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New page: left|200px<br /> <applet load="1zjp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1zjp, resolution 1.59Å" /> '''Crystal Structure o...
 
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[[Image:1zjp.gif|left|200px]]<br />
[[Image:1zjp.gif|left|200px]]<br /><applet load="1zjp" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1zjp" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1zjp, resolution 1.59&Aring;" />
caption="1zjp, resolution 1.59&Aring;" />
'''Crystal Structure of Human Galactosyltransferase (GTB) Complexed with Galactose-grease'''<br />
'''Crystal Structure of Human Galactosyltransferase (GTB) Complexed with Galactose-grease'''<br />


==Overview==
==Overview==
The human ABO(H) blood group A and B antigens are generated by the, homologous glycosyltransferases A (GTA) and B (GTB), which add the, monosaccharides GalNAc and Gal, respectively, to the cell-surface H, antigens. In the first comprehensive structural study of the recognition, by a glycosyltransferase of a panel of substrates corresponding to, acceptor fragments, 14 high resolution crystal structures of GTA and GTB, have been determined in the presence of oligosaccharides corresponding to, different segments of the type I, (alpha-l-Fucp-(1--&gt;2)-beta-D-Galp-(1--&gt;3)-beta-D-GlcNAcp-OR, where R is a, glycoprotein or glycolipid in natural acceptors) and type II, (alpha-l-Fucp-(1--&gt;2)-beta-D-Galp-(1--&gt;4)-beta-d-GlcNAcp-OR) H antigen, trisaccharides. GTA and GTB differ in only four "critical" amino acid, residues (Arg/Gly-176, Gly/Ser-235, Leu/Met-266, and Gly/Ala-268). As, these enzymes both utilize the H antigen acceptors, the four critical, residues had been thought to be involved strictly in donor recognition;, however, we now report that acceptor binding and subsequent transfer are, significantly influenced by two of these residues: Gly/Ser-235 and, Leu/Met-266. Furthermore, these structures show that acceptor recognition, is dominated by the central Gal residue despite the fact that the L-Fuc, residue is required for efficient catalysis and give direct insight into, the design of model inhibitors for GTA and GTB.
The human ABO(H) blood group A and B antigens are generated by the homologous glycosyltransferases A (GTA) and B (GTB), which add the monosaccharides GalNAc and Gal, respectively, to the cell-surface H antigens. In the first comprehensive structural study of the recognition by a glycosyltransferase of a panel of substrates corresponding to acceptor fragments, 14 high resolution crystal structures of GTA and GTB have been determined in the presence of oligosaccharides corresponding to different segments of the type I (alpha-l-Fucp-(1--&gt;2)-beta-D-Galp-(1--&gt;3)-beta-D-GlcNAcp-OR, where R is a glycoprotein or glycolipid in natural acceptors) and type II (alpha-l-Fucp-(1--&gt;2)-beta-D-Galp-(1--&gt;4)-beta-d-GlcNAcp-OR) H antigen trisaccharides. GTA and GTB differ in only four "critical" amino acid residues (Arg/Gly-176, Gly/Ser-235, Leu/Met-266, and Gly/Ala-268). As these enzymes both utilize the H antigen acceptors, the four critical residues had been thought to be involved strictly in donor recognition; however, we now report that acceptor binding and subsequent transfer are significantly influenced by two of these residues: Gly/Ser-235 and Leu/Met-266. Furthermore, these structures show that acceptor recognition is dominated by the central Gal residue despite the fact that the L-Fuc residue is required for efficient catalysis and give direct insight into the design of model inhibitors for GTA and GTB.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1ZJP 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 HG, CL, MN, DR4 and UDP as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ZJP OCA].  
1ZJP 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=HG:'>HG</scene>, <scene name='pdbligand=CL:'>CL</scene>, <scene name='pdbligand=MN:'>MN</scene>, <scene name='pdbligand=DR4:'>DR4</scene> and <scene name='pdbligand=UDP:'>UDP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZJP OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Barry, C.H.]]
[[Category: Barry, C H.]]
[[Category: Borisova, S.N.]]
[[Category: Borisova, S N.]]
[[Category: Evans, S.V.]]
[[Category: Evans, S V.]]
[[Category: Fang, Y.R.]]
[[Category: Fang, Y R.]]
[[Category: Letts, J.A.]]
[[Category: Letts, J A.]]
[[Category: Palcic, M.M.]]
[[Category: Palcic, M M.]]
[[Category: Rose, N.L.]]
[[Category: Rose, N L.]]
[[Category: Seto, N.O.]]
[[Category: Seto, N O.]]
[[Category: CL]]
[[Category: CL]]
[[Category: DR4]]
[[Category: DR4]]
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[[Category: retaining]]
[[Category: retaining]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:35:40 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:16:15 2008''

Revision as of 17:16, 21 February 2008

File:1zjp.gif


1zjp, resolution 1.59Å

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Crystal Structure of Human Galactosyltransferase (GTB) Complexed with Galactose-grease

OverviewOverview

The human ABO(H) blood group A and B antigens are generated by the homologous glycosyltransferases A (GTA) and B (GTB), which add the monosaccharides GalNAc and Gal, respectively, to the cell-surface H antigens. In the first comprehensive structural study of the recognition by a glycosyltransferase of a panel of substrates corresponding to acceptor fragments, 14 high resolution crystal structures of GTA and GTB have been determined in the presence of oligosaccharides corresponding to different segments of the type I (alpha-l-Fucp-(1-->2)-beta-D-Galp-(1-->3)-beta-D-GlcNAcp-OR, where R is a glycoprotein or glycolipid in natural acceptors) and type II (alpha-l-Fucp-(1-->2)-beta-D-Galp-(1-->4)-beta-d-GlcNAcp-OR) H antigen trisaccharides. GTA and GTB differ in only four "critical" amino acid residues (Arg/Gly-176, Gly/Ser-235, Leu/Met-266, and Gly/Ala-268). As these enzymes both utilize the H antigen acceptors, the four critical residues had been thought to be involved strictly in donor recognition; however, we now report that acceptor binding and subsequent transfer are significantly influenced by two of these residues: Gly/Ser-235 and Leu/Met-266. Furthermore, these structures show that acceptor recognition is dominated by the central Gal residue despite the fact that the L-Fuc residue is required for efficient catalysis and give direct insight into the design of model inhibitors for GTA and GTB.

DiseaseDisease

Known disease associated with this structure: Blood group, ABO system OMIM:[110300]

About this StructureAbout this Structure

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

ReferenceReference

Differential recognition of the type I and II H antigen acceptors by the human ABO(H) blood group A and B glycosyltransferases., Letts JA, Rose NL, Fang YR, Barry CH, Borisova SN, Seto NO, Palcic MM, Evans SV, J Biol Chem. 2006 Feb 10;281(6):3625-32. Epub 2005 Dec 2. PMID:16326711

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