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Received: 2005-08-12

Revision Accepted: 2005-10-23

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Journal of Zhejiang University SCIENCE B 2006 Vol.7 No.1 P.1-6

http://doi.org/10.1631/jzus.2006.B0001


EHPred: an SVM-based method for epoxide hydrolases recognition and classification


Author(s):  Jia Jia, Yang Liang, Zhang Zi-zhang

Affiliation(s):  James. D. Watson Institute of Genome Sciences, Zhejiang University, Hangzhou 310008, China; more

Corresponding email(s):   zhangzz@zju.edu.cn

Key Words:  Epoxide hydrolases (EHs), Amino acid composition (AAC), Dipeptide composition (DPC), Pseudo-amino acid composition (PAAC), Support vector machines (SVM)


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Jia Jia, Yang Liang, Zhang Zi-zhang. EHPred: an SVM-based method for epoxide hydrolases recognition and classification[J]. Journal of Zhejiang University Science B, 2006, 7(1): 1-6.

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journal="Journal of Zhejiang University Science B",
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publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.2006.B0001"
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%A Jia Jia
%A Yang Liang
%A Zhang Zi-zhang
%J Journal of Zhejiang University SCIENCE B
%V 7
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%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.2006.B0001

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PB - Zhejiang University Press & Springer
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DOI - 10.1631/jzus.2006.B0001


Abstract: 
A two-layer method based on support vector machines (SVMs) has been developed to distinguish epoxide hydrolases (EHs) from other enzymes and to classify its subfamilies using its primary protein sequences. SVM classifiers were built using three different feature vectors extracted from the primary sequence of EHs: the amino acid composition (AAC), the dipeptide composition (DPC), and the pseudo-amino acid composition (PAAC). Validated by 5-fold cross tests, the first layer SVM classifier can differentiate EHs and non-EHs with an accuracy of 94.2% and has a Matthew’s correlation coefficient (MCC) of 0.84. Using 2-fold cross validation, PAAC-based second layer SVM can further classify EH subfamilies with an overall accuracy of 90.7% and MCC of 0.87 as compared to AAC (80.0%) and DPC (84.9%). A program called EHPred has also been developed to assist readers to recognize EHs and to classify their subfamilies using primary protein sequences with greater accuracy.

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