 Enoyl-CoA Hydratase
"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
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| MeSH Number(s) |
D08.811.520.241.300.250
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| 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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Enoyl-CoA Hydratase" by people in Profiles.
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Gilani A, Hove JLV, Thomas JA, Kleinschmidt-DeMasters BK. Distinguishing Encephaloclastic Lesions Resulting From Primary or Secondary Pyruvate Dehydrogenase Deficiency From Other Neonatal or Infantile Cavitary Brain Lesions. Pediatr Dev Pathol. 2020 May-Jun; 23(3):189-196.
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Campbell NV, Weitzenkamp DA, Campbell IL, Schmidt RF, Hicks C, Morgan MJ, Irwin DC, Tentler JJ. "Omics" data integration and functional analyses link Enoyl-CoA hydratase, short chain 1 to drug refractory dilated cardiomyopathy. BMC Med Genomics. 2018 Dec 12; 11(1):110.
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Ferdinandusse S, Friederich MW, Burlina A, Ruiter JP, Coughlin CR, Dishop MK, Gallagher RC, Bedoyan JK, Vaz FM, Waterham HR, Gowan K, Chatfield K, Bloom K, Bennett MJ, Elpeleg O, Van Hove JL, Wanders RJ. Clinical and biochemical characterization of four patients with mutations in ECHS1. Orphanet J Rare Dis. 2015 Jun 18; 10:79.
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Sakata M, Kurachi H, Morishige K, Ogura K, Yamaguchi M, Nishio Y, Ikegami H, Miyake A, Murata Y. Messenger RNA differential display reverse-transcriptase-polymerase-chain-reaction analysis of a progestogen-suppressive gene in a human endometrial-cancer cell line. Int J Cancer. 1998 Sep 25; 78(1):125-9.
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