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使用蛋白质-配体相互作用指纹图谱分析多靶点活性景观:相互作用悬崖

Analyzing multitarget activity landscapes using protein-ligand interaction fingerprints: interaction cliffs.

作者信息

Méndez-Lucio Oscar, Kooistra Albert J, de Graaf Chris, Bender Andreas, Medina-Franco José L

机构信息

Centre for Molecular Informatics, Department of Chemistry, University of Cambridge , Lensfield Road, Cambridge CB2 1EW, United Kingdom.

出版信息

J Chem Inf Model. 2015 Feb 23;55(2):251-62. doi: 10.1021/ci500721x. Epub 2015 Feb 6.

Abstract

Activity landscape modeling is mostly a descriptive technique that allows rationalizing continuous and discontinuous SARs. Nevertheless, the interpretation of some landscape features, especially of activity cliffs, is not straightforward. As the nature of activity cliffs depends on the ligand and the target, information regarding both should be included in the analysis. A specific way to include this information is using protein-ligand interaction fingerprints (IFPs). In this paper we report the activity landscape modeling of 507 ligand-kinase complexes (from the KLIFS database) including IFP, which facilitates the analysis and interpretation of activity cliffs. Here we introduce the structure-activity-interaction similarity (SAIS) maps that incorporate information on ligand-target contact similarity. We also introduce the concept of interaction cliffs defined as ligand-target complexes with high structural and interaction similarity but have a large potency difference of the ligands. Moreover, the information retrieved regarding the specific interaction allowed the identification of activity cliff hot spots, which help to rationalize activity cliffs from the target point of view. In general, the information provided by IFPs provides a structure-based understanding of some activity landscape features. This paper shows examples of analyses that can be carried out when IFPs are added to the activity landscape model.

摘要

活性景观建模主要是一种描述性技术,可用于对连续和不连续的构效关系进行合理化分析。然而,对某些景观特征的解释,尤其是对活性断崖的解释并不简单。由于活性断崖的性质取决于配体和靶点,分析中应同时包含有关两者的信息。包含此信息的一种特定方法是使用蛋白质-配体相互作用指纹(IFP)。在本文中,我们报告了507种配体-激酶复合物(来自KLIFS数据库)的活性景观建模,其中包括IFP,这有助于对活性断崖进行分析和解释。在这里,我们引入了结构-活性-相互作用相似性(SAIS)图,该图纳入了配体-靶点接触相似性的信息。我们还引入了相互作用断崖的概念,定义为具有高结构和相互作用相似性但配体效力差异很大的配体-靶点复合物。此外,所检索到的关于特定相互作用的信息有助于识别活性断崖热点,这有助于从靶点角度对活性断崖进行合理化分析。一般来说,IFP提供的信息有助于基于结构理解某些活性景观特征。本文展示了在将IFP添加到活性景观模型时可以进行的分析示例。

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