8rqf: Difference between revisions
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New page: '''Unreleased structure''' The entry 8rqf is ON HOLD Authors: Description: Category: Unreleased Structures |
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==Cryo-EM structure of human NTCP-Bulevirtide complex== | |||
<StructureSection load='8rqf' size='340' side='right'caption='[[8rqf]], [[Resolution|resolution]] 3.41Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8rqf]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens], [https://en.wikipedia.org/wiki/Lama_glama Lama glama] and [https://en.wikipedia.org/wiki/Hepatitis_B_virus_genotype_C Hepatitis B virus genotype C]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8RQF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8RQF FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.41Å</td></tr> | |||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BJU:2-(tetradecanoylamino)ethanoic+acid'>BJU</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=8rqf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8rqf OCA], [https://pdbe.org/8rqf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8rqf RCSB], [https://www.ebi.ac.uk/pdbsum/8rqf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8rqf ProSAT]</span></td></tr> | |||
</table> | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Cellular entry of the hepatitis B and D viruses (HBV/HDV) requires binding of the viral surface polypeptide preS1 to the hepatobiliary transporter Na(+)-taurocholate co-transporting polypeptide (NTCP). This interaction can be blocked by bulevirtide (BLV, formerly Myrcludex B), a preS1 derivative and approved drug for treating HDV infection. Here, to elucidate the basis of this inhibitory function, we determined a cryo-EM structure of BLV-bound human NTCP. BLV forms two domains, a plug lodged in the bile salt transport tunnel of NTCP and a string that covers the receptor's extracellular surface. The N-terminally attached myristoyl group of BLV interacts with the lipid-exposed surface of NTCP. Our structure reveals how BLV inhibits bile salt transport, rationalizes NTCP mutations that decrease the risk of HBV/HDV infection, and provides a basis for understanding the host specificity of HBV/HDV. Our results provide opportunities for structure-guided development of inhibitors that target HBV/HDV docking to NTCP. | |||
Structure of antiviral drug bulevirtide bound to hepatitis B and D virus receptor protein NTCP.,Liu H, Zakrzewicz D, Nosol K, Irobalieva RN, Mukherjee S, Bang-Sorensen R, Goldmann N, Kunz S, Rossi L, Kossiakoff AA, Urban S, Glebe D, Geyer J, Locher KP Nat Commun. 2024 Mar 20;15(1):2476. doi: 10.1038/s41467-024-46706-w. PMID:38509088<ref>PMID:38509088</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
[[Category: | </div> | ||
<div class="pdbe-citations 8rqf" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Hepatitis B virus genotype C]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Lama glama]] | |||
[[Category: Large Structures]] | |||
[[Category: Bang-Soerensen R]] | |||
[[Category: Geyer J]] | |||
[[Category: Glebe D]] | |||
[[Category: Goldmann N]] | |||
[[Category: Irobalieva RN]] | |||
[[Category: Kossiakoff AA]] | |||
[[Category: Kunz S]] | |||
[[Category: Liu H]] | |||
[[Category: Locher KP]] | |||
[[Category: Mukherjee S]] | |||
[[Category: Nosol K]] | |||
[[Category: Rossi L]] | |||
[[Category: Urban S]] | |||
[[Category: Zakrzewicz D]] | |||