|
77
|
257
|
5wlvA |
Carbonic anhydrase ii in complex with aryloxy-2-hydroxypropylammine sulfonamide |
|
79
|
258
|
5vgyA |
Identification of a new zinc binding chemotype by fragment screening |
|
78
|
267
|
5cjfA |
The crystal structure of the human carbonic anhydrase xiv in complex with a 1,1'-biphenyl-4-sulfonamide inhibitor. |
|
78
|
256
|
5cacA |
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution |
|
77
|
257
|
5dsqA |
Structure of co2 released apo-form of human carbonic anhydrase ii with 3 min warming |
|
75
|
255
|
5ca2A |
Conformational mobility of his-64 in the thr-200 (right arrow) ser mutant of human carbonic anhydrase ii |
|
79
|
257
|
5byiA |
Human carbonic anhydrase ii with an azobenzene inhibitor (1d) |
|
75
|
257
|
5c8iA |
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with methazolamide |
|
79
|
258
|
5brwA |
Catalytic improvement of an artificial metalloenzyme by computational design |
|
74
|
209
|
5bq1A |
Capturing carbon dioxide in beta carbonic anhydrase |
|
78
|
258
|
5bruA |
Catalytic improvement of an artificial metalloenzyme by computational design |
|
76
|
257
|
5bnlA |
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins |
|
78
|
257
|
5amdA |
Three dimensional structure of human carbonic anhydrase ii in complex with 2-((2-phenylethyl)sulfamoyl)-4-sulfamoylbenzoic acid |
|
76
|
258
|
5a25A |
Rational engineering of a mesophilic carbonic anhydrase to an extreme halotolerant biocatalyst |
|
76
|
257
|
4zwyA |
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor |
|
77
|
257
|
4zwzA |
Engineered carbonic anhydrase ix mimic in complex with a glucosyl sulfamate inhibitor |
|
56
|
163
|
4yf5A |
Crystal structure of rv1284 in the presence of polycarpine at acidic ph |
|
79
|
257
|
4yxoA |
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (3). |
|
77
|
257
|
4z1kA |
Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv) |
|
76
|
257
|
4yxiA |
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (2). |
|
77
|
257
|
4yytA |
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (5). |
|
76
|
258
|
4z1nA |
Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv) |
|
76
|
257
|
4yx4A |
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (1). |
|
54
|
163
|
4yf4A |
Crystal structure of rv1284 in the presence of polycarpine at mildly acidic ph |
|
73
|
257
|
4ygnA |
Nai--interactions between hofmeister anions and the binding pocket of a protein |
|
76
|
258
|
4yglA |
Naclo4--interactions between hofmeister anions and the binding pocket of a protein |
|
53
|
163
|
4yf6A |
Crystal structure of oxidised rv1284 |
|
72
|
261
|
4qjwA |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor |
|
76
|
257
|
4q7wA |
Crystal structure of 1-hydroxy-6-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii |
|
77
|
260
|
4qsjA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide |
|
75
|
257
|
4e4aA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
73
|
257
|
4dz7A |
Hca ii in complex with novel sulfonamide inhibitors set d |
|
74
|
257
|
4e3fA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
71
|
257
|
4e5qA |
Human carbonic anhydrase ii in complex with cyanate |
|
76
|
257
|
4e3dA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
75
|
257
|
4e3gA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
78
|
257
|
4e49A |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
77
|
257
|
4e3hA |
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors |
|
75
|
257
|
4dz9A |
Hca ii in complex with novel sulfonamide inhibitors set d |
|
77
|
256
|
4cq0A |
Cyclic secondary sulfonamides: unusually good inhibitors of cancer- related carbonic anhydrase enzymes |
|
78
|
257
|
4cnvA |
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture |
|
79
|
257
|
4cnxA |
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture |
|
67
|
225
|
4coqA |
The complex of alpha-carbonic anhydrase from thermovibrio ammonificans with inhibitor sulfanilamide. |
|
78
|
256
|
4cacA |
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution |
|
75
|
257
|
4cnwA |
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture |
|
75
|
255
|
4ca2A |
Engineering the hydrophobic pocket of carbonic anhydrase ii |
|
79
|
257
|
4cnrA |
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture |
|
66
|
225
|
4c3tA |
The carbonic anhydrase from thermovibrio ammonificans reveals an interesting intermolecular disulfide contributing to increasing thermal stability of this enzyme |
|
79
|
257
|
4bf1A |
Three dimensional structure of human carbonic anhydrase ii in complex with 5-(1-naphthalen-1-yl-1,2,3-triazol-4-yl)thiophene-2-sulfonamide |
|
78
|
257
|
4bcwA |
Carbonic anhydrase ix mimic in complex with (e)-2-(5-bromo-2- hydroxyphenyl)ethenesulfonic acid |
