2-Methylbutyryl-CoA: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
 
No edit summary
 
(2 intermediate revisions by the same user not shown)
Line 28: Line 28:


{{stub}}
{{stub}}
<gallery>
File:2-Methylbutanoyl-CoA.png|2-Methylbutanoyl-CoA
</gallery>

Latest revision as of 18:46, 16 March 2025

2-Methylbutyryl-CoA is a metabolite involved in the metabolism of amino acids. It is a substrate in the metabolic pathway of isoleucine, an essential amino acid in humans.

Metabolic Pathway[edit]

2-Methylbutyryl-CoA is produced from 2-Methylbutyryl-CoA dehydrogenase, an enzyme that catalyzes the chemical reaction in the metabolism of isoleucine. This reaction is part of the larger branched-chain amino acid degradation pathway, which is responsible for the breakdown of the essential amino acids leucine, isoleucine, and valine.

The metabolic pathway of isoleucine includes several steps:

  1. Isoleucine is first transaminated to 2-Ketoisocaproate.
  2. 2-Ketoisocaproate is then reduced to 2-Methylbutyryl-CoA.
  3. 2-Methylbutyryl-CoA is converted to Tiglyl-CoA by the enzyme 2-Methylbutyryl-CoA dehydrogenase.
  4. Tiglyl-CoA is further metabolized to form acetyl-CoA, which enters the citric acid cycle.

Clinical Significance[edit]

Deficiency in the enzyme 2-Methylbutyryl-CoA dehydrogenase can lead to a buildup of 2-Methylbutyryl-CoA, resulting in 2-Methylbutyrylglycinuria, a rare metabolic disorder. Symptoms of this disorder can include developmental delay, seizures, and hypotonia.

See Also[edit]

This article is a medical stub. You can help WikiMD by expanding it!
PubMed
Wikipedia