Protein sectors: statistical coupling analysis versus conservation
arXiv:1405.7081 · doi:10.1371/journal.pcbi.1004091
Abstract
Statistical coupling analysis (SCA) is a method for analyzing multiple sequence alignments that was used to identify groups of coevolving residues termed "sectors". The method applies spectral analysis to a matrix obtained by combining correlation information with sequence conservation. It has been asserted that the protein sectors identified by SCA are functionally significant, with different sectors controlling different biochemical properties of the protein. Here we reconsider the available experimental data and note that it involves almost exclusively proteins with a single sector. We show that in this case sequence conservation is the dominating factor in SCA, and can alone be used to make statistically equivalent functional predictions. Therefore, we suggest shifting the experimental focus to proteins for which SCA identifies several sectors. Correlations in protein alignments, which have been shown to be informative in a number of independent studies, would then be less dominated by sequence conservation.
36 pages, 17 figures
References in corpus (4)
- Direct-coupling analysis of residue co-evolution captures native contacts across many protein families
- Identification of direct residue contacts in protein-protein interaction by message passing
- Financial Applications of Random Matrix Theory: a short review
- Elements of Coevolution in Biological Sequences
Cited by in corpus (8)
- Architecture and Co-Evolution of Allosteric Materials
- Green function of correlated genes in a minimal mechanical model of protein evolution
- Physical model of the genotype-to-phenotype map of proteins
- Proteins: the physics of amorphous evolving matter
- Revealing evolutionary constraints on proteins through sequence analysis
- Physical networks become what they learn
- Impact of phylogeny on the inference of functional sectors from protein sequence data
- Symmetry, Rigidity, and Allosteric Signaling: From Monomeric Proteins to Molecular Machines