4JG6
RSK2 CTD bound to 2-cyano-3-(1H-indazol-5-yl)acrylamide
Summary for 4JG6
Entry DOI | 10.2210/pdb4jg6/pdb |
Descriptor | Ribosomal protein S6 kinase alpha-3, (2S)-2-cyano-3-(1H-indazol-5-yl)propanamide, SODIUM ION, ... (4 entities in total) |
Functional Keywords | protein kinase, phosphorylation, covalent inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Nucleus (By similarity): P51812 |
Total number of polymer chains | 1 |
Total formula weight | 40304.76 |
Authors | Miller, R.M.,Paavilainen, V.O.,Krishnan, S.,Serafimova, I.M.,Taunton, J. (deposition date: 2013-02-28, release date: 2013-04-10, Last modification date: 2013-04-24) |
Primary citation | Miller, R.M.,Paavilainen, V.O.,Krishnan, S.,Serafimova, I.M.,Taunton, J. Electrophilic fragment-based design of reversible covalent kinase inhibitors. J.Am.Chem.Soc., 135:5298-5301, 2013 Cited by PubMed: 23540679DOI: 10.1021/ja401221b PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.6 Å) |
Structure validation
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