S +31
|
S 3x +31
|
|
4mo8A
|
The crystal structure of the human carbonic anhydrase ii in complex with n-[2-(2-methyl-5-nitro-1h-imidazol-1-yl)ethyl]sulfamide
|
S +31
|
S 3x +31
|
|
3s78B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 3x +31
|
|
3v3jA
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
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
|
S +31
|
S 3x +31
|
|
5a6hA
|
Synthesis, carbonic anhydrase inhibition and protein x-ray structure of the unusual natural product primary sulfonamide psammaplin c
|
S +31
|
S 11x +31
|
|
4qy3A
|
The crystal structure of the complex of hcaii with an ortho-substituted benzoic acid
|
S +31
|
S 4x +31
|
|
5ulnA
|
Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography
|
S +31
|
S 3x +31
|
|
4g0cA
|
Neutron structure of acetazolamide-bound human carbonic anhydrase ii reveal molecular details of drug binding.
|
S +31
|
S 3x +31
|
|
5u0dA
|
Identification of a new zinc binding chemotype by fragment screening
|
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
|
S +31
|
S 3x +31
|
|
3dvdA
|
X-ray crystal structure of mutant n62d of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
4zx1A
|
Engineered carbonic anhydrase ix mimic in complex with a glucosyl sulfamate 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
|
S +31
|
S 3x +31
|
|
3hkuA
|
Human carbonic anhydrase ii in complex with topiramate
|
S +31
|
S 3x +31
|
|
4itoA
|
Human ca ii inhibition by novel sulfonamide
|
S +31
|
S 3x +31
|
|
3v3hB
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
K +31
|
K 3x +31
|
|
3v2mA
|
Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5bnlA
|
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins
|
S +31
|
S 3x +31
|
|
4ilxA
|
Structure of human carbonic anhydrase ii in complex with an adamantyl sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
2povA
|
The crystal structure of the human carbonic anhydrase ii in complex with 4-amino-6-chloro-benzene-1,3-disulfonamide
|
K +31
|
K 3x +31
|
|
5tyaA
|
Identification of a new zinc binding chemotype by fragment screening
|
S +31
|
S 3x +31
|
|
5n1rA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4'-pyrazol-1-ylmethyl-biphenyl-4-sulfonamide
|
S +31
|
S 3x +31
|
|
5jq0A
|
Crystal structure of human carbonic anhydrase ii in complex with benzoxaborole at ph=8.7
|
S +31
|
S 11x +31
|
|
2hncA
|
Crystal structure of the human carbonic anhydrase ii in complex with the 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor.
|
K +31
|
K 3x +31
|
|
4pyxA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
S +31
|
S 3x +31
|
|
2fmzA
|
Carbonic anhydrase activators. activation of isoforms i, ii, iv, va, vii and xiv with l- and d- phenylalanine, structure with d-phenylalanine.
|
S +31
|
S 3x +31
|
|
5flqA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 15x +31
|
|
4q8yA
|
Crystal structure of 2-hydroxyisoquinoline-1(2h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5o07A
|
The crystal structure of the human carbonic anhydrase ii in complex with a nitroimidazole sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
3qykA
|
Human carbonic anhydrase ii complexed with triple ring benzene sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
5n1sA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(1h-indol-2-yl)-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5e2rA
|
The crystal structure of the human carbonic anhydrase ii in complex with a 1,1'-biphenyl-4-sulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
3ryxB
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
S 11x +31
|
|
4yxuA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (4).
|
S +31
|
S 7x +31
|
|
4q78A
|
Structure-assisted design of carborane-based inhibitors of carbonic anhydrase
|
S +31
|
S 3x +31
|
|
4rh2A
|
Crystal structure of human carbonic anhydrase ii in complex with 2-(6-hydroxy-3-oxo-3h-xanthen-9-yl)-5-{3-1-(4-sulfamoyl-phenyl)-1h-[1,2,3]triazol-4-ylmethyl-thioureido}-benzoic acid
|
K +31
|
K 3x +31
|
|
4e4aA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
S +31
|
S 23x +31
|
|
4jsaA
|
Benzenesulfonamide complexed with hcaii h94d
|
K +31
|
K 3x +31
|
|
2fnmA
|
Activation of human carbonic anhdyrase ii by exogenous proton donors
|
S +31
|
S 3x +31
|
|
5a25A
|
Rational engineering of a mesophilic carbonic anhydrase to an extreme halotolerant biocatalyst
|
S +31
|
S 3x +31
|
|
3ni5A
|
Carbonic anhydrase inhibitor: c1 family
|
S +31
|
S 3x +31
|
|
3k7kA
|
Crystal structure of the complex between carbonic anhydrase ii and anions
|
K +31
|
K 3x +31
|
|
3r16A
|
Human caii bound to n-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
S +31
|
S 11x +31
|
|
4fvnA
|
Carbonic anhydrase ii in complex with n-(tetrahydropyrimidin-2(1h)-ylidene)sulfuric diamide
|
S +31
|
S 3x +31
|
|
5jmzA
|
Carbonic anhydrase ix-mimic in complex with u-no2
|
S +31
|
S 3x +31
|
|
3v3iB
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
K +31
|
K 3x +31
|
|
6d1lA
|
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects
|
S +31
|
S 15x +31
|
|
4q7wA
|
Crystal structure of 1-hydroxy-6-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
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
|
S +31
|
S 3x +31
|
|
5amgA
|
Three dimensional structure of human carbonic anhydrase ii in complex with 2-(pentylsulfamoyl)-4-sulfamoylbenzoic acid
|
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
|
S +31
|
S 3x +31
|
|
5e2kA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-(3-aminophenyl)benzenesulfonamide inhibitor
|
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
|
S +31
|
S 3x +31
|
|
4n16A
|
Structure of cholate bound to human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
3m1qA
|
Carbonic anhydrase ii mutant w5c-h64c with opened disulfide bond
|
K +31
|
K 1x +31
|
|
2eu2A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
S +31
|
S 3x +31
|
|
3t82A
|
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
|
S +31
|
S 3x +31
|
|
4jszA
|
Benzenesulfonamide bound to hcaii h94c
|
K +31
|
K 3x +31
|
|
4e3fA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
S +31
|
S 7x +31
|
|
3m2yA
|
Carbonic anhydrase ii in complex with novel sulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
2wejA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
S +31
|
S 3x +31
|
|
3k2fA
|
Nitric oxide-donating carbonic anhydrase inhibitors for the treatment of open-angle glaucoma
|
S +31
|
S 3x +31
|
|
3kigA
|
Mutant carbonic anhydrase ii in complex with an azide and an alkyne
|
S +31
|
S 3x +31
|
|
3d9zA
|
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
|
|
2q38A
|
Carbonic anhydrase ii in complex with saccharin at 1.95 angstrom
|
S +31
|
S 3x +31
|
|
2osmA
|
Inhibition of carbonic anhydrase ii by thioxolone: a mechanistic and structural study
|
S +31
|
S 23x +31
|
|
3rj7A
|
Human carbonic anhydrase ii complexed with its inhibitor rhenium(i)triscarbonyl-cyclopentadienyl-carboxy-4-aminomethylbenzene-sulfonamide
|
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.
|
S +31
|
S 3x +31
|
|
3rldA
|
Crystal structure of the y7i mutant of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
2iliA
|
Refine atomic structure of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5wgpA
|
Human carbonic anhydrase ix-mimic complexed with acek
|
S +31
|
S 7x +31
|
|
5eoiA
|
Crystal structure of copper bound human carbonic anhydrase ii
|
S +31
|
S 7x +31
|
|
4q7sA
|
Crystal structure of 1-hydroxy-4-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5ekjA
|
Human carbonic anhydrase ii complexed with a two-faced guest
|
S +31
|
S 3x +31
|
4
|
4zwiA
|
Surface lysine acetylated human carbonic anhydrase ii in complex with a sulfamate-based inhibitor
|
S +31
|
S 3x +31
|
|
4zwyA
|
Human carbonic anhydrase ii in complex with a glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
3tvoX
|
Human carbonic anhydrase ii proton transfer double mutant
|
S +31
|
S 3x +31
|
|
4jswA
|
Human carbonic anhydrase ii h94c
|
K +31
|
K 3x +31
|
|
4fikA
|
Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
|
S +31
|
S 3x +31
|
|
3t83A
|
Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
|
S +31
|
S 3x +31
|
|
4hf3A
|
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
|
|
3u7cA
|
Crystal structure of the v143i mutant of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3u45X
|
Human carbonic anhydrase ii v143a
|
K +31
|
K 3x +31
|
|
3p55A
|
Human carbonic anhydrase ii in complex with p-(4-ferrocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
3hktA
|
Human carbonic anhydrase ii in complex with alpha-d-glucopyranosyl-(1->4)-1-thio-beta-d-glucopyranosylsulfonamide
|
S +31
|
S 3x +31
|
|
3p4vA
|
Human carbonic anhydrase ii in complex with (+)-xylariamide a
|
S +31
|
S 3x +31
|
|
3l14A
|
Human carbonic anhydrase ii complexed with althiazide
|
S +31
|
S 3x +31
|
|
3oilA
|
Human carbonic anhydrase ii mutant a65s, n67q (ca ix mimic) bound by 2-ethylestradiol 3-o-sulfamate
|
K +31
|
K 3x +31
|
|
2nwzA
|
Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3dvcA
|
X-ray crystal structure of mutant n62t of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3v3gB
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
K +31
|
K 3x +31
|
|
5t71A
|
Human carboanhydrase f131c_c206s double mutant in complex with sa-2
|
S +31
|
S 3x +31
|
|
3hfpA
|
Crystal structure of teh complex between ca ii and the activator mai
|
S +31
|
S 15x +31
|
|
4q8xA
|
Crystal structure of 1-hydroxy-5-(trifluoromethyl)pyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
5dsmA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 25 min warming
|
S +31
|
S 3x +31
|
|
5dslA
|
Structure of co2 released holo-form of human carbonic anhydrase ii with 10 min warming
|
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
|
S +31
|
S 3x +31
|
|
4m2vA
|
Genetically engineered carbonic anhydrase ix in complex with brinzolamide
|
S +31
|
S 3x +31
|
|
3s77B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 3x +31
|
|
5yuiA
|
Co2 release in human carbonic anhydrase ii crystals: reveal histidine 64 and solvent dynamics
|
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
|
S +31
|
S 3x +31
|
|
5n0eA
|
Crystal structure of human carbonic anhydrase ii in complex with (s)-4-(6,7-dihydroxy-1-phenyl-3,4-tetrahydroisoquinoline-1h-2-carbonyl)benzenesulfonamide.
|
S +31
|
S 3x +31
|
|
5llhA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-(1,3-benzothiazol-2-ylthio)-2,3,5,6-tetrafluorobenzenesulfonamide
|
K +31
|
K 3x +31
|
|
5brwA
|
Catalytic improvement of an artificial metalloenzyme by computational design
|
S +31
|
S 7x +31
|
|
5fnkA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
6d1mA
|
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects
|
S +31
|
S 3x +31
|
|
3m1wA
|
Carbonic anhyrdase ii mutant w5ch64c with closed disulfide bond in complex with sulfate
|
S +31
|
S 3x +31
|
|
5fngA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
3m5sA
|
Carbonic anhydrase ii mutant h64c in complex with carbonate
|
S +31
|
S 3x +31
|
|
2weoA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
K +31
|
K 3x +31
|
|
5wexA
|
Discovery of new selenoureido analogs of 4-(4-fluorophenylureido) benzenesulfonamides as carbonic anhydrase inhibitors
|
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
|
|
4zwxA
|
Engineered carbonic anhydrase ix mimic in complex with glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
4riuA
|
A carbonic anhydrase ix mimic in complex with a saccharin-based inhibitor
|
K +31
|
K 3x +31
|
|
4q06A
|
Crystal structure of chimeric carbonic anhydrase ix with 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 11x +31
|
|
2hkkA
|
Carbonic anhydrase activators: solution and x-ray crystallography for the interaction of andrenaline with various carbonic anhydrase isoforms
|
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
|
K +31
|
K 3x +31
|
|
3p5aA
|
Human carbonic anhydrase complexed with sodium morpholinocarbodithioate
|
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
|
K +31
|
K 3x +31
|
|
5je7B
|
Human carbonic anhydrase ii (f131y) 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
|
K +31
|
K 3x +31
|
|
5ekmA
|
Human carbonic anhydrase ii complexed with a two-faced guest
|
S +31
|
S 3x +31
|
|
4y0jA
|
H/d exchanged human carbonic anhydrase ii ph 6 room temperature neutron crystal structure.
|
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)
|
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
|