7L5P
Crystal structure of the covalently bonded complex of rilzabrutinib with BTK
Summary for 7L5P
Entry DOI | 10.2210/pdb7l5p/pdb |
Descriptor | Tyrosine-protein kinase BTK, (2E)-2-{(3R)-3-[4-amino-3-(2-fluoro-4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carbonyl}-4-methyl-4-[4-(oxetan-3-yl)piperazin-1-yl]pent-2-enenitrile, SULFATE ION, ... (5 entities in total) |
Functional Keywords | protein kinase inhibitor, transferase-transferase inhibitor complex, transferase, transferase/transferase inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 64940.42 |
Authors | Bradshaw, J.M.,Brameld, K.A.,Mrosek, M.,Lammens, A.,Blaesse, M. (deposition date: 2020-12-22, release date: 2022-06-29, Last modification date: 2024-10-23) |
Primary citation | Owens, T.D. The Discovery Rilzabrutinib (PRN1008): A Reversible Covalent BTK Inhibitor for Immune Mediated Diseases To Be Published, |
Experimental method | X-RAY DIFFRACTION (2.14 Å) |
Structure validation
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