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首页> 外文期刊>Journal of Computer-Aided Molecular Design >PLASS: Protein-ligand affinity statistical score - a knowledge-based force-field model of interaction derived from the PDB
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PLASS: Protein-ligand affinity statistical score - a knowledge-based force-field model of interaction derived from the PDB

机译:PLASS:蛋白质-配体亲和力统计评分-源自PDB的基于知识的相互作用力场模型

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摘要

We have developed PLASS (Protein-Ligand Affinity Statistical Score), a pair-wise potential of mean-force for rapid estimation of the binding affinity of a ligand molecule to a protein active site. This scoring function is derived from the frequency of occurrence of atom-type pairs in crystallographic complexes taken from the Protein Data Bank (PDB). Statistical distributions are converted into distance-dependent contributions to the Gibbs free interaction energy for 10 atomic types using the Boltzmann hypothesis, with only one adjustable parameter. For a representative set of 72 protein-ligand structures, PLASS scores correlate well with the experimentally measured dissociation constants: a correlation coefficient R of 0.82 and RMS error of 2.0 kcal/mol. Such high accuracy results from our novel treatment of the volume correction term, which takes into account the inhomogeneous properties of the protein-ligand complexes. PLASS is able to rank reliably the affinity of complexes which have as much diversity as in the PDB.
机译:我们已经开发出PLASS(蛋白质-配体亲和力统计评分),这是平均力的成对潜力,用于快速估算配体分子与蛋白质活性位点的结合亲和力。该得分函数是从蛋白质数据库(PDB)提取的晶体复合物中原子型对的出现频率得出的。使用Boltzmann假设,仅使用一个可调参数,就可以将统计分布转换为10种原子类型对Gibbs自由相互作用能的距离相关贡献。对于72个蛋白质-配体结构的代表性集合,PLASS评分与实验测得的解离常数相关性很好:相关系数R为0.82,RMS误差为2.0 kcal / mol。如此高的准确性源自我们对体积校正项的新颖处理,该处理考虑了蛋白质-配体复合物的不均匀特性。 PLASS能够可靠地对具有与PDB一样多的多样性的复合物的亲和力进行排名。

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