Insights into the Interactions between Maleimide Derivates and GSK3 beta Combining Molecular Docking and QSAR

Quesada-Romero, L.; Mena-Ulecia, K.; Tiznado, W.; Caballero, J.

Abstract

Many protein kinase (PK) inhibitors have been reported in recent years, but only a few have been approved for clinical use. The understanding of the available molecular information using computational tools is an alternative to contribute to this process. With this in mind, we studied the binding modes of 77 maleimide derivates inside the PK glycogen synthase kinase 3 beta (GSK3 beta) using docking experiments. We found that the orientations that these compounds adopt inside GSK3 beta binding site prioritize the formation of hydrogen bond (HB) interactions between the maleimide group and the residues at the hinge region (residues Val135 and Asp133), and adopt propeller-like conformations (where the maleimide is the propeller axis and the heterocyclic substituents are two slanted blades). In addition, quantitative structure-activity relationship (QSAR) models using CoMSIA methodology were constructed to explain the trend of the GSK3 beta inhibitory activities for the studied compounds. We found a model to explain the structure-activity relationship of non-cyclic maleimide (NCM) derivatives (54 compounds). The best CoMSIA model (training set included 44 compounds) included steric, hydrophobic, and HB donor fields and had a good Q(2) value of 0.539. It also predicted adequately the most active compounds contained in the test set. Furthermore, the analysis of the plots of the steric CoMSIA field describes the elements involved in the differential potency of the inhibitors that can be considered for the selection of suitable inhibitors.

Más información

Título según WOS: Insights into the Interactions between Maleimide Derivates and GSK3 beta Combining Molecular Docking and QSAR
Título según SCOPUS: Insights into the interactions between maleimide derivates and GSK3? combining molecular docking and QSAR
Título de la Revista: PLOS ONE
Volumen: 9
Número: 7
Editorial: PUBLIC LIBRARY SCIENCE
Fecha de publicación: 2014
Idioma: English
URL: http://dx.plos.org/10.1371/journal.pone.0102212
DOI:

10.1371/journal.pone.0102212

Notas: ISI, SCOPUS - ISI, SCOPUS