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Identification of residue pairing in interacting ß-strands from a predicted residue contact map.
Mao, Wenzhi; Wang, Tong; Zhang, Wenxuan; Gong, Haipeng.
Afiliação
  • Mao W; MOE Key Laboratory of Bioinformatics, School of Life Sciences, Tsinghua University, Beijing, China.
  • Wang T; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, China.
  • Zhang W; MOE Key Laboratory of Bioinformatics, School of Life Sciences, Tsinghua University, Beijing, China.
  • Gong H; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, China.
BMC Bioinformatics ; 19(1): 146, 2018 04 19.
Article em En | MEDLINE | ID: mdl-29673311
ABSTRACT

BACKGROUND:

Despite the rapid progress of protein residue contact prediction, predicted residue contact maps frequently contain many errors. However, information of residue pairing in ß strands could be extracted from a noisy contact map, due to the presence of characteristic contact patterns in ß-ß interactions. This information may benefit the tertiary structure prediction of mainly ß proteins. In this work, we propose a novel ridge-detection-based ß-ß contact predictor to identify residue pairing in ß strands from any predicted residue contact map.

RESULTS:

Our algorithm RDb2C adopts ridge detection, a well-developed technique in computer image processing, to capture consecutive residue contacts, and then utilizes a novel multi-stage random forest framework to integrate the ridge information and additional features for prediction. Starting from the predicted contact map of CCMpred, RDb2C remarkably outperforms all state-of-the-art methods on two conventional test sets of ß proteins (BetaSheet916 and BetaSheet1452), and achieves F1-scores of ~ 62% and ~ 76% at the residue level and strand level, respectively. Taking the prediction of the more advanced RaptorX-Contact as input, RDb2C achieves impressively higher performance, with F1-scores reaching ~ 76% and ~ 86% at the residue level and strand level, respectively. In a test of structural modeling using the top 1 L predicted contacts as constraints, for 61 mainly ß proteins, the average TM-score achieves 0.442 when using the raw RaptorX-Contact prediction, but increases to 0.506 when using the improved prediction by RDb2C.

CONCLUSION:

Our method can significantly improve the prediction of ß-ß contacts from any predicted residue contact maps. Prediction results of our algorithm could be directly applied to effectively facilitate the practical structure prediction of mainly ß proteins.

AVAILABILITY:

All source data and codes are available at http//166.111.152.91/Downloads.html or the GitHub address of https//github.com/wzmao/RDb2C .
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas / Biologia Computacional / Aminoácidos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas / Biologia Computacional / Aminoácidos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article