ⓘ 3-hydroxyacyl-CoA dehydrogenase

                                     

ⓘ 3-hydroxyacyl-CoA dehydrogenase

In enzymology, a 3-hydroxyacyl-CoA dehydrogenase is an enzyme that catalyzes the chemical reaction

S-3-hydroxyacyl-CoA + NAD + ⇌ {\displaystyle \rightleftharpoons } 3-oxoacyl-CoA + NADH + H +

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.

This enzyme belongs to the family of oxidoreductases, to be specific individuals acting on CH-Oh group of donor with Nad or NADP as acceptor.

                                     
  • 3 - hydroxyacyl - coenzyme A dehydrogenase deficiency is a rare condition that prevents the body from converting certain fats to energy, particularly during
  • to inadequate levels of an enzyme called long - chain 3 - hydroxyacyl - coenzyme A CoA dehydrogenase which is part of a protein complex known as mitochondrial
  • deficiency is associated with 3 - hydroxyacyl - coenzyme A dehydrogenase deficiency. Mutations also cause 3 - hydroxyacyl - CoA dehydrogenase deficiency. There are a
  • subunit alpha, mitochondrial also known as hydroxyacyl - CoA dehydrogenase 3 - ketoacyl - CoA thiolase enoyl - CoA hydratase trifunctional protein alpha subunit
  • reductase, beta - ketoacyl - CoA reductase, D - 3 - hydroxyacyl - CoA reductase, and R - 3 - hydroxyacyl - CoA dehydrogenase This enzyme participates in butanoate
  • Physiological role of D - 3 - hydroxyacyl - CoA dehydratase D - 3 - hydroxyacyl - CoA dehydrogenase bifunctional protein Journal of Biochemistry. 121 3 506 13. doi: 10
  • 17 - β - Hydroxysteroid dehydrogenase X HSD10 also known as 3 - hydroxyacyl - CoA dehydrogenase type - 2 is a mitochondrial enzyme that in humans is encoded by
  • coenzyme A dehydrogenase short - chain acyl CoA dehydrogenase short - chain acyl - coenzyme A dehydrogenase 3 - hydroxyacyl CoA reductase, butanoyl - CoA acceptor
  • long - chain 3 - hydroxyacyl - CoA dehydrogenase LCHAD long - chain enoyl - CoA hydratase, and long - chain thiolase. This deficiency can be classified into 3 main clinical
  • multifunctional enzyme including enoyl - CoA isomerase, enoyl - CoA hydratase, and L - - 3 - hydroxyacyl - CoA dehydrogenase Three different enzymes reside on this
  • 3 - hydroxy 3 - methyl glutaryl - coa lyase deficiency 3 - hydroxyacyl - coa dehydrogenase deficiency 3 hydroxyisobutyric aciduria, rare NIH 3 - methyl crotonyl - coa carboxylase
  • coenzyme A dehydrogenase short - chain acyl CoA dehydrogenase short - chain acyl - coenzyme A dehydrogenase 3 - hydroxyacyl CoA reductase, butanoyl - CoA acceptor