|
105
|
402
|
4yzcA |
Crystal structure of pire1alpha in complex with staurosporine |
|
269
|
949
|
4xx5A |
Structure of pi3k gamma in complex with an inhibitor |
|
121
|
400
|
4yvcA |
Rock 1 bound to thiazole inhibitor |
|
260
|
949
|
4xz4A |
Structure of pi3k gamma in complex with an inhibitor |
|
336
|
1060
|
4wafA |
Crystal structure of a novel tetrahydropyrazolo[1,5-a]pyrazine in an engineered pi3k alpha |
|
76
|
272
|
4xv2A |
B-raf kinase v600e oncogenic mutant in complex with dabrafenib |
|
97
|
367
|
4xhlA |
Structure of s. cerevisiae hrr25 1-394 (k38r mutant) |
|
85
|
322
|
4y0xA |
Crystal structure of the s/t protein kinase pkng from mycobacterium tuberculosis in complex with adp |
|
84
|
275
|
4xv9A |
B-raf kinase domain in complex with plx5568 |
|
86
|
289
|
4xx9A |
Crystal structure of pdk1 in complex with atp and the pif-pocket ligand rf4 |
|
82
|
274
|
4xhkB |
Pim1 kinase in complex with compound 1s |
|
65
|
270
|
4xv3A |
B-raf kinase v600e oncogenic mutant in complex with plx7922 |
|
80
|
273
|
4xh6A |
Crystal structure of proto-oncogene kinase pim1 bound to hispidulin |
|
84
|
322
|
4y12A |
Crystal structure of the s/t protein kinase pkng from mycobacterium tuberculosis in complex with ags |
|
126
|
395
|
4xh0A |
Structure of c. glabrata hrr25 bound to adp (so4 condition) |
|
100
|
343
|
4xbrA |
In cellulo crystal structure of pak4 in complex with inka |
|
92
|
297
|
4xs2A |
Irak4-inhibitor co-structure |
|
275
|
945
|
4wwnA |
Crystal structure of human pi3k-gamma in complex with (s)-n-(1-(7-fluoro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)-9h-purin-6-amine amg319 inhibitor |
|
105
|
297
|
4y73A |
Crystal structure of irak4 kinase domain with inhibitor |
|
71
|
268
|
4xv1A |
B-raf kinase v600e oncogenic mutant in complex with plx7904 |
|
263
|
944
|
4wwoA |
Crystal structure of human pi3k-gamma in complex with phenylquinoline inhibitor n-{(1s)-1-[8-chloro-2-(3-fluorophenyl)quinolin-3-yl]ethyl}-9h-purin-6-amine |
|
93
|
293
|
4xbuA |
In vitro crystal structure of pak4 in complex with inka peptide |
|
74
|
256
|
4ww9A |
Crystal structure of binary complex bud32-cgi121 in complex with adp |
|
68
|
250
|
4wwaA |
Crystal structure of binary complex bud32-cgi121 |
|
76
|
273
|
4wsyA |
Crystal structure of human pim-1 kinase in complex with a thiazolamine-indazole inhibitor. |
|
87
|
262
|
4uzdA |
Sar156497 an exquisitely selective inhibitor of aurora kinases |
|
18
|
97
|
4uow0 |
Crystal structure of the titin m10-obscurin ig domain 1 complex |
|
81
|
273
|
4wt6A |
Crystal structure of human pim-1 kinase in complex with a thiadiazolamine-indole inhibitor. |
|
86
|
304
|
4w9xA |
Crystal structure of bmp-2-inducible kinase in complex with baricitinib |
|
92
|
300
|
4uv0A |
Structure of a semisynthetic phosphorylated dapk |
|
82
|
292
|
4x7oA |
Co-crystal structure of perk bound to 1-[5-(4-amino-2,7-dimethyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)-2,3-dihydro-1h-indol-1-yl]-2-[3-fluoro-5-(trifluoromethyl)phenyl]ethanone inhibitor |
|
17
|
93
|
4uow1 |
Crystal structure of the titin m10-obscurin ig domain 1 complex |
|
75
|
287
|
4x3fA |
Crystal structure of the intracellular domain of the m. tuberculosis ser/thr kinase pkna |
|
76
|
254
|
4ww7A |
Crystal structure of binary complex bud32-cgi121 in complex with amp |
|
75
|
274
|
4wo5A |
Crystal structure of a braf kinase domain monomer |
|
83
|
268
|
4uzhA |
Sar156497 an exquisitely selective inhibitor of aurora kinases |
|
106
|
331
|
4umtA |
Structure of melk in complex with inhibitors |
|
87
|
298
|
4x7kA |
Co-crystal structure of perk bound to 4-{2-amino-3-[5-fluoro-2-(methylamino)quinazolin-6-yl]-4-methylbenzoyl}-1-methyl-2,5-diphenyl-1,2-dihydro-3h-pyrazol-3-one inhibitor |
|
117
|
370
|
4wuaA |
Crystal structure of human srpk1 complexed to an inhibitor srpin340 |
|
88
|
306
|
4w9wA |
Crystal structure of bmp-2-inducible kinase in complex with small molecule azd-7762 |
|
272
|
940
|
4tv3A |
Isolated p110a subunit of pi3ka provides a platform for structure-based drug design |
|
72
|
291
|
4usdA |
Human stk10 (lok) with sb-633825 |
|
80
|
288
|
4x3fC |
Crystal structure of the intracellular domain of the m. tuberculosis ser/thr kinase pkna |
|
106
|
396
|
4wotA |
Rock2 in complex with 1426382-07-1 |
|
81
|
274
|
4wnpA |
Structure of ulk1 bound to a potent inhibitor |
|
95
|
291
|
4w8eA |
Structure of mst3 with a pyrrolopyrimidine inhibitor (pf-06645342) |
|
66
|
256
|
4x7qA |
Pim2 kinase in complex with compound 1s |
|
79
|
267
|
4uynA |
Sar156497 an exquisitely selective inhibitor of aurora kinases |
|
95
|
329
|
4umqA |
Structure of melk in complex with inhibitors |
|
86
|
298
|
4x7lA |
Co-crystal structure of perk bound to 4-{2-amino-4-methyl-3-[2-(methylamino)-1,3-benzothiazol-6-yl]benzoyl}-1-methyl-2,5-diphenyl-1,2-dihydro-3h-pyrazol-3-one inhibitor |
