An Improved Integration of Template-Based and Template-Free Protein Structure Modeling Methods and its Assessment in CASP11

被引:8
|
作者
Li, Jilong [1 ]
Adhikari, Badri [1 ]
Cheng, Jianlin [1 ,2 ]
机构
[1] Univ Missouri, Dept Comp Sci, Columbia, MO 65211 USA
[2] Univ Missouri, Inst Informat, Columbia, MO 65211 USA
来源
PROTEIN AND PEPTIDE LETTERS | 2015年 / 22卷 / 07期
关键词
Model generation; model selection; protein structure prediction; sequence alignment; template-based modeling; template-free modeling; STRUCTURE PREDICTION; QUALITY ASSESSMENT; SOFTWARE SUITE; FEATURES; MULTICOM; SATISFACTION; SECONDARY; ALIGNMENT; SEQUENCE; SINGLE;
D O I
10.2174/0929866522666150520145717
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
Most computational protein structure prediction methods are designed for either template-based or template-free (ab initio) structure prediction. The approaches that integrate the prediction capabilities of both template-based modeling and template-free modeling are needed to synergistically combine the two kinds of methods to improve protein structure prediction. In this work, we develop a new method to integrate several protein structure prediction methods including our template-based MULTICOM server, our ab initio contact-based protein structure prediction method CONFOLD, our multi-template-based model generation tool MTMG, and locally installed external Rosetta, I-TASSER and RaptorX protein structure prediction tools to improve protein structure prediction of a full-spectrum difficulty ranging from easy, to medium and to hard. Our method participated in the 11th community-wide Critical Assessment of Techniques for Protein Structure Prediction (CASP11) in 2014 as MULTICOM-NOVEL server. It was ranked among top 10 methods for protein tertiary structure prediction according to the official CASP11 assessment, which demonstrates that integrating complementary modeling methods is useful for advancing protein structure prediction.
引用
收藏
页码:586 / 593
页数:8
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