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PROSPER: An Integrated Feature-Based Tool for Predicting Protease Substrate Cleavage Sites

Author

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  • Jiangning Song
  • Hao Tan
  • Andrew J Perry
  • Tatsuya Akutsu
  • Geoffrey I Webb
  • James C Whisstock
  • Robert N Pike

Abstract

The ability to catalytically cleave protein substrates after synthesis is fundamental for all forms of life. Accordingly, site-specific proteolysis is one of the most important post-translational modifications. The key to understanding the physiological role of a protease is to identify its natural substrate(s). Knowledge of the substrate specificity of a protease can dramatically improve our ability to predict its target protein substrates, but this information must be utilized in an effective manner in order to efficiently identify protein substrates by in silico approaches. To address this problem, we present PROSPER, an integrated feature-based server for in silico identification of protease substrates and their cleavage sites for twenty-four different proteases. PROSPER utilizes established specificity information for these proteases (derived from the MEROPS database) with a machine learning approach to predict protease cleavage sites by using different, but complementary sequence and structure characteristics. Features used by PROSPER include local amino acid sequence profile, predicted secondary structure, solvent accessibility and predicted native disorder. Thus, for proteases with known amino acid specificity, PROSPER provides a convenient, pre-prepared tool for use in identifying protein substrates for the enzymes. Systematic prediction analysis for the twenty-four proteases thus far included in the database revealed that the features we have included in the tool strongly improve performance in terms of cleavage site prediction, as evidenced by their contribution to performance improvement in terms of identifying known cleavage sites in substrates for these enzymes. In comparison with two state-of-the-art prediction tools, PoPS and SitePrediction, PROSPER achieves greater accuracy and coverage. To our knowledge, PROSPER is the first comprehensive server capable of predicting cleavage sites of multiple proteases within a single substrate sequence using machine learning techniques. It is freely available at http://lightning.med.monash.edu.au/PROSPER/.

Suggested Citation

  • Jiangning Song & Hao Tan & Andrew J Perry & Tatsuya Akutsu & Geoffrey I Webb & James C Whisstock & Robert N Pike, 2012. "PROSPER: An Integrated Feature-Based Tool for Predicting Protease Substrate Cleavage Sites," PLOS ONE, Public Library of Science, vol. 7(11), pages 1-23, November.
  • Handle: RePEc:plo:pone00:0050300
    DOI: 10.1371/journal.pone.0050300
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    References listed on IDEAS

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    1. Xiao-Feng Wang & Zhen Chen & Chuan Wang & Ren-Xiang Yan & Ziding Zhang & Jiangning Song, 2011. "Predicting Residue-Residue Contacts and Helix-Helix Interactions in Transmembrane Proteins Using an Integrative Feature-Based Random Forest Approach," PLOS ONE, Public Library of Science, vol. 6(10), pages 1-11, October.
    2. Jianlin Shao & Dong Xu & Sau-Na Tsai & Yifei Wang & Sai-Ming Ngai, 2009. "Computational Identification of Protein Methylation Sites through Bi-Profile Bayes Feature Extraction," PLOS ONE, Public Library of Science, vol. 4(3), pages 1-7, March.
    3. Phaedra Agius & Aaron Arvey & William Chang & William Stafford Noble & Christina Leslie, 2010. "High Resolution Models of Transcription Factor-DNA Affinities Improve In Vitro and In Vivo Binding Predictions," PLOS Computational Biology, Public Library of Science, vol. 6(9), pages 1-12, September.
    4. Yanay Ofran & Burkhard Rost, 2007. "Protein–Protein Interaction Hotspots Carved into Sequences," PLOS Computational Biology, Public Library of Science, vol. 3(7), pages 1-8, July.
    5. Avner Schlessinger & Jinfeng Liu & Burkhard Rost, 2007. "Natively Unstructured Loops Differ from Other Loops," PLOS Computational Biology, Public Library of Science, vol. 3(7), pages 1-12, July.
    6. Jiangning Song & Hao Tan & Khalid Mahmood & Ruby H P Law & Ashley M Buckle & Geoffrey I Webb & Tatsuya Akutsu & James C Whisstock, 2009. "Prodepth: Predict Residue Depth by Support Vector Regression Approach from Protein Sequences Only," PLOS ONE, Public Library of Science, vol. 4(9), pages 1-14, September.
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    1. Sonu Kumar & Boris I Ratnikov & Marat D Kazanov & Jeffrey W Smith & Piotr Cieplak, 2015. "CleavPredict: A Platform for Reasoning about Matrix Metalloproteinases Proteolytic Events," PLOS ONE, Public Library of Science, vol. 10(5), pages 1-19, May.
    2. Huilin Wang & Mingjun Wang & Hao Tan & Yuan Li & Ziding Zhang & Jiangning Song, 2014. "PredPPCrys: Accurate Prediction of Sequence Cloning, Protein Production, Purification and Crystallization Propensity from Protein Sequences Using Multi-Step Heterogeneous Feature Fusion and Selection," PLOS ONE, Public Library of Science, vol. 9(8), pages 1-17, August.
    3. Sheng-Hung Juan & Teng-Ruei Chen & Wei-Cheng Lo, 2020. "A simple strategy to enhance the speed of protein secondary structure prediction without sacrificing accuracy," PLOS ONE, Public Library of Science, vol. 15(6), pages 1-26, June.
    4. Julian E Fuchs & Susanne von Grafenstein & Roland G Huber & Christian Kramer & Klaus R Liedl, 2013. "Substrate-Driven Mapping of the Degradome by Comparison of Sequence Logos," PLOS Computational Biology, Public Library of Science, vol. 9(11), pages 1-15, November.

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