A conformation ensemble approach to protein residue-residue contact

被引:15
|
作者
Eickholt, Jesse [1 ]
Wang, Zheng [1 ]
Cheng, Jianlin [1 ,2 ,3 ]
机构
[1] Univ Missouri, Dept Comp Sci, Columbia, MO 65211 USA
[2] Univ Missouri, Inst Informat, Columbia, MO 65211 USA
[3] Univ Missouri, C Bond Life Sci Ctr, Columbia, MO 65211 USA
关键词
CORRELATED MUTATIONS; PREDICTION; QUALITY;
D O I
10.1186/1472-6807-11-38
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Background: Protein residue-residue contact prediction is important for protein model generation and model evaluation. Here we develop a conformation ensemble approach to improve residue-residue contact prediction. We collect a number of structural models stemming from a variety of methods and implementations. The various models capture slightly different conformations and contain complementary information which can be pooled together to capture recurrent, and therefore more likely, residue-residue contacts. Results: We applied our conformation ensemble approach to free modeling targets from both CASP8 and CASP9. Given a diverse ensemble of models, the method is able to achieve accuracies of. 48 for the top L/5 medium range contacts and. 36 for the top L/5 long range contacts for CASP8 targets (L being the target domain length). When applied to targets from CASP9, the accuracies of the top L/5 medium and long range contact predictions were. 34 and. 30 respectively. Conclusions: When operating on a moderately diverse ensemble of models, the conformation ensemble approach is an effective means to identify medium and long range residue-residue contacts. An immediate benefit of the method is that when tied with a scoring scheme, it can be used to successfully rank models.
引用
收藏
页数:8
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