|
89
|
299
|
1k3aA |
Structure of the insulin-like growth factor 1 receptor kinase |
|
81
|
286
|
1jsuA |
P27(kip1)/cyclin a/cdk2 complex |
|
82
|
298
|
1i44A |
Crystallographic studies of an activation loop mutant of the insulin receptor tyrosine kinase |
|
109
|
362
|
1howA |
The x-ray crystal structure of sky1p, an sr protein kinase in yeast |
|
80
|
275
|
1ia8A |
The 1.7 a crystal structure of human cell cycle checkpoint kinase chk1 |
|
100
|
330
|
1iasA |
Cytoplasmic domain of unphosphorylated type i tgf-beta receptor crystallized without fkbp12 |
|
86
|
274
|
1iepA |
Crystal structure of the c-abl kinase domain in complex with sti-571. |
|
89
|
360
|
1i09A |
Structure of glycogen synthase kinase-3 (gsk3b) |
|
85
|
298
|
1hckA |
Human cyclin-dependent kinase 2 |
|
74
|
286
|
1h4lA |
Structure and regulation of the cdk5-p25(nck5a) complex |
|
77
|
298
|
1hclA |
Human cyclin-dependent kinase 2 |
|
82
|
296
|
1gy3A |
Pcdk2/cyclin a in complex with mgadp, nitrate and peptide substrate |
|
87
|
297
|
1h1rA |
Structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6086 |
|
84
|
297
|
1h1pA |
Structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu2058 |
|
81
|
298
|
1h0vA |
Human cyclin dependent protein kinase 2 in complex with the inhibitor 2-amino-6-[(r)-pyrrolidino-5'-yl]methoxypurine |
|
72
|
296
|
1gzkA |
Molecular mechanism for the regulation of protein kinase b/akt by hydrophobic motif phosphorylation |
|
82
|
296
|
1h07A |
Cdk2 in complex with a disubstituted 4, 6-bis anilino pyrimidine cdk4 inhibitor |
|
110
|
357
|
1golA |
Coordinates of rat map kinase erk2 with an arginine mutation at position 52 |
|
78
|
297
|
1h1qA |
Structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6094 |
|
80
|
298
|
1h0wA |
Human cyclin dependent protein kinase 2 in complex with the inhibitor 2-amino-6-[cyclohex-3-enyl]methoxypurine |
|
69
|
296
|
1gznA |
Structure of pkb kinase domain |
|
100
|
349
|
1gngA |
Glycogen synthase kinase-3 beta (gsk3) complex with frattide peptide |
|
82
|
294
|
1h25A |
Cdk2/cyclin a in complex with an 11-residue recruitment peptide from retinoblastoma-associated protein |
|
85
|
297
|
1h26A |
Cdk2/cyclina in complex with an 11-residue recruitment peptide from p53 |
|
88
|
297
|
1h1sA |
Structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6102 |
|
78
|
296
|
1h01A |
Cdk2 in complex with a disubstituted 2, 4-bis anilino pyrimidine cdk4 inhibitor |
|
103
|
352
|
1h8fA |
Glycogen synthase kinase 3 beta. |
|
72
|
297
|
1h28A |
Cdk2/cyclina in complex with an 11-residue recruitment peptide from p107 |
|
81
|
298
|
1h00A |
Cdk2 in complex with a disubstituted 4, 6-bis anilino pyrimidine cdk4 inhibitor |
|
68
|
296
|
1gzoA |
Structure of protein kinase b unphosphorylated |
|
79
|
294
|
1h24A |
Cdk2/cyclina in complex with a 9 residue recruitment peptide from e2f |
|
75
|
298
|
1h08A |
Cdk2 in complex with a disubstituted 2, 4-bis anilino pyrimidine cdk4 inhibitor |
|
82
|
298
|
1gz8A |
Human cyclin dependent kinase 2 complexed with the inhibitor 2-amino-6-(3'-methyl-2'-oxo)butoxypurine |
|
81
|
297
|
1h27A |
Cdk2/cyclina in complex with an 11-residue recruitment peptide from p27 |
|
79
|
289
|
1h1wA |
High resolution crystal structure of the human pdk1 catalytic domain |
|
83
|
298
|
1gjoA |
The fgfr2 tyrosine kinase domain |
|
82
|
298
|
1giiA |
Human cyclin dependent kinase 2 complexed with the cdk4 inhibitor |
|
68
|
258
|
1k2pA |
Crystal structure of bruton's tyrosine kinase domain |
|
87
|
303
|
1gagA |
Crystal structure of the insulin receptor kinase in complex with a bisubstrate inhibitor |
|
77
|
298
|
1gihA |
Human cyclin dependent kinase 2 complexed with the cdk4 inhibitor |
|
77
|
298
|
1gijA |
Human cyclin dependent kinase 2 complexed with the cdk4 inhibitor |
|
73
|
298
|
1g5sA |
Crystal structure of human cyclin dependent kinase 2 (cdk2) in complex with the inhibitor h717 |
|
82
|
298
|
1fvvA |
The structure of cdk2/cyclin a in complex with an oxindole inhibitor |
|
132
|
452
|
1fmkA |
Crystal structure of human tyrosine-protein kinase c-src |
|
65
|
296
|
1fq1B |
Crystal structure of kinase associated phosphatase (kap) in complex with phospho-cdk2 |
|
97
|
356
|
1jnkA |
The c-jun n-terminal kinase (jnk3s) complexed with mgamp-pnp |
|
108
|
338
|
1fmoE |
Crystal structure of a polyhistidine-tagged recombinant catalytic subunit of camp-dependent protein kinase complexed with the peptide inhibitor pki(5-24) and adenosine |
|
98
|
309
|
1fvrA |
Tie2 kinase domain |
|
87
|
316
|
1fotA |
Structure of the unliganded camp-dependent protein kinase catalytic subunit from saccharomyces cerevisiae |
|
63
|
291
|
1jowB |
Crystal structure of a complex of human cdk6 and a viral cyclin |
