|
87
|
288
|
3wf9A |
Crystal structure of s6k1 kinase domain in complex with a quinoline derivative 1-oxo-1-[(4-sulfamoylphenyl)amino]propan-2-yl-2-methyl-1,2,3,4-tetrahydroacridine-9-carboxylate |
|
116
|
334
|
3wikA |
Crystal structure of the ck2alpha/compound10 complex |
|
13
|
51
|
3wwsA |
Crystal structure of serine/threonine-protein kinase 3 |
|
84
|
290
|
3wf6A |
Crystal structure of s6k1 kinase domain in complex with a pyrazolopyrimidine derivative 4-[4-(1h-indol-3-yl)-3,6-dihydropyridin-1(2h)-yl]-1h-pyrazolo[3,4-d]pyrimidine |
|
99
|
349
|
3zdiA |
Glycogen synthase kinase 3 beta complexed with axin peptide and inhibitor 7d |
|
90
|
290
|
3we4A |
Crystal structure of s6k1 kinase domain in complex with a pyrimidine derivative pf-4708671 2-{[4-(5-ethylpyrimidin-4-yl)piperazin-1-yl]methyl}-5-(trifluoromethyl)-1h-benzimidazole |
|
85
|
273
|
3we8A |
Pim-1 kinase in complex with ruthenium-based inhibitor |
|
74
|
275
|
3zhpC |
Human mst3 (stk24) in complex with mo25beta |
|
89
|
288
|
3wf8A |
Crystal structure of s6k1 kinase domain in complex with a quinoline derivative 2-oxo-2-[(4-sulfamoylphenyl)amino]ethyl 7,8,9,10-tetrahydro-6h-cyclohepta[b]quinoline-11-carboxylate |
|
121
|
334
|
3warA |
Crystal structure of human ck2a |
|
78
|
263
|
3w10A |
Aurora kinase a complexed to pyrazole aminoquinoline i |
|
24
|
66
|
3w8hB |
Crystal structure of ccm3 in complex with the c-terminal regulatory domain of stk25 |
|
29
|
67
|
3w8iB |
Crystal structure of ccm3 in complex with the c-terminal regulatory domain of mst4 |
|
52
|
261
|
3w2cA |
Structure of aurora kinase a complexed to benzoimidazole-indazole inhibitor xv |
|
67
|
263
|
3w18A |
Structure of aurora kinase a complexed to benzoimidazole-indazole inhibitor xiii |
|
71
|
263
|
3w16A |
Structure of aurora kinase a complexed to pyrazole-aminoquinoline inhibitor iii |
|
157
|
566
|
3utoA |
Twitchin kinase region from c.elegans (fn31-nl-kin-crd-ig26) |
|
78
|
271
|
3vbyA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
96
|
292
|
3uzpA |
Crystal structure of ck1d with pf670462 from p21 crystal form |
|
123
|
395
|
3v8sA |
Human rho-associated protein kinase 1 (rock 1) in complex with indazole derivative (compound 18) |
|
80
|
274
|
3vc4A |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
79
|
271
|
3vbwA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
81
|
271
|
3vbvA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
81
|
271
|
3vbtA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
82
|
271
|
3vbxA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
83
|
291
|
3uysA |
Crystal structure of apo human ck1d |
|
90
|
290
|
3uytA |
Crystal structure of ck1d with pf670462 from p1 crystal form |
|
80
|
271
|
3vbqA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
76
|
262
|
3vapA |
Synthesis and sar studies of imidazo-[1,2-a]-pyrazine aurora kinase inhibitors with improved off target kinase selectivity |
|
70
|
264
|
3up7A |
Aurora a in complex with yl1-038-09 |
|
103
|
329
|
3u87A |
Structure of a chimeric construct of human ck2alpha and human ck2alpha' in complex with a non-hydrolysable atp-analogue |
|
48
|
125
|
3uv4A |
Crystal structure of the second bromodomain of human transcription initiation factor tfiid subunit 1 (taf1) |
|
67
|
264
|
3uohA |
Aurora a in complex with rpm1722 |
|
59
|
288
|
3uiuA |
Crystal structure of apo-pkr kinase domain |
|
89
|
309
|
3uc3A |
The crystal structure of snf1-related kinase 2.3 |
|
71
|
264
|
3uo6A |
Aurora a in complex with yl5-083 |
|
87
|
266
|
3uodA |
Aurora a in complex with rpm1693 |
|
73
|
265
|
3uokA |
Aurora a in complex with yl5-81-1 |
|
77
|
302
|
3uimA |
Structural basis for the impact of phosphorylation on plant receptor-like kinase bak1 activation |
|
85
|
353
|
3uibA |
Map kinase lmampk10 from leishmania major in complex with sb203580 |
|
78
|
269
|
3uixA |
Crystal structure of pim1 kinase in complex with small molecule inhibitor |
|
78
|
266
|
3uo4A |
Aurora a in complex with rpm1680 |
|
82
|
268
|
3umxA |
Crystal structure of pim1 kinase in complex with inhibitor (z)-2-[(1h-indol-3-yl)methylene]-7-(azepan-1-ylmethyl)-6-hydroxybenzofuran-3(2h)-one |
|
103
|
331
|
3u9cA |
Structure of a c-terminal deletion mutant of human protein kinase ck2 catalytic subunit with the atp-competitive inhibitor resorufin |
|
81
|
268
|
3umwA |
Crystal structure of pim1 kinase in complex with inhibitor (z)-2-[(1h-indazol-3-yl)methylene]-6-methoxy-7-(piperazin-1-ylmethyl)benzofuran-3(2h)-one |
|
71
|
263
|
3unzA |
Aurora a in complex with rpm1679 |
|
79
|
299
|
3ujgA |
Crystal structure of snrk2.6 in complex with hab1 |
|
79
|
306
|
3udbA |
Crystal structure of snrk2.6 |
|
75
|
263
|
3uolA |
Aurora a in complex with so2-162 |
|
77
|
302
|
3ulzA |
Crystal structure of apo bak1 |
