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New page: left|200px<br /><applet load="1rkx" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rkx, resolution 1.80Å" /> '''Crystal Structure at...
 
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[[Image:1rkx.gif|left|200px]]<br /><applet load="1rkx" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1rkx.gif|left|200px]]<br /><applet load="1rkx" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1rkx, resolution 1.80&Aring;" />
caption="1rkx, resolution 1.80&Aring;" />
'''Crystal Structure at 1.8 Angstrom of CDP-D-glucose 4,6-dehydratase from Yersinia pseudotuberculosis'''<br />
'''Crystal Structure at 1.8 Angstrom of CDP-D-glucose 4,6-dehydratase from Yersinia pseudotuberculosis'''<br />


==Overview==
==Overview==
CDP-D-glucose 4,6-dehydratase catalyzes the conversion of CDP-D-glucose to, CDP-4-keto-6-deoxyglucose in an NAD(+)-dependent manner. The product of, this conversion is a building block for a variety of primary antigenic, determinants in bacteria, possibly implicated directly in reactive, arthritis. Here, we describe the solution of the high-resolution crystal, structure of CDP-D-glucose 4,6-dehydratase from Yersinia, pseudotuberculosis in the resting state. This structure represents the, first CDP nucleotide utilizing dehydratase of the short-chain, dehydrogenase/reductase (SDR) family to be determined, as well as the, first tetrameric structure of the subfamily of SDR enzymes in which NAD(+), undergoes a full reaction cycle. On the basis of a comparison of this, structure with structures of homologous enzymes, a chemical mechanism is, proposed in which Tyr157 acts as the catalytic base, initiating hydride, transfer by abstraction of the proton from the sugar 4'-hydroxyl., Concomitant with the removal of the proton from the 4'-hydroxyl oxygen, the sugar 4'-hydride is transferred to the B face of the NAD(+) cofactor, forming the reduced cofactor and a CDP-4-keto-d-glucose intermediate. A, conserved Lys161 most likely acts to position the NAD(+) cofactor so that, hydride transfer is favorable and/or to reduce the pK(a) of Tyr157., Following substrate oxidation, we propose that Lys134, acting as a base, would abstract the 5'-hydrogen of CDP-4-keto-D-glucose, priming the, intermediate for the spontaneous loss of water. Finally, the resulting, Delta(5,6)-glucoseen intermediate would be reduced suprafacially by the, cofactor, and reprotonation at C-5' is likely mediated by Lys134.
CDP-D-glucose 4,6-dehydratase catalyzes the conversion of CDP-D-glucose to CDP-4-keto-6-deoxyglucose in an NAD(+)-dependent manner. The product of this conversion is a building block for a variety of primary antigenic determinants in bacteria, possibly implicated directly in reactive arthritis. Here, we describe the solution of the high-resolution crystal structure of CDP-D-glucose 4,6-dehydratase from Yersinia pseudotuberculosis in the resting state. This structure represents the first CDP nucleotide utilizing dehydratase of the short-chain dehydrogenase/reductase (SDR) family to be determined, as well as the first tetrameric structure of the subfamily of SDR enzymes in which NAD(+) undergoes a full reaction cycle. On the basis of a comparison of this structure with structures of homologous enzymes, a chemical mechanism is proposed in which Tyr157 acts as the catalytic base, initiating hydride transfer by abstraction of the proton from the sugar 4'-hydroxyl. Concomitant with the removal of the proton from the 4'-hydroxyl oxygen, the sugar 4'-hydride is transferred to the B face of the NAD(+) cofactor, forming the reduced cofactor and a CDP-4-keto-d-glucose intermediate. A conserved Lys161 most likely acts to position the NAD(+) cofactor so that hydride transfer is favorable and/or to reduce the pK(a) of Tyr157. Following substrate oxidation, we propose that Lys134, acting as a base, would abstract the 5'-hydrogen of CDP-4-keto-D-glucose, priming the intermediate for the spontaneous loss of water. Finally, the resulting Delta(5,6)-glucoseen intermediate would be reduced suprafacially by the cofactor, and reprotonation at C-5' is likely mediated by Lys134.


==About this Structure==
==About this Structure==
1RKX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Yersinia_pseudotuberculosis Yersinia pseudotuberculosis] with NAD as [http://en.wikipedia.org/wiki/ligand ligand]. 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=1RKX OCA].  
1RKX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Yersinia_pseudotuberculosis Yersinia pseudotuberculosis] with <scene name='pdbligand=NAD:'>NAD</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. 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=1RKX OCA].  


==Reference==
==Reference==
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[[Category: Bellamacina, C.]]
[[Category: Bellamacina, C.]]
[[Category: He, X.]]
[[Category: He, X.]]
[[Category: Liu, H.W.]]
[[Category: Liu, H W.]]
[[Category: Petsko, G.A.]]
[[Category: Petsko, G A.]]
[[Category: Ringe, D.]]
[[Category: Ringe, D.]]
[[Category: Vogan, E.M.]]
[[Category: Vogan, E M.]]
[[Category: NAD]]
[[Category: NAD]]
[[Category: cdp glucose dehydratase]]
[[Category: cdp glucose dehydratase]]
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[[Category: sdr]]
[[Category: sdr]]


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