|
78
|
256
|
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 |
|
75
|
209
|
3bobA |
Carbonic anhydrase from marine diatom thalassiosira weissflogii- cadmium bound domain 2 |
|
76
|
209
|
3bojA |
Carbonic anhydrase from marine diatom thalassiosira weissflogii- cadmium bound domain 1 without bound metal (cdca1-r1) |
|
78
|
213
|
3bohA |
Carbonic anhydrase from marine diatom thalassiosira weissflogii- cadmium bound domain 1 with acetate (cdca1-r1) |
|
71
|
256
|
3bl1A |
Carbonic anhydrase inhibitors. sulfonamide diuretics revisited old leads for new applications |
|
77
|
209
|
3bocA |
Carbonic anhydrase from marine diatom thalassiosira weissflogii- zinc bound domain 2 (cdca1-r2) |
|
75
|
209
|
3boeA |
Carbonic anhydrase from marine diatom thalassiosira weissflogii- cadmium bound domain 2 with acetate (cdca1-r2) |
|
76
|
257
|
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 |
|
74
|
258
|
3betA |
Crystal structure of the human carbonic anhydrase ii in complex with stx 641 at 1.85 angstroms resolution |
|
91
|
357
|
3b1bA |
The unique structure of wild type carbonic anhydrase alpha-ca1 from chlamydomonas reinhardtii |
|
80
|
256
|
3b4fA |
Carbonic anhydrase inhibitors. interaction of 2-(hydrazinocarbonyl)-3-phenyl-1h-indole-5-sulfonamide with twelve mammalian isoforms: kinetic and x-ray crystallographic studies |
|
62
|
258
|
2zncA |
Murine carbonic anhydrase iv |
|
75
|
257
|
2x7sA |
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors. |
|
75
|
257
|
2x7tA |
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors. |
|
73
|
257
|
2x7uA |
Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors. |
|
77
|
258
|
2wehA |
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors |
|
75
|
258
|
2wejA |
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors |
|
76
|
257
|
2weoA |
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors |
|
70
|
230
|
2w3nA |
Structure and inhibition of the co2-sensing carbonic anhydrase can2 from the pathogenic fungus cryptococcus neoformans |
|
75
|
258
|
2wegA |
Thermodynamic optimisation of carbonic anhydrase fragment inhibitors |
|
73
|
234
|
2w3qA |
Structure and inhibition of the co2-sensing carbonic anhydrase can2 from the pathogenic fungus cryptococcus neoformans |
|
74
|
257
|
2wd3A |
Highly potent first examples of dual aromatase-steroid sulfatase inhibitors based on a biphenyl template |
|
73
|
258
|
2wd2A |
A chimeric microtubule disruptor with efficacy on a taxane resistant cell line |
|
78
|
268
|
2w2jA |
Crystal structure of the human carbonic anhydrase related protein viii |
|
76
|
258
|
2vvbX |
Human carbonic anhydrase ii in complex with bicarbonate |
|
77
|
258
|
2vvaX |
Human carbonic anhydrase in complex with co2 |
|
76
|
258
|
2qp6A |
The crystal structure of the complex of hcaii with a bioreductive antitumor derivative |
|
76
|
259
|
2qo8A |
Crystal structure of the complex of hcaii with an indane-sulfonamide inhibitor |
|
76
|
257
|
2qoaA |
Crystal structure of the complex of hcaii with an indane-sulfonamide inhibitor |
|
77
|
256
|
2q1bA |
Carbonic anhydrase ii in complex with saccharin |
|
75
|
256
|
2q38A |
Carbonic anhydrase ii in complex with saccharin at 1.95 angstrom |
|
75
|
258
|
2pouA |
The crystal structure of the human carbonic anhydrase ii in complex with 4,5-dichloro-benzene-1,3-disulfonamide |
|
73
|
257
|
2powA |
The crystal structure of the human carbonic anhydrase ii in complex with 4-amino-6-trifluoromethyl-benzene-1,3-disulfonamide |
|
77
|
257
|
2q1qA |
Carbonic anhydrase inhibitors. interaction of the antiepileptic drug sulthiame with twelve mammalian isoforms: kinetic and x-ray crystallographic studies |
|
74
|
257
|
2povA |
The crystal structure of the human carbonic anhydrase ii in complex with 4-amino-6-chloro-benzene-1,3-disulfonamide |
|
74
|
257
|
2osfA |
Inhibition of carbonic anhydrase ii by thioxolone: a mechanistic and structural study |
|
75
|
258
|
2osmA |
Inhibition of carbonic anhydrase ii by thioxolone: a mechanistic and structural study |
|
76
|
256
|
2o4zA |
Crystal structure of the carbonic anhydrase ii complexed with hydroxysulfamide inhibitor |
|
78
|
258
|
2nxrA |
Structural effects of hydrophobic mutations on the active site of human carbonic anhydrase ii |
|
75
|
258
|
2nwoA |
Structural and kinetic effect of hydrophobic mutations in the active site of human carbonic anhydrase ii |
|
77
|
258
|
2nngA |
Structure of inhibitor binding to carbonic anhydrase ii |
|
76
|
258
|
2nwzA |
Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii |
|
73
|
258
|
2nn1A |
Structure of inhibitor binding to carbonic anhydrase i |
|
74
|
258
|
2nxsA |
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii |
|
74
|
258
|
2nmxA |
Structure of inhibitor binding to carbonic anhydrase i |
|
73
|
258
|
2nwpA |
Structural and kinetic effects of hydrophobic mutations in the active site of human carbonic anhydrase ii |
|
74
|
258
|
2nn7A |
Structure of inhibitor binding to carbonic anhydrase i |
|
77
|
259
|
2nnsA |
Structure of inhibitor binding to carbonic anhydrase ii |
|
76
|
258
|
2nwyA |
Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii |
|
74
|
259
|
2nnvA |
Structure of inhibitor binding to carbonic anhydrase ii |
