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

被引:25
作者
Hazarika, Ridip [1 ]
Parida, Pratap [2 ]
Neog, Bijoy [1 ]
Yadav, Raj Narain Singh [2 ]
机构
[1] Dibrugarh Univ, Dept Life Sci, Dibrugarh 786004, Assam, India
[2] Dibrugarh Univ, BIF, Ctr Studies Biotechnol, Dibrugarh 786004, Assam, India
关键词
anti-diabetic; docking; Exome (TM) Horizon suite; GSK-3; Momordica charantia;
D O I
10.6026/97320630008251
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
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 Exome (TM) Horizon suite. The study recorded minimum binding energy by momordicilin in comparison to the others.
引用
收藏
页码:251 / 254
页数:4
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