"Enoyl-CoA Hydratase" 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 catalyzes reversibly the hydration of unsaturated fatty acyl-CoA to yield beta-hydroxyacyl-CoA. It plays a role in the oxidation of fatty acids and in mitochondrial fatty acid synthesis, has broad specificity, and is most active with crotonyl-CoA. EC 4.2.1.17.
| Descriptor ID |
D004746
|
| MeSH Number(s) |
D08.811.520.241.300.250
|
| Concept/Terms |
Enoyl-CoA Hydratase- Enoyl-CoA Hydratase
- Enoyl CoA Hydratase
- Hydratase, Enoyl-CoA
- 3-Hydroxyacyl Dehydratases
- 3 Hydroxyacyl Dehydratases
- Dehydratases, 3-Hydroxyacyl
- beta-Hydroxyacyl Dehydratases
- Dehydratases, beta-Hydroxyacyl
- beta Hydroxyacyl Dehydratases
- beta-Hydroxyacyl-CoA Dehydrases
- Dehydrases, beta-Hydroxyacyl-CoA
- beta Hydroxyacyl CoA Dehydrases
- trans-2-Enoyl-Coenzyme A Hydratase
- Hydratase, trans-2-Enoyl-Coenzyme A
- trans 2 Enoyl Coenzyme A Hydratase
- Enoyl CoA Hydratases
- CoA Hydratases, Enoyl
- Hydratases, Enoyl CoA
- Enoyl Hydrase
- Hydrase, Enoyl
- 3-Hydroxyacyl CoA Hydrolyases
- 3 Hydroxyacyl CoA Hydrolyases
- CoA Hydrolyases, 3-Hydroxyacyl
- Hydrolyases, 3-Hydroxyacyl CoA
- Crotonase
|
Below are MeSH descriptors whose meaning is more general than "Enoyl-CoA Hydratase".
Below are MeSH descriptors whose meaning is more specific than "Enoyl-CoA Hydratase".
This graph shows the total number of publications written about "Enoyl-CoA Hydratase" by people in this website by year, and whether "Enoyl-CoA Hydratase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 1 | 2 |
| 2019 | 1 | 1 | 2 |
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Below are the most recent publications written about "Enoyl-CoA Hydratase" by people in Profiles.
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SIRT3 controls brown fat thermogenesis by deacetylation regulation of pathways upstream of UCP1. Mol Metab. 2019 07; 25:35-49.
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Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency. Am J Med Genet A. 2019 05; 179(5):803-807.
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Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. Hum Mol Genet. 2018 08 15; 27(16):2940-2953.
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Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiency. Am J Med Genet A. 2018 05; 176(5):1115-1127.
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Chemical genetic identification of the IGF-linked pathway that is mediated by STAT6 and MFP2. Chem Biol. 2006 Mar; 13(3):241-9.
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Animal fatty acid synthetase. A novel arrangement of the beta-ketoacyl synthetase sites comprising domains of the two subunits. J Biol Chem. 1981 May 25; 256(10):5128-33.