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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
C9JK35 AGPAT3 1-acylglycerol-3-phosphate O-acyltransferase 3 Homo sapiens (Human) 38 aa

Protein Details: C9JK35 (AGPAT3)

Protein Information
AccessionC9JK35
Protein Names1-acylglycerol-3-phosphate O-acyltransferase 3
Gene SymbolAGPAT3
OrganismHomo sapiens (Human)
Length38 aa
IsoformsNo isoforms
Related PMIDs 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
1-381MGLLAFLKTQ11FVLHLLVGFV21FVVSGLVINF31VQLCTLAL
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
34 - - -
Deep-Palm: 0.03
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
2
PC3
Specificity: 1.000
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
254 C → C 0.002294 SNP Silent OV
306 W → C 0.002545 SNP Missense Mutation GBM
314 W → C 0.002506 SNP Missense Mutation COAD
353 R → C 0.002506 SNP Missense Mutation COAD
353 R → C 0.007299 SNP Missense Mutation READ
353 R → C 0.002141 SNP Missense Mutation SKCM
353 R → C 0.003774 SNP Missense Mutation UCEC
353 R → C 0.005618 SNP Missense Mutation PAAD