Kinome‐Wide Profiling Prediction of Small Molecules

• DOI: 10.1002/cmdc.201700180
• Publication Date: 2017-05-24T01:05:53Z
• Authors: Frieda A. Sorgenfrei; Simone Fulle; Benjamin Merget
• Keywords: Small Molecule Libraries; 0301 basic medicine; 03 medical and health sciences; Humans; Quantitative Structure-Activity Relationship; Protein Kinase Inhibitors; Protein Kinases

AbstractExtensive kinase profiling data, covering more than half of the human kinome, are available nowadays and allow the construction of activity prediction models of high practical utility. Proteochemometric (PCM) approaches use compound and protein descriptors, which enables the extrapolation of bioactivity values to thus far unexplored kinases. In this study, the potential of PCM to make large‐scale predictions on the entire kinome is explored, considering the applicability on novel compounds and kinases, including clinically relevant mutants. A rigorous validation indicates high predictive power on left‐out kinases and superiority over individual kinase QSAR models for new compounds. Furthermore, external validation on clinically relevant mutant kinases reveals an excellent predictive power for mutations spread across the ATP binding site.