2off

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[[Image:2off.jpg|left|200px]]
[[Image:2off.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 2off |SIZE=350|CAPTION= <scene name='initialview01'>2off</scene>, resolution 2.20&Aring;
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The line below this paragraph, containing "STRUCTURE_2off", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=LLP:2-LYSINE(3-HYDROXY-2-METHYL-5-PHOSPHONOOXYMETHYL-PYRIDIN-4-YLMETHANE)'>LLP</scene>, <scene name='pdbligand=OFF:2-DEOXY-3,4-BIS-O-[3-(4-HYDROXYPHENYL)PROPANOYL]-L-THREO-PENTARIC+ACID'>OFF</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Phosphorylase Phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.1.1 2.4.1.1] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_2off| PDB=2off | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2off FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2off OCA], [http://www.ebi.ac.uk/pdbsum/2off PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2off RCSB]</span>
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}}
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'''The crystal structure of Glycogen Phosphorylase b in complex with a potent allosteric inhibitor'''
'''The crystal structure of Glycogen Phosphorylase b in complex with a potent allosteric inhibitor'''
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[[Category: Tiraidis, C.]]
[[Category: Tiraidis, C.]]
[[Category: Zographos, S E.]]
[[Category: Zographos, S E.]]
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[[Category: glycogenolysis]]
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[[Category: Glycogenolysis]]
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[[Category: transferase]]
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[[Category: Transferase]]
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[[Category: type 2 diabetes]]
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[[Category: Type 2 diabetes]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 10:47:46 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:17:01 2008''
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Revision as of 07:47, 4 May 2008

Template:STRUCTURE 2off

The crystal structure of Glycogen Phosphorylase b in complex with a potent allosteric inhibitor


Overview

FR258900 has been discovered as a novel inhibitor of human liver glycogen phosphorylase a and proved to suppress hepatic glycogen breakdown and reduce plasma glucose concentrations in diabetic mice models. To elucidate the mechanism of inhibition, we have determined the crystal structure of the cocrystallized rabbit muscle glycogen phosphorylase b-FR258900 complex and refined it to 2.2 A resolution. The structure demonstrates that the inhibitor binds at the allosteric activator site, where the physiological activator AMP binds. The contacts from FR258900 to glycogen phosphorylase are dominated by nonpolar van der Waals interactions with Gln71, Gln72, Phe196, and Val45' (from the symmetry-related subunit), and also by ionic interactions from the carboxylate groups to the three arginine residues (Arg242, Arg309, and Arg310) that form the allosteric phosphate-recognition subsite. The binding of FR258900 to the protein promotes conformational changes that stabilize an inactive T-state quaternary conformation of the enzyme. The ligand-binding mode is different from those of the potent phenoxy-phthalate and acyl urea inhibitors, previously described, illustrating the broad specificity of the allosteric site.

About this Structure

2OFF is a Single protein structure of sequence from Oryctolagus cuniculus. Full crystallographic information is available from OCA.

Reference

FR258900, a potential anti-hyperglycemic drug, binds at the allosteric site of glycogen phosphorylase., Tiraidis C, Alexacou KM, Zographos SE, Leonidas DD, Gimisis T, Oikonomakos NG, Protein Sci. 2007 Aug;16(8):1773-82. Epub 2007 Jun 28. PMID:17600143 Page seeded by OCA on Sun May 4 10:47:46 2008

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