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We utilized site-directed mutagenesis to determine the deposits critical for the copper binding of individual tyrosinase. Seven histidine mutants in the two copper-binding websites were generated, and catalytic tasks were characterised. The tyrosine hydroxylase tasks of this CuA website mutants had been roughly 50% less than those of this wild-type tyrosinase, as the dopa oxidation tasks associated with the mutants weren't dramatically distinct from that of wild-type tyrosinase. By contrast, mutations
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