|
85
|
292
|
3dgkA |
Crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain |
|
79
|
263
|
3dj7A |
Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 130. |
|
112
|
329
|
3dlzA |
Crystal structure of human haspin in complex with amp |
|
46
|
123
|
3dd7A |
Structure of doch66y in complex with the c-terminal domain of phd |
|
76
|
261
|
3dj6A |
Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 823. |
|
67
|
268
|
3daeA |
Crystal structure of phosphorylated snf1 kinase domain |
|
82
|
274
|
3cxwA |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a beta carboline ligand i |
|
86
|
269
|
3d14A |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-{5-[2-(thieno[3,2-d]pyrimidin-4-ylamino)-ethyl]- thiazol-2-yl}-3-(3-trifluoromethyl-phenyl)-urea |
|
108
|
400
|
3d9vA |
Crystal structure of rock i bound to h-1152p a di-methylated variant of fasudil |
|
80
|
276
|
3d4qA |
Pyrazole-based inhibitors of b-raf kinase |
|
103
|
335
|
3d0eA |
Crystal structure of human akt2 in complex with gsk690693 |
|
268
|
945
|
3cstA |
Crystal structure of pi3k p110gamma catalytical domain in complex with organoruthenium inhibitor e5e2 |
|
78
|
263
|
3d15A |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-(3-chloro-phenyl)-3-{5-[2-(thieno[3,2-d]pyrimidin-4-ylamino)- ethyl]-thiazol-2-yl}-urea [sns-314] |
|
80
|
273
|
3cy2A |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a beta carboline ligand ii |
|
85
|
290
|
3dakA |
Crystal structure of domain-swapped osr1 kinase domain |
|
76
|
261
|
3d2kA |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with [7-(2-{2-[3-(3-chloro-phenyl)-ureido]-thiazol-5-yl}-ethylamino)-pyrazolo[4,3-d]pyrimidin-1-yl]-acetic acid |
|
73
|
262
|
3dajA |
Crystal structure of aurora a complexed with an inhibitor discovered through site-directed dynamic tethering |
|
22
|
171
|
3d6tB |
Structure of the roc domain from the parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric gtpase |
|
75
|
262
|
3d2iA |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-{5-[2-(1-methyl-1h-pyrazolo[4,3-d]pyrimidin-7-ylamino)-ethyl]-thiazol-2-yl}-3-(3-trifluoromethyl-phenyl)-urea |
|
82
|
273
|
3cy3A |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and the jnk inhibitor v |
|
271
|
945
|
3csfA |
Crystal structure of pi3k p110gamma catalytical domain in complex with organoruthenium inhibitor dw2 |
|
0
|
10
|
3cqwC |
Crystal structure of akt-1 complexed with substrate peptide and inhibitor |
|
79
|
261
|
3cohA |
Crystal structure of aurora-a in complex with a pentacyclic inhibitor |
|
98
|
335
|
3cqwA |
Crystal structure of akt-1 complexed with substrate peptide and inhibitor |
|
81
|
279
|
3ckwA |
Crystal structure of sterile 20-like kinase 3 (mst3, stk24) |
|
94
|
335
|
3cquA |
Crystal structure of akt-1 complexed with substrate peptide and inhibitor |
|
85
|
270
|
3comA |
Crystal structure of mst1 kinase |
|
0
|
10
|
3cquC |
Crystal structure of akt-1 complexed with substrate peptide and inhibitor |
|
84
|
279
|
3ckxA |
Crystal structure of sterile 20-like kinase 3 (mst3, stk24) in complex with staurosporine |
|
95
|
300
|
3c0hA |
Cask cam-kinase domain- amppnp complex, p1 form |
|
79
|
273
|
3c4eA |
Pim-1 kinase domain in complex with 3-aminophenyl-7-azaindole |
|
61
|
275
|
3c4cA |
B-raf kinase in complex with plx4720 |
|
112
|
328
|
3c13A |
Low ph-value crystal structure of emodin in complex with the catalytic subunit of protein kinase ck2 |
|
90
|
317
|
3c0gA |
Cask cam-kinase domain- 3'-amp complex, p1 form |
|
96
|
298
|
3c0iA |
Cask cam-kinase domain- 3'-amp complex, p212121 form |
|
88
|
278
|
3bqrA |
Crystal structure of human death associated protein kinase 3 (dapk3) in complex with an imidazo-pyridazine ligand |
|
112
|
328
|
3bqcA |
High ph-value crystal structure of emodin in complex with the catalytic subunit of protein kinase ck2 |
|
78
|
273
|
3bgzA |
Human pim-1 kinase in complex with diphenyl indole inhibitor vx3 |
|
87
|
276
|
3bhyA |
Crystal structure of human death associated protein kinase 3 (dapk3) in complex with a beta-carboline ligand |
|
110
|
328
|
3be9A |
Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase ck2 and their anticancer activities |
|
82
|
273
|
3bgpA |
Human pim-1 complexed with a benzoisoxazole inhibitor vx1 |
|
81
|
370
|
3begA |
Crystal structure of sr protein kinase 1 complexed to its substrate asf/sf2 |
|
79
|
273
|
3bgqA |
Human pim-1 kinase in complex with an triazolo pyridazine inhibitor vx2 |
|
241
|
949
|
3apfA |
Crystal structure of human pi3k-gamma in complex with ch5039699 |
|
264
|
950
|
3apdA |
Crystal structure of human pi3k-gamma in complex with ch5108134 |
|
92
|
569
|
3b43A |
I-band fragment i65-i70 from titin |
|
267
|
950
|
3apcA |
Crystal structure of human pi3k-gamma in complex with ch5132799 |
|
106
|
329
|
3axwA |
Crystal structure of human ck2alpha complexed with a potent inhibitor |
|
116
|
334
|
3at2A |
Crystal structure of ck2alpha |
|
113
|
332
|
3at3A |
Crystal structure of ck2alpha with pyradine derivative |
