5LWN
Crystal structure of JAK3 in complex with Compound 5 (FM409)
Summary for 5LWN
Entry DOI | 10.2210/pdb5lwn/pdb |
Descriptor | Tyrosine-protein kinase JAK3, 1-phenylurea, 1,2-ETHANEDIOL, ... (6 entities in total) |
Functional Keywords | transferase, jak3, covalent inhibitor, reversible covalent inhibitor, induced pocket, arginine pocket, structural genomics, structural genomics consortium, sgc |
Biological source | Homo sapiens (Human) |
Cellular location | Endomembrane system ; Peripheral membrane protein : P52333 |
Total number of polymer chains | 1 |
Total formula weight | 34812.88 |
Authors | Chaikuad, A.,Forster, M.,Mukhopadhyay, S.,Kupinska, K.,Ellis, K.,Mahajan, P.,Burgess-Brown, N.,Edwards, A.M.,Arrowsmith, C.H.,Bountra, C.,Laufer, S.A.,Knapp, S.,Structural Genomics Consortium (SGC) (deposition date: 2016-09-18, release date: 2016-10-26, Last modification date: 2016-11-30) |
Primary citation | Forster, M.,Chaikuad, A.,Bauer, S.M.,Holstein, J.,Robers, M.B.,Corona, C.R.,Gehringer, M.,Pfaffenrot, E.,Ghoreschi, K.,Knapp, S.,Laufer, S.A. Selective JAK3 Inhibitors with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket. Cell Chem Biol, 23:1335-1340, 2016 Cited by PubMed: 27840070DOI: 10.1016/j.chembiol.2016.10.008 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.6 Å) |
Structure validation
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