73
|
257
|
3qykA |
Human carbonic anhydrase ii complexed with triple ring benzene sulfonamide inhibitor |
59
|
236
|
3q31A |
Structure of fungal alpha carbonic anhydrase from aspergillus oryzae |
75
|
258
|
3pykA |
Human carbonic anhydrase ii as host for pianostool complexes bearing a sulfonamide anchor |
69
|
258
|
3pjjA |
Synthetic dimer of human carbonic anhydrase ii |
80
|
258
|
3po6A |
Crystal structure of human carbonic anhydrase ii with 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinoline-2(1h)-sulfonamide |
76
|
257
|
3oysA |
Human carbonic anhydrase ii complexed with 2-{[4-amino-3-(3-hydroxyprop-1-yn-1-yl)-1h-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-5-methyl-3-(2-methylphenyl)quinazolin-4(3h)-one |
78
|
258
|
3oimA |
Human carbonic anhydrase ii bound by 2-ethylestradiol 3-o-sulfamate |
75
|
258
|
3p3hA |
Human carbonic anhydrase ii in complex with p-(5-ferrocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide |
73
|
257
|
3p44A |
Human carbonic anhydrase ii in complex with p-(4-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide |
77
|
257
|
3oilA |
Human carbonic anhydrase ii mutant a65s, n67q (ca ix mimic) bound by 2-ethylestradiol 3-o-sulfamate |
76
|
257
|
3p55A |
Human carbonic anhydrase ii in complex with p-(4-ferrocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide |
76
|
257
|
3p3jA |
Human carbonic anhydrase ii in complex with p-(5-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide |
80
|
258
|
3okuA |
Human carbonic anhydrase ii in complex with 2-ethylestrone-3-o-sulfamate |
75
|
257
|
3p4vA |
Human carbonic anhydrase ii in complex with (+)-xylariamide a |
75
|
257
|
3p5aA |
Human carbonic anhydrase complexed with sodium morpholinocarbodithioate |
80
|
257
|
3okvA |
Human carbonic anhydrase ii a65s, n67q (ca ix mimic) bound with 2-ethylestrone 3-o-sulfamate |
78
|
257
|
3p5lA |
Human carbonic anhydrase complexed with sodium 4-cyano-4-phenylpiperidine-1-carbodithioate |
78
|
257
|
3oy0A |
Human carbonic anhydrase ii complexed with 1-(4-(4-(2-(isopropylsulfonyl)phenylamino)-1h-pyrrolo[2,3-b]pyridin-6-ylamino)-3-methoxyphenyl)piperidin-4-ol |
79
|
258
|
3oikA |
Human carbonic anhydrase ii mutant a65s, n67q (ca ix mimic) bound by 2-ethylestradiol 3,17-o,o-bis-sulfamate |
78
|
257
|
3p58A |
Human carbonic anhydrase in complex with benzyl (methyl) carbamodithoic acid |
77
|
257
|
3oyqA |
Structure of human carbonic anhydrase ii complexed with 5,6-dihydro-benzo[h]cinnolin-3-ylamine |
76
|
257
|
3nj9A |
Crystal structure of carbonic anhydrase ii in complex with a nir inhibitor |
73
|
256
|
3ni5A |
Carbonic anhydrase inhibitor: c1 family |
77
|
258
|
3n4bA |
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor |
78
|
258
|
3n2pA |
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor |
76
|
257
|
3mzcA |
Human carbonic ahydrase ii in complex with a benzenesulfonamide inhibitor |
72
|
258
|
3n3jA |
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor |
75
|
257
|
3nb5A |
Human carbonic anhydrase ii in complex with 2-(3-chloro-4-hydroxyphenyl)-n-(4-sulfamoylphenethyl)acetamide |
75
|
258
|
3mnkA |
Human carbonic anhydrase ii mutant k170h |
74
|
257
|
3mnaA |
The crystal structure of human carbonic anhydrase ii in complex with a 1,3,5-triazine-substituted benzenesulfonamide inhibitor |
77
|
257
|
3myqA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-[(1h-imidazo[4,5-c]quinolin-2-ylsulfanyl)acetyl]benzenesulfonamide |
72
|
257
|
3mnuA |
Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron containing aromatic sulfamide with mammalian isoforms i-xv |
75
|
262
|
3ml5A |
Crystal structure of the c183s/c217s mutant of human ca vii in complex with acetazolamide |
75
|
258
|
3mniA |
Human carbonic anhydrase ii mutant k170d |
74
|
257
|
3mmfA |
Crystal structure of human carbonic anhydrase ii in complex with a 1,3,5-triazine-substituted benzenesulfonamide inhibitor |
73
|
257
|
3mwoA |
Human carbonic anhydrase ii in a doubled monoclinic cell: a re-determination |
74
|
258
|
3mnhA |
Human carbonic anhydrase ii mutant k170a |
77
|
258
|
3n0nA |
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor |
74
|
258
|
3mnjA |
Human carbonic anhydrase ii mutant k170e |
72
|
257
|
3ml2A |
Human carbonic anhydsase ii in complex with an aryl sulfonamide inhibitor |
77
|
257
|
3m5tA |
Fragment tethered to carbonic anhydrase ii h64c mutant |
77
|
257
|
3m96A |
Crystal structure of human carbonic anhydrase isozyme ii with 5-{[(5-bromo-1h-benzimidazol-2-yl)sulfanyl]acetyl}-2-chlorobenzenesulfonamide |
77
|
257
|
3m14A |
Carbonic anhydrase ii in complex with novel sulfonamide inhibitor |
79
|
257
|
3mhcA |
Crystal structure of human cabonic anhydrase ii in adduct with an adamantyl analogue of acetazolamide in a novel hydrophobic binding pocket |
79
|
257
|
3m5sA |
Carbonic anhydrase ii mutant h64c in complex with carbonate |
78
|
256
|
3m1kA |
Carbonic anhydrase in complex with fragment |
75
|
257
|
3mhlA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[n-(6-methoxy-5-nitropyrimidin-4-yl)amino]methyl}benzenesulfonamide |
75
|
257
|
3m67A |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-[(6,7-dihydro-1h-[1,4]dioxino[2,3-f]benzimidazol-2-ylsulfanyl)acetyl]benzenesulfonamide |
78
|
256
|
3mhoA |
Crystal structure of human carbonic anhydrase isozyme ii with 4-[n-(6-chloro-5-formyl-2-methylthiopyrimidin-4-yl)amino]benzenesulfonamide |
63
|
259
|
3mdzA |
Crystal structure of human carbonic anhydrase vii [isoform 1], ca7 |