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7PSU

Structure of protein kinase CK2alpha mutant K198R associated with the Okur-Chung Neurodevelopmental Syndrome

Summary for 7PSU
Entry DOI10.2210/pdb7psu/pdb
DescriptorCasein kinase II subunit alpha, 1,2-ETHANEDIOL, SULFATE ION, ... (5 entities in total)
Functional Keywordsprotein kinase ck2, casein kinase 2, csnk2a1 mutant k198r, okur-chung neurodevelopmental syndrome, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight96309.94
Authors
Werner, C.,Gast, A.,Lindenblatt, D.,Nickelsen, K.,Niefind, K.,Jose, J.,Hochscherf, J. (deposition date: 2021-09-23, release date: 2022-03-23, Last modification date: 2024-01-31)
Primary citationWerner, C.,Gast, A.,Lindenblatt, D.,Nickelsen, A.,Niefind, K.,Jose, J.,Hochscherf, J.
Structural and Enzymological Evidence for an Altered Substrate Specificity in Okur-Chung Neurodevelopmental Syndrome Mutant CK2 alpha Lys198Arg.
Front Mol Biosci, 9:831693-831693, 2022
Cited by
PubMed: 35445078
DOI: 10.3389/fmolb.2022.831693
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.77 Å)
Structure validation

221051

數據於2024-06-12公開中

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