Search results query ec: 4.2.1.1

Found 1300 chains in Genus chains table. Displaying 551 - 600. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
76	258	3tvoX	Human carbonic anhydrase ii proton transfer double mutant
80	256	3t5uA	Crystal structure of the human carbonic anhydrase ii in complex with n-hydroxy benzenesulfonamide
77	257	3t83A	Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
73	257	3t85A	Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
74	258	3t5zA	Crystal structure of the human carbonic anhydrase ii in complex with n-methoxy-benzenesulfonamide
75	257	3t82A	Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
75	257	3t84A	Human carbonic anhydrase ii in complex with acetylated carbohydrate sulfamates
78	259	3sbhA	Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4,6-dimethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
73	257	3s75B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
79	258	3saxA	Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(5-ethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
71	257	3s73B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
78	257	3s74B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
73	258	3s71B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
76	257	3s72B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
75	258	3s78B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
75	258	3s77B	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
75	257	3sapA	Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(5-butyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
76	257	3s76A	The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
77	258	3sbiA	Crystal structure of human carbonic anhydrase isozyme ii with 4-[(2-pyrimidinylsulfanyl)acetyl]benzenesulfonamide
73	258	3ryzA	Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
74	257	3ryvB	Carbonic anhydrase complexed with n-ethyl-4-sulfamoylbenzamide
77	258	3rz5A	Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
74	257	3ryjB	Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide
74	257	3ryyA	Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
77	257	3rz8A	Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
71	258	3rz0B	Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
74	258	3ryxB	Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
75	257	3rldA	Crystal structure of the y7i mutant of human carbonic anhydrase ii
68	257	3rg4A	Crystal structure of the w5f mutant of human carbonic anhydrase ii
75	256	3rgeA	Crystal structure of the w5h mutant of human carbonic anhydrase ii
71	255	3rg3A	Crystal structure of the w5e mutant of human carbonic anhydrase ii
78	258	3rj7A	Human carbonic anhydrase ii complexed with its inhibitor rhenium(i)triscarbonyl-cyclopentadienyl-carboxy-4-aminomethylbenzene-sulfonamide
79	257	3dbuA	Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
75	257	5y2rA	2.5 atm co2-pressurized human carbonic anhydrase ii
79	257	3m1qA	Carbonic anhydrase ii mutant w5c-h64c with opened disulfide bond
76	257	3dcwA	Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
78	259	3igpA	Structure of inhibitor binding to carbonic anhydrase ii
75	257	5y2sA	7.0 atm co2-pressurized human carbonic anhydrase ii
80	257	5wlrA	Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide
78	257	5wluA	Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide
76	257	5wltA	Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide
78	257	5w8bA	Carbonic anhydrase ii in complex with activating histamine pyridinium derivative
78	258	5wexA	Discovery of new selenoureido analogs of 4-(4-fluorophenylureido) benzenesulfonamides as carbonic anhydrase inhibitors
75	257	5wg7A	Human carbonic anhydrase ii complexed with acek
78	258	5umcA	Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography
78	259	5ulnA	Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography
79	258	5ty9A	Identification of a new zinc binding chemotype by fragment screening
79	258	5u0dA	Identification of a new zinc binding chemotype by fragment screening
77	258	5u0fA	Identification of a new zinc binding chemotype by fragment screening
81	258	5ty8A	Identification of a new zinc binding chemotype by fragment screening