2n9x

</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=2n9x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n9x OCA], [https://pdbe.org/2n9x PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2n9x RCSB], [https://www.ebi.ac.uk/pdbsum/2n9x PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2n9x ProSAT]</span></td></tr>

<div style="background-color:#fffaf0;">

== Publication Abstract from PubMed ==

Mitophagy is a fundamental process that determines mitochondrial quality and homeostasis. Several mitophagy receptors, including the newly identified FUNDC1, mediate selective removal of damaged or superfluous mitochondria through their specific interaction with LC3. However, the precise mechanism by which this interaction is regulated to initiate mitophagy is not understood. Here, we report the solution structure of LC3 in complex with a peptide containing the FUNDC1 LC3-interacting region (LIR) motif. The structure reveals a noncanonical LC3-LIR binding conformation, in which the third LIR residue (Val20) is also inserted into the hydrophobic pocket of LC3, together with the conserved residues Tyr18 and Leu21. This enables Tyr18 to be positioned near Asp19 of LC3, and thus phosphorylation of Tyr18 significantly weakens the binding affinity due to electrostatic repulsion. Functional analysis revealed that mitochondrial targeting of the LIR-containing cytosolic portion of FUNDC1 is necessary and sufficient to initiate mitophagy when Tyr18 is unphosphorylated, even in the absence of mitochondrial fragmentation. Thus, we demonstrated that phosphorylation of Tyr18 of FUNDC1 serves as a molecular switch for mitophagy. This may represent a novel target for therapeutic intervention.

Structural basis for the phosphorylation of FUNDC1 LIR as a molecular switch of mitophagy.,Kuang Y, Ma K, Zhou C, Ding P, Zhu Y, Chen Q, Xia B Autophagy. 2016 Dec;12(12):2363-2373. Epub 2016 Sep 21. PMID:27653272<ref>PMID:27653272</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>

</div>

<div class="pdbe-citations 2n9x" style="background-color:#fffaf0;"></div>

== References ==

<references/>