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Using Phylogenetic Analysis to Investigate Eukaryotic Gene Origin
Published on: August 14, 2018
Reducing phylogenetic bias in correlated mutation analysis
Haim Ashkenazy1, Yossef Kliger
1Compugen Ltd, 72 Pinchas Rosen, Tel Aviv 69512, Israel.
Protein Engineering, Design & Selection : PEDS
|January 14, 2010
Summary
Correlated mutation analysis (CMA) improves protein contact map prediction by reducing noise in sequence alignments. A refined Pearson
Area of Science:
- Computational biology
- Structural bioinformatics
- Protein science
Background:
- Correlated mutation analysis (CMA) predicts protein contacts from sequence data.
- CMA relies on correlations between mutations in interacting amino acid residues.
- Estimating these correlations often involves Pearson's correlation coefficient (PCC) or mutual information (MI) from multiple sequence alignments (MSAs).
Purpose of the Study:
- To investigate if noise reduction techniques, successful for MI-based predictors, can enhance PCC-based CMA.
- To compare the performance of improved PCC-based CMA against MI-based methods.
Main Methods:
- Applied a noise reduction procedure to a PCC-based correlated mutation analysis method.
- Evaluated performance across four major SCOP protein classes.
- Compared the improved PCC method with existing MI-based predictors using MSAs of varying sizes.
Main Results:
- The noise reduction approach significantly improved PCC-based CMA performance across all tested SCOP classes.
- The enhanced PCC-based method demonstrated superior performance compared to MI-based methods for proteins with up to 100 sequences in their MSAs.
Conclusions:
- Noise reduction is a viable strategy to improve PCC-based correlated mutation analysis for protein contact map prediction.
- The refined PCC-based method offers a more effective approach than MI-based methods for proteins with limited homologous sequences.
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