|
266
|
743
|
3rj0A |
Plant steroid receptor bri1 ectodomain in complex with brassinolide |
|
263
|
743
|
3rizA |
Crystal structure of the plant steroid receptor bri1 ectodomain |
|
82
|
267
|
3uo5A |
Aurora a in complex with yl1-038-31 |
|
265
|
745
|
3rgzA |
Structural insight into brassinosteroid perception by bri1 |
|
76
|
263
|
3uojA |
Aurora a in complex with rpm1715 |
|
255
|
742
|
3rgxA |
Structural insight into brassinosteroid perception by bri1 |
|
343
|
2533
|
5zcsA |
4.9 angstrom cryo-em structure of human mtor complex 2 |
|
3
|
29
|
6g5iz |
Cryo-em structure of a late human pre-40s ribosomal subunit - state r |
|
309
|
1052
|
5xgiA |
Crystal structure of pi3k complex with an inhibitor |
|
295
|
1048
|
5xghA |
Crystal structure of pi3k complex with an inhibitor |
|
292
|
1048
|
5xgjA |
Crystal structure of pi3k complex with an inhibitor |
|
298
|
1079
|
5swoA |
Crystal structure of pi3kalpha in complex with fragments 4 and 19 |
|
85
|
271
|
5vjaA |
Crystal structure of human zipper-interacting protein kinase (zipk, alias dapk3) in complex with a pyrazolo[3,4-d]pyrimidinone ligand (hs38) |
|
89
|
290
|
5ng3A |
Structure of inactive kinase rip2k(k47r) |
|
89
|
289
|
5ng3B |
Structure of inactive kinase rip2k(k47r) |
|
84
|
294
|
5ng2A |
Structure of rip2k(d146n) with bound staurosporine |
|
81
|
276
|
5u94A |
Crystal structure of the mycobacterium tuberculosis pasta kinase pknb in complex with the potential theraputic kinase inhibitor gsk690693. |
|
101
|
491
|
5nclA |
Crystal structure of the cbk1-mob2 kinase-coactivator complex with an ssd1 peptide |
|
82
|
273
|
5ndtA |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule (e)-3-(2-(thiophen-2-yl)vinyl)-3,4-dihydroquinoxalin-2(1h)-one |
|
80
|
273
|
5n4rA |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule 2-(azepan-1-yl)-1-(1h-indol-3-yl)propan-1-one |
|
82
|
273
|
5n4vA |
Crystal structure of human pim-1 kinase in complex with a consensuspeptide and fragment like molekule 2-cyclopropyl-4,5-dimethylthieno[5,4-d]pyrimidine-6-carboxylic acid |
|
110
|
329
|
5n9nA |
Crystal structure of human protein kinase ck2 catalytic subunit in complex with the atp-competitive, tight-binding dibenzofuran inhibitor tf85 (4a) |
|
78
|
273
|
5n4yA |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule 2,5-dihydro-1h-isothiochromeno[3,4-d]pyrazol-3-one |
|
111
|
331
|
5n1vA |
Crystal structure of the protein kinase ck2 catalytic subunit in complex with pyrazolo-pyrimidine macrocyclic ligand |
|
110
|
329
|
5n9lA |
Crystal structure of human protein kinase ck2 catalytic subunit in complex with the atp-competitive dibenzofuran inhibitor tf (4b) |
|
81
|
273
|
5n50A |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule 2-(4-chlorophenyl)sulfanylacetohydrazide |
|
82
|
273
|
5n51A |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule 3,4-dibromothiophene-2-carboxylic acid |
|
121
|
375
|
5my8A |
Crystal structure of srpk1 in complex with sphinx31 |
|
81
|
284
|
5mrdA |
Human pdk1-pkciota kinase chimera in complex with allosteric compound ps267 bound to the pif-pocket |
|
88
|
483
|
5n8yA |
Kaicba circadian clock backbone model based on a cryo-em density |
|
125
|
383
|
5mxxA |
Crystal structure of human sr protein kinase 1 (srpk1) in complex with compound 1 |
|
79
|
273
|
5n5mA |
Crystal structure of human pim-1 kinase in complex with a consensuspeptide and (r)-3-(2-((isoquinolin-5-ylmethyl)(methyl)carbamoyl)phenyl)pyrrolidin-1-ium |
|
78
|
273
|
5mzlA |
Crystal structure of human pim-1 kinase in complex with a consensuspeptide and fragment like molekule n-quinolin-5-ylpyridine-3-carboxamide |
|
1
|
12
|
5mycP |
Crystal structure of human 14-3-3 sigma in complex with lrrk2 peptide ps910 |
|
34
|
90
|
5ncmB |
Crystal structure cbk1(ntr)-mob2 complex |
|
82
|
272
|
5n4uA |
Crystal structure of human pim-1 kinase in complex with a consensuspeptide and fragment like molekule 5-(2-amino-1,3-thiazol-4-yl)-1,3-dihydrobenzimidazol-2-one |
|
82
|
273
|
5n52A |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule (e)-3-(2,3-dimethoxyphenyl)acrylic acid |
|
66
|
218
|
5n6rA |
Solution structure of the dbl-homology domain of bcr-abl |
|
82
|
273
|
5n4nA |
Crystal structure of human pim-1 kinase in complex with a consensus peptide and fragment like molecule 3,4-dimethyl-5-(1h-1,2,4-triazol-3-yl)thiophene-2-carbonitrile |
|
108
|
370
|
5myvA |
Crystal structure of srpk2 in complex with compound 1 |
|
30
|
76
|
5ncnB |
Crystal structure dbf2(ntr)-mob1 complex |
|
116
|
331
|
5m56A |
Monoclinic complex structure of human protein kinase ck2 catalytic subunit (isoform ck2alpha') with the inhibitor 4'-carboxy-6,8-chloro-flavonol (flc21) |
|
104
|
327
|
5mo7A |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
57
|
137
|
5mg2A |
Crystal structure of the second bromodomain of human taf1 in complex with bay-299 chemical probe |
|
111
|
332
|
5m5aA |
Crystal structure of melk in complex with an inhibitor |
|
110
|
327
|
5modA |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
|
115
|
332
|
5mahA |
Crystal structure of melk in complex with an inhibitor |
|
113
|
332
|
5m4uA |
Orthorhombic complex structure of human protein kinase ck2 catalytic subunit (isoform ck2alpha') with the inhibitor 4'-carboxy-6,8-chloro- flavonol (flc21) |
|
103
|
326
|
5mpjA |
1-(2-chloro-[1,1'-biphenyl]-4-yl)-n-methylethanamine |
|
111
|
325
|
5mo8A |
Crystal structure of ck2alpha with n-(3-(((2-chloro-[1,1'-biphenyl]-4-yl)methyl)amino)propyl)methanesulfonamide bound |
