A multistep docking and scoring protocol for congeneric series: Implementation on kinase DFG-out type II inhibitors

Author:

Granadino-Roldán José M1,Garzón Andrés2,Gomez-Gutierrez Patricia3,Pasamontes-Funez Ignacio4,Santos Tomas Maria5,Rubio-Martinez Jaime4

Affiliation:

1. Departamento de Química Física, Facultad de Ciencias Experimentales, Universidad de Jaén, Campus ‘Las Lagunillas’ s/n, 23071 Jaén, Spain

2. Departamento de Química Física, Facultad de Farmacia, Universidad de Castilla-La Mancha, Paseo de los Estudiantes, s/n, 02071 Albacete, Spain

3. Department of Chemical Engineering, Universitat Politecnica de Catalunya, ETSEIB. Av. Diagonal, 647, 08028 Barcelona, Spain

4. Departament de Ciència dels Materials i Química Física, Universitat de Barcelona (UB) & the Institut de Recerca en Quimica Teorica i Computacional (IQTCUB), Martí i Franqués 1, 08028 Barcelona, Spain

5. Department of Architecture Technology, Universitat Politecnica de Catalunya, Av. Diagonal 649, 08028 Barcelona, Spain

Abstract

Aim: Rescoring of docking-binding poses can significantly improve molecular docking results. Our aim was to evaluate postprocessing docking protocols in order to determine the most suitable methodology for the study of the binding of congeneric compounds to protein kinases. Materials & methods: Diverse ligand-receptor poses generated after docking were submitted to different relaxation protocols. The Molecular Mechanics Poisson–Boltzmann (Generalized Born) Surface Area approach was applied for the evaluation of the binding affinity of complexes obtained. The performance of various Molecular Mechanics Poisson–Boltzmann (Generalized Born) Surface Area methodologies was compared. Results: The inclusion of a postprocessing protocol after docking enhances the quality of the results, although the best methodology is system dependent. Conclusion: An examination of the interactions established has allowed us to suggest useful modifications for the design of new type II inhibitors.

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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