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ADP-ribosylation, a mechanism regulating nitrogenase activity

期刊

FEBS JOURNAL
卷 280, 期 15, 页码 3484-3490

出版社

WILEY
DOI: 10.1111/febs.12279

关键词

activity regulation; crystallography; DraG; DraT; manganese; metalloprotein; nitrogenase; nitrogen fixation; post-translational modification; Rhodospirillum rubrum

资金

  1. Swedish Foundation for Strategic Research
  2. Knut and Alice Wallenberg Foundation
  3. Swedish Research Council

向作者/读者索取更多资源

Nitrogen fixation is the vital biochemical process in which atmospheric molecular nitrogen is made available to the biosphere. The process is highly energetically costly and thus tightly regulated. The activity of the key enzyme, nitrogenase, is controlled by reversible mono-ADP-ribosylation of one of its components, the Fe protein. This protein provides the other component, the MoFe protein, with the electrons required for the reduction of molecular nitrogen. The Fe-protein is ADP-ribosylated and de-ADP-ribosylated by dinitrogenase reductase ADP-ribosyl transferase and dinitrogenase reductase activating glycohydrolase, respectively. Here we review the current biochemical and structural knowledge of this central regulatory reaction.

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