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1F0Q

CRYSTAL STRUCTURE OF THE ALPHA SUBUNIT OF PROTEIN KINASE CK2 IN COMPLEX WITH THE NUCLEOTIDE COMPETITIVE INHIBITOR EMODIN

Summary for 1F0Q
Entry DOI10.2210/pdb1f0q/pdb
Related1A6O 1DAW 1DAY 1DS5
DescriptorPROTEIN KINASE CK2, ALPHA SUBUNIT, 3-METHYL-1,6,8-TRIHYDROXYANTHRAQUINONE (3 entities in total)
Functional Keywordsprotein kinase-inhibitor complex, transferase
Biological sourceZea mays
Total number of polymer chains1
Total formula weight39561.40
Authors
Battistutta, R.,Sarno, S.,De Moliner, E.,Papinutto, E.,Zanotti, G.,Pinna, L.A. (deposition date: 2000-05-17, release date: 2001-05-23, Last modification date: 2024-02-07)
Primary citationBattistutta, R.,Sarno, S.,De Moliner, E.,Papinutto, E.,Zanotti, G.,Pinna, L.A.
The replacement of ATP by the competitive inhibitor emodin induces conformational modifications in the catalytic site of protein kinase CK2.
J.Biol.Chem., 275:29618-29622, 2000
Cited by
PubMed: 10882732
DOI: 10.1074/jbc.M004257200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.63 Å)
Structure validation

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