Summary for 7I9B
| Entry DOI | 10.2210/pdb7i9b/pdb |
| Group deposition | Btk ph domain (G_1002333) |
| Descriptor | Tyrosine-protein kinase BTK, (6R)-6-(5-chlorothiophen-2-yl)-4,5,6,7-tetrahydro-1-benzofuran-3-carboxylic acid, MAGNESIUM ION, ... (5 entities in total) |
| Functional Keywords | fragment based drug discovery, ph domain, hydrolase |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 4 |
| Total formula weight | 81333.32 |
| Authors | Brear, P.,West, R.M.,Nicolescu, R.C.B.,Blaszczyk, B.K.,Anwar, A.,Deingruber, T.,Sanders, M.G.,Perez-Areales, F.J.,Stephens, L.R.,Hawkins, P.T.,Spring, D.R.,Hyvonen, M. (deposition date: 2025-03-24, release date: 2026-05-20) |
| Primary citation | Brear, P.,West, R.M.,Nicolescu, R.C.B.,Blaszczyk, B.K.,Anwar, A.,Deingruber, T.,Sanders, M.G.,Perez-Areales, F.J.,Stephens, L.R.,Hawkins, P.T.,Spring, D.R.,Hyvonen, M. Inhibition of a Pleckstrin Homology Domain by Lysine-reactive Covalent Inhibitor To be published, |
| Experimental method | X-RAY DIFFRACTION (2.769 Å) |
Structure validation
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