6o88: Difference between revisions

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<StructureSection load='6o88' size='340' side='right'caption='[[6o88]], [[Resolution|resolution]] 1.99&Aring;' scene=''>
<StructureSection load='6o88' size='340' side='right'caption='[[6o88]], [[Resolution|resolution]] 1.99&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[6o88]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Eupatorium_rebaudianum Eupatorium rebaudianum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6O88 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6O88 FirstGlance]. <br>
<table><tr><td colspan='2'>[[6o88]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Stevia_rebaudiana Stevia rebaudiana]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6O88 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6O88 FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=LRV:(8alpha,9beta,10alpha,13alpha)-13-{[alpha-L-allopyranosyl-(1- 2)-[beta-D-mannopyranosyl-(1- 3)]-beta-D-allopyranosyl]oxy}kauran-18-oic+acid'>LRV</scene>, <scene name='pdbligand=UDP:URIDINE-5-DIPHOSPHATE'>UDP</scene></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.99&#8491;</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">UGT76G1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=55670 Eupatorium rebaudianum])</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=LRV:(8alpha,9beta,10alpha,13alpha)-13-{[alpha-L-allopyranosyl-(1- 2)-[beta-D-mannopyranosyl-(1- 3)]-beta-D-allopyranosyl]oxy}kauran-18-oic+acid'>LRV</scene>, <scene name='pdbligand=UDP:URIDINE-5-DIPHOSPHATE'>UDP</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6o88 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6o88 OCA], [http://pdbe.org/6o88 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6o88 RCSB], [http://www.ebi.ac.uk/pdbsum/6o88 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6o88 ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6o88 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6o88 OCA], [https://pdbe.org/6o88 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6o88 RCSB], [https://www.ebi.ac.uk/pdbsum/6o88 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6o88 ProSAT]</span></td></tr>
</table>
</table>
<div style="background-color:#fffaf0;">
== Function ==
== Publication Abstract from PubMed ==
[https://www.uniprot.org/uniprot/U76G1_STERE U76G1_STERE]
Steviol glucosides, such as stevioside and rebaudioside A, are natural products roughly 200-fold sweeter than sugar and are used as natural, noncaloric sweeteners. Biosynthesis of rebaudioside A, and other related stevia glucosides, involves formation of the steviol diterpenoid followed by a series of glycosylations catalyzed by uridine diphosphate (UDP)-dependent glucosyltransferases. UGT76G1 from Stevia rebaudiana catalyzes the formation of the branched-chain glucoside that defines the stevia molecule and is critical for its high-intensity sweetness. Here, we report the 3D structure of the UDP-glucosyltransferase UGT76G1, including a complex of the protein with UDP and rebaudioside A bound in the active site. The X-ray crystal structure and biochemical analysis of site-directed mutants identifies a catalytic histidine and how the acceptor site of UGT76G1 achieves regioselectivity for branched-glucoside synthesis. The active site accommodates a two-glucosyl side chain and provides a site for addition of a third sugar molecule to the C3' position of the first C13 sugar group of stevioside. This structure provides insight on the glycosylation of other naturally occurring sweeteners, such as the mogrosides from monk fruit, and a possible template for engineering of steviol biosynthesis.


Molecular basis for branched steviol glucoside biosynthesis.,Lee SG, Salomon E, Yu O, Jez JM Proc Natl Acad Sci U S A. 2019 Jun 10. pii: 1902104116. doi:, 10.1073/pnas.1902104116. PMID:31182573<ref>PMID:31182573</ref>
==See Also==
 
*[[Glycosyltransferase 3D structures|Glycosyltransferase 3D structures]]
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 6o88" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Eupatorium rebaudianum]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Jez, J M]]
[[Category: Stevia rebaudiana]]
[[Category: Lee, S G]]
[[Category: Jez JM]]
[[Category: Plant biochemistry]]
[[Category: Lee SG]]
[[Category: Transferase]]

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