Enzyme engineering plays a central role in developing efficient biocatalysts for biotechnology, biomedicine, and life sciences. Apart from classical rational design and …
A Marabotti, B Scafuri, A Facchiano - Briefings in Bioinformatics, 2021 - academic.oup.com
A very large number of computational methods to predict the change in thermodynamic stability of proteins due to mutations have been developed during the last 30 years, and …
B Li, YT Yang, JA Capra… - PLoS computational …, 2020 - journals.plos.org
Predicting mutation-induced changes in protein thermodynamic stability (ΔΔG) is of great interest in protein engineering, variant interpretation, and protein biophysics. We introduce …
M Musil, A Jezik, J Horackova, S Borko… - Briefings in …, 2024 - academic.oup.com
Thermostable proteins find their use in numerous biomedical and biotechnological applications. However, the computational design of stable proteins often results in single …
F Pucci, KV Bernaerts, JM Kwasigroch… - …, 2018 - academic.oup.com
Motivation Bioinformatics tools that predict protein stability changes upon point mutations have made a lot of progress in the last decades and have become accurate and fast enough …
F Pucci, R Bourgeas, M Rooman - Scientific reports, 2016 - nature.com
The accurate prediction of the impact of an amino acid substitution on the thermal stability of a protein is a central issue in protein science, and is of key relevance for the rational …
Prediction of protein stability changes caused by mutation is of major importance to protein engineering and for understanding protein misfolding diseases and protein evolution. The …
Accurately predicting the protein thermostability changes upon single point mutations in silico is a challenge that has implications for understanding diseases as well as industrial …
The understanding of the molecular mechanisms driving the fitness of the SARS-CoV-2 virus and its mutational evolution is still a critical issue. We built a simplified computational model …