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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
C9JJM7 HACL1 2-hydroxyacyl-CoA lyase 1 Homo sapiens (Human) 157 aa

Protein Details: C9JJM7 (HACL1)

Protein Information
AccessionC9JJM7
Protein Names2-hydroxyacyl-CoA lyase 1
Gene SymbolHACL1
OrganismHomo sapiens (Human)
Length157 aa
IsoformsNo isoforms
Related PMIDs 31251020 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
1-501MPDSNFAERS11EEQVSGAKVI21AQALKTQDVE31YIFGIVGIPV41TEIAIAAQQL
51-10051GIKYIGMRNE61QAVEACRLYT71KFSARPSSIE81AIPFVIEKAV91RSSIYGRPGA
101-150101CYVDIPADFV111NLQVNVNSIK121YMERCMSPPI131SMAETSAVCT141AASVIRNAKQ
151-157151PLLIIGK
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
66 - - -
GPS-Palm: 0.89
Deep-Palm: 0.93
101 - - -
Deep-Palm: 0.85
125 - - -
GPS-Palm: 0.68
Deep-Palm: 0.08
139 - - -
GPS-Palm: 0.82
Deep-Palm: 0.91
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
LNCaP
Specificity: 0.800
4/4 (100.0%)
1
PC3
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.
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
140 R → C 0.002506 SNP Missense Mutation COAD
166 C → C 0.001887 SNP Silent UCEC
183 S → C 0.002427 SNP Missense Mutation BLCA
223 G → C 0.001887 SNP Missense Mutation UCEC
289 F → C 0.002506 SNP Missense Mutation COAD
301 F → C 0.002545 SNP Missense Mutation GBM
392 C → C 0.001887 SNP Silent UCEC
432 F → C 0.005435 SNP Missense Mutation ESCA