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2fhy

From Proteopedia

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[[Image:2fhy.png|left|200px]]
 
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{{STRUCTURE_2fhy| PDB=2fhy | SCENE= }}
{{STRUCTURE_2fhy| PDB=2fhy | SCENE= }}
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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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{{ABSTRACT_PUBMED_16442285}}
{{ABSTRACT_PUBMED_16442285}}
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==Reference==
==Reference==
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<ref group="xtra">PMID:016442285</ref><ref group="xtra">PMID:016446092</ref><references group="xtra"/>
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<ref group="xtra">PMID:016442285</ref><ref group="xtra">PMID:016446092</ref><references group="xtra"/><references/>
[[Category: Fructose-bisphosphatase]]
[[Category: Fructose-bisphosphatase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]

Revision as of 05:26, 25 March 2013

Template:STRUCTURE 2fhy

Contents

Structure of human liver FPBase complexed with a novel benzoxazole as allosteric inhibitor

Template:ABSTRACT PUBMED 16442285

About this Structure

2fhy is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • von Geldern TW, Lai C, Gum RJ, Daly M, Sun C, Fry EH, Abad-Zapatero C. Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding mode. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1811-5. Epub 2006 Jan 25. PMID:16442285 doi:10.1016/j.bmcl.2006.01.015
  • Lai C, Gum RJ, Daly M, Fry EH, Hutchins C, Abad-Zapatero C, von Geldern TW. Benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1807-10. Epub 2006 Jan 30. PMID:16446092 doi:10.1016/j.bmcl.2006.01.014

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OCA

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