Journal article
Pervasive Cryptic Epistasis in Molecular Evolution
Abstract
The functional effects of most amino acid replacements accumulated during molecular evolution are unknown, because most are not observed naturally and the possible combinations are too numerous. We created 168 single mutations in wild-type Escherichia coli isopropymalate dehydrogenase (IMDH) that match the differences found in wild-type Pseudomonas aeruginosa IMDH. 104 mutant enzymes performed similarly to E. coli wild-type IMDH, one was …
Authors
Lunzer M; Golding GB; Dean AM
Journal
PLOS Genetics, Vol. 6, No. 10,
Publisher
Public Library of Science (PLoS)
DOI
10.1371/journal.pgen.1001162
ISSN
1553-7390
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
3-Isopropylmalate DehydrogenaseAmino Acid SequenceAmino Acid SubstitutionBacterial ProteinsBase SequenceBinding SitesEpistasis, GeneticEscherichia coliEscherichia coli ProteinsEvolution, MolecularKineticsModels, MolecularMolecular Sequence DataMutagenesis, Site-DirectedMutationNADPhylogenyProtein Structure, TertiaryPseudomonas aeruginosaSequence Homology, Amino Acid