9S8J
Structure of protein kinase CK2alpha mutant R191Q associated with the Okur-Chung Neurodevelopmental Syndrome
Summary for 9S8J
| Entry DOI | 10.2210/pdb9s8j/pdb |
| Descriptor | Casein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, SULFATE ION, ... (5 entities in total) |
| Functional Keywords | protein kinase ck2, ck2, casein kinase ii, kinase, okur-chung neurodevelopmental syndrome, transferase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 2 |
| Total formula weight | 96387.69 |
| Authors | Werner, C.,Gast, A.,Meyer, S.C.,Jose, J.,Niefind, K. (deposition date: 2025-08-05, release date: 2026-08-19) |
| Primary citation | Werner, C.,Gast, A.,Caefer, D.,Fellhoefer, J.,Meyer, S.C.,Jordan, S.,Buchwald, L.M.,Than, T.L.,Schwartz, D.,Jose, J.,Niefind, K. Investigation of the structure-dysfunction relationship of various OCNDS-related CK2alpha mutants To Be Published, |
| Experimental method | X-RAY DIFFRACTION (2.48 Å) |
Structure validation
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