|
132
|
452
|
1fmkA |
Crystal structure of human tyrosine-protein kinase c-src |
|
76
|
298
|
1fvtA |
The structure of cyclin-dependent kinase 2 (cdk2) in complex with an oxindole inhibitor |
|
83
|
293
|
1g3nA |
Structure of a p18(ink4c)-cdk6-k-cyclin ternary complex |
|
104
|
339
|
1jluE |
Crystal structure of the catalytic subunit of camp-dependent protein kinase complexed with a phosphorylated substrate peptide and detergent |
|
87
|
293
|
1jksA |
1.5a x-ray structure of apo form of a catalytic domain of death-associated protein kinase |
|
88
|
299
|
1fgkA |
Crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 |
|
86
|
292
|
1jkkA |
2.4a x-ray structure of ternary complex of a catalytic domain of death-associated protein kinase with atp analogue and mg. |
|
94
|
299
|
1fgiA |
Crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 in complex with su5402 inhibitor |
|
46
|
276
|
1jktA |
Tetragonal crystal form of a catalytic domain of death-associated protein kinase |
|
83
|
298
|
1finA |
Cyclin a-cyclin-dependent kinase 2 complex |
|
86
|
293
|
1jklA |
1.6a x-ray structure of binary complex of a catalytic domain of death-associated protein kinase with atp analogue |
|
110
|
357
|
1erkA |
Structure of signal-regulated kinase |
|
82
|
294
|
1f3mC |
Crystal structure of human serine/threonine kinase pak1 |
|
97
|
329
|
1f0qA |
Crystal structure of the alpha subunit of protein kinase ck2 in complex with the nucleotide competitive inhibitor emodin |
|
76
|
298
|
1f5qA |
Crystal structure of murine gamma herpesvirus cyclin complexed to human cyclin dependent kinase 2 |
|
79
|
293
|
1eh4A |
Binary complex of casein kinase-1 from s. pombe with an atp competitive inhibitor, ic261 |
|
83
|
296
|
1e9hA |
Thr 160 phosphorylated cdk2 - human cyclin a3 complex with the inhibitor indirubin-5-sulphonate bound |
|
99
|
328
|
1ds5A |
Dimeric crystal structure of the alpha subunit in complex with two beta peptides mimicking the architecture of the tetrameric protein kinase ck2 holoenzyme. |
|
113
|
342
|
1jbpE |
Crystal structure of the catalytic subunit of camp-dependent protein kinase complexed with a substrate peptide, adp and detergent |
|
103
|
327
|
1jamA |
Crystal structure of apo-form of z. mays ck2 protein kinase alpha subunit |
|
82
|
298
|
1e1xA |
Human cyclin dependent kinase 2 complexed with the inhibitor nu6027 |
|
108
|
327
|
1j91A |
Crystal structure of z. mays ck2 kinase alpha subunit in complex with the atp-competitive inhibitor 4,5,6,7-tetrabromobenzotriazole |
|
84
|
298
|
1e1vA |
Human cyclin dependent kinase 2 complexed with the inhibitor nu2058 |
|
107
|
327
|
1dayA |
Crystal structure of a binary complex of protein kinase ck2 (alpha-subunit) and mg-gmppnp |
|
111
|
327
|
1dawA |
Crystal structure of a binary complex of protein kinase ck2 (alpha-subunit) and mg-amppnp |
|
83
|
298
|
1di8A |
The structure of cyclin-dependent kinase 2 (cdk2) in complex with 4-[3-hydroxyanilino]-6,7-dimethoxyquinazoline |
|
104
|
348
|
1di9A |
The structure of p38 mitogen-activated protein kinase in complex with 4-[3-methylsulfanylanilino]-6,7-dimethoxyquinazoline |
|
81
|
298
|
1dm2A |
Human cyclin-dependent kinase 2 complexed with the inhibitor hymenialdisine |
|
88
|
342
|
1j3hA |
Crystal structure of apoenzyme camp-dependent protein kinase catalytic subunit |
|
93
|
296
|
1ckjA |
Casein kinase i delta truncation mutant containing residues 1-317 complex with bound tungstate |
|
92
|
354
|
1j1bA |
Binary complex structure of human tau protein kinase i with amppnp |
|
95
|
299
|
1ckiA |
Recombinant casein kinase i delta truncation mutant containing residues 1-317 |
|
105
|
350
|
1cmkE |
Crystal structures of the myristylated catalytic subunit of camp-dependent protein kinase reveal open and closed conformations |
|
92
|
354
|
1j1cA |
Binary complex structure of human tau protein kinase i with adp |
|
97
|
344
|
1ctpE |
Structure of the mammalian catalytic subunit of camp-dependent protein kinase and an inhibitor peptide displays an open conformation |
|
93
|
346
|
1cm8A |
Phosphorylated map kinase p38-gamma |
|
80
|
298
|
1ckpA |
Human cyclin dependent kinase 2 complexed with the inhibitor purvalanol b |
|
92
|
293
|
1csnA |
Binary complex of casein kinase-1 with mgatp |
|
75
|
294
|
1buhA |
Crystal structure of the human cdk2 kinase complex with cell cycle-regulatory protein ckshs1 |
|
76
|
262
|
1bygA |
Kinase domain of human c-terminal src kinase (csk) in complex with inhibitor staurosporine |
|
94
|
339
|
1bx6A |
Crystal structure of the potent natural product inhibitor balanol in complex with the catalytic subunit of camp-dependent protein kinase |
|
114
|
343
|
1cdkA |
Camp-dependent protein kinase catalytic subunit (e.c.2.7.1.37) (protein kinase a) complexed with protein kinase inhibitor peptide fragment 5-24 (pki(5-24) isoelectric variant ca) and mn2+ adenylyl imidodiphosphate (mnamp-pnp) at ph 5.6 and 7c and 4c |
|
93
|
303
|
1ir3A |
Phosphorylated insulin receptor tyrosine kinase in complex with peptide substrate and atp analog |
|
88
|
305
|
1blxA |
P19ink4d/cdk6 complex |
|
106
|
351
|
1bmkA |
The complex structure of the map kinase p38/sb218655 |
|
67
|
292
|
1bi7A |
Mechanism of g1 cyclin dependent kinase inhibition from the structure of the cdk6-p16ink4a tumor suppressor complex |
|
101
|
326
|
1b6cB |
Crystal structure of the cytoplasmic domain of the type i tgf-beta receptor in complex with fkbp12 |
|
68
|
291
|
1bi8A |
Mechanism of g1 cyclin dependent kinase inhibition from the structures cdk6-p19ink4d inhibitor complex |
|
82
|
298
|
1b38A |
Human cyclin-dependent kinase 2 |
|
88
|
339
|
1bkxA |
A binary complex of the catalytic subunit of camp-dependent protein kinase and adenosine further defines conformational flexibility |
