5eri: Difference between revisions
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==MarR Protein from Peptoclostridium difficile DA00132== | |||
<StructureSection load='5eri' size='340' side='right'caption='[[5eri]], [[Resolution|resolution]] 2.30Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[5eri]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Clostridioides_difficile Clostridioides difficile]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5ERI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5ERI 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]] 2.3Å</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=5eri FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5eri OCA], [https://pdbe.org/5eri PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5eri RCSB], [https://www.ebi.ac.uk/pdbsum/5eri PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5eri ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/A0A031WDA8_CLODI A0A031WDA8_CLODI] | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Regulators of multiple antibiotic resistance (MarRs) are key players against toxins in prokaryotes. MarR homologues have been identified in many bacterial and archaeal species which pose daunting antibiotic resistance issues that threaten public health. The continuous prevalence of Clostridium difficile infection (CDI) throughout the world is associated with the abuse of antibiotics, and antibiotic treatments of CDI have limited effect. In the genome of C. difficile strain 630, the marR gene (ID 4913953) encodes a MarR protein. Here, MarR from C. difficile (MarRC.difficile) was subcloned and crystallized for the first time. MarRC.difficile was successfully expressed in Escherichia coli in a soluble form and was purified to near-homogeneity (>95%) by a two-step purification protocol. The structure of MarRC.difficile has been solved at 2.3 A resolution. The crystal belonged to the monoclinic space group P43212, with unit-cell parameters a = b = 66.569, c = 83.654 A. The structure reported reveals MarRC.difficile to be a dimer, with each subunit consisting of six alpha-helices and three antiparallel beta-hairpins. MarRC.difficile shows high structural similarity to the MarR proteins from E. coli and Staphylococcus aureus, indicating that MarRC.difficile might be a DNA-binding protein. | |||
Crystal structure of the multiple antibiotic resistance regulator MarR from Clostridium difficile.,Peng JW, Yuan H, Tan XS Acta Crystallogr F Struct Biol Commun. 2017 Jun 1;73(Pt 6):363-368. doi:, 10.1107/S2053230X1700766X. Epub 2017 May 31. PMID:28580925<ref>PMID:28580925</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
[[Category: | </div> | ||
[[Category: Peng | <div class="pdbe-citations 5eri" style="background-color:#fffaf0;"></div> | ||
[[Category: | |||
[[Category: | ==See Also== | ||
*[[Transcriptional activator 3D structures|Transcriptional activator 3D structures]] | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Clostridioides difficile]] | |||
[[Category: Large Structures]] | |||
[[Category: Peng JW]] | |||
[[Category: Tan XS]] | |||
[[Category: Yuan H]] | |||
Latest revision as of 11:18, 12 July 2023
MarR Protein from Peptoclostridium difficile DA00132MarR Protein from Peptoclostridium difficile DA00132
Structural highlights
FunctionPublication Abstract from PubMedRegulators of multiple antibiotic resistance (MarRs) are key players against toxins in prokaryotes. MarR homologues have been identified in many bacterial and archaeal species which pose daunting antibiotic resistance issues that threaten public health. The continuous prevalence of Clostridium difficile infection (CDI) throughout the world is associated with the abuse of antibiotics, and antibiotic treatments of CDI have limited effect. In the genome of C. difficile strain 630, the marR gene (ID 4913953) encodes a MarR protein. Here, MarR from C. difficile (MarRC.difficile) was subcloned and crystallized for the first time. MarRC.difficile was successfully expressed in Escherichia coli in a soluble form and was purified to near-homogeneity (>95%) by a two-step purification protocol. The structure of MarRC.difficile has been solved at 2.3 A resolution. The crystal belonged to the monoclinic space group P43212, with unit-cell parameters a = b = 66.569, c = 83.654 A. The structure reported reveals MarRC.difficile to be a dimer, with each subunit consisting of six alpha-helices and three antiparallel beta-hairpins. MarRC.difficile shows high structural similarity to the MarR proteins from E. coli and Staphylococcus aureus, indicating that MarRC.difficile might be a DNA-binding protein. Crystal structure of the multiple antibiotic resistance regulator MarR from Clostridium difficile.,Peng JW, Yuan H, Tan XS Acta Crystallogr F Struct Biol Commun. 2017 Jun 1;73(Pt 6):363-368. doi:, 10.1107/S2053230X1700766X. Epub 2017 May 31. PMID:28580925[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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