|
81
|
295
|
4oboA |
Map4k4 in complex with inhibitor (compound 22), 6-(3-chlorophenyl)quinazolin-4-amine |
|
319
|
1051
|
4l1bA |
Crystal structure of p110alpha complexed with nish2 of p85alpha |
|
74
|
267
|
4o0wA |
Crystal structures of human kinase aurora a |
|
32
|
106
|
4nxfA |
Crystal structure of ilov-i486(2lt) at ph 8.0 |
|
40
|
123
|
4otnA |
Crystal structure of the c-terminal regulatory domain of murine gcn2 |
|
96
|
330
|
4nh1A |
Crystal structure of a heterotetrameric ck2 holoenzyme complex carrying the andante-mutation in ck2beta and consistent with proposed models of autoinhibition and trans-autophosphorylation |
|
84
|
273
|
4n6zA |
Pim1 complexed with a pyridylcarboxamide |
|
84
|
292
|
4o0tA |
Back pocket flexibility provides group-ii pak selectivity for type 1 kinase inhibitors |
|
31
|
104
|
4nxeA |
Crystal structure of ilov-i486(2lt) at ph 6.5 |
|
32
|
103
|
4nxgA |
Crystal structure of ilov-i486z(2lt) at ph 9.0 |
|
111
|
329
|
4oucA |
Structure of human haspin in complex with histone h3 substrate |
|
18
|
102
|
4o00A |
Crystal structure of the titin a-band domain a3 |
|
108
|
361
|
4nm5A |
Crystal structure of gsk-3/axin complex bound to phosphorylated wnt receptor lrp6 c-motif |
|
66
|
268
|
4otpA |
Crystal structure of the catalytic domain of the human riok1 atypical protein kinase in complex with adp/mg2+ |
|
18
|
51
|
4oh9A |
Crystal structure of the human mst2 sarah homodimer |
|
79
|
275
|
4n70A |
Pim1 complexed with a pyridylcarboxamide |
|
84
|
309
|
4oh4A |
Crystal structure of bri1 in complex with bki1 |
|
87
|
293
|
4o0rA |
Back pocket flexibility provides group-ii pak selectivity for type 1 kinase inhibitors |
|
147
|
455
|
4mvfA |
Crystal structure of plasmodium falciparum cdpk2 complexed with inhibitor staurosporine |
|
111
|
332
|
4md8E |
Crystal structure of full-length symmetric ck2 holoenzyme with mutated alpha subunit (f121e) |
|
81
|
303
|
4m8tA |
Rsk2 t493m c-terminal kinase domain in complex with 3-(3-(1h-pyrazol-4-yl)phenyl)-2-cyanoacrylamide |
|
61
|
186
|
4lscA |
Isolated serk1 co-receptor ectodomain at high resolution |
|
246
|
949
|
4kz0A |
Structure of pi3k gamma with imidazopyridine inhibitors |
|
128
|
371
|
4mwhA |
Crystal structure of scck2 alpha in complex with atp |
|
96
|
359
|
4lgdA |
Structural basis for autoactivation of human mst2 kinase and its regulation by rassf5 |
|
77
|
272
|
4mnfA |
Crystal structure of braf-v600e bound to gdc0879 |
|
240
|
949
|
4kzcA |
Structure of pi3k gamma with imidazopyridine inhibitors |
|
86
|
298
|
4maoA |
Rsk2 t493m c-terminal kinase domain in complex with rmm58 |
|
87
|
301
|
4m69A |
Crystal structure of the mouse rip3-mlkl complex |
|
59
|
468
|
4lqqA |
Crystal structure of the cbk1(t743e)-mob2 kinase-coactivator complex in crystal form b |
|
82
|
272
|
4ll5A |
Crystal structure of pim-1 in complex with the fluorescent compound skf86002 |
|
371
|
1165
|
4jsnA |
Structure of mtordeltan-mlst8 complex |
|
340
|
1060
|
4jpsA |
Co-crystal structures of the lipid kinase pi3k alpha with pan and isoform selective inhibitors |
|
77
|
273
|
4medA |
Crystal structure of ser/thr kinase pim1 in complex with thioridazine derivatives |
|
81
|
286
|
4m7iA |
Crystal structure of gsk6157 bound to perk (r587-r1092, delete a660-t867) at 2.34a resolution |
|
51
|
163
|
4lrjA |
Bacterial effector nleh1 kinase domain with amppnp and mg2+ |
|
62
|
456
|
4lqsA |
Crystal structure of the cbk1-mob2 kinase-coactivator complex |
|
82
|
273
|
4mtaA |
Crystal structure of pim-1 kinase domain in complex with 2-methyl-5-phenylfuran-3-carboxylic acid |
|
358
|
1165
|
4jsvA |
Mtor kinase structure, mechanism and regulation. |
|
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 |
|
60
|
468
|
4lqpA |
Crystal structure of the cbk1(t743e)-mob2 kinase-coactivator complex, in crystal form a |
|
308
|
1046
|
4l2yA |
Crystal structure of p110alpha complexed with nish2 of p85alpha and compound 9d |
|
77
|
271
|
4lm5A |
Crystal structure of pim1 in complex with 2-{4-[(3-aminopropyl)amino]quinazolin-2-yl}phenol (resulting from displacement of skf86002) |
|
367
|
1165
|
4jspA |
Structure of mtordeltan-mlst8-atpgammas-mg complex |
|
110
|
332
|
4md7E |
Crystal structure of full-length symmetric ck2 holoenzyme |
|
62
|
276
|
4mbjA |
Human b-raf kinase domain in complex with an imidazopyridine-based inhibitor |
|
76
|
274
|
4mblA |
Discovery of pyrazolo[1,5a]pyrimidine-based pim1 inhibitors |
|
47
|
162
|
4lrkA |
Bacterial effector nleh2 kinase domain |
