Literature DB >> 2254939

Machine learning approach for the prediction of protein secondary structure.

R D King1, M J Sternberg.   

Abstract

PROMIS (protein machine induction system), a program for machine learning, was used to generalize rules that characterize the relationship between primary and secondary structure in globular proteins. These rules can be used to predict an unknown secondary structure from a known primary structure. The symbolic induction method used by PROMIS was specifically designed to produce rules that are meaningful in terms of chemical properties of the residues. The rules found were compared with existing knowledge of protein structure: some features of the rules were already recognized (e.g. amphipathic nature of alpha-helices). Other features are not understood, and are under investigation. The rules produced a prediction accuracy for three states (alpha-helix, beta-strand and coil) of 60% for all proteins, 73% for proteins of known alpha domain type, 62% for proteins of known beta domain type and 59% for proteins of known alpha/beta domain type. We conclude that machine learning is a useful tool in the examination of the large databases generated in molecular biology.

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Year:  1990        PMID: 2254939     DOI: 10.1016/S0022-2836(05)80333-X

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  14 in total

1.  Cascaded multiple classifiers for secondary structure prediction.

Authors:  M Ouali; R D King
Journal:  Protein Sci       Date:  2000-06       Impact factor: 6.725

2.  Characterization and prediction of linker sequences of multi-domain proteins by a neural network.

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Journal:  J Struct Funct Genomics       Date:  2002

3.  Modelling of peptide and protein structures.

Authors:  S Fraga; J M Parker
Journal:  Amino Acids       Date:  1994-06       Impact factor: 3.520

4.  Immunization of mice with a TolA-like surface protein of Trypanosoma cruzi generates CD4(+) T-cell-dependent parasiticidal activity.

Authors:  N M Quanquin; C Galaviz; D L Fouts; R A Wrightsman; J E Manning
Journal:  Infect Immun       Date:  1999-09       Impact factor: 3.441

5.  Peptide design in machina: development of artificial mitochondrial protein precursor cleavage sites by simulated molecular evolution.

Authors:  G Schneider; J Schuchhardt; P Wrede
Journal:  Biophys J       Date:  1995-02       Impact factor: 4.033

6.  Improving protein secondary structure prediction with aligned homologous sequences.

Authors:  V Di Francesco; J Garnier; P J Munson
Journal:  Protein Sci       Date:  1996-01       Impact factor: 6.725

7.  A preference-based free-energy parameterization of enzyme-inhibitor binding. Applications to HIV-1-protease inhibitor design.

Authors:  A Wallqvist; R L Jernigan; D G Covell
Journal:  Protein Sci       Date:  1995-09       Impact factor: 6.725

8.  Development of artificial neural filters for pattern recognition in protein sequences.

Authors:  G Schneider; P Wrede
Journal:  J Mol Evol       Date:  1993-06       Impact factor: 2.395

9.  Dehydration-specific induction of hydrophilic protein genes in the anhydrobiotic nematode Aphelenchus avenae.

Authors:  John A Browne; Katharine M Dolan; Trevor Tyson; Kshamata Goyal; Alan Tunnacliffe; Ann M Burnell
Journal:  Eukaryot Cell       Date:  2004-08

Review 10.  Protein function in precision medicine: deep understanding with machine learning.

Authors:  Burkhard Rost; Predrag Radivojac; Yana Bromberg
Journal:  FEBS Lett       Date:  2016-08-06       Impact factor: 4.124

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