2bpi: Difference between revisions

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[[Image:2bpi.png|left|200px]]


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==Structure of Iron dependent superoxide dismutase from P. falciparum.==
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<StructureSection load='2bpi' size='340' side='right'caption='[[2bpi]], [[Resolution|resolution]] 2.52&Aring;' scene=''>
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== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[2bpi]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Plasmodium_falciparum_3D7 Plasmodium falciparum 3D7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BPI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2BPI FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.52&#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=FE:FE+(III)+ION'>FE</scene></td></tr>
{{STRUCTURE_2bpi|  PDB=2bpi  |  SCENE=  }}
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2bpi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2bpi OCA], [https://pdbe.org/2bpi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2bpi RCSB], [https://www.ebi.ac.uk/pdbsum/2bpi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2bpi ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/SODF_PLAF7 SODF_PLAF7] Destroys superoxide anion radicals which are normally produced within the cells and which are toxic to biological systems.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/bp/2bpi_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</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=2bpi ConSurf].
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== Publication Abstract from PubMed ==
BACKGROUND: Superoxide dismutases (SODs) are important enzymes in defence against oxidative stress. In Plasmodium falciparum, they may be expected to have special significance since part of the parasite life cycle is spent in red blood cells where the formation of reactive oxygen species is likely to be promoted by the products of haemoglobin breakdown. Thus, inhibitors of P. falciparum SODs have potential as anti-malarial compounds. As a step towards their development we have determined the crystal structure of the parasite's cytosolic iron superoxide dismutase. RESULTS: The cytosolic iron superoxide dismutase from P. falciparum (PfFeSOD) has been overexpressed in E. coli in a catalytically active form. Its crystal structure has been solved by molecular replacement and refined against data extending to 2.5 A resolution. The structure reveals a two-domain organisation and an iron centre in which the metal is coordinated by three histidines, an aspartate and a solvent molecule. Consistent with ultracentrifugation analysis the enzyme is a dimer in which a hydrogen bonding lattice links the two active centres. CONCLUSION: The tertiary structure of PfFeSOD is very similar to those of a number of other iron-and manganese-dependent superoxide dismutases, moreover the active site residues are conserved suggesting a common mechanism of action. Comparison of the dimer interfaces of PfFeSOD with the human manganese-dependent superoxide dismutase reveals a number of differences, which may underpin the design of parasite-selective superoxide dismutase inhibitors.


===STUCTURE OF IRON DEPENDENT SUPEROXIDE DISMUTASE FROM P. FALCIPARUM.===
The crystal structure of superoxide dismutase from Plasmodium falciparum.,Boucher IW, Brzozowski AM, Brannigan JA, Schnick C, Smith DJ, Kyes SA, Wilkinson AJ BMC Struct Biol. 2006 Oct 4;6:20. PMID:17020617<ref>PMID:17020617</ref>


From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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<div class="pdbe-citations 2bpi" style="background-color:#fffaf0;"></div>


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==See Also==
The line below this paragraph, {{ABSTRACT_PUBMED_17020617}}, adds the Publication Abstract to the page
*[[Superoxide dismutase 3D structures|Superoxide dismutase 3D structures]]
(as it appears on PubMed at http://www.pubmed.gov), where 17020617 is the PubMed ID number.
== References ==
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<references/>
{{ABSTRACT_PUBMED_17020617}}
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</StructureSection>
==About this Structure==
[[Category: Large Structures]]
2BPI is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Plasmodium_falciparum Plasmodium falciparum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BPI OCA].
[[Category: Plasmodium falciparum 3D7]]
 
[[Category: Boucher IW]]
==Reference==
[[Category: Brannigan J]]
The crystal structure of superoxide dismutase from Plasmodium falciparum., Boucher IW, Brzozowski AM, Brannigan JA, Schnick C, Smith DJ, Kyes SA, Wilkinson AJ, BMC Struct Biol. 2006 Oct 4;6:20. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17020617 17020617]
[[Category: Brzozowski M]]
[[Category: Plasmodium falciparum]]
[[Category: Wilkinson AJ]]
[[Category: Single protein]]
[[Category: Superoxide dismutase]]
[[Category: Boucher, I W.]]
[[Category: Brannigan, J A.]]
[[Category: Brzozowski, A M.]]
[[Category: Wilkinson, A J.]]
[[Category: Dismutase]]
[[Category: Metal-binding]]
[[Category: Oxidoreductase]]
 
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