PDB ID: 6D20
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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FQD | 5-(4-fluorophenyl)thieno[2,3-D]pyrimidin-4(3h)-one | PoSSuM | |||
FQG | 5-{[2,4-dichloro-5-(pyridin-2-yl)benzene-1-carbonyl]amino}-N-(2-hydroxy-2-methylpropyl)-1-phenyl-1h-pyrazole-3-carboxamide | PoSSuM |
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Download interaction data: 6D20
Structure summary
Code : | 6D20 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE/Inhibitor | ||||||||||||
Title : | Crystal structure of Tyrosine-protein kinase receptor in complex with 5-(4-fluorophenyl)thieno[2,3-D]pyrimidin-4(3H)-one and 5-{[2,4-dichloro-5-(pyridin-2-yl)benzene-1-carbonyl]amino}-N-(2-hydroxy-2-methylpropyl)-1-phenyl-1H-pyrazole-3-carboxamide Inhibitors | ||||||||||||
Release Data : | 2018-05-02 | ||||||||||||
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Authors : | Greasley, S.E., Johnson, E., Kraus, M.L., Cronin, C.N. | ||||||||||||
Keywords : | Allosteric Inhibitor Complex Tyrosine kinase, TRANSFERASE, TRANSFERASE-Inhibitor complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.9400 Å ) | ||||||||||||
Citation : |
Discovery of Allosteric, Potent, Subtype Selective, and Peripherally Restricted TrkA Kinase Inhibitors.
Bagal, S.K.,Omoto, K.,Blakemore, D.C.
et al.
PubMed: 29672039 |
Reaction
Chain : | A | ||||||||
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UniProt : | P04629 (NTRK1_HUMAN) | ||||||||
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