1GZF

Structure of the Clostridium botulinum C3 exoenzyme (wild-type) in complex with NAD

1GZF の概要

• エントリーDOI: 10.2210/pdb1gzf/pdb
• 関連するPDBエントリー: 1G24 1GZE
• 分子名称: MONO-ADP-RIBOSYLTRANSFERASE C3, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, SULFATE ION, ... (6 entities in total)
• 機能のキーワード: transferase, adp-ribosyltransferase, bacterial toxin, c3 exoenzyme
• 由来する生物種: CLOSTRIDIUM BOTULINUM
• 細胞内の位置: Secreted: P15879
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 96983.53

構造登録者

Menetrey, J.,Flatau, G.,Stura, E.A.,Charbonnier, J.B.,Gas, F.,Teulon, J.M.,Le Du, M.H.,Boquet, P.,Menez, A. (登録日: 2002-05-21, 公開日: 2002-08-29, 最終更新日: 2024-05-08)

主引用文献

Menetrey, J.,Flatau, G.,Stura, E.A.,Charbonnier, J.B.,Gas, F.,Teulon, J.M.,Le Du, M.H.,Boquet, P.,Menez, A.
Nad Binding Induces Conformational Changes in Rho Adp-Ribosylating Clostridium Botulinum C3 Exoenzyme
J.Biol.Chem., 277:30950-, 2002

PubMed Abstract: We have solved the crystal structures of Clostridium botulinum C3 exoenzyme free and complexed to NAD in the same crystal form, at 2.7 and 1.95 A, respectively. The asymmetric unit contains four molecules, which, in the free form, share the same conformation. Upon NAD binding, C3 underwent various conformational changes, whose amplitudes were differentially limited in the four molecules of the crystal unit. A major rearrangement concerns the loop that contains the functionally important ARTT motif (ADP-ribosyltransferase toxin turn-turn). The ARTT loop undergoes an ample swinging motion to adopt a conformation that covers the nicotinamide moiety of NAD. In particular, Gln-212, which belongs to the ARTT motif, flips over from a solvent-exposed environment to a buried conformation in the NAD binding pocket. Mutational experiments showed that Gln-212 is neither involved in NAD binding nor in the NAD-glycohydrolase activity of C3, whereas it plays a critical role in the ADP-ribosyl transfer to the substrate Rho. We observed additional NAD-induced movements, including a crab-claw motion of a subdomain that closes the NAD binding pocket. The data emphasized a remarkable NAD-induced plasticity of the C3 binding pocket and suggest that the NAD-induced ARTT loop conformation may be favored by the C3-NAD complex to bind to the substrate Rho. Our structural observations, together with a number of mutational experiments suggest that the mechanisms of Rho ADP-ribosylation by C3-NAD may be more complex than initially anticipated.

PubMed: 12029083
DOI: 10.1074/JBC.M201844200

実験手法

X-RAY DIFFRACTION (1.95 Å)