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PDBsum entry 2hl4

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Lyase PDB id
2hl4
Jmol
Contents
Protein chain
257 a.a.
Ligands
BO1
MBO
GOL
Metals
_ZN
_CL
Waters ×321

References listed in PDB file
Key reference
Title 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.
Authors A.Di fiore, A.Scozzafava, J.Y.Winum, J.L.Montero, C.Pedone, C.T.Supuran, G.De simone.
Ref. Bioorg Med Chem Lett, 2007, 17, 1726-1731. [DOI no: 10.1016/j.bmcl.2006.12.099]
PubMed id 17251017
Abstract
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.
Secondary reference #1
Title Refined structure of human carbonic anhydrase ii at 2.0 a resolution.
Authors A.E.Eriksson, T.A.Jones, A.Liljas.
Ref. Proteins, 1988, 4, 274-282.
PubMed id 3151019
Abstract
PROCHECK
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