3E62
Fragment based discovery of JAK-2 inhibitors
Summary for 3E62
Entry DOI | 10.2210/pdb3e62/pdb |
Related | 3E63 3E64 |
Descriptor | Tyrosine-protein kinase JAK2, 5-bromo-1H-indazol-3-amine (3 entities in total) |
Functional Keywords | drug discovery, jak2, fragment based, atp-binding, disease mutation, kinase, membrane, nucleotide-binding, phosphoprotein, proto-oncogene, sh2 domain, transferase, tyrosine-protein kinase |
Biological source | Homo sapiens (human) |
Cellular location | Endomembrane system; Peripheral membrane protein (By similarity): O60674 |
Total number of polymer chains | 1 |
Total formula weight | 34890.54 |
Authors | Antonysamy, S.,Fang, W.,Hirst, G.,Park, F.,Russell, M.,Smyth, L.,Sprengeler, P.,Stappenbeck, F.,Steensma, R.,Thompson, D.A.,Wilson, M.,Wong, M.,Zhang, A.,Zhang, F. (deposition date: 2008-08-14, release date: 2008-10-14, Last modification date: 2012-02-08) |
Primary citation | Antonysamy, S.,Hirst, G.,Park, F.,Sprengeler, P.,Stappenbeck, F.,Steensma, R.,Wilson, M.,Wong, M. Fragment-based discovery of JAK-2 inhibitors. Bioorg.Med.Chem.Lett., 19:279-282, 2009 Cited by PubMed: 19019674DOI: 10.1016/j.bmcl.2008.08.064 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.922 Å) |
Structure validation
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