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Histidine ammonia-lyase

Histidine ammonia-lyase is an enzyme that in humans is encoded by the HAL gene. It converts histidine into ammonia and urocanic acid. Its systematic name is L-histidine ammonia-lyase (urocanate-forming).

Function
Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid., from the tripeptide Ala-Ser-Gly by two water elimination steps.|center == Pathology ==
Pathology
Mutations in the gene for histidase are associated with histidinemia and urocanic aciduria. == See also ==
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