|
107
|
329
|
9epyA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgc3330 |
|
107
|
329
|
9epzA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgc3337 |
|
108
|
329
|
9epvA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgc333 |
|
110
|
331
|
9epwB |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgc3336 |
|
103
|
329
|
9epxA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgc3331 |
|
102
|
328
|
9eq0A |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgjg12 |
|
109
|
331
|
9eq1A |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with allosteric ligand fgjm24 |
|
110
|
328
|
8c6mA |
Human protein kinase ck2 alpha in complex with ck2-tn02 |
|
110
|
328
|
8c6lA |
Human protein kinase ck2 alpha in complex with ck2-tn01 |
|
107
|
328
|
8c6nA |
Human protein kinase ck2 alpha in complex with ck2-tn03 |
|
104
|
329
|
8c5qA |
Ck2 kinase bound to inhibitor ab668 |
|
108
|
330
|
8qwzA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with 4-(6-(6-isopropoxy-1h-indol-1-yl)pyrazin-2-yl)benzoic acid |
|
110
|
331
|
8qwyA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with 4-(6-((5-isopropoxy-2-methoxyphenyl)amino)pyrazin-2-yl)benzoic acid |
|
110
|
331
|
7ay9A |
Crystal structure of ck2 bound by compound 7 |
|
109
|
331
|
7ayaA |
Crystal structure of ck2 bound by compound 9 |
|
111
|
330
|
6z83AAA |
Ck2 alpha bound to chemical probe sgc-ck2-1 |
|
115
|
332
|
7psuA |
Structure of protein kinase ck2alpha mutant k198r associated with the okur-chung neurodevelopmental syndrome |
|
112
|
329
|
6z84AAA |
Ck2 alpha bound to chemical probe sgc-ck2-1 derivative |
|
109
|
327
|
7zwgA |
The crystal structure of ro4493940 bound to ck2alpha |
|
106
|
327
|
7zweA |
The crystal structure of gw8695 bound to ck2alpha |
|
111
|
331
|
8p07A |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with 5-((3-(4h-1,2,4-triazol-4-yl)phenyl)amino)-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrile |
|
108
|
329
|
8p05A |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with leucettinib-92 |
|
111
|
327
|
8ae7A |
The strucuture of compound 15 bound to ck2alpha |
|
107
|
327
|
8aemA |
Structure of compound 13 bound to ck2alpha |
|
104
|
327
|
7a4qA |
The crystal structure of ro4613269 bound to ck2alpha |
|
1
|
8
|
7quxD |
Crystal structure of p7c8 bound to ck2alpha |
|
113
|
330
|
7quxA |
Crystal structure of p7c8 bound to ck2alpha |
|
108
|
327
|
7zykA |
Compound 9 bound to ck2alpha |
|
104
|
329
|
8bgcA |
Crystal structure of human casein kinase ii subunit alpha (ck2a1) in complex with compound 2 (aa-cs-9-003) |
|
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 |
|
111
|
327
|
8aekA |
Structure of compound 14 bound to ck2alpha |
|
110
|
327
|
7zy2A |
Crystal structure of compound 7 bound to ck2alpha |
|
109
|
327
|
7zy0A |
Crystal structure of compound 7 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 |
|
110
|
327
|
7zydA |
Structure of compound 6 bound to ck2alpha |
|
112
|
326
|
7zy5A |
Crystal structure of compound 2 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 |
|
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 |
