2fhy
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Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor
OverviewOverview
We have identified benzoxazole benzenesulfonamide 1 as a novel allosteric, inhibitor of fructose-1,6-bisphosphatase (FBPase-1). X-ray, crystallographic and biological studies of 1 indicate a distinct binding, mode that recapitulates features of several previously reported FBPase-1, inhibitor classes.
DiseaseDisease
Known disease associated with this structure: Fructose-bisphosphatase deficiency OMIM:[229700]
About this StructureAbout this Structure
2FHY is a Single protein structure of sequence from Homo sapiens with MG and A37 as ligands. Active as Fructose-bisphosphatase, with EC number 3.1.3.11 Full crystallographic information is available from OCA.
ReferenceReference
Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding mode., von Geldern TW, Lai C, Gum RJ, Daly M, Sun C, Fry EH, Abad-Zapatero C, Bioorg Med Chem Lett. 2006 Apr 1;16(7):1811-5. Epub 2006 Jan 25. PMID:16442285
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