|
90
|
269
|
2yexA |
Synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors |
|
66
|
272
|
2y4pA |
Dimeric structure of dapk-1 catalytic domain |
|
120
|
350
|
2y9qA |
Crystal structure of human erk2 complexed with a mapk docking peptide |
|
106
|
309
|
2xzsA |
Death associated protein kinase 1 residues 1-312 |
|
102
|
360
|
2xs0A |
Linear binding motifs for jnk and for calcineurin antagonistically control the nuclear shuttling of nfat4 |
|
108
|
350
|
2y8oA |
Crystal structure of human p38alpha complexed with a mapk docking peptide |
|
95
|
300
|
2y0aA |
Structure of dapk1 construct residues 1-304 |
|
84
|
282
|
2xvdA |
Ephb4 kinase domain inhibitor complex |
|
88
|
277
|
2yakA |
Structure of death-associated protein kinase 1 (dapk1) in complex with a ruthenium octasporine ligand (osv) |
|
56
|
279
|
2y4iB |
Ksr2-mek1 heterodimer |
|
95
|
301
|
2xuuA |
Crystal structure of a dap-kinase 1 mutant |
|
92
|
299
|
2yabA |
Crystal structure of the autoinhibited form of mouse dapk2 in complex with amp |
|
98
|
300
|
2yaaA |
Crystal structure of the autoinhibited form of mouse dapk2 in complex with atp |
|
78
|
266
|
2xynA |
Human abl2 in complex with aurora kinase inhibitor vx-680 |
|
83
|
283
|
2y6oA |
Crystal structure of epha4 kinase domain in complex with dasatinib. |
|
84
|
290
|
2yacA |
Crystal structure of polo-like kinase 1 in complex with nms-p937 |
|
79
|
345
|
2y4iC |
Ksr2-mek1 heterodimer |
|
80
|
280
|
2xyuA |
Crystal structure of epha4 kinase domain in complex with vuf 12058 |
|
98
|
299
|
2ya9A |
Crystal structure of the autoinhibited form of mouse dapk2 |
|
83
|
283
|
2y6mA |
Crystal structure of epha4 kinase domain |
|
93
|
284
|
2y7jA |
Structure of human phosphorylase kinase, gamma 2 |
|
82
|
274
|
2xiyA |
Protein kinase pim-1 in complex with fragment-2 from crystallographic fragment screen |
|
69
|
263
|
2xruA |
Aurora-a t288e complexed with pha-828300 |
|
79
|
277
|
2xnoA |
Structure of nek2 bound to cct243779 |
|
78
|
277
|
2xkdA |
Structure of nek2 bound to aminopyrazine compound 12 |
|
68
|
274
|
2xj0A |
Protein kinase pim-1 in complex with fragment-4 from crystallographic fragment screen |
|
69
|
264
|
2xeyA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
82
|
300
|
2xk9A |
Structural analysis of checkpoint kinase 2 (chk2) in complex with inhibitor pv1533 |
|
78
|
277
|
2xkcA |
Structure of nek2 bound to aminopyrazine compound 14 |
|
92
|
290
|
2xikA |
Structure of human ysk1 (yeast sps1-ste20-related kinase 1) |
|
82
|
277
|
2xnmA |
Structure of nek2 bound to cct |
|
58
|
293
|
2xm8A |
Co-crystal structure of a small molecule inhibitor bound to the kinase domain of chk2 |
|
96
|
307
|
2xbaA |
Structure of human anaplastic lymphoma kinase in complex with pha- e429 |
|
79
|
277
|
2xnpA |
Structure of nek2 bound to cct244858 |
|
90
|
302
|
2xm9A |
Structure of a small molecule inhibitor with the kinase domain of chk2 |
|
81
|
274
|
2xj2A |
Protein kinase pim-1 in complex with small molecule inhibitor |
|
73
|
277
|
2xk4A |
Structure of nek2 bound to aminopyrazine compound 17 |
|
83
|
274
|
2xj1A |
Protein kinase pim-1 in complex with small molecule inibitor |
|
74
|
264
|
2xezA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
73
|
277
|
2xk3A |
Structure of nek2 bound to aminopyrazine compound 35 |
|
75
|
277
|
2xk7A |
Structure of nek2 bound to aminopyrazine compound 23 |
|
128
|
435
|
2xarA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with ip6. |
|
79
|
277
|
2xk8A |
Structure of nek2 bound to aminopyrazine compound 15 |
|
79
|
277
|
2xkfA |
Structure of nek2 bound to aminopyrazine compound 2 |
|
116
|
365
|
2xrwA |
Linear binding motifs for jnk and for calcineurin antagonistically control the nuclear shuttling of nfat4 |
|
141
|
435
|
2xanA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with amp pnp and ip5 |
|
75
|
262
|
2xneA |
Structure of aurora-a bound to an imidazopyrazine inhibitor |
|
75
|
298
|
2xnbA |
Discovery and characterisation of 2-anilino-4-(thiazol-5-yl) pyrimidine transcriptional cdk inhibitors as anticancer agents |
|
100
|
303
|
2xirA |
Crystal structure of the vegfr2 kinase domain in complex with pf- 00337210 (n,2-dimethyl-6-(7-(2-morpholinoethoxy)quinolin-4-yloxy) benzofuran-3-carboxamide) |
|
68
|
267
|
2xf0A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
