4.6 Review

Glycyl radical activating enzymes: Structure, mechanism, and substrate interactions

Journal

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 546, Issue -, Pages 64-71

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2014.01.020

Keywords

Radical S-adenosylmethionine (SAM) enzyme; Glycyl radical enzyme activating enzyme (GRE-AE); Glycyl radical enzyme (GRE); Pyruvate formate lyase activating enzyme (PFL-AE)

Funding

  1. National Institutes of Health [GM54608]

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The glycyl radical enzyme activating enzymes (GRE-AEs) are a group of enzymes that belong to the radical S-adenosylmethionine (SAM) superfamily and utilize a [4Fe-4S] cluster and SAM to catalyze H-atom abstraction from their substrate proteins. GRE-AEs activate homodimeric proteins known as glycyl radical enzymes (GREs) through the production of a glycyl radical. After activation, these GREs catalyze diverse reactions through the production of their own substrate radicals. The GRE-AE pyruvate formate lyase activating enzyme (PFL-AE) is extensively characterized and has provided insights into the active site structure of radical SAM enzymes including GRE-AEs, illustrating the nature of the interactions with their corresponding substrate GREs and external electron donors. This review will highlight research on PFL-AE and will also discuss a few GREs and their respective activating enzymes. (C) 2014 Published by Elsevier Inc.

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