6hp5

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m (Protected "6hp5" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6hp5 is ON HOLD
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==ARBITRIUM PEPTIDE RECEPTOR FROM SPBETA PHAGE==
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<StructureSection load='6hp5' size='340' side='right'caption='[[6hp5]], [[Resolution|resolution]] 2.28&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6hp5]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Bacsu Bacsu]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6HP5 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6HP5 FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<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>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">yopK, BSU20860 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=224308 BACSU])</td></tr>
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<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=6hp5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6hp5 OCA], [http://pdbe.org/6hp5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6hp5 RCSB], [http://www.ebi.ac.uk/pdbsum/6hp5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6hp5 ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Bacillus phages use a communication system, termed "arbitrium," to coordinate lysis-lysogeny decisions. Arbitrium communication is mediated by the production and secretion of a hexapeptide (AimP) during lytic cycle. Once internalized, AimP reduces the expression of the negative regulator of lysogeny, AimX, by binding to the transcription factor, AimR, promoting lysogeny. We have elucidated the crystal structures of AimR from the Bacillus subtilis SPbeta phage in its apo form, bound to its DNA operator and in complex with AimP. AimR presents intrinsic plasticity, sharing structural features with the RRNPP quorum-sensing family. Remarkably, AimR binds to an unusual operator with a long spacer that interacts nonspecifically with the receptor TPR domain, while the HTH domain canonically recognizes two inverted repeats. AimP stabilizes a compact conformation of AimR that approximates the DNA-recognition helices, preventing AimR binding to the aimX promoter region. Our results establish the molecular basis of the arbitrium communication system.
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Authors: Marina, A., Gallego del Sol, F.
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Deciphering the Molecular Mechanism Underpinning Phage Arbitrium Communication Systems.,Gallego Del Sol F, Penades JR, Marina A Mol Cell. 2019 Feb 6. pii: S1097-2765(19)30045-0. doi:, 10.1016/j.molcel.2019.01.025. PMID:30745087<ref>PMID:30745087</ref>
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Description: ARBITRIUM PEPTIDE RECEPTOR FROM SPBETA PHAGE
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Gallego Del Sol, F]]
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<div class="pdbe-citations 6hp5" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Bacsu]]
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[[Category: Large Structures]]
[[Category: Marina, A]]
[[Category: Marina, A]]
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[[Category: Sol, F Gallego del]]
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[[Category: Arbitrium peptide receptor]]
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[[Category: Dna binding protein]]
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[[Category: Spbeta phage]]

Current revision

ARBITRIUM PEPTIDE RECEPTOR FROM SPBETA PHAGE

PDB ID 6hp5

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