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2fhy
From Proteopedia
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[[Image:2fhy.gif|left|200px]] | [[Image:2fhy.gif|left|200px]] | ||
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'''Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor''' | '''Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor''' | ||
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[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Abad-Zapatero, C.]] | [[Category: Abad-Zapatero, C.]] | ||
| - | [[Category: | + | [[Category: Allosteric inhibitors human fbpase]] |
| - | [[Category: | + | [[Category: Benzoxazole]] |
| - | [[Category: | + | [[Category: Intersubunit allosteric inhibition of human fpbase]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 03:55:10 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 00:55, 4 May 2008
Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor
Overview
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.
About this Structure
2FHY is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
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 Page seeded by OCA on Sun May 4 03:55:10 2008
