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(New page: 200px<br /><applet load="1wvg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1wvg, resolution 1.8&Aring;" /> '''Structure of CDP-D-gl...)
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'''Structure of CDP-D-glucose 4,6-dehydratase from Salmonella typhi'''<br />
'''Structure of CDP-D-glucose 4,6-dehydratase from Salmonella typhi'''<br />
==Overview==
==Overview==
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Tyvelose is a unique 3,6-dideoxyhexose found in the O antigens of some, pathogenic species of Yersinia and Salmonella. It is produced via a, complex biochemical pathway that employs CDP-D-glucose as the starting, ligand. CDP-D-glucose 4,6-dehydratase catalyzes the first irreversible, step in the synthesis of this 3,6-dideoxysugar by converting CDP-D-glucose, to CDP-4-keto-6-deoxyglucose via an NAD+ -dependent intramolecular, oxidation-reduction reaction. Here, the cloning, protein purification and, X-ray crystallographic analysis of CDP-D-glucose 4,6-dehydratase from, Salmonella typhi complexed with the substrate analog CDP-D-xylose are, described. Each subunit of the tetrameric enzyme folds into two domains., The N-terminal region contains a Rossmann fold and provides the platform, for NAD(H) binding. The C-terminal motif is primarily composed of, alpha-helices and houses the binding pocket for the CDP portion of the, CDP-D-xylose ligand. The xylose moiety extends into the active-site cleft, that is located between the two domains. Key residues involved in, anchoring the sugar group to the protein include Ser134, Tyr159, Asn197, and Arg208. Strikingly, Ser134 O gamma and Tyr159 O eta sit within 2.9 A, of the 4'-hydroxyl group of xylose. Additionally, the side chains of, Asp135 and Lys136 are located at 3.5 and 3.2 A, respectively, from C-5 of, xylose. In the structurally related dTDP-D-glucose 4,6-dehydratase, the, Asp/Lys pair is replaced with an Asp/Glu couple. On the basis of this, investigation, it can be speculated that Tyr159 serves as the catalytic, base to abstract the 4'-hydroxyl proton from the sugar and that Asp135 and, Lys136 play critical roles in the subsequent dehydration step that leads, to the final product.
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Tyvelose is a unique 3,6-dideoxyhexose found in the O antigens of some pathogenic species of Yersinia and Salmonella. It is produced via a complex biochemical pathway that employs CDP-D-glucose as the starting ligand. CDP-D-glucose 4,6-dehydratase catalyzes the first irreversible step in the synthesis of this 3,6-dideoxysugar by converting CDP-D-glucose to CDP-4-keto-6-deoxyglucose via an NAD+ -dependent intramolecular oxidation-reduction reaction. Here, the cloning, protein purification and X-ray crystallographic analysis of CDP-D-glucose 4,6-dehydratase from Salmonella typhi complexed with the substrate analog CDP-D-xylose are described. Each subunit of the tetrameric enzyme folds into two domains. The N-terminal region contains a Rossmann fold and provides the platform for NAD(H) binding. The C-terminal motif is primarily composed of alpha-helices and houses the binding pocket for the CDP portion of the CDP-D-xylose ligand. The xylose moiety extends into the active-site cleft that is located between the two domains. Key residues involved in anchoring the sugar group to the protein include Ser134, Tyr159, Asn197 and Arg208. Strikingly, Ser134 O gamma and Tyr159 O eta sit within 2.9 A of the 4'-hydroxyl group of xylose. Additionally, the side chains of Asp135 and Lys136 are located at 3.5 and 3.2 A, respectively, from C-5 of xylose. In the structurally related dTDP-D-glucose 4,6-dehydratase, the Asp/Lys pair is replaced with an Asp/Glu couple. On the basis of this investigation, it can be speculated that Tyr159 serves as the catalytic base to abstract the 4'-hydroxyl proton from the sugar and that Asp135 and Lys136 play critical roles in the subsequent dehydration step that leads to the final product.
==About this Structure==
==About this Structure==
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1WVG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Salmonella_enterica_subsp._enterica_serovar_typhi Salmonella enterica subsp. enterica serovar typhi] with APR and CXY as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/CDP-glucose_4,6-dehydratase CDP-glucose 4,6-dehydratase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.2.1.45 4.2.1.45] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1WVG OCA].
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1WVG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Salmonella_enterica_subsp._enterica_serovar_typhi Salmonella enterica subsp. enterica serovar typhi] with <scene name='pdbligand=APR:'>APR</scene> and <scene name='pdbligand=CXY:'>CXY</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/CDP-glucose_4,6-dehydratase CDP-glucose 4,6-dehydratase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.2.1.45 4.2.1.45] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WVG OCA].
==Reference==
==Reference==
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[[Category: Salmonella enterica subsp. enterica serovar typhi]]
[[Category: Salmonella enterica subsp. enterica serovar typhi]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Holden, H.M.]]
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[[Category: Holden, H M.]]
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[[Category: Koropatkin, N.M.]]
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[[Category: Koropatkin, N M.]]
[[Category: APR]]
[[Category: APR]]
[[Category: CXY]]
[[Category: CXY]]
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[[Category: short-chain dehydrogenase/reductase]]
[[Category: short-chain dehydrogenase/reductase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 05:42:05 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:48:29 2008''

Revision as of 13:48, 21 February 2008


1wvg, resolution 1.8Å

Drag the structure with the mouse to rotate

Structure of CDP-D-glucose 4,6-dehydratase from Salmonella typhi

Overview

Tyvelose is a unique 3,6-dideoxyhexose found in the O antigens of some pathogenic species of Yersinia and Salmonella. It is produced via a complex biochemical pathway that employs CDP-D-glucose as the starting ligand. CDP-D-glucose 4,6-dehydratase catalyzes the first irreversible step in the synthesis of this 3,6-dideoxysugar by converting CDP-D-glucose to CDP-4-keto-6-deoxyglucose via an NAD+ -dependent intramolecular oxidation-reduction reaction. Here, the cloning, protein purification and X-ray crystallographic analysis of CDP-D-glucose 4,6-dehydratase from Salmonella typhi complexed with the substrate analog CDP-D-xylose are described. Each subunit of the tetrameric enzyme folds into two domains. The N-terminal region contains a Rossmann fold and provides the platform for NAD(H) binding. The C-terminal motif is primarily composed of alpha-helices and houses the binding pocket for the CDP portion of the CDP-D-xylose ligand. The xylose moiety extends into the active-site cleft that is located between the two domains. Key residues involved in anchoring the sugar group to the protein include Ser134, Tyr159, Asn197 and Arg208. Strikingly, Ser134 O gamma and Tyr159 O eta sit within 2.9 A of the 4'-hydroxyl group of xylose. Additionally, the side chains of Asp135 and Lys136 are located at 3.5 and 3.2 A, respectively, from C-5 of xylose. In the structurally related dTDP-D-glucose 4,6-dehydratase, the Asp/Lys pair is replaced with an Asp/Glu couple. On the basis of this investigation, it can be speculated that Tyr159 serves as the catalytic base to abstract the 4'-hydroxyl proton from the sugar and that Asp135 and Lys136 play critical roles in the subsequent dehydration step that leads to the final product.

About this Structure

1WVG is a Single protein structure of sequence from Salmonella enterica subsp. enterica serovar typhi with and as ligands. Active as CDP-glucose 4,6-dehydratase, with EC number 4.2.1.45 Full crystallographic information is available from OCA.

Reference

Structure of CDP-D-glucose 4,6-dehydratase from Salmonella typhi complexed with CDP-D-xylose., Koropatkin NM, Holden HM, Acta Crystallogr D Biol Crystallogr. 2005 Apr;61(Pt 4):365-73. Epub 2005, Mar 24. PMID:15805590

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