|
91
|
329
|
4md9E |
Crystal structure of symmetric ck2 holoenzyme with mutated alpha subunit (f121e truncated at aa 336) |
|
80
|
274
|
4mbiA |
Discovery of pyrazolo[1,5a]pyrimidine-based pim1 inhibitors |
|
76
|
298
|
4m66A |
Crystal structure of the mouse rip3 kinase domain |
|
92
|
291
|
4kb8A |
Ck1d in complex with 1-{4-[3-(4-fluorophenyl)-1-methyl-1h-pyrazol-4-yl]pyridin-2-yl}-n-methylmethanamine ligand |
|
81
|
338
|
4l46A |
Crystal structures of human p70s6k1-wt |
|
92
|
291
|
4l3lA |
Crystal structures of human p70s6k1 kinase domain (zinc anomalous) |
|
98
|
292
|
4kbcA |
Ck1d in complex with {4-[3-(4-fluorophenyl)-1h-pyrazol-4-yl]pyridin-2-yl}methanol inhibitor |
|
137
|
370
|
4lfiA |
Crystal structure of scck2 alpha in complex with gmppnp |
|
86
|
291
|
4l3jA |
Crystal structures of human p70s6k1 kinase domain |
|
90
|
334
|
4l42A |
Crystal structures of human p70s6k1-pif |
|
94
|
291
|
4kbaA |
Ck1d in complex with 9-[3-(4-fluorophenyl)-1-methyl-1h-pyrazol-4-yl]-2,3,4,5-tetrahydropyrido[2,3-f][1,4]oxazepine inhibitor |
|
20
|
51
|
4l0nA |
Crystal structure of stk3 (mst2) sarah domain |
|
88
|
337
|
4l44A |
Crystal structures of human p70s6k1-t389a (form ii) |
|
95
|
291
|
4kbkA |
Ck1d in complex with (3s)-3-{4-[3-(4-fluorophenyl)-1-methyl-1h-pyrazol-4-yl]pyridin-2-yl}morpholine inhibitor |
|
101
|
329
|
4kwpA |
Crystal structure of human ck2-alpha in complex with a benzimidazole inhibitor (k164) at 1.25 a resolution |
|
76
|
290
|
4l67A |
Crystal structure of catalytic domain of pak4 |
|
91
|
287
|
4ks8A |
Pak6 kinase domain in complex with sunitinib |
|
200
|
657
|
4jl9A |
Crystal structure of mouse tbk1 bound to bx795 |
|
85
|
337
|
4l43A |
Crystal structures of human p70s6k1-t389a (form i) |
|
76
|
275
|
4kspA |
Crystal structure of human b-raf bound to a dfg-out inhibitor tak-632 |
|
264
|
945
|
4j6iA |
Discovery of thiazolobenzoxepin pi3-kinase inhibitors that spare the pi3-kinase beta isoform |
|
80
|
274
|
4jx7A |
Crystal structure of pim1 kinase in complex with inhibitor 2-[(trans-4-aminocyclohexyl)amino]-4-{[3-(trifluoromethyl)phenyl]amino}pyrido[4,3-d]pyrimidin-5(6h)-one |
|
110
|
391
|
4l6qA |
Rock2 in complex with benzoxaborole |
|
96
|
287
|
4ks7A |
Pak6 kinase domain in complex with pf-3758309 |
|
136
|
427
|
4kqbA |
Crystal structure of the golgi casein kinase with mn/adp bound |
|
79
|
273
|
4k1bA |
Structure of pim-1 kinase bound to n-(5-(2-fluorophenyl)-1h-pyrrolo[2,3-b]pyridin-3-yl)-5-((((3r,4r)-3-fluoropiperidin-4-yl)methyl)amino)pyrazolo[1,5-a]pyrimidine-3-carboxamide |
|
31
|
67
|
4l2wA |
Crystal structure of the shroom-binding domain of human rock1 |
|
124
|
426
|
4kqaA |
Crystal structure of the golgi casein kinase |
|
209
|
657
|
4jlcA |
Crystal structure of mouse tbk1 bound to su6668 |
|
91
|
291
|
4lg4A |
Structural basis for autoactivation of human mst2 kinase and its regulation by rassf5 |
|
1
|
20
|
4l67B |
Crystal structure of catalytic domain of pak4 |
|
83
|
337
|
4l45A |
Crystal structures of human p70s6k1-t389e |
|
74
|
275
|
4ksqA |
Crystal structure of human b-raf bound to a dfg-out inhibitor 5b |
|
96
|
348
|
4j1rA |
Crystal structure of gsk3b in complex with inhibitor 15r |
|
82
|
277
|
4k18A |
Structure of pim-1 kinase bound to 5-(4-cyanobenzyl)-n-(4-fluorophenyl)-7-hydroxypyrazolo[1,5-a]pyrimidine-3-carboxamide |
|
189
|
659
|
4iwqA |
Crystal structure and mechanism of activation of tbk1 |
|
98
|
297
|
4jjrA |
A p21 crystal form of mammalian casein kinase 1 delta |
|
83
|
289
|
4i93A |
Structure of the bsk8 kinase domain (semet labeled) |
|
86
|
309
|
4jg7A |
Structure of rsk2 ctd bound to 3-(3-(1h-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)-2-cyanoacrylamide |
|
212
|
659
|
4im2A |
Structure of tank-binding kinase 1 |
|
76
|
266
|
4j8mA |
Aurora a in complex with cd532 |
|
75
|
287
|
4ithA |
Crystal structure of rip1 kinase in complex with necrostatin-1 analog |
|
130
|
369
|
4jqeA |
Crystal structure of scck2 alpha in complex with amppn |
|
94
|
336
|
4ijpA |
Crystal structure of human prpf4b kinase domain in complex with 4-{5-[(2-chloro-pyridin-4-ylmethyl)-carbamoyl]-thiophen-2-yl}-benzo[b]thiophene-2-carboxylic acid amine |
|
100
|
320
|
4jnwA |
Bacterially expressed titin kinase |
|
110
|
331
|
4ib5A |
Structure of human protein kinase ck2 catalytic subunit in complex with a ck2beta-competitive cyclic peptide |
|
91
|
332
|
4hzsA |
Crystal structure of ack1 kinase domain with c-terminal sh3 domain |
|
93
|
290
|
4jdkA |
Crystal structure of serine/threonine-protein kinase pak 4 f461v mutant in complex with paktide s peptide substrate |
|
71
|
266
|
4j8nA |
Aurora a kinase apo |
|
70
|
275
|
4jvgA |
B-raf kinase in complex with birb796 |
