PDB ID: 6EBW
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J3Y | [6-{[(1s)-1-(5-fluoropyridin-2-yl)ethyl]amino}-1-(5-methyl-1h-pyrazol-3-yl)-1h-pyrrolo[2,3-B]pyridin-3-yl](morpholin-4-yl)methanone | PoSSuM |
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Download interaction data: 6EBW
Structure summary
Code : | 6EBW PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE/INHIBITOR | ||||||||||||
Title : | hALK in complex with compound 9 (6-(((1S)-1-(5-Fluoropyridin-2-yl)ethyl)amino)-1-(3-methyl-1H-pyrazol-5-yl)-1H-pyrrolo[2,3-B]pyridin-3-yl)(morpholin-4-yl)methanone | ||||||||||||
Release Data : | 2019-05-01 | ||||||||||||
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Authors : | Lane, W., Saikatendu, K. | ||||||||||||
Keywords : | Inhibitor, complex, kinase, sbdd, TRANSFERASE-INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.455 Å ) | ||||||||||||
Citation : |
Discovery of Potent, Selective, and Brain-Penetrant 1 H-Pyrazol-5-yl-1 H-pyrrolo[2,3- b]pyridines as Anaplastic Lymphoma Kinase (ALK) Inhibitors.
Fushimi, M.,Fujimori, I.,Wakabayashi, T.
et al.
PubMed: 31009559 |
Reaction
Chain : | A | ||||||||
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UniProt : | Q9UM73 (ALK_HUMAN) | ||||||||
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