9S6G
Structure of protein kinase CK2alpha mutant R47Q associated with the Okur-Chung Neurodevelopmental Syndrome
Summary for 9S6G
| Entry DOI | 10.2210/pdb9s6g/pdb |
| Descriptor | Casein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, SULFATE ION, ... (5 entities in total) |
| Functional Keywords | okur-chung neurodevelopmental syndrome, ocnds, ck2, protein kinase, casein kinase ii, transferase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 2 |
| Total formula weight | 96939.77 |
| Authors | Werner, C.,Gast, A.,Buchwald, L.,Niefind, K. (deposition date: 2025-08-01, release date: 2026-08-12) |
| Primary citation | Werner, C.,Gast, A.,Caefer, D.,Fellhoefer, J.,Jordan, S.,Meyer, S.C.,Buchwald, L.,Than, T.L.,Schwartz, D.,Niefind, K. Structure of protein kinase CK2alpha mutant R47Q associated with the Okur-Chung Neurodevelopmental Syndrome To Be Published, |
| Experimental method | X-RAY DIFFRACTION (1.81 Å) |
Structure validation
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