1b9w: Difference between revisions

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New page: left|200px<br /><applet load="1b9w" size="450" color="white" frame="true" align="right" spinBox="true" caption="1b9w, resolution 1.800Å" /> '''C-TERMINAL MEROZOIT...
 
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[[Image:1b9w.jpg|left|200px]]<br /><applet load="1b9w" size="450" color="white" frame="true" align="right" spinBox="true"
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'''C-TERMINAL MEROZOITE SURFACE PROTEIN 1 FROM PLASMODIUM CYNOMOLGI'''<br />


==Overview==
==C-TERMINAL MEROZOITE SURFACE PROTEIN 1 FROM PLASMODIUM CYNOMOLGI==
The C-terminal proteolytic processing product of merozoite surface protein, 1 (MSP1) appears essential for successful erythrocyte invasion by the, malarial parasite, Plasmodium. We have determined the crystal structure at, 1.8 A resolution of a soluble baculovirus-recombinant form of the protein, from P. cynomolgi, which confers excellent protective efficacy in primate, vaccination trials. The structure comprises two EGF-like domains, and, sequence comparisons strongly suggest that the same conformation is, present in all species of Plasmodium, including P. falciparum and P., vivax, which are pathogenic in man. In particular, conserved interdomain, contacts between the two EGF modules should preserve the compact form of, the molecule in all species. Implications of the crystal structure for, anti-malarial vaccine development are discussed.
<StructureSection load='1b9w' size='340' side='right'caption='[[1b9w]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1b9w]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Plasmodium_cynomolgi Plasmodium cynomolgi]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1B9W OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1B9W FirstGlance]. <br>
</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>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1b9w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1b9w OCA], [https://pdbe.org/1b9w PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1b9w RCSB], [https://www.ebi.ac.uk/pdbsum/1b9w PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1b9w ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/Q25659_9APIC Q25659_9APIC]
== 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/b9/1b9w_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.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=1b9w ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The C-terminal proteolytic processing product of merozoite surface protein 1 (MSP1) appears essential for successful erythrocyte invasion by the malarial parasite, Plasmodium. We have determined the crystal structure at 1.8 A resolution of a soluble baculovirus-recombinant form of the protein from P. cynomolgi, which confers excellent protective efficacy in primate vaccination trials. The structure comprises two EGF-like domains, and sequence comparisons strongly suggest that the same conformation is present in all species of Plasmodium, including P. falciparum and P. vivax, which are pathogenic in man. In particular, conserved interdomain contacts between the two EGF modules should preserve the compact form of the molecule in all species. Implications of the crystal structure for anti-malarial vaccine development are discussed.


==About this Structure==
The crystal structure of C-terminal merozoite surface protein 1 at 1.8 A resolution, a highly protective malaria vaccine candidate.,Chitarra V, Holm I, Bentley GA, Petres S, Longacre S Mol Cell. 1999 Apr;3(4):457-64. PMID:10230398<ref>PMID:10230398</ref>
1B9W is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Plasmodium_cynomolgi Plasmodium cynomolgi]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1B9W OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
The crystal structure of C-terminal merozoite surface protein 1 at 1.8 A resolution, a highly protective malaria vaccine candidate., Chitarra V, Holm I, Bentley GA, Petres S, Longacre S, Mol Cell. 1999 Apr;3(4):457-64. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=10230398 10230398]
</div>
<div class="pdbe-citations 1b9w" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Plasmodium cynomolgi]]
[[Category: Plasmodium cynomolgi]]
[[Category: Single protein]]
[[Category: Bentley GA]]
[[Category: Bentley, G.A.]]
[[Category: Chitarra V]]
[[Category: Chitarra, V.]]
[[Category: Holm I]]
[[Category: Holm, I.]]
[[Category: Longacre S]]
[[Category: Longacre, S.]]
[[Category: candidate malaria vaccine]]
[[Category: msp-1]]
[[Category: surface antigen]]
 
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 23:55:28 2007''

Latest revision as of 10:12, 9 October 2024

C-TERMINAL MEROZOITE SURFACE PROTEIN 1 FROM PLASMODIUM CYNOMOLGIC-TERMINAL MEROZOITE SURFACE PROTEIN 1 FROM PLASMODIUM CYNOMOLGI

Structural highlights

1b9w is a 1 chain structure with sequence from Plasmodium cynomolgi. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 1.8Å
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

Q25659_9APIC

Evolutionary Conservation

Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf.

Publication Abstract from PubMed

The C-terminal proteolytic processing product of merozoite surface protein 1 (MSP1) appears essential for successful erythrocyte invasion by the malarial parasite, Plasmodium. We have determined the crystal structure at 1.8 A resolution of a soluble baculovirus-recombinant form of the protein from P. cynomolgi, which confers excellent protective efficacy in primate vaccination trials. The structure comprises two EGF-like domains, and sequence comparisons strongly suggest that the same conformation is present in all species of Plasmodium, including P. falciparum and P. vivax, which are pathogenic in man. In particular, conserved interdomain contacts between the two EGF modules should preserve the compact form of the molecule in all species. Implications of the crystal structure for anti-malarial vaccine development are discussed.

The crystal structure of C-terminal merozoite surface protein 1 at 1.8 A resolution, a highly protective malaria vaccine candidate.,Chitarra V, Holm I, Bentley GA, Petres S, Longacre S Mol Cell. 1999 Apr;3(4):457-64. PMID:10230398[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Chitarra V, Holm I, Bentley GA, Petres S, Longacre S. The crystal structure of C-terminal merozoite surface protein 1 at 1.8 A resolution, a highly protective malaria vaccine candidate. Mol Cell. 1999 Apr;3(4):457-64. PMID:10230398

1b9w, resolution 1.80Å

Drag the structure with the mouse to rotate

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