3TJD
co-crystal structure of Jak2 with thienopyridine 19
Summary for 3TJD
Entry DOI | 10.2210/pdb3tjd/pdb |
Related | 3TJC |
Descriptor | Tyrosine-protein kinase JAK2, 4-amino-2-[4-(tert-butylsulfamoyl)phenyl]-N-methylthieno[3,2-c]pyridine-7-carboxamide (3 entities in total) |
Functional Keywords | jak2, kinase, inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Endomembrane system; Peripheral membrane protein (By similarity): O60674 |
Total number of polymer chains | 2 |
Total formula weight | 71084.81 |
Authors | Huang, X. (deposition date: 2011-08-24, release date: 2011-11-30, Last modification date: 2011-12-28) |
Primary citation | Schenkel, L.B.,Huang, X.,Cheng, A.,Deak, H.L.,Doherty, E.,Emkey, R.,Gu, Y.,Gunaydin, H.,Kim, J.L.,Lee, J.,Loberg, R.,Olivieri, P.,Pistillo, J.,Tang, J.,Wan, Q.,Wang, H.L.,Wang, S.W.,Wells, M.C.,Wu, B.,Yu, V.,Liu, L.,Geuns-Meyer, S. Discovery of potent and highly selective thienopyridine janus kinase 2 inhibitors. J.Med.Chem., 54:8440-8450, 2011 Cited by PubMed: 22087750DOI: 10.1021/jm200911r PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.9 Å) |
Structure validation
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