Automated evaluation of quaternary structures from protein crystals.
Ontology highlight
ABSTRACT: A correct assessment of the quaternary structure of proteins is a fundamental prerequisite to understanding their function, physico-chemical properties and mode of interaction with other proteins. Currently about 90% of structures in the Protein Data Bank are crystal structures, in which the correct quaternary structure is embedded in the crystal lattice among a number of crystal contacts. Computational methods are required to 1) classify all protein-protein contacts in crystal lattices as biologically relevant or crystal contacts and 2) provide an assessment of how the biologically relevant interfaces combine into a biological assembly. In our previous work we addressed the first problem with our EPPIC (Evolutionary Protein Protein Interface Classifier) method. Here, we present our soluti
SUBMITTER: Bliven S
PROVIDER: S-EPMC5945228 | biostudies-literature | 2018 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA