Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
J3QQJ4 CPD Carboxypeptidase D Homo sapiens (Human) 184 aa

Protein Details: J3QQJ4 (CPD)

Protein Information
AccessionJ3QQJ4
Protein NamesCarboxypeptidase D
Gene SymbolCPD
OrganismHomo sapiens (Human)
Length184 aa
IsoformsNo isoforms
Related PMIDs 19137006 31251020 32944167
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501VHQGVRGFVL11DATDGRGILN21ATISVAEINH31PVTTYKTGDY41WRLLVPGTYK
51-10051ITASARGYNP61VTKNVTVKSE71GAIQVNFTLV81RSSTDSNNES91KKGKGASSST
101-150101NDASDPTTKE111FETLIKDLSA121ENGLESLMLR131SSSNLALALY141RYHSYKDLSE
151-184151FLRGLVMNYP161HITNLTNLGP171KNLLLSSQIV181FYIH
Palmitoylation Sites Details

No known palmitoylation sites

Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.400
4
LNCaP
Specificity: 0.400
4/4 (100.0%)
4
PC3
Specificity: 0.400
4/4 (100.0%)
2
Jurkat T cell
Specificity: 0.200
2/2 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
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.
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
288 F → C 0.002545 SNP Missense Mutation GBM
704 A → Cfs*15 0.001014 INS Frame Shift Ins BRCA
739 W → C 0.002545 SNP Missense Mutation GBM
988 R → C 0.002141 SNP Missense Mutation SKCM
1049 C → S 0.002427 SNP Missense Mutation BLCA
1184 C → C 0.002141 SNP Silent SKCM
1206 S → C 0.002427 SNP Missense Mutation BLCA
1218 F → C 0.001887 SNP Missense Mutation UCEC
1246 G → C 0.002506 SNP Missense Mutation COAD
1321 C → G 0.002288 SNP Missense Mutation STAD
1323 C → C 0.001764 SNP Silent LUAD
1349 R → C 0.002141 SNP Missense Mutation SKCM
1376 Y → C 0.001764 SNP Missense Mutation LUAD
1323* C → ? 0.002545 SNP Nonsense Mutation GBM