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Binding Energy calculation of GSK-3 protein of Human against some anti-diabetic compounds of Momordica charantia linn (Bitter melon)

机译:人的GSK-3蛋白对苦瓜的某些抗糖尿病化合物的结合能计算

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摘要

Diabetes is one of the major life threatening diseases worldwide. It creates major health problems in urban India. Glycogen Synthase Kinase-3 (GSK-3) protein of human is known for phosphorylating and inactivating glycogen synthase which also acts as a negative regulator in the hormonal control of glucose homeostasis. In traditional medicine, Momordica charantia is used as antidiabetic plant because of its hypoglycemic effect. Hence to block the active site of the GSK-3 protein three anti-diabetic compounds namely, charantin, momordenol & momordicilin were taken from Momordica charantia for docking study and calculation of binding energy. The aim of present investigation is to find the binding energy of three major insulin-like active compounds against glycogen synthase kinase-3 (GSK-3), one of the key proteins involved in carbohydrate metabolism, with the help of molecular docking using ExomeTM Horizon suite. The study recorded minimum binding energy by momordicilin in comparison to the others.
机译:糖尿病是全世界主要的威胁生命的疾病之一。它在印度城市造成严重的健康问题。已知人类的糖原合酶激酶3(GSK-3)蛋白可使糖原合酶磷酸化和失活,该糖原合酶在激素稳态的葡萄糖稳态中也起着负调节剂的作用。在传统医学中,苦瓜由于其降血糖作用而被用作抗糖尿病植物。因此,为了阻断GSK-3蛋白的活性位点,从苦瓜中提取了三种抗糖尿病化合物,即苦瓜素,苦瓜酚和苦瓜素,用于对接研究和计算结合能。本研究的目的是借助ExomeTM Horizo​​n进行分子对接,发现三种主要的胰岛素样活性化合物与糖原合酶激酶3(GSK-3)的结合能,糖原合酶激酶3是参与碳水化合物代谢的关键蛋白质之一。套房。该研究记录了莫莫地林与其他药物相比具有的最小结合能。

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