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Structural Evidence for Asymmetrical Nucleotide Interactions in Nitrogenase
Author(s) -
F. Akif Tezcan,
Jens T. Kaiser,
James B. Howard,
Douglas C. Rees
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja511945e
Subject(s) - chemistry , nitrogenase , nucleotide , atp hydrolysis , enzyme , stereochemistry , substrate (aquarium) , protein structure , crystallography , sequence (biology) , biophysics , hydrolysis , biochemistry , electron transfer , photochemistry , atpase , nitrogen fixation , nitrogen , oceanography , organic chemistry , biology , gene , geology
The roles of ATP hydrolysis in electron-transfer (ET) reactions of the nitrogenase catalytic cycle remain obscure. Here, we present a new structure of a nitrogenase complex crystallized with MgADP and MgAMPPCP, an ATP analogue. In this structure the two nucleotides are bound asymmetrically by the Fe-protein subunits connected to the two different MoFe-protein subunits. This binding mode suggests that ATP hydrolysis and phosphate release may proceed by a stepwise mechanism. Through the associated Fe-protein conformational changes, a stepwise mechanism is anticipated to prolong the lifetime of the Fe-protein-MoFe-protein complex and, in turn, could orchestrate the sequence of intracomplex ET required for substrate reduction.

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