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4BYI

Aurora A kinase bound to a highly selective imidazopyridine inhibitor

Summary for 4BYI
Entry DOI10.2210/pdb4byi/pdb
Related4BYJ
DescriptorAURORA KINASE A, (S)-N-((1-(6-chloro-2-(1,3-dimethyl-1H-pyrazol-4-yl)-3H-imidazo[4,5-b]pyridin-7-yl)pyrrolidin-3-yl)methyl)acetamide (2 entities in total)
Functional Keywordstransferase, cell cycle, inhibitor
Biological sourceHOMO SAPIENS (HUMAN)
Cellular locationCytoplasm, cytoskeleton, microtubule organizing center, centrosome: O14965
Total number of polymer chains1
Total formula weight33336.65
Authors
Joshi, A.,Kosmopoulou, M.,Bayliss, R. (deposition date: 2013-07-19, release date: 2013-11-20, Last modification date: 2023-12-20)
Primary citationBavetsias, V.,Faisal, A.,Crumpler, S.,Brown, N.,Kosmopoulou, M.,Joshi, A.,Atrash, B.,Perez-Fuertes, Y.,Schmitt, J.A.,Boxall, K.J.,Burke, R.,Sun, C.,Avery, S.,Bush, K.,Henley, A.,Raynaud, F.I.,Workman, P.,Bayliss, R.,Linardopoulos, S.,Blagg, J.
Aurora Isoform Selectivity: Design and Synthesis of Imidazo[4,5-B]Pyridine Derivatives as Highly Selective Inhibitors of Aurora-A Kinase in Cells.
J.Med.Chem., 56:9122-, 2013
Cited by
PubMed: 24195668
DOI: 10.1021/JM401115G
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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