Evidence map›Paper›PMID 26634993›Full record

ArticleScientific reports2015

Improving Protein Fold Recognition by Deep Learning Networks.

Taeho Jo, Jie Hou, Jesse Eickholt, Jianlin Cheng

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

  1. Protein Structure Prediction Methods.Advances in experimental medicine and biology · 2026
    Review
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  8. Review
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  11. Local Alignment of DNA Sequence Based on Deep Reinforcement Learning.IEEE open journal of engineering in medicine and biology · 2021
    Article
  12. Article
  13. Network-based protein structural classification.Royal Society open science · 2020
    Article
  14. Article
  15. Article
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  19. Article
  20. Deep learning improves antimicrobial peptide recognition.Bioinformatics (Oxford, England) · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Taeho JoDepartment of Computer Science, University of Missouri, Columbia, MO 65211, USA.
Jie HouDepartment of Computer Science, University of Missouri, Columbia, MO 65211, USA.
Jesse EickholtDepartment of Computer Science, Central Michigan University, Mount Pleasant, MI 48859, USA.
Jianlin ChengDepartment of Computer Science, University of Missouri, Columbia, MO 65211, USA.

Funding

Integrated Prediction of Protein Struture at 1D, 2D and 3D LevelsR01GM093123 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHENG, JIANLIN · 2010 to 2023
$3.8M
NIGMS NIH HHS R01 GM093123NIGMS NIH HHS R01GM093123
6 · The paper itself

Abstract

For accurate recognition of protein folds, a deep learning network method (DN-Fold) was developed to predict if a given query-template protein pair belongs to the same structural fold. The input used stemmed from the protein sequence and structural features extracted from the protein pair. We evaluated the performance of DN-Fold along with 18 different methods on Lindahl's benchmark dataset and on a large benchmark set extracted from SCOP 1.75 consisting of about one million protein pairs, at three different levels of fold recognition (i.e., protein family, superfamily, and fold) depending on the evolutionary distance between protein sequences. The correct recognition rate of ensembled DN-Fold for Top 1 predictions is 84.5%, 61.5%, and 33.6% and for Top 5 is 91.2%, 76.5%, and 60.7% at family, superfamily, and fold levels, respectively. We also evaluated the performance of single DN-Fold (DN-FoldS), which showed the comparable results at the level of family and superfamily, compared to ensemble DN-Fold. Finally, we extended the binary classification problem of fold recognition to real-value regression task, which also show a promising performance. DN-Fold is freely available through a web server at http://iris.rnet.missouri.edu/dnfold.

Indexed as

Protein ConformationProtein FoldingSoftwareAlgorithmsAmino Acid SequenceArtificial IntelligenceComputational BiologyDatabases, ProteinPattern Recognition, AutomatedProteinsSequence Analysis, ProteinProteins

Identifiers

PMID26634993
PMCPMC4669437

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.