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The First Glimpse of a Complex of Nitrogenase Component Proteins by Solution X-ray Scattering: Conformation of the Electron Transfer Transition State Complex of Klebsiella Pneumoniae Nitrogenase

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Journal J Mol Biol
Publisher Elsevier
Date 1997 Mar 7
PMID 9102457
Citations 4
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Abstract

An essential feature of the mechanism of nitrogenase, the enzyme responsible for biological nitrogen fixation, is the formation of a transient electron transfer complex between the MoFe protein containing the active site at which N2 is reduced, and the Fe protein, which functions as a specific electron donor to the MoFe protein. We have obtained high quality solution X-ray scattering data using synchrotron X-rays of a stable putative electron transfer complex, (MoFe-protein)(Fe-protein.ADP.AIF4)2, of Klebsiella pneumoniae and used the model-independent approach based on the multipole expansion method to provide a stable and unique shape restoration at approximately 15 A resolution. The biological significance of this first molecular structure of a nitrogenase complex is discussed.

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