Show simple item record

dc.creatorShapovalov, M
dc.creatorDunbrack, RL
dc.creatorVucetic, S
dc.date.accessioned2020-12-15T20:49:50Z
dc.date.available2020-12-15T20:49:50Z
dc.date.issued2020-05-01
dc.identifier.issn1932-6203
dc.identifier.issn1932-6203
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/4463
dc.identifier.other32374785 (pubmed)
dc.identifier.urihttp://hdl.handle.net/20.500.12613/4481
dc.description.abstract© 2020 Shapovalov et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Protein secondary structure prediction remains a vital topic with broad applications. Due to lack of a widely accepted standard in secondary structure predictor evaluation, a fair comparison of predictors is challenging. A detailed examination of factors that contribute to higher accuracy is also lacking. In this paper, we present: (1) new test sets, Test2018, Test2019, and Test2018-2019, consisting of proteins from structures released in 2018 and 2019 with less than 25% identity to any protein published before 2018; (2) a 4-layer convolutional neural network, SecNet, with an input window of ±14 amino acids which was trained on proteins ≤25% identical to proteins in Test2018 and the commonly used CB513 test set; (3) an additional test set that shares no homologous domains with the training set proteins, according to the Evolutionary Classification of Proteins (ECOD) database; (4) a detailed ablation study where we reverse one algorithmic choice at a time in SecNet and evaluate the effect on the prediction accuracy; (5) new 4- and 5-label prediction alphabets that may be more practical for tertiary structure prediction methods. The 3-label accuracy (helix, sheet, coil) of the leading predictors on both Test2018 and CB513 is 81–82%, while SecNet’s accuracy is 84% for both sets. Accuracy on the non-homologous ECOD set is only 0.6 points (83.9%) lower than the results on the Test2018-2019 set (84.5%). The ablation study of features, neural network architecture, and training hyper-parameters suggests the best accuracy results are achieved with good choices for each of them while the neural network architecture is not as critical as long as it is not too simple. Protocols for generating and using unbiased test, validation, and training sets are provided. Our data sets, including input features and assigned labels, and SecNet software including third-party dependencies and databases, are downloadable from dunbrack.fccc.edu/ss and github.com/sh-maxim/ss.
dc.format.extente0232528-e0232528
dc.language.isoen
dc.relation.haspartPLoS ONE
dc.relation.isreferencedbyPublic Library of Science (PLoS)
dc.rightsCC BY
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAlgorithms
dc.subjectAmino Acid Sequence
dc.subjectAmino Acids
dc.subjectDatabases, Protein
dc.subjectDeep Learning
dc.subjectNeural Networks, Computer
dc.subjectProtein Structure, Secondary
dc.subjectProteins
dc.subjectSoftware
dc.titleMultifaceted analysis of training and testing convolutional neural networks for protein secondary structure prediction
dc.typeArticle
dc.type.genreJournal Article
dc.relation.doi10.1371/journal.pone.0232528
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.date.updated2020-12-15T20:49:46Z
refterms.dateFOA2020-12-15T20:49:51Z


Files in this item

Thumbnail
Name:
Multifaceted analysis of training ...
Size:
2.698Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

CC BY
Except where otherwise noted, this item's license is described as CC BY