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The Inhibition of Folylpolyglutamate Synthetase (folC) in the Prevention of Drug Resistance inMycobacterium tuberculosisby Traditional Chinese Medicine

机译:抑制福利聚氨酸盐合成酶(FOLC)在预防耐药性结核病中药中药

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摘要

Tuberculosis (TB) is an infectious disease caused by many strains of mycobacteria, but commonly Mycobacterium tuberculosis. As a possible method of reducing the drug resistance of M. tuberculosis, this research investigates the inhibition of Folylpolyglutamate synthetase, a protein transcript from the resistance association gene folC. After molecular docking to screen the traditional Chinese medicine (TCM) database, the candidate TCM compounds, with Folylpolyglutamate synthetase, were selected by molecular dynamics. The 10,000 ps simulation in association with RMSD analysis and total energy and structural variation defined the protein-ligand interaction. The selected TCM compounds Saussureamine C, methyl 3-O-feruloylquinate, and Labiatic acid have been found to inhibit the activity of bacteria and viruses and to regulate immunity. We also suggest the possible pathway in protein for each ligand. Compared with the control, similar interactions and structural variations indicate that these compounds might have an effect on Folylpolyglutamate synthetase. Finally, we suggest Saussureamine C is the best candidate compound as the complex has a high score, maintains its structural composition, and has a larger variation value than the control, thus inhibiting the drug resistance ability of Mycobacterium tuberculosis.
机译:结核病(TB)是由许多菌株的分枝杆菌引起的传染病,但常见的结核分枝杆菌。作为降低结核分枝杆菌的耐药性的可能的方法中,此研究调查叶酰聚谷氨酸合成酶,从电阻关联基因FOLC蛋白质转录物的抑制。在分子对接后筛选中药(TCM)数据库,通过分子动力学选择候选TCM化合物,用福利戊酰胺合成酶选择。与RMSD分析和总能量和结构变化相关联的10,000 PS模拟限定了蛋白质 - 配体相互作用。已经发现所选的TCM化合物Saussureamin C,甲基3-O-离子链和少清酸抑制细菌和病毒的活性并调节免疫。我们还提出了每个配体的蛋白质中可能的途径。与对照相比,类似的相互作用和结构变化表明这些化合物可能对亚芳基谷氨酸合成酶产生影响。最后,我们建议索斯脲胺C是最佳的候选化合物,因为复合物具有高分,保持其结构组合物,并且具有比对照更大的变化值,从而抑制结核分枝杆菌的耐药能力。

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