Christianson D W, Lipscomb W N
Proc Natl Acad Sci U S A. 1986 Oct;83(20):7568-72. doi: 10.1073/pnas.83.20.7568.
A high-resolution x-ray crystallographic investigation of the complex between carboxypeptidase A (CPA; peptidyl-L-amino-acid hydrolase, EC 3.4.17.1) and the slowly hydrolyzed substrate glycyl-L-tyrosine was done at -9 degrees C. Although this enzyme-substrate complex has been the subject of earlier crystallographic investigation, a higher resolution electron-density map of the complex with greater occupancy of the substrate was desired. All crystal chemistry (i.e., crystal soaking and x-ray data collection) was performed on a diffractometer-mounted flow cell, in which the crystal was immobilized. The x-ray data to 1.6-A resolution have yielded a well-resolved structure in which the zinc ion of the active site is five-coordinate: three enzyme residues (glutamate-72, histidine-69, and histidine-196) and the carbonyl oxygen and amino terminus of glycyl-L-tyrosine complete the coordination polyhedron of the metal. These results confirm that this substrate may be bound in a nonproductive manner, because the hydrolytically important zinc-bound water has been displaced and excluded from the active site. It is likely that all dipeptide substrates of carboxypeptidase A that carry an unprotected amino terminus are poor substrates because of such favorable bidentate coordination to the metal ion of the active site.
在-9℃下对羧肽酶A(CPA;肽基-L-氨基酸水解酶,EC 3.4.17.1)与缓慢水解的底物甘氨酰-L-酪氨酸之间的复合物进行了高分辨率X射线晶体学研究。尽管这种酶-底物复合物一直是早期晶体学研究的对象,但仍需要一个分辨率更高、底物占有率更高的复合物电子密度图。所有晶体化学操作(即晶体浸泡和X射线数据收集)均在安装在衍射仪上的流动池中进行,晶体在该流动池中固定。分辨率达到1.6埃的X射线数据产生了一个分辨率良好的结构,其中活性位点的锌离子为五配位:三个酶残基(谷氨酸-72、组氨酸-69和组氨酸-196)以及甘氨酰-L-酪氨酸的羰基氧和氨基末端完成了金属的配位多面体。这些结果证实该底物可能以非生产性方式结合,因为水解重要的锌结合水已被取代并排除在活性位点之外。由于与活性位点的金属离子形成如此有利的双齿配位,羧肽酶A的所有带有未保护氨基末端的二肽底物可能都是不良底物。