1iir: Difference between revisions

New page: left|200px<br /><applet load="1iir" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iir, resolution 1.8Å" /> '''Crystal Structure of ...
 
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[[Image:1iir.gif|left|200px]]<br /><applet load="1iir" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1iir.gif|left|200px]]<br /><applet load="1iir" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1iir, resolution 1.8&Aring;" />
caption="1iir, resolution 1.8&Aring;" />
'''Crystal Structure of UDP-glucosyltransferase GtfB'''<br />
'''Crystal Structure of UDP-glucosyltransferase GtfB'''<br />


==Overview==
==Overview==
BACKGROUND: Members of the vancomycin group of glycopeptide antibiotics, have an oxidatively crosslinked heptapeptide scaffold decorated at the, hydroxyl groups of 4-OH-Phegly4 or beta-OH-Tyr6 with mono- (residue 6) or, disaccharides (residue 4). The disaccharide in vancomycin itself is, L-vancosamine-1,2-glucose, and in chloroeremomycin it is, L-4-epi-vancosamine-1,2-glucose. The sugars and their substituents play an, important role in efficacy, particularly against vancomycin-resistant, pathogenic enterococci. RESULTS: The glucosyltransferase, GtfB, that, transfers the glucose residue from UDP-glucose to the 4-OH-Phegly4 residue, of the vancomycin aglycone, initiating the glycosylation pathway in, chloroeremomycin maturation, has been crystallized, and its structure has, been determined by X-ray analysis at 1.8 A resolution. The enzyme has a, two-domain structure, with a deep interdomain cleft identified as the, likely site of UDP-glucose binding. A hydrophobic patch on the surface of, the N-terminal domain is proposed to be the binding site of the aglycone, substrate. Mutagenesis has revealed Asp332 as the best candidate for the, general base in the glucosyltransfer reaction. CONCLUSIONS: The structure, of GtfB places it in a growing group of glycosyltransferases, including, Escherichia coli MurG and a beta-glucosyltransferase from T4 phage, which, together form a subclass of the glycosyltransferase superfamily and give, insights into the recognition of the NDP-sugar and aglycone cosubstrates., A single major interdomain linker between the N- and C- terminal domains, suggests that reprogramming of sugar transfer or aglycone recognition in, the antibiotic glycosyltransferases, including the glycopeptide and also, the macrolide antibiotics, will be facilitated by this structural, information.
BACKGROUND: Members of the vancomycin group of glycopeptide antibiotics have an oxidatively crosslinked heptapeptide scaffold decorated at the hydroxyl groups of 4-OH-Phegly4 or beta-OH-Tyr6 with mono- (residue 6) or disaccharides (residue 4). The disaccharide in vancomycin itself is L-vancosamine-1,2-glucose, and in chloroeremomycin it is L-4-epi-vancosamine-1,2-glucose. The sugars and their substituents play an important role in efficacy, particularly against vancomycin-resistant pathogenic enterococci. RESULTS: The glucosyltransferase, GtfB, that transfers the glucose residue from UDP-glucose to the 4-OH-Phegly4 residue of the vancomycin aglycone, initiating the glycosylation pathway in chloroeremomycin maturation, has been crystallized, and its structure has been determined by X-ray analysis at 1.8 A resolution. The enzyme has a two-domain structure, with a deep interdomain cleft identified as the likely site of UDP-glucose binding. A hydrophobic patch on the surface of the N-terminal domain is proposed to be the binding site of the aglycone substrate. Mutagenesis has revealed Asp332 as the best candidate for the general base in the glucosyltransfer reaction. CONCLUSIONS: The structure of GtfB places it in a growing group of glycosyltransferases, including Escherichia coli MurG and a beta-glucosyltransferase from T4 phage, which together form a subclass of the glycosyltransferase superfamily and give insights into the recognition of the NDP-sugar and aglycone cosubstrates. A single major interdomain linker between the N- and C- terminal domains suggests that reprogramming of sugar transfer or aglycone recognition in the antibiotic glycosyltransferases, including the glycopeptide and also the macrolide antibiotics, will be facilitated by this structural information.


==About this Structure==
==About this Structure==
1IIR is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Amycolatopsis_orientalis Amycolatopsis orientalis] with SO4 and MG as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IIR OCA].  
1IIR is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Amycolatopsis_orientalis Amycolatopsis orientalis] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=MG:'>MG</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IIR OCA].  


==Reference==
==Reference==
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[[Category: Amycolatopsis orientalis]]
[[Category: Amycolatopsis orientalis]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Garavito, R.M.]]
[[Category: Garavito, R M.]]
[[Category: Losey, H.C.]]
[[Category: Losey, H C.]]
[[Category: Mulichak, A.M.]]
[[Category: Mulichak, A M.]]
[[Category: Walsh, C.T.]]
[[Category: Walsh, C T.]]
[[Category: MG]]
[[Category: MG]]
[[Category: SO4]]
[[Category: SO4]]
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[[Category: rossmann fold]]
[[Category: rossmann fold]]


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