Here, we provide a comprehensive overview of the selectivity profiles of 242 kinase inhibitors currently in clinical trials. We screened available inhibitors against human protein kinases by using the Kinobead technology resulting in a drug matrix identifying the druggable kinome and related proteins.
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Kinase inhibitors ; chemical proteomics ; clinical kinase inhibitors ; selectivity ; target ; LC-MS/MS ; mass spectrometry
Principal Investigators: (in alphabetical order) |
Bernhard Kuster, Chair of Proteomics and Bioanalytics, Technische Universit�t M�nchen, Germany, N/A |
Submitting User: | ccms |
Klaeger S, Heinzlmeir S, Wilhelm M, Polzer H, Vick B, Koenig PA, Reinecke M, Ruprecht B, Petzoldt S, Meng C, Zecha J, Reiter K, Qiao H, Helm D, Koch H, Schoof M, Canevari G, Casale E, Depaolini SR, Feuchtinger A, Wu Z, Schmidt T, Rueckert L, Becker W, Huenges J, Garz AK, Gohlke BO, Zolg DP, Kayser G, Vooder T, Preissner R, Hahne H, Tõnisson N, Kramer K, Götze K, Bassermann F, Schlegl J, Ehrlich HC, Aiche S, Walch A, Greif PA, Schneider S, Felder ER, Ruland J, Médard G, Jeremias I, Spiekermann K, Kuster B.
The target landscape of clinical kinase drugs.
Science.
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Experimental Design | ||
Conditions:
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Identification Results | ||
Proteins (Human, Remapped):
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Proteins (Reported):
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PSMs:
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Quantification Results | ||
Differential Proteins:
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Quantified Proteins:
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