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| <StructureSection load='4yiz' size='340' side='right'caption='[[4yiz]], [[Resolution|resolution]] 2.20Å' scene=''> | | <StructureSection load='4yiz' size='340' side='right'caption='[[4yiz]], [[Resolution|resolution]] 2.20Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[4yiz]] is a 6 chain structure with sequence from [http://en.wikipedia.org/wiki/Coccidian_parasite Coccidian parasite] and [http://en.wikipedia.org/wiki/Toxgm Toxgm]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4YIZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4YIZ FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4yiz]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Eimeria_tenella Eimeria tenella] and [https://en.wikipedia.org/wiki/Toxoplasma_gondii_ME49 Toxoplasma gondii ME49]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4YIZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4YIZ FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=A2G:N-ACETYL-2-DEOXY-2-AMINO-GALACTOSE'>A2G</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</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]] 2.2Å</td></tr> |
- | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4yiv|4yiv]]</td></tr>
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A2G:N-ACETYL-2-DEOXY-2-AMINO-GALACTOSE'>A2G</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">TGME49_255260 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=508771 TOXGM]), ETH_00012760 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5802 Coccidian parasite])</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=4yiz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4yiz OCA], [https://pdbe.org/4yiz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4yiz RCSB], [https://www.ebi.ac.uk/pdbsum/4yiz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4yiz ProSAT]</span></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=4yiz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4yiz OCA], [http://pdbe.org/4yiz PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4yiz RCSB], [http://www.ebi.ac.uk/pdbsum/4yiz PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4yiz ProSAT]</span></td></tr> | + | |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/S8GKS3_TOXGM S8GKS3_TOXGM] |
| <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: Coccidian parasite]] | + | [[Category: Eimeria tenella]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Toxgm]] | + | [[Category: Toxoplasma gondii ME49]] |
- | [[Category: Boulanger, M J]] | + | [[Category: Boulanger MJ]] |
- | [[Category: Parker, M L]] | + | [[Category: Parker ML]] |
- | [[Category: Apicomplexa]]
| + | |
- | [[Category: Immune system]]
| + | |
- | [[Category: Invasion]]
| + | |
- | [[Category: Moving junction]]
| + | |
- | [[Category: Pan domain]]
| + | |
- | [[Category: Parasite]]
| + | |
- | [[Category: Protein engineering]]
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| Structural highlights
Function
S8GKS3_TOXGM
Publication Abstract from PubMed
Apicomplexan parasites are the causative agents of globally prevalent diseases including malaria and toxoplasmosis. These obligate intracellular pathogens have evolved a sophisticated host cell invasion strategy that relies on a parasite-host cell junction anchored by interactions between apical membrane antigens (AMAs) on the parasite surface and rhoptry neck 2 (RON2) proteins discharged from the parasite and embedded in the host cell membrane. Key to formation of the AMA1-RON2 complex is displacement of an extended surface loop on AMA1 called the DII loop. While conformational flexibility of the DII loop is required to expose the mature RON2 binding groove, a definitive role of this substructure has not been elucidated. To establish a role of the DII loop in Toxoplasma gondii AMA1, we engineered a form of the protein where the mobile portion of the loop was replaced with a short Gly-Ser linker (TgAMA1DeltaDIIloop). Isothermal titration calorimetry measurements with a panel of RON2 peptides revealed an influential role for the DII loop in governing selectivity. Most notably, an Eimeria tenella RON2 (EtRON2) peptide that showed only weak binding to TgAMA1 bound with high affinity to TgAMA1DeltaDIIloop. To define the molecular basis for the differential binding, we determined the crystal structure of TgAMA1DeltaDIIloop in complex with the EtRON2 peptide. When analyzed in the context of existing AMA1-RON2 structures, spatially distinct anchor points in the AMA1 groove were identified that, when engaged, appear to provide the necessary traction to outcompete the DII loop. Collectively, these data support a model where the AMA1 DII loop serves as a structural gatekeeper to selectively filter out ligands otherwise capable of binding with high affinity in the AMA1 apical groove. These data also highlight the importance of considering the functional implications of the DII loop in the ongoing development of therapeutic intervention strategies targeting the AMA1-RON2 invasion complex.
An Extended Surface Loop on Toxoplasma gondii Apical Membrane Antigen 1 (AMA1) Governs Ligand Binding Selectivity.,Parker ML, Boulanger MJ PLoS One. 2015 May 8;10(5):e0126206. doi: 10.1371/journal.pone.0126206., eCollection 2015. PMID:25955165[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Parker ML, Boulanger MJ. An Extended Surface Loop on Toxoplasma gondii Apical Membrane Antigen 1 (AMA1) Governs Ligand Binding Selectivity. PLoS One. 2015 May 8;10(5):e0126206. doi: 10.1371/journal.pone.0126206., eCollection 2015. PMID:25955165 doi:http://dx.doi.org/10.1371/journal.pone.0126206
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