Abstract
The enzymes adenylate deaminase (AMPDA) and adenosine deaminase (ADA) are able to catalyze the stereoselective hydrolytic deamination of (5 ′ R, S)-methyl-2 ′,3 ′-isopropylidene adenosine, but the 5 ′-butyl analog is a substrate only for AMPDA, which stereospecifically converts the (5 ′ S)-isomer to the corresponding inosine derivative.
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