"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.
- 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".
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Below are the most recent publications written about "Glutaryl-CoA Dehydrogenase" by people in Profiles.
Glutaric aciduria type 1 and nonaccidental head injury. Pediatrics. 2002 Mar; 109(3):554.