Ontology highlight
ABSTRACT:
SUBMITTER: Werner M
PROVIDER: S-EPMC8041375 | biostudies-literature | 2021 Apr
REPOSITORIES: biostudies-literature
Werner Martin M Gapsys Vytautas V de Groot Bert L BL
The journal of physical chemistry letters 20210324 12
Correlated mutations have played a pivotal role in the recent success in protein fold prediction. Understanding nonadditive effects of mutations is crucial for altering protein structure, as mutations of multiple residues may change protein stability or binding affinity in a manner unforeseen by the investigation of single mutants. While the couplings between amino acids can be inferred from homologous protein sequences, the physical mechanisms underlying these correlations remain elusive. In th ...[more]