S +31
|
S 3x +31
|
|
2weoA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
S +31
|
S 3x +31
|
|
2nn7A
|
Structure of inhibitor binding to carbonic anhydrase i
|
S +31
|
S 3x +31
|
|
5ogoA
|
Crystal structure of chimeric carbonic anhydrase i with 3-(benzylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4xfwA
|
Crystal structure of the monoclinic form of alpha-carbonic anhydrase from the human pathogen helicobacter pylori
|
S +31
|
S 3x +31
|
|
4zwxA
|
Engineered carbonic anhydrase ix mimic in complex with glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
4xiwA
|
Carbonic anhydrase cah3 from chlamydomonas reinhardtii in complex with acetazolamide
|
S +31
|
S 3x +31
|
|
4riuA
|
A carbonic anhydrase ix mimic in complex with a saccharin-based inhibitor
|
S +31
|
S 3x +31
|
|
4cq0A
|
Cyclic secondary sulfonamides: unusually good inhibitors of cancer- related carbonic anhydrase enzymes
|
S +31
|
S 3x +31
|
|
4cnxA
|
Surface residue engineering of bovine carbonic anhydrase to an extreme halophilic enzyme for potential application in postcombustion co2 capture
|
S +31
|
S 15x +31
|
|
3kwaA
|
Polyamines inhibit carbonic anhydrases
|
S +31
|
S 3x +31
|
|
3dccA
|
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
|
|
1i9qA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(3,4,5-trifluorophenyl)methyl]-benzamide
|
S +31
|
S 15x +31
|
|
1i9lA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(4-fluorophenyl)methyl]-benzamide
|
S +31
|
S 11x +31
|
|
2hkkA
|
Carbonic anhydrase activators: solution and x-ray crystallography for the interaction of andrenaline with various carbonic anhydrase isoforms
|
S +31
|
S 3x +31
|
|
1fljA
|
Crystal structure of s-glutathiolated carbonic anhydrase iii
|
S +31
|
S 3x +31
|
|
2aw1A
|
Carbonic anhydrase inhibitors: valdecoxib binds to a different active site region of the human isoform ii as compared to the structurally related cyclooxygenase ii "selective" inhibitor celecoxib
|
S +31
|
S 11x +31
|
|
1cnwA
|
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants
|
S +31
|
S 3x +31
|
|
1crmA
|
Structure and function of carbonic anhydrases
|
S +31
|
S 3x +31
|
|
1fr7A
|
X-ray crystal structure of zinc-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
|
S +31
|
S 11x +31
|
|
2hl4A
|
Crystal structure analysis of human carbonic anhydrase ii in complex with a benzenesulfonamide derivative
|
S +31
|
S 3x +31
|
|
3mnhA
|
Human carbonic anhydrase ii mutant k170a
|
S +31
|
S 3x +31
|
|
3p58A
|
Human carbonic anhydrase in complex with benzyl (methyl) carbamodithoic acid
|
S +31
|
S 3x +31
|
|
6bc9A
|
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with dorzolamide
|
S +31
|
S 3x +31
|
|
5wg7A
|
Human carbonic anhydrase ii complexed with acek
|
S +31
|
S 3x +31
|
|
5mjnA
|
Three dimensional structure of human carbonic anhydrase ii in complex with 5-[(4chlorobenzyl)sulfanyl]thiophene-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5jg3B
|
Human carbonic anhydrase ii (121t/n67q) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5jegB
|
Human carbonic anhydrase ii (v121i) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5j8zA
|
Human carbonic anhydrase ii in complex with ligand
|
S +31
|
S 3x +31
|
|
4y0jA
|
H/d exchanged human carbonic anhydrase ii ph 6 room temperature neutron crystal structure.
|
S +31
|
S 7x +31
|
|
5byiA
|
Human carbonic anhydrase ii with an azobenzene inhibitor (1d)
|
S +31
|
S 3x +31
|
|
5c8iA
|
Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with methazolamide
|
S +31
|
S 3x +31
|
|
4zx0A
|
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
4rfdA
|
Human carbonic anhydrase ii in complex with 4-(4-sulfamoyl-phenoxy)-butylammonium
|
S +31
|
S 3x +31
|
|
4q0lA
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
S +31
|
S 3x +31
|
|
4l5wA
|
Structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4cacA
|
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution
|
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
|
S +31
|
S 23x +31
|
|
1ydbA
|
Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1tg3A
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
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
|
|
1yo1A
|
Proton transfer from his200 in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1cvcA
|
Redesigning the zinc binding site of human carbonic anhydrase ii: structure of a his2asp-zn2+ metal coordination polyhedron
|
S +31
|
S 3x +31
|
|
1hecA
|
Structural consequences of hydrophilic amino-acid substitutions in the hydrophobic pocket of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1teuX
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1tg9A
|
Effect of shuttle location and ph environment on h+ transfer in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1lzvA
|
Site-specific mutant (tyr7 replaced with his) of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1rzeA
|
X-ray analysis of metal substituted human carbonic anhydrase ii derivatives
|
S +31
|
S 3x +31
|
|
1kwrA
|
Human carbonic anhydrase ii complexed with inhibitor 0134-36
|
S +31
|
S 3x +31
|
|
1cajA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
S +31
|
S 2x +31
|
|
1cilA
|
The positions of his-64 and a bound water in human carbonic anhydrase ii upon binding three structurally related inhibitors
|
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
|
|
1camA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
1cvaA
|
Structural and functional importance of a conserved hydrogen bond network in human carbonic anhydrase ii
|
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
|
|
5llaA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 4-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
5ll5A
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-(1h-benzimidazol-1-ylacetyl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5gmmA
|
Crystal structure of human carbonic anhydrase i in complex with polmacoxib
|
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 3x +31
|
|
4qjxA
|
Crystal structure of human carbonic anhydrase isozyme xiii with inhibitor
|
S +31
|
S 3x +31
|
|
4knmA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-{[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetyl}benzenesulfonamide
|
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
|
S +31
|
S 3x +31
|
|
3mdzA
|
Crystal structure of human carbonic anhydrase vii [isoform 1], ca7
|
S +31
|
S 3x +31
|
|
1xegA
|
Crystal structure of human carbonic anhydrase ii complexed with an acetate ion
|
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
|
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 3x +31
|
|
1ccuA
|
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity
|
S +31
|
S 7x +31
|
|
1ugeA
|
Human carbonic anhydrase ii [hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by leu (a65l)
|
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
|
|
1bnmA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 23x +31
|
|
1cimA
|
The positions of his-64 and a bound water in human carbonic anhydrase ii upon binding three structurally related inhibitors
|
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
|
S +31
|
S 11x +31
|
|
8ca2A
|
Engineering the hydrophobic pocket of carbonic anhydrase ii
|
S +31
|
S 1x +31
|
|
3da2A
|
X-ray structure of human carbonic anhydrase 13 in complex with inhibitor
|
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
|
|
|
6ctfA
|
Crystal structure of gltph fast mutant - r276s/m395r
|
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
|
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
|
S +31
|
S 3x +31
|
|
1ca2A
|
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution
|
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
|
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
|
|
4qjoA
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with inhibitor
|
S +31
|
S 3x +31
|
|
4qjpA
|
Crystal structure of human carbonic anhydrase isozyme xiii with inhibitor
|
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
|
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
|
S +31
|
S 19x +31
|
|
1i9pA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,4,6-trifluorophenyl)methyl]-benzamide
|
S +31
|
S 7x +31
|
|
1i9mA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,4-difluorophenyl)methyl]-benzamide
|
S +31
|
S 15x +31
|
|
1ydcA
|
Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
|
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
|
S +31
|
S 23x +31
|
|
1if5A
|
Carbonic anhydrase ii complexed with 2,6-difluorobenzenesulfonamide
|
S +31
|
S 10x +31
|
|
2ca2A
|
Crystallographic studies of inhibitor binding sites in human carbonic anhydrase ii. a pentacoordinated binding of the scn-ion to the zinc at high p*h
|
S +31
|
S 23x +31
|
|
1g1dA
|
Carbonic anhydrase ii complexed with 4-(aminosulfonyl)-n-[(2-fluorophenyl)methyl]-benzamide
|
S +31
|
S 22x +31
|
|
1hcaA
|
Unexpected ph-dependent conformation of his-64, the proton shuttle of carbonic anhydrase ii.
|
S +31
|
S 19x +31
|
|
1i9oA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,3,4-trifluorophenyl)methyl]-benzamide
|
S +31
|
S 19x +31
|
|
1hedA
|
Structural consequences of hydrophilic amino-acid substitutions in the hydrophobic pocket of human carbonic anhydrase ii
|
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 3x +31
|
|
2cbbA
|
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
|
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 11x +31
|
|
1hebA
|
Structural consequences of hydrophilic amino-acid substitutions in the hydrophobic pocket of human carbonic anhydrase ii
|
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
|
S +31
|
S 22x +31
|
|
1cnxA
|
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants
|
S +31
|
S 15x +31
|
|
6ca2A
|
Engineering the hydrophobic pocket of carbonic anhydrase ii
|
S +31
|
S 22x +31
|
|
3ca2A
|
Crystallographic studies of inhibitor binding sites in human carbonic anhydrase ii. a pentacoordinated binding of the scn-ion to the zinc at high p*h
|
S +31
|
S 3x +31
|
|
3tmjA
|
Joint x-ray/neutron structure of human carbonic anhydrase ii at ph 7.8
|