Ontology highlight
ABSTRACT:
SUBMITTER: Ung PM
PROVIDER: S-EPMC6054563 | biostudies-literature | 2018 Jul
REPOSITORIES: biostudies-literature
Ung Peter Man-Un PM Rahman Rayees R Schlessinger Avner A
Cell chemical biology 20180531 7
Protein kinases are dynamic, adopting different conformational states that are critical for their catalytic activity. We assess a range of structural features derived from the conserved αC helix and DFG motif to define the conformational space of the catalytic domain of protein kinases. We then construct Kinformation, a random forest classifier, to annotate the conformation of 3,708 kinase structures in the PDB. Our classification scheme captures known active and inactive kinase conformations an ...[more]