S +31
|
S 3x +31
|
|
6ymbA
|
Microed structure of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6ufdA
|
Carbonic anhydrase 2 with inhibitor (2z)-3-oxo-n-(4-sulfamoylphenyl)-2-[(thiophen-2-yl)methylidene]butanamide (11g/d7)
|
S +31
|
S 3x +31
|
|
6ufbA
|
Carbonic anhydrase 2 with inhibitor (2z)-2-benzylidene-3-oxo-n-(4-sulfamoylphenyl)butanamide (11a/d1)
|
S +31
|
S 3x +31
|
|
6ufcA
|
Carbonic anhydrase 2 with inhibitor (2z)-2-[(4-methoxyphenyl)methylidene]-3-oxo-n-(4-sulfamoylphenyl)butanamide (11d/d4)
|
S +31
|
S 3x +31
|
|
6klzA
|
Human carbonic anhydrase ii v143i variant 00 atm co2
|
S +31
|
S 3x +31
|
|
6km0A
|
Human carbonic anhydrase ii v143i variant 07 atm co2
|
S +31
|
S 3x +31
|
|
6km4A
|
Human carbonic anhydrase ii native 07 atm co2
|
S +31
|
S 3x +31
|
|
6km6A
|
Human carbonic anhydrase ii native 15 atm co2
|
S +31
|
S 3x +31
|
|
6wq4A
|
Carbonic anhydrase ii complexed with 2-((2-cyanoethyl)(phenethyl)amino)-n-phenethyl-n-(4-sulfamoylphenethyl)acetamide
|
S +31
|
S 3x +31
|
|
6wq8A
|
Carbonic anhydrase ii complexed with 3-((2-((furan-2-ylmethyl)(4-sulfamoylphenethyl)amino)-2-oxoethyl)(phenethyl)amino)propanoic acid
|
S +31
|
S 3x +31
|
|
6wq9A
|
Carbonic anhydrase ii complexed with 3-((2-((naphthalen-2-ylmethyl)(4-sulfamoylphenethyl)amino)-2-oxoethyl)(phenethyl)amino)propanoic acid
|
S +31
|
S 3x +31
|
|
6t7uA
|
Carborane inhibitor of carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
6t9zA
|
Nidocarborane inhibitor of carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
6rmxA
|
Human carbonic anhydrase ii mutant t199v bound by 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6otkA
|
Carbonic anhydrase ix mimic complexed with ureido benzene sulfonamide mb10-596b
|
S +31
|
S 3x +31
|
|
6otoA
|
Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb9-561b
|
S +31
|
S 3x +31
|
|
6otqA
|
Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb10-596b
|
S +31
|
S 3x +31
|
|
6oubA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb11-694b
|
S +31
|
S 3x +31
|
|
6otpA
|
Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb10-586b
|
S +31
|
S 3x +31
|
|
6ouhA
|
Carbonic anhydrase ii mimic complexed with benzene sulfonamide mb11-710a
|
S +31
|
S 3x +31
|
|
6oudA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-694b
|
S +31
|
S 3x +31
|
|
6oufA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-707a
|
S +31
|
S 3x +31
|
|
6oukA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb10-580b
|
S +31
|
S 3x +31
|
|
6ouiA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-710a
|
S +31
|
S 3x +31
|
|
6oujA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb11-689a
|
S +31
|
S 3x +31
|
|
6oumA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb10-580b
|
S +31
|
S 3x +31
|
|
6rg3A
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzylpiperazin-1-yl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6rmyA
|
Human carbonic anhydrase ii mutant t199v bound by 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6rhkA
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(3-benzylimidazolidine-1-carbonyl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6rzxA
|
Carbonic anhydrase caix mimic in complex with inhibitor fbsa
|
S +31
|
S 3x +31
|
|
6s03A
|
Carbonic anhydrase caix mimic in complex with inhibitor i39lt379
|
S +31
|
S 3x +31
|
|
6sdsA
|
Human carbonic anhydrase ii in complex with a sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
6r6jA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-(benzenesulfonyl)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6r71A
|
Crystal structure of human carbonic anhydrase isozyme xii with 2-(benzenesulfonyl)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6rm1A
|
Human carbonic anhydrase ii in complex with fragment.
|
S +31
|
S 3x +31
|
|
6qutA
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6vkgA
|
Human carbonic anhydrase ix mimic with epacadostat bound
|
S +31
|
S 3x +31
|
|
6ugpA
|
Human carbonic anhydrase 2 complexed with sb4-206
|
S +31
|
S 3x +31
|
|
6ugqA
|
Human carbonic anhydrase ix-mimic complexed with sb4-206
|
S +31
|
S 3x +31
|
|
6ugrA
|
Human carbonic anhydrase 2 complexed with sb4-208
|
S +31
|
S 3x +31
|
|
6ugzA
|
Human carbonic anhydrase ix-mimic complexed with sb4-208
|
S +31
|
S 3x +31
|
|
6ugoA
|
Human carbonic anhydrase ix-mimic complexed with sb4-205
|
S +31
|
S 3x +31
|
|
6uh0A
|
Human carbonic anhydrase 2 in complex with sb4-202
|
S +31
|
S 3x +31
|
|
6r6fA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-chloro-2-cyclohexylsulfanyl-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6qn0A
|
Three dimensional structure of human carbonic anhydrase xii in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6qn2A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6qn6A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6u4qA
|
Carbonic anhydrase 2 in complex with sb4197
|
S +31
|
S 3x +31
|
|
6u4tA
|
Carbonic anhydrase 9 in complex with sb4197
|
S +31
|
S 3x +31
|
|
6nm0A
|
Selective inhibition of carbonic anhydrase ix activity, using compound slc-149, displays limited anticancer effects in breast cancer cell lines
|
S +31
|
S 3x +31
|
|
6nlvA
|
Selective inhibition of carbonic anhydrase ix activity, using compound slc-149, displays limited anticancer effects in breast cancer cell lines
|
S +31
|
S 3x +31
|
|
6i0lA
|
Crystal structure of human carbonic anhydrase i in complex with the 1-[4-chloro-3-(trifluoromethyl)phenyl]-3-[2-(4-sulfamoylphenyl)ethyl]urea inhibitor
|
S +31
|
S 3x +31
|
4
|
6nj3A
|
Thermostable variant of human carbonic anhydrase with ordered tetrazine 2.0 at site 233
|
S +31
|
S 3x +31
|
4
|
6nj6A
|
Thermostable variant of human carbonic anhydrase with tetrazine 2.0 at site 186 reacted with stco in crystallo
|
S +31
|
S 3x +31
|
|
6ql2A
|
Crystal structure of chimeric carbonic anhydrase vi with ethoxzolamide.
|
S +31
|
S 3x +31
|
|
6ql1A
|
Crystal structure of chimeric carbonic anhydrase vi with 4-[(4,6-dimethylpyrimidin-2-yl)thio]-2,3,5,6-tetrafluorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
6hd2A
|
Active-site conformational dynamics of carbonic anhydrase ii under native conditions: an nmr perspective
|
S +31
|
S 3x +31
|
|
6gxbA
|
Carbonic anhydrase caix mimic in complex with inhibitor js13
|
S +31
|
S 3x +31
|
|
6gxeA
|
Carbonic anhydrase caix mimic in complex with inhibitor js14
|
S +31
|
S 3x +31
|
|
6qfwA
|
Human carbonic anhydrase ii with bound ircp* complex (cofactor 9) to generate an artificial transfer hydrogenase (athase)
|
S +31
|
S 3x +31
|
|
6qfuA
|
Human carbonic anhydrase ii with bound ircp* complex (cofactor 7) to generate an artificial transfer hydrogenase (athase)
|
S +31
|
S 3x +31
|
|
6qfvA
|
Human carbonic anhydrase ii with bound ircp* complex (cofactor 8) to generate an artificial transfer hydrogenase (athase)
|
S +31
|
S 3x +31
|
|
6qfxA
|
Human carbonic anhydrase ii with bound ircp* complex (cofactor 10) to generate an artificial transfer hydrogenase (athase)
|
S +31
|
S 3x +31
|
|
6mbyA
|
Carbonic anhydrase ii in complex with ferulic acid
|
S +31
|
S 3x +31
|
|
6g6tA
|
Crystal structure of human carbonic anhydrase isozyme ii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6g5uA
|
Crystal structure of human carbonic anhydrase isozyme xiii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6g5lA
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-chloro-2-(cyclohexylamino)-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6g7aA
|
Crystal structure of human carbonic anhydrase isozyme xii 2-(benzylamino)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6mbvA
|
Carbonic anhydrase ii in complex with nicotinic acid
|
S +31
|
S 3x +31
|
|
6qebA
|
Assessment of a large enzyme-drug complex by proton-detected solid-state nmr without deuteration
|
S +31
|
S 3x +31
|
|
6fjjA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin).
|
S +31
|
S 3x +31
|
|
6fjiA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (apo).
|
S +31
|
S 3x +31
|
|
6gcyA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin-sugar conjugate complex)
|
S +31
|
S 3x +31
|
|
6h6sA
|
Sad phasing on nickel-substituted human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6hwzA
|
Selenols: a new class of carbonic anhydrase inhibitors
|
S +31
|
S 3x +31
|
|
6hx5A
|
Selenols: a new class of carbonic anhydrase inhibitors
|
S +31
|
S 3x +31
|
|
6h33A
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide.
|
S +31
|
S 3x +31
|
|
6h34A
|
The crystal structure of human carbonic anhydrase ii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
|
S +31
|
S 3x +31
|
4
|
6g3qA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor famotidine
|
S +31
|
S 3x +31
|
|
6g3vA
|
Crystal structure of human carbonic anhydrase i in complex with the inhibitor famotidine
|
S +31
|
S 3x +31
|
|
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.
|
S +31
|
S 3x +31
|
|
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.
|
S +31
|
S 3x +31
|
|
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.
|
S +31
|
S 3x +31
|
|
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.
|
S +31
|
S 3x +31
|
|
4yglA
|
Naclo4--interactions between hofmeister anions and the binding pocket of a protein
|
S +31
|
S 3x +31
|
|
1ttmA
|
Human carbonic anhydrase ii complexed with 667-coumate
|
S +31
|
S 3x +31
|
|
1azmA
|
Drug-protein interactions: structure of sulfonamide drug complexed with human carbonic anhydrase i
|
S +31
|
S 3x +31
|
|
5neaA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(2-methyl-1,3-oxazol-5-yl)benzene-1-sulfonammide
|
S +31
|
S 3x +31
|
|
6b59A
|
Carbonic anhydrase ii in complex with nitrogenous base-bearing benezenesulfonamide
|
S +31
|
S 3x +31
|
|
5e2mA
|
Crystal structure of human carbonic anhydrase isozyme i with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4qsjA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide
|
S +31
|
S 3x +31
|
|
1rzbA
|
X-ray analysis of metal substituted human carbonic anhydrase ii derivatives
|
S +31
|
S 3x +31
|
|
5ohhA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5n25A
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-pyridin-3-yl-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4qizA
|
Crystal structure of human carbonic anhydrase isozyme xiii with inhibitor
|
S +31
|
S 3x +31
|
|
6evrA
|
Crystal structure of human carbonic anhydrase i in complex with the 4-(4 acetyl-3-benzylpiperazine-1 carbonyl)benzene-1-sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4cnvA
|
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture
|
S +31
|
S 3x +31
|
|
4bcwA
|
Carbonic anhydrase ix mimic in complex with (e)-2-(5-bromo-2- hydroxyphenyl)ethenesulfonic acid
|
S +31
|
S 3x +31
|
|
3s75B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 3x +31
|
|
3dc3A
|
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
S +31
|
S 3x +31
|
|
1th9A
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4gl1X
|
Structure of h64a/n62l/n67l human carbonic anhydrase ii triple mutant
|
S +31
|
S 3x +31
|
|
6fe2A
|
Three dimensional structure of human carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
4z0qA
|
Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv)
|
S +31
|
S 3x +31
|
|
4qj0A
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
S +31
|
S 3x +31
|
|
4qk2A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - e234p
|
S +31
|
S 3x +31
|
|
4bf1A
|
Three dimensional structure of human carbonic anhydrase ii in complex with 5-(1-naphthalen-1-yl-1,2,3-triazol-4-yl)thiophene-2-sulfonamide
|
S +31
|
S 3x +31
|
|
3d92A
|
Human carbonic anhydrase ii bound with substrate carbon dioxide
|
S +31
|
S 3x +31
|
|
2f14A
|
Tne crystal structure of the human carbonic anhydrase ii in complex with a fluorescent inhibitor
|
S +31
|
S 3x +31
|
|
5ogjA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
4
|
5neeA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 5-[2-(morpholine-4-carbonyl)1,3-oxazol-5-yl)]thiophene-2-sulfonammide
|
S +31
|
S 3x +31
|
|
5ljqA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-(4-(phenoxymethyl)-1h-1,2,3-triazol-1-yl)benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4n0xB
|
Room temperature crystal structure of human carbonic anhydrase ii in complex with thiophene-2-sulfonamide
|
S +31
|
S 3x +31
|
|
3mnaA
|
The crystal structure of human carbonic anhydrase ii in complex with a 1,3,5-triazine-substituted benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4knjA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5bu6A
|
Structure of bpsb deaceylase domain from bordetella bronchiseptica
|
S +31
|
S 3x +31
|
|
4k0zA
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with methazolamide
|
S +31
|
S 3x +31
|
|
5fnlA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
5eheA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-(benzylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
1j9wA
|
Solution structure of the cai michigan 1 variant
|
S +31
|
S 3x +31
|
|
3mzcA
|
Human carbonic ahydrase ii in complex with a benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4k0sA
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with acetazolamide
|
S +31
|
S 3x +31
|
|
5cluA
|
The crystal structure of the complex of hcaii with a saccharine derivative
|
S +31
|
S 3x +31
|
|
4k0tA
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with chlorzolamide
|
S +31
|
S 3x +31
|
|
3w6hA
|
Crystal structure of 19f probe-labeled hcai in complex with acetazolamide
|
S +31
|
S 3x +31
|
|
5fnhA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
6ekiA
|
Structure of a hyperthermostable carbonic anhydrase identified from an active hydrothermal vent chimney
|
S +31
|
S 3x +31
|
|
3igpA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5ogpA
|
Metalacarborane inhibitors of carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
4xixA
|
Carbonic anhydrase cah3 from chlamydomonas reinhardtii in complex with phosphate.
|
S +31
|
S 3x +31
|
|
4q09A
|
Crystal structure of chimeric carbonic anhydrase xii with inhibitor
|
S +31
|
S 3x +31
|
|
4e3hA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
S +31
|
S 3x +31
|
|
4m2wA
|
Genetically engineered carbonic anhydrase ix in complex with dorzolamide
|
S +31
|
S 3x +31
|
|
4q08A
|
Crystal structure of chimeric carbonic anhydrase xii with inhibitor
|
S +31
|
S 3x +31
|
|
4q07A
|
Crystal structure of chimeric carbonic anhydrase ix with inhibitor
|
S +31
|
S 3x +31
|
|
3r17B
|
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
S +31
|
S 3x +31
|
|
2cbdA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
S +31
|
S 3x +31
|
|
3f4xA
|
Carbonic anhydrase inhibitors. comparison of chlorthalidone and indapamide x-ray crystal structures in adducts with isozyme ii: when three water molecules make the difference
|
S +31
|
S 3x +31
|
|
2wehA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
S +31
|
S 3x +31
|
4
|
2nnvA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
2fw4A
|
Carbonic anhydrase activators. the first x-ray crystallographic study of an activator of isoform i, structure with l-histidine.
|
S +31
|
S 3x +31
|
|
3dc9A
|
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
S +31
|
S 3x +31
|
|
1zscA
|
Carbonic anhydrase ii mutant e117q, holo form
|
S +31
|
S 3x +31
|
|
2cbaA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
S +31
|
S 3x +31
|
|
1rj5A
|
Crystal structure of the extracellular domain of murine carbonic anhydrase xiv
|
S +31
|
S 3x +31
|
|
2eu3A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
S +31
|
S 3x +31
|
|
3mnkA
|
Human carbonic anhydrase ii mutant k170h
|
S +31
|
S 3x +31
|
|
5jepB
|
Human carbonic anhydrase ii (t199s) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
4qk3A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - [delta]230-240
|
S +31
|
S 3x +31
|
|
5ekhA
|
Human carbonic anhydrase ii complexed with a two-faced guest
|