丝氨酸
化学
蛋白质水解
脚手架
丝氨酸蛋白酶抑制剂
机制(生物学)
生物化学
酶
支架蛋白
立体化学
蛋白酶抑制剂
生物物理学
生物
丝氨酸蛋白酶
信号转导
计算机科学
物理
量子力学
数据库
蛋白酶
作者
Clyde Kelly,M. Laskowski,Mohammad Qasim
出处
期刊:Protein and Peptide Letters
[Bentham Science]
日期:2005-07-01
卷期号:12 (5): 465-471
被引量:11
标识
DOI:10.2174/0929866054395383
摘要
In single domain, “standard mechanism” protein inhibitors of serine proteinases, about a dozen residues make contact with the cognate enzyme. The remainder of the molecule, the scaffolding, holds the reactive site region of the inhibitor in a canonical conformation, improves the binding by about six orders of magnitude and protects it from proteolysis. However, the stability and global structure of the scaffolding is irrelevant to inhibition, provided that inhibition is measured much below the melting temperature,™. Keywords: standard mechanism inhibitors, scaffolding, serine proteinases, inhibitor stability
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