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Protein & Peptide Letters

Editor-in-Chief

ISSN (Print): 0929-8665
ISSN (Online): 1875-5305

Fold Prediction Problem: The Application of New Physical and Physicochemical- Based Features

Author(s): Abdollah Dehzangi and Somnuk Phon-Amnuaisuk

Volume 18, Issue 2, 2011

Page: [174 - 185] Pages: 12

DOI: 10.2174/092986611794475101

Price: $65

Abstract

One of the most important goals in bioinformatics is the ability to predict tertiary structure of a protein from its amino acid sequence. In this paper, new feature groups based on the physical and physicochemical properties of amino acids (size of the amino acids side chains, predicted secondary structure based on normalized frequency of β-Strands, Turns, and Reverse Turns) are proposed to tackle this task. The proposed features are extracted using a modified feature extraction method adapted from Dubchak et al. To study the effectiveness of the proposed features and the modified feature extraction method, AdaBoost.M1, Multi Layer Perceptron (MLP), and Support Vector Machine (SVM) that have been commonly and successfully applied to the protein folding problem are employed. Our experimental results show that the new feature groups altogether with the modified feature extraction method are capable of enhancing the protein fold prediction accuracy better than the previous works found in the literature.

Keywords: Protein fold prediction problem, feature extraction, size of the amino acids' side chain, distribution factor, multi layer perceptron, support vector machine, AdaBoost.M1, protein secondary structure, Strands, KNN, HMM, ANN, SVM, Helix, WEKA, MLP, MMH, complexity parameter, SMO, PKF, SCOP, Van Der Waals bonds, amino acid, Degree of Freedom, Hydrophobicity, Polarity, Polarizability, LDA, Cytochrome C, KnottinsProtein fold prediction problem, feature extraction, size of the amino acids' side chain, distribution factor, multi layer perceptron, support vector machine, AdaBoost.M1, protein secondary structure, Strands, KNN, HMM, ANN, SVM, Helix, WEKA, MLP, MMH, complexity parameter, SMO, PKF, SCOP, Van Der Waals bonds, amino acid, Degree of Freedom, Hydrophobicity, Polarity, Polarizability, LDA, Cytochrome C, Knottins


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