|
8
|
54
|
2cosA |
Solution structure of rsgi ruh-038, a uba domain from mouse lats2 (large tumor suppressor homolog 2) |
|
86
|
292
|
2cdzA |
Crystal structure of the human p21-activated kinase 4 in complex with cgp74514a |
|
88
|
293
|
2csnA |
Binary complex of casein kinase-1 with cki7 |
|
94
|
296
|
2cmwA |
Structure of human casein kinase 1 gamma-1 in complex with 2-(2- hydroxyethylamino)-6-(3-chloroanilino)-9-isopropylpurine |
|
75
|
268
|
2cgxA |
Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening |
|
14
|
115
|
2cr6A |
Solution structure of the ig domain (2998-3100) of human obscurin |
|
91
|
301
|
2ckeA |
Human death-associated drp-1 kinase in complex with inhibitor |
|
78
|
272
|
2c3lA |
Identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification |
|
84
|
297
|
2cn5A |
Crystal structure of human chk2 in complex with adp |
|
77
|
267
|
2cgvA |
Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening |
|
76
|
263
|
2c6eA |
Aurora a kinase activated mutant (t287d) in complex with a 5- aminopyrimidinyl quinazoline inhibitor |
|
100
|
298
|
2chlA |
Structure of casein kinase 1 gamma 3 |
|
84
|
269
|
2c3iB |
Crystal structure of human pim1 in complex with imidazopyridazin i |
|
78
|
266
|
2cgwA |
Identification of chemically diverse chk1 inhibitors by receptor- based virtual screening |
|
78
|
264
|
2c6dA |
Aurora a kinase activated mutant (t287d) in complex with adpnp |
|
92
|
290
|
2c30A |
Crystal structure of the human p21-activated kinase 6 |
|
84
|
273
|
2bziB |
Crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru2 |
|
78
|
265
|
2c3jA |
Identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification |
|
83
|
275
|
2bzhB |
Crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru1 |
|
95
|
295
|
2c47A |
Structure of casein kinase 1 gamma 2 |
|
73
|
265
|
2c3kA |
Identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification |
|
78
|
275
|
2brbA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
76
|
275
|
2broA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
80
|
275
|
2br1A |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
82
|
273
|
2bzkB |
Crystal structure of the human pim1 in complex with amppnp and pimtide |
|
74
|
263
|
2brgA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
84
|
273
|
2bzjA |
Crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru3 |
|
61
|
288
|
2bvaA |
Crystal structure of the human p21-activated kinase 4 |
|
82
|
287
|
2biyA |
Structure of pdk1-s241a mutant kinase domain |
|
87
|
273
|
2bikB |
Human pim1 phosphorylated on ser261 |
|
87
|
295
|
2bujA |
Crystal structure of the human serine-threonine kinase 16 in complex with staurosporine |
|
24
|
97
|
2bk8A |
M1 domain from titin |
|
73
|
268
|
2brmA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
76
|
268
|
2bmcA |
Aurora-2 t287d t288d complexed with pha-680632 |
|
87
|
271
|
2bfyA |
Complex of aurora-b with incenp and hesperadin. |
|
75
|
271
|
2brnA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
79
|
266
|
2brhA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
81
|
274
|
2bilB |
The human protein kinase pim1 in complex with its consensus peptide pimtide |
|
88
|
270
|
2bfxA |
Mechanism of aurora-b activation by incenp and inhibition by hesperadin. |
|
76
|
268
|
2aypA |
Crystal structure of chk1 with an indol inhibitor |
|
61
|
339
|
2be1A |
Structure of the compact lumenal domain of yeast ire1 |
|
252
|
949
|
2a5uA |
Crystal structure of human pi3kgamma complexed with as605240 |
|
34
|
105
|
2a9iA |
Molecular structure of the interleukin-1 receptor-associated kinase-4 death domain |
|
222
|
944
|
2a4zA |
Crystal structure of human pi3kgamma complexed with as604850 |
|
75
|
301
|
2ac5A |
Structure of human mnk2 kinase domain mutant d228g |
|
107
|
325
|
1zogA |
Crystal structure of protein kinase ck2 in complex with tbb-derivatives |
|
14
|
54
|
1zl8B |
Nmr structure of l27 heterodimer from c. elegans lin-7 and h. sapiens lin-2 scaffold proteins |
|
0
|
22
|
1zsgB |
Beta pix-sh3 complexed with an atypical peptide from alpha-pak |
|
103
|
325
|
1zoeA |
Crystal structure of protein kinase ck2 in complex with tbb-derivatives inhibitors |
|
92
|
280
|
1zarA |
Crystal structure of a.fulgidus rio2 kinase complexed with adp and manganese ions |
