Krause K L, Volz K W, Lipscomb W N
J Mol Biol. 1987 Feb 5;193(3):527-53. doi: 10.1016/0022-2836(87)90265-8.
In an X-ray diffraction study using the method of multiple isomorphous replacement, the structure of aspartate carbamoyltransferase (EC 2.1.3.2) complexed with the bisubstrate analog N-(phosphonacetyl)-L-aspartate (PALA) has been solved to 2.5 A. Ten rounds of model building and 123 cycles of restrained reciprocal space refinement have resulted in a model containing 94.4% of the theoretical atoms of the protein-inhibitor complex with an R-factor of 0.231. The fit of the model to the density is excellent, except for occasional side-chains and two sections of the regulatory chains that may be disordered. The electron density for the PALA molecule is readily identifiable for both catalytic (c) chains of the asymmetric unit and bonding interactions with several important residues including Ser52, Arg54, Thr55, Ser80, Lys84, Arg105, His134, Arg165, Arg229 and Gln231 are apparent. The carboxylate groups of the PALA molecule are in a nearly cis conformation. Gross quaternary changes between the T and R forms are noted and in agreement with earlier work from this laboratory. Namely, in the new structure the catalytic trimers move apart by 12 A along the 3-fold axis of the enzyme and relocate by 10 degrees relative to each other, adopting a more eclipsed position. The regulatory (r) chains in the new structure reorient about their 2-fold axis by 15 degrees. Large tertiary changes that include domain migration and rearrangement are also present between these two forms. In the R form both domains of the catalytic chain relocate closer to each other in order to bind to the inhibitor. The polar domain seems to bind primarily to the carbamoyl phosphate moiety of PALA, and the equatorial domain binds primarily to the L-aspartate moiety. Other changes in tertiary structure bring the 80s loop (from an adjacent catalytic chain) and the 240s loop into a position to interact with the PALA molecule. Changes have been searched for in all interface regions of the enzyme. While the C1-C4 and C1-R4 regions have been completely altered, most of the other interchain interfaces are similar in the T and R forms. The intrachain interfaces, between domains of the same catalytic chains, have undergone some reorganization as these domains move closer to each other when the inhibitor is bound. This new structure allows a reinterpretation of genetic and chemical modification studies done to date.(ABSTRACT TRUNCATED AT 400 WORDS)
在一项采用多同晶置换法的X射线衍射研究中,天冬氨酸氨甲酰基转移酶(EC 2.1.3.2)与双底物类似物N-(膦酰乙酰基)-L-天冬氨酸(PALA)复合物的结构已解析至2.5埃分辨率。经过十轮模型构建和123个循环的受限倒易空间精修,得到了一个包含蛋白质-抑制剂复合物理论原子数94.4%的模型,其R因子为0.231。该模型与电子密度的拟合效果极佳,只是偶尔会出现侧链以及两条可能无序的调节链区域。对于不对称单元的两条催化(c)链,PALA分子的电子密度易于识别,并且与包括Ser52、Arg54、Thr55、Ser80、Lys84、Arg105、His134、Arg165、Arg229和Gln231在内的几个重要残基的键合相互作用也很明显。PALA分子的羧基处于近乎顺式的构象。注意到T态和R态之间存在明显的四级结构变化,这与本实验室早期的研究结果一致。具体而言,在新结构中,催化三聚体沿酶的三重轴彼此分开12埃,并相对于彼此重新定位10度,采取了更重叠的位置。新结构中的调节(r)链围绕其二重轴重新定向了15度。这两种形式之间还存在包括结构域迁移和重排在内的较大三级结构变化。在R态中,催化链的两个结构域彼此靠近重新定位以结合抑制剂。极性结构域似乎主要与PALA的氨甲酰磷酸部分结合,而赤道结构域主要与L-天冬氨酸部分结合。三级结构的其他变化使(来自相邻催化链的)80s环和240s环处于与PALA分子相互作用的位置。已在酶的所有界面区域寻找变化。虽然C1-C4和C1-R4区域已完全改变,但大多数其他链间界面在T态和R态中相似。当抑制剂结合时,同一催化链的结构域彼此靠近,这些结构域之间的链内界面发生了一些重组。这个新结构使得对迄今为止所做的遗传和化学修饰研究有了新的解读。(摘要截选至400字)