6 relations: Enoyl-CoA hydratase, Gene, Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, Mitochondrion, Protein, 3-hydroxyacyl-CoA dehydrogenase.
Enoyl-CoA hydratase
Enoyl-CoA hydratase is an enzyme that hydrates the double bond between the second and third carbons on acyl-CoA.
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Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, often shortened to LCHAD deficiency, is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats into energy.
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Mitochondrion
The mitochondrion (plural mitochondria) is a double-membrane-bound organelle found in most eukaryotic organisms.
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Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
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3-hydroxyacyl-CoA dehydrogenase
In enzymology, a 3-hydroxyacyl-CoA dehydrogenase is an enzyme that catalyzes the chemical reaction Thus, the two substrates of this enzyme are (S)-3-hydroxyacyl-CoA and NAD+, whereas its 3 products are 3-oxoacyl-CoA, NADH, and H+.
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Redirects here:
Hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit, LCEH, Long-chain 3-hydroxy acyl-coenzyme A dehydrogenase, Long-chain-(S)-3-hydroxyacyl-CoA:NAD+ oxidoreductase, TP-ALPHA, Trifunctional enzyme subunit alpha, mitochondrial.