S +31
|
S 11x +31
|
|
4yytA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (5).
|
S +31
|
S 3x +31
|
|
4ruyA
|
Crystal structure of human carbonic anhydrase ii in complex with 4-propoxybenzenesulfonamide
|
S +31
|
S 1x +31
|
|
3da2A
|
X-ray structure of human carbonic anhydrase 13 in complex with inhibitor
|
K +31
|
K 3x +31
|
|
6gotA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(phenethylthio)benzenesulfonamide
|
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
|
K +31
|
K 3x +31
|
|
3s73B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 7x +31
|
|
1g4jA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,3,4,5,6-pentafluorophenyl)methyl]-benzamide
|
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 15x +31
|
|
1kwqA
|
Human carbonic anhydrase ii complexed with inhibitor 2000-07
|
S +31
|
S 11x +31
|
|
1avnA
|
Human carbonic anhydrase ii complexed with the histamine activator
|
K +31
|
K 3x +31
|
|
5yujA
|
Co2 release in human carbonic anhydrase ii crystals: reveal histidine 64 and solvent dynamics
|
S +31
|
S 7x +31
|
|
4q99A
|
Crystal structure of 2-mercapto-4-methylphenol bound to human carbonic anhydrase ii
|
S +31
|
S 15x +31
|
|
4q87A
|
Crystal structure of 1-hydroxy-4-(trifluoromethyl)pyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 15x +31
|
|
4q83A
|
Crystal structure of 1-hydroxy-3-(trifluoromethyl)pyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 15x +31
|
|
4q9yA
|
Crystal structure of 3-methylthiophenol bound to human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
2osfA
|
Inhibition of carbonic anhydrase ii by thioxolone: a mechanistic and structural study
|
S +31
|
S 7x +31
|
|
3zp9A
|
Human carbonic anhydrase ii as a scaffold for an artificial transfer hydrogenase
|
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
|
K +31
|
K 3x +31
|
|
4kapA
|
The binding of benzoarylsulfonamide ligands to human carbonic anhydrase is insensitive to formal fluorination of the ligand
|
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 19x +31
|
|
1i9pA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,4,6-trifluorophenyl)methyl]-benzamide
|
K +31
|
K 23x +31
|
|
1g0eA
|
Site-specific mutant (his64 replaced with ala) of human carbonic anhydrase ii complexed with 4-methylimidazole
|
S +31
|
S 7x +31
|
|
1i9mA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,4-difluorophenyl)methyl]-benzamide
|
K +31
|
K 7x +31
|
|
2ez7A
|
Carbonic anhydrase activators. activation of isozymes i, ii, iv, va, vii and xiv with l- and d-histidine and crystallographic analysis of their adducts with isoform ii: engineering proton transfer processes within the active site of an enzyme
|
S +31
|
S 3x +31
|
4
|
2fouA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
S +31
|
S 23x +31
|
|
1i91A
|
Carbonic anhydrase ii complexed with al-6619 2h-thieno[3,2-e]-1,2-thiazine-6-sulfonamide, 2-(3-hydroxyphenyl)-3-(4-morpholinyl)-, 1,1-dioxide
|
K +31
|
K 23x +31
|
|
1if9A
|
Carbonic anhydrase ii complexed with n-[2-(1h-indol-5-yl)-butyl]-4-sulfamoyl-benzamide
|
K +31
|
K 23x +31
|
|
1if7A
|
Carbonic anhydrase ii complexed with (r)-n-(3-indol-1-yl-2-methyl-propyl)-4-sulfamoyl-benzamide
|
S +31
|
S 23x +31
|
|
1if5A
|
Carbonic anhydrase ii complexed with 2,6-difluorobenzenesulfonamide
|
S +31
|
S 23x +31
|
|
1g1dA
|
Carbonic anhydrase ii complexed with 4-(aminosulfonyl)-n-[(2-fluorophenyl)methyl]-benzamide
|
S +31
|
S 19x +31
|
|
1i9oA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,3,4-trifluorophenyl)methyl]-benzamide
|
S +31
|
S 15x +31
|
|
1g4oA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-phenylmethylbenzamide
|
S +31
|
S 1x +31
|
|
1v9eA
|
Crystal structure analysis of bovine carbonic anhydrase ii
|
S +31
|
S 11x +31
|
|
1i8zA
|
Carbonic anhydrase ii complexed with al-6629 2h-thieno[3,2-e]-1,2-thiazine-6-sulfonamide, 2-(3-methoxyphenyl)-3-(4-morpholinyl)-, 1,1-dioxide
|
S +31
|
S 7x +31
|
|
1i90A
|
Carbonic anhydrase ii complexed with al-8520 2h-thieno[3,2-e]-1,2-thiazine-6-sulfonamide, 4-amino-3,4-dihydro-2-(3-methoxypropyl)-, 1,1-dioxide, (r)
|
S +31
|
S 7x +31
|
|
1g52A
|
Carbonic anhydrase ii complexed with 4-(aminosulfonyl)-n-[(2,3-difluorophenyl)methyl]-benzamide
|
S +31
|
S 11x +31
|
|
1if8A
|
Carbonic anhydrase ii complexed with (s)-n-(3-indol-1-yl-2-methyl-propyl)-4-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
1jd0A
|
Crystal structure of the extracellular domain of human carbonic anhydrase xii complexed with acetazolamide
|
S +31
|
S 11x +31
|
|
2fmgA
|
Carbonic anhydrase activators. activation of isoforms i, ii, iv, va, vii and xiv with l- and d- phenylalanine and crystallographic analysis of their adducts with isozyme ii: sterospecific recognition within the active site of an enzyme and its consequences for the drug design, structure with l-phenylalanine
|
K +31
|
K 1x +31
|
|
1thkA
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
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
|
K +31
|
K 3x +31
|
|
3rz0B
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
S 7x +31
|
|
2o4zA
|
Crystal structure of the carbonic anhydrase ii complexed with hydroxysulfamide inhibitor
|
S +31
|
S 23x +31
|
|
3f8eA
|
Coumarins are a novel class of suicide carbonic anhydrase inhibitors
|
K +31
|
K 3x +31
|
|
3czvA
|
Crystal structure of the human carbonic anhydrase xiii in complex with acetazolamide
|
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
|
K +31
|
K 3x +31
|
|
3okvA
|
Human carbonic anhydrase ii a65s, n67q (ca ix mimic) bound with 2-ethylestrone 3-o-sulfamate
|
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
|
K +31
|
K 3x +31
|
|
3bl0A
|
Carbonic anhydrase inhibitors. interaction of 2-n,n-dimethylamino-1,3,4-thiadiazole-5-methanesulfonamide with twelve mammalian isoforms: kinetic and x-ray crystallographic studies
|
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 11x +31
|
|
2q1qA
|
Carbonic anhydrase inhibitors. interaction of the antiepileptic drug sulthiame with twelve mammalian isoforms: kinetic and x-ray crystallographic studies
|
S +31
|
S 3x +31
|
|
6h29A
|
Human carbonic anhydrase ii in complex with benzyl carbamate
|
S +31
|
S 8x +31
|
|
1jv0A
|
The crystal structure of the zinc(ii) adduct of the cai michigan 1 variant
|
K +31
|
K 3x +31
|
4
|
2fosA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
S +31
|
S 11x +31
|
|
1ugfA
|
Human carbonic anhydrase ii [hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by thr (a65t)
|
S +31
|
S 2x +31
|
|
1kopA
|
Neisseria gonorrhoeae carbonic anhydrase
|
K +31
|
K 23x +31
|
|
1fqmA
|
X-ray crystal structure of zinc-bound f93i/f95m/w97v carbonic anhydrase (caii) variant
|
S +31
|
S 3x +31
|
|
1lg5A
|
Crystal structure analysis of the hca ii mutant t199p in complex with beta-mercaptoethanol
|
S +31
|
S 23x +31
|
|
1lugA
|
Full matrix error analysis of carbonic anhydrase
|
S +31
|
S 7x +31
|
|
2hd6A
|
Crystal structure of the human carbonic anhydrase ii in complex with a hypoxia-activatable sulfonamide.
|
K +31
|
K 3x +31
|
|
1xevA
|
Crystal structure of human carbonic anhydrase ii in a new crystal form
|
S +31
|
S 3x +31
|
|
1tbtX
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
2nxtA
|
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1yo2A
|
Proton transfer from his200 in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3d8wA
|
Use of a carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
S +31
|
S 3x +31
|
|
3dd8A
|
Carbonic anhydrase inhibitors. interaction of the antitumor sulfamate emd-486019 with twelve mammalian isoforms: kinetic and x-ray crystallographic studies
|
S +31
|
S 3x +31
|
4
|
2wd2A
|
A chimeric microtubule disruptor with efficacy on a taxane resistant cell line
|
S +31
|
S 3x +31
|
|
2x7uA
|
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors.
|
S +31
|
S 3x +31
|
|
3u47A
|
Human carbonic anhydrase ii v143l
|
S +31
|
S 3x +31
|
|
4rivA
|
A carbonic anhydrase ix mimic in complex with saccharin
|
S +31
|
S 7x +31
|
|
1f2wA
|
The mechanism of cyanamide hydration catalyzed by carbonic anhydrase ii revealed by cryogenic x-ray diffraction
|
S +31
|
S 3x +31
|
|
5dsnA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 1 hr warming
|
S +31
|
S 3x +31
|
|
5dskA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 3 min warming
|
S +31
|
S 3x +31
|
|
5ljtA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-((1-phenyl-1h-1,2,3-triazol-4-yl)methoxy)benzenesulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
5gmnA
|
Crystal structure of human carbonic anhydrase ii in complex with polmacoxib
|
K +31
|
K 3x +31
|
|
2ax2A
|
Production and x-ray crystallographic analysis of fully deuterated human carbonic anhydrase ii
|
S +31
|
S 11x +31
|
|
2abeA
|
Carbonic anhydrase activators: x-ray crystal structure of the adduct of human isozyme ii with l-histidine as a platform for the design of stronger activators
|
K +31
|
|
|
3m98A
|
Crystal structure of human carbonic anhydrase isozyme ii with 5-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
|
K +31
|
|
|
3m96A
|
Crystal structure of human carbonic anhydrase isozyme ii with 5-{[(5-bromo-1h-benzimidazol-2-yl)sulfanyl]acetyl}-2-chlorobenzenesulfonamide
|
S +31
|
|
|
3c7pA
|
Crystal structure of human carbonic anhydrase ii in complex with stx237
|
K +31
|
|
|
2w2jA
|
Crystal structure of the human carbonic anhydrase related protein viii
|
K +31
|
|
|
3betA
|
Crystal structure of the human carbonic anhydrase ii in complex with stx 641 at 1.85 angstroms resolution
|
S +31
|
|
|
3d93A
|
Apo human carbonic anhydrase ii bound with substrate carbon dioxide
|
K +31
|
|
|
3cajA
|
Crystal structure of the human carbonic anhydrase ii in complex with ethoxzolamide
|
S +31
|
|
|
3iaiA
|
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase ix
|
S +31
|
|
|
4bf6A
|
Three dimensional structure of human carbonic anhydrase ii in complex with 5-(1-(3-cyanophenyl)-1h-1,2,3-triazol-4-yl)thiophene-2- sulfonamide
|
K +31
|
|
|
5dsqA
|
Structure of co2 released apo-form of human carbonic anhydrase ii with 3 min warming
|
K +31
|
|
|
5dsoA
|
Structure of co2 bound apo-form of human carbonic anhydrase ii with 0 sec (no) warming
|
K +31
|
|
|
1fsnA
|
X-ray crystal structure of metal-free f93s/f95l/w97m carbonic anhydrase (caii) variant
|
S +31
|
|
|
1fqnA
|
X-ray crystal structure of metal-free f93i/f95m/w97v carbonic anhydrase (caii) variant
|
K +31
|
|
|
3rz5A
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
K +31
|
|
|
3rz7A
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
K +31
|
|
|
3s76A
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
|
|
3rz8A
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
|
|
3ryzA
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
|
|
3ryyA
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
|
|
5dspA
|
Structure of co2 released apo-form of human carbonic anhydrase ii with 40 sec warming
|
K +31
|
|
|
5dsrA
|
Structure of co2 released apo-form of human carbonic anhydrase ii with 10 min warming
|
K 41 41
|
|
|
6fhtA
|
Crystal structure of an artificial phytochrome regulated adenylate/guanylate cyclase in its dark adapted pr form
|
K +31
|
|
|
5y2rA
|
2.5 atm co2-pressurized human carbonic anhydrase ii
|
K +31
|
|
|
5y2sA
|
7.0 atm co2-pressurized human carbonic anhydrase ii
|
K +31
|
|
|
5msbA
|
Crystal structure of human carbonic anhydrase isozyme xii with 2,3,5,6-tetrafluoro-4[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
|
|
5nxgA
|
Carbonic anhydrase ii inhibitor ra1
|
K +31
|
|
|
5nxiA
|
Carbonic anhydrase ii inhibitor ra2
|
K +31
|
|
|
5nxoA
|
Carbonic anhydrase ii inhibitor ra6
|
K +31
|
|
|
5nxpA
|
Carbonic anhydrase ii inhibitor ra7
|
K +31
|
|
|
5nxvA
|
Carbonic anhydrase ii inhibitor ra8
|
K +31
|
|
|
5nxwA
|
Carbonic anhydrase ii inhibitor ra9
|
K +31
|
|
|
5ny1A
|
Carbonic anhydrase ii inhibitor ra10
|
K +31
|
|
|
5ny3A
|
Carbonic anhydrase ii inhibitor ra11
|
K +31
|
|
|
5ny6A
|
Carbonic anhydrase ii inhibitor ra12
|
K +31
|
|
|
5nyaA
|
Carbonic anhydrase ii inhibitor ra13
|
K +31
|
|
|
5m78A
|
Human carbonic anhydrase ii in complex with fragment-like inhibitor.
|
K +31
|
|
|
5t75A
|
Human carbonic anhydrase ii g132c_c206s double mutant in complex with sa-2
|
K +31
|
|
1
|
5tt8A
|
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with benzolamide
|
K +31
|
|
|
5lleA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-(1-adamantylamino)-2,3,5,6-tetrafluorobenzenesulfonamide
|
K +31
|
|
|
5llgA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-propylthiobenzenesulfonamide
|
K +31
|
|
|
5lloA
|
Crystal structure of human carbonic anhydrase isozyme xii with 3-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-2,5,6-trifluoro-4-[(2-hy-droxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
|
|
5llnA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2,3,5,6-tetrafluoro-4-(propylthio)benzenesulfonamide
|
K +31
|
|
|
5llpA
|
Crystal structure of human carbonic anhydraseisozyme xii with 3-[(1s)-1,2,3,4-tetrahydronapthalen-1-ylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
|
1
|
5ipzA
|
Crystal structure of human carbonic anhydrase isozyme iv with 5-(2-amino-1,3-thiazol-4-yl)-2-chlorobenzenesulfonamide
|
K +31
|
|
|
5l6kA
|
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer
|
K +31
|
|
|
5drsA
|
Crystal structure of human carbonic anhydraseisozyme ii with 3-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
|
|
5dogA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-(benzylamino)-3,5,6-trifluoro-4-[(2-phenylethyl)thio]benzene- sulfonamide
|
K +31
|
|
|
5dohA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
K +31
|
|
|
5g03A
|
An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
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S +31
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1n2mA
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The s53a proenzyme structure of methanococcus jannaschii.
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S +31
|
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2qqdC
|
N47a mutant of pyruvoyl-dependent arginine decarboxylase from methanococcus jannashii
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K +31
|
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1y7wA
|
Crystal structure of a halotolerant carbonic anhydrase from dunaliella salina
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K +31
|
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1zncA
|
Human carbonic anhydrase iv
|
K +31
|
|
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2hfyA
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Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase iii
|
K +31
|
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1
|
2zncA
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Murine carbonic anhydrase iv
|
K +31
|
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1
|
3b1bA
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The unique structure of wild type carbonic anhydrase alpha-ca1 from chlamydomonas reinhardtii
|
K +31
|
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1
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3f7bA
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Crystal structure of soluble domain of ca4 in complex with small molecule.
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S +31
|
|
1
|
3f7uA
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Crystal structure of soluble domain of ca4 in complex with small molecule.
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K +31
|
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1
|
3fw3A
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Crystal structure of soluble domain of ca4 in complex with dorzolamide
|
K +31
|
|
1
|
3zncA
|
Murine carbonic anhydrase iv complexed with brinzolamide
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