Found 1300 chains in Genus chains table. Displaying 301 - 350. Applied filters: Proteins

Search results query ec: 4.2.1.1

Total Genus Sequence Length pdb Title
77 257 6wq4A Carbonic anhydrase ii complexed with 2-((2-cyanoethyl)(phenethyl)amino)-n-phenethyl-n-(4-sulfamoylphenethyl)acetamide
78 257 6t9zA Nidocarborane inhibitor of carbonic anhydrase ix
80 257 6t7uA Carborane inhibitor of carbonic anhydrase ix
78 259 6sdtA Human carbonic anhydrase vii in complex with a sulfonamide inhibitor
78 260 6sdsA Human carbonic anhydrase ii in complex with a sulfonamide inhibitor
78 257 6s03A Carbonic anhydrase caix mimic in complex with inhibitor i39lt379
81 258 6rzxA Carbonic anhydrase caix mimic in complex with inhibitor fbsa
75 258 6rofA Human carbonic anhydrase ii mutant t199v bound by 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
73 257 6rfhA Human carbonic anhydrase ii in complex with 4-carboxybenzenesulfonamide
78 259 6rg3A Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzylpiperazin-1-yl)benzenesulfonamide
71 257 6rigA Human carbonic anhydrase ii in complex with 4-hydroxybenzenesulfonamide
79 257 6rmxA Human carbonic anhydrase ii mutant t199v bound by 2-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
76 258 6rmyA Human carbonic anhydrase ii mutant t199v bound by 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
77 257 6rhkA The crystal structure of human carbonic anhydrase ii in complex with 4-(3-benzylimidazolidine-1-carbonyl)benzenesulfonamide
76 258 6rg4A Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzyl-4-methylpiperazin-1-yl)benzenesulfonamide
73 257 6rg5A Human carbonic anhydrase ii in complex with 4-(2-hydroxyethyl)benzenesulfonamide
78 257 6rhjA Crystal structure of human carbonic anhydrase isozyme ii with 4-(4-benzyl-1,4-diazepane-1-carbonyl)benzenesulfonamide
79 257 6oudA Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-694b
79 257 6ouiA Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-710a
75 257 6ouhA Carbonic anhydrase ii mimic complexed with benzene sulfonamide mb11-710a
75 257 6oujA Carbonic anhydrase ii complexed with benzene sulfonamide mb11-689a
78 257 6otoA Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb9-561b
80 257 6otiA Carbonic anhydrase ix mimic complexed with ureic benzene sulfonamide mb9-561b
81 257 6oufA Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb11-707a
76 257 6otpA Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb10-586b
80 257 6otmA Carbonic anhydrase ix mimic complexed with ureic benzene sulfonamide mb10-586b
79 257 6oukA Carbonic anhydrase ii complexed with benzene sulfonamide mb10-580b
80 257 6otkA Carbonic anhydrase ix mimic complexed with ureido benzene sulfonamide mb10-596b
77 257 6oumA Carbonic anhydrase ix mimic complexed with benzene sulfonamide mb10-580b
75 257 6oueA Carbonic anhydrase ii complexed with benzene sulfonamide mb11-707a
75 257 6otqA Carbonic anhydrase ii complexed with ureic benzene sulfonamide mb10-596b
77 257 6oubA Carbonic anhydrase ii complexed with benzene sulfonamide mb11-694b
84 277 6qqmA Crystal structure of the alpha carbonic anhydrase from schistosoma mansoni
75 257 6hxdA Human carbonic anhydrase ii in complex with 4-butylbenzenesulfonamide
76 257 6ebeA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
79 260 6g3qA Crystal structure of human carbonic anhydrase ii in complex with the inhibitor famotidine
76 257 6edaA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
68 208 6gwuA Carbonic anhydrase cance103p from candida albicans
77 257 6eczA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
74 257 6f3bA Crystal structure of human carbonic anhydrase i in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-[(4-methylphenyl)methyl]urea inhibitor
76 257 6eeoA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
71 256 6g3vA Crystal structure of human carbonic anhydrase i in complex with the inhibitor famotidine
76 257 6ex1A 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
76 257 6fagA Crystal structure of human carbonic anhydrase i in complex with the 1-(2-hydroxy-5-sulfamoylphenyl)-3-(2-methoxyphenyl)urea inhibitor
78 257 6eehA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
76 257 6eeaA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
73 257 6fafA Crystal structure of human carbonic anhydrase i in complex with the 3-(2,5-dimethylphenyl)-1-(2-hydroxy-5-sulfamoylphenyl)urea inhibitor
19 260 6qebA Assessment of a large enzyme-drug complex by proton-detected solid-state nmr without deuteration
74 257 6mbvA Carbonic anhydrase ii in complex with nicotinic acid
76 257 6mbyA Carbonic anhydrase ii in complex with ferulic acid