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4D2S

Human TTK in complex with a Dyrk1B inhibitor

Summary for 4D2S
Entry DOI10.2210/pdb4d2s/pdb
Related4D2R
DescriptorDUAL SPECIFICITY PROTEIN KINASE TTK, N-{2-methoxy-4-[(1-methylpiperidin-4-yl)oxy]phenyl}-4-(1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine (3 entities in total)
Functional Keywordstransferase, oncology
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains1
Total formula weight33089.01
Authors
Primary citationKettle, J.G.,Ballard, P.,Bardelle, C.,Cockerill, M.,Colclough, N.,Critchlow, S.E.,Debreczeni, J.E.,Fairley, G.,Fillery, S.,Graham, M.A.,Goodwin, L.,Guichard, S.,Hudson, K.,Ward, R.A.,Whittaker, D.
Discovery and Optimization of a Novel Series of Dyrk1B Kinase Inhibitors to Explore a Mek Resistance Hypothesis.
J.Med.Chem., 58:2834-, 2015
Cited by
PubMed Abstract: Potent and selective inhibitors of Dyrk1B kinase were developed to explore the hypothesis, based on siRNA studies, that Dyrk1B may be a resistance mechanism in cells undergoing a stress response.
PubMed: 25738750
DOI: 10.1021/ACS.JMEDCHEM.5B00098
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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