| Literature DB >> 24292428 |
Kenneth M Light1, John A Hangasky, Michael J Knapp, Edward I Solomon.
Abstract
Non-heme Fe(II) enzymes exhibit a general mechanistic strategy where binding all cosubstrates opens a coordination site on the Fe(II) for O2 activation. This study shows that strong-donor ligands, steric interactions with the substrate and second-sphere H-bonding to the facial triad carboxylate allow for five-coordinate site formation in this enzyme superfamily.Entities:
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Year: 2014 PMID: 24292428 PMCID: PMC3976902 DOI: 10.1039/c3dt53201a
Source DB: PubMed Journal: Dalton Trans ISSN: 1477-9226 Impact factor: 4.390