Glutaryl-CoA Dehydrogenase
"Glutaryl-CoA Dehydrogenase" 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.
A flavoprotein enzyme that is responsible for the catabolism of LYSINE; HYDROXYLYSINE; and TRYPTOPHAN. It catalyzes the oxidation of GLUTARYL-CoA to crotonoyl-CoA using FAD as a cofactor. Glutaric aciduria type I is an inborn error of metabolism due to the deficiency of glutaryl-CoA dehydrogenase.
| Descriptor ID |
D050770
|
| MeSH Number(s) |
D08.811.682.660.425
|
| Concept/Terms |
Glutaryl-CoA Dehydrogenase- Glutaryl-CoA Dehydrogenase
- Dehydrogenase, Glutaryl-CoA
- Glutaryl-Coenzyme A Dehydrogenase
- Dehydrogenase, Glutaryl-Coenzyme A
- Glutaryl Coenzyme A Dehydrogenase
- Glutaryl CoA Dehydrogenase
- CoA Dehydrogenase, Glutaryl
- Dehydrogenase, Glutaryl CoA
|
Below are MeSH descriptors whose meaning is more general than "Glutaryl-CoA Dehydrogenase".
Below are MeSH descriptors whose meaning is more specific than "Glutaryl-CoA Dehydrogenase".
This graph shows the total number of publications written about "Glutaryl-CoA Dehydrogenase" by people in this website by year, and whether "Glutaryl-CoA Dehydrogenase" was a major or minor topic of these publications.
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Below are the most recent publications written about "Glutaryl-CoA Dehydrogenase" by people in Profiles.
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Knapp JF, Soden SE, Dasouki MJ, Walsh IR. A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay. Pediatr Emerg Care. 2002 Feb; 18(1):44-7.