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9S6G

Structure of protein kinase CK2alpha mutant R47Q associated with the Okur-Chung Neurodevelopmental Syndrome

Summary for 9S6G
Entry DOI10.2210/pdb9s6g/pdb
DescriptorCasein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, SULFATE ION, ... (5 entities in total)
Functional Keywordsokur-chung neurodevelopmental syndrome, ocnds, ck2, protein kinase, casein kinase ii, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight96939.77
Authors
Werner, C.,Gast, A.,Buchwald, L.,Niefind, K. (deposition date: 2025-08-01, release date: 2026-08-12)
Primary citationWerner, 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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PDB entries from 2026-08-12

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