|
74
|
257
|
2foqA |
Human carbonic anhydrase ii complexed with two-prong inhibitors |
|
79
|
257
|
2fmgA |
Carbonic anhydrase activators. activation of isoforms i, ii, iv, va, vii and xiv with l- and d- phenylalanine and crystallographic analysis of their adducts with isozyme ii: sterospecific recognition within the active site of an enzyme and its consequences for the drug design, structure with l-phenylalanine |
|
75
|
258
|
2fnkA |
Activation of human carbonic anhydrase ii by exogenous proton donors |
|
188
|
477
|
2fgyA |
Beta carbonic anhydrase from the carboxysomal shell of halothiobacillus neapolitanus (csosca) |
|
69
|
257
|
2fw4A |
Carbonic anhydrase activators. the first x-ray crystallographic study of an activator of isoform i, structure with l-histidine. |
|
65
|
173
|
2fkoA |
Structure of ph1591 from pyrococcus horikoshii ot3 |
|
72
|
256
|
2foyA |
Human carbonic anhydrase i complexed with a two-prong inhibitor |
|
74
|
257
|
2eu2A |
Human carbonic anhydrase ii in complex with novel inhibitors |
|
78
|
258
|
2ez7A |
Carbonic anhydrase activators. activation of isozymes i, ii, iv, va, vii and xiv with l- and d-histidine and crystallographic analysis of their adducts with isoform ii: engineering proton transfer processes within the active site of an enzyme |
|
77
|
213
|
2esfA |
Identification of a novel non-catalytic bicarbonate binding site in eubacterial beta-carbonic anhydrase |
|
74
|
257
|
2f14A |
Tne crystal structure of the human carbonic anhydrase ii in complex with a fluorescent inhibitor |
|
74
|
256
|
2eu3A |
Human carbonic anhydrase ii in complex with novel inhibitors |
|
80
|
258
|
2cbbA |
Structure of native and apo carbonic anhydrase ii and some of its anion-ligand complexes |
|
75
|
256
|
2cabA |
Structure, refinement and function of carbonic anhydrase isozymes. refinement of human carbonic anhydrase i |
|
80
|
258
|
2cbdA |
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 |
|
78
|
258
|
2cbaA |
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 |
|
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 |
|
80
|
221
|
2a8cA |
Haemophilus influenzae beta-carbonic anhydrase |
|
68
|
262
|
1zncA |
Human carbonic anhydrase iv |
|
73
|
256
|
1zfkA |
Carbonic anhydrase ii in complex with n-4-sulfonamidphenyl-n'-4-methylbenzosulfonylurease 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 |
|
74
|
256
|
1zh9A |
Carbonic anhydrase ii in complex with n-4-methyl-1-piperazinyl-n'-(p-sulfonamide)phenylthiourea as sulfonamide inhibitor |
|
86
|
221
|
2a8dA |
Haemophilus influenzae beta-carbonic anhydrase complexed with bicarbonate |
|
70
|
257
|
1zsaA |
Carbonic anhydrase ii mutant e117q, apo form |
|
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 |
|
75
|
256
|
1zfqA |
Carbonic anhydrase ii in complex with ethoxzolamidphenole as sulfonamide inhibitor |
|
69
|
210
|
2a5vA |
Crystal structure of m. tuberculosis beta carbonic anhydrase, rv3588c, tetrameric form |
|
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 |
|
76
|
256
|
1z9yA |
Carbonic anhydrase ii in complex with furosemide as sulfonamide inhibitor |
|
73
|
263
|
1z97A |
Human carbonic anhydrase iii: structural and kinetic study of catalysis and proton transfer. |
|
67
|
263
|
1z93A |
Human carbonic anhydrase iii:structural and kinetic study of catalysis and proton transfer. |
|
76
|
258
|
1yo1A |
Proton transfer from his200 in human carbonic anhydrase ii |
|
77
|
258
|
1yo0A |
Proton transfer from his200 in human carbonic anhydrase ii |
|
55
|
163
|
1ylkA |
Crystal structure of rv1284 from mycobacterium tuberculosis in complex with thiocyanate |
|
76
|
258
|
1yo2A |
Proton transfer from his200 in human carbonic anhydrase ii |
|
78
|
255
|
1ydbA |
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 |
|
71
|
203
|
1ym3A |
Crystal structure of carbonic anhydrase rv3588c from mycobacterium tuberculosis |
|
76
|
256
|
1yddA |
Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii |
|
73
|
255
|
1ydaA |
Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii |
|
78
|
274
|
1y7wA |
Crystal structure of a halotolerant carbonic anhydrase from dunaliella salina |
|
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 |
