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9S7A

Structure of protein kinase CK2alpha mutant R80C associated with the Okur-Chung Neurodevelopmental Syndrome

Summary for 9S7A
Entry DOI10.2210/pdb9s7a/pdb
DescriptorCasein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, SULFATE ION, ... (5 entities in total)
Functional Keywordsokur-chung neurodevelopmental syndrome, ocnds, protein kinase, ck2, casein kinase ck2, csnk2a1, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight96697.67
Authors
Werner, C.,Gast, A.,Meyer, S.C.,Jose, J.,Niefind, K. (deposition date: 2025-08-04, release date: 2026-08-19)
Primary citationWerner, 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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PDB entries from 2026-08-19

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