Turk D, Guncar G, Podobnik M, Turk B
Department of Biochemistry and Molecular Biology, Jozef Stefan Institute, Ljubljana, Slovenia.
Biol Chem. 1998 Feb;379(2):137-47. doi: 10.1515/bchm.1998.379.2.137.
A review of kinetic and structural data has enabled us to reconsider the definition of substrate binding sites in papain-like cysteine proteases. Only three substrate binding sites, S2, S1 and S1', involve main as well as side chain contacts between substrate and enzyme residues. Interactions between the enzymes and the substrate P3 and P2' residues are based on side chains (an exception is cathepsin B which is a carboxydipeptidase), so their interaction surface spreads over a relatively wide area. The location and definition of substrate binding sites beyond S3 and S2' is even more questionable.
对动力学和结构数据的综述使我们能够重新审视木瓜蛋白酶样半胱氨酸蛋白酶中底物结合位点的定义。只有三个底物结合位点,即S2、S1和S1',涉及底物与酶残基之间的主链以及侧链接触。酶与底物P3和P2'残基之间的相互作用基于侧链(组织蛋白酶B是一种羧基二肽酶,属于例外情况),因此它们的相互作用表面分布在相对较宽的区域。S3和S2'之外的底物结合位点的位置和定义更值得怀疑。