ATP Citrate (pro-S)-Lyase
"ATP Citrate (pro-S)-Lyase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An enzyme that, in the presence of ATP and COENZYME A, catalyzes the cleavage of citrate to yield acetyl CoA, oxaloacetate, ADP, and ORTHOPHOSPHATE. This reaction represents an important step in fatty acid biosynthesis. This enzyme was formerly listed as EC 4.1.3.8.
| Descriptor ID |
D001275
|
| MeSH Number(s) |
D08.811.913.050.331
|
| Concept/Terms |
ATP Citrate (pro-S)-Lyase- ATP Citrate (pro-S)-Lyase
- Citrate Cleavage Enzyme
- Cleavage Enzyme, Citrate
- ATP Citrate Synthase
- Citrate Synthase, ATP
- Synthase, ATP Citrate
- ATP-Dependent Citrate Lyase
- ATP Dependent Citrate Lyase
- Citrate Lyase, ATP-Dependent
- Lyase, ATP-Dependent Citrate
- ATP Citrate (pro-3S)-Lyase
- ATP Citrate Lyase
- Citrate Lyase, ATP
- Lyase, ATP Citrate
|
Below are MeSH descriptors whose meaning is more general than "ATP Citrate (pro-S)-Lyase".
Below are MeSH descriptors whose meaning is more specific than "ATP Citrate (pro-S)-Lyase".
This graph shows the total number of publications written about "ATP Citrate (pro-S)-Lyase" by people in this website by year, and whether "ATP Citrate (pro-S)-Lyase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "ATP Citrate (pro-S)-Lyase" by people in Profiles.
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Hatipoglu A, Menon D, Levy T, Frias MA, Foster DA. Inhibiting glutamine utilization creates a synthetic lethality for suppression of ATP citrate lyase in KRas-driven cancer cells. PLoS One. 2022; 17(10):e0276579.
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Shara M, Ohia SE, Yasmin T, Zardetto-Smith A, Kincaid A, Bagchi M, Chatterjee A, Bagchi D, Stohs SJ. Dose- and time-dependent effects of a novel (-)-hydroxycitric acid extract on body weight, hepatic and testicular lipid peroxidation, DNA fragmentation and histopathological data over a period of 90 days. Mol Cell Biochem. 2003 Dec; 254(1-2):339-46.