2gc0: Difference between revisions

New page: left|200px<br /><applet load="2gc0" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gc0, resolution 2.000Å" /> '''The crystal structu...
 
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[[Image:2gc0.gif|left|200px]]<br /><applet load="2gc0" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2gc0.gif|left|200px]]<br /><applet load="2gc0" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2gc0, resolution 2.000&Aring;" />
caption="2gc0, resolution 2.000&Aring;" />
'''The crystal structure of phosphoglucose isomerase from Pyrococcus furiosus in complex with 5-phospho-D-arabinonohydroxamate and zinc'''<br />
'''The crystal structure of phosphoglucose isomerase from Pyrococcus furiosus in complex with 5-phospho-D-arabinonohydroxamate and zinc'''<br />


==Overview==
==Overview==
The enzymatic aldose ketose isomerisation of glucose and fructose sugars, involves the transfer of a hydrogen between their C1 and C2 carbon atoms, and, in principle, can proceed through either a direct hydride shift or, via a cis-enediol intermediate. Pyrococcus furiosus phosphoglucose, isomerase (PfPGI), an archaeal metalloenzyme, which catalyses the, interconversion of glucose 6-phosphate and fructose 6-phosphate, has been, suggested to operate via a hydride shift mechanism. In contrast, the, structurally distinct PGIs of eukaryotic or bacterial origin are thought, to catalyse isomerisation via a cis-enediol intermediate. We have shown by, NMR that hydrogen exchange between substrate and solvent occurs during the, reaction catalysed by PfPGI eliminating the possibility of a, hydride-shift-based mechanism. In addition, kinetic measurements on this, enzyme have shown that 5-phospho-d-arabinonohydroxamate, a stable analogue, of the putative cis-enediol intermediate, is the most potent inhibitor of, the enzyme yet discovered. Furthermore, determination and analysis of, crystal structures of PfPGI with bound zinc and the substrate F6P, and, with a number of competitive inhibitors, and EPR analysis of the, coordination of the metal ion within PfPGI, have suggested that a, cis-enediol intermediate-based mechanism is used by PfPGI with Glu97, acting as the catalytic base responsible for isomerisation.
The enzymatic aldose ketose isomerisation of glucose and fructose sugars involves the transfer of a hydrogen between their C1 and C2 carbon atoms and, in principle, can proceed through either a direct hydride shift or via a cis-enediol intermediate. Pyrococcus furiosus phosphoglucose isomerase (PfPGI), an archaeal metalloenzyme, which catalyses the interconversion of glucose 6-phosphate and fructose 6-phosphate, has been suggested to operate via a hydride shift mechanism. In contrast, the structurally distinct PGIs of eukaryotic or bacterial origin are thought to catalyse isomerisation via a cis-enediol intermediate. We have shown by NMR that hydrogen exchange between substrate and solvent occurs during the reaction catalysed by PfPGI eliminating the possibility of a hydride-shift-based mechanism. In addition, kinetic measurements on this enzyme have shown that 5-phospho-d-arabinonohydroxamate, a stable analogue of the putative cis-enediol intermediate, is the most potent inhibitor of the enzyme yet discovered. Furthermore, determination and analysis of crystal structures of PfPGI with bound zinc and the substrate F6P, and with a number of competitive inhibitors, and EPR analysis of the coordination of the metal ion within PfPGI, have suggested that a cis-enediol intermediate-based mechanism is used by PfPGI with Glu97 acting as the catalytic base responsible for isomerisation.


==About this Structure==
==About this Structure==
2GC0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pyrococcus_furiosus Pyrococcus furiosus] with ZN and PAN as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glucose-6-phosphate_isomerase Glucose-6-phosphate isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.9 5.3.1.9] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2GC0 OCA].  
2GC0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pyrococcus_furiosus Pyrococcus furiosus] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=PAN:'>PAN</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glucose-6-phosphate_isomerase Glucose-6-phosphate isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.9 5.3.1.9] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GC0 OCA].  


==Reference==
==Reference==
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[[Category: Pyrococcus furiosus]]
[[Category: Pyrococcus furiosus]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Baker, P.J.]]
[[Category: Baker, P J.]]
[[Category: Berrisford, J.M.]]
[[Category: Berrisford, J M.]]
[[Category: Rice, D.W.]]
[[Category: Rice, D W.]]
[[Category: PAN]]
[[Category: PAN]]
[[Category: ZN]]
[[Category: ZN]]
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[[Category: phosphoglucose isomerase]]
[[Category: phosphoglucose isomerase]]


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