5K3Y
Crystal structure of AuroraB/INCENP in complex with BI 811283
Summary for 5K3Y
Entry DOI | 10.2210/pdb5k3y/pdb |
Descriptor | Aurora kinase B-A, Inner centromere protein A, N-methyl-N-(1-methylpiperidin-4-yl)-4-{[4-({(1R,2S)-2-[(propan-2-yl)carbamoyl]cyclopentyl}amino)-5-(trifluoromethyl)pyrimidin-2-yl]amino}benzamide, ... (4 entities in total) |
Functional Keywords | kinase, inhibitor, transferase |
Biological source | Xenopus laevis (African clawed frog) More |
Cellular location | Nucleus: Q6DE08 O13024 |
Total number of polymer chains | 4 |
Total formula weight | 81388.26 |
Authors | Bader, G.,Zahn, S.K.,Zoephel, A. (deposition date: 2016-05-20, release date: 2016-08-17, Last modification date: 2022-12-07) |
Primary citation | Sini, P.,Gurtler, U.,Zahn, S.K.,Baumann, C.,Rudolph, D.,Baumgartinger, R.,Strauss, E.,Haslinger, C.,Tontsch-Grunt, U.,Waizenegger, I.C.,Solca, F.,Bader, G.,Zoephel, A.,Treu, M.,Reiser, U.,Garin-Chesa, P.,Boehmelt, G.,Kraut, N.,Quant, J.,Adolf, G.R. Pharmacological Profile of BI 847325, an Orally Bioavailable, ATP-Competitive Inhibitor of MEK and Aurora Kinases. Mol.Cancer Ther., 15:2388-2398, 2016 Cited by PubMed: 27496137DOI: 10.1158/1535-7163.MCT-16-0066 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.6 Å) |
Structure validation
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