蛋白质-蛋白质相互作用
变构调节
药物发现
小分子
灵活性(工程)
蛋白质聚集
自噬相关蛋白13
化学
囊泡相关膜蛋白8
计算生物学
生物
生物化学
蛋白激酶A
蛋白质磷酸化
膜蛋白
酶
统计
数学
膜
作者
A. V. Veselovsky,Alexander I. Archakov
出处
期刊:Current Computer - Aided Drug Design
[Bentham Science Publishers]
日期:2007-02-28
卷期号:3 (1): 51-58
被引量:23
标识
DOI:10.2174/157340907780058754
摘要
Protein-protein interactions play a crucial role in numerous vital cell functions. However proteinprotein interactions are also responsible for pathological formation of protein aggregates, which determine the development of several diseases. The key role of protein-protein interactions for manifestation of numerous cell functions attracts much attention to protein complexes as perspective drug targets. So design or discovery of small molecules that would regulate protein-protein interactions represents great pharmacological interest. The recent progress in understanding of mechanism protein-protein interaction, including role of flexibility of protein-protein interfaces, thermodynamic of complex formation, discovery of small molecules modifying protein-protein interactions, the advantages and limitation of protein-protein inhibitors as potential drugs are discussed in this review. Keywords: Protein-protein interaction, inhibitors, target, dimerization, drug, flexibility, allosteric inhibition
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