Evidence map›Paper›PMID 17888163›Full record

ArticleBMC bioinformatics2007

An evolutionary method for learning HMM structure: prediction of protein secondary structure.

Kyoung-Jae Won, Thomas Hamelryck, Adam Prügel-Bennett, Anders Krogh

Abstract read
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Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Tokenization and deep learning architectures in genomics: A comprehensive review.Computational and structural biotechnology journal · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Article
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  13. Article
  14. Template-based protein modeling: recent methodological advances.Current topics in medicinal chemistry · 2010
    Review
  15. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kyoung-Jae WonBioinformatics Centre, Department of Molecular Biology, University of Copenhagen, Ole Maaloes Vej 5, DK-2200 Copenhagen, Denmark. won@binf.ku.dk
Thomas Hamelryck
Adam Prügel-Bennett
Anders Krogh

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prediction of the secondary structure of proteins is one of the most studied problems in bioinformatics. Despite their success in many problems of biological sequence analysis, Hidden Markov Models (HMMs) have not been used much for this problem, as the complexity of the task makes manual design of HMMs difficult. Therefore, we have developed a method for evolving the structure of HMMs automatically, using Genetic Algorithms (GAs).

resultsIn the GA procedure, populations of HMMs are assembled from biologically meaningful building blocks. Mutation and crossover operators were designed to explore the space of such Block-HMMs. After each step of the GA, the standard HMM estimation algorithm (the Baum-Welch algorithm) was used to update model parameters. The final HMM captures several features of protein sequence and structure, with its own HMM grammar. In contrast to neural network based predictors, the evolved HMM also calculates the probabilities associated with the predictions. We carefully examined the performance of the HMM based predictor, both under the multiple- and single-sequence condition.

conclusionWe have shown that the proposed evolutionary method can automatically design the topology of HMMs. The method reads the grammar of protein sequences and converts it into the grammar of an HMM. It improved previously suggested evolutionary methods and increased the prediction quality. Especially, it shows good performance under the single-sequence condition and provides probabilistic information on the prediction result. The protein secondary structure predictor using HMMs (P.S.HMM) is on-line available http://www.binf.ku.dk/~won/pshmm.htm. It runs under the single-sequence condition.

Indexed as

AlgorithmsModels, ChemicalModels, MolecularProtein Structure, SecondaryAmino Acid SequenceComputer SimulationMarkov ChainsMolecular Sequence DataProteinsSequence Analysis, ProteinProteins

Identifiers

PMID17888163
PMCPMC2072961

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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.