|
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 |
|
77
|
257
|
4k0sA |
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with acetazolamide |
|
76
|
257
|
4jsaA |
Benzenesulfonamide complexed with hcaii h94d |
|
74
|
257
|
4js6A |
Crystal structure of inhibitor-free hcaii h94d |
|
77
|
257
|
4itpA |
Structure of human carbonic anhydrase ii bound to a benzene sulfonamide |
|
78
|
257
|
4iwzA |
Structure of hcaii in complex with an acetazolamide derivative |
|
78
|
257
|
4k0tA |
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with chlorzolamide |
|
76
|
257
|
4ilxA |
Structure of human carbonic anhydrase ii in complex with an adamantyl sulfonamide inhibitor |
|
75
|
257
|
4itoA |
Human ca ii inhibition by novel sulfonamide |
|
76
|
258
|
4idrX |
Human carbonic anhydrase ii proton transfer double mutant |
|
76
|
257
|
4jssA |
Human carbonic anhydrase ii h94d bound to a bidentate inhibitor |
|
74
|
257
|
4jswA |
Human carbonic anhydrase ii h94c |
|
75
|
257
|
4jszA |
Benzenesulfonamide bound to hcaii h94c |
|
75
|
261
|
4ht2A |
Crystal structure of human carbonic anhydrase isozyme xii with the inhibitor. |
|
79
|
259
|
4hu1A |
Crystal structure of human carbonic anhydrase isozyme xiii with the inhibitor. |
|
77
|
257
|
4ht0A |
Crystal structure of human carbonic anhydrase isozyme ii with the inhibitor. |
|
72
|
257
|
4hewA |
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure |
|
74
|
257
|
4heyA |
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure |
|
75
|
257
|
4hf3A |
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure |
|
74
|
257
|
4hbaA |
Structural and catalytic characterization of a thermal and acid stable variant of human carbonic anhydrase ii containing an engineered disulfide bond |
|
73
|
257
|
4hezA |
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure |
|
61
|
224
|
4g7aA |
The crystal structure of an alpha carbonic anhydrase from the extremophilic bacterium sulfurihydrogenibium yellowstonense yo3aop1 |
|
76
|
258
|
4gl1X |
Structure of h64a/n62l/n67l human carbonic anhydrase ii triple mutant |
|
79
|
257
|
4fvoA |
Carbonic anhydrase ii in complex with n-[(2e)-3,4-dihydroquinazolin-2(1h)-ylidene]sulfuric diamide |
|
77
|
257
|
4g0cA |
Neutron structure of acetazolamide-bound human carbonic anhydrase ii reveal molecular details of drug binding. |
|
78
|
257
|
4fu5A |
Carbonic anhydrase ii in complex with n-[(2z)-1,3-oxazolidin-2-ylidene]sulfuric diamide |
|
77
|
257
|
4frcA |
Carbonic anhydrase ii in complex with n'-sulfamoylpyrrolidine-1-carboximidamide |
|
77
|
257
|
4fvnA |
Carbonic anhydrase ii in complex with n-(tetrahydropyrimidin-2(1h)-ylidene)sulfuric diamide |
|
75
|
257
|
4fl7A |
The crystal structure of human carbonic anhydrase ii in complex with n-(hydroxy)-benzamide |
|
77
|
257
|
3r16A |
Human caii bound to n-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide |
|
78
|
257
|
3r17B |
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide |
|
78
|
257
|
4fikA |
Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products |
|
78
|
257
|
4fptA |
Carbonic anhydrase ii in complex with ethyl (2z,4r)-2-(sulfamoylimino)-1,3-thiazolidine-4-carboxylate |
|
81
|
215
|
3qy1A |
1.54a resolution crystal structure of a beta-carbonic anhydrase from salmonella enterica subsp. enterica serovar typhimurium str. lt2 |
|
73
|
257
|
3qykA |
Human carbonic anhydrase ii complexed with triple ring benzene sulfonamide inhibitor |
|
75
|
258
|
3pykA |
Human carbonic anhydrase ii as host for pianostool complexes bearing a sulfonamide anchor |
|
59
|
236
|
3q31A |
Structure of fungal alpha carbonic anhydrase from aspergillus oryzae |
|
80
|
258
|
3po6A |
Crystal structure of human carbonic anhydrase ii with 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinoline-2(1h)-sulfonamide |
|
69
|
258
|
3pjjA |
Synthetic dimer of human carbonic anhydrase ii |
|
73
|
257
|
3p44A |
Human carbonic anhydrase ii in complex with p-(4-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide |
|
73
|
205
|
3otmA |
Crystal structures of wild-type gamma-carbonic anhydrase from methanosarcina thermophila |
|
70
|
205
|
3oupA |
Crystal structure of the gamma-carbonic anhydrase w19n mutant from methanosarcina thermophila |
|
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
|
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 |
