9w2t: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
 
Line 1: Line 1:
'''Unreleased structure'''


The entry 9w2t is ON HOLD  until Paper Publication
==Cryo-EM structure of Fo domain of FoF1-ATPase monomer state on the bovine heart submitochondrial particles==
<StructureSection load='9w2t' size='340' side='right'caption='[[9w2t]], [[Resolution|resolution]] 4.10&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9w2t]] is a 17 chain structure with sequence from [https://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9W2T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9W2T 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]] 4.1&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=M3L:N-TRIMETHYLLYSINE'>M3L</scene></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=9w2t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9w2t OCA], [https://pdbe.org/9w2t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9w2t RCSB], [https://www.ebi.ac.uk/pdbsum/9w2t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9w2t ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/ATP8_BOVIN ATP8_BOVIN] Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F(0) domain. Minor subunit located with subunit a in the membrane (By similarity).
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Understanding the functional mechanisms of membrane protein complexes requires structural analysis within their native membrane environment. Here, we applied cryo-electron microscopy to determine the structures of F(o)F(1) ATP synthase and respiratory supercomplexes (SCs) on sub-mitochondrial particles (SMPs) isolated from bovine heart mitochondria. Most F(o)F(1) complexes were observed as dimers stabilized by the regulatory factor IF(1), and a tetrameric assembly comprising two F(o)F(1)-IF(1) dimers arranged linearly was also identified. This finding indicates that the tetrameric units of F(o)F(1) are present in the mitochondrial inner membrane and contribute to shaping cristae tips in mammalian mitochondria. F(o) domain maps resolve the e-subunit- c(8)-ring interface and show no discrete density for a tightly bound lipid within the c(8)-ring. In addition to the previously reported SCs compositions CI(1)CIII(2)CIV(1) and CI(1)CIII(2)CIV(2), our analysis identified an additional assembly with the composition CI(1)CIII(2)CIV(3), as well as a CI(2)CIII(2)CIV(6) mega-complex. This approach enables rapid structural determination of F(o)F(1) ATP synthase and SCs from minimal membrane fractions, providing a foundation for elucidating the molecular basis of metabolic disorders and mitochondrial diseases at the level of higher-order architecture.


Authors: Nakano, A., Masuya, T., Akisada, S., Ishikawa-Fukuda, M., Mitsuoka, K., Miyoshi, H., Murai, M., Yokoyama, K.
Structures of respiratory supercomplexes and ATP synthase oligomers in mammalian mitochondrial inner membrane.,Nakano A, Masuya T, Akisada S, Ishikawa-Fukuda M, Mitsuoka K, Miyoshi H, Murai M, Yokoyama K Nat Commun. 2026 Mar 17. doi: 10.1038/s41467-026-70578-x. PMID:41844608<ref>PMID:41844608</ref>


Description: Cryo-EM structure of Fo domain of FoF1-ATPase monomer state on the bovine heart submitochondrial particles
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Mitsuoka, K]]
<div class="pdbe-citations 9w2t" style="background-color:#fffaf0;"></div>
[[Category: Ishikawa-Fukuda, M]]
== References ==
[[Category: Masuya, T]]
<references/>
[[Category: Akisada, S]]
__TOC__
[[Category: Nakano, A]]
</StructureSection>
[[Category: Yokoyama, K]]
[[Category: Bos taurus]]
[[Category: Miyoshi, H]]
[[Category: Large Structures]]
[[Category: Murai, M]]
[[Category: Akisada S]]
[[Category: Ishikawa-Fukuda M]]
[[Category: Masuya T]]
[[Category: Mitsuoka K]]
[[Category: Miyoshi H]]
[[Category: Murai M]]
[[Category: Nakano A]]
[[Category: Yokoyama K]]