|
61
|
186
|
4z64C |
The plant peptide hormone receptor complex in arabidopsis |
|
30
|
297
|
4yzsA |
Crystal structures reveal transient perk luminal domain tetramerization in er stress signaling |
|
93
|
294
|
4yo4A |
Crystal structure of dapk1 catalytic domain in complex with the hinge binding fragment phthalazine |
|
54
|
130
|
4yynA |
Crystal structure of taf1 bd2 bromodomain bound to a crotonyllysine peptide |
|
57
|
185
|
4z61C |
The plant peptide hormone receptor complex |
|
279
|
951
|
4ezlA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
98
|
328
|
4umrA |
Structure of melk in complex with inhibitors |
|
97
|
333
|
4umpA |
Structure of melk in complex with inhibitors |
|
264
|
947
|
4hvbA |
Catalytic unit of pi3kg in complex with pi3k/mtor dual inhibitor pf-04979064 |
|
107
|
331
|
4umuA |
Structure of melk in complex with inhibitors |
|
247
|
759
|
4mn8A |
Crystal structure of flg22 in complex with the fls2 and bak1 ectodomains |
|
273
|
951
|
4ezjA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
216
|
740
|
4lsxA |
Plant steroid receptor ectodomain bound to brassinolide and serk1 co-receptor ectodomain |
|
267
|
949
|
4fa6A |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
242
|
743
|
4lsaA |
Crystal structure of bri1 sud1 (gly643glu) bound to brassinolide |
|
275
|
949
|
4ezkA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
265
|
945
|
4f1sA |
Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine-sulfonamide inhibitor |
|
253
|
950
|
4fadA |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
88
|
300
|
4tl0A |
Crystal structure of death-associated protein kinase 1 with a crucial phosphomimicking mutation |
|
80
|
276
|
4f0fA |
Crystal structure of the roco4 kinase domain bound to appcp from d. discoideum |
|
34
|
175
|
4m7eC |
Structural insight into bl-induced activation of the bri1-bak1 complex |
|
93
|
308
|
4euuA |
Structure of bx-795 complexed with human tbk1 kinase domain phosphorylated on ser172 |
|
108
|
386
|
4eutA |
Structure of bx-795 complexed with unphosphorylated human tbk1 kinase-uld domain |
|
75
|
276
|
4f1oA |
Crystal structure of the l1180t mutant roco4 kinase domain from d. discoideum bound to appcp |
|
97
|
290
|
4qmqA |
Mst3 in complex with cp-673451 |
|
71
|
274
|
4pp7A |
Highly potent and selective 3-n-methylquinazoline-4(3h)-one based inhibitors of b-rafv600e kinase |
|
102
|
354
|
4f9cA |
Human cdc7 kinase in complex with dbf4 and xl413 |
|
81
|
277
|
4f0gA |
Crystal structure of the roco4 kinase domain from d. discoideum |
|
78
|
275
|
4ewhA |
Co-crystal structure of ack1 with inhibitor |
|
195
|
639
|
4mnaA |
Crystal structure of the free fls2 ectodomains |
|
38
|
94
|
4fapB |
Atomic structures of the rapamycin analogs in complex with both human fkbp12 and frb domain of frap |
|
77
|
278
|
4f1mA |
Crystal structure of the g1179s roco4 kinase domain bound to appcp from d. discoideum. |
|
87
|
284
|
4qmnA |
Mst3 in complex with bosutinib |
|
100
|
356
|
4f9bA |
Human cdc7 kinase in complex with dbf4 and pha767491 |
|
68
|
276
|
4f1tA |
Crystal structure of the roco4 kinase domain from d. discoideum bound to the rock inhibitor h1152 |
|
214
|
733
|
4m7eA |
Structural insight into bl-induced activation of the bri1-bak1 complex |
|
42
|
175
|
4mn8B |
Crystal structure of flg22 in complex with the fls2 and bak1 ectodomains |
|
100
|
356
|
4f9aA |
Human cdc7 kinase in complex with dbf4 and nucleotide |
|
17
|
61
|
4f2lA |
Structure of a regulatory domain of ampk |
|
246
|
727
|
4j0mA |
Crystal structure of brl1 (lrr) in complex with brassinolide |
|
46
|
185
|
4lsxC |
Plant steroid receptor ectodomain bound to brassinolide and serk1 co-receptor ectodomain |
|
96
|
354
|
4f99A |
Human cdc7 kinase in complex with dbf4 and nucleotide |
|
256
|
945
|
4dk5A |
Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine inhibitor |
|
106
|
435
|
4ejnA |
Crystal structure of autoinhibited form of akt1 in complex with n-(4-(5-(3-acetamidophenyl)-2-(2-aminopyridin-3-yl)-3h-imidazo[4,5-b]pyridin-3-yl)benzyl)-3-fluorobenzamide |
|
23
|
100
|
4eaiA |
Co-crystal structure of an ampk core with amp |
|
135
|
500
|
4dugD |
Crystal structure of circadian clock protein kaic e318a mutant |
|
39
|
95
|
4drhB |
Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor at low ph |
|
52
|
194
|
4esqA |
Crystal structure of the extracellular domain of pknh from mycobacterium tuberculosis |
|
38
|
96
|
4driB |
Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor |
|
81
|
269
|
4enyA |
Crystal structure of pim-1 kinase in complex with (2e,5z)-2-(2-chlorophenylimino)-5-(4-hydroxy-3-methoxybenzylidene)thiazolidin-4-one |
