SKEMPI 2.0: an updated benchmark of changes in protein–protein binding energy, kinetics and thermodynamics upon mutation
Author(s) -
Justina Jankauskaitė,
Brian JiménezGarcía,
Justas Dapkūnas,
Juan FernándezRecio,
Iain H. Moal
Publication year - 2018
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/bty635
Subject(s) - kinetics , mutation , protein data bank , enthalpy , binding energy , computational biology , entropy (arrow of time) , chemistry , thermodynamics , protein structure , biology , biochemistry , physics , gene , quantum mechanics , nuclear physics
Understanding the relationship between the sequence, structure, binding energy, binding kinetics and binding thermodynamics of protein-protein interactions is crucial to understanding cellular signaling, the assembly and regulation of molecular complexes, the mechanisms through which mutations lead to disease, and protein engineering.
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