|
111
|
334
|
6l24A |
Crystal structure of ck2a1 h115y/v116i with hematein |
|
112
|
331
|
6l21A |
Crystal structure of ck2a1 h160a with hematein |
|
112
|
334
|
6l22A |
Crystal structure of ck2a1 h115y 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 |
|
109
|
328
|
6hotA |
Human protein kinase ck2 alpha in complex with ferulic aldehyde |
|
111
|
328
|
6hopA |
Human protein kinase ck2 alpha in complex with curcumin degradation products |
|
109
|
328
|
6houA |
Human protein kinase ck2 alpha in complex with vanillin |
|
110
|
328
|
6hnyA |
Human protein kinase ck2 alpha in complex with boldine |
|
114
|
327
|
6jwaA |
Crystal structure of ck2a1 with 5-iodotubercidin |
|
112
|
325
|
6qs5A |
Crystal structure of maize ck2 in complex with tyrphostin ag99 |
|
107
|
327
|
5zn2A |
X-ray structure of protein kinase ck2 alpha subunit h148a mutant |
|
108
|
327
|
5zn1A |
X-ray structure of protein kinase ck2 alpha subunit in d2o |
|
105
|
327
|
5zn3A |
X-ray structure of protein kinase ck2 alpha subunit h148s mutant |
|
111
|
327
|
5zn5A |
X-ray structure of protein kinase ck2 alpha subunit h148a mutant |
|
105
|
327
|
5zn4A |
X-ray structure of protein kinase ck2 alpha subunit h148n mutant |
|
107
|
327
|
5zn0A |
Joint x-ray/neutron structure of protein kinase ck2 alpha subunit |
|
120
|
334
|
6a1cA |
Crystal structure of the ck2a1-go289 complex |
|
106
|
327
|
6q38A |
The crystal structure of ck2a bound to p1-c4 |
|
1
|
8
|
6q38C |
The crystal structure of ck2a bound to p1-c4 |
|
1
|
8
|
6q4qC |
The crystal structure of ck2a bound to p2-c4 |
|
115
|
327
|
6q4qA |
The crystal structure of ck2a bound to p2-c4 |
|
109
|
327
|
6fvfA |
The structure of ck2alpha with cch503 bound |
|
114
|
332
|
6hmeA |
Low-salt structure of protein kinase ck2 catalytic subunit (isoform ck2alpha; csnk2a1 gene product) in complex with the indenoindole-type inhibitor thn27 |
|
108
|
327
|
6fvgA |
The structure of ck2alpha with cch507 bound |
|
118
|
333
|
6hbnA |
High-salt structure of protein kinase ck2 catalytic subunit (isoform ck2alpha/cskn2a1 gene product) in complex with the indenoindole-type inhibitor thn27 |
|
111
|
331
|
5n1vA |
Crystal structure of the protein kinase ck2 catalytic subunit in complex with pyrazolo-pyrimidine macrocyclic ligand |
|
110
|
329
|
5n9lA |
Crystal structure of human protein kinase ck2 catalytic subunit in complex with the atp-competitive dibenzofuran inhibitor tf (4b) |
|
110
|
329
|
5n9nA |
Crystal structure of human protein kinase ck2 catalytic subunit in complex with the atp-competitive, tight-binding dibenzofuran inhibitor tf85 (4a) |
|
109
|
326
|
5mmrA |
Crystal structure of ck2alpha with n-((2-chloro-[1,1'-biphenyl]-4-yl)methyl)butane-1,4-diamine bound |
|
111
|
325
|
5mo8A |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
113
|
326
|
5mmfA |
Crystal structure of ck2alpha with compound 7 bound |
|
103
|
326
|
5mpjA |
1-(2-chloro-[1,1'-biphenyl]-4-yl)-n-methylethanamine |
|
104
|
327
|
5mo7A |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
110
|
327
|
5modA |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
109
|
326
|
5mo5A |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
105
|
325
|
5movA |
Crystal structure of ck2alpha with zt0633 bound |
|
115
|
329
|
5m4cA |
Complex structure of human protein kinase ck2 catalytic subunit with a thieno[2,3-d]pyrimidin inhibitor crystallized under low-salt conditions |
|
116
|
325
|
5moeA |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
113
|
325
|
5mo6A |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
104
|
328
|
5motA |
Crystal structure of ck2alpha with zt0627 bound |
