| Literature DB >> 28993150 |
John M Nicoludis1, Rachelle Gaudet2.
Abstract
Recently, protein sequence coevolution analysis has matured into a predictive powerhouse for protein structure and function. Direct methods, which use global statistical models of sequence coevolution, have enabled the prediction of membrane and disordered protein structures, protein complex architectures, and the functional effects of mutations in proteins. The field of membrane protein biochemistry and structural biology has embraced these computational techniques, which provide functional and structural information in an otherwise experimentally-challenging field. Here we review recent applications of protein sequence coevolution analysis to membrane protein structure and function and highlight the promising directions and future obstacles in these fields. We provide insights and guidelines for membrane protein biochemists who wish to apply sequence coevolution analysis to a given experimental system.Entities:
Keywords: ABC transporters; Clustered protocadherin; Conformational changes; Membrane proteins; Protein-protein interactions; Sequence coevolution analysis
Mesh:
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Year: 2017 PMID: 28993150 PMCID: PMC5807202 DOI: 10.1016/j.bbamem.2017.10.004
Source DB: PubMed Journal: Biochim Biophys Acta Biomembr ISSN: 0005-2736 Impact factor: 3.747