BTK
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 |
|---|---|---|---|---|
| A0A2R8Y4L2 | S95 | Sugiyama | HNRNPA1L3 HNRNPA1P48 | RPHKVDGRVVEPKRAVSREDsQRPDAHLTVKKIFVGGIKED |
| A0MZ66 | Y24 | Sugiyama | SHTN1 KIAA1598 | sDEEKQLQLITsLKEQAIGEyEDLRAENQKTKEKCDKIRQE |
| 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 |
| O00165 | S153 | Sugiyama | HAX1 HS1BP1 | PDSHQPRIFGGVLESDARSEsPQPAPDWGsQRPFHRFDDVW |
| O00170 | Y202 | Sugiyama | AIP XAP2 | IHQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPE |
| O00170 | Y203 | Sugiyama | AIP XAP2 | HQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPEW |
| O00193 | Y84 | Sugiyama | SMAP C11orf58 | TSHFRTGEEDKKINEELEsQyQQsMDsKLSGRYRRHCGLGF |
| O00231 | Y397 | Sugiyama | PSMD11 | ILDQGEGVLIIFDEPPVDKtyEAALETIQNMSKVVDSLyNK |
| O00233 | Y70 | Sugiyama | PSMD9 | IGMNEPLVDCEGyPRSDVDLyQVRTARHNIICLQNDHKAVM |
| O00264 | Y113 | Sugiyama | PGRMC1 HPR6.6 PGRMC | INGKVFDVTKGRKFyGPEGPyGVFAGRDASRGLATFCLDKE |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00469 | Y586 | Sugiyama | PLOD2 | FWFPIFSEKACDELVEEMEHyGKWSGGKHHDsRIsGGyENV |
| O00567 | Y408 | Sugiyama | NOP56 NOL5A | VPTSVFGEKLREQVEERLSFyETGEIPRKNLDVMKEAMVQA |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O14579 | Y304 | Sugiyama | COPE | HPFIKEYQAKENDFDRLVLQyAPsA________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14744 | Y502 | Sugiyama | PRMT5 HRMT1L5 IBP72 JBP1 SKB1 | NEVRACREKDRDPEAQFEMPyVVRLHNFHQLSAPQPCFTFS |
| O14818 | Y176 | Sugiyama | PSMA7 HSPC | WKANAIGRGAKSVREFLEKNyTDEAIETDDLTIKLVIKALL |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14950 | Y143 | Sugiyama | MYL12B MRLC2 MYLC2B | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14964 | Y216 | Sugiyama | HGS HRS | KYSTIPKFGIEKEVRVCEPCyEQLNRKAEGKAtsttELPPE |
| O14979 | Y167 | Sugiyama | HNRNPDL HNRPDL JKTBP | DGKMFIGGLSWDTsKKDLtEyLSRFGEVVDCtIKTDPVTGR |
| O15013 | Y1307 | Sugiyama | ARHGEF10 KIAA0294 | sLsLsHGsssLEHRSEDsTIyDLLKDPVSLRSKARRAKKAK |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15230 | Y81 | Sugiyama | LAMA5 KIAA0533 KIAA1907 | SATCGEEAPARGSPRPTEDLyCKLVGGPVAGGDPNQTIRGQ |
| O15294 | Y316 | Sugiyama | OGT | YCNLANALKEKGSVAEAEDCyNTALRLCPTHADSLNNLANI |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15460 | Y342 | Sugiyama | P4HA2 UNQ290/PRO330 | LLIAPFKEEDEWDSPHIVRYyDVMsDEEIERIKEIAKPKLA |
| O43143 | Y485 | Sugiyama | DHX15 DBP1 DDX15 | SAQQRAGRAGRTRPGKCFRLyTEKAYKTEMQDNTYPEILRS |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43390 | Y435 | Sugiyama | HNRNPR HNRPR | KRKERQAARQAsRstAyEDyyyHPPPRMPPPIRGRGRGGGR |
| O43615 | Y435 | Sugiyama | TIMM44 MIMT44 TIM44 | KVLRMLYVWALCRDQDELNPyAAWRLLDISASSTEQIL___ |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43776 | Y45 | Sugiyama | NARS1 NARS NRS | PFKTGLKALMTVGKEPFPtIyVDsQKENERWNVISKsQLKN |
| O43823 | Y311 | Sugiyama | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43865 | Y291 | Sugiyama | AHCYL1 DCAL IRBIT XPVKONA | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDVMFGG |
| O60264 | Y80 | Sugiyama | SMARCA5 SNF2H WCRF135 | EIFDDAsPGKQKEIQEPDPtyEEKMQTDRANRFEYLLKQTE |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60488 | S584 | Sugiyama | ACSL4 ACS4 FACL4 LACS4 | CLQIIDRKKDLVKLQAGEyVsLGKVEAALKNCPLIDNICAF |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y276 | Sugiyama | SYNCRIP HNRPQ NSAP1 | KEQILEEFSKVTEGLTDVILyHQPDDKKKNRGFCFLEyEDH |
| O60506 | Y293 | Sugiyama | SYNCRIP HNRPQ NSAP1 | VILyHQPDDKKKNRGFCFLEyEDHKTAAQARRRLMSGKVKV |
| O60506 | Y47 | Sugiyama | SYNCRIP HNRPQ NSAP1 | FQTLLDAGLPQKVAEKLDEIyVAGLVAHsDLDERAIEALKE |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60716 | Y280 | Sugiyama | CTNND1 KIAA0384 | QPQVRVGGssVDLHRFHPEPyGLEDDQRsMGyDDLDyGMMs |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60841 | S135 | Sugiyama | EIF5B IF2 KIAA0741 | ELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKAQ |
| O60841 | Y134 | Sugiyama | EIF5B IF2 KIAA0741 | EELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKA |
| O75116 | Y722 | Sugiyama | ROCK2 KIAA0619 | EQEEAEHKATKARLADKNKIyEsIEEAKSEAMKEMEKKLLE |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75323 | Y187 | Sugiyama | NIPSNAP2 GBAS | QLLLEFSFWNEPVPRSGPNIyELRSYQLRPGTMIEWGNYWA |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75369 | T1575 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | QITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYG |
| O75369 | Y2502 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | ANEtssILVEsVTRsstETCysAIPKASSDASKVTSKGAGL |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75390 | Y80 | Sugiyama | CS | VGQITVDMMYGGMRGMKGLVyEtsVLDPDEGIRFRGFsIPE |
| O75436 | Y40 | Sugiyama | VPS26A VPS26 | DGETRKMAEMKTEDGKVEKHyLFyDGEsVSGKVNLAFKQPG |
| O75436 | Y43 | Sugiyama | VPS26A VPS26 | TRKMAEMKTEDGKVEKHyLFyDGEsVSGKVNLAFKQPGKRL |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75688 | Y367 | Sugiyama | PPM1B PP2CB | IPNLPPGGGLAGKRNVIEAVySRLNPHREsDGAsDEAEEsG |
| O75874 | Y391 | Sugiyama | IDH1 PICD | FMTKDLAACIKGLPNVQRsDyLNTFEFMDKLGENLKIKLAQ |
| O75976 | S1377 | Sugiyama | CPD | KsLLsHEFQDEtDtEEEtLyssKH_________________ |
| O75976 | Y1376 | Sugiyama | CPD | KKsLLsHEFQDEtDtEEEtLyssKH________________ |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| O95149 | Y334 | Sugiyama | SNUPN RNUT1 SPN1 | KSQKEGMKEKLTHKAsENGHyELEHLstPKLKGssHsPDHP |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95573 | S593 | Sugiyama | ACSL3 ACS3 FACL3 LACS3 | CLKIIDRKKDLVKLQAGEyVsLGKVEAALKNLPLVDNICAY |
| O95757 | Y600 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | IDLPIQssLCRQLGQDLLNsyIENEGKMIMQDKLEKERNDA |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O95757 | Y663 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | ITPEDLSKLSAVLEDTENWLyEDGEDQPKQVYVDKLQELKK |
| O95834 | Y352 | Sugiyama | EML2 EMAP2 EMAPL2 | EVPEDFGPVRTVAEGHGDtLyVGtTRNSILQGSVHTGFSLL |
| O95861 | Y293 | Sugiyama | BPNT1 | HKDVKHMNSAGVLAtLRNyDyyASRVPESIKNALVP_____ |
| O96019 | T67 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | RDDGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsP |
| O96019 | Y69 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | DGsTLMEIDGDKGKQGGPtyyIDtNALRVPRENMEAIsPLK |
| P00338 | Y10 | Sugiyama | LDHA PIG19 | ___________MAtLKDQLIyNLLKEEQtPQNKITVVGVGA |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00390 | Y371 | Sugiyama | GSR GLUR GRD1 | TDDKGHIIVDEFQNtNVKGIyAVGDVCGKALLtPVAIAAGR |
| P00491 | Y166 | Sugiyama | PNP NP | PLRGPNDERFGDRFPAMsDAyDRtMRQRALstWKQMGEQRE |
| P00505 | Y96 | Sugiyama | GOT2 KYAT4 | VLPSVRKAEAQIAAKNLDKEyLPIGGLAEFCKASAELALGE |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00558 | Y196 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | MVGVNLPQKAGGFLMKKELNyFAKALEsPERPFLAILGGAK |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P02545 | Y45 | Sugiyama | LMNA LMN1 | RItRLQEKEDLQELNDRLAVyIDRVRsLETENAGLRLRItE |
| P02786 | Y168 | Sugiyama | TFRC | NENsyVPREAGsQKDENLALyVENQFREFKLSKVWRDQHFV |
| P04075 | S46 | Sugiyama | ALDOA ALDA | PGKGILAADEstGsIAKRLQsIGtENtEENRRFyRQLLLtA |
| P04181 | Y50 | Sugiyama | OAT | TKKtVQGPPtSDDIFEREyKyGAHNyHPLPVALERGKGIyL |
| P04181 | Y55 | Sugiyama | OAT | QGPPtSDDIFEREyKyGAHNyHPLPVALERGKGIyLWDVEG |
| P04406 | Y314 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | tFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsK |
| P04406 | Y320 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsKE_____ |
| P04406 | Y94 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | ItIFQERDPsKIKWGDAGAEyVVEstGVFttMEKAGAHLQG |
| P04637 | S15 | EPSD|PSP | TP53 P53 | ______MEEPQsDPsVEPPLsQEtFsDLWKLLPENNVLsPL |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P04818 | Y135 | Sugiyama | TYMS TS OK/SW-cl.29 | RDFLDsLGFsTREEGDLGPVyGFQWRHFGAEyRDMEsDysG |
| P04843 | Y387 | Sugiyama | RPN1 | SLTVKIILPEGAKNIEIDsPyEISRAPDELHYTYLDTFGRP |
| P05187 | Y182 | Sugiyama | ALPP PLAP | GKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADVPASARQ |
| P05362 | Y455 | Sugiyama | ICAM1 | GtFPLPIGEsVtVtRDLEGtyLCRARSTQGEVTRKVTVNVL |
| P05787 | S280 | Sugiyama | KRT8 CYK8 | IAEVKAQyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDL |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y282 | Sugiyama | KRT8 CYK8 | EVKAQyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRR |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06576 | Y418 | Sugiyama | ATP5F1B ATP5B ATPMB ATPSB | VDPLDSTSRIMDPNIVGsEHyDVARGVQKILQDYKSLQDII |
| P06730 | Y34 | Sugiyama | EIF4E EIF4EL1 EIF4F | PPttEEEKtEsNQEVANPEHyIKHPLQNRWALWFFKNDKsK |
| P06733 | S272 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | FRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsI |
| P06733 | T41 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EVDLFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKG |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07205 | Y196 | Sugiyama | PGK2 PGKB | MVGVNLPHKASGFLMKKELDyFAKALENPVRPFLAILGGAK |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07355 | Y199 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RAEDGsVIDyELIDQDARDLyDAGVKRKGTDVPKWIsIMTE |
| P07437 | T107 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAESC |
| P07437 | Y106 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAES |
| P07437 | Y50 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IDPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEP |
| P07437 | Y51 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPG |
| P07686 | Y547 | Sugiyama | HEXB HCC7 | DRLTRHRCRMVERGIAAQPLyAGyCNHENM___________ |
| P07711 | Y112 | Sugiyama | CTSL CTSL1 | MNGFQNRKPRKGKVFQEPLFyEAPRSVDWREKGyVTPVKNQ |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07814 | Y1505 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PLCELQPGAKCVCGKNPAKyytLFGRsy_____________ |
| P07814 | Y684 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | LKKGDIIQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPD |
| P07814 | Y690 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | IQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPDGHtKEM |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07858 | Y244 | Sugiyama | CTSB CPSB | HYGYNSYSVSNSEKDIMAEIyKNGPVEGAFSVYSDFLLYKS |
| P07900 | S53 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | IINtFySNKEIFLRELIsNssDALDKIRyEsLtDPsKLDsG |
| 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 | Y445 | Sugiyama | LAMB1 | QCRCKLNVEGEHCDVCKEGFyDLssEDPFGCKSCACNPLGT |
| P07954 | Y54 | Sugiyama | FH | PSFWPPNAARMAsQNSFRIEyDtFGELKVPNDKYYGAQTVR |
| 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 | Y457 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | LKLGIHEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMK |
| 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 |
| P08670 | Y291 | Sugiyama | VIM | DVRQQyEsVAAKNLQEAEEWyKSKFADLsEAANRNNDALRQ |
| P08670 | Y53 | Sugiyama | VIM | tsTRtYsLGsALRPstsRsLyAssPGGVyAtRssAVRLRss |
| P08670 | Y61 | Sugiyama | VIM | GsALRPstsRsLyAssPGGVyAtRssAVRLRssVPGVRLLQ |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| P08758 | S135 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | AsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRMLVV |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P09001 | Y265 | Sugiyama | MRPL3 MRL3 RPML3 | TGDIGRVWPGTKMPGKMGNIyRTEYGLKVWRINTKHNIIYV |
| P09104 | T41 | Sugiyama | ENO2 | EVDLyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKG |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09651 | S95 | Sugiyama | HNRNPA1 HNRPA1 | RPHKVDGRVVEPKRAVsREDsQRPGAHLtVKKIFVGGIKED |
| P09651 | Y253 | Sugiyama | HNRNPA1 HNRPA1 | GGGGYGGSGDGyNGFGNDGGyGGGGPGYSGGSRGYGSGGQG |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09874 | Y794 | Sugiyama | PARP1 ADPRT PPOL | AySLLRGGsDDssKDPIDVNyEKLKTDIKVVDRDSEEAEII |
| P09923 | Y179 | Sugiyama | ALPI | GKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADMPASARQ |
| P09960 | Y233 | Sugiyama | LTA4H LTA4 | RQIGPRTLVWSEKEQVEKSAyEFsETEsMLKIAEDLGGPYV |
| P09972 | Y358 | Sugiyama | ALDOC ALDC | AAQGKYEGSGEDGGAAAQsLyIANHAY______________ |
| P0C0L4 | Y946 | Sugiyama | C4A CO4 CPAMD2 | AVSKVLQIEKEGAIHREELVyELNPLDHRGRTLEIPGNSDP |
| P0C0L5 | Y946 | Sugiyama | C4B CO4 CPAMD3; C4B_2 | AVSKVLQIEKEGAIHREELVyELNPLDHRGRTLEIPGNSDP |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG38 | Y791 | Sugiyama | POTEI | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y754 | Sugiyama | POTEJ | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0DPH7 | Y103 | Sugiyama | TUBA3C TUBA2 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIVDLVLDRIR |
| P0DPH7 | Y224 | Sugiyama | TUBA3C TUBA2 | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| P10398 | Y155 | Sugiyama | ARAF ARAF1 PKS PKS2 | HCSSKVPTVCVDMSTNRQQFyHsVQDLsGGsRQHEAPsNRP |
| P10586 | Y224 | Sugiyama | PTPRF LAR | KYECVATNSAGTRYSAPANLyVRVRRVAPRFSIPPSSQEVM |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11142 | S40 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P11142 | Y149 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | EIAEAyLGKtVTNAVVtVPAyFNDsQRQAtKDAGtIAGLNV |
| P11142 | Y371 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | QDFFNGKELNKsINPDEAVAyGAAVQAAILsGDKSENVQDL |
| P11142 | Y41 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11413 | Y112 | Sugiyama | G6PD | PEEKLKLEDFFARNsyVAGQyDDAAsyQRLNsHMNALHLGs |
| P11940 | Y194 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLFGKF |
| P11940 | Y297 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLRKEFsPF |
| P11940 | Y382 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | PLyVALAQRKEERQAHLtNQyMQRMASVRAVPNPVINPYQP |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y422 | Sugiyama | ACTN1 | KAsIHEAWtDGKEAMLRQKDyEtAtLsEIKALLKKHEAFEs |
| P12814 | Y842 | Sugiyama | ACTN1 | DTDTADQVMASFKILAGDKNyITMDELRRELPPDQAEyCIA |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P12956 | Y103 | Sugiyama | XRCC6 G22P1 | LAVVFYGTEKDKNSVNFKNIyVLQELDNPGAKRILELDQFK |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | S732 | Sugiyama | EEF2 EF2 | DAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQCP |
| P13639 | T582 | Sugiyama | EEF2 EF2 | EEDHACIPIKKSDPVVsyREtVsEEsNVLCLsKsPNKHNRL |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y579 | Sugiyama | EEF2 EF2 | KDLEEDHACIPIKKSDPVVsyREtVsEEsNVLCLsKsPNKH |
| P13639 | Y639 | Sugiyama | EEF2 EF2 | KGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGPDGTGP |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | Y323 | Sugiyama | PDIA4 ERP70 ERP72 | GDDVIIIGVFKGESDPAyQQyQDAANNLREDYKFHHTFSTE |
| P13667 | Y448 | Sugiyama | PDIA4 ERP70 ERP72 | RAATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLs |
| P13667 | Y458 | Sugiyama | PDIA4 ERP70 ERP72 | VLEVAKDFPEytFAIADEEDyAGEVKDLGLsEsGEDVNAAI |
| P13674 | Y141 | Sugiyama | P4HA1 P4HA | FPNDEDQVGAAKALLRLQDtyNLDTDtIsKGNLPGVKHKSF |
| P13674 | Y282 | Sugiyama | P4HA1 P4HA | ASDDQSDQKTTPKKKGVAVDyLPERQKyEMLCRGEGIKMTP |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13929 | T41 | Sugiyama | ENO3 | EVDLHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKG |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y87 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | FEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTSL |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| 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 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14625 | Y678 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | MERIMKAQAYQtGKDIstNyyAsQKKTFEINPRHPLIRDML |
| P14649 | S87 | Sugiyama | MYL6B MLC1SA | EEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVLK |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14868 | Y143 | Sugiyama | DARS1 DARS PIG40 | VNQKIGSCTQQDVELHVQKIyVISLAEPRLPLQLDDAVRPE |
| P14868 | Y389 | Sugiyama | DARS1 DARS PIG40 | stPNEKLLGHLVKEKyDTDFyILDKYPLAVRPFYTMPDPRN |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15311 | Y424 | Sugiyama | EZR VIL2 | ERQAVDQIKsQEQLAAELAEytAKIALLEEARRRKEDEVEE |
| P15391 | Y500 | iPTMNet | CD19 | SPHGSAWDPSREATSLGSQsyEDMRGILyAAPQLRSIRGQP |
| P15391 | Y531 | iPTMNet | CD19 | PQLRSIRGQPGPNHEEDADSyENMDNPDGPDPAWGGGGRMG |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y250 | Sugiyama | RPS2 RPS4 | tAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEFt |
| P16885 | Y1197 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | PLCG2 | LASLLVFCEMRPVLESEEELySSCRQLRRRQEELNNQLFLy |
| P16885 | Y1217 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PLCG2 | ySSCRQLRRRQEELNNQLFLyDtHQNLRNANRDALVKEFsV |
| P16885 | Y753 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PLCG2 | YPVTPELLERyNMERDINSLyDVSRMyVDPSEINPSMPQRT |
| P16885 | Y759 | SIGNOR|ELM|iPTMNet|EPSD|PSP | PLCG2 | LLERyNMERDINSLyDVSRMyVDPSEINPSMPQRTVKALYD |
| P17066 | S42 | Sugiyama | HSPA6 HSP70B' | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P17066 | Y43 | Sugiyama | HSPA6 HSP70B' | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P17812 | S575 | Sugiyama | CTPS1 CTPS | LQKGCRLsPRDtysDRsGsssPDsEItELKFPsINHD____ |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17980 | T163 | Sugiyama | PSMC3 TBP1 | EKLKPGDLVGVNKDSyLILEtLPtEyDsRVKAMEVDERPtE |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18031 | Y20 | Sugiyama | PTPN1 PTP1B | _MEMEKEFEQIDKsGsWAAIyQDIRHEASDFPCRVAKLPKN |
| 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 | Y26 | Sugiyama | PGAM1 PGAMA CDABP0006 | LVLIRHGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALR |
| P18669 | Y92 | Sugiyama | PGAM1 PGAMA CDABP0006 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| P18754 | Y89 | Sugiyama | RCC1 CHC1 | VVQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSE |
| P19105 | Y142 | Sugiyama | MYL12A MLCB MRLC3 RLC | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19338 | Y462 | Sugiyama | NCL | AEKTFEEKQGtEIDGRsIsLyytGEKGQNQDYRGGKNSTWs |
| P19784 | Y13 | Sugiyama | CSNK2A2 CK2A2 | ________MPGPAAGSRARVyAEVNsLRsREYWDYEAHVPS |
| P19838 | Y240 | Sugiyama | NFKB1 | LPDSTGSFTRRLEPVVSDAIyDSKAPNASNLKIVRMDRTAG |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20700 | Y46 | Sugiyama | LMNB1 LMN2 LMNB | RLsRLQEKEELRELNDRLAVyIDKVRsLEtENsALQLQVTE |
| P21127 | Y449 | Sugiyama | CDK11B CDC2L1 CDK11 PITSLREA PK58 | LQGCRsVEEFQCLNRIEEGtyGVVYRAKDKKTDEIVALKRL |
| P21333 | Y2379 | Sugiyama | FLNA FLN FLN1 | GAKGAIDAKVHsPsGALEECyVtEIDQDKYAVRFIPRENGV |
| P21333 | Y373 | Sugiyama | FLNA FLN FLN1 | THKVTVLFAGQHIAKsPFEVyVDKsQGDASKVTAQGPGLEP |
| P21333 | Y643 | Sugiyama | FLNA FLN FLN1 | CDDKGDGsCDVRyWPQEAGEyAVHVLCNsEDIRLsPFMADI |
| P21333 | Y731 | Sugiyama | FLNA FLN FLN1 | VQDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWGG |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P21980 | Y583 | Sugiyama | TGM2 | VRALLVEPVINSYLLAERDLyLENPEIKIRILGEPKQKRKL |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22314 | Y560 | Sugiyama | UBA1 A1S9T UBE1 | NPHIRVTSHQNRVGPDtERIyDDDFFQNLDGVANALDNVDA |
| P22314 | Y60 | Sugiyama | UBA1 A1S9T UBE1 | GMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSVLVSGL |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22626 | S259 | Sugiyama | HNRNPA2B1 HNRPA2B1 | GFGDGyNGyGGGPGGGNFGGsPGyGGGRGGYGGGGPGYGNQ |
| P22626 | Y247 | Sugiyama | HNRNPA2B1 HNRPA2B1 | FRGGsDGyGsGRGFGDGyNGyGGGPGGGNFGGsPGyGGGRG |
| P22626 | Y331 | Sugiyama | HNRNPA2B1 HNRPA2B1 | SNYGPMKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRs |
| P22626 | Y336 | Sugiyama | HNRNPA2B1 HNRPA2B1 | MKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRsRy___ |
| P23193 | Y126 | Sugiyama | TCEA1 GTF2S TFIIS | EsTSsGNVsNRKDETNARDTyVsSFPRAPstsDsVRLKCRE |
| P23246 | Y488 | Sugiyama | SFPQ PSF | PMYQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQV |
| P23246 | Y490 | Sugiyama | SFPQ PSF | YQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQVEK |
| P23284 | Y119 | Sugiyama | PPIB CYPB | DFMIQGGDFtRGDGtGGKsIyGERFPDENFKLKHyGPGWVs |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23468 | Y224 | Sugiyama | PTPRD | KYECVATNSAGTRYSAPANLyVRELREVRRVPPRFSIPPTN |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | T70 | Sugiyama | CFL1 CFL | EEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAtyE |
| P23528 | Y140 | Sugiyama | CFL1 CFL | SKDAIKKKLtGIKHELQANCyEEVKDRCTLAEKLGGsAVIs |
| P23528 | Y68 | Sugiyama | CFL1 CFL | ILEEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAt |
| P23528 | Y85 | Sugiyama | CFL1 CFL | DDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWA |
| P23528 | Y89 | Sugiyama | CFL1 CFL | AtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| 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 | T220 | Sugiyama | ACAT1 ACAT MAT | TAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNEVIPVtV |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24752 | Y90 | Sugiyama | ACAT1 ACAT MAT | IAIQGAIEKAGIPKEEVKEAyMGNVLQGGEGQAPTRQAVLG |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P25205 | Y188 | Sugiyama | MCM3 | FPSSSVYPTKDEENNPLETEyGLSVyKDHQtITIQEMPEKA |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y45 | Sugiyama | MCM3 | DEEDQGIyQsKVRELIsDNQyRLIVNVNDLRRKNEKRANRL |
| P25205 | Y456 | Sugiyama | MCM3 | AGIHARLNARCsVLAAANPVyGRyDQyKTPMENIGLQDSLL |
| P25205 | Y708 | Sugiyama | MCM3 | KRKRRKTRQPDAKDGDsyDPyDFsDtEEEMPQVHtPKTADs |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25685 | Y176 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | ARKKQDPPVTHDLRVsLEEIysGCtKKMKISHKRLNPDGKS |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P25787 | Y57 | Sugiyama | PSMA2 HC3 PSC3 | GIKAANGVVLATEKKQKSILyDERSVHKVEPITKHIGLVys |
| P25963 | Y289 | PSP | NFKBIA IKBA MAD3 NFKBI | LGQLTLENLQMLPEsEDEEsyDtEsEFTEFtEDELPyDDCV |
| P25963 | Y305 | PSP | NFKBIA IKBA MAD3 NFKBI | DEEsyDtEsEFTEFtEDELPyDDCVFGGQRLTL________ |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26373 | S77 | Sugiyama | RPL13 BBC1 OK/SW-cl.46 | PIVRCPTVRYHTKVRAGRGFsLEELRVAGIHKKVARTIGIs |
| P26599 | Y127 | Sugiyama | PTBP1 PTB | ANTMVNYYTSVTPVLRGQPIyIQFsNHKELKtDSSPNQARA |
| P26639 | Y252 | Sugiyama | TARS1 TARS | YNKFKCRILNEKVNtPtttVyRCGPLIDLCRGPHVRHTGKI |
| 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 | Y211 | Sugiyama | YWHAQ | LAKTAFDEAIAELDtLNEDsyKDstLIMQLLRDNLTLWtsD |
| 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 |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P27824 | Y70 | Sugiyama | CANX | TAPPSSPKVTYKAPVPtGEVyFADsFDRGTLSGWILSKAKK |
| P28062 | Y271 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | MKEDGWVKVEsTDVSDLLHQyREANQ_______________ |
| P28066 | Y185 | Sugiyama | PSMA5 | CDARAIGsAsEGAQssLQEVyHKSMTLKEAIKSSLIILKQV |
| P28074 | Y212 | Sugiyama | PSMB5 LMPX MB1 X | VYAYGVMDRGYSYDLEVEQAyDLARRAIyQATYRDAysGGA |
| P28074 | Y236 | Sugiyama | PSMB5 LMPX MB1 X | RRAIyQATYRDAysGGAVNLyHVREDGWIRVSsDNVADLHE |
| P29144 | Y1042 | Sugiyama | TPP2 | TEALRDLKIQWMTKLDSsDIyNELKEtyPNyLPLyVARLHQ |
| P29144 | Y1056 | Sugiyama | TPP2 | LDSsDIyNELKEtyPNyLPLyVARLHQLDAEKERMKRLNEI |
| 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 | Y205 | Sugiyama | BLVRB FLR SCAN | MLRCLttDEyDGHstyPsHQyQ___________________ |
| P30084 | Y112 | Sugiyama | ECHS1 | KAFAAGADIKEMQNLsFQDCySSKFLKHWDHLTQVKKPVIA |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| P30086 | Y176 | Sugiyama | PEBP1 PBP PEBP | KKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK_________ |
| P30086 | Y181 | Sugiyama | PEBP1 PBP PEBP | RAPVAGtCyQAEWDDyVPKLyEQLsGK______________ |
| P30086 | Y64 | Sugiyama | PEBP1 PBP PEBP | tQVKNRPtsIsWDGLDsGKLytLVLtDPDAPsRKDPKYREW |
| P30101 | S478 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | ANKKLNPKKyEGGRELsDFIsyLQREAtNPPVIQEEKPKKK |
| P30101 | Y115 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | yGVsGyPtLKIFRDGEEAGAyDGPRtADGIVsHLKKQAGPA |
| P30101 | Y445 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KDPNIVIAKMDAtANDVPsPyEVRGFPtIyFsPANKKLNPK |
| P30101 | Y479 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | NKKLNPKKyEGGRELsDFIsyLQREAtNPPVIQEEKPKKKK |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30876 | Y845 | Sugiyama | POLR2B | QEEVFEKPTRETCQGMRHAIyDKLDDDGLIAPGVRVSGDDV |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31483 | Y10 | Sugiyama | TIA1 | ___________MEDEMPKTLyVGNLSRDVTEALILQLFSQI |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31946 | Y213 | Sugiyama | YWHAB | LAKTAFDEAIAELDtLNEEsyKDstLIMQLLRDNLtLWtSE |
| P31946 | Y50 | Sugiyama | YWHAB | AVtEQGHELsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P31947 | Y151 | Sugiyama | SFN HME1 | LAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIRLG |
| P31947 | Y19 | Sugiyama | SFN HME1 | __MERASLIQKAKLAEQAERyEDMAAFMKGAVEKGEELsCE |
| P31947 | Y213 | Sugiyama | SFN HME1 | LAKTtFDEAMADLHtLsEDsyKDstLIMQLLRDNLtLWTAD |
| P31947 | Y48 | Sugiyama | SFN HME1 | GAVEKGEELsCEERNLLsVAyKNVVGGQRAAWRVLSsIEQK |
| P31948 | Y323 | Sugiyama | STIP1 | YARIGNSyFKEEKYKDAIHFyNKSLAEHRtPDVLKKCQQAE |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33121 | Y693 | Sugiyama | ACSL1 FACL1 FACL2 LACS LACS1 LACS2 | TMKAKRPELRNYFRSQIDDLyStIKV_______________ |
| P33176 | Y62 | Sugiyama | KIF5B KNS KNS1 | ASKPYAFDRVFQSsTsQEQVyNDCAKKIVKDVLEGyNGtIF |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33991 | Y193 | Sugiyama | MCM4 CDC21 | FIDPLAKEEENVGIDITEPLyMQRLGEINVIGEPFLNVNCE |
| P33992 | Y403 | Sugiyama | MCM5 CDC46 | PGTAKSQLLKFVEKCsPIGVytsGKGSSAAGLtAsVMRDPs |
| P33993 | Y102 | Sugiyama | MCM7 CDC47 MCM2 | QELLPQYKEREVVNKDVLDVyIEHRLMMEQRSRDPGMVRsP |
| P33993 | Y333 | Sugiyama | MCM7 CDC47 MCM2 | EsGAGELtREELRQIAEEDFyEKLAASIAPEIYGHEDVKKA |
| P34896 | Y34 | Sugiyama | SHMT1 | LWSsHDKMLAQPLKDSDVEVyNIIKKESNRQRVGLELIASE |
| P34931 | S42 | Sugiyama | HSPA1L | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P34931 | Y43 | Sugiyama | HSPA1L | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P34931 | Y547 | Sugiyama | HSPA1L | YKAEDEVQREKIAAKNALEsyAFNMKSVVSDEGLKGKISES |
| P34932 | Y30 | Sugiyama | HSPA4 APG2 HSPH2 | FQSCYVAVARAGGIETIANEysDRCtPACIsFGPKNRSIGA |
| P34932 | Y336 | Sugiyama | HSPA4 APG2 HSPH2 | RVEPPLRSVLEQTKLKKEDIyAVEIVGGATRIPAVKEKISK |
| P34932 | Y597 | Sugiyama | HSPA4 APG2 HSPH2 | VDLPIENQLLWQIDREMLNLyIENEGKMIMQDKLEKERNDA |
| P34932 | Y626 | Sugiyama | HSPA4 APG2 HSPH2 | MQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDDRN |
| P34932 | Y660 | Sugiyama | HSPA4 APG2 HSPH2 | VSEDDRNsFtLKLEDTENWLyEDGEDQPKQVYVDKLAELKN |
| P35080 | Y79 | Sugiyama | PFN2 | FFtNGLtLGAKKCSVIRDSLyVDGDCtMDIRTKsQGGEPTy |
| P35221 | S641 | Sugiyama | CTNNA1 | GIRDIRKAVLMIRtPEELDDsDFEtEDFDVRsRtsVQtEDD |
| P35270 | Y259 | Sugiyama | SPR | QKLLSLLEKDEFKSGAHVDFyDK__________________ |
| P35579 | Y11 | Sugiyama | MYH9 | __________MAQQAADKyLyVDKNFINNPLAQADWAAKKL |
| P35579 | Y754 | Sugiyama | MYH9 | MDGKQACVLMIKALELDsNLyRIGQSKVFFRAGVLAHLEEE |
| P35637 | Y325 | Sugiyama | FUS TLS | FKQIGIIKTNKKTGQPMINLyTDRETGKLKGEAtVsFDDPP |
| P35637 | Y468 | Sugiyama | FUS TLS | KAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRGGYRGRG |
| P36578 | Y211 | Sugiyama | RPL4 RPL1 | AGKGKMRNRRRIQRRGPCIIyNEDNGIIKAFRNIPGITLLN |
| P37802 | T190 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | GKNVIGLQMGtNRGAsQAGMtGyGMPRQIL___________ |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P38646 | T120 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | LVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIKNV |
| P38646 | T87 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | VAVMEGKQAKVLENAEGARttPsVVAFtADGERLVGMPAKR |
| P38646 | Y118 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | ERLVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIK |
| P38646 | Y196 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | EtAENyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNV |
| P38919 | Y54 | Sugiyama | EIF4A3 DDX48 KIAA0111 | VDVTPTFDTMGLREDLLRGIyAyGFEKPsAIQQRAIKQIIK |
| P38919 | Y56 | Sugiyama | EIF4A3 DDX48 KIAA0111 | VTPTFDTMGLREDLLRGIyAyGFEKPsAIQQRAIKQIIKGR |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P39023 | S13 | Sugiyama | RPL3 OK/SW-cl.32 | ________MSHRKFSAPRHGsLGFLPRKRSSRHRGKVKSFP |
| P39023 | S265 | Sugiyama | RPL3 OK/SW-cl.32 | HRGLRKVACIGAWHPARVAFsVARAGQKGYHHRTEINKKIY |
| P39687 | T143 | Sugiyama | ANP32A C15orf1 LANP MAPM PHAP1 | CEVtNLNDyRENVFKLLPQLtyLDGyDRDDKEAPDsDAEGY |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41219 | Y287 | Sugiyama | PRPH NEF4 PRPH1 | DIRAQYESIAAKNLQEAEEWyKSKYADLSDAANRNHEALRQ |
| P41227 | Y138 | Sugiyama | NAA10 ARD1 ARD1A TE2 | ALHLYSNTLNFQISEVEPKyyADGEDAyAMKRDLtQMADEL |
| P41227 | Y145 | Sugiyama | NAA10 ARD1 ARD1A TE2 | TLNFQISEVEPKyyADGEDAyAMKRDLtQMADELRRHLELK |
| P41252 | Y680 | Sugiyama | IARS1 IARS | YRFLIQNVLRLQKEEEIEFLyNENTVRESPNITDRWILSFM |
| P42166 | S159 | Sugiyama | TMPO LAP2 | RKLYEKKLLKLREQGtEsRsstPLPtIsssAENtRQNGsND |
| P42166 | T160 | Sugiyama | TMPO LAP2 | KLYEKKLLKLREQGtEsRsstPLPtIsssAENtRQNGsNDs |
| P42167 | S159 | Sugiyama | TMPO LAP2 | RKLYEKKLLKLREQGTESRsstPLPTISsSAENTRQNGSND |
| P42167 | T160 | Sugiyama | TMPO LAP2 | KLYEKKLLKLREQGTESRsstPLPTISsSAENTRQNGSNDS |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P42229 | Y694 | SIGNOR|iPTMNet | STAT5A STAT5 | PKDEVFSKYYTPVLAKAVDGyVKPQIKQVVPEFVNASADAG |
| P42680 | Y206 | SIGNOR|ELM|iPTMNet|EPSD|PSP | TEC PSCTK4 | AMyDFQAAEGHDLRLERGQEyLILEKNDVHWWRARDKYGNE |
| P42768 | Y291 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | WAS IMD2 | FSRAGIsEAQLtDAETsKLIyDFIEDQGGLEAVRQEMRRQE |
| P43121 | Y222 | Sugiyama | MCAM MUC18 | YTLQSILKAQLVKEDKDAQFyCELNYRLPSGNHMKEsREVT |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43487 | S60 | Sugiyama | RANBP1 | TLEEDEEELFKMRAKLFRFAsENDLPEWKERGTGDVKLLKH |
| P45974 | Y851 | Sugiyama | USP5 ISOT | IYNDQKVCASEKPPKDLGyIyFyQRVAS_____________ |
| P46776 | Y52 | Sugiyama | RPL27A | RGNAGGLHHHRINFDKyHPGyFGKVGMKHYHLKRNQsFCPt |
| P46777 | Y219 | Sugiyama | RPL5 MSTP030 | IMGQNVADyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEM |
| P46777 | Y226 | Sugiyama | RPL5 MSTP030 | DyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEMyKKAHAA |
| P46777 | Y240 | Sugiyama | RPL5 MSTP030 | KKQFsQyIKNsVtPDMMEEMyKKAHAAIRENPVyEKKPKKE |
| P46777 | Y253 | Sugiyama | RPL5 MSTP030 | PDMMEEMyKKAHAAIRENPVyEKKPKKEVKKKRWNRPKMsL |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46781 | Y35 | Sugiyama | RPS9 | TPRRPFEKSRLDQELKLIGEyGLRNKREVWRVKFTLAKIRK |
| P46940 | Y1095 | Sugiyama | IQGAP1 KIAA0051 | VVKEIMDDKSLNIKTDPVDIyKsWVNQMESQTGEASKLPyD |
| P46940 | Y140 | Sugiyama | IQGAP1 KIAA0051 | LNAMDEIGLPKIFYPETTDIyDRKNMPRCIYCIHALSLYLF |
| P47224 | Y114 | Sugiyama | RABIF MSS4 RASGRF3 | CADCEIGPIGWHCLDDKNSFyVALERVSHE___________ |
| P47756 | Y59 | Sugiyama | CAPZB | LLSSVDQPLKIARDKVVGKDyLLCDyNRDGDSyRsPWSNKy |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48163 | Y208 | Sugiyama | ME1 | CLPVILDVGTENEELLKDPLyIGLRQRRVRGsEYDDFLDEF |
| P48637 | Y375 | Sugiyama | GSS | LAAPSRFVLKPQREGGGNNLyGEEMVQALKQLKDSEERAsy |
| P48741 | S42 | Sugiyama | HSPA7 HSP70B | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P48741 | Y43 | Sugiyama | HSPA7 HSP70B | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| 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 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49458 | Y18 | Sugiyama | SRP9 | ___MPQYQTWEEFSRAAEKLyLADPMKARVVLKYRHsDGNL |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y535 | Sugiyama | AARS1 AARS | FVEEVSTGQECGVVLDKTCFyAEQGGQIyDEGYLVKVDDss |
| P49588 | Y543 | Sugiyama | AARS1 AARS | QECGVVLDKTCFyAEQGGQIyDEGYLVKVDDssEDKTEFTV |
| P49588 | Y667 | Sugiyama | AARS1 AARS | QQIKKAEEIANEMIEAAKAVyTQDCPLAAAKAIQGLRAVFD |
| P49591 | Y248 | Sugiyama | SARS1 SARS SERS | FMRKEVMQEVAQLsQFDEELyKVIGKGSEKSDDNSYDEKYL |
| P49736 | Y234 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | VFKERIsDMCKENREsLVVNyEDLAAREHVLAYFLPEAPAE |
| P49792 | S3137 | Sugiyama | RANBP2 NUP358 | IPDFVCQGGDITKHDGTGGQsIyGDKFEDENFDVKHTGPGL |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50395 | Y404 | Sugiyama | GDI2 RABGDIB | SDLLVPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRM |
| P50454 | Y135 | Sugiyama | SERPINH1 CBP1 CBP2 HSP47 SERPINH2 PIG14 | LRSLSNSTARNVTWKLGsRLyGPssVsFADDFVRssKQHYN |
| P50454 | Y246 | Sugiyama | SERPINH1 CBP1 CBP2 HSP47 SERPINH2 PIG14 | VTRSYTVGVMMMHRTGLyNyyDDEKEKLQIVEMPLAHKLsS |
| P50502 | Y185 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | NAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50990 | Y426 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | KRLVPGGGAtEIELAKQItsyGETCPGLEQyAIKKFAEAFE |
| P50990 | Y436 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | EIELAKQItsyGETCPGLEQyAIKKFAEAFEAIPRALAENS |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50995 | Y365 | Sugiyama | ANXA11 ANX11 | NRDESTNVDMSLAQRDAQELyAAGENRLGTDESKFNAVLCS |
| P51116 | S620 | Sugiyama | FXR2 FMR1L2 | GsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPsEDsLsG |
| P51116 | T610 | Sugiyama | FXR2 FMR1L2 | RRRNRGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLER |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51452 | Y38 | Sugiyama | DUSP3 VHR | DGSGCYsLPSQPCNEVTPRIyVGNAsVAQDIPKLQKLGITH |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51813 | Y216 | SIGNOR|ELM|iPTMNet|EPSD|PSP | BMX | NESKKNyGSQPPsSSTSLAQyDSNSKKIyGSQPNFNMQYIP |
| P51813 | Y224 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | BMX | SQPPsSSTSLAQyDSNSKKIyGSQPNFNMQYIPREDFPDWW |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P51991 | Y360 | Sugiyama | HNRNPA3 HNRPA3 | QSNYGPMKGGsFGGRssGsPyGGGyGsGGGsGGyGsRRF__ |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52565 | Y144 | Sugiyama | ARHGDIA GDIA1 | SGMKYIQHTyRKGVKIDKtDyMVGsYGPRAEEyEFLtPVEE |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52948 | Y1215 | Sugiyama | NUP98 ADAR2 | KVHLEKLSLRQRKPDEDMKLyQTPLELKLKHSTVHVDELCP |
| P53041 | Y313 | Sugiyama | PPP5C PPP5 | YPDHFHLLRGNHETDNMNQIyGFEGEVKAKYTAQMYELFSE |
| P53396 | Y252 | Sugiyama | ACLY | KWGDIEFPPPFGREAyPEEAyIADLDAKSGASLKLTLLNPK |
| P53396 | Y659 | Sugiyama | ACLY | TGGMLDNILASKLyRPGsVAyVSRsGGMsNELNNIISRTTD |
| P53621 | Y391 | Sugiyama | COPA | NPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGK |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P53675 | Y921 | Sugiyama | CLTCL1 CLH22 CLTCL CLTD | DSSVVGRYCEKRDPHLACVAyERGQCDLELIKVCNENSLFK |
| P54105 | Y38 | Sugiyama | CLNS1A CLCI ICLN | RQQPDTEAVLNGKGLGtGtLyIAEsRLSWLDGsGLGFSLEY |
| P54136 | Y384 | Sugiyama | RARS1 RARS | VFVPGCSIPLTIVKsDGGytyDtSDLAAIKQRLFEEKADMI |
| P54577 | Y134 | Sugiyama | YARS1 YARS | KLKFIKGTDYQLSKEytLDVyRLSSVVTQHDSKKAGAEVVK |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54577 | Y388 | Sugiyama | YARS1 YARS | LDIRVGKIITVEKHPDADsLyVEKIDVGEAEPRTVVSGLVQ |
| P54652 | S41 | Sugiyama | HSPA2 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P54652 | Y42 | Sugiyama | HSPA2 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P55060 | Y278 | Sugiyama | CSE1L CAS XPO2 | EEEAGLLELLKSQICDNAALyAQKyDEEFQRYLPRFVTAIW |
| P55084 | T359 | Sugiyama | HADHB MSTP029 | DFMYVSQDPKDQLLLGPtYAtPKVLEKAGLTMNDIDAFEFH |
| P55084 | Y244 | Sugiyama | HADHB MSTP029 | GHSADRLAAAFAVSRLEQDEyALRsHSLAKKAQDEGLLSDV |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y66 | Sugiyama | NAP1L1 NRP | PQILAALQERLDGLVEtPtGyIEsLPRVVKRRVNALKNLQV |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55884 | Y768 | Sugiyama | EIF3B EIF3S9 | ERRRTMMEDFRKYRKMAQELyMEQKNERLELRGGVDTDELD |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58753 | Y106 | EPSD|PSP | TIRAP MAL | yDVCVCHSEEDLVAAQDLVSyLEGSTASLRCFLQLRDATPG |
| P58753 | Y187 | EPSD|PSP | TIRAP MAL | EAPGAEGCTIPLLSGLSRAAyPPELRFMYYVDGRGPDGGFR |
| P58753 | Y86 | EPSD|PSP | TIRAP MAL | SPSLPPTHASDSGSSRWSKDyDVCVCHSEEDLVAAQDLVSy |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60174 | Y68 | Sugiyama | TPI1 TPI | yIDFARQKLDPKIAVAAQNCyKVTNGAFtGEIsPGMIKDCG |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60660 | S30 | Sugiyama | MYL6 | AEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVLK |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | Y198 | Sugiyama | ACTB | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P60709 | Y240 | Sugiyama | ACTB | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P60709 | Y294 | Sugiyama | ACTB | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P60709 | Y362 | Sugiyama | ACTB | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P60709 | Y91 | Sugiyama | ACTB | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P60842 | T393 | Sugiyama | EIF4A1 DDX2A EIF4A | INMVTEEDKRTLRDIEtFyNtsIEEMPLNVADLI_______ |
| P60842 | Y197 | Sugiyama | EIF4A1 DDX2A EIF4A | KMFVLDEADEMLsRGFKDQIyDIFQKLNsNtQVVLLSATMP |
| P60842 | Y48 | Sugiyama | EIF4A1 DDX2A EIF4A | NEIVDSFDDMNLSESLLRGIyAyGFEKPsAIQQRAILPCIK |
| P60842 | Y50 | Sugiyama | EIF4A1 DDX2A EIF4A | IVDSFDDMNLSESLLRGIyAyGFEKPsAIQQRAILPCIKGy |
| P60842 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60900 | Y160 | Sugiyama | PSMA6 PROS27 | LIGIDEEQGPQVYKCDPAGyyCGFKATAAGVKQtEstsFLE |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| P61353 | Y75 | Sugiyama | RPL27 | AAMGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtV |
| P61353 | Y77 | Sugiyama | RPL27 | MGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVN |
| P61604 | T79 | Sugiyama | HSPE1 | EIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDILGK |
| P61604 | Y76 | Sugiyama | HSPE1 | KGGEIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDI |
| P61604 | Y88 | Sugiyama | HSPE1 | GDKVLLPEyGGtKVVLDDKDyFLFRDGDILGKyVD______ |
| P61758 | Y112 | Sugiyama | VBP1 PFDN3 | QKKKESTNSMETRFLLADNLyCKASVPPTDKVCLWLGANVM |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | S215 | Sugiyama | YWHAG | HLAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWts |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y216 | Sugiyama | YWHAG | LAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWtsD |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62191 | Y439 | Sugiyama | PSMC1 | FKKSKENVLyKKQEGtPEGLyL___________________ |
| P62241 | Y113 | Sugiyama | RPS8 OK/SW-cl.83 | TKTLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEE |
| P62241 | Y117 | Sugiyama | RPS8 OK/SW-cl.83 | VKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEEIL |
| P62249 | Y115 | Sugiyama | RPS16 | YYQKYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGP |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y214 | Sugiyama | YWHAE | LAKAAFDDAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P62258 | Y49 | Sugiyama | YWHAE | KVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssIEQK |
| P62263 | S70 | Sugiyama | RPS14 PRO2640 | KETICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELGI |
| P62269 | S96 | Sugiyama | RPS18 D6S218E | QYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLKK |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62277 | Y18 | Sugiyama | RPS13 | ___MGRMHAPGKGLsQsALPyRRsVPtWLKLTsDDVKEQIy |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62312 | Y72 | Sugiyama | LSM6 | VNGQLKNKyGDAFIRGNNVLyIstQKRRM____________ |
| P62495 | Y345 | Sugiyama | ETF1 ERF1 RF1 SUP45L1 | NLDIMRYVLHCQGTEEEKILyLTPEQEKDKSHFTDKETGQE |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y144 | Sugiyama | RPL23A | VNtLIRPDGEKKAYVRLAPDyDALDVANKIGII________ |
| P62750 | Y74 | Sugiyama | RPL23A | LRRQPKYPRKSAPRRNKLDHyAIIKFPLTTEsAMKKIEDNN |
| 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 |
| P62829 | Y38 | Sugiyama | RPL23 | LGLPVGAVINCADNTGAKNLyIIsVKGIKGRLNRLPAAGVG |
| P62847 | Y76 | Sugiyama | RPS24 | FVFGFRTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGL |
| P62899 | Y103 | Sugiyama | RPL31 | RIRVRLSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVD |
| P62899 | Y108 | Sugiyama | RPL31 | LSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVDEN___ |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62979 | T147 | Sugiyama | RPS27A UBA80 UBCEP1 | GAGVFMAsHFDRHyCGKCCLtyCFNKPEDK___________ |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63220 | T52 | Sugiyama | RPS21 | IQMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRL |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | Y198 | Sugiyama | ACTG1 ACTG | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P63261 | Y240 | Sugiyama | ACTG1 ACTG | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P63261 | Y294 | Sugiyama | ACTG1 ACTG | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P63261 | Y362 | Sugiyama | ACTG1 ACTG | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P63261 | Y91 | Sugiyama | ACTG1 ACTG | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68032 | Y93 | Sugiyama | ACTC1 ACTC | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68104 | Y254 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68133 | Y93 | Sugiyama | ACTA1 ACTA | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68363 | Y103 | Sugiyama | TUBA1B | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| P68363 | Y224 | Sugiyama | TUBA1B | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68363 | Y451 | Sugiyama | TUBA1B | DyEEVGVDsVEGEGEEEGEEy____________________ |
| P68366 | Y103 | Sugiyama | TUBA4A TUBA1 | YRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDPVLDRIR |
| P68366 | Y224 | Sugiyama | TUBA4A TUBA1 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| P68400 | Y12 | Sugiyama | CSNK2A1 CK2A1 | _________MSGPVPSRARVytDVNTHRPREYWDYESHVVE |
| P68400 | Y125 | Sugiyama | CSNK2A1 CK2A1 | VSRTPALVFEHVNNTDFKQLyQtLTDYDIRFYMYEILKALD |
| P68400 | Y255 | Sugiyama | CSNK2A1 CK2A1 | GHDNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGR |
| P78347 | Y248 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | GTF2I BAP135 WBSCR6 | SGIsLEMAAVTVKEESEDPDyyQYNIQAGPSETDDVDEKQP |
| P78347 | Y398 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | GTF2I BAP135 WBSCR6 | KAKGPVTIPYPLFQsHVEDLyVEGLPEGIPFRRPstYGIPR |
| P78347 | Y503 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | GTF2I BAP135 WBSCR6 | GSTEAKAVPYQKFEAHPNDLyVEGLPENIPFRsPsWyGIPR |
| P84103 | Y13 | Sugiyama | SRSF3 SFRS3 SRP20 | ________MHRDsCPLDCKVyVGNLGNNGNKtELERAFGyy |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| P98179 | Y118 | Sugiyama | RBM3 RNPL | GRGRSYSRGGGDQGYGSGRyyDsRPGGyGyGyGRSRDYNGR |
| Q00169 | Y140 | Sugiyama | PITPNA PITPN | GTQENVHKLEPEAWKHVEAVyIDIADRSQVLSKDYKAEEDP |
| Q00341 | Y358 | Sugiyama | HDLBP HBP VGL | SETVILRGEPEKLGQALTEVyAKANsFTVSSVAAPSWLHRF |
| Q00341 | Y40 | Sugiyama | HDLBP HBP VGL | VPQQIKVAtLNsEEEsDPPtyKDAFPPLPEKAACLESAQEP |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00610 | Y1487 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LNNLFITEEDyQALRTsIDAyDNFDNIsLAQRLEKHELIEF |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00610 | Y900 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | AKIyIDsNNNPERFLRENPyyDsRVVGKYCEKRDPHLACVA |
| Q00610 | Y921 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | DsRVVGKYCEKRDPHLACVAyERGQCDLELINVCNENSLFK |
| Q00613 | S363 | Sugiyama | HSF1 HSTF1 | AsVTALtDARGHTDtEGRPPsPPPtstPEKCLsVACLDKNE |
| 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 |
| Q01082 | T779 | Sugiyama | SPTBN1 SPTB2 | WMLDILKIVssSDVGHDEystQsLVKKHKDVAEEIANYRPT |
| Q01082 | Y777 | Sugiyama | SPTBN1 SPTB2 | DAWMLDILKIVssSDVGHDEystQsLVKKHKDVAEEIANYR |
| Q01085 | Y12 | Sugiyama | TIAL1 | _________MMEDDGQPRTLyVGNLSRDVTEVLILQLFSQI |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01518 | Y164 | Sugiyama | CAP1 CAP | VAMAPKPGPYVKEMNDAAMFytNRVLKEYKDVDKKHVDWVK |
| Q02952 | S629 | Sugiyama | AKAP12 AKAP250 | PWAsFKKMVtPKKRVRRPsEsDKEDELDKVKsAtLsstEst |
| Q04206 | Y100 | Sugiyama | RELA NFKB3 | DPPHRPHPHELVGKDCRDGFyEAELCPDRCIHSFQNLGIQC |
| Q04446 | Y200 | Sugiyama | GBE1 | PEHSYEFKHSRPKKPRSLRIyESHVGISSHEGKVASYKHFT |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04724 | Y770 | Sugiyama | TLE1 | DDKYIVTGSGDKKATVYEVIy____________________ |
| Q04726 | Y772 | Sugiyama | TLE3 KIAA1547 | DDKYIVTGSGDKKATVYEVIy____________________ |
| Q04727 | Y773 | Sugiyama | TLE4 GRG4 KIAA1261 | DDKYIVTGSGDKKATVYEVIy____________________ |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | S215 | Sugiyama | YWHAH YWHA1 | LLAKQAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWTS |
| Q04917 | Y154 | Sugiyama | YWHAH YWHA1 | LAEVASGEKKNsVVEAsEAAyKEAFEISKEQMQPTHPIRLG |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05639 | Y254 | Sugiyama | EEF1A2 EEF1AL STN | TILPPTRPTDKPLRLPLQDVyKIGGIGtVPVGRVETGILRP |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q06187 | S342 | Sugiyama | BTK AGMX1 ATK BPK | KsTGDPQGVIRHyVVCSTPQsQyyLAEKHLFSTIPELINyH |
| Q06187 | S543 | Sugiyama | BTK AGMX1 ATK BPK | AARNCLVNDQGVVKVSDFGLsRyVLDDEytssVGsKFPVRW |
| Q06187 | S557 | Sugiyama | BTK AGMX1 ATK BPK | VSDFGLsRyVLDDEytssVGsKFPVRWSPPEVLMYSKFSSK |
| Q06187 | S604 | Sugiyama | BTK AGMX1 ATK BPK | GVLMWEIYSLGKMPYERFtNsEtAEHIAQGLRLyRPHLASE |
| Q06187 | T316 | Sugiyama | BTK AGMX1 ATK BPK | KQEGKEGGFIVRDSSKAGKytVSVFAKsTGDPQGVIRHyVV |
| Q06187 | T602 | Sugiyama | BTK AGMX1 ATK BPK | AFGVLMWEIYSLGKMPYERFtNsEtAEHIAQGLRLyRPHLA |
| Q06187 | T606 | Sugiyama | BTK AGMX1 ATK BPK | LMWEIYSLGKMPYERFtNsEtAEHIAQGLRLyRPHLASEKV |
| Q06187 | Y106 | Sugiyama | BTK AGMX1 ATK BPK | SSEMEQISIIERFPYPFQVVyDEGPLyVFSPTEELRKRWIH |
| Q06187 | Y112 | Sugiyama | BTK AGMX1 ATK BPK | ISIIERFPYPFQVVyDEGPLyVFSPTEELRKRWIHQLKNVI |
| Q06187 | Y134 | Sugiyama | BTK AGMX1 ATK BPK | FSPTEELRKRWIHQLKNVIRyNSDLVQKYHPCFWIDGQyLC |
| Q06187 | Y152 | Sugiyama | BTK AGMX1 ATK BPK | IRyNSDLVQKYHPCFWIDGQyLCCSQTAKNAMGCQILENRN |
| Q06187 | Y223 | ELM|iPTMNet|EPSD|PSP|Sugiyama | BTK AGMX1 ATK BPK | PPEPAAAPVSTSELKKVVALyDyMPMNANDLQLRKGDEYFI |
| Q06187 | Y225 | Sugiyama | BTK AGMX1 ATK BPK | EPAAAPVSTSELKKVVALyDyMPMNANDLQLRKGDEYFILE |
| Q06187 | Y315 | Sugiyama | BTK AGMX1 ATK BPK | LKQEGKEGGFIVRDSSKAGKytVSVFAKsTGDPQGVIRHyV |
| Q06187 | Y334 | Sugiyama | BTK AGMX1 ATK BPK | KytVSVFAKsTGDPQGVIRHyVVCSTPQsQyyLAEKHLFST |
| Q06187 | Y344 | Sugiyama | BTK AGMX1 ATK BPK | TGDPQGVIRHyVVCSTPQsQyyLAEKHLFSTIPELINyHQH |
| Q06187 | Y345 | Sugiyama | BTK AGMX1 ATK BPK | GDPQGVIRHyVVCSTPQsQyyLAEKHLFSTIPELINyHQHN |
| Q06187 | Y39 | Sugiyama | BTK AGMX1 ATK BPK | KTsPLNFKKRLFLLTVHKLSyyEyDFERGRRGsKKGsIDVE |
| Q06187 | Y392 | Sugiyama | BTK AGMX1 ATK BPK | RLKyPVSQQNKNAPSTAGLGyGSWEIDPKDLTFLKELGTGQ |
| Q06187 | Y40 | Sugiyama | BTK AGMX1 ATK BPK | TsPLNFKKRLFLLTVHKLSyyEyDFERGRRGsKKGsIDVEK |
| Q06187 | Y42 | Sugiyama | BTK AGMX1 ATK BPK | PLNFKKRLFLLTVHKLSyyEyDFERGRRGsKKGsIDVEKIT |
| Q06187 | Y425 | Sugiyama | BTK AGMX1 ATK BPK | LKELGTGQFGVVKYGKWRGQyDVAIKMIKEGSMSEDEFIEE |
| Q06187 | Y461 | Sugiyama | BTK AGMX1 ATK BPK | EFIEEAKVMMNLSHEKLVQLyGVCTKQRPIFIITEYMANGC |
| Q06187 | Y511 | Sugiyama | BTK AGMX1 ATK BPK | HRFQtQQLLEMCKDVCEAMEyLESKQFLHRDLAARNCLVND |
| Q06187 | Y545 | Sugiyama | BTK AGMX1 ATK BPK | RNCLVNDQGVVKVSDFGLsRyVLDDEytssVGsKFPVRWSP |
| Q06187 | Y551 | SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | BTK AGMX1 ATK BPK | DQGVVKVSDFGLsRyVLDDEytssVGsKFPVRWSPPEVLMY |
| Q06187 | Y617 | Sugiyama | BTK AGMX1 ATK BPK | PYERFtNsEtAEHIAQGLRLyRPHLASEKVyTIMySCWHEK |
| Q06187 | Y627 | Sugiyama | BTK AGMX1 ATK BPK | AEHIAQGLRLyRPHLASEKVyTIMySCWHEKADERPTFKIL |
| Q06187 | Y631 | Sugiyama | BTK AGMX1 ATK BPK | AQGLRLyRPHLASEKVyTIMySCWHEKADERPTFKILLSNI |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q07157 | Y669 | Sugiyama | TJP1 ZO1 | IFGPIADVAREKLAREEPDIyQIAKSEPRDAGTDQRSsGII |
| Q07666 | S20 | Sugiyama | KHDRBS1 SAM68 | _MQRRDDPAARMsRssGRsGsMDPsGAHPsVRQtPsRQPPL |
| Q07666 | T33 | Sugiyama | KHDRBS1 SAM68 | RssGRsGsMDPsGAHPsVRQtPsRQPPLPHRSRGGGGGSRG |
| Q07666 | Y145 | Sugiyama | KHDRBS1 SAM68 | LtAEIEKIQKGDSKKDDEENyLDLFsHKNMKLKERVLIPVK |
| Q07866 | Y449 | Sugiyama | KLC1 KLC KNS2 | HAEEREECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKN |
| Q07866 | Y453 | Sugiyama | KLC1 KLC KNS2 | REECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKNLGAL |
| Q07866 | Y474 | Sugiyama | KLC1 KLC KNS2 | KACKVDsPtVTTtLKNLGALyRRQGKFEAAETLEEAAMRSR |
| Q07955 | Y149 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | PPSGsWQDLKDHMREAGDVCyADVYRDGTGVVEFVRKEDMT |
| Q07955 | Y37 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | RIyVGNLPPDIRtKDIEDVFyKYGAIRDIDLKNRRGGPPFA |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08170 | Y53 | Sugiyama | SRSF4 SFRS4 SRP75 | LKNGYGFVEFDDLRDADDAVyELNGKDLCGERVIVEHARGP |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q08881 | Y180 | SIGNOR|ELM|iPTMNet|EPSD|PSP | ITK EMT LYK | TPEDNRRPLWEPEETVVIALyDYQTNDPQELALRRNEEyCL |
| Q08J23 | Y51 | Sugiyama | NSUN2 SAKI TRM4 | EAGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALR |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q12792 | Y309 | Sugiyama | TWF1 PTK9 | MDVIRKIEIDNGDELtADFLyEEVHPKQHAHKQSFAKPKGP |
| Q12805 | Y369 | Sugiyama | EFEMP1 FBLN3 FBNL | MCWNYHGGFRCYPRNPCQDPyILTPENRCVCPVsNAMCREL |
| Q12904 | Y288 | Sugiyama | AIMP1 EMAP2 SCYE1 | KKIWEQIQPDLHtNDECVAtyKGVPFEVKGKGVCRAQTMSN |
| Q12913 | S843 | Sugiyama | PTPRJ DEP1 | PNITSVSHNSVKVKFSGFEAsHGPIKAYAVILTTGEAGHPS |
| Q12931 | Y498 | Sugiyama | TRAP1 HSP75 HSPC5 | GQLtsLsEyASRMRAGtRNIyyLCAPNRHLAEHsPyyEAMK |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q12996 | Y708 | Sugiyama | CSTF3 | NEDsDEDEEKGAVVPPVHDIyRARQQKRIR___________ |
| Q13098 | Y172 | Sugiyama | GPS1 COPS1 CSN1 | YKGNSIKESIRRGHDDLGDHyLDCGDLSNALKCYSRARDYC |
| Q13112 | S410 | Sugiyama | CHAF1B CAF1A CAF1P60 MPHOSPH7 MPP7 | LNMRtPDtAKKTKsQtHRGssPGPRPVEGtPASRtQDPssP |
| Q13162 | Y191 | Sugiyama | PRDX4 | PIRIPLLSDLTHQISKDyGVyLEDSGHTLRGLFIIDDKGIL |
| Q13162 | Y54 | Sugiyama | PRDX4 | AVQGWETEERPRTREEECHFyAGGQVyPGEAsRVsVADHsL |
| Q13200 | Y434 | Sugiyama | PSMD2 TRAP2 | LGMILLWDVDGGLTQIDKyLySsEDyIKSGALLACGIVNSG |
| Q13228 | Y28 | Sugiyama | SELENBP1 SBP | CGPGySTPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVD |
| Q13228 | Y33 | Sugiyama | SELENBP1 SBP | STPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVDVDPKs |
| Q13242 | Y70 | Sugiyama | SRSF9 SFRS9 SRP30C | GLVPFAFVRFEDPRDAEDAIyGRNGyDYGQCRLRVEFPRTY |
| Q13247 | S303 | Sugiyama | SRSF6 SFRS6 SRP55 | ENGKGDIKsKSRsRsQsRsNsPLPVPPsKARsVsPPPKRAT |
| Q13247 | Y53 | Sugiyama | SRSF6 SFRS6 SRP55 | LKNGYGFVEFEDsRDADDAVyELNGKELCGERVIVEHARGP |
| Q13263 | Y133 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TVVDCPVCKQQCFSKDIVENyFMRDsGsKAATDAQDANQCC |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13283 | S232 | Sugiyama | G3BP1 G3BP | EEKPEPVLEETAPEDAQKsssPAPADIAQtVQEDLRtFsWA |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13283 | Y40 | PSP | G3BP1 G3BP | ytLLNQAPDMLHRFYGKNssyVHGGLDsNGKPADAVyGQKE |
| Q13283 | Y56 | Sugiyama | G3BP1 G3BP | KNssyVHGGLDsNGKPADAVyGQKEIHRKVMsQNFtNCHTK |
| Q13287 | T229 | Sugiyama | NMI | EIGVADKILKKKEYPLYINQtCHRVTVSPYTEIHLKKYQIF |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13422 | S214 | EPSD|PSP | IKZF1 IK1 IKAROS LYF1 ZNFN1A1 | THSVGKPHKCGYCGRSYKQRssLEEHKERCHNYLESMGLPG |
| Q13422 | S215 | EPSD|PSP | IKZF1 IK1 IKAROS LYF1 ZNFN1A1 | HSVGKPHKCGYCGRSYKQRssLEEHKERCHNYLESMGLPGT |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13439 | Y2148 | Sugiyama | GOLGA4 | EFREQIHNLEDRLKKYEKNVyATTVGtPyKGGNLyHtDVSL |
| Q13442 | T18 | Sugiyama | PDAP1 HASPP28 | ___MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEE |
| Q13509 | T107 | Sugiyama | TUBB3 TUBB4 | PDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECENC |
| Q13509 | Y106 | Sugiyama | TUBB3 TUBB4 | RPDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECEN |
| Q13510 | Y305 | Sugiyama | ASAH1 ASAH HSD-33 HSD33 | GNQSGEGCVITRDRKESLDVyELDAKQGRWYVVQTNYDRWK |
| Q13546 | Y387 | Sugiyama | RIPK1 RIP RIP1 | QEENEPSLQSKLQDEANyHLyGsRMDRQTKQQPRQNVAYNR |
| Q13561 | Y207 | Sugiyama | DCTN2 DCTN50 | SKGGSGGKttGtPPDssLVtyELHsRPEQDKFSQAAKVAEL |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13573 | Y430 | Sugiyama | SNW1 SKIIP SKIP | RLFNQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRP |
| Q13573 | Y433 | Sugiyama | SNW1 SKIIP SKIP | NQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRPSKN |
| Q13630 | Y316 | Sugiyama | GFUS SDR4E1 TSTA3 | FRFTPFKQAVKETCAWFTDNyEQARK_______________ |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13642 | Y9 | Sugiyama | FHL1 SLIM1 | ____________MAEKFDCHyCRDPLQGKKYVQKDGHHCCL |
| Q13765 | S117 | Sugiyama | NACA HSD48 | RKSKNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQL |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q13885 | T107 | Sugiyama | TUBB2A TUBB2 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q13885 | Y106 | Sugiyama | TUBB2A TUBB2 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q14152 | S584 | Sugiyama | EIF3A EIF3S10 KIAA0139 | EHQRILARRQtIEERKERLEsLNIQREKEELEQREAELQKV |
| Q14152 | Y697 | Sugiyama | EIF3A EIF3S10 KIAA0139 | LEKEKKELQERLKNQEKKIDyFERAKRLEEIPLIKSAYEEQ |
| 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 | Y49 | Sugiyama | EIF4A2 DDX2B EIF4F | NEIVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIK |
| Q14240 | Y51 | Sugiyama | EIF4A2 DDX2B EIF4F | IVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIKGy |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | S447 | Sugiyama | CTTN EMS1 | FKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYATE |
| 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________________ |
| Q14432 | S402 | Sugiyama | PDE3A | STQLTFQAIHKPRVNPVtsLsENytCsDsEESSEKDKLAIP |
| Q14566 | Y510 | Sugiyama | MCM6 | KATLNARTsILAAANPIsGHyDRSKSLKQNINLSAPIMSRF |
| Q14566 | Y810 | Sugiyama | MCM6 | LTQAGLKGstEGsEsYEEDPyLVVNPNyLLED_________ |
| Q14568 | S53 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | IINTFYSNKEIFLRELIsNssDALDKIWYESLTDPSKLDSG |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14651 | Y463 | Sugiyama | PLS1 | VNKPPYPALGGNMKKIENCNyAVELGKNKAKFSLVGIAGQD |
| Q14677 | Y106 | Sugiyama | CLINT1 ENTH EPN4 EPNR KIAA0171 | LAYLIRNGSERVVTSAREHIyDLRSLENyHFVDEHGKDQGI |
| Q14764 | Y389 | Sugiyama | MVP LRP | AKVEVVEERQAIPLDENEGIyVQDVKTGKVRAVIGSTYMLT |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q14980 | Y1836 | Sugiyama | NUMA1 NMP22 NUMA | NITMTKKLDVEEPDsANssFystRsAPAsQAsLRAtsstQs |
| Q15024 | Y13 | Sugiyama | EXOSC7 KIAA0116 RRP42 | ________MASVTLSEAEKVyIVHGVQEDLRVDGRGCEDYR |
| Q15024 | Y187 | Sugiyama | EXOSC7 KIAA0116 RRP42 | RVRVLEDEEGsKDIELSDDPyDCIRLSVENVPCIVTLCKIG |
| Q15029 | Y167 | Sugiyama | EFTUD2 KIAA0031 SNRP116 | DCLIEQTHPEIRKRyDQDLCyTDILFTEQERGVGIKSTPVT |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15149 | Y3362 | Sugiyama | PLEC PLEC1 | TGLsLLPLSEKAARARQEELySELQAREtFEKTPVEVPVGG |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15417 | Y10 | Sugiyama | CNN3 | ___________MTHFNKGPsyGLsAEVKNKIASKYDHQAEE |
| Q15427 | T14 | Sugiyama | SF3B4 SAP49 | _______MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFL |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15631 | Y210 | Sugiyama | TSN | sLRKRYDGLKYDVKKVEEVVyDLSIRGFNKETAAACVEK__ |
| Q15637 | Y87 | Sugiyama | SF1 ZFM1 ZNF162 | tGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFRTRKKLEE |
| Q15785 | Y25 | Sugiyama | TOMM34 URCC3 | FPDsVEELRAAGNESFRNGQyAEASALyGRALRVLQAQGss |
| Q15785 | Y32 | Sugiyama | TOMM34 URCC3 | LRAAGNESFRNGQyAEASALyGRALRVLQAQGssDPEEEsV |
| Q15785 | Y54 | Sugiyama | TOMM34 URCC3 | RALRVLQAQGssDPEEEsVLysNRAACHLKDGNCRDCIKDC |
| Q16181 | Y306 | Sugiyama | SEPTIN7 CDC10 SEPT7 | RNMLIRTHMQDLKDVTNNVHyENyRSRKLAAVtyNGVDNNK |
| Q16555 | Y499 | Sugiyama | DPYSL2 CRMP2 ULIP2 | yKRIKARSRLAELRGVPRGLyDGPVCEVsVtPKtVtPAssA |
| Q16658 | Y493 | Sugiyama | FSCN1 FAN1 HSN SNL | DHAGVLKASAEtVDPAsLWEy____________________ |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16740 | Y209 | Sugiyama | CLPP | TDIAIQAEEIMKLKKQLYNIyAKHTKQSLQVIEsAMERDRY |
| 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 | Y281 | Sugiyama | TXNRD1 GRIM12 KDRF | SLNWGYRVALREKKVVyENAyGQFIGPHRIKATNNKGKEKI |
| Q1KMD3 | Y610 | Sugiyama | HNRNPUL2 HNRPUL2 | LEMKANFsLPEKCDYMDEVTyGELEKEEAQPIVTKYKEEAR |
| Q32P51 | S95 | Sugiyama | HNRNPA1L2 HNRNPA1L | TPHKVDGRVVEPKRAVsREDsQRPGAHLtVKKIFVGGIKED |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q53H82 | Y99 | Sugiyama | LACTB2 CGI-83 | HRDHSGGIGDICKSINNDtTyCIKKLPRNPQREEIIGNGEQ |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | 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 |
| Q5F1R6 | Y5 | Sugiyama | DNAJC21 DNAJA5 | ________________MKCHyEALGVRRDASEEELKKAYRK |
| Q5JTH9 | Y1251 | Sugiyama | RRP12 KIAA0690 | AEYKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQG |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5T035 | S66 | Sugiyama | FAM120A2P C9orf129 | LSEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERSLPI |
| 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 |
| Q63HQ0 | Y110 | Sugiyama | AP1AR C4orf16 PRO0971 | KIQKELALQEEKLRLEEEALyAAQREAARAAKQRKLLEQER |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6L8Q7 | Y235 | Sugiyama | PDE12 | sLsPssPsssWtEtDVEERVytPSNADIGLRLKLHCTPGDG |
| Q6NW29 | S28 | Sugiyama | RWDD4 FAM28A RWDD4A | EMELEALRSIyEGDEsFRELsPVSFQyRIGENGDPKAFLIE |
| Q6NW29 | Y18 | Sugiyama | RWDD4 FAM28A RWDD4A | ___MsANEDQEMELEALRSIyEGDEsFRELsPVSFQyRIGE |
| Q6PEY2 | Y224 | Sugiyama | TUBA3E | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| Q6PIW4 | Y663 | Sugiyama | FIGNL1 | DFENAFRTVRPSVSPKDLELyENWNKTFGCGK_________ |
| Q6PKG0 | Y633 | Sugiyama | LARP1 KIAA0731 LARP | MEQMDGRKNtFtAWsDEEsDyEIDDRDVNKILIVtQtPHyM |
| Q6PKG0 | Y777 | Sugiyama | LARP1 KIAA0731 LARP | APEPstIARsLPttVPEsPNyRNtRtPRtPRtPQLKDSSQT |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y791 | Sugiyama | POTEE A26C1A POTE2 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6UN15 | S492 | Sugiyama | FIP1L1 FIP1 RHE | DRDRDRERERTRERERERDHsPtPsVFNsDEERyRYREYAE |
| Q6UN15 | S496 | Sugiyama | FIP1L1 FIP1 RHE | DRERERTRERERERDHsPtPsVFNsDEERyRYREYAERGYE |
| Q6UN15 | T494 | Sugiyama | FIP1L1 FIP1 RHE | DRDRERERTRERERERDHsPtPsVFNsDEERyRYREYAERG |
| Q71RC2 | Y72 | Sugiyama | LARP4 PP13296 | AHPEGNAELSEDICKEYEVMySssCETTRNTTGIEESTDGM |
| Q71U36 | Y103 | Sugiyama | TUBA1A TUBA3 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q71U36 | Y224 | Sugiyama | TUBA1A TUBA3 | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q71U36 | Y451 | Sugiyama | TUBA1A TUBA3 | DyEEVGVDsVEGEGEEEGEEy____________________ |
| Q7KZ85 | Y633 | Sugiyama | SUPT6H KIAA0162 SPT6H | RAKLNItPTKKGRKDVDEAHyAYSFKYLKNKPVKELRDDQF |
| Q7KZF4 | Y113 | Sugiyama | SND1 TDRD11 | KEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVAEGLA |
| 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 |
| Q86V21 | Y117 | Sugiyama | AACS ACSF1 | SRLNYAENLLRHKENDRVALyIAREGKEEIVKVTFEELRQE |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q8IV50 | T210 | Sugiyama | LYSMD2 | STQAAKKLKEESRDEEsPyAtSLyHs_______________ |
| Q8IWW6 | S240 | Sugiyama | ARHGAP12 | SSSsTEQIRAttPPNQGRPDsPVyANLQELKISQSALPPLP |
| Q8IWW6 | T231 | Sugiyama | ARHGAP12 | QDSEsGDELSSSsTEQIRAttPPNQGRPDsPVyANLQELKI |
| Q8IWW6 | Y243 | Sugiyama | ARHGAP12 | sTEQIRAttPPNQGRPDsPVyANLQELKISQSALPPLPGSP |
| Q8IXH6 | Y211 | Sugiyama | TP53INP2 C20orf110 DOR PINH | RQNRARESRPRRSKNQSsFIyQPCQRQFNY___________ |
| Q8IZ21 | S118 | Sugiyama | PHACTR4 PRO2963 | PSDAMLKNGHTTPIGNARsssPVQVEEEPVRLAsLRKAIPE |
| Q8N0Y7 | S134 | Sugiyama | PGAM4 PGAM3 | IWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYE |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N5M4 | Y11 | Sugiyama | TTC9C | __________MEKRLQEAQLyKEEGNQRYREGKYRDAVSRY |
| Q8N5P1 | Y76 | Sugiyama | ZC3H8 ZC3HDC8 | SAISPKSSLHRKSRSKDYDVysDNDICsQEsEDNFAKELQQ |
| Q8N684 | S205 | Sugiyama | CPSF7 | IPPRAHsRDssDsADGRAtPsENLVPSSARVDKPPSVLPYF |
| Q8N684 | T203 | Sugiyama | CPSF7 | GGIPPRAHsRDssDsADGRAtPsENLVPSSARVDKPPSVLP |
| Q8N7H5 | Y169 | Sugiyama | PAF1 PD2 | EKPEVKIGVSVKQQFTEEEIyKDRDSQITAIEKTFEDAQKS |
| Q8NBF2 | Y39 | Sugiyama | NHLRC2 | TSLEYALLDAVTQQEKDSLVyQyLQKVDGWEQDLSVPEFPE |
| Q8NBP7 | Y521 | Sugiyama | PCSK9 NARC1 PSEC0052 | EAQGGKLVCRAHNAFGGEGVyAIARCCLLPQANCSVHTAPP |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NBS9 | Y289 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | RDGKKVDQYKGKRDLEsLREyVEsQLQRTETGATETVTPSE |
| Q8NDI1 | Y585 | Sugiyama | EHBP1 KIAA0903 NACSIN | TYKVGNYETDTNssVDQEKFyAELSDLKREPELQQPISGAV |
| Q8NFI4 | Y185 | Sugiyama | ST13P5 FAM10A5 | NAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TD19 | Y52 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PSASQGPRAGGGAAEQEELHyIPIRVLGRGAFGEAtLyRRT |
| Q8TEW0 | S720 | Sugiyama | PARD3 PAR3 PAR3A | ELPIETALDDRERRIsHsLysGIEGLDEsPsRNAALsRIMG |
| Q8WUM4 | Y39 | Sugiyama | PDCD6IP AIP1 ALIX KIAA1375 | KPLVKFIQQTYPSGGEEQAQyCRAAEELSKLRRAAVGRPLD |
| Q8WVJ2 | Y145 | Sugiyama | NUDCD2 | ERFQKENPGFDFsGAEIsGNytKGGPDFsNLEK________ |
| Q8WWM7 | Y264 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | ESDMSNGWDPNEMFKFNEENyGVKTtyDssLssytVPLEKD |
| Q8WWM7 | Y270 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | GWDPNEMFKFNEENyGVKTtyDssLssytVPLEKDNsEEFR |
| Q8WWM7 | Y277 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | FKFNEENyGVKTtyDssLssytVPLEKDNsEEFRQRELRAA |
| Q8WX92 | Y541 | Sugiyama | NELFB COBRA1 KIAA1182 | EALQKALEPTGQSGEAVKELysQLGEKLEQLDHRKPsPAQA |
| Q92574 | S505 | Sugiyama | TSC1 KIAA0243 TSC | ELsEITTAEAEPVVPRGGFDsPFyRDsLPGsQRKtHsAAss |
| Q92574 | Y508 | Sugiyama | TSC1 KIAA0243 TSC | EITTAEAEPVVPRGGFDsPFyRDsLPGsQRKtHsAAsssQG |
| Q92598 | Y641 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MIMQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQD |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y89 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | RFHGRAFNDPFIQKEKENLsyDLVPLKNGGVGIKVMYMGEE |
| Q92905 | Y203 | Sugiyama | COPS5 CSN5 JAB1 | LGAFRTYPKGYKPPDEGPsEyQtIPLNKIEDFGVHCKQYYA |
| Q93052 | Y301 | Sugiyama | LPP | LQPEPGYGYAPNQGRyyEGyyAAGPGyGGRNDsDPtyGQQG |
| Q93052 | Y317 | Sugiyama | LPP | yEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPGA |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96AY3 | Y201 | Sugiyama | FKBP10 FKBP65 PSEC0056 | YNGTLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGM |
| Q96AY3 | Y204 | Sugiyama | FKBP10 FKBP65 PSEC0056 | TLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGMCPG |
| Q96BP3 | Y274 | Sugiyama | PPWD1 KIAA0073 | PHEYKFPKNVNWEYKTDTDLyEFAKCKAYPTSVCFsPDGKK |
| Q96C19 | T84 | Sugiyama | EFHD2 SWS1 | DLNQGIGEPQsPsRRVFNPytEFKEFSRKQIKDMEKMFKQy |
| Q96D15 | Y125 | Sugiyama | RCN3 UNQ239/PRO272 | WIAHTQQRHIRDsVsAAWDtyDtDRDGRVGWEELRNATYGH |
| Q96DG6 | Y165 | Sugiyama | CMBL | YSEFRAGVSVYGIVKDSEDIyNLKNPTLFIFAENDVVIPLK |
| Q96EB1 | Y147 | Sugiyama | ELP4 C11orf19 PAXNEB | QELPAPLLDDKCKKEFDEDVyNHKtPEsNIKMKIAWRYQLL |
| Q96EU6 | Y138 | Sugiyama | RRP36 C6orf153 HSPC253 | RDPRFDDLSGEYNPEVFDKtyQFLNDIRAKEKELVKKQLKK |
| Q96FW1 | Y68 | Sugiyama | OTUB1 OTB1 OTU1 HSPC263 | VSERLELsVLyKEYAEDDNIyQQKIKDLHKKYSYIRKTRPD |
| Q96G03 | Y177 | Sugiyama | PGM2 MSTP006 | CAGIMItAsHNPKQDNGYKVyWDNGAQIIsPHDKGISQAIE |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96HN2 | Y372 | Sugiyama | AHCYL2 KIAA0828 | LCVPAMNVNDSVTKQKFDNLyCCRESILDGLKRTTDMMFGG |
| Q96KR1 | Y667 | Sugiyama | ZFR | RRREEEERWRMEMRRYEEDMyWRRMEEEQHHWDDRRRMPDG |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | S890 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | GINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWTN |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q96QK1 | Y791 | Sugiyama | VPS35 MEM3 TCCCTA00141 | HNtLEHLRLRREsPEsEGPIyEGLIL_______________ |
| Q96S44 | T8 | Sugiyama | TP53RK C20orf64 PRPK | _____________MAAARAttPADGEEPAPEAEALAAARER |
| Q99426 | Y114 | Sugiyama | TBCB CG22 CKAP1 | RLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKRsKLGRyN |
| Q99439 | Y12 | Sugiyama | CNN2 | _________MsstQFNKGPsyGLsAEVKNRLLSKYDPQKEA |
| Q99459 | Y511 | Sugiyama | CDC5L KIAA0432 PCDC5RP | EIVLPENAEKELEEREIDDtyIEDAADVDARKQAIRDAERV |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99497 | T140 | Sugiyama | PARK7 | GSKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPGT |
| Q99497 | Y139 | Sugiyama | PARK7 | FGSKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPG |
| Q99497 | Y67 | Sugiyama | PARK7 | sRDVVICPDAsLEDAKKEGPyDVVVLPGGNLGAQNLSESAA |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99733 | Y55 | Sugiyama | NAP1L4 NAP2 | PRVLAALQERLDNVPHtPssyIEtLPKAVKRRINALKQLQV |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| Q99848 | Y265 | Sugiyama | EBNA1BP2 EBP2 | NQKFGFGGKKKGSKWNtREsyDDVssFRAKTAHGRGLKRPG |
| Q99877 | Y41 | Sugiyama | H2BC15 H2BFD HIST1H2BN | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99877 | Y43 | Sugiyama | H2BC15 H2BFD HIST1H2BN | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99879 | Y41 | Sugiyama | H2BC14 H2BFE HIST1H2BM | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99879 | Y43 | Sugiyama | H2BC14 H2BFE HIST1H2BM | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99880 | Y41 | Sugiyama | H2BC13 H2BFC HIST1H2BL | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99880 | Y43 | Sugiyama | H2BC13 H2BFC HIST1H2BL | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q9BQE3 | Y103 | Sugiyama | TUBA1C TUBA6 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q9BQE3 | Y224 | Sugiyama | TUBA1C TUBA6 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BQE3 | Y449 | Sugiyama | TUBA1C TUBA6 | EKDyEEVGADsADGEDEGEEy____________________ |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BSU3 | Y138 | Sugiyama | NAA11 ARD1B ARD2 | ALHLYSNTLNFQISEVEPKyyADGEDAyAMKRDLSQMADEL |
| Q9BSU3 | Y145 | Sugiyama | NAA11 ARD1B ARD2 | TLNFQISEVEPKyyADGEDAyAMKRDLSQMADELRRQMDLK |
| Q9BT78 | Y167 | Sugiyama | COPS4 CSN4 | TYLKIARLYLEDDDPVQAEAyINRASLLQNESTNEQLQIHY |
| Q9BUJ2 | Y111 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | GYSGPDGHYAMDNITRQNQFyDtQVIKQENESGyERRPLEM |
| Q9BUJ2 | Y510 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | RLIQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIV |
| Q9BVA1 | T107 | Sugiyama | TUBB2B | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q9BVA1 | Y106 | Sugiyama | TUBB2B | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BYX7 | Y91 | Sugiyama | POTEKP ACTBL3 FKSG30 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q9C0C9 | Y355 | Sugiyama | UBE2O KIAA1734 | RVKRLGCFDHAQRQLGERCLyVFPAKVEPAKIAWECPEKNC |
| Q9GZL7 | Y380 | Sugiyama | WDR12 | SGSLDNIVKLWDTRSCKAPLyDLAAHEDKVLSVDWTDTGLL |
| Q9H0H5 | Y384 | Sugiyama | RACGAP1 KIAA1478 MGCRACGAP | SIVVHCVNEIEQRGLTETGLyRIsGCDRTVKELKEKFLRVK |
| Q9H0W8 | Y147 | Sugiyama | SMG9 C19orf61 | PAAPAPPKGEKEGQRPTQPVyQIQNRGMGTAAPAAMDPVVG |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H3P7 | Y492 | Sugiyama | ACBD3 GCP60 GOCAP1 GOLPH1 | NKPLLDEIVPVYRRDCHEEVyAGSHQYPGRGVYLLKFDNSY |
| Q9H4A3 | Y2102 | Sugiyama | WNK1 HSN2 KDP KIAA0344 PRKWNK1 | KHLKEIQDLQSRQKHEIEsLyTKLGKVPPAVIIPPAAPLsG |
| Q9H4M9 | Y339 | Sugiyama | EHD1 PAST PAST1 CDABP0131 | PNVFGKESKKKELVNNLGEIyQKIEREHQIsPGDFPsLRKM |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HAS0 | Y38 | Sugiyama | C17orf75 | ssEEGGsAEERRLEPPSSSHyCLysYRGSRLAQQRGDsEDG |
| Q9HAS0 | Y41 | Sugiyama | C17orf75 | EGGsAEERRLEPPSSSHyCLysYRGSRLAQQRGDsEDGsPs |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HCN8 | Y81 | Sugiyama | SDF2L1 UNQ1941/PRO4424 | GSGSGQQSVtGVEAsDDANSyWRIRGGSEGGCPRGSPVRCG |
| Q9NQR4 | Y202 | Sugiyama | NIT2 CUA002 | TTGPAHWELLQRSRAVDNQVyVAtAsPARDDKASYVAWGHS |
| Q9NR46 | Y77 | Sugiyama | SH3GLB2 KIAA1848 PP578 | LRQTEVLLQPNPSARVEEFLyEKLDRKVPSRVTNGELLAQY |
| Q9NRX4 | Y116 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AyGPAQHAISTEKIKAKyPDyEVtWANDGy___________ |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NSK0 | Y474 | Sugiyama | KLC4 KNSL8 | KACKVssPTVNTTLRNLGALyRRQGKLEAAETLEECALRSR |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVD7 | Y124 | Sugiyama | PARVA MXRA2 | WINDVLVGERIIVKDLAEDLyDGQVLQKLFEKLESEKLNVA |
| Q9NVS9 | Y157 | Sugiyama | PNPO | NRQVRVEGPVKKLPEEEAECyFHSRPKssQIGAVVSHQSSV |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NWS0 | Y194 | Sugiyama | PIH1D1 NOP17 | IsQQNIRSEQRPRIQELGDLytPAPGRAESGPEKPHLNLWL |
| Q9NXV6 | T114 | Sugiyama | CDKN2AIP CARF | QKVMDKILSMAEGIKVtDAPtyTTRDELVAKVKKRGIsssN |
| Q9NXV6 | Y115 | Sugiyama | CDKN2AIP CARF | KVMDKILSMAEGIKVtDAPtyTTRDELVAKVKKRGIsssNE |
| Q9NY65 | Y103 | Sugiyama | TUBA8 TUBAL2 | YRQLFHPEQLItGKEDAANNyARGHYTVGKESIDLVLDRIR |
| Q9NY65 | Y224 | Sugiyama | TUBA8 TUBAL2 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| Q9NYU2 | Y449 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | IEGLSLHNVLKLNIQPsEADyAVDIRSPAISWVNNLEVDSR |
| Q9NYU2 | Y779 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | RPVTFWIVGDFDSPSGRQLLyDAIKHQKSSNNVRISMINNP |
| Q9NZB2 | S417 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | LSEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERssPI |
| Q9NZB2 | Y418 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | SEPAPLTLDTSGKNLtEQNsysNIPHEGKHtPLyERssPIN |
| Q9NZB2 | Y9 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | ____________MGVQGFQDyIEKHCPsAVVPVELQKLARG |
| Q9P0U4 | Y405 | Sugiyama | CXXC1 CFP1 CGBP PCCX1 PHF18 | QPSSKYCSDDCGMKLAANRIyEILPQRIQQWQQSPCIAEEH |
| Q9UBB9 | Y51 | Sugiyama | TFIP11 STIP HSPC006 | LQNEFNPNRQRHWQTKEEAtyGVWAERDsDDERPSFGGKRA |
| Q9UBQ7 | Y255 | Sugiyama | GRHPR GLXR MSTP035 | KETAVFINISRGDVVNQDDLyQALAsGKIAAAGLDVtsPEP |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y352 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | TEEAREGIKQLLKQGSVQKVyNGLQGY______________ |
| Q9UBS4 | Y89 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | DLGAAyEVLsDSEKRKQyDTyGEEGLKDGHQSSHGDIFSHF |
| Q9UBT2 | Y159 | Sugiyama | UBA2 SAE2 UBLE1B HRIHFB2115 | SGTAGYLGQVTTIKKGVtECyECHPKPTQRTFPGCtIRNTP |
| Q9UDY4 | Y172 | Sugiyama | DNAJB4 DNAJW HLJ1 | SRLKQDPPVIHELRVsLEEIySGCTKRMKISRKRLNADGRS |
| Q9UGI8 | Y251 | Sugiyama | TES | RTQYSCYCCKLSMKEGDPAIyAERAGyDKLWHPACFVCSTC |
| Q9UHG3 | Y498 | Sugiyama | PCYOX1 KIAA0908 PCL1 UNQ597/PRO1183 | ALLAYHRWNGHTDMIDQDGLyEKLKTEL_____________ |
| Q9UI15 | T190 | Sugiyama | TAGLN3 NP25 | GQNVIGLQMGSNKGAsQAGMtGyGMPRQIM___________ |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UII2 | Y58 | Sugiyama | ATP5IF1 ATPI ATPIF1 | GsIREAGGAFGKREQAEEERyFRAQsREQLAALKKHHEEEI |
| Q9UJU6 | Y16 | Sugiyama | DBNL CMAP SH3P7 PP5423 | _____MAANLSRNGPALQEAyVRVVtEKsPtDWALFTyEGN |
| Q9UJV9 | Y414 | SIGNOR|EPSD|PSP | DDX41 ABS | VTINVGRAGAASLDVIQEVEyVKEEAKMVYLLECLQKTPPP |
| Q9UKF6 | Y677 | Sugiyama | CPSF3 CPSF73 | EGsEDDESLREMVELAAQRLyEALtPVH_____________ |
| Q9UKV3 | Y1086 | Sugiyama | ACIN1 ACINUS KIAA0670 | RTALHGVKWPQSNPKFLCADyAEQDELDyHRGLLVDRPsEt |
| Q9UL25 | Y150 | Sugiyama | RAB21 KIAA0118 | VGNKIDLEKERHVsIQEAESyAESVGAKHYHTSAKQNKGIE |
| Q9ULT8 | Y841 | Sugiyama | HECTD1 KIAA1131 | KLKSKLEKTKQKVRTMARDLyDDHFKAVESMPRGVVVTLRN |
| Q9UMS0 | Y194 | Sugiyama | NFU1 HIRIP5 CGI-33 | KELLDTRIRPTVQEDGGDVIyKGFEDGIVQLKLQGSCTSCP |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UN19 | Y139 | SIGNOR|iPTMNet | DAPP1 BAM32 HSPC066 | tGtLMVLKHPYPRKVEEPsIyEsVRVHTAMQTGRTEDDLVP |
| Q9UNZ2 | Y167 | Sugiyama | NSFL1C UBXN2C | PRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLKLW |
| Q9UQ35 | S1102 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | EsPsLQSKSQTsPKGGRsRsssPVtELAsRsPIRQDRGEFs |
| Q9UQ35 | S1112 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | TsPKGGRsRsssPVtELAsRsPIRQDRGEFsAsPMLKsGMs |
| Q9UQ35 | S1648 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | APRALPRRSRSGSSSKGRGPsPEGssstEssPEHPPKSRTA |
| Q9UQ35 | S2132 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | SRMsCFsRPsMsPtPLDRCRsPGMLEPLGssRtPMsVLQQA |
| Q9UQ35 | S876 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | tsPQANEQsVtPQRRsCFEssPDPELKsRtPsRHsCsGssP |
| Q9UQ80 | Y343 | Sugiyama | PA2G4 EBP1 | VLLMPNGPMRITsGPFEPDLyKsEMEVQDAELKALLQssAs |
| Q9UQB8 | Y164 | Sugiyama | BAIAP2 | LRKKSQGSKNPQKYSDKELQyIDAISNKQGELENyVSDGYK |
| Q9UQE7 | Y228 | Sugiyama | SMC3 BAM BMH CSPG6 SMC3L1 | EELAQYQKWDKMRRALEyTIyNQELNETRAKLDELSAKRET |
| Q9Y230 | Y172 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | TGTGSKVGKLTLKTTEMETIyDLGTKMIESLTKDKVQAGDV |
| Q9Y265 | Y220 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | VKRQGRCDTYAtEFDLEAEEyVPLPKGDVHKKKEIIQDVtL |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2S7 | Y203 | Sugiyama | POLDIP2 PDIP38 POLD4 HSPC017 | PYTSTDQVPIQHELFERFLLyDQTKAPPFVARETLRAWQEK |
| Q9Y2T3 | Y441 | Sugiyama | GDA KIAA1258 | SEAVIQKFLyLGDDRNIEEVyVGGKQVVPFSSsV_______ |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2W1 | T230 | Sugiyama | THRAP3 BCLAF2 TRAP150 | tsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERsPA |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y399 | Y271 | Sugiyama | MRPS2 CGI-91 | RLFQTAITRAKEKRQQVEALyRLQGQKEPGDQGPAHPPGAD |
| Q9Y3F4 | Y280 | Sugiyama | STRAP MAWD UNRIP | syKGHFGPIHCVRFSPDGELyAsGSEDGTLRLWQTVVGKty |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3P9 | Y472 | Sugiyama | RABGAP1 HSPC094 | FFLKLKQIKQRERKNNTDTLyEVVCLESESERERRKTTAsP |
| Q9Y3S2 | Y315 | Sugiyama | ZNF330 NOA36 | ssDLFTNLNLGRTYAsGYAHyEEQEN_______________ |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y4L1 | Y116 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | TLRYFQHLLGKQADNPHVALyQARFPEHELTFDPQRQTVHF |
| Q9Y4L1 | Y759 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | AANsLEAFIFEtQDKLyQPEyQEVsTEEQREEISGKLSAAS |
| Q9Y5Q8 | Y393 | Sugiyama | GTF3C5 CDABP0017 | SGtsGARKPASSKYKLKDSVyIFREGALPPYRQMFYQLCDL |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | Y244 | Sugiyama | CLIC4 | AysRDEFtNtCPsDKEVEIAysDVAKRLTK___________ |
| Q9Y6I3 | Y101 | Sugiyama | EPN1 | MEYLIKTGSERVSQQCKENMyAVQTLKDFQYVDRDGKDQGV |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Axon guidance | R-HSA-422475 | 9.268494e-07 | 6.033 | 0 | 0 |
| Immune System | R-HSA-168256 | 1.173496e-06 | 5.931 | 1 | 0 |
| Nervous system development | R-HSA-9675108 | 2.493142e-06 | 5.603 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 3.036350e-05 | 4.518 | 1 | 0 |
| Signal Transduction | R-HSA-162582 | 7.520975e-05 | 4.124 | 1 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.139939e-04 | 3.943 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 1.220488e-04 | 3.913 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.552380e-04 | 3.809 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.718170e-04 | 3.765 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.892537e-04 | 3.723 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 2.975344e-04 | 3.526 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 2.975344e-04 | 3.526 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 3.238866e-04 | 3.490 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.281464e-04 | 3.642 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 2.226340e-04 | 3.652 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 3.378919e-04 | 3.471 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 3.271564e-04 | 3.485 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 3.818561e-04 | 3.418 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 4.230953e-04 | 3.374 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 4.990050e-04 | 3.302 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 4.825210e-04 | 3.316 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 4.825210e-04 | 3.316 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 6.005054e-04 | 3.221 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 6.561397e-04 | 3.183 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 7.723905e-04 | 3.112 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 8.138878e-04 | 3.089 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 8.955423e-04 | 3.048 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 9.094692e-04 | 3.041 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 1.075875e-03 | 2.968 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 1.075875e-03 | 2.968 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.191064e-03 | 2.924 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 1.214569e-03 | 2.916 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 1.214569e-03 | 2.916 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.118922e-03 | 2.951 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 1.384620e-03 | 2.859 | 0 | 0 |
| MET activates PTPN11 | R-HSA-8865999 | 1.384620e-03 | 2.859 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 1.280275e-03 | 2.893 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 1.392015e-03 | 2.856 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 1.392015e-03 | 2.856 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 1.446507e-03 | 2.840 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 1.503984e-03 | 2.823 | 0 | 0 |
| Depurination | R-HSA-73927 | 1.510386e-03 | 2.821 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 1.767837e-03 | 2.753 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 1.767837e-03 | 2.753 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 1.676820e-03 | 2.776 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 1.657864e-03 | 2.780 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 1.745001e-03 | 2.758 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 1.907322e-03 | 2.720 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 1.907322e-03 | 2.720 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.324273e-03 | 2.634 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 2.371221e-03 | 2.625 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 2.371221e-03 | 2.625 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 2.208816e-03 | 2.656 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 2.208816e-03 | 2.656 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 2.443605e-03 | 2.612 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.522888e-03 | 2.598 | 1 | 1 |
| DAP12 interactions | R-HSA-2172127 | 2.541663e-03 | 2.595 | 1 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 3.060590e-03 | 2.514 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 3.237811e-03 | 2.490 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 3.307668e-03 | 2.480 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 3.454055e-03 | 2.462 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 3.577246e-03 | 2.446 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 3.577246e-03 | 2.446 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 3.943469e-03 | 2.404 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 3.609697e-03 | 2.443 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 3.975939e-03 | 2.401 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 4.468877e-03 | 2.350 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 4.217545e-03 | 2.375 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 4.361641e-03 | 2.360 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 4.468877e-03 | 2.350 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 4.193374e-03 | 2.377 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 4.568814e-03 | 2.340 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 5.001425e-03 | 2.301 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 5.167048e-03 | 2.287 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 5.282987e-03 | 2.277 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 4.813740e-03 | 2.318 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 5.282987e-03 | 2.277 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 4.730112e-03 | 2.325 | 0 | 0 |
| MET activates PI3K/AKT signaling | R-HSA-8851907 | 5.347060e-03 | 2.272 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 5.379451e-03 | 2.269 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 5.841570e-03 | 2.233 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 6.053651e-03 | 2.218 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 6.190858e-03 | 2.208 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 5.597958e-03 | 2.252 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 5.632259e-03 | 2.249 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 6.065335e-03 | 2.217 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 5.877538e-03 | 2.231 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 5.532552e-03 | 2.257 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 5.837840e-03 | 2.234 | 0 | 0 |
| MET receptor recycling | R-HSA-8875656 | 6.424704e-03 | 2.192 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 6.515091e-03 | 2.186 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 6.615819e-03 | 2.179 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 6.950661e-03 | 2.158 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 7.001201e-03 | 2.155 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 7.042278e-03 | 2.152 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 7.143467e-03 | 2.146 | 1 | 1 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 7.196928e-03 | 2.143 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 7.196928e-03 | 2.143 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 7.854134e-03 | 2.105 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 7.554843e-03 | 2.122 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 8.430196e-03 | 2.074 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 8.439127e-03 | 2.074 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 8.698365e-03 | 2.061 | 0 | 0 |
| MET activates RAP1 and RAC1 | R-HSA-8875555 | 8.848464e-03 | 2.053 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 8.911623e-03 | 2.050 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 9.103282e-03 | 2.041 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 1.039120e-02 | 1.983 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 1.138665e-02 | 1.944 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 1.138665e-02 | 1.944 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 1.015056e-02 | 1.994 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 9.520302e-03 | 2.021 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 9.949563e-03 | 2.002 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 1.084533e-02 | 1.965 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 1.084533e-02 | 1.965 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.120273e-02 | 1.951 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 9.944666e-03 | 2.002 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 1.131210e-02 | 1.946 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 1.130353e-02 | 1.947 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 9.520302e-03 | 2.021 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 1.033299e-02 | 1.986 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 1.152951e-02 | 1.938 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 1.161683e-02 | 1.935 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.161683e-02 | 1.935 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 1.179161e-02 | 1.928 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.179161e-02 | 1.928 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 1.212843e-02 | 1.916 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.228400e-02 | 1.911 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.234663e-02 | 1.908 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 1.274225e-02 | 1.895 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 1.278937e-02 | 1.893 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 1.278937e-02 | 1.893 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 1.278937e-02 | 1.893 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 1.301121e-02 | 1.886 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.471423e-02 | 1.832 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 1.330160e-02 | 1.876 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 1.551495e-02 | 1.809 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 1.542311e-02 | 1.812 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 1.587298e-02 | 1.799 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 1.330785e-02 | 1.876 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 1.551495e-02 | 1.809 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 1.494299e-02 | 1.826 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 1.438455e-02 | 1.842 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 1.610053e-02 | 1.793 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 1.330160e-02 | 1.876 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 1.610053e-02 | 1.793 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.638158e-02 | 1.786 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.638158e-02 | 1.786 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 1.679882e-02 | 1.775 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 1.679882e-02 | 1.775 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 1.701887e-02 | 1.769 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 1.783290e-02 | 1.749 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 1.793994e-02 | 1.746 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.812558e-02 | 1.742 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.812558e-02 | 1.742 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.825379e-02 | 1.739 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 1.858092e-02 | 1.731 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 1.881890e-02 | 1.725 | 1 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 1.994441e-02 | 1.700 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 1.998381e-02 | 1.699 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 2.085940e-02 | 1.681 | 0 | 0 |
| Drug-mediated inhibition of MET activation | R-HSA-9734091 | 2.125879e-02 | 1.672 | 0 | 0 |
| Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) | R-HSA-5619110 | 2.125879e-02 | 1.672 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 2.131892e-02 | 1.671 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 2.199123e-02 | 1.658 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 2.199123e-02 | 1.658 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 2.272479e-02 | 1.644 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 2.346575e-02 | 1.630 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 2.583227e-02 | 1.588 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.583227e-02 | 1.588 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5619101 | 3.171907e-02 | 1.499 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5660686 | 3.171907e-02 | 1.499 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 3.233131e-02 | 1.490 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 3.462577e-02 | 1.461 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 3.443917e-02 | 1.463 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 3.009983e-02 | 1.521 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 2.747420e-02 | 1.561 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 3.233646e-02 | 1.490 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 2.992137e-02 | 1.524 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 3.592473e-02 | 1.445 | 1 | 1 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.462577e-02 | 1.461 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 3.592473e-02 | 1.445 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 3.168356e-02 | 1.499 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 3.733011e-02 | 1.428 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 3.733011e-02 | 1.428 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 3.827926e-02 | 1.417 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 3.939730e-02 | 1.405 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 4.035675e-02 | 1.394 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 4.072631e-02 | 1.390 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 4.440208e-02 | 1.353 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 4.681757e-02 | 1.330 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 4.698819e-02 | 1.328 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 4.794715e-02 | 1.319 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 4.962816e-02 | 1.304 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 4.962816e-02 | 1.304 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 4.962816e-02 | 1.304 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 4.962816e-02 | 1.304 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 5.086597e-02 | 1.294 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 5.182498e-02 | 1.285 | 0 | 0 |
| Defective CYP19A1 causes AEXS | R-HSA-5579030 | 5.230735e-02 | 1.281 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.230735e-02 | 1.281 | 0 | 0 |
| MET activates STAT3 | R-HSA-8875791 | 5.230735e-02 | 1.281 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 5.232055e-02 | 1.281 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 5.261572e-02 | 1.279 | 0 | 0 |
| TLR3-mediated TICAM1-dependent programmed cell death | R-HSA-9013957 | 6.243768e-02 | 1.205 | 0 | 0 |
| TGFBR1 KD Mutants in Cancer | R-HSA-3656532 | 6.243768e-02 | 1.205 | 0 | 0 |
| SMAD2/3 Phosphorylation Motif Mutants in Cancer | R-HSA-3304356 | 7.246034e-02 | 1.140 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.237647e-02 | 1.084 | 0 | 0 |
| Defective CSF2RA causes SMDP4 | R-HSA-5688890 | 8.237647e-02 | 1.084 | 0 | 0 |
| Defective CSF2RB causes SMDP5 | R-HSA-5688849 | 8.237647e-02 | 1.084 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 7.003705e-02 | 1.155 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 6.532963e-02 | 1.185 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 6.532963e-02 | 1.185 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 6.532963e-02 | 1.185 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 7.246034e-02 | 1.140 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 7.246034e-02 | 1.140 | 0 | 0 |
| SLC15A4:TASL-dependent IRF5 activation | R-HSA-9860276 | 8.237647e-02 | 1.084 | 0 | 0 |
| SARS-CoV-1-mediated effects on programmed cell death | R-HSA-9692913 | 6.243768e-02 | 1.205 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 7.558319e-02 | 1.122 | 0 | 0 |
| Loss of Function of TGFBR1 in Cancer | R-HSA-3656534 | 7.246034e-02 | 1.140 | 0 | 0 |
| Loss of Function of SMAD2/3 in Cancer | R-HSA-3304349 | 8.237647e-02 | 1.084 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 7.983769e-02 | 1.098 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 7.764972e-02 | 1.110 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 6.652054e-02 | 1.177 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 7.157181e-02 | 1.145 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 5.839916e-02 | 1.234 | 1 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 5.758912e-02 | 1.240 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 7.868690e-02 | 1.104 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 6.804878e-02 | 1.167 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 7.252007e-02 | 1.140 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 6.243768e-02 | 1.205 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 8.182999e-02 | 1.087 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 7.801897e-02 | 1.108 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.237647e-02 | 1.084 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 7.366039e-02 | 1.133 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 6.652054e-02 | 1.177 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 7.868690e-02 | 1.104 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 6.069836e-02 | 1.217 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 7.150471e-02 | 1.146 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 7.383423e-02 | 1.132 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 6.949877e-02 | 1.158 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 8.082302e-02 | 1.092 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 5.601691e-02 | 1.252 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 6.804878e-02 | 1.167 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 6.915990e-02 | 1.160 | 1 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 6.808792e-02 | 1.167 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 5.503986e-02 | 1.259 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 8.765103e-02 | 1.057 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 8.765103e-02 | 1.057 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 9.025550e-02 | 1.045 | 1 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 9.025550e-02 | 1.045 | 1 | 1 |
| Parasite infection | R-HSA-9664407 | 9.025550e-02 | 1.045 | 1 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 9.148384e-02 | 1.039 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 9.184654e-02 | 1.037 | 0 | 0 |
| MET Receptor Activation | R-HSA-6806942 | 9.218720e-02 | 1.035 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex in Cancer | R-HSA-3304351 | 9.218720e-02 | 1.035 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 9.389987e-02 | 1.027 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 9.477283e-02 | 1.023 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 9.602276e-02 | 1.018 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 9.669973e-02 | 1.015 | 0 | 0 |
| TRIF-mediated programmed cell death | R-HSA-2562578 | 1.018936e-01 | 0.992 | 0 | 0 |
| Activated NTRK2 signals through PI3K | R-HSA-9028335 | 1.114969e-01 | 0.953 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.209980e-01 | 0.917 | 0 | 0 |
| CASP8 activity is inhibited | R-HSA-5218900 | 1.209980e-01 | 0.917 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 1.303982e-01 | 0.885 | 0 | 0 |
| Highly calcium permeable postsynaptic nicotinic acetylcholine receptors | R-HSA-629594 | 1.303982e-01 | 0.885 | 0 | 0 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | R-HSA-933543 | 1.396983e-01 | 0.855 | 0 | 0 |
| RHOBTB3 ATPase cycle | R-HSA-9706019 | 1.396983e-01 | 0.855 | 0 | 0 |
| MET activates RAS signaling | R-HSA-8851805 | 1.580031e-01 | 0.801 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.580031e-01 | 0.801 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.580031e-01 | 0.801 | 0 | 0 |
| InlB-mediated entry of Listeria monocytogenes into host cell | R-HSA-8875360 | 1.847366e-01 | 0.733 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.847366e-01 | 0.733 | 0 | 0 |
| TICAM1, RIP1-mediated IKK complex recruitment | R-HSA-168927 | 1.847366e-01 | 0.733 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.934588e-01 | 0.713 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.934588e-01 | 0.713 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 1.047077e-01 | 0.980 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 1.069260e-01 | 0.971 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.777072e-01 | 0.750 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.777072e-01 | 0.750 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.892438e-01 | 0.723 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 1.253127e-01 | 0.902 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 1.373441e-01 | 0.862 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 1.397967e-01 | 0.855 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.303982e-01 | 0.885 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.396983e-01 | 0.855 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 1.114969e-01 | 0.953 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 1.488996e-01 | 0.827 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 1.397967e-01 | 0.855 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 1.329442e-01 | 0.876 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 1.151764e-01 | 0.939 | 0 | 0 |
| ATF6 (ATF6-alpha) activates chaperone genes | R-HSA-381183 | 1.488996e-01 | 0.827 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.759205e-01 | 0.755 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.847366e-01 | 0.733 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.847366e-01 | 0.733 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 1.069260e-01 | 0.971 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 1.512813e-01 | 0.820 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.580031e-01 | 0.801 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 1.777072e-01 | 0.750 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 1.650964e-01 | 0.782 | 0 | 0 |
| Caspase activation via Death Receptors in the presence of ligand | R-HSA-140534 | 1.934588e-01 | 0.713 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 1.650964e-01 | 0.782 | 0 | 0 |
| Regulation by c-FLIP | R-HSA-3371378 | 1.114969e-01 | 0.953 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 1.114969e-01 | 0.953 | 0 | 0 |
| Defective RIPK1-mediated regulated necrosis | R-HSA-9693928 | 1.303982e-01 | 0.885 | 0 | 0 |
| Membrane binding and targetting of GAG proteins | R-HSA-174490 | 1.670097e-01 | 0.777 | 0 | 0 |
| Postsynaptic nicotinic acetylcholine receptors | R-HSA-622327 | 1.670097e-01 | 0.777 | 0 | 0 |
| RIP-mediated NFkB activation via ZBP1 | R-HSA-1810476 | 1.847366e-01 | 0.733 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 1.154894e-01 | 0.937 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 1.625069e-01 | 0.789 | 1 | 1 |
| Microbial modulation of RIPK1-mediated regulated necrosis | R-HSA-9686347 | 1.018936e-01 | 0.992 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 9.816523e-02 | 1.008 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 1.003270e-01 | 0.999 | 1 | 1 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.488996e-01 | 0.827 | 0 | 0 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | R-HSA-174495 | 1.759205e-01 | 0.755 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 1.047077e-01 | 0.980 | 0 | 0 |
| Estrogen biosynthesis | R-HSA-193144 | 1.580031e-01 | 0.801 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.847366e-01 | 0.733 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 1.497527e-01 | 0.825 | 0 | 0 |
| Dimerization of procaspase-8 | R-HSA-69416 | 1.114969e-01 | 0.953 | 0 | 0 |
| Activation of RAC1 downstream of NMDARs | R-HSA-9619229 | 1.209980e-01 | 0.917 | 0 | 0 |
| Acetylcholine binding and downstream events | R-HSA-181431 | 1.670097e-01 | 0.777 | 0 | 0 |
| Activation of SMO | R-HSA-5635838 | 1.934588e-01 | 0.713 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 1.137186e-01 | 0.944 | 0 | 0 |
| ATF6 (ATF6-alpha) activates chaperones | R-HSA-381033 | 1.670097e-01 | 0.777 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 1.447461e-01 | 0.839 | 0 | 0 |
| Diseases associated with surfactant metabolism | R-HSA-5687613 | 1.580031e-01 | 0.801 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 1.206129e-01 | 0.919 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 1.082547e-01 | 0.966 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 1.668194e-01 | 0.778 | 0 | 0 |
| PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | R-HSA-8849469 | 1.114969e-01 | 0.953 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.209980e-01 | 0.917 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.488996e-01 | 0.827 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.580031e-01 | 0.801 | 0 | 0 |
| Synthesis of GDP-mannose | R-HSA-446205 | 1.580031e-01 | 0.801 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 1.276873e-01 | 0.894 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 1.226929e-01 | 0.911 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.082547e-01 | 0.966 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 1.402169e-01 | 0.853 | 0 | 0 |
| Nef Mediated CD4 Down-regulation | R-HSA-167590 | 1.018936e-01 | 0.992 | 0 | 0 |
| Synthesis of PIPs at the ER membrane | R-HSA-1483248 | 1.396983e-01 | 0.855 | 0 | 0 |
| Signaling by FGFR4 in disease | R-HSA-5655291 | 1.759205e-01 | 0.755 | 0 | 0 |
| Retrograde transport at the Trans-Golgi-Network | R-HSA-6811440 | 1.186790e-01 | 0.926 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 1.276873e-01 | 0.894 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 1.303982e-01 | 0.885 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 1.208741e-01 | 0.918 | 0 | 0 |
| Positive Regulation of CDH1 Gene Transcription | R-HSA-9764790 | 1.303982e-01 | 0.885 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.303982e-01 | 0.885 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 1.908034e-01 | 0.719 | 1 | 0 |
| Protein methylation | R-HSA-8876725 | 1.847366e-01 | 0.733 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 1.349066e-01 | 0.870 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 1.756367e-01 | 0.755 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.580031e-01 | 0.801 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.847366e-01 | 0.733 | 0 | 0 |
| Attachment and Entry | R-HSA-9678110 | 1.934588e-01 | 0.713 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 1.119601e-01 | 0.951 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 1.119601e-01 | 0.951 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 1.533175e-01 | 0.814 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 1.154894e-01 | 0.937 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 1.738868e-01 | 0.760 | 0 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 1.257624e-01 | 0.900 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 1.662884e-01 | 0.779 | 0 | 0 |
| Atorvastatin ADME | R-HSA-9754706 | 1.934588e-01 | 0.713 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 1.588494e-01 | 0.799 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 1.553214e-01 | 0.809 | 1 | 0 |
| Disease | R-HSA-1643685 | 1.671622e-01 | 0.777 | 1 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.373441e-01 | 0.862 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.222079e-01 | 0.913 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 1.402169e-01 | 0.853 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 1.077842e-01 | 0.967 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.373441e-01 | 0.862 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 1.229545e-01 | 0.910 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 1.293415e-01 | 0.888 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.396983e-01 | 0.855 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.396983e-01 | 0.855 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 1.573349e-01 | 0.803 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 2.016993e-01 | 0.695 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 2.020883e-01 | 0.694 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 2.020883e-01 | 0.694 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 2.020883e-01 | 0.694 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 2.020883e-01 | 0.694 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 2.020883e-01 | 0.694 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 2.047768e-01 | 0.689 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.106260e-01 | 0.676 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 2.106260e-01 | 0.676 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.106260e-01 | 0.676 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.106260e-01 | 0.676 | 0 | 0 |
| Modulation of host responses by IFN-stimulated genes | R-HSA-9909505 | 2.106260e-01 | 0.676 | 0 | 0 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 2.106260e-01 | 0.676 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 2.172564e-01 | 0.663 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.190729e-01 | 0.659 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.190729e-01 | 0.659 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.190729e-01 | 0.659 | 0 | 0 |
| FOXO-mediated transcription of cell death genes | R-HSA-9614657 | 2.190729e-01 | 0.659 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.190729e-01 | 0.659 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 2.241120e-01 | 0.650 | 1 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 2.241120e-01 | 0.650 | 1 | 0 |
| DNA Repair | R-HSA-73894 | 2.261237e-01 | 0.646 | 0 | 0 |
| PI-3K cascade:FGFR3 | R-HSA-5654710 | 2.274299e-01 | 0.643 | 0 | 0 |
| IKK complex recruitment mediated by RIP1 | R-HSA-937041 | 2.274299e-01 | 0.643 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.274299e-01 | 0.643 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.274299e-01 | 0.643 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 2.274299e-01 | 0.643 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.274299e-01 | 0.643 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 2.331964e-01 | 0.632 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.356979e-01 | 0.628 | 0 | 0 |
| PI-3K cascade:FGFR4 | R-HSA-5654720 | 2.356979e-01 | 0.628 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.356979e-01 | 0.628 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.356979e-01 | 0.628 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.356979e-01 | 0.628 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.360269e-01 | 0.627 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 2.417061e-01 | 0.617 | 1 | 1 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 2.438780e-01 | 0.613 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.438780e-01 | 0.613 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.438780e-01 | 0.613 | 0 | 0 |
| Assembly Of The HIV Virion | R-HSA-175474 | 2.519711e-01 | 0.599 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.519711e-01 | 0.599 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 2.577698e-01 | 0.589 | 0 | 0 |
| PI-3K cascade:FGFR1 | R-HSA-5654689 | 2.599780e-01 | 0.585 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 2.599780e-01 | 0.585 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.599780e-01 | 0.585 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 2.599780e-01 | 0.585 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 2.646330e-01 | 0.577 | 1 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 2.678831e-01 | 0.572 | 0 | 0 |
| Organic anion transport by SLCO transporters | R-HSA-879518 | 2.678997e-01 | 0.572 | 0 | 0 |
| Constitutive Signaling by AKT1 E17K in Cancer | R-HSA-5674400 | 2.678997e-01 | 0.572 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 2.718467e-01 | 0.566 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 2.751129e-01 | 0.560 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.757371e-01 | 0.560 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.757371e-01 | 0.560 | 0 | 0 |
| Complex III assembly | R-HSA-9865881 | 2.757371e-01 | 0.560 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 2.797716e-01 | 0.553 | 0 | 0 |
| PI-3K cascade:FGFR2 | R-HSA-5654695 | 2.834910e-01 | 0.547 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.834910e-01 | 0.547 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.834910e-01 | 0.547 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 2.834910e-01 | 0.547 | 0 | 0 |
| HDMs demethylate histones | R-HSA-3214842 | 2.834910e-01 | 0.547 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 2.834910e-01 | 0.547 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 2.849072e-01 | 0.545 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.876905e-01 | 0.541 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.911625e-01 | 0.536 | 0 | 0 |
| TRP channels | R-HSA-3295583 | 2.911625e-01 | 0.536 | 0 | 0 |
| Caspase activation via extrinsic apoptotic signalling pathway | R-HSA-5357769 | 2.911625e-01 | 0.536 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.911625e-01 | 0.536 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.911625e-01 | 0.536 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 2.916468e-01 | 0.535 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 2.932858e-01 | 0.533 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 2.936388e-01 | 0.532 | 1 | 0 |
| TNFR1-induced NF-kappa-B signaling pathway | R-HSA-5357956 | 2.987522e-01 | 0.525 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 2.987522e-01 | 0.525 | 0 | 0 |
| Signaling by FGFR3 in disease | R-HSA-5655332 | 2.987522e-01 | 0.525 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 2.987522e-01 | 0.525 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 2.987522e-01 | 0.525 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 2.994703e-01 | 0.524 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 3.061843e-01 | 0.514 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 3.062612e-01 | 0.514 | 0 | 0 |
| ATF4 activates genes in response to endoplasmic reticulum stress | R-HSA-380994 | 3.062612e-01 | 0.514 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 3.092142e-01 | 0.510 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 3.111514e-01 | 0.507 | 0 | 0 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | R-HSA-917729 | 3.136902e-01 | 0.503 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 3.136902e-01 | 0.503 | 0 | 0 |
| Downstream signaling of activated FGFR3 | R-HSA-5654708 | 3.136902e-01 | 0.503 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.136902e-01 | 0.503 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.136902e-01 | 0.503 | 0 | 0 |
| Termination of translesion DNA synthesis | R-HSA-5656169 | 3.136902e-01 | 0.503 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 3.192431e-01 | 0.496 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.210401e-01 | 0.493 | 0 | 0 |
| Downstream signaling of activated FGFR4 | R-HSA-5654716 | 3.210401e-01 | 0.493 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 3.210401e-01 | 0.493 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.210401e-01 | 0.493 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 3.210401e-01 | 0.493 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.231672e-01 | 0.491 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.283117e-01 | 0.484 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 3.283117e-01 | 0.484 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 3.283117e-01 | 0.484 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 3.316218e-01 | 0.479 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 3.349043e-01 | 0.475 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.355060e-01 | 0.474 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.426236e-01 | 0.465 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.426236e-01 | 0.465 | 0 | 0 |
| Recycling of bile acids and salts | R-HSA-159418 | 3.426236e-01 | 0.465 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 3.496654e-01 | 0.456 | 0 | 0 |
| Translation | R-HSA-72766 | 3.546015e-01 | 0.450 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.566322e-01 | 0.448 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.566322e-01 | 0.448 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 3.579124e-01 | 0.446 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 3.581933e-01 | 0.446 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 3.618855e-01 | 0.441 | 0 | 0 |
| Downstream signaling of activated FGFR2 | R-HSA-5654696 | 3.635247e-01 | 0.439 | 0 | 0 |
| Downstream signaling of activated FGFR1 | R-HSA-5654687 | 3.635247e-01 | 0.439 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.635247e-01 | 0.439 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.703439e-01 | 0.431 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.703439e-01 | 0.431 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 3.703439e-01 | 0.431 | 0 | 0 |
| Voltage gated Potassium channels | R-HSA-1296072 | 3.770904e-01 | 0.424 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 3.770904e-01 | 0.424 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 3.773755e-01 | 0.423 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 3.773755e-01 | 0.423 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.837651e-01 | 0.416 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 3.840653e-01 | 0.416 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 3.849833e-01 | 0.415 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 3.903686e-01 | 0.409 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 3.903686e-01 | 0.409 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 3.969018e-01 | 0.401 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 3.969018e-01 | 0.401 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 3.969018e-01 | 0.401 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 3.998772e-01 | 0.398 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 4.013725e-01 | 0.396 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 4.033654e-01 | 0.394 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 4.033654e-01 | 0.394 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 4.033654e-01 | 0.394 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 4.033654e-01 | 0.394 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 4.033654e-01 | 0.394 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 4.033654e-01 | 0.394 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 4.078793e-01 | 0.389 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 4.097601e-01 | 0.387 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 4.097601e-01 | 0.387 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 4.097601e-01 | 0.387 | 0 | 0 |
| Intra-Golgi traffic | R-HSA-6811438 | 4.097601e-01 | 0.387 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 4.097601e-01 | 0.387 | 0 | 0 |
| SLC-mediated transport of neurotransmitters | R-HSA-442660 | 4.097601e-01 | 0.387 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.160866e-01 | 0.381 | 0 | 0 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | R-HSA-381676 | 4.160866e-01 | 0.381 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.160866e-01 | 0.381 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 4.185444e-01 | 0.378 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 4.186990e-01 | 0.378 | 0 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 4.223458e-01 | 0.374 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.223458e-01 | 0.374 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 4.223458e-01 | 0.374 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.223458e-01 | 0.374 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 4.244281e-01 | 0.372 | 1 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 4.270716e-01 | 0.369 | 1 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 4.285382e-01 | 0.368 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 4.285382e-01 | 0.368 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.285382e-01 | 0.368 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 4.327325e-01 | 0.364 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 4.346646e-01 | 0.362 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.346646e-01 | 0.362 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 4.346646e-01 | 0.362 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.346646e-01 | 0.362 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 4.370265e-01 | 0.359 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 4.390037e-01 | 0.358 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 4.407257e-01 | 0.356 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 4.407257e-01 | 0.356 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 4.467222e-01 | 0.350 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.467222e-01 | 0.350 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 4.478731e-01 | 0.349 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 4.526548e-01 | 0.344 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 4.585241e-01 | 0.339 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 4.585241e-01 | 0.339 | 0 | 0 |
| Chemokine receptors bind chemokines | R-HSA-380108 | 4.585241e-01 | 0.339 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 4.643309e-01 | 0.333 | 0 | 0 |
| Signaling by FGFR2 in disease | R-HSA-5655253 | 4.643309e-01 | 0.333 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.700757e-01 | 0.328 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 4.717517e-01 | 0.326 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 4.757593e-01 | 0.323 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.757593e-01 | 0.323 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 4.757593e-01 | 0.323 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 4.757593e-01 | 0.323 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 4.813822e-01 | 0.318 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 4.813822e-01 | 0.318 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 4.813822e-01 | 0.318 | 0 | 0 |
| Amino acids regulate mTORC1 | R-HSA-9639288 | 4.813822e-01 | 0.318 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 4.843933e-01 | 0.315 | 1 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 4.869452e-01 | 0.313 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 4.869452e-01 | 0.313 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 4.869452e-01 | 0.313 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 4.924489e-01 | 0.308 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 4.924489e-01 | 0.308 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 4.934790e-01 | 0.307 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 4.978938e-01 | 0.303 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 4.978938e-01 | 0.303 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 4.978938e-01 | 0.303 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 4.988766e-01 | 0.302 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 5.032807e-01 | 0.298 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 5.032807e-01 | 0.298 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 5.032807e-01 | 0.298 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 5.086102e-01 | 0.294 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.086102e-01 | 0.294 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 5.095314e-01 | 0.293 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 5.137179e-01 | 0.289 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 5.137179e-01 | 0.289 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.138827e-01 | 0.289 | 0 | 0 |
| Amino acid transport across the plasma membrane | R-HSA-352230 | 5.138827e-01 | 0.289 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 5.190990e-01 | 0.285 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 5.226833e-01 | 0.282 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.242597e-01 | 0.280 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 5.242597e-01 | 0.280 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.242597e-01 | 0.280 | 0 | 0 |
| Endogenous sterols | R-HSA-211976 | 5.242597e-01 | 0.280 | 0 | 0 |
| Collagen degradation | R-HSA-1442490 | 5.242597e-01 | 0.280 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 5.293653e-01 | 0.276 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 5.293653e-01 | 0.276 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 5.301747e-01 | 0.276 | 0 | 0 |
| Activation of gene expression by SREBF (SREBP) | R-HSA-2426168 | 5.344164e-01 | 0.272 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.344164e-01 | 0.272 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.344164e-01 | 0.272 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 5.394136e-01 | 0.268 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.394136e-01 | 0.268 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 5.430672e-01 | 0.265 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 5.443575e-01 | 0.264 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 5.443575e-01 | 0.264 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 5.484034e-01 | 0.261 | 0 | 0 |
| Metabolism of steroid hormones | R-HSA-196071 | 5.540876e-01 | 0.256 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.540876e-01 | 0.256 | 0 | 0 |
| SLC-mediated transport of amino acids | R-HSA-9958863 | 5.540876e-01 | 0.256 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 5.588749e-01 | 0.253 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.588749e-01 | 0.253 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 5.588749e-01 | 0.253 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 5.617278e-01 | 0.250 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 5.619441e-01 | 0.250 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.711729e-01 | 0.243 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 5.729322e-01 | 0.242 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 5.729322e-01 | 0.242 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 5.729322e-01 | 0.242 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 5.729322e-01 | 0.242 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 5.775183e-01 | 0.238 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.820555e-01 | 0.235 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.820555e-01 | 0.235 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 5.832590e-01 | 0.234 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.865441e-01 | 0.232 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 5.865441e-01 | 0.232 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 5.921590e-01 | 0.228 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.040246e-01 | 0.219 | 0 | 0 |
| SLC-mediated transport of organic anions | R-HSA-9955298 | 6.040246e-01 | 0.219 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 6.040246e-01 | 0.219 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 6.048604e-01 | 0.218 | 1 | 0 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | R-HSA-1655829 | 6.082787e-01 | 0.216 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.082787e-01 | 0.216 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 6.123758e-01 | 0.213 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 6.123758e-01 | 0.213 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 6.124873e-01 | 0.213 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.207701e-01 | 0.207 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 6.250096e-01 | 0.204 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 6.263456e-01 | 0.203 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 6.328655e-01 | 0.199 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 6.330761e-01 | 0.199 | 1 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 6.368114e-01 | 0.196 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 6.368114e-01 | 0.196 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 6.407151e-01 | 0.193 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.407151e-01 | 0.193 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 6.445772e-01 | 0.191 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 6.445772e-01 | 0.191 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 6.559174e-01 | 0.183 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 6.582836e-01 | 0.182 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 6.633905e-01 | 0.178 | 0 | 0 |
| Protein folding | R-HSA-391251 | 6.668978e-01 | 0.176 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 6.668978e-01 | 0.176 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 6.704800e-01 | 0.174 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 6.731681e-01 | 0.172 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 6.740238e-01 | 0.171 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 6.844296e-01 | 0.165 | 0 | 0 |
| Potassium Channels | R-HSA-1296071 | 6.844296e-01 | 0.165 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.880137e-01 | 0.162 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 6.911827e-01 | 0.160 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 6.911827e-01 | 0.160 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 6.945051e-01 | 0.158 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 6.977920e-01 | 0.156 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 6.977920e-01 | 0.156 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 6.977920e-01 | 0.156 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 7.010437e-01 | 0.154 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 7.033278e-01 | 0.153 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 7.042607e-01 | 0.152 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 7.095286e-01 | 0.149 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 7.105917e-01 | 0.148 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 7.133808e-01 | 0.147 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 7.133808e-01 | 0.147 | 0 | 0 |
| Post-translational modification: synthesis of GPI-anchored proteins | R-HSA-163125 | 7.137065e-01 | 0.146 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 7.137065e-01 | 0.146 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 7.169420e-01 | 0.145 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.198364e-01 | 0.143 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 7.221701e-01 | 0.141 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 7.228523e-01 | 0.141 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 7.232437e-01 | 0.141 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 7.243319e-01 | 0.140 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.258359e-01 | 0.139 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 7.287875e-01 | 0.137 | 0 | 0 |
| Bile acid and bile salt metabolism | R-HSA-194068 | 7.317076e-01 | 0.136 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 7.402815e-01 | 0.131 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 7.485829e-01 | 0.126 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 7.485829e-01 | 0.126 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 7.512910e-01 | 0.124 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 7.566205e-01 | 0.121 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.566205e-01 | 0.121 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 7.669412e-01 | 0.115 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 7.719372e-01 | 0.112 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.743951e-01 | 0.111 | 0 | 0 |
| Synthesis of substrates in N-glycan biosythesis | R-HSA-446219 | 7.953642e-01 | 0.099 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 7.975710e-01 | 0.098 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 7.975710e-01 | 0.098 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 7.975710e-01 | 0.098 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 8.082551e-01 | 0.092 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 8.109820e-01 | 0.091 | 1 | 1 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 8.143945e-01 | 0.089 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 8.171106e-01 | 0.088 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 8.179191e-01 | 0.087 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.241955e-01 | 0.084 | 0 | 0 |
| S Phase | R-HSA-69242 | 8.334817e-01 | 0.079 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 8.334817e-01 | 0.079 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 8.370582e-01 | 0.077 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.405583e-01 | 0.075 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 8.405583e-01 | 0.075 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 8.408706e-01 | 0.075 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 8.422802e-01 | 0.075 | 0 | 0 |
| PPARA activates gene expression | R-HSA-1989781 | 8.456687e-01 | 0.073 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 8.464684e-01 | 0.072 | 0 | 0 |
| Regulation of lipid metabolism by PPARalpha | R-HSA-400206 | 8.489848e-01 | 0.071 | 0 | 0 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | R-HSA-446193 | 8.489848e-01 | 0.071 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 8.552664e-01 | 0.068 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 8.569685e-01 | 0.067 | 0 | 0 |
| Cytochrome P450 - arranged by substrate type | R-HSA-211897 | 8.645324e-01 | 0.063 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.716985e-01 | 0.060 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 8.716985e-01 | 0.060 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 8.723116e-01 | 0.059 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 8.771590e-01 | 0.057 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 8.850715e-01 | 0.053 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 8.855789e-01 | 0.053 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 8.910127e-01 | 0.050 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 8.927530e-01 | 0.049 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 8.945135e-01 | 0.048 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 8.963868e-01 | 0.048 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 8.987216e-01 | 0.046 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 9.016877e-01 | 0.045 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 9.067120e-01 | 0.043 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.094284e-01 | 0.041 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 9.123407e-01 | 0.040 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.132907e-01 | 0.039 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.217578e-01 | 0.035 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.263709e-01 | 0.033 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 9.368626e-01 | 0.028 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.407156e-01 | 0.027 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.548479e-01 | 0.020 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.605022e-01 | 0.018 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.695540e-01 | 0.013 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.890776e-01 | 0.005 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.905370e-01 | 0.004 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.933548e-01 | 0.003 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 9.944332e-01 | 0.002 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.951475e-01 | 0.002 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.973821e-01 | 0.001 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.987452e-01 | 0.001 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.995060e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999996e-01 | 0.000 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 1.000000e+00 | 0.000 | 1 | 1 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 1.000000e+00 | 0.000 | 1 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 1.000000e+00 | 0.000 | 1 | 1 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 1.000000e+00 | 0.000 | 1 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 1.000000e+00 | 0.000 | 1 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 1.000000e+00 | 0.000 | 1 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 1.000000e+00 | 0.000 | 1 | 0 |
| Diseases of Immune System | R-HSA-5260271 | 1.000000e+00 | 0.000 | 1 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 1.000000e+00 | 0.000 | 1 | 0 |
| MyD88 deficiency (TLR2/4) | R-HSA-5602498 | 1.000000e+00 | 0.000 | 1 | 1 |
| IRAK4 deficiency (TLR2/4) | R-HSA-5603041 | 1.000000e+00 | 0.000 | 1 | 1 |
| G beta:gamma signalling through BTK | R-HSA-8964315 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 1.110223e-16 | 15.955 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 1.110223e-16 | 15.955 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 1.110223e-16 | 15.955 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 1.110223e-16 | 15.955 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 1.110223e-16 | 15.955 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 1.110223e-16 | 15.955 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 1.110223e-16 | 15.955 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 1.110223e-16 | 15.955 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.110223e-16 | 15.955 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 1.110223e-16 | 15.955 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 1.110223e-16 | 15.955 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 1.110223e-16 | 15.955 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.110223e-16 | 15.955 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 1.110223e-16 | 15.955 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 1.110223e-16 | 15.955 | 0 | 0 |
| 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 |
| M Phase | R-HSA-68886 | 1.110223e-16 | 15.955 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 1.110223e-16 | 15.955 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.110223e-16 | 15.955 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 1.110223e-16 | 15.955 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.110223e-16 | 15.955 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 1.110223e-16 | 15.955 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 1.110223e-16 | 15.955 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 1.110223e-16 | 15.955 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 1.110223e-16 | 15.955 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 1.110223e-16 | 15.955 | 1 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 1.110223e-16 | 15.955 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 1.110223e-16 | 15.955 | 1 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 1.110223e-16 | 15.955 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 2.220446e-16 | 15.654 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 2.220446e-16 | 15.654 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 1.665335e-15 | 14.778 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 2.331468e-15 | 14.632 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 8.104628e-15 | 14.091 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 2.098322e-14 | 13.678 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 2.098322e-14 | 13.678 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 3.641532e-14 | 13.439 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 4.130030e-14 | 13.384 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 9.303669e-14 | 13.031 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 1.050271e-13 | 12.979 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 1.374456e-13 | 12.862 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.362244e-13 | 12.866 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 1.336709e-13 | 12.874 | 0 | 0 |
| Kinesins | R-HSA-983189 | 1.389999e-13 | 12.857 | 0 | 0 |
| Protein folding | R-HSA-391251 | 1.452172e-13 | 12.838 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 1.791900e-13 | 12.747 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 1.832978e-13 | 12.737 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 2.662315e-13 | 12.575 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 3.251843e-13 | 12.488 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 3.701484e-13 | 12.432 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 3.701484e-13 | 12.432 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 6.930012e-13 | 12.159 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 8.456569e-13 | 12.073 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 9.057199e-13 | 12.043 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 1.014522e-12 | 11.994 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 1.661449e-12 | 11.780 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 1.706635e-12 | 11.768 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 2.188916e-12 | 11.660 | 0 | 0 |
| Disease | R-HSA-1643685 | 2.569167e-12 | 11.590 | 1 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 3.335443e-12 | 11.477 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 3.718692e-12 | 11.430 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 3.718692e-12 | 11.430 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 4.125811e-12 | 11.384 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 6.154188e-12 | 11.211 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 7.845502e-12 | 11.105 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 7.845502e-12 | 11.105 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 9.177992e-12 | 11.037 | 0 | 0 |
| Depurination | R-HSA-73927 | 9.945045e-12 | 11.002 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 1.308487e-11 | 10.883 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 1.341904e-11 | 10.872 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 1.341904e-11 | 10.872 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 1.572542e-11 | 10.803 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 1.572542e-11 | 10.803 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 1.962486e-11 | 10.707 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 1.962486e-11 | 10.707 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 2.107281e-11 | 10.676 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 2.369283e-11 | 10.625 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 3.013545e-11 | 10.521 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 3.013545e-11 | 10.521 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 3.709433e-11 | 10.431 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 4.337153e-11 | 10.363 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 4.604783e-11 | 10.337 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 5.347078e-11 | 10.272 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 5.550416e-11 | 10.256 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 5.550416e-11 | 10.256 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 6.390266e-11 | 10.194 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 6.390266e-11 | 10.194 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 9.868317e-11 | 10.006 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.016366e-10 | 9.993 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 9.868317e-11 | 10.006 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 1.080275e-10 | 9.966 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 1.197537e-10 | 9.922 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 1.241897e-10 | 9.906 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 1.260124e-10 | 9.900 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 1.883044e-10 | 9.725 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 1.988421e-10 | 9.701 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 2.024659e-10 | 9.694 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 2.491443e-10 | 9.604 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 2.596288e-10 | 9.586 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 2.846124e-10 | 9.546 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 3.295999e-10 | 9.482 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 3.334253e-10 | 9.477 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 3.359852e-10 | 9.474 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 3.539828e-10 | 9.451 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 3.633788e-10 | 9.440 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 4.328579e-10 | 9.364 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 5.438060e-10 | 9.265 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 6.352031e-10 | 9.197 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 7.401454e-10 | 9.131 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 9.414847e-10 | 9.026 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 9.961012e-10 | 9.002 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.043854e-09 | 8.981 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 1.065772e-09 | 8.972 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 1.359722e-09 | 8.867 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 1.411626e-09 | 8.850 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 1.481792e-09 | 8.829 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 1.766220e-09 | 8.753 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 1.523288e-09 | 8.817 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 2.026747e-09 | 8.693 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 2.321160e-09 | 8.634 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 2.446137e-09 | 8.612 | 1 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 2.763627e-09 | 8.559 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 2.872463e-09 | 8.542 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 2.989710e-09 | 8.524 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 3.027306e-09 | 8.519 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 3.027306e-09 | 8.519 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 3.447815e-09 | 8.462 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 3.885486e-09 | 8.411 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 3.885486e-09 | 8.411 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 3.885486e-09 | 8.411 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 3.919819e-09 | 8.407 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 4.719308e-09 | 8.326 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 5.585315e-09 | 8.253 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 6.439772e-09 | 8.191 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 7.925483e-09 | 8.101 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 8.176040e-09 | 8.087 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 9.100238e-09 | 8.041 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 1.031886e-08 | 7.986 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 9.680481e-09 | 8.014 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 1.156760e-08 | 7.937 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 1.181691e-08 | 7.927 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 1.297157e-08 | 7.887 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.622014e-08 | 7.790 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.622014e-08 | 7.790 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 1.645159e-08 | 7.784 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 2.271691e-08 | 7.644 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 2.380817e-08 | 7.623 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 2.467608e-08 | 7.608 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 2.535153e-08 | 7.596 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 2.685349e-08 | 7.571 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 3.374880e-08 | 7.472 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 3.374880e-08 | 7.472 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 3.611387e-08 | 7.442 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 3.731673e-08 | 7.428 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 4.203315e-08 | 7.376 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 4.226662e-08 | 7.374 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 4.904057e-08 | 7.309 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 4.966116e-08 | 7.304 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 5.423412e-08 | 7.266 | 1 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 6.170993e-08 | 7.210 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 6.914678e-08 | 7.160 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.931132e-08 | 7.159 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 7.523885e-08 | 7.124 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 7.635592e-08 | 7.117 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 8.116885e-08 | 7.091 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 8.785382e-08 | 7.056 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 9.121886e-08 | 7.040 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 9.213880e-08 | 7.036 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 1.292442e-07 | 6.889 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 1.292442e-07 | 6.889 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 1.292442e-07 | 6.889 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.256023e-07 | 6.901 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 1.256023e-07 | 6.901 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 1.496413e-07 | 6.825 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 1.496488e-07 | 6.825 | 0 | 0 |
| Immune System | R-HSA-168256 | 1.560987e-07 | 6.807 | 1 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 1.625828e-07 | 6.789 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 1.625828e-07 | 6.789 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.753660e-07 | 6.756 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 2.883269e-07 | 6.540 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 3.378781e-07 | 6.471 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 3.390266e-07 | 6.470 | 1 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 4.766770e-07 | 6.322 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 5.350856e-07 | 6.272 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 6.820171e-07 | 6.166 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 7.462357e-07 | 6.127 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 7.680612e-07 | 6.115 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 8.071145e-07 | 6.093 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 1.042818e-06 | 5.982 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 1.107192e-06 | 5.956 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 1.231455e-06 | 5.910 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 1.967054e-06 | 5.706 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 3.046292e-06 | 5.516 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 3.388794e-06 | 5.470 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 4.853651e-06 | 5.314 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 5.378570e-06 | 5.269 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 5.823181e-06 | 5.235 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 7.286304e-06 | 5.137 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 7.938582e-06 | 5.100 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 1.110198e-05 | 4.955 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 1.230500e-05 | 4.910 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 1.254757e-05 | 4.901 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 1.475911e-05 | 4.831 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 2.012257e-05 | 4.696 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 2.376601e-05 | 4.624 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 2.663752e-05 | 4.575 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 3.142674e-05 | 4.503 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 4.742592e-05 | 4.324 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 7.011286e-05 | 4.154 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 8.216195e-05 | 4.085 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 8.216195e-05 | 4.085 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 1.368364e-04 | 3.864 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 1.496404e-04 | 3.825 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 1.576951e-04 | 3.802 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.701377e-04 | 3.769 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 2.249636e-04 | 3.648 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 2.019802e-04 | 3.695 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.332244e-04 | 3.632 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 2.430836e-04 | 3.614 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 2.495212e-04 | 3.603 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 2.723966e-04 | 3.565 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.557191e-04 | 3.449 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 4.978843e-04 | 3.303 | 1 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 5.079399e-04 | 3.294 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 5.570299e-04 | 3.254 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 5.813733e-04 | 3.236 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 5.813733e-04 | 3.236 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 5.873566e-04 | 3.231 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 5.961828e-04 | 3.225 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 6.008552e-04 | 3.221 | 1 | 1 |
| Signaling by Interleukins | R-HSA-449147 | 6.258321e-04 | 3.204 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 6.312578e-04 | 3.200 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 6.586046e-04 | 3.181 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 8.152782e-04 | 3.089 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 8.184536e-04 | 3.087 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 8.761166e-04 | 3.057 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 9.241143e-04 | 3.034 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 9.241143e-04 | 3.034 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 1.007860e-03 | 2.997 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 1.009339e-03 | 2.996 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.060501e-03 | 2.974 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 1.063901e-03 | 2.973 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 1.106869e-03 | 2.956 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 1.153774e-03 | 2.938 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 1.374686e-03 | 2.862 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 1.459991e-03 | 2.836 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 1.526674e-03 | 2.816 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 1.593306e-03 | 2.798 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 1.663006e-03 | 2.779 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.734860e-03 | 2.761 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 1.858843e-03 | 2.731 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.884914e-03 | 2.725 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 1.998377e-03 | 2.699 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 2.019090e-03 | 2.695 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 2.211550e-03 | 2.655 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 2.399225e-03 | 2.620 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 2.511871e-03 | 2.600 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 2.575259e-03 | 2.589 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 2.650196e-03 | 2.577 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 2.771646e-03 | 2.557 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 2.771646e-03 | 2.557 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 3.147876e-03 | 2.502 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 3.421905e-03 | 2.466 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 3.855021e-03 | 2.414 | 1 | 1 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 3.908750e-03 | 2.408 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 3.908750e-03 | 2.408 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 3.908750e-03 | 2.408 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 3.908750e-03 | 2.408 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 3.908750e-03 | 2.408 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 4.967749e-03 | 2.304 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 5.124687e-03 | 2.290 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 5.901093e-03 | 2.229 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 7.539474e-03 | 2.123 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 7.539474e-03 | 2.123 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 8.904499e-03 | 2.050 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.720244e-03 | 2.173 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.998125e-03 | 2.155 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 8.190156e-03 | 2.087 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 8.508845e-03 | 2.070 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 8.956592e-03 | 2.048 | 1 | 1 |
| Translation | R-HSA-72766 | 7.017120e-03 | 2.154 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 6.278667e-03 | 2.202 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 6.308942e-03 | 2.200 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 6.278667e-03 | 2.202 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 8.904499e-03 | 2.050 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 7.436509e-03 | 2.129 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 8.956592e-03 | 2.048 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 7.883524e-03 | 2.103 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 9.306155e-03 | 2.031 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 6.466729e-03 | 2.189 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 9.642134e-03 | 2.016 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 9.869586e-03 | 2.006 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 1.022502e-02 | 1.990 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 1.023180e-02 | 1.990 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 1.037118e-02 | 1.984 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 1.060303e-02 | 1.975 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.101627e-02 | 1.958 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 1.137295e-02 | 1.944 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.160731e-02 | 1.935 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.160731e-02 | 1.935 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.160731e-02 | 1.935 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.160731e-02 | 1.935 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.160731e-02 | 1.935 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.160731e-02 | 1.935 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 1.177184e-02 | 1.929 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 1.177184e-02 | 1.929 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 1.180229e-02 | 1.928 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.193700e-02 | 1.923 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 1.257915e-02 | 1.900 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 1.346254e-02 | 1.871 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 1.359948e-02 | 1.866 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.359948e-02 | 1.866 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.359948e-02 | 1.866 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.493083e-02 | 1.826 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.535620e-02 | 1.814 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.535620e-02 | 1.814 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 1.545808e-02 | 1.811 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.555288e-02 | 1.808 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 1.579698e-02 | 1.801 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 1.579698e-02 | 1.801 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.619102e-02 | 1.791 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.627374e-02 | 1.789 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 1.669253e-02 | 1.777 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 1.680183e-02 | 1.775 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.914282e-02 | 1.718 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 1.919082e-02 | 1.717 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 1.949741e-02 | 1.710 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 2.116809e-02 | 1.674 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 2.116809e-02 | 1.674 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 2.116809e-02 | 1.674 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.133042e-02 | 1.671 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 2.302978e-02 | 1.638 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.327828e-02 | 1.633 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.359542e-02 | 1.627 | 1 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.430442e-02 | 1.614 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 2.477495e-02 | 1.606 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 2.547119e-02 | 1.594 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 2.547119e-02 | 1.594 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 2.600067e-02 | 1.585 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 2.698023e-02 | 1.569 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.774463e-02 | 1.557 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.945243e-02 | 1.531 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 2.970167e-02 | 1.527 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 2.971432e-02 | 1.527 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 3.009645e-02 | 1.521 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 3.252455e-02 | 1.488 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 3.252455e-02 | 1.488 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 3.390575e-02 | 1.470 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 3.390575e-02 | 1.470 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 3.533413e-02 | 1.452 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 3.553279e-02 | 1.449 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 3.679319e-02 | 1.434 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 3.760137e-02 | 1.425 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 3.760137e-02 | 1.425 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.760137e-02 | 1.425 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 3.803954e-02 | 1.420 | 1 | 1 |
| Parasite infection | R-HSA-9664407 | 3.803954e-02 | 1.420 | 1 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 3.803954e-02 | 1.420 | 1 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 3.854617e-02 | 1.414 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 3.980285e-02 | 1.400 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 4.024606e-02 | 1.395 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 4.024606e-02 | 1.395 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 4.096347e-02 | 1.388 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 4.295898e-02 | 1.367 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 4.386565e-02 | 1.358 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 4.440251e-02 | 1.353 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.563127e-02 | 1.341 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.563127e-02 | 1.341 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.563127e-02 | 1.341 | 0 | 0 |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.563127e-02 | 1.341 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.563127e-02 | 1.341 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.563127e-02 | 1.341 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 4.573822e-02 | 1.340 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 4.721929e-02 | 1.326 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 4.785372e-02 | 1.320 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 4.858187e-02 | 1.314 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 4.858187e-02 | 1.314 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 4.955281e-02 | 1.305 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 4.955281e-02 | 1.305 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 4.964653e-02 | 1.304 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.766409e-02 | 1.170 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.849002e-02 | 1.105 | 0 | 0 |
| Plus-strand DNA synthesis | R-HSA-164525 | 8.919090e-02 | 1.050 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.919090e-02 | 1.050 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.919090e-02 | 1.050 | 0 | 0 |
| Uncoating of the HIV Virion | R-HSA-162585 | 9.976817e-02 | 1.001 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.976817e-02 | 1.001 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.976817e-02 | 1.001 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 8.017061e-02 | 1.096 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 7.677917e-02 | 1.115 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 7.013995e-02 | 1.154 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 9.061391e-02 | 1.043 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 7.849002e-02 | 1.105 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.919090e-02 | 1.050 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 5.748103e-02 | 1.240 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.671167e-02 | 1.246 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.671167e-02 | 1.246 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.919090e-02 | 1.050 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 5.748103e-02 | 1.240 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 5.316022e-02 | 1.274 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 5.526695e-02 | 1.258 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 6.613178e-02 | 1.180 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 6.613178e-02 | 1.180 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 9.417973e-02 | 1.026 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 8.278861e-02 | 1.082 | 0 | 0 |
| NADE modulates death signalling | R-HSA-205025 | 6.766409e-02 | 1.170 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 7.205333e-02 | 1.142 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 8.360788e-02 | 1.078 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 7.849002e-02 | 1.105 | 0 | 0 |
| Signaling by LTK in cancer | R-HSA-9842640 | 9.976817e-02 | 1.001 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.976817e-02 | 1.001 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 5.113967e-02 | 1.291 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 9.853534e-02 | 1.006 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.919090e-02 | 1.050 | 0 | 0 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 8.919090e-02 | 1.050 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 9.976817e-02 | 1.001 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 7.013995e-02 | 1.154 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 9.778553e-02 | 1.010 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 8.271472e-02 | 1.082 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 7.677917e-02 | 1.115 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 6.035278e-02 | 1.219 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.671253e-02 | 1.246 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 8.233679e-02 | 1.084 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 9.778553e-02 | 1.010 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 9.667119e-02 | 1.015 | 0 | 0 |
| Nectin/Necl trans heterodimerization | R-HSA-420597 | 7.849002e-02 | 1.105 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 5.785901e-02 | 1.238 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 8.360788e-02 | 1.078 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 7.013995e-02 | 1.154 | 0 | 0 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | R-HSA-9818027 | 8.017061e-02 | 1.096 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 8.017061e-02 | 1.096 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 9.061391e-02 | 1.043 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 8.055178e-02 | 1.094 | 1 | 1 |
| Regulation of TP53 Activity | R-HSA-5633007 | 5.893720e-02 | 1.230 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 9.061391e-02 | 1.043 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 1.014299e-01 | 0.994 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.014299e-01 | 0.994 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 1.051115e-01 | 0.978 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.051115e-01 | 0.978 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 1.088289e-01 | 0.963 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 1.090936e-01 | 0.962 | 1 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 1.102233e-01 | 0.958 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.102233e-01 | 0.958 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 1.105248e-01 | 0.957 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.163661e-01 | 0.934 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 1.201833e-01 | 0.920 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.201833e-01 | 0.920 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 1.201833e-01 | 0.920 | 0 | 0 |
| Reverse Transcription of HIV RNA | R-HSA-162589 | 1.205576e-01 | 0.919 | 0 | 0 |
| Minus-strand DNA synthesis | R-HSA-164516 | 1.205576e-01 | 0.919 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 1.205576e-01 | 0.919 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 1.205576e-01 | 0.919 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 1.205576e-01 | 0.919 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 1.208843e-01 | 0.918 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 1.230441e-01 | 0.910 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.240313e-01 | 0.906 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.240313e-01 | 0.906 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 1.281911e-01 | 0.892 | 0 | 0 |
| Lipophagy | R-HSA-9613354 | 1.307725e-01 | 0.883 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.307725e-01 | 0.883 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.307725e-01 | 0.883 | 0 | 0 |
| Calcineurin activates NFAT | R-HSA-2025928 | 1.307725e-01 | 0.883 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.307725e-01 | 0.883 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.307725e-01 | 0.883 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 1.307725e-01 | 0.883 | 0 | 0 |
| HuR (ELAVL1) binds and stabilizes mRNA | R-HSA-450520 | 1.307725e-01 | 0.883 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 1.318145e-01 | 0.880 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 1.370779e-01 | 0.863 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 1.391616e-01 | 0.856 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.397065e-01 | 0.855 | 0 | 0 |
| Binding and entry of HIV virion | R-HSA-173107 | 1.408693e-01 | 0.851 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.408693e-01 | 0.851 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.408693e-01 | 0.851 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.408693e-01 | 0.851 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.408693e-01 | 0.851 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.408693e-01 | 0.851 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.408693e-01 | 0.851 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 1.423853e-01 | 0.847 | 1 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 1.423853e-01 | 0.847 | 1 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 1.436904e-01 | 0.843 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.436904e-01 | 0.843 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.436904e-01 | 0.843 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 1.476980e-01 | 0.831 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.508495e-01 | 0.821 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.508495e-01 | 0.821 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.508495e-01 | 0.821 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 1.519261e-01 | 0.818 | 1 | 0 |
| RSV-host interactions | R-HSA-9833110 | 1.550103e-01 | 0.810 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 1.557804e-01 | 0.807 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.557804e-01 | 0.807 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.557804e-01 | 0.807 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 1.598530e-01 | 0.796 | 0 | 0 |
| APOBEC3G mediated resistance to HIV-1 infection | R-HSA-180689 | 1.607144e-01 | 0.794 | 0 | 0 |
| Integration of provirus | R-HSA-162592 | 1.607144e-01 | 0.794 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.633767e-01 | 0.787 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.633767e-01 | 0.787 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 1.639452e-01 | 0.785 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 1.641873e-01 | 0.785 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 1.648571e-01 | 0.783 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 1.680561e-01 | 0.775 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.704653e-01 | 0.768 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.704653e-01 | 0.768 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.704653e-01 | 0.768 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.704653e-01 | 0.768 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.704653e-01 | 0.768 | 0 | 0 |
| Advanced glycosylation endproduct receptor signaling | R-HSA-879415 | 1.704653e-01 | 0.768 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.704653e-01 | 0.768 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.704653e-01 | 0.768 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 1.718754e-01 | 0.765 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 1.721845e-01 | 0.764 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.721845e-01 | 0.764 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 1.721845e-01 | 0.764 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 1.721845e-01 | 0.764 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 1.737142e-01 | 0.760 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.801035e-01 | 0.744 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.801035e-01 | 0.744 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.801035e-01 | 0.744 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.801035e-01 | 0.744 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.801035e-01 | 0.744 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.801035e-01 | 0.744 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.896303e-01 | 0.722 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.896303e-01 | 0.722 | 0 | 0 |
| Respiratory syncytial virus genome transcription | R-HSA-9828642 | 1.896303e-01 | 0.722 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.896303e-01 | 0.722 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.896303e-01 | 0.722 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 1.972730e-01 | 0.705 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.990470e-01 | 0.701 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 1.990470e-01 | 0.701 | 0 | 0 |
| Protein lipoylation | R-HSA-9857492 | 1.990470e-01 | 0.701 | 0 | 0 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 1.990470e-01 | 0.701 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.990470e-01 | 0.701 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.990470e-01 | 0.701 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 2.010502e-01 | 0.697 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 2.014991e-01 | 0.696 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 2.057357e-01 | 0.687 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 2.067748e-01 | 0.685 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 2.083548e-01 | 0.681 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 2.083548e-01 | 0.681 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 2.083548e-01 | 0.681 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 2.083548e-01 | 0.681 | 0 | 0 |
| KSRP (KHSRP) binds and destabilizes mRNA | R-HSA-450604 | 2.083548e-01 | 0.681 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 2.083548e-01 | 0.681 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 2.100238e-01 | 0.678 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 2.160552e-01 | 0.665 | 0 | 0 |
| G beta:gamma signalling through CDC42 | R-HSA-8964616 | 2.175551e-01 | 0.662 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 2.175551e-01 | 0.662 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 2.175551e-01 | 0.662 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 2.175551e-01 | 0.662 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 2.175551e-01 | 0.662 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 2.190848e-01 | 0.659 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 2.227713e-01 | 0.652 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.266489e-01 | 0.645 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.266489e-01 | 0.645 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.266489e-01 | 0.645 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.266489e-01 | 0.645 | 0 | 0 |
| Metabolism of ingested H2SeO4 and H2SeO3 into H2Se | R-HSA-2408550 | 2.266489e-01 | 0.645 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.266489e-01 | 0.645 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 2.270487e-01 | 0.644 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 2.313320e-01 | 0.636 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 2.313320e-01 | 0.636 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 2.343588e-01 | 0.630 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 2.356205e-01 | 0.628 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.356377e-01 | 0.628 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.356377e-01 | 0.628 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.356377e-01 | 0.628 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.356377e-01 | 0.628 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 2.356377e-01 | 0.628 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 2.388589e-01 | 0.622 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 2.399135e-01 | 0.620 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 2.405220e-01 | 0.619 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 2.442103e-01 | 0.612 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.445225e-01 | 0.612 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.445225e-01 | 0.612 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.445225e-01 | 0.612 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.445225e-01 | 0.612 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.445225e-01 | 0.612 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 2.477744e-01 | 0.606 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 2.497023e-01 | 0.603 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 2.498170e-01 | 0.602 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.533046e-01 | 0.596 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.533046e-01 | 0.596 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.533046e-01 | 0.596 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.533046e-01 | 0.596 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.571172e-01 | 0.590 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 2.615969e-01 | 0.582 | 1 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.619851e-01 | 0.582 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.619851e-01 | 0.582 | 0 | 0 |
| Early Phase of HIV Life Cycle | R-HSA-162594 | 2.619851e-01 | 0.582 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 2.657292e-01 | 0.576 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 2.667077e-01 | 0.574 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.705652e-01 | 0.568 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.705652e-01 | 0.568 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 2.705652e-01 | 0.568 | 0 | 0 |
| Assembly Of The HIV Virion | R-HSA-175474 | 2.705652e-01 | 0.568 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.748463e-01 | 0.561 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.790461e-01 | 0.554 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 2.790461e-01 | 0.554 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.790461e-01 | 0.554 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.874290e-01 | 0.541 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.874290e-01 | 0.541 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 2.874290e-01 | 0.541 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 2.874614e-01 | 0.541 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.957148e-01 | 0.529 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.957148e-01 | 0.529 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.957148e-01 | 0.529 | 0 | 0 |
| Mitochondrial RNA degradation | R-HSA-9836573 | 2.957148e-01 | 0.529 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 2.958438e-01 | 0.529 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 3.039049e-01 | 0.517 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 3.039049e-01 | 0.517 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 3.039049e-01 | 0.517 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 3.039049e-01 | 0.517 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 3.039049e-01 | 0.517 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 3.064644e-01 | 0.514 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 3.096378e-01 | 0.509 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 3.120002e-01 | 0.506 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 3.120002e-01 | 0.506 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 3.128124e-01 | 0.505 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 3.191642e-01 | 0.496 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 3.200018e-01 | 0.495 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 3.200018e-01 | 0.495 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 3.200018e-01 | 0.495 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 3.200018e-01 | 0.495 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 3.200018e-01 | 0.495 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 3.200018e-01 | 0.495 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 3.200018e-01 | 0.495 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 3.279109e-01 | 0.484 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 3.279109e-01 | 0.484 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 3.279109e-01 | 0.484 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.279109e-01 | 0.484 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.279109e-01 | 0.484 | 0 | 0 |
| Iron assimilation using enterobactin | R-HSA-9638334 | 3.279109e-01 | 0.484 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 3.350483e-01 | 0.475 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 3.357284e-01 | 0.474 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.357284e-01 | 0.474 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.357284e-01 | 0.474 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.357284e-01 | 0.474 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.357284e-01 | 0.474 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 3.385134e-01 | 0.470 | 1 | 1 |
| Mitochondrial protein degradation | R-HSA-9837999 | 3.427425e-01 | 0.465 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.434555e-01 | 0.464 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.434555e-01 | 0.464 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.434555e-01 | 0.464 | 0 | 0 |
| GABA synthesis, release, reuptake and degradation | R-HSA-888590 | 3.434555e-01 | 0.464 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.434555e-01 | 0.464 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.434555e-01 | 0.464 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 3.510932e-01 | 0.455 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.510932e-01 | 0.455 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 3.586425e-01 | 0.445 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.586425e-01 | 0.445 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 3.586425e-01 | 0.445 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.595705e-01 | 0.444 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 3.661045e-01 | 0.436 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 3.661045e-01 | 0.436 | 1 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.661045e-01 | 0.436 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.661045e-01 | 0.436 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.661045e-01 | 0.436 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 3.734801e-01 | 0.428 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.734801e-01 | 0.428 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.807703e-01 | 0.419 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 3.807703e-01 | 0.419 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.807703e-01 | 0.419 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.807703e-01 | 0.419 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 3.807703e-01 | 0.419 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 3.807703e-01 | 0.419 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.807703e-01 | 0.419 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.879761e-01 | 0.411 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 3.879761e-01 | 0.411 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.879761e-01 | 0.411 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 3.879761e-01 | 0.411 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 3.879761e-01 | 0.411 | 0 | 0 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | R-HSA-2408508 | 3.879761e-01 | 0.411 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 3.950985e-01 | 0.403 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 3.950985e-01 | 0.403 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 3.950985e-01 | 0.403 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 3.950985e-01 | 0.403 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 3.968227e-01 | 0.401 | 0 | 0 |
| Voltage gated Potassium channels | R-HSA-1296072 | 4.021385e-01 | 0.396 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 4.021385e-01 | 0.396 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 4.021385e-01 | 0.396 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 4.021385e-01 | 0.396 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 4.021385e-01 | 0.396 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 4.021385e-01 | 0.396 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 4.049694e-01 | 0.393 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 4.090970e-01 | 0.388 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 4.090970e-01 | 0.388 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 4.159749e-01 | 0.381 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 4.159749e-01 | 0.381 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 4.159749e-01 | 0.381 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 4.159749e-01 | 0.381 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 4.159749e-01 | 0.381 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 4.170904e-01 | 0.380 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 4.170904e-01 | 0.380 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 4.227732e-01 | 0.374 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 4.227732e-01 | 0.374 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 4.227732e-01 | 0.374 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 4.227732e-01 | 0.374 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 4.227732e-01 | 0.374 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 4.251023e-01 | 0.372 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 4.294927e-01 | 0.367 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 4.294927e-01 | 0.367 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 4.294927e-01 | 0.367 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 4.361345e-01 | 0.360 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 4.361345e-01 | 0.360 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 4.361345e-01 | 0.360 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 4.361345e-01 | 0.360 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 4.361345e-01 | 0.360 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.426993e-01 | 0.354 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 4.448786e-01 | 0.352 | 1 | 1 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 4.448786e-01 | 0.352 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.491881e-01 | 0.348 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 4.556017e-01 | 0.341 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.556017e-01 | 0.341 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.556017e-01 | 0.341 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.556017e-01 | 0.341 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 4.604265e-01 | 0.337 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 4.619411e-01 | 0.335 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 4.619411e-01 | 0.335 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.619411e-01 | 0.335 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 4.619411e-01 | 0.335 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.619411e-01 | 0.335 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 4.619411e-01 | 0.335 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 4.619411e-01 | 0.335 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 4.619411e-01 | 0.335 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 4.623685e-01 | 0.335 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 4.681056e-01 | 0.330 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 4.682070e-01 | 0.330 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.682070e-01 | 0.330 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.682070e-01 | 0.330 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 4.682070e-01 | 0.330 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 4.708903e-01 | 0.327 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 4.744003e-01 | 0.324 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.744003e-01 | 0.324 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.805219e-01 | 0.318 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.805219e-01 | 0.318 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.805219e-01 | 0.318 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 4.822868e-01 | 0.317 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 4.925532e-01 | 0.308 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 4.925532e-01 | 0.308 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 4.984644e-01 | 0.302 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 4.984644e-01 | 0.302 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.984644e-01 | 0.302 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 5.043072e-01 | 0.297 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 5.043072e-01 | 0.297 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 5.043072e-01 | 0.297 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 5.100822e-01 | 0.292 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 5.100822e-01 | 0.292 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 5.100822e-01 | 0.292 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 5.270089e-01 | 0.278 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 5.325208e-01 | 0.274 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 5.325208e-01 | 0.274 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.379689e-01 | 0.269 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 5.433538e-01 | 0.265 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.433538e-01 | 0.265 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.433538e-01 | 0.265 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 5.486762e-01 | 0.261 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 5.486762e-01 | 0.261 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 5.539370e-01 | 0.257 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.539370e-01 | 0.257 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 5.591367e-01 | 0.252 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 5.642762e-01 | 0.249 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.642762e-01 | 0.249 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.642762e-01 | 0.249 | 0 | 0 |
| Ion transport by P-type ATPases | R-HSA-936837 | 5.693560e-01 | 0.245 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 5.693560e-01 | 0.245 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.693560e-01 | 0.245 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.693560e-01 | 0.245 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 5.743770e-01 | 0.241 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 5.743770e-01 | 0.241 | 0 | 0 |
| S Phase | R-HSA-69242 | 5.783155e-01 | 0.238 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 5.783155e-01 | 0.238 | 1 | 0 |
| Kidney development | R-HSA-9830369 | 5.842448e-01 | 0.233 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.848291e-01 | 0.233 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.890931e-01 | 0.230 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 5.944606e-01 | 0.226 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 5.986215e-01 | 0.223 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 5.986215e-01 | 0.223 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 6.033030e-01 | 0.219 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 6.033030e-01 | 0.219 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 6.033030e-01 | 0.219 | 0 | 0 |
| Metal ion assimilation from the host | R-HSA-9638482 | 6.033030e-01 | 0.219 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 6.079301e-01 | 0.216 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 6.079301e-01 | 0.216 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 6.079301e-01 | 0.216 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 6.162851e-01 | 0.210 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 6.170240e-01 | 0.210 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 6.214919e-01 | 0.207 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 6.345870e-01 | 0.198 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.345870e-01 | 0.198 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 6.345870e-01 | 0.198 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 6.388512e-01 | 0.195 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.388512e-01 | 0.195 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 6.430658e-01 | 0.192 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.430658e-01 | 0.192 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 6.472314e-01 | 0.189 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 6.554183e-01 | 0.183 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.594405e-01 | 0.181 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.634161e-01 | 0.178 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 6.673455e-01 | 0.176 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 6.712293e-01 | 0.173 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 6.750679e-01 | 0.171 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.826120e-01 | 0.166 | 1 | 1 |
| Neurotransmitter release cycle | R-HSA-112310 | 6.863185e-01 | 0.163 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 6.971815e-01 | 0.157 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 6.996710e-01 | 0.155 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 7.007186e-01 | 0.154 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 7.046607e-01 | 0.152 | 1 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 7.076702e-01 | 0.150 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 7.144611e-01 | 0.146 | 0 | 0 |
| Potassium Channels | R-HSA-1296071 | 7.144611e-01 | 0.146 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 7.144611e-01 | 0.146 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 7.177975e-01 | 0.144 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 7.210951e-01 | 0.142 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 7.275757e-01 | 0.138 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 7.307597e-01 | 0.136 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 7.307597e-01 | 0.136 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 7.339066e-01 | 0.134 | 0 | 0 |
| Mitochondrial ribosome-associated quality control | R-HSA-9937383 | 7.370169e-01 | 0.133 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 7.400911e-01 | 0.131 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.461326e-01 | 0.127 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.491007e-01 | 0.125 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.549339e-01 | 0.122 | 1 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.549339e-01 | 0.122 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 7.675367e-01 | 0.115 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.743077e-01 | 0.111 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 7.795578e-01 | 0.108 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 7.846863e-01 | 0.105 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.846863e-01 | 0.105 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 7.888843e-01 | 0.103 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 7.949742e-01 | 0.100 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 8.086024e-01 | 0.092 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 8.216635e-01 | 0.085 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 8.338378e-01 | 0.079 | 0 | 0 |
| Mitochondrial translation | R-HSA-5368287 | 8.377093e-01 | 0.077 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.505663e-01 | 0.070 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 8.557614e-01 | 0.068 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.748057e-01 | 0.058 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 8.841752e-01 | 0.053 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.926231e-01 | 0.049 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 8.926231e-01 | 0.049 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 8.951307e-01 | 0.048 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 8.951307e-01 | 0.048 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 9.011477e-01 | 0.045 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 9.079164e-01 | 0.042 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 9.172146e-01 | 0.038 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 9.264542e-01 | 0.033 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.264542e-01 | 0.033 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.401554e-01 | 0.027 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.412759e-01 | 0.026 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.508448e-01 | 0.022 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.525636e-01 | 0.021 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.568604e-01 | 0.019 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 9.575638e-01 | 0.019 | 1 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.682955e-01 | 0.014 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.701538e-01 | 0.013 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 9.715408e-01 | 0.013 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 9.778737e-01 | 0.010 | 1 | 0 |
| Biological oxidations | R-HSA-211859 | 9.881599e-01 | 0.005 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.915772e-01 | 0.004 | 1 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.936825e-01 | 0.003 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.936825e-01 | 0.003 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.994836e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.998159e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999937e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999981e-01 | 0.000 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 1.000000e+00 | 0.000 | 1 | 1 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 1.000000e+00 | 0.000 | 1 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 1.000000e+00 | 0.000 | 1 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 1.000000e+00 | 0.000 | 1 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 1.000000e+00 | 0.000 | 1 | 1 |
| Diseases of Immune System | R-HSA-5260271 | 1.000000e+00 | 0.000 | 1 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 1.000000e+00 | 0.000 | 1 | 0 |
| MyD88 deficiency (TLR2/4) | R-HSA-5602498 | 1.000000e+00 | 0.000 | 1 | 1 |
| IRAK4 deficiency (TLR2/4) | R-HSA-5603041 | 1.000000e+00 | 0.000 | 1 | 1 |
| G beta:gamma signalling through BTK | R-HSA-8964315 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
