Predicting the Strongest Domain-Domain Contact in Interacting Protein Pairs
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Tom M. W. Nye
Experiments to determine the complete 3-dimensional structures of protein complexes are difficult to perform and only a limited range of such structures are available.In contrast, large-scale screening experiments have identified thousands of pairwise interactions between proteins, but such experiments do not produce explicit structural information.In addition, the data produced by these high through-put experiments contain large numbers of false positive results, and can be biased against detection of certain types of interaction.Several methods exist that analyse such pairwise interaction data in terms of the constituent domains within proteins, scoring pairs of domain superfamilies according to their propensity to interact.These scores can be used to predict the strongest domain-domain contact (the contact with the largest surface area) between interacting proteins for which the domain-level structures of the individual proteins are known.We test this predictive approach on a set of pairwise protein interactions taken from the Protein Quaternary Structure (PQS) database for which the true domain-domain contacts are known.While the overall prediction success rate across the whole test data set is poor, we shown how interactions in the test data set for which the training data are not informative can be automatically excluded from the prediction process, giving improved prediction success rates at the expense of restricted coverage of the test data.
©2011 Walter de Gruyter GmbH & Co. KG, Berlin/Boston
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- A Generalized Clustering Problem, with Application to DNA Microarrays
- A Bayes Regression Approach to Array-CGH Data
- Statistical Selection of Maintenance Genes for Normalization of Gene Expressions
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- Dimension Reduction for Classification with Gene Expression Microarray Data
- A New Type of Stochastic Dependence Revealed in Gene Expression Data
- A New Order Estimator for Fixed and Variable Length Markov Models with Applications to DNA Sequence Similarity
- Quality Optimised Analysis of General Paired Microarray Experiments
- Issues of Processing and Multiple Testing of SELDI-TOF MS Proteomic Data
- Cross-Validated Bagged Prediction of Survival
- Treatment of Uninformative Families in Mean Allele Sharing Tests for Linkage
- Quantile-Function Based Null Distribution in Resampling Based Multiple Testing
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- Pseudo-likelihood for Non-reversible Nucleotide Substitution Models with Neighbour Dependent Rates
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- Numerical Solutions for Patterns Statistics on Markov Chains
- A Heuristic Bayesian Method for Segmenting DNA Sequence Alignments and Detecting Evidence for Recombination and Gene Conversion
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