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Ligands
Code Name Style Show Link
CC3 N-{3-[(4-{[3-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)amino]phenyl}cyclopropanecarboxamide
SO4 Sulfate ion
Non-standard Residues
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Glycosylation
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Code : 2NP8   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : Structural Basis for the Inhibition of Aurora A Kinase by a Novel Class of High Affinity Disubstituted Pyrimidine Inhibitors
Release Data : 2006-12-26
Compound :
mol_id molecule chains synonym
1 Serine/threonine-protein kinase 6 A Serine/threonine kinase 15, Aurora/IPL1-related kinase 1, Aurora-related kinase 1, hARK1, Aurora-A, Breast-tumor-amplified kinase
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: AIK
expression_system_strain: BL21(DE3)
expression_system_vector_type: plasmid
expression_system_plasmid: pET28
Authors : Tari, L.W., Hoffman, I.D., Bensen, D.C., Hunter, M.J., Nix, J., Nelson, K.J., McRee, D.E., Swanson, R.V.
Keywords : Aurora A kinase, AIK, aurora 2 kinase, kinase, kinase inhibitor, Transferase
Exp. method : X-RAY DIFFRACTION ( 2.25 Å )
Citation :

Structural basis for the inhibition of Aurora A kinase by a novel class of high affinity disubstituted pyrimidine inhibitors.

Tari, L.W.,Hoffman, I.D.,Bensen, D.C.  et al.
(2007)  Bioorg.Med.Chem.Lett.  17 : 688 - 691

PubMed: 17157005
DOI: 10.1016/j.bmcl.2006.10.086

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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