6n1b: Difference between revisions

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<StructureSection load='6n1b' size='340' side='right'caption='[[6n1b]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
<StructureSection load='6n1b' size='340' side='right'caption='[[6n1b]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[6n1b]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N1B OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N1B FirstGlance]. <br>
<table><tr><td colspan='2'>[[6n1b]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Flavonifractor_plautii Flavonifractor plautii]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N1B OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6N1B 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=FUC:ALPHA-L-FUCOSE'>FUC</scene>, <scene name='pdbligand=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=GLA:ALPHA+D-GALACTOSE'>GLA</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</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]] 1.3&#8491;</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=6n1b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n1b OCA], [http://pdbe.org/6n1b PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n1b RCSB], [http://www.ebi.ac.uk/pdbsum/6n1b PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n1b ProSAT]</span></td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=FUC:ALPHA-L-FUCOSE'>FUC</scene>, <scene name='pdbligand=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=GLA:ALPHA+D-GALACTOSE'>GLA</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</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=6n1b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n1b OCA], [https://pdbe.org/6n1b PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6n1b RCSB], [https://www.ebi.ac.uk/pdbsum/6n1b PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6n1b ProSAT]</span></td></tr>
</table>
</table>
== Function ==
[https://www.uniprot.org/uniprot/G9YSP4_FLAPL G9YSP4_FLAPL]
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Access to efficient enzymes that can convert A and B type red blood cells to 'universal' donor O would greatly increase the supply of blood for transfusions. Here we report the functional metagenomic screening of the human gut microbiome for enzymes that can remove the cognate A and B type sugar antigens. Among the genes encoded in our library of 19,500 expressed fosmids bearing gut bacterial DNA, we identify an enzyme pair from the obligate anaerobe Flavonifractor plautii that work in concert to efficiently convert the A antigen to the H antigen of O type blood, via a galactosamine intermediate. The X-ray structure of the N-acetylgalactosamine deacetylase reveals the active site and mechanism of the founding member of an esterase family. The galactosaminidase expands activities within the CAZy family GH36. Their ability to completely convert A to O of the same rhesus type at very low enzyme concentrations in whole blood will simplify their incorporation into blood transfusion practice, broadening blood supply.
An enzymatic pathway in the human gut microbiome that converts A to universal O type blood.,Rahfeld P, Sim L, Moon H, Constantinescu I, Morgan-Lang C, Hallam SJ, Kizhakkedathu JN, Withers SG Nat Microbiol. 2019 Jun 10. pii: 10.1038/s41564-019-0469-7. doi:, 10.1038/s41564-019-0469-7. PMID:31182795<ref>PMID:31182795</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 6n1b" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Flavonifractor plautii]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Rahfeld, P]]
[[Category: Rahfeld P]]
[[Category: Sim, L]]
[[Category: Sim L]]
[[Category: Withers, S G]]
[[Category: Withers SG]]
[[Category: A blood antigen]]
[[Category: Cazy]]
[[Category: Hydrolase]]
[[Category: N-acetylgalactosamine deacetylase]]

Latest revision as of 06:43, 11 October 2023

Crystal structure of an N-acetylgalactosamine deacetylase from F. plautii in complex with blood group B trisaccharide

6n1b, resolution 1.30Å

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