• Title of article

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

  • Author/Authors

    Shisler، نويسنده , , Krista A. and Broderick، نويسنده , , Joan B.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2014
  • Pages
    8
  • From page
    64
  • To page
    71
  • Abstract
    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.
  • Keywords
    Glycyl radical enzyme (GRE) , Glycyl radical enzyme activating enzyme (GRE–AE) , Pyruvate formate lyase activating enzyme (PFL-AE) , Radical S-adenosylmethionine (SAM) enzyme
  • Journal title
    Archives of Biochemistry and Biophysics
  • Serial Year
    2014
  • Journal title
    Archives of Biochemistry and Biophysics
  • Record number

    1634119