Literature DB >> 20035768

Prediction of the parallel/antiparallel orientation of beta-strands using amino acid pairing preferences and support vector machines.

Ning Zhang1, Guangyou Duan, Shan Gao, Jishou Ruan, Tao Zhang.   

Abstract

In principle, structural information of protein sequences with no detectable homology to a protein of known structure could be obtained by predicting the arrangement of their secondary structural elements. Although some ab initio methods for protein structure prediction have been reported, the long-range interactions required to accurately predict tertiary structures of beta-sheet containing proteins are still difficult to simulate. To remedy this problem and facilitate de novo prediction of beta-sheet containing protein structures, we developed a support vector machine (SVM) approach that classified parallel and antiparallel orientation of beta-strands by using the information of interstrand amino acid pairing preferences. Based on a second-order statistics on the relative frequencies of each possible interstrand amino acid pair, we defined an average amino acid pairing encoding matrix (APEM) for encoding beta-strands as input in the prediction model. As a result, a prediction accuracy of 86.89% and a Matthew's correlation coefficient value of 0.71 have been achieved through 7-fold cross-validation on a non-redundant protein dataset from PISCES. Although several issues still remain to be studied, the method presented here to some extent could indicate the important contribution of the amino acid pairs to the beta-strand orientation, and provide a possible way to further be combined with other algorithms making a full 'identification' of beta-strands. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 20035768     DOI: 10.1016/j.jtbi.2009.12.019

Source DB:  PubMed          Journal:  J Theor Biol        ISSN: 0022-5193            Impact factor:   2.691


  8 in total

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7.  Statistical Analysis of Terminal Extensions of Protein β-Strand Pairs.

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8.  New insights regarding protein folding as learned from beta-sheets.

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  8 in total

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