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| ==Crystal structure of the conserved staphylococcal antigen 1B, Csa1B== | | ==Crystal structure of the conserved staphylococcal antigen 1B, Csa1B== |
- | <StructureSection load='4big' size='340' side='right' caption='[[4big]], [[Resolution|resolution]] 2.27Å' scene=''> | + | <StructureSection load='4big' size='340' side='right'caption='[[4big]], [[Resolution|resolution]] 2.27Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[4big]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Staa8 Staa8]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BIG OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4BIG FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4big]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_aureus_subsp._aureus_NCTC_8325 Staphylococcus aureus subsp. aureus NCTC 8325]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BIG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BIG FirstGlance]. <br> |
- | </td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.274Å</td></tr> |
- | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4bih|4bih]]</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> |
- | <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=4big FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4big OCA], [http://pdbe.org/4big PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4big RCSB], [http://www.ebi.ac.uk/pdbsum/4big PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4big ProSAT]</span></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=4big FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4big OCA], [https://pdbe.org/4big PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4big RCSB], [https://www.ebi.ac.uk/pdbsum/4big PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4big ProSAT]</span></td></tr> |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/Y053_STAA8 Y053_STAA8] |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Staa8]] | + | [[Category: Large Structures]] |
- | [[Category: Bottomley, M J]] | + | [[Category: Staphylococcus aureus subsp. aureus NCTC 8325]] |
- | [[Category: Liberatori, S]] | + | [[Category: Bottomley MJ]] |
- | [[Category: Malito, E]] | + | [[Category: Liberatori S]] |
- | [[Category: Schluepen, C]] | + | [[Category: Malito E]] |
- | [[Category: Immune system]]
| + | [[Category: Schluepen C]] |
- | [[Category: Protective immunity]]
| + | |
- | [[Category: Tandem lipoprotein]]
| + | |
| Structural highlights
Function
Y053_STAA8
Publication Abstract from PubMed
In the human pathogen Staphylococcus aureus there exists an enormous diversity of proteins containing domains of unknown function (DUF). Here, we characterized the family of conserved staphylococcal antigens (Csa) classified as DUF576 and taxonomically restricted to S. aureus. The 18 Csa paralogs in S. aureus Newman are highly similar at the sequence level yet were found to be expressed in multiple cellular localizations. Extracellular Csa1A was shown to be post-translationally processed and released. Molecular interaction studies revealed Csa1A interacts with other Csa paralogs, suggesting that these proteins are involved in the same cellular process. The structures of Csa1A and Csa1B were determined by X-ray crystallography, unveiling a peculiar structure with limited structural similarity to other known proteins. Our results provide the first detailed biological characterization of this family and confirm the uniqueness of this family also at the structural level. We also provide evidence that Csa family members elicit protective immunity in in vivo animal models of Staphylococcal infections, indicating a possible important role of these proteins in S.aureus biology and pathogenesis. These findings identify the Csa family as new potential vaccine candidates, and underline the importance of mining the bacterial unknown proteome to identify new targets for preventive vaccines.
Mining the bacterial unknown proteome: identification and characterization of a novel family of highly conserved protective antigens in Staphylococcus aureus.,Schluepen C, Malito E, Marongiu A, Schirle M, McWhinnie E, Lo Surdo P, Biancucci M, Falugi F, Nardi-Dei V, Marchi S, Fontana MR, Lombardi B, De Falco MG, Rinaudo CD, Spraggon G, Nissum M, Bagnoli F, Grandi G, Bottomley MJ, Liberatori S Biochem J. 2013 Jul 29. PMID:23895222[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Schluepen C, Malito E, Marongiu A, Schirle M, McWhinnie E, Lo Surdo P, Biancucci M, Falugi F, Nardi-Dei V, Marchi S, Fontana MR, Lombardi B, De Falco MG, Rinaudo CD, Spraggon G, Nissum M, Bagnoli F, Grandi G, Bottomley MJ, Liberatori S. Mining the bacterial unknown proteome: identification and characterization of a novel family of highly conserved protective antigens in Staphylococcus aureus. Biochem J. 2013 Jul 29. PMID:23895222 doi:10.1042/BJ20130540
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