Hart P J, Liu H, Pellegrini M, Nersissian A M, Gralla E B, Valentine J S, Eisenberg D
UCLA-DOE Laboratory of Structural Biology and Molecular Medicine, University of California, Los Angeles 90095, USA.
Protein Sci. 1998 Mar;7(3):545-55. doi: 10.1002/pro.5560070302.
The X-ray crystal structure of a human copper/zinc superoxide dismutase mutant (G37R CuZnSOD) found in some patients with the inherited form of Lou Gehrig's disease (FALS) has been determined to 1.9 angstroms resolution. The two SOD subunits have distinct environments in the crystal and are different in structure at their copper binding sites. One subunit (subunit[intact]) shows a four-coordinate ligand geometry of the copper ion, whereas the other subunit (subunit[broken]) shows a three-coordinate geometry of the copper ion. Also, subunit(intact) displays higher atomic displacement parameters for backbone atoms ((B) = 30 +/- 10 angstroms2) than subunit(broken) ((B) = 24 +/- 11 angstroms2). This structure is the first CuZnSOD to show large differences between the two subunits. Factors that may contribute to these differences are discussed and a possible link of a looser structure to FALS is suggested.
已确定在某些患有遗传性卢伽雷氏病(家族性肌萎缩侧索硬化症,FALS)的患者中发现的一种人类铜/锌超氧化物歧化酶突变体(G37R CuZnSOD)的X射线晶体结构,分辨率达到1.9埃。两个超氧化物歧化酶亚基在晶体中具有不同的环境,并且它们的铜结合位点在结构上有所不同。一个亚基(完整亚基)显示铜离子的四配位配体几何结构,而另一个亚基(断裂亚基)显示铜离子的三配位几何结构。此外,完整亚基主链原子的原子位移参数((B) = 30 +/- 10埃²)高于断裂亚基((B) = 24 +/- 11埃²)。这种结构是首个显示两个亚基之间存在巨大差异的铜锌超氧化物歧化酶。文中讨论了可能导致这些差异的因素,并提出了结构较松散与家族性肌萎缩侧索硬化症之间的可能联系。