Synechocystis ferredoxin/ferredoxin-NADP+-reductase/NADP+ complex:: Structural model obtained by NMR-restrained docking

被引:22
|
作者
Palma, PN
Lagoutte, B
Krippahl, L
Moura, JJG
Guerlesquin, F
机构
[1] CNRS, IBSM, Unite Bioenerget & Ingn Prot, F-13402 Marseille, France
[2] CEA Saclay, CNRS, Dept Biol Joliot Curie, Serv Bioenerget,URA 2096, F-91191 Gif Sur Yvette, France
[3] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, REQUIMTE, P-2859516 Caparica, Portugal
关键词
ferredoxin; ferredoxin NADP(+)-reductase; complex; docking and NMR;
D O I
10.1016/j.febslet.2005.07.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2005 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:4585 / 4590
页数:6
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