Target intelligence / Profile preview

Hydroxyacid oxidase (glycolate oxidase) 1 (HAO1)

Target
HAO1
Molecular classification
Enzyme, Oxidoreductase, Peroxisomal protein
01

Overview

Hydroxyacid oxidase (glycolate oxidase) 1 is a peroxisomal enzyme, encoded by the HAO1 gene and primarily expressed in the liver and pancreas, that catalyzes the oxidation of glycolate to glyoxylate as part of glyoxylate metabolism. By facilitating the conversion of glycolate, the enzyme plays a key role in the regulation of oxalate production. Aberrant HAO1 activity can lead to pathological accumulation of oxalate, predisposing to disorders such as primary hyperoxaluria and kidney stones. The enzyme can also oxidize other 2-hydroxy acids with lower catalytic efficiency and is implicated as a potential therapeutic target for diseases related to oxalate metabolism[1][2][6][8].

Other names
HAO1Glycolate oxidaseGOXGOX1HAOX1GO
02

Mechanism of action

Enzyme inhibition reduces oxidation of glycolate to glyoxylate, lowering oxalate production and potentially reducing risk of calcium oxalate kidney stones and systemic oxalosis

03

Biological functions

Glyoxylate metabolismGlycine degradationPeroxisomal fatty acid metabolismOxidative stress response
04

Disease associations

Primary hyperoxaluriaCalcium oxalate nephrolithiasis (kidney stones)Potential biomarker or mechanistic contributor in liver cirrhosis and prostatic neoplasms
05

Safety considerations

Off-target inhibition may disrupt peroxisomal metabolism and induce accumulation of glycolate or other 2-hydroxy acidsPotential metabolic disturbances in liver and pancreasRisk of unintended alteration of glycine and oxalate balance
06

Interacting drugs

4-carboxy-5-[(4-chlorophenyl)sulfanyl]-1,2,3-thiadiazole (experimental inhibitor)

1 more in the full profile.

07

Biomarkers

Glycolate (substrate levels used as indirect biomarker)Oxalate (product, used as biomarker of HAO1 activity)HAO1 mRNA/protein (in research settings)

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