K +31
|
|
|
7nh8AAA
|
Crystal structure of human carbonic anhydrase ii with n-((1-(6-((3ar,7r,7as)-7-hydroxy-2,2-dimethyltetrahydro-[1,3]dioxolo[4,5-c]pyridin-5(4h)-yl)hexyl)-1h-1,2,3-triazol-4-yl)methyl)-4-sulfamoylbenzamide
|
K +31
|
K 3x +31
|
|
7mu3A
|
Human carbonic anhydrase 9 mimic with compound
|
K +31
|
K 15x +31
|
|
6rrgA
|
Human carbonic anhydrase ii in complex with fluorinated benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6yj3A
|
Metala-carborane di-propyl-sulfonamide
|
K +31
|
K 3x +31
|
|
6yokA
|
Para-carborane di-propyl-sulfonamide in complex with ca ix mimic
|
S +31
|
S 3x +31
|
|
6ymbA
|
Microed structure of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
6ymaA
|
Microed structure of acetazolamide-bound human carbonic anhydrase ii
|
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
|
|
6ufbA
|
Carbonic anhydrase 2 with inhibitor (2z)-2-benzylidene-3-oxo-n-(4-sulfamoylphenyl)butanamide (11a/d1)
|
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
|
|
6km6A
|
Human carbonic anhydrase ii native 15 atm co2
|
K +31
|
K 3x +31
|
|
6km5A
|
Human carbonic anhydrase ii native 13 atm co2
|
S +31
|
S 3x +31
|
|
6km4A
|
Human carbonic anhydrase ii native 07 atm co2
|
K +31
|
K 3x +31
|
|
6km3A
|
Human carbonic anhydrase ii native 00 atm co2
|
K +31
|
K 3x +31
|
|
6km2A
|
Human carbonic anhydrase ii v143i variant 15 atm co2
|
K +31
|
K 3x +31
|
|
6km1A
|
Human carbonic anhydrase ii v143i variant 13 atm co2
|
S +31
|
S 3x +31
|
|
6km0A
|
Human carbonic anhydrase ii v143i variant 07 atm co2
|
S +31
|
S 3x +31
|
|
6klzA
|
Human carbonic anhydrase ii v143i variant 00 atm co2
|
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
|
|
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
|
|
6wq4A
|
Carbonic anhydrase ii complexed with 2-((2-cyanoethyl)(phenethyl)amino)-n-phenethyl-n-(4-sulfamoylphenethyl)acetamide
|
K +31
|
K 3x +31
|
|
6wq7A
|
Carbonic anhydrase ii complexed with 2-((3-aminopropyl)(phenethyl)amino)-n-(4-fluorobenzyl)-n-(4-sulfamoylphenethyl)acetamide
|
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
|
|
6t9zA
|
Nidocarborane inhibitor of carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
6t7uA
|
Carborane inhibitor of carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
6sdsA
|
Human carbonic anhydrase ii in complex with a sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
6s03A
|
Carbonic anhydrase caix mimic in complex with inhibitor i39lt379
|
S +31
|
S 3x +31
|
|
6rzxA
|
Carbonic anhydrase caix mimic in complex with inhibitor fbsa
|
S +31
|
S 3x +31
|
|
6rhkA
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(3-benzylimidazolidine-1-carbonyl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6rofA
|
Human carbonic anhydrase ii mutant t199v bound by 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]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
|
K +31
|
K 3x +31
|
|
6rhjA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-(4-benzyl-1,4-diazepane-1-carbonyl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6rg3A
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzylpiperazin-1-yl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6rg4A
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzyl-4-methylpiperazin-1-yl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6oueA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb11-707a
|
S +31
|
S 3x +31
|
|
6oumA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb10-580b
|
S +31
|
S 3x +31
|
|
6oujA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb11-689a
|
S +31
|
S 3x +31
|
|
6ouiA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-710a
|
S +31
|
S 3x +31
|
|
6oukA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb10-580b
|
S +31
|
S 3x +31
|
|
6oufA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-707a
|
S +31
|
S 3x +31
|
|
6oudA
|
Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-694b
|
S +31
|
S 3x +31
|
|
6ouhA
|
Carbonic anhydrase ii mimic complexed with benzene sulfonamide mb11-710a
|
S +31
|
S 3x +31
|
|
6otpA
|
Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb10-586b
|
S +31
|
S 3x +31
|
|
6oubA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb11-694b
|
S +31
|
S 3x +31
|
|
6otqA
|
Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb10-596b
|
K +31
|
K 3x +31
|
|
6otiA
|
Carbonic anhydrase ix mimic complexed with ureic benzene sulfonamide mb9-561b
|
K +31
|
K 3x +31
|
|
6otmA
|
Carbonic anhydrase ix mimic complexed with ureic benzene sulfonamide mb10-586b
|
S +31
|
S 3x +31
|
|
6otoA
|
Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb9-561b
|
S +31
|
S 3x +31
|
|
6otkA
|
Carbonic anhydrase ix mimic complexed with ureido benzene sulfonamide mb10-596b
|
K +31
|
K 3x +31
|
|
6ux1A
|
Carbonic anhydrase ii complexed with salicylic acid
|
S +31
|
S 3x +31
|
|
6rm1A
|
Human carbonic anhydrase ii in complex with fragment.
|
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
|
K +31
|
K 3x +31
|
|
6vj3A
|
Carbonic anhydrase ii in complex with pyrimidine-based inhibitor
|
S +31
|
S 3x +31
|
|
6uh0A
|
Human carbonic anhydrase 2 in complex with sb4-202
|
S +31
|
S 3x +31
|
|
6ugrA
|
Human carbonic anhydrase 2 complexed with sb4-208
|
K +31
|
K 3x +31
|
|
6ugnA
|
Human carbonic anhydrase 2 complexed with sb4-205
|
S +31
|
S 3x +31
|
|
6ugpA
|
Human carbonic anhydrase 2 complexed with sb4-206
|
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 7x +31
|
|
6pdvA
|
Cu-carbonic anhydrase ii, a nitrite reductase
|
S +31
|
|
|
6peaA
|
High resolution apo carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6u4tA
|
Carbonic anhydrase 9 in complex with sb4197
|
S +31
|
S 3x +31
|
|
6u4qA
|
Carbonic anhydrase 2 in complex with sb4197
|
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
|
|
6nm0A
|
Selective inhibition of carbonic anhydrase ix activity, using compound slc-149, displays limited anticancer effects in breast cancer cell lines
|
S +31
|
S 19x +31
|
|
6i2fA
|
Human carbonic anhydrase ii in complex with 4-propoxybenzenesulfonamide
|
S +31
|
S 15x +31
|
|
6i1uA
|
Human carbonic anhydrase ii in complex with 4-ethoxybenzenesulfonamide
|
K +31
|
K 31x +31
|
|
6i0wA
|
Human carbonic anhydrase ii in complex with 4-methoxybenzenesulfonamide
|
S +31
|
S 15x +31
|
|
6hxdA
|
Human carbonic anhydrase ii in complex with 4-butylbenzenesulfonamide
|
K +31
|
K 15x +31
|
|
6hr3A
|
Human carbonic anhydrase ii in complex with 4-propylbenzenesulfonamide
|
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
|
4
|
6nj3A
|
Thermostable variant of human carbonic anhydrase with ordered tetrazine 2.0 at site 233
|
K +31
|
K 3x +31
|
4
|
6nj2A
|
Thermostable carbonic anhydrase ii variant with tetrazine 2.0 at site 186
|
K +31
|
K 3x +31
|
3
|
6nj5A
|
Thermostable variant of human carbonic anhydrase ii with disordered tetrazine 2.0 at site 233
|
K +31
|
K 3x +31
|
4
|
6nj4A
|
Thermostable variant of human carbonic anhydrase with disordered tetrazine 2.0 reacted with strained trans-cyclooctene at site 233
|
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
|
|
6ql2A
|
Crystal structure of chimeric carbonic anhydrase vi with ethoxzolamide.
|
K +31
|
K 3x +31
|
|
6ql3A
|
Crystal structure of chimeric carbonic anhydrase vi with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6hzxA
|
Protein-aromatic foldamer complex crystal structure
|
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
|
|
6gxeA
|
Carbonic anhydrase caix mimic in complex with inhibitor js14
|
S +31
|
S 3x +31
|
|
6gxbA
|
Carbonic anhydrase caix mimic in complex with inhibitor js13
|
S +31
|
S 15x +31
|
|
6gdcA
|
Human carbonic anhydrase ii in complex with benzenesulfonamide
|
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
|
|
6qfvA
|
Human carbonic anhydrase ii with bound ircp* complex (cofactor 8) 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
|
|
6qfwA
|
Human carbonic anhydrase ii with bound ircp* complex (cofactor 9) to generate an artificial transfer hydrogenase (athase)
|
S +31
|
S 3x +31
|
|
6mbvA
|
Carbonic anhydrase ii in complex with nicotinic 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
|
|
6mbyA
|
Carbonic anhydrase ii in complex with ferulic 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
|
|
6gcyA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin-sugar conjugate complex)
|
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
|
|
6fjjA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin).
|
S +31
|
S 3x +31
|
|
6h6sA
|
Sad phasing on nickel-substituted human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6hx5A
|
Selenols: a new class of carbonic anhydrase inhibitors
|
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 2x +31
|
|
6h2zA
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide.
|
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
|
|
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.
|
K +31
|
K 3x +31
|
|
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.
|
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
|
|
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.
|
K +31
|
K 3x +31
|
|
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.
|
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
|
4
|
6g3qA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor famotidine
|
S +31
|
S 7x +31
|
|
5thiA
|
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2 l198g
|
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
|
|
5n25A
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-pyridin-3-yl-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6b59A
|
Carbonic anhydrase ii in complex with nitrogenous base-bearing benezenesulfonamide
|
S +31
|
S 3x +31
|
|
4yglA
|
Naclo4--interactions between hofmeister anions and the binding pocket of a protein
|
K +31
|
K 3x +31
|
|
3iqkA
|
Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
|
K +31
|
K 3x +31
|
|
5tfxA
|
New method for synthesis of benzoxazole amide inhibitors of carbonic anhydrase
|
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
|
K +31
|
K 11x +31
|
|
4mdlA
|
Meta carborane carbonic anhydrase 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
|
K +31
|
K 11x +31
|
|
4fptA
|
Carbonic anhydrase ii in complex with ethyl (2z,4r)-2-(sulfamoylimino)-1,3-thiazolidine-4-carboxylate
|
S +31
|
S 6x +31
|
|
3ieoA
|
The coumarin-binding site in carbonic anhydrase: the antiepileptic lacosamide as an example
|
K +31
|
K 3x +31
|
4
|
3s72B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 11x +31
|
|
3nj9A
|
Crystal structure of carbonic anhydrase ii in complex with a nir inhibitor
|
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
|
K +31
|
K 3x +31
|
|
3dazA
|
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
|
4
|
2nnvA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
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
|
|
2eu3A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
S +31
|
S 3x +31
|
|
3mnkA
|
Human carbonic anhydrase ii mutant k170h
|
K +31
|
K 3x +31
|
|
2vvbX
|
Human carbonic anhydrase ii in complex with bicarbonate
|
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
|
S +31
|
S 7x +31
|
|
4xe1A
|
Human carbonic anhydrase ii in complex with 6-sulfamoyl-saccharin
|
S +31
|
S 3x +31
|
|
5eh5A
|
Human carbonic anhydrase ii in complex with ligand
|
K +31
|
K 3x +31
|
|
4z1eA
|
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
|
|
4rn4A
|
Human carbonic anhydrases ii in complex with a acetazolamide derivative comprising one hydrophobic and one hydrophilic tail moiety
|
S +31
|
S 3x +31
|
|
4pq7A
|
The crystal structure of the human carbonic anhydrase ii in complex with a sulfamide inhibitor
|
K +31
|
K 3x +31
|
|
3kkxA
|
Neutron structure of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
4l5vA
|
The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
3u3aX
|
Structure of human carbonic anhydrase ii v143i
|
K +31
|
K 3x +31
|
|
3hknA
|
Human carbonic anhydrase ii in complex with (2,3,4,6-tetra-o-acetyl-beta-d-galactopyranosyl) -(1-4)-1,2,3,6-tetra-o-acetyl-1-thio-beta-d-glucopyranosylsulfonamide
|
S +31
|
S 3x +31
|
|
3hljA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-methylthiobenzimidazo[1,2-c][1,2,3]thiadiazol-7-sulfonamide
|
S +31
|
S 3x +31
|
|
3oikA
|
Human carbonic anhydrase ii mutant a65s, n67q (ca ix mimic) bound by 2-ethylestradiol 3,17-o,o-bis-sulfamate
|
S +31
|
S 3x +31
|
|
4k13A
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with dorzolamide
|
S +31
|
S 3x +31
|
|
5txyA
|
Identification of a new zinc binding chemotype of by fragment screening on human carbonic anhydrase
|
K +31
|
K 3x +31
|
|
3ryjB
|
Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide
|
K +31
|
K 3x +31
|
|
5sz5A
|
Carbonic anhydrase ix-mimic in complex with 4-(2-methylphenyl)-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
3rz1B
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|