9S7A
Structure of protein kinase CK2alpha mutant R80C associated with the Okur-Chung Neurodevelopmental Syndrome
Summary for 9S7A
| Entry DOI | 10.2210/pdb9s7a/pdb |
| Descriptor | Casein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, SULFATE ION, ... (5 entities in total) |
| Functional Keywords | okur-chung neurodevelopmental syndrome, ocnds, protein kinase, ck2, casein kinase ck2, csnk2a1, transferase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 2 |
| Total formula weight | 96697.67 |
| Authors | Werner, C.,Gast, A.,Meyer, S.C.,Jose, J.,Niefind, K. (deposition date: 2025-08-04, release date: 2026-08-19) |
| Primary citation | Werner, C.,Gast, A.,Caefer, D.,Fellhoefer, J.M.,Jordan, S.,Buchwald, L.M.,Meyer, S.C.,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 (2.03 Å) |
Structure validation
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