CASP9 assessment of free modeling target predictions

被引:73
作者
Kinch, Lisa [1 ]
Shi, Shuo Yong [2 ]
Cong, Qian [2 ]
Cheng, Hua [2 ]
Liao, Yuxing [2 ]
Grishin, Nick V. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
protein-fold prediction; structure comparison; alignment quality; ab-initio; domain structure; CASP9; PROTEIN-STRUCTURE PREDICTION; ALL-ATOM REFINEMENT; SECONDARY STRUCTURE; STRUCTURE ALIGNMENT; I-TASSER; ROSETTA; RECOGNITION;
D O I
10.1002/prot.23181
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
We present an overview of the ninth round of Critical Assessment of Protein Structure Prediction (CASP9) "Template free modeling" category (FM). Prediction models were evaluated using a combination of established structural and sequence comparison measures and a novel automated method designed to mimic manual inspection by capturing both global and local structural features. These scores were compared to those assigned manually over a diverse subset of target domains. Scores were combined to compare overall performance of participating groups and to estimate rank significance. Moreover, we discuss a few examples of free modeling targets to highlight the progress and bottlenecks of current prediction methods. Notably, a server prediction model for a single target (T0581) improved significantly over the closest structure template (44% GDT increase). This accomplishment represents the "winner" of the CASP9 FM category. A number of human expert groups submitted slight variations of this model, highlighting a trend for human experts to act as "meta predictors" by correctly selecting among models produced by the top-performing automated servers. The details of evaluation are available at http://prodata.swmed.edu/CASP9/. Proteins 2011; 79(Suppl 10):59-73. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:59 / 73
页数:15
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