PDB ID: 4G5J
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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0WN | N-{4-[(3-chloro-4-fluorophenyl)amino]-7-[(3s)-tetrahydrofuran-3-yloxy]quinazolin-6-yl}-4-(dimethylamino)butanamide | PoSSuM | |||
0WM | (2e)-N-{4-[(3-chloro-4-fluorophenyl)amino]-7-[(3s)-tetrahydrofuran-3-yloxy]quinazolin-6-yl}-4-(dimethylamino)but-2-enamide | PoSSuM |
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Download interaction data: 4G5J
Structure summary
Code : | 4G5J PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE/TRANSFERASE INHIBITOR | ||||||||||||
Title : | Crystal structure of EGFR kinase in complex with BIBW2992 | ||||||||||||
Release Data : | 2012-08-29 | ||||||||||||
Compound : |
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Source : |
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Authors : | Solca, F., Dahl, G., Zoephel, A., Bader, G., Sanderson, M., Klein, C., Kraemer, O., Himmelsbach, F., Haaksma, E., Adolf, G.R. | ||||||||||||
Keywords : | PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.8 Å ) | ||||||||||||
Citation : |
Target Binding Properties and Cellular Activity of Afatinib (BIBW 2992), an Irreversible ErbB Family Blocker.
Solca, F.,Dahl, G.,Zoephel, A.
et al.
PubMed: 22888144 |
Reaction
Chain : | A | ||||||||
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UniProt : | P00533 (EGFR_HUMAN) | ||||||||
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