|
K +31
|
K 3x +31
|
|
4kp8A
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 3-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
|
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)
|
|
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
|
|
K +31
|
K 3x +31
|
|
6b00A
|
Thermostabilized mutant of human carbonic anhydrase ii - a65t l100h k154n l224s l240p a248t
|
|
K +31
|
K 3x +31
|
|
5u0eA
|
Identification of a new zinc binding chemotype by fragment screening
|
|
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
|
|
4m2uA
|
Carbonic anhydrase ii in complex with dorzolamide
|
|
K +31
|
K 3x +31
|
4
|
4r5aA
|
A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
|
|
K +31
|
K 3x +31
|
|
2fnkA
|
Activation of human carbonic anhydrase ii by exogenous proton donors
|
|
K +31
|
K 3x +31
|
|
5fnmA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
|
K +31
|
K 3x +31
|
|
4iwzA
|
Structure of hcaii in complex with an acetazolamide derivative
|
|
K +31
|
K 3x +31
|
|
4ht2A
|
Crystal structure of human carbonic anhydrase isozyme xii with the inhibitor.
|
|
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
|
|
3v7xA
|
Complex of human carbonic anhydrase ii with n-[2-(3,4-dimethoxyphenyl)ethyl]-4-sulfamoylbenzamide
|
|
K +31
|
K 3x +31
|
|
3dv7A
|
Role of hydrophilic residues in proton transfer during catalysis by human carbonic anhydrase ii (n62a)
|
|
K +31
|
K 3x +31
|
|
4qjmA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
|
K +31
|
K 3x +31
|
|
6bbsA
|
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with brinzolamide
|
|
K +31
|
K 3x +31
|
|
4mdmA
|
Nido-carborane carbonic anhydrase inhibitor
|
|
K +31
|
K 3x +31
|
|
3n0nA
|
Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor
|
|
K +31
|
K 7x +31
|
|
4q8zA
|
Crystal structure of 1-hydroxy-4-methylpyridin-2(1h)-one bound to human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
4fl7A
|
The crystal structure of human carbonic anhydrase ii in complex with n-(hydroxy)-benzamide
|
|
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.
|
|
K +31
|
K 4x +31
|
|
5vgyA
|
Identification of a new zinc binding chemotype by fragment screening
|
|
K +31
|
K 3x +31
|
|
2wd3A
|
Highly potent first examples of dual aromatase-steroid sulfatase inhibitors based on a biphenyl template
|
|
K +31
|
K 3x +31
|
|
4e5qA
|
Human carbonic anhydrase ii in complex with cyanate
|
|
K +31
|
K 3x +31
|
|
4wl4A
|
Crystal structure of human carbonic anhydrase ii in complex with the 6-hydroxy-chromene-2-thione inhibitor
|
|
K +31
|
K 3x +31
|
|
5u0fA
|
Identification of a new zinc binding chemotype by fragment screening
|
|
K +31
|
K 3x +31
|
|
4kuyA
|
Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(o-tolylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor
|
|
K +31
|
K 3x +31
|
|
3v2mA
|
Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
|
|
K +31
|
K 11x +31
|
|
1g0fA
|
Site-specific mutant (his64 replaced with ala) of human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
5tyaA
|
Identification of a new zinc binding chemotype by fragment screening
|
|
K +31
|
K 3x +31
|
|
4pyxA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
|
K +31
|
K 3x +31
|
|
6fe1A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide.
|
|
K +31
|
K 3x +31
|
|
3ryxB
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
|
K +31
|
K 3x +31
|
|
1razA
|
The structure of human carbonic anhydrase ii in complex with bromide and azide
|
|
K +31
|
K 3x +31
|
|
4e4aA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
|
K +31
|
K 3x +31
|
|
2fnmA
|
Activation of human carbonic anhdyrase ii by exogenous proton donors
|
|
K +31
|
K 3x +31
|
|
3r16A
|
Human caii bound to n-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
|
K +31
|
K 3x +31
|
|
5wlrA
|
Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide
|
|
K +31
|
K 3x +31
|
|
6d1lA
|
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects
|
|
K +31
|
K 3x +31
|
|
3vbdA
|
Complex of human carbonic anhydrase ii with 4-(6-methoxy-3,4-dihydroisoquinolin-1-yl)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
5jehB
|
Human carbonic anhydrase ii (l198a) complexed with benzo[d]thiazole-2-sulfonamide
|
|
K +31
|
K 3x +31
|
|
4q90A
|
Crystal structure of 4-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
4
|
2nnsA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
3myqA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-[(1h-imidazo[4,5-c]quinolin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
3m1qA
|
Carbonic anhydrase ii mutant w5c-h64c with opened disulfide bond
|
|
K +31
|
K 3x +31
|
4
|
5tuoA
|
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor.
|
|
K +31
|
K 1x +31
|
|
2eu2A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
|
K +31
|
K 3x +31
|
|
4e3fA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
|
K +31
|
K 3x +31
|
|
2wejA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
|
K +31
|
K 11x +31
|
|
3k34A
|
Human carbonic anhydrase ii with a sulfonamide inhibitor
|
|
K +31
|
K 3x +31
|
|
4e3gA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
|
K +31
|
K 2x +31
|
|
2x7tA
|
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors.
|
|
K +31
|
K 3x +31
|
|
2iliA
|
Refine atomic structure of human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
4fikA
|
Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
|
|
K +31
|
K 3x +31
|
|
3p55A
|
Human carbonic anhydrase ii in complex with p-(4-ferrocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
2nwzA
|
Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
3uynA
|
Hca 3
|
|
K +31
|
K 3x +31
|
|
5t71A
|
Human carboanhydrase f131c_c206s double mutant in complex with sa-2
|
|
K +31
|
K 1x +31
|
|
2hfxA
|
Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase iii
|
|
K +31
|
K 3x +31
|
|
3ml2A
|
Human carbonic anhydsase ii in complex with an aryl sulfonamide inhibitor
|
|
K +31
|
K 3x +31
|
|
4k1qA
|
Structure of hcaix mimic (hcaii with 5 mutations in active site)
|
|
K +31
|
K 3x +31
|
|
5ty8A
|
Identification of a new zinc binding chemotype by fragment screening
|
|
K +31
|
K 3x +31
|
|
5g0cA
|
An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
|
|
K +31
|
K 3x +31
|
|
1fsrA
|
X-ray crystal structure of copper-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
|
|
K +31
|
K 3x +31
|
|
6g98A
|
Three dimensional structure of human carbonic anhydrase ix in complex with sulfonamide
|
|
K +31
|
K 3x +31
|
|
5dvxA
|
Crystal structure of the catalytic-domain of human carbonic anhydrase ix at 1.6 angstrom resolution
|
|
K +31
|
K 3x +31
|
|
5amdA
|
Three dimensional structure of human carbonic anhydrase ii in complex with 2-((2-phenylethyl)sulfamoyl)-4-sulfamoylbenzoic acid
|
|
K +31
|
K 3x +31
|
|
4qefA
|
Human carbonic anhydrase ii v207i - cyanate inhibitor complex
|
|
K +31
|
K 3x +31
|
|
4hewA
|
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
|
|
3okuA
|
Human carbonic anhydrase ii in complex with 2-ethylestrone-3-o-sulfamate
|
|
K +31
|
K 3x +31
|
|
1z93A
|
Human carbonic anhydrase iii:structural and kinetic study of catalysis and proton transfer.
|
|
K +31
|
K 3x +31
|
|
5brwA
|
Catalytic improvement of an artificial metalloenzyme by computational design
|
|
K +31
|
K 3x +31
|
|
5wexA
|
Discovery of new selenoureido analogs of 4-(4-fluorophenylureido) benzenesulfonamides as carbonic anhydrase inhibitors
|
|
K +31
|
K 3x +31
|
|
4q06A
|
Crystal structure of chimeric carbonic anhydrase ix with inhibitor
|
|
K +31
|
K 3x +31
|
|
3p5aA
|
Human carbonic anhydrase complexed with sodium morpholinocarbodithioate
|
|
K +31
|
K 3x +31
|
|
5je7B
|
Human carbonic anhydrase ii (f131y) complexed with benzo[d]thiazole-2-sulfonamide
|
|
K +31
|
K 3x +31
|
|
5ekmA
|
Human carbonic anhydrase ii complexed with a two-faced guest
|
|
K +31
|
K 3x +31
|
|
4z1jA
|
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
|
|
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
|
|
K +31
|
K 3x +31
|
|
4itpA
|
Structure of human carbonic anhydrase ii bound to a benzene sulfonamide
|
|
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
|
|
K +31
|
|
|
1urtA
|
Murine carbonic anhydrase v
|
|
K +31
|
K 3x +31
|
|
4knnA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
|
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
|
|
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
|
|
K +31
|
K 3x +31
|
|
6gotA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(phenethylthio)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
3s73B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
|
K +31
|
K 3x +31
|
|
5yujA
|
Co2 release in human carbonic anhydrase ii crystals: reveal histidine 64 and solvent dynamics
|
|
K +31
|
K 3x +31
|
|
2osfA
|
Inhibition of carbonic anhydrase ii by thioxolone: a mechanistic and structural study
|
|
K +31
|
K 3x +31
|
|
4kapA
|
The binding of benzoarylsulfonamide ligands to human carbonic anhydrase is insensitive to formal fluorination of the ligand
|
|
K +31
|
K 23x +31
|
|
1g0eA
|
Site-specific mutant (his64 replaced with ala) of human carbonic anhydrase ii complexed with 4-methylimidazole
|
|
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
|
|
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
|
|
K +31
|
K 7x +31
|
|
2cbcA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
|
K +31
|
K 3x +31
|
|
4lu3A
|
The crystal structure of the human carbonic anhydrase xiv
|
|
K +31
|
K 1x +31
|
|
1thkA
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
|
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
|
|
K +31
|
K 3x +31
|
|
3czvA
|
Crystal structure of the human carbonic anhydrase xiii in complex with acetazolamide
|
|
K +31
|
K 3x +31
|
|
3okvA
|
Human carbonic anhydrase ii a65s, n67q (ca ix mimic) bound with 2-ethylestrone 3-o-sulfamate
|
|
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
|
|
K +31
|
K 3x +31
|
4
|
2fosA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
|
K +31
|
K 23x +31
|
|
1fqmA
|
X-ray crystal structure of zinc-bound f93i/f95m/w97v carbonic anhydrase (caii) variant
|
|
K +31
|
K 3x +31
|
|
1xevA
|
Crystal structure of human carbonic anhydrase ii in a new crystal form
|
|
K +31
|
K 3x +31
|
|
2nxtA
|
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
|
K +31
|
|
|
4v7hBE
|
Structure of the 80s rrna and proteins and p/e trna for eukaryotic ribosome based on cryo-em map of thermomyces lanuginosus ribosome at 8.9a resolution
|
|
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
|
|
K +31
|
K 3x +31
|
|
5l70A
|
Crystal structure of human carbonic anhydrase ii in complex with a quinoline oligoamide foldamer
|
|
K +31
|
|
|
4cndB
|
Crystal structure of e.coli trmj
|
|
K +31
|
|
1
|
4cneB
|
Crystal structure of e.coli trmj in complex with s-adenosyl-l- homocysteine
|
|
K +31
|
|
1
|
4cnfB
|
Crystal structure of sulfolobus acidocaldarius trmj
|
|
K +31
|
|
1
|
4cngB
|
Crystal structure of sulfolobus acidocaldarius trmj in complex with s-adenosyl-l-homocysteine
|
|
K +31
|
|
1
|
6emsA
|
Crystal structure of dual specific trm10 construct from thermococcus kodakaraensis.
|
|
K +31
|
|
|
5vm8A
|
Crystal structure of a ribosomal rna small subunit methyltransferase e from neisseria gonorrhoeae bound to s-adenosyl methionine
|
|
K +31
|
|
1
|
6emtA
|
Crystal structure of dual specific trm10 construct from thermococcus kodakaraensis.
|
|
K +31
|
|
1
|
6emvA
|
Crystal structure of dual specific trm10 construct from thermococcus kodakaraensis.
|
|
K +31
|
|
1
|
5a19A
|
The structure of mat2a in complex with ppnp.
|
|
K +31
|
|
|
1cngA
|
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site
|
|
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
|
|
K +31
|
|
|
3m98A
|
Crystal structure of human carbonic anhydrase isozyme ii with 5-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
|
|
K +31
|
|
|
3m2nA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{2-[n-(6-chloro-5-nitropyrimidin-4-yl)amino]ethyl}benzenesulfonamide
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K +31
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3mhmA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-{[n-(6-benzylamino-5-nitropyrimidin-4-yl)amino]methyl}benzenesulfonamide
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K +31
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3m96A
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Crystal structure of human carbonic anhydrase isozyme ii with 5-{[(5-bromo-1h-benzimidazol-2-yl)sulfanyl]acetyl}-2-chlorobenzenesulfonamide
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K +31
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3po6A
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Crystal structure of human carbonic anhydrase ii with 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinoline-2(1h)-sulfonamide
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K +31
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1hvaA
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Engineering the zinc binding site of human carbonic anhydrase ii: structure of the his-94-> cys apoenzyme in a new crystalline form
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K +31
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2w2jA
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Crystal structure of the human carbonic anhydrase related protein viii
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K +31
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3betA
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Crystal structure of the human carbonic anhydrase ii in complex with stx 641 at 1.85 angstroms resolution
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K +31
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3cajA
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Crystal structure of the human carbonic anhydrase ii in complex with ethoxzolamide
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K +31
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3ibuA
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The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic sulfamate inhibitor
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K +31
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3ibnA
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The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic bis-sulfamate inhibitor
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K +31
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3iblA
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The crystal structure of the human carbonic anhydrase ii in complex with an aliphatic bis-sulfamate inhibitor
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K +31
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5dsqA
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Structure of co2 released apo-form of human carbonic anhydrase ii with 3 min warming
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K +31
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5dsoA
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Structure of co2 bound apo-form of human carbonic anhydrase ii with 0 sec (no) warming
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K +31
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1fsnA
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X-ray crystal structure of metal-free f93s/f95l/w97m carbonic anhydrase (caii) variant
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K +31
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2cbeA
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Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
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K +31
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3rz5A
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Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
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K +31
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3rz7A
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Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
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K +31
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3s76A
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The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
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K +31
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1zsaA
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Carbonic anhydrase ii mutant e117q, apo form
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