S +31
|
S 3x +31
|
|
4zx0A
|
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor
|
K +31
|
K 3x +31
|
|
3oysA
|
Human carbonic anhydrase ii complexed with 2-{[4-amino-3-(3-hydroxyprop-1-yn-1-yl)-1h-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-5-methyl-3-(2-methylphenyl)quinazolin-4(3h)-one
|
S +31
|
S 3x +31
|
|
4rfdA
|
Human carbonic anhydrase ii in complex with 4-(4-sulfamoyl-phenoxy)-butylammonium
|
S +31
|
S 3x +31
|
|
4l5wA
|
Structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
4itpA
|
Structure of human carbonic anhydrase ii bound to a benzene sulfonamide
|
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
|
K +31
|
K 3x +31
|
|
3dvbA
|
X-ray crystal structure of mutant n62v human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
2powA
|
The crystal structure of the human carbonic anhydrase ii in complex with 4-amino-6-trifluoromethyl-benzene-1,3-disulfonamide
|
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
|
|
6b4dA
|
Crystal structure of human carbonic anhydrase ii in complex with a heteroaryl-pyrazole carboxylic acid derivative.
|
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 15x +31
|
|
5jqtA
|
Crystal structure of human carbonic anhydrase ii in complex with benzoxaborole at ph 7.4
|
S +31
|
S 3x +31
|
|
5zxwA
|
Crystal structure of human carbonic anhydrase ii crystallized by ammonium sulfate
|
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 7x +31
|
|
4lp6A
|
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer
|
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
|
K +31
|
K 3x +31
|
|
3saxA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(5-ethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
|
K +31
|
K 3x +31
|
|
4qsaA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide
|
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
|
K +31
|
K 3x +31
|
|
3s8xA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4-methyl-6-oxo-1,6-dihydro-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4ht0A
|
Crystal structure of human carbonic anhydrase isozyme ii with the inhibitor.
|
S +31
|
S 23x +31
|
|
2gehA
|
N-hydroxyurea, a versatile zinc binding function in the design of metalloenzyme inhibitors
|
S +31
|
S 7x +31
|
|
5thnA
|
Crystal structure of 2-hydroxycyclohepta-2,4,6-triene-1-thione bound to human carbonic anhydrase 2
|
S +31
|
S 11x +31
|
|
2h15A
|
Carbonic anhydrase inhibitors: clashing with ala65 as a means of designing isozyme-selective inhibitors that show low affinity for the ubiquitous isozyme ii
|
S +31
|
S 3x +31
|
|
3n3jA
|
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor
|
S +31
|
S 11x +31
|
|
4yxoA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (3).
|
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
|
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
|
|
2nwpA
|
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
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 3x +31
|
|
2nwyA
|
Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
5yujA
|
Co2 release in human carbonic anhydrase ii crystals: reveal histidine 64 and solvent dynamics
|
S +31
|
S 23x +31
|
|
4fu5A
|
Carbonic anhydrase ii in complex with n-[(2z)-1,3-oxazolidin-2-ylidene]sulfuric diamide
|
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 3x +31
|
|
4kv0A
|
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-tosylureido)pyridine-2-sulfonamide inhibitor
|
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 11x +31
|
|
4fvoA
|
Carbonic anhydrase ii in complex with n-[(2e)-3,4-dihydroquinazolin-2(1h)-ylidene]sulfuric diamide
|
S +31
|
S 7x +31
|
|
5l9eA
|
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer
|
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
|
|
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
|
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 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
|
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
|
K +31
|
K 3x +31
|
|
3t85A
|
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
|
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
|
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
|
S +31
|
S 3x +31
|
|
3v5gA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-sulfamido-benzenesulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
3sbiA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-[(2-pyrimidinylsulfanyl)acetyl]benzenesulfonamide
|
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 7x +31
|
|
2hd6A
|
Crystal structure of the human carbonic anhydrase ii in complex with a hypoxia-activatable sulfonamide.
|
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
|
|
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
|
|
3pykA
|
Human carbonic anhydrase ii as host for pianostool complexes bearing a sulfonamide anchor
|
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 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
|
|
5l70A
|
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer
|
K +31
|
|
|
3mhlA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[n-(6-methoxy-5-nitropyrimidin-4-yl)amino]methyl}benzenesulfonamide
|
K +31
|
|
|
3m5eA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[n-(6-chloro-5-formyl-2-methylthiopyrimidin-4-yl)amino]methyl}benzenesulfonamide
|
K +31
|
|
|
3m40A
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-[n-(6-chloro-5-nitropyrimidin-4-yl)amino]benzenesulfonamide
|
K +31
|
|
|
3m3xA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{2-[n-(6-methoxy-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide
|
K +31
|
|
|
3m67A
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-[(6,7-dihydro-1h-[1,4]dioxino[2,3-f]benzimidazol-2-ylsulfanyl)acetyl]benzenesulfonamide
|
S +31
|
|
|
3mhoA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-[n-(6-chloro-5-formyl-2-methylthiopyrimidin-4-yl)amino]benzenesulfonamide
|
K +31
|
|
|
3m98A
|
Crystal structure of human carbonic anhydrase isozyme ii with 5-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
|
S +31
|
|
|
3mhiA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(5-nitro-6-oxo-1,6-dihydro-4-pyrimidinyl)amino]methyl}benzenesulfonamide
|
K +31
|
|
|
3m2nA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{2-[n-(6-chloro-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide
|
K +31
|
|
|
3mhmA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[n-(6-benzylamino-5-nitropyrimidin-4-yl)amino]methyl}benzenesulfonamide
|
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
|
|
|
3po6A
|
Crystal structure of human carbonic anhydrase ii with 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinoline-2(1h)-sulfonamide
|
K +31
|
|
|
3betA
|
Crystal structure of the human carbonic anhydrase ii in complex with stx 641 at 1.85 angstroms resolution
|
K +31
|
|
|
3cajA
|
Crystal structure of the human carbonic anhydrase ii in complex with ethoxzolamide
|
K +31
|
|
|
3ibuA
|
The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic sulfamate inhibitor
|
S +31
|
|
|
3ibiA
|
The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic sulfamate inhibitor
|
K +31
|
|
|
3ibnA
|
The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic bis-sulfamate inhibitor
|
K +31
|
|
|
3iblA
|
The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic bis-sulfamate inhibitor
|
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
|
|
|
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 +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
|
|
|
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
|
|
|
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
|
|
|
5thjA
|
Crystal structure of 2-hydroxycyclohepta-2,4,6-trien-1-one bound to human carbonic anhydrase 2
|
K +31
|
|
|
5jn3A
|
Carbonic anhydrase ix-mimic in complex with u-f
|
K +31
|
|
|
5l6kA
|
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer
|
K +31
|
|
|
5sz7A
|
Carbonic anhydrase ix-mimic in complex with 4-(3-quinolinyl)-benzenesulfonamide
|
K +31
|
|
|
5sz0A
|
Carbonic anhydrase ii in complex with 4-(phenyl)-benzenesulfonamide
|