Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P08581 MET Hepatocyte growth factor receptor (HGF … Homo sapiens (Human) 1390 aa

Protein Details: P08581 (MET)

Protein Information
AccessionP08581
Protein NamesHepatocyte growth factor receptor (HGF receptor) (EC 2.7.10.1) (HGF/SF receptor) (Proto-oncogene c-Met) (Scatter factor receptor) (SF receptor) (Tyrosine-protein kinase Met)
Gene SymbolMET
OrganismHomo sapiens (Human)
Length1390 aa
IsoformsNo isoforms
Related PMIDs 31251020 (mass) 32651440 (mass) 36430497 (mass)
Database SourcesdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MKAPAVLAPG11ILVLLFTLVQ21RSNGECKEAL31AKSEMNVNMK41YQLPNFTAET
51-10051PIQNVILHEH61HIFLGATNYI71YVLNEEDLQK81VAEYKTGPVL91EHPDCFPCQD
101-150101CSSKANLSGG111VWKDNINMAL121VVDTYYDDQL131ISCGSVNRGT141CQRHVFPHNH
151-200151TADIQSEVHC161IFSPQIEEPS171QCPDCVVSAL181GAKVLSSVKD191RFINFFVGNT
201-250201INSSYFPDHP211LHSISVRRLK221ETKDGFMFLT231DQSYIDVLPE241FRDSYPIKYV
251-300251HAFESNNFIY261FLTVQRETLD271AQTFHTRIIR281FCSINSGLHS291YMEMPLECIL
301-350301TEKRKKRSTK311KEVFNILQAA321YVSKPGAQLA331RQIGASLNDD341ILFGVFAQSK
351-400351PDSAEPMDRS361AMCAFPIKYV371NDFFNKIVNK381NNVRCLQHFY391GPNHEHCFNR
401-450401TLLRNSSGCE411ARRDEYRTEF421TTALQRVDLF431MGQFSEVLLT441SISTFIKGDL
451-500451TIANLGTSEG461RFMQVVVSRS471GPSTPHVNFL481LDSHPVSPEV491IVEHTLNQNG
501-550501YTLVITGKKI511TKIPLNGLGC521RHFQSCSQCL531SAPPFVQCGW541CHDKCVRSEE
551-600551CLSGTWTQQI561CLPAIYKVFP571NSAPLEGGTR581LTICGWDFGF591RRNNKFDLKK
601-650601TRVLLGNESC611TLTLSESTMN621TLKCTVGPAM631NKHFNMSIII641SNGHGTTQYS
651-700651TFSYVDPVIT661SISPKYGPMA671GGTLLTLTGN681YLNSGNSRHI691SIGGKTCTLK
701-750701SVSNSILECY711TPAQTISTEF721AVKLKIDLAN731RETSIFSYRE741DPIVYEIHPT
751-800751KSFISGGSTI761TGVGKNLNSV771SVPRMVINVH781EAGRNFTVAC791QHRSNSEIIC
801-850801CTTPSLQQLN811LQLPLKTKAF821FMLDGILSKY831FDLIYVHNPV841FKPFEKPVMI
851-900851SMGNENVLEI861KGNDIDPEAV871KGEVLKVGNK881SCENIHLHSE891AVLCTVPNDL
901-950901LKLNSELNIE911WKQAISSTVL921GKVIVQPDQN931FTGLIAGVVS941ISTALLLLLG
951-1000951FFLWLKKRKQ961IKDLGSELVR971YDARVHTPHL981DRLVSARSVS991PTTEMVSNES
1001-10501001VDYRATFPED1011QFPNSSQNGS1021CRQVQYPLTD1031MSPILTSGDS1041DISSPLLQNT
1051-11001051VHIDLSALNP1061ELVQAVQHVV1071IGPSSLIVHF1081NEVIGRGHFG1091CVYHGTLLDN
1101-11501101DGKKIHCAVK1111SLNRITDIGE1121VSQFLTEGII1131MKDFSHPNVL1141SLLGICLRSE
1151-12001151GSPLVVLPYM1161KHGDLRNFIR1171NETHNPTVKD1181LIGFGLQVAK1191GMKYLASKKF
1201-12501201VHRDLAARNC1211MLDEKFTVKV1221ADFGLARDMY1231DKEYYSVHNK1241TGAKLPVKWM
1251-13001251ALESLQTQKF1261TTKSDVWSFG1271VLLWELMTRG1281APPYPDVNTF1291DITVYLLQGR
1301-13501301RLLQPEYCPD1311PLYEVMLKCW1321HPKAEMRPSF1331SELVSRISAI1341FSTFIGEHYV
1351-13901351HVNATYVNVK1361CVAPYPSLLS1371SEDNADDEVD1381TRPASFWETS
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
26 - - -
GPS-Palm: 0.66
Deep-Palm: 0.92
95 - - -
Deep-Palm: 0.68
98 - - -
Deep-Palm: 0.21
101 - - -
Deep-Palm: 0.16
133 - - -
Deep-Palm: 0.09
141 - - -
Deep-Palm: 0.04
160 - - -
Deep-Palm: 0.02
172 - - -
Deep-Palm: 0.77
175 - - -
Deep-Palm: 0.93
282 - - -
GPS-Palm: 0.83
Deep-Palm: 0.37
298 - - -
GPS-Palm: 0.90
Deep-Palm: 0.90
363 - - -
GPS-Palm: 0.77
Deep-Palm: 0.36
385 - - -
Deep-Palm: 0.02
397 - - -
Deep-Palm: 0.08
409 - - -
GPS-Palm: 0.78
Deep-Palm: 0.68
520 - - -
GPS-Palm: 0.76
Deep-Palm: 0.92
526 - - -
Deep-Palm: 0.06
529 - - -
Deep-Palm: 0.03
538 - - -
Deep-Palm: 0.05
541 - - -
Deep-Palm: 0.06
545 - - -
Deep-Palm: 0.08
551 - -
Jurkat T (32651440)
Deep-Palm: 0.05
561 - - -
GPS-Palm: 0.77
Deep-Palm: 0.91
584 - - -
GPS-Palm: 0.81
Deep-Palm: 0.55
610 - - -
GPS-Palm: 0.78
Deep-Palm: 0.94
624 DBPTM SWISSPALM IPT/TIG domain - -
GPS-Palm: 0.80
Deep-Palm: 0.14
697 - - -
GPS-Palm: 0.78
Deep-Palm: 0.26
709 - - -
GPS-Palm: 0.69
Deep-Palm: 0.85
790 - - -
Deep-Palm: 0.20
800 - - -
GPS-Palm: 0.83
Deep-Palm: 0.63
801 - - -
GPS-Palm: 0.89
Deep-Palm: 0.54
882 - - -
Deep-Palm: 0.91
894 DBPTM SWISSPALM - - -
GPS-Palm: 0.75
Deep-Palm: 0.86
1021 - - -
Deep-Palm: 0.13
1091 - - -
Deep-Palm: 0.34
1107 - - -
GPS-Palm: 0.69
Deep-Palm: 0.72
1146 - - -
GPS-Palm: 0.75
Deep-Palm: 0.88
1210 - - -
GPS-Palm: 0.87
Deep-Palm: 0.88
1308 - - -
Deep-Palm: 0.23
1319 - - -
Deep-Palm: 0.07
1361 - - -
Deep-Palm: 0.11
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
1
Jurkat T cells (Mass)
Specificity: 1.000
1/10 (10.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). Blue bars: Literature data, Orange bars: Mass Spectrometry data. The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
26 C → R 0.002545 SNP Missense Mutation GBM
95 C → F 0.002427 SNP Missense Mutation BLCA
98 C → F 0.001764 SNP Missense Mutation LUAD
172 C → Y 0.001887 SNP Missense Mutation UCEC
187 S → C 0.003460 SNP Missense Mutation CESC
205 Y → C 0.001969 SNP Missense Mutation HNSC
228 F → C 0.002506 SNP Missense Mutation COAD
396 H → _C397insSCGLAPSPL 0.002294 INS In Frame Ins OV
412 R → C 0.003774 SNP Missense Mutation UCEC
441 S → C 0.001764 SNP Missense Mutation LUAD
697 C → C 0.001887 SNP Silent UCEC
800 C → C 0.005618 SNP Silent PAAD
882 C → W 0.002020 SNP Missense Mutation PRAD
894 C → Y 0.001887 SNP Missense Mutation UCEC
1230 Y → C 0.003559 SNP Missense Mutation KIRP
1308 C → S 0.005435 SNP Missense Mutation ESCA
1319 C → Y 0.002506 SNP Missense Mutation COAD
1327 R → C 0.001887 SNP Missense Mutation UCEC
1356 Y → C 0.002141 SNP Missense Mutation SKCM
1319* C → ? 0.002288 SNP Nonsense Mutation STAD