2ji3

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[[Image:2ji3.jpg|left|200px]]<br /><applet load="2ji3" size="350" color="white" frame="true" align="right" spinBox="true"
 
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caption="2ji3, resolution 1.95&Aring;" />
 
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'''X-RAY STRUCTURE OF THE IRON-PEROXIDE INTERMEDIATE OF SUPEROXIDE REDUCTASE (E114A MUTANT) FROM DESULFOARCULUS BAARSII'''<br />
 
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==About this Structure==
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==X-ray structure of the iron-peroxide intermediate of superoxide reductase (E114A mutant) from Desulfoarculus baarsii==
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2JI3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Desulfovibrio_baarsii Desulfovibrio baarsii] with <scene name='pdbligand=FE:'>FE</scene>, <scene name='pdbligand=CA:'>CA</scene>, <scene name='pdbligand=NO3:'>NO3</scene> and <scene name='pdbligand=PER:'>PER</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Superoxide_reductase Superoxide reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.2 1.15.1.2] Known structural/functional Site: <scene name='pdbsite=AC1:Per Binding Site For Chain D'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2JI3 OCA].
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<StructureSection load='2ji3' size='340' side='right'caption='[[2ji3]], [[Resolution|resolution]] 1.95&Aring;' scene=''>
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[[Category: Desulfovibrio baarsii]]
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== Structural highlights ==
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[[Category: Single protein]]
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<table><tr><td colspan='2'>[[2ji3]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Desulfarculus_baarsii Desulfarculus baarsii]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2JI3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2JI3 FirstGlance]. <br>
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[[Category: Superoxide reductase]]
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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]] 1.95&#8491;</td></tr>
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[[Category: Adam, V.]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene>, <scene name='pdbligand=NO3:NITRATE+ION'>NO3</scene>, <scene name='pdbligand=PER:PEROXIDE+ION'>PER</scene></td></tr>
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[[Category: Amara, P.]]
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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=2ji3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ji3 OCA], [https://pdbe.org/2ji3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ji3 RCSB], [https://www.ebi.ac.uk/pdbsum/2ji3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ji3 ProSAT]</span></td></tr>
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[[Category: Bourgeois, D.]]
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</table>
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[[Category: Carpentier, P.]]
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== Function ==
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[[Category: Katona, G.]]
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[https://www.uniprot.org/uniprot/DFX_DESB2 DFX_DESB2] Catalyzes the one-electron reduction of superoxide anion radical to hydrogen peroxide at a nonheme ferrous iron center. Plays a fundamental role in case of oxidative stress via its superoxide detoxification activity.<ref>PMID:10617593</ref>
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[[Category: Niviere, V.]]
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== Evolutionary Conservation ==
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[[Category: Ohana, J.]]
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[[Image:Consurf_key_small.gif|200px|right]]
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[[Category: Tsanov, N.]]
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Check<jmol>
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[[Category: CA]]
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<jmolCheckbox>
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[[Category: FE]]
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/ji/2ji3_consurf.spt"</scriptWhenChecked>
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[[Category: NO3]]
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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[[Category: PER]]
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<text>to colour the structure by Evolutionary Conservation</text>
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[[Category: detoxification]]
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</jmolCheckbox>
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[[Category: electron transport]]
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2ji3 ConSurf].
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[[Category: intermediate trapping]]
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<div style="clear:both"></div>
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[[Category: iron]]
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<div style="background-color:#fffaf0;">
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[[Category: metal-binding]]
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== Publication Abstract from PubMed ==
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[[Category: microspectrophotometry]]
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Iron-peroxide intermediates are central in the reaction cycle of many iron-containing biomolecules. We trapped iron(III)-(hydro)peroxo species in crystals of superoxide reductase (SOR), a nonheme mononuclear iron enzyme that scavenges superoxide radicals. X-ray diffraction data at 1.95 angstrom resolution and Raman spectra recorded in crystallo revealed iron-(hydro)peroxo intermediates with the (hydro)peroxo group bound end-on. The dynamic SOR active site promotes the formation of transient hydrogen bond networks, which presumably assist the cleavage of the iron-oxygen bond in order to release the reaction product, hydrogen peroxide.
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[[Category: oxidoreductase]]
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[[Category: raman spectroscopy]]
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[[Category: redox states]]
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[[Category: superoxide reductase]]
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[[Category: transport]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 15:27:52 2008''
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Raman-assisted crystallography reveals end-on peroxide intermediates in a nonheme iron enzyme.,Katona G, Carpentier P, Niviere V, Amara P, Adam V, Ohana J, Tsanov N, Bourgeois D Science. 2007 Apr 20;316(5823):449-53. PMID:17446401<ref>PMID:17446401</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 2ji3" style="background-color:#fffaf0;"></div>
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==See Also==
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*[[Superoxide Reductase|Superoxide Reductase]]
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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: Desulfarculus baarsii]]
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[[Category: Large Structures]]
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[[Category: Adam V]]
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[[Category: Amara P]]
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[[Category: Bourgeois D]]
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[[Category: Carpentier P]]
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[[Category: Katona G]]
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[[Category: Niviere V]]
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[[Category: Ohana J]]
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[[Category: Tsanov N]]

Current revision

X-ray structure of the iron-peroxide intermediate of superoxide reductase (E114A mutant) from Desulfoarculus baarsii

PDB ID 2ji3

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