Literature DB >> 1438176

Limits on alpha-helix prediction with neural network models.

S Hayward1, J F Collins.   

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.

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Year:  1992        PMID: 1438176     DOI: 10.1002/prot.340140306

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  2 in total

1.  Improved prediction of protein secondary structure by use of sequence profiles and neural networks.

Authors:  B Rost; C Sander
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-15       Impact factor: 11.205

2.  Analysis of protein transmembrane helical regions by a neural network.

Authors:  G W Dombi; J Lawrence
Journal:  Protein Sci       Date:  1994-04       Impact factor: 6.725

  2 in total

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