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Results 1 - 10 of 21 > >>
EC Number Substrates Commentary Substrates Products Commentary (Products) Reversibility
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54allophanate + H2O - NH3 + CO2 - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54allophanate + H2O - 2 CO2 + 2 NH3 - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54allophanate + H2O the enzyme exhibits high specificity for allophanate 2 CO2 + 2 NH3 - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54biuret + H2O - ? - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54malonamic acid + H2O - ? - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54malonamic acid + hydroxylamine hydroxylamine trapping activity malonohydroxamate + ? - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54malonamide + H2O - ? - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54more allophanate also shows nonenzymatic decomposition, half-life at pH 8.0 is 50 h ? - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54more substrate specificity, no activity with methyl allophanate, hydantoic acid, oxamic acid, hydroxyurea, methyl carbamate, N-methylurea, acetylurea, 1-acetyl-2-thiourea, and semicarbazide, no activity with rhodanine, rhodanine-3-acetic acid, 3-aminorhodanine, (4R)-(-)-2-thioxo-4-thiazolidinecarboxylic acid, (-)-2-oxo-4-thiazolinecarboxylic acid, and 2-amino-5-bromothiazol ? - ?
Show all pathways known for 3.5.1.54Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.54more allophanate is produced at the active site of the UC C-terminal domain and is translocated to that of the AH N-domain for subsequent reaction. Allophanate is translocated from the active site of UC C-terminal domain to that of the AH N-domain via diffusion through solvent, instead of being channeled through the dimer ? - ?
Results 1 - 10 of 21 > >>