|
107
|
338
|
3fhiA |
Crystal structure of a complex between the catalytic and regulatory (ri{alpha}) subunits of pka |
|
79
|
264
|
3f9nA |
Crystal structure of chk1 kinase in complex with inhibitor 38 |
|
112
|
329
|
3fmdA |
Crystal structure of human haspin with an isoquinoline ligand |
|
94
|
288
|
3f7wA |
Crystal structure of putative fructosamine-3-kinase (yp_290396.1) from thermobifida fusca yx-er1 at 1.85 a resolution |
|
113
|
349
|
3fmmA |
P38 kinase crystal structure in complex with ro6226 |
|
67
|
288
|
3fmeA |
Crystal structure of human mitogen-activated protein kinase kinase 6 (mek6) activated mutant (s207d, t211d) |
|
80
|
277
|
3f3tA |
Kinase domain of csrc in complex with inhibitor rl38 (type iii) |
|
108
|
349
|
3fmnA |
P38 kinase crystal structure in complex with ro2530 |
|
81
|
277
|
3f3vA |
Kinase domain of csrc in complex with inhibitor rl45 (type ii) |
|
93
|
293
|
3f5uA |
Crystal structure of the death associated protein kinase in complex with amppnp and mg2+ |
|
105
|
325
|
3fl5A |
Protein kinase ck2 in complex with the inhibitor quinalizarin |
|
87
|
272
|
3f3zA |
Crystal structure of cryptosporidium parvum calcium dependent protein kinase cgd7_1840 in presence of indirubin e804 |
|
112
|
349
|
3fknA |
P38 kinase crystal structure in complex with ro7125 |
|
86
|
330
|
3faaA |
Crystal structure of tgfbri complexed with a 2-aminoimidazole inhibitor |
|
111
|
349
|
3flyA |
P38 kinase crystal structure in complex with 6-(2,4-difluoro-phenoxy)-2-isopropylamino-8-methyl-8h-pyrido[2,3-d]pyrimidin-7-one |
|
107
|
349
|
3fmjA |
P38 kinase crystal structure in complex with 4-(5-methyl-3-phenyl-isoxazol-4-yl)-pyrimidin-2-ylamine |
|
109
|
349
|
3flzA |
P38 kinase crystal structure in complex with 8-methyl-6-phenoxy-2-(tetrahydro-pyran-4-ylamino)-8h-pyrido[2,3-d]pyrimidin-7-one |
|
84
|
277
|
3f3wA |
Drug resistant csrc kinase domain in complex with inhibitor rl45 (type ii) |
|
130
|
347
|
3fegA |
Crystal structure of human choline kinase beta in complex with phosphorylated hemicholinium-3 and adenosine nucleotide |
|
82
|
293
|
3fc2A |
Plk1 in complex with bi6727 |
|
109
|
349
|
3flwA |
P38 kinase crystal structure in complex with pamapimod |
|
110
|
349
|
3flqA |
P38 kinase crystal structure in complex with 6-(2,4-difluoro-phenoxy)-2-((s)-2-methanesulfonyl-1-methyl-ethylamino)-8-methyl-8h-pyrido[2,3-d]pyrimidin |
|
112
|
328
|
3f2nA |
Crystal structure of human haspin with an imidazo-pyridazine ligand |
|
100
|
345
|
3fi2A |
Crystal structure of jnk3 with amino-pyrazole inhibitor, sr-3451 |
|
112
|
418
|
3fbvA |
Crystal structure of the oligomer formed by the kinase-ribonuclease domain of ire1 |
|
98
|
350
|
3f7zA |
X-ray co-crystal structure of glycogen synthase kinase 3beta in complex with an inhibitor |
|
110
|
350
|
3flnC |
P38 kinase crystal structure in complex with r1487 |
|
108
|
349
|
3fmlA |
P38 kinase crystal structure in complex with ro6224 |
|
81
|
290
|
3f61A |
Crystal structure of m. tuberculosis pknb leu33asp/val222asp double mutant in complex with adp |
|
102
|
317
|
3fe3A |
Crystal structure of the kinase mark3/par-1: t211a-s215a double mutant |
|
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 |
|
73
|
288
|
3enmA |
The structure of the map2k mek6 reveals an autoinhibitory dimer |
|
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 |
