Bott R, Subramanian E, Davies D R
Biochemistry. 1982 Dec 21;21(26):6956-62. doi: 10.1021/bi00269a052.
An X-ray diffraction analysis has been carried out at 2.5-A resolution of the three-dimensional structure of the Rhizopus chinensis carboxyl proteinase complexed with pepstatin. The resulting model of the complex supports the hypothesis [Marciniszyn, J., Hartsuck, J.A., & Tang, J. (1976) J. Biol. Chem. 251, 7088-7094] that statine (3-hydroxy-4-amino-6-methylheptanoic acid) approaches an analogue of the transition state for catalysis. The way in which pepstatin binds to the enzyme can be extended to provide a model of substrate binding and a model of the transition-state complex. This in turn has led to a proposed mechanism of action based on general acid-base catalysis with no covalent intermediates. These predictions are in general agreement with kinetic studies using several carboxyl proteinases, which together with their sequence homology and their common three-dimensional structures suggest that this mechanism can be extrapolated to all carboxyl proteinases.
已对与胃蛋白酶抑制剂复合的华根霉羧基蛋白酶的三维结构进行了2.5埃分辨率的X射线衍射分析。所得的复合物模型支持以下假设[Marciniszyn, J., Hartsuck, J.A., & Tang, J. (1976) J. Biol. Chem. 251, 7088 - 7094],即静抑素(3 - 羟基 - 4 - 氨基 - 6 - 甲基庚酸)接近催化过渡态的类似物。胃蛋白酶抑制剂与酶结合的方式可扩展以提供底物结合模型和过渡态复合物模型。这进而导致了基于无共价中间体的一般酸碱催化作用机制的提出。这些预测总体上与使用几种羧基蛋白酶的动力学研究一致,这些研究连同它们的序列同源性和共同的三维结构表明,该机制可外推至所有羧基蛋白酶。