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 ... |
No edit summary |
||
Line 1: | Line 1: | ||
[[Image:1iir.gif|left|200px]]<br /><applet load="1iir" size=" | [[Image:1iir.gif|left|200px]]<br /><applet load="1iir" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1iir, resolution 1.8Å" /> | caption="1iir, resolution 1.8Å" /> | ||
'''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 | 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:// | 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== | ||
Line 13: | Line 13: | ||
[[Category: Amycolatopsis orientalis]] | [[Category: Amycolatopsis orientalis]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Garavito, R | [[Category: Garavito, R M.]] | ||
[[Category: Losey, H | [[Category: Losey, H C.]] | ||
[[Category: Mulichak, A | [[Category: Mulichak, A M.]] | ||
[[Category: Walsh, C | [[Category: Walsh, C T.]] | ||
[[Category: MG]] | [[Category: MG]] | ||
[[Category: SO4]] | [[Category: SO4]] | ||
Line 22: | Line 22: | ||
[[Category: rossmann fold]] | [[Category: rossmann fold]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:12:17 2008'' |