Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101219
Title: Prediction of protein structural classes for low-homology sequences based on predicted secondary structure
Authors: Yang, Jian-Yi
Peng, Zhen-Ling
Chen, Xin
Keywords: Mathematical Sciences
Issue Date: 2010
Source: Yang, J. Y., Peng, Z. L., & Chen, X. (2010). Prediction of protein structural classes for low-homology sequences based on predicted secondary structure. BMC Bioinformatics, 11(Suppl 1):S9.
Series/Report no.: BMC bioinformatics
Abstract: Background: Prediction of protein structural classes (a, b, a + b and a/b) from amino acid sequences is of great importance, as it is beneficial to study protein function, regulation and interactions. Many methods have been developed for high-homology protein sequences, and the prediction accuracies can achieve up to 90%. However, for low-homology sequences whose average pairwise sequence identity lies between 20% and 40%, they perform relatively poorly, yielding the prediction accuracy often below 60%. Results: We propose a new method to predict protein structural classes on the basis of features extracted from the predicted secondary structures of proteins rather than directly from their amino acid sequences. It first uses PSIPRED to predict the secondary structure for each protein sequence. Then, the chaos game representation is employed to represent the predicted secondary structure as two time series, from which we generate a comprehensive set of 24 features using recurrence quantification analysis, K-string based information entropy and segment-based analysis. The resulting feature vectors are finally fed into a simple yet powerful Fisher’s discriminant algorithm for the prediction of protein structural classes. We tested the proposed method on three benchmark datasets in low homology and achieved the overall prediction accuracies of 82.9%, 83.1% and 81.3%, respectively. Comparisons with ten existing methods showed that our method consistently performs better for all the tested datasets and the overall accuracy improvements range from 2.3% to 27.5%. A web server that implements the proposed method is freely available at http://www1.spms.ntu.edu.sg/~chenxin/RKS_PPSC/. Conclusion: The high prediction accuracy achieved by our proposed method is attributed to the design of a comprehensive feature set on the predicted secondary structure sequences, which is capable of characterizing the sequence order information, local interactions of the secondary structural elements, and spacial arrangements of a helices and b strands. Thus, it is a valuable method to predict protein structural classes particularly for low-homology amino acid sequences.
URI: https://hdl.handle.net/10356/101219
http://hdl.handle.net/10220/17874
ISSN: 1471-2105
DOI: 10.1186/1471-2105-11-S1-S9
Rights: © 2010 Yang et al; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

Files in This Item:
File Description SizeFormat 
1471-2105-11-S1-S9.pdf907.8 kBAdobe PDFThumbnail
View/Open

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.