HCK
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 |
|---|---|---|---|---|
| A0MZ66 | Y24 | Sugiyama | SHTN1 KIAA1598 | sDEEKQLQLITsLKEQAIGEyEDLRAENQKTKEKCDKIRQE |
| A1L429 | Y9 | Sugiyama | GAGE12B; GAGE12C; GAGE12D; GAGE12E | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A4FU28 | Y433 | Sugiyama | CTAGE9 | EEKLSRVEEKISHATEELETyRKLAKDLEEELERTVHFYQK |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y851 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | QVWPEANQHFSKEIDDEANSyFQRIYNHPPHPTMSVDEVLE |
| A6NDE8 | Y9 | Sugiyama | GAGE12H | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A6NER3 | Y9 | Sugiyama | GAGE12J | ____________MSWRGRsTyyWPRPRPYVQPPEMIGPMRP |
| A6NHL2 | Y319 | Sugiyama | TUBAL3 | TTACFESSNQLVKCDPRLGKyMACCLLyRGDVVPKEVNAAI |
| A6NMY6 | Y238 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | TERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENAFLN |
| A6NMY6 | Y24 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | VHEILCKLsLEGDHstPPsAyGsVKAytNFDAERDALNIEt |
| A8K0Z3 | Y103 | Sugiyama | WASHC1 FAM39E WASH1 | KKAIKVFSSAKYPAPGRLQEyGsIFTGAQDPGLQRRPRHRI |
| C4AMC7 | Y103 | Sugiyama | WASH3P FAM39DP | KKAIKVFSSAKYPAPERLQEyGsIFTGAQDPGLQRRPRHRI |
| O00231 | Y397 | Sugiyama | PSMD11 | ILDQGEGVLIIFDEPPVDKtyEAALETIQNMSKVVDSLyNK |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00410 | Y33 | Sugiyama | IPO5 KPNB3 RANBP5 | LLLGNLLsPDNVVRKQAEEtyENIPGQSKITFLLQAIRNTT |
| O00429 | Y101 | Sugiyama | DNM1L DLP1 DRP1 | EENGVEAEEWGKFLHTKNKLyTDFDEIRQEIENETERISGN |
| O00469 | Y586 | Sugiyama | PLOD2 | FWFPIFSEKACDELVEEMEHyGKWSGGKHHDsRIsGGyENV |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O00764 | Y66 | Sugiyama | PDXK C21orf124 C21orf97 PKH PNK PRED79 | HTGYAHWKGQVLNSDELQELyEGLRLNNMNKyDyVLTGYTR |
| O14579 | Y202 | Sugiyama | COPE | TQLATAWVSLATGGEKLQDAyyIFQEMADKCSPTLLLLNGQ |
| O14579 | Y203 | Sugiyama | COPE | QLATAWVSLATGGEKLQDAyyIFQEMADKCSPTLLLLNGQA |
| O14602 | Y35 | Sugiyama | EIF1AY | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEALCFDGV |
| O14744 | Y502 | Sugiyama | PRMT5 HRMT1L5 IBP72 JBP1 SKB1 | NEVRACREKDRDPEAQFEMPyVVRLHNFHQLSAPQPCFTFS |
| O14818 | Y106 | Sugiyama | PSMA7 HSPC | RARVECQsHRLTVEDPVTVEyITRYIASLKQRYTQSNGRRP |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| O14950 | Y143 | Sugiyama | MYL12B MRLC2 MYLC2B | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14964 | Y216 | Sugiyama | HGS HRS | KYSTIPKFGIEKEVRVCEPCyEQLNRKAEGKAtsttELPPE |
| O14974 | Y901 | Sugiyama | PPP1R12A MBS MYPT1 | EtQtDsIsRyETssTsAGDRyDsLLGRsGsysYLEERKPYS |
| O15013 | Y1307 | Sugiyama | ARHGEF10 KIAA0294 | sLsLsHGsssLEHRSEDsTIyDLLKDPVSLRSKARRAKKAK |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15226 | Y657 | Sugiyama | NKRF ITBA4 NRF | HQIAQKYGLKSKSHGVGHDRyLVVGRKRRKEDLLDQLKQEG |
| O15230 | Y81 | Sugiyama | LAMA5 KIAA0533 KIAA1907 | SATCGEEAPARGSPRPTEDLyCKLVGGPVAGGDPNQTIRGQ |
| O15234 | Y240 | Sugiyama | CASC3 MLN51 | HDKFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRK |
| O15234 | Y242 | Sugiyama | CASC3 MLN51 | KFREDEQAPKSRQELIALyGyDIRSAHNPDDIKPRRIRKPR |
| O15294 | Y316 | Sugiyama | OGT | YCNLANALKEKGSVAEAEDCyNTALRLCPTHADSLNNLANI |
| O15350 | Y28 | GPS6|EPSD|PSP | TP73 P73 | SPDGGTTFEHLWSSLEPDStyFDLPQSSRGNNEVVGGTDss |
| O15357 | Y1135 | Sugiyama | INPPL1 SHIP2 | SGDDRSCSVLQMAKTLSEVDyAPAGPARSALLPGPLELQPP |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15372 | Y350 | Sugiyama | EIF3H EIF3S3 | IKEFTAQNLGKLFMAQALQEyNN__________________ |
| O15460 | Y79 | Sugiyama | P4HA2 UNQ290/PRO330 | KSWANKMEALTSKSAADAEGyLAHPVNAyKLVKRLNTDWPA |
| O15460 | Y87 | Sugiyama | P4HA2 UNQ290/PRO330 | ALTSKSAADAEGyLAHPVNAyKLVKRLNTDWPALEDLVLQD |
| O15541 | Y120 | Sugiyama | RNF113A RNF113 ZNF183 | yKSTRSAKPVGPEDMGATAVyELDTEKERDAQAIFERSQKI |
| O43390 | Y136 | Sugiyama | HNRNPR HNRPR | QESTKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O43390 | Y296 | Sugiyama | HNRNPR HNRPR | VILYHQPDDKKKNRGFCFLEyEDHKSAAQARRRLMSGKVKV |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y533 | Sugiyama | ACTN4 | REALEKTEKQLEAIDQLHLEyAKRAAPFNNWMESAMEDLQD |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43707 | Y886 | Sugiyama | ACTN4 | ELRRELPPDQAEyCIARMAPyQGPDAVPGALDyKsFStALy |
| O43707 | Y898 | Sugiyama | ACTN4 | yCIARMAPyQGPDAVPGALDyKsFStALyGEsDL_______ |
| O43707 | Y906 | Sugiyama | ACTN4 | yQGPDAVPGALDyKsFStALyGEsDL_______________ |
| O43719 | Y634 | Sugiyama | HTATSF1 | EGsEREFDEDsDEKEEEEDtyEKVFDDEsDEKEDEEyADEK |
| O43765 | Y195 | Sugiyama | SGTA SGT SGT1 | HVEAVAYYKKALELDPDNEtyKsNLKIAELKLREAPSPTGG |
| O43776 | Y508 | Sugiyama | NARS1 NARS NRS | GYKREGIDPTPyyWytDQRKyGTCPHGGYGLGLERFLTWIL |
| O43852 | S219 | Sugiyama | CALU | DIDKNADGFIDLEEyIGDMysHDGNtDEPEWVKTEREQFVE |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y129 | Sugiyama | CALU | VERQWKGHDLNEDGLVsWEEyKNATYGYVLDDPDPDDGFNY |
| O43852 | Y185 | Sugiyama | CALU | KDGDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNAD |
| O43852 | Y213 | Sugiyama | CALU | VQEtMEDIDKNADGFIDLEEyIGDMysHDGNtDEPEWVKTE |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O60264 | Y80 | Sugiyama | SMARCA5 SNF2H WCRF135 | EIFDDAsPGKQKEIQEPDPtyEEKMQTDRANRFEYLLKQTE |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60488 | Y507 | Sugiyama | ACSL4 ACS4 FACL4 LACS4 | RVGAPLICCEIKLKDWQEGGytINDKPNPRGEIVIGGQNIS |
| O60496 | Y271 | iPTMNet|EPSD | DOK2 | ATPQPQPATIPASLPRPDsPySRPHDsLPPPsPTTPVPAPR |
| O60496 | Y299 | iPTMNet|EPSD | DOK2 | PPPsPTTPVPAPRPRGQEGEyAVPFDAVARSLGKNFRGILA |
| O60496 | Y345 | iPTMNet|EPSD | DOK2 | LADPLYDSIEETLPPRPDHIyDEPEGVAALSLYDSPQEPRG |
| O60506 | Y133 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ADSSKGPDEAKIKALLERtGytLDVttGQRKYGGPPPDSVY |
| O60506 | Y293 | Sugiyama | SYNCRIP HNRPQ NSAP1 | VILyHQPDDKKKNRGFCFLEyEDHKTAAQARRRLMSGKVKV |
| O60506 | Y373 | Sugiyama | SYNCRIP HNRPQ NSAP1 | ILEKAFsQFGKLERVKKLKDyAFIHFDERDGAVKAMEEMNG |
| O60610 | Y374 | Sugiyama | DIAPH1 DIAP1 | ENEDMRVQLNVFDEQGEEDsyDLKGRLDDIRMEMDDFNEVF |
| O60664 | S93 | Sugiyama | PLIN3 M6PRBP1 TIP47 | AAVsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQP |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60841 | Y134 | Sugiyama | EIF5B IF2 KIAA0741 | EELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKA |
| O60884 | Y66 | Sugiyama | DNAJA2 CPR3 HIRIP4 | KFKEISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDD |
| O60884 | Y69 | Sugiyama | DNAJA2 CPR3 HIRIP4 | EISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDDIFS |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75131 | Y162 | Sugiyama | CPNE3 CPN3 KIAA0636 | LFEMEARKLDNKDLFGKSDPyLEFHKQTSDGNWLMVHRTEV |
| O75208 | Y93 | Sugiyama | COQ9 C16orf49 HSPC326 PSEC0129 | PEssHsPPRYTDQGGEEEEDyEsEEQLQHRILTAALEFVPA |
| O75347 | Y48 | Sugiyama | TBCA | KEAKQQEEKIEKMRAEDGENyDIKKQAEILQEsRMMIPDCQ |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75348 | Y47 | Sugiyama | ATP6V1G1 ATP6G ATP6G1 ATP6J | KRKNRRLKQAKEEAQAEIEQyRLQREKEFKAKEAAALGsRG |
| O75390 | Y345 | Sugiyama | CS | DEKLRDYIWNtLNSGRVVPGyGHAVLRKTDPRYTCQREFAL |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75822 | Y143 | Sugiyama | EIF3J EIF3S1 PRO0391 | LQEEsDLELAKEtFGVNNAVyGIDAMNPSSRDDFtEFGKLL |
| O76087 | Y9 | Sugiyama | GAGE7 GAGE12I GAGE7B | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| O94776 | T439 | Sugiyama | MTA2 MTA1L1 PID | EPHSRGHLsRPEAQsLsPyttsANRAKLLAKNRQtFLLQtT |
| O94776 | Y437 | Sugiyama | MTA2 MTA1L1 PID | tTEPHSRGHLsRPEAQsLsPyttsANRAKLLAKNRQtFLLQ |
| O95218 | Y114 | Sugiyama | ZRANB2 ZIS ZNF265 | AKLEERtGYGGGFNERENVEyIEREEsDGEyDEFGRKKKKY |
| O95218 | Y124 | Sugiyama | ZRANB2 ZIS ZNF265 | GGFNERENVEyIEREEsDGEyDEFGRKKKKYRGKAVGPAsI |
| O95218 | Y167 | Sugiyama | ZRANB2 ZIS ZNF265 | EVEDKEsEGEEEDEDEDLsKyKLDEDEDEDDADLsKyNLDA |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| P00338 | Y172 | Sugiyama | LDHA PIG19 | GFPKNRVIGsGCNLDsARFRyLMGERLGVHPLSCHGWVLGE |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00491 | Y166 | Sugiyama | PNP NP | PLRGPNDERFGDRFPAMsDAyDRtMRQRALstWKQMGEQRE |
| P00505 | Y401 | Sugiyama | GOT2 KYAT4 | FCFTGLKPEQVERLIKEFSIyMtKDGRISVAGVTSsNVGYL |
| P00519 | Y115 | EPSD|PSP | ABL1 ABL JTK7 | HNGEWCEAQTKNGQGWVPSNyITPVNSLEKHSWyHGPVSRN |
| P00519 | Y128 | EPSD|PSP | ABL1 ABL JTK7 | QGWVPSNyITPVNSLEKHSWyHGPVSRNAAEyLLSSGINGS |
| P00519 | Y139 | EPSD|PSP | ABL1 ABL JTK7 | VNSLEKHSWyHGPVSRNAAEyLLSSGINGSFLVRESESSPG |
| P00519 | Y172 | EPSD|PSP | ABL1 ABL JTK7 | RESESSPGQRSISLRYEGRVyHYRINtASDGKLyVSSESRF |
| P00519 | Y185 | EPSD|PSP | ABL1 ABL JTK7 | LRYEGRVyHYRINtASDGKLyVSSESRFNTLAELVHHHSTV |
| P00519 | Y215 | EPSD|PSP | ABL1 ABL JTK7 | LAELVHHHSTVADGLITTLHyPAPKRNKPTVyGVSPNyDKW |
| P00519 | Y226 | EPSD|PSP | ABL1 ABL JTK7 | ADGLITTLHyPAPKRNKPTVyGVSPNyDKWEMERTDITMKH |
| P00519 | Y393 | EPSD|PSP | ABL1 ABL JTK7 | ENHLVKVADFGLSRLMtGDtytAHAGAKFPIKWTAPESLAy |
| P00519 | Y70 | EPSD|PSP | ABL1 ABL JTK7 | SKENLLAGPsENDPNLFVALyDFVAsGDNTLSITKGEKLRV |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00568 | T35 | Sugiyama | AK1 | GGPGSGKGTQCEKIVQKyGytHLstGDLLRSEVSSGSARGK |
| P00568 | Y32 | Sugiyama | AK1 | FVVGGPGSGKGTQCEKIVQKyGytHLstGDLLRSEVSSGSA |
| P00813 | Y348 | Sugiyama | ADA ADA1 | NAAKSSFLPEDEKRELLDLLyKAYGMPPSASAGQNL_____ |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P02786 | Y168 | Sugiyama | TFRC | NENsyVPREAGsQKDENLALyVENQFREFKLSKVWRDQHFV |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P02786 | Y683 | Sugiyama | TFRC | AEKTDRFVMKKLNDRVMRVEyHFLSPyVSPKESPFRHVFWG |
| P02786 | Y689 | Sugiyama | TFRC | FVMKKLNDRVMRVEyHFLSPyVSPKESPFRHVFWGSGSHTL |
| P04406 | S312 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | sstFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMA |
| P04632 | Y87 | Sugiyama | CAPNS1 CAPN4 CAPNS | sAISEAAAQYNPEPPPPRtHysNIEANEsEEVRQFRRLFAQ |
| P05023 | Y542 | Sugiyama | ATP1A1 | LLHGKEQPLDEELKDAFQNAyLELGGLGERVLGFCHLFLPD |
| P05198 | Y150 | Sugiyama | EIF2S1 EIF2A | LFQRTAWVFDDKyKRPGyGAyDAFKHAVsDPsILDsLDLNE |
| P05362 | Y455 | Sugiyama | ICAM1 | GtFPLPIGEsVtVtRDLEGtyLCRARSTQGEVTRKVTVNVL |
| P05455 | Y104 | Sugiyama | SSB | EDKTKIRRsPsKPLPEVTDEyKNDVKNRsVYIKGFPtDAtL |
| P05783 | Y168 | Sugiyama | KRT18 CYK18 PIG46 | ARIVLQIDNARLAADDFRVKyETELAMRQsVENDIHGLRKV |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y282 | Sugiyama | KRT8 CYK8 | EVKAQyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRR |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P06733 | S254 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | AGYTDKVVIGMDVAASEFFRsGKyDLDFKsPDDPsRyIsPD |
| P06733 | S272 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | FRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsI |
| P06733 | Y131 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ILGVsLAVCKAGAVEKGVPLyRHIADLAGNsEVILPVPAFN |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y257 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | TDKVVIGMDVAASEFFRsGKyDLDFKsPDDPsRyIsPDQLA |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y287 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | PsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDDWGAWQKF |
| P06733 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07237 | Y327 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LKKEECPAVRLITLEEEMTKyKPEsEELtAERItEFCHRFL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07237 | Y99 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPKEytAG |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07355 | Y199 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RAEDGsVIDyELIDQDARDLyDAGVKRKGTDVPKWIsIMTE |
| P07355 | Y238 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | TERSVPHLQKVFDRYKsysPyDMLEsIRKEVKGDLENAFLN |
| P07355 | Y24 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | VHEILCKLsLEGDHstPPsAyGsVKAytNFDAERDALNIEt |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | T107 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAESC |
| P07437 | Y106 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAES |
| P07437 | 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___________ |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07814 | T376 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | LYRCKIQPHPRTGNKyNVyPtyDFACPIVDSIEGVTHALRT |
| P07814 | Y1028 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PKKQTRLGLEAKKEENLADWysQVITKSEMIEYHDISGCYI |
| P07814 | Y1127 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | SGKTELAEPIAIRPTsEtVMyPAyAKWVQSHRDLPIKLNQW |
| P07814 | Y1130 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | TELAEPIAIRPTsEtVMyPAyAKWVQSHRDLPIKLNQWCNV |
| P07814 | Y1504 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | KPLCELQPGAKCVCGKNPAKyytLFGRsy____________ |
| P07814 | Y1505 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PLCELQPGAKCVCGKNPAKyytLFGRsy_____________ |
| P07814 | Y371 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | MRDPtLYRCKIQPHPRTGNKyNVyPtyDFACPIVDSIEGVT |
| P07814 | Y374 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PtLYRCKIQPHPRTGNKyNVyPtyDFACPIVDSIEGVTHAL |
| P07814 | Y684 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | LKKGDIIQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPD |
| P07814 | Y690 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | IQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPDGHtKEM |
| P07814 | Y754 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | ERPtPsLNNNCttsEDsLVLyNRVAVQGDVVRELKAKKAPK |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07858 | Y244 | Sugiyama | CTSB CPSB | HYGYNSYSVSNSEKDIMAEIyKNGPVEGAFSVYSDFLLYKS |
| P07900 | S63 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | IFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLIPN |
| 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 |
| P07900 | Y627 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | TANMERIMKAQALRDNstMGyMAAKKHLEINPDHsIIEtLR |
| P07942 | Y1002 | Sugiyama | LAMB1 | IDTTDPEACDKETGRCLKCLyHtEGEHCQFCRFGyyGDALQ |
| P07942 | Y445 | Sugiyama | LAMB1 | QCRCKLNVEGEHCDVCKEGFyDLssEDPFGCKSCACNPLGT |
| P07948 | T398 | Sugiyama | LYN JTK8 | SLMCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINFG |
| P07948 | Y397 | Sugiyama | LYN JTK8 | ESLMCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINF |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | S58 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | IFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDIIPN |
| P08238 | Y211 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EyLEERRVKEVVKKHsQFIGyPItLyLEKEREKEIsDDEAE |
| P08238 | Y216 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | RRVKEVVKKHsQFIGyPItLyLEKEREKEIsDDEAEEEKGE |
| P08238 | Y276 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P08238 | Y301 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | ELNKtKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHF |
| P08238 | Y426 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KNIVKKCLELFsELAEDKENyKKFyEAFSKNLKLGIHEDst |
| 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 |
| P08243 | Y140 | Sugiyama | ASNS TS11 | VFAFVLLDTANKKVFLGRDTyGVRPLFKAMTEDGFLAVCSE |
| P08559 | S300 | Sugiyama | PDHA1 PHE1A | ILMELQTYRyHGHsMsDPGVsyRtREEIQEVRsKsDPIMLL |
| P08621 | Y126 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | FVARVNYDTTEsKLRREFEVyGPIKRIHMVYSKRsGKPRGy |
| P08631 | S130 | Sugiyama | HCK | ESGEWWKARSLATRKEGyIPsNyVARVDsLETEEWFFKGIS |
| P08631 | S138 | Sugiyama | HCK | RSLATRKEGyIPsNyVARVDsLETEEWFFKGISRKDAERQL |
| P08631 | S78 | Sugiyama | HCK | TIKPGPNSHNSNTPGIREAGsEDIIVVALyDyEAIHHEDLs |
| P08631 | S98 | Sugiyama | HCK | sEDIIVVALyDyEAIHHEDLsFQKGDQMVVLEESGEWWKAR |
| P08631 | T412 | Sugiyama | HCK | SLVCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINFG |
| P08631 | Y127 | Sugiyama | HCK | VLEESGEWWKARSLATRKEGyIPsNyVARVDsLETEEWFFK |
| P08631 | Y132 | Sugiyama | HCK | GEWWKARSLATRKEGyIPsNyVARVDsLETEEWFFKGISRK |
| P08631 | Y209 | GPS6|ELM|iPTMNet|EPSD|Sugiyama | HCK | PRQGDTVKHYKIRtLDNGGFyISPRstFSTLQELVDHyKKG |
| P08631 | Y411 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | HCK | ASLVCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINF |
| P08631 | Y487 | Sugiyama | HCK | IRALERGYRMPRPENCPEELyNIMMRCWKNRPEERPTFEYI |
| P08631 | Y51 | GPS6|SIGNOR|iPTMNet|EPSD | HCK | QVGGNtFsKTETsAsPHCPVyVPDPTSTIKPGPNSHNSNTP |
| P08631 | Y522 | SIGNOR|ELM|iPTMNet|EPSD|PSP | HCK | PTFEYIQSVLDDFYTAtEsQyQQQP________________ |
| P08631 | Y87 | Sugiyama | HCK | NSNTPGIREAGsEDIIVVALyDyEAIHHEDLsFQKGDQMVV |
| P08631 | Y89 | Sugiyama | HCK | NTPGIREAGsEDIIVVALyDyEAIHHEDLsFQKGDQMVVLE |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P08865 | Y202 | Sugiyama | RPSA LAMBR LAMR1 | VLRMRGTISREHPWEVMPDLyFyRDPEEIEKEEQAAAEKAV |
| P08865 | Y204 | Sugiyama | RPSA LAMBR LAMR1 | RMRGTISREHPWEVMPDLyFyRDPEEIEKEEQAAAEKAVTK |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09211 | Y64 | Sugiyama | GSTP1 FAEES3 GST3 | LKASCLyGQLPKFQDGDLtLyQsNtILRHLGRTLGLYGKDQ |
| P09234 | T11 | Sugiyama | SNRPC | __________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHK |
| P09234 | T14 | Sugiyama | SNRPC | _______MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKENV |
| P09234 | Y12 | Sugiyama | SNRPC | _________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKE |
| P09234 | Y8 | Sugiyama | SNRPC | _____________MPKFyCDyCDtyLtHDsPsVRKTHCSGR |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09874 | Y794 | Sugiyama | PARP1 ADPRT PPOL | AySLLRGGsDDssKDPIDVNyEKLKTDIKVVDRDSEEAEII |
| P09917 | Y43 | PSP | ALOX5 LOG5 | YLSLVGSAGCSEKHLLDKPFyNDFERGAVDSyDVTVDEELG |
| P09917 | Y54 | PSP | ALOX5 LOG5 | EKHLLDKPFyNDFERGAVDSyDVTVDEELGEIQLVRIEKRK |
| P09917 | Y95 | PSP | ALOX5 LOG5 | YWLNDDWYLKYITLKTPHGDyIEFPCYRWITGDVEVVLRDG |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CL80 | Y9 | Sugiyama | GAGE12F | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P0DPH7 | T94 | Sugiyama | TUBA3C TUBA2 | VVDEVRtGtyRQLFHPEQLItGKEDAANNyARGHYTIGKEI |
| P0DPH7 | Y103 | Sugiyama | TUBA3C TUBA2 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIVDLVLDRIR |
| P0DPH7 | Y224 | Sugiyama | TUBA3C TUBA2 | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| P0DSO3 | Y9 | Sugiyama | GAGE4 | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P10412 | Y71 | Sugiyama | H1-4 H1F4 HIST1H1E | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P11047 | Y854 | Sugiyama | LAMC1 LAMB2 | IDPNAVGNCNRLTGECLKCIyNtAGFyCDRCKDGFFGNPLA |
| P11142 | S153 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | AyLGKtVTNAVVtVPAyFNDsQRQAtKDAGtIAGLNVLRII |
| P11142 | S40 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P11142 | S432 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | VLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGERAMTKD |
| P11142 | T427 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | GGVMTVLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGER |
| P11142 | Y183 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | tIAGLNVLRIINEPtAAAIAyGLDKKVGAERNVLIFDLGGG |
| P11142 | Y443 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KQtQtFttysDNQPGVLIQVyEGERAMTKDNNLLGKFELTG |
| P11274 | Y177 | ELM|iPTMNet|EPSD|PSP | BCR BCR1 D22S11 | NFERIRKGHGQPGADAEKPFyVNVEFHHERGLVKVNDKEVS |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11413 | Y503 | Sugiyama | G6PD | IYGsRGPTEADELMKRVGFQyEGtyKWVNPHKL________ |
| P11413 | Y507 | Sugiyama | G6PD | RGPTEADELMKRVGFQyEGtyKWVNPHKL____________ |
| P11586 | Y834 | Sugiyama | MTHFD1 MTHFC MTHFD | LLYDLKLPVEDKIRIIAQKIyGADDIELLPEAQHKAEVYTK |
| P11940 | Y194 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLFGKF |
| P11940 | Y382 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | PLyVALAQRKEERQAHLtNQyMQRMASVRAVPNPVINPYQP |
| P12268 | Y509 | Sugiyama | IMPDH2 IMPD2 | KFEKRtssAQVEGGVHsLHsyEKRLF_______________ |
| P12277 | S129 | Sugiyama | CKB CKBB | DLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPHCsRG |
| P12814 | Y193 | Sugiyama | ACTN1 | WKDGLGFCALIHRHRPELIDyGKLRKDDPLTNLNTAFDVAE |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y842 | Sugiyama | ACTN1 | DTDTADQVMASFKILAGDKNyITMDELRRELPPDQAEyCIA |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P12956 | Y103 | Sugiyama | XRCC6 G22P1 | LAVVFYGTEKDKNSVNFKNIyVLQELDNPGAKRILELDQFK |
| P13010 | Y295 | Sugiyama | XRCC5 G22P2 | TWTVVDAKTLKKEDIQKETVyCLNDDDETEVLKEDIIQGFR |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | Y367 | Sugiyama | EEF2 EF2 | GDALLQMITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKs |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y411 | Sugiyama | EEF2 EF2 | KGPLMMYISKMVPTSDKGRFyAFGRVFsGLVsTGLKVRIMG |
| P13639 | Y639 | Sugiyama | EEF2 EF2 | KGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGPDGTGP |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | S135 | Sugiyama | PDIA4 ERP70 ERP72 | IPVAKIDAtsAsVLAsRFDVsGyPtIKILKKGQAVDyEGsR |
| P13667 | Y137 | Sugiyama | PDIA4 ERP70 ERP72 | VAKIDAtsAsVLAsRFDVsGyPtIKILKKGQAVDyEGsRtQ |
| P13667 | Y273 | Sugiyama | PDIA4 ERP70 ERP72 | PTLKIFRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTL |
| P13667 | Y278 | Sugiyama | PDIA4 ERP70 ERP72 | FRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTLKQVQE |
| P13667 | Y448 | Sugiyama | PDIA4 ERP70 ERP72 | RAATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLs |
| P13667 | Y458 | Sugiyama | PDIA4 ERP70 ERP72 | VLEVAKDFPEytFAIADEEDyAGEVKDLGLsEsGEDVNAAI |
| P13674 | Y141 | Sugiyama | P4HA1 P4HA | FPNDEDQVGAAKALLRLQDtyNLDTDtIsKGNLPGVKHKSF |
| P13693 | Y18 | Sugiyama | TPT1 | ___MIIYRDLIsHDEMFsDIyKIREIADGLCLEVEGKMVSR |
| P13797 | Y601 | Sugiyama | PLS3 | DKHNNAKYAVSMARRIGARVyALPEDLVEVKPKMVMTVFAC |
| P13929 | Y131 | Sugiyama | ENO3 | ILGVSLAVCKAGAAEKGVPLyRHIADLAGNPDLILPVPAFN |
| P13929 | Y189 | Sugiyama | ENO3 | MILPVGAsSFKEAMRIGAEVyHHLKGVIKAKYGKDATNVGD |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y86 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | KFEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTS |
| P13987 | Y87 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | FEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTSL |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14324 | Y349 | Sugiyama | FDPS FPS KIAA1293 | QDNKCSWLVVQCLQRATPEQyQILKENYGQKEAEKVARVKA |
| P14618 | Y105 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | AEtIKNVRtAtEsFAsDPILyRPVAVALDTKGPEIRtGLIK |
| P14625 | Y258 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | GNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFINFP |
| P14625 | Y401 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | VTFKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDD |
| P14625 | Y429 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | IKLYVRRVFITDDFHDMMPKyLNFVKGVVDsDDLPLNVsRE |
| P14625 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14635 | Y175 | Sugiyama | CCNB1 CCNB | DVDAEDGADPNLCSEYVKDIyAYLRQLEEEQAVRPKYLLGR |
| P14649 | S87 | Sugiyama | MYL6B MLC1SA | EEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVLK |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14866 | Y257 | Sugiyama | HNRNPL HNRPL P/OKcl.14 | EFDSVQSAQRAKASLNGADIysGCCTLKIEYAKPTRLNVFK |
| P14868 | S33 | Sugiyama | DARS1 DARS PIG40 | KPREIMDAAEDyAKERyGIssMIQsQEKPDRVLVRVRDLtI |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15531 | Y142 | Sugiyama | NME1 NDPKA NM23 | sVEsAEKEIGLWFHPEELVDyTsCAQNWIyE__________ |
| P15531 | Y151 | Sugiyama | NME1 NDPKA NM23 | GLWFHPEELVDyTsCAQNWIyE___________________ |
| P15586 | Y344 | Sugiyama | GNS | TSDNGYHTGQFSLPIDKRQLyEFDIKVPLLVRGPGIKPNQT |
| P15880 | Y223 | Sugiyama | RPS2 RPS4 | GIVsAPVPKKLLMMAGIDDCytsARGCtAtLGNFAKATFDA |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P16070 | Y79 | Sugiyama | CD44 LHR MDU2 MDU3 MIC4 | TLPTMAQMEKALsIGFEtCRyGFIEGHVVIPRIHPNSICAA |
| P16152 | Y253 | Sugiyama | CBR1 CBR CRN SDR21C1 | TDMAGPKATKSPEEGAEtPVyLALLPPDAEGPHGQFVSEKR |
| P16402 | Y72 | Sugiyama | H1-3 H1F3 HIST1H1D | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P16403 | Y71 | Sugiyama | H1-2 H1F2 HIST1H1C | SKERsGVsLAALKKALAAAGyDVEKNNSRIKLGLKsLVsKG |
| P16885 | Y1217 | PSP | PLCG2 | ySSCRQLRRRQEELNNQLFLyDtHQNLRNANRDALVKEFsV |
| P16885 | Y753 | SIGNOR|iPTMNet|EPSD | PLCG2 | YPVTPELLERyNMERDINSLyDVSRMyVDPSEINPSMPQRT |
| P16885 | Y759 | SIGNOR|iPTMNet|EPSD | PLCG2 | LLERyNMERDINSLyDVSRMyVDPSEINPSMPQRTVKALYD |
| P17066 | S42 | Sugiyama | HSPA6 HSP70B' | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P17066 | Y185 | Sugiyama | HSPA6 HSP70B' | AIAGLNVLRIINEPTAAAIAyGLDRRGAGERNVLIFDLGGG |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18077 | Y106 | Sugiyama | RPL35A GIG33 | AKFRsNLPAKAIGHRIRVMLyPSRI________________ |
| P18124 | T196 | Sugiyama | RPL7 | ARSLGKyGIICMEDLIHEIytVGKRFKEANNFLWPFKLSSP |
| P18124 | Y155 | Sugiyama | RPL7 | IVEPYIAWGYPNLKsVNELIyKRGYGKINKKRIALtDNALI |
| P18124 | Y182 | Sugiyama | RPL7 | INKKRIALtDNALIARSLGKyGIICMEDLIHEIytVGKRFK |
| P18206 | Y822 | Sugiyama | VCL | KAVAGNIsDPGLQKsFLDsGyRILGAVAKVREAFQPQEPDF |
| P18615 | Y170 | Sugiyama | NELFE RD RDBP | GEEAEGPGAGDGPPRsFDWGyEERSGAHSsAsPPRsRSRDR |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18621 | Y4 | Sugiyama | RPL17 | _________________MVRysLDPENPtKsCKSRGSNLRV |
| P18669 | S137 | Sugiyama | PGAM1 PGAMA CDABP0006 | RsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLK |
| P18669 | Y119 | Sugiyama | PGAM1 PGAMA CDABP0006 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| P18669 | Y26 | Sugiyama | PGAM1 PGAMA CDABP0006 | LVLIRHGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALR |
| P18669 | Y92 | Sugiyama | PGAM1 PGAMA CDABP0006 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| P18754 | Y89 | Sugiyama | RCC1 CHC1 | VVQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSE |
| P19105 | Y142 | Sugiyama | MYL12A MLCB MRLC3 RLC | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19174 | Y1253 | SIGNOR|iPTMNet|EPSD | PLCG1 PLC1 | sDASGQLFHGRAREGsFEsRyQQPFEDFRIsQEHLADHFDs |
| P19174 | Y771 | SIGNOR|iPTMNet|EPSD | PLCG1 PLC1 | KLRYPINEEALEKIGTAEPDyGALyEGRNPGFyVEANPMPT |
| P19174 | Y783 | SIGNOR|iPTMNet|EPSD | PLCG1 PLC1 | KIGTAEPDyGALyEGRNPGFyVEANPMPTFKCAVKALFDYK |
| P19838 | Y240 | Sugiyama | NFKB1 | LPDSTGSFTRRLEPVVSDAIyDSKAPNASNLKIVRMDRTAG |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21333 | Y731 | Sugiyama | FLNA FLN FLN1 | VQDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWGG |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P22059 | Y456 | Sugiyama | OSBP OSBP1 | MPVNFNEPLSMLQRLTEDLEyHELLDRAAKCENSLEQLCYV |
| P22059 | Y767 | Sugiyama | OSBP OSBP1 | RKKREAEAMKATEDGtPYDPyKALWFERKKDPVTKELTHIy |
| P22059 | Y787 | Sugiyama | OSBP OSBP1 | yKALWFERKKDPVTKELTHIyRGEyWECKEKQDWSsCPDIF |
| P22059 | Y791 | Sugiyama | OSBP OSBP1 | WFERKKDPVTKELTHIyRGEyWECKEKQDWSsCPDIF____ |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y60 | Sugiyama | UBA1 A1S9T UBE1 | GMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSVLVSGL |
| P22314 | Y666 | Sugiyama | UBA1 A1S9T UBE1 | QWARDEFEGLFKQPAENVNQyLtDPKFVERtLRLAGtQPLE |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22492 | Y75 | Sugiyama | H1-6 H1FT H1T HIST1H1T | SQERVGMSLVALKKALAAAGyDVEKNNSRIKLSLKSLVNKG |
| P22681 | Y731 | iPTMNet|EPSD | CBL CBL2 RNF55 | LDTsQSsRACDCDQQIDSCTyEAMYNIQSQAPSITESSTFG |
| P23142 | Y175 | Sugiyama | FBLN1 PP213 | VGGLQETDKIIEVEEEQEDPyLNDRCRGGGPCKQQCRDTGD |
| P23193 | Y177 | Sugiyama | TCEA1 GTF2S TFIIS | DYIAIGADEEELGSQIEEAIyQEIRNTDMKYKNRVRSRISN |
| P23246 | Y488 | Sugiyama | SFPQ PSF | PMYQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQV |
| P23246 | Y490 | Sugiyama | SFPQ PSF | YQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQVEK |
| P23284 | Y119 | Sugiyama | PPIB CYPB | DFMIQGGDFtRGDGtGGKsIyGERFPDENFKLKHyGPGWVs |
| P23396 | Y87 | Sugiyama | RPS3 OK/SW-cl.26 | RELtAVVQKRFGFPEGsVELyAEKVAtRGLCAIAQAEsLRy |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23434 | Y164 | Sugiyama | GCSH | LIKMtLsNPsELDELMsEEAyEKYIKSIEE___________ |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | T70 | Sugiyama | CFL1 CFL | EEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAtyE |
| P23528 | Y140 | Sugiyama | CFL1 CFL | SKDAIKKKLtGIKHELQANCyEEVKDRCTLAEKLGGsAVIs |
| P23528 | Y68 | Sugiyama | CFL1 CFL | ILEEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAt |
| P23528 | Y82 | Sugiyama | CFL1 CFL | QtVDDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFI |
| P23528 | Y85 | Sugiyama | CFL1 CFL | DDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWA |
| P23528 | Y89 | Sugiyama | CFL1 CFL | AtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| P23588 | Y211 | Sugiyama | EIF4B | DsDKtDTDWRARPAtDsFDDyPPRRGDDsFGDKYRDRYDsD |
| P23921 | Y556 | Sugiyama | RRM1 RR1 | yyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPT |
| P24534 | Y18 | Sugiyama | EEF1B2 EEF1B EF1B | ___MGFGDLKsPAGLQVLNDyLADKSYIEGYVPsQADVAVF |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24752 | Y90 | Sugiyama | ACAT1 ACAT MAT | IAIQGAIEKAGIPKEEVKEAyMGNVLQGGEGQAPTRQAVLG |
| P25205 | Y19 | Sugiyama | MCM3 | __MAGtVVLDDVELREAQRDyLDFLDDEEDQGIyQsKVREL |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y45 | Sugiyama | MCM3 | DEEDQGIyQsKVRELIsDNQyRLIVNVNDLRRKNEKRANRL |
| P25205 | Y456 | Sugiyama | MCM3 | AGIHARLNARCsVLAAANPVyGRyDQyKTPMENIGLQDSLL |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P25787 | Y57 | Sugiyama | PSMA2 HC3 PSC3 | GIKAANGVVLATEKKQKSILyDERSVHKVEPITKHIGLVys |
| P25788 | Y105 | Sugiyama | PSMA3 HC8 PSC8 | ARSLADIAREEAsNFRSNFGyNIPLKHLADRVAMYVHAYTL |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26639 | T574 | Sugiyama | TARS1 TARS | RYHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAIL |
| P26639 | T629 | Sugiyama | TARS1 TARS | GGKWPFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMAD |
| P26639 | Y633 | Sugiyama | TARS1 TARS | PFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMADIDLD |
| P26640 | Y601 | Sugiyama | VARS1 G7A VARS VARS2 | VDMDFGTGAVKITPAHDQNDyEVGQRHGLEAIsIMDsRGAL |
| P26641 | Y297 | Sugiyama | EEF1G EF1G PRO1608 | KDPFAHLPKstFVLDEFKRKysNEDtLsVALPyFWEHFDKD |
| P26641 | Y309 | Sugiyama | EEF1G EF1G PRO1608 | VLDEFKRKysNEDtLsVALPyFWEHFDKDGWSLWySEYRFP |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27348 | Y19 | Sugiyama | YWHAQ | __MEKTELIQKAKLAEQAERyDDMAtCMKAVtEQGAELsNE |
| 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 |
| P28066 | Y185 | Sugiyama | PSMA5 | CDARAIGsAsEGAQssLQEVyHKSMTLKEAIKSSLIILKQV |
| P28066 | Y8 | Sugiyama | PSMA5 | _____________MFLTRsEyDRGVNtFsPEGRLFQVEyAI |
| P28074 | Y171 | Sugiyama | PSMB5 LMPX MB1 X | GMGLSMGTMICGWDKRGPGLyyVDsEGNRISGATFSVGSGS |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | Y202 | Sugiyama | TKT | LDINRLGQsDPAPLQHQMDIyQKRCEAFGWHAIIVDGHSVE |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P29803 | S298 | Sugiyama | PDHA2 PDHAL | ILMELQTYRyHGHsMsDPGVsyRtREEIQEVRsKRDPIIIL |
| P30040 | Y115 | Sugiyama | ERP29 C12orf8 ERP28 | DyGDKLNMELSEKYKLDKESyPVFyLFRDGDFENPVPyTGA |
| P30040 | Y119 | Sugiyama | ERP29 C12orf8 ERP28 | KLNMELSEKYKLDKESyPVFyLFRDGDFENPVPyTGAVKVG |
| P30043 | S202 | Sugiyama | BLVRB FLR SCAN | GHFMLRCLttDEyDGHstyPsHQyQ________________ |
| P30043 | T199 | Sugiyama | BLVRB FLR SCAN | HDLGHFMLRCLttDEyDGHstyPsHQyQ_____________ |
| P30043 | Y194 | Sugiyama | BLVRB FLR SCAN | RVISKHDLGHFMLRCLttDEyDGHstyPsHQyQ________ |
| P30043 | Y200 | Sugiyama | BLVRB FLR SCAN | DLGHFMLRCLttDEyDGHstyPsHQyQ______________ |
| P30043 | Y205 | Sugiyama | BLVRB FLR SCAN | MLRCLttDEyDGHstyPsHQyQ___________________ |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| P30086 | T65 | Sugiyama | PEBP1 PBP PEBP | QVKNRPtsIsWDGLDsGKLytLVLtDPDAPsRKDPKYREWH |
| P30086 | Y106 | Sugiyama | PEBP1 PBP PEBP | HFLVVNMKGNDIssGtVLsDyVGsGPPKGtGLHRyVWLVyE |
| P30086 | Y120 | Sugiyama | PEBP1 PBP PEBP | GtVLsDyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsN |
| P30086 | Y125 | Sugiyama | PEBP1 PBP PEBP | DyVGsGPPKGtGLHRyVWLVyEQDRPLKCDEPILsNRsGDH |
| P30086 | Y176 | Sugiyama | PEBP1 PBP PEBP | KKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK_________ |
| P30086 | Y181 | Sugiyama | PEBP1 PBP PEBP | RAPVAGtCyQAEWDDyVPKLyEQLsGK______________ |
| P30086 | Y64 | Sugiyama | PEBP1 PBP PEBP | tQVKNRPtsIsWDGLDsGKLytLVLtDPDAPsRKDPKYREW |
| P30101 | Y115 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | yGVsGyPtLKIFRDGEEAGAyDGPRtADGIVsHLKKQAGPA |
| P30101 | Y356 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | FVMQEEFsRDGKALERFLQDyFDGNLKRyLKsEPIPESNDG |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30622 | Y269 | Sugiyama | CLIP1 CYLN1 RSN | PLGKNDGAVAGtRyFQCQPKyGLFAPVHKVTKIGFPsttPA |
| P30876 | Y845 | Sugiyama | POLR2B | QEEVFEKPTRETCQGMRHAIyDKLDDDGLIAPGVRVSGDDV |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31327 | Y162 | Sugiyama | CPS1 | HWLATKsLGQWLQEEKVPAIyGVDtRMLTKIIRDKGTMLGK |
| P31939 | Y185 | Sugiyama | ATIC PURH OK/SW-cl.86 | DTSLETRRQLALKAFTHtAQyDEAISDyFRKQYSKGVsQMP |
| P31939 | Y192 | Sugiyama | ATIC PURH OK/SW-cl.86 | RQLALKAFTHtAQyDEAISDyFRKQYSKGVsQMPLRyGMNP |
| P31943 | Y276 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | GSDRFGRDLNyCFsGMsDHRyGDGGstFQsttGHCVHMRGL |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31947 | S149 | Sugiyama | SFN HME1 | RyLAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIR |
| P31947 | Y151 | Sugiyama | SFN HME1 | LAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIRLG |
| P31947 | Y19 | Sugiyama | SFN HME1 | __MERASLIQKAKLAEQAERyEDMAAFMKGAVEKGEELsCE |
| P31947 | Y213 | Sugiyama | SFN HME1 | LAKTtFDEAMADLHtLsEDsyKDstLIMQLLRDNLtLWTAD |
| P31948 | S28 | Sugiyama | STIP1 | KEKGNKALsVGNIDDALQCysEAIKLDPHNHVLysNRsAAy |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32929 | Y114 | Sugiyama | CTH | TVTITHLLKAGDQIICMDDVyGGTNRYFRQVASEFGLKISF |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33176 | Y516 | Sugiyama | KIF5B KNS KNS1 | EELAVNyDQKSQEVEDKTKEyELLSDELNQKsATLAsIDAE |
| P33176 | Y62 | Sugiyama | KIF5B KNS KNS1 | ASKPYAFDRVFQSsTsQEQVyNDCAKKIVKDVLEGyNGtIF |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33993 | Y102 | Sugiyama | MCM7 CDC47 MCM2 | QELLPQYKEREVVNKDVLDVyIEHRLMMEQRSRDPGMVRsP |
| P33993 | Y333 | Sugiyama | MCM7 CDC47 MCM2 | EsGAGELtREELRQIAEEDFyEKLAASIAPEIYGHEDVKKA |
| P34741 | Y131 | Sugiyama | SDC2 HSPG1 | KVHLSDSERKMDPAEEDtNVyTEKHSDSLFKRTEVLAAVIA |
| P34931 | S42 | Sugiyama | HSPA1L | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P34931 | Y185 | Sugiyama | HSPA1L | VIAGLNVLRIINEPtAAAIAyGLDKGGQGERHVLIFDLGGG |
| P34932 | Y597 | Sugiyama | HSPA4 APG2 HSPH2 | VDLPIENQLLWQIDREMLNLyIENEGKMIMQDKLEKERNDA |
| P34932 | Y624 | Sugiyama | HSPA4 APG2 HSPH2 | MIMQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDD |
| P34932 | Y626 | Sugiyama | HSPA4 APG2 HSPH2 | MQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDDRN |
| P34932 | Y660 | Sugiyama | HSPA4 APG2 HSPH2 | VSEDDRNsFtLKLEDTENWLyEDGEDQPKQVYVDKLAELKN |
| P35244 | Y99 | Sugiyama | RPA3 REPA3 RPA14 | ILCTSYVQFKEDSHPFDLGLyNEAVKIIHDFPQFYPLGIVQ |
| P35270 | Y259 | Sugiyama | SPR | QKLLSLLEKDEFKSGAHVDFyDK__________________ |
| P35579 | Y297 | Sugiyama | MYH9 | FYYLLSGAGEHLKTDLLLEPyNKyRFLsNGHVtIPGQQDKD |
| P35637 | Y468 | Sugiyama | FUS TLS | KAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRGGYRGRG |
| P36578 | S55 | Sugiyama | RPL4 RPL1 | DIVNFVHTNLRKNNRQPyAVsELAGHQtsAEsWGtGRAVAR |
| P36578 | Y211 | Sugiyama | RPL4 RPL1 | AGKGKMRNRRRIQRRGPCIIyNEDNGIIKAFRNIPGITLLN |
| P36578 | Y52 | Sugiyama | RPL4 RPL1 | IRPDIVNFVHTNLRKNNRQPyAVsELAGHQtsAEsWGtGRA |
| P36871 | Y476 | Sugiyama | PGM1 | GKQFSANDKVYtVEKADNFEysDPVDGsIsRNQGLRLIFTD |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P38117 | Y192 | Sugiyama | ETFB FP585 | tLRLKLPAVVTADLRLNEPRyAtLPNIMKAKKKKIEVIKPG |
| 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 |
| P39687 | Y148 | Sugiyama | ANP32A C15orf1 LANP MAPM PHAP1 | LNDyRENVFKLLPQLtyLDGyDRDDKEAPDsDAEGYVEGLD |
| P40227 | Y109 | Sugiyama | CCT6A CCT6 CCTZ | GDGTTsNVLIIGELLKQADLyISEGLHPRIITEGFEAAKEK |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40763 | Y176 | Sugiyama | STAT3 APRF | QDLEQKMKVVENLQDDFDFNyKTLKsQGDMQDLNGNNQsVT |
| P40763 | Y705 | SIGNOR|EPSD | STAT3 APRF | KyCRPEsQEHPEADPGsAAPyLKTKFICVtPttCsNtIDLP |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P41091 | Y102 | Sugiyama | EIF2S3 EIF2G | GYANAKIYKLDDPSCPRPECyRSCGsstPDEFPtDIPGtKG |
| P41227 | Y145 | Sugiyama | NAA10 ARD1 ARD1A TE2 | TLNFQISEVEPKyyADGEDAyAMKRDLtQMADELRRHLELK |
| P41252 | Y680 | Sugiyama | IARS1 IARS | YRFLIQNVLRLQKEEEIEFLyNENTVRESPNITDRWILSFM |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P42229 | Y694 | EPSD|PSP | STAT5A STAT5 | PKDEVFSKYYTPVLAKAVDGyVKPQIKQVVPEFVNASADAG |
| P42684 | Y116 | GPS6 | ABL2 ABLL ARG | ssKENLLGATESDPNLFVALyDFVAsGDNTLSITKGEKLRV |
| P42684 | Y161 | GPS6 | ABL2 ABLL ARG | QNGEWsEVRSKNGQGWVPSNyITPVNSLEKHSWyHGPVSRS |
| P42684 | Y174 | GPS6 | ABL2 ABLL ARG | QGWVPSNyITPVNSLEKHSWyHGPVSRSAAEyLLSSLINGS |
| P42684 | Y185 | GPS6 | ABL2 ABLL ARG | VNSLEKHSWyHGPVSRSAAEyLLSSLINGSFLVREsEssPG |
| P42684 | Y218 | GPS6 | ABL2 ABLL ARG | REsEssPGQLsISLRYEGRVyHYRINTTADGKVyVTAESRF |
| P42684 | Y231 | GPS6 | ABL2 ABLL ARG | LRYEGRVyHYRINTTADGKVyVTAESRFSTLAELVHHHSTV |
| P42684 | Y261 | GPS6 | ABL2 ABLL ARG | LAELVHHHSTVADGLVTTLHyPAPKCNKPTVyGVsPIHDKW |
| P42768 | Y291 | SIGNOR|ELM|iPTMNet|EPSD | WAS IMD2 | FSRAGIsEAQLtDAETsKLIyDFIEDQGGLEAVRQEMRRQE |
| P43243 | Y202 | Sugiyama | MATR3 KIAA0723 | RHFRRDsFDDRGPsLNPVLDyDHGsRsQEsGyyDRMDyEDD |
| P43490 | Y188 | Sugiyama | NAMPT PBEF PBEF1 | QKKILAKyLLEtsGNLDGLEyKLHDFGyRGVSSQETAGIGA |
| P43686 | Y191 | Sugiyama | PSMC4 MIP224 TBP7 | DIQKQEVREAVELPLTHFELyKQIGIDPPRGVLMYGPPGCG |
| P46063 | Y61 | Sugiyama | RECQL RECQ1 RECQL1 | VLTKKIKQCLEDsDAGAsNEyDssPAAWNKEDFPWSGKVKD |
| P46776 | Y48 | Sugiyama | RPL27A | HPGGRGNAGGLHHHRINFDKyHPGyFGKVGMKHYHLKRNQs |
| P46777 | Y207 | Sugiyama | RPL5 MSTP030 | sKEFNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyI |
| P46777 | Y210 | Sugiyama | RPL5 MSTP030 | FNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyIKNs |
| P46777 | Y219 | Sugiyama | RPL5 MSTP030 | IMGQNVADyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEM |
| P46777 | Y240 | Sugiyama | RPL5 MSTP030 | KKQFsQyIKNsVtPDMMEEMyKKAHAAIRENPVyEKKPKKE |
| P46777 | Y253 | Sugiyama | RPL5 MSTP030 | PDMMEEMyKKAHAAIRENPVyEKKPKKEVKKKRWNRPKMsL |
| P46778 | Y156 | Sugiyama | RPL21 | REAHFVRTNGKEPELLEPIPyEFMA________________ |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46940 | T663 | Sugiyama | IQGAP1 KIAA0051 | LsALRsPDVGLyGVIPECGEtyHsDLAEAKKKKLAVGDNNS |
| P46940 | Y1478 | Sugiyama | IQGAP1 KIAA0051 | KIQTGLKKLTELGtVDPKNKyQELINDIARDIRNQRRYRQR |
| P46940 | Y41 | Sugiyama | IQGAP1 KIAA0051 | LDNERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGED |
| P46940 | Y654 | Sugiyama | IQGAP1 KIAA0051 | VESGDVGKtLsALRsPDVGLyGVIPECGEtyHsDLAEAKKK |
| P47224 | Y114 | Sugiyama | RABIF MSS4 RASGRF3 | CADCEIGPIGWHCLDDKNSFyVALERVSHE___________ |
| P47813 | Y35 | Sugiyama | EIF1AX EIF1A EIF4C | GKNENESEKRELVFKEDGQEyAQVIKMLGNGRLEAMCFDGV |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | S42 | Sugiyama | HSPA7 HSP70B | VFQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAA |
| P49023 | Y118 | Sugiyama | PXN | sNPQDsVGsPCsRVGEEEHVysFPNKQKsAEPsPtVMstsL |
| P49023 | Y88 | Sugiyama | PXN | QWQPSSSRFIHQQPQsssPVyGssAKtssVsNPQDsVGsPC |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49327 | S279 | Sugiyama | FASN FAS | QGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGTKV |
| P49327 | Y2034 | Sugiyama | FASN FAS | DYFVVFSSVSCGRGNAGQsNyGFANsAMERICEKRRHEGLP |
| P49327 | Y277 | Sugiyama | FASN FAS | KEQGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGT |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y667 | Sugiyama | AARS1 AARS | QQIKKAEEIANEMIEAAKAVyTQDCPLAAAKAIQGLRAVFD |
| P49589 | Y32 | Sugiyama | CARS1 CARS | RRVQPQWsPPAGtQPCRLHLyNsLtRNKEVFIPQDGKKVTW |
| P49736 | Y137 | Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | MRQRDREAGRGLGRMRRGLLyDsDEEDEERPARKRRQVERA |
| P49792 | S3137 | Sugiyama | RANBP2 NUP358 | IPDFVCQGGDITKHDGTGGQsIyGDKFEDENFDVKHTGPGL |
| P49792 | Y3139 | Sugiyama | RANBP2 NUP358 | DFVCQGGDITKHDGTGGQsIyGDKFEDENFDVKHTGPGLLS |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50502 | Y185 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | NAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50914 | Y14 | Sugiyama | RPL14 | _______MVFRRFVEVGRVAyVsFGPHAGKLVAIVDVIDQN |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50990 | Y426 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | KRLVPGGGAtEIELAKQItsyGETCPGLEQyAIKKFAEAFE |
| P50990 | Y436 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | EIELAKQItsyGETCPGLEQyAIKKFAEAFEAIPRALAENS |
| P50995 | Y365 | Sugiyama | ANXA11 ANX11 | NRDESTNVDMSLAQRDAQELyAAGENRLGTDESKFNAVLCS |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51532 | Y718 | Sugiyama | SMARCA4 BAF190A BRG1 SNF2B SNF2L4 | VsEVDARHIIENAKQDVDDEyGVsQALARGLQSyyAVAHAV |
| P51692 | Y699 | ELM|iPTMNet|EPSD|PSP | STAT5B | ySKyytPVPCESATAKAVDGyVKPQIKQVVPEFVNASADAG |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P52209 | Y137 | Sugiyama | PGD PGDH | KAKGILFVGsGVsGGEEGARyGPSLMPGGNKEAWPHIKTIF |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52597 | S265 | Sugiyama | HNRNPF HNRPF | EySGLSDGYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQs |
| P52597 | Y266 | Sugiyama | HNRNPF HNRPF | ySGLSDGYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQsT |
| P52597 | Y272 | Sugiyama | HNRNPF HNRPF | GYGFTTDLFGRDLsyCLsGMyDHRYGDsEFtVQsTTGHCVH |
| P52788 | Y336 | Sugiyama | SMS | GNCVNLTEALSLYEEQLGRLyCPVEFSKEIVCVPSYLELWV |
| P52888 | Y576 | Sugiyama | THOP1 | VLAKVDQALHTQTDADPAEEyARLCQEILGVPATPGTNMPA |
| P52943 | Y198 | Sugiyama | CRIP2 CRP2 | CYGILFGPKGVNTGAVGsyIyDRDPEGKVQP__________ |
| P52948 | Y1215 | Sugiyama | NUP98 ADAR2 | KVHLEKLSLRQRKPDEDMKLyQTPLELKLKHSTVHVDELCP |
| P52948 | Y627 | Sugiyama | NUP98 ADAR2 | NsNLFsPVNRDsENLAsPsEyPENGERFsFLSKPVDENHQQ |
| P53396 | Y213 | Sugiyama | ACLY | EDLYFTYLEINPLVVTKDGVyVLDLAAKVDATADyICKVKW |
| P53396 | Y652 | Sugiyama | ACLY | GCFKIGNTGGMLDNILASKLyRPGsVAyVSRsGGMsNELNN |
| P53396 | Y659 | Sugiyama | ACLY | TGGMLDNILASKLyRPGsVAyVSRsGGMsNELNNIISRTTD |
| P53597 | Y78 | Sugiyama | SUCLG1 | IICQGFTGKQGtFHSQQALEyGtKLVGGTTPGKGGQTHLGL |
| P53621 | Y249 | Sugiyama | COPA | VKIWRMNESKAWEVDTCRGHyNNVSCAVFHPRQELILsNsE |
| P53634 | Y438 | Sugiyama | CTSC CPPI | SGMDYWIVKNsWGtGWGENGyFRIRRGtDECAIEsIAVAAt |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y388 | Sugiyama | YARS1 YARS | LDIRVGKIITVEKHPDADsLyVEKIDVGEAEPRTVVSGLVQ |
| P54652 | S41 | Sugiyama | HSPA2 | VFQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVA |
| P54652 | Y184 | Sugiyama | HSPA2 | tITGLNVLRIINEPtAAAIAyGLDKKGCAGGEKNVLIFDLG |
| P55060 | Y278 | Sugiyama | CSE1L CAS XPO2 | EEEAGLLELLKSQICDNAALyAQKyDEEFQRYLPRFVTAIW |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55209 | S69 | Sugiyama | NAP1L1 NRP | LAALQERLDGLVEtPtGyIEsLPRVVKRRVNALKNLQVKCA |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55209 | Y66 | Sugiyama | NAP1L1 NRP | PQILAALQERLDGLVEtPtGyIEsLPRVVKRRVNALKNLQV |
| P55209 | Y96 | Sugiyama | NAP1L1 NRP | RRVNALKNLQVKCAQIEAKFyEEVHDLERKyAVLyQPLFDK |
| P55809 | Y43 | Sugiyama | OXCT1 OXCT SCOT | TWYKGCVCSFSTSAHRHTKFyTDPVEAVKDIPDGATVLVGG |
| P55884 | Y768 | Sugiyama | EIF3B EIF3S9 | ERRRTMMEDFRKYRKMAQELyMEQKNERLELRGGVDTDELD |
| P56945 | Y387 | Sugiyama | BCAR1 CAS CASS1 CRKAS | PAPDLyDVPPGLRRPGPGtLyDVPRERVLPPEVADGGVVDs |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60510 | Y124 | Sugiyama | PPP4C PPP4 PPX | YPDRITLIRGNHESRQITQVyGFyDECLRKYGSVTVWRYCT |
| P60510 | Y127 | Sugiyama | PPP4C PPP4 PPX | RITLIRGNHESRQITQVyGFyDECLRKYGSVTVWRYCTEIF |
| P60660 | S30 | Sugiyama | MYL6 | AEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVLK |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | Y188 | Sugiyama | ACTB | GyALPHAILRLDLAGRDLTDyLMKILtERGysFtttAEREI |
| P60709 | Y198 | Sugiyama | ACTB | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P60709 | Y240 | Sugiyama | ACTB | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P60709 | Y294 | Sugiyama | ACTB | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P60709 | Y362 | Sugiyama | ACTB | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| 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 |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61247 | S236 | Sugiyama | RPS3A FTE1 MFTL | KMLKKPKFELGKLMELHGEGsssGKAtGDEtGAKVERADGy |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| 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 |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62140 | Y304 | Sugiyama | PPP1CB | VDETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPP |
| P62140 | Y306 | Sugiyama | PPP1CB | ETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPPKK |
| P62191 | Y184 | Sugiyama | PSMC1 | MDDTDPLVTVMKVEKAPQETyADIGGLDNQIQEIKESVELP |
| P62241 | Y113 | Sugiyama | RPS8 OK/SW-cl.83 | TKTLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEE |
| P62241 | Y117 | Sugiyama | RPS8 OK/SW-cl.83 | VKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEEIL |
| P62241 | Y198 | Sugiyama | RPS8 OK/SW-cl.83 | RPGQCGRADGyVLEGKELEFyLRKIKARKGK__________ |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y214 | Sugiyama | YWHAE | LAKAAFDDAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P62263 | Y72 | Sugiyama | RPS14 PRO2640 | TICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELGITA |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62277 | Y18 | Sugiyama | RPS13 | ___MGRMHAPGKGLsQsALPyRRsVPtWLKLTsDDVKEQIy |
| P62280 | T54 | Sugiyama | RPS11 | PRYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILs |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62312 | Y72 | Sugiyama | LSM6 | VNGQLKNKyGDAFIRGNNVLyIstQKRRM____________ |
| P62495 | Y345 | Sugiyama | ETF1 ERF1 RF1 SUP45L1 | NLDIMRYVLHCQGTEEEKILyLTPEQEKDKSHFTDKETGQE |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62633 | Y75 | Sugiyama | CNBP RNF163 ZNF9 | YRCGESGHLAKDCDLQEDACyNCGRGGHIAKDCKEPKRERE |
| P62714 | Y127 | Sugiyama | PPP2CB | YPERITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFT |
| P62714 | Y130 | Sugiyama | PPP2CB | RITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFTDLF |
| P62736 | Y190 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | GyALPHAIMRLDLAGRDLTDyLMKILTERGysFVttAEREI |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y117 | Sugiyama | RPL23A | VFIVDVKANKHQIKQAVKKLyDIDVAKVNtLIRPDGEKKAY |
| P62750 | Y144 | Sugiyama | RPL23A | VNtLIRPDGEKKAYVRLAPDyDALDVANKIGII________ |
| P62750 | Y74 | Sugiyama | RPL23A | LRRQPKYPRKSAPRRNKLDHyAIIKFPLTTEsAMKKIEDNN |
| P62753 | Y156 | Sugiyama | RPS6 OK/SW-cl.2 | KRASRIRKLFNLsKEDDVRQyVVRKPLNKEGKKPRTKAPKI |
| P62753 | Y28 | Sugiyama | RPS6 OK/SW-cl.2 | PAtGCQKLIEVDDERKLRtFyEKRMAtEVAADALGEEWKGY |
| P62807 | 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 | Y147 | Sugiyama | RAN ARA24 OK/SW-cl.81 | KDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLARK |
| P62829 | Y38 | Sugiyama | RPL23 | LGLPVGAVINCADNTGAKNLyIIsVKGIKGRLNRLPAAGVG |
| P62841 | Y30 | Sugiyama | RPS15 RIG | RTFRKFTYRGVDLDQLLDMsyEQLMQLySARQRRRLNRGLR |
| P62841 | Y37 | Sugiyama | RPS15 RIG | YRGVDLDQLLDMsyEQLMQLySARQRRRLNRGLRRKQHSLL |
| P62847 | Y76 | Sugiyama | RPS24 | FVFGFRTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGL |
| P62847 | Y81 | Sugiyama | RPS24 | RTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGLYEKKK |
| P62899 | T26 | Sugiyama | RPL31 | KGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRAL |
| P62899 | Y103 | Sugiyama | RPL31 | RIRVRLSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVD |
| P62899 | Y108 | Sugiyama | RPL31 | LSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVDEN___ |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62910 | Y95 | Sugiyama | RPL32 PP9932 | RKFLVHNVKELEVLLMCNKsyCAEIAHNVSsKNRKAIVERA |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62942 | Y27 | Sugiyama | FKBP1A FKBP1 FKBP12 | tIsPGDGRtFPKRGQtCVVHytGMLEDGKKFDSSRDRNKPF |
| P62979 | T147 | Sugiyama | RPS27A UBA80 UBCEP1 | GAGVFMAsHFDRHyCGKCCLtyCFNKPEDK___________ |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P62993 | Y160 | PSP | GRB2 ASH | VSRNQQIFLRDIEQVPQQPtyVQALFDFDPQEDGELGFRRG |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y19 | Sugiyama | YWHAZ | __MDKNELVQKAKLAEQAERyDDMAACMKsVtEQGAELsNE |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63173 | T44 | Sugiyama | RPL38 | KIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLPPGL |
| P63173 | Y43 | Sugiyama | RPL38 | VKIKKNKDNVKFKVRCSRyLytLVItDKEKAEKLKQSLPPG |
| P63220 | T52 | Sugiyama | RPS21 | IQMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRL |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | Y188 | Sugiyama | ACTG1 ACTG | GyALPHAILRLDLAGRDLTDyLMKILtERGysFtttAEREI |
| P63261 | Y198 | Sugiyama | ACTG1 ACTG | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P63261 | Y240 | Sugiyama | ACTG1 ACTG | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P63261 | Y294 | Sugiyama | ACTG1 ACTG | IHETTFNSIMKCDVDIRKDLyANtVLsGGttMyPGIADRMQ |
| P63261 | Y362 | Sugiyama | ACTG1 ACTG | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P63267 | Y189 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | GyALPHAIMRLDLAGRDLTDyLMKILTERGysFVttAEREI |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67775 | Y127 | Sugiyama | PPP2CA | YRERITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFT |
| P67775 | Y130 | Sugiyama | PPP2CA | RITILRGNHESRQITQVyGFyDECLRKYGNANVWKYFTDLF |
| P67809 | S209 | Sugiyama | YBX1 NSEP1 YB1 | RRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGEQ |
| P67809 | Y196 | Sugiyama | YBX1 NSEP1 YB1 | sAPEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGE |
| P67809 | Y197 | Sugiyama | YBX1 NSEP1 YB1 | APEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGEV |
| P67809 | Y72 | Sugiyama | YBX1 NSEP1 YB1 | KKVIATKVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| P68032 | Y190 | Sugiyama | ACTC1 ACTC | GyALPHAIMRLDLAGRDLTDyLMKILTERGysFVttAEREI |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68104 | T88 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | ERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGTSQ |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68133 | Y190 | Sugiyama | ACTA1 ACTA | GyALPHAIMRLDLAGRDLTDyLMKILTERGysFVttAEREI |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68363 | T94 | Sugiyama | TUBA1B | VIDEVRtGtyRQLFHPEQLItGKEDAANNyARGHYTIGKEI |
| P68363 | Y103 | Sugiyama | TUBA1B | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| P68363 | Y224 | Sugiyama | TUBA1B | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| P68363 | Y312 | Sugiyama | TUBA1B | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P68366 | T94 | Sugiyama | TUBA4A TUBA1 | VIDEIRNGPYRQLFHPEQLItGKEDAANNyARGHYTIGKEI |
| P68366 | Y103 | Sugiyama | TUBA4A TUBA1 | YRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDPVLDRIR |
| P68366 | Y224 | Sugiyama | TUBA4A TUBA1 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| P68366 | Y312 | Sugiyama | TUBA4A TUBA1 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| P78316 | Y119 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | EKMMKRFALEQQRHHEKKSIyNLNEDEELTHyGQsLADIEK |
| P78316 | Y130 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | QRHHEKKSIyNLNEDEELTHyGQsLADIEKHNDIVDsDsDA |
| P78345 | Y29 | Sugiyama | RPP38 | GRGsLRKTRPLVVKTSLNNPyIIRWSALESEDMHFILQTLE |
| P80303 | Y350 | Sugiyama | NUCB2 NEFA | PDsWEtLDQQQFFtEEELKEyENIIALQENELKKKADELQK |
| P83731 | Y11 | Sugiyama | RPL24 | __________MKVELCsFsGyKIYPGHGRRYARTDGKVFQF |
| P83731 | Y55 | Sugiyama | RPL24 | KCEsAFLSKRNPRQINWtVLyRRKHKKGQsEEIQKKRTRRA |
| P84103 | Y32 | Sugiyama | SRSF3 SFRS3 SRP20 | VyVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVE |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| Q00653 | Y247 | Sugiyama | NFKB2 LYT10 | NLKISRMDKTAGSVRGGDEVyLLCDKVQKDDIEVRFYEDDE |
| Q00839 | Y257 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | QKGGDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVE |
| Q00839 | Y260 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | GDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVEEED |
| Q00839 | Y525 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | LPGAGKTTWVTKHAAENPGKyNILGtNtIMDKMMVAGFKKQ |
| Q00839 | Y654 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | LKMKGNFTLPEVAECFDEITyVELQKEEAQKLLEQYKEESK |
| Q01082 | Y1408 | Sugiyama | SPTBN1 SPTB2 | sCADLDKWLHGLESQIQSDDyGKDLTsVNILLKKQQMLENQ |
| Q01082 | Y777 | Sugiyama | SPTBN1 SPTB2 | DAWMLDILKIVssSDVGHDEystQsLVKKHKDVAEEIANYR |
| Q01105 | Y140 | Sugiyama | SET | LTRVEVtEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNE |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01814 | Y1152 | Sugiyama | ATP2B2 PMCA2 | RGLNRIQtQIRVVKAFRssLyEGLEKPEsRtsIHNFMAHPE |
| Q01844 | Y278 | Sugiyama | EWSR1 EWS | SSSYGQQSsFRQDHPssMGVyGQESGGFSGPGENRSMSGPD |
| Q02539 | Y74 | Sugiyama | H1-1 H1F1 HIST1H1A | SKERGGVSLAALKKALAAAGyDVEKNNSRIKLGIKsLVsKG |
| Q02790 | Y111 | Sugiyama | FKBP4 FKBP52 | DIAIATMKVGEVCHItCKPEyAyGsAGsPPKIPPNATLVFE |
| Q02790 | Y113 | Sugiyama | FKBP4 FKBP52 | AIATMKVGEVCHItCKPEyAyGsAGsPPKIPPNATLVFEVE |
| Q02790 | Y202 | Sugiyama | FKBP4 FKBP52 | LFDQRELRFEIGEGENLDLPyGLERAIQRMEKGEHsIVyLK |
| Q02878 | Y116 | Sugiyama | RPL6 TXREB1 | VGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQH |
| Q02878 | Y216 | Sugiyama | RPL6 TXREB1 | AtsTKIDISNVKIPKHLtDAyFKKKKLRKPRHQEGEIFDtE |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04446 | Y73 | Sugiyama | GBE1 | sQILKNIGENEGGIDKFSRGyEsFGVHRCADGGLYCKEWAP |
| Q04637 | Y1424 | Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | KEFLPEGQDIGAFVAEQKVEyTLGEEsEAPGQRALPsEELN |
| Q04637 | Y594 | Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | WDSKEDKIHNAENIQPGEQKyEyKsDQWKPLNLEEKKRYDR |
| Q04637 | Y596 | Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | SKEDKIHNAENIQPGEQKyEyKsDQWKPLNLEEKKRYDREF |
| Q04837 | S67 | Sugiyama | SSBP1 SSBP | QVEGKNPVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRI |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y20 | Sugiyama | YWHAH YWHA1 | _MGDREQLLQRARLAEQAERyDDMAsAMKAVtELNEPLsNE |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q07021 | Y188 | Sugiyama | C1QBP GC1QBP HABP1 SF2P32 | FVVEVIKNDDGKKALVLDCHyPEDEVGQEDEAEsDIFsIRE |
| Q07157 | Y1165 | Sugiyama | TJP1 ZO1 | RYEQAPRAsALRHEEQPAPGyDtHGRLRPEAQPHPsAGPKP |
| Q07666 | Y145 | Sugiyama | KHDRBS1 SAM68 | LtAEIEKIQKGDSKKDDEENyLDLFsHKNMKLKERVLIPVK |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08211 | Y370 | Sugiyama | DHX9 DDX9 LKP NDH2 | GPLAFATPEQISMDLKNELMyQLEQDHDLQAILQERELLPV |
| Q08211 | Y616 | Sugiyama | DHX9 DDX9 LKP NDH2 | KDDDGGEDDDANCNLICGDEyGPETRLsMsQLNEKETPFEL |
| Q08211 | Y68 | Sugiyama | DHX9 DDX9 LKP NDH2 | MGNSTNKKDAQSNAARDFVNyLVRINEIKsEEVPAFGVAsP |
| Q08752 | Y323 | Sugiyama | PPID CYP40 CYPD | DPSNTKALYRRAQGWQGLKEyDQALADLKKAQGIAPEDKAI |
| Q08J23 | Y262 | Sugiyama | NSUN2 SAKI TRM4 | DASSIPRLQIDVDGRKEILFyDRILCDVPCSGDGtMRKNID |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q12797 | Y90 | Sugiyama | ASPH BAH | VAVVWFDLVDYEEVLGKLGIyDADGDGDFDVDDAKVLLGLK |
| Q12805 | Y369 | Sugiyama | EFEMP1 FBLN3 FBNL | MCWNYHGGFRCYPRNPCQDPyILTPENRCVCPVsNAMCREL |
| Q12874 | Y136 | Sugiyama | SF3A3 SAP61 | ARENPSEEAQNLVEFtDEEGyGRYLDLHDCYLKYINLKASE |
| Q12874 | Y85 | Sugiyama | SF3A3 SAP61 | DGLRKEELNAIsGPNEFAEFyNRLKQIKEFHRKHPNEICVP |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q12974 | Y145 | Sugiyama | PTP4A2 PRL2 PTPCAAX2 BM-008 | DAVQFIRQKRRGAFNSKQLLyLEKYRPKMRLRFRDTNGHCC |
| Q12996 | Y708 | Sugiyama | CSTF3 | NEDsDEDEEKGAVVPPVHDIyRARQQKRIR___________ |
| Q13069 | Y9 | Sugiyama | GAGE5 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13070 | Y9 | Sugiyama | GAGE6 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13098 | Y172 | Sugiyama | GPS1 COPS1 CSN1 | YKGNSIKESIRRGHDDLGDHyLDCGDLSNALKCYSRARDYC |
| Q13162 | Y54 | Sugiyama | PRDX4 | AVQGWETEERPRTREEECHFyAGGQVyPGEAsRVsVADHsL |
| Q13228 | Y28 | Sugiyama | SELENBP1 SBP | CGPGySTPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVD |
| Q13228 | Y33 | Sugiyama | SELENBP1 SBP | STPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVDVDPKs |
| Q13242 | Y17 | Sugiyama | SRSF9 SFRS9 SRP30C | ____MsGWADERGGEGDGRIyVGNLPTDVREKDLEDLFyKY |
| Q13242 | Y214 | Sugiyama | SRSF9 SFRS9 SRP30C | RsRSGsRGRDsPyQsRGsPHyFsPFRPy_____________ |
| Q13242 | Y221 | Sugiyama | SRSF9 SFRS9 SRP30C | GRDsPyQsRGsPHyFsPFRPy____________________ |
| Q13263 | Y133 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TVVDCPVCKQQCFSKDIVENyFMRDsGsKAATDAQDANQCC |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13263 | Y458 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | GssQPMEVQEGyGFGsGDDPyssAEPHVsGVKRsRsGEGEV |
| Q13263 | Y517 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | LtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQPGtA |
| Q13263 | Y755 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | GGTLDLTLIRARLQEKLsPPyssPQEFAQDVGRMFKQFNKL |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13310 | Y238 | Sugiyama | PABPC4 APP1 PABP4 | LSVKVMRDPNGKSKGFGFVSyEKHEDANKAVEEMNGKEISG |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13442 | S19 | Sugiyama | PDAP1 HASPP28 | __MPKGGRKGGHKGRARQytsPEEIDAQLQAEKQKAREEEE |
| Q13444 | Y715 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | ADAM15 MDC15 | TTGLLLSLLVLLVLVMLGASyWYRARLHQRLCQLKGPTCQy |
| Q13444 | Y735 | GPS6|SIGNOR|EPSD | ADAM15 MDC15 | yWYRARLHQRLCQLKGPTCQyRAAQSGPSERPGPPQRALLA |
| Q13509 | T107 | Sugiyama | TUBB3 TUBB4 | PDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECENC |
| Q13509 | Y106 | Sugiyama | TUBB3 TUBB4 | RPDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECEN |
| Q13510 | Y305 | Sugiyama | ASAH1 ASAH HSD-33 HSD33 | GNQSGEGCVITRDRKESLDVyELDAKQGRWYVVQTNYDRWK |
| Q13561 | Y207 | Sugiyama | DCTN2 DCTN50 | SKGGSGGKttGtPPDssLVtyELHsRPEQDKFSQAAKVAEL |
| Q13561 | Y313 | Sugiyama | DCTN2 DCTN50 | IAKHKASVEDADTQSKVHQLyEtIQRWsPIASTLPELVQRL |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13885 | T107 | Sugiyama | TUBB2A TUBB2 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q13885 | Y106 | Sugiyama | TUBB2A TUBB2 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q13905 | Y504 | SIGNOR|ELM|iPTMNet|EPSD|PSP | RAPGEF1 GRF2 | QYDNISGEDLQSTAPIPSVPyAPFAAILPFQHGGSSAPVEF |
| Q14152 | Y697 | Sugiyama | EIF3A EIF3S10 KIAA0139 | LEKEKKELQERLKNQEKKIDyFERAKRLEEIPLIKSAYEEQ |
| Q14157 | Y858 | Sugiyama | UBAP2L KIAA0144 NICE4 | PFPtPttPLtGRDGsLAsNPysGDLtKFGRGDASSPAPATT |
| Q14240 | Y49 | Sugiyama | EIF4A2 DDX2B EIF4F | NEIVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIK |
| Q14240 | Y51 | Sugiyama | EIF4A2 DDX2B EIF4F | IVDNFDDMNLKESLLRGIyAyGFEKPsAIQQRAIIPCIKGy |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | S332 | Sugiyama | CTTN EMS1 | VQKDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRA |
| Q14247 | Y141 | Sugiyama | CTTN EMS1 | FGGKFGVQMDRVDQsAVGFEyQGKtEKHAsQKDyssGFGGK |
| Q14247 | Y334 | Sugiyama | CTTN EMS1 | KDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRANF |
| Q14247 | Y421 | Sugiyama | CTTN EMS1 | tPPVsPAPQPtEERLPssPVyEDAAsFKAELsyRGPVsGtE |
| Q14247 | Y446 | Sugiyama | CTTN EMS1 | sFKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYAT |
| Q14257 | Y30 | Sugiyama | RCN2 ERC55 | LGLLLLCAAAAGAGKAEELHyPLGERRsDyDREALLGVQED |
| Q14257 | Y303 | Sugiyama | RCN2 ERC55 | LsEEEILENPDLFLtsEAtDyGRQLHDDyFyHDEL______ |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14566 | Y276 | Sugiyama | MCM6 | KLSTPGARAEtNsRVsGVDGyEtEGIRGLRALGVRDLSYRL |
| Q14566 | Y510 | Sugiyama | MCM6 | KATLNARTsILAAANPIsGHyDRSKSLKQNINLSAPIMSRF |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14974 | Y752 | Sugiyama | KPNB1 NTF97 | LEVVLNTLQQASQAQVDKSDyDMVDYLNELRESCLEAYTGI |
| Q14CX7 | Y19 | Sugiyama | NAA25 C12orf30 MDM20 NAP1 | __MATRGHVQDPNDRRLRPIyDyLDNGNNKMAIQQADKLLK |
| Q15024 | Y187 | Sugiyama | EXOSC7 KIAA0116 RRP42 | RVRVLEDEEGsKDIELSDDPyDCIRLSVENVPCIVTLCKIG |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15181 | Y169 | Sugiyama | PPA1 IOPPP PP | EGETDWKVIAINVDDPDAANyNDINDVKRLKPGYLEATVDW |
| Q15293 | Y148 | Sugiyama | RCN1 RCN | DRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKML |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15435 | Y327 | Sugiyama | PPP1R7 SDS22 | LLESWSDLDELKGARsLETVyLERNPLQKDPQYRRKVMLAL |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15631 | Y210 | Sugiyama | TSN | sLRKRYDGLKYDVKKVEEVVyDLSIRGFNKETAAACVEK__ |
| Q15637 | Y87 | Sugiyama | SF1 ZFM1 ZNF162 | tGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFRTRKKLEE |
| Q16543 | Y248 | Sugiyama | CDC37 CDC37A | VDPRACFRQFFTKIKtADRQyMEGFNDELEAFKERVRGRAK |
| Q16595 | Y95 | Sugiyama | FXN FRDA X25 | LMNLRKsGtLGHPGsLDEttyERLAEETLDSLAEFFEDLAD |
| Q16643 | Y163 | Sugiyama | DBN1 D0S117E | PVLHRLRLREDENAEPVGttyQKTDAAVEMKRINREQFWEQ |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16763 | Y144 | Sugiyama | UBE2S E2EPF OK/SW-cl.73 | NPESALNEEAGRLLLENyEEyAARARLLtEIHGGAGGPSGR |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q562R1 | Y189 | Sugiyama | ACTBL2 | GYALPHAILRLDLAGRDLTDyLMKILTERGYNFTTTAEREI |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | S58 | Sugiyama | HSP90AB3P HSP90BC | IFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPN |
| Q58FF7 | Y190 | Sugiyama | HSP90AB3P HSP90BC | EyLEERRVKEVVKKHsQFIGyPItLyLEKEQDKEIsDDEAE |
| Q58FF7 | Y195 | Sugiyama | HSP90AB3P HSP90BC | RRVKEVVKKHsQFIGyPItLyLEKEQDKEIsDDEAEEEKGE |
| Q58FF7 | Y492 | Sugiyama | HSP90AB3P HSP90BC | TANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIMETLR |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | S58 | Sugiyama | HSP90AB2P HSP90BB | IFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPN |
| Q58FF8 | Y198 | Sugiyama | HSP90AB2P HSP90BB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKTKPIWTRNTEDI |
| Q58FF8 | Y260 | Sugiyama | HSP90AB2P HSP90BB | VRYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVW |
| Q58FF8 | Y261 | Sugiyama | HSP90AB2P HSP90BB | RYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVWK |
| Q58FF8 | Y56 | Sugiyama | HSP90AB2P HSP90BB | KEIFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FG0 | Y177 | Sugiyama | HSP90AA5P HSP90AE | GQLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQ |
| Q58FG0 | Y178 | Sugiyama | HSP90AA5P HSP90AE | QLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQK |
| Q5JTH9 | Y1251 | Sugiyama | RRP12 KIAA0690 | AEYKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQG |
| Q5JTH9 | Y1253 | Sugiyama | RRP12 KIAA0690 | YKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQGQF |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5VTE0 | T88 | Sugiyama | EEF1A1P5 EEF1AL3 | ERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGTSQ |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6PEY2 | Y224 | Sugiyama | TUBA3E | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6UVK1 | Y1511 | Sugiyama | CSPG4 MCSP | PIPAEALRSTDGDSGSEDLVyTIEQPSNGRVVLRGAPGTEV |
| Q6VEQ5 | Y103 | Sugiyama | WASH2P FAM39B | KKAIKVFSSAKYPAPERLQEyGsIFTGAQDPGLQRRPRHRI |
| Q71RC2 | Y425 | Sugiyama | LARP4 PP13296 | SRNFPAERHNPTVTGHQEQtyLQKETSTLQVEQNGDYGRGR |
| Q71U36 | T94 | Sugiyama | TUBA1A TUBA3 | VIDEVRtGtyRQLFHPEQLItGKEDAANNyARGHYTIGKEI |
| Q71U36 | Y103 | Sugiyama | TUBA1A TUBA3 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q71U36 | Y224 | Sugiyama | TUBA1A TUBA3 | VDNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRF |
| Q71U36 | Y312 | Sugiyama | TUBA1A TUBA3 | tNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q7KZF4 | S473 | Sugiyama | SND1 TDRD11 | ALVSKGLATVIRYRQDDDQRssHyDELLAAEARAIKNGKGL |
| Q7KZF4 | Y109 | Sugiyama | SND1 TDRD11 | KLIGKEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVA |
| Q7KZF4 | Y113 | Sugiyama | SND1 TDRD11 | KEVCFtIENKtPQGREyGMIyLGKDTNGENIAEsLVAEGLA |
| Q7RTV0 | Y100 | Sugiyama | PHF5A | KDRDGCPKIVNLGSsKTDLFyERKKYGFKKR__________ |
| Q7Z2W4 | Y642 | Sugiyama | ZC3HAV1 ZC3HDC2 PRO1677 | GEEKDKRKNsNVDssyLEsLyQSCPRGVVPFQAGSRNYELS |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q8IWX8 | Y714 | Sugiyama | CHERP DAN26 SCAF6 | YsPPSHDRPRNsEGWEQNGLyEFFRAKMRARRRKGQEKRNS |
| Q8IWX8 | Y894 | Sugiyama | CHERP DAN26 SCAF6 | GDVRDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDE |
| Q8IWX8 | Y897 | Sugiyama | CHERP DAN26 SCAF6 | RDKWDQYKGVGVALDDPyENyRRNKsysFIARMKARDECK_ |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N8S7 | Y87 | Sugiyama | ENAH MENA | GLKYNQAtQtFHQWRDARQVyGLNFGSKEDANVFASAMMHA |
| Q8NBF2 | Y39 | Sugiyama | NHLRC2 | TSLEYALLDAVTQQEKDSLVyQyLQKVDGWEQDLSVPEFPE |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NFD5 | S1744 | Sugiyama | ARID1B BAF250B DAN15 KIAA1235 OSA2 | ALDTINILLYDDSTVATFNLsQLSGFLELLVEYFRKCLIDI |
| Q8NFI4 | Y185 | Sugiyama | ST13P5 FAM10A5 | NAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| Q8NI22 | Y135 | Sugiyama | MCFD2 SDNSF | DELINIIDGVLRDDDKNNDGyIDyAEFAKSLQ_________ |
| Q8WUA2 | Y401 | Sugiyama | PPIL4 | TSKKHKKKTHHCsEEKEDEDyMPIKNTNQDIYREMGFGHYE |
| Q92522 | Y48 | Sugiyama | H1-10 H1FX | AALsPsKKRKNSKKKNQPGKySQLVVEtIRRLGERNGSSLA |
| Q92526 | Y109 | Sugiyama | CCT6B | GDGTTSNVLIIGELLKQADLyISEGLHPRIIAEGFEAAKIK |
| Q92556 | Y18 | SIGNOR|EPSD|PSP | ELMO1 KIAA0281 | ___MPPPADIVKVAIEWPGAyPKLMEIDQKKPLSAIIKEVC |
| Q92556 | Y216 | SIGNOR|EPSD|PSP | ELMO1 KIAA0281 | SILQRSLAILESMVLNSHDLyQKVAQEITIGQLIPHLQGSD |
| Q92556 | Y395 | SIGNOR|EPSD|PSP | ELMO1 KIAA0281 | PPGMLALDNMLYFAKHHQDAyIRIVLENSSREDKHECPFGR |
| Q92556 | Y511 | SIGNOR|EPSD|PSP | ELMO1 KIAA0281 | ALTTKPSSLDQFKSKLQNLsyTEILKIRQSERMNQEDFQSR |
| Q92556 | Y720 | SIGNOR|EPSD|PSP | ELMO1 KIAA0281 | DLENIQIPDAPPPIPKEPSNyDFVyDCN_____________ |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y846 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | EDLEDKNNFGAEPPHQNGECyPNEKNsVNMDLD________ |
| Q92615 | Y596 | Sugiyama | LARP4B KIAA0217 LARP5 | LPVVVSREPsVPAsCAVsAtyERsPsPAHLPDDPKVAEKQR |
| Q92796 | S615 | Sugiyama | DLG3 KIAA1232 | GLSDDYYGAKNLKGQEDAILsYEPVTRQEIHYARPVIILGP |
| Q92878 | Y308 | Sugiyama | RAD50 | ELEEKMEKVFQGTDEQLNDLyHNHQRTVREKERKLVDCHRE |
| Q92905 | Y203 | Sugiyama | COPS5 CSN5 JAB1 | LGAFRTYPKGYKPPDEGPsEyQtIPLNKIEDFGVHCKQYYA |
| Q93052 | T316 | Sugiyama | LPP | yyEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPG |
| Q93052 | Y317 | Sugiyama | LPP | yEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPGA |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q93096 | Y148 | Sugiyama | PTP4A1 PRL1 PTPCAAX1 | DAVQFIRQKRRGAFNSKQLLyLEKYRPKMRLRFKDSNGHRN |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96AE4 | Y60 | Sugiyama | FUBP1 | QIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKVAP |
| Q96CT7 | Y38 | Sugiyama | CCDC124 | RRAEAKAAADAKKQKELEDAyWKDDDKHVMRKEQRKEEKEK |
| Q96F86 | Y225 | Sugiyama | EDC3 LSM16 YJDC YJEFN2 PP844 | DFEGNLALFDKAAVFEEIDtyERRSGTRsRGIPNERPTRYR |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96IK1 | Y82 | Sugiyama | BOD1 FAM44B | RGLFDSFRRDCLADVDTKPAyQNLRQKVDNFVStHLDKQEW |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96ST3 | Y13 | Sugiyama | SIN3A | ________MKRRLDDQEsPVyAAQQRRIPGstEAFPHQHRV |
| Q99062 | Y752 | SIGNOR|EPSD | CSF3R GCSFR | DPRAVSTQPQSQSGTSDQVLyGQLLGSPTSPGPGHyLRCDS |
| Q99062 | Y787 | SIGNOR|EPSD | CSF3R GCSFR | yLRCDSTQPLLAGLTPSPKSyENLWFQASPLGTLVTPAPSQ |
| Q99426 | Y114 | Sugiyama | TBCB CG22 CKAP1 | RLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKRsKLGRyN |
| Q99459 | Y788 | Sugiyama | CDC5L KIAA0432 PCDC5RP | ECLKEDVQRQQEREKELQHRyADLLLEKETLKSKF______ |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99497 | T140 | Sugiyama | PARK7 | GSKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPGT |
| Q99497 | Y139 | Sugiyama | PARK7 | FGSKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPG |
| Q99497 | Y141 | Sugiyama | PARK7 | SKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPGTS |
| Q99497 | Y67 | Sugiyama | PARK7 | sRDVVICPDAsLEDAKKEGPyDVVVLPGGNLGAQNLSESAA |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99614 | Y96 | Sugiyama | TTC1 TPR1 | ADKVENKsNEDVNssELDEEyLIELEKNMSDEEKQKRREES |
| Q99733 | Y85 | Sugiyama | NAP1L4 NAP2 | RRINALKQLQVRCAHIEAKFyEEVHDLERKyAALyQPLFDK |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| 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 | T94 | Sugiyama | TUBA1C TUBA6 | VIDEVRtGtyRQLFHPEQLItGKEDAANNyARGHYTIGKEI |
| Q9BQE3 | Y103 | Sugiyama | TUBA1C TUBA6 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q9BQE3 | Y224 | Sugiyama | TUBA1C TUBA6 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| Q9BQE3 | Y312 | Sugiyama | TUBA1C TUBA6 | TNACFEPANQMVKCDPRHGKyMACCLLyRGDVVPKDVNAAI |
| Q9BQE3 | Y449 | Sugiyama | TUBA1C TUBA6 | EKDyEEVGADsADGEDEGEEy____________________ |
| Q9BRK5 | Y162 | Sugiyama | SDF4 CAB45 PSEC0034 | sKTHFRAVDPDGDGHVsWDEyKVKFLASKGHSEKEVADAIR |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BS40 | Y20 | Sugiyama | LXN | _MEIPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQA |
| Q9BS40 | Y23 | Sugiyama | LXN | IPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQAsME |
| Q9BSU3 | Y145 | Sugiyama | NAA11 ARD1B ARD2 | TLNFQISEVEPKyyADGEDAyAMKRDLSQMADELRRQMDLK |
| Q9BTD8 | Y424 | Sugiyama | RBM42 | FPsFLKAKVIRDKRTGKTKGyGFVSFKDPsDyVRAMREMNG |
| Q9BTD8 | Y435 | Sugiyama | RBM42 | DKRTGKTKGyGFVSFKDPsDyVRAMREMNGKYVGSRPIKLR |
| Q9BUJ2 | Y111 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | GYSGPDGHYAMDNITRQNQFyDtQVIKQENESGyERRPLEM |
| Q9BUJ2 | Y510 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | RLIQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIV |
| Q9BVA1 | T107 | Sugiyama | TUBB2B | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q9BVA1 | Y106 | Sugiyama | TUBB2B | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q9BWF3 | Y194 | Sugiyama | RBM4 RBM4A | ECPIDRSGRVADLTEQYNEQyGAVRTPYTMSYGDSLYYNNA |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BZZ5 | Y28 | Sugiyama | API5 MIG8 | YRNyGILADATEQVGQHKDAyQVILDGVKGGTKEKRLAAQF |
| Q9C0C2 | Y855 | Sugiyama | TNKS1BP1 KIAA1741 TAB182 | RsQEADVQDWEFRKRDsQGtyssRDAELQDQEFGKRDsLGt |
| Q9C0C9 | Y604 | Sugiyama | UBE2O KIAA1734 | FCPGDFVVDKRVQSCPDPAVyGVVQSGDHIGRTCMVKWFKL |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H2H8 | Y75 | Sugiyama | PPIL3 | DPTGTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPN |
| Q9H2H8 | Y78 | Sugiyama | PPIL3 | GTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPNTNG |
| Q9H3S7 | Y1165 | Sugiyama | PTPN23 KIAA1471 | KVDAAEGRRPQALRLIERDPyEHPERLRQLQQELEAFRGQL |
| Q9H446 | Y67 | Sugiyama | RWDD1 DFRP2 CGI-24 PTD013 | TVQTTLKFTYSEKYPDEAPLyEIFSQENLEDNDVSDILKLL |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9H814 | Y309 | Sugiyama | PHAX RNUXA | FLNLLKNtPsISEEQIKDIFyIENQKEYENKKAARKRRTQV |
| Q9HB71 | Y165 | Sugiyama | CACYBP S100A6BP SIP PNAS-107 | VKTDTVLILCRKKVENTRWDyLtQVEKECKEKEKPsYDtEt |
| Q9HC35 | T554 | Sugiyama | EML4 C2orf2 EMAPL4 | ILWDHDLNPEREIEVPDQyGtIRAVAEGKADQFLVGTSRNF |
| Q9NPD3 | Y53 | Sugiyama | EXOSC4 RRP41 SKI6 | AQADGSAYIEQGNTKALAVVyGPHEIRGsRARALPDRALVN |
| Q9NQA3 | Y85 | Sugiyama | WASH6P CXYorf1 FAM39A | KKAIKVFSSAKYPAPERLQEyGsIFTGAQDPGLQRRPRHRI |
| Q9NRX4 | Y52 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | RSGAPAAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCE |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NSE4 | Y260 | Sugiyama | IARS2 | YKPVFWSPSSRTALAEAELEyNPEHVSRSIYVKFPLLKPSP |
| Q9NSE4 | Y97 | Sugiyama | IARS2 | GRQQPDtELEIQQKCGFSELysWQRERKVKTEFCLHDGPPY |
| Q9NVS9 | Y195 | Sugiyama | PNPO | SSVIPDREYLRKKNEELEQLyQDQEVPKPKSWGGYVLYPQV |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NY65 | T94 | Sugiyama | TUBA8 TUBAL2 | VVDEVRAGTYRQLFHPEQLItGKEDAANNyARGHYTVGKES |
| Q9NY65 | Y103 | Sugiyama | TUBA8 TUBAL2 | YRQLFHPEQLItGKEDAANNyARGHYTVGKESIDLVLDRIR |
| Q9NY65 | Y224 | Sugiyama | TUBA8 TUBAL2 | VDNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRF |
| Q9NYF8 | Y219 | Sugiyama | BCLAF1 BTF KIAA0164 | IDEFNKssAtsGDIWPGLsAyDNsPRsPHsPsPIAtPPSQS |
| Q9NYU2 | Y966 | Sugiyama | UGGT1 GT UGCGL1 UGGT UGT1 UGTR | LVMKVDALLsAQPKGDPRIEyQFFEDRHSAIKLRPKEGETY |
| Q9P270 | Y293 | Sugiyama | SLAIN2 KIAA1458 | NDVTDVQILARMQEESLRQEyAATTSRRSSGSSCNSTRRGt |
| Q9UBQ5 | Y42 | Sugiyama | EIF3K EIF3S12 ARG134 HSPC029 MSTP001 PTD001 | NPENLAtLERYVETQAKENAyDLEANLAVLKLYQFNPAFFQ |
| Q9UBQ7 | Y255 | Sugiyama | GRHPR GLXR MSTP035 | KETAVFINISRGDVVNQDDLyQALAsGKIAAAGLDVtsPEP |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y74 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | PDRNPDDPQAQEKFQDLGAAyEVLsDSEKRKQyDTyGEEGL |
| Q9UBS4 | Y89 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | DLGAAyEVLsDSEKRKQyDTyGEEGLKDGHQSSHGDIFSHF |
| Q9UBT2 | Y159 | Sugiyama | UBA2 SAE2 UBLE1B HRIHFB2115 | SGTAGYLGQVTTIKKGVtECyECHPKPTQRTFPGCtIRNTP |
| Q9UGI8 | Y251 | Sugiyama | TES | RTQYSCYCCKLSMKEGDPAIyAERAGyDKLWHPACFVCSTC |
| Q9UHD2 | Y354 | SIGNOR|EPSD|PSP | TBK1 NAK | IFHELVyKQTKIISsNQELIyEGRRLVLEPGRLAQHFPKTT |
| Q9UHD2 | Y394 | SIGNOR|EPSD|PSP | TBK1 NAK | TEENPIFVVsREPLNtIGLIyEKISLPKVHPRYDLDGDAsM |
| Q9UHR5 | Y46 | Sugiyama | SAP30BP HCNGP HTRG HTRP | AGIEAVGSAAEEKGGLVsDAyGEDDFsRLGGDEDGYEEEED |
| Q9UHX1 | Y269 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | FGKIKSCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNL |
| Q9UHX1 | Y274 | Sugiyama | PUF60 FIR ROBPI SIAHBP1 | SCTLARDPTTGKHKGyGFIEyEKAQSSQDAVSSMNLFDLGG |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UII2 | Y58 | Sugiyama | ATP5IF1 ATPI ATPIF1 | GsIREAGGAFGKREQAEEERyFRAQsREQLAALKKHHEEEI |
| Q9UIQ6 | Y70 | Sugiyama | LNPEP OTASE | GsRLLVRGLGEHEMEEDEEDyEssAKLLGMsFMNRssGLRN |
| Q9UKY7 | Y244 | Sugiyama | CDV3 H41 | NRGRDEVSKNQALKLQLDNQyAVLENQKSSHSQYN______ |
| Q9UL25 | Y150 | Sugiyama | RAB21 KIAA0118 | VGNKIDLEKERHVsIQEAESyAESVGAKHYHTSAKQNKGIE |
| Q9UL46 | Y33 | Sugiyama | PSME2 | ARKQVEVFRQNLFQEAEEFLyRFLPQKIIYLNQLLQEDSLN |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UN86 | Y125 | Sugiyama | G3BP2 KIAA0660 | ERKFMQTFVLAPEGSVPNKFyVHNDMFRYEDEVFGDsEPEL |
| Q9UNH7 | Y220 | Sugiyama | SNX6 | VSGVKDVDDFFEHERTFLLEyHNRVKDASAKSDRMTRSHKS |
| Q9UNZ2 | Y167 | Sugiyama | NSFL1C UBXN2C | PRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLKLW |
| Q9UQ35 | S172 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | DPQRRAREAKQPAPEPPKPYsLVREssssRsPTPKQKKKKK |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2B0 | Y71 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | IQMGsFRINPDGsQsVVEVPyARsEAHLtELLEEICDRMKE |
| Q9Y2T7 | Y107 | Sugiyama | YBX2 CSDA3 MSY2 | KPVLAIQVLGTVKWFNVRNGyGFINRNDtKEDVFVHQtAIK |
| Q9Y2W1 | T230 | Sugiyama | THRAP3 BCLAF2 TRAP150 | tsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERsPA |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y2W2 | Y236 | Sugiyama | WBP11 NPWBP SIPP1 SNP70 | GRKVGFALDLPPRRRDEDMLysPELAQRGHDDDVSSTSEDD |
| Q9Y2X3 | Y428 | Sugiyama | NOP58 NOL5 NOP5 HSPC120 | GTGKALAKTEKYEHKSEVKtyDPSGDstLPtCsKKRKIEQV |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y490 | Y1893 | Sugiyama | TLN1 KIAA1027 TLN | TKsNtsPEELGPLANQLTsDyGRLAsEAKPAAVAAENEEIG |
| Q9Y4L1 | Y116 | Sugiyama | HYOU1 GRP170 HSPH4 ORP150 | TLRYFQHLLGKQADNPHVALyQARFPEHELTFDPQRQTVHF |
| Q9Y5K5 | Y176 | Sugiyama | UCHL5 UCH37 AD-019 CGI-70 | SAKEEDAFHFVSyVPVNGRLyELDGLREGPIDLGACNQDDW |
| Q9Y5S9 | S56 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWILF |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y639 | Y216 | Sugiyama | NPTN SDFR1 SDR1 | KNASNMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKA |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | S245 | Sugiyama | CLIC4 | ysRDEFtNtCPsDKEVEIAysDVAKRLTK____________ |
| Q9Y6D5 | Y819 | Sugiyama | ARFGEF2 ARFGEP2 BIG2 | KMNRGINDSKDLPEEyLSsIyEEIEGKKIAMKETKELTIAT |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
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| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Signal Transduction | R-HSA-162582 | 8.921246e-09 | 8.050 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.912551e-08 | 7.718 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 6.186997e-08 | 7.209 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.541869e-07 | 6.812 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 9.621004e-06 | 5.017 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 2.002644e-05 | 4.698 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 3.779950e-05 | 4.423 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 5.288417e-05 | 4.277 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 5.380467e-05 | 4.269 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 8.738915e-05 | 4.059 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 8.652135e-05 | 4.063 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 1.041733e-04 | 3.982 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 1.000506e-04 | 4.000 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.013063e-04 | 3.994 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 1.108532e-04 | 3.955 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 1.587935e-04 | 3.799 | 1 | 1 |
| EPH-Ephrin signaling | R-HSA-2682334 | 1.534536e-04 | 3.814 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.811132e-04 | 3.742 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 1.796015e-04 | 3.746 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 2.006983e-04 | 3.697 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 2.167410e-04 | 3.664 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.535041e-04 | 3.596 | 1 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 2.843232e-04 | 3.546 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 2.774355e-04 | 3.557 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 2.843232e-04 | 3.546 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 3.051267e-04 | 3.516 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.237851e-04 | 3.373 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 4.587904e-04 | 3.338 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 5.257191e-04 | 3.279 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 6.012275e-04 | 3.221 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 6.540124e-04 | 3.184 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 7.258278e-04 | 3.139 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 6.943982e-04 | 3.158 | 0 | 0 |
| Immune System | R-HSA-168256 | 7.861055e-04 | 3.105 | 1 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 8.256490e-04 | 3.083 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 8.795029e-04 | 3.056 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 9.336801e-04 | 3.030 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 1.170379e-03 | 2.932 | 1 | 1 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 1.112095e-03 | 2.954 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.097492e-03 | 2.960 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 1.216700e-03 | 2.915 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 1.170379e-03 | 2.932 | 0 | 0 |
| TRKA activation by NGF | R-HSA-187042 | 1.448385e-03 | 2.839 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 1.450463e-03 | 2.838 | 1 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.475628e-03 | 2.831 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 1.903671e-03 | 2.720 | 1 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 1.903671e-03 | 2.720 | 1 | 1 |
| Leishmania phagocytosis | R-HSA-9664417 | 1.903671e-03 | 2.720 | 1 | 0 |
| Innate Immune System | R-HSA-168249 | 1.811680e-03 | 2.742 | 1 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.920903e-03 | 2.716 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 2.105092e-03 | 2.677 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 2.154983e-03 | 2.667 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 2.392321e-03 | 2.621 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 2.233784e-03 | 2.651 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 2.398280e-03 | 2.620 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 2.393899e-03 | 2.621 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 2.467259e-03 | 2.608 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.759083e-03 | 2.559 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 2.759083e-03 | 2.559 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.656740e-03 | 2.576 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 2.749138e-03 | 2.561 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.779926e-03 | 2.556 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 2.779926e-03 | 2.556 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 2.798205e-03 | 2.553 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 3.407593e-03 | 2.468 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 3.147508e-03 | 2.502 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 3.620562e-03 | 2.441 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 3.754689e-03 | 2.425 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 4.232427e-03 | 2.373 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 4.571344e-03 | 2.340 | 0 | 0 |
| Activation of TRKA receptors | R-HSA-187015 | 5.588735e-03 | 2.253 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 5.512921e-03 | 2.259 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 5.697698e-03 | 2.244 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 5.721817e-03 | 2.242 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 5.998080e-03 | 2.222 | 0 | 0 |
| Activated NTRK2 signals through FYN | R-HSA-9032500 | 6.713996e-03 | 2.173 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 7.050928e-03 | 2.152 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 6.950024e-03 | 2.158 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 6.458792e-03 | 2.190 | 1 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 6.458792e-03 | 2.190 | 1 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 6.508002e-03 | 2.187 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 7.785905e-03 | 2.109 | 0 | 0 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | R-HSA-428542 | 7.933103e-03 | 2.101 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 8.171570e-03 | 2.088 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 8.189336e-03 | 2.087 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 9.243895e-03 | 2.034 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 8.801207e-03 | 2.055 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 9.839010e-03 | 2.007 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 1.002294e-02 | 1.999 | 0 | 0 |
| Drug resistance of ALK mutants | R-HSA-9700649 | 1.093189e-02 | 1.961 | 0 | 0 |
| crizotinib-resistant ALK mutants | R-HSA-9717326 | 1.093189e-02 | 1.961 | 0 | 0 |
| NVP-TAE684-resistant ALK mutants | R-HSA-9717301 | 1.093189e-02 | 1.961 | 0 | 0 |
| brigatinib-resistant ALK mutants | R-HSA-9717319 | 1.093189e-02 | 1.961 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 1.093189e-02 | 1.961 | 0 | 0 |
| ASP-3026-resistant ALK mutants | R-HSA-9717264 | 1.093189e-02 | 1.961 | 0 | 0 |
| lorlatinib-resistant ALK mutants | R-HSA-9717329 | 1.093189e-02 | 1.961 | 0 | 0 |
| alectinib-resistant ALK mutants | R-HSA-9717316 | 1.093189e-02 | 1.961 | 0 | 0 |
| ceritinib-resistant ALK mutants | R-HSA-9717323 | 1.093189e-02 | 1.961 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 1.151198e-02 | 1.939 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 1.058998e-02 | 1.975 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 1.079439e-02 | 1.967 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 1.171307e-02 | 1.931 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 1.171307e-02 | 1.931 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 1.188641e-02 | 1.925 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.213206e-02 | 1.916 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 1.225645e-02 | 1.912 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 1.225645e-02 | 1.912 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 1.225645e-02 | 1.912 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 1.370528e-02 | 1.863 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.370528e-02 | 1.863 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.536189e-02 | 1.814 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 1.465265e-02 | 1.834 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.465265e-02 | 1.834 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 1.550606e-02 | 1.809 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 1.447847e-02 | 1.839 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.638696e-02 | 1.786 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.709989e-02 | 1.767 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.891733e-02 | 1.723 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.891733e-02 | 1.723 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.891733e-02 | 1.723 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.932854e-02 | 1.714 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 1.979915e-02 | 1.703 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 2.018698e-02 | 1.695 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 2.018698e-02 | 1.695 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 2.018698e-02 | 1.695 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 2.081228e-02 | 1.682 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 2.081228e-02 | 1.682 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.081228e-02 | 1.682 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 2.081228e-02 | 1.682 | 0 | 0 |
| TGFBR2 MSI Frameshift Mutants in Cancer | R-HSA-3642279 | 2.174494e-02 | 1.663 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 2.556157e-02 | 1.592 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 2.556157e-02 | 1.592 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 2.556157e-02 | 1.592 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 2.291273e-02 | 1.640 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 2.437593e-02 | 1.613 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.671980e-02 | 1.573 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.694347e-02 | 1.570 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.694347e-02 | 1.570 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 2.694347e-02 | 1.570 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 2.694347e-02 | 1.570 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 2.771513e-02 | 1.557 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 2.778358e-02 | 1.556 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 2.911932e-02 | 1.536 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 2.911932e-02 | 1.536 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.912988e-02 | 1.536 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5660686 | 3.244044e-02 | 1.489 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5619101 | 3.244044e-02 | 1.489 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 3.036051e-02 | 1.518 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 3.292541e-02 | 1.482 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 3.424896e-02 | 1.465 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 3.162923e-02 | 1.500 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 3.370606e-02 | 1.472 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 3.138466e-02 | 1.503 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 3.503673e-02 | 1.455 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 3.036051e-02 | 1.518 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.609239e-02 | 1.443 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 3.138466e-02 | 1.503 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 3.702999e-02 | 1.431 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.122608e-02 | 1.505 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 3.335198e-02 | 1.477 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 3.559980e-02 | 1.449 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.370606e-02 | 1.472 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.609239e-02 | 1.443 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 3.854196e-02 | 1.414 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.900074e-02 | 1.409 | 0 | 0 |
| Loss of Function of TGFBR2 in Cancer | R-HSA-3642278 | 4.301965e-02 | 1.366 | 0 | 0 |
| Regulation of cortical dendrite branching | R-HSA-8985801 | 4.301965e-02 | 1.366 | 0 | 0 |
| TGFBR2 Kinase Domain Mutants in Cancer | R-HSA-3645790 | 4.301965e-02 | 1.366 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 4.301965e-02 | 1.366 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 4.301965e-02 | 1.366 | 0 | 0 |
| TGFBR1 LBD Mutants in Cancer | R-HSA-3656535 | 4.301965e-02 | 1.366 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 4.301965e-02 | 1.366 | 0 | 0 |
| The NLRP1 inflammasome | R-HSA-844455 | 5.348384e-02 | 1.272 | 0 | 0 |
| PLC-gamma1 signalling | R-HSA-167021 | 5.348384e-02 | 1.272 | 0 | 0 |
| Signalling to STAT3 | R-HSA-198745 | 5.348384e-02 | 1.272 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 5.348384e-02 | 1.272 | 0 | 0 |
| Defective CYP19A1 causes AEXS | R-HSA-5579030 | 5.348384e-02 | 1.272 | 0 | 0 |
| Defective ABCC2 causes DJS | R-HSA-5679001 | 5.348384e-02 | 1.272 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 4.105312e-02 | 1.387 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 4.427147e-02 | 1.354 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 4.427147e-02 | 1.354 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 4.896567e-02 | 1.310 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 4.625375e-02 | 1.335 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 4.275935e-02 | 1.369 | 0 | 0 |
| The AIM2 inflammasome | R-HSA-844615 | 4.301965e-02 | 1.366 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.348384e-02 | 1.272 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.348384e-02 | 1.272 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 5.168164e-02 | 1.287 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 4.895461e-02 | 1.310 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 4.275935e-02 | 1.369 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 4.427147e-02 | 1.354 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 4.068925e-02 | 1.391 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 4.598425e-02 | 1.337 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 5.168164e-02 | 1.287 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 4.730384e-02 | 1.325 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 4.809889e-02 | 1.318 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 5.168164e-02 | 1.287 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 4.625375e-02 | 1.335 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 4.625375e-02 | 1.335 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 4.427147e-02 | 1.354 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 4.427147e-02 | 1.354 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 5.133998e-02 | 1.290 | 0 | 0 |
| Formation of the nephric duct | R-HSA-9830364 | 4.625375e-02 | 1.335 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 4.127379e-02 | 1.384 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 4.217656e-02 | 1.375 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 4.894006e-02 | 1.310 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 5.168164e-02 | 1.287 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 5.447696e-02 | 1.264 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 5.503562e-02 | 1.259 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 5.629874e-02 | 1.250 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 5.732455e-02 | 1.242 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 5.739253e-02 | 1.241 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 5.986946e-02 | 1.223 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 6.022294e-02 | 1.220 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 6.022294e-02 | 1.220 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 6.081823e-02 | 1.216 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 6.202835e-02 | 1.207 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 6.202835e-02 | 1.207 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 6.261154e-02 | 1.203 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 6.383425e-02 | 1.195 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.383425e-02 | 1.195 | 0 | 0 |
| TGFBR1 KD Mutants in Cancer | R-HSA-3656532 | 6.383425e-02 | 1.195 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 7.407210e-02 | 1.130 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 7.407210e-02 | 1.130 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.407210e-02 | 1.130 | 0 | 0 |
| NTRK2 activates RAC1 | R-HSA-9032759 | 7.407210e-02 | 1.130 | 0 | 0 |
| Loss of Function of TGFBR1 in Cancer | R-HSA-3656534 | 7.407210e-02 | 1.130 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 7.407210e-02 | 1.130 | 0 | 0 |
| SMAD2/3 Phosphorylation Motif Mutants in Cancer | R-HSA-3304356 | 7.407210e-02 | 1.130 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 8.419862e-02 | 1.075 | 0 | 0 |
| NGF-independant TRKA activation | R-HSA-187024 | 8.419862e-02 | 1.075 | 0 | 0 |
| Signalling to p38 via RIT and RIN | R-HSA-187706 | 8.419862e-02 | 1.075 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.419862e-02 | 1.075 | 0 | 0 |
| SLIT2:ROBO1 increases RHOA activity | R-HSA-8985586 | 8.419862e-02 | 1.075 | 0 | 0 |
| Defective CSF2RB causes SMDP5 | R-HSA-5688849 | 8.419862e-02 | 1.075 | 0 | 0 |
| Defective CSF2RA causes SMDP4 | R-HSA-5688890 | 8.419862e-02 | 1.075 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 9.421501e-02 | 1.026 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.421501e-02 | 1.026 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.421501e-02 | 1.026 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 6.920868e-02 | 1.160 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 9.231841e-02 | 1.035 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 8.731161e-02 | 1.059 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.920868e-02 | 1.160 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 8.185235e-02 | 1.087 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 6.920868e-02 | 1.160 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 6.383425e-02 | 1.195 | 0 | 0 |
| MDK and PTN in ALK signaling | R-HSA-9851151 | 6.383425e-02 | 1.195 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex in Cancer | R-HSA-3304351 | 9.421501e-02 | 1.026 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 7.407210e-02 | 1.130 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 8.507168e-02 | 1.070 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 6.383425e-02 | 1.195 | 0 | 0 |
| CLEC7A/inflammasome pathway | R-HSA-5660668 | 8.419862e-02 | 1.075 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.419862e-02 | 1.075 | 0 | 0 |
| Loss of Function of SMAD2/3 in Cancer | R-HSA-3304349 | 8.419862e-02 | 1.075 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 9.169696e-02 | 1.038 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 6.616641e-02 | 1.179 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 7.411960e-02 | 1.130 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 6.977896e-02 | 1.156 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 8.836556e-02 | 1.054 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 7.121084e-02 | 1.147 | 1 | 1 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 8.597400e-02 | 1.066 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 6.383425e-02 | 1.195 | 1 | 1 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 7.407210e-02 | 1.130 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.421501e-02 | 1.026 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 6.442929e-02 | 1.191 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 7.002697e-02 | 1.155 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 8.181655e-02 | 1.087 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 6.287302e-02 | 1.202 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 9.421501e-02 | 1.026 | 1 | 1 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 6.574465e-02 | 1.182 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 7.387695e-02 | 1.131 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 7.229616e-02 | 1.141 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 8.507168e-02 | 1.070 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 7.860140e-02 | 1.105 | 0 | 0 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 6.383425e-02 | 1.195 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 9.421501e-02 | 1.026 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 6.423094e-02 | 1.192 | 0 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 9.421501e-02 | 1.026 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 7.387695e-02 | 1.131 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 8.181655e-02 | 1.087 | 0 | 0 |
| Formation of WDR5-containing histone-modifying complexes | R-HSA-9772755 | 7.860140e-02 | 1.105 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 8.008425e-02 | 1.096 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 8.996437e-02 | 1.046 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 6.423094e-02 | 1.192 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 1.139221e-01 | 0.943 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.236152e-01 | 0.908 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.236152e-01 | 0.908 | 0 | 0 |
| Inactivation of CDC42 and RAC1 | R-HSA-428543 | 1.236152e-01 | 0.908 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 1.236152e-01 | 0.908 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 1.332029e-01 | 0.875 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 1.332029e-01 | 0.875 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 1.520664e-01 | 0.818 | 0 | 0 |
| Activation of RAC1 | R-HSA-428540 | 1.520664e-01 | 0.818 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.613445e-01 | 0.792 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 1.705217e-01 | 0.768 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.705217e-01 | 0.768 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 1.795990e-01 | 0.746 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 1.795990e-01 | 0.746 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 1.885775e-01 | 0.725 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 1.195589e-01 | 0.922 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 1.231763e-01 | 0.909 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 1.454016e-01 | 0.837 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 9.665305e-02 | 1.015 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 1.041225e-01 | 0.982 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.124073e-01 | 0.949 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 1.124536e-01 | 0.949 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 1.570396e-01 | 0.804 | 0 | 0 |
| Activated NTRK3 signals through PI3K | R-HSA-9603381 | 1.041225e-01 | 0.982 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.332029e-01 | 0.875 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 1.416402e-01 | 0.849 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 1.570396e-01 | 0.804 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 1.139221e-01 | 0.943 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 1.019043e-01 | 0.992 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.195589e-01 | 0.922 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.195589e-01 | 0.922 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.195589e-01 | 0.922 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 1.243022e-01 | 0.906 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.159689e-01 | 0.936 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 1.024121e-01 | 0.990 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 1.139221e-01 | 0.943 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 1.520664e-01 | 0.818 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 9.846751e-02 | 1.007 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 1.019043e-01 | 0.992 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 1.454016e-01 | 0.837 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 1.419361e-01 | 0.848 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 1.304895e-01 | 0.884 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.885775e-01 | 0.725 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 1.341833e-01 | 0.872 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 1.088754e-01 | 0.963 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.195589e-01 | 0.922 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 1.124073e-01 | 0.949 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 1.722613e-01 | 0.764 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 1.722613e-01 | 0.764 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 1.722613e-01 | 0.764 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 1.722613e-01 | 0.764 | 0 | 0 |
| TGFBR3 regulates TGF-beta signaling | R-HSA-9839389 | 1.041225e-01 | 0.982 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.041225e-01 | 0.982 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 1.139221e-01 | 0.943 | 0 | 0 |
| Conjugation of benzoate with glycine | R-HSA-177135 | 1.426862e-01 | 0.846 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.613445e-01 | 0.792 | 0 | 0 |
| Conjugation of salicylate with glycine | R-HSA-177128 | 1.613445e-01 | 0.792 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.705217e-01 | 0.768 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.885775e-01 | 0.725 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 1.159689e-01 | 0.936 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.416402e-01 | 0.849 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.606450e-01 | 0.794 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 9.506467e-02 | 1.022 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.426862e-01 | 0.846 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.520664e-01 | 0.818 | 0 | 0 |
| p38MAPK events | R-HSA-171007 | 1.885775e-01 | 0.725 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.705217e-01 | 0.768 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.865735e-01 | 0.729 | 0 | 0 |
| Estrogen biosynthesis | R-HSA-193144 | 1.613445e-01 | 0.792 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.885775e-01 | 0.725 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.846751e-02 | 1.007 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 1.606450e-01 | 0.794 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.575394e-01 | 0.803 | 0 | 0 |
| Diseases associated with surfactant metabolism | R-HSA-5687613 | 1.613445e-01 | 0.792 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 1.722613e-01 | 0.764 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.441417e-01 | 0.841 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 1.379005e-01 | 0.860 | 0 | 0 |
| Netrin mediated repulsion signals | R-HSA-418886 | 1.041225e-01 | 0.982 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 1.236152e-01 | 0.908 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.236152e-01 | 0.908 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.332029e-01 | 0.875 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.520664e-01 | 0.818 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 1.613445e-01 | 0.792 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.705217e-01 | 0.768 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 1.416402e-01 | 0.849 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.236152e-01 | 0.908 | 0 | 0 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | R-HSA-2032785 | 1.795990e-01 | 0.746 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 1.492576e-01 | 0.826 | 0 | 0 |
| Kinesins | R-HSA-983189 | 1.722613e-01 | 0.764 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 1.416402e-01 | 0.849 | 0 | 0 |
| Downregulation of ERBB4 signaling | R-HSA-1253288 | 1.139221e-01 | 0.943 | 0 | 0 |
| Synthesis of PIPs at the ER membrane | R-HSA-1483248 | 1.426862e-01 | 0.846 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.705217e-01 | 0.768 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.800808e-01 | 0.745 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 1.340928e-01 | 0.873 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 1.879532e-01 | 0.726 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.441417e-01 | 0.841 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 1.243022e-01 | 0.906 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 1.441417e-01 | 0.841 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 1.124073e-01 | 0.949 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 1.332029e-01 | 0.875 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.705217e-01 | 0.768 | 0 | 0 |
| Physiological factors | R-HSA-5578768 | 1.795990e-01 | 0.746 | 0 | 0 |
| RNA Polymerase I Transcription Initiation | R-HSA-73762 | 1.053740e-01 | 0.977 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 1.055652e-01 | 0.976 | 1 | 1 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 9.779456e-02 | 1.010 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 1.623115e-01 | 0.790 | 1 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 1.623115e-01 | 0.790 | 1 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.800808e-01 | 0.745 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 9.885112e-02 | 1.005 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 1.218969e-01 | 0.914 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 1.671029e-01 | 0.777 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 1.041225e-01 | 0.982 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 1.520664e-01 | 0.818 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 1.613445e-01 | 0.792 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 1.613445e-01 | 0.792 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 1.596613e-01 | 0.797 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.426862e-01 | 0.846 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 1.236152e-01 | 0.908 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 9.779456e-02 | 1.010 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 1.885775e-01 | 0.725 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 1.226744e-01 | 0.911 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.562544e-01 | 0.806 | 1 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 1.311759e-01 | 0.882 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 1.529854e-01 | 0.815 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 1.014143e-01 | 0.994 | 1 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 9.558741e-02 | 1.020 | 1 | 0 |
| Autophagy | R-HSA-9612973 | 1.264320e-01 | 0.898 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 1.606450e-01 | 0.794 | 0 | 0 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | R-HSA-9615017 | 1.019043e-01 | 0.992 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 9.846751e-02 | 1.007 | 1 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 1.411403e-01 | 0.850 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 1.233777e-01 | 0.909 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 1.218969e-01 | 0.914 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.268202e-01 | 0.897 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 1.122790e-01 | 0.950 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.233777e-01 | 0.909 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.919074e-01 | 0.717 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 1.919074e-01 | 0.717 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 1.974583e-01 | 0.705 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.974583e-01 | 0.705 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 1.974583e-01 | 0.705 | 0 | 0 |
| Activation of SMO | R-HSA-5635838 | 1.974583e-01 | 0.705 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.974583e-01 | 0.705 | 0 | 0 |
| Attachment and Entry | R-HSA-9678110 | 1.974583e-01 | 0.705 | 0 | 0 |
| Atorvastatin ADME | R-HSA-9754706 | 1.974583e-01 | 0.705 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 1.974583e-01 | 0.705 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 1.974583e-01 | 0.705 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 1.974583e-01 | 0.705 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 2.010987e-01 | 0.697 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 2.038331e-01 | 0.691 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 2.059137e-01 | 0.686 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 2.060690e-01 | 0.686 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 2.060690e-01 | 0.686 | 0 | 0 |
| Antigen processing: Ub, ATP-independent proteasomal degradation | R-HSA-9912633 | 2.062424e-01 | 0.686 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 2.062424e-01 | 0.686 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 2.062424e-01 | 0.686 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 2.062424e-01 | 0.686 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 2.062424e-01 | 0.686 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 2.062424e-01 | 0.686 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 2.062424e-01 | 0.686 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 2.062424e-01 | 0.686 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 2.078272e-01 | 0.682 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 2.118295e-01 | 0.674 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.149310e-01 | 0.668 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.149310e-01 | 0.668 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 2.149310e-01 | 0.668 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 2.158394e-01 | 0.666 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 2.158394e-01 | 0.666 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 2.198563e-01 | 0.658 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 2.231327e-01 | 0.651 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 2.231327e-01 | 0.651 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.235249e-01 | 0.651 | 0 | 0 |
| Synaptic adhesion-like molecules | R-HSA-8849932 | 2.235249e-01 | 0.651 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.235249e-01 | 0.651 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 2.235249e-01 | 0.651 | 0 | 0 |
| Aspirin ADME | R-HSA-9749641 | 2.238795e-01 | 0.650 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 2.260043e-01 | 0.646 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 2.279085e-01 | 0.642 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 2.319426e-01 | 0.635 | 0 | 0 |
| Conjugation of carboxylic acids | R-HSA-159424 | 2.320254e-01 | 0.634 | 0 | 0 |
| Amino Acid conjugation | R-HSA-156587 | 2.320254e-01 | 0.634 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.320254e-01 | 0.634 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 2.320254e-01 | 0.634 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 2.320254e-01 | 0.634 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.320254e-01 | 0.634 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.320254e-01 | 0.634 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.320254e-01 | 0.634 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 2.337315e-01 | 0.631 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 2.359812e-01 | 0.627 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.359812e-01 | 0.627 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 2.359812e-01 | 0.627 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.359812e-01 | 0.627 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.404332e-01 | 0.619 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 2.404332e-01 | 0.619 | 0 | 0 |
| Creatine metabolism | R-HSA-71288 | 2.404332e-01 | 0.619 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 2.404332e-01 | 0.619 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.404332e-01 | 0.619 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 2.433772e-01 | 0.614 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 2.433772e-01 | 0.614 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 2.440698e-01 | 0.612 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.462944e-01 | 0.609 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 2.487496e-01 | 0.604 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 2.487496e-01 | 0.604 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 2.487496e-01 | 0.604 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 2.521698e-01 | 0.598 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 2.521698e-01 | 0.598 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 2.569754e-01 | 0.590 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 2.569754e-01 | 0.590 | 0 | 0 |
| Signaling by NTRK3 (TRKC) | R-HSA-9034015 | 2.569754e-01 | 0.590 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.569754e-01 | 0.590 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.569754e-01 | 0.590 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 2.600665e-01 | 0.585 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 2.602769e-01 | 0.585 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.609594e-01 | 0.583 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.651116e-01 | 0.577 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 2.651116e-01 | 0.577 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.651116e-01 | 0.577 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.724418e-01 | 0.565 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 2.724418e-01 | 0.565 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 2.724418e-01 | 0.565 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 2.724418e-01 | 0.565 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.731592e-01 | 0.564 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 2.731592e-01 | 0.564 | 1 | 0 |
| S Phase | R-HSA-69242 | 2.757356e-01 | 0.560 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 2.764960e-01 | 0.558 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 2.764960e-01 | 0.558 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 2.787017e-01 | 0.555 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 2.805490e-01 | 0.552 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.811192e-01 | 0.551 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.811192e-01 | 0.551 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.811192e-01 | 0.551 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.811192e-01 | 0.551 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.811192e-01 | 0.551 | 0 | 0 |
| ADP signalling through P2Y purinoceptor 1 | R-HSA-418592 | 2.811192e-01 | 0.551 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 2.811192e-01 | 0.551 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 2.816710e-01 | 0.550 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 2.846003e-01 | 0.546 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 2.846003e-01 | 0.546 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 2.846432e-01 | 0.546 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 2.876181e-01 | 0.541 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 2.889925e-01 | 0.539 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 2.889925e-01 | 0.539 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 2.905956e-01 | 0.537 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 2.935753e-01 | 0.532 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.967801e-01 | 0.528 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 2.967801e-01 | 0.528 | 0 | 0 |
| Metalloprotease DUBs | R-HSA-5689901 | 2.967801e-01 | 0.528 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.967801e-01 | 0.528 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 3.007805e-01 | 0.522 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 3.044829e-01 | 0.516 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 3.044829e-01 | 0.516 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 3.044829e-01 | 0.516 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 3.058871e-01 | 0.514 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 3.121017e-01 | 0.506 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.121017e-01 | 0.506 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 3.121017e-01 | 0.506 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 3.128775e-01 | 0.505 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 3.161149e-01 | 0.500 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.196376e-01 | 0.495 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.196376e-01 | 0.495 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 3.196376e-01 | 0.495 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 3.206932e-01 | 0.494 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 3.270913e-01 | 0.485 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.270913e-01 | 0.485 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.270913e-01 | 0.485 | 0 | 0 |
| Thrombin signalling through proteinase activated receptors (PARs) | R-HSA-456926 | 3.270913e-01 | 0.485 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.270913e-01 | 0.485 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 3.270913e-01 | 0.485 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 3.289359e-01 | 0.483 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.329354e-01 | 0.478 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 3.344639e-01 | 0.476 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 3.344639e-01 | 0.476 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 3.344639e-01 | 0.476 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 3.344639e-01 | 0.476 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 3.369283e-01 | 0.472 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 3.369283e-01 | 0.472 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 3.380350e-01 | 0.471 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 3.417561e-01 | 0.466 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 3.417561e-01 | 0.466 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 3.417561e-01 | 0.466 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 3.429984e-01 | 0.465 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 3.488631e-01 | 0.457 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.489689e-01 | 0.457 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 3.489689e-01 | 0.457 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.489689e-01 | 0.457 | 0 | 0 |
| Cardiogenesis | R-HSA-9733709 | 3.489689e-01 | 0.457 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 3.489689e-01 | 0.457 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 3.503703e-01 | 0.455 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 3.528258e-01 | 0.452 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 3.528258e-01 | 0.452 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 3.533561e-01 | 0.452 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 3.561031e-01 | 0.448 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 3.561031e-01 | 0.448 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.607261e-01 | 0.443 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.631595e-01 | 0.440 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 3.631595e-01 | 0.440 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 3.631595e-01 | 0.440 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 3.631595e-01 | 0.440 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.631595e-01 | 0.440 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 3.631595e-01 | 0.440 | 0 | 0 |
| Signal amplification | R-HSA-392518 | 3.631595e-01 | 0.440 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.701391e-01 | 0.432 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 3.701391e-01 | 0.432 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.701391e-01 | 0.432 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 3.701391e-01 | 0.432 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 3.701391e-01 | 0.432 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 3.742045e-01 | 0.427 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 3.770425e-01 | 0.424 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 3.770425e-01 | 0.424 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 3.770425e-01 | 0.424 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.770425e-01 | 0.424 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.770425e-01 | 0.424 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 3.838708e-01 | 0.416 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 3.838708e-01 | 0.416 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 3.838708e-01 | 0.416 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 3.838708e-01 | 0.416 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 3.838708e-01 | 0.416 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 3.842054e-01 | 0.415 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 3.901483e-01 | 0.409 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 3.973048e-01 | 0.401 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 3.973048e-01 | 0.401 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 3.973048e-01 | 0.401 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 4.034874e-01 | 0.394 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 4.037515e-01 | 0.394 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 4.039121e-01 | 0.394 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 4.039121e-01 | 0.394 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 4.039121e-01 | 0.394 | 0 | 0 |
| Nuclear signaling by ERBB4 | R-HSA-1251985 | 4.039121e-01 | 0.394 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 4.059513e-01 | 0.392 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 4.073100e-01 | 0.390 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 4.104475e-01 | 0.387 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 4.104475e-01 | 0.387 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 4.104475e-01 | 0.387 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 4.104475e-01 | 0.387 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 4.169116e-01 | 0.380 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 4.169116e-01 | 0.380 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 4.169116e-01 | 0.380 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 4.169116e-01 | 0.380 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 4.169116e-01 | 0.380 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 4.169116e-01 | 0.380 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 4.169116e-01 | 0.380 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 4.169116e-01 | 0.380 | 0 | 0 |
| SLC-mediated transport of neurotransmitters | R-HSA-442660 | 4.169116e-01 | 0.380 | 0 | 0 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | R-HSA-381676 | 4.233052e-01 | 0.373 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.233052e-01 | 0.373 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 4.246309e-01 | 0.372 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 4.262429e-01 | 0.370 | 0 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 4.296291e-01 | 0.367 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.296291e-01 | 0.367 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 4.296291e-01 | 0.367 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 4.328953e-01 | 0.364 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 4.328953e-01 | 0.364 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 4.337284e-01 | 0.363 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.358840e-01 | 0.361 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 4.374517e-01 | 0.359 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 4.420707e-01 | 0.355 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 4.420707e-01 | 0.355 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 4.420707e-01 | 0.355 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 4.420707e-01 | 0.355 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 4.420707e-01 | 0.355 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.420707e-01 | 0.355 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 4.420707e-01 | 0.355 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 4.420707e-01 | 0.355 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 4.447245e-01 | 0.352 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 4.448585e-01 | 0.352 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 4.476974e-01 | 0.349 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 4.481900e-01 | 0.349 | 0 | 0 |
| Signaling by TGFBR3 | R-HSA-9839373 | 4.481900e-01 | 0.349 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.481900e-01 | 0.349 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.481900e-01 | 0.349 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 4.481900e-01 | 0.349 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 4.481900e-01 | 0.349 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 4.485417e-01 | 0.348 | 1 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 4.542425e-01 | 0.343 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 4.542425e-01 | 0.343 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 4.558670e-01 | 0.341 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 4.558670e-01 | 0.341 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 4.558670e-01 | 0.341 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.602290e-01 | 0.337 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.602290e-01 | 0.337 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 4.661502e-01 | 0.331 | 0 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 4.661502e-01 | 0.331 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 4.661502e-01 | 0.331 | 0 | 0 |
| Chemokine receptors bind chemokines | R-HSA-380108 | 4.661502e-01 | 0.331 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 4.775044e-01 | 0.321 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 4.777995e-01 | 0.321 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 4.777995e-01 | 0.321 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 4.777995e-01 | 0.321 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.835290e-01 | 0.316 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 4.891960e-01 | 0.311 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 4.969817e-01 | 0.304 | 1 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 5.003452e-01 | 0.301 | 0 | 0 |
| Paracetamol ADME | R-HSA-9753281 | 5.003452e-01 | 0.301 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 5.055295e-01 | 0.296 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 5.058287e-01 | 0.296 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 5.058287e-01 | 0.296 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 5.058287e-01 | 0.296 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 5.058287e-01 | 0.296 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 5.113816e-01 | 0.291 | 1 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.166168e-01 | 0.287 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 5.180910e-01 | 0.286 | 1 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.219228e-01 | 0.282 | 0 | 0 |
| Peroxisomal protein import | R-HSA-9033241 | 5.219228e-01 | 0.282 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.219228e-01 | 0.282 | 0 | 0 |
| Amino acid transport across the plasma membrane | R-HSA-352230 | 5.219228e-01 | 0.282 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 5.219228e-01 | 0.282 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 5.221003e-01 | 0.282 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 5.271708e-01 | 0.278 | 0 | 0 |
| Sphingolipid de novo biosynthesis | R-HSA-1660661 | 5.271708e-01 | 0.278 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.323615e-01 | 0.274 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.323615e-01 | 0.274 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.323615e-01 | 0.274 | 0 | 0 |
| Endogenous sterols | R-HSA-211976 | 5.323615e-01 | 0.274 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 5.374955e-01 | 0.270 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 5.374955e-01 | 0.270 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 5.424476e-01 | 0.266 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 5.457084e-01 | 0.263 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 5.521814e-01 | 0.258 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 5.525638e-01 | 0.258 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 5.585897e-01 | 0.253 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 5.617695e-01 | 0.250 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 5.617695e-01 | 0.250 | 0 | 0 |
| Metabolism of steroid hormones | R-HSA-196071 | 5.623371e-01 | 0.250 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.623371e-01 | 0.250 | 0 | 0 |
| SLC-mediated transport of amino acids | R-HSA-9958863 | 5.623371e-01 | 0.250 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 5.623371e-01 | 0.250 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 5.628669e-01 | 0.250 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.671439e-01 | 0.246 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 5.671439e-01 | 0.246 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.766004e-01 | 0.239 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 5.766004e-01 | 0.239 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 5.766004e-01 | 0.239 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 5.766004e-01 | 0.239 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 5.812514e-01 | 0.236 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.835704e-01 | 0.234 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.858516e-01 | 0.232 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 5.858516e-01 | 0.232 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.858516e-01 | 0.232 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 5.896517e-01 | 0.229 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.904015e-01 | 0.229 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.949017e-01 | 0.226 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 5.949017e-01 | 0.226 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 6.032647e-01 | 0.219 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 6.124161e-01 | 0.213 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 6.124161e-01 | 0.213 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 6.124161e-01 | 0.213 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 6.166757e-01 | 0.210 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.166757e-01 | 0.210 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 6.190719e-01 | 0.208 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 6.208888e-01 | 0.207 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 6.250559e-01 | 0.204 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.291774e-01 | 0.201 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 6.332538e-01 | 0.198 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 6.491189e-01 | 0.188 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 6.507452e-01 | 0.187 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 6.522149e-01 | 0.186 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 6.529773e-01 | 0.185 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 6.567935e-01 | 0.183 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 6.567935e-01 | 0.183 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.605680e-01 | 0.180 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 6.643013e-01 | 0.178 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.679937e-01 | 0.175 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.716457e-01 | 0.173 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 6.730172e-01 | 0.172 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 6.748565e-01 | 0.171 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 6.752577e-01 | 0.171 | 0 | 0 |
| Protein folding | R-HSA-391251 | 6.752577e-01 | 0.171 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.858586e-01 | 0.164 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 6.858586e-01 | 0.164 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.893151e-01 | 0.162 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 6.893151e-01 | 0.162 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 6.927339e-01 | 0.159 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.927339e-01 | 0.159 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 6.946262e-01 | 0.158 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 6.961152e-01 | 0.157 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 6.994596e-01 | 0.155 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.999690e-01 | 0.155 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 7.060389e-01 | 0.151 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 7.092746e-01 | 0.149 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 7.092746e-01 | 0.149 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 7.093056e-01 | 0.149 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 7.114123e-01 | 0.148 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 7.124749e-01 | 0.147 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 7.124749e-01 | 0.147 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.156402e-01 | 0.145 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 7.187708e-01 | 0.143 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 7.218672e-01 | 0.142 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 7.238879e-01 | 0.140 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 7.249297e-01 | 0.140 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 7.250636e-01 | 0.140 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 7.272552e-01 | 0.138 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.279586e-01 | 0.138 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 7.287734e-01 | 0.137 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.309543e-01 | 0.136 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 7.339173e-01 | 0.134 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 7.339173e-01 | 0.134 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.339173e-01 | 0.134 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 7.339173e-01 | 0.134 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 7.397462e-01 | 0.131 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 7.397462e-01 | 0.131 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 7.442634e-01 | 0.128 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 7.454481e-01 | 0.128 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 7.591653e-01 | 0.120 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 7.618192e-01 | 0.118 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 7.618192e-01 | 0.118 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 7.623868e-01 | 0.118 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 7.746589e-01 | 0.111 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 7.746589e-01 | 0.111 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 7.795999e-01 | 0.108 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.820299e-01 | 0.107 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 7.901532e-01 | 0.102 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 8.027348e-01 | 0.095 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 8.154393e-01 | 0.089 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 8.154393e-01 | 0.089 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 8.208890e-01 | 0.086 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 8.232259e-01 | 0.084 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 8.292362e-01 | 0.081 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 8.292362e-01 | 0.081 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.329863e-01 | 0.079 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 8.521947e-01 | 0.069 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 8.554433e-01 | 0.068 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 8.570408e-01 | 0.067 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 8.662464e-01 | 0.062 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 8.662640e-01 | 0.062 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 8.675212e-01 | 0.062 | 0 | 0 |
| Cytochrome P450 - arranged by substrate type | R-HSA-211897 | 8.706513e-01 | 0.060 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 8.706513e-01 | 0.060 | 0 | 0 |
| Translation | R-HSA-72766 | 8.743546e-01 | 0.058 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 8.762790e-01 | 0.057 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 8.880671e-01 | 0.052 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 8.926288e-01 | 0.049 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 8.964575e-01 | 0.047 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 8.987377e-01 | 0.046 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 8.998590e-01 | 0.046 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.070237e-01 | 0.042 | 0 | 0 |
| Sphingolipid metabolism | R-HSA-428157 | 9.123894e-01 | 0.040 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.143206e-01 | 0.039 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 9.149010e-01 | 0.039 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.180569e-01 | 0.037 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 9.233597e-01 | 0.035 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 9.358904e-01 | 0.029 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.386905e-01 | 0.027 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.413691e-01 | 0.026 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.433013e-01 | 0.025 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.456217e-01 | 0.024 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.588909e-01 | 0.018 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 9.626258e-01 | 0.017 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.633458e-01 | 0.016 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.669123e-01 | 0.015 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.730592e-01 | 0.012 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 9.781189e-01 | 0.010 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 9.797737e-01 | 0.009 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.835980e-01 | 0.007 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 9.897067e-01 | 0.004 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.901608e-01 | 0.004 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.989248e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.998441e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.999994e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000e+00 | 0.000 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 1.000000e+00 | 0.000 | 1 | 1 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
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| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Cell Cycle, Mitotic | R-HSA-69278 | 2.242651e-14 | 13.649 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 4.130030e-14 | 13.384 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 1.147971e-13 | 12.940 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 1.147971e-13 | 12.940 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 2.153833e-13 | 12.667 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 2.227107e-13 | 12.652 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.932898e-13 | 12.714 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 2.124967e-13 | 12.673 | 0 | 0 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 2.594591e-13 | 12.586 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 3.157474e-13 | 12.501 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 3.157474e-13 | 12.501 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 5.181411e-13 | 12.286 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 6.833423e-13 | 12.165 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 9.451329e-13 | 12.025 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 9.673373e-13 | 12.014 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 1.167288e-12 | 11.933 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 1.163514e-12 | 11.934 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 1.163514e-12 | 11.934 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 1.929679e-12 | 11.715 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.953215e-12 | 11.709 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 2.462586e-12 | 11.609 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 2.614797e-12 | 11.583 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 2.462586e-12 | 11.609 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 2.208012e-12 | 11.656 | 0 | 0 |
| Depurination | R-HSA-73927 | 3.125056e-12 | 11.505 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 3.831380e-12 | 11.417 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 4.952039e-12 | 11.305 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 4.952039e-12 | 11.305 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 4.901413e-12 | 11.310 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 5.123679e-12 | 11.290 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 6.186607e-12 | 11.209 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 6.186607e-12 | 11.209 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 6.826428e-12 | 11.166 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 7.771117e-12 | 11.110 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 8.897660e-12 | 11.051 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 9.520496e-12 | 11.021 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 9.520496e-12 | 11.021 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 1.173162e-11 | 10.931 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 1.178679e-11 | 10.929 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 1.300005e-11 | 10.886 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.240341e-11 | 10.906 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 1.324751e-11 | 10.878 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.326039e-11 | 10.877 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 1.439526e-11 | 10.842 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 1.759193e-11 | 10.755 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 1.759193e-11 | 10.755 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 1.842415e-11 | 10.735 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.842415e-11 | 10.735 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 2.119660e-11 | 10.674 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 2.770351e-11 | 10.557 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 3.137857e-11 | 10.503 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 3.778189e-11 | 10.423 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 4.475853e-11 | 10.349 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 5.320433e-11 | 10.274 | 1 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 6.465639e-11 | 10.189 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 7.253642e-11 | 10.139 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 7.289780e-11 | 10.137 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 7.685497e-11 | 10.114 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 9.108525e-11 | 10.041 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 1.076419e-10 | 9.968 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 1.089080e-10 | 9.963 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.104257e-10 | 9.957 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 1.392507e-10 | 9.856 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 1.747861e-10 | 9.757 | 0 | 0 |
| Immune System | R-HSA-168256 | 1.950039e-10 | 9.710 | 1 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 1.969627e-10 | 9.706 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 2.043818e-10 | 9.690 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 2.339171e-10 | 9.631 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 2.384042e-10 | 9.623 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 2.770907e-10 | 9.557 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 3.200132e-10 | 9.495 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 4.530040e-10 | 9.344 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 5.600397e-10 | 9.252 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 5.725884e-10 | 9.242 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 6.577547e-10 | 9.182 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 7.243233e-10 | 9.140 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 7.541126e-10 | 9.123 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 7.541126e-10 | 9.123 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 7.702798e-10 | 9.113 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 8.837034e-10 | 9.054 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 9.856449e-10 | 9.006 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 9.856449e-10 | 9.006 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 1.123763e-09 | 8.949 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 1.261796e-09 | 8.899 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 1.278978e-09 | 8.893 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 1.542596e-09 | 8.812 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 1.550797e-09 | 8.809 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 1.593028e-09 | 8.798 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.110245e-09 | 8.676 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 2.110245e-09 | 8.676 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 2.381011e-09 | 8.623 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 2.520327e-09 | 8.599 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 2.914549e-09 | 8.535 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 2.684959e-09 | 8.571 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 3.102864e-09 | 8.508 | 1 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 3.395927e-09 | 8.469 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 3.810977e-09 | 8.419 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 3.918094e-09 | 8.407 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 4.073862e-09 | 8.390 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 4.826385e-09 | 8.316 | 1 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 6.906316e-09 | 8.161 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 7.603764e-09 | 8.119 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 8.230226e-09 | 8.085 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 1.123850e-08 | 7.949 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 1.167978e-08 | 7.933 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 1.287571e-08 | 7.890 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 1.243996e-08 | 7.905 | 0 | 0 |
| Protein folding | R-HSA-391251 | 1.519207e-08 | 7.818 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 1.711936e-08 | 7.767 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 2.002244e-08 | 7.698 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 2.020934e-08 | 7.694 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 2.131881e-08 | 7.671 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 2.133057e-08 | 7.671 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 2.509952e-08 | 7.600 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 2.717420e-08 | 7.566 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 3.052336e-08 | 7.515 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 3.184068e-08 | 7.497 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 4.019279e-08 | 7.396 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 4.019279e-08 | 7.396 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 4.019279e-08 | 7.396 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 4.307819e-08 | 7.366 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 4.245798e-08 | 7.372 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 4.307819e-08 | 7.366 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 4.513707e-08 | 7.345 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 4.595208e-08 | 7.338 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 5.226407e-08 | 7.282 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 5.513540e-08 | 7.259 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 5.513540e-08 | 7.259 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 6.300851e-08 | 7.201 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 6.637288e-08 | 7.178 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 6.669993e-08 | 7.176 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 1.052297e-07 | 6.978 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 1.052297e-07 | 6.978 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 1.055314e-07 | 6.977 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 1.156898e-07 | 6.937 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 1.348779e-07 | 6.870 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 1.512021e-07 | 6.820 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 1.585762e-07 | 6.800 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 1.663324e-07 | 6.779 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.758911e-07 | 6.755 | 1 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 2.847147e-07 | 6.546 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 2.398420e-07 | 6.620 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 2.860130e-07 | 6.544 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 2.835762e-07 | 6.547 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 3.353013e-07 | 6.475 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 3.563825e-07 | 6.448 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 4.021170e-07 | 6.396 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 5.523161e-07 | 6.258 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 7.039600e-07 | 6.152 | 0 | 0 |
| Kinesins | R-HSA-983189 | 7.716503e-07 | 6.113 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 7.850453e-07 | 6.105 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 1.007521e-06 | 5.997 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 1.239525e-06 | 5.907 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 1.279542e-06 | 5.893 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 1.577568e-06 | 5.802 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 1.651771e-06 | 5.782 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 2.304353e-06 | 5.637 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 2.323293e-06 | 5.634 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 2.425085e-06 | 5.615 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 3.160123e-06 | 5.500 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 3.488043e-06 | 5.457 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 3.747651e-06 | 5.426 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 4.323798e-06 | 5.364 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 4.929948e-06 | 5.307 | 1 | 0 |
| Chromatin organization | R-HSA-4839726 | 6.424982e-06 | 5.192 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 6.648607e-06 | 5.177 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 8.012364e-06 | 5.096 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 8.016210e-06 | 5.096 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 9.506239e-06 | 5.022 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 1.161639e-05 | 4.935 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.196763e-05 | 4.922 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.531448e-05 | 4.815 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 1.913445e-05 | 4.718 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 2.054630e-05 | 4.687 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 2.660232e-05 | 4.575 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 3.015097e-05 | 4.521 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 3.120948e-05 | 4.506 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 3.215175e-05 | 4.493 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 3.224606e-05 | 4.492 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 4.856470e-05 | 4.314 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 5.441835e-05 | 4.264 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 6.028769e-05 | 4.220 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 7.553344e-05 | 4.122 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 7.596536e-05 | 4.119 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 7.774775e-05 | 4.109 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 8.338978e-05 | 4.079 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 9.362460e-05 | 4.029 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 1.309508e-04 | 3.883 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.319416e-04 | 3.880 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.400671e-04 | 3.854 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 1.863393e-04 | 3.730 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 2.111266e-04 | 3.675 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 2.283464e-04 | 3.641 | 1 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 2.314084e-04 | 3.636 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 2.382052e-04 | 3.623 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 2.610449e-04 | 3.583 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 2.710571e-04 | 3.567 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 2.981297e-04 | 3.526 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 3.099358e-04 | 3.509 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 4.419102e-04 | 3.355 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 5.046217e-04 | 3.297 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 5.501783e-04 | 3.259 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 5.657837e-04 | 3.247 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 7.461112e-04 | 3.127 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 9.312802e-04 | 3.031 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 1.016980e-03 | 2.993 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.121478e-03 | 2.950 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.174795e-03 | 2.930 | 0 | 0 |
| Signaling by FGFR1 amplification mutants | R-HSA-1839120 | 1.322239e-03 | 2.879 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 1.517152e-03 | 2.819 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 1.581488e-03 | 2.801 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 1.581488e-03 | 2.801 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 1.929376e-03 | 2.715 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.730639e-03 | 2.762 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.730639e-03 | 2.762 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 1.628368e-03 | 2.788 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 2.138110e-03 | 2.670 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.440141e-03 | 2.613 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 2.971913e-03 | 2.527 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 3.215237e-03 | 2.493 | 0 | 0 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | R-HSA-9758919 | 3.315814e-03 | 2.479 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 3.315814e-03 | 2.479 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 3.350620e-03 | 2.475 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 3.350620e-03 | 2.475 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 3.882693e-03 | 2.411 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 4.108552e-03 | 2.386 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 4.114854e-03 | 2.386 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 4.114854e-03 | 2.386 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 4.167865e-03 | 2.380 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 4.356222e-03 | 2.361 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 4.356222e-03 | 2.361 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 4.606964e-03 | 2.337 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 4.856827e-03 | 2.314 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 4.867243e-03 | 2.313 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 4.867243e-03 | 2.313 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 4.969132e-03 | 2.304 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 5.110336e-03 | 2.292 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 5.167587e-03 | 2.287 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 5.207570e-03 | 2.283 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 5.280185e-03 | 2.277 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 5.417060e-03 | 2.266 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 6.400965e-03 | 2.194 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 6.414504e-03 | 2.193 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 6.528681e-03 | 2.185 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 6.700537e-03 | 2.174 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 6.700537e-03 | 2.174 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 6.969539e-03 | 2.157 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 6.969539e-03 | 2.157 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 7.258740e-03 | 2.139 | 0 | 0 |
| HuR (ELAVL1) binds and stabilizes mRNA | R-HSA-450520 | 7.258740e-03 | 2.139 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 7.258740e-03 | 2.139 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 7.480401e-03 | 2.126 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 8.029006e-03 | 2.095 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 8.092580e-03 | 2.092 | 0 | 0 |
| FGFR1 mutant receptor activation | R-HSA-1839124 | 8.327331e-03 | 2.079 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 8.460846e-03 | 2.073 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 8.460846e-03 | 2.073 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 8.790997e-03 | 2.056 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 8.916587e-03 | 2.050 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 9.719846e-03 | 2.012 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.045337e-02 | 1.981 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 1.045337e-02 | 1.981 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 1.082815e-02 | 1.965 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 1.089852e-02 | 1.963 | 0 | 0 |
| Signaling by activated point mutants of FGFR1 | R-HSA-1839122 | 1.111153e-02 | 1.954 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 1.111153e-02 | 1.954 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 1.117117e-02 | 1.952 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 1.135574e-02 | 1.945 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 1.227943e-02 | 1.911 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.909221e-02 | 1.719 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 1.973666e-02 | 1.705 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 1.973666e-02 | 1.705 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.789133e-02 | 1.747 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.567659e-02 | 1.805 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.450299e-02 | 1.839 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 1.531243e-02 | 1.815 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.661517e-02 | 1.779 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.448703e-02 | 1.839 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.667592e-02 | 1.778 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.909221e-02 | 1.719 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 1.789133e-02 | 1.747 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.567659e-02 | 1.805 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 1.425456e-02 | 1.846 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 1.382668e-02 | 1.859 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 1.606548e-02 | 1.794 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.789133e-02 | 1.747 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 1.657906e-02 | 1.780 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 1.921943e-02 | 1.716 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 2.069727e-02 | 1.684 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.107390e-02 | 1.676 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 2.107390e-02 | 1.676 | 0 | 0 |
| Translation | R-HSA-72766 | 2.114243e-02 | 1.675 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 2.168320e-02 | 1.664 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 2.269447e-02 | 1.644 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 2.269447e-02 | 1.644 | 0 | 0 |
| Phospholipase C-mediated cascade: FGFR1 | R-HSA-5654219 | 2.278984e-02 | 1.642 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 2.318859e-02 | 1.635 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.373106e-02 | 1.625 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 2.373106e-02 | 1.625 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 2.394268e-02 | 1.621 | 0 | 0 |
| FGFR1 ligand binding and activation | R-HSA-190242 | 2.474031e-02 | 1.607 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.474031e-02 | 1.607 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 2.542800e-02 | 1.595 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 2.588022e-02 | 1.587 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 2.588022e-02 | 1.587 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 2.621990e-02 | 1.581 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.675643e-02 | 1.573 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 2.699273e-02 | 1.569 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.883662e-02 | 1.540 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 2.923740e-02 | 1.534 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 3.048156e-02 | 1.516 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 3.097936e-02 | 1.509 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.097936e-02 | 1.509 | 0 | 0 |
| PTEN Loss of Function in Cancer | R-HSA-5674404 | 3.099717e-02 | 1.509 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.099717e-02 | 1.509 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 3.169477e-02 | 1.499 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.232812e-02 | 1.490 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.318311e-02 | 1.479 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.318311e-02 | 1.479 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 3.371143e-02 | 1.472 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 3.443881e-02 | 1.463 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 3.544639e-02 | 1.450 | 0 | 0 |
| PI-3K cascade:FGFR1 | R-HSA-5654689 | 3.544639e-02 | 1.450 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 3.544639e-02 | 1.450 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 3.544639e-02 | 1.450 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 3.660201e-02 | 1.436 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 3.679710e-02 | 1.434 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 3.679710e-02 | 1.434 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 3.756168e-02 | 1.425 | 0 | 0 |
| Regulation of PTEN mRNA translation | R-HSA-8943723 | 3.776774e-02 | 1.423 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 3.776774e-02 | 1.423 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 3.853574e-02 | 1.414 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 3.853574e-02 | 1.414 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 3.853574e-02 | 1.414 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 3.949677e-02 | 1.403 | 0 | 0 |
| SHC-mediated cascade:FGFR1 | R-HSA-5654688 | 4.014570e-02 | 1.396 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 4.088339e-02 | 1.388 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 4.088339e-02 | 1.388 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 4.088339e-02 | 1.388 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.111581e-02 | 1.386 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.111581e-02 | 1.386 | 0 | 0 |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.111581e-02 | 1.386 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.111581e-02 | 1.386 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.111581e-02 | 1.386 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.111581e-02 | 1.386 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 4.229437e-02 | 1.374 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 4.229437e-02 | 1.374 | 0 | 0 |
| Signaling by plasma membrane FGFR1 fusions | R-HSA-8853336 | 5.112940e-02 | 1.291 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.103903e-02 | 1.214 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.084578e-02 | 1.150 | 0 | 0 |
| FGFR1c and Klotho ligand binding and activation | R-HSA-190374 | 7.084578e-02 | 1.150 | 0 | 0 |
| Plus-strand DNA synthesis | R-HSA-164525 | 8.055070e-02 | 1.094 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.055070e-02 | 1.094 | 0 | 0 |
| FRS-mediated FGFR1 signaling | R-HSA-5654693 | 4.257886e-02 | 1.371 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 7.507301e-02 | 1.125 | 0 | 0 |
| Downstream signaling of activated FGFR1 | R-HSA-5654687 | 7.260321e-02 | 1.139 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 4.906845e-02 | 1.309 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 4.906845e-02 | 1.309 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.386841e-02 | 1.195 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 5.826037e-02 | 1.235 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.284298e-02 | 1.277 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 4.971051e-02 | 1.304 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 7.084578e-02 | 1.150 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 5.552456e-02 | 1.256 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 6.965018e-02 | 1.157 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 7.862776e-02 | 1.104 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.055070e-02 | 1.094 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 7.541203e-02 | 1.123 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.112940e-02 | 1.291 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.112940e-02 | 1.291 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.055070e-02 | 1.094 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 4.760522e-02 | 1.322 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 5.826037e-02 | 1.235 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 7.559611e-02 | 1.122 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 6.622335e-02 | 1.179 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 7.260321e-02 | 1.139 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 6.104207e-02 | 1.214 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 8.457162e-02 | 1.073 | 1 | 1 |
| Leishmania phagocytosis | R-HSA-9664417 | 8.457162e-02 | 1.073 | 1 | 0 |
| Parasite infection | R-HSA-9664407 | 8.457162e-02 | 1.073 | 1 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 6.104207e-02 | 1.214 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 7.260321e-02 | 1.139 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 7.260321e-02 | 1.139 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 7.914931e-02 | 1.102 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 5.771581e-02 | 1.239 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 7.862776e-02 | 1.104 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 8.480276e-02 | 1.072 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 5.938587e-02 | 1.226 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 6.386841e-02 | 1.195 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 7.277570e-02 | 1.138 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 7.084578e-02 | 1.150 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 7.084578e-02 | 1.150 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 7.559611e-02 | 1.122 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 7.559611e-02 | 1.122 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 7.862776e-02 | 1.104 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 7.862776e-02 | 1.104 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 5.606853e-02 | 1.251 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 6.673818e-02 | 1.176 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 6.965018e-02 | 1.157 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 6.965018e-02 | 1.157 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 7.260321e-02 | 1.139 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 6.754520e-02 | 1.170 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 4.760522e-02 | 1.322 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 6.279364e-02 | 1.202 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 7.920841e-02 | 1.101 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 7.815402e-02 | 1.107 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 4.684679e-02 | 1.329 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 4.559857e-02 | 1.341 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 6.386841e-02 | 1.195 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 7.862776e-02 | 1.104 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 8.480276e-02 | 1.072 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 8.169701e-02 | 1.088 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 4.971051e-02 | 1.304 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 7.449976e-02 | 1.128 | 1 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 5.134747e-02 | 1.289 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 6.965018e-02 | 1.157 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 5.826037e-02 | 1.235 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.559611e-02 | 1.122 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 8.480276e-02 | 1.072 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 8.480276e-02 | 1.072 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 6.104207e-02 | 1.214 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 7.541203e-02 | 1.123 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 5.487321e-02 | 1.261 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 7.559611e-02 | 1.122 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 5.484840e-02 | 1.261 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 8.480276e-02 | 1.072 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 8.480276e-02 | 1.072 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 8.589335e-02 | 1.066 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 8.794394e-02 | 1.056 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 8.794394e-02 | 1.056 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 8.794394e-02 | 1.056 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 8.794394e-02 | 1.056 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 8.840393e-02 | 1.054 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.015485e-02 | 1.045 | 0 | 0 |
| Uncoating of the HIV Virion | R-HSA-162585 | 9.015485e-02 | 1.045 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.015485e-02 | 1.045 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.015485e-02 | 1.045 | 0 | 0 |
| Signaling by LTK in cancer | R-HSA-9842640 | 9.015485e-02 | 1.045 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 9.067277e-02 | 1.043 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.111947e-02 | 1.040 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 9.111947e-02 | 1.040 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 9.111947e-02 | 1.040 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 9.313034e-02 | 1.031 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 9.432830e-02 | 1.025 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 9.432830e-02 | 1.025 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 9.432830e-02 | 1.025 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 9.432830e-02 | 1.025 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 9.432830e-02 | 1.025 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 9.432830e-02 | 1.025 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 9.519691e-02 | 1.021 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 9.728226e-02 | 1.012 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 9.756940e-02 | 1.011 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 9.756940e-02 | 1.011 | 1 | 0 |
| S Phase | R-HSA-69242 | 9.858770e-02 | 1.006 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 9.965926e-02 | 1.001 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 9.965926e-02 | 1.001 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 9.965926e-02 | 1.001 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 9.965926e-02 | 1.001 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 1.002084e-01 | 0.999 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 1.008418e-01 | 0.996 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.008418e-01 | 0.996 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 1.036487e-01 | 0.984 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 1.041444e-01 | 0.982 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.041444e-01 | 0.982 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 1.074763e-01 | 0.969 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 1.074763e-01 | 0.969 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 1.074763e-01 | 0.969 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 1.074763e-01 | 0.969 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 1.074763e-01 | 0.969 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 1.074763e-01 | 0.969 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.084959e-01 | 0.965 | 0 | 0 |
| Reverse Transcription of HIV RNA | R-HSA-162589 | 1.090650e-01 | 0.962 | 0 | 0 |
| Minus-strand DNA synthesis | R-HSA-164516 | 1.090650e-01 | 0.962 | 0 | 0 |
| FGFR1b ligand binding and activation | R-HSA-190370 | 1.090650e-01 | 0.962 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 1.090650e-01 | 0.962 | 0 | 0 |
| Interleukin-23 signaling | R-HSA-9020933 | 1.090650e-01 | 0.962 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 1.090650e-01 | 0.962 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.090650e-01 | 0.962 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.108365e-01 | 0.955 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.108365e-01 | 0.955 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.108365e-01 | 0.955 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.108365e-01 | 0.955 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 1.108365e-01 | 0.955 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 1.108365e-01 | 0.955 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 1.123863e-01 | 0.949 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 1.123863e-01 | 0.949 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 1.168577e-01 | 0.932 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.176382e-01 | 0.929 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 1.183730e-01 | 0.927 | 0 | 0 |
| MAPK1 (ERK2) activation | R-HSA-112411 | 1.183730e-01 | 0.927 | 0 | 0 |
| Calcineurin activates NFAT | R-HSA-2025928 | 1.183730e-01 | 0.927 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 1.183730e-01 | 0.927 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 1.188344e-01 | 0.925 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 1.199437e-01 | 0.921 | 1 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 1.210777e-01 | 0.917 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 1.213951e-01 | 0.916 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 1.223728e-01 | 0.912 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 1.236879e-01 | 0.908 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 1.245420e-01 | 0.905 | 0 | 0 |
| Binding and entry of HIV virion | R-HSA-173107 | 1.275844e-01 | 0.894 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.275844e-01 | 0.894 | 0 | 0 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | R-HSA-5140745 | 1.275844e-01 | 0.894 | 0 | 0 |
| Interleukin-27 signaling | R-HSA-9020956 | 1.275844e-01 | 0.894 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.275844e-01 | 0.894 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.275844e-01 | 0.894 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 1.280299e-01 | 0.893 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 1.280299e-01 | 0.893 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 1.280299e-01 | 0.893 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 1.280299e-01 | 0.893 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 1.315408e-01 | 0.881 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 1.315408e-01 | 0.881 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.315408e-01 | 0.881 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 1.351101e-01 | 0.869 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.367000e-01 | 0.864 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.367000e-01 | 0.864 | 0 | 0 |
| Dissolution of Fibrin Clot | R-HSA-75205 | 1.367000e-01 | 0.864 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 1.408998e-01 | 0.851 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 1.443339e-01 | 0.841 | 0 | 0 |
| APOBEC3G mediated resistance to HIV-1 infection | R-HSA-180689 | 1.457210e-01 | 0.836 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 1.457210e-01 | 0.836 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.457210e-01 | 0.836 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 1.457210e-01 | 0.836 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.457210e-01 | 0.836 | 0 | 0 |
| Integration of provirus | R-HSA-162592 | 1.457210e-01 | 0.836 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 1.457963e-01 | 0.836 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 1.457963e-01 | 0.836 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 1.457963e-01 | 0.836 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 1.474449e-01 | 0.831 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.494092e-01 | 0.826 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 1.494092e-01 | 0.826 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.546483e-01 | 0.811 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.546483e-01 | 0.811 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.546483e-01 | 0.811 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.546483e-01 | 0.811 | 0 | 0 |
| VLDLR internalisation and degradation | R-HSA-8866427 | 1.546483e-01 | 0.811 | 0 | 0 |
| Advanced glycosylation endproduct receptor signaling | R-HSA-879415 | 1.546483e-01 | 0.811 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.546483e-01 | 0.811 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 1.546483e-01 | 0.811 | 0 | 0 |
| Interleukin-35 Signalling | R-HSA-8984722 | 1.546483e-01 | 0.811 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.546483e-01 | 0.811 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 1.598413e-01 | 0.796 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 1.603527e-01 | 0.795 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 1.603527e-01 | 0.795 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 1.603527e-01 | 0.795 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.634828e-01 | 0.787 | 0 | 0 |
| Interleukin-6 signaling | R-HSA-1059683 | 1.634828e-01 | 0.787 | 0 | 0 |
| FGFR1c ligand binding and activation | R-HSA-190373 | 1.634828e-01 | 0.787 | 0 | 0 |
| IL-6-type cytokine receptor ligand interactions | R-HSA-6788467 | 1.634828e-01 | 0.787 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.634828e-01 | 0.787 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.634828e-01 | 0.787 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.634828e-01 | 0.787 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.634828e-01 | 0.787 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.634828e-01 | 0.787 | 0 | 0 |
| Replication of the SARS-CoV-1 genome | R-HSA-9682706 | 1.634828e-01 | 0.787 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 1.640331e-01 | 0.785 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 1.648872e-01 | 0.783 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 1.677285e-01 | 0.775 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 1.677285e-01 | 0.775 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 1.722255e-01 | 0.764 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.722255e-01 | 0.764 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.722255e-01 | 0.764 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.722255e-01 | 0.764 | 0 | 0 |
| SARS-CoV-1 Genome Replication and Transcription | R-HSA-9679514 | 1.722255e-01 | 0.764 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 1.751183e-01 | 0.757 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 1.777038e-01 | 0.750 | 1 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 1.788979e-01 | 0.747 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.808774e-01 | 0.743 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.808774e-01 | 0.743 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.808774e-01 | 0.743 | 0 | 0 |
| Protein lipoylation | R-HSA-9857492 | 1.808774e-01 | 0.743 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.808774e-01 | 0.743 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.808774e-01 | 0.743 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.808774e-01 | 0.743 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 1.870342e-01 | 0.728 | 0 | 0 |
| Entry of Influenza Virion into Host Cell via Endocytosis | R-HSA-168275 | 1.894394e-01 | 0.723 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.894394e-01 | 0.723 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 1.894394e-01 | 0.723 | 0 | 0 |
| WNT5A-dependent internalization of FZD4 | R-HSA-5099900 | 1.894394e-01 | 0.723 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.894394e-01 | 0.723 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 1.900123e-01 | 0.721 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 1.901779e-01 | 0.721 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 1.907856e-01 | 0.719 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 1.939594e-01 | 0.712 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 1.977507e-01 | 0.704 | 0 | 0 |
| Antigen processing: Ub, ATP-independent proteasomal degradation | R-HSA-9912633 | 1.979125e-01 | 0.704 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 1.979125e-01 | 0.704 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 1.979125e-01 | 0.704 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 1.979125e-01 | 0.704 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 1.979125e-01 | 0.704 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 1.979125e-01 | 0.704 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 1.979125e-01 | 0.704 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.979125e-01 | 0.704 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 2.015510e-01 | 0.696 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 2.041042e-01 | 0.690 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 2.053599e-01 | 0.687 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.062975e-01 | 0.686 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.062975e-01 | 0.686 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.062975e-01 | 0.686 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.062975e-01 | 0.686 | 0 | 0 |
| Replication of the SARS-CoV-2 genome | R-HSA-9694686 | 2.062975e-01 | 0.686 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 2.070036e-01 | 0.684 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 2.091767e-01 | 0.679 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 2.107091e-01 | 0.676 | 1 | 0 |
| Leishmania infection | R-HSA-9658195 | 2.107091e-01 | 0.676 | 1 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 2.125700e-01 | 0.672 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.145953e-01 | 0.668 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.145953e-01 | 0.668 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.145953e-01 | 0.668 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.145953e-01 | 0.668 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 2.145953e-01 | 0.668 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 2.176316e-01 | 0.662 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.228069e-01 | 0.652 | 1 | 1 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.228069e-01 | 0.652 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.228069e-01 | 0.652 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.228069e-01 | 0.652 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.228069e-01 | 0.652 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 2.228069e-01 | 0.652 | 0 | 0 |
| SARS-CoV-2 Genome Replication and Transcription | R-HSA-9694682 | 2.228069e-01 | 0.652 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 2.230949e-01 | 0.652 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.283597e-01 | 0.641 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 2.283597e-01 | 0.641 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.309331e-01 | 0.637 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.309331e-01 | 0.637 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.309331e-01 | 0.637 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.309331e-01 | 0.637 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 2.368689e-01 | 0.625 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.389749e-01 | 0.622 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.389749e-01 | 0.622 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 2.389749e-01 | 0.622 | 0 | 0 |
| Early Phase of HIV Life Cycle | R-HSA-162594 | 2.389749e-01 | 0.622 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 2.389749e-01 | 0.622 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 2.469331e-01 | 0.607 | 1 | 1 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.469331e-01 | 0.607 | 0 | 0 |
| Ribavirin ADME | R-HSA-9755088 | 2.469331e-01 | 0.607 | 0 | 0 |
| Assembly Of The HIV Virion | R-HSA-175474 | 2.469331e-01 | 0.607 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 2.476588e-01 | 0.606 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 2.535866e-01 | 0.596 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 2.548085e-01 | 0.594 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.591978e-01 | 0.586 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 2.592682e-01 | 0.586 | 0 | 0 |
| Interleukin-20 family signaling | R-HSA-8854691 | 2.626021e-01 | 0.581 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 2.626021e-01 | 0.581 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.626021e-01 | 0.581 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.626021e-01 | 0.581 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 2.626021e-01 | 0.581 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 2.648258e-01 | 0.577 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 2.676456e-01 | 0.572 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 2.703146e-01 | 0.568 | 0 | 0 |
| Interleukin-6 family signaling | R-HSA-6783589 | 2.703146e-01 | 0.568 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.703146e-01 | 0.568 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.703146e-01 | 0.568 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.703146e-01 | 0.568 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 2.708849e-01 | 0.567 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 2.747567e-01 | 0.561 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.779470e-01 | 0.556 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 2.779470e-01 | 0.556 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.779470e-01 | 0.556 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.779470e-01 | 0.556 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.779470e-01 | 0.556 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.779470e-01 | 0.556 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 2.789588e-01 | 0.554 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 2.824972e-01 | 0.549 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.854999e-01 | 0.544 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.854999e-01 | 0.544 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.854999e-01 | 0.544 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 2.929744e-01 | 0.533 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 2.929744e-01 | 0.533 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 2.929744e-01 | 0.533 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 2.929744e-01 | 0.533 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 2.929744e-01 | 0.533 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 2.929744e-01 | 0.533 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 2.979551e-01 | 0.526 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 3.003711e-01 | 0.522 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 3.003711e-01 | 0.522 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 3.003711e-01 | 0.522 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.003711e-01 | 0.522 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.003711e-01 | 0.522 | 0 | 0 |
| Iron assimilation using enterobactin | R-HSA-9638334 | 3.003711e-01 | 0.522 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 3.056665e-01 | 0.515 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 3.056665e-01 | 0.515 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 3.076908e-01 | 0.512 | 1 | 1 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.076908e-01 | 0.512 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.076908e-01 | 0.512 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.076908e-01 | 0.512 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 3.133624e-01 | 0.504 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.149345e-01 | 0.502 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.149345e-01 | 0.502 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 3.149345e-01 | 0.502 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 3.149345e-01 | 0.502 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.149345e-01 | 0.502 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 3.172037e-01 | 0.499 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 3.172037e-01 | 0.499 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 3.210401e-01 | 0.493 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 3.216972e-01 | 0.493 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 3.221027e-01 | 0.492 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.221027e-01 | 0.492 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 3.221027e-01 | 0.492 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 3.286971e-01 | 0.483 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 3.325171e-01 | 0.478 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.362164e-01 | 0.473 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.362164e-01 | 0.473 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 3.401385e-01 | 0.468 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.401385e-01 | 0.468 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.431633e-01 | 0.464 | 0 | 0 |
| Effects of PIP2 hydrolysis | R-HSA-114508 | 3.431633e-01 | 0.464 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 3.445523e-01 | 0.463 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.500379e-01 | 0.456 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 3.500379e-01 | 0.456 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.500379e-01 | 0.456 | 1 | 1 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.568410e-01 | 0.448 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 3.568410e-01 | 0.448 | 0 | 0 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | R-HSA-2408508 | 3.568410e-01 | 0.448 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 3.590708e-01 | 0.445 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.635733e-01 | 0.439 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.635733e-01 | 0.439 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 3.635733e-01 | 0.439 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 3.702355e-01 | 0.432 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 3.740749e-01 | 0.427 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.768284e-01 | 0.424 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 3.768284e-01 | 0.424 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.768284e-01 | 0.424 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.833527e-01 | 0.416 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 3.833527e-01 | 0.416 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 3.833527e-01 | 0.416 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.833527e-01 | 0.416 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 3.852353e-01 | 0.414 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 3.898091e-01 | 0.409 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 3.898091e-01 | 0.409 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 3.898091e-01 | 0.409 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 3.898091e-01 | 0.409 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 3.926281e-01 | 0.406 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 3.926281e-01 | 0.406 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 3.926281e-01 | 0.406 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 3.961982e-01 | 0.402 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 3.961982e-01 | 0.402 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 3.961982e-01 | 0.402 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.087778e-01 | 0.389 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 4.124711e-01 | 0.385 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.149695e-01 | 0.382 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.149695e-01 | 0.382 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 4.185187e-01 | 0.378 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 4.210967e-01 | 0.376 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.210967e-01 | 0.376 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 4.210967e-01 | 0.376 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.210967e-01 | 0.376 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.271602e-01 | 0.369 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.271602e-01 | 0.369 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 4.329318e-01 | 0.364 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.331605e-01 | 0.363 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.331605e-01 | 0.363 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 4.429262e-01 | 0.354 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.449743e-01 | 0.352 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.449743e-01 | 0.352 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.449743e-01 | 0.352 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 4.565715e-01 | 0.340 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.678726e-01 | 0.330 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 4.678726e-01 | 0.330 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 4.734489e-01 | 0.325 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 4.734489e-01 | 0.325 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 4.789671e-01 | 0.320 | 0 | 0 |
| G alpha (z) signalling events | R-HSA-418597 | 4.844278e-01 | 0.315 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.004709e-01 | 0.301 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 5.057075e-01 | 0.296 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.057075e-01 | 0.296 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 5.079097e-01 | 0.294 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.160176e-01 | 0.287 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.160176e-01 | 0.287 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.210922e-01 | 0.283 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 5.210922e-01 | 0.283 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 5.261139e-01 | 0.279 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 5.261139e-01 | 0.279 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 5.261139e-01 | 0.279 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.310832e-01 | 0.275 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 5.336743e-01 | 0.273 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.430975e-01 | 0.265 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.456826e-01 | 0.263 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.456826e-01 | 0.263 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 5.504479e-01 | 0.259 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 5.523886e-01 | 0.258 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 5.554561e-01 | 0.255 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 5.598300e-01 | 0.252 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.598300e-01 | 0.252 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 5.644478e-01 | 0.248 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.644478e-01 | 0.248 | 0 | 0 |
| Metal ion assimilation from the host | R-HSA-9638482 | 5.644478e-01 | 0.248 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.690174e-01 | 0.245 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.690174e-01 | 0.245 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 5.705713e-01 | 0.244 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.735394e-01 | 0.241 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.780142e-01 | 0.238 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 5.954514e-01 | 0.225 | 0 | 0 |
| Interleukin-10 signaling | R-HSA-6783783 | 5.954514e-01 | 0.225 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 5.954514e-01 | 0.225 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 5.996976e-01 | 0.222 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 6.038995e-01 | 0.219 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.038995e-01 | 0.219 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.121722e-01 | 0.213 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.202731e-01 | 0.207 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 6.321102e-01 | 0.199 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 6.321102e-01 | 0.199 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 6.443433e-01 | 0.191 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.510289e-01 | 0.186 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.546949e-01 | 0.184 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 6.583227e-01 | 0.182 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.689802e-01 | 0.175 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 6.689802e-01 | 0.175 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.724587e-01 | 0.172 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.759009e-01 | 0.170 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 6.793071e-01 | 0.168 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 6.893138e-01 | 0.162 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 6.925799e-01 | 0.160 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 6.925799e-01 | 0.160 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 6.990100e-01 | 0.156 | 0 | 0 |
| Mitochondrial ribosome-associated quality control | R-HSA-9937383 | 6.990100e-01 | 0.156 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 7.021747e-01 | 0.154 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 7.084053e-01 | 0.150 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.084053e-01 | 0.150 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.114718e-01 | 0.148 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.145063e-01 | 0.146 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 7.209807e-01 | 0.142 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 7.234206e-01 | 0.141 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 7.234206e-01 | 0.141 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 7.292092e-01 | 0.137 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 7.292092e-01 | 0.137 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 7.292092e-01 | 0.137 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 7.385604e-01 | 0.132 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.485371e-01 | 0.126 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.589592e-01 | 0.120 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 7.718436e-01 | 0.112 | 0 | 0 |
| Mitochondrial translation | R-HSA-5368287 | 8.049687e-01 | 0.094 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 8.070246e-01 | 0.093 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 8.264348e-01 | 0.083 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 8.300773e-01 | 0.081 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 8.471809e-01 | 0.072 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 8.640238e-01 | 0.063 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.654603e-01 | 0.063 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.751015e-01 | 0.058 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 8.876949e-01 | 0.052 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 8.912207e-01 | 0.050 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 8.943424e-01 | 0.048 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 9.042568e-01 | 0.044 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.061302e-01 | 0.043 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 9.235973e-01 | 0.035 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 9.281845e-01 | 0.032 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.304450e-01 | 0.031 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.333493e-01 | 0.030 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.354481e-01 | 0.029 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.408251e-01 | 0.026 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.505681e-01 | 0.022 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 9.560964e-01 | 0.019 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 9.574380e-01 | 0.019 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.792479e-01 | 0.009 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.830737e-01 | 0.007 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.894603e-01 | 0.005 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.915058e-01 | 0.004 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.941138e-01 | 0.003 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.993593e-01 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.999374e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999992e-01 | 0.000 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 1.000000e+00 | 0.000 | 1 | 1 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 1.000000e+00 | 0.000 | 1 | 0 |
| FCGR activation | R-HSA-2029481 | 1.000000e+00 | 0.000 | 1 | 1 |
| FLT3 Signaling | R-HSA-9607240 | 1.000000e+00 | 0.000 | 1 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 1.000000e+00 | 0.000 | 1 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 1.000000e+00 | 0.000 | 1 | 1 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 1.000000e+00 | 0.000 | 1 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
