6f4f: Difference between revisions
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<StructureSection load='6f4f' size='340' side='right' caption='[[6f4f]], [[Resolution|resolution]] 1.75Å' scene=''> | <StructureSection load='6f4f' size='340' side='right' caption='[[6f4f]], [[Resolution|resolution]] 1.75Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6f4f]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6F4F OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6F4F FirstGlance]. <br> | <table><tr><td colspan='2'>[[6f4f]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Bjerkandera_versicolor Bjerkandera versicolor]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6F4F OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6F4F FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=GDN:GLUTATHIONE+S-(2,4+DINITROBENZENE)'>GDN</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=GDN:GLUTATHIONE+S-(2,4+DINITROBENZENE)'>GDN</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr> | ||
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6f43|6f43]], [[6f4b|6f4b]]</td></tr> | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6f43|6f43]], [[6f4b|6f4b]]</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=6f4f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f4f OCA], [http://pdbe.org/6f4f PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6f4f RCSB], [http://www.ebi.ac.uk/pdbsum/6f4f PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6f4f ProSAT]</span></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=6f4f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f4f OCA], [http://pdbe.org/6f4f PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6f4f RCSB], [http://www.ebi.ac.uk/pdbsum/6f4f PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6f4f ProSAT]</span></td></tr> | ||
</table> | </table> | ||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Wood decay fungi have complex detoxification systems that enable them to cope with secondary metabolites produced by plants. Although the number of genes encoding for glutathione transferases is especially expanded in lignolytic fungi, little is known about their target molecules. In this study, by combining biochemical, enzymatic and structural approaches, interactions between polyphenols and six glutathione transferases from the white-rot fungus Trametes versicolor have been demonstrated. Two isoforms, named TvGSTO3S and TvGSTO6S have been deeply studied at the structural level. Each isoform shows two distinct ligand-binding sites, a narrow L-site at the dimer interface and a peculiar deep hydrophobic H-site. In TvGSTO3S, the latter appears optimized for aromatic ligand binding such as hydroxybenzophenones. Affinity crystallography revealed that this H-site retains the flavonoid dihydrowogonin from a partially purified wild-cherry extract. Besides, TvGSTO6S binds two molecules of the flavonoid naringenin in the L-site. These data suggest that TvGSTO isoforms could interact with plant polyphenols released during wood degradation. | |||
Molecular recognition of wood polyphenols by phase II detoxification enzymes of the white rot Trametes versicolor.,Schwartz M, Perrot T, Aubert E, Dumarcay S, Favier F, Gerardin P, Morel-Rouhier M, Mulliert G, Saiag F, Didierjean C, Gelhaye E Sci Rep. 2018 May 31;8(1):8472. doi: 10.1038/s41598-018-26601-3. PMID:29855494<ref>PMID:29855494</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
</div> | |||
<div class="pdbe-citations 6f4f" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Bjerkandera versicolor]] | ||
[[Category: | [[Category: Didierjean, C]] | ||
[[Category: | [[Category: Favier, F]] | ||
[[Category: Schwartz, M]] | |||
[[Category: Fungi]] | [[Category: Fungi]] | ||
[[Category: Glutathione]] | [[Category: Glutathione]] |