Glutaryl-CoA Dehydrogenase

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.

Year introduced: 2006(1973)

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Tree Number(s): D08.811.682.660.425

MeSH Unique ID: D050770

Registry Number: EC 1.3.8.6

Entry Terms:

• Dehydrogenase, Glutaryl-CoA
• Glutaryl CoA Dehydrogenase
• CoA Dehydrogenase, Glutaryl
• Dehydrogenase, Glutaryl CoA
• Glutaryl-Coenzyme A Dehydrogenase
• Dehydrogenase, Glutaryl-Coenzyme A
• Glutaryl Coenzyme A Dehydrogenase

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)

All MeSH Categories
Chemicals and Drugs Category
Enzymes and Coenzymes
Enzymes
Oxidoreductases
Oxidoreductases Acting on CH-CH Group Donors
Glutaryl-CoA Dehydrogenase