Ontology highlight
ABSTRACT:
INSTRUMENT(S): Orbitrap Fusion, Q Exactive HF, LTQ Orbitrap Elite, Q Exactive
ORGANISM(S): Homo Sapiens (ncbitaxon:9606)
SUBMITTER: Bernhard Kuster
PROVIDER: MSV000081932 | MassIVE | Fri Jan 12 21:28:00 GMT 2018
SECONDARY ACCESSION(S): PXD005336
REPOSITORIES: MassIVE
Klaeger Susan S Heinzlmeir Stephanie S Wilhelm Mathias M Polzer Harald H Vick Binje B Koenig Paul-Albert PA Reinecke Maria M Ruprecht Benjamin B Petzoldt Svenja S Meng Chen C Zecha Jana J Reiter Katrin K Qiao Huichao H Helm Dominic D Koch Heiner H Schoof Melanie M Canevari Giulia G Casale Elena E Depaolini Stefania Re SR Feuchtinger Annette A Wu Zhixiang Z Schmidt Tobias T Rueckert Lars L Becker Wilhelm W Huenges Jan J Garz Anne-Kathrin AK Gohlke Bjoern-Oliver BO Zolg Daniel Paul DP Kayser Gian G Vooder Tonu T Preissner Robert R Hahne Hannes H Tõnisson Neeme N Kramer Karl K Götze Katharina K Bassermann Florian F Schlegl Judith J Ehrlich Hans-Christian HC Aiche Stephan S Walch Axel A Greif Philipp A PA Schneider Sabine S Felder Eduard Rudolf ER Ruland Juergen J Médard Guillaume G Jeremias Irmela I Spiekermann Karsten K Kuster Bernhard B
Science (New York, N.Y.) 20171201 6367
Kinase inhibitors are important cancer therapeutics. Polypharmacology is commonly observed, requiring thorough target deconvolution to understand drug mechanism of action. Using chemical proteomics, we analyzed the target spectrum of 243 clinically evaluated kinase drugs. The data revealed previously unknown targets for established drugs, offered a perspective on the "druggable" kinome, highlighted (non)kinase off-targets, and suggested potential therapeutic applications. Integration of phosphop ...[more]