| Literature DB >> 27939289 |
Jieming Chen1, Bo Wang2, Lynne Regan3, Mark Gerstein4.
Abstract
Large-scale genome sequencing holds great promise for the interpretation of protein structures through the discovery of many, rare functional variants in the human population. However, because protein-coding regions are under high selective constraints, these variants occur at low frequencies, such that there is often insufficient statistics for downstream calculations. To address this problem, we develop the Intensification approach, which uses the modular structure of repeat protein domains to amplify signals of selection from population genetics and traditional interspecies conservation. In particular, we are able to aggregate variants at the codon level to identify important positions in repeat domains that show strong conservation signals. This allows us to compare conservation over different evolutionary timescales. It also enables us to visualize population-genetic measures on protein structures. We make available the Intensification results as an online resource (http://intensification.gersteinlab.org) and illustrate the approach through a case study on the tetratricopeptide repeat.Entities:
Keywords: database; exome sequencing; population genetics; protein repeat domain; protein structure
Mesh:
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Year: 2016 PMID: 27939289 PMCID: PMC5420328 DOI: 10.1016/j.jmb.2016.12.003
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469