|
107
|
348
|
3p79A |
P38 inhibitor-bound |
|
75
|
276
|
3ppkA |
Human b-raf kinase in complex with a non-oxime furopyridine inhibitor |
|
89
|
288
|
3pp0A |
Crystal structure of the kinase domain of human her2 (erbb2). |
|
80
|
269
|
3pa5A |
X-ray crystal structure of compound 1 bound to human chk1 kinase domain |
|
76
|
276
|
3prfA |
Crystal structure of human b-raf kinase domain in complex with a non-oxime furopyridine inhibitor |
|
73
|
271
|
3ppzA |
Crystal structure of ctr1 kinase domain in complex with staurosporine |
|
83
|
267
|
3pa3A |
X-ray crystal structure of compound 70 bound to human chk1 kinase domain |
|
103
|
348
|
3p78A |
P38 inhibitor-bound |
|
75
|
276
|
3psbA |
Furo[2,3-c]pyridine-based indanone oximes as potent and selective b-raf inhibitors |
|
109
|
356
|
3pg1A |
Map kinase lmampk10 from leishmania major (1.95 angs resolution) |
|
106
|
348
|
3p7bA |
P38 inhibitor-bound |
|
109
|
337
|
3pooA |
Human camp-dependent protein kinase in complex with an inhibitor |
|
84
|
322
|
3pp1A |
Crystal structure of the human mitogen-activated protein kinase kinase 1 (mek 1) in complex with ligand and mgatp |
|
100
|
348
|
3p7cA |
P38 inhibitor-bound |
|
100
|
348
|
3p7aA |
P38 inhibitor-bound |
|
74
|
276
|
3priA |
Crystal structure of human b-raf kinase in complex with a non-oxime furopyridine inhibitor |
|
64
|
276
|
3omvA |
Crystal structure of c-raf (raf-1) |
|
95
|
355
|
3oxiA |
Design and synthesis of disubstituted thiophene and thiazole based inhibitors of jnk for the treatment of neurodegenerative diseases |
|
111
|
328
|
3owjA |
Human ck2 catalytic domain in complex with a pyridocarbazole derivative inhibitor |
|
88
|
284
|
3oy3A |
Crystal structure of abl t315i mutant kinase domain bound with a dfg-out inhibitor ap24589 |
|
73
|
272
|
3og7A |
B-raf kinase v600e oncogenic mutant in complex with plx4032 |
|
70
|
254
|
3otvA |
Crystal structure of the intracellular domain of rv3910 from mycobacterium tuberculosis |
|
85
|
289
|
3ortA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 6) |
|
89
|
284
|
3oxzA |
Crystal structure of abl kinase domain bound with a dfg-out inhibitor ap24534 |
|
104
|
330
|
3owlA |
Human ck2 catalytic domain in complex with a benzopyridoindole derivative inhibitor |
|
83
|
267
|
3ot8A |
X-ray crystal structure of compound 17r bound to human chk1 kinase domain |
|
81
|
285
|
3orxA |
Pdk1 mutant bound to allosteric disulfide fragment inhibitor 1f8 |
|
105
|
350
|
3p4kA |
The third conformation of p38a map kinase observed in phosphorylated p38a and in solution |
|
80
|
265
|
3p08A |
Crystal structure of the human btk kinase domain |
|
111
|
336
|
3owpA |
Human camp-dependent protein kinase in complex with an inhibitor |
|
94
|
335
|
3ow4A |
Discovery of dihydrothieno- and dihydrofuropyrimidines as potent pan akt inhibitors |
|
81
|
267
|
3ot3A |
X-ray crystal structure of compound 22k bound to human chk1 kinase domain |
|
58
|
248
|
3oukA |
Crystal structure of rv3910 from mycobacterium tuberculosis |
|
114
|
325
|
3ofmA |
Structure of a human ck2alpha prime, the paralog isoform of the catalytic subunit of protein kinase ck2 from homo sapiens |
|
106
|
330
|
3owkA |
Human ck2 catalytic domain in complex with a benzopyridoindole derivative inhibitor |
|
69
|
257
|
3ounB |
Crystal structure of the fhaa fha domain complexed with the intracellular domain of rv3910 |
|
85
|
283
|
3otuA |
Pdk1 mutant bound to allosteric disulfide fragment activator js30 |
|
105
|
401
|
3p23A |
Crystal structure of the human kinase and rnase domains in complex with adp |
|
106
|
355
|
3oy1A |
Highly selective c-jun n-terminal kinase (jnk) 2 and 3 inhibitors with in vitro cns-like pharmacokinetic properties |
|
78
|
280
|
3ormA |
Mycobacterium tuberculosis pknb kinase domain d76a mutant |
|
89
|
288
|
3ornA |
Mitogen-activated protein kinase kinase 1 (mek1) in complex with ch4987655 and mgamp-pnp |
|
105
|
348
|
3p5kA |
P38 inhibitor-bound |
|
81
|
280
|
3oroA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 4) |
|
116
|
378
|
3oz6A |
Crystal structure of mapk from cryptosporidium parvum, cgd2_1960 |
|
102
|
297
|
3oomA |
Crystal structure of the acvr1 kinase domain in complex with the imidazo[1,2-b]pyridazine inhibitor k00507 |
|
110
|
336
|
3ow3A |
Discovery of dihydrothieno- and dihydrofuropyrimidines as potent pan akt inhibitors |
|
71
|
287
|
3orlA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 3) |
|
106
|
321
|
3op5A |
Human vaccinia-related kinase 1 |
|
107
|
337
|
3p0mA |
Human camp-dependent protein kinase in complex with an inhibitor |
|
95
|
348
|
3ohtA |
Crystal structure of salmo salar p38alpha |
