来自着色植物(Stenochlaena palutris)的化学物质作为农药暴露导致的 ALK 蛋白损伤的竞争者的潜力:硅研究

Sarmila Sarmila, Nafisah Nafisah, Hanna Habibah, Indah Saputri, Indah Setiawati, N. Komari
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引用次数: 0

摘要

农药活性成分对目标生物和非目标生物具有广泛的毒性影响。持续接触杀虫剂会导致癌症。Kelakai 被认为对癌细胞的生长具有潜在的细胞毒性活性。本研究的目的是在硅学中检验暴露于有机磷农药的无性淋巴瘤激酶(ALK)蛋白上的化合物的潜在活性。使用 Chimera 程序制备蛋白质和配体,使用 SwissDock 进行对接,以及使用 pkCSM 网络和 ProTox 进行虚拟筛选。乙硫磷和新对二甲苯的 ∆G 值最负,分别为 -8.62 kcal/mol 和 -8.39 kcal/mol。乙硫磷和新对二甲苯化合物与 ALK 蛋白的结合位点正好位于 ALK 蛋白的活性位点。乙硫磷是毒性最大的有机磷农药,具有细胞致病性。凯拉凯化合物中的新对二甲苯有可能成为抑制 ALK 蛋白的竞争者。乙硫磷和新戊二烯在 ALK 蛋白质中的结合残基类型和数量相似,这表明乙硫磷和新戊二烯之间存在竞争。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential of Chemical Compounds from Coloring Plants (Stenochlaena palutris) as Competitors for ALK Protein Damage Due To Pesticide Exposure: In Silico Study
Pesticide active ingredients have widespread toxicity effects on target and non-target organisms. Continuous exposure to pesticides causes cancer. Kelakai is thought to have potential cytotoxic activity against the growth of cancer cells. The aim of this research is to examine the potential activity of chemical compounds on Anaplastic Lymphoma Kinase (ALK) proteins exposed to organophosphate pesticides in silico. Protein and ligand preparation with the Chimera program, Docking using SwissDock, as well as virtual screening using the pkCSM web and ProTox. Ethion and neophytadiene have the most negative ∆G values of -8.62 kcal/mol and -8.39 kcal/mol, respectively. The binding site for ethion and neophytadiene compounds with the ALK protein is right at the active site of the ALK protein. Ethion is the most toxic organophosphate pesticide and has the potential to be cytogenic. Neophytadiene from kelakai compounds has the potential to act as a competitor in inhibiting the ALK protein. The similarity in the type and number of binding residues in ethion and neophytadiene in the ALK protein indicates competition between ethion and neophytadiene.
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