Skip to search formSkip to main contentSkip to account menu

Pyruvate Dehydrogenase E2 Deficiency

Known as: LACTIC ACIDEMIA DUE TO DEFECT OF E2 LIPOYL TRANSACETYLASE OF THE PYRUVATE DEHYDROGENASE COMPLEX, PDHDD 
National Institutes of Health

Related topics

Related topics

12 relations

Broader (2)

Acidosis, LacticPyruvate Dehydrogenase Complex Deficiency Disease
AtaxiaAutosomal recessive inheritanceBlepharoptosisDLAT, 3-BP DEL, 361GAA

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1990
1990
Lipoamidase (lipoyl-X hydrolase) from pig brain.
Although the optimum substrate for lipoamidase (lipoyl-X hydrolase) has not yet been determined, it is known that lipoamidase… 
1990
1990
Lipoamidase is a multiple hydrolase.
The substrate specificity of lipoamidase, purified from the pig brain membrane with lipoyl 4-aminobenzoate (LPAB) as a substrate… 
1988
1988
Structure function studies on the lipoate-acetyltransferase--component-X-core assembly of the ox heart pyruvate dehydrogenase complex.
Component X, the recently recognised subunit of mammalian pyruvate dehydrogenase complex, was shown by immune blotting to be… 
1977
1977
Determination of the chain stoichiometries from the number of reactive sulfhydryl groups in the pyruvate dehydrogenase complexes of Azotobacter vinelandii and Escherichia coli.
The pyruvate dehydrogenase complex from Azotobacter vinelandii incubated with 0.05–0.7 mM [2-14C]pyruvate, magnesium chloride and… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)