|
84
|
277
|
6qqmA |
Crystal structure of the alpha carbonic anhydrase from schistosoma mansoni |
|
75
|
257
|
6hxdA |
Human carbonic anhydrase ii in complex with 4-butylbenzenesulfonamide |
|
76
|
257
|
6ebeA |
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines. |
|
79
|
260
|
6g3qA |
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor famotidine |
|
76
|
257
|
6edaA |
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines. |
|
77
|
257
|
6eczA |
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines. |
|
74
|
257
|
6f3bA |
Crystal structure of human carbonic anhydrase i in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-[(4-methylphenyl)methyl]urea inhibitor |
|
76
|
257
|
6eeoA |
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines. |
|
71
|
256
|
6g3vA |
Crystal structure of human carbonic anhydrase i in complex with the inhibitor famotidine |
|
76
|
257
|
6ex1A |
Crystal structure of human carbonic anhydrase i in complex with the 4-[(3s)-3 benzyl-4-(4-sulfamoylbenzoyl)piperazine -1-carbonyl]benzene-1-sulfonamide inhibitor |
|
76
|
257
|
6fagA |
Crystal structure of human carbonic anhydrase i in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-(2-methoxyphenyl)urea inhibitor |
|
78
|
257
|
6eehA |
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines. |
|
76
|
257
|
6eeaA |
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines. |
|
73
|
257
|
6fafA |
Crystal structure of human carbonic anhydrase i in complex with the 3-(2,5-dimethylphenyl)-1-(2-hydroxy-5-sulfamoylphenyl)urea inhibitor |
|
19
|
260
|
6qebA |
Assessment of a large enzyme-drug complex by proton-detected solid-state nmr without deuteration |
|
74
|
257
|
6mbvA |
Carbonic anhydrase ii in complex with nicotinic acid |
|
76
|
257
|
6mbyA |
Carbonic anhydrase ii in complex with ferulic acid |
|
77
|
257
|
6hx5A |
Selenols: a new class of carbonic anhydrase inhibitors |
|
70
|
256
|
6hwzA |
Selenols: a new class of carbonic anhydrase inhibitors |
|
76
|
257
|
6h34A |
The crystal structure of human carbonic anhydrase ii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide. |
|
79
|
259
|
6h36A |
The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide. |
|
77
|
258
|
6h37A |
The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide |
|
76
|
256
|
6h2zA |
The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide. |
|
78
|
259
|
6h38A |
The crystal structure of human carbonic anhydrase vii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide. |
|
76
|
260
|
6h33A |
The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide. |
|
69
|
258
|
6h6sA |
Sad phasing on nickel-substituted human carbonic anhydrase ii |
|
72
|
261
|
6g5lA |
Crystal structure of human carbonic anhydrase isozyme xii with 4-chloro-2-(cyclohexylamino)-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide |
|
78
|
258
|
6g5uA |
Crystal structure of human carbonic anhydrase isozyme xiii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide |
|
79
|
258
|
6gcyA |
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin-sugar conjugate complex) |
|
76
|
257
|
6g6tA |
Crystal structure of human carbonic anhydrase isozyme ii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide |
|
76
|
262
|
6g7aA |
Crystal structure of human carbonic anhydrase isozyme xii 2-(benzylamino)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide |
|
77
|
258
|
6fjiA |
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (apo). |
|
77
|
258
|
6fjjA |
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin). |
|
77
|
256
|
6qfuA |
Human carbonic anhydrase ii with bound ircp* complex (cofactor 7) to generate an artificial transfer hydrogenase (athase) |
|
78
|
256
|
6qfxA |
Human carbonic anhydrase ii with bound ircp* complex (cofactor 10) to generate an artificial transfer hydrogenase (athase) |
|
80
|
255
|
6qfvA |
Human carbonic anhydrase ii with bound ircp* complex (cofactor 8) to generate an artificial transfer hydrogenase (athase) |
|
78
|
256
|
6qfwA |
Human carbonic anhydrase ii with bound ircp* complex (cofactor 9) to generate an artificial transfer hydrogenase (athase) |
|
79
|
257
|
6gxbA |
Carbonic anhydrase caix mimic in complex with inhibitor js13 |
|
73
|
257
|
6e91A |
Ca ix mimic complexed with steroidal sulfamate compound stx 2484 |
|
79
|
257
|
6gxeA |
Carbonic anhydrase caix mimic in complex with inhibitor js14 |
|
77
|
257
|
6e8xA |
Ca ix mimic complexed with steroidal sulfamate compound stx 140 |
|
78
|
258
|
6ic2A |
Polypharmacology of epacadostat: a potent and selective inhibitor of the tumor associated carbonic anhydrases ix and xii |
|
74
|
257
|
6gdcA |
Human carbonic anhydrase ii in complex with benzenesulfonamide |
|
74
|
257
|
6e8pA |
Ca ix mimic complexed with steroidal sulfamate compound stx 49 |
|
77
|
257
|
6e92A |
Ca ix mimic complexed with steroidal sulfamate compound stx 2845 |
|
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 |
