Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
H3BND9 PCBP2 Poly(rC) binding protein 2 Homo sapiens (Human) 112 aa

Protein Details: H3BND9 (PCBP2)

Protein Information
AccessionH3BND9
Protein NamesPoly(rC) binding protein 2
Gene SymbolPCBP2
OrganismHomo sapiens (Human)
Length112 aa
IsoformsNo isoforms
Related PMIDs 32944167
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MAGPTNAIFK11AFAMIIDKLE21EDISSSMTNS31TAASRPPVTL41RLVVPASQCG
51-10051SLIGKGGCKI61KEIREAGVQW71RSHGSLQQNI81DLPSLRRSSH91LSLPRSRDCR
101-112101LPPPHPNFCI111FL
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
49 SWISSPALM DBPTM CYSMODDB KH domain -
cerebral cortex (36430497)
GPS-Palm: 0.90
Deep-Palm: 0.97
58 - - -
GPS-Palm: 0.80
Deep-Palm: 0.94
99 - - -
Deep-Palm: 0.71
109 - - -
GPS-Palm: 0.95
Deep-Palm: 0.02
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): 1.000
3
PC3
Specificity: 1.000
3/3 (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
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