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2XRU

AURORA-A T288E COMPLEXED WITH PHA-828300

Summary for 2XRU
Entry DOI10.2210/pdb2xru/pdb
Related1MQ4 1MUO 1OL5 1OL6 1OL7 2BMC 2C6D 2C6E 2J4Z 2J50 2W1C 2W1D 2W1E 2W1F 2W1G 2WQE 2WTV 2WTW 2X6D 2X6E 2X81 2XNE 2XNG
DescriptorSERINE/THREONINE-PROTEIN KINASE 6, 3-({[4-(4-METHYLPIPERAZIN-1-YL)PHENYL]CARBONYL}AMINO)-N-[(1R)-1-PHENYLPROPYL]-1H-THIENO[3,2-C]PYRAZOLE-5-CARBOXAMIDE (2 entities in total)
Functional Keywordsnucleotide-binding, kinase, cell cycle, transferase
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains1
Total formula weight32899.71
Authors
Primary citationBindi, S.,Fancelli, D.,Alli, C.,Berta, D.,Bertrand, J.A.,Cameron, A.D.,Cappella, P.,Carpinelli, P.,Cervi, G.,Croci, V.,D'Anello, M.,Forte, B.,Laura Giorgini, M.,Marsiglio, A.,Moll, J.,Pesenti, E.,Pittala, V.,Pulici, M.,Riccardi-Sirtori, F.,Roletto, F.,Soncini, C.,Storici, P.,Varasi, M.,Volpi, D.,Zugnoni, P.,Vianello, P.
Thieno[3,2-C]Pyrazoles: A Novel Class of Aurora Inhibitors with Favorable Antitumor Activity.
Bioorg.Med.Chem., 18:7113-, 2010
Cited by
PubMed: 20817473
DOI: 10.1016/J.BMC.2010.07.048
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.9 Å)
Structure validation

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