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      Prediction of Enzyme Mutant Activity Using Computational Mutagenesis and Incremental Transduction

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      Advances in Bioinformatics
      Hindawi Publishing Corporation

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          Abstract

          Wet laboratory mutagenesis to determine enzyme activity changes is expensive and time consuming. This paper expands on standard one-shot learning by proposing an incremental transductive method (T2bRF) for the prediction of enzyme mutant activity during mutagenesis using Delaunay tessellation and 4-body statistical potentials for representation. Incremental learning is in tune with both eScience and actual experimentation, as it accounts for cumulative annotation effects of enzyme mutant activity over time. The experimental results reported, using cross-validation, show that overall the incremental transductive method proposed, using random forest as base classifier, yields better results compared to one-shot learning methods. T2bRF is shown to yield 90% on T4 and LAC (and 86% on HIV-1). This is significantly better than state-of-the-art competing methods, whose performance yield is at 80% or less using the same datasets.

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          Boosting the margin: a new explanation for the effectiveness of voting methods

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            Statitical Learning Theory

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              Accurate prediction of stability changes in protein mutants by combining machine learning with structure based computational mutagenesis.

              Accurate predictive models for the impact of single amino acid substitutions on protein stability provide insight into protein structure and function. Such models are also valuable for the design and engineering of new proteins. Previously described methods have utilized properties of protein sequence or structure to predict the free energy change of mutants due to thermal (DeltaDeltaG) and denaturant (DeltaDeltaG(H2O)) denaturations, as well as mutant thermal stability (DeltaT(m)), through the application of either computational energy-based approaches or machine learning techniques. However, accuracy associated with applying these methods separately is frequently far from optimal. We detail a computational mutagenesis technique based on a four-body, knowledge-based, statistical contact potential. For any mutation due to a single amino acid replacement in a protein, the method provides an empirical normalized measure of the ensuing environmental perturbation occurring at every residue position. A feature vector is generated for the mutant by considering perturbations at the mutated position and it's ordered six nearest neighbors in the 3-dimensional (3D) protein structure. These predictors of stability change are evaluated by applying machine learning tools to large training sets of mutants derived from diverse proteins that have been experimentally studied and described. Predictive models based on our combined approach are either comparable to, or in many cases significantly outperform, previously published results. A web server with supporting documentation is available at http://proteins.gmu.edu/automute.
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                Author and article information

                Journal
                Adv Bioinformatics
                ABI
                Advances in Bioinformatics
                Hindawi Publishing Corporation
                1687-8027
                1687-8035
                2011
                9 October 2011
                : 2011
                : 958129
                Affiliations
                Department of Computer Science, George Mason University, 4400 University Drive, Fairfax, VA 22030, USA
                Author notes

                Academic Editor: Sandor Vajda

                Article
                10.1155/2011/958129
                3189455
                22007208
                0803ed90-1a25-444f-8df1-ba1c59aa2032
                Copyright © 2011 N. Basit and H. Wechsler.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 8 May 2011
                : 27 June 2011
                : 4 August 2011
                Categories
                Research Article

                Bioinformatics & Computational biology
                Bioinformatics & Computational biology

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