|
84
|
297
|
1oi9A |
Structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor |
|
77
|
276
|
1o6yA |
Catalytic domain of pknb kinase from mycobacterium tuberculosis |
|
77
|
286
|
1ob3A |
Structure of p. falciparum pfpk5 |
|
80
|
271
|
1nvqA |
The complex structure of checkpoint kinase chk1/ucn-01 |
|
78
|
271
|
1nvsA |
The complex structure of checkpoint kinase chk1/sb218078 |
|
71
|
304
|
1nxkA |
Crystal structure of staurosporine bound to map kap kinase 2 |
|
96
|
326
|
1na7A |
Crystal structure of the catalytic subunit of human protein kinase ck2 |
|
75
|
300
|
1ny3A |
Crystal structure of adp bound to map kap kinase 2 |
|
80
|
271
|
1nvrA |
The complex structure of checkpoint kinase chk1/staurosporine |
|
80
|
283
|
1mqbA |
Crystal structure of ephrin a2 (epha2) receptor protein kinase |
|
82
|
273
|
1mp8A |
Crystal structure of focal adhesion kinase (fak) |
|
81
|
263
|
1mq4A |
Crystal structure of aurora-a protein kinase |
|
74
|
295
|
1mryA |
Crystal structure of an inactive akt2 kinase domain |
|
57
|
261
|
1muoA |
Crystal structure of aurora-2, an oncogenic serine-threonine kinase |
|
67
|
294
|
1mrvA |
Crystal structure of an inactive akt2 kinase domain |
|
72
|
284
|
1mruA |
Intracellular ser/thr protein kinase domain of mycobacterium tuberculosis pknb. |
|
80
|
271
|
1m52A |
Crystal structure of the c-abl kinase domain in complex with pd173955 |
|
110
|
350
|
1lezA |
Crystal structure of map kinase p38 complexed to the docking site on its activator mkk3b |
|
107
|
348
|
1m7qA |
Crystal structure of p38 map kinase in complex with a dihydroquinazolinone inhibitor |
|
108
|
327
|
1m2rA |
Crystal structure of 5,8-di-amino-1,4-di-hydroxy-anthraquinone/ck2 kinase complex |
|
107
|
327
|
1m2qA |
Crystal structure of 1,8-di-hydroxy-4-nitro-xanten-9-one/ck2 kinase complex |
|
107
|
350
|
1lewA |
Crystal structure of map kinase p38 complexed to the docking site on its nuclear substrate mef2a |
|
108
|
327
|
1lp4A |
Crystal structure of a binary complex of the catalytic subunit of protein kinase ck2 with mg-amppnp |
|
107
|
325
|
1m2pA |
Crystal structure of 1,8-di-hydroxy-4-nitro-anthraquinone/ck2 kinase complex |
|
88
|
324
|
1m17A |
Epidermal growth factor receptor tyrosine kinase domain with 4-anilinoquinazoline inhibitor erlotinib |
|
115
|
327
|
1lpuA |
Low temperature crystal structure of the apo-form of the catalytic subunit of protein kinase ck2 from zea mays |
|
95
|
301
|
1lufA |
Crystal structure of the musk tyrosine kinase: insights into receptor autoregulation |
|
90
|
305
|
1m7nA |
Crystal structure of unactivated apo insulin-like growth factor-1 receptor kinase domain |
|
88
|
325
|
1m14A |
Tyrosine kinase domain from epidermal growth factor receptor |
|
113
|
327
|
1lr4A |
Room temperature crystal structure of the apo-form of the catalytic subunit of protein kinase ck2 from zea mays |
|
89
|
348
|
1kv2A |
Human p38 map kinase in complex with birb 796 |
|
78
|
340
|
1kwpA |
Crystal structure of mapkap2 |
|
99
|
348
|
1kv1A |
P38 map kinase in complex with inhibitor 1 |
|
109
|
350
|
1l3rE |
Crystal structure of a transition state mimic of the catalytic subunit of camp-dependent protein kinase |
|
129
|
450
|
1kswA |
Structure of human c-src tyrosine kinase (thr338gly mutant) in complex with n6-benzyl adp |
|
76
|
298
|
1ke9A |
Cyclin-dependent kinase 2 (cdk2) complexed with 3-{[4-({[amino(imino)methyl]aminosulfonyl)anilino]methylene}-2-oxo-2,3-dihydro-1h-indole |
|
80
|
298
|
1ke7A |
Cyclin-dependent kinase 2 (cdk2) complexed with 3-{[(2,2-dioxido-1,3-dihydro-2-benzothien-5-yl)amino]methylene}-5-(1,3-oxazol-5-yl)-1,3-dihydro-2h-indol-2-one |
|
117
|
445
|
1k9aA |
Crystal structure analysis of full-length carboxyl-terminal src kinase at 2.5 a resolution |
|
79
|
298
|
1ke8A |
Cyclin-dependent kinase 2 (cdk2) complexed with 4-{[(2-oxo-1,2-dihydro-3h-indol-3-ylidene)methyl]amino}-n-(1,3-thiazol-2-yl)benzenesulfonamide |
|
104
|
352
|
1kobA |
Twitchin kinase fragment (aplysia), autoregulated protein kinase domain |
|
78
|
298
|
1ke6A |
Cyclin-dependent kinase 2 (cdk2) complexed with n-methyl-{4-[2-(7-oxo-6,7-dihydro-8h-[1,3]thiazolo[5,4-e]indol-8-ylidene)hydrazino]phenyl}methanesulfonamide |
|
76
|
298
|
1ke5A |
Cdk2 complexed with n-methyl-4-{[(2-oxo-1,2-dihydro-3h-indol-3-ylidene)methyl]amino}benzenesulfonamide |
|
113
|
447
|
1koaA |
Twitchin kinase fragment (c.elegans), autoregulated protein kinase and immunoglobulin domains |
|
76
|
298
|
1jsvA |
The structure of cyclin-dependent kinase 2 (cdk2) in complex with 4-[(6-amino-4-pyrimidinyl)amino]benzenesulfonamide |
|
91
|
293
|
1ig1A |
1.8a x-ray structure of ternary complex of a catalytic domain of death-associated protein kinase with atp analogue and mn. |
|
87
|
336
|
1jwhA |
Crystal structure of human protein kinase ck2 holoenzyme |
|
90
|
303
|
1jqhA |
Igf-1 receptor kinase domain |
|
80
|
298
|
1jvpP |
Crystal structure of human cdk2 (unphosphorylated) in complex with pkf049-365 |
|
85
|
299
|
1jpaA |
Crystal structure of unphosphorylated ephb2 receptor tyrosine kinase and juxtamembrane region |
|
89
|
299
|
1k3aA |
Structure of the insulin-like growth factor 1 receptor kinase |
