|
224
|
715
|
7y4gA |
Sit-bound btdpp4 |
|
68
|
219
|
7yhaA |
Crystal structure of imp-1 mbl in complex with (3-(4-(p-tolyl)-1h-1,2,3-triazol-1-yl)benzyl)phosphonic acid |
|
71
|
231
|
7yhdA |
Crystal structure of vim-2 mbl in complex with 3-(4-(4-(2-aminoethoxy)phenyl)-1h-1,2,3-triazol-1-yl)phthalic acid |
|
72
|
231
|
7yhbA |
Crystal structure of vim-2 mbl in complex with (2-(4-phenyl-1h-1,2,3-triazol-1-yl)benzyl)phosphonic acid |
|
68
|
219
|
7yh9A |
Crystal structure of imp-1 mbl in complex with 3-(4-benzyl-1h-1,2,3-triazol-1-yl)phthalic acid |
|
73
|
231
|
7yhcA |
Crystal structure of vim-2 mbl in complex with 3-(4-(3-aminophenyl)-1h-1,2,3-triazol-1-yl)phthalic acid |
|
18
|
99
|
8fuiA |
Hiv-1 wild type protease with grl-02519a, with n-(2,5-dimethylphenyl)-4-(pyridin-3-yl)pyrimidin-2-amine as p2-p3 group |
|
18
|
99
|
8fujA |
Hiv-1 wild type protease with grl-03419a, with n-(2,5-dimethylphenyl)-4-(pyridin-3-yl)pyrimidin-2-amine as p2-p3 group and 3,5-difluorophenylmethyl as the p1 group |
|
88
|
306
|
8dmdA |
Room temperature x-ray structure of sars-cov-2 main protease in complex with compound zz4461624291 |
|
60
|
319
|
8gmnA |
Crystal structure of human c1s in complex with inhibitor |
|
92
|
300
|
7t1dA |
Human sirt2 in complex with small molecule 359 |
|
28
|
99
|
8g45A |
Structure of hdac6 zinc-finger ubiquitin binding domain in complex with sgc-ubd253 chemical probe |
|
28
|
99
|
8g44A |
Structure of hdac6 zinc-finger ubiquitin binding domain in complex with 3-(3-(2-(benzylamino)-2-oxoethyl)-4-oxo-3,4-dihydroquinazolin-2-yl)propanoic acid |
|
28
|
99
|
8g43A |
Structure of hdac6 zinc-finger ubiquitin binding domain in complex with 3-(3-(2-(methylamino)-2-oxoethyl)-4-oxo-3,4-dihydroquinazolin-2-yl)propanoic acid |
|
40
|
218
|
8g25B |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 7.5 |
|
51
|
223
|
8g26A |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 8.5 |
|
24
|
103
|
8g26C |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 8.5 |
|
42
|
218
|
8g24B |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 5.5 |
|
24
|
103
|
8g24C |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 5.5 |
|
42
|
218
|
8g26B |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 8.5 |
|
55
|
223
|
8g25A |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 7.5 |
|
53
|
223
|
8g24A |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 5.5 |
|
25
|
103
|
8g25C |
Crystal structure of cathepsin-g and neutrophil elastase inhibited by s. aureus eaph2 at ph 7.5 |
|
139
|
356
|
8eqiA |
Crystal structure of danio rerio histone deacetylase 6 catalytic domain 2 complexed with cyclopeptide des4.2.0 |
|
81
|
244
|
8culA |
Xray ray crystal structure of oxa-24/40 in complex with cr167 |
|
89
|
311
|
8euaA |
Structure of sars-cov2 plpro bound to a covalent inhibitor |
|
82
|
244
|
8cumA |
X-ray crystal structure of oxa-24/40 in complex with sulfonamidoboronic acid 6d |
|
121
|
358
|
8cuqA |
X-ray crystal structure of adc-33 in complex with sulfonamidoboronic acid 6e |
|
120
|
358
|
8cupA |
X-ray crystal structure of adc-33 in complex with sulfonamidoboronic acid 6d |
|
84
|
244
|
8cuoA |
X-ray crystal structure of oxa-24/40 in complex with sulfonamidoboronic acid 6e |
|
18
|
99
|
8esxA |
Hiv protease in complex with benzoxaborolone analog of darunavir |
|
54
|
245
|
8f7uA |
Macrocyclic plasmin inhibitor |
|
18
|
99
|
8esyA |
D30n mutant hiv protease in complex with benzoxaborolone analog of darunavir |
|
107
|
287
|
7y8oA |
Structure of scired-r3-v4 from streptomyces clavuligerus in complex with 5-(3-fluorophenyl)-3,4-dihydro-2h-pyrrole |
|
69
|
229
|
7u8yA |
Trex1 structural studies capture small molecule inhibition and implicate novel dna dynamics |
|
88
|
265
|
8ebrA |
Xfel structure of mycobacterium tuberculosis beta lactamase microcrystals mixed with sulbactam for 30ms |
|
79
|
265
|
8ecfA |
Cryo structure of mycobacterium tuberculosis beta lactamase microcrystals mixed with sulbactam for 3 hours |
|
106
|
317
|
8e5nA |
Structure of arg1 complex with pyrrolidine-based non-boronic acid inhibitor 10 |
|
260
|
778
|
7rd2A |
Co-crystal structure of chaetomium glucosidase with compound 2 |
|
85
|
265
|
8ec4A |
Xfel structure of mycobacterium tuberculosis beta lactamase microcrystals mixed with sulbactam for 240ms |
|
18
|
99
|
8f0fA |
Hiv-1 wild type protease with grl-110-19a, a chloroacetamide derivative based on darunavir as p2' group |
|
266
|
778
|
8eudA |
Co-crystal structure of chaetomium glucosidase with compound 22 |
|
259
|
776
|
8eutA |
Co-crystal structure of chaetomium glucosidase with compound 27 |
|
265
|
776
|
8eidA |
Co-crystal structure of chaetomium glucosidase with compound 14 |
|
257
|
778
|
8eqxA |
Co-crystal structure of chaetomium glucosidase with compound 21 |
|
267
|
778
|
8etoA |
Co-crystal structure of chaetomium glucosidase with compound 25 |
|
259
|
778
|
8euxA |
Co-crystal structure of chaetomium glucosidase with compound 28 |
|
269
|
778
|
8eurA |
Co-crystal structure of chaetomium glucosidase with compound 26 |
|
264
|
778
|
8etlA |
Co-crystal structure of chaetomium glucosidase with compound 24 |
|
259
|
778
|
8ecwA |
Co-crystal structure of chaetomium glucosidase with compound 11 |
