|
79
|
258
|
5tyaA |
Identification of a new zinc binding chemotype by fragment screening |
|
79
|
258
|
5ty9A |
Identification of a new zinc binding chemotype by fragment screening |
|
77
|
256
|
5txyA |
Identification of a new zinc binding chemotype of by fragment screening on human carbonic anhydrase |
|
80
|
258
|
5u0eA |
Identification of a new zinc binding chemotype by fragment screening |
|
80
|
258
|
5ty1A |
Identification of a new zinc binding chemotype by fragment screening |
|
51
|
227
|
5tuoA |
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor. |
|
76
|
257
|
5th4A |
Crystal structure of 1-hydroxypyridine-2(1h)-thione bound to human carbonic anhydrase 2 l198g |
|
77
|
257
|
5thnA |
Crystal structure of 2-hydroxycyclohepta-2,4,6-triene-1-thione bound to human carbonic anhydrase 2 |
|
76
|
257
|
5ti0A |
Crystal structure of 2-hydroxycyclohepta-2,4,6-triene-1-thione bound to human carbonic anhydrase 2 l198g |
|
75
|
258
|
5tfxA |
New method for synthesis of benzoxazole amide inhibitors of carbonic anhydrase |
|
38
|
226
|
5tv3A |
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with (e)-5-(((4-(tert-butyl)phenyl)sulfonyl)imino)-4-methyl-4,5-dihydro-1,3,4-thiadiazole-2-sulfonamide |
|
78
|
257
|
5thjA |
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2 |
|
79
|
257
|
5thiA |
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2 l198g |
|
79
|
257
|
5t72A |
Human carboanhydrase f131c_c206s double mutant in complex with 2 |
|
77
|
257
|
5t75A |
Human carbonic anhydrase ii g132c_c206s double mutant in complex with sa-2 |
|
78
|
257
|
5t71A |
Human carboanhydrase f131c_c206s double mutant in complex with sa-2 |
|
75
|
257
|
5t74A |
Human carboanhydrase f131c_c206s double mutant in complex with 14 |
|
81
|
257
|
5sz7A |
Carbonic anhydrase ix-mimic in complex with 4-(3-quinolinyl)-benzenesulfonamide |
|
76
|
257
|
5sz6A |
Carbonic anhydrase ix-mimic in complex with 4-(3-formylphenyl)-benzenesulfonamide |
|
78
|
257
|
5sz1A |
Carbonic anhydrase ii in complex with 4-(2-methylphenyl)-benzenesulfonamide |
|
72
|
223
|
5swcA |
The structure of the beta-carbonic anhydrase ccaa |
|
78
|
257
|
5sz0A |
Carbonic anhydrase ii in complex with 4-(phenyl)-benzenesulfonamide |
|
79
|
257
|
5sz3A |
Carbonic anhydrase ii in complex with 4-(3-quinolinyl)-benzenesulfonamide |
|
77
|
257
|
5sz2A |
Carbonic anhydrase ii in complex with 4-(3-formylphenyl)-benzenesulfonamide |
|
75
|
259
|
5ohhA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide |
|
79
|
259
|
5ognA |
Metalacarborane inhibitors of carbonic anhydrase ix |
|
82
|
259
|
5ogjA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide |
|
80
|
259
|
5ogpA |
Metalacarborane inhibitors of carbonic anhydrase ix |
|
79
|
258
|
5ogoA |
Crystal structure of chimeric carbonic anhydrase i with 3-(benzylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide |
|
77
|
258
|
5ny6A |
Carbonic anhydrase ii inhibitor ra12 |
|
78
|
258
|
5ny3A |
Carbonic anhydrase ii inhibitor ra11 |
|
75
|
258
|
5nxoA |
Carbonic anhydrase ii inhibitor ra6 |
|
76
|
259
|
5nxiA |
Carbonic anhydrase ii inhibitor ra2 |
|
78
|
257
|
5nyaA |
Carbonic anhydrase ii inhibitor ra13 |
|
76
|
257
|
5nxgA |
Carbonic anhydrase ii inhibitor ra1 |
|
78
|
258
|
5nxpA |
Carbonic anhydrase ii inhibitor ra7 |
|
77
|
257
|
5ny1A |
Carbonic anhydrase ii inhibitor ra10 |
|
78
|
257
|
5nxwA |
Carbonic anhydrase ii inhibitor ra9 |
|
79
|
258
|
5nxmA |
Carbonic anhydrase ii inhibitor ra1 |
|
75
|
256
|
5o07A |
The crystal structure of the human carbonic anhydrase ii in complex with a nitroimidazole sulfamate inhibitor |
|
77
|
258
|
5nxvA |
Carbonic anhydrase ii inhibitor ra8 |
|
79
|
258
|
5n1sA |
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(1h-indol-2-yl)-benzenesulfonamide |
|
73
|
258
|
5l6tA |
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer |
|
75
|
257
|
5lmdA |
The crystal structure of hca ii in complex with a benzoxaborole inhibitor |
|
69
|
259
|
5l9eA |
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer |
|
72
|
259
|
5lvsA |
Self-assembled protein-aromatic foldamer complexes with 2:3 and 2:2:1 stoichiometries |
|
73
|
258
|
5jdvB |
Human carbonic anhydrase ii (f131w) complexed with benzo[d]thiazole-2-sulfonamide |
|
78
|
258
|
5brvA |
Catalytic improvement of an artificial metalloenzyme by computational design |
|
72
|
259
|
5l3oA |
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer |
|
76
|
261
|
5j8zA |
Human carbonic anhydrase ii in complex with ligand |
