6wtz: Difference between revisions

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'''Unreleased structure'''


The entry 6wtz is ON HOLD
==Cryo-EM structure of E. Coli OmpF==
<StructureSection load='6wtz' size='340' side='right'caption='[[6wtz]], [[Resolution|resolution]] 3.15&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WTZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6WTZ 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]] 3.15&#8491;</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=6wtz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6wtz OCA], [https://pdbe.org/6wtz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6wtz RCSB], [https://www.ebi.ac.uk/pdbsum/6wtz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6wtz ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Single-particle cryo-electron microscopy (cryo-EM) has become a powerful technique in the field of structural biology. However, the inability to reliably produce pure, homogeneous membrane protein samples hampers the progress of their structural determination. Here, we develop a bottom-up iterative method, Build and Retrieve (BaR), that enables the identification and determination of cryo-EM structures of a variety of inner and outer membrane proteins, including membrane protein complexes of different sizes and dimensions, from a heterogeneous, impure protein sample. We also use the BaR methodology to elucidate structural information from Escherichia coli K12 crude membrane and raw lysate. The findings demonstrate that it is possible to solve high-resolution structures of a number of relatively small (&lt;100 kDa) and less abundant (&lt;10%) unidentified membrane proteins within a single, heterogeneous sample. Importantly, these results highlight the potential of cryo-EM for systems structural proteomics.


Authors: Morgan, C.E., Su, C.-C., Lyu, M., Yu, E.W.
A 'Build and Retrieve' methodology to simultaneously solve cryo-EM structures of membrane proteins.,Su CC, Lyu M, Morgan CE, Bolla JR, Robinson CV, Yu EW Nat Methods. 2021 Jan;18(1):69-75. doi: 10.1038/s41592-020-01021-2. Epub 2021 Jan, 6. PMID:33408407<ref>PMID:33408407</ref>


Description: Cryo-EM structure of E. Coli OmpF
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Morgan, C.E]]
<div class="pdbe-citations 6wtz" style="background-color:#fffaf0;"></div>
[[Category: Lyu, M]]
 
[[Category: Yu, E.W]]
==See Also==
[[Category: Su, C.-C]]
*[[Porin 3D structures|Porin 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Lyu M]]
[[Category: Morgan CE]]
[[Category: Su C-C]]
[[Category: Yu EW]]

Latest revision as of 05:58, 14 May 2025

Cryo-EM structure of E. Coli OmpF

6wtz, resolution 3.15Å

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