Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
7 entry terms
- Glutaryl CoA Dehydrogenase
- Glutaryl-Coenzyme A Dehydrogenase
- CoA Dehydrogenase, Glutaryl
- Dehydrogenase, Glutaryl CoA
- Dehydrogenase, Glutaryl-CoA
- Dehydrogenase, Glutaryl-Coenzyme A
- Glutaryl Coenzyme A Dehydrogenase
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2006(1973)
MeSH Record
Previous Indexing
- Acyl Coenzyme A (1973-1979)
- Coenzymes (1973-1979)
- Glutarates (1973-1980)
- Oxidoreductases (1983-2003)
- Oxidoreductases Acting on CH-CH Group Donors (2004-2005)
MeSH Hierarchy
Tree Number
AMA Style
References
- National Library of Medicine. Glutaryl-CoA Dehydrogenase. Medical Subject Headings (MeSH). 2026. Unique ID D050770. http://id.nlm.nih.gov/mesh/2026/D050770
- Glutaryl-CoA Dehydrogenase. In: Wikidata. https://www.wikidata.org/wiki/Q58543827