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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.


This graph shows the total number of publications written about "Glutaryl-CoA Dehydrogenase" by people in Harvard Catalyst Profiles by year, and whether "Glutaryl-CoA Dehydrogenase" was a major or minor topic of these publication.
Bar chart showing 12 publications over 12 distinct years, with a maximum of 1 publications in 1991 and 1994 and 1995 and 2001 and 2004 and 2005 and 2010 and 2012 and 2014 and 2016 and 2017 and 2018
To see the data from this visualization as text, click here.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.