ACLY


Summary: ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Dec 2014].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:108728
PHARMGKB IDPA24441
Map Location17q21.2

Gene Categories:

DRUGGABLE GENOME

GO terms in ACLY


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Term Type
Evidence Type
GO Term ID
GO Des.
MF IBA GO:0003878 ATP citrate synthase activity
MF IDA GO:0003878 ATP citrate synthase activity
MF TAS GO:0003878 ATP citrate synthase activity
MF IPI GO:0005515 protein binding
MF TAS GO:0005524 ATP binding
MF IEA GO:0046872 metal ion binding
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Gene expression in normal tissue: ACLY

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 1

Gene-drug pathway distribution

ERK MAPK signaling1

Pathways in ACLY


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Database
Pathway ID
Pathway Des.
wikipathways WP1982 Sterol Regulatory Element-Binding Proteins (SREBP) signalling
wikipathways WP2453 TCA Cycle and Deficiency of Pyruvate Dehydrogenase complex (PDHc)
wikipathways WP357 Fatty Acid Biosynthesis
wikipathways WP3925 Amino Acid metabolism
wikipathways WP3965 Lipid Metabolism Pathway
wikipathways WP4010 Liver steatosis AOP
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD353 PD0325901 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in ACLY

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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