Found 169 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: carbonic anhydrase ii

Total Genus Sequence Length pdb Title
73 255 12caA Altering the mouth of a hydrophobic pocket. structure and kinetics of human carbonic anhydrase ii mutants at residue val-121
73 255 8ca2A Engineering the hydrophobic pocket of carbonic anhydrase ii
76 255 9ca2A Engineering the hydrophobic pocket of carbonic anhydrase ii
74 255 7ca2A Engineering the hydrophobic pocket of carbonic anhydrase ii
77 255 6ca2A Engineering the hydrophobic pocket of carbonic anhydrase ii
75 255 5ca2A Conformational mobility of his-64 in the thr-200 (right arrow) ser mutant of human carbonic anhydrase ii
75 255 4ca2A Engineering the hydrophobic pocket of carbonic anhydrase ii
76 257 3d93A Apo human carbonic anhydrase ii bound with substrate carbon dioxide
75 257 3d8wA Use of a carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
74 257 3d92A Human carbonic anhydrase ii bound with substrate carbon dioxide
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
75 257 2h4nA H94n carbonic anhydrase ii complexed with acetazolamide
75 260 2fouA Human carbonic anhydrase ii complexed with two-prong inhibitors
74 259 2fosA Human carbonic anhydrase ii complexed with two-prong inhibitors
74 259 2fovA Human carbonic anhydrase ii complexed with two-prong inhibitors
80 258 2cbdA Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
80 258 2cbbA Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
75 256 2ca2A 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
78 258 2cbaA Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
79 258 2cbeA Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
78 258 2cbcA Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes
77 258 2ax2A Production and x-ray crystallographic analysis of fully deuterated human carbonic anhydrase ii
75 257 2aw1A Carbonic anhydrase inhibitors: valdecoxib binds to a different active site region of the human isoform ii as compared to the structurally related cyclooxygenase ii "selective" inhibitor celecoxib
77 257 1zsbA Carbonic anhydrase ii mutant e117q, transition state analogue acetazolamide
70 257 1zsaA Carbonic anhydrase ii mutant e117q, apo form
73 256 1zfkA Carbonic anhydrase ii in complex with n-4-sulfonamidphenyl-n'-4-methylbenzosulfonylurease as sulfonamide inhibitor
74 256 1zh9A Carbonic anhydrase ii in complex with n-4-methyl-1-piperazinyl-n'-(p-sulfonamide)phenylthiourea as sulfonamide inhibitor
75 257 2abeA Carbonic anhydrase activators: x-ray crystal structure of the adduct of human isozyme ii with l-histidine as a platform for the design of stronger activators
75 258 1ze8A Carbonic anhydrase ii in complex with a membrane-impermeant sulfonamide inhibitor
78 256 1zgfA Carbonic anhydrase ii in complex with trichloromethiazide as sulfonamide inhibitor
75 256 1zfqA Carbonic anhydrase ii in complex with ethoxzolamidphenole as sulfonamide inhibitor
74 256 1zgeA Carbonic anhydrase ii in complex with p-sulfonamido-o,o'-dichloroaniline as sulfonamide inhibitor
77 257 1zscA Carbonic anhydrase ii mutant e117q, holo form
76 256 1z9yA Carbonic anhydrase ii in complex with furosemide as sulfonamide inhibitor
77 258 1yo0A Proton transfer from his200 in human carbonic anhydrase ii
76 258 1yo1A Proton transfer from his200 in human carbonic anhydrase ii
76 256 1yddA Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
78 255 1ydbA Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
76 258 1yo2A Proton transfer from his200 in human carbonic anhydrase ii
73 255 1ydaA Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
78 255 1ydcA Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
76 258 1xpzA Structure of human carbonic anhydrase ii with 4-[4-o-sulfamoylbenzyl)(4-cyanophenyl)amino]-4h-[1,2,4]-triazole
72 258 1xq0A Structure of human carbonic anhydrase ii with 4-[(3-bromo-4-o-sulfamoylbenzyl)(4-cyanophenyl)amino]-4h-[1,2,4]-triazole
75 258 1xegA Crystal structure of human carbonic anhydrase ii complexed with an acetate ion
72 258 1xevA Crystal structure of human carbonic anhydrase ii in a new crystal form
69 261 1v9iC Crystal structure analysis of the site specific mutant (q253c) of bovine carbonic anhydrase ii
75 259 1v9eA Crystal structure analysis of bovine carbonic anhydrase ii
77 258 1ugaA Human carbonic anhydrase ii[hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by phe (a65f)
79 258 1ugeA Human carbonic anhydrase ii [hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by leu (a65l)
76 258 1ugbA Human carbonic anhydrase ii[hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by gly (a65g)