Abstract
Abstract The catalytic activity, 6β-hydroxylation, toward testosterone of engineered cytochrome P-450d was three-times increased by Thr319Ala mutation at the putative distal site, While that was abolished Ala315Ser and important role the steroid of while that was abolished by mutations Thr322Ala at the same site, suggesting the of this region in catalytic activity toward cytochrome P-450d.
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