| Literature DB >> 16087182 |
P Nuno Palma1, Bernard Lagoutte, Ludwig Krippahl, José J G Moura, Françoise Guerlesquin.
Abstract
Ferredoxin (Fd) and ferredoxin-NADP(+)-reductase (FNR) are two terminal physiological partners of the photosynthetic electron transport chain. Based on a nuclear magnetic resonance (NMR)-restrained-docking approach, two alternative structural models of the Fd-FNR complex in the presence of NADP+ are proposed. The protein docking simulations were performed with the software BiGGER. NMR titration revealed a 1:1 stoichiometry for the complex and allowed the mapping of the interacting residues at the surface of Fd. The NMR chemical shifts were encoded into distance constraints and used with theoretically calculated electronic coupling between the redox cofactors to propose experimentally validated docked complexes.Entities:
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Year: 2005 PMID: 16087182 DOI: 10.1016/j.febslet.2005.07.027
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124