Literature DB >> 26233307

Identification of Heat Shock Protein families and J-protein types by incorporating Dipeptide Composition into Chou's general PseAAC.

Saeed Ahmad1, Muhammad Kabir1, Maqsood Hayat2.   

Abstract

Heat Shock Proteins (HSPs) are the substantial ingredients for cell growth and viability, which are found in all living organisms. HSPs manage the process of folding and unfolding of proteins, the quality of newly synthesized proteins and protecting cellular homeostatic processes from environmental stress. On the basis of functionality, HSPs are categorized into six major families namely: (i) HSP20 or sHSP (ii) HSP40 or J-proteins types (iii) HSP60 or GroEL/ES (iv) HSP70 (v) HSP90 and (vi) HSP100. Identification of HSPs family and sub-family through conventional approaches is expensive and laborious. It is therefore, highly desired to establish an automatic, robust and accurate computational method for prediction of HSPs quickly and reliably. Regard, a computational model is developed for the prediction of HSPs family. In this model, protein sequences are formulated using three discrete methods namely: Split Amino Acid Composition, Pseudo Amino Acid Composition, and Dipeptide Composition. Several learning algorithms are utilized to choice the best one for high throughput computational model. Leave one out test is applied to assess the performance of the proposed model. The empirical results showed that support vector machine achieved quite promising results using Dipeptide Composition feature space. The predicted outcomes of proposed model are 90.7% accuracy for HSPs dataset and 97.04% accuracy for J-protein types, which are higher than existing methods in the literature so far.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Heat Shock Proteins; J-protein; KNN; PNN; SVM

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Year:  2015        PMID: 26233307     DOI: 10.1016/j.cmpb.2015.07.005

Source DB:  PubMed          Journal:  Comput Methods Programs Biomed        ISSN: 0169-2607            Impact factor:   5.428


  14 in total

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Journal:  J Membr Biol       Date:  2016-01-08       Impact factor: 1.843

5.  iPhos-PseEn: identifying phosphorylation sites in proteins by fusing different pseudo components into an ensemble classifier.

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6.  Multi-label Learning for Predicting the Activities of Antimicrobial Peptides.

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7.  Relapse-related long non-coding RNA signature to improve prognosis prediction of lung adenocarcinoma.

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8.  iRNA-3typeA: Identifying Three Types of Modification at RNA's Adenosine Sites.

Authors:  Wei Chen; Pengmian Feng; Hui Yang; Hui Ding; Hao Lin; Kuo-Chen Chou
Journal:  Mol Ther Nucleic Acids       Date:  2018-03-30       Impact factor: 8.886

9.  PredHSP: Sequence Based Proteome-Wide Heat Shock Protein Prediction and Classification Tool to Unlock the Stress Biology.

Authors:  Ravindra Kumar; Bandana Kumari; Manish Kumar
Journal:  PLoS One       Date:  2016-05-19       Impact factor: 3.240

10.  ir-HSP: Improved Recognition of Heat Shock Proteins, Their Families and Sub-types Based On g-Spaced Di-peptide Features and Support Vector Machine.

Authors:  Prabina K Meher; Tanmaya K Sahu; Shachi Gahoi; Atmakuri R Rao
Journal:  Front Genet       Date:  2018-01-11       Impact factor: 4.599

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