76
|
257
|
4q8zA |
Crystal structure of 1-hydroxy-4-methylpyridin-2(1h)-one bound to human carbonic anhydrase ii |
77
|
258
|
4q49A |
Room temperature neutron crystal structure of apo human carbonic anhydrase at ph 7.5 |
77
|
260
|
4pq7A |
The crystal structure of the human carbonic anhydrase ii in complex with a sulfamide inhibitor |
76
|
257
|
4q8xA |
Crystal structure of 1-hydroxy-5-(trifluoromethyl)pyridine-2(1h)-thione bound to human carbonic anhydrase ii |
74
|
257
|
4q6eA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[3-(3,5-dimethyl-1h-pyrazol-1-yl)-3-oxopropyl]amino}benzene-1-sulfonamide |
78
|
257
|
4pyxA |
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor |
72
|
257
|
4qefA |
Human carbonic anhydrase ii v207i - cyanate inhibitor complex |
74
|
257
|
4q90A |
Crystal structure of 4-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii |
75
|
257
|
4pyyA |
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor |
76
|
257
|
4q99A |
Crystal structure of 2-mercapto-4-methylphenol bound to human carbonic anhydrase ii |
77
|
257
|
4q7vA |
Crystal structure of 1-hydroxy-5-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii |
78
|
257
|
4q08A |
Crystal structure of chimeric carbonic anhydrase xii with inhibitor |
74
|
258
|
4q78A |
Structure-assisted design of carborane-based inhibitors of carbonic anhydrase |
80
|
258
|
4pzhA |
Crystal structure of human carbonic anhydrase isozyme ii with 2,3,5,6-tetrafluoro-4[(2-hydroxyethyl)sulfonyl]benzenesulfonamide |
80
|
257
|
4q07A |
Crystal structure of chimeric carbonic anhydrase ix with inhibitor |
76
|
257
|
4q7sA |
Crystal structure of 1-hydroxy-4-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii |
77
|
258
|
4q06A |
Crystal structure of chimeric carbonic anhydrase ix with inhibitor |
75
|
257
|
4q87A |
Crystal structure of 1-hydroxy-4-(trifluoromethyl)pyridine-2(1h)-thione bound to human carbonic anhydrase ii |
73
|
261
|
4q0lA |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor |
83
|
211
|
4o1kA |
Crystal structures of two tetrameric beta-carbonic anhydrases from the filamentous ascomycete sordaria macrospora. |
67
|
197
|
4o1jA |
Crystal structures of two tetrameric beta-carbonic anhydrases from the filamentous ascomycete sordaria macrospora. |
74
|
258
|
4n16A |
Structure of cholate bound to human carbonic anhydrase ii |
74
|
258
|
4n0xB |
Room temperature crystal structure of human carbonic anhydrase ii in complex with thiophene-2-sulfonamide |
76
|
258
|
4mdlA |
Meta carborane carbonic anhydrase inhibitor |
78
|
266
|
4lu3A |
The crystal structure of the human carbonic anhydrase xiv |
81
|
258
|
4mdmA |
Nido-carborane carbonic anhydrase inhibitor |
72
|
257
|
4m2wA |
Genetically engineered carbonic anhydrase ix in complex with dorzolamide |
73
|
257
|
4mltA |
Structure of a monodentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii |
73
|
257
|
4m2vA |
Genetically engineered carbonic anhydrase ix in complex with brinzolamide |
72
|
257
|
4lp6A |
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer |
75
|
258
|
4mtyA |
Structure at 1a resolution of a helical aromatic foldamer-protein complex. |
76
|
258
|
4mdgA |
Closo carborane carbonic anhydrase inhibitor |
74
|
257
|
4m2rA |
Human carbonic anhydrase ii in complex with brinzolamide |
76
|
257
|
4mlxA |
Structure of a bidentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii |
71
|
257
|
4m2uA |
Carbonic anhydrase ii in complex with dorzolamide |
77
|
257
|
4mo8A |
The crystal structure of the human carbonic anhydrase ii in complex with n-[2-(2-methyl-5-nitro-1h-imidazol-1-yl)ethyl]sulfamide |
71
|
261
|
4kp8A |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 3-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
76
|
257
|
4knjA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
75
|
261
|
4kp5A |
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
78
|
258
|
4knnA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide |
75
|
257
|
4l5vA |
The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii |
78
|
257
|
4kv0A |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-tosylureido)pyridine-2-sulfonamide inhibitor |
78
|
259
|
4knmA |
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide |
79
|
256
|
4kuvA |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(4-chlorophenylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor |
71
|
258
|
4k1qA |
Structure of hcaix mimic (hcaii with 5 mutations in active site) |
74
|
257
|
4l5uA |
The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii |
72
|
257
|
4l5wA |
Structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii |
79
|
257
|
4kuyA |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(o-tolylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor |
76
|
257
|
4k13A |
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with dorzolamide |
80
|
257
|
4kuwA |
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(4-fluorophenylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor |