PDB ID: 6CZ3
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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ACT | Acetate ion | PoSSuM | |||
FLJ | (3-fluoro-4-{[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]amino}phenyl)(morpholin-4-yl)methanone | PoSSuM | |||
K | Potassium ion | PoSSuM |
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Download interaction data: 6CZ3
Structure summary
Code : | 6CZ3 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | Transferase/Transferase Inhibitor | ||||||||||||
Title : | Structure of the PTK6 kinase domain bound to a type I inhibitor (3-fluoro-4-{[6-methyl-3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]amino}phenyl)(morpholin-4-yl)methanone | ||||||||||||
Release Data : | 2018-06-20 | ||||||||||||
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Authors : | Gajiwala, K.S., Johnson, E., Cronin, C.N. | ||||||||||||
Keywords : | Protein kinase, PTK6, Transferase-Transferase Inhibitor complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.80 Å ) | ||||||||||||
Citation : |
Small molecule inhibitors reveal PTK6 kinase is not an oncogenic driver in breast cancers.
Qiu, L.,Levine, K.,Gajiwala, K.S.
et al.
PubMed: 29879184 |
Reaction
Chain : | A | ||||||||
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UniProt : | Q13882 (PTK6_HUMAN) | ||||||||
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