...
首页> 外文期刊>Journal of computational biology: A journal of computational molecular cell biology >An Effective Exact Algorithm and a New Upper Bound for the Number of Contacts in the Hydrophobic-Polar Two-Dimensional Lattice Model
【24h】

An Effective Exact Algorithm and a New Upper Bound for the Number of Contacts in the Hydrophobic-Polar Two-Dimensional Lattice Model

机译:疏水-极性二维晶格模型中接触数的有效精确算法和新的上限

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Protein Structure Prediction (PSP) is the problem of predicting the three-dimensional native structure of a protein given its primary structure, i.e., the corresponding sequence of amino acids. Different approaches have been proposed to model this problem, and this research explores the prediction of optimal structures using the well studied simplified lattice Hydrophobic and Polar (HP) model—in particular, on the 2D square lattice. We present a twofold result. First, we devise a new upper bound for the number of contacts achievable by an HP sequence, and show that it is in several cases more stringent than the upper bound previously known in literature. Then, we present an innovative algorithm that outperforms the state of the art in exact approaches for the prediction of optimal structures in lattice protein model, for 2D square lattices. The algorithm, called minwalk and based on a heavily pruned exhaustive search, also outperforms the state of the art in non-exact approaches in several cases. Due to this algorithm, it is now possible to prove optimal results in the square 2D lattice, for standard HP sequences of size up to 80 elements, which were only best-known-results previously. Furthermore, we provide the degeneracy (i.e. all optimal solutions) of such benchmark sequences, which was unknown in literature. These results can be a useful tool to foster advances in further research.
机译:蛋白质结构预测(PSP)是在给定蛋白质的一级结构即相应的氨基酸序列的情况下预测蛋白质的三维天然结构的问题。已经提出了不同的方法来对该问题进行建模,并且本研究使用经过充分研究的简化晶格疏水和极性(HP)模型(尤其是在2D方格上)探索了最佳结构的预测。我们提出了双重结果。首先,我们为HP序列可达到的接触数量设计了一个新的上限,并表明在某些情况下它比以前文献中已知的上限更严格。然后,我们提出了一种创新的算法,该算法在精确方法上优于2D正方形晶格的晶格蛋白质模型中最佳结构的预测方法。该算法称为minwalk,它基于严重修剪的穷举搜索,在某些情况下,它在非精确方法中也优于现有技术。由于采用了这种算法,现在有可能在正方形2D晶格中证明最佳结果,对于标准HP序列,其大小最多为80个元素,而这只是以前的最佳结果。此外,我们提供了此类基准序列的简并性(即所有最优解),这在文献中是未知的。这些结果可能是促进进一步研究进展的有用工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号