| 1AZM |
2.0 |
DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I |
| 1BZM |
2.0 |
DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I |
| 1CRM |
2.0 |
STRUCTURE AND FUNCTION OF CARBONIC ANHYDRASES |
| 1CZM |
2.0 |
DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I |
| 1HCB |
1.6 |
ENZYME-SUBSTRATE INTERACTIONS: STRUCTURE OF HUMAN CARBONIC ANHYDRASE I COMPLEXED WITH BICARBONATE |
| 1HUG |
2.0 |
Differences in anionic inhibition of Human Carbonic Anhydrase I revealed from the structures of iodide and gold cyanide inhibitor complexes |
| 1HUH |
2.2 |
DIFFERENCES IN ANIONIC INHIBITION OF HUMAN CARBONIC ANHYDRASE I REVEALED FROM THE STRUCTURES OF IODIDE AND GOLD CYANIDE INHIBITOR COMPLEXES |
| 1J9W |
2.6 |
Solution Structure of the CAI Michigan 1 Variant |
| 1JV0 |
2.0 |
THE CRYSTAL STRUCTURE OF THE ZINC(II) ADDUCT OF THE CAI MICHIGAN 1 VARIANT |
| 2CAB |
2.0 |
STRUCTURE, REFINEMENT AND FUNCTION OF CARBONIC ANHYDRASE ISOZYMES. REFINEMENT OF HUMAN CARBONIC ANHYDRASE I |
| 2FOY |
1.55 |
Human Carbonic Anhydrase I complexed with a two-prong inhibitor |
| 2FW4 |
2.0 |
Carbonic anhydrase activators. The first X-ray crystallographic study of an activator of isoform I, structure with L-histidine. |
| 2IT4 |
2.0 |
X ray structure of the complex between Carbonic Anhydrase I and the phosphonate antiviral drug foscarnet |
| 2NMX |
1.55 |
Structure of inhibitor binding to Carbonic Anhydrase I |
| 2NN1 |
1.65 |
Structure of inhibitor binding to Carbonic Anhydrase I |
| 2NN7 |
1.85 |
Structure of inhibitor binding to Carbonic Anhydrase I |
| 3LXE |
1.9 |
Human Carbonic Anhydrase I in complex with topiramate |
| 3W6H |
2.964 |
Crystal structure of 19F probe-labeled hCAI in complex with acetazolamide |
| 3W6I |
2.693 |
Crystal structure of 19F probe-labeled hCAI |
| 4WR7 |
1.5 |
Crystal structure of human carbonic anhydrase isozyme I with 2,3,5,6-Tetrafluoro-4-(propylthio)benzenesulfonamide. |
| 4WUP |
1.75 |
Crystal structure of human carbonic anhydrase isozyme I with 4-[(2-Hydroxyethyl)thio]benzenesulfonamide |
| 4WUQ |
1.75 |
Crystal structure of human carbonic anhydrase isozyme I with 2,3,5,6-Tetrafluoro-4-piperidin-1-ylbenzenesulfonamide |
| 5E2M |
1.41 |
Crystal structure of human carbonic anhydrase isozyme I with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide |
| 5GMM |
2.003 |
Crystal structure of human Carbonic anhydrase I in complex with polmacoxib |
| 6EVR |
1.5 |
Crystal structure of human carbonic anhydrase I in complex with the 4-(4 acetyl-3-benzylpiperazine-1 carbonyl)benzene-1-sulfonamide inhibitor |
| 6EX1 |
1.6 |
Crystal structure of human carbonic anhydrase I in complex with the 4-[(3S)-3 benzyl-4-(4-sulfamoylbenzoyl)piperazine -1-carbonyl]benzene-1-sulfonamide inhibitor |
| 6F3B |
1.4 |
Crystal structure of human carbonic anhydrase I in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-[(4-methylphenyl)methyl]urea inhibitor |
| 6FAF |
1.99 |
Crystal structure of human carbonic anhydrase I in complex with the 3-(2,5-dimethylphenyl)-1-(2-hydroxy-5-sulfamoylphenyl)urea inhibitor |
| 6FAG |
1.79 |
Crystal structure of human carbonic anhydrase I in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-(2-methoxyphenyl)urea inhibitor |
| 6G3V |
1.69 |
Crystal structure of human carbonic anhydrase I in complex with the inhibitor famotidine |
| 6HWZ |
1.64 |
Selenols: a new class of Carbonic Anhydrase inhibitors |
| 6I0J |
1.35 |
Crystal structure of human carbonic anhydrase I in complex with the 4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)phenyl sulfamate inhibitor |
| 6I0L |
1.4 |
Crystal structure of human carbonic anhydrase I in complex with the 1-[4-chloro-3-(trifluoromethyl)phenyl]-3-[2-(4-sulfamoylphenyl)ethyl]urea inhibitor |
| 6SWM |
2.77 |
selenol bound carbonic anhydrase I |
| 6XZE |
1.54 |
crystal structure of human carbonic anhydrase I in complex with 4-(3-(2-((2-fluorobenzyl)amino)ethyl)ureido) benzenesulfonamide |
| 6XZO |
1.44 |
Crystal structure of human carbonic anhydrase I in complex with 4-(3-(2-((4-bromo-2-hydroxybenzyl)amino)ethyl)ureido) benzenesulfonamide |
| 6XZS |
1.53 |
Crystal structure of human carbonic anhydrase I in complex with 4-(3-(2-((4-fluorobenzyl)amino)ethyl)ureido) benzenesulfonamide |
| 6XZX |
1.55 |
crystal structure of human carbonic anhydrase I in complex with 4-(3-(2-((2-fluorobenzyl)amino)ethyl)ureido) benzenesulfonamide |
| 6XZY |
1.66 |
crystal structure of human carbonic anhydrase I in complex with 4-(3-(2-((2-fluorobenzyl)amino)ethyl)ureido) benzenesulfonamide |
| 6Y00 |
1.37 |
crystal structure of human carbonic anhydrase I in complex with 4-(3-(2-((2-fluorobenzyl)amino)ethyl)ureido) benzenesulfonamide |
| 7PLF |
1.461 |
Human Carbonic Anhydrase I in complex with clorsulon |
| 7Q0D |
1.24 |
Human carbonic anhydrase I in complex with Methyl 2-(benzenesulfonyl)-4-chloro-5-sulfamoylbenzoate |
| 7QOB |
1.8 |
Human Carbonic Anhydrase I in complex with benzoselenoate |
