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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
K7ESG8 ACLY ATP citrate lyase Homo sapiens (Human) 109 aa

Protein Details: K7ESG8 (ACLY)

Protein Information
AccessionK7ESG8
Protein NamesATP citrate lyase
Gene SymbolACLY
OrganismHomo sapiens (Human)
Length109 aa
IsoformsNo isoforms
Related PMIDs 29575903 31251020 32944167 36430497
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MSAKAISEQT11GKELLYKFIC21TTSAIQNRFK31YARVTPDTDW41ARLLQDHPWL
51-10051LSQNLVVKPD61QLIKRRGKLG71LVGVNLTLDG81VKSWLKPRLG91QEATVGKATG
101-109101FLKNFLIEP
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
20 SWISSPALM DBPTM CYSMODDB ATP-citrate synthase ATP-grasp domain - -
GPS-Palm: 0.91
Deep-Palm: 0.86
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): 0.333
3
PC3
Specificity: 0.333
3/3 (100.0%)
3
cerebral cortex
Specificity: 0.333
3/3 (100.0%)
2
LNCaP
Specificity: 0.222
2/2 (100.0%)
1
HeLa cell
Specificity: 0.111
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
20 C → C 0.002288 SNP Silent STAD
184 F → C 0.001887 SNP Missense Mutation UCEC
576 R → C 0.002033 SNP Missense Mutation LUSC
653 R → C 0.002506 SNP Missense Mutation COAD
728 C → Y 0.001887 SNP Missense Mutation UCEC
887 C → Y 0.001887 SNP Missense Mutation UCEC
893 C → Y 0.002747 SNP Missense Mutation LIHC
1033 F → C 0.001887 SNP Missense Mutation UCEC