|
74
|
257
|
3ryjB |
Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide |
|
74
|
257
|
3ryyA |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
77
|
257
|
3rz8A |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
71
|
258
|
3rz0B |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
74
|
258
|
3ryxB |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
77
|
258
|
3rz5A |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
75
|
257
|
3rldA |
Crystal structure of the y7i mutant of human carbonic anhydrase ii |
|
68
|
257
|
3rg4A |
Crystal structure of the w5f mutant of human carbonic anhydrase ii |
|
75
|
256
|
3rgeA |
Crystal structure of the w5h mutant of human carbonic anhydrase ii |
|
71
|
255
|
3rg3A |
Crystal structure of the w5e mutant of human carbonic anhydrase ii |
|
78
|
258
|
3rj7A |
Human carbonic anhydrase ii complexed with its inhibitor rhenium(i)triscarbonyl-cyclopentadienyl-carboxy-4-aminomethylbenzene-sulfonamide |
|
79
|
257
|
3dbuA |
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties |
|
75
|
257
|
5y2rA |
2.5 atm co2-pressurized human carbonic anhydrase ii |
|
79
|
257
|
3m1qA |
Carbonic anhydrase ii mutant w5c-h64c with opened disulfide bond |
|
76
|
257
|
3dcwA |
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties |
|
78
|
259
|
3igpA |
Structure of inhibitor binding to carbonic anhydrase ii |
|
75
|
257
|
5y2sA |
7.0 atm co2-pressurized human carbonic anhydrase ii |
|
80
|
257
|
5wlrA |
Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide |
|
76
|
257
|
5wltA |
Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide |
|
78
|
257
|
5wluA |
Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide |
|
78
|
258
|
5wexA |
Discovery of new selenoureido analogs of 4-(4-fluorophenylureido) benzenesulfonamides as carbonic anhydrase inhibitors |
|
78
|
257
|
5w8bA |
Carbonic anhydrase ii in complex with activating histamine pyridinium derivative |
|
75
|
257
|
5wg7A |
Human carbonic anhydrase ii complexed with acek |
|
78
|
258
|
5umcA |
Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography |
|
78
|
259
|
5ulnA |
Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography |
|
79
|
258
|
5u0dA |
Identification of a new zinc binding chemotype by fragment screening |
|
77
|
258
|
5u0fA |
Identification of a new zinc binding chemotype by fragment screening |
|
81
|
258
|
5ty8A |
Identification of a new zinc binding chemotype by fragment screening |
|
81
|
258
|
5u0gA |
Identification of a new zinc binding chemotype by fragment screening |
|
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 |
|
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 |
