2hl4
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Crystal structure analysis of human carbonic anhydrase II in complex with a benzenesulfonamide derivative
OverviewOverview
N-(4-Sulfamoylphenyl)-alpha-d-glucopyranosylamine, a promising topical, antiglaucoma agent, is a potent inhibitor of the zinc enzyme carbonic, anhydrase (CA, EC 4.2.1.1). The high resolution X-ray crystal structure of, its adduct with the target isoform involved in glaucoma, CA II, is, reported here. The sugar sulfanilamide derivative binds to the enzyme in a, totally new manner as compared to other CA-inhibitor adducts investigated, earlier. The sulfonamide anchor was coordinated to the active site metal, ion, and the phenylene ring of the inhibitor filled the channel leading to, the active site cavity. The glycosyl moiety responsible for the high water, solubility of the compound was oriented towards a hydrophilic region of, the active site, where no other inhibitors were observed to be bound up to, now. A network of seven hydrogen bonds with four water molecules and the, amino acid residues Pro201, Pro202 and Gln92 further stabilize the, enzyme-inhibitor adduct. Topiramate, another sugar-based CA inhibitor, binds in a completely different manner to CA II as compared to the, sulfonamide investigated here. These findings are useful for the design of, potent, sugar-derived enzyme inhibitors.
About this StructureAbout this Structure
2HL4 is a Single protein structure of sequence from Homo sapiens with , , , and as ligands. Active as Carbonate dehydratase, with EC number 4.2.1.1 Full crystallographic information is available from OCA.
ReferenceReference
Carbonic anhydrase inhibitors: binding of an antiglaucoma glycosyl-sulfanilamide derivative to human isoform II and its consequences for the drug design of enzyme inhibitors incorporating sugar moieties., Di Fiore A, Scozzafava A, Winum JY, Montero JL, Pedone C, Supuran CT, De Simone G, Bioorg Med Chem Lett. 2007 Mar 15;17(6):1726-31. Epub 2007 Jan 8. PMID:17251017
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