S +31
|
S 3x +31
|
|
5fnhA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
K +31
|
K 3x +31
|
|
5flsA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
3igpA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
5umcA
|
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
|
|
5ogpA
|
Metalacarborane inhibitors of carbonic anhydrase ix
|
K +31
|
K 3x +31
|
|
5g01A
|
An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
|
K +31
|
K 3x +31
|
|
4ywpA
|
Sucrose binding site in genetically engineered carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
4q09A
|
Crystal structure of chimeric carbonic anhydrase xii with inhibitor
|
S +31
|
S 3x +31
|
|
4e3hA
|
Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
|
S +31
|
S 3x +31
|
|
4m2wA
|
Genetically engineered carbonic anhydrase ix in complex with dorzolamide
|
S +31
|
S 3x +31
|
|
4q08A
|
Crystal structure of chimeric carbonic anhydrase xii with inhibitor
|
K +31
|
K 11x +31
|
|
4mdlA
|
Meta carborane carbonic anhydrase inhibitor
|
S +31
|
S 3x +31
|
|
4q07A
|
Crystal structure of chimeric carbonic anhydrase ix with inhibitor
|
S +31
|
S 3x +31
|
|
3r17B
|
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
K +31
|
K 11x +31
|
|
4fptA
|
Carbonic anhydrase ii in complex with ethyl (2z,4r)-2-(sulfamoylimino)-1,3-thiazolidine-4-carboxylate
|
S +31
|
S 6x +31
|
|
3ieoA
|
The coumarin-binding site in carbonic anhydrase: the antiepileptic lacosamide as an example
|
K +31
|
K 3x +31
|
4
|
3s72B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
S +31
|
S 11x +31
|
|
3nj9A
|
Crystal structure of carbonic anhydrase ii in complex with a nir inhibitor
|
S +31
|
S 3x +31
|
|
3f4xA
|
Carbonic anhydrase inhibitors. comparison of chlorthalidone and indapamide x-ray crystal structures in adducts with isozyme ii: when three water molecules make the difference
|
S +31
|
S 3x +31
|
|
2wehA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
K +31
|
K 3x +31
|
|
3dazA
|
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
|
4
|
2nnvA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
3dc9A
|
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
|
|
2eu3A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
S +31
|
S 3x +31
|
|
3mnkA
|
Human carbonic anhydrase ii mutant k170h
|
K +31
|
K 3x +31
|
|
2vvbX
|
Human carbonic anhydrase ii in complex with bicarbonate
|
S +31
|
S 3x +31
|
|
5jepB
|
Human carbonic anhydrase ii (t199s) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
4qk3A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - [delta]230-240
|
S +31
|
S 3x +31
|
|
5ekhA
|
Human carbonic anhydrase ii complexed with a two-faced guest
|
S +31
|
S 7x +31
|
|
4xe1A
|
Human carbonic anhydrase ii in complex with 6-sulfamoyl-saccharin
|
S +31
|
S 3x +31
|
|
5eh5A
|
Human carbonic anhydrase ii in complex with ligand
|
K +31
|
K 3x +31
|
|
4z1eA
|
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 3x +31
|
|
4rn4A
|
Human carbonic anhydrases ii in complex with a acetazolamide derivative comprising one hydrophobic and one hydrophilic tail moiety
|
S +31
|
S 3x +31
|
|
4pq7A
|
The crystal structure of the human carbonic anhydrase ii in complex with a sulfamide inhibitor
|
K +31
|
K 3x +31
|
|
3kkxA
|
Neutron structure of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
4l5vA
|
The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
3u3aX
|
Structure of human carbonic anhydrase ii v143i
|
K +31
|
K 3x +31
|
|
3hknA
|
Human carbonic anhydrase ii in complex with (2,3,4,6-tetra-o-acetyl-beta-d-galactopyranosyl) -(1-4)-1,2,3,6-tetra-o-acetyl-1-thio-beta-d-glucopyranosylsulfonamide
|
S +31
|
S 3x +31
|
|
3hljA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-methylthiobenzimidazo[1,2-c][1,2,3]thiadiazol-7-sulfonamide
|
S +31
|
S 3x +31
|
|
3oikA
|
Human carbonic anhydrase ii mutant a65s, n67q (ca ix mimic) bound by 2-ethylestradiol 3,17-o,o-bis-sulfamate
|
K +31
|
K 3x +31
|
|
5tfxA
|
New method for synthesis of benzoxazole amide inhibitors of carbonic anhydrase
|
S +31
|
S 3x +31
|
|
3mnjA
|
Human carbonic anhydrase ii mutant k170e
|
K +31
|
K 3x +31
|
|
2fnnA
|
Activation of human carbonic anhydrase ii by exogenous proton donors
|
S +31
|
S 3x +31
|
|
4pyyA
|
Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
|
S +31
|
S 3x +31
|
4
|
2x7sA
|
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors.
|
S +31
|
S 15x +31
|
|
4mtyA
|
Structure at 1a resolution of a helical aromatic foldamer-protein complex.
|
S +31
|
S 3x +31
|
|
3mniA
|
Human carbonic anhydrase ii mutant k170d
|
S +31
|
S 7x +31
|
|
5fdiA
|
Crystal structure of human carbonic anhydrase ii with the anticonvulsant sulfamide jnj-26990990 and its s,s-dioxide analog.
|
S +31
|
S 3x +31
|
4
|
2nngA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6b5aA
|
Carbonic anhydrase ix-mimic in complex with nitrogenous base-bearing benezenesulfonamide
|
K +31
|
K 3x +31
|
|
3p3jA
|
Human carbonic anhydrase ii in complex with p-(5-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
5jesB
|
Human carbonic anhydrase ii (v121t) complexed with benzo[d]thiazole-2-sulfonamide
|
K +31
|
K 3x +31
|
|
3gz0A
|
Apo-human carbonic anhydrase ii revisited: implications of the loss of a metal in protein structure, stability and solvent network
|
K +31
|
K 3x +31
|
|
4qk1A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - k170p
|
K +31
|
K 3x +31
|
|
5floA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
K +31
|
K 3x +31
|
|
5th4A
|
Crystal structure of 1-hydroxypyridine-2(1h)-thione bound to human carbonic anhydrase 2 l198g
|
S +31
|
S 3x +31
|
4
|
2foqA
|
Human carbonic anhydrase ii complexed with two-prong inhibitors
|
S +31
|
S 3x +31
|
|
4q49A
|
Room temperature neutron crystal structure of apo human carbonic anhydrase at ph 7.5
|
S +31
|
S 3x +31
|
|
4zwzA
|
Engineered carbonic anhydrase ix mimic in complex with a glucosyl sulfamate inhibitor
|
S +31
|
S 3x +31
|
|
3ryvB
|
Carbonic anhydrase complexed with n-ethyl-4-sulfamoylbenzamide
|
K +31
|
K 3x +31
|
|
5sz5A
|
Carbonic anhydrase ix-mimic in complex with 4-(2-methylphenyl)-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5txyA
|
Identification of a new zinc binding chemotype of by fragment screening on human carbonic anhydrase
|
K +31
|
K 3x +31
|
|
3ryjB
|
Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide
|
S +31
|
S 3x +31
|
|
4k13A
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with dorzolamide
|
S +31
|
S 3x +31
|
|
3rz1B
|
Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
|
S +31
|
S 3x +31
|
|
3bl1A
|
Carbonic anhydrase inhibitors. sulfonamide diuretics revisited old leads for new applications
|
S +31
|
S 3x +31
|
|
3p44A
|
Human carbonic anhydrase ii in complex with p-(4-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4z1nA
|
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
|
|
4ygnA
|
Nai--interactions between hofmeister anions and the binding pocket of a protein
|
K +31
|
K 3x +31
|
|
5lmdA
|
The crystal structure of hca ii in complex with a benzoxaborole inhibitor
|
S +31
|
S 3x +31
|
|
5fnjA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 3x +31
|
|
6equA
|
X-ray crystal structure of the human carbonic anhydrase ii adduct with a membrane-impermeant inhibitor
|
K +31
|
K 3x +31
|
4
|
5jgsB
|
Human carbonic anhydrase ii (f131y/l198a) complexed with benzo[d]thiazole-2-sulfonamide
|
S +31
|
S 11x +31
|
|
2gd8A
|
Crystal structure analysis of the human carbonic anhydrase ii in complex with a 2-substituted estradiol bis-sulfamate
|
S +31
|
S 3x +31
|
|
3mwoA
|
Human carbonic anhydrase ii in a doubled monoclinic cell: a re-determination
|
S +31
|
S 3x +31
|
|
5e2sA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-(2-iso-propylphenyl)benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
3s71B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
K +31
|
K 3x +31
|
|
3m1qA
|
Carbonic anhydrase ii mutant w5c-h64c with opened disulfide bond
|
S +31
|
S 3x +31
|
|
3dcwA
|
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
|
|
4idrX
|
Human carbonic anhydrase ii proton transfer double mutant
|
S +31
|
S 7x +31
|
|
3m1jA
|
The crystal structure of a nami a-carbonic anhydrase ii adduct discloses the mode of action of this novel anticancer metallodrug
|
S +31
|
S 3x +31
|
|
3hs4A
|
Human carbonic anhydrase ii complexed with acetazolamide
|
S +31
|
S 3x +31
|
|
6cjvA
|
Carbonic anhydrase ix-mimic in complex with sucralose
|
S +31
|
S 3x +31
|
|
4ruxA
|
Crystal structure of human carbonic anhydrase ii in complex with 4-(allyloxy)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5jgtB
|
Human carbonic anhydrase ii (f131y/l198a) complexed with 1,3-thiazole-2-sulfonamide
|
S +31
|
S 3x +31
|
|
5dsiA
|
Structure of co2 bound holo-form of human carbonic anhydrase ii with 0 sec (no) warming
|
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
|
S +31
|
S 3x +31
|
|
5llcA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-(methylamino)-2,5,6-trifluoro-4-[(2-phenylethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
3dd0A
|
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
K +31
|
K 3x +31
|
|
4fl7A
|
The crystal structure of human carbonic anhydrase ii in complex with n-(hydroxy)-benzamide
|
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
|
|
4jszA
|
Benzenesulfonamide bound to hcaii h94c
|
S +31
|
S 3x +31
|
|
4n16A
|
Structure of cholate bound to human 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
|
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
|
4
|
2nnsA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
4q90A
|
Crystal structure of 4-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
|
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
|
|
5jehB
|
Human carbonic anhydrase ii (l198a) complexed with benzo[d]thiazole-2-sulfonamide
|
K +31
|
K 3x +31
|
|
3vbdA
|
Complex of human carbonic anhydrase ii with 4-(6-methoxy-3,4-dihydroisoquinolin-1-yl)benzenesulfonamide
|
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
|
|
6d1lA
|
Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects
|
S +31
|
S 3x +31
|
|
3v3iB
|
Kinetic and structural studies of thermostabilized mutants of hca ii.
|
S +31
|
S 3x +31
|
|
5jmzA
|
Carbonic anhydrase ix-mimic in complex with u-no2
|
S +31
|
S 11x +31
|
|
4fvnA
|
Carbonic anhydrase ii in complex with n-(tetrahydropyrimidin-2(1h)-ylidene)sulfuric diamide
|
K +31
|
K 3x +31
|
|
3r16A
|
Human caii bound to n-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
S +31
|
S 3x +31
|
|
3k7kA
|
Crystal structure of the complex between carbonic anhydrase ii and anions
|
S +31
|
S 3x +31
|
|
3ni5A
|
Carbonic anhydrase inhibitor: c1 family
|
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
|
|
3mmfA
|
Crystal structure of human carbonic anhydrase ii in complex with a 1,3,5-triazine-substituted benzenesulfonamide inhibitor
|
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
|
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.
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S +31
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S 3x +31
|
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5flqA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 15x +31
|
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4q8yA
|
Crystal structure of 2-hydroxyisoquinoline-1(2h)-thione bound to human carbonic anhydrase ii
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S +31
|
S 3x +31
|
|
5o07A
|
The crystal structure of the human carbonic anhydrase ii in complex with a nitroimidazole sulfamate inhibitor
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S +31
|
S 3x +31
|
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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
|
|
5a25A
|
Rational engineering of a mesophilic carbonic anhydrase to an extreme halotolerant biocatalyst
|
S +31
|
S 23x +31
|
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4jsaA
|
Benzenesulfonamide complexed with hcaii h94d
|
K +31
|
K 3x +31
|
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2fnmA
|
Activation of human carbonic anhdyrase ii by exogenous proton donors
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