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| | ==Solution structure of the LysM region of the E. coli Intimin periplasmic domain== | | ==Solution structure of the LysM region of the E. coli Intimin periplasmic domain== |
| - | <StructureSection load='2mpw' size='340' side='right' caption='[[2mpw]], [[NMR_Ensembles_of_Models | 23 NMR models]]' scene=''> | + | <StructureSection load='2mpw' size='340' side='right'caption='[[2mpw]], [[NMR_Ensembles_of_Models | 23 NMR models]]' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[2mpw]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/"bacillus_coli"_migula_1895 "bacillus coli" migula 1895]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MPW OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2MPW FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[2mpw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/"bacillus_coli"_migula_1895 "bacillus coli" migula 1895]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MPW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2MPW FirstGlance]. <br> |
| - | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">eae, eaeA, E2348C_3939 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 "Bacillus coli" Migula 1895])</td></tr> | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">eae, eaeA, E2348C_3939 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 "Bacillus coli" Migula 1895])</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=2mpw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mpw OCA], [http://pdbe.org/2mpw PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2mpw RCSB], [http://www.ebi.ac.uk/pdbsum/2mpw PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2mpw 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=2mpw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mpw OCA], [https://pdbe.org/2mpw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mpw RCSB], [https://www.ebi.ac.uk/pdbsum/2mpw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mpw ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/EAE_ECO27 EAE_ECO27]] Necessary for the production of attaching and effacing lesions on tissue culture cells. Believed to mediate adherence. | + | [[https://www.uniprot.org/uniprot/EAE_ECO27 EAE_ECO27]] Necessary for the production of attaching and effacing lesions on tissue culture cells. Believed to mediate adherence. |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | </StructureSection> | | </StructureSection> |
| | [[Category: Bacillus coli migula 1895]] | | [[Category: Bacillus coli migula 1895]] |
| | + | [[Category: Large Structures]] |
| | [[Category: Autenrieth, I B]] | | [[Category: Autenrieth, I B]] |
| | [[Category: Chaubey, M]] | | [[Category: Chaubey, M]] |
| Structural highlights
Function
[EAE_ECO27] Necessary for the production of attaching and effacing lesions on tissue culture cells. Believed to mediate adherence.
Publication Abstract from PubMed
Intimin and Invasin are prototypical inverse (Type Ve) autotransporters and important virulence factors of enteropathogenic Escherichia coli and Yersinia spp., respectively. In addition to a C-terminal extracellular domain and a beta-barrel transmembrane domain, both proteins also contain a short N-terminal periplasmic domain that, in Intimin, includes a lysin motif (LysM), which is thought to mediate binding to peptidoglycan. We show that the periplasmic domain of Intimin does bind to peptidoglycan both in vitro and in vivo, but only under acidic conditions. We were able to determine a dissociation constant of 0.8 muM for this interaction, whereas the Invasin periplasmic domain, which lacks a LysM, bound only weakly in vitro and failed to bind peptidoglycan in vivo. We present the solution structure of the Intimin LysM, which has an additional alpha-helix conserved within inverse autotransporter LysMs but lacking in others. In contrast to previous reports, we demonstrate that the periplasmic domain of Intimin mediates dimerisation. We further show that dimerisation and peptidoglycan binding are general features of LysM-containing inverse autotransporters. Peptidoglycan binding by the periplasmic domain in the infection process may aid in resisting mechanical and chemical stress during transit through the gastrointestinal tract.
The Intimin periplasmic domain mediates dimerisation and binding to peptidoglycan.,Leo JC, Oberhettinger P, Chaubey M, Schutz M, Kuhner D, Bertsche U, Schwarz H, Gotz F, Autenrieth IB, Coles M, Linke D Mol Microbiol. 2014 Oct 29. doi: 10.1111/mmi.12840. PMID:25353290[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Leo JC, Oberhettinger P, Chaubey M, Schutz M, Kuhner D, Bertsche U, Schwarz H, Gotz F, Autenrieth IB, Coles M, Linke D. The Intimin periplasmic domain mediates dimerisation and binding to peptidoglycan. Mol Microbiol. 2014 Oct 29. doi: 10.1111/mmi.12840. PMID:25353290 doi:http://dx.doi.org/10.1111/mmi.12840
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