A possible iron delivery function of the dinuclear iron center of HcgD in 
[Fe]-hydrogenase cofactor biosynthesis

Fujishiro, T.; Ermler, U.; Shima, S.

doi:10.1016/j.febslet.2014.05.059

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A possible iron delivery function of the dinuclear iron center of HcgD in [Fe]-hydrogenase cofactor biosynthesis

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Fujishiro, T.
Department-Independent Research Group Microbial Protein Structure, Max Planck Institute for Terrestrial Microbiology, Max Planck Society;

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Shima, S.
Department-Independent Research Group Microbial Protein Structure, Max Planck Institute for Terrestrial Microbiology, Max Planck Society;

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Citation

Fujishiro, T., Ermler, U., & Shima, S. (2014). A possible iron delivery function of the dinuclear iron center of HcgD in [Fe]-hydrogenase cofactor biosynthesis. FEBS Letters, 588(17), 2789-2793. doi:10.1016/j.febslet.2014.05.059.

Cite as: https://hdl.handle.net/21.11116/0000-0007-BDD1-8

Abstract

HcgD, a homolog of the ubiquitous Nif3-like protein family, is found in a gene cluster involved in the biosynthesis of the iron-guanylylpyridinol (FeGP) cofactor of [Fe]-hydrogenase. The presented crystal structure and biochemical analyses indicated that HcgD has a dinuclear iron-center, which provides a pronounced binding site for anionic ligands. HcgD contains a stronger and a weaker bound iron; the latter being removable by chelating reagents preferentially in the oxidized state. Therefore, we propose HcgD as an iron chaperone in FeGP cofactor biosynthesis, which might also stimulate investigations on the functionally unknown but physiologically important eukaryotic Nif3-like protein family members.