Sekhar Pagadala Nataraj, Kishor Polavarapu B Kavi, Reddy Lakkireddy Ananda, Mondal Prosenjit, Dash Ardhendu K, Kar Manoranjan, Mohanty Satya, Sabat Surendra C
Department of Genetics, Osmania University, Hyderabad - 500 007, India.
In Silico Biol. 2006;6(5):435-47.
Homology modeling of the catalase, CatC cloned and sequenced from rice (Oryza sativa L., cv Ratna an Indica cultivar) has been performed based on the crystal structure of the catalase CatF (PDB code 1m7s) by using the software MODELLER. With the aid of molecular mechanics and molecular dynamics methods, the final model is obtained and is further assessed by PROCHECK and VERIFY - 3D graph, which show that the final refined model is reliable. With this model, a flexible docking study with the hydrogen peroxide, the substrate for catalase, is performed and the results indicate that Arg310, Asp343 and Arg346 in catalase are three important determinant residues in binding as they have strong hydrogen bonding contacts with the substrate. These hydrogen-bonding interactions play an important role for the stability of the complex. Our results may be helpful for further experimental investigations.
基于过氧化氢酶CatF(蛋白质数据银行代码1m7s)的晶体结构,利用MODELLER软件对从水稻(籼稻品种Ratna)中克隆并测序的过氧化氢酶CatC进行了同源建模。借助分子力学和分子动力学方法获得了最终模型,并通过PROCHECK和VERIFY - 3D图进一步评估,结果表明最终优化后的模型是可靠的。利用该模型,对过氧化氢酶的底物过氧化氢进行了柔性对接研究,结果表明过氧化氢酶中的精氨酸310、天冬氨酸343和精氨酸346是结合过程中的三个重要决定残基,因为它们与底物有很强的氢键接触。这些氢键相互作用对复合物的稳定性起着重要作用。我们的结果可能有助于进一步的实验研究。