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5nku

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'''Unreleased structure'''
 
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The entry 5nku is ON HOLD
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==Joint neutron/X-ray structure of dimeric chlorite dismutase from Cyanothece sp. PCC7425==
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<StructureSection load='5nku' size='340' side='right' caption='[[5nku]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5nku]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5NKU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5NKU FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>, <scene name='pdbligand=OH:HYDROXIDE+ION'>OH</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5nku FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5nku OCA], [http://pdbe.org/5nku PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5nku RCSB], [http://www.ebi.ac.uk/pdbsum/5nku PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5nku ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The heme enzyme chlorite dismutase (Cld) catalyzes the degradation of chlorite to chloride and dioxygen. Although structure and steady-state kinetics of Clds have been elucidated, many questions remain (e.g., the mechanism of chlorite cleavage and the pH dependence of the reaction). Here, we present high-resolution X-ray crystal structures of a dimeric Cld at pH 6.5 and 8.5, its fluoride and isothiocyanate complexes and the neutron structure at pH 9.0 together with the pH dependence of the Fe(III)/Fe(II) couple, and the UV-vis and resonance Raman spectral features. We demonstrate that the distal Arg127 cannot act as proton acceptor and is fully ionized even at pH 9.0 ruling out its proposed role in dictating the pH dependence of chlorite degradation. Stopped-flow studies show that (i) Compound I and hypochlorite do not recombine and (ii) Compound II is the immediately formed redox intermediate that dominates during turnover. Homolytic cleavage of chlorite is proposed.
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Authors: Puehringer, D., Schaffner, I., Mlynek, G., Obinger, C., Djinovic-Carugo, K.
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Molecular Mechanism of Enzymatic Chlorite Detoxification: Insights from Structural and Kinetic Studies.,Schaffner I, Mlynek G, Flego N, Puhringer D, Libiseller-Egger J, Coates L, Hofbauer S, Bellei M, Furtmuller PG, Battistuzzi G, Smulevich G, Djinovic-Carugo K, Obinger C ACS Catal. 2017 Nov 3;7(11):7962-7976. doi: 10.1021/acscatal.7b01749. Epub 2017, Oct 13. PMID:29142780<ref>PMID:29142780</ref>
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Description: Joint neutron/X-ray structure of dimeric chlorite dismutase from Cyanothece sp. PCC7425
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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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<div class="pdbe-citations 5nku" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Djinovic-Carugo, K]]
[[Category: Djinovic-Carugo, K]]
[[Category: Mlynek, G]]
[[Category: Mlynek, G]]
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[[Category: Obinger, C]]
[[Category: Puehringer, D]]
[[Category: Puehringer, D]]
[[Category: Schaffner, I]]
[[Category: Schaffner, I]]
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[[Category: Obinger, C]]
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[[Category: Chlorite dismutase]]
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[[Category: Cyanobacteria]]
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[[Category: Ferredoxin-like fold]]
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[[Category: Heme]]
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[[Category: Oxidoreductase]]

Revision as of 06:18, 28 February 2018

Joint neutron/X-ray structure of dimeric chlorite dismutase from Cyanothece sp. PCC7425

5nku, resolution 2.00Å

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