101
|
328
|
7l1xA |
Structure of human ck2 alpha kinase (catalytic subunit) with the inhibitor 108600. |
117
|
332
|
7at5A |
Structure of protein kinase ck2 catalytic subunit (csnk2a1 gene product) in complex with the bivalent inhibitor kn2 |
109
|
328
|
6z19B |
Crystal structure of p8c9 bound to ck2alpha |
0
|
7
|
6z19C |
Crystal structure of p8c9 bound to ck2alpha |
112
|
360
|
6yzhA |
Crystal structure of p8c9 bound to ck2alpha |
1
|
8
|
6yzhD |
Crystal structure of p8c9 bound to ck2alpha |
121
|
334
|
6l23A |
Crystal structure of ck2a1 v116i with hematein |
115
|
332
|
7b8iA |
Tetragonal structure of human protein kinase ck2 catalytic subunit in complex with a heparin oligo saccharide |
112
|
329
|
7b8hA |
Monoclinic structure of human protein kinase ck2 catalytic subunit in complex with a heparin oligo saccharide |
110
|
334
|
7a4cA |
Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the atp-competitive inhibitor 5,6,7-tribromo-1h-triazolo[4,5-b]pyridine |
115
|
334
|
7a49A |
Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the atp-competitive inhibitor 6-bromo-5-chloro-1h-triazolo[4,5-b]pyridine |
112
|
333
|
7a4bA |
Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the atp-competitive inhibitor 5,6-dibromo-1h-triazolo[4,5-b]pyridine |
122
|
333
|
6tluAAA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5-dibromobenzotriazole |
129
|
333
|
6tlsA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,6-dibromobenzotriazole |
128
|
333
|
6tlvA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5-bromobenzotriazole |
126
|
333
|
6tloA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5,6-tribromobenzotriazole |
124
|
333
|
6tlwA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4-bromobenzotriazole |
123
|
333
|
6tlrA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,7-dibromobenzotriazole |
122
|
333
|
6tlpA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6-dibromobenzotriazole |
123
|
333
|
6tllA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5,6,7-tetrabromobenzotriazole (tbbt) |
105
|
330
|
6k77A |
Crystal structure of amppnp bound ck1a alpha from c. neoformans |
107
|
330
|
6k74A |
Crystal structure of amppnp bound ck1a alpha from c. neoformans |
111
|
327
|
6ypkA |
Crystal structure of ck2alpha with gtp bound |
106
|
327
|
6ypjA |
Crystal structure of ck2alpha with compound 1 bound |
106
|
331
|
6yumAAA |
Ck2 alpha bound to unclosed macrocycle |
110
|
326
|
6yphA |
Crystal structure of ck2alpha with compound 2 bound |
104
|
327
|
6ypgA |
Crystal structure of ck2alpha with compound 2 bound to second crystal form |
107
|
326
|
6ypnB |
Crystal structure of ck2alpha with 2 molecules of adp bound |
114
|
331
|
6yulAAA |
Ck2 alpha bound to macrocycle |
113
|
331
|
6teiA |
Crystal structure of human protein kinase ck2alpha (csnk2a1 gene product) in complex with the 2-aminothiazole-type inhibitor 17 |
112
|
328
|
6rfeA |
Human protein kinase ck2 alpha in complex with 2-cyano-2-propenamide compound 4 |
110
|
329
|
6rb1A |
Human protein kinase ck2 alpha in complex with 2-cyano-2-propenamide compound 1 |
104
|
328
|
6rcbA |
Human protein kinase ck2 alpha in complex with 2-cyano-2-propenamide compound 14 |
105
|
328
|
6rffA |
Human protein kinase ck2 alpha in complex with 2-cyano-2-propenamide compound 7 |
108
|
328
|
6rcmA |
Human protein kinase ck2 alpha in complex with 2-cyano-2-propenamide compound 3 |
116
|
334
|
6qy7A |
Human csnk2a1 bound to erb-041 |
111
|
334
|
6l24A |
Crystal structure of ck2a1 h115y/v116i with hematein |
112
|
334
|
6l22A |
Crystal structure of ck2a1 h115y with hematein |
112
|
331
|
6l21A |
Crystal structure of ck2a1 h160a with hematein |
115
|
327
|
6spwA |
Structure of protein kinase ck2 catalytic subunit with the ck2beta-competitive bisubstrate inhibitor arc3140 |
0
|
6
|
6spwB |
Structure of protein kinase ck2 catalytic subunit with the ck2beta-competitive bisubstrate inhibitor arc3140 |
106
|
329
|
6spxA |
Structure of protein kinase ck2 catalytic subunit in complex with the ck2beta-competitive bisubstrate inhibitor arc1502 |
0
|
6
|
6spxB |
Structure of protein kinase ck2 catalytic subunit in complex with the ck2beta-competitive bisubstrate inhibitor arc1502 |
105
|
326
|
6isjA |
Crystal structure of cx-4945 bound ck2 alpha from c. neoformans |
104
|
327
|
6iseA |
Crystal structure of amppnp bound ck2 alpha from c. neoformans |
111
|
329
|
6k3lB |
Crystal structure of cx-4945 bound cka1 from c. neoformans |
104
|
330
|
6ko6B |
Crystal structure of amppnp bound cka1 from c. neoformans |
111
|
328
|
6horA |
Human protein kinase ck2 alpha in complex with feruloylmethane |
112
|
328
|
6hnwA |
Human protein kinase ck2 alpha in complex with coumestrol |
109
|
328
|
6hoqA |
Human protein kinase ck2 alpha in complex with ferulic acid |