Evidence map›Paper›PMID 34641786›Full record

ArticleBMC bioinformatics2021

FoldHSphere: deep hyperspherical embeddings for protein fold recognition.

Amelia Villegas-Morcillo, Victoria Sanchez, Angel M Gomez

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Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Amelia Villegas-MorcilloDepartment of Signal Theory, Telematics and Communications, University of Granada, Periodista Daniel Saucedo Aranda, 18071, Granada, Spain. ameliavm@ugr.es.
Victoria SanchezDepartment of Signal Theory, Telematics and Communications, University of Granada, Periodista Daniel Saucedo Aranda, 18071, Granada, Spain.
Angel M GomezDepartment of Signal Theory, Telematics and Communications, University of Granada, Periodista Daniel Saucedo Aranda, 18071, Granada, Spain.

Funding

Spanish Ministry of Science, Innovation and Universities Project No. PID2019-104206GB-I00 / SRA (State Research Agency) / 10.13039/501100011033
6 · The paper itself

Abstract

backgroundCurrent 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.

resultsIn 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.

conclusionsOur 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.

Indexed as

AlgorithmsNeural Networks, ComputerProteinsProteinsDeep neural networksEmbedding learningHyperspherical spaceProtein fold recognitionResidual convolutionsThomson problem

Identifiers

PMID34641786
PMCPMC8507389

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