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Secondary structure specific simpler prediction models for protein backbone angles

MOTIVATION: Protein backbone angle prediction has achieved significant accuracy improvement with the development of deep learning methods. Usually the same deep learning model is used in making prediction for all residues regardless of the categories of secondary structures they belong to. In this p...

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Autores principales: Newton, M. A. Hakim, Mataeimoghadam, Fereshteh, Zaman, Rianon, Sattar, Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728911/
https://www.ncbi.nlm.nih.gov/pubmed/34983370
http://dx.doi.org/10.1186/s12859-021-04525-6
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author Newton, M. A. Hakim
Mataeimoghadam, Fereshteh
Zaman, Rianon
Sattar, Abdul
author_facet Newton, M. A. Hakim
Mataeimoghadam, Fereshteh
Zaman, Rianon
Sattar, Abdul
author_sort Newton, M. A. Hakim
collection PubMed
description MOTIVATION: Protein backbone angle prediction has achieved significant accuracy improvement with the development of deep learning methods. Usually the same deep learning model is used in making prediction for all residues regardless of the categories of secondary structures they belong to. In this paper, we propose to train separate deep learning models for each category of secondary structures. Machine learning methods strive to achieve generality over the training examples and consequently loose accuracy. In this work, we explicitly exploit classification knowledge to restrict generalisation within the specific class of training examples. This is to compensate the loss of generalisation by exploiting specialisation knowledge in an informed way. RESULTS: The new method named SAP4SS obtains mean absolute error (MAE) values of 15.59, 18.87, 6.03, and 21.71 respectively for four types of backbone angles [Formula: see text] , [Formula: see text] , [Formula: see text] , and [Formula: see text] . Consequently, SAP4SS significantly outperforms existing state-of-the-art methods SAP, OPUS-TASS, and SPOT-1D: the differences in MAE for all four types of angles are from 1.5 to 4.1% compared to the best known results. AVAILABILITY: SAP4SS along with its data is available from https://gitlab.com/mahnewton/sap4ss.
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spelling pubmed-87289112022-01-06 Secondary structure specific simpler prediction models for protein backbone angles Newton, M. A. Hakim Mataeimoghadam, Fereshteh Zaman, Rianon Sattar, Abdul BMC Bioinformatics Research MOTIVATION: Protein backbone angle prediction has achieved significant accuracy improvement with the development of deep learning methods. Usually the same deep learning model is used in making prediction for all residues regardless of the categories of secondary structures they belong to. In this paper, we propose to train separate deep learning models for each category of secondary structures. Machine learning methods strive to achieve generality over the training examples and consequently loose accuracy. In this work, we explicitly exploit classification knowledge to restrict generalisation within the specific class of training examples. This is to compensate the loss of generalisation by exploiting specialisation knowledge in an informed way. RESULTS: The new method named SAP4SS obtains mean absolute error (MAE) values of 15.59, 18.87, 6.03, and 21.71 respectively for four types of backbone angles [Formula: see text] , [Formula: see text] , [Formula: see text] , and [Formula: see text] . Consequently, SAP4SS significantly outperforms existing state-of-the-art methods SAP, OPUS-TASS, and SPOT-1D: the differences in MAE for all four types of angles are from 1.5 to 4.1% compared to the best known results. AVAILABILITY: SAP4SS along with its data is available from https://gitlab.com/mahnewton/sap4ss. BioMed Central 2022-01-04 /pmc/articles/PMC8728911/ /pubmed/34983370 http://dx.doi.org/10.1186/s12859-021-04525-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Newton, M. A. Hakim
Mataeimoghadam, Fereshteh
Zaman, Rianon
Sattar, Abdul
Secondary structure specific simpler prediction models for protein backbone angles
title Secondary structure specific simpler prediction models for protein backbone angles
title_full Secondary structure specific simpler prediction models for protein backbone angles
title_fullStr Secondary structure specific simpler prediction models for protein backbone angles
title_full_unstemmed Secondary structure specific simpler prediction models for protein backbone angles
title_short Secondary structure specific simpler prediction models for protein backbone angles
title_sort secondary structure specific simpler prediction models for protein backbone angles
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728911/
https://www.ncbi.nlm.nih.gov/pubmed/34983370
http://dx.doi.org/10.1186/s12859-021-04525-6
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