| Literature DB >> 31494759 |
William E Broderick1, Joan B Broderick2.
Abstract
As the field of radical SAM enzymology has grown from a few examples in the 1990s to hundreds of thousands today, a fundamental question has remained: how does Nature use S-adenosyl-L-methionine to initiate radical reactions? This was a driving question when we first began studying pyruvate formate-lyase activating enzyme in 1993, and our journey for answers has brought us to many surprising discoveries, from the direct coordination of SAM to a unique iron in a [4Fe-4S] cluster, to our recent discovery of an organometallic intermediate and our ability to quantitatively produce and characterize the long-sought 5'-deoxyadenosyl radical intermediate. These adventures and what we have learned along the way about this fundamentally novel chemistry is described in this review.Entities:
Keywords: Deoxyadenosyl radical; Organometallic; Radical SAM; S-adenosylmethionine
Mesh:
Substances:
Year: 2019 PMID: 31494759 PMCID: PMC8837180 DOI: 10.1007/s00775-019-01706-w
Source DB: PubMed Journal: J Biol Inorg Chem ISSN: 0949-8257 Impact factor: 3.358