Ontology highlight
ABSTRACT: Background
Functionally relevant artificial or natural mutations are difficult to assess or predict if no structure-function information is available for a protein. This is especially important to correctly identify functionally significant non-synonymous single nucleotide polymorphisms (nsSNPs) or to design a site-directed mutagenesis strategy for a target protein. A new and powerful methodology is proposed to guide these two decision strategies, based only on conservation rules of physicochemical properties of amino acids extracted from a multiple alignment of a protein family where the target protein belongs, with no need of explicit structure-function relationships.Results
A statistical analysis is performed over each amino acid position in the multiple protein alignmen
SUBMITTER: Olivera-Nappa A
PROVIDER: S-EPMC3123232 | biostudies-literature | 2011 Apr
REPOSITORIES: biostudies-literature