Cargando…

FoldHSphere: deep hyperspherical embeddings for protein fold recognition

BACKGROUND: Current state-of-the-art deep learning approaches for protein fold recognition learn protein embeddings that improve prediction performance at the fold level. However, there still exists aperformance gap at the fold level and the (relatively easier) family level, suggesting that it might...

Descripción completa

Detalles Bibliográficos
Autores principales: Villegas-Morcillo, Amelia, Sanchez, Victoria, Gomez, Angel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507389/
https://www.ncbi.nlm.nih.gov/pubmed/34641786
http://dx.doi.org/10.1186/s12859-021-04419-7
_version_ 1784581846228533248
author Villegas-Morcillo, Amelia
Sanchez, Victoria
Gomez, Angel M.
author_facet Villegas-Morcillo, Amelia
Sanchez, Victoria
Gomez, Angel M.
author_sort Villegas-Morcillo, Amelia
collection PubMed
description BACKGROUND: Current state-of-the-art deep learning approaches for protein fold recognition learn protein embeddings that improve prediction performance at the fold level. However, there still exists aperformance gap at the fold level and the (relatively easier) family level, suggesting that it might be possible to learn an embedding space that better represents the protein folds. RESULTS: In this paper, we propose the FoldHSphere method to learn a better fold embedding space through a two-stage training procedure. We first obtain prototype vectors for each fold class that are maximally separated in hyperspherical space. We then train a neural network by minimizing the angular large margin cosine loss to learn protein embeddings clustered around the corresponding hyperspherical fold prototypes. Our network architectures, ResCNN-GRU and ResCNN-BGRU, process the input protein sequences by applying several residual-convolutional blocks followed by a gated recurrent unit-based recurrent layer. Evaluation results on the LINDAHL dataset indicate that the use of our hyperspherical embeddings effectively bridges the performance gap at the family and fold levels. Furthermore, our FoldHSpherePro ensemble method yields an accuracy of 81.3% at the fold level, outperforming all the state-of-the-art methods. CONCLUSIONS: Our methodology is efficient in learning discriminative and fold-representative embeddings for the protein domains. The proposed hyperspherical embeddings are effective at identifying the protein fold class by pairwise comparison, even when amino acid sequence similarities are low. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04419-7.
format Online
Article
Text
id pubmed-8507389
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85073892021-10-20 FoldHSphere: deep hyperspherical embeddings for protein fold recognition Villegas-Morcillo, Amelia Sanchez, Victoria Gomez, Angel M. BMC Bioinformatics Research BACKGROUND: Current state-of-the-art deep learning approaches for protein fold recognition learn protein embeddings that improve prediction performance at the fold level. However, there still exists aperformance gap at the fold level and the (relatively easier) family level, suggesting that it might be possible to learn an embedding space that better represents the protein folds. RESULTS: In this paper, we propose the FoldHSphere method to learn a better fold embedding space through a two-stage training procedure. We first obtain prototype vectors for each fold class that are maximally separated in hyperspherical space. We then train a neural network by minimizing the angular large margin cosine loss to learn protein embeddings clustered around the corresponding hyperspherical fold prototypes. Our network architectures, ResCNN-GRU and ResCNN-BGRU, process the input protein sequences by applying several residual-convolutional blocks followed by a gated recurrent unit-based recurrent layer. Evaluation results on the LINDAHL dataset indicate that the use of our hyperspherical embeddings effectively bridges the performance gap at the family and fold levels. Furthermore, our FoldHSpherePro ensemble method yields an accuracy of 81.3% at the fold level, outperforming all the state-of-the-art methods. CONCLUSIONS: Our methodology is efficient in learning discriminative and fold-representative embeddings for the protein domains. The proposed hyperspherical embeddings are effective at identifying the protein fold class by pairwise comparison, even when amino acid sequence similarities are low. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04419-7. BioMed Central 2021-10-12 /pmc/articles/PMC8507389/ /pubmed/34641786 http://dx.doi.org/10.1186/s12859-021-04419-7 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
Villegas-Morcillo, Amelia
Sanchez, Victoria
Gomez, Angel M.
FoldHSphere: deep hyperspherical embeddings for protein fold recognition
title FoldHSphere: deep hyperspherical embeddings for protein fold recognition
title_full FoldHSphere: deep hyperspherical embeddings for protein fold recognition
title_fullStr FoldHSphere: deep hyperspherical embeddings for protein fold recognition
title_full_unstemmed FoldHSphere: deep hyperspherical embeddings for protein fold recognition
title_short FoldHSphere: deep hyperspherical embeddings for protein fold recognition
title_sort foldhsphere: deep hyperspherical embeddings for protein fold recognition
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507389/
https://www.ncbi.nlm.nih.gov/pubmed/34641786
http://dx.doi.org/10.1186/s12859-021-04419-7
work_keys_str_mv AT villegasmorcilloamelia foldhspheredeephypersphericalembeddingsforproteinfoldrecognition
AT sanchezvictoria foldhspheredeephypersphericalembeddingsforproteinfoldrecognition
AT gomezangelm foldhspheredeephypersphericalembeddingsforproteinfoldrecognition