Tomita Takeo, Fushinobu Shinya, Kuzuyama Tomohisa, Nishiyama Makoto
Biotechnology Research Center, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.
Biochem Biophys Res Commun. 2005 Aug 26;334(2):613-8. doi: 10.1016/j.bbrc.2005.06.133.
For better understanding of the coenzyme specificity in NAD-dependent MDH (tMDH) from Thermus flavus AT-62, we determined the crystal structures of tMDH-NADP(H) complex at maximally 1.65 A resolution. The overall structure is almost the same as that of the tMDH-NADH complex. However, NADP(H) binds to tMDH in the reverse orientation, where adenine occupies the position near the catalytic center and nicotinamide is positioned at the adenine binding site of the tMDH-NADH complex. Consistent with this, kinetic analysis of the malate-oxidizing reaction revealed that NADP(+) inhibited tMDH at high concentrations. This has provided the first evidence for the alternative binding mode of the nicotinamide coenzyme, that has pseudo-symmetry in its structure, in a single enzyme.
为了更好地理解嗜热黄杆菌AT-62中依赖NAD的苹果酸脱氢酶(tMDH)的辅酶特异性,我们测定了tMDH-NADP(H)复合物的晶体结构,分辨率最高为1.65 Å。其整体结构与tMDH-NADH复合物几乎相同。然而,NADP(H)以相反的方向与tMDH结合,其中腺嘌呤占据靠近催化中心的位置,烟酰胺位于tMDH-NADH复合物的腺嘌呤结合位点。与此一致,苹果酸氧化反应的动力学分析表明,高浓度的NADP(+)会抑制tMDH。这首次证明了烟酰胺辅酶在单一酶中具有结构伪对称性的替代结合模式。