|
110
|
350
|
3flnC |
P38 kinase crystal structure in complex with r1487 |
|
108
|
349
|
3fmlA |
P38 kinase crystal structure in complex with ro6224 |
|
80
|
277
|
3f3tA |
Kinase domain of csrc in complex with inhibitor rl38 (type iii) |
|
73
|
273
|
3et7A |
Crystal structure of pyk2 complexed with pf-2318841 |
|
74
|
298
|
3eocA |
Cdk2/cyclina complexed with a imidazo triazin-2-amine |
|
96
|
290
|
3eyhA |
Crystal structures of jak1 and jak2 inhibitor complexes |
|
85
|
276
|
3eqrA |
Crystal structure of ack1 with compound t74 |
|
101
|
344
|
3eqiA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a binary complex with adp and mg2p |
|
83
|
277
|
3f2aA |
Crystal structure of human pim-1 in complex with dappa |
|
104
|
312
|
3ewhA |
Crystal structure of the vegfr2 kinase domain in complex with a pyridyl-pyrimidine benzimidazole inhibitor |
|
148
|
534
|
3enhA |
Crystal structure of cgi121/bud32/kae1 complex |
|
77
|
298
|
3ezrA |
Cdk-2 with indazole inhibitor 17 bound at its active site |
|
101
|
344
|
3eqdA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a binary complex with atp-gs and mg2p |
|
178
|
537
|
3en9A |
Structure of the methanococcus jannaschii kae1-bud32 fusion protein |
|
116
|
358
|
3eljA |
Jnk1 complexed with a bis-anilino-pyrrolopyrimidine inhibitor. |
|
103
|
344
|
3eqcA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a ternary complex with compound 1, atp-gs and mg2p |
|
91
|
290
|
3eygA |
Crystal structures of jak1 and jak2 inhibitor complexes |
|
88
|
343
|
3eqfA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a binary complex with k252a and mg2p |
|
77
|
276
|
3en4A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with pp121, a multitargeted kinase inhibitor |
|
85
|
322
|
3eqbA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp |
|
70
|
278
|
3en7A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with s1, a multitargeted kinase inhibitor |
|
97
|
343
|
3eqhA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a ternary complex with u0126, adp and mg2p |
|
83
|
274
|
3eqpA |
Crystal structure of ack1 with compound t95 |
|
97
|
294
|
3etaA |
Kinase domain of insulin receptor complexed with a pyrrolo pyridine inhibitor |
|
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 |
|
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 |
|
92
|
293
|
3eh9A |
Crystal structure of death associated protein kinase complexed with adp |
|
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 |
|
101
|
293
|
3e64A |
Fragment based discovery of jak-2 inhibitors |
|
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 |
|
99
|
311
|
3dtwA |
Crystal structure of the vegfr2 kinase domain in complex with a benzisoxazole inhibitor |
|
111
|
350
|
3e93A |
Crystal structure of p38 kinase in complex with a biaryl amide inhibitor |