9S7H

Structure of protein kinase CK2alpha mutant H160R associated with the Okur-Chung Neurodevelopmental Syndrome

Summary for 9S7H

• Entry DOI: 10.2210/pdb9s7h/pdb
• Descriptor: Casein kinase II subunit alpha, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, MAGNESIUM ION, ... (5 entities in total)
• Functional Keywords: protein kinase ck2, ck2, casein kinase ii, epk, csnk2a1, ocnds, okur-chung neurodevelopmental syndrome, transferase
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 2
• Total formula weight: 97060.30

Authors

Werner, C.,Gast, A.,Jose, J.,Niefind, K. (deposition date: 2025-08-04, release date: 2026-08-19)

• Primary citation: Werner, C.,Gast, A.,Caefer, D.,Fellhoefer, J.,Meyer, S.C.,Jordan, S.,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 (2.09 Å)