A highly accurate protein structural class prediction approach using auto cross covariance transformation and recursive feature elimination

[Display omitted] •Prediction performance of protein structural class has been improved.•A high-quality feature extraction technique has been designed.•A recursive feature selection has been used to reduce feature abundance. Structural class characterizes the overall folding type of a protein or its...

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Veröffentlicht in:Computational biology and chemistry 2015-12, Vol.59, p.95-100
Hauptverfasser: Li, Xiaowei, Liu, Taigang, Tao, Peiying, Wang, Chunhua, Chen, Lanming
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Sprache:eng
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Zusammenfassung:[Display omitted] •Prediction performance of protein structural class has been improved.•A high-quality feature extraction technique has been designed.•A recursive feature selection has been used to reduce feature abundance. Structural class characterizes the overall folding type of a protein or its domain. Many methods have been proposed to improve the prediction accuracy of protein structural class in recent years, but it is still a challenge for the low-similarity sequences. In this study, we introduce a feature extraction technique based on auto cross covariance (ACC) transformation of position-specific score matrix (PSSM) to represent a protein sequence. Then support vector machine-recursive feature elimination (SVM-RFE) is adopted to select top K features according to their importance and these features are input to a support vector machine (SVM) to conduct the prediction. Performance evaluation of the proposed method is performed using the jackknife test on three low-similarity datasets, i.e., D640, 1189 and 25PDB. By means of this method, the overall accuracies of 97.2%, 96.2%, and 93.3% are achieved on these three datasets, which are higher than those of most existing methods. This suggests that the proposed method could serve as a very cost-effective tool for predicting protein structural class especially for low-similarity datasets.
ISSN:1476-9271
1476-928X
DOI:10.1016/j.compbiolchem.2015.08.012