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Fructose-1,6-bisphosphatase

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Line 26: Line 26:
**[[1d9q]] – peFBP – pea<br />
**[[1d9q]] – peFBP – pea<br />
**[[1dbz]], [[1dcu]] – peFBP (mutant)<br />
**[[1dbz]], [[1dcu]] – peFBP (mutant)<br />
-
**[[1fj6]], [[1fj9]], [[1yxi]], [[2f3b]], [[2f3d]], [[2f3h]] - pFBP (mutant) – pig<br />
+
**[[1fj6]], [[1fj9]], [[1yxi]], [[2f3b]], [[2f3d]] - pFBP (mutant) – pig<br />
**[[3bih]] - EcFBP GlpX (mutant) - ''Escherichia coli''<br />
**[[3bih]] - EcFBP GlpX (mutant) - ''Escherichia coli''<br />

Revision as of 08:49, 17 November 2016

Human liver fructose-1,6-bisphosphatase complex with inhibitor (PDB entry 3kc0)

Drag the structure with the mouse to rotate

3D Structures of Fructose-1,6-bisphosphatase

Updated on 17-November-2016

References

  1. ↑ Zhang Y, Liang JY, Lipscomb WN. Structural similarities between fructose-1,6-bisphosphatase and inositol monophosphatase. Biochem Biophys Res Commun. 1993 Feb 15;190(3):1080-3. PMID:8382485
  2. ↑ Storey KB. Metabolic regulation in mammalian hibernation: enzyme and protein adaptations. Comp Biochem Physiol A Physiol. 1997 Dec;118(4):1115-24. PMID:9505421
  3. ↑ van Poelje PD, Potter SC, Chandramouli VC, Landau BR, Dang Q, Erion MD. Inhibition of fructose 1,6-bisphosphatase reduces excessive endogenous glucose production and attenuates hyperglycemia in Zucker diabetic fatty rats. Diabetes. 2006 Jun;55(6):1747-54. PMID:16731838 doi:http://dx.doi.org/10.2337/db05-1443
  4. ↑ van Poelje PD, Potter SC, Erion MD. Fructose-1, 6-bisphosphatase inhibitors for reducing excessive endogenous glucose production in type 2 diabetes. Handb Exp Pharmacol. 2011;(203):279-301. doi: 10.1007/978-3-642-17214-4_12. PMID:21484576 doi:http://dx.doi.org/10.1007/978-3-642-17214-4_12
  5. ↑ Tsukada T, Takahashi M, Takemoto T, Kanno O, Yamane T, Kawamura S, Nishi T. Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1004-7. Epub 2009 Dec 21. PMID:20045638 doi:10.1016/j.bmcl.2009.12.056

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