9Y56
Co-crystal structure of BTK kinase domain with non-covalent inhibitor
This is a non-PDB format compatible entry.
Entity
| Entity ID | Chain ID | Description | Type | Chain length | Formula weight | Number of molecules | DB Name (Accession) | Biological source | Descriptive keywords |
| 1 | A (A) | Tyrosine-protein kinase BTK | polymer | 278 | 32269.0 | 1 | UniProt (Q06187) Pfam (PF07714) | Homo sapiens (human) | Agammaglobulinemia tyrosine kinase,ATK,B-cell progenitor kinase,BPK,Bruton tyrosine kinase |
| 2 | B (A) | IMIDAZOLE | non-polymer | 69.1 | 1 | Chemie (IMD) | |||
| 3 | C (A) | 1-{4-[(5-fluoro-2-methoxybenzamido)methyl]phenyl}-4-({6-[(1S)-1-methoxyethyl]-5-[4-(2-methoxyethyl)piperazin-1-yl]pyridin-2-yl}amino)-1H-pyrazole-5-carboxamide | non-polymer | 660.7 | 1 | Chemie (A1CSI) | |||
| 4 | D (A) | water | water | 18.0 | 428 | Chemie (HOH) |
Sequence viewer
Contents of the asymmetric unit
| Polymers | Number of chains | 1 |
| Total formula weight | 32269.0 | |
| Non-Polymers* | Number of molecules | 2 |
| Total formula weight | 729.8 | |
| All* | Total formula weight | 32998.8 |
