|
52
|
206
|
5z9nA |
S.aureus gyrb atpase domain in complex with 4,6-dichloro-2-(methylthio)pyrimidine |
|
61
|
203
|
5z4oA |
Bacterial gyrb atpase domain in complex with a chemical fragment |
|
59
|
204
|
5z9lA |
Bacterial gyrb atpase domain in complex with a chemical fragment |
|
58
|
203
|
5z9fA |
Bacterial gyrb atpase domain in complex with a chemical fragment |
|
54
|
203
|
5z9qA |
Bacterial gyrb atpase domain in complex with a chemical fragment |
|
67
|
210
|
6cygA |
Hsp90-alpha n-domain bound to neoca |
|
115
|
385
|
6enhA |
Crystal structure of the 43k atpase domain of thermus thermophilus gyrase b in complex with an aminocoumarin |
|
60
|
225
|
6dk8A |
Rets kinase region without cobalt |
|
124
|
381
|
6engA |
Crystal structure of the 43k atpase domain of escherichia coli gyrase b in complex with an aminocoumarin |
|
65
|
226
|
6dk7A |
Rets histidine kinase region with cobalt |
|
66
|
210
|
6cyhA |
Hsp90-alpha n-domain bound to neaca |
|
68
|
265
|
6cyiA |
Grp94 n-domain bound to neoca |
|
66
|
208
|
5j20A |
Hsp90 in complex with 5-[4-(2-fluoro-phenyl)-5-oxo-4,5-dihydro-1h-[1,2,4]triazol-3-yl]-n-furan-2-ylmethyl-2,4-dihydroxy-n-methyl-benzamide |
|
68
|
207
|
4cwpA |
Human hsp90 alpha n-terminal domain in complex with an aminotriazoloquinazoline inhibitor |
|
70
|
219
|
3u67A |
Crystal structure of the n-terminal domain of hsp90 from leishmania major(lmjf33.0312)in complex with adp |
|
68
|
209
|
3tuhA |
Crystal structure of the n-terminal domain of an hsp90 in the presence of an the inhibitor ganetespib |
|
26
|
320
|
3ur1A |
The structure of a ternary complex between chea domains p4 and p5 with chew and with a truncated fragment of tm14, a chemoreceptor analog from thermotoga maritima. |
|
65
|
210
|
6b99A |
Hsp90-alpha n-domain bound to neca |
|
121
|
361
|
5m4kA |
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase |
|
66
|
213
|
5mmoA |
E. coli dna gyrase b 24 kda atpase domain in complex with [3-(3-ethyl-ureido)-5-(pyridin-4-yl)-isoquinolin-8-yl-methyl]-carbamic acid prop-2-ynyl ester |
|
122
|
361
|
5m4pA |
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase |
|
64
|
213
|
5mmnA |
E. coli dna gyrase b 24 kda atpase domain in complex with 1-ethyl-3-[8-methyl-5-(2-methyl-pyridin-4-yl)-isoquinolin-3-yl]-urea |
|
59
|
210
|
5mmpA |
E. coli dna gyrase b 24 kda atpase domain in complex with 1-ethyl-3-[5-pyridin-4-yl-8-(pyridin-3-ylamino)-isoquinolin-3-yl]-urea |
|
63
|
207
|
5lo6A |
Hsp90 with indazole derivative |
|
65
|
207
|
5lo0A |
Hsp90 with indazole derivative |
|
67
|
208
|
5lr1A |
Crystal structure of hsp90 in complex with a003498614a. |
|
122
|
361
|
5m4nA |
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase |
|
82
|
243
|
5lfkA |
Crystal structure of cpxahdc (hemiphosphorylated form) |
|
70
|
207
|
5lq9A |
Crystal structure of hsp90 in complex with sar200323. |
|
67
|
208
|
5lrlA |
Crystal structure of hsp90 in complex with a003492875 |
|
69
|
207
|
5lrzA |
Crystal structure of hsp90 in complex with a003643501 |
|
74
|
240
|
5lfkB |
Crystal structure of cpxahdc (hemiphosphorylated form) |
|
67
|
208
|
5m4hA |
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase |
|
67
|
207
|
5lnzA |
Hsp90 with indazole derivative |
|
67
|
207
|
5lr7A |
Crystal structure of hsp90 in complex with sar567530 |
|
69
|
207
|
5lnyA |
Hsp90 with indazole derivative |
|
66
|
208
|
5m4eA |
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase |
|
69
|
207
|
5lo5A |
Hsp90 with indole derivative |
|
122
|
361
|
5m4mA |
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase |
|
112
|
378
|
5l3jA |
Escherichia coli dna gyrase b in complex with benzothiazole-based inhibitor |
|
60
|
208
|
5j82A |
Crystal structure of hsp90-alpha n-domain in complex 5-[4-(2-fluoro-phenyl)-5-oxo-4,5-dihydro-1h-[1,2,4]triazol-3-yl]-2,4-dihydroxy-n-isopropyl-n-methyl-benzenesulfonamide |
|
66
|
208
|
5j8uA |
Crystal structure of hsp90-alpha n-domain l107a mutant in complex with 5-(2,4-dihydroxy-phenyl)-4-(2-fluoro-phenyl)-2,4-dihydro-[1,2,4]triazol-3-one |
|
66
|
208
|
5j9xA |
Hsp90 in complex with n-butyl-5-[4-(2-fluoro-phenyl)-5-oxo-4,5-dihydro-1h-[1,2,4]triazol-3-yl]-2,4-dihydroxy-n-methyl-benzamide |
|
124
|
381
|
5j71A |
Crystal structure of pyruvate dehydrogenase kinase isoform 2 in complex with inhibitor ps35 |
|
68
|
208
|
5j6lA |
Crystal structure of hsp90-alpha n-domain in complex with n-butyl-5-[4-(2-fluoro-phenyl)-5-oxo-4,5-dihydro-1h-[1,2,4]triazol-3-yl]-2,4-dihydroxy-n-methyl-benzamide |
|
69
|
209
|
5j2xA |
Crystal structure of hsp90-alpha n-domain in complex with 5-(5-bromo-2,4-dihydroxy-phenyl)-4-(2-fluoro-phenyl)-2,4-dihydro-[1,2,4]triazol-3-one |
|
64
|
208
|
5j64A |
Crystal structure of hsp90-alpha n-domain in complex with 5-(2,4-dihydroxy-phenyl)-4-(2-fluoro-phenyl)-2,4-dihydro-[1,2,4]triazol-3-one |
|
70
|
209
|
5j6nA |
Crystal structure of hsp90-alpha n-domain l107a mutant in complex with 5-[4-(2-fluoro-phenyl)-5-oxo-4,5-dihydro-1h-[1,2,4]triazol-3-yl]-2,4-dihydroxy-n-methyl-n-propyl-benzenesulfonamide |
|
131
|
363
|
5j6aA |
Crystal structure of pyruvate dehydrogenase kinase isoform 2 in complex with inhibitor ps46 |
|
67
|
227
|
5in9A |
Crystal structure of grp94 bound to methyl 3-chloro-2-(2-(1-((5-chlorofuran-2-yl)methyl)-1h-imidazol-2-yl)ethyl)-4,6-dihydroxybenzoate, an inhibitor based on the bnim and radamide scaffolds. |
