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2ncl
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Solution structure of BOLA3 from Homo sapiens== | |
| + | <StructureSection load='2ncl' size='340' side='right' caption='[[2ncl]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[2ncl]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NCL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2NCL 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=2ncl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ncl OCA], [http://pdbe.org/2ncl PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2ncl RCSB], [http://www.ebi.ac.uk/pdbsum/2ncl PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2ncl ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/BOLA3_HUMAN BOLA3_HUMAN]] Fatal multiple mitochondrial dysfunction syndrome type 2. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Assembly of mitochondrial iron-sulfur (Fe/S) proteins is a key process of cells, and defects cause many rare diseases. In the first phase of this pathway, ten Fe/S cluster (ISC) assembly components synthesize and insert [2Fe-2S] clusters. The second phase is dedicated to the assembly of [4Fe-4S] proteins, yet this part is poorly understood. Here, we characterize the BOLA family proteins Bol1 and Bol3 as specific mitochondrial ISC assembly factors that facilitate [4Fe-4S] cluster insertion into a subset of mitochondrial proteins such as lipoate synthase and succinate dehydrogenase. Bol1-Bol3 perform largely overlapping functions, yet cannot replace the ISC protein Nfu1 that also participates in this phase of Fe/S protein biogenesis. Bol1 and Bol3 form dimeric complexes with both monothiol glutaredoxin Grx5 and Nfu1. Complex formation differentially influences the stability of the Grx5-Bol-shared Fe/S clusters. Our findings provide the biochemical basis for explaining the pathological phenotypes of patients with mutations in BOLA3. | ||
| - | + | Mitochondrial Bol1 and Bol3 function as assembly factors for specific iron-sulfur proteins.,Uzarska MA, Nasta V, Weiler BD, Spantgar F, Ciofi-Baffoni S, Saviello MR, Gonnelli L, Muhlenhoff U, Banci L, Lill R Elife. 2016 Aug 17;5. pii: e16673. doi: 10.7554/eLife.16673. PMID:27532772<ref>PMID:27532772</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | + | </div> | |
| - | + | <div class="pdbe-citations 2ncl" style="background-color:#fffaf0;"></div> | |
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
[[Category: Banci, L]] | [[Category: Banci, L]] | ||
[[Category: Ciofi-Baffoni, S]] | [[Category: Ciofi-Baffoni, S]] | ||
| + | [[Category: Nasta, V]] | ||
| + | [[Category: Class ii kh-like fold]] | ||
| + | [[Category: Fe/s protein biogenesis]] | ||
| + | [[Category: Mitochondrial protein]] | ||
| + | [[Category: Protein binding]] | ||
Revision as of 20:59, 10 September 2016
Solution structure of BOLA3 from Homo sapiens
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