|
82
|
274
|
2jkmA |
Focal adhesion kinase catalytic domain in complex with bis-anilino pyrimidine inhibitor |
|
91
|
288
|
2jflA |
Crystal structure of human ste20-like kinase (diphosphorylated form) bound to 5- amino-3-((4-(aminosulfonyl)phenyl)amino)-n-(2,6- difluorophenyl)-1h-1,2,4-triazole-1-carbothioamide |
|
109
|
337
|
2jdsA |
Structure of camp-dependent protein kinase complexed with a-443654 |
|
74
|
289
|
2jgzA |
Crystal structure of phospho-cdk2 in complex with cyclin b |
|
88
|
303
|
2jc6A |
Crystal structure of human calmodulin-dependent protein kinase 1d |
|
86
|
324
|
2j6mA |
Crystal structure of egfr kinase domain in complex with aee788 |
|
85
|
285
|
2jamA |
Crystal structure of human calmodulin-dependent protein kinase i g |
|
73
|
261
|
2j50A |
Structure of aurora-2 in complex with pha-739358 |
|
102
|
351
|
2jldA |
Extremely tight binding of ruthenium complex to glycogen synthase kinase 3 |
|
46
|
285
|
2jivA |
Crystal structure of egfr kinase domain t790m mutation in compex with hki-272 |
|
107
|
336
|
2jdvA |
Structure of pka-pkb chimera complexed with a-443654 |
|
78
|
321
|
2jitA |
Crystal structure of egfr kinase domain t790m mutation |
|
91
|
322
|
2itqA |
Crystal structure of egfr kinase domain g719s mutation in complex with afn941 |
|
72
|
277
|
2javA |
Human kinase with pyrrole-indolinone ligand |
|
89
|
313
|
2ivtA |
Crystal structure of phosphorylated ret tyrosine kinase domain |
|
88
|
323
|
2itzA |
Crystal structure of egfr kinase domain l858r mutation in complex with iressa |
|
81
|
303
|
2jboA |
Protein kinase mk2 in complex with an inhibitor (crystal form-1, soaking) |
|
91
|
324
|
2itoA |
Crystal structure of egfr kinase domain g719s mutation in complex with iressa |
|
81
|
293
|
2j7tA |
Crystal structure of human serine threonine kinase-10 bound to su11274 |
|
85
|
325
|
2j5eA |
Crystal structure of egfr kinase domain in complex with an irreversible inhibitor 13-jab |
|
88
|
290
|
2j0iA |
Crystal structure of the human p21-activated kinase 4 |
|
99
|
298
|
2iztA |
Structure of casein kinase gamma 3 in complex with inhibitor |
|
90
|
324
|
2ituA |
Crystal structure of egfr kinase domain l858r mutation in complex with afn941 |
|
80
|
274
|
2j90A |
Crystal structure of human zip kinase in complex with a tetracyclic pyridone inhibitor (pyridone 6) |
|
89
|
288
|
2j51A |
Crystal structure of human ste20-like kinase bound to 5-amino-3-((4-(aminosulfonyl)phenyl)amino) -n-(2,6-difluorophenyl)-1h-1,2,4-triazole- 1-carbothioamide |
|
88
|
322
|
2itwA |
Crystal structure of egfr kinase domain in complex with afn941 |
|
185
|
652
|
2j0jA |
Crystal structure of a fragment of focal adhesion kinase containing the ferm and kinase domains. |
|
92
|
300
|
2ivsA |
Crystal structure of non-phosphorylated ret tyrosine kinase domain |
|
90
|
323
|
2ittA |
Crystal structure of egfr kinase domain l858r mutation in complex with aee788 |
|
77
|
298
|
2j9mA |
Crystal structure of cdk2 in complex with macrocyclic aminopyrimidine |
|
89
|
324
|
2j5fA |
Crystal structure of egfr kinase domain in complex with an irreversible inhibitor 34-jab |
|
81
|
273
|
2j2iB |
Crystal structure of the humab pim1 in complex with ly333531 |
|
100
|
299
|
2izrA |
Structure of casein kinase gamma 3 in complex with inhibitor |
|
81
|
296
|
2iw6A |
Structure of human thr160-phospho cdk2-cyclin a complexed with a bisanilinopyrimidine inhibitor |
|
94
|
322
|
2itpA |
Crystal structure of egfr kinase domain g719s mutation in complex with aee788 |
|
83
|
279
|
2io6A |
Wee1 kinase complexed with inhibitor pd330961 |
|
78
|
273
|
2j0mB |
Crystal structure a two-chain complex between the ferm and kinase domains of focal adhesion kinase. |
|
88
|
313
|
2ivuA |
Crystal structure of phosphorylated ret tyrosine kinase domain complexed with the inhibitor zd6474 |
|
59
|
257
|
2iwiA |
Crystal structure of the human pim2 in complex with a ruthenium organometallic ligand ru1 |
|
92
|
323
|
2ityA |
Crystal structure of egfr kinase domain in complex with iressa |
|
80
|
279
|
2in6A |
Wee1 kinase complex with inhibitor pd311839 |
|
102
|
298
|
2izsA |
Structure of casein kinase gamma 3 in complex with inhibitor |
|
90
|
312
|
2ivvA |
Crystal structure of phosphorylated ret tyrosine kinase domain complexed with the inhibitor pp1 |
|
94
|
324
|
2itvA |
Crystal structure of egfr kinase domain l858r mutation in complex with amp-pnp |
|
92
|
324
|
2itnA |
Crystal structure of egfr kinase domain g719s mutation in complex with amp-pnp |
|
77
|
276
|
2j0lA |
Crystal structure of a the active conformation of the kinase domain of focal adhesion kinase with a phosphorylated activation loop. |
|
100
|
299
|
2izuA |
Structure of casein kinase gamma 3 in complex with inhibitor |
|
92
|
323
|
2itxA |
Crystal structure of egfr kinase domain in complex with amp-pnp |
|
82
|
275
|
2ijmA |
Crystal structure of focal adhesion kinase domain with 2 molecules in the asymmetric unit complexed with adp and atp |
|
81
|
264
|
2hyyA |
Human abl kinase domain in complex with imatinib (sti571, glivec) |
