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9S76

Structure of protein kinase CK2alpha mutant Y50C associated with the Okur-Chung Neurodevelopmental Syndrome

Summary for 9S76
Entry DOI10.2210/pdb9s76/pdb
DescriptorCasein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, MAGNESIUM ION, ... (5 entities in total)
Functional Keywordsokur-chung neurodevelopmental syndrome, ocnds, ck2, protein kinase ck2, casein kinase ii, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight96517.89
Authors
Werner, C.,Gast, A.,Jose, J.,Niefind, K. (deposition date: 2025-08-04, release date: 2026-08-19)
Primary citationWerner, C.,Gast, A.,Caefer, D.,Fellhoefer, J.,Jordan, S.,Meyer, S.C.,Buchwald, L.M.,Than, T.L.,Schwartz, D.,Jose, J.,Niefind, K.
Structure of protein kinase CK2alpha mutant Y50C associated with the Okur-Chung Neurodevelopmental Syndrome
To Be Published,
Experimental method
X-RAY DIFFRACTION (1.73 Å)
Structure validation

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