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ABSTRACT: Background
Predicting the effect of single point variations on protein stability constitutes a crucial step toward understanding the relationship between protein structure and function. To this end, several methods have been developed to predict changes in the Gibbs free energy of unfolding (∆∆G) between wild type and variant proteins, using sequence and structure information. Most of the available methods however do not exhibit the anti-symmetric prediction property, which guarantees that the predicted ∆∆G value for a variation is the exact opposite of that predicted for the reverse variation, i.e., ∆∆G(A → B) = -∆∆G(B → A), where A and B are amino acids.Results
Here we introduce simple anti-symmetric features, based on evolutionary information, which are combined to defin
SUBMITTER: Montanucci L
PROVIDER: S-EPMC6606456 | biostudies-literature | 2019 Jul
REPOSITORIES: biostudies-literature