1sg3

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(New page: 200px<br /><applet load="1sg3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1sg3, resolution 2.60&Aring;" /> '''Structure of allanto...)
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[[Image:1sg3.gif|left|200px]]<br /><applet load="1sg3" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1sg3, resolution 2.60&Aring;" />
caption="1sg3, resolution 2.60&Aring;" />
'''Structure of allantoicase'''<br />
'''Structure of allantoicase'''<br />
==Overview==
==Overview==
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Allantoicase (EC 3.5.3.4) catalyzes the conversion of allantoate into, ureidoglycolate and urea, one of the final steps in the degradation of, purines to urea. The mechanism of most enzymes involved in this pathway, which has been known for a long time, is unknown. In this paper we, describe the three-dimensional crystal structure of the yeast allantoicase, determined at a resolution of 2.6 A by single anomalous diffraction. This, constitutes the first structure for an enzyme of this pathway. The, structure reveals a repeated jelly roll beta-sheet motif, also present in, proteins of unrelated biochemical function. Allantoicase has a hexameric, arrangement in the crystal (dimer of trimers). Analysis of the protein, sequence against the structural data reveals the presence of two totally, conserved surface patches, one on each jelly roll motif. The hexameric, packing concentrates these patches into conserved pockets that probably, constitute the active site.
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Allantoicase (EC 3.5.3.4) catalyzes the conversion of allantoate into ureidoglycolate and urea, one of the final steps in the degradation of purines to urea. The mechanism of most enzymes involved in this pathway, which has been known for a long time, is unknown. In this paper we describe the three-dimensional crystal structure of the yeast allantoicase determined at a resolution of 2.6 A by single anomalous diffraction. This constitutes the first structure for an enzyme of this pathway. The structure reveals a repeated jelly roll beta-sheet motif, also present in proteins of unrelated biochemical function. Allantoicase has a hexameric arrangement in the crystal (dimer of trimers). Analysis of the protein sequence against the structural data reveals the presence of two totally conserved surface patches, one on each jelly roll motif. The hexameric packing concentrates these patches into conserved pockets that probably constitute the active site.
==About this Structure==
==About this Structure==
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1SG3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Active as [http://en.wikipedia.org/wiki/Allantoicase Allantoicase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.3.4 3.5.3.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SG3 OCA].
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1SG3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Active as [http://en.wikipedia.org/wiki/Allantoicase Allantoicase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.3.4 3.5.3.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SG3 OCA].
==Reference==
==Reference==
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[[Category: Quevillon-Cheruel, S.]]
[[Category: Quevillon-Cheruel, S.]]
[[Category: Sorel, I.]]
[[Category: Sorel, I.]]
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[[Category: Tilbeurgh, H.van.]]
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[[Category: Tilbeurgh, H van.]]
[[Category: allantoicase]]
[[Category: allantoicase]]
[[Category: hexamer]]
[[Category: hexamer]]
[[Category: jelly roll]]
[[Category: jelly roll]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 02:21:40 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:01:08 2008''

Revision as of 13:01, 21 February 2008


1sg3, resolution 2.60Å

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Structure of allantoicase

Overview

Allantoicase (EC 3.5.3.4) catalyzes the conversion of allantoate into ureidoglycolate and urea, one of the final steps in the degradation of purines to urea. The mechanism of most enzymes involved in this pathway, which has been known for a long time, is unknown. In this paper we describe the three-dimensional crystal structure of the yeast allantoicase determined at a resolution of 2.6 A by single anomalous diffraction. This constitutes the first structure for an enzyme of this pathway. The structure reveals a repeated jelly roll beta-sheet motif, also present in proteins of unrelated biochemical function. Allantoicase has a hexameric arrangement in the crystal (dimer of trimers). Analysis of the protein sequence against the structural data reveals the presence of two totally conserved surface patches, one on each jelly roll motif. The hexameric packing concentrates these patches into conserved pockets that probably constitute the active site.

About this Structure

1SG3 is a Single protein structure of sequence from Saccharomyces cerevisiae. Active as Allantoicase, with EC number 3.5.3.4 Full crystallographic information is available from OCA.

Reference

Crystal structure of yeast allantoicase reveals a repeated jelly roll motif., Leulliot N, Quevillon-Cheruel S, Sorel I, Graille M, Meyer P, Liger D, Blondeau K, Janin J, van Tilbeurgh H, J Biol Chem. 2004 May 28;279(22):23447-52. Epub 2004 Mar 12. PMID:15020593

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