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Coenzyme B12‐dependent enzymes such as ethanolamine ammonia lyase have remarkable catalytic power and some unique properties that enable detailed analysis of the reaction chemistry and associated dynamics. By selectively deuterating the substrate (ethanolamine) and/or the β‐carbon of the 5′‐deoxyadenosyl moiety of the intrinsic coenzyme B12, it was possible to experimentally probe both the forward...
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