Yuan Y R, Blecker S, Martsinkevich O, Millen L, Thomas P J, Hunt J F
Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
J Biol Chem. 2001 Aug 24;276(34):32313-21. doi: 10.1074/jbc.M100758200. Epub 2001 Jun 11.
The crystal structure of the MJ0796 ATP-binding cassette, a member of the o228/LolD transporter family, has been determined at 2.7-A resolution with MgADP bound at its active site. Comparing this structure with that of the ATP-bound form of the HisP ATP-binding cassette (Hung, L. W., Wang, I. X., Nikaido, K., Liu, P. Q., Ames, G. F., and Kim, S. H. (1998) Nature 396, 703-707) shows a 5-A withdrawal of a phylogenetically invariant glutamine residue from contact with the gamma-phosphate of ATP in the active site. This glutamine is located in a protein segment that links the rigid F(1)-type ATP-binding core of the enzyme to an ABC transporter-specific alpha-helical subdomain that moves substantially away from the active site in the MgADP-bound structure of MJ0796 compared with the ATP-bound structure of HisP. A similar conformational effect is observed in the MgADP-bound structure of MJ1267 (Karpowich, N., et al. (2001) Structure, in press), establishing the withdrawal of the glutamine and the coupled outward rotation of the alpha-helical subdomain as consistent consequences of gamma-phosphate release from the active site of the transporter. Considering this subdomain movement in the context of a leading model for the physiological dimer of cassettes present in ABC transporters indicates that it produces a modest mechanical change that is likely to play a role in facilitating nucleotide exchange out of the ATPase active site. Finally, it is noteworthy that one of the intersubunit packing interactions in the MJ0796 crystal involves antiparallel beta-type hydrogen bonding interactions between the outermost beta-strands in the two core beta-sheets, leading to their fusion into a single extended beta-sheet, a type of structural interaction that has been proposed to play a role in mediating the aggregation of beta-sheet-containing proteins.
已确定o228/LolD转运蛋白家族成员MJ0796 ATP结合盒的晶体结构,分辨率为2.7埃,其活性位点结合有MgADP。将此结构与HisP ATP结合盒的ATP结合形式(Hung, L. W., Wang, I. X., Nikaido, K., Liu, P. Q., Ames, G. F., and Kim, S. H. (1998) Nature 396, 703 - 707)进行比较,结果显示一个系统发育上不变的谷氨酰胺残基从与活性位点中ATP的γ - 磷酸基团接触处撤回了5埃。该谷氨酰胺位于一个蛋白质片段中,该片段将酶的刚性F(1)型ATP结合核心与ABC转运蛋白特有的α - 螺旋亚结构域相连,与HisP的ATP结合结构相比,在MJ0796的MgADP结合结构中,该α - 螺旋亚结构域从活性位点大幅移开。在MJ1267的MgADP结合结构中也观察到了类似的构象效应(Karpowich, N., et al. (2001) Structure, in press),证实谷氨酰胺的撤回以及α - 螺旋亚结构域的向外旋转是转运蛋白活性位点γ - 磷酸基团释放的一致结果。在ABC转运蛋白中存在的盒式结构生理二聚体的主导模型背景下考虑这种亚结构域运动表明,它会产生适度的机械变化,这可能在促进核苷酸从ATP酶活性位点交换出去中发挥作用。最后,值得注意 的是,MJ0796晶体中的一个亚基间堆积相互作用涉及两个核心β - 折叠中最外层β - 链之间的反平行β型氢键相互作用,导致它们融合成一个单一的延伸β - 折叠,这种结构相互作用类型已被提出在介导含β - 折叠蛋白质的聚集过程中发挥作用。