Urocanase (also known as imidazolonepropionate hydrolase or urocanate hydratase) is the enzyme (EC 4.2.1.49 4.2.1.49) that catalyzes the second step in...
4 KB (381 words) - 16:37, 27 July 2022
Urocanic aciduria (redirect from Urocanase deficiency)
autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase. It is a secondary disorder of histidine metabolism. Urocanic aciduria...
4 KB (301 words) - 00:59, 25 April 2022
Urinary calculi Urinary tract neoplasm Urioste–Martinez–Frias syndrome Urocanase deficiency Urogenital adysplasia Urophathy distal obstructive polydactyly...
2 KB (232 words) - 19:32, 1 May 2024
prokaryotes, histidine is first converted to urocanate by histidase. Then, urocanase converts urocanate to 4-imidazolone-5-propionate. Imidazolonepropionase...
24 KB (2,533 words) - 10:53, 5 August 2024
urocanate hydratase (or urocanase) to 4-imidazolone-5-propionic acid and subsequently to glutamic acid. Inherited deficiency of urocanase leads to elevated...
7 KB (671 words) - 04:03, 25 March 2024
accession codes 1XFK and 2A0M. Kaminskas E, Kimhi Y, Magasanik B (1970). "Urocanase and N-formimino-L-glutamate formiminohydrolase of Bacillus subtilis, two...
2 KB (188 words) - 14:04, 26 August 2023
The compound features an imidazolone ring. It arises via the action of urocanase on urocanic acid. Hydrolysis of the heterocycle to the glutamic acid derivative...
3 KB (200 words) - 21:46, 21 June 2024
severe limb deficiency; 276820; WNT7A Ulnar–mammary syndrome; 181450; TBX3 Urocanase deficiency; 276880; UROC1 Urofacial syndrome; 236730; HPSE2 Usher syndrome...
234 KB (18,877 words) - 15:43, 9 May 2024