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UniProt ID Gene Symbol Protein Name Organism Length Action
B1AM21 GNAQ G protein subunit alpha q Homo sapiens (Human) 170 aa

Protein Details: B1AM21 (GNAQ)

Protein Information
AccessionB1AM21
Protein NamesG protein subunit alpha q
Gene SymbolGNAQ
OrganismHomo sapiens (Human)
Length170 aa
IsoformsNo isoforms
Related PMIDs 29575903 36430497
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MGERWADSQL11DSRSTHGTGE21SGKSTFIKQM31RIIHGSGYSD41EDKRGFTKLV
51-10051YQNIFTAMQA61MIRAMDTLKI71PYKYEHNKAH81AQLVREVDVE91KVSAFENPYV
101-150101DAIKSLWNDP111GIQECYDRRR121EYQLSDSTKY131YLNDLDRVAD141PAYLPTQQDV
151-170151LRVRVPTTGI161IEYPFDLQSV
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
115 SWISSPALM DBPTM CYSMODDB G-protein alpha subunit
HeLa (29575903)
cerebral cortex (36430497)
GPS-Palm: 0.80
Deep-Palm: 0.66
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): 0.800
4
cerebral cortex
Specificity: 0.800
4/4 (100.0%)
1
HeLa cell
Specificity: 0.200
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.
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
10 C → Y 0.001887 SNP Missense Mutation UCEC
356 Y → C 0.002141 SNP Missense Mutation SKCM