Zhang Ming, Chen Changjun, He Yi, Xiao Yi
Biomolecular Physics and Modeling Group, Department of Physics, Huazhong University of Science and Technology, Wuhan 430074, Hubei, China.
Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Nov;72(5 Pt 1):051919. doi: 10.1103/PhysRevE.72.051919. Epub 2005 Nov 16.
Improvements were made on a simplified protein model--the Ramachandran model-to achieve better computer simulation of protein folding. To check the validity of such improvements, we chose the ultrafast folding protein Engrailed Homeodomain as an example and explored several aspects of its folding. The engrailed homeodomain is a mainly alpha-helical protein of 61 residues from Drosophila melanogaster. We found that the simplified model of Engrailed Homeodomain can fold into a global minimum state with a tertiary structure in good agreement with its native structure.
为了更好地对蛋白质折叠进行计算机模拟,对一个简化的蛋白质模型——拉马钱德兰模型进行了改进。为检验这些改进的有效性,我们选择超快速折叠蛋白果蝇Engrailed同源域作为示例,并对其折叠的几个方面进行了探索。Engrailed同源域是一种来自黑腹果蝇的主要由61个残基组成的α螺旋蛋白。我们发现,Engrailed同源域的简化模型能够折叠成一个全局最小状态,其三级结构与其天然结构高度吻合。