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 4x +31
|
|
6sdtA
|
Human carbonic anhydrase vii 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
|
|
|
6peaA
|
High resolution apo carbonic anhydrase ii
|
S +31
|
S 7x +31
|
|
6pdvA
|
Cu-carbonic anhydrase ii, a nitrite reductase
|
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 15x +31
|
|
6i1uA
|
Human carbonic anhydrase ii in complex with 4-ethoxybenzenesulfonamide
|
S +31
|
S 19x +31
|
|
6i2fA
|
Human carbonic anhydrase ii in complex with 4-propoxybenzenesulfonamide
|
S +31
|
S 15x +31
|
|
6hxdA
|
Human carbonic anhydrase ii in complex with 4-butylbenzenesulfonamide
|
S +31
|
|
|
6scfA
|
A viral anti-crispr subverts type iii crispr immunity by rapid degradation of cyclic oligoadenylate
|
S +31
|
|
1
|
6tysA
|
A potent cross-neutralizing antibody targeting the fusion glycoprotein inhibits nipah virus and hendra virus infection
|
S +31
|
|
|
6qd7A
|
Em structure of a ebov-gp bound to 3t0331 neutralizing antibody
|
S +31
|
|
|
6qd8A
|
Em structure of a ebov-gp bound to 4m0368 neutralizing antibody
|
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
|
|
|
6psoA
|
Crystal structure of pss1_19b c77s in complex with iota-neocarratetraose
|
S +31
|
|
|
6prmA
|
Crystal structure of apo pss1_19b
|
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
|
|
1
|
6dc5A
|
Rsv prefusion f in complex with am22 fab
|
S +31
|
S 3x +31
|
|
6hd2A
|
Active-site conformational dynamics of carbonic anhydrase ii under native conditions: an nmr perspective
|
S +31
|
|
1
|
6eajF
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant t400a stabilized in the prefusion state
|
S +31
|
|
1
|
6eamF
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant e487d stabilized in the prefusion state
|
S +31
|
|
1
|
6eakF
|
Crystal structure of fusion inhibitor jnj-2408068 in complex with human respiratory syncytial virus fusion glycoprotein escape variant t400a stabilized in the prefusion state
|
S +31
|
|
1
|
6eaiA
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant s398l stabilized in the prefusion state
|
S +31
|
|
1
|
6eahA
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant k394r-s398l stabilized in the prefusion state
|
S +31
|
|
1
|
6eagF
|
Crystal structure of fusion inhibitor jnj-2408068 in complex with human respiratory syncytial virus fusion glycoprotein escape variant g143s stabilized in the prefusion state
|
S +31
|
|
1
|
6eafA
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant g143s stabilized in the prefusion state
|
S +31
|
|
1
|
6eadF
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant f140i stabilized in the prefusion state
|
S +31
|
|
1
|
6eanF
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant f488i stabilized in the prefusion state
|
S +31
|
|
1
|
6ealF
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant d486n stabilized in the prefusion state
|
S +31
|
|
1
|
6eaeF
|
Crystal structure of human respiratory syncytial virus fusion glycoprotein inhibitor escape variant l141w stabilized in the prefusion state
|
S +31
|
|
1
|
6dc3F
|
Rsv prefusion f bound to rsd5 fab
|
S +31
|
|
|
6hhmA
|
Crystal structure of the family s1_7 ulvan-specific sulfatase fa22070 from formosa agariphila
|
S +31
|
|
1
|
6j66A
|
Chondroitin sulfate/dermatan sulfate endolytic 4-o-sulfatase
|
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 15x +31
|
|
6gdcA
|
Human carbonic anhydrase ii in complex with benzenesulfonamide
|
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
|
|
1
|
6o0hA
|
Cryo-em structure of human atp-citrate lyase in complex with inhibitor ndi-091143
|
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 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
|
|
6h34A
|
The crystal structure of human carbonic anhydrase ii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
|
S +31
|
S 4x +31
|
|
6h37A
|
The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide
|
S +31
|
S 4x +31
|
|
6h38A
|
The crystal structure of human carbonic anhydrase vii 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 7x +31
|
|
5thiA
|
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2 l198g
|
S +31
|
|
1
|
6mlkA
|
Structure of thioesterase from debs with a thioesterase-specific antibody
|
S +31
|
S 3x +31
|
|
4yglA
|
Naclo4--interactions between hofmeister anions and the binding pocket of a protein
|
S +31
|
S 23x +31
|
|
1bnnA
|
Carbonic anhydrase ii inhibitor
|
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 7x +31
|
|
1bv3A
|
Human carbonic anhydrase ii complexed with urea
|
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 1x +31
|
|
12caA
|
Altering the mouth of a hydrophobic pocket. structure and kinetics of human carbonic anhydrase ii mutants at residue val-121
|
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
|
|
3w6iA
|
Crystal structure of 19f probe-labeled hcai
|
S +31
|
S 3x +31
|
4
|
2foqA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
S +31
|
S 3x +31
|
|
5bu6B
|
Structure of bpsb deaceylase domain from bordetella bronchiseptica
|
S +31
|
S 11x +31
|
|
1bn4A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
4q49A
|
Room temperature neutron crystal structure of apo human carbonic anhydrase at ph 7.5
|
S +31
|
S 3x +31
|
|
1yo0A
|
Proton transfer from his200 in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4zwzA
|
Engineered carbonic anhydrase ix mimic in complex with a glucosyl sulfamate inhibitor
|
S +31
|
S 11x +31
|
|
1heaA
|
Carbonic anhydrase ii (carbonate dehydratase) (hca ii) (e.c.4.2.1.1) mutant with leu 198 replaced by arg (l198r)
|
S +31
|
S 3x +31
|
|
3ryvB
|
Carbonic anhydrase complexed with n-ethyl-4-sulfamoylbenzamide
|
S +31
|
S 3x +31
|
|
4g7aA
|
The crystal structure of an alpha carbonic anhydrase from the extremophilic bacterium sulfurihydrogenibium yellowstonense yo3aop1
|
S +31
|
S 3x +31
|
|
5txyA
|
Identification of a new zinc binding chemotype of by fragment screening on human carbonic anhydrase
|
S +31
|
S 3x +31
|
|
1te3X
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4k13A
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with dorzolamide
|
S +31
|
S 11x +31
|
|
1fqlA
|
X-ray crystal structure of zinc-bound f95m/w97v carbonic anhydrase (caii) variant
|
S +31
|
S 3x +31
|
|
1hugA
|
Differences in anionic inhibition of human carbonic anhydrase i revealed from the structures of iodide and gold cyanide inhibitor complexes
|
S +31
|
S 3x +31
|
|
3rz1B
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
S 3x +31
|
4
|
3fe4A
|
Crystal structure of human carbonic anhydrase vi
|