Evidence map›Paper›PMID 33203392›Full record

ArticleBMC bioinformatics2020

DeepFrag-k: a fragment-based deep learning approach for protein fold recognition.

Wessam Elhefnawy, Min Li, Jianxin Wang, Yaohang Li

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wessam ElhefnawyDepartment of Computer Science, Old Dominion University, Norfolk, U.S.A.
Min LiDepartment of Computer Science, Central South University, Changsha, China.
Jianxin WangDepartment of Computer Science, Central South University, Changsha, China.
Yaohang LiDepartment of Computer Science, Old Dominion University, Norfolk, U.S.A.. yaohang@cs.odu.edu.ORCID http://orcid.org/0000-0003-0178-1876

Funding

National Natural Science Foundation of China 61728211National Natural Science Foundation of China 61832019
6 · The paper itself

Abstract

backgroundOne of the most essential problems in structural bioinformatics is protein fold recognition. In this paper, we design a novel deep learning architecture, so-called DeepFrag-k, which identifies fold discriminative features at fragment level to improve the accuracy of protein fold recognition. DeepFrag-k is composed of two stages: the first stage employs a multi-modal Deep Belief Network (DBN) to predict the potential structural fragments given a sequence, represented as a fragment vector, and then the second stage uses a deep convolutional neural network (CNN) to classify the fragment vector into the corresponding fold.

resultsOur results show that DeepFrag-k yields 92.98% accuracy in predicting the top-100 most popular fragments, which can be used to generate discriminative fragment feature vectors to improve protein fold recognition.

conclusionsThere is a set of fragments that can serve as structural "keywords" distinguishing between major protein folds. The deep learning architecture in DeepFrag-k is able to accurately identify these fragments as structure features to improve protein fold recognition.

Indexed as

Computational BiologyDeep LearningProtein FoldingNeural Networks, ComputerProteinsProteinsDeep learningFold recognitionProtein fragments

Identifiers

PMID33203392
PMCPMC7672895

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.