S +31
|
S 3x +31
|
|
3mnjA
|
Human carbonic anhydrase ii mutant k170e
|
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
|
|
3hljA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-methylthiobenzimidazo[1,2-c][1,2,3]thiadiazol-7-sulfonamide
|
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
|
K +31
|
K 3x +31
|
|
3u3aX
|
Structure of human carbonic anhydrase ii v143i
|
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
|
|
4kp5A
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
K +31
|
K 3x +31
|
|
3kkxA
|
Neutron structure of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4pq7A
|
The crystal structure of the human carbonic anhydrase ii in complex with a sulfamide inhibitor
|
S +31
|
S 3x +31
|
|
4rn4A
|
Human carbonic anhydrases ii in complex with a acetazolamide derivative comprising one hydrophobic and one hydrophilic tail moiety
|
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 7x +31
|
|
4xe1A
|
Human carbonic anhydrase ii in complex with 6-sulfamoyl-saccharin
|
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
|
K +31
|
K 3x +31
|
|
2vvbX
|
Human carbonic anhydrase ii in complex with bicarbonate
|
S +31
|
S 3x +31
|
|
3mnkA
|
Human carbonic anhydrase ii mutant k170h
|
S +31
|
S 7x +31
|
|
1bnqA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
2eu3A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
S +31
|
S 3x +31
|
|
1rj5A
|
Crystal structure of the extracellular domain of murine carbonic anhydrase xiv
|
S +31
|
S 3x +31
|
|
2cbaA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
S +31
|
S 11x +31
|
|
1bn3A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
1zscA
|
Carbonic anhydrase ii mutant e117q, holo form
|
S +31
|
S 7x +31
|
|
1g3zA
|
Carbonic anhydrase ii (f131v)
|
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
|
|
2fw4A
|
Carbonic anhydrase activators. the first x-ray crystallographic study of an activator of isoform i, structure with l-histidine.
|
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
|
|
2wehA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
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
|
|
2cbdA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
S +31
|
S 11x +31
|
|
3nj9A
|
Crystal structure of carbonic anhydrase ii in complex with a nir inhibitor
|
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 6x +31
|
|
3ieoA
|
The coumarin-binding site in carbonic anhydrase: the antiepileptic lacosamide as an example
|
S +31
|
S 10x +31
|
|
4ca2A
|
Engineering the hydrophobic pocket of carbonic anhydrase ii
|
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 3x +31
|
|
3r17B
|
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
S +31
|
S 3x +31
|
|
4q07A
|
Crystal structure of chimeric carbonic anhydrase ix with inhibitor
|
K +31
|
K 11x +31
|
|
4mdlA
|
Meta carborane carbonic anhydrase inhibitor
|
S +31
|
S 3x +31
|
|
4q08A
|
Crystal structure of chimeric carbonic anhydrase xii with inhibitor
|
S +31
|
S 3x +31
|
|
4m2wA
|
Genetically engineered carbonic anhydrase ix in complex with dorzolamide
|
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
|
|
4q09A
|
Crystal structure of chimeric carbonic anhydrase xii with inhibitor
|
K +31
|
K 3x +31
|
|
4ywpA
|
Sucrose binding site in genetically engineered carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
4xixA
|
Carbonic anhydrase cah3 from chlamydomonas reinhardtii in complex with phosphate.
|
S +31
|
S 3x +31
|
4
|
2nnvA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
S +31
|
S 7x +31
|
|
1g46A
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,3-difluorophenyl)methyl]-benzamide
|
S +31
|
S 15x +31
|
|
1if6A
|
Carbonic anhydrase ii complexed with 3,5-difluorobenzenesulfonamide
|
S +31
|
S 15x +31
|
|
1i9nA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,5-difluorophenyl)methyl]-benzamide
|
S +31
|
S 23x +31
|
|
1if4A
|
Carbonic anhydrase ii complexed with 4-fluorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
3w6hA
|
Crystal structure of 19f probe-labeled hcai in complex with acetazolamide
|
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
|
|
5cluA
|
The crystal structure of the complex of hcaii with a saccharine derivative
|
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
|
|
3mzcA
|
Human carbonic ahydrase ii in complex with a benzenesulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
3mhcA
|
Crystal structure of human cabonic anhydrase ii in adduct with an adamantyl analogue of acetazolamide in a novel hydrophobic binding pocket
|
K +31
|
K 5x +31
|
|
1cnjA
|
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site
|
S +31
|
S 3x +31
|
|
1j9wA
|
Solution structure of the cai michigan 1 variant
|
K +31
|
K 3x +31
|
|
4qsbA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide
|
K +31
|
K 4x +31
|
|
3ml5A
|
Crystal structure of the c183s/c217s mutant of human ca vii in complex with acetazolamide
|
S +31
|
S 5x +31
|
|
1cniA
|
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site
|
S +31
|
S 7x +31
|
|
2hocA
|
Crystal structure of the human carbonic anhydrase ii in complex with the 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
4xz5A
|
Structure of the thermostable alpha-carbonic anydrase from thiomicrospira crunogena xcl-2 gammaproteobacterium
|
S +31
|
S 3x +31
|
|
4k0zA
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with methazolamide
|
S +31
|
S 11x +31
|
|
1bn1A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 15x +31
|
|
4q7pA
|
Crystal structure of 1-hydroxy-3-methylpyridine-2(1h)-thione bound to hcaii
|
S +31
|
S 5x +31
|
|
1ccsA
|
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity
|
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
|
|
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
|
|
4n0xB
|
Room temperature crystal structure of human carbonic anhydrase ii in complex with thiophene-2-sulfonamide
|
S +31
|
S 1x +31
|
|
2hfwA
|
Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase iii
|
S +31
|
S 3x +31
|
|
2f14A
|
Tne crystal structure of the human carbonic anhydrase ii in complex with a fluorescent inhibitor
|
K +31
|
K 3x +31
|
|
2nwoA
|
Structural and kinetic effect of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3d92A
|
Human carbonic anhydrase ii bound with substrate carbon dioxide
|
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
|
K +31
|
K 3x +31
|
|
4m2rA
|
Human carbonic anhydrase ii in complex with brinzolamide
|
K +31
|
K 3x +31
|
|
3konA
|
Crystal structure of cobalt (ii) human carbonic anhydrase ii at ph 11.0
|
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
|
|
4qj0A
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
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)
|
K +31
|
K 3x +31
|
|
3v2jA
|
Effect of sucrose and glycerol as cryoprotectans, on the inhibition of 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
|
|
1th9A
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
1caoA
|
Crystallographic studies of the binding of protonated and unprotonated inhibitors to carbonic anhydrase using hydrogen sulphide and nitrate anions
|
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
|
K +31
|
K 3x +31
|
4
|
2nnoA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
3mnuA
|
Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron containing aromatic sulfamide with mammalian isoforms i-xv
|
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
|
|
4bcwA
|
Carbonic anhydrase ix mimic in complex with (e)-2-(5-bromo-2- hydroxyphenyl)ethenesulfonic acid
|
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
|
K +31
|
K 3x +31
|
|
4mdgA
|
Closo carborane carbonic anhydrase inhibitor
|
K +31
|
K 3x +31
|
|
4r59A
|
A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
|
K +31
|
K 3x +31
|
|
4mltA
|
Structure of a monodentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii
|
S +31
|
S 3x +31
|
|
4pyyA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
S +31
|
S 3x +31
|
|
4idrX
|
Human carbonic anhydrase ii proton transfer double mutant
|
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
|
|
3s71B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 11x +31
|
|
1okmA
|
Carbonic anhydrase ii complex with the 1okm inhibitor 4-sulfonamide-[1-(4-aminobutane)]benzamide
|
S +31
|
S 11x +31
|
|
2q1bA
|
Carbonic anhydrase ii in complex with saccharin
|
S +31
|
S 3x +31
|
|
3mmfA
|
Crystal structure of human carbonic anhydrase ii in complex with a 1,3,5-triazine-substituted benzenesulfonamide inhibitor
|
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 3x +31
|
|
3ks3A
|
High resolution structure of human carbonic anhydrase ii at 0.9 a
|
K +31
|
K 3x +31
|
|
4qjmA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
S +31
|
S 3x +31
|
|
1calA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3sbhA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4,6-dimethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
|
S +31
|
S 15x +31
|
|
4mlxA
|
Structure of a bidentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii
|
S +31
|
S 7x +31
|
|
1bnuA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
4kniA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide
|
K +31
|
K 3x +31
|
|
3dv7A
|
Role of hydrophilic residues in proton transfer during catalysis by human carbonic anhydrase ii (n62a)
|
S +31
|
S 3x +31
|
|
3p5lA
|
Human carbonic anhydrase complexed with sodium 4-cyano-4-phenylpiperidine-1-carbodithioate
|
K +31
|
K 3x +31
|
|
3v7xA
|
Complex of human carbonic anhydrase ii with n-[2-(3,4-dimethoxyphenyl)ethyl]-4-sulfamoylbenzamide
|
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
|
|
4ht2A
|
Crystal structure of human carbonic anhydrase isozyme xii with the inhibitor.
|
S +31
|
S 3x +31
|
|
3m2zA
|
Fragment tethered to carbonic anhydrase ii h64c mutant
|
S +31
|
S 3x +31
|
|
4qtlA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
S +31
|
S 6x +31
|
|
1cctA
|
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity
|
K +31
|
K 3x +31
|
|
4iwzA
|
Structure of hcaii in complex with an acetazolamide derivative
|
S +31
|
S 3x +31
|
|
3sapA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(5-butyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4qsiA
|
Crystal structure of human carbonic anhydrase isozyme ii with 5-{[(4-tert-buthyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}-2-chlorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
1cayA
|
Wild-type and e106q mutant carbonic anhydrase complexed with acetate
|
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
|
|
4qjwA
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
S +31
|
S 3x +31
|
|
3hkqA
|
Human carbonic anhydrase ii in complex with 1-s-d-galactopyranosylsulfonamide
|
K +31
|
K 3x +31
|
|
2fnkA
|
Activation of human carbonic anhydrase ii by exogenous proton donors
|
S +31
|
S 7x +31
|
|
1g48A
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,6-difluorophenyl)methyl]-benzamide
|
S +31
|
S 3x +31
|
|
3s9tA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(4,6-dimethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
|
K +31
|
K 3x +31
|
4
|
4r5aA
|
A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
|
S +31
|
S 3x +31
|
|
1dcbA
|
Structure of an engineered metal binding site in human carbonic anhydrase ii reveals the architecture of a regulatory cysteine switch
|
K +31
|
K 3x +31
|
|
4m2uA
|
Carbonic anhydrase ii in complex with dorzolamide
|
S +31
|
S 15x +31
|
|
1am6A
|
Carbonic anhydrase ii inhibitor: acetohydroxamate
|
S +31
|
S 3x +31
|
|
3t5zA
|
Crystal structure of the human carbonic anhydrase ii in complex with n-methoxy-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4dz7A
|
Hca ii in complex with novel sulfonamide inhibitors set d
|
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 6x +31
|
|
1dcaA
|
Structure of an engineered metal binding site in human carbonic anhydrase ii reveals the architecture of a regulatory cysteine switch
|
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
|
K +31
|
K 3x +31
|
|
4kp8A
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 3-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
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 11x +31
|
|
1muaA
|
Structure and energetics of a non-proline cis-peptidyl linkage in an engineered protein
|
S +31
|
S 11x +31
|
|
4jssA
|
Human carbonic anhydrase ii h94d bound to a bidentate inhibitor
|
S +31
|
S 3x +31
|
|
2cabA
|
Structure, refinement and function of carbonic anhydrase isozymes. refinement of human carbonic anhydrase i
|
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
|
|
1bzmA
|
Drug-protein interactions: structure of sulfonamide drug complexed with human carbonic anhydrase i
|
S +31
|
S 3x +31
|
|
4q6dA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-[(z)-azepan-1-yldiazenyl]benzenesulfonamide
|
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
|
|
1caiA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1oq5A
|
Carbonic anhydrase ii in complex with nanomolar inhibitor
|
S +31
|
S 23x +31
|
|
4frcA
|
Carbonic anhydrase ii in complex with n'-sulfamoylpyrrolidine-1-carboximidamide
|
S +31
|
S 3x +31
|
|
4r5bA
|
Human carbonic anhydrase ii in complex with a carbohydrate-based sulfamate
|
S +31
|
S 3x +31
|
|
1rayA
|
The structure of human carbonic anhydrase ii in complex with bromide and azide
|
S +31
|
S 3x +31
|
|
4pxxA
|
Crystal structure of a highly thermal stabilized variant of human carbonic anhydrase ii
|