Propionyl-CoA: Difference between revisions

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[[Category:Metabolism]]
[[Category:Metabolism]]
[[Category:Coenzymes]]
[[Category:Coenzymes]]
<gallery>
File:Propionyl-Coenzyme_A.png|Propionyl-Coenzyme A structure
File:Odd-chain_FA_oxydation.png|Odd-chain fatty acid oxidation
File:Nihms213291f1.jpg|Propionyl-CoA
File:Methylcitrate_Cycle_with_Intermediates_and_Enzymes.png|Methylcitrate cycle with intermediates and enzymes
File:3-hydroxypropionic-acid-3D-balls.png|3-Hydroxypropionic acid 3D model
File:Aspergillus_nidulans.jpg|Aspergillus nidulans
File:5H84_as_recorded_by_PYMOL_from_the_Protein_Data_Bank.png|5H84 structure from the Protein Data Bank
</gallery>

Latest revision as of 11:34, 18 February 2025

Propionyl-CoA is a significant intermediate in the metabolic pathway known as the tricarboxylic acid cycle (TCA cycle) or Krebs cycle. It is derived from the catabolism of odd-chain fatty acids, branched-chain amino acids, and from the side chain of cholesterol.

Structure[edit]

Propionyl-CoA is a Coenzyme A (CoA) derivative in which the terminal sulfhydryl group (-SH) is linked to the carboxyl group (-COOH) of propionic acid through a high-energy thioester bond. The molecule is composed of an adenosine 3',5'-bisphosphate moiety, a pantothenic acid moiety, and a cysteamine moiety.

Metabolism[edit]

Propionyl-CoA is metabolized in a series of reactions known as the propionyl-CoA carboxylase pathway. This pathway converts propionyl-CoA to methylmalonyl-CoA, which is then converted to succinyl-CoA, a key intermediate in the TCA cycle. The conversion of propionyl-CoA to succinyl-CoA requires several enzymes and cofactors, including biotin, adenosylcobalamin, and methylmalonyl-CoA mutase.

Clinical significance[edit]

Defects in the metabolism of propionyl-CoA can lead to several metabolic disorders, including propionic acidemia and methylmalonic acidemia. These disorders are characterized by the accumulation of propionyl-CoA and its metabolites in the body, leading to various symptoms such as developmental delay, intellectual disability, and metabolic acidosis.

See also[edit]


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