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- W2056552040 abstract "When the pKm of alpha-mannosidase was determined at different pH values, the results indicated that ionizable groups with pK values of approx. 3.8 and 5.7 could be essential. Modification with carbodiimide or Woodward's Reagent K abolished the enzyme activity. The substrate analogue, alpha-methyl-D-mannoside, protected the enzyme against inactivation. Incorporation of a 14C-labeled nucleophile reagent in the presence or absence of the analogue suggested that 2--4 carboxyl groups were protected. Exchange studies indicated that the essential Zn2+ could be bound to such groups. There was no indication that hydroxyl groups, sulphydryl groups, guanidino groups or amino groups take part in the catalytic activity." @default.
- W2056552040 created "2016-06-24" @default.
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- W2056552040 date "1978-10-01" @default.
- W2056552040 modified "2023-09-27" @default.
- W2056552040 title "Reaction of α-mannosidase from Phaseolus vulgaris with group-specific reagents. Essential carboxyl groups" @default.
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- W2056552040 doi "https://doi.org/10.1016/0005-2744(78)90141-9" @default.
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