Found 968 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query ec: 4.2.1.1

Total Genus Sequence Length pdb Title
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
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.
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.
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
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.
19 260 6qebA Assessment of a large enzyme-drug complex by proton-detected solid-state nmr without deuteration
76 257 6mbyA Carbonic anhydrase ii in complex with ferulic acid
74 257 6mbvA Carbonic anhydrase ii in complex with nicotinic acid
77 257 6hx5A Selenols: a new class of carbonic anhydrase inhibitors
70 256 6hwzA Selenols: a new class of carbonic anhydrase inhibitors
76 260 6h33A The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide.
69 258 6h6sA Sad phasing on nickel-substituted human carbonic anhydrase ii
76 257 6h34A The crystal structure of human carbonic anhydrase ii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
79 259 6h36A The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide.
77 258 6h37A The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenyl)-4-hydroxy-1-piperidine-1-carbonyl)benzenesulfonamide
76 256 6h2zA The crystal structure of human carbonic anhydrase ii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide.
78 259 6h38A The crystal structure of human carbonic anhydrase vii in complex with 4-[(4-fluorophenyl)methyl]-1-piperazinyl]benzenesulfonamide.
76 257 6g6tA Crystal structure of human carbonic anhydrase isozyme ii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide
72 261 6g5lA Crystal structure of human carbonic anhydrase isozyme xii with 4-chloro-2-(cyclohexylamino)-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
78 258 6g5uA Crystal structure of human carbonic anhydrase isozyme xiii with n-butyl-2,4-dichloro-5-sulfamoyl-benzamide
79 258 6gcyA Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin-sugar conjugate complex)
77 258 6fjjA Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (saccharin).
76 262 6g7aA Crystal structure of human carbonic anhydrase isozyme xii 2-(benzylamino)-4-chloro-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
77 258 6fjiA Joint neutron and x-ray crystal structure of human carbonic anhydrase ix mimic (apo).
77 256 6qfuA Human carbonic anhydrase ii with bound ircp* complex (cofactor 7) to generate an artificial transfer hydrogenase (athase)
80 255 6qfvA Human carbonic anhydrase ii with bound ircp* complex (cofactor 8) to generate an artificial transfer hydrogenase (athase)
78 256 6qfwA Human carbonic anhydrase ii with bound ircp* complex (cofactor 9) to generate an artificial transfer hydrogenase (athase)
78 256 6qfxA Human carbonic anhydrase ii with bound ircp* complex (cofactor 10) to generate an artificial transfer hydrogenase (athase)
79 257 6gxeA Carbonic anhydrase caix mimic in complex with inhibitor js14
79 257 6gxbA Carbonic anhydrase caix mimic in complex with inhibitor js13
73 257 6e91A Ca ix mimic complexed with steroidal sulfamate compound stx 2484
74 257 6e8pA Ca ix mimic complexed with steroidal sulfamate compound stx 49
77 257 6e92A Ca ix mimic complexed with steroidal sulfamate compound stx 2845
77 257 6e8xA Ca ix mimic complexed with steroidal sulfamate compound stx 140
78 258 6ic2A Polypharmacology of epacadostat: a potent and selective inhibitor of the tumor associated carbonic anhydrases ix and xii
74 257 6gdcA Human carbonic anhydrase ii in complex with benzenesulfonamide
77 258 3s9tA Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(4,6-dimethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
75 257 3rz1B Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
79 257 3s8xA Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4-methyl-6-oxo-1,6-dihydro-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
77 257 3rz7A Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase