Improved beta-protein structure prediction by multilevel optimization of NonLocal strand pairings and local backbone conformation

被引:47
作者
Bradley, Philip [1 ]
Baker, David [1 ]
机构
[1] Univ Washington, Dept Biochem & HHMI, Seattle, WA 98195 USA
关键词
protein structure prediction; beta-sheet; fragment assembly; Rosetta;
D O I
10.1002/prot.21133
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins with complex, nonlocal beta-sheets are challenging for de novo structure prediction, due in part to the difficulty of efficiently sampling long-range strand pairings. We present a new, multilevel approach to beta-sheet structure prediction that circumvents this difficulty by reformulating structure generation in terms of a folding tree. Nonlocal connections in this tree allow us to explicitly sample alternative beta-strand pairings while simultaneously exploring local conformational space using backbone torsion-space moves. An iterative, energy-biased resampling strategy is used to explore the space of beta-strand pairings; we expect that such a strategy will be generally useful for searching large conformational spaces with a high degree of combinatorial complexity.
引用
收藏
页码:922 / 929
页数:8
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