Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
B4DKB2 ECE1 Endothelin-converting enzyme 1 (EC 3.4.24.71) Homo sapiens (Human) 738 aa

Protein Details: B4DKB2 (ECE1)

Protein Information
AccessionB4DKB2
Protein NamesEndothelin-converting enzyme 1 (EC 3.4.24.71)
Gene SymbolECE1
OrganismHomo sapiens (Human)
Length738 aa
IsoformsNo isoforms
Related PMIDs 19801377 22496122 29575903 31251020 32651440 31251020 (mass) 32651440 (mass) 36430497 (mass)
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MRGVWPPPVS11ALLSALGMST21YKRATLDEED31LVDSLSEGDA41YPNGLQVNFH
51-10051SPRSGQRCWA61ARTQVEKRLV71VLVVLLAAGL81VACLAALGIQ91YQTRSPSVCL
101-150101SEACVSVTSS111ILSSMDPTVD121PCHDFFSYAC131GGWIKANPVP141DGHSRWGTFS
151-200151NLWEHNQAII161KHLLENSTAS171VSEAERKAQV181YYRACMNETR191IEELRAKPLM
201-250201ELIERLGGWN211ITGPWAKDNF221QDTLQVVTAH231YRTSPFFSVY241VSADSKNSNS
251-300251NVIQVDQSGL261GLPSRDYYLN271KTENEKVLTG281YLNYMVQLGK291LLGGGDEEAI
301-350301RPQMQQILDF311ETALANITIP321QEKRRDEELI331YHKVTAAELQ341TLAPAINWLP
351-400351FLNTIFYPVE361INESEPIVVY371DKEYLEQIST381LINTTDRCLL391NNYMIWNLVR
401-450401KTSSFLDQRF411QDADEKFMEV421MYGTKKTCLP431RWKFCVSDTE441NNLGFALGPM
451-500451FVKATFAEDS461KSIATEIILE471IKKAFEESLS481TLKWMDEETR491KSAKEKADAI
501-550501YNMIGYPNFI511MDPKELDKVF521NDYTAVPDLY531FENAMRFFNF541SWRVTADQLR
551-600551KAPNRDQWSM561TPPMVNAYYS571PTKNEIVFPA581GILQAPFYTR591SSPKALNFGG
601-650601IGVVVGHELT611HAFDDQGREY621DKDGNLRPWW631KNSSVEAFKR641QTECMVEQYS
651-700651NYSVNGEPVN661GRHTLGENIA671DNGGLKAAYR681VWCSVRTPES691SHEGLITDPH
701-738701SPSRFRVIGS711LSNSKEFSEH721FRCPPGSPMN731PPHKCEVW
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
58 SWISSPALM DBPTM CYSMODDB -
HeLa (29575903)
-
GPS-Palm: 0.72
Deep-Palm: 0.95
83 - - -
GPS-Palm: 0.86
Deep-Palm: 0.98
99 - - -
Deep-Palm: 0.90
104 - - -
Deep-Palm: 0.74
122 - - -
Deep-Palm: 0.09
130 - - -
Deep-Palm: 0.11
185 - - -
GPS-Palm: 0.70
Deep-Palm: 0.96
388 - - -
Deep-Palm: 0.24
428 - - -
GPS-Palm: 0.83
Deep-Palm: 0.37
435 - -
LNCaP (31251020)
GPS-Palm: 0.92
Deep-Palm: 0.68
644 - - -
Deep-Palm: 0.13
683 - - -
GPS-Palm: 0.73
Deep-Palm: 0.95
723 - -
LNCaP (31251020)
Deep-Palm: 0.63
735 - - -
GPS-Palm: 0.87
Deep-Palm: 0.01
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): 0.500
4
LNCaP
Specificity: 0.400
4/4 (100.0%)
1
HeLa cell
Specificity: 0.100
1/1 (100.0%)
1
Jurkat T cell
Specificity: 0.100
1/1 (100.0%)
1
EC cell
Specificity: 0.100
1/1 (100.0%)
1
DU145 cell
Specificity: 0.100
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
2
LNCaP cells (Mass)
Specificity: 0.200
2/4 (50.0%)
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
83 C → Y 0.002288 SNP Missense Mutation STAD
83 C → F 0.002141 SNP Missense Mutation SKCM
104 C → C 0.002288 SNP Silent STAD
183 R → C 0.001887 SNP Missense Mutation UCEC
208 G → C 0.002506 SNP Missense Mutation COAD
232 R → C 0.002506 SNP Missense Mutation COAD
409 R → C 0.002141 SNP Missense Mutation SKCM
509 F → C 0.002141 SNP Missense Mutation SKCM
630 W → C 0.002427 SNP Missense Mutation BLCA
736 R → C 0.002141 SNP Missense Mutation SKCM
767 C → C 0.002506 SNP Silent COAD