5l71

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'''Unreleased structure'''
 
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The entry 5l71 is ON HOLD until Paper Publication
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==Crystal structure of mouse phospholipid hydroperoxide glutathione peroxidase 4 (GPx4)==
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<StructureSection load='5l71' size='340' side='right'caption='[[5l71]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5l71]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5L71 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5L71 FirstGlance]. <br>
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</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>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></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=5l71 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5l71 OCA], [https://pdbe.org/5l71 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5l71 RCSB], [https://www.ebi.ac.uk/pdbsum/5l71 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5l71 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/GPX4_MOUSE GPX4_MOUSE] Essential antioxidant peroxidase that directly reduces phospholipid hydroperoxide even if they are incorporated in membranes and lipoproteins (PubMed:29290465). Can also reduce fatty acid hydroperoxide, cholesterol hydroperoxide and thymine hydroperoxide (By similarity). Plays a key role in protecting cells from oxidative damage by preventing membrane lipid peroxidation (PubMed:12566075). Required to prevent cells from ferroptosis, a non-apoptotic cell death resulting from an iron-dependent accumulation of lipid reactive oxygen species (PubMed:12566075, PubMed:24439385, PubMed:25402683, PubMed:25922076, PubMed:29290465). The presence of selenocysteine (Sec) versus Cys at the active site is essential for life: it provides resistance to overoxidation and prevents cells against ferroptosis (PubMed:29290465). The presence of Sec at the active site is also essential for the survival of a specific type of parvalbumin-positive interneurons, thereby preventing against fatal epileptic seizures (PubMed:29290465). May be required to protect cells from the toxicity of ingested lipid hydroperoxides (PubMed:12566075). Required for normal sperm development and male fertility (PubMed:19783653, PubMed:25922076). Essential for maturation and survival of photoreceptor cells (PubMed:22207760). Plays a role in a primary T-cell response to viral and parasitic infection by protecting T-cells from ferroptosis and by supporting T-cell expansion (PubMed:25824823). Plays a role of glutathione peroxidase in platelets in the arachidonic acid metabolism (By similarity). Reduces hydroperoxy ester lipids formed by a 15-lipoxygenase that may play a role as down-regulator of the cellular 15-lipoxygenase pathway (By similarity).[UniProtKB:P36968][UniProtKB:P36969]<ref>PMID:12566075</ref> <ref>PMID:18762024</ref> <ref>PMID:19783653</ref> <ref>PMID:22207760</ref> <ref>PMID:24439385</ref> <ref>PMID:25402683</ref> <ref>PMID:25824823</ref> <ref>PMID:25922076</ref> <ref>PMID:29290465</ref> Specifically able to suppress the production of leukotriene and prostaglandin in response to several stimuli by reducing fatty acid hydroperoxide.[UniProtKB:P36970] Specifically required to prevent mitochondrial cell death by mediating reduction of cardiolipin hydroperoxide (By similarity). Also required for normal sperm development and male fertility (PubMed:19417079).[UniProtKB:P36970]<ref>PMID:19417079</ref> Required for male fertility by stabilizing the condensed chromatin in sperm nuclei (PubMed:12566075).<ref>PMID:12566075</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The mammalian glutathione peroxidase (GPx) family is a key component of the cellular antioxidative defence system. Within this family, GPx4 has unique features as it accepts a large class of hydroperoxy lipid substrates and has a plethora of biological functions, including sperm maturation, regulation of apoptosis and cerebral embryogenesis. In this paper, the structure of the cytoplasmic isoform of mouse phospholipid hydroperoxide glutathione peroxidase (O70325-2 GPx4) with selenocysteine 46 mutated to cysteine is reported solved at 1.8 A resolution using X-ray crystallography. Furthermore, solution data of an isotope-labelled GPx protein are presented.
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Authors: Janowski, R., Scanu, S., Madl, T., Niessing, D.
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Crystal and solution structural studies of mouse phospholipid hydroperoxide glutathione peroxidase 4.,Janowski R, Scanu S, Niessing D, Madl T Acta Crystallogr F Struct Biol Commun. 2016 Oct 1;72(Pt 10):743-749. Epub 2016, Sep 22. PMID:27710939<ref>PMID:27710939</ref>
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Description: Crystal structure of mouse phospholipid hydroperoxide glutathione peroxidase 4 (GPx4)
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Niessing, D]]
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<div class="pdbe-citations 5l71" style="background-color:#fffaf0;"></div>
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[[Category: Scanu, S]]
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[[Category: Madl, T]]
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==See Also==
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[[Category: Janowski, R]]
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*[[Glutathione peroxidase|Glutathione peroxidase]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Mus musculus]]
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[[Category: Janowski R]]
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[[Category: Madl T]]
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[[Category: Niessing D]]
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[[Category: Scanu S]]

Current revision

Crystal structure of mouse phospholipid hydroperoxide glutathione peroxidase 4 (GPx4)

PDB ID 5l71

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