1ec7: Difference between revisions

New page: left|200px<br /><applet load="1ec7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ec7, resolution 1.9Å" /> '''E. COLI GLUCARATE DEH...
 
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caption="1ec7, resolution 1.9&Aring;" />
caption="1ec7, resolution 1.9&Aring;" />
'''E. COLI GLUCARATE DEHYDRATASE NATIVE ENZYME'''<br />
'''E. COLI GLUCARATE DEHYDRATASE NATIVE ENZYME'''<br />


==Overview==
==Overview==
D-Glucarate dehydratase (GlucD) from Escherichia coli catalyzes the, dehydration of both D-glucarate and L-idarate as well as their, interconversion via epimerization. GlucD is a member of the mandelate, racemase (MR) subgroup of the enolase superfamily, the members of which, catalyze reactions that are initiated by abstraction of the alpha-proton, of a carboxylate anion substrate. Alignment of the sequence of GlucD with, that of MR reveals a conserved Lys-X-Lys motif and a His-Asp dyad, homologous to the S- and R-specific bases in the active site of MR., Crystals of GlucD have been obtained into which the substrate D-glucarate, and two competitive inhibitors, 4-deoxy-D-glucarate and xylarohydroxamate, could be diffused; D-glucarate is converted to the dehydration product, 5-keto-4-deoxy-D-glucarate (KDG). The structures of these complexes have, been determined and reveal the identities of the ligands for the required, Mg(2+) (Asp(235), Glu(266), and Asn(289)) as well as confirm the expected, presence of Lys(207) and His(339), the catalytic bases that are properly, positioned to abstract the proton from C5 of L-idarate and D-glucarate, respectively. Surprisingly, the C6 carboxylate group of KDG is a bidentate, ligand to the Mg(2+), with the resulting geometry of the bound KDG, suggesting that stereochemical roles of Lys(207) and His(339) are reversed, from the predictions made on the basis of the established, structure-function relationships for the MR-catalyzed reaction. The, catalytic roles of these residues have been examined by characterization, of mutant enzymes, although we were unable to use these to demonstrate the, catalytic independence of Lys(207) and His(339) as was possible for the, homologous Lys(166) and His(297) in the MR-catalyzed reaction.
D-Glucarate dehydratase (GlucD) from Escherichia coli catalyzes the dehydration of both D-glucarate and L-idarate as well as their interconversion via epimerization. GlucD is a member of the mandelate racemase (MR) subgroup of the enolase superfamily, the members of which catalyze reactions that are initiated by abstraction of the alpha-proton of a carboxylate anion substrate. Alignment of the sequence of GlucD with that of MR reveals a conserved Lys-X-Lys motif and a His-Asp dyad homologous to the S- and R-specific bases in the active site of MR. Crystals of GlucD have been obtained into which the substrate D-glucarate and two competitive inhibitors, 4-deoxy-D-glucarate and xylarohydroxamate, could be diffused; D-glucarate is converted to the dehydration product, 5-keto-4-deoxy-D-glucarate (KDG). The structures of these complexes have been determined and reveal the identities of the ligands for the required Mg(2+) (Asp(235), Glu(266), and Asn(289)) as well as confirm the expected presence of Lys(207) and His(339), the catalytic bases that are properly positioned to abstract the proton from C5 of L-idarate and D-glucarate, respectively. Surprisingly, the C6 carboxylate group of KDG is a bidentate ligand to the Mg(2+), with the resulting geometry of the bound KDG suggesting that stereochemical roles of Lys(207) and His(339) are reversed from the predictions made on the basis of the established structure-function relationships for the MR-catalyzed reaction. The catalytic roles of these residues have been examined by characterization of mutant enzymes, although we were unable to use these to demonstrate the catalytic independence of Lys(207) and His(339) as was possible for the homologous Lys(166) and His(297) in the MR-catalyzed reaction.


==About this Structure==
==About this Structure==
1EC7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with MG and IPA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glucarate_dehydratase Glucarate dehydratase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.2.1.40 4.2.1.40] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1EC7 OCA].  
1EC7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=MG:'>MG</scene> and <scene name='pdbligand=IPA:'>IPA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glucarate_dehydratase Glucarate dehydratase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.2.1.40 4.2.1.40] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EC7 OCA].  


==Reference==
==Reference==
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[[Category: Glucarate dehydratase]]
[[Category: Glucarate dehydratase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Gerlt, J.A.]]
[[Category: Gerlt, J A.]]
[[Category: Gulick, A.M.]]
[[Category: Gulick, A M.]]
[[Category: Hubbard, B.K.]]
[[Category: Hubbard, B K.]]
[[Category: Rayment, I.]]
[[Category: Rayment, I.]]
[[Category: IPA]]
[[Category: IPA]]
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[[Category: glucarate dehydratase enolase enzyme superfamily tim barrel (beta/alpha)7beta barrel]]
[[Category: glucarate dehydratase enolase enzyme superfamily tim barrel (beta/alpha)7beta barrel]]


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