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AcalPred: A Sequence-Based Tool for Discriminating between Acidic and Alkaline Enzymes

Author

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  • Hao Lin
  • Wei Chen
  • Hui Ding

Abstract

The structure and activity of enzymes are influenced by pH value of their surroundings. Although many enzymes work well in the pH range from 6 to 8, some specific enzymes have good efficiencies only in acidic (pH 9) solution. Studies have demonstrated that the activities of enzymes correlate with their primary sequences. It is crucial to judge enzyme adaptation to acidic or alkaline environment from its amino acid sequence in molecular mechanism clarification and the design of high efficient enzymes. In this study, we developed a sequence-based method to discriminate acidic enzymes from alkaline enzymes. The analysis of variance was used to choose the optimized discriminating features derived from g-gap dipeptide compositions. And support vector machine was utilized to establish the prediction model. In the rigorous jackknife cross-validation, the overall accuracy of 96.7% was achieved. The method can correctly predict 96.3% acidic and 97.1% alkaline enzymes. Through the comparison between the proposed method and previous methods, it is demonstrated that the proposed method is more accurate. On the basis of this proposed method, we have built an online web-server called AcalPred which can be freely accessed from the website (http://lin.uestc.edu.cn/server/AcalPred). We believe that the AcalPred will become a powerful tool to study enzyme adaptation to acidic or alkaline environment.

Suggested Citation

  • Hao Lin & Wei Chen & Hui Ding, 2013. "AcalPred: A Sequence-Based Tool for Discriminating between Acidic and Alkaline Enzymes," PLOS ONE, Public Library of Science, vol. 8(10), pages 1-6, October.
  • Handle: RePEc:plo:pone00:0075726
    DOI: 10.1371/journal.pone.0075726
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    Cited by:

    1. Qiqige Wuyun & Wei Zheng & Yanping Zhang & Jishou Ruan & Gang Hu, 2016. "Improved Species-Specific Lysine Acetylation Site Prediction Based on a Large Variety of Features Set," PLOS ONE, Public Library of Science, vol. 11(5), pages 1-21, May.

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