Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A286SD53 COMT catechol O-methyltransferase (EC 2.1.1.6) Homo sapiens (Human) 64 aa

Protein Details: A0A286SD53 (COMT)

Protein Information
AccessionA0A286SD53
Protein Namescatechol O-methyltransferase (EC 2.1.1.6)
Gene SymbolCOMT
OrganismHomo sapiens (Human)
Length64 aa
IsoformsNo isoforms
Related PMIDs 19801377
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501KIVDAVIQEH11QPSVLLELGA21YCGYSAVRMA31RLLSPGARLI41TIEINPDCAA
51-6451ITQRMVDFAG61MKDK
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
22 Class I-like SAM-dependent O-methyltransferase S-adenosyl-L-methionine-dependent methyltransferase superfamily CATECHOL O-METHYLTRANSFERASE 1-RELATED -
Unknown (32651440)
GPS-Palm: 0.80
Deep-Palm: 0.98
48 - -
Unknown (32651440)
GPS-Palm: 0.83
Deep-Palm: 0.97
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
1
DU145 cell
Specificity: 1.000
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
82 Y → C 0.002288 SNP Missense Mutation STAD
234 R → C 0.002288 SNP Missense Mutation STAD