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POVME 2.0: An Enhanced Tool for Determining Pocket Shape and Volume Characteristics
Author(s) -
Jacob D. Durrant,
Lane Votapka,
Jesper Givskov Sørensen,
Rommie E. Amaro
Publication year - 2014
Publication title -
journal of chemical theory and computation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.001
H-Index - 185
eISSN - 1549-9626
pISSN - 1549-9618
DOI - 10.1021/ct500381c
Subject(s) - druggability , computer science , drug discovery , interface (matter) , volume (thermodynamics) , computational biology , emulation , bioinformatics , data mining , chemistry , biology , physics , biochemistry , operating system , bubble , quantum mechanics , maximum bubble pressure method , gene , economics , economic growth
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.

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