PDB ID: 3VAP
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0FY | 3-(1-{2-[(3-fluoropyridinium-4-yl)amino]-2-oxoethyl}-1h-pyrazol-4-yl)-6-methyl-8-[(3-{[(1r,3r)-3-methylpiperidinium-1-yl]methyl}-1,2-thiazol-5-yl)amino]imidazo[1,2-a]pyrazin-1-ium | PoSSuM |
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Download interaction data: 3VAP
Structure summary
Code : | 3VAP PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE/TRANSFERASE INHIBITOR | ||||||||||||
Title : | Synthesis and SAR Studies of imidazo-[1,2-a]-pyrazine Aurora kinase inhibitors with improved off target kinase selectivity | ||||||||||||
Release Data : | 2012-05-02 | ||||||||||||
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Authors : | Voss, M.E., Rainka, M.P., Fleming, M., Peterson, L.H., Belanger, D.B., Siddiqui, M.A., Hruza, A., Voigt, J., Basso, A.D., Gray, K. | ||||||||||||
Keywords : | kinase, cell cycle, inhibitor, transferase, TRANSFERASE-TRANSFERASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.66 Å ) | ||||||||||||
Citation : |
Synthesis and SAR studies of imidazo-[1,2-a]-pyrazine Aurora kinase inhibitors with improved off-target kinase selectivity.
Voss, M.E.,Rainka, M.P.,Fleming, M.
et al.
PubMed: 22503250 |
Reaction
Chain : | A | ||||||||||||
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UniProt : | O14965 (AURKA_HUMAN) | ||||||||||||
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