1fgg

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(New page: 200px<br /> <applet load="1fgg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fgg, resolution 2.30&Aring;" /> '''CRYSTAL STRUCTURE O...)
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<applet load="1fgg" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1fgg, resolution 2.30&Aring;" />
caption="1fgg, resolution 2.30&Aring;" />
'''CRYSTAL STRUCTURE OF 1,3-GLUCURONYLTRANSFERASE I (GLCAT-I) COMPLEXED WITH GAL-GAL-XYL, UDP, AND MN2+'''<br />
'''CRYSTAL STRUCTURE OF 1,3-GLUCURONYLTRANSFERASE I (GLCAT-I) COMPLEXED WITH GAL-GAL-XYL, UDP, AND MN2+'''<br />
==Overview==
==Overview==
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Human beta1,3-glucuronyltransferase I (GlcAT-I) is a central enzyme in the, initial steps of proteoglycan synthesis. GlcAT-I transfers a glucuronic, acid moiety from the uridine diphosphate-glucuronic acid (UDP-GlcUA) to, the common linkage region trisaccharide Gal beta 1-3Gal beta 1-4Xyl, covalently bound to a Ser residue at the glycosaminylglycan attachment, site of proteoglycans. We have now determined the crystal structure of, GlcAT-1 at 2.3 A in the presence of the donor substrate product UDP, the, catalytic Mn(2+) ion, and the acceptor substrate analog Gal beta 1-3Gal, beta 1-4Xyl. The enzyme is a alpha/beta protein with two subdomains that, constitute the donor and acceptor substrate binding site. The active site, residues lie in a cleft extending across both subdomains in which the, trisaccharide molecule is oriented perpendicular to the UDP. Residues, Glu(227), Asp(252), and Glu(281) dictate the binding orientation of the, terminal Gal-2 moiety. Residue Glu(281) is in position to function as a, catalytic base by deprotonating the incoming 3-hydroxyl group of the, acceptor. The conserved DXD motif (Asp(194), Asp(195), Asp(196)) has, direct interaction with the ribose of the UDP molecule as well as with the, Mn(2+) ion. The key residues involved in substrate binding and catalysis, are conserved in the glucuronyltransferase family as well as other, glycosyltransferases.
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Human beta1,3-glucuronyltransferase I (GlcAT-I) is a central enzyme in the initial steps of proteoglycan synthesis. GlcAT-I transfers a glucuronic acid moiety from the uridine diphosphate-glucuronic acid (UDP-GlcUA) to the common linkage region trisaccharide Gal beta 1-3Gal beta 1-4Xyl covalently bound to a Ser residue at the glycosaminylglycan attachment site of proteoglycans. We have now determined the crystal structure of GlcAT-1 at 2.3 A in the presence of the donor substrate product UDP, the catalytic Mn(2+) ion, and the acceptor substrate analog Gal beta 1-3Gal beta 1-4Xyl. The enzyme is a alpha/beta protein with two subdomains that constitute the donor and acceptor substrate binding site. The active site residues lie in a cleft extending across both subdomains in which the trisaccharide molecule is oriented perpendicular to the UDP. Residues Glu(227), Asp(252), and Glu(281) dictate the binding orientation of the terminal Gal-2 moiety. Residue Glu(281) is in position to function as a catalytic base by deprotonating the incoming 3-hydroxyl group of the acceptor. The conserved DXD motif (Asp(194), Asp(195), Asp(196)) has direct interaction with the ribose of the UDP molecule as well as with the Mn(2+) ion. The key residues involved in substrate binding and catalysis are conserved in the glucuronyltransferase family as well as other glycosyltransferases.
==About this Structure==
==About this Structure==
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1FGG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with MN, UDP and UNX as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FGG OCA].
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1FGG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=MN:'>MN</scene>, <scene name='pdbligand=UDP:'>UDP</scene> and <scene name='pdbligand=UNX:'>UNX</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FGG OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Darden, T.A.]]
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[[Category: Darden, T A.]]
[[Category: Kitagawa, H.]]
[[Category: Kitagawa, H.]]
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[[Category: Pedersen, L.C.]]
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[[Category: Pedersen, L C.]]
[[Category: Sugahara, K.]]
[[Category: Sugahara, K.]]
[[Category: Tsuchida, K]]
[[Category: Tsuchida, K]]
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[[Category: udp]]
[[Category: udp]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:52:56 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:38:24 2008''

Revision as of 10:38, 21 February 2008


1fgg, resolution 2.30Å

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CRYSTAL STRUCTURE OF 1,3-GLUCURONYLTRANSFERASE I (GLCAT-I) COMPLEXED WITH GAL-GAL-XYL, UDP, AND MN2+

Overview

Human beta1,3-glucuronyltransferase I (GlcAT-I) is a central enzyme in the initial steps of proteoglycan synthesis. GlcAT-I transfers a glucuronic acid moiety from the uridine diphosphate-glucuronic acid (UDP-GlcUA) to the common linkage region trisaccharide Gal beta 1-3Gal beta 1-4Xyl covalently bound to a Ser residue at the glycosaminylglycan attachment site of proteoglycans. We have now determined the crystal structure of GlcAT-1 at 2.3 A in the presence of the donor substrate product UDP, the catalytic Mn(2+) ion, and the acceptor substrate analog Gal beta 1-3Gal beta 1-4Xyl. The enzyme is a alpha/beta protein with two subdomains that constitute the donor and acceptor substrate binding site. The active site residues lie in a cleft extending across both subdomains in which the trisaccharide molecule is oriented perpendicular to the UDP. Residues Glu(227), Asp(252), and Glu(281) dictate the binding orientation of the terminal Gal-2 moiety. Residue Glu(281) is in position to function as a catalytic base by deprotonating the incoming 3-hydroxyl group of the acceptor. The conserved DXD motif (Asp(194), Asp(195), Asp(196)) has direct interaction with the ribose of the UDP molecule as well as with the Mn(2+) ion. The key residues involved in substrate binding and catalysis are conserved in the glucuronyltransferase family as well as other glycosyltransferases.

About this Structure

1FGG is a Single protein structure of sequence from Homo sapiens with , and as ligands. Full crystallographic information is available from OCA.

Reference

Heparan/chondroitin sulfate biosynthesis. Structure and mechanism of human glucuronyltransferase I., Pedersen LC, Tsuchida K, Kitagawa H, Sugahara K, Darden TA, Negishi M, J Biol Chem. 2000 Nov 3;275(44):34580-5. PMID:10946001

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