2vt5

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[[Image:2vt5.png|left|200px]]
[[Image:2vt5.png|left|200px]]
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{{STRUCTURE_2vt5| PDB=2vt5 | SCENE= }}
{{STRUCTURE_2vt5| PDB=2vt5 | SCENE= }}
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===FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH A DUAL BINDING AMP SITE INHIBITOR===
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===FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE -1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH A DUAL BINDING AMP SITE INHIBITOR===
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{{ABSTRACT_PUBMED_18650089}}
{{ABSTRACT_PUBMED_18650089}}
==About this Structure==
==About this Structure==
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2VT5 is a 8 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2VT5 OCA].
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[[2vt5]] is a 8 chain structure of [[Fructose-1%2C6-bisphosphatase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2VT5 OCA].
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==See Also==
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*[[Fructose-1%2C6-bisphosphatase|Fructose-1%2C6-bisphosphatase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:18650089</ref><references group="xtra"/>
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<ref group="xtra">PMID:018650089</ref><references group="xtra"/>
[[Category: Fructose-bisphosphatase]]
[[Category: Fructose-bisphosphatase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Gluconeogenesis]]
[[Category: Gluconeogenesis]]
[[Category: Hydrolase]]
[[Category: Hydrolase]]
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[[Category: Polymorphism]]
 
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[[Category: Zinc]]
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 13:24:58 2009''
 

Revision as of 13:15, 25 July 2012

Template:STRUCTURE 2vt5

Contents

FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE -1-PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH A DUAL BINDING AMP SITE INHIBITOR

Template:ABSTRACT PUBMED 18650089

About this Structure

2vt5 is a 8 chain structure of Fructose-1,6-bisphosphatase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Hebeisen P, Kuhn B, Kohler P, Gubler M, Huber W, Kitas E, Schott B, Benz J, Joseph C, Ruf A. Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sites. Bioorg Med Chem Lett. 2008 Aug 15;18(16):4708-12. Epub 2008 Jul 5. PMID:18650089 doi:10.1016/j.bmcl.2008.06.103

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