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PMID: 1438176 Published · ppublish English Journal Article

Limits on alpha-helix prediction with neural network models.

Proteins ·Vol. 14 ·No. 3 ·1992-11-00 ·Pages 372-81

Hayward S, Collins JF

Abstract

Using a backpropagation neural network model we have found a limit for secondary structure prediction from local sequence. By including only sequences from whole alpha-helix and non-alpha-helix structures in our training and test sets--sequences spanning boundaries between these two structures were excluded--it was possible to investigate directly the relationship between sequence and structure for alpha-helix. A group of non-alpha-helix sequences, that was disrupting overall prediction success, was indistinguishable to the network from alpha-helix sequences. These sequences were found to occur at regions adjacent to the termini of alpha-helices with statistical significance, suggesting that potentially longer alpha-helices are disrupted by global constraints. Some of these regions spanned more than 20 residues. On these whole structure sequences, 10 residues in length, a comparatively high prediction success of 78% with a correlation coefficient of 0.52 was achieved. In addition, the structure of the input space, the distribution of beta-sheet in this space, and the effect of segment length were also investigated.

MeSH Terms
Amino Acid Sequence Forecasting Mathematical Computing Models, Chemical Models, Molecular Molecular Sequence Data Neural Networks, Computer Oligopeptides/chemistry Protein Structure, Secondary Proteins/chemistry Reproducibility of Results Software
Chemicals
Oligopeptides Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hayward S
Biocomputing Research Unit, Institute of Cell and Molecular Biology, Edinburgh, Scotland.
Collins J F
Article Info
Journal
Proteins
Abbr.
Proteins
ISSN
0887-3585
Published
1992-11-00
Pages
372-81
Language
English
Region
United States
NLM ID
8700181
Subset
IM
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