7c39: Difference between revisions
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<StructureSection load='7c39' size='340' side='right'caption='[[7c39]], [[Resolution|resolution]] 1.85Å' scene=''> | <StructureSection load='7c39' size='340' side='right'caption='[[7c39]], [[Resolution|resolution]] 1.85Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[7c39]] is a 2 chain structure with sequence from [ | <table><tr><td colspan='2'>[[7c39]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Orbilia_oligospora_ATCC_24927 Orbilia oligospora ATCC 24927]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7C39 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7C39 FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.85Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CIT:CITRIC+ACID'>CIT</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MFU:ALPHA-L-METHYL-FUCOSE'>MFU</scene></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=7c39 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7c39 OCA], [https://pdbe.org/7c39 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7c39 RCSB], [https://www.ebi.ac.uk/pdbsum/7c39 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7c39 ProSAT]</span></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Function == | |||
[https://www.uniprot.org/uniprot/G1XA82_ARTOA G1XA82_ARTOA] | |||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Cheng | [[Category: Orbilia oligospora ATCC 24927]] | ||
[[Category: Liu | [[Category: Cheng X]] | ||
[[Category: Wang | [[Category: Liu M]] | ||
[[Category: Wang | [[Category: Wang J]] | ||
[[Category: Zhang | [[Category: Wang M]] | ||
[[Category: Zhang M]] | |||
Latest revision as of 18:53, 29 November 2023
Crystal structure of AofleA from Arthrobotrys oligospora in complex with methylated L-fucoseCrystal structure of AofleA from Arthrobotrys oligospora in complex with methylated L-fucose
Structural highlights
FunctionPublication Abstract from PubMedFungal lectin can bind specific carbohydrate structures of the host and work in recognition and adhesion or as a toxic factor. AofleA, as a fucose-specific lectin from widely studied nematode predatory fungus Arthrobotrys oligospora, possibly plays a key role in the event of capturing nematodes, but the mechanism remains unknown. Here we report the crystal structure of AofleA, which exists as a homodimer with each subunit folds as a six-bladed beta-propeller. Our structural and biological results revealed that three of the six putative binding sites of AofleA had fucose-binding abilities. In addition, we found that AofleA could bind to the pharynx and intestine of the nematode in a fucose-binding-dependent manner. Our results facilitate the understanding of the mechanism that fucose-specific lectin mediates fungi-nematodes interaction, and provide structural information for the development of potential applications of AofleA. Structural insights into the fungi-nematodes interaction mediated by fucose-specific lectin AofleA from Arthrobotrys oligospora.,Liu M, Cheng X, Wang J, Tian D, Tang K, Xu T, Zhang M, Wang Y, Wang M Int J Biol Macromol. 2020 Jul 19;164:783-793. doi:, 10.1016/j.ijbiomac.2020.07.173. PMID:32698064[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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