQTGEASKLPyD |
| P46940 | Y140 | Sugiyama | IQGAP1 KIAA0051 | LNAMDEIGLPKIFYPETTDIyDRKNMPRCIYCIHALSLYLF |
| P46940 | Y1478 | Sugiyama | IQGAP1 KIAA0051 | KIQTGLKKLTELGtVDPKNKyQELINDIARDIRNQRRYRQR |
| P47712 | Y535 | Sugiyama | PLA2G4A CPLA2 PLA2G4 | sFDDDELDAAVADPDEFERIyEPLDVKSKKIHVVDSGLTFN |
| P47756 | Y232 | Sugiyama | CAPZB | NIGRLVEDMENKIRstLNEIyFGKTKDIVNGLRSVQTFADK |
| P47756 | Y64 | Sugiyama | CAPZB | DQPLKIARDKVVGKDyLLCDyNRDGDSyRsPWSNKyDPPLE |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47813 | Y35 | Sugiyama | EIF1AX EIF1A EIF4C | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEAMCFDGV |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48556 | Y225 | Sugiyama | PSMD8 | VAEFHTELERLPAKDIQTNVyIKHPVSLEQYLMEGSYNKVF |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | Y43 | Sugiyama | HSPA7 HSP70B | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P49023 | Y88 | Sugiyama | PXN | QWQPSSSRFIHQQPQsssPVyGssAKtssVsNPQDsVGsPC |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | T2450 | Sugiyama | FASN FAS | AEQYtPKAKyHGNVMLLRAKtGGAyGEDLGADyNLsQVCDG |
| P49327 | Y2034 | Sugiyama | FASN FAS | DYFVVFSSVSCGRGNAGQsNyGFANsAMERICEKRRHEGLP |
| P49327 | Y2454 | Sugiyama | FASN FAS | tPKAKyHGNVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsV |
| P49327 | Y2462 | Sugiyama | FASN FAS | NVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsVHVIEGDHR |
| P49327 | Y277 | Sugiyama | FASN FAS | KEQGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGT |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49327 | Y959 | Sugiyama | FASN FAS | EASRAFEVSENGNLVVSGKVyQWDDPDPRLFDHPEsPtPNP |
| P49419 | Y55 | Sugiyama | ALDH7A1 ATQ1 | NQPQYAWLKELGLREENEGVyNGSWGGRGEVIttyCPANNE |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y667 | Sugiyama | AARS1 AARS | QQIKKAEEIANEMIEAAKAVyTQDCPLAAAKAIQGLRAVFD |
| P49588 | Y690 | Sugiyama | AARS1 AARS | DCPLAAAKAIQGLRAVFDEtyPDPVRVVSIGVPVSELLDDP |
| P49591 | Y294 | Sugiyama | SARS1 SARS SERS | QPIAALHRDEWLRPEDLPIKyAGLsTCFRQEVGSHGRDTRG |
| P49736 | Y137 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | MRQRDREAGRGLGRMRRGLLyDsDEEDEERPARKRRQVERA |
| P49736 | Y234 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | VFKERIsDMCKENREsLVVNyEDLAAREHVLAYFLPEAPAE |
| P50395 | T408 | Sugiyama | GDI2 RABGDIB | VPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRMtGsE |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50395 | Y404 | Sugiyama | GDI2 RABGDIB | SDLLVPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRM |
| P50402 | Y95 | Sugiyama | EMD EDMD STA | DLPKKEDALLyQsKGyNDDyyEEsyFTTRTyGEPEsAGPSR |
| P50454 | Y135 | Sugiyama | SERPINH1 CBP1 CBP2 HSP47 SERPINH2 PIG14 | LRSLSNSTARNVTWKLGsRLyGPssVsFADDFVRssKQHYN |
| P50502 | Y185 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | NAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50995 | Y365 | Sugiyama | ANXA11 ANX11 | NRDESTNVDMSLAQRDAQELyAAGENRLGTDESKFNAVLCS |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51451 | S190 | Sugiyama | BLK | QGELIKHYKIRCLDEGGyyIsPRITFPSLQALVQHySKKGD |
| P51451 | S24 | Sugiyama | BLK | VSSKKPDKEKPIKEKDKGQWsPLKVSAQDKDAPPLPPLVVF |
| P51451 | S387 | Sugiyama | BLK | LVSEALCCKIADFGLARIIDsEytAQEGAKFPIKWTAPEAI |
| P51451 | T169 | Sugiyama | BLK | LIRESETNKGAFSLSVKDVTtQGELIKHYKIRCLDEGGyyI |
| P51451 | T390 | Sugiyama | BLK | EALCCKIADFGLARIIDsEytAQEGAKFPIKWTAPEAIHFG |
| P51451 | Y107 | Sugiyama | BLK | VLKGTGDWWLARSLVTGREGyVPSNFVARVESLEMERWFFR |
| P51451 | Y187 | Sugiyama | BLK | VTtQGELIKHYKIRCLDEGGyyIsPRITFPSLQALVQHySK |
| P51451 | Y188 | Sugiyama | BLK | TtQGELIKHYKIRCLDEGGyyIsPRITFPSLQALVQHySKK |
| P51451 | Y300 | Sugiyama | BLK | AFLGEANVMKALQHERLVRLyAVVTKEPIyIVTEyMARGCL |
| P51451 | Y309 | Sugiyama | BLK | KALQHERLVRLyAVVTKEPIyIVTEyMARGCLLDFLKTDEG |
| P51451 | Y314 | Sugiyama | BLK | ERLVRLyAVVTKEPIyIVTEyMARGCLLDFLKTDEGSRLSL |
| P51451 | Y389 | Sugiyama | BLK | SEALCCKIADFGLARIIDsEytAQEGAKFPIKWTAPEAIHF |
| P51511 | Y60 | Sugiyama | MMP15 | LGLGVAAEDAEVHAENWLRLyGYLPQPSRHMSTMRSAQILA |
| P51532 | Y718 | Sugiyama | SMARCA4 BAF190A BRG1 SNF2B SNF2L4 | VsEVDARHIIENAKQDVDDEyGVsQALARGLQSyyAVAHAV |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52298 | Y14 | Sugiyama | NCBP2 CBP20 PIG55 | _______MSGGLLKALRsDsyVELSQYRDQHFRGDNEEQEK |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | Y82 | Sugiyama | HNRNPF HNRPF | GsEDDVKMALKKDRESMGHRyIEVFKSHRTEMDWVLKHsGP |
| P52888 | Y576 | Sugiyama | THOP1 | VLAKVDQALHTQTDADPAEEyARLCQEILGVPATPGTNMPA |
| P52948 | Y848 | Sugiyama | NUP98 ADAR2 | PTDKTSRCLIKsPDRLADINyEGRLEAVSRKQGAQFKEyRP |
| P53396 | Y659 | Sugiyama | ACLY | TGGMLDNILASKLyRPGsVAyVSRsGGMsNELNNIISRTTD |
| P53621 | Y391 | Sugiyama | COPA | NPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGK |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P53675 | Y921 | Sugiyama | CLTCL1 CLH22 CLTCL CLTD | DSSVVGRYCEKRDPHLACVAyERGQCDLELIKVCNENSLFK |
| P54105 | Y214 | Sugiyama | CLNS1A CLCI ICLN | QsVssQYNMAGVRtEDsIRDyEDGMEVDttPtVAGQFEDAD |
| P54136 | Y384 | Sugiyama | RARS1 RARS | VFVPGCSIPLTIVKsDGGytyDtSDLAAIKQRLFEEKADMI |
| P54277 | Y563 | Sugiyama | PMS1 PMSL1 | EDSCNKKSNVIDNKSGKVTAyDLLSNRVIKKPMSASALFVQ |
| P54577 | Y198 | Sugiyama | YARS1 YARS | KVDAQFGGIDQRKIFTFAEKyLPALGySKRVHLMNPMVPGL |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54577 | Y388 | Sugiyama | YARS1 YARS | LDIRVGKIITVEKHPDADsLyVEKIDVGEAEPRTVVSGLVQ |
| P54652 | Y42 | Sugiyama | HSPA2 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55084 | Y244 | Sugiyama | HADHB MSTP029 | GHSADRLAAAFAVSRLEQDEyALRsHSLAKKAQDEGLLSDV |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55786 | Y173 | Sugiyama | NPEPPS PSA | NDKMKGFYRSKYTTPSGEVRyAAVTQFEATDARRAFPCWDE |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55884 | Y306 | Sugiyama | EIF3B EIF3S9 | PFKDLGNLRYWLEEAECRDQysVIFESGDRTSIFWNDVKDP |
| P55884 | Y768 | Sugiyama | EIF3B EIF3S9 | ERRRTMMEDFRKYRKMAQELyMEQKNERLELRGGVDTDELD |
| P57053 | Y38 | Sugiyama | H2BC12L H2BFS H2BS1 | AVTKAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y38 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60174 | Y48 | Sugiyama | TPI1 TPI | tLNAAKVPADtEVVCAPPtAyIDFARQKLDPKIAVAAQNCy |
| P60174 | Y68 | Sugiyama | TPI1 TPI | yIDFARQKLDPKIAVAAQNCyKVTNGAFtGEIsPGMIKDCG |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60510 | Y124 | Sugiyama | PPP4C PPP4 PPX | YPDRITLIRGNHESRQITQVyGFyDECLRKYGSVTVWRYCT |
| P60510 | Y127 | Sugiyama | PPP4C PPP4 PPX | RITLIRGNHESRQITQVyGFyDECLRKYGSVTVWRYCTEIF |
| P60660 | S30 | Sugiyama | MYL6 | AEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVLK |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | S239 | Sugiyama | ACTB | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| 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 |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61158 | S232 | Sugiyama | ACTR3 ARP3 | EVGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSKW |
| P61158 | Y231 | Sugiyama | ACTR3 ARP3 | REVGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSK |
| P61158 | Y273 | Sugiyama | ACTR3 ARP3 | IKQYTGINAISKKEFSIDVGyERFLGPEIFFHPEFANPDFT |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61163 | Y33 | Sugiyama | ACTR1A CTRN1 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALE |
| P61163 | Y38 | Sugiyama | ACTR1A CTRN1 | SGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALEGDIFI |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61247 | Y31 | Sugiyama | RPS3A FTE1 MFTL | KGGKKGAKKKVVDPFSKKDWyDVKAPAMFNIRNIGKTLVTR |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| P61353 | Y38 | Sugiyama | RPL27 | YSGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMG |
| P61604 | T79 | Sugiyama | HSPE1 | EIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDILGK |
| P61604 | Y76 | Sugiyama | HSPE1 | KGGEIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDI |
| P61978 | T70 | Sugiyama | HNRNPK HNRPK | QSKNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsI |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62191 | Y439 | Sugiyama | PSMC1 | FKKSKENVLyKKQEGtPEGLyL___________________ |
| P62249 | Y115 | Sugiyama | RPS16 | YYQKYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGP |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y49 | Sugiyama | YWHAE | KVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssIEQK |
| P62263 | S69 | Sugiyama | RPS14 PRO2640 | GKETICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELG |
| P62269 | S96 | Sugiyama | RPS18 D6S218E | QYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLKK |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62277 | Y18 | Sugiyama | RPS13 | ___MGRMHAPGKGLsQsALPyRRsVPtWLKLTsDDVKEQIy |
| P62280 | T54 | Sugiyama | RPS11 | PRYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILs |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62312 | Y72 | Sugiyama | LSM6 | VNGQLKNKyGDAFIRGNNVLyIstQKRRM____________ |
| P62333 | Y328 | Sugiyama | PSMC6 SUG2 | ARLDILKIHAGPITKHGEIDyEAIVKLSDGFNGADLRNVCT |
| P62495 | Y345 | Sugiyama | ETF1 ERF1 RF1 SUP45L1 | NLDIMRYVLHCQGTEEEKILyLTPEQEKDKSHFTDKETGQE |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62714 | Y127 | Sugiyama | PPP2CB | YPERITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFT |
| P62714 | Y130 | Sugiyama | PPP2CB | RITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFTDLF |
| P62714 | Y284 | Sugiyama | PPP2CB | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRT |
| P62736 | S241 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y144 | Sugiyama | RPL23A | VNtLIRPDGEKKAYVRLAPDyDALDVANKIGII________ |
| P62750 | Y74 | Sugiyama | RPL23A | LRRQPKYPRKSAPRRNKLDHyAIIKFPLTTEsAMKKIEDNN |
| P62753 | Y156 | Sugiyama | RPS6 OK/SW-cl.2 | KRASRIRKLFNLsKEDDVRQyVVRKPLNKEGKKPRTKAPKI |
| P62805 | Y52 | Sugiyama | H4C1 H4/A H4FA HIST1H4A; H4C2 H4/I H4FI HIST1H4B; H4C3 H4/G H4FG HIST1H4C; H4C4 H4/B H4FB HIST1H4D; H4C5 H4/J H4FJ HIST1H4E; H4C6 H4/C H4FC HIST1H4F; H4C8 H4/H H4FH HIST1H4H; H4C9 H4/M H4FM HIST1H4I; H4C11 H4/E H4FE HIST1H4J; H4C12 H4/D H4FD HIST1H4K; H4C13 H4/K H4FK HIST1H4L; H4C14 H4/N H4F2 H4FN HIST2H4 HIST2H4A; H4C15 H4/O H4FO HIST2H4B; H4C16 H4-16 HIST4H4 | KPAIRRLARRGGVKRIsGLIyEETRGVLKVFLENVIRDAVt |
| P62807 | 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 |
| P62899 | T26 | Sugiyama | RPL31 | KGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRAL |
| P62899 | Y25 | Sugiyama | RPL31 | KKGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRA |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63010 | Y526 | Sugiyama | AP2B1 ADTB2 CLAPB1 | VLSLATQDSDNPDLRDRGyIyWRLLsTDPVTAKEVVLSEKP |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63220 | T52 | Sugiyama | RPS21 | IQMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRL |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | S239 | Sugiyama | ACTG1 ACTG | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| 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 | S240 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67775 | Y127 | Sugiyama | PPP2CA | YRERITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFT |
| P67775 | Y130 | Sugiyama | PPP2CA | RITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFTDLF |
| P67775 | Y284 | Sugiyama | PPP2CA | NyCyRCGNQAAIMELDDTLKySFLQFDPAPRRGEPHVTRRt |
| 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 | S241 | Sugiyama | ACTC1 ACTC | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68032 | Y93 | Sugiyama | ACTC1 ACTC | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68104 | Y254 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | S241 | Sugiyama | ACTA1 ACTA | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68133 | Y93 | Sugiyama | ACTA1 ACTA | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68363 | Y312 | Sugiyama | TUBA1B | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68363 | Y451 | Sugiyama | TUBA1B | DyEEVGVDsVEGEGEEEGEEy____________________ |
| P68366 | Y312 | Sugiyama | TUBA4A TUBA1 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68400 | Y255 | Sugiyama | CSNK2A1 CK2A1 | GHDNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGR |
| P83731 | Y11 | Sugiyama | RPL24 | __________MKVELCsFsGyKIYPGHGRRYARTDGKVFQF |
| 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 |
| Q00341 | Y358 | Sugiyama | HDLBP HBP VGL | SETVILRGEPEKLGQALTEVyAKANsFTVSSVAAPSWLHRF |
| Q00526 | T14 | Sugiyama | CDK3 CDKN3 | _______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKK |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00526 | Y19 | Sugiyama | CDK3 CDKN3 | __MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKIRLDL |
| Q00534 | Y13 | Sugiyama | CDK6 CDKN6 | ________MEKDGLCRADQQyECVAEIGEGAyGKVFKARDL |
| Q00534 | Y24 | Sugiyama | CDK6 CDKN6 | DGLCRADQQyECVAEIGEGAyGKVFKARDLKNGGRFVALKR |
| Q00610 | Y1487 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LNNLFITEEDyQALRTsIDAyDNFDNIsLAQRLEKHELIEF |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00610 | Y921 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | DsRVVGKYCEKRDPHLACVAyERGQCDLELINVCNENSLFK |
| 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 |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01518 | T165 | Sugiyama | CAP1 CAP | AMAPKPGPYVKEMNDAAMFytNRVLKEYKDVDKKHVDWVKA |
| Q01518 | Y164 | Sugiyama | CAP1 CAP | VAMAPKPGPYVKEMNDAAMFytNRVLKEYKDVDKKHVDWVK |
| Q01581 | Y84 | Sugiyama | HMGCS1 HMGCS | DINSLCMTVVQNLMERNNLsyDCIGRLEVGTEtIIDKSKSV |
| Q01814 | Y1152 | Sugiyama | ATP2B2 PMCA2 | RGLNRIQtQIRVVKAFRssLyEGLEKPEsRtsIHNFMAHPE |
| Q01844 | Y278 | Sugiyama | EWSR1 EWS | SSSYGQQSsFRQDHPssMGVyGQESGGFSGPGENRSMSGPD |
| Q02878 | Y216 | Sugiyama | RPL6 TXREB1 | AtsTKIDISNVKIPKHLtDAyFKKKKLRKPRHQEGEIFDtE |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y154 | Sugiyama | YWHAH YWHA1 | LAEVASGEKKNsVVEAsEAAyKEAFEISKEQMQPTHPIRLG |
| Q04917 | Y20 | Sugiyama | YWHAH YWHA1 | _MGDREQLLQRARLAEQAERyDDMAsAMKAVtELNEPLsNE |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05639 | Y254 | Sugiyama | EEF1A2 EEF1AL STN | TILPPTRPTDKPLRLPLQDVyKIGGIGtVPVGRVETGILRP |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q07157 | Y1165 | Sugiyama | TJP1 ZO1 | RYEQAPRAsALRHEEQPAPGyDtHGRLRPEAQPHPsAGPKP |
| Q07866 | Y449 | Sugiyama | KLC1 KLC KNS2 | HAEEREECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKN |
| Q07866 | Y453 | Sugiyama | KLC1 KLC KNS2 | REECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKNLGAL |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q08378 | Y329 | Sugiyama | GOLGA3 | EVDGNDsDsSSYSSASTRGTyGILSKTVGTQDTPYMVNGQE |
| Q08378 | Y747 | Sugiyama | GOLGA3 | TLTQEALQSREQsLDALQTHyDELQARLGELQGEAASREDT |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q10567 | Y526 | Sugiyama | AP1B1 ADTB1 BAM22 CLAPB2 | VLSLATQDSDNPDLRDRGyIyWRLLsTDPVAAKEVVLAEKP |
| Q12797 | Y90 | Sugiyama | ASPH BAH | VAVVWFDLVDYEEVLGKLGIyDADGDGDFDVDDAKVLLGLK |
| Q12805 | Y369 | Sugiyama | EFEMP1 FBLN3 FBNL | MCWNYHGGFRCYPRNPCQDPyILTPENRCVCPVsNAMCREL |
| Q12874 | Y479 | Sugiyama | SF3A3 SAP61 | WAKLKLQKASERWQPDtEEEyEDssGNVVNKKTYEDLKRQG |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q12996 | Y708 | Sugiyama | CSTF3 | NEDsDEDEEKGAVVPPVHDIyRARQQKRIR___________ |
| Q13017 | Y1109 | Sugiyama | ARHGAP5 RHOGAP5 | DNyAEPIDTIFKQKGYsDEIyVVPDDsQNRIKIRNsFVNNt |
| Q13162 | Y188 | Sugiyama | PRDX4 | GLGPIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDK |
| Q13162 | Y191 | Sugiyama | PRDX4 | PIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDKGIL |
| Q13162 | Y54 | Sugiyama | PRDX4 | AVQGWETEERPRTREEECHFyAGGQVyPGEAsRVsVADHsL |
| Q13200 | Y110 | Sugiyama | PSMD2 TRAP2 | TSVPKPLKFLRPHyGKLKEIyENMAPGENKRFAADIISVLA |
| Q13200 | Y434 | Sugiyama | PSMD2 TRAP2 | LGMILLWDVDGGLTQIDKyLySsEDyIKSGALLACGIVNSG |
| Q13228 | Y28 | Sugiyama | SELENBP1 SBP | CGPGySTPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVD |
| Q13228 | Y56 | Sugiyama | SELENBP1 SBP | tGtEAPDyLATVDVDPKsPQyCQVIHRLPMPNLKDELHHSG |
| Q13263 | Y133 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TVVDCPVCKQQCFSKDIVENyFMRDsGsKAATDAQDANQCC |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13283 | Y56 | Sugiyama | G3BP1 G3BP | KNssyVHGGLDsNGKPADAVyGQKEIHRKVMsQNFtNCHTK |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13310 | Y238 | Sugiyama | PABPC4 APP1 PABP4 | LSVKVMRDPNGKSKGFGFVSyEKHEDANKAVEEMNGKEISG |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13442 | S19 | Sugiyama | PDAP1 HASPP28 | __MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEEE |
| Q13510 | Y305 | Sugiyama | ASAH1 ASAH HSD-33 HSD33 | GNQSGEGCVITRDRKESLDVyELDAKQGRWYVVQTNYDRWK |
| Q13547 | S88 | Sugiyama | HDAC1 RPD3L1 | HSDDyIKFLRSIRPDNMsEysKQMQRFNVGEDCPVFDGLFE |
| Q13561 | Y313 | Sugiyama | DCTN2 DCTN50 | IAKHKASVEDADTQSKVHQLyEtIQRWsPIASTLPELVQRL |
| Q13561 | Y6 | Sugiyama | DCTN2 DCTN50 | _______________MADPKyADLPGIARNEPDVYETSDLP |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13573 | Y430 | Sugiyama | SNW1 SKIIP SKIP | RLFNQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRP |
| Q13573 | Y433 | Sugiyama | SNW1 SKIIP SKIP | NQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRPSKN |
| Q13573 | Y459 | Sugiyama | SNW1 SKIIP SKIP | GGKDMAQsIyRPSKNLDKDMyGDDLEARIKTNRFVPDKEFS |
| Q13642 | Y117 | Sugiyama | FHL1 SLIM1 | DsPKCKGCFKAIVAGDQNVEyKGtVWHKDCFTCSNCKQVIG |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q13907 | Y173 | Sugiyama | IDI1 | LLVRKNVTLNPDPNEIKSYCyVSKEELKELLKKAASGEIKI |
| Q14157 | Y858 | Sugiyama | UBAP2L KIAA0144 NICE4 | PFPtPttPLtGRDGsLAsNPysGDLtKFGRGDASSPAPATT |
| Q14194 | Y479 | Sugiyama | CRMP1 DPYSL1 ULIP3 | INVNKGMGRFIPRKAFPEHLyQRVKIRNKVFGLQGVSRGMY |
| Q14204 | Y2265 | Sugiyama | DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325 | EGVEGVAHIIDPKAISKDHLyGtLDPNTREWTDGLFTHVLR |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | S447 | Sugiyama | CTTN EMS1 | FKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYATE |
| Q14247 | Y215 | Sugiyama | CTTN EMS1 | FGGKyGIDKDKVDKsAVGFEyQGKtEKHESQKDyVKGFGGK |
| Q14247 | Y334 | Sugiyama | CTTN EMS1 | KDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRANF |
| Q14247 | Y421 | Sugiyama | CTTN EMS1 | tPPVsPAPQPtEERLPssPVyEDAAsFKAELsyRGPVsGtE |
| Q14247 | Y446 | Sugiyama | CTTN EMS1 | sFKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYAT |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14566 | T278 | Sugiyama | MCM6 | STPGARAEtNsRVsGVDGyEtEGIRGLRALGVRDLSYRLVF |
| Q14568 | Y160 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | SAYLVAEKVTVITKHNDDEQyAWEssAGGsFtVRTDTGERM |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14677 | Y106 | Sugiyama | CLINT1 ENTH EPN4 EPNR KIAA0171 | LAYLIRNGSERVVTSAREHIyDLRSLENyHFVDEHGKDQGI |
| Q14738 | Y580 | Sugiyama | PPP2R5D | KDIKKEKVLLRRKsELPQDVyTIKALEAHKRAEEFLTAsQE |
| Q14764 | Y389 | Sugiyama | MVP LRP | AKVEVVEERQAIPLDENEGIyVQDVKTGKVRAVIGSTYMLT |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q15019 | Y211 | Sugiyama | SEPTIN2 DIFF6 KIAA0158 NEDD5 SEPT2 | ERERLKKRILDEIEEHNIKIyHLPDAEsDEDEDFKEQtRLL |
| Q15024 | Y187 | Sugiyama | EXOSC7 KIAA0116 RRP42 | RVRVLEDEEGsKDIELSDDPyDCIRLSVENVPCIVTLCKIG |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15149 | Y3362 | Sugiyama | PLEC PLEC1 | TGLsLLPLSEKAARARQEELySELQAREtFEKTPVEVPVGG |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15181 | Y17 | Sugiyama | PPA1 IOPPP PP | ____MSGFSTEERAAPFsLEyRVFLKNEKGQyIsPFHDIPI |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15392 | Y507 | Sugiyama | DHCR24 KIAA0018 | GSLYHKLREKLGCQDAFPEVyDKICKAARH___________ |
| Q15417 | Y261 | Sugiyama | CNN3 | STISLQMGTNKVAsQKGMsVyGLGRQVYDPKYCAAPTEPVI |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15436 | Y678 | Sugiyama | SEC23A | IYHGETIAQWRKSGYQDMPEyENFRHLLQAPVDDAQEILHS |
| 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 |
| Q15691 | Y217 | Sugiyama | MAPRE1 | MQQVNVLKLtVEDLEKERDFyFGKLRNIELICQENEGENDP |
| Q15785 | Y32 | Sugiyama | TOMM34 URCC3 | LRAAGNESFRNGQyAEASALyGRALRVLQAQGssDPEEEsV |
| Q15785 | Y54 | Sugiyama | TOMM34 URCC3 | RALRVLQAQGssDPEEEsVLysNRAACHLKDGNCRDCIKDC |
| Q15819 | Y143 | Sugiyama | UBE2V2 MMS2 UEV2 | RRLMMSKENMKLPQPPEGQtyNN__________________ |
| Q16181 | Y306 | Sugiyama | SEPTIN7 CDC10 SEPT7 | RNMLIRTHMQDLKDVTNNVHyENyRSRKLAAVtyNGVDNNK |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16740 | Y209 | Sugiyama | CLPP | TDIAIQAEEIMKLKKQLYNIyAKHTKQSLQVIEsAMERDRY |
| Q16762 | Y165 | Sugiyama | TST | PSRPEPAVFKATLDRSLLKTyEQVLENLESKRFQLVDSRSQ |
| Q16762 | Y37 | Sugiyama | TST | AESIRTGKLGPGLRVLDAsWysPGTREARKEYLERHVPGAS |
| Q16763 | Y144 | Sugiyama | UBE2S E2EPF OK/SW-cl.73 | NPESALNEEAGRLLLENyEEyAARARLLtEIHGGAGGPSGR |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q16881 | Y277 | Sugiyama | TXNRD1 GRIM12 KDRF | NHIGSLNWGYRVALREKKVVyENAyGQFIGPHRIKATNNKG |
| Q16881 | Y281 | Sugiyama | TXNRD1 GRIM12 KDRF | SLNWGYRVALREKKVVyENAyGQFIGPHRIKATNNKGKEKI |
| Q1KMD3 | Y610 | Sugiyama | HNRNPUL2 HNRPUL2 | LEMKANFsLPEKCDYMDEVTyGELEKEEAQPIVTKYKEEAR |
| Q3V6T2 | Y1153 | Sugiyama | CCDC88A APE GRDN KIAA1212 | SSLENENESVIKEREDLKSLyDSLIKDHEKLELLHERQAsE |
| Q4VXU2 | Y291 | Sugiyama | PABPC1L C20orf119 | ERQNELKRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLR |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q53GQ0 | Y115 | Sugiyama | HSD17B12 SDR12C1 | KEKFKVETRTIAVDFASEDIyDKIKTGLAGLEIGILVNNVG |
| Q562R1 | S240 | Sugiyama | ACTBL2 | VALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPE |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | Y167 | Sugiyama | HSP90AB4P | GEPIDRDTKVILHLKEDQtEyLEERWVKEVVKKHPQFIGCL |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | Y171 | Sugiyama | HSP90AB3P HSP90BC | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| Q58FF7 | Y492 | Sugiyama | HSP90AB3P HSP90BC | TANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIMETLR |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | Y198 | Sugiyama | HSP90AB2P HSP90BB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKTKPIWTRNTEDI |
| Q58FF8 | Y260 | Sugiyama | HSP90AB2P HSP90BB | VRYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVW |
| Q58FF8 | Y261 | Sugiyama | HSP90AB2P HSP90BB | RYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVWK |
| Q58FF8 | Y56 | Sugiyama | HSP90AB2P HSP90BB | KEIFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FG0 | Y177 | Sugiyama | HSP90AA5P HSP90AE | GQLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQ |
| Q58FG0 | Y178 | Sugiyama | HSP90AA5P HSP90AE | QLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQK |
| Q5JTH9 | Y1251 | Sugiyama | RRP12 KIAA0690 | AEYKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQG |
| Q5JTH9 | Y1253 | Sugiyama | RRP12 KIAA0690 | YKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQGQF |
| Q5QNW6 | Y38 | Sugiyama | H2BC18 HIST2H2BF | AVTKVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5T035 | Y67 | Sugiyama | FAM120A2P C9orf129 | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERSLPIN |
| Q5VTE0 | Y254 | Sugiyama | EEF1A1P5 EEF1AL3 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VV41 | Y216 | Sugiyama | ARHGEF16 EPHEXIN4 NBR | KKTLGRKRGHKGsFKDDPQLyQEIQERGLNtsQEsDDDILD |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6PKG0 | Y633 | Sugiyama | LARP1 KIAA0731 LARP | MEQMDGRKNtFtAWsDEEsDyEIDDRDVNKILIVtQtPHyM |
| Q6PKG0 | Y699 | Sugiyama | LARP1 KIAA0731 LARP | INDGLFyyEQDLWAEKFEPEysQIKQEVENFKKVNMISREQ |
| Q6S8J3 | S939 | Sugiyama | POTEE A26C1A POTE2 | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y791 | Sugiyama | POTEE A26C1A POTE2 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6UN15 | Y454 | Sugiyama | FIP1L1 FIP1 RHE | LPGSAPsWPSLVDTSKQWDyyARREKDRDRERDRDRERDRD |
| Q6UVK1 | Y1511 | Sugiyama | CSPG4 MCSP | PIPAEALRSTDGDSGSEDLVyTIEQPSNGRVVLRGAPGTEV |
| Q71U36 | Y312 | Sugiyama | TUBA1A TUBA3 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q71U36 | Y451 | Sugiyama | TUBA1A TUBA3 | DyEEVGVDsVEGEGEEEGEEy____________________ |
| Q7KZF4 | Y476 | Sugiyama | SND1 TDRD11 | SKGLATVIRYRQDDDQRssHyDELLAAEARAIKNGKGLHSK |
| Q7RTV0 | Y100 | Sugiyama | PHF5A | KDRDGCPKIVNLGSsKTDLFyERKKYGFKKR__________ |
| Q7RTV0 | Y51 | Sugiyama | PHF5A | VICDSyVRPCTLVRICDECNyGsyQGRCVICGGPGVSDAyy |
| Q7Z2W4 | Y642 | Sugiyama | ZC3HAV1 ZC3HDC2 PRO1677 | GEEKDKRKNsNVDssyLEsLyQSCPRGVVPFQAGSRNYELS |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86UK7 | Y306 | Sugiyama | ZNF598 | QFSYAPRHSRRNEGVVGGEDyEEVDRysRQGRVARAGTRGA |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q8IWA5 | Y308 | Sugiyama | SLC44A2 CTL2 PSEC0210 | GEAGSDVSLVDLGFQTDFRVyLHLRQTWLAFMIILSILEVI |
| Q8IWX8 | Y894 | Sugiyama | CHERP DAN26 SCAF6 | GDVRDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDE |
| Q8IWX8 | Y897 | Sugiyama | CHERP DAN26 SCAF6 | RDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDECK_ |
| Q8IZV5 | Y126 | Sugiyama | RDH10 SDR16C4 UNQ9375/PRO34191 | PHCNLQVFTYTCDVGKRENVyLTAERVRKEVGEVSVLVNNA |
| Q8N0Y7 | S134 | Sugiyama | PGAM4 PGAM3 | IWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYE |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N6H7 | Y278 | Sugiyama | ARFGAP2 ZNF289 Nbla10535 | QAADAKKQAEESMVASMRLAyQELQIDRKKEEKKLQNLEGK |
| Q8N7H5 | Y169 | Sugiyama | PAF1 PD2 | EKPEVKIGVSVKQQFTEEEIyKDRDSQITAIEKTFEDAQKS |
| Q8N884 | Y215 | SIGNOR|PSP | CGAS C6orf150 MB21D1 | LRLKCDsAFRGVGLLNTGSyyEHVKIsAPNEFDVMFKLEVP |
| Q8NBP7 | Y521 | Sugiyama | PCSK9 NARC1 PSEC0052 | EAQGGKLVCRAHNAFGGEGVyAIARCCLLPQANCSVHTAPP |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NCN5 | Y463 | Sugiyama | PDPR KIAA1990 | DLKVPRWDFQTGRQLRTSPLyDRLDAQGARWMEKHGFERPK |
| Q8NFI4 | Y185 | Sugiyama | ST13P5 FAM10A5 | NAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TD19 | Y52 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PSASQGPRAGGGAAEQEELHyIPIRVLGRGAFGEAtLyRRT |
| Q8TD19 | Y845 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PDsPsPLsAAFsEsEKDTLPyEELQGLKVAsEAPLEHKPQV |
| Q8TF05 | Y54 | Sugiyama | PPP4R1 MEG1 PP4R1 | SALDFVSQDEMLTPLGRLDKyAAsENIFNRQMVARSLLDTL |
| Q8WUM4 | Y39 | Sugiyama | PDCD6IP AIP1 ALIX KIAA1375 | KPLVKFIQQTYPSGGEEQAQyCRAAEELSKLRRAAVGRPLD |
| Q8WWF6 | Y53 | Sugiyama | DNAJB3 HCG3 | DKNPENKEEAERRFKQVAEAyEVLSDAKKRDIYDRYGEAGA |
| Q8WWM7 | Y270 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | GWDPNEMFKFNEENyGVKTtyDssLssytVPLEKDNsEEFR |
| Q8WWM7 | Y277 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | FKFNEENyGVKTtyDssLssytVPLEKDNsEEFRQRELRAA |
| Q8WX92 | Y541 | Sugiyama | NELFB COBRA1 KIAA1182 | EALQKALEPTGQSGEAVKELysQLGEKLEQLDHRKPsPAQA |
| 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 |
| Q92626 | Y264 | Sugiyama | PXDN KIAA0230 MG50 PRG2 PXD01 VPO VPO1 | ERPRITSEPQDADVTSGNTVyFTCRAEGNPKPEIIWLRNNN |
| Q92769 | S89 | Sugiyama | HDAC2 | HSDEYIKFLRSIRPDNMsEysKQMQRFNVGEDCPVFDGLFE |
| Q92796 | S615 | Sugiyama | DLG3 KIAA1232 | GLSDDYYGAKNLKGQEDAILsYEPVTRQEIHYARPVIILGP |
| Q92945 | Y317 | Sugiyama | KHSRP FUBP2 | EMVMDILRERDQGGFGDRNEyGsRIGGGIDVPVPRHsVGVV |
| Q93052 | Y301 | Sugiyama | LPP | LQPEPGYGYAPNQGRyyEGyyAAGPGyGGRNDsDPtyGQQG |
| Q93052 | Y317 | Sugiyama | LPP | yEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPGA |
| Q93079 | Y38 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | AVTKAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssK |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96AE4 | Y58 | Sugiyama | FUBP1 | ARQIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKV |
| Q96AY3 | Y201 | Sugiyama | FKBP10 FKBP65 PSEC0056 | YNGTLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGM |
| Q96AY3 | Y204 | Sugiyama | FKBP10 FKBP65 PSEC0056 | TLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGMCPG |
| Q96C19 | T84 | Sugiyama | EFHD2 SWS1 | DLNQGIGEPQsPsRRVFNPytEFKEFSRKQIKDMEKMFKQy |
| Q96CT7 | Y38 | Sugiyama | CCDC124 | RRAEAKAAADAKKQKELEDAyWKDDDKHVMRKEQRKEEKEK |
| Q96D15 | T127 | Sugiyama | RCN3 UNQ239/PRO272 | AHTQQRHIRDsVsAAWDtyDtDRDGRVGWEELRNATYGHYA |
| Q96D46 | Y459 | Sugiyama | NMD3 CGI-07 | YQDFLEDLEEDEAIRKNVNIyRDsAIPVEsDtDDEGAPRIS |
| Q96DG6 | Y165 | Sugiyama | CMBL | YSEFRAGVSVYGIVKDSEDIyNLKNPTLFIFAENDVVIPLK |
| Q96EU6 | Y138 | Sugiyama | RRP36 C6orf153 HSPC253 | RDPRFDDLSGEYNPEVFDKtyQFLNDIRAKEKELVKKQLKK |
| Q96FW1 | Y26 | Sugiyama | OTUB1 OTB1 OTU1 HSPC263 | PQQQKQEPLGsDsEGVNCLAyDEAIMAQQDRIQQEIAVQNP |
| Q96FW1 | Y68 | Sugiyama | OTUB1 OTB1 OTU1 HSPC263 | VSERLELsVLyKEYAEDDNIyQQKIKDLHKKYSYIRKTRPD |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96HE7 | Y73 | Sugiyama | ERO1A ERO1L UNQ434/PRO865 | IDRFNNYRLFPRLQKLLEsDyFRyyKVNLKRPCPFWNDISQ |
| Q96HN2 | Y372 | Sugiyama | AHCYL2 KIAA0828 | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDMMFGG |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q96QK1 | Y791 | Sugiyama | VPS35 MEM3 TCCCTA00141 | HNtLEHLRLRREsPEsEGPIyEGLIL_______________ |
| Q96ST3 | Y13 | Sugiyama | SIN3A | ________MKRRLDDQEsPVyAAQQRRIPGstEAFPHQHRV |
| Q99426 | Y114 | Sugiyama | TBCB CG22 CKAP1 | RLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKRsKLGRyN |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99470 | Y69 | Sugiyama | SDF2 | GSGSGQQSVTGVTSVDDSNSyWRIRGKSATVCERGTPIKCG |
| Q99536 | Y240 | Sugiyama | VAT1 | TASASKHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIV |
| Q99536 | Y245 | Sugiyama | VAT1 | KHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIVMDPLG |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99700 | Y454 | Sugiyama | ATXN2 ATX2 SCA2 TNRC13 | FLKREARANQLAEEIESsAQyKARVALENDDRsEEEKyTAV |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y432 | Sugiyama | ACO2 | SQFtITPGSEQIRAtIERDGyAQILRDLGGIVLANACGPCI |
| Q99798 | Y544 | Sugiyama | ACO2 | LEAPDADELPKGEFDPGQDtyQHPPKDSsGQHVDVsPtsQR |
| Q99798 | Y665 | Sugiyama | ACO2 | DtARYYKKHGIRWVVIGDENyGEGSSREHAALEPRHLGGRA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| 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 |
| Q9BPX3 | Y929 | Sugiyama | NCAPG CAPG NYMEL3 | QDATLTTTTFQNEDEKNKEVyMtPLRGVKATQASKSTQLKT |
| Q9BQE3 | Y312 | Sugiyama | TUBA1C TUBA6 | TNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BQS8 | Y646 | Sugiyama | FYCO1 ZFYVE7 | QNVVGRNQLLEGKLQALQADyQALQQRESAIQGsLASLEAE |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BRL6 | Y44 | Sugiyama | SRSF8 SFRS2B SRP46 | RtsPDsLRRVFEKYGRVGDVyIPREPHTKAPRGFAFVRFHD |
| Q9BS26 | T398 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | VASSPPESSFQKLAPsEyRytLLRDRDEL____________ |
| Q9BS26 | Y395 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | AQDVASSPPESSFQKLAPsEyRytLLRDRDEL_________ |
| Q9BS40 | Y20 | Sugiyama | LXN | _MEIPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQA |
| Q9BS40 | Y23 | Sugiyama | LXN | IPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQAsME |
| Q9BSU3 | Y145 | Sugiyama | NAA11 ARD1B ARD2 | TLNFQISEVEPKyyADGEDAyAMKRDLSQMADELRRQMDLK |
| Q9BT78 | Y167 | Sugiyama | COPS4 CSN4 | TYLKIARLYLEDDDPVQAEAyINRASLLQNESTNEQLQIHY |
| Q9BUJ2 | S512 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | IQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIVIC |
| Q9BUJ2 | Y111 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | GYSGPDGHYAMDNITRQNQFyDtQVIKQENESGyERRPLEM |
| Q9BUJ2 | Y510 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | RLIQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIV |
| Q9BW91 | Y140 | Sugiyama | NUDT9 NUDT10 PSEC0099 UNQ3012/PRO9771 | FsPKFNEKDGHVERKSKNGLyEIENGRPRNPAGRTGLVGRG |
| Q9BWF3 | Y194 | Sugiyama | RBM4 RBM4A | ECPIDRSGRVADLTEQYNEQyGAVRTPYTMSYGDSLYYNNA |
| Q9BXJ9 | Y247 | Sugiyama | NAA15 GA19 NARG1 NATH TBDN100 | EETKGELLLQLCRLEDAADVyRGLQERNPENWAYYKGLEKA |
| Q9BYX7 | S239 | Sugiyama | POTEKP ACTBL3 FKSG30 | VALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPE |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BYX7 | Y91 | Sugiyama | POTEKP ACTBL3 FKSG30 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q9GZZ9 | S54 | Sugiyama | UBA5 UBE1DC1 | GGGRVRIEKMssEVVDSNPysRLMALKRMGIVSDYEKIRTF |
| Q9H0B6 | S436 | Sugiyama | KLC2 | EEREESKDKRRDsAPyGEyGsWYKACKVDsPtVNTTLRSLG |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H4M9 | Y339 | Sugiyama | EHD1 PAST PAST1 CDABP0131 | PNVFGKESKKKELVNNLGEIyQKIEREHQIsPGDFPsLRKM |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9H814 | T151 | Sugiyama | PHAX RNUXA | ATELGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDL |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HC35 | T554 | Sugiyama | EML4 C2orf2 EMAPL4 | ILWDHDLNPEREIEVPDQyGtIRAVAEGKADQFLVGTSRNF |
| Q9HCN8 | Y81 | Sugiyama | SDF2L1 UNQ1941/PRO4424 | GSGSGQQSVtGVEAsDDANSyWRIRGGSEGGCPRGSPVRCG |
| Q9NQE9 | Y44 | Sugiyama | HINT3 | TTVssVGTCEAAGKsPEPKDyDstCVFCRIAGRQDPGTELL |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NSE4 | Y260 | Sugiyama | IARS2 | YKPVFWSPSSRTALAEAELEyNPEHVSRSIYVKFPLLKPSP |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NWS0 | Y194 | Sugiyama | PIH1D1 NOP17 | IsQQNIRSEQRPRIQELGDLytPAPGRAESGPEKPHLNLWL |
| Q9NX40 | Y199 | Sugiyama | OCIAD1 ASRIJ OCIA | HIVQGPDPNLEEsPKRKNITyEELRNKNREsyEVSLTQKTD |
| Q9NY12 | Y145 | Sugiyama | GAR1 NOLA1 | FSVKLSENMKASSFKKLQKFyIDPyKLLPLQRFLPRPPGEK |
| Q9NY12 | Y149 | Sugiyama | GAR1 NOLA1 | LSENMKASSFKKLQKFyIDPyKLLPLQRFLPRPPGEKGPPR |
| Q9NYB9 | T24 | Sugiyama | ABI2 ARGBPIA | LQMLLEEEIPGGRRALFDsytNLERVADyCENNyIQSADKQ |
| Q9NYU2 | Y1516 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | PMTKEPKLEAAVRIVPEWQDyDQEIKQLQIRFQKEKETGAL |
| Q9NYU2 | Y449 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | IEGLSLHNVLKLNIQPsEADyAVDIRSPAISWVNNLEVDSR |
| Q9NYU2 | Y779 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | RPVTFWIVGDFDSPSGRQLLyDAIKHQKSSNNVRISMINNP |
| Q9NZB2 | Y418 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERssPIN |
| Q9UBQ7 | Y255 | Sugiyama | GRHPR GLXR MSTP035 | KETAVFINISRGDVVNQDDLyQALAsGKIAAAGLDVtsPEP |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y352 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | TEEAREGIKQLLKQGSVQKVyNGLQGY______________ |
| Q9UBS4 | Y74 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | PDRNPDDPQAQEKFQDLGAAyEVLsDSEKRKQyDTyGEEGL |
| Q9UGI8 | Y251 | Sugiyama | TES | RTQYSCYCCKLSMKEGDPAIyAERAGyDKLWHPACFVCSTC |
| Q9UHG3 | Y498 | Sugiyama | PCYOX1 KIAA0908 PCL1 UNQ597/PRO1183 | ALLAYHRWNGHTDMIDQDGLyEKLKTEL_____________ |
| Q9UHI6 | Y659 | Sugiyama | DDX20 DP103 GEMIN3 | RVPVLASSsQsGDsEsDSDSySSRTSSQSKGNKsyLEGssD |
| Q9UHX1 | Y269 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | FGKIKSCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNL |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UIQ6 | Y70 | Sugiyama | LNPEP OTASE | GsRLLVRGLGEHEMEEDEEDyEssAKLLGMsFMNRssGLRN |
| Q9UK59 | Y533 | Sugiyama | DBR1 | LsDEHEPEQRKKIKRRNQAIyAAVDDDDDDAA_________ |
| Q9UKF6 | Y677 | Sugiyama | CPSF3 CPSF73 | EGsEDDESLREMVELAAQRLyEALtPVH_____________ |
| Q9UKS6 | Y206 | Sugiyama | PACSIN3 | RKLQERVERCAKEAEKTKAQyEQtLAELHRYTPRYMEDMEQ |
| Q9UMS0 | Y194 | Sugiyama | NFU1 HIRIP5 CGI-33 | KELLDTRIRPTVQEDGGDVIyKGFEDGIVQLKLQGSCTSCP |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UNZ2 | Y167 | Sugiyama | NSFL1C UBXN2C | PRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLKLW |
| Q9UQ80 | Y98 | Sugiyama | PA2G4 EBP1 | TSISVNNCVCHFsPLKSDQDyILKEGDLVKIDLGVHVDGFI |
| Q9Y230 | Y172 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | TGTGSKVGKLTLKTTEMETIyDLGTKMIESLTKDKVQAGDV |
| Q9Y262 | Y247 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | VLNVLHSLVDKSNINRQLEVytsGGDPEsVAGEyGRHSLYK |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y262 | Y415 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | GDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNY |
| Q9Y262 | Y89 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QKVYELQASRVssDVIDQKVyEIQDIyENSWTKLTERFFKN |
| Q9Y262 | Y95 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QASRVssDVIDQKVyEIQDIyENSWTKLTERFFKNTPWPEA |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2B0 | Y71 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | IQMGsFRINPDGsQsVVEVPyARsEAHLtELLEEICDRMKE |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y2X3 | Y428 | Sugiyama | NOP58 NOL5 NOP5 HSPC120 | GTGKALAKTEKYEHKSEVKtyDPSGDstLPtCsKKRKIEQV |
| Q9Y371 | Y80 | Sugiyama | SH3GLB1 KIAA0491 CGI-61 | MKQTEVLLQPNPNARIEEFVyEKLDRKAPSRINNPELLGQY |
| Q9Y3C1 | Y118 | Sugiyama | NOP16 CGI-117 HSPC111 | EAEASLPEKKGNTLSRDLIDyVRYMVENHGEDYKAMARDEK |
| Q9Y3D8 | Y31 | Sugiyama | AK6 CINAP AD-004 CGI-137 | TPGVGKTTLGKELASKSGLKyINVGDLAREEQLYDGYDEEY |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y490 | Y127 | Sugiyama | TLN1 KIAA1027 TLN | TVTDMLMTICARIGITNHDEysLVRELMEEKKEEItGtLRK |
| Q9Y490 | Y1893 | Sugiyama | TLN1 KIAA1027 TLN | TKsNtsPEELGPLANQLTsDyGRLAsEAKPAAVAAENEEIG |
| Q9Y4L1 | Y116 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | TLRYFQHLLGKQADNPHVALyQARFPEHELTFDPQRQTVHF |
| Q9Y5Q8 | Y393 | Sugiyama | GTF3C5 CDABP0017 | SGtsGARKPASSKYKLKDSVyIFREGALPPYRQMFYQLCDL |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y639 | Y216 | Sugiyama | NPTN SDFR1 SDR1 | KNASNMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKA |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | Y244 | Sugiyama | CLIC4 | AysRDEFtNtCPsDKEVEIAysDVAKRLTK___________ |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.246749e-08 | 7.904 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 6.240103e-06 | 5.205 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 6.240103e-06 | 5.205 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 7.906051e-06 | 5.102 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 7.156837e-05 | 4.145 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 9.178092e-05 | 4.037 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 1.071871e-04 | 3.970 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 1.605898e-04 | 3.794 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 2.132467e-04 | 3.671 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 2.537317e-04 | 3.596 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 3.480269e-04 | 3.458 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 3.892696e-04 | 3.410 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 5.060539e-04 | 3.296 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 5.887669e-04 | 3.230 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 5.749513e-04 | 3.240 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 6.406045e-04 | 3.193 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 7.090170e-04 | 3.149 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 8.146910e-04 | 3.089 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 8.721420e-04 | 3.059 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 9.939702e-04 | 3.003 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 9.940174e-04 | 3.003 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 9.897934e-04 | 3.004 | 1 | 0 |
| Regulation of MITF-M dependent genes involved in metabolism | R-HSA-9854907 | 1.353256e-03 | 2.869 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 1.297119e-03 | 2.887 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.279260e-03 | 2.893 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.238086e-03 | 2.907 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 1.467944e-03 | 2.833 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 1.694570e-03 | 2.771 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 1.855193e-03 | 2.732 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.828450e-03 | 2.738 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 2.060740e-03 | 2.686 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 2.077683e-03 | 2.682 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 2.365549e-03 | 2.626 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.615708e-03 | 2.582 | 0 | 0 |
| Regulation of MITF-M dependent genes involved in invasion | R-HSA-9854909 | 2.615708e-03 | 2.582 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.522526e-03 | 2.598 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 3.062912e-03 | 2.514 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 3.382403e-03 | 2.471 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 3.658788e-03 | 2.437 | 0 | 0 |
| Immune System | R-HSA-168256 | 3.758155e-03 | 2.425 | 1 | 0 |
| Selective autophagy | R-HSA-9663891 | 3.992745e-03 | 2.399 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 5.125092e-03 | 2.290 | 1 | 1 |
| Nervous system development | R-HSA-9675108 | 5.310089e-03 | 2.275 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 6.257592e-03 | 2.204 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 5.995904e-03 | 2.222 | 0 | 0 |
| Kinesins | R-HSA-983189 | 6.257592e-03 | 2.204 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 6.228908e-03 | 2.206 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 6.662288e-03 | 2.176 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 7.007824e-03 | 2.154 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 6.919892e-03 | 2.160 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 7.424773e-03 | 2.129 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 8.014376e-03 | 2.096 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 8.014376e-03 | 2.096 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 8.597633e-03 | 2.066 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 9.205195e-03 | 2.036 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 9.300864e-03 | 2.031 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 9.545360e-03 | 2.020 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 1.056328e-02 | 1.976 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 9.967028e-03 | 2.001 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 1.032369e-02 | 1.986 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 9.837262e-03 | 2.007 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.062351e-02 | 1.974 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 1.087044e-02 | 1.964 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 1.117564e-02 | 1.952 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 1.136554e-02 | 1.944 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 1.283952e-02 | 1.891 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.270470e-02 | 1.896 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 1.283952e-02 | 1.891 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 1.239884e-02 | 1.907 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.337121e-02 | 1.874 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 1.337121e-02 | 1.874 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.415373e-02 | 1.849 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.665477e-02 | 1.778 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.726962e-02 | 1.763 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 1.773109e-02 | 1.751 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 1.605731e-02 | 1.794 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 1.773513e-02 | 1.751 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 1.813470e-02 | 1.741 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 1.845079e-02 | 1.734 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.951634e-02 | 1.710 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 1.951634e-02 | 1.710 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 2.035026e-02 | 1.691 | 0 | 0 |
| TGFBR2 MSI Frameshift Mutants in Cancer | R-HSA-3642279 | 2.101563e-02 | 1.677 | 0 | 0 |
| SARS-CoV-1 targets PDZ proteins in cell-cell junction | R-HSA-9692912 | 2.101563e-02 | 1.677 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.188982e-02 | 1.660 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 2.156165e-02 | 1.666 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.446027e-02 | 1.612 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.528387e-02 | 1.597 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.528387e-02 | 1.597 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 2.528387e-02 | 1.597 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 2.598716e-02 | 1.585 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 2.650953e-02 | 1.577 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 2.667081e-02 | 1.574 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 2.752187e-02 | 1.560 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 2.781488e-02 | 1.556 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5619101 | 3.135819e-02 | 1.504 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5660686 | 3.135819e-02 | 1.504 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 3.264880e-02 | 1.486 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.390142e-02 | 1.470 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.165246e-02 | 1.500 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.390142e-02 | 1.470 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.159212e-02 | 1.381 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.159212e-02 | 1.381 | 0 | 0 |
| Loss of Function of TGFBR2 in Cancer | R-HSA-3642278 | 4.159212e-02 | 1.381 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.159212e-02 | 1.381 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.159212e-02 | 1.381 | 0 | 0 |
| TGFBR2 Kinase Domain Mutants in Cancer | R-HSA-3645790 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.159212e-02 | 1.381 | 0 | 0 |
| TGFBR1 LBD Mutants in Cancer | R-HSA-3656535 | 4.159212e-02 | 1.381 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.159212e-02 | 1.381 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.159212e-02 | 1.381 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.159212e-02 | 1.381 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 3.857921e-02 | 1.414 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 4.066459e-02 | 1.391 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 4.066459e-02 | 1.391 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 4.100505e-02 | 1.387 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 3.621084e-02 | 1.441 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 4.068683e-02 | 1.391 | 1 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 3.789162e-02 | 1.421 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 3.906489e-02 | 1.408 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 4.066459e-02 | 1.391 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 4.066459e-02 | 1.391 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 4.066459e-02 | 1.391 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 3.795327e-02 | 1.421 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 4.094066e-02 | 1.388 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 3.912879e-02 | 1.408 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 4.348688e-02 | 1.362 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 5.171856e-02 | 1.286 | 0 | 0 |
| Defective ABCC2 causes DJS | R-HSA-5679001 | 5.171856e-02 | 1.286 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 4.501100e-02 | 1.347 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 4.602328e-02 | 1.337 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 5.394583e-02 | 1.268 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.171856e-02 | 1.286 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 4.861283e-02 | 1.313 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 5.427019e-02 | 1.265 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 5.394583e-02 | 1.268 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 5.512587e-02 | 1.259 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 5.512587e-02 | 1.259 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 4.861283e-02 | 1.313 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.600615e-02 | 1.252 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 5.668656e-02 | 1.247 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 5.668656e-02 | 1.247 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 5.668656e-02 | 1.247 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 5.668656e-02 | 1.247 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 5.668656e-02 | 1.247 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 5.711468e-02 | 1.243 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.173862e-02 | 1.209 | 0 | 0 |
| TGFBR1 KD Mutants in Cancer | R-HSA-3656532 | 6.173862e-02 | 1.209 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 6.173862e-02 | 1.209 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 7.165341e-02 | 1.145 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 7.165341e-02 | 1.145 | 1 | 1 |
| Loss of Function of TGFBR1 in Cancer | R-HSA-3656534 | 7.165341e-02 | 1.145 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.165341e-02 | 1.145 | 0 | 0 |
| SMAD2/3 Phosphorylation Motif Mutants in Cancer | R-HSA-3304356 | 7.165341e-02 | 1.145 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 7.165341e-02 | 1.145 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 8.146404e-02 | 1.089 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.146404e-02 | 1.089 | 0 | 0 |
| Defective CSF2RA causes SMDP4 | R-HSA-5688890 | 8.146404e-02 | 1.089 | 0 | 0 |
| Defective CSF2RB causes SMDP5 | R-HSA-5688849 | 8.146404e-02 | 1.089 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 9.117159e-02 | 1.040 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.117159e-02 | 1.040 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.117159e-02 | 1.040 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 1.102818e-01 | 0.957 | 0 | 0 |
| Type I hemidesmosome assembly | R-HSA-446107 | 1.102818e-01 | 0.957 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.196865e-01 | 0.922 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 1.289924e-01 | 0.889 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 1.289924e-01 | 0.889 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.563273e-01 | 0.806 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.563273e-01 | 0.806 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 1.652481e-01 | 0.782 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.652481e-01 | 0.782 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 1.740751e-01 | 0.759 | 0 | 0 |
| Defective GALNT3 causes HFTC | R-HSA-5083625 | 1.914516e-01 | 0.718 | 0 | 0 |
| Defective GALNT12 causes CRCS1 | R-HSA-5083636 | 1.914516e-01 | 0.718 | 0 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 7.108037e-02 | 1.148 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.084647e-01 | 0.681 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.084647e-01 | 0.681 | 0 | 0 |
| Defective C1GALT1C1 causes TNPS | R-HSA-5083632 | 2.084647e-01 | 0.681 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.251218e-01 | 0.648 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 9.950471e-02 | 1.002 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 8.535585e-02 | 1.069 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 1.935806e-01 | 0.713 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 1.227955e-01 | 0.911 | 1 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 1.007771e-01 | 0.997 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.828093e-01 | 0.738 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.518991e-02 | 1.186 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 7.165341e-02 | 1.145 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 1.102818e-01 | 0.957 | 0 | 0 |
| Nef mediated downregulation of MHC class I complex cell surface expression | R-HSA-164940 | 1.102818e-01 | 0.957 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 1.783467e-01 | 0.749 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex in Cancer | R-HSA-3304351 | 9.117159e-02 | 1.040 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.333192e-01 | 0.632 | 0 | 0 |
| VxPx cargo-targeting to cilium | R-HSA-5620916 | 2.333192e-01 | 0.632 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.652481e-01 | 0.782 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 1.376400e-01 | 0.861 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.168373e-01 | 0.664 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 2.089749e-01 | 0.680 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 1.234147e-01 | 0.909 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.740751e-01 | 0.759 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.828093e-01 | 0.738 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 1.633157e-01 | 0.787 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 1.633157e-01 | 0.787 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 1.633157e-01 | 0.787 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 1.633157e-01 | 0.787 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 6.173862e-02 | 1.209 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 6.173862e-02 | 1.209 | 0 | 0 |
| Loss of Function of SMAD2/3 in Cancer | R-HSA-3304349 | 8.146404e-02 | 1.089 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.146404e-02 | 1.089 | 0 | 0 |
| TGFBR3 regulates TGF-beta signaling | R-HSA-9839389 | 1.007771e-01 | 0.997 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.007771e-01 | 0.997 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.382005e-01 | 0.859 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.563273e-01 | 0.806 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.563273e-01 | 0.806 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.652481e-01 | 0.782 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.914516e-01 | 0.718 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.251218e-01 | 0.648 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.522032e-01 | 0.818 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 2.000031e-01 | 0.699 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 7.713658e-02 | 1.113 | 0 | 0 |
| RAB geranylgeranylation | R-HSA-8873719 | 1.633157e-01 | 0.787 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.740881e-01 | 0.759 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.652481e-01 | 0.782 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.828093e-01 | 0.738 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.234147e-01 | 0.909 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.234147e-01 | 0.909 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.872536e-01 | 0.728 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 8.921578e-02 | 1.050 | 0 | 0 |
| VLDL clearance | R-HSA-8964046 | 1.007771e-01 | 0.997 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.828093e-01 | 0.738 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 2.000031e-01 | 0.699 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.164461e-01 | 0.934 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 1.834595e-01 | 0.736 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 7.182489e-02 | 1.144 | 0 | 0 |
| Diseases associated with surfactant metabolism | R-HSA-5687613 | 1.563273e-01 | 0.806 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 2.084647e-01 | 0.681 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.333192e-01 | 0.632 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 1.708030e-01 | 0.768 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 2.051135e-01 | 0.688 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 1.633157e-01 | 0.787 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 2.244902e-01 | 0.649 | 0 | 0 |
| M Phase | R-HSA-68886 | 6.705392e-02 | 1.174 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.740881e-01 | 0.759 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 2.051135e-01 | 0.688 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 2.051135e-01 | 0.688 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.168373e-01 | 0.664 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 2.251218e-01 | 0.648 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.752381e-01 | 0.756 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 7.165341e-02 | 1.145 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.117159e-02 | 1.040 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 1.007771e-01 | 0.997 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.196865e-01 | 0.922 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 1.289924e-01 | 0.889 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.289924e-01 | 0.889 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.473118e-01 | 0.832 | 0 | 0 |
| Mitotic Telophase/Cytokinesis | R-HSA-68884 | 1.473118e-01 | 0.832 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 1.563273e-01 | 0.806 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.563273e-01 | 0.806 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 2.251218e-01 | 0.648 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.251218e-01 | 0.648 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 1.450064e-01 | 0.839 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 5.931149e-02 | 1.227 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.745682e-01 | 0.758 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 2.333192e-01 | 0.632 | 0 | 0 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | R-HSA-2032785 | 1.740751e-01 | 0.759 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 7.713658e-02 | 1.113 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 8.893935e-02 | 1.051 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 1.007771e-01 | 0.997 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 1.196865e-01 | 0.922 | 0 | 0 |
| Synthesis of PIPs at the ER membrane | R-HSA-1483248 | 1.382005e-01 | 0.859 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.652481e-01 | 0.782 | 0 | 0 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 2.084647e-01 | 0.681 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.708030e-01 | 0.768 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 1.248793e-01 | 0.904 | 0 | 0 |
| STAT3 nuclear events downstream of ALK signaling | R-HSA-9701898 | 1.828093e-01 | 0.738 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 1.925915e-01 | 0.715 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 2.322817e-01 | 0.634 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 1.399049e-01 | 0.854 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 1.289924e-01 | 0.889 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.652481e-01 | 0.782 | 0 | 0 |
| Physiological factors | R-HSA-5578768 | 1.740751e-01 | 0.759 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.294089e-02 | 1.032 | 0 | 0 |
| RNA Polymerase I Transcription Initiation | R-HSA-73762 | 9.950471e-02 | 1.002 | 0 | 0 |
| Creatine metabolism | R-HSA-71288 | 2.333192e-01 | 0.632 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 7.943069e-02 | 1.100 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 2.225821e-01 | 0.653 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.708030e-01 | 0.768 | 0 | 0 |
| HuR (ELAVL1) binds and stabilizes mRNA | R-HSA-450520 | 1.196865e-01 | 0.922 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 8.022386e-02 | 1.096 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.251218e-01 | 0.648 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 2.115622e-01 | 0.675 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 1.485336e-01 | 0.828 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 9.146373e-02 | 1.039 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 8.970868e-02 | 1.047 | 0 | 0 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 6.173862e-02 | 1.209 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 9.117159e-02 | 1.040 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.740751e-01 | 0.759 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 8.540189e-02 | 1.069 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 1.717334e-01 | 0.765 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 1.633157e-01 | 0.787 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.914516e-01 | 0.718 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 1.637556e-01 | 0.786 | 0 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 9.117159e-02 | 1.040 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 1.007771e-01 | 0.997 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 1.473118e-01 | 0.832 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 1.563273e-01 | 0.806 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.828093e-01 | 0.738 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 9.563416e-02 | 1.019 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 1.486265e-01 | 0.828 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 1.270523e-01 | 0.896 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 7.438208e-02 | 1.129 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.102818e-01 | 0.957 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 1.196865e-01 | 0.922 | 0 | 0 |
| Attachment and Entry | R-HSA-9678110 | 1.914516e-01 | 0.718 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.084647e-01 | 0.681 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 2.333192e-01 | 0.632 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 2.244902e-01 | 0.649 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 2.049229e-01 | 0.688 | 0 | 0 |
| Disease | R-HSA-1643685 | 7.773482e-02 | 1.109 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 7.108037e-02 | 1.148 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 2.000031e-01 | 0.699 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 2.168373e-01 | 0.664 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.251218e-01 | 0.648 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 2.012602e-01 | 0.696 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 7.108037e-02 | 1.148 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.828093e-01 | 0.738 | 0 | 0 |
| Atorvastatin ADME | R-HSA-9754706 | 1.914516e-01 | 0.718 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 1.914516e-01 | 0.718 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 2.168373e-01 | 0.664 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.333192e-01 | 0.632 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 2.115028e-01 | 0.675 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 1.448827e-01 | 0.839 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.028342e-01 | 0.988 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 7.406440e-02 | 1.130 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.713658e-02 | 1.113 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 8.651104e-02 | 1.063 | 0 | 0 |
| TBC/RABGAPs | R-HSA-8854214 | 1.028342e-01 | 0.988 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 1.522032e-01 | 0.818 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 2.322817e-01 | 0.634 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 1.670520e-01 | 0.777 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 8.459098e-02 | 1.073 | 0 | 0 |
| Formation of WDR5-containing histone-modifying complexes | R-HSA-9772755 | 7.408835e-02 | 1.130 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 1.340499e-01 | 0.873 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.340499e-01 | 0.873 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 1.914516e-01 | 0.718 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 1.914516e-01 | 0.718 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 1.688985e-01 | 0.772 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 1.890226e-01 | 0.723 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 1.221059e-01 | 0.913 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 1.164461e-01 | 0.934 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 1.119683e-01 | 0.951 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 1.051369e-01 | 0.978 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.612023e-01 | 0.793 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.309215e-01 | 0.637 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 1.038280e-01 | 0.984 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 2.167197e-01 | 0.664 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 8.282655e-02 | 1.082 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 8.045430e-02 | 1.094 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 7.043346e-02 | 1.152 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 1.273598e-01 | 0.895 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 1.068263e-01 | 0.971 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.110120e-01 | 0.955 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 1.897554e-01 | 0.722 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 8.835660e-02 | 1.054 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 2.181421e-01 | 0.661 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 2.337144e-01 | 0.631 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 2.337144e-01 | 0.631 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 2.337144e-01 | 0.631 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 2.400901e-01 | 0.620 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 2.400901e-01 | 0.620 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 2.400901e-01 | 0.620 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.414304e-01 | 0.617 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.414304e-01 | 0.617 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 2.414304e-01 | 0.617 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 2.421291e-01 | 0.616 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 2.429445e-01 | 0.614 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 2.444519e-01 | 0.612 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 2.452315e-01 | 0.610 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 2.475234e-01 | 0.606 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.494563e-01 | 0.603 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 2.534251e-01 | 0.596 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.573977e-01 | 0.589 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 2.573977e-01 | 0.589 | 0 | 0 |
| WNT ligand biogenesis and trafficking | R-HSA-3238698 | 2.573977e-01 | 0.589 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 2.573977e-01 | 0.589 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.573977e-01 | 0.589 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 2.573977e-01 | 0.589 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 2.596579e-01 | 0.586 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 2.635756e-01 | 0.579 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 2.635756e-01 | 0.579 | 0 | 0 |
| Termination of O-glycan biosynthesis | R-HSA-977068 | 2.652557e-01 | 0.576 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 2.652557e-01 | 0.576 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.652557e-01 | 0.576 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 2.674937e-01 | 0.573 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 2.674937e-01 | 0.573 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 2.706862e-01 | 0.568 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 2.714116e-01 | 0.566 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.730309e-01 | 0.564 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.730309e-01 | 0.564 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.730309e-01 | 0.564 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.730309e-01 | 0.564 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 2.753290e-01 | 0.560 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 2.807243e-01 | 0.552 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.807243e-01 | 0.552 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.807243e-01 | 0.552 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.883368e-01 | 0.540 | 0 | 0 |
| Metalloprotease DUBs | R-HSA-5689901 | 2.883368e-01 | 0.540 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.883368e-01 | 0.540 | 0 | 0 |
| Protein folding | R-HSA-391251 | 2.948932e-01 | 0.530 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 2.958692e-01 | 0.529 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 2.958692e-01 | 0.529 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 2.992326e-01 | 0.524 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 3.009294e-01 | 0.522 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 3.027008e-01 | 0.519 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.033223e-01 | 0.518 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 3.104937e-01 | 0.508 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 3.104937e-01 | 0.508 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 3.106970e-01 | 0.508 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.106970e-01 | 0.508 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.143837e-01 | 0.503 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.179941e-01 | 0.498 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.179941e-01 | 0.498 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.179941e-01 | 0.498 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 3.252144e-01 | 0.488 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 3.252144e-01 | 0.488 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.252144e-01 | 0.488 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 3.260240e-01 | 0.487 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 3.260240e-01 | 0.487 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 3.298931e-01 | 0.482 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 3.298931e-01 | 0.482 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 3.310136e-01 | 0.480 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 3.323587e-01 | 0.478 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.323587e-01 | 0.478 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 3.376556e-01 | 0.472 | 0 | 0 |
| Nuclear RNA decay | R-HSA-9930044 | 3.394277e-01 | 0.469 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.394277e-01 | 0.469 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.394277e-01 | 0.469 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.394277e-01 | 0.469 | 0 | 0 |
| Cardiogenesis | R-HSA-9733709 | 3.394277e-01 | 0.469 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 3.453062e-01 | 0.462 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.453062e-01 | 0.462 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.453062e-01 | 0.462 | 0 | 0 |
| Effects of PIP2 hydrolysis | R-HSA-114508 | 3.464224e-01 | 0.460 | 0 | 0 |
| Miscellaneous transport and binding events | R-HSA-5223345 | 3.464224e-01 | 0.460 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 3.464224e-01 | 0.460 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.533434e-01 | 0.452 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.533434e-01 | 0.452 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.533434e-01 | 0.452 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 3.550433e-01 | 0.450 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 3.567915e-01 | 0.448 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.601916e-01 | 0.443 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 3.601916e-01 | 0.443 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 3.601916e-01 | 0.443 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 3.637821e-01 | 0.439 | 1 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 3.644088e-01 | 0.438 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 3.644088e-01 | 0.438 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 3.644088e-01 | 0.438 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 3.659424e-01 | 0.437 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 3.669676e-01 | 0.435 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 3.669676e-01 | 0.435 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.669676e-01 | 0.435 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.669676e-01 | 0.435 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 3.682048e-01 | 0.434 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 3.736724e-01 | 0.428 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 3.736724e-01 | 0.428 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 3.795393e-01 | 0.421 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 3.795393e-01 | 0.421 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.803065e-01 | 0.420 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.803065e-01 | 0.420 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 3.868707e-01 | 0.412 | 0 | 0 |
| Expression of BMAL (ARNTL), CLOCK, and NPAS2 | R-HSA-9931509 | 3.868707e-01 | 0.412 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 3.868707e-01 | 0.412 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 3.870487e-01 | 0.412 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 3.933658e-01 | 0.405 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 3.933658e-01 | 0.405 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 3.970783e-01 | 0.401 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 3.970783e-01 | 0.401 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 3.982382e-01 | 0.400 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 3.997925e-01 | 0.398 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 3.997925e-01 | 0.398 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 3.997925e-01 | 0.398 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 3.997925e-01 | 0.398 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 4.019473e-01 | 0.396 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 4.019473e-01 | 0.396 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 4.061515e-01 | 0.391 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 4.061515e-01 | 0.391 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 4.061515e-01 | 0.391 | 0 | 0 |
| SLC-mediated transport of neurotransmitters | R-HSA-442660 | 4.061515e-01 | 0.391 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 4.093332e-01 | 0.388 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.124436e-01 | 0.385 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 4.126699e-01 | 0.384 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 4.166748e-01 | 0.380 | 0 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 4.186693e-01 | 0.378 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.186693e-01 | 0.378 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.186693e-01 | 0.378 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 4.186693e-01 | 0.378 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 4.248295e-01 | 0.372 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 4.248295e-01 | 0.372 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 4.248295e-01 | 0.372 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.248295e-01 | 0.372 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.248295e-01 | 0.372 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 4.248295e-01 | 0.372 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 4.276012e-01 | 0.369 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 4.309248e-01 | 0.366 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.309248e-01 | 0.366 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.309248e-01 | 0.366 | 0 | 0 |
| Vasopressin regulates renal water homeostasis via Aquaporins | R-HSA-432040 | 4.309248e-01 | 0.366 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 4.326938e-01 | 0.364 | 0 | 0 |
| mRNA Splicing - Minor Pathway | R-HSA-72165 | 4.369558e-01 | 0.360 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 4.369558e-01 | 0.360 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 4.369558e-01 | 0.360 | 0 | 0 |
| Signaling by TGFBR3 | R-HSA-9839373 | 4.369558e-01 | 0.360 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 4.384205e-01 | 0.358 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 4.384205e-01 | 0.358 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 4.384205e-01 | 0.358 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 4.455718e-01 | 0.351 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.488279e-01 | 0.348 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.488279e-01 | 0.348 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 4.544215e-01 | 0.343 | 1 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 4.546703e-01 | 0.342 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 4.546703e-01 | 0.342 | 0 | 0 |
| Chemokine receptors bind chemokines | R-HSA-380108 | 4.546703e-01 | 0.342 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 4.554697e-01 | 0.342 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 4.562036e-01 | 0.341 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 4.563192e-01 | 0.341 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 4.597217e-01 | 0.338 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 4.604511e-01 | 0.337 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 4.661710e-01 | 0.331 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.661710e-01 | 0.331 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 4.661710e-01 | 0.331 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 4.718307e-01 | 0.326 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 4.718307e-01 | 0.326 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 4.718307e-01 | 0.326 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 4.718307e-01 | 0.326 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.718307e-01 | 0.326 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 4.718307e-01 | 0.326 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 4.774306e-01 | 0.321 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 4.774306e-01 | 0.321 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 4.774306e-01 | 0.321 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 4.829715e-01 | 0.316 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 4.829715e-01 | 0.316 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 4.883956e-01 | 0.311 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 4.884541e-01 | 0.311 | 0 | 0 |
| G alpha (z) signalling events | R-HSA-418597 | 4.884541e-01 | 0.311 | 0 | 0 |
| Paracetamol ADME | R-HSA-9753281 | 4.884541e-01 | 0.311 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 4.907801e-01 | 0.309 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 4.938788e-01 | 0.306 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 4.938788e-01 | 0.306 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 5.045572e-01 | 0.297 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.045572e-01 | 0.297 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.098121e-01 | 0.293 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.098121e-01 | 0.293 | 0 | 0 |
| Assembly of collagen fibrils and other multimeric structures | R-HSA-2022090 | 5.098121e-01 | 0.293 | 0 | 0 |
| Amino acid transport across the plasma membrane | R-HSA-352230 | 5.098121e-01 | 0.293 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 5.108581e-01 | 0.292 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 5.149075e-01 | 0.288 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.201563e-01 | 0.284 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.201563e-01 | 0.284 | 0 | 0 |
| Aquaporin-mediated transport | R-HSA-445717 | 5.201563e-01 | 0.284 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 5.226856e-01 | 0.282 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 5.239545e-01 | 0.281 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 5.252468e-01 | 0.280 | 0 | 0 |
| Heme signaling | R-HSA-9707616 | 5.252468e-01 | 0.280 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.252468e-01 | 0.280 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 5.304145e-01 | 0.275 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.336222e-01 | 0.273 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.399930e-01 | 0.268 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 5.399930e-01 | 0.268 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 5.405689e-01 | 0.267 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 5.463039e-01 | 0.263 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 5.482704e-01 | 0.261 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.494368e-01 | 0.260 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.499047e-01 | 0.260 | 0 | 0 |
| SLC-mediated transport of amino acids | R-HSA-9958863 | 5.499047e-01 | 0.260 | 0 | 0 |
| O-linked glycosylation of mucins | R-HSA-913709 | 5.546813e-01 | 0.256 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 5.546813e-01 | 0.256 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.546813e-01 | 0.256 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 5.546813e-01 | 0.256 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 5.618170e-01 | 0.250 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 5.640839e-01 | 0.249 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.640839e-01 | 0.249 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 5.640839e-01 | 0.249 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 5.687109e-01 | 0.245 | 0 | 0 |
| Diseases associated with O-glycosylation of proteins | R-HSA-3906995 | 5.687109e-01 | 0.245 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 5.687109e-01 | 0.245 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.687109e-01 | 0.245 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 5.687109e-01 | 0.245 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 5.687109e-01 | 0.245 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 5.687109e-01 | 0.245 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.732890e-01 | 0.242 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 5.732890e-01 | 0.242 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.732890e-01 | 0.242 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 5.732890e-01 | 0.242 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.732890e-01 | 0.242 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 5.769501e-01 | 0.239 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.778189e-01 | 0.238 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 5.778189e-01 | 0.238 | 0 | 0 |
| Aspirin ADME | R-HSA-9749641 | 5.778189e-01 | 0.238 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 5.799717e-01 | 0.237 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.823009e-01 | 0.235 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 5.823009e-01 | 0.235 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 5.823009e-01 | 0.235 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 5.867357e-01 | 0.232 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 5.867357e-01 | 0.232 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 5.867357e-01 | 0.232 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 5.911236e-01 | 0.228 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 5.974936e-01 | 0.224 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 5.997610e-01 | 0.222 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 5.997610e-01 | 0.222 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 6.060677e-01 | 0.217 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 6.082169e-01 | 0.216 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 6.082169e-01 | 0.216 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.082169e-01 | 0.216 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 6.123781e-01 | 0.213 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 6.123781e-01 | 0.213 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 6.164953e-01 | 0.210 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 6.228019e-01 | 0.206 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 6.240278e-01 | 0.205 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 6.245997e-01 | 0.204 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 6.255374e-01 | 0.204 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.285878e-01 | 0.202 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 6.285878e-01 | 0.202 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 6.325338e-01 | 0.199 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 6.336521e-01 | 0.198 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 6.393189e-01 | 0.194 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 6.441235e-01 | 0.191 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 6.468724e-01 | 0.189 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 6.521575e-01 | 0.186 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.553497e-01 | 0.184 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 6.584545e-01 | 0.181 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.590129e-01 | 0.181 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 6.626375e-01 | 0.179 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 6.626375e-01 | 0.179 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 6.686979e-01 | 0.175 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 6.697721e-01 | 0.174 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.732829e-01 | 0.172 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 6.732829e-01 | 0.172 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.767567e-01 | 0.170 | 0 | 0 |
| Scavenging of heme from plasma | R-HSA-2168880 | 6.767567e-01 | 0.170 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 6.801937e-01 | 0.167 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.801937e-01 | 0.167 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.818903e-01 | 0.166 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 6.835944e-01 | 0.165 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 6.835944e-01 | 0.165 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 6.842805e-01 | 0.165 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 6.869591e-01 | 0.163 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 6.869591e-01 | 0.163 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 6.968413e-01 | 0.157 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 6.968413e-01 | 0.157 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 7.000660e-01 | 0.155 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 7.000660e-01 | 0.155 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 7.000660e-01 | 0.155 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 7.003017e-01 | 0.155 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.032566e-01 | 0.153 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 7.064134e-01 | 0.151 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 7.066511e-01 | 0.151 | 1 | 0 |
| RSV-host interactions | R-HSA-9833110 | 7.095368e-01 | 0.149 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.187102e-01 | 0.143 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 7.187102e-01 | 0.143 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 7.187102e-01 | 0.143 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.217036e-01 | 0.142 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 7.223388e-01 | 0.141 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 7.246653e-01 | 0.140 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 7.333636e-01 | 0.135 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 7.390101e-01 | 0.131 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 7.393963e-01 | 0.131 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.417887e-01 | 0.130 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 7.472578e-01 | 0.127 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 7.493868e-01 | 0.125 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 7.532906e-01 | 0.123 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 7.552464e-01 | 0.122 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 7.629838e-01 | 0.117 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 7.680065e-01 | 0.115 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.704781e-01 | 0.113 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 7.704781e-01 | 0.113 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 7.750849e-01 | 0.111 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 7.777367e-01 | 0.109 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 7.798431e-01 | 0.108 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 7.809377e-01 | 0.107 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 7.824485e-01 | 0.107 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 7.915763e-01 | 0.102 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 7.955926e-01 | 0.099 | 0 | 0 |
| O-linked glycosylation | R-HSA-5173105 | 8.066431e-01 | 0.093 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 8.087052e-01 | 0.092 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 8.186923e-01 | 0.087 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.225404e-01 | 0.085 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 8.281609e-01 | 0.082 | 0 | 0 |
| S Phase | R-HSA-69242 | 8.299948e-01 | 0.081 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 8.299948e-01 | 0.081 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 8.299948e-01 | 0.081 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 8.371377e-01 | 0.077 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 8.388763e-01 | 0.076 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 8.388763e-01 | 0.076 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 8.388763e-01 | 0.076 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 8.405358e-01 | 0.075 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 8.456482e-01 | 0.073 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 8.456482e-01 | 0.073 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 8.472965e-01 | 0.072 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 8.505407e-01 | 0.070 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 8.518862e-01 | 0.070 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 8.568251e-01 | 0.067 | 0 | 0 |
| Translation | R-HSA-72766 | 8.591759e-01 | 0.066 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 8.613653e-01 | 0.065 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 8.714101e-01 | 0.060 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 8.714101e-01 | 0.060 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 8.857525e-01 | 0.053 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 8.881838e-01 | 0.051 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 8.917347e-01 | 0.050 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 8.940394e-01 | 0.049 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.108046e-01 | 0.041 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 9.135334e-01 | 0.039 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 9.148151e-01 | 0.039 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 9.163873e-01 | 0.038 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.164960e-01 | 0.038 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.241165e-01 | 0.034 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.354516e-01 | 0.029 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.381073e-01 | 0.028 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 9.445058e-01 | 0.025 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.522963e-01 | 0.021 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.526862e-01 | 0.021 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 9.879794e-01 | 0.005 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.884921e-01 | 0.005 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.920634e-01 | 0.003 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.948730e-01 | 0.002 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.986445e-01 | 0.001 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999914e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.999991e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000e+00 | 0.000 | 0 | 0 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.110223e-16 | 15.955 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 2.109424e-15 | 14.676 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.787459e-14 | 13.748 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.787459e-14 | 13.748 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 2.131628e-14 | 13.671 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 3.175238e-14 | 13.498 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 8.815171e-14 | 13.055 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 8.815171e-14 | 13.055 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 9.081624e-14 | 13.042 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.241229e-13 | 12.906 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 1.409983e-13 | 12.851 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 1.655343e-13 | 12.781 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.918465e-13 | 12.717 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 3.983480e-13 | 12.400 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 4.296563e-13 | 12.367 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 5.253575e-13 | 12.280 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 7.107648e-13 | 12.148 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 7.449596e-13 | 12.128 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 8.949508e-13 | 12.048 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 8.949508e-13 | 12.048 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 1.044276e-12 | 11.981 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 1.484923e-12 | 11.828 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 1.895595e-12 | 11.722 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 1.968647e-12 | 11.706 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 1.895595e-12 | 11.722 | 0 | 0 |
| Depurination | R-HSA-73927 | 2.405964e-12 | 11.619 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 2.553513e-12 | 11.593 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 2.885803e-12 | 11.540 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 3.814282e-12 | 11.419 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 3.814282e-12 | 11.419 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 4.308776e-12 | 11.366 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 4.766298e-12 | 11.322 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 4.766298e-12 | 11.322 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 7.338241e-12 | 11.134 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 7.338241e-12 | 11.134 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 8.440137e-12 | 11.074 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 9.044543e-12 | 11.044 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 9.994228e-12 | 11.000 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 1.356859e-11 | 10.867 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 1.356859e-11 | 10.867 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 1.390599e-11 | 10.857 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.390599e-11 | 10.857 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.527189e-11 | 10.816 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 2.048250e-11 | 10.689 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 2.421874e-11 | 10.616 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 3.045875e-11 | 10.516 | 0 | 0 |
| M Phase | R-HSA-68886 | 3.649681e-11 | 10.438 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 4.994871e-11 | 10.301 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 5.486078e-11 | 10.261 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 5.938594e-11 | 10.226 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 7.039758e-11 | 10.152 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 8.321277e-11 | 10.080 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 1.352105e-10 | 9.869 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 1.701752e-10 | 9.769 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 1.845075e-10 | 9.734 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 1.921219e-10 | 9.716 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 2.100484e-10 | 9.678 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 2.380892e-10 | 9.623 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 3.437127e-10 | 9.464 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 3.877587e-10 | 9.411 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 4.437445e-10 | 9.353 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 5.846867e-10 | 9.233 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 5.595548e-10 | 9.252 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 7.645470e-10 | 9.117 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 7.645470e-10 | 9.117 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 7.722042e-10 | 9.112 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 8.718797e-10 | 9.060 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 9.065561e-10 | 9.043 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 9.925295e-10 | 9.003 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 1.061595e-09 | 8.974 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 1.072383e-09 | 8.970 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 1.570664e-09 | 8.804 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 1.570664e-09 | 8.804 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 1.570664e-09 | 8.804 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 1.574605e-09 | 8.803 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 1.639103e-09 | 8.785 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 1.812758e-09 | 8.742 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 2.086448e-09 | 8.681 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 2.132984e-09 | 8.671 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 2.219973e-09 | 8.654 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 2.640126e-09 | 8.578 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 2.986400e-09 | 8.525 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 2.963471e-09 | 8.528 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 3.154167e-09 | 8.501 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 3.154167e-09 | 8.501 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 3.154167e-09 | 8.501 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 3.713697e-09 | 8.430 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 3.736001e-09 | 8.428 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 4.705988e-09 | 8.327 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 5.271240e-09 | 8.278 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 8.926057e-09 | 8.049 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 8.758997e-09 | 8.058 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 9.024278e-09 | 8.045 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 1.474709e-08 | 7.831 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 1.497388e-08 | 7.825 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 1.563668e-08 | 7.806 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 2.081632e-08 | 7.682 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 2.509112e-08 | 7.600 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 3.236012e-08 | 7.490 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 3.319539e-08 | 7.479 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 3.460339e-08 | 7.461 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 3.510985e-08 | 7.455 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 3.952171e-08 | 7.403 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 4.313630e-08 | 7.365 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 4.313630e-08 | 7.365 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 4.838735e-08 | 7.315 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 7.829281e-08 | 7.106 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 1.146781e-07 | 6.941 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 1.190384e-07 | 6.924 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.735640e-07 | 6.761 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 2.095192e-07 | 6.679 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 2.238086e-07 | 6.650 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 2.493947e-07 | 6.603 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 2.535236e-07 | 6.596 | 0 | 0 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 2.897987e-07 | 6.538 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 3.145221e-07 | 6.502 | 1 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 4.241339e-07 | 6.372 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 7.259600e-07 | 6.139 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 7.981744e-07 | 6.098 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 8.648134e-07 | 6.063 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 1.160457e-06 | 5.935 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.178388e-06 | 5.929 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 1.212985e-06 | 5.916 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 1.249946e-06 | 5.903 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 1.351748e-06 | 5.869 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 1.599228e-06 | 5.796 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 2.333338e-06 | 5.632 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 2.752538e-06 | 5.560 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 2.787609e-06 | 5.555 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 2.787609e-06 | 5.555 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 3.036500e-06 | 5.518 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 3.489715e-06 | 5.457 | 1 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 4.263308e-06 | 5.370 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 4.366274e-06 | 5.360 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 5.258780e-06 | 5.279 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 5.645911e-06 | 5.248 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 5.811811e-06 | 5.236 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 6.447533e-06 | 5.191 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 8.597585e-06 | 5.066 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 9.521032e-06 | 5.021 | 1 | 0 |
| DNA Repair | R-HSA-73894 | 1.017883e-05 | 4.992 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.024451e-05 | 4.990 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 1.141724e-05 | 4.942 | 0 | 0 |
| Protein folding | R-HSA-391251 | 1.231121e-05 | 4.910 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.265138e-05 | 4.898 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 1.408445e-05 | 4.851 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 1.443164e-05 | 4.841 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 1.555499e-05 | 4.808 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 1.580732e-05 | 4.801 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 1.869505e-05 | 4.728 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 2.519261e-05 | 4.599 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 2.552308e-05 | 4.593 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 2.856489e-05 | 4.544 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 3.109631e-05 | 4.507 | 0 | 0 |
| Immune System | R-HSA-168256 | 3.156461e-05 | 4.501 | 1 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 3.982298e-05 | 4.400 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 3.561995e-05 | 4.448 | 1 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 4.517007e-05 | 4.345 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 4.524431e-05 | 4.344 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 4.617596e-05 | 4.336 | 1 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 7.673333e-05 | 4.115 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 8.122934e-05 | 4.090 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 8.703659e-05 | 4.060 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.015882e-04 | 3.993 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.031505e-04 | 3.987 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.032734e-04 | 3.986 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.032734e-04 | 3.986 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 1.242684e-04 | 3.906 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 1.252767e-04 | 3.902 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.290950e-04 | 3.889 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 1.378404e-04 | 3.861 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 1.378404e-04 | 3.861 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 1.417167e-04 | 3.849 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 1.632865e-04 | 3.787 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 1.670102e-04 | 3.777 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 1.670102e-04 | 3.777 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 1.670102e-04 | 3.777 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 1.798083e-04 | 3.745 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 1.910353e-04 | 3.719 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 1.984087e-04 | 3.702 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 1.984087e-04 | 3.702 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 2.060286e-04 | 3.686 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 2.126045e-04 | 3.672 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 2.485805e-04 | 3.605 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 2.824335e-04 | 3.549 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 2.605747e-04 | 3.584 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 2.605747e-04 | 3.584 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 2.605747e-04 | 3.584 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 2.605747e-04 | 3.584 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 2.832823e-04 | 3.548 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 2.522127e-04 | 3.598 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 3.142996e-04 | 3.503 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 3.557118e-04 | 3.449 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 3.572859e-04 | 3.447 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 3.894425e-04 | 3.410 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 4.037956e-04 | 3.394 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 4.088701e-04 | 3.388 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 4.100458e-04 | 3.387 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 4.514211e-04 | 3.345 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 4.757404e-04 | 3.323 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 5.029210e-04 | 3.299 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 5.119424e-04 | 3.291 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 5.402535e-04 | 3.267 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 5.927240e-04 | 3.227 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 6.005194e-04 | 3.221 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 6.605130e-04 | 3.180 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 6.824213e-04 | 3.166 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 7.150227e-04 | 3.146 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 7.172171e-04 | 3.144 | 0 | 0 |
| Kinesins | R-HSA-983189 | 7.358199e-04 | 3.133 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 7.511770e-04 | 3.124 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 8.362756e-04 | 3.078 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 9.031373e-04 | 3.044 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 9.467058e-04 | 3.024 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 9.907653e-04 | 3.004 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.007198e-03 | 2.997 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.046927e-03 | 2.980 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.046927e-03 | 2.980 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.181660e-03 | 2.928 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.392582e-03 | 2.856 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 1.423607e-03 | 2.847 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 1.528331e-03 | 2.816 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 1.532559e-03 | 2.815 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 1.632212e-03 | 2.787 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.673832e-03 | 2.776 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 1.685240e-03 | 2.773 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.802435e-03 | 2.744 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 1.857668e-03 | 2.731 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.032679e-03 | 2.692 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 2.142638e-03 | 2.669 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 2.452863e-03 | 2.610 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 2.618979e-03 | 2.582 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.872156e-03 | 2.542 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 2.830170e-03 | 2.548 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.439061e-03 | 2.613 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 2.792657e-03 | 2.554 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 2.861544e-03 | 2.543 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 2.546113e-03 | 2.594 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 2.972054e-03 | 2.527 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 3.092402e-03 | 2.510 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 3.196918e-03 | 2.495 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 3.209342e-03 | 2.494 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 3.285272e-03 | 2.483 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 3.285272e-03 | 2.483 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 3.291631e-03 | 2.483 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 3.454994e-03 | 2.462 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 3.560534e-03 | 2.448 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 3.566303e-03 | 2.448 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 3.796517e-03 | 2.421 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 3.796517e-03 | 2.421 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 3.890156e-03 | 2.410 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 3.978211e-03 | 2.400 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 4.002769e-03 | 2.398 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 4.233972e-03 | 2.373 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 4.237233e-03 | 2.373 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 4.474028e-03 | 2.349 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 4.562051e-03 | 2.341 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 4.723093e-03 | 2.326 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 4.866280e-03 | 2.313 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 4.941719e-03 | 2.306 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 4.981317e-03 | 2.303 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 5.169065e-03 | 2.287 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 5.243294e-03 | 2.280 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 5.554533e-03 | 2.255 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 5.793135e-03 | 2.237 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 5.863729e-03 | 2.232 | 0 | 0 |
| Interleukin-18 signaling | R-HSA-9012546 | 5.863729e-03 | 2.232 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 6.012465e-03 | 2.221 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 6.078987e-03 | 2.216 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 6.468555e-03 | 2.189 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 6.931822e-03 | 2.159 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 6.931822e-03 | 2.159 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 6.931822e-03 | 2.159 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 6.980973e-03 | 2.156 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 7.057637e-03 | 2.151 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 7.197432e-03 | 2.143 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 7.801935e-03 | 2.108 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 8.081098e-03 | 2.093 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 8.255994e-03 | 2.083 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 8.255994e-03 | 2.083 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 8.313333e-03 | 2.080 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 8.536623e-03 | 2.069 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 9.236780e-03 | 2.034 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 9.637927e-03 | 2.016 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 1.015222e-02 | 1.993 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.019454e-02 | 1.992 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.019454e-02 | 1.992 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.019454e-02 | 1.992 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.019454e-02 | 1.992 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.019454e-02 | 1.992 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.019454e-02 | 1.992 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.061624e-02 | 1.974 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 1.061624e-02 | 1.974 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.136528e-02 | 1.944 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.136528e-02 | 1.944 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 1.165161e-02 | 1.934 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.199870e-02 | 1.921 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.199870e-02 | 1.921 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.215644e-02 | 1.915 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 1.215644e-02 | 1.915 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 1.318457e-02 | 1.880 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 1.360973e-02 | 1.866 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.360973e-02 | 1.866 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 1.396431e-02 | 1.855 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.405642e-02 | 1.852 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH3 | R-HSA-5632927 | 2.028577e-02 | 1.693 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH6 | R-HSA-5632968 | 2.028577e-02 | 1.693 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 1.825585e-02 | 1.739 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.179846e-02 | 1.662 | 0 | 0 |
| Inhibition of PKR | R-HSA-169131 | 2.028577e-02 | 1.693 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.519124e-02 | 1.818 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.825585e-02 | 1.739 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 1.680125e-02 | 1.775 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 1.680125e-02 | 1.775 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 1.881045e-02 | 1.726 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | R-HSA-2892247 | 1.999395e-02 | 1.699 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 2.037641e-02 | 1.691 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.179846e-02 | 1.662 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 2.230278e-02 | 1.652 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 2.284487e-02 | 1.641 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 2.290539e-02 | 1.640 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 2.351335e-02 | 1.629 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 2.351335e-02 | 1.629 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 2.351335e-02 | 1.629 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.366786e-02 | 1.626 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 2.427520e-02 | 1.615 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 2.501027e-02 | 1.602 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.560065e-02 | 1.592 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.560065e-02 | 1.592 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 2.746573e-02 | 1.561 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 2.808428e-02 | 1.552 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 2.868453e-02 | 1.542 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 3.021640e-02 | 1.520 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH2 | R-HSA-5632928 | 3.027473e-02 | 1.519 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.027473e-02 | 1.519 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.176481e-02 | 1.498 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 3.393671e-02 | 1.469 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 3.579254e-02 | 1.446 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 3.592370e-02 | 1.445 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 3.643593e-02 | 1.438 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 3.643593e-02 | 1.438 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 3.726008e-02 | 1.429 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.016246e-02 | 1.396 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.016246e-02 | 1.396 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.016246e-02 | 1.396 | 0 | 0 |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.016246e-02 | 1.396 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.016246e-02 | 1.396 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.016246e-02 | 1.396 | 0 | 0 |
| Translation | R-HSA-72766 | 4.321724e-02 | 1.364 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.561346e-02 | 1.341 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 4.561346e-02 | 1.341 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 4.671961e-02 | 1.331 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 4.836736e-02 | 1.315 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 4.836736e-02 | 1.315 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 4.986461e-02 | 1.302 | 0 | 0 |
| Diseases of Mismatch Repair (MMR) | R-HSA-5423599 | 4.994998e-02 | 1.301 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 4.994998e-02 | 1.301 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 5.064108e-02 | 1.295 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 5.138431e-02 | 1.289 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 5.322632e-02 | 1.274 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 5.585756e-02 | 1.253 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 5.585756e-02 | 1.253 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 5.963829e-02 | 1.224 | 0 | 0 |
| NADE modulates death signalling | R-HSA-205025 | 5.963829e-02 | 1.224 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 6.125327e-02 | 1.213 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 6.125327e-02 | 1.213 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 6.401541e-02 | 1.194 | 0 | 0 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | R-HSA-9818027 | 6.401541e-02 | 1.194 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 6.401541e-02 | 1.194 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 6.681888e-02 | 1.175 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 6.681888e-02 | 1.175 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 6.681888e-02 | 1.175 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 6.922840e-02 | 1.160 | 0 | 0 |
| Biosynthesis of DPAn-3-derived 13-series resolvins | R-HSA-9026403 | 6.922840e-02 | 1.160 | 0 | 0 |
| Nectin/Necl trans heterodimerization | R-HSA-420597 | 6.922840e-02 | 1.160 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 6.932681e-02 | 1.159 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 7.872129e-02 | 1.104 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 8.811794e-02 | 1.055 | 0 | 0 |
| Metabolism of ingested MeSeO2H into MeSeH | R-HSA-5263617 | 8.811794e-02 | 1.055 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 8.811794e-02 | 1.055 | 0 | 0 |
| PP2A-mediated dephosphorylation of key metabolic factors | R-HSA-163767 | 9.741933e-02 | 1.011 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 9.741933e-02 | 1.011 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 9.741933e-02 | 1.011 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 9.741933e-02 | 1.011 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 1.066264e-01 | 0.972 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 1.066264e-01 | 0.972 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.247614e-01 | 0.904 | 0 | 0 |
| Truncations of AMER1 destabilize the destruction complex | R-HSA-5467348 | 1.336913e-01 | 0.874 | 0 | 0 |
| APC truncation mutants have impaired AXIN binding | R-HSA-5467337 | 1.336913e-01 | 0.874 | 0 | 0 |
| AXIN missense mutants destabilize the destruction complex | R-HSA-5467340 | 1.336913e-01 | 0.874 | 0 | 0 |
| Signaling by GSK3beta mutants | R-HSA-5339716 | 1.425305e-01 | 0.846 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 1.265560e-01 | 0.898 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 1.355234e-01 | 0.868 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 1.355234e-01 | 0.868 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.000782e-01 | 1.000 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 7.862835e-02 | 1.104 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.032956e-01 | 0.986 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 8.179933e-02 | 1.087 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 9.373170e-02 | 1.028 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 7.872129e-02 | 1.104 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 1.368741e-01 | 0.864 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 1.403541e-01 | 0.853 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 7.872129e-02 | 1.104 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 9.741933e-02 | 1.011 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.336913e-01 | 0.874 | 0 | 0 |
| Signaling by APC mutants | R-HSA-4839744 | 1.336913e-01 | 0.874 | 0 | 0 |
| Signaling by AMER1 mutants | R-HSA-4839748 | 1.425305e-01 | 0.846 | 0 | 0 |
| Signaling by AXIN mutants | R-HSA-4839735 | 1.425305e-01 | 0.846 | 0 | 0 |
| ERKs are inactivated | R-HSA-202670 | 1.425305e-01 | 0.846 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.265560e-01 | 0.898 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 1.299743e-01 | 0.886 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 1.334139e-01 | 0.875 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.157401e-01 | 0.937 | 0 | 0 |
| Chylomicron assembly | R-HSA-8963888 | 1.336913e-01 | 0.874 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 1.152210e-01 | 0.938 | 0 | 0 |
| LDL remodeling | R-HSA-8964041 | 9.741933e-02 | 1.011 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.157401e-01 | 0.937 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.247614e-01 | 0.904 | 0 | 0 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | R-HSA-113501 | 1.425305e-01 | 0.846 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 8.444644e-02 | 1.073 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 7.254539e-02 | 1.139 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 9.157228e-02 | 1.038 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 8.811794e-02 | 1.055 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.157401e-01 | 0.937 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.247614e-01 | 0.904 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.425305e-01 | 0.846 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 7.311540e-02 | 1.136 | 0 | 0 |
| VLDL assembly | R-HSA-8866423 | 8.811794e-02 | 1.055 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 9.741933e-02 | 1.011 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 1.157401e-01 | 0.937 | 0 | 0 |
| Biosynthesis of DPAn-3-derived maresins | R-HSA-9026290 | 1.336913e-01 | 0.874 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 1.231600e-01 | 0.910 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 1.000782e-01 | 1.000 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 1.182681e-01 | 0.927 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 7.842405e-02 | 1.106 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 9.060438e-02 | 1.043 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 1.157401e-01 | 0.937 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 1.299743e-01 | 0.886 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 7.493313e-02 | 1.125 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.247614e-01 | 0.904 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.336913e-01 | 0.874 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 1.403541e-01 | 0.853 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 1.022693e-01 | 0.990 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 7.842405e-02 | 1.106 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.164376e-01 | 0.934 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.164376e-01 | 0.934 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.403541e-01 | 0.853 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 7.131783e-02 | 1.147 | 0 | 0 |
| Interleukin-23 signaling | R-HSA-9020933 | 1.066264e-01 | 0.972 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 7.599002e-02 | 1.119 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.254539e-02 | 1.139 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.265560e-01 | 0.898 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 8.337270e-02 | 1.079 | 0 | 0 |
| Transcriptional regulation of pluripotent stem cells | R-HSA-452723 | 7.842405e-02 | 1.106 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 9.417759e-02 | 1.026 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 1.197869e-01 | 0.922 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.274401e-02 | 1.033 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 9.079572e-02 | 1.042 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 1.152210e-01 | 0.938 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.336913e-01 | 0.874 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 9.688998e-02 | 1.014 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.000782e-01 | 1.000 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 1.003112e-01 | 0.999 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.044874e-01 | 0.981 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.017002e-01 | 0.993 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.438532e-01 | 0.842 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 1.470078e-01 | 0.833 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 1.472994e-01 | 0.832 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.472994e-01 | 0.832 | 0 | 0 |
| Signaling by CTNNB1 phospho-site mutants | R-HSA-4839743 | 1.512801e-01 | 0.820 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.512801e-01 | 0.820 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.512801e-01 | 0.820 | 0 | 0 |
| CTNNB1 T41 mutants aren't phosphorylated | R-HSA-5358752 | 1.512801e-01 | 0.820 | 0 | 0 |
| CTNNB1 S37 mutants aren't phosphorylated | R-HSA-5358749 | 1.512801e-01 | 0.820 | 0 | 0 |
| CTNNB1 S33 mutants aren't phosphorylated | R-HSA-5358747 | 1.512801e-01 | 0.820 | 0 | 0 |
| CTNNB1 S45 mutants aren't phosphorylated | R-HSA-5358751 | 1.512801e-01 | 0.820 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 1.512801e-01 | 0.820 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.512801e-01 | 0.820 | 0 | 0 |
| Biosynthesis of DPAn-3-derived protectins and resolvins | R-HSA-9026286 | 1.512801e-01 | 0.820 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 1.521010e-01 | 0.818 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 1.569521e-01 | 0.804 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 1.580254e-01 | 0.801 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.599410e-01 | 0.796 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.599410e-01 | 0.796 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.599410e-01 | 0.796 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.599410e-01 | 0.796 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.599410e-01 | 0.796 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.599410e-01 | 0.796 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 1.616089e-01 | 0.792 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.652072e-01 | 0.782 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.685140e-01 | 0.773 | 0 | 0 |
| Biosynthesis of E-series 18(R)-resolvins | R-HSA-9023661 | 1.685140e-01 | 0.773 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.685140e-01 | 0.773 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.685140e-01 | 0.773 | 0 | 0 |
| CLEC7A (Dectin-1) induces NFAT activation | R-HSA-5607763 | 1.685140e-01 | 0.773 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.685140e-01 | 0.773 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.770001e-01 | 0.752 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.770001e-01 | 0.752 | 0 | 0 |
| Beta-catenin phosphorylation cascade | R-HSA-196299 | 1.770001e-01 | 0.752 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 1.770001e-01 | 0.752 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 1.770001e-01 | 0.752 | 0 | 0 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 1.770001e-01 | 0.752 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.770001e-01 | 0.752 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.770001e-01 | 0.752 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.770001e-01 | 0.752 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 1.818884e-01 | 0.740 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 1.833976e-01 | 0.737 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 1.833976e-01 | 0.737 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.854000e-01 | 0.732 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 1.854000e-01 | 0.732 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 1.854000e-01 | 0.732 | 0 | 0 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | R-HSA-9634600 | 1.854000e-01 | 0.732 | 0 | 0 |
| KSRP (KHSRP) binds and destabilizes mRNA | R-HSA-450604 | 1.854000e-01 | 0.732 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 1.854000e-01 | 0.732 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.854000e-01 | 0.732 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 1.870710e-01 | 0.728 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 1.907548e-01 | 0.720 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 1.907548e-01 | 0.720 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 1.924431e-01 | 0.716 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 1.937148e-01 | 0.713 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 1.937148e-01 | 0.713 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 1.937148e-01 | 0.713 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 1.940371e-01 | 0.712 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 1.944484e-01 | 0.711 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 1.945128e-01 | 0.711 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 1.945128e-01 | 0.711 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 1.947362e-01 | 0.711 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 1.981511e-01 | 0.703 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 1.981511e-01 | 0.703 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 2.018625e-01 | 0.695 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.019452e-01 | 0.695 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.019452e-01 | 0.695 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.019452e-01 | 0.695 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | R-HSA-5358606 | 2.019452e-01 | 0.695 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | R-HSA-5358565 | 2.019452e-01 | 0.695 | 0 | 0 |
| Biosynthesis of aspirin-triggered D-series resolvins | R-HSA-9020265 | 2.019452e-01 | 0.695 | 0 | 0 |
| Metabolism of ingested H2SeO4 and H2SeO3 into H2Se | R-HSA-2408550 | 2.019452e-01 | 0.695 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.019452e-01 | 0.695 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 2.093089e-01 | 0.679 | 0 | 0 |
| Mismatch Repair | R-HSA-5358508 | 2.100920e-01 | 0.678 | 0 | 0 |
| Synaptic adhesion-like molecules | R-HSA-8849932 | 2.100920e-01 | 0.678 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.100920e-01 | 0.678 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.100920e-01 | 0.678 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.100920e-01 | 0.678 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.100920e-01 | 0.678 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.130429e-01 | 0.672 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 2.130832e-01 | 0.671 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 2.157349e-01 | 0.666 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.181562e-01 | 0.661 | 0 | 0 |
| Strand-asynchronous mitochondrial DNA replication | R-HSA-9913635 | 2.181562e-01 | 0.661 | 0 | 0 |
| Synthesis of 5-eicosatetraenoic acids | R-HSA-2142688 | 2.181562e-01 | 0.661 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.181562e-01 | 0.661 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 2.205297e-01 | 0.657 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 2.205297e-01 | 0.657 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.205297e-01 | 0.657 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 2.242816e-01 | 0.649 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.261386e-01 | 0.646 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.261386e-01 | 0.646 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 2.261386e-01 | 0.646 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.261386e-01 | 0.646 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.261386e-01 | 0.646 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.261386e-01 | 0.646 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 2.280383e-01 | 0.642 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 2.280383e-01 | 0.642 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.290955e-01 | 0.640 | 0 | 0 |
| Transcriptional activation of mitochondrial biogenesis | R-HSA-2151201 | 2.317995e-01 | 0.635 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.340400e-01 | 0.631 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.340400e-01 | 0.631 | 0 | 0 |
| Biosynthesis of E-series 18(S)-resolvins | R-HSA-9018896 | 2.340400e-01 | 0.631 | 0 | 0 |
| ERK/MAPK targets | R-HSA-198753 | 2.340400e-01 | 0.631 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.340400e-01 | 0.631 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 2.418611e-01 | 0.616 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 2.418611e-01 | 0.616 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.418611e-01 | 0.616 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.418611e-01 | 0.616 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 2.418611e-01 | 0.616 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 2.426081e-01 | 0.615 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.480503e-01 | 0.605 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 2.496029e-01 | 0.603 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 2.496029e-01 | 0.603 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.496029e-01 | 0.603 | 0 | 0 |
| Biosynthesis of D-series resolvins | R-HSA-9018676 | 2.496029e-01 | 0.603 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.496029e-01 | 0.603 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.496029e-01 | 0.603 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 2.535114e-01 | 0.596 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 2.535114e-01 | 0.596 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 2.535114e-01 | 0.596 | 0 | 0 |
| XBP1(S) activates chaperone genes | R-HSA-381038 | 2.544344e-01 | 0.594 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 2.562486e-01 | 0.591 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 2.572661e-01 | 0.590 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.572661e-01 | 0.590 | 0 | 0 |
| Biosynthesis of maresins | R-HSA-9018682 | 2.572661e-01 | 0.590 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 2.617354e-01 | 0.582 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.648516e-01 | 0.577 | 0 | 0 |
| Plasma lipoprotein assembly | R-HSA-8963898 | 2.648516e-01 | 0.577 | 0 | 0 |
| Mitochondrial RNA degradation | R-HSA-9836573 | 2.648516e-01 | 0.577 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 2.699938e-01 | 0.569 | 1 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 2.699938e-01 | 0.569 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 2.723600e-01 | 0.565 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.723600e-01 | 0.565 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.723600e-01 | 0.565 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.723600e-01 | 0.565 | 0 | 0 |
| Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives | R-HSA-9027604 | 2.723600e-01 | 0.565 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 2.723600e-01 | 0.565 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.723600e-01 | 0.565 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.723600e-01 | 0.565 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 2.733370e-01 | 0.563 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 2.755162e-01 | 0.560 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 2.763052e-01 | 0.559 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 2.771169e-01 | 0.557 | 0 | 0 |
| IRE1alpha activates chaperones | R-HSA-381070 | 2.771169e-01 | 0.557 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.797922e-01 | 0.553 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 2.797922e-01 | 0.553 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.797922e-01 | 0.553 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 2.846733e-01 | 0.546 | 1 | 1 |
| Cristae formation | R-HSA-8949613 | 2.871489e-01 | 0.542 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 2.871489e-01 | 0.542 | 0 | 0 |
| Biosynthesis of DPAn-3 SPMs | R-HSA-9025094 | 2.871489e-01 | 0.542 | 0 | 0 |
| Insulin processing | R-HSA-264876 | 2.871489e-01 | 0.542 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 2.871489e-01 | 0.542 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 2.871489e-01 | 0.542 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 2.922224e-01 | 0.534 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 2.944309e-01 | 0.531 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 2.944309e-01 | 0.531 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 2.944309e-01 | 0.531 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 2.944309e-01 | 0.531 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 2.959934e-01 | 0.529 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 2.959934e-01 | 0.529 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 2.997615e-01 | 0.523 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 3.016390e-01 | 0.521 | 0 | 0 |
| Biosynthesis of EPA-derived SPMs | R-HSA-9018679 | 3.016390e-01 | 0.521 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.016390e-01 | 0.521 | 0 | 0 |
| MAPK targets/ Nuclear events mediated by MAP kinases | R-HSA-450282 | 3.016390e-01 | 0.521 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 3.035264e-01 | 0.518 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 3.072879e-01 | 0.512 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 3.072879e-01 | 0.512 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.087739e-01 | 0.510 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.087739e-01 | 0.510 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.087739e-01 | 0.510 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.087739e-01 | 0.510 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 3.087739e-01 | 0.510 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.087739e-01 | 0.510 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 3.139153e-01 | 0.503 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 3.147990e-01 | 0.502 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.158363e-01 | 0.501 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.158363e-01 | 0.501 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 3.158363e-01 | 0.501 | 0 | 0 |
| Biosynthesis of DPA-derived SPMs | R-HSA-9018683 | 3.158363e-01 | 0.501 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.158363e-01 | 0.501 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 3.158363e-01 | 0.501 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 3.185480e-01 | 0.497 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 3.228271e-01 | 0.491 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 3.228271e-01 | 0.491 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.228271e-01 | 0.491 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 3.228271e-01 | 0.491 | 0 | 0 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | R-HSA-2173795 | 3.228271e-01 | 0.491 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 3.260316e-01 | 0.487 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 3.297468e-01 | 0.482 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 3.297468e-01 | 0.482 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.297468e-01 | 0.482 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.297468e-01 | 0.482 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 3.297468e-01 | 0.482 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 3.365962e-01 | 0.473 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.365962e-01 | 0.473 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 3.433760e-01 | 0.464 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 3.433760e-01 | 0.464 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.433760e-01 | 0.464 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 3.433760e-01 | 0.464 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 3.433760e-01 | 0.464 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.433760e-01 | 0.464 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 3.433760e-01 | 0.464 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 3.446427e-01 | 0.463 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 3.446427e-01 | 0.463 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.500870e-01 | 0.456 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 3.500870e-01 | 0.456 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.500870e-01 | 0.456 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 3.500870e-01 | 0.456 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 3.500870e-01 | 0.456 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.500870e-01 | 0.456 | 0 | 0 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | R-HSA-2408508 | 3.500870e-01 | 0.456 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 3.557318e-01 | 0.449 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 3.567298e-01 | 0.448 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 3.567298e-01 | 0.448 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 3.567298e-01 | 0.448 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 3.567298e-01 | 0.448 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 3.621913e-01 | 0.441 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 3.630879e-01 | 0.440 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 3.633051e-01 | 0.440 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 3.633051e-01 | 0.440 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 3.633051e-01 | 0.440 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 3.633051e-01 | 0.440 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 3.633051e-01 | 0.440 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.698136e-01 | 0.432 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.698136e-01 | 0.432 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 3.740628e-01 | 0.427 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.762560e-01 | 0.425 | 0 | 0 |
| NS1 Mediated Effects on Host Pathways | R-HSA-168276 | 3.762560e-01 | 0.425 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 3.762560e-01 | 0.425 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 3.762560e-01 | 0.425 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 3.762560e-01 | 0.425 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.762560e-01 | 0.425 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 3.826329e-01 | 0.417 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 3.826329e-01 | 0.417 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 3.889450e-01 | 0.410 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 3.889450e-01 | 0.410 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 3.951930e-01 | 0.403 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 3.951930e-01 | 0.403 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 3.951930e-01 | 0.403 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 3.951930e-01 | 0.403 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.013774e-01 | 0.396 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 4.013774e-01 | 0.396 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 4.041275e-01 | 0.393 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 4.074990e-01 | 0.390 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.074990e-01 | 0.390 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.074990e-01 | 0.390 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 4.100645e-01 | 0.387 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 4.109899e-01 | 0.386 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 4.128986e-01 | 0.384 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.135584e-01 | 0.383 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 4.135584e-01 | 0.383 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.135584e-01 | 0.383 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 4.195561e-01 | 0.377 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.195561e-01 | 0.377 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 4.195561e-01 | 0.377 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 4.195561e-01 | 0.377 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.195561e-01 | 0.377 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 4.195561e-01 | 0.377 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 4.195561e-01 | 0.377 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 4.195561e-01 | 0.377 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 4.195561e-01 | 0.377 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.195561e-01 | 0.377 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 4.254929e-01 | 0.371 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.254929e-01 | 0.371 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.254929e-01 | 0.371 | 0 | 0 |
| Diseases of DNA repair | R-HSA-9675135 | 4.254929e-01 | 0.371 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 4.254929e-01 | 0.371 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 4.254929e-01 | 0.371 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 4.313694e-01 | 0.365 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.313694e-01 | 0.365 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.371861e-01 | 0.359 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.371861e-01 | 0.359 | 0 | 0 |
| Plasma lipoprotein remodeling | R-HSA-8963899 | 4.371861e-01 | 0.359 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.371861e-01 | 0.359 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 4.381317e-01 | 0.358 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 4.429436e-01 | 0.354 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 4.429436e-01 | 0.354 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 4.486426e-01 | 0.348 | 0 | 0 |
| Complex IV assembly | R-HSA-9864848 | 4.542837e-01 | 0.343 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 4.542837e-01 | 0.343 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 4.542837e-01 | 0.343 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.598673e-01 | 0.337 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.598673e-01 | 0.337 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 4.598673e-01 | 0.337 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 4.653942e-01 | 0.332 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 4.654647e-01 | 0.332 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 4.708649e-01 | 0.327 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 4.755128e-01 | 0.323 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 4.762799e-01 | 0.322 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 4.816399e-01 | 0.317 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 4.816399e-01 | 0.317 | 0 | 0 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | R-HSA-2173793 | 4.816399e-01 | 0.317 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 4.816399e-01 | 0.317 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 4.911816e-01 | 0.309 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 4.921967e-01 | 0.308 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 4.973948e-01 | 0.303 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 4.973948e-01 | 0.303 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 4.973948e-01 | 0.303 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 5.025399e-01 | 0.299 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 5.025399e-01 | 0.299 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 5.025399e-01 | 0.299 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 5.025399e-01 | 0.299 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 5.025399e-01 | 0.299 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 5.025399e-01 | 0.299 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 5.025399e-01 | 0.299 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.076327e-01 | 0.294 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.076327e-01 | 0.294 | 0 | 0 |
| MAP kinase activation | R-HSA-450294 | 5.076327e-01 | 0.294 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.076327e-01 | 0.294 | 0 | 0 |
| S Phase | R-HSA-69242 | 5.081692e-01 | 0.294 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 5.113620e-01 | 0.291 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.126736e-01 | 0.290 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.145413e-01 | 0.289 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.176632e-01 | 0.286 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.176632e-01 | 0.286 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 5.226021e-01 | 0.282 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.226021e-01 | 0.282 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 5.274907e-01 | 0.278 | 0 | 0 |
| PPARA activates gene expression | R-HSA-1989781 | 5.302332e-01 | 0.276 | 0 | 0 |
| Regulation of lipid metabolism by PPARalpha | R-HSA-400206 | 5.364135e-01 | 0.271 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.371191e-01 | 0.270 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.371191e-01 | 0.270 | 0 | 0 |
| Collagen biosynthesis and modifying enzymes | R-HSA-1650814 | 5.418599e-01 | 0.266 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 5.438263e-01 | 0.265 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 5.511973e-01 | 0.259 | 0 | 0 |
| Interleukin-17 signaling | R-HSA-448424 | 5.511973e-01 | 0.259 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 5.557948e-01 | 0.255 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.557948e-01 | 0.255 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 5.557948e-01 | 0.255 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.603455e-01 | 0.252 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 5.640898e-01 | 0.249 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.648498e-01 | 0.248 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 5.780894e-01 | 0.238 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 5.781045e-01 | 0.238 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 5.809761e-01 | 0.236 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 5.866926e-01 | 0.232 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 5.866926e-01 | 0.232 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 5.909286e-01 | 0.228 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 5.909286e-01 | 0.228 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 5.951215e-01 | 0.225 | 0 | 0 |
| Biosynthesis of DHA-derived SPMs | R-HSA-9018677 | 5.992716e-01 | 0.222 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 5.992716e-01 | 0.222 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.033794e-01 | 0.219 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 6.074454e-01 | 0.216 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 6.074454e-01 | 0.216 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.114699e-01 | 0.214 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.154534e-01 | 0.211 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.193964e-01 | 0.208 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.193964e-01 | 0.208 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 6.193964e-01 | 0.208 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 6.232991e-01 | 0.205 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.232991e-01 | 0.205 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 6.271621e-01 | 0.203 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 6.276083e-01 | 0.202 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.347703e-01 | 0.197 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 6.385163e-01 | 0.195 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 6.495268e-01 | 0.187 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 6.566813e-01 | 0.183 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 6.566813e-01 | 0.183 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 6.602039e-01 | 0.180 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 6.678539e-01 | 0.175 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 6.739387e-01 | 0.171 | 0 | 0 |
| MyD88 cascade initiated on plasma membrane | R-HSA-975871 | 6.739387e-01 | 0.171 | 0 | 0 |
| Toll Like Receptor 10 (TLR10) Cascade | R-HSA-168142 | 6.739387e-01 | 0.171 | 0 | 0 |
| Toll Like Receptor 5 (TLR5) Cascade | R-HSA-168176 | 6.739387e-01 | 0.171 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 6.805977e-01 | 0.167 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 6.838763e-01 | 0.165 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 6.838763e-01 | 0.165 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 6.997745e-01 | 0.155 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 6.997745e-01 | 0.155 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 7.021627e-01 | 0.154 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.028574e-01 | 0.153 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 7.059089e-01 | 0.151 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 7.059089e-01 | 0.151 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.089292e-01 | 0.149 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.089292e-01 | 0.149 | 0 | 0 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | R-HSA-975138 | 7.089292e-01 | 0.149 | 0 | 0 |
| MyD88 dependent cascade initiated on endosome | R-HSA-975155 | 7.119187e-01 | 0.148 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 7.148777e-01 | 0.146 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 7.148777e-01 | 0.146 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 7.176560e-01 | 0.144 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 7.213645e-01 | 0.142 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 7.235746e-01 | 0.141 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 7.315776e-01 | 0.136 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 7.320078e-01 | 0.135 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 7.347616e-01 | 0.134 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 7.401852e-01 | 0.131 | 0 | 0 |
| Peptide hormone metabolism | R-HSA-2980736 | 7.401852e-01 | 0.131 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 7.428555e-01 | 0.129 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 7.454985e-01 | 0.128 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 7.454985e-01 | 0.128 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.507038e-01 | 0.125 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 7.532667e-01 | 0.123 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 7.532667e-01 | 0.123 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.583140e-01 | 0.120 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 7.583140e-01 | 0.120 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 7.656933e-01 | 0.116 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 7.797866e-01 | 0.108 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 7.872412e-01 | 0.104 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 7.930371e-01 | 0.101 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 8.074973e-01 | 0.093 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.094794e-01 | 0.092 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.114412e-01 | 0.091 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 8.114513e-01 | 0.091 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 8.169628e-01 | 0.088 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 8.172069e-01 | 0.088 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 8.190896e-01 | 0.087 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.264295e-01 | 0.083 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 8.286334e-01 | 0.082 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 8.351895e-01 | 0.078 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.589187e-01 | 0.066 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 8.618144e-01 | 0.065 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 8.618144e-01 | 0.065 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.687980e-01 | 0.061 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 8.767166e-01 | 0.057 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 8.829512e-01 | 0.054 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 8.853564e-01 | 0.053 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 8.877124e-01 | 0.052 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 8.908102e-01 | 0.050 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 8.987899e-01 | 0.046 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.029104e-01 | 0.044 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.062165e-01 | 0.043 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.169308e-01 | 0.038 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.196700e-01 | 0.036 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 9.235654e-01 | 0.035 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.289370e-01 | 0.032 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.311226e-01 | 0.031 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.353746e-01 | 0.029 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.366297e-01 | 0.028 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.455911e-01 | 0.024 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 9.560120e-01 | 0.020 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 9.615980e-01 | 0.017 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.848902e-01 | 0.007 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.928697e-01 | 0.003 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.995649e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.996105e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.998337e-01 | 0.000 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
