|
80
|
279
|
2qhmA |
Crystal structure of chek1 in complex with inhibitor 2a |
|
113
|
327
|
2pvjA |
Structure-based design of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase ck2 |
|
29
|
127
|
2qrdA |
Crystal structure of the adenylate sensor from amp-activated protein kinase in complex with adp and atp |
|
82
|
279
|
2qhnA |
Crystal structure of chek1 in complex with inhibitor 1a |
|
109
|
328
|
2pvnA |
Structure-based design of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase ck2 |
|
83
|
286
|
2pe1A |
Crystal structure of human phosphoinositide-dependent protein kinase 1 (pdk1) {2-oxo-3-[1-(1h-pyrrol-2-yl)-eth-(z)-ylidene]-2,3-dihydro-1h-indol-5-yl}-urea {bx-517} complex |
|
114
|
328
|
2pvkA |
Structure-based design of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase ck2 |
|
111
|
328
|
2pvrA |
Crystal structure of the catalytic subunit of protein kinase ck2 (c-terminal deletion mutant 1-335) in complex with two sulfate ions |
|
84
|
277
|
2phkA |
The crystal structure of a phosphorylase kinase peptide substrate complex: kinase substrate recognition |
|
112
|
328
|
2pvmA |
Structure-based design of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase ck2 |
|
86
|
286
|
2pe0A |
Crystal structure of human phosphoinositide-dependent protein kinase 1 (pdk1) 5-hydroxy-3-[1-(1h-pyrrol-2-yl)-eth-(z)-ylidene]-1,3-dihydro-indol-2-one complex |
|
95
|
294
|
2q0nA |
Structure of human p21 activating kinase 4 (pak4) in complex with a consensus peptide |
|
57
|
320
|
2p3gX |
Crystal structure of a pyrrolopyridine inhibitor bound to mapkap kinase-2 |
|
2
|
34
|
2ov2I |
The crystal structure of the human rac3 in complex with the crib domain of human p21-activated kinase 4 (pak4) |
|
82
|
286
|
2pe2A |
Crystal structure of human phosphoinositide-dependent protein kinase 1 (pdk1) 3-{5-[2-oxo-5-ureido-1,2-dihydro-indol-(3z)-ylidenemethyl]-1h-pyrrol-3-yl}-n-(2-piperidin-1-yl-ethyl)-benzamide complex |
|
93
|
340
|
2ozaA |
Structure of p38alpha complex |
|
98
|
325
|
2oxxA |
Protein kinase ck2 in complex with tetrabromobenzoimidazole derivatives k17, k22 and k32 |
|
80
|
274
|
2o63A |
Crystal structure of pim1 with myricetin |
|
98
|
325
|
2oxdA |
Protein kinase ck2 in complex with tetrabromobenzoimidazole k17, k22 and k32 inhibitors |
|
71
|
348
|
2onlC |
Crystal structure of the p38a-mapkap kinase 2 heterodimer |
|
79
|
274
|
2o3pA |
Crystal structure of pim1 with quercetin |
|
86
|
351
|
2ow3A |
Glycogen synthase kinase-3 beta in complex with bis-(indole)maleimide pyridinophane inhibitor |
|
27
|
129
|
2ooyA |
Crystal structure of the adenylate sensor from amp-activated protein kinase complexed with atp |
|
91
|
296
|
2oicA |
Crystal structure of irak4 kinase domain complexed with staurosporine |
|
81
|
274
|
2o64A |
Crystal structure of pim1 with quercetagetin |
|
91
|
305
|
2nz8B |
N-terminal dhph cassette of trio in complex with nucleotide-free rac1 |
|
6
|
24
|
2okrC |
Crystal structure of the p38a-mapkap kinase 2 heterodimer |
|
82
|
273
|
2objA |
Crystal structure of human pim-1 kinase in complex with inhibitor |
|
85
|
275
|
2oi4X |
Crystal structure of human pim1 in complex with fluorinated ruthenium pyridocarbazole |
|
79
|
350
|
2o5kA |
Crystal structure of gsk3beta in complex with a benzoimidazol inhibitor |
|
29
|
128
|
2ooxA |
Crystal structure of the adenylate sensor from amp-activated protein kinase complexed with amp |
|
84
|
295
|
2oidA |
Crystal structure of irak4 kinase domain complexed with amppnp |
|
90
|
295
|
2o8yA |
Apo irak4 kinase domain |
|
95
|
297
|
2oibA |
Crystal structure of irak4 kinase domain apo form |
|
1
|
35
|
2odbB |
The crystal structure of human cdc42 in complex with the crib domain of human p21-activated kinase 6 (pak6) |
|
77
|
274
|
2o65A |
Crystal structure of pim1 with pentahydroxyflavone |
|
21
|
62
|
2ltuA |
Solution structure of autoinhibitory domain of human amp-activated protein kinase catalytic subunit |
|
86
|
295
|
2nruA |
Crystal structure of irak-4 |
|
9
|
104
|
2n56A |
Ig59 domain of human obscurin a |
|
55
|
292
|
2nziA |
Crystal structure of domains a168-a170 from titin |
|
34
|
106
|
2n7zA |
Solution structure of rip2 card |
|
32
|
136
|
2kufA |
Nmr structure of the pasta domain 3 and 4 of mycobacterium tuberculosis of pknb |
|
7
|
33
|
2kioA |
Nmr structure of the oxidized yeast tor1 fatc domain bound to dpc micelles at 318k |
|
93
|
360
|
2kulA |
Solution structure of human vaccinia related kinase 1(vrk1) |
|
61
|
272
|
2kuiA |
Nmr structure of the pasta domain of mycobacterium tuberculosis of pknb |
|
33
|
171
|
2kbxA |
Solution structure of ilk-pinch complex |
|
12
|
96
|
2kylA |
Solution structure of mast2-pdz complexed with the c-terminus of pten |
|
26
|
105
|
2n83B |
P75ntr dd:rip2 card |
|
0
|
16
|
2kymB |
Solution structure of the bem1p sh3-ci domain from l.elongisporus in complex with ste20p peptide |
|
82
|
262
|
2np8A |
Structural basis for the inhibition of aurora a kinase by a novel class of high affinity disubstituted pyrimidine inhibitors |
