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首页> 外文期刊>Journal of chemical information and modeling >Knowledge-based scoring functions in drug design. 1. Developing a target-specific method for kinase-ligand interactions
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Knowledge-based scoring functions in drug design. 1. Developing a target-specific method for kinase-ligand interactions

机译:药物设计中基于知识的评分功能。 1.开发激酶-配体相互作用的靶标特异性方法

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Protein kinases are attractive targets for therapeutic interventions in many diseases. Due to their importance ?n drug discovery, a kinase family-specific potential of mean force (PMF) scoring function, kinase-PMF, was developed to assess the binding of ATP-competitive kinase inhibitors. It is hypothesized that target-specific PMF scoring functions may achieve increased performance in scoring along with the growth of the PDB database. The kinase-PMF inherits the functions and atom types in PMF04 and uses a kinase data set of 872 complexes to derive the potentials. The performance of kinase-PMF was evaluated with an external test set containing 128 kinase crystal structures. We compared it with eight scoring functions commonly used in computer-aided drug design, either in terms of the retrieval rate of retrieving "right" conformations or a virtual screening study. The evaluation results clearly demonstrate that a target-specific scoring function is a promising way to improve prediction power in structure-based drug design compared with other general scoring functions. To provide this rescoring service for researchers, a publicly accessible Web site was established at http://202.127.30.184:8080/ scoring/index.jsp.
机译:蛋白激酶是许多疾病中治疗干预的有吸引力的靶标。由于它们在药物发现中的重要性,开发了一种激酶家族特异的平均力(PMF)评分功能,即激酶-PMF,以评估ATP竞争性激酶抑制剂的结合。假设随着PDB数据库的增长,特定于目标的PMF评分功能可以在评分方面实现更高的性能。激酶-PMF继承了PMF04中的功能和原子类型,并使用872个配合物的激酶数据集来推导电势。使用包含128个激酶晶体结构的外部测试仪评估了激酶PMF的性能。我们将其与计算机辅助药物设计中常用的八种评分功能进行了比较,无论是检索“正确”构象的检索率还是虚拟筛选研究。评估结果清楚地表明,与其他一般评分功能相比,特定于目标的评分功能是提高基于结构的药物设计预测能力的一种有前途的方法。为了向研究人员提供这种评分服务,在http://202.127.30.184:8080/ scoring / index.jsp上建立了可公开访问的网站。

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