3X41

Copper amine oxidase from Arthrobacter globiformis: Product Schiff-base form produced by anaerobic reduction in the presence of sodium bromide

3X41 の概要

• エントリーDOI: 10.2210/pdb3x41/pdb
• 関連するPDBエントリー: 3X3X 3X3Y 3X3Z 3X40 3X42
• 分子名称: Phenylethylamine oxidase, COPPER (II) ION, BROMIDE ION, ... (7 entities in total)
• 機能のキーワード: copper amine oxidase, topaquinone, tpq, oxidoreductase
• 由来する生物種: Arthrobacter globiformis
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 140487.86

構造登録者

Okajima, T.,Nakanishi, S.,Murakawa, T.,Kataoka, M.,Hayashi, H.,Hamaguchi, A.,Nakai, T.,Kawano, Y.,Yamaguchi, H.,Tanizawa, K. (登録日: 2015-03-10, 公開日: 2015-08-19, 最終更新日: 2024-11-13)

主引用文献

Murakawa, T.,Hamaguchi, A.,Nakanishi, S.,Kataoka, M.,Nakai, T.,Kawano, Y.,Yamaguchi, H.,Hayashi, H.,Tanizawa, K.,Okajima, T.
Probing the Catalytic Mechanism of Copper Amine Oxidase from Arthrobacter globiformis with Halide Ions.
J.Biol.Chem., 290:23094-23109, 2015

PubMed Abstract: The catalytic reaction of copper amine oxidase proceeds through a ping-pong mechanism comprising two half-reactions. In the initial half-reaction, the substrate amine reduces the Tyr-derived cofactor, topa quinone (TPQ), to an aminoresorcinol form (TPQamr) that is in equilibrium with a semiquinone radical (TPQsq) via an intramolecular electron transfer to the active-site copper. We have analyzed this reductive half-reaction in crystals of the copper amine oxidase from Arthrobacter globiformis. Anerobic soaking of the crystals with an amine substrate shifted the equilibrium toward TPQsq in an "on-copper" conformation, in which the 4-OH group ligated axially to the copper center, which was probably reduced to Cu(I). When the crystals were soaked with substrate in the presence of halide ions, which act as uncompetitive and noncompetitive inhibitors with respect to the amine substrate and dioxygen, respectively, the equilibrium in the crystals shifted toward the "off-copper" conformation of TPQamr. The halide ion was bound to the axial position of the copper center, thereby preventing TPQamr from adopting the on-copper conformation. Furthermore, transient kinetic analyses in the presence of viscogen (glycerol) revealed that only the rate constant in the step of TPQamr/TPQsq interconversion is markedly affected by the viscogen, which probably perturbs the conformational change. These findings unequivocally demonstrate that TPQ undergoes large conformational changes during the reductive half-reaction.

PubMed: 26269595
DOI: 10.1074/jbc.M115.662726

実験手法

X-RAY DIFFRACTION (1.87 Å)