K +31
|
|
|
7priAAA
|
Carbonic anhydrase from schistosoma mansoni in complex with clorsulon
|
K +31
|
|
|
7plfAAA
|
Human carbonic anhydrase i in complex with clorsulon
|
K +31
|
|
|
7nh8AAA
|
Crystal structure of human carbonic anhydrase ii with n-((1-(6-((3ar,7r,7as)-7-hydroxy-2,2-dimethyltetrahydro-[1,3]dioxolo[4,5-c]pyridin-5(4h)-yl)hexyl)-1h-1,2,3-triazol-4-yl)methyl)-4-sulfamoylbenzamide
|
K +31
|
K 3x +31
|
|
7ng1A
|
Crystal structure of alpha carbonic anhydrase from schistoso ma mansoni bound to 1-(4-iodophenyl)-3-[2-(4-sulfamoylphenyl)ethyl]selenourea
|
K +31
|
K 3x +31
|
|
7mu3A
|
Human carbonic anhydrase 9 mimic with compound
|
K +31
|
K 4x +31
|
|
6zr9A
|
The crystal structure of the complex of hcavii with 2-(4-benzhydrylpiperazin-1-yl)-n-(4-sulfamoylphenyl)acetamide
|
K +31
|
K 15x +31
|
|
6rrgA
|
Human carbonic anhydrase ii in complex with fluorinated benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6yj3A
|
Metala-carborane di-propyl-sulfonamide
|
K +31
|
K 3x +31
|
|
6yokA
|
Para-carborane di-propyl-sulfonamide in complex with ca ix mimic
|
S +31
|
S 3x +31
|
|
6ymbA
|
Microed structure of human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
6ymaA
|
Microed structure of acetazolamide-bound human carbonic anhydrase ii
|
K +31
|
K 3x +31
|
|
6y74A
|
X-ray crystal structure of human carbonic anhydrase ix catalytic domain.
|
S +31
|
S 3x +31
|
|
6km6A
|
Human carbonic anhydrase ii native 15 atm co2
|
K +31
|
K 3x +31
|
|
6km5A
|
Human carbonic anhydrase ii native 13 atm co2
|
S +31
|
S 3x +31
|
|
6km4A
|
Human carbonic anhydrase ii native 07 atm co2
|
K +31
|
K 3x +31
|
|
6km3A
|
Human carbonic anhydrase ii native 00 atm co2
|
K +31
|
K 3x +31
|
|
6km2A
|
Human carbonic anhydrase ii v143i variant 15 atm co2
|
K +31
|
K 3x +31
|
|
6km1A
|
Human carbonic anhydrase ii v143i variant 13 atm co2
|
S +31
|
S 3x +31
|
|
6km0A
|
Human carbonic anhydrase ii v143i variant 07 atm co2
|
S +31
|
S 3x +31
|
|
6klzA
|
Human carbonic anhydrase ii v143i variant 00 atm co2
|
S +31
|
S 3x +31
|
|
6rmxA
|
Human carbonic anhydrase ii mutant t199v bound by 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6t9zA
|
Nidocarborane inhibitor of carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
6t7uA
|
Carborane inhibitor of carbonic anhydrase ix
|
S +31
|
S 4x +31
|
|
6sdtA
|
Human carbonic anhydrase vii in complex with a sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
6sdsA
|
Human carbonic anhydrase ii in complex with a sulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
6s03A
|
Carbonic anhydrase caix mimic in complex with inhibitor i39lt379
|
S +31
|
S 3x +31
|
|
6rzxA
|
Carbonic anhydrase caix mimic in complex with inhibitor fbsa
|
S +31
|
S 3x +31
|
|
6rhkA
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(3-benzylimidazolidine-1-carbonyl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6rofA
|
Human carbonic anhydrase ii mutant t199v bound by 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6rmyA
|
Human carbonic anhydrase ii mutant t199v bound by 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6rhjA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-(4-benzyl-1,4-diazepane-1-carbonyl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6rg3A
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzylpiperazin-1-yl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6rg4A
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzyl-4-methylpiperazin-1-yl)benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6ux1A
|
Carbonic anhydrase ii complexed with salicylic acid
|
S +31
|
S 3x +31
|
|
6rm1A
|
Human carbonic anhydrase ii in complex with fragment.
|
S +31
|
S 3x +31
|
|
6r71A
|
Crystal structure of human carbonic anhydrase isozyme xii with 2-(benzenesulfonyl)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
K +31
|
K 3x +31
|
|
6r6yA
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-chloro-2-cyclohexylsulfanyl-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6r6jA
|
Crystal structure of human carbonic anhydrase isozyme ii with 2-(benzenesulfonyl)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6qutA
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6qnlA
|
Three dimensional structure of human carbonic anhydrase xii in complex with benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6qngA
|
Three dimensional structure of human carbonic anhydrase xii in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6r6fA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-chloro-2-cyclohexylsulfanyl-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 7x +31
|
|
6pdvA
|
Cu-carbonic anhydrase ii, a nitrite reductase
|
S +31
|
|
|
6peaA
|
High resolution apo carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6qn6A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
K +31
|
K 3x +31
|
|
6qn5A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6qn2A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6qn0A
|
Three dimensional structure of human carbonic anhydrase xii in complex with benzenesulfonamide
|
S +31
|
S 19x +31
|
|
6i2fA
|
Human carbonic anhydrase ii in complex with 4-propoxybenzenesulfonamide
|
S +31
|
S 15x +31
|
|
6i1uA
|
Human carbonic anhydrase ii in complex with 4-ethoxybenzenesulfonamide
|
S +31
|
S 3x +31
|
|
6i0lA
|
Crystal structure of human carbonic anhydrase i in complex with the 1-[4-chloro-3-(trifluoromethyl)phenyl]-3-[2-(4-sulfamoylphenyl)ethyl]urea inhibitor
|
K +31
|
K 3x +31
|
|
6i0jA
|
Crystal structure of human carbonic anhydrase i in complex with the 4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)phenyl sulfamate inhibitor
|
K +31
|
K 31x +31
|
|
6i0wA
|
Human carbonic anhydrase ii in complex with 4-methoxybenzenesulfonamide
|
K +31
|
K 3x +31
|
|
6qqmA
|
Crystal structure of the alpha carbonic anhydrase from schistosoma mansoni
|
S +31
|
S 15x +31
|
|
6hxdA
|
Human carbonic anhydrase ii in complex with 4-butylbenzenesulfonamide
|
K +31
|
K 15x +31
|
|
6hr3A
|
Human carbonic anhydrase ii in complex with 4-propylbenzenesulfonamide
|
K +31
|
K 3x +31
|
4
|
6nj4A
|
Thermostable variant of human carbonic anhydrase with disordered tetrazine 2.0 reacted with strained trans-cyclooctene at site 233
|
K +31
|
K 3x +31
|
3
|
6nj5A
|
Thermostable variant of human carbonic anhydrase ii with disordered tetrazine 2.0 at site 233
|
K +31
|
K 3x +31
|
4
|
6nj2A
|
Thermostable carbonic anhydrase ii variant with tetrazine 2.0 at site 186
|
S +31
|
S 3x +31
|
4
|
6nj3A
|
Thermostable variant of human carbonic anhydrase with ordered tetrazine 2.0 at site 233
|
S +31
|
S 3x +31
|
4
|
6nj6A
|
Thermostable variant of human carbonic anhydrase with tetrazine 2.0 at site 186 reacted with stco in crystallo
|
S +31
|
S 3x +31
|
|
6ql2A
|
Crystal structure of chimeric carbonic anhydrase vi with ethoxzolamide.
|
K +31
|
K 3x +31
|
|
6ql3A
|
Crystal structure of chimeric carbonic anhydrase vi with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6ql1A
|
Crystal structure of chimeric carbonic anhydrase vi with 4-[(4,6-dimethylpyrimidin-2-yl)thio]-2,3,5,6-tetrafluorobenzenesulfonamide
|
K +31
|
K 3x +31
|
|
6hzxA
|
Protein-aromatic foldamer complex crystal structure
|
S +31
|
S 3x +31
|
|
6gxeA
|
Carbonic anhydrase caix mimic in complex with inhibitor js14
|
S +31
|
S 3x +31
|
|
6gxbA
|
Carbonic anhydrase caix mimic in complex with inhibitor js13
|
S +31
|
S 15x +31
|
|
6gdcA
|
Human carbonic anhydrase ii in complex with benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6g5uA
|
Crystal structure of human carbonic anhydrase isozyme xiii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6g6tA
|
Crystal structure of human carbonic anhydrase isozyme ii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6g7aA
|
Crystal structure of human carbonic anhydrase isozyme xii 2-(benzylamino)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6mbyA
|
Carbonic anhydrase ii in complex with ferulic acid
|
S +31
|
S 3x +31
|
|
6mbvA
|
Carbonic anhydrase ii in complex with nicotinic acid
|
S +31
|
S 3x +31
|
|
6g5lA
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-chloro-2-(cyclohexylamino)-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
S +31
|
S 3x +31
|
|
6gcyA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin-sugar conjugate complex)
|
S +31
|
S 3x +31
|
|
6fjiA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (apo).
|
S +31
|
S 3x +31
|
|
6fjjA
|
Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin).
|
S +31
|
S 3x +31
|
|
6hwzA
|
Selenols: a new class of carbonic anhydrase inhibitors
|
S +31
|
S 4x +31
|
|
6h38A
|
The crystal structure of human carbonic anhydrase vii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
|
K +31
|
K 4x +31
|
|
6h36A
|
The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide.
|
S +31
|
S 4x +31
|
|
6h37A
|
The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
6h34A
|
The crystal structure of human carbonic anhydrase ii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
|
S +31
|
S 2x +31
|
|
6h2zA
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide.
|
S +31
|
S 3x +31
|
|
6h33A
|
The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide.
|
S +31
|
S 3x +31
|
|
6g3vA
|
Crystal structure of human carbonic anhydrase i in complex with the inhibitor famotidine
|
S +31
|
S 3x +31
|
4
|
6g3qA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor famotidine
|
S +31
|
S 3x +31
|
|
6evrA
|
Crystal structure of human carbonic anhydrase i in complex with the 4-(4 acetyl-3-benzylpiperazine-1 carbonyl)benzene-1-sulfonamide inhibitor
|
K +31
|
K 3x +31
|
|
3iqkA
|
Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
|
S +31
|
S 3x +31
|
|
4yglA
|
Naclo4--interactions between hofmeister anions and the binding pocket of a protein
|
S +31
|
S 23x +31
|
|
1bnnA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
1ttmA
|
Human carbonic anhydrase ii complexed with 667-coumate
|
K +31
|
K 3x +31
|
|
5fl5A
|
Three dimensional structure of human carbonic anhydrase ix in complex with 5-(1-(4-methoxyphenyl)-1h-1,2,3-triazol-4-yl)thiophene-2- sulfonamide
|
S +31
|
S 3x +31
|
|
5neaA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(2-methyl-1,3-oxazol-5-yl)benzene-1-sulfonammide
|
S +31
|
S 7x +31
|
|
1bv3A
|
Human carbonic anhydrase ii complexed with urea
|
S +31
|
S 3x +31
|
|
5e2mA
|
Crystal structure of human carbonic anhydrase isozyme i with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5ohhA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5n25A
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-pyridin-3-yl-benzenesulfonamide
|
S +31
|
S 3x +31
|
|
4gl1X
|
Structure of h64a/n62l/n67l human carbonic anhydrase ii triple mutant
|
K +31
|
K 3x +31
|
|
3v2jA
|
Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
6fe2A
|
Three dimensional structure of human carbonic anhydrase ix
|
S +31
|
S 3x +31
|
|
4z0qA
|
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
|
|
4qk2A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - e234p
|
K +31
|
K 3x +31
|
|
3konA
|
Crystal structure of cobalt (ii) human carbonic anhydrase ii at ph 11.0
|
S +31
|
S 3x +31
|
|
4bf1A
|
Three dimensional structure of human carbonic anhydrase ii in complex with 5-(1-naphthalen-1-yl-1,2,3-triazol-4-yl)thiophene-2-sulfonamide
|
S +31
|
S 3x +31
|
|
3d92A
|
Human carbonic anhydrase ii bound with substrate carbon dioxide
|
K +31
|
K 3x +31
|
|
2nwoA
|
Structural and kinetic effect of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
S +31
|
S 3x +31
|
|
2f14A
|
Tne crystal structure of the human carbonic anhydrase ii in complex with a fluorescent inhibitor
|
S +31
|
S 1x +31
|
|
2hfwA
|
Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase iii
|
S +31
|
S 3x +31
|
|
5ogjA
|
Crystal structure of human carbonic anhydrase isozyme xiii with 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
S +31
|
S 3x +31
|
4
|
5neeA
|
Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 5-[2-(morpholine-4-carbonyl)1,3-oxazol-5-yl)]thiophene-2-sulfonammide
|
K +31
|
K 3x +31
|
|
5msaA
|
Crystal structure of human carbonic anhydrase isozyme xii with 2,3,5,6-tetrafluoro-4-(propylthio)benzenesulfonamide
|
S +31
|
S 3x +31
|
|
5ljqA
|
Crystal structure of human carbonic anhydrase ii in complex with the 4-(4-(phenoxymethyl)-1h-1,2,3-triazol-1-yl)benzenesulfonamide inhibitor
|
S +31
|
S 3x +31
|
|
4n0xB
|
Room temperature crystal structure of human carbonic anhydrase ii in complex with thiophene-2-sulfonamide
|
S +31
|
S 15x +31
|
|
4q7pA
|
Crystal structure of 1-hydroxy-3-methylpyridine-2(1h)-thione bound to hcaii
|
S +31
|
S 11x +31
|
|
1bn1A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
4k0zA
|
Structure of hcaix mimic (hcaii with 5 mutations in active site) in complex with methazolamide
|
K +31
|
K 3x +31
|
|
5flpA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
K +31
|
K 3x +31
|
|
5flrA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
K +31
|
K 3x +31
|
|
4xz5A
|
Structure of the thermostable alpha-carbonic anydrase from thiomicrospira crunogena xcl-2 gammaproteobacterium
|
S +31
|
S 3x +31
|
|
5fnlA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 11x +31
|
|
4yxiA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (2).
|
S +31
|
S 7x +31
|
|
2hocA
|
Crystal structure of the human carbonic anhydrase ii in complex with the 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide inhibitor
|
K +31
|
K 4x +31
|
|
3ml5A
|
Crystal structure of the c183s/c217s mutant of human ca vii in complex with acetazolamide
|
S +31
|
S 3x +31
|
|
5eheA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-(benzylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
K +31
|
K 3x +31
|
|
5ty1A
|
Identification of a new zinc binding chemotype by fragment screening
|
K +31
|
K 3x +31
|
|
4ywpA
|
Sucrose binding site in genetically engineered carbonic anhydrase ix
|
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
|
|
5eh5A
|
Human carbonic anhydrase ii in complex with ligand
|
S +31
|
S 7x +31
|
|
4xe1A
|
Human carbonic anhydrase ii in complex with 6-sulfamoyl-saccharin
|
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
|
|
5jepB
|
Human carbonic anhydrase ii (t199s) complexed with benzo[d]thiazole-2-sulfonamide
|
K +31
|
K 3x +31
|
|
2vvbX
|
Human carbonic anhydrase ii in complex with bicarbonate
|
S +31
|
S 7x +31
|
|
1bnqA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 3x +31
|
|
2eu3A
|
Human carbonic anhydrase ii in complex with novel inhibitors
|
S +31
|
S 3x +31
|
|
1rj5A
|
Crystal structure of the extracellular domain of murine carbonic anhydrase xiv
|
S +31
|
S 11x +31
|
|
1bn3A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 7x +31
|
|
1g3zA
|
Carbonic anhydrase ii (f131v)
|
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
|
|
2fw4A
|
Carbonic anhydrase activators. the first x-ray crystallographic study of an activator of isoform i, structure with l-histidine.
|
S +31
|
S 3x +31
|
4
|
2nnvA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
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
|
|
2wehA
|
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
|
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
|
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 3x +31
|
|
3r17B
|
Hcarbonic anhydrase ii bound to n-(2-fluoro.4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
|
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
|
|
5fnhA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
S +31
|
S 23x +31
|
|
1if4A
|
Carbonic anhydrase ii complexed with 4-fluorobenzenesulfonamide
|
S +31
|
S 3x +31
|
|
3w6hA
|
Crystal structure of 19f probe-labeled hcai in complex with acetazolamide
|
S +31
|
S 15x +31
|
|
1i9nA
|
Carbonic anhydrase ii (f131v) complexed with 4-(aminosulfonyl)-n-[(2,5-difluorophenyl)methyl]-benzamide
|