A Novel Average Measure Approach to the Identification of Native-Like Protein Structures Among Decoy Sets

被引:1
|
作者
Li, Juan [2 ]
Fang, Caiyun [1 ]
Fang, Huisheng [1 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Med, Affiliated Hosp, Dept Hematol,Nanjing Drum Tower Hosp, Nanjing 210008, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Ab initio prediction; CASP; decoy; native-like protein structures; STRUCTURE PREDICTION; FOLD RECOGNITION; QUALITY ASSESSMENT; ENERGY FUNCTIONS; MODELS; CONSENSUS; REFINEMENT; CORRECT; PCONS;
D O I
10.2174/1574893608666131203224654
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It is a great challenge to predict a protein structure and this challenge has fascinated researchers in different disciplines for many years. Basically the prediction process mainly includes two steps. With the first step that the generation of prediction model increasing fast, the second step that the quality estimation of predicted model i.e. identification of models' native like structure becomes more and more important. In this study, we developed a simple and effective approach to identify the native-like protein structures among a set of decoys. Three different average measures were used in our study as follows: the average rmsd (armsd), the average alignment score (AAS) and MAXSUB. This approach was evaluated by decoy set (Park-Levitt). Comparison of model quality revealed that a significant correlation existed between these parameters. For example, the average measure could be effectively used to identify native-like protein models. The performance of both armsd and AAS was better than that of clustering. Since many other measures could be used to assess the similarity between protein structures, other analogous approaches might be also useful for the identification of native-like proteins. Finally, data showed that its performance was better than that of other servers in predicting the targets in CASP6, CASP7, CASP9 and CASP10.
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页码:194 / 201
页数:8
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