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Título

MM-ISMSA: An ultrafast and accurate scoring function for protein-protein docking

Autor Klett, Javier ; Núñez, Alfonso; Dos Santos, Helena G.; Cortés Cabrera, Álvaro; Gil Redondo, Rubén ; Abia, David; Gago, Federico ; Morreale, Antonio
Fecha de publicación 2012
EditorAmerican Chemical Society
Citación Journal of Chemical Theory and Computation 8: 3395- 3408 (2012)
ResumenAn ultrafast and accurate scoring function for protein-protein docking is presented. It includes (1) a molecular mechanics (MM) part based on a 12-6 Lennard-Jones potential; (2) an electrostatic component based on an implicit solvent model (ISM) with individual desolvation penalties for each partner in the protein-protein complex plus a hydrogen bonding term; and (3) a surface area (SA) contribution to account for the loss of water contacts upon protein-protein complex formation. The accuracy and performance of the scoring function, termed MM-ISMSA, have been assessed by (1) comparing the total binding energies, the electrostatic term, and its components (charge-charge and individual desolvation energies), as well as the per residue contributions, to results obtained with well-established methods such as APBSA or MM-PB(GB)SA for a set of 1242 decoy protein-protein complexes and (2) testing its ability to recognize the docking solution closest to the experimental structure as that providing the most favorable total binding energy. For this purpose, a test set consisting of 15 protein-protein complexes with known 3D structure mixed with 10 decoys for each complex was used. The correlation between the values afforded by MM-ISMSA and those from the other methods is quite remarkable (r 2 ∼ 0.9), and only 0.2-5.0 s (depending on the number of residues) are spent on a single calculation including an all vs all pairwise energy decomposition. On the other hand, MM-ISMSA correctly identifies the best docking solution as that closest to the experimental structure in 80% of the cases. Finally, MM-ISMSA can process molecular dynamics trajectories and reports the results as averaged values with their standard deviations. MM-ISMSA has been implemented as a plugin to the widely used molecular graphics program PyMOL, although it can also be executed in command-line mode. MM-ISMSA is distributed free of charge to nonprofit organizations. © 2012 American Chemical Society.
URI http://hdl.handle.net/10261/113939
DOI10.1021/ct300497z
Identificadoresdoi: 10.1021/ct300497z
issn: 1549-9618
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