9O7Q
Crystal structure of human adenosine kinase (ADK) in complex with inhibitor BKI-1676
This is a non-PDB format compatible entry.
Summary for 9O7Q
| Entry DOI | 10.2210/pdb9o7q/pdb |
| Descriptor | Isoform 2 of Adenosine kinase, 1-[(3P)-3-[6-(cyclopropyloxy)naphthalen-2-yl]-4-(methylamino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-2-methylpropan-2-ol, SULFATE ION, ... (4 entities in total) |
| Functional Keywords | ssgcid, structural genomics, seattle structural genomics center for infectious disease, adenosine kinase (adk), inhibitor, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 54095.64 |
| Authors | Seattle Structural Genomics Center for Infectious Disease (SSGCID) (deposition date: 2025-04-15, release date: 2026-05-06) |
| Primary citation | Liu, L.,Lovell, S.,Battaile, K.P. Crystal structure of human adenosine kinase (ADK) in complex with inhibitor BKI-1676 To be published, |
| Experimental method | X-RAY DIFFRACTION (2.81 Å) |
Structure validation
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