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Selection shapes the robustness of ligand-binding amino acids
- Source :
- Journal of molecular evolution
- Publication Year :
- 2013
-
Abstract
- The phenotypes of biological systems are to some extent robust to genotypic changes. Such robustness exists on multiple levels of biological organization. We analyzed this robustness for two categories of amino acids in proteins. Specifically, we studied the codons of amino acids that bind or do not bind small molecular ligands. We asked to what extent codon changes caused by mutation or mistranslation may affect physicochemical amino acid properties or protein folding. We found that the codons of ligand-binding amino acids are on average more robust than those of non-binding amino acids. Because mistranslation is usually more frequent than mutation, we speculate that selection for error mitigation at the translational level stands behind this phenomenon. Our observations suggest that natural selection can affect the robustness of very small units of biological organization. © 2013 Springer Science+Business Media New York.
- Subjects :
- Protein Folding
Genotype
Codon bias
Biology
Ligands
03 medical and health sciences
10127 Institute of Evolutionary Biology and Environmental Studies
0302 clinical medicine
1311 Genetics
Genetics
Protein biosynthesis
1312 Molecular Biology
Humans
Binding site
Amino Acids
Selection, Genetic
Codon
Molecular Biology
Ecology, Evolution, Behavior and Systematics
Ligand binding
030304 developmental biology
chemistry.chemical_classification
0303 health sciences
Natural selection
Binding Sites
Robustness (evolution)
High-Throughput Nucleotide Sequencing
Proteins
Amino acid
Phenotype
1105 Ecology, Evolution, Behavior and Systematics
chemistry
Codon usage bias
Protein Biosynthesis
Mutation
570 Life sciences
biology
590 Animals (Zoology)
Protein folding
Synonymous substitution
030217 neurology & neurosurgery
Codon robustness
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Journal of molecular evolution
- Accession number :
- edsair.doi.dedup.....6bc7093ad195c4a9a6fec101905ac86d