Redefining the Protein Kinase Conformational Space with Machine Learning.

ABSTRACT: 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 and defines an additional conformational state, thereby refining the current understanding of the kinase conformational space. Furthermore, network analysis of the small molecules recognized by each conformation captures chemical substructures that are associated with each conformation type. Our descr

SUBMITTER: Ung PM 

PROVIDER: S-EPMC6054563 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature