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2BMC

Aurora-2 T287D T288D complexed with PHA-680632

Summary for 2BMC
Entry DOI10.2210/pdb2bmc/pdb
Related1MQ4 1MUO 1OL5 1OL6 1OL7
DescriptorSERINE THREONINE-PROTEIN KINASE 6, (3E)-N-(2,6-DIETHYLPHENYL)-3-{[4-(4-METHYLPIPERAZIN-1-YL)BENZOYL]IMINO}PYRROLO[3,4-C]PYRAZOLE-5(3H)-CARBOXAMIDE (3 entities in total)
Functional Keywordscell cycle, transferase, serine/threonine-protein kinase, atp-binding, phosphorylation
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains6
Total formula weight214816.53
Authors
Primary citationFancelli, D.,Berta, D.,Bindi, S.,Cameron, A.,Cappella, P.,Carpinelli, P.,Catana, C.,Forte, B.,Giordano, P.,Giorgini, M.L.,Mantegani, S.,Marsiglio, A.,Meroni, M.,Moll, J.,Pittala, V.,Roletto, F.,Severino, D.,Soncini, C.,Storici, P.,Tonani, R.,Varasi, M.,Vulpetti, A.,Vianello, P.
Potent and Selective Aurora Inhibitors Identified by the Expansion of a Novel Scaffold for Protein Kinase Inhibition.
J.Med.Chem., 48:3080-, 2005
Cited by
PubMed: 15828847
DOI: 10.1021/JM049076M
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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