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New page: left|200px<br /><applet load="1fx5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fx5, resolution 2.2Å" /> '''CRYSTAL STRUCTURE ANA...
 
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[[Image:1fx5.gif|left|200px]]<br /><applet load="1fx5" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1fx5.gif|left|200px]]<br /><applet load="1fx5" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1fx5, resolution 2.2&Aring;" />
caption="1fx5, resolution 2.2&Aring;" />
'''CRYSTAL STRUCTURE ANALYSIS OF ULEX EUROPAEUS LECTIN I'''<br />
'''CRYSTAL STRUCTURE ANALYSIS OF ULEX EUROPAEUS LECTIN I'''<br />


==Overview==
==Overview==
The tertiary and quaternary structure of the lectin I from Ulex europaeus, (UE-I) has been determined to 2.2 A resolution. UE-I is a dimeric, metalloglycoprotein that binds the H-type 2 human blood group determinant, [alpha-L-Fucalpha(1--&gt;2)-beta-D-Galbeta(1--&gt;4)-beta-D-Glc NAcalpha-]. Nine, changes from the published amino acid sequence were necessary to account, for the electron density. The quaternary structural organization of UE-I, is that of the most commonly occurring legume lectin dimer. The tertiary, structure of the monomeric subunits is similar to that in the conventional, lectin subunit; however, some structural differences are noted. These, differences include a four-stranded anti-parallel "S" sheet in UE-I versus, the five-stranded S sheet in other lectin monomers. The Ala residue of the, Ala-Asp cis-peptide bond present in the carbohydrate-binding site of the, conventional lectin monomer is replaced with a Thr in the UE-I structure., Also, a novel disulfide bridge linking Cys115 and Cys150 is present. There, are two metallic ions, one calcium and the other manganese, per subunit., N-linked oligosaccharides are at residues 23 and 111 of each subunit. One, molecule of R-2-methyl-2, 4-pentanediol (R-MPD) is present in a shallow, depression on the surface of each subunit. In order to examine the binding, of the H-type 2 blood group determinant by UE-I, its beta-methyl glycoside, (H-type 2-OMe) was docked into the binding site of R-MPD. The epitope, previously identified for H-type 2-OMe by chemical mapping proved, with, only minor adjustment of amino acid residues, to be complementary to the, shallow cavity occupied by R-MPD in the structure. Several key, interactions have been proposed between the H-type 2-OMe and UE-I.
The tertiary and quaternary structure of the lectin I from Ulex europaeus (UE-I) has been determined to 2.2 A resolution. UE-I is a dimeric metalloglycoprotein that binds the H-type 2 human blood group determinant [alpha-L-Fucalpha(1--&gt;2)-beta-D-Galbeta(1--&gt;4)-beta-D-Glc NAcalpha-]. Nine changes from the published amino acid sequence were necessary to account for the electron density. The quaternary structural organization of UE-I is that of the most commonly occurring legume lectin dimer. The tertiary structure of the monomeric subunits is similar to that in the conventional lectin subunit; however, some structural differences are noted. These differences include a four-stranded anti-parallel "S" sheet in UE-I versus the five-stranded S sheet in other lectin monomers. The Ala residue of the Ala-Asp cis-peptide bond present in the carbohydrate-binding site of the conventional lectin monomer is replaced with a Thr in the UE-I structure. Also, a novel disulfide bridge linking Cys115 and Cys150 is present. There are two metallic ions, one calcium and the other manganese, per subunit. N-linked oligosaccharides are at residues 23 and 111 of each subunit. One molecule of R-2-methyl-2, 4-pentanediol (R-MPD) is present in a shallow depression on the surface of each subunit. In order to examine the binding of the H-type 2 blood group determinant by UE-I, its beta-methyl glycoside (H-type 2-OMe) was docked into the binding site of R-MPD. The epitope previously identified for H-type 2-OMe by chemical mapping proved, with only minor adjustment of amino acid residues, to be complementary to the shallow cavity occupied by R-MPD in the structure. Several key interactions have been proposed between the H-type 2-OMe and UE-I.


==About this Structure==
==About this Structure==
1FX5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Ulex_europaeus Ulex europaeus] with MN, CA and MRD as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FX5 OCA].  
1FX5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Ulex_europaeus Ulex europaeus] with <scene name='pdbligand=MN:'>MN</scene>, <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=MRD:'>MRD</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FX5 OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Ulex europaeus]]
[[Category: Ulex europaeus]]
[[Category: Audette, G.F.]]
[[Category: Audette, G F.]]
[[Category: Delbaere, L.T.J.]]
[[Category: Delbaere, L T.J.]]
[[Category: Vandonselaar, M.]]
[[Category: Vandonselaar, M.]]
[[Category: CA]]
[[Category: CA]]
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[[Category: ue-i]]
[[Category: ue-i]]


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