|
75
|
257
|
3rz1B |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
77
|
258
|
3s9tA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(4,6-dimethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide |
|
79
|
257
|
3s8xA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4-methyl-6-oxo-1,6-dihydro-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide |
|
77
|
257
|
3rz7A |
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase |
|
73
|
255
|
12caA |
Altering the mouth of a hydrophobic pocket. structure and kinetics of human carbonic anhydrase ii mutants at residue val-121 |
|
81
|
257
|
5sz4A |
Carbonic anhydrase ix-mimic in complex with 4-(phenyl)-benzenesulfonamide |
|
76
|
257
|
5sz5A |
Carbonic anhydrase ix-mimic in complex with 4-(2-methylphenyl)-benzenesulfonamide |
|
75
|
259
|
5l6kA |
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer |
|
77
|
259
|
5jg5B |
Human carbonic anhydrase ii (v121t/f131y) complexed with benzo[d]thiazole-2-sulfonamide |
|
76
|
259
|
5jegB |
Human carbonic anhydrase ii (v121i) complexed with benzo[d]thiazole-2-sulfonamide |
|
79
|
257
|
5jq0A |
Crystal structure of human carbonic anhydrase ii in complex with benzoxaborole at ph=8.7 |
|
74
|
259
|
5jg3B |
Human carbonic anhydrase ii (121t/n67q) complexed with benzo[d]thiazole-2-sulfonamide |
|
76
|
259
|
5jgtB |
Human carbonic anhydrase ii (f131y/l198a) complexed with 1,3-thiazole-2-sulfonamide |
|
75
|
259
|
5jehB |
Human carbonic anhydrase ii (l198a) complexed with benzo[d]thiazole-2-sulfonamide |
|
79
|
260
|
5jqtA |
Crystal structure of human carbonic anhydrase ii in complex with benzoxaborole at ph 7.4 |
|
74
|
258
|
5jesB |
Human carbonic anhydrase ii (v121t) complexed with benzo[d]thiazole-2-sulfonamide |
|
75
|
257
|
5jgsB |
Human carbonic anhydrase ii (f131y/l198a) complexed with benzo[d]thiazole-2-sulfonamide |
|
74
|
265
|
5ipzA |
Crystal structure of human carbonic anhydrase isozyme iv with 5-(2-amino-1,3-thiazol-4-yl)-2-chlorobenzenesulfonamide |
|
57
|
217
|
5hpjA |
Photobacterium profundum alpha-carbonic anhydrase |
|
79
|
259
|
5a6hA |
Synthesis, carbonic anhydrase inhibition and protein x-ray structure of the unusual natural product primary sulfonamide psammaplin c |
|
73
|
255
|
8ca2A |
Engineering the hydrophobic pocket of carbonic anhydrase ii |
|
76
|
255
|
9ca2A |
Engineering the hydrophobic pocket of carbonic anhydrase ii |
|
74
|
255
|
7ca2A |
Engineering the hydrophobic pocket of carbonic anhydrase ii |
|
77
|
255
|
6ca2A |
Engineering the hydrophobic pocket of carbonic anhydrase ii |
|
78
|
267
|
5cjfA |
The crystal structure of the human carbonic anhydrase xiv in complex with a 1,1'-biphenyl-4-sulfonamide inhibitor. |
|
78
|
257
|
5dsjA |
Structure of co2 released holo-form of human carbonic anhydrase ii with 50 sec warming |
|
75
|
257
|
5dsiA |
Structure of co2 bound holo-form of human carbonic anhydrase ii with 0 sec (no) warming |
|
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 |
|
75
|
257
|
5c8iA |
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with methazolamide |
|
79
|
257
|
5byiA |
Human carbonic anhydrase ii with an azobenzene inhibitor (1d) |
|
79
|
258
|
5brwA |
Catalytic improvement of an artificial metalloenzyme by computational design |
|
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 |
|
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) |
|
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 |
|
76
|
257
|
4yx4A |
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (1). |
|
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 |
|
59
|
233
|
4etqC |
Vaccinia virus d8l imv envelope protein in complex with fab of murine igg2a la5 |
