6z1o

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==AL amyloid fibril from a lambda 3 light chain in conformation A==
==AL amyloid fibril from a lambda 3 light chain in conformation A==
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<StructureSection load='6z1o' size='340' side='right'caption='[[6z1o]]' scene=''>
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<StructureSection load='6z1o' size='340' side='right'caption='[[6z1o]], [[Resolution|resolution]] 3.20&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6Z1O OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6Z1O FirstGlance]. <br>
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6Z1O OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6Z1O FirstGlance]. <br>
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</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=6z1o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6z1o OCA], [https://pdbe.org/6z1o PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6z1o RCSB], [https://www.ebi.ac.uk/pdbsum/6z1o PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6z1o ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.2&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6z1o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6z1o OCA], [https://pdbe.org/6z1o PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6z1o RCSB], [https://www.ebi.ac.uk/pdbsum/6z1o PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6z1o ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Systemic AL amyloidosis is a debilitating and potentially fatal disease that arises from the misfolding and fibrillation of immunoglobulin light chains (LCs). The disease is patient-specific with essentially each patient possessing a unique LC sequence. In this study, we present two ex vivo fibril structures of a lambda3 LC. The fibrils were extracted from the explanted heart of a patient (FOR005) and consist of 115-residue fibril proteins, mainly from the LC variable domain. The fibril structures imply that a 180 degrees rotation around the disulfide bond and a major unfolding step are necessary for fibrils to form. The two fibril structures show highly similar fibril protein folds, differing in only a 12-residue segment. Remarkably, the two structures do not represent separate fibril morphologies, as they can co-exist at different z-axial positions within the same fibril. Our data imply the presence of structural breaks at the interface of the two structural forms.
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Cryo-EM reveals structural breaks in a patient-derived amyloid fibril from systemic AL amyloidosis.,Radamaker L, Baur J, Huhn S, Haupt C, Hegenbart U, Schonland S, Bansal A, Schmidt M, Fandrich M Nat Commun. 2021 Feb 8;12(1):875. doi: 10.1038/s41467-021-21126-2. PMID:33558536<ref>PMID:33558536</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 6z1o" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>

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AL amyloid fibril from a lambda 3 light chain in conformation A

PDB ID 6z1o

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