K +31
|
K 3x +31
|
4
|
5tt3A
|
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with ethoxzolamide
|
K +31
|
K 3x +31
|
|
5g01A
|
An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
|
S +31
|
S 3x +31
|
|
4xixA
|
Carbonic anhydrase cah3 from chlamydomonas reinhardtii in complex with phosphate.
|
K +31
|
K 3x +31
|
|
4ywpA
|
Sucrose binding site in genetically engineered carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
3r17B
|
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
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 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
|
|
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 7x +31
|
|
1g3zA
|
Carbonic anhydrase ii (f131v)
|
S +31
|
S 11x +31
|
|
1bn3A
|
Carbonic anhydrase ii inhibitor
|
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 7x +31
|
|
1bnqA
|
Carbonic anhydrase ii inhibitor
|
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 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)
|
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
|
K +31
|
K 3x +31
|
|
2fnnA
|
Activation of human carbonic anhydrase ii by exogenous proton donors
|
S +31
|
S 3x +31
|
4
|
2x7sA
|
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors.
|
S +31
|
S 7x +31
|
|
5fdiA
|
Crystal structure of human carbonic anhydrase ii with the anticonvulsant sulfamide jnj-26990990 and its s,s-dioxide analog.
|
S +31
|
S 3x +31
|
4
|
2nngA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
3p3jA
|
Human carbonic anhydrase ii in complex with p-(5-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
5jesB
|
Human carbonic anhydrase ii (v121t) complexed with benzo[d]thiazole-2-sulfonamide
|
K +31
|
K 3x +31
|
|
3gz0A
|
Apo-human carbonic anhydrase ii revisited: implications of the loss of a metal in protein structure, stability and solvent network
|
S +31
|
S 3x +31
|
|
3w6iA
|
Crystal structure of 19f probe-labeled hcai
|
K +31
|
K 3x +31
|
|
4qk1A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - k170p
|
K +31
|
K 3x +31
|
|
5floA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
4
|
2foqA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
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
|
K +31
|
K 3x +31
|
|
5cjfA
|
The crystal structure of the human carbonic anhydrase xiv in complex with a 1,1'-biphenyl-4-sulfonamide inhibitor.
|
K +31
|
K 3x +31
|
|
1z97A
|
Human carbonic anhydrase iii: structural and kinetic study of catalysis and proton transfer.
|
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
|
K +31
|
K 3x +31
|
|
1fsqA
|
X-ray crystal structure of cobalt-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
|
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
|
K +31
|
K 3x +31
|
|
3ryjB
|
Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide
|
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
|
|
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
|
S +31
|
S 3x +31
|
|
3bl1A
|
Carbonic anhydrase inhibitors. sulfonamide diuretics revisited old leads for new applications
|
S +31
|
S 3x +31
|
|
3p44A
|
Human carbonic anhydrase ii in complex with p-(4-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
K +31
|
K 7x +31
|
|
1ze8A
|
Carbonic anhydrase ii in complex with a membrane-impermeant sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4z1nA
|
Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv)
|
K +31
|
K 3x +31
|
|
4ygnA
|
Nai--interactions between hofmeister anions and the binding pocket of a protein
|
K +31
|
K 3x +31
|
|
5lmdA
|
The crystal structure of hca ii in complex with a benzoxaborole inhibitor
|
S +31
|
S 3x +31
|
|
1lgdA
|
Crystal structure analysis of hca ii mutant t199p in complex with bicarbonate
|
S +31
|
S 3x +31
|
|
5fnjA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
6equA
|
X-ray crystal structure of the human carbonic anhydrase ii adduct with a membrane-impermeant inhibitor
|
K +31
|
K 3x +31
|
4
|
5jgsB
|
Human carbonic anhydrase ii (f131y/l198a) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 11x +31
|
|
2gd8A
|
Crystal structure analysis of the human carbonic anhydrase ii in complex with a 2-substituted estradiol bis-sulfamate
|
S +31
|
S 3x +31
|
|
3mwoA
|
Human carbonic anhydrase ii in a doubled monoclinic cell: a re-determination
|
S +31
|
S 3x +31
|
|
5e2sA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-(2-iso-propylphenyl)benzenesulfonamide inhibitor
|
S +31
|
S 15x +31
|
|
4q81A
|
Crystal structure of 1-hydroxy-4,6-dimethylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4heyA
|
Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure
|
S +31
|
S 7x +31
|
|
1g45A
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2-fluorophenyl)methyl]-benzamide
|
K +31
|
K 3x +31
|
|
4z1kA
|
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 22x +31
|
|
1bntA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 15x +31
|
|
4js6A
|
Crystal structure of inhibitor-free hcaii h94d
|
S +31
|
S 3x +31
|
|
2vvaX
|
Human carbonic anhydrase in complex with co2
|
S +31
|
S 3x +31
|
|
5amlA
|
Three dimensional structure of human carbonic anhydrase ii in complex with 2-(but-2-yn-1-ylsulfamoyl)-4-sulfamoylbenzoic acid
|
S +31
|
S 3x +31
|
|
5eh8A
|
Human carbonic anhydrase ii in complex with ligand
|
S +31
|
S 3x +31
|
|
5e2nA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
K 3x +31
|
|
2pouA
|
The crystal structure of the human carbonic anhydrase ii in complex with 4,5-dichloro-benzene-1,3-disulfonamide
|
S +31
|
S 3x +31
|
|
3dcsA
|
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
S +31
|
S 15x +31
|
|
1g53A
|
Carbonic anhydrase ii complexed with 4-(aminosulfonyl)-n-[(2,6-difluorophenyl)methyl]-benzamide
|
S +31
|
S 3x +31
|
|
5fl6A
|
Three dimensional structure of human carbonic anhydrase ix in complex with 5-(1-(4-methylphenyl)-1h-1,2,3-triazol-4-yl)thiophene-2- sulfonamide
|
S +31
|
S 3x +31
|
|
1eouA
|
Crystal structure of human carbonic anhydrase ii complexed with an anticonvulsant sugar sulfamate
|
K +31
|
K 3x +31
|
|
6b00A
|
Thermostabilized mutant of human carbonic anhydrase ii - a65t l100h k154n l224s l240p a248t
|
S +31
|
S 3x +31
|
|
4zaoA
|
Genetically engineered carbonic anhydrase ix
|
K +31
|
K 3x +31
|
|
5u0eA
|
Identification of a new zinc binding chemotype by fragment screening
|
S +31
|
S 11x +31
|
|
4yx4A
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (1).
|
S +31
|
S 3x +31
|
|
5fniA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
4r5bA
|
Human carbonic anhydrase ii in complex with a carbohydrate-based sulfamate
|
S +31
|
S 3x +31
|
|
3m5tA
|
Fragment tethered to carbonic anhydrase ii h64c mutant
|
K +31
|
K 3x +31
|
|
5g0bA
|
An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
|
K +31
|
K 3x +31
|
|
5ll9A
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
|
K +31
|
K 3x +31
|
4
|
4r5aA
|
A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
|
S +31
|
S 3x +31
|
|
5dsjA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 50 sec warming
|
S +31
|
S 7x +31
|
|
1g48A
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,6-difluorophenyl)methyl]-benzamide
|
K +31
|
K 3x +31
|
|
2fnkA
|
Activation of human carbonic anhydrase ii by exogenous proton donors
|
S +31
|
S 3x +31
|
|
3hkqA
|
Human carbonic anhydrase ii in complex with 1-s-d-galactopyranosylsulfonamide
|
K +31
|
K 3x +31
|
|
5fnmA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 7x +31
|
|
4q7vA
|
Crystal structure of 1-hydroxy-5-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3m2zA
|
Fragment tethered to carbonic anhydrase ii h64c mutant
|
K +31
|
K 3x +31
|
|
3s74B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
K +31
|
K 3x +31
|
|
3dv7A
|
Role of hydrophilic residues in proton transfer during catalysis by human carbonic anhydrase ii (n62a)
|
S +31
|
S 7x +31
|
|
1bnuA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 15x +31
|
|
4mlxA
|
Structure of a bidentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii
|
S +31
|
S 3x +31
|
|
5jg5B
|
Human carbonic anhydrase ii (v121t/f131y) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
3ks3A
|
High resolution structure of human carbonic anhydrase ii at 0.9 a
|
S +31
|
S 3x +31
|
|
4cnrA
|
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture
|
S +31
|
S 11x +31
|
|
2q1bA
|
Carbonic anhydrase ii in complex with saccharin
|
S +31
|
S 11x +31
|
|
1okmA
|
Carbonic anhydrase ii complex with the 1okm inhibitor 4-sulfonamide-[1-(4-aminobutane)]benzamide
|
S +31
|
S 3x +31
|
|
3s71B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 3x +31
|
|
3dcwA
|
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
|
|
4idrX
|
Human carbonic anhydrase ii proton transfer double mutant
|
S +31
|
S 7x +31
|
|
3m1jA
|
The crystal structure of a nami a-carbonic anhydrase ii adduct discloses the mode of action of this novel anticancer metallodrug
|
S +31
|
S 3x +31
|
|
3hs4A
|
Human carbonic anhydrase ii complexed with acetazolamide
|
S +31
|
S 3x +31
|
|
6cjvA
|
Carbonic anhydrase ix-mimic in complex with sucralose
|
S +31
|
S 3x +31
|
|
4ruxA
|
Crystal structure of human carbonic anhydrase ii in complex with 4-(allyloxy)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5jgtB
|
Human carbonic anhydrase ii (f131y/l198a) complexed with 1,3-thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5dsiA
|
Structure of co2 bound holo-form of human carbonic anhydrase ii with 0 sec (no) warming
|
S +31
|
S 3x +31
|
|
1rj6A
|
Crystal structure of the extracellular domain of murine carbonic anhydrase xiv in complex with acetazolamide
|
K +31
|
K 7x +31
|
|
4q8zA
|
Crystal structure of 1-hydroxy-4-methylpyridin-2(1h)-one bound to human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5llcA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-(methylamino)-2,5,6-trifluoro-4-[(2-phenylethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
3dd0A
|
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
K +31
|
K 3x +31
|
|
4fl7A
|
The crystal structure of human carbonic anhydrase ii in complex with n-(hydroxy)-benzamide
|
S +31
|
S 3x +31
|
|
3s78B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 3x +31
|
|
3v3jA
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
K +31
|
K 7x +31
|
|
5fdcA
|
Crystal structure of human carbonic anhydrase ii in complex with the anticonvulsant sulfamide jnj-26990990 and its s,s-dioxide analog.
|
S +31
|
S 3x +31
|
|
2it4A
|
X ray structure of the complex between carbonic anhydrase i and the phosphonate antiviral drug foscarnet
|
K +31
|
K 3x +31
|
|
2wd3A
|
Highly potent first examples of dual aromatase-steroid sulfatase inhibitors based on a biphenyl template
|
S +31
|
S 3x +31
|
|
5a6hA
|
Synthesis, carbonic anhydrase inhibition and protein x-ray structure of the unusual natural product primary sulfonamide psammaplin c
|
S +31
|
S 1x +31 +31
|
|
1koqA
|
Neisseria gonorrhoeae carbonic anhydrase
|
S +31
|
S 4x +31
|
|
5ulnA
|
Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography
|
S +31
|
S 3x +31
|
|
5u0dA
|
Identification of a new zinc binding chemotype by fragment screening
|
K +31
|
K 3x +31
|
|
4e5qA
|
Human carbonic anhydrase ii in complex with cyanate
|
S +31
|
S 3x +31
|
|
1v9iC
|
Crystal structure analysis of the site specific mutant (q253c) of bovine carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
4wl4A
|
Crystal structure of human carbonic anhydrase ii in complex with the 6-hydroxy-chromene-2-thione inhibitor
|
S +31
|
S 3x +31
|
|
1h9nA
|
H119n carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3dvdA
|
X-ray crystal structure of mutant n62d of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
5u0fA
|
Identification of a new zinc binding chemotype by fragment screening
|
S +31
|
S 3x +31
|
|
3hkuA
|
Human carbonic anhydrase ii in complex with topiramate
|
S +31
|
S 3x +31
|
|
3v3hB
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
K +31
|
K 3x +31
|
|
3v2mA
|
Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5bnlA
|
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins
|
K +31
|
K 11x +31
|
|
1g0fA
|
Site-specific mutant (his64 replaced with ala) of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
2povA
|
The crystal structure of the human carbonic anhydrase ii in complex with 4-amino-6-chloro-benzene-1,3-disulfonamide
|
K +31
|
K 3x +31
|
|
5tyaA
|
Identification of a new zinc binding chemotype by fragment screening
|
S +31
|
S 3x +31
|
|
5n1rA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4'-pyrazol-1-ylmethyl-biphenyl-4-sulfonamide
|
S +31
|
S 3x +31
|
|
5jq0A
|
Crystal structure of human carbonic anhydrase ii in complex with benzoxaborole at ph=8.7
|
S +31
|
S 11x +31
|
|
2hncA
|
Crystal structure of the human carbonic anhydrase ii in complex with the 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor.
|
S +31
|
S 3x +31
|
|
2fmzA
|
Carbonic anhydrase activators. activation of isoforms i, ii, iv, va, vii and xiv with l- and d- phenylalanine, structure with d-phenylalanine.
|
S +31
|
S 3x +31
|
|
5flqA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|