A docking score function for estimating ligand-protein interactions: Application to acetylcholinesterase inhibition

被引:54
作者
Guo, JX
Hurley, MM
Wright, JB
Lushington, GH [1 ]
机构
[1] Univ Kansas, Mol Graphics & Modeling Lab, Lawrence, KS 66045 USA
[2] USA, Res Lab, Aberdeen Proving Ground, MD 21005 USA
[3] USA, RDECOM, Natick Soldier Ctr, Natick, MA 01760 USA
关键词
D O I
10.1021/jm049695v
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Acetylcholinesterase (AChE) inhibition is an important research topic because of its wide range of associated health implications. A receptor-specific scoring function was developed herein for predicting binding affinities for human AChE (huAChE) inhibitors. This method entails a statistically trained weighted sum of electrostatic and van der Waals (VDW) interactions between ligands and the receptor residues. Within the 53 ligand training set, a strong correlation was found (R-2 = 0.89) between computed and experimental inhibition constants. Leave-one-out cross-validation indicated high predictive power (Q(2) = 0.72), and analysis of a separate 16-compound test set also produced very good correlation with experiment (R-2 = 0.69). Scoring function analysis has permitted identification and characterization of important ligand-receptor interactions, producing a list of those residues making the most important electrostatic and VDW contributions within the main active site, gorge area, acyl binding pocket, and periferal site. These analyses are consistent with X-ray crystallographic and site-directed mutagenesis studies.
引用
收藏
页码:5492 / 5500
页数:9
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