PDB ID: 3FV8
Hetero Atom Contents
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Color scheme of protein:
Code | Name | Style | Show | Link | |
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EDO | 1,2-ethanediol | PoSSuM | |||
JK3 | 5-bromo-N-(3-chloro-2-(4-(prop-2-ynyl)piperazin-1-yl)phenyl)furan-2-carboxamide | PoSSuM |
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OCY | Hydroxyethylcysteine |
Code | Name | Emphasize |
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Download interaction data: 3FV8
Structure summary
Code : | 3FV8 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE | ||||||||||||
Title : | JNK3 bound to piperazine amide inhibitor, SR2774. | ||||||||||||
Release Data : | 2009-04-07 | ||||||||||||
Compound : |
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Source : |
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Authors : | Habel, J.E. | ||||||||||||
Keywords : | JNK3, protein-inhibitor complex, Alternative splicing, ATP-binding, Chromosomal rearrangement, Cytoplasm, Epilepsy, Kinase, Nucleotide-binding, Phosphoprotein, Serine/threonine-protein kinase, Transferase | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.280 Å ) | ||||||||||||
Citation : |
Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitors.
Shin, Y.,Chen, W.,Habel, J.
et al.
PubMed: 19433357 |
Reaction
Chain : | A | ||||||||||||
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UniProt : | P53779 (MK10_HUMAN) | ||||||||||||
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