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'''Unreleased structure'''


The entry 9szq is ON HOLD
==Crystal structure of the E336K mutant of human Apoptosis Inducing Factor==
 
<StructureSection load='9szq' size='340' side='right'caption='[[9szq]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
Authors: Martinez-Julvez, M., Ferreira, P., Ferrer, M.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9szq]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9SZQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9SZQ FirstGlance]. <br>
Description: Crystal structure of the E336K mutant of human Apoptosis Inducing Factor
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
[[Category: Martinez-Julvez, M]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9szq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9szq OCA], [https://pdbe.org/9szq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9szq RCSB], [https://www.ebi.ac.uk/pdbsum/9szq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9szq ProSAT]</span></td></tr>
[[Category: Ferreira, P]]
</table>
[[Category: Ferrer, M]]
== Disease ==
[https://www.uniprot.org/uniprot/AIFM1_HUMAN AIFM1_HUMAN] Defects in AIFM1 are the cause of combined oxidative phosphorylation deficiency type 6 (COXPD6) [MIM:[https://omim.org/entry/300816 300816]. It is a mitochondrial disease resulting in a neurodegenerative disorder characterized by psychomotor delay, hypotonia, areflexia, muscle weakness and wasting.<ref>PMID:20362274</ref> <ref>PMID:22019070</ref>
== Function ==
[https://www.uniprot.org/uniprot/AIFM1_HUMAN AIFM1_HUMAN] Probable oxidoreductase that has a dual role in controlling cellular life and death; during apoptosis, it is translocated from the mitochondria to the nucleus to function as a proapoptotic factor in a caspase-independent pathway, while in normal mitochondria, it functions as an antiapoptotic factor via its oxidoreductase activity. The soluble form (AIFsol) found in the nucleus induces 'parthanatos' i.e. caspase-independent fragmentation of chromosomal DNA. Interacts with EIF3G,and thereby inhibits the EIF3 machinery and protein synthesis, and activates casapse-7 to amplify apoptosis. Plays a critical role in caspase-independent, pyknotic cell death in hydrogen peroxide-exposed cells. Binds to DNA in a sequence-independent manner.<ref>PMID:17094969</ref> <ref>PMID:19418225</ref> <ref>PMID:20362274</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ferreira P]]
[[Category: Ferrer M]]
[[Category: Martinez-Julvez M]]
Retrieved from "https://proteopedia.org/9szq"