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Article

An Investigation of Molecular Docking and Molecular Dynamic Simulation on Imidazopyridines as B-Raf Kinase Inhibitors

1
Department of Chemistry, Yunnan University, Kunming 650091, China
2
Department of Chemistry, School of Pharmaceutical Science & Yunnan Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming 650500, China
*
Authors to whom correspondence should be addressed.
Academic Editor: Christo Z. Christov
Int. J. Mol. Sci. 2015, 16(11), 27350-27361; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms161126026
Received: 26 September 2015 / Revised: 31 October 2015 / Accepted: 6 November 2015 / Published: 16 November 2015
In the recent cancer treatment, B-Raf kinase is one of key targets. Nowadays, a group of imidazopyridines as B-Raf kinase inhibitors have been reported. In order to investigate the interaction between this group of inhibitors and B-Raf kinase, molecular docking, molecular dynamic (MD) simulation and binding free energy (ΔGbind) calculation were performed in this work. Molecular docking was carried out to identify the key residues in the binding site, and MD simulations were performed to determine the detail binding mode. The results obtained from MD simulation reveal that the binding site is stable during the MD simulations, and some hydrogen bonds (H-bonds) in MD simulations are different from H-bonds in the docking mode. Based on the obtained MD trajectories, ΔGbind was computed by using Molecular Mechanics Generalized Born Surface Area (MM-GBSA), and the obtained energies are consistent with the activities. An energetic analysis reveals that both electrostatic and van der Waals contributions are important to ΔGbind, and the unfavorable polar solvation contribution results in the instability of the inhibitor with the lowest activity. These results are expected to understand the binding between B-Raf and imidazopyridines and provide some useful information to design potential B-Raf inhibitors. View Full-Text
Keywords: imidazopyridine; B-Raf kinase; molecular docking; molecular dynamic simulation imidazopyridine; B-Raf kinase; molecular docking; molecular dynamic simulation
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MDPI and ACS Style

Xie, H.; Li, Y.; Yu, F.; Xie, X.; Qiu, K.; Fu, J. An Investigation of Molecular Docking and Molecular Dynamic Simulation on Imidazopyridines as B-Raf Kinase Inhibitors. Int. J. Mol. Sci. 2015, 16, 27350-27361. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms161126026

AMA Style

Xie H, Li Y, Yu F, Xie X, Qiu K, Fu J. An Investigation of Molecular Docking and Molecular Dynamic Simulation on Imidazopyridines as B-Raf Kinase Inhibitors. International Journal of Molecular Sciences. 2015; 16(11):27350-27361. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms161126026

Chicago/Turabian Style

Xie, Huiding, Yupeng Li, Fang Yu, Xiaoguang Xie, Kaixiong Qiu, and Jijun Fu. 2015. "An Investigation of Molecular Docking and Molecular Dynamic Simulation on Imidazopyridines as B-Raf Kinase Inhibitors" International Journal of Molecular Sciences 16, no. 11: 27350-27361. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms161126026

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