Evidence map›Paper›PMID 32603341›Full record

ArticlePloS one2020

A simple strategy to enhance the speed of protein secondary structure prediction without sacrificing accuracy.

Sheng-Hung Juan, Teng-Ruei Chen, Wei-Cheng Lo

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. SeqCP: A sequence-based algorithm for searching circularly permuted proteins.Computational and structural biotechnology journal · 2023
    Article
  3. Deep learning for protein secondary structure prediction: Pre and post-AlphaFold.Computational and structural biotechnology journal · 2022
    Review
  4. Article
  5. Article
  6. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sheng-Hung JuanInstitute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan.
Teng-Ruei ChenInstitute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan.ORCID 0000-0001-8995-334X
Wei-Cheng LoInstitute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan.ORCID 0000-0001-8865-5113

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The secondary structure prediction of proteins is a classic topic of computational structural biology with a variety of applications. During the past decade, the accuracy of prediction achieved by state-of-the-art algorithms has been >80%; meanwhile, the time cost of prediction increased rapidly because of the exponential growth of fundamental protein sequence data. Based on literature studies and preliminary observations on the relationships between the size/homology of the fundamental protein dataset and the speed/accuracy of predictions, we raised two hypotheses that might be helpful to determine the main influence factors of the efficiency of secondary structure prediction. Experimental results of size and homology reductions of the fundamental protein dataset supported those hypotheses. They revealed that shrinking the size of the dataset could substantially cut down the time cost of prediction with a slight decrease of accuracy, which could be increased on the contrary by homology reduction of the dataset. Moreover, the Shannon information entropy could be applied to explain how accuracy was influenced by the size and homology of the dataset. Based on these findings, we proposed that a proper combination of size and homology reductions of the protein dataset could speed up the secondary structure prediction while preserving the high accuracy of state-of-the-art algorithms. Testing the proposed strategy with the fundamental protein dataset of the year 2018 provided by the Universal Protein Resource, the speed of prediction was enhanced over 20 folds while all accuracy measures remained equivalently high. These findings are supposed helpful for improving the efficiency of researches and applications depending on the secondary structure prediction of proteins. To make future implementations of the proposed strategy easy, we have established a database of size and homology reduced protein datasets at http://10.life.nctu.edu.tw/UniRefNR.

Indexed as

Protein Structure, SecondaryAlgorithmsComputational BiologyData AccuracyDatabases, ProteinProteinsSequence AlignmentSequence Homology, Amino AcidProteins

Identifiers

PMID32603341
PMCPMC7326220

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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.