|
138
|
488
|
3k09C |
Crystal structure of the phosphorylation-site mutant s431d of the kaic circadian clock protein |
|
130
|
506
|
3k0cA |
Crystal structure of the phosphorylation-site double mutant s431a/t432e of the kaic circadian clock protein |
|
83
|
269
|
3k5uA |
Identification, sar studies and x-ray cocrystal analysis of a novel furano-pyrimidine aurora kinase a inhibitor |
|
133
|
491
|
3k0aB |
Crystal structure of the phosphorylation-site mutant s431a of the kaic circadian clock protein |
|
73
|
178
|
3k21A |
Crystal structure of carboxy-terminus of pfc0420w. |
|
81
|
274
|
3jyaA |
Discovery of 3h-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as potent, highly selective and orally bioavailable pim kinases inhibitors |
|
114
|
334
|
3juhA |
Crystal structure of a mutant of human protein kinase ck2alpha with altered cosubstrate specificity |
|
82
|
273
|
3jpvA |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a pyrrolo[2,3-a]carbazole ligand |
|
81
|
271
|
3jvrA |
Characterization of the chk1 allosteric inhibitor binding site |
|
237
|
950
|
3ibeA |
Crystal structure of a pyrazolopyrimidine inhibitor bound to pi3 kinase gamma |
|
80
|
285
|
3iopA |
Pdk-1 in complex with the inhibitor compound-8i |
|
59
|
171
|
3ixeA |
Structural basis of competition between pinch1 and pinch2 for binding to the ankyrin repeat domain of integrin-linked kinase |
|
113
|
328
|
3iq7A |
Crystal structure of human haspin in complex with 5-iodotubercidin |
|
306
|
1084
|
3hhmA |
Crystal structure of p110alpha h1047r mutant in complex with nish2 of p85alpha and the drug wortmannin |
|
81
|
285
|
3ionA |
Pdk1 in complex with compound 8h |
|
72
|
272
|
3idpA |
B-raf v600e kinase domain in complex with an aminoisoquinoline inhibitor |
|
281
|
1089
|
3hizA |
Crystal structure of p110alpha h1047r mutant in complex with nish2 of p85alpha |
|
101
|
315
|
3iecA |
Helicobacter pylori caga inhibits par1/mark family kinases by mimicking host substrates |
|
75
|
273
|
3ii5A |
The complex of wild-type b-raf with pyrazolo pyrimidine inhibitor |
|
71
|
262
|
3hyhA |
Crystal structure of the protein kinase domain of yeast amp-activated protein kinase snf1 |
|
84
|
284
|
3hrcA |
Crystal structure of a mutant of human pdk1 kinase domain in complex with atp |
|
103
|
410
|
3i6wA |
Structure and activation mechanism of the chk2 dna-damage checkpoint kinase |
|
86
|
285
|
3hrfA |
Crystal structure of human pdk1 kinase domain in complex with an allosteric activator bound to the pif-pocket |
|
106
|
361
|
3i4bA |
Crystal structure of gsk3b in complex with a pyrimidylpyrrole inhibitor |
|
107
|
413
|
3i6uA |
Structure and activation mechanism of the chk2 dna-damage checkpoint kinase |
|
80
|
293
|
3hdnA |
Crystal structure of serum and glucocorticoid-regulated kinase 1 in complex with compound 2 |
|
108
|
333
|
3h30A |
Crystal structure of the catalytic subunit of human protein kinase ck2 with 5,6-dichloro-1-beta-d-ribofuranosylbenzimidazole |
|
80
|
285
|
3h9oA |
Phosphoinositide-dependent protein kinase 1 (pdk-1) in complex with compound 9 |
|
74
|
263
|
3h0yA |
Aurora a in complex with a bisanilinopyrimidine |
|
89
|
265
|
3ha6A |
Crystal structure of aurora a in complex with tpx2 and compound 10 |
|
84
|
268
|
3h10A |
Aurora a inhibitor complex |
|
77
|
327
|
3h4jA |
Crystal structure of pombe ampk kdaid fragment |
|
0
|
9
|
3h9hC |
Human class i mhc hla-a2(a150p) in complex with the tel1p peptide |
|
68
|
261
|
3h0zA |
Aurora a in complex with a bisanilinopyrimidine |
|
80
|
298
|
3hdmA |
Crystal structure of serum and glucocorticoid-regulated kinase 1 in complex with compound 1 |
|
75
|
284
|
3ggfA |
Crystal structure of human serine/threonine-protein kinase mst4 in complex with an quinazolin |
|
92
|
293
|
3gu7A |
Crystal structure of dapkq23v-adp-mg2+ |
|
97
|
424
|
3greA |
Crystal structure of saccharomyces cerevisiae vps15 wd repeat domain |
|
93
|
293
|
3gu6A |
Crystal structure of dapkq23v-adp |
|
75
|
305
|
3gokA |
Binding site mapping of protein ligands |
|
86
|
292
|
3gubA |
Crystal structure of dapkl93g complexed with n6-(2-phenylethyl)adenosine |
|
88
|
292
|
3gu8A |
Crystal structure of dapkl93g with n6-cyclopentyladenosine |
|
95
|
293
|
3gu5A |
Crystal structure of dapkq23v-amppnp-mg2+ |
|
91
|
293
|
3gu4A |
Crystal structure of dapkq23v-amppnp |
|
95
|
349
|
3gb2A |
Gsk3beta inhibitor complex |
|
88
|
317
|
3fxwA |
High resolution crystal structure of mitogen-activated protein kinase-activated protein kinase 3/inhibitor 2 complex |
|
106
|
334
|
3fwqA |
Inactive conformation of human protein kinase ck2 catalytic subunit |
|
67
|
320
|
3fykX |
Crystal structure of a benzthiophene lead bound to mapkap kinase-2 (mk-2) |
|
96
|
293
|
3fy0A |
Crystal structure of pak1 kinase domain with ruthenium complex dw1 |
|
73
|
302
|
3fpmA |
Crystal structure of a squarate inhibitor bound to mapkap kinase-2 |
