Abstract

BackgroundThe prediction of the secondary structure of a protein is a critical step in the prediction of its tertiary structure and, potentially, its function. Moreover, the backbone dihedral angles, highly correlated with secondary structures, provide crucial information about the local three-dimensional structure.ResultsWe predict independently both the secondary structure and the backbone dihedral angles and combine the results in a loop to enhance each prediction reciprocally. Support vector machines, a state-of-the-art supervised classification technique, achieve secondary structure predictive accuracy of 80% on a non-redundant set of 513 proteins, significantly higher than other methods on the same dataset. The dihedral angle space is divided into a number of regions using two unsupervised clustering techniques in order to predict the region in which a new residue belongs. The performance of our method is comparable to, and in some cases more accurate than, other multi-class dihedral prediction methods.ConclusionsWe have created an accurate predictor of backbone dihedral angles and secondary structure. Our method, called DISSPred, is available online at http://comp.chem.nottingham.ac.uk/disspred/.

Highlights

  • The prediction of the secondary structure of a protein is a critical step in the prediction of its tertiary structure and, potentially, its function

  • In 1988, Qian and Sejnowski pioneered the application of artificial neural networks (ANNs) to predict secondary structure [3]

  • The support vector machine method (SVM) can find non-linear boundaries between two classes by using a kernel function, which maps the data from the input space into a richer feature space, where linear boundaries can be implemented

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Summary

Results

We predict independently both the secondary structure and the backbone dihedral angles and combine the results in a loop to enhance each prediction reciprocally. A state-of-the-art supervised classification technique, achieve secondary structure predictive accuracy of 80% on a non-redundant set of 513 proteins, significantly higher than other methods on the same dataset. The dihedral angle space is divided into a number of regions using two unsupervised clustering techniques in order to predict the region in which a new residue belongs. The performance of our method is comparable to, and in some cases more accurate than, other multi-class dihedral prediction methods

Background
Methods
Results and Discussion
Method
Conclusions
Rost B
Jones DT
12. Pan XM
21. Karypis G: YASSPP
44. Vapnik V
62. Matthews BW
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