S +31
|
S 3x +31
|
|
5wgpA
|
Human carbonic anhydrase ix-mimic complexed with acek
|
S +31
|
S 3x +31
|
|
5fl4A
|
Three dimensional structure of human carbonic anhydrase ix in complex with 5-(1-naphthalen-1-yl-1,2,3-triazol-4-yl)thiophene-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5ekjA
|
Human carbonic anhydrase ii complexed with a two-faced guest
|
S +31
|
S 3x +31
|
4
|
4zwiA
|
Surface lysine acetylated human carbonic anhydrase ii in complex with a sulfamate-based inhibitor
|
S +31
|
S 3x +31
|
|
4zwyA
|
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
3tvoX
|
Human carbonic anhydrase ii proton transfer double mutant
|
S +31
|
S 3x +31
|
|
4jswA
|
Human carbonic anhydrase ii h94c
|
S +31
|
S 3x +31
|
|
3t83A
|
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
|
S +31
|
S 3x +31
|
|
4hf3A
|
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure
|
S +31
|
S 3x +31
|
|
3lxeA
|
Human carbonic anhydrase i in complex with topiramate
|
S +31
|
S 3x +31
|
|
3u7cA
|
Crystal structure of the v143i mutant of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3u45X
|
Human carbonic anhydrase ii v143a
|
S +31
|
S 3x +31
|
|
1xpzA
|
Structure of human carbonic anhydrase ii with 4-[4-o-sulfamoylbenzyl)(4-cyanophenyl)amino]-4h-[1,2,4]-triazole
|
S +31
|
S 3x +31
|
|
3hktA
|
Human carbonic anhydrase ii in complex with alpha-d-glucopyranosyl-(1->4)-1-thio-beta-d-glucopyranosylsulfonamide
|
S +31
|
S 3x +31
|
|
3p4vA
|
Human carbonic anhydrase ii in complex with (+)-xylariamide a
|
S +31
|
S 3x +31
|
|
3l14A
|
Human carbonic anhydrase ii complexed with althiazide
|
S +31
|
S 3x +31
|
|
1ugbA
|
Human carbonic anhydrase ii[hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by gly (a65g)
|
S +31
|
S 3x +31
|
|
3oilA
|
Human carbonic anhydrase ii mutant a65s, n67q (ca ix mimic) bound by 2-ethylestradiol 3-o-sulfamate
|
S +31
|
S 3x +31
|
|
3dvcA
|
X-ray crystal structure of mutant n62t of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1cncA
|
Compensatory plastic effects in the redesign of protein-zinc binding sites
|
S +31
|
S 3x +31
|
|
1lg6A
|
Crystal structure analysis of hca ii mutant t199p in complex with thiocyanate
|
S +31
|
S 3x +31
|
|
3v3gB
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
S +31
|
S 3x +31
|
|
3hfpA
|
Crystal structure of teh complex between ca ii and the activator mai
|
S +31
|
S 3x +31
|
|
2nn1A
|
Structure of inhibitor binding to carbonic anhydrase i
|
S +31
|
S 3x +31
|
|
5dsmA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 25 min warming
|
S +31
|
S 3x +31
|
|
5dslA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 10 min warming
|
S +31
|
S 3x +31
|
|
4m2vA
|
Genetically engineered carbonic anhydrase ix in complex with brinzolamide
|
S +31
|
S 3x +31
|
|
3s77B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 3x +31
|
|
5yuiA
|
Co2 release in human carbonic anhydrase ii crystals: reveal histidine 64 and solvent dynamics
|
S +31
|
S 3x +31
|
|
5n0eA
|
Crystal structure of human carbonic anhydrase ii in complex with (s)-4-(6,7-dihydroxy-1-phenyl-3,4-tetrahydroisoquinoline-1h-2-carbonyl)benzenesulfonamide.
|
S +31
|
S 3x +31
|
|
5llhA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-(1,3-benzothiazol-2-ylthio)-2,3,5,6-tetrafluorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
6d1mA
|
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects
|
S +31
|
S 3x +31
|
|
1cvdA
|
Structural consequences of redesigning a protein-zinc binding site
|
S +31
|
S 3x +31
|
|
3m1wA
|
Carbonic anhyrdase ii mutant w5ch64c with closed disulfide bond in complex with sulfate
|
S +31
|
S 3x +31
|
|
5fngA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
3uyqA
|
Hca 3
|
S +31
|
S 3x +31
|
|
3m5sA
|
Carbonic anhydrase ii mutant h64c in complex with carbonate
|
S +31
|
S 3x +31
|
|
2weoA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
S +31
|
S 3x +31
|
|
2nn7A
|
Structure of inhibitor binding to carbonic anhydrase i
|
S +31
|
S 3x +31
|
|
5ogoA
|
Crystal structure of chimeric carbonic anhydrase i with 3-(benzylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4xfwA
|
Crystal structure of the monoclinic form of alpha-carbonic anhydrase from the human pathogen helicobacter pylori
|
S +31
|
S 3x +31
|
|
4zwxA
|
Engineered carbonic anhydrase ix mimic in complex with glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
4xiwA
|
Carbonic anhydrase cah3 from chlamydomonas reinhardtii in complex with acetazolamide
|
S +31
|
S 3x +31
|
|
4riuA
|
A carbonic anhydrase ix mimic in complex with a saccharin-based inhibitor
|
S +31
|
S 3x +31
|
|
4cq0A
|
Cyclic secondary sulfonamides: unusually good inhibitors of cancer- related carbonic anhydrase enzymes
|
S +31
|
S 3x +31
|
|
4cnxA
|
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture
|
S +31
|
S 3x +31
|
|
3dccA
|
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
|
|
1fljA
|
Crystal structure of s-glutathiolated carbonic anhydrase iii
|
S +31
|
S 3x +31
|
|
2aw1A
|
Carbonic anhydrase inhibitors: valdecoxib binds to a different active site region of the human isoform ii as compared to the structurally related cyclooxygenase ii "selective" inhibitor celecoxib
|
S +31
|
S 3x +31
|
|
1crmA
|
Structure and function of carbonic anhydrases
|
S +31
|
S 3x +31
|
|
1fr7A
|
X-ray crystal structure of zinc-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
|
S +31
|
S 3x +31
|
|
3mnhA
|
Human carbonic anhydrase ii mutant k170a
|
S +31
|
S 3x +31
|
|
3p58A
|
Human carbonic anhydrase in complex with benzyl (methyl) carbamodithoic acid
|
S +31
|
S 3x +31
|
|
6bc9A
|
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with dorzolamide
|
S +31
|
S 3x +31
|
|
5wg7A
|
Human carbonic anhydrase ii complexed with acek
|
S +31
|
S 3x +31
|
|
5mjnA
|
Three dimensional structure of human carbonic anhydrase ii in complex with 5-[(4chlorobenzyl)sulfanyl]thiophene-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5jg3B
|
Human carbonic anhydrase ii (121t/n67q) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5jegB
|
Human carbonic anhydrase ii (v121i) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5j8zA
|
Human carbonic anhydrase ii in complex with ligand
|
S +31
|
S 3x +31
|
|
4y0jA
|
H/d exchanged human carbonic anhydrase ii ph 6 room temperature neutron crystal structure.
|
S +31
|
S 3x +31
|
|
5c8iA
|
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with methazolamide
|
S +31
|
S 3x +31
|
|
4zx0A
|
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
4rfdA
|
Human carbonic anhydrase ii in complex with 4-(4-sulfamoyl-phenoxy)-butylammonium
|
S +31
|
S 3x +31
|
|
4q0lA
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
S +31
|
S 3x +31
|
|
4l5wA
|
Structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4cacA
|
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution
|
S +31
|
S 3x +31
|
|
3tvnX
|
Human carbonic anhydrase ii proton transfer mutant
|
S +31
|
S 3x +31
|
|
4hezA
|
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure
|
S +31
|
S 3x +31
|
|
3rg3A
|
Crystal structure of the w5e mutant of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3t84A
|
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
|
S +31
|
S 3x +31
|
|
3oimA
|
Human carbonic anhydrase ii bound by 2-ethylestradiol 3-o-sulfamate
|
S +31
|
S 3x +31
|
|
3rg4A
|
Crystal structure of the w5f mutant of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3rgeA
|
Crystal structure of the w5h mutant of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3p3hA
|
Human carbonic anhydrase ii in complex with p-(5-ferrocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
3oy0A
|
Human carbonic anhydrase ii complexed with 1-(4-(4-(2-(isopropylsulfonyl)phenylamino)-1h-pyrrolo[2,3-b]pyridin-6-ylamino)-3-methoxyphenyl)piperidin-4-ol
|
S +31
|
S 3x +31
|
|
2nxrA
|
Structural effects of hydrophobic mutations on the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1tg3A
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
2nxsA
|
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1yo1A
|
Proton transfer from his200 in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1cvcA
|
Redesigning the zinc binding site of human carbonic anhydrase ii: structure of a his2asp-zn2+ metal coordination polyhedron
|
S +31
|
S 3x +31
|
|
1hecA
|
Structural consequences of hydrophilic amino-acid substitutions in the hydrophobic pocket of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1teuX
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1tg9A
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1lzvA
|
Site-specific mutant (tyr7 replaced with his) of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1rzeA
|
X-ray analysis of metal substituted human carbonic anhydrase ii derivatives
|
S +31
|
S 3x +31
|
|
1kwrA
|
Human carbonic anhydrase ii complexed with inhibitor 0134-36
|
S +31
|
S 3x +31
|
|
1cajA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6b4dA
|
Crystal structure of human carbonic anhydrase ii in complex with a heteroaryl-pyrazole carboxylic acid derivative.
|
S +31
|
S 3x +31
|
|
1camA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1cvaA
|
Structural and functional importance of a conserved hydrogen bond network in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5n0dA
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(6,7-dihydroxy-1-phenyl-3,4-tetrahydroisoquinoline-1h-2-carbonyl)benzenesulfonamide.
|
S +31
|
S 3x +31
|
|
5zxwA
|
Crystal structure of human carbonic anhydrase ii crystallized by ammonium sulfate
|
S +31
|
S 3x +31
|
|
5llaA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 4-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
5ll5A
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-(1h-benzimidazol-1-ylacetyl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5gmmA
|
Crystal structure of human carbonic anhydrase i in complex with polmacoxib
|
S +31
|
S 3x +31
|
|
5e28A
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-(4-aminophenyl)benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4yvyA
|
Crystal structure of human carbonic anhydrase ii in complex with hydroxylamine-o-sulfonamide, a molecule incorporating two zinc-binding groups.
|
S +31
|
S 3x +31
|
|
4qjxA
|
Crystal structure of human carbonic anhydrase isozyme xiii with inhibitor
|
S +31
|
S 3x +31
|
|
4knmA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4kuwA
|
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(4-fluorophenylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
3n4bA
|
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
3mdzA
|
Crystal structure of human carbonic anhydrase vii [isoform 1], ca7
|
S +31
|
S 3x +31
|
|
1xegA
|
Crystal structure of human carbonic anhydrase ii complexed with an acetate ion
|
S +31
|
S 3x +31
|
|
4qiyA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
S +31
|
S 3x +31
|
|
4pzhA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2,3,5,6-tetrafluoro-4[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4q6eA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[3-(3,5-dimethyl-1h-pyrazol-1-yl)-3-oxopropyl]amino}benzene-1-sulfonamide
|
S +31
|
S 3x +31
|
|
4ht0A
|
Crystal structure of human carbonic anhydrase isozyme ii with the inhibitor.
|
S +31
|
S 3x +31
|
|
1ccuA
|
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity
|
S +31
|
S 3x +31
|
|
3n3jA
|
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4ruyA
|
Crystal structure of human carbonic anhydrase ii in complex with 4-propoxybenzenesulfonamide
|
S +31
|
S 3x +31
|
|
6fagA
|
Crystal structure of human carbonic anhydrase i in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-(2-methoxyphenyl)urea inhibitor
|
S +31
|
S 3x +31
|
|
6ex1A
|
Crystal structure of human carbonic anhydrase i in complex with the 4-[(3s)-3 benzyl-4-(4-sulfamoylbenzoyl)piperazine -1-carbonyl]benzene-1-sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
6fafA
|
Crystal structure of human carbonic anhydrase i in complex with the 3-(2,5-dimethylphenyl)-1-(2-hydroxy-5-sulfamoylphenyl)urea inhibitor
|
S +31
|
S 3x +31
|
|
6f3bA
|
Crystal structure of human carbonic anhydrase i in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-[(4-methylphenyl)methyl]urea inhibitor
|
S +31
|
S 3x +31
|
|
2nwpA
|
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1h4nA
|
H94n carbonic anhydrase ii complexed with tris
|
S +31
|
S 3x +31
|
|
3pjjA
|
Synthetic dimer of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
2nwyA
|
Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1ca2A
|
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution
|
S +31
|
S 3x +31
|
|
4kv0A
|
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-tosylureido)pyridine-2-sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4qjoA
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
S +31
|
S 3x +31
|
|
4qjpA
|
Crystal structure of human carbonic anhydrase isozyme xiii with inhibitor
|
S +31
|
S 3x +31
|
|
4hbaA
|
Structural and catalytic characterization of a thermal and acid stable variant of human carbonic anhydrase ii containing an engineered disulfide bond
|
S +31
|
S 3x +31
|
|
4l5uA
|
The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4kuvA
|
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(4-chlorophenylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
5n24A
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor b4'-cyano-biphenyl-4-sulfonic acid amide
|
S +31
|
S 3x +31
|
|
4rfcA
|
Human carbonic anhydrase ii in complex with tert-butyl 4-(4-sulfamoylphenoxy)butylcarbamate
|
S +31
|
S 3x +31
|
|
5sz6A
|
Carbonic anhydrase ix-mimic in complex with 4-(3-formylphenyl)-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4e49A
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
S +31
|
S 3x +31
|
4
|
2fouA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
S +31
|
S 3x +31
|
|
2cbbA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
S +31
|
S 3x +31
|
|
1jd0A
|
Crystal structure of the extracellular domain of human carbonic anhydrase xii complexed with acetazolamide
|
S +31
|
S 3x +31
|
|
3tmjA
|
Joint x-ray/neutron structure of human carbonic anhydrase ii at ph 7.8
|
S +31
|
S 3x +31
|
|
3b4fA
|
Carbonic anhydrase inhibitors. interaction of 2-(hydrazinocarbonyl)-3-phenyl-1h-indole-5-sulfonamide with twelve mammalian isoforms: kinetic and x-ray crystallographic studies
|
S +31
|
S 3x +31
|
|
3efiA
|
Carbonic anhydrase activators: kinetic and x-ray crystallographic study for the interaction of d- and l-tryptophan with the mammalian isoforms i-xiv
|
S +31
|
S 3x +31
|
|
3dbuA
|
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
|
|
3kokA
|
Crystal structure of cobalt (ii) human carbonic anhydrase ii at ph 8.5
|
S +31
|
S 3x +31
|
4
|
3eftA
|
Crystal structure of the complex between carbonic anhydrase ii and a spin-labeled sulfonamide incorporating tempo moiety
|
S +31
|
S 3x +31
|
|
2wegA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
S +31
|
S 3x +31
|
|
3ffpX
|
X ray structure of the complex between carbonic anhydrase ii and lc inhibitors
|
S +31
|
S 3x +31
|
|
3v5gA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-sulfamido-benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4cnwA
|
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture
|
S +31
|
S 3x +31
|
|
3d0nA
|
Crystal structure of human carbonic anhydrase xiii
|
S +31
|
S 3x +31
|
|
6h29A
|
Human carbonic anhydrase ii in complex with benzyl carbamate
|
S +31
|
S 3x +31
|
|
1bcdA
|
X-ray crystallographic structure of a complex between human carbonic anhydrase ii and a new topical inhibitor, trifluoromethane sulphonamide
|
S +31
|
S 3x +31
|
|
1rzaA
|
X-ray analysis of metal substituted human carbonic anhydrase ii derivatives
|
S +31
|
S 3x +31
|
|
1rzcA
|
X-ray analysis of metal substituted human carbonic anhydrase ii derivatives
|
S +31
|
S 3x +31
|
|
1rzdA
|
X-ray analysis of metal substituted human carbonic anhydrase ii derivatives
|
S +31
|
S 3x +31
|
|
1lg5A
|
Crystal structure analysis of the hca ii mutant t199p in complex with beta-mercaptoethanol
|
S +31
|
S 3x +31
|
|
1tbtX
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|