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UniProt ID Gene Symbol Protein Name Organism Length Action
F8VTZ0 PCBP2 Poly(rC) binding protein 2 Homo sapiens (Human) 64 aa

Protein Details: F8VTZ0 (PCBP2)

Protein Information
AccessionF8VTZ0
Protein NamesPoly(rC) binding protein 2
Gene SymbolPCBP2
OrganismHomo sapiens (Human)
Length64 aa
IsoformsNo isoforms
Related PMIDs 31251020 32944167
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MDTGVIEGGL11NVTLTIRLLM21HGKEVGSIIG31KKGESVKKMR41EESGARINIS
51-6451EGNCPERIIT61LAGP
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
54 SWISSPALM DBPTM CYSMODDB KH domain -
cerebral cortex (36430497)
LNCaP (31251020)
Deep-Palm: 0.55
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): 0.750
3
PC3
Specificity: 0.750
3/3 (100.0%)
1
LNCaP
Specificity: 0.250
1/1 (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.
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
109 C → W 0.002545 SNP Missense Mutation GBM
148 I → Cfs*9 0.002288 DEL Frame Shift Del STAD
305 R → C 0.002020 SNP Missense Mutation PRAD
314 R → C 0.002141 SNP Missense Mutation SKCM