POVME 2.0: An Enhanced Tool for Determining Pocket Shape and Volume Characteristics

被引:203
作者
Durrant, Jacob D. [1 ,2 ]
Votapka, Lane [1 ]
Sorensen, Jesper [1 ]
Amaro, Rommie E. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Ctr Res Biol Syst, Natl Biomed Computat Resource, La Jolla, CA 92093 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
PROTEIN-PROTEIN INTERACTION; MOLECULAR-DYNAMICS; TRYPANOSOMA-BRUCEI; BIOMOLECULAR SIMULATIONS; DRUG DESIGN; STRUCTURAL ENSEMBLES; BINDING POCKETS; CAVITIES; IDENTIFICATION; RECEPTOR;
D O I
10.1021/ct500381c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Analysis of macromolecular/small-molecule binding pockets can provide important insights into molecular recognition and receptor dynamics. Since its release in 2011, the POVME (POcket Volume MEasurer) algorithm has been widely adopted as a simple-to-use tool for measuring and characterizing pocket volumes and shapes. We here present POVME 2.0, which is an order of magnitude faster, has improved accuracy, includes a graphical user interface, and can produce volumetric density maps for improved pocket analysis. To demonstrate the utility of the algorithm, we use it to analyze the binding pocket of RNA editing ligase 1 from the unicellular parasite Trypanosoma brucei, the etiological agent of African sleeping sickness. The POVME analysis characterizes the full dynamics of a potentially druggable transient binding pocket and so may guide future antitrypanosomal drug-discovery efforts. We are hopeful that this new version will be a useful tool for the computational- and medicinal-chemist community.
引用
收藏
页码:5047 / 5056
页数:10
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