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Ligands
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9YQ 4-(propanoylamino)-~{N}-[4-[(5,8,11-trimethyl-6-oxidanylidene-pyrimido[4,5-B][1,4]benzodiazepin-2-yl)amino]phenyl]benzamide
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Code : 5ONE   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : Crystal structure of Aurora-A in complex with FMF-03-145-1 (compound 2)
Release Data : 2017-09-06
Compound :
mol_id molecule chains synonym
1 Aurora kinase A A Aurora 2,Aurora/IPL1-related kinase 1,hARK1,Breast tumor-amplified kinase,Serine/threonine-protein kinase 15,Serine/threonine-protein kinase 6,Serine/threonine-protein kinase aurora-A
ec: 2.7.11.1
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:469008)
gene: AURKA, AIK, AIRK1, ARK1, AURA, AYK1, BTAK, IAK1, STK15, STK6
expression_system_strain: BL21(DE3)
expression_system_variant: R3-pRARE2
expression_system_vector_type: plasmid
Authors : Chaikuad, A., Ferguson, F.M., Gray, N.S., Knapp, S.
Keywords : aurora kinase, kinase, inhibitor complex, cell cycle, TRANSFERASE
Exp. method : X-RAY DIFFRACTION ( 2.60 Å )
Citation :

Characterization of a highly selective inhibitor of the Aurora kinases.

Ferguson, F.M.,Doctor, Z.M.,Chaikuad, A.  et al.
(2017)  Bioorg. Med. Chem. Lett.  27 : 4405 - 4408

PubMed: 28818446
DOI: 10.1016/j.bmcl.2017.08.016

Chain : A
UniProt : O14965 (AURKA_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.11.1 PubMed:12237287, PubMed:16337122, PubMed:19140666, PubMed:19402633, PubMed:27837025, PubMed:28218735
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ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.11.1 PubMed:12237287, PubMed:16337122, PubMed:19140666, PubMed:19402633, PubMed:27837025, PubMed:28218735
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