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9S8J

Structure of protein kinase CK2alpha mutant R191Q associated with the Okur-Chung Neurodevelopmental Syndrome

Summary for 9S8J
Entry DOI10.2210/pdb9s8j/pdb
DescriptorCasein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, SULFATE ION, ... (5 entities in total)
Functional Keywordsprotein kinase ck2, ck2, casein kinase ii, kinase, okur-chung neurodevelopmental syndrome, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight96387.69
Authors
Werner, C.,Gast, A.,Meyer, S.C.,Jose, J.,Niefind, K. (deposition date: 2025-08-05, release date: 2026-08-19)
Primary citationWerner, 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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PDB entries from 2026-08-19

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