|
75
|
298
|
3ezvA |
Cdk-2 with indazole inhibitor 9 bound at its active site |
|
113
|
350
|
3erkA |
The complex structure of the map kinase erk2/sb220025 |
|
92
|
343
|
3eqgA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a ternary complex with pd, adp and mg2p |
|
73
|
288
|
3enmA |
The structure of the map2k mek6 reveals an autoinhibitory dimer |
|
91
|
290
|
3eygA |
Crystal structures of jak1 and jak2 inhibitor complexes |
|
110
|
344
|
3e8eA |
Crystal structures of the kinase domain of pka in complex with atp-competitive inhibitors |
|
68
|
263
|
3efwA |
Structure of auroraa with pyridyl-pyrimidine urea inhibitor |
|
71
|
274
|
3en6A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with pp102, a multitargeted kinase inhibitor |
|
97
|
370
|
3eb0A |
Crystal structure of cgd4_240 from cryptosporidium parvum in complex with indirubin e804 |
|
78
|
276
|
3el8A |
Crystal structure of c-src in complex with pyrazolopyrimidine 5 |
|
84
|
297
|
3eidA |
Cdk2/cyclina complexed with a pyrazolopyridazine inhibitor |
|
82
|
298
|
3efjA |
Structure of c-met with pyrimidone inhibitor 7 |
|
72
|
274
|
3en5A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with pp494, a multitargeted kinase inhibitor |
|
87
|
303
|
3ekkA |
Insulin receptor kinase complexed with an inhibitor |
|
68
|
277
|
3el7A |
Crystal structure of c-src in complex with pyrazolopyrimidine 3 |
|
92
|
312
|
3eflA |
Crystal structure of the vegfr2 kinase domain in complex with motesanib |
|
81
|
267
|
3emgA |
Discovery and sar of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (syk) |
|
80
|
298
|
3ej1A |
Cdk2/cyclina complexed with a pyrazolopyridazine inhibitor |
|
94
|
293
|
3ehaA |
Crystal structure of death associated protein kinase complexed with amppnp |
|
85
|
300
|
3eknA |
Insulin receptor kinase complexed with an inhibitor |
|
86
|
298
|
3efkA |
Structure of c-met with pyrimidone inhibitor 50 |
|
92
|
293
|
3eh9A |
Crystal structure of death associated protein kinase complexed with adp |
|
101
|
293
|
3e64A |
Fragment based discovery of jak-2 inhibitors |
|
80
|
340
|
3dxpA |
Crystal structure of a putative aminoglycoside phosphotransferase (reut_a1007) from ralstonia eutropha jmp134 at 2.32 a resolution |
|
99
|
311
|
3dtwA |
Crystal structure of the vegfr2 kinase domain in complex with a benzisoxazole inhibitor |
|
98
|
335
|
3e8dA |
Crystal structures of the kinase domain of akt2 in complex with atp-competitive inhibitors |
|
82
|
265
|
3e5aA |
Crystal structure of aurora a in complex with vx-680 and tpx2 |
|
89
|
322
|
3dv3A |
Mek1 with pf-04622664 bound |
|
111
|
350
|
3e93A |
Crystal structure of p38 kinase in complex with a biaryl amide inhibitor |
|
110
|
344
|
3e8cA |
Crystal structures of the kinase domain of pka in complex with atp-competitive inhibitors |
|
97
|
370
|
3dzoA |
Crystal structure of a rhoptry kinase from toxoplasma gondii |
|
100
|
348
|
3du8A |
Crystal structure of gsk-3 beta in complex with nms-869553a |
|
109
|
356
|
3dt1A |
P38 complexed with a quinazoline inhibitor |
|
98
|
353
|
3e7oA |
Crystal structure of jnk2 |
|
68
|
270
|
3dtcA |
Crystal structure of mixed-lineage kinase mlk1 complexed with compound 16 |
|
110
|
350
|
3e92A |
Crystal structure of p38 kinase in complex with a biaryl amide inhibitor |
|
109
|
328
|
3e7vA |
Crystal structure of human haspin with a pyrazolo-pyrimidine ligand |
|
99
|
293
|
3e62A |
Fragment based discovery of jak-2 inhibitors |
|
90
|
335
|
3e88A |
Crystal structures of the kinase domain of akt2 in complex with atp-competitive inhibitors |
|
83
|
334
|
3e3bX |
Crystal structure of catalytic subunit of human protein kinase ck2alpha prime with a potent indazole-derivative inhibitor |
|
100
|
335
|
3e87A |
Crystal structures of the kinase domain of akt2 in complex with atp-competitive inhibitors |
|
76
|
303
|
3dy7A |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp |
|
99
|
292
|
3e63A |
Fragment based discovery of jak-2 inhibitors |
|
89
|
322
|
3e8nA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) complexed with a potent inhibitor rdea119 and mgatp |
|
107
|
347
|
3e3pA |
Glycogen synthase kinase from leishmania major |
|
87
|
300
|
3dxqA |
Crystal structure of choline/ethanolamine kinase family protein (np_106042.1) from mesorhizobium loti at 2.55 a resolution |
|
92
|
296
|
3dzqA |
Human epha3 kinase domain in complex with inhibitor awl-ii-38.3 |
|
74
|
269
|
3dxnA |
Crystal structure of the calcium-dependent kinase from toxoplasma gondii, 541.m00134, kinase domain. |
|
104
|
349
|
3ds6A |
P38 complex with a phthalazine inhibitor |
|
105
|
336
|
3dndA |
Camp-dependent protein kinase pka catalytic subunit with pki-5-24 |
