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InterPro results for 1.13.11.5

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Homogentisate 1,2-dioxygenase (IPR005708) Alkaptonuria (AKU), a rare hereditary disorder, was the first disease to be interpreted as an inborn error of metabolism. The deficiency causes homogentisic aciduria, ochronosis, ...

Homogentisate 1,2-dioxygenase, bacterial (IPR022950) This entry represents bacterial homogentisate 1,2-dioxygenase . This enzyme mediates the conversion of homogentisate to maleylacetoacetate; a step in the catabolism of both tyrosi...