PDB ID: 4D9T
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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0JG | Methyl (2s)-3-{4-amino-7-[(1e)-3-hydroxyprop-1-en-1-yl]-5-(4-methylphenyl)-7h-pyrrolo[2,3-D]pyrimidin-6-yl}-2-cyanopropanoate | PoSSuM | |||
NA | Sodium ion | PoSSuM |
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Download interaction data: 4D9T
Structure summary
Code : | 4D9T PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE/TRANSFERASE INHIBITOR | ||||||||||||
Title : | Rsk2 C-terminal Kinase Domain with inhibitor (E)-methyl 3-(4-amino-7-(3-hydroxypropyl)-5-P-tolyl-7H-pyrrolo[2,3-D]pyrimidin-6-yl)-2-cyanoacrylate | ||||||||||||
Release Data : | 2012-04-25 | ||||||||||||
Compound : |
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Authors : | Serafimova, I.M., Pufall, M.A., Krishnan, S., Duda, K., Cohen, M.S., Maglathlin, R.L., McFarland, J.M., Miller, R.M., Frodin, M., Taunton, J. | ||||||||||||
Keywords : | kinase, inhibitor, reversible, thiol, phosphorylation, migration, TRANSFERASE-TRANSFERASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.4000 Å ) | ||||||||||||
Citation : |
Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles.
Serafimova, I.M.,Pufall, M.A.,Krishnan, S.
et al.
PubMed: 22466421 |
Reaction
Chain : | A | ||||||||||||
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UniProt : | P51812 (KS6A3_HUMAN) | ||||||||||||
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