1a9y: Difference between revisions

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New page: left|200px<br /><applet load="1a9y" size="450" color="white" frame="true" align="right" spinBox="true" caption="1a9y, resolution 1.8Å" /> '''UDP-GALACTOSE 4-EPIME...
 
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[[Image:1a9y.gif|left|200px]]<br /><applet load="1a9y" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1a9y.gif|left|200px]]<br /><applet load="1a9y" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1a9y, resolution 1.8&Aring;" />
caption="1a9y, resolution 1.8&Aring;" />
'''UDP-GALACTOSE 4-EPIMERASE MUTANT S124A/Y149F COMPLEXED WITH UDP-GLUCOSE'''<br />
'''UDP-GALACTOSE 4-EPIMERASE MUTANT S124A/Y149F COMPLEXED WITH UDP-GLUCOSE'''<br />


==Overview==
==Overview==
UDP-galactose 4-epimerase catalyzes the interconversion of UDP-galactose, and UDP-glucose during normal galactose metabolism. Within recent years, the enzyme from Escherichia coli has been studied extensively by both, biochemical and X-ray crystallographic techniques. One of several key, features in the catalytic mechanism of the enzyme involves the putative, rotation of a 4'-ketopyranose intermediate within the active site region., The mode of binding of UDP-glucose to epimerase is well understood on the, basis of previous high-resolution X-ray crystallographic investigations, from this laboratory with an enzyme/NADH/UDP-glucose abortive complex., Attempts to prepare an enzyme/NADH/UDP-galactose abortive complex always, failed, however, in that UDP-glucose rather than UDP-galactose was, observed binding in the active site. In an effort to prepare an abortive, complex with UDP-galactose, a site-directed mutant protein was constructed, in which Ser 124 and Tyr 149, known to play critical roles in catalysis, were substituted with alanine and phenylalanine residues, respectively., With this double mutant it was possible to crystallize and solve the, three-dimensional structures of reduced epimerase in the presence of, UDP-glucose or UDP-galactose to high resolution. This study represents the, first direct observation of UDP-galactose binding to epimerase and lends, strong structural support for a catalytic mechanism in which there is free, rotation of a 4'-ketopyranose intermediate within the active site cleft of, the enzyme.
UDP-galactose 4-epimerase catalyzes the interconversion of UDP-galactose and UDP-glucose during normal galactose metabolism. Within recent years the enzyme from Escherichia coli has been studied extensively by both biochemical and X-ray crystallographic techniques. One of several key features in the catalytic mechanism of the enzyme involves the putative rotation of a 4'-ketopyranose intermediate within the active site region. The mode of binding of UDP-glucose to epimerase is well understood on the basis of previous high-resolution X-ray crystallographic investigations from this laboratory with an enzyme/NADH/UDP-glucose abortive complex. Attempts to prepare an enzyme/NADH/UDP-galactose abortive complex always failed, however, in that UDP-glucose rather than UDP-galactose was observed binding in the active site. In an effort to prepare an abortive complex with UDP-galactose, a site-directed mutant protein was constructed in which Ser 124 and Tyr 149, known to play critical roles in catalysis, were substituted with alanine and phenylalanine residues, respectively. With this double mutant it was possible to crystallize and solve the three-dimensional structures of reduced epimerase in the presence of UDP-glucose or UDP-galactose to high resolution. This study represents the first direct observation of UDP-galactose binding to epimerase and lends strong structural support for a catalytic mechanism in which there is free rotation of a 4'-ketopyranose intermediate within the active site cleft of the enzyme.


==About this Structure==
==About this Structure==
1A9Y 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 NA, NAD and UPG as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/UDP-glucose_4-epimerase UDP-glucose 4-epimerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.1.3.2 5.1.3.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1A9Y OCA].  
1A9Y 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=NA:'>NA</scene>, <scene name='pdbligand=NAD:'>NAD</scene> and <scene name='pdbligand=UPG:'>UPG</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/UDP-glucose_4-epimerase UDP-glucose 4-epimerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.1.3.2 5.1.3.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A9Y OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: UDP-glucose 4-epimerase]]
[[Category: UDP-glucose 4-epimerase]]
[[Category: Holden, H.M.]]
[[Category: Holden, H M.]]
[[Category: Thoden, J.B.]]
[[Category: Thoden, J B.]]
[[Category: NA]]
[[Category: NA]]
[[Category: NAD]]
[[Category: NAD]]
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[[Category: galactose metabolism]]
[[Category: galactose metabolism]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:42:31 2008''