1F0Q
CRYSTAL STRUCTURE OF THE ALPHA SUBUNIT OF PROTEIN KINASE CK2 IN COMPLEX WITH THE NUCLEOTIDE COMPETITIVE INHIBITOR EMODIN
Summary for 1F0Q
Entry DOI | 10.2210/pdb1f0q/pdb |
Related | 1A6O 1DAW 1DAY 1DS5 |
Descriptor | PROTEIN KINASE CK2, ALPHA SUBUNIT, 3-METHYL-1,6,8-TRIHYDROXYANTHRAQUINONE (3 entities in total) |
Functional Keywords | protein kinase-inhibitor complex, transferase |
Biological source | Zea mays |
Total number of polymer chains | 1 |
Total formula weight | 39561.40 |
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 citation | Battistutta, 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: 10882732DOI: 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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