3-hydroxyanthranilate oxidase: Difference between revisions

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Latest revision as of 02:47, 17 March 2025

3-hydroxyanthranilate oxidase






3-hydroxyanthranilate oxidase is an enzyme that catalyzes the oxidation of 3-hydroxyanthranilic acid to quinolinic acid, a key intermediate in the kynurenine pathway of tryptophan metabolism. This enzyme is classified under the oxidoreductases, specifically those acting on diphenols and related substances as donors with oxygen as the acceptor.

Function[edit]

3-hydroxyanthranilate oxidase plays a crucial role in the kynurenine pathway, which is the major route of tryptophan degradation in mammals. The enzyme facilitates the conversion of 3-hydroxyanthranilic acid into quinolinic acid, which is a precursor for the synthesis of nicotinamide adenine dinucleotide (NAD+), an essential coenzyme in cellular metabolism.

Mechanism[edit]

The enzyme catalyzes the following reaction:

3-hydroxyanthranilate + O₂ → quinolinic acid + H₂O₂

In this reaction, 3-hydroxyanthranilate oxidase uses molecular oxygen (O₂) to oxidize 3-hydroxyanthranilic acid, producing quinolinic acid and hydrogen peroxide (H₂O₂) as byproducts.

Clinical Significance[edit]

Dysregulation of the kynurenine pathway, and consequently the activity of 3-hydroxyanthranilate oxidase, has been implicated in several neurological disorders, including Alzheimer's disease, Huntington's disease, and Parkinson's disease. Elevated levels of quinolinic acid, a neurotoxin, can lead to excitotoxicity and neuronal damage.

Research[edit]

Research into 3-hydroxyanthranilate oxidase includes studies on its structure, function, and role in disease. Understanding the enzyme's activity and regulation could lead to therapeutic targets for diseases associated with tryptophan metabolism.

Also see[edit]



Template:Tryptophan metabolism