|
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) |
|
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 |
|
76
|
257
|
4lhiA |
Crystal structure of human carbonic anhydrase isozyme ii with 5-(phenylsulfonyl)thiophene-2-sulfonamide |
|
76
|
257
|
4kniA |
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide |
|
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 |
|
74
|
258
|
4kapA |
The binding of benzoarylsulfonamide ligands to human carbonic anhydrase is insensitive to formal fluorination of the ligand |
|
75
|
258
|
4k0zA |
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with methazolamide |
|
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 |
|
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 |
|
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 |
|
76
|
258
|
4idrX |
Human carbonic anhydrase ii proton transfer double mutant |
|
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 |
|
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 |
|
75
|
257
|
4hf3A |
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure |
|
76
|
258
|
4gl1X |
Structure of h64a/n62l/n67l human carbonic anhydrase ii triple mutant |
|
61
|
224
|
4g7aA |
The crystal structure of an alpha carbonic anhydrase from the extremophilic bacterium sulfurihydrogenibium yellowstonense yo3aop1 |
|
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 |
|
79
|
257
|
4fvoA |
Carbonic anhydrase ii in complex with n-[(2e)-3,4-dihydroquinazolin-2(1h)-ylidene]sulfuric diamide |
|
77
|
257
|
4fvnA |
Carbonic anhydrase ii in complex with n-(tetrahydropyrimidin-2(1h)-ylidene)sulfuric diamide |
|
77
|
257
|
4frcA |
Carbonic anhydrase ii in complex with n'-sulfamoylpyrrolidine-1-carboximidamide |
|
78
|
257
|
3r17B |
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide |
|
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
|
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 |
