|
111
|
327
|
7z39A |
Structure of belumosudil bound to ck2alpha |
|
107
|
327
|
7zyrA |
Compound 20 bound to ck2alpha |
|
119
|
332
|
7qgbA |
H. sapiens ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6-dibromobenzotriazole at ph 6.5 |
|
117
|
333
|
7qgdA |
H. sapiens ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6-dibromobenzotriazole at ph 8.5 |
|
109
|
327
|
7zy0A |
Crystal structure of compound 7 bound to ck2alpha |
|
110
|
327
|
7zy2A |
Crystal structure of compound 7 bound to ck2alpha |
|
111
|
327
|
8aekA |
Structure of compound 14 bound to ck2alpha |
|
109
|
327
|
7zyoA |
Compound 9 bound to ck2alpha |
|
113
|
325
|
7zy8A |
Crystal structure of compound 2 bound to ck2alpha |
|
122
|
333
|
7qgeA |
H. sapiens ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6,7,8-tetrabromobenzotriazole (tbbt) at ph 8.5 |
|
112
|
327
|
8aecA |
Structure of compound 17 bound to ck2alpha |
|
112
|
326
|
7zy5A |
Crystal structure of compound 2 bound to ck2alpha |
|
110
|
327
|
7zydA |
Structure of compound 6 bound to ck2alpha |
|
118
|
333
|
7qgcA |
H. sapiens ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6-dibromobenzotriazole at ph 5.5 |
|
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 |
|
1
|
8
|
6yzhD |
Crystal structure of p8c9 bound to ck2alpha |
|
112
|
360
|
6yzhA |
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 |
|
123
|
333
|
6tllA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5,6,7-tetrabromobenzotriazole (tbbt) |
|
122
|
333
|
6tlpA |
Human ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 5,6-dibromobenzotriazole |
|
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 |
|
104
|
327
|
6ypgA |
Crystal structure of ck2alpha with compound 2 bound to second crystal form |
|
110
|
326
|
6yphA |
Crystal structure of ck2alpha with compound 2 bound |
|
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 |
