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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
D6RIW1 HMGCS1 3-hydroxy-3-methylglutaryl-CoA synthase 1 Homo sapiens (Human) 95 aa

Protein Details: D6RIW1 (HMGCS1)

Protein Information
AccessionD6RIW1
Protein Names3-hydroxy-3-methylglutaryl-CoA synthase 1
Gene SymbolHMGCS1
OrganismHomo sapiens (Human)
Length95 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
1-501MPGSLPLNAE11ACWPKDVGIV21ALEIYFPSQY31VDQAELEKYD41GVDAGKYTIG
51-9551LGQAKMGFCT61DREDINSLCM71TVVQNLMERN81NLSYDCIGRL91EVGTE
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
12 - - -
Deep-Palm: 0.11
59 - - -
Deep-Palm: 0.90
69 - - -
GPS-Palm: 0.69
Deep-Palm: 0.27
86 - - -
Deep-Palm: 0.17
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
PC3
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.
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
84 Y → C 0.001969 SNP Missense Mutation HNSC
268 C → S 0.001969 SNP Missense Mutation HNSC
352 S → C 0.003559 SNP Missense Mutation KIRP