5xy3 - Revision history

OCA at 22:39, 10 April 2020

OCA — Fri, 10 Apr 2020 22:39:09 GMT

OCA at 20:12, 6 March 2020

OCA — Fri, 06 Mar 2020 20:12:10 GMT

OCA at 09:14, 18 December 2019

OCA — Wed, 18 Dec 2019 09:14:18 GMT

OCA: Protected "5xy3" [edit=sysop:move=sysop]

OCA — Wed, 30 Aug 2017 04:12:43 GMT

Protected "5xy3" [edit=sysop:move=sysop]

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Revision as of 04:12, 30 August 2017

OCA: New page: {{Large structure}} ==Large subunit of Trichomonas vaginalis ribosome==
OCA — Wed, 30 Aug 2017 04:12:41 GMT

New page: {{Large structure}} ==Large subunit of Trichomonas vaginalis ribosome== <StructureSection load='5xy3' size='340' side='right' caption='5xy3, resolution 3.20Å' scen...

New page
{{Large structure}}
==Large subunit of Trichomonas vaginalis ribosome==
<StructureSection load='5xy3' size='340' side='right' caption='[[5xy3]], [[Resolution|resolution]] 3.20Å' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[5xy3]] is a 43 chain structure with sequence from [http://en.wikipedia.org/wiki/Trichomonas_vaginalis Trichomonas vaginalis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5XY3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5XY3 FirstGlance]. <br>
</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=5xy3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5xy3 OCA], [http://pdbe.org/5xy3 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5xy3 RCSB], [http://www.ebi.ac.uk/pdbsum/5xy3 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5xy3 ProSAT]</span></td></tr>
</table>
{{Large structure}}
== Function ==
[[http://www.uniprot.org/uniprot/A2F8Y8_TRIVA A2F8Y8_TRIVA]] Binds to the 23S rRNA.[RuleBase:RU000576]
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
As an indispensable molecular machine universal in all living organisms, the ribosome has been selected by evolution to be the natural target of many antibiotics and small-molecule inhibitors. High-resolution structures of pathogen ribosomes are crucial for understanding the general and unique aspects of translation control in disease-causing microbes. With cryo-electron microscopy technique, we have determined structures of the cytosolic ribosomes from two human parasites, Trichomonas vaginalis and Toxoplasma gondii, at resolution of 3.2-3.4 A. Although the ribosomal proteins from both pathogens are typical members of eukaryotic families, with a co-evolution pattern between certain species-specific insertions/extensions and neighboring ribosomal RNA (rRNA) expansion segments, the sizes of their rRNAs are sharply different. Very interestingly, rRNAs of T. vaginalis are in size comparable to prokaryotic counterparts, with nearly all the eukaryote-specific rRNA expansion segments missing. These structures facilitate the dissection of evolution path for ribosomal proteins and RNAs, and may aid in design of novel translation inhibitors.Cell Research advance online publication 15 August 2017; doi:10.1038/cr.2017.104.

Cryo-EM structures of the 80S ribosomes from human parasites Trichomonas vaginalis and Toxoplasma gondii.,Li Z, Guo Q, Zheng L, Ji Y, Xie YT, Lai DH, Lun ZR, Suo X, Gao N Cell Res. 2017 Aug 15. doi: 10.1038/cr.2017.104. PMID:28809395<ref>PMID:28809395</ref>

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 5xy3" style="background-color:#fffaf0;"></div>
== References ==
<references/>
TOC
</StructureSection>
[[Category: Trichomonas vaginalis]]
[[Category: Gao, N]]
[[Category: Guo, Q]]
[[Category: Ji, Y]]
[[Category: Lai, D]]
[[Category: Li, Z]]
[[Category: Lun, Z]]
[[Category: Suo, X]]
[[Category: Xie, Y]]
[[Category: Zheng, L]]
[[Category: Ribosome]]
[[Category: Rprotein]]
[[Category: Rrna]]
[[Category: Trichomonas vaginalis ribosome]]