6n0f

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'''Unreleased structure'''
 
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The entry 6n0f is ON HOLD until Paper Publication
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==Cryo-EM structure of the HO BMC shell: subregion classified for BMC-T: TD-TSTSTS==
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<StructureSection load='6n0f' size='340' side='right'caption='[[6n0f]], [[Resolution|resolution]] 3.90&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6n0f]] is a 51 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N0F OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N0F FirstGlance]. <br>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6mzx|6mzx]], [[6mzy|6mzy]], [[6n06|6n06]], [[6mzu|6mzu]], [[6mzv|6mzv]], [[6n07|6n07]], [[6n09|6n09]], [[6n0g|6n0g]]</td></tr>
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<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=6n0f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n0f OCA], [http://pdbe.org/6n0f PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n0f RCSB], [http://www.ebi.ac.uk/pdbsum/6n0f PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n0f ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Bacterial microcompartments (BMCs) are composed of an enzymatic core encapsulated by a selectively permeable protein shell that enhances catalytic efficiency. Many pathogenic bacteria derive competitive advantages from their BMC-based catabolism, implicating BMCs as drug targets. BMC shells are of interest for bioengineering due to their diverse and selective permeability properties and because they self-assemble. A complete understanding of shell composition and organization is a prerequisite for biotechnological applications. Here, we report the cryoelectron microscopy structure of a BMC shell at 3.0-A resolution, using an image-processing strategy that allowed us to determine the previously uncharacterized structural details of the interactions formed by the BMC-T(S) and BMC-T(D) shell subunits in the context of the assembled shell. We found unexpected structural plasticity among these interactions, resulting in distinct shell populations assembled from varying numbers of the BMC-T(S) and BMC-T(D) subunits. We discuss the implications of these findings on shell assembly and function.
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Authors: Greber, B.J., Sutter, M., Kerfeld, C.A.
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The Plasticity of Molecular Interactions Governs Bacterial Microcompartment Shell Assembly.,Greber BJ, Sutter M, Kerfeld CA Structure. 2019 Feb 12. pii: S0969-2126(19)30017-6. doi:, 10.1016/j.str.2019.01.017. PMID:30833088<ref>PMID:30833088</ref>
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Description: Cryo-EM structure of the HO BMC shell: subregion classified for BMC-T: TD-TSTSTS
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 6n0f" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Greber, B J]]
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[[Category: Kerfeld, C A]]
[[Category: Sutter, M]]
[[Category: Sutter, M]]
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[[Category: Greber, B.J]]
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[[Category: Bmc fold]]
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[[Category: Kerfeld, C.A]]
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[[Category: Compartmentalization]]
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[[Category: Microcompartment]]
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[[Category: Shell]]
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[[Category: Structural protein]]

Revision as of 12:09, 13 March 2019

Cryo-EM structure of the HO BMC shell: subregion classified for BMC-T: TD-TSTSTS

PDB ID 6n0f

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