Horovitz A, Rigbi M
J Theor Biol. 1985 Sep 7;116(1):149-59. doi: 10.1016/s0022-5193(85)80135-1.
Additivity of contributions to the free energies of association of ovomucoid third domain inhibitors with elastase, chymotrypsin and subtilisin (Laskowski, 1980; Laskowski et al., 1981, 1983; Empie & Laskowski, 1982) is fully demonstrated by applying the mathematical method of Free and Wilson (1964) for calculating the effects of substitutions in a family of drugs. Also demonstrated is the ability to predict the activity of third domain sequences. Sensitive regions in the contact area of inhibitor and enzyme are mapped, and a sequence is suggested for a new, more powerful and selective ovomucoid third domain inhibitor of subtilisin.
通过应用弗里和威尔逊(1964年)的数学方法来计算一类药物中取代基的效应,充分证明了卵类粘蛋白第三结构域抑制剂与弹性蛋白酶、胰凝乳蛋白酶和枯草杆菌蛋白酶结合时对自由能贡献的加和性(拉斯科夫斯基,1980年;拉斯科夫斯基等人,1981年、1983年;恩皮和拉斯科夫斯基,1982年)。还证明了预测第三结构域序列活性的能力。绘制了抑制剂与酶接触区域中的敏感区域,并提出了一种针对枯草杆菌蛋白酶的新型、更强效且更具选择性的卵类粘蛋白第三结构域抑制剂的序列。