Department of Chemistry, Seoul National University, Seoul 08826, Korea.
Nucleic Acids Res. 2019 Jul 2;47(W1):W451-W455. doi: 10.1093/nar/gkz288.
The 3D structure of a protein can be predicted from its amino acid sequence with high accuracy for a large fraction of cases because of the availability of large quantities of experimental data and the advance of computational algorithms. Recently, deep learning methods exploiting the coevolution information obtained by comparing related protein sequences have been successfully used to generate highly accurate model structures even in the absence of template structure information. However, structures predicted based on either template structures or related sequences require further improvement in regions for which information is missing. Refining a predicted protein structure with insufficient information on certain regions is critical because these regions may be connected to functional specificity that is not conserved among related proteins. The GalaxyRefine2 web server, freely available via http://galaxy.seoklab.org/refine2, is an upgraded version of the GalaxyRefine protein structure refinement server and reflects recent developments successfully tested through CASP blind prediction experiments. This method adopts an iterative optimization approach involving various structure move sets to refine both local and global structures. The estimation of local error and hybridization of available homolog structures are also employed for effective conformation search.
由于大量实验数据的可用性和计算算法的进步,蛋白质的 3D 结构可以从其氨基酸序列中以高精度预测,对于很大一部分情况都是如此。最近,利用通过比较相关蛋白质序列获得的共进化信息的深度学习方法已成功用于生成高度准确的模型结构,即使在没有模板结构信息的情况下也是如此。然而,基于模板结构或相关序列预测的结构需要在信息缺失的区域进一步改进。对于某些区域信息不足的预测蛋白质结构进行细化至关重要,因为这些区域可能与功能特异性有关,而功能特异性在相关蛋白质中并不保守。GalaxyRefine2 网络服务器可通过 http://galaxy.seoklab.org/refine2 免费获得,是 GalaxyRefine 蛋白质结构细化服务器的升级版,反映了通过 CASP 盲预测实验成功测试的最新发展。该方法采用涉及各种结构移动集的迭代优化方法来细化局部和全局结构。还利用局部误差估计和可用同源结构的杂交来进行有效的构象搜索。