|
75
|
255
|
1cveA |
Structural consequences of redesigning a protein-zinc binding site |
|
78
|
257
|
1cnjA |
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site |
|
70
|
255
|
1cnbA |
Compensatory plastic effects in the redesign of protein-zinc binding sites |
|
72
|
257
|
1cngA |
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site |
|
79
|
256
|
1cnxA |
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants |
|
74
|
260
|
1czmA |
Drug-protein interactions: structure of sulfonamide drug complexed with human carbonic anhydrase i |
|
77
|
255
|
1cvfA |
Structural consequences of redesigning a protein-zinc binding site |
|
77
|
257
|
1cniA |
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site |
|
71
|
256
|
1cnyA |
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants |
|
75
|
257
|
1cnkA |
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site |
|
79
|
256
|
1cnwA |
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants |
|
76
|
256
|
1cilA |
The positions of his-64 and a bound water in human carbonic anhydrase ii upon binding three structurally related inhibitors |
|
76
|
255
|
1cvaA |
Structural and functional importance of a conserved hydrogen bond network in human carbonic anhydrase ii |
|
78
|
259
|
1craA |
The complex between human carbonic anhydrase ii and the aromatic inhibitor 1,2,4-triazole |
|
75
|
255
|
1cvcA |
Redesigning the zinc binding site of human carbonic anhydrase ii: structure of a his2asp-zn2+ metal coordination polyhedron |
|
72
|
255
|
1cvdA |
Structural consequences of redesigning a protein-zinc binding site |
|
78
|
257
|
1cnhA |
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site |
|
76
|
256
|
1ca2A |
Refined structure of human carbonic anhydrase ii at 2.0 angstroms resolution |
|
74
|
255
|
1ca3A |
Unexpected ph-dependent conformation of his-64, the proton shuttle of carbonic anhydrase ii. |
|
73
|
255
|
1ccuA |
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity |
|
78
|
259
|
1canA |
Crystallographic studies of the binding of protonated and unprotonated inhibitors to carbonic anhydrase using hydrogen sulphide and nitrate anions |
|
79
|
256
|
1bntA |
Carbonic anhydrase ii inhibitor |
|
75
|
255
|
1cctA |
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity |
|
78
|
258
|
1cazA |
Wild-type and e106q mutant carbonic anhydrase complexed with acetate |
|
81
|
259
|
1caoA |
Crystallographic studies of the binding of protonated and unprotonated inhibitors to carbonic anhydrase using hydrogen sulphide and nitrate anions |
|
75
|
258
|
1cakA |
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii |
|
77
|
258
|
1camA |
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii |
|
75
|
258
|
1calA |
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii |
|
77
|
258
|
1cajA |
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii |
|
79
|
258
|
1caiA |
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii |
|
64
|
260
|
1bzmA |
Drug-protein interactions: structure of sulfonamide drug complexed with human carbonic anhydrase i |
|
74
|
255
|
1ccsA |
Structure-assisted redesign of a protein-zinc binding site with femtomolar affinity |
|
80
|
258
|
1cayA |
Wild-type and e106q mutant carbonic anhydrase complexed with acetate |
|
80
|
258
|
1cahA |
Structure of cobalt carbonic anhydrase complexed with bicarbonate |
|
75
|
257
|
1bv3A |
Human carbonic anhydrase ii complexed with urea |
|
71
|
257
|
1bnvA |
Carbonic anhydrase ii inhibitor |
|
75
|
257
|
1avnA |
Human carbonic anhydrase ii complexed with the histamine activator |
|
73
|
256
|
1bnwA |
Carbonic anhydrase ii inhibitor |
|
76
|
256
|
1bnqA |
Carbonic anhydrase ii inhibitor |
|
74
|
257
|
1bn4A |
Carbonic anhydrase ii inhibitor |
|
66
|
258
|
1azmA |
Drug-protein interactions: structure of sulfonamide drug complexed with human carbonic anhydrase i |
|
75
|
257
|
1bnnA |
Carbonic anhydrase ii inhibitor |
|
75
|
257
|
1bn1A |
Carbonic anhydrase ii inhibitor |
|
72
|
257
|
1bnmA |
Carbonic anhydrase ii inhibitor |
|
76
|
258
|
1bicA |
Crystallographic analysis of thr-200-> his human carbonic anhydrase ii and its complex with the substrate, hco3- |
|
75
|
256
|
1bnuA |
Carbonic anhydrase ii inhibitor |
|
76
|
257
|
1bn3A |
Carbonic anhydrase ii inhibitor |
|
78
|
258
|
1bcdA |
X-ray crystallographic structure of a complex between human carbonic anhydrase ii and a new topical inhibitor, trifluoromethane sulphonamide |
|
73
|
258
|
1am6A |
Carbonic anhydrase ii inhibitor: acetohydroxamate |
|
78
|
256
|
1a42A |
Human carbonic anhydrase ii complexed with brinzolamide |
