Structure of T4moF, the Toluene 4-Monooxygenase Ferredoxin Oxidoreductase

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• 作者：Justin F. Acheson ; Hannah Moseson ; Brian G. Fox
• 刊名：Biochemistry
• 出版年：2015
• 出版时间：September 29, 2015
• 年：2015
• 卷：54
• 期：38
• 页码：5980-5988
• 全文大小：425K
• ISSN：1520-4995

文摘

The 1.6 脜 crystal structure of toluene 4-monooxygenase reductase T4moF is reported. The structure includes ferredoxin, flavin, and NADH binding domains. The position of the ferredoxin domain relative to the other two domains represents a new configuration for the iron鈥搒ulfur flavoprotein family. Close contacts between the C8 methyl group of FAD and [2Fe-2S] ligand Cys36-O represent a plausible pathway for electron transfer between the redox cofactors. Energy-minimized docking of NADH and calculation of hingelike motions between domains suggest how simple coordinated shifts of residues at the C-terminus of the enzyme could expose the N5 position of FAD for productive interaction with the nicotinamide ring. The domain configuration revealed by the T4moF structure provides an excellent steric and electrostatic match to the obligate electron acceptor, Rieske-type [2Fe-2S] ferredoxin T4moC. Protein鈥損rotein docking and energy minimization of the T4moFC complex indicate that T4moF [2Fe-2S] ligand Cys41 and T4moC [2Fe-2S] ligand His67, along with other electrostatic interactions between the protein partners, form the functional electron transfer interface.