RDb2C2: an improved method to identify the residue-residue pairing in β strands
Autor: | Yaoguang Xing, Di Shao, Haipeng Gong, Wenzhi Mao |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Improved method
β-β residue pairing lcsh:Computer applications to medicine. Medical informatics Biochemistry Residual neural network 03 medical and health sciences 0302 clinical medicine Structural Biology Molecular Biology lcsh:QH301-705.5 030304 developmental biology Mathematics 0303 health sciences Residue (complex analysis) Applied Mathematics A protein Percentage point Protein structure prediction Mainly β proteins Computer Science Applications Random forest Ridge detection lcsh:Biology (General) Pairing lcsh:R858-859.7 Algorithm 030217 neurology & neurosurgery |
Zdroj: | BMC Bioinformatics, Vol 21, Iss 1, Pp 1-12 (2020) |
ISSN: | 1471-2105 |
DOI: | 10.1186/s12859-020-3476-z |
Popis: | Background Despite the great advance of protein structure prediction, accurate prediction of the structures of mainly β proteins is still highly challenging, but could be assisted by the knowledge of residue-residue pairing in β strands. Previously, we proposed a ridge-detection-based algorithm RDb2C that adopted a multi-stage random forest framework to predict the β-β pairing given the amino acid sequence of a protein. Results In this work, we developed a second version of this algorithm, RDb2C2, by employing the residual neural network to further enhance the prediction accuracy. In the benchmark test, this new algorithm improves the F1-score by > 10 percentage points, reaching impressively high values of ~ 72% and ~ 73% in the BetaSheet916 and BetaSheet1452 sets, respectively. Conclusion Our new method promotes the prediction accuracy of β-β pairing to a new level and the prediction results could better assist the structure modeling of mainly β proteins. We prepared an online server of RDb2C2 at http://structpred.life.tsinghua.edu.cn/rdb2c2.html. |
Databáze: | OpenAIRE |
Externí odkaz: | |
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