Rykunov Dmitry, Steinberger Elliot, Madrid-Aliste Carlos J, Fiser András
Department of Systems and Computational Biology, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, NY 10461, USA.
J Struct Funct Genomics. 2009 Mar;10(1):95-9. doi: 10.1007/s10969-008-9044-9. Epub 2008 Nov 5.
Improvements in comparative protein structure modeling for the remote target-template sequence similarity cases are possible through the optimal combination of multiple template structures and by improving the quality of target-template alignment. Recently developed MMM and M4T methods were designed to address these problems. Here we describe new developments in both the alignment generation and the template selection parts of the modeling algorithms. We set up a new scoring function in MMM to deliver more accurate target-template alignments. This was achieved by developing and incorporating into the composite scoring function a novel statistical pairwise potential that combines local and non-local terms. The non-local term of the statistical potential utilizes a shuffled reference state definition that helped to eliminate most of the false positive signal from the background distribution of pairwise contacts. The accuracy of the scoring function was further increased by using BLOSUM mutation table scores.
通过多个模板结构的最佳组合以及提高目标-模板比对的质量,可以改进针对远程目标-模板序列相似性情况的比较蛋白质结构建模。最近开发的MMM和M4T方法旨在解决这些问题。在此,我们描述了建模算法中比对生成和模板选择部分的新进展。我们在MMM中设置了一个新的评分函数,以提供更准确的目标-模板比对。这是通过开发一种新颖的统计成对势并将其纳入复合评分函数来实现的,该统计成对势结合了局部和非局部项。统计势的非局部项利用了一种洗牌参考状态定义,有助于从成对接触的背景分布中消除大部分假阳性信号。通过使用BLOSUM突变表分数,评分函数的准确性进一步提高。