以InhA、MabA和PanK为受体的酒精类化合物作为分枝杆菌剂的分子对接和分子动力学研究

G. Syahputra, A. Arwansyah, W. Kusharyoto
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引用次数: 1

摘要

结核病感染是许多发展中国家的主要传染病之一;甚至在一些发达国家也有轻微的病例。结核病感染通过空气传播,当对与结核病研究有关的医疗和实验室设备使用不适当的消毒剂时,感染的可能性更大。实验室设备中常用的适当消毒剂可以减少结核病传播的风险。酒精类化合物是常用的消毒剂之一,对微生物、病毒和真菌具有广谱活性。通过分子对接和分子动力学模拟,支持虚拟筛选和配体-受体复合物结合观察,寻找合适的杀菌剂。基于分子对接和分子动力学分析,戊烷醇具有以PanK为特异性受体的抗菌活性。pentadecanol与pankl相互作用的吉布斯自由能∆G为-5.5 kcal/mol。分子动力学分析表明,在300K和1atm作用5ns时,结合位点的确认变化不大,而五戊醇仍然被其结合位点PanK结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Docking and Molecular Dynamics Study of Alcoholic Compounds as Mycobactericidal Agents Using InhA, MabA and PanK as Receptors
     Tuberculosis (TB) infection is one of the primaryinfectious diseases in many developing countries; even there are minor cases in some developed countries. TB infection spread through the air and ismore probable when using improper disinfectant on medical and laboratory equipment which related to TB research. The appropriate disinfectants which are commonly usedin laboratory equipment can reduce the risk of transmission of TB disease. Alcoholic compoundsare one of the common disinfectants with a broad spectrum activity towardsmicrobes,viruses, and fungus. We employed molecular docking and molecular dynamics simulation to support virtual screening and ligand-receptor complex binding observation in searching for an appropriate mycobactericidal agent.Based on the analysis of molecular docking and molecular dynamics, pentadecanol has potency as a mycobactericidal agent with PanK as itsspecific receptor. The Gibbs free energy (∆G) for the interaction of pentadecanol with PanKhas been found to be -5.5 kcal/mol. Molecular dynamics analysis at 300K and 1 atm for 5 ns showed a little change in the confirmation of the binding site, whilepentadecanolwas still being bound by its binding siteon PanK.
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