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New page: left|200px<br /><applet load="2p5t" size="350" color="white" frame="true" align="right" spinBox="true" caption="2p5t, resolution 3.20Å" /> '''Molecular and struct...
 
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[[Image:2p5t.gif|left|200px]]<br /><applet load="2p5t" size="350" color="white" frame="true" align="right" spinBox="true"
caption="2p5t, resolution 3.20&Aring;" />
'''Molecular and structural characterization of the PezAT chromosomal toxin-antitoxin system of the human pathogen Streptococcus pneumoniae'''<br />


==Overview==
==Molecular and structural characterization of the PezAT chromosomal toxin-antitoxin system of the human pathogen Streptococcus pneumoniae==
The chromosomal pezT gene of the Gram-positive pathogen Streptococcus, pneumoniae encodes a protein that is homologous to the zeta toxin of the, Streptococcus pyogenes plasmid pSM19035-encoded epsilon-zeta, toxin-antitoxin system. Overexpression of pezT in Escherichia coli led to, severe growth inhibition from which the bacteria recovered approximately 3, h after induction of expression. The toxicity of PezT was counteracted by, PezA, which is encoded immediately upstream of pezT and shares weak, sequence similarities in the C-terminal region with the epsilon antitoxin., The pezAT genes form a bicistronic operon that is co-transcribed from a, sigma(70)-like promoter upstream of pezA and is negatively autoregulated, with PezA functioning as a transcriptional repressor and PezT as a, co-repressor. Both PezA and the non-toxic PezA(2)PezT(2) protein complex, bind to a palindrome sequence that overlaps the promoter. This differs, from the epsilon-zeta system in which epsilon functions solely as the, antitoxin and transcriptional regulation is carried out by another protein, designated omega. Results from site-directed mutagenesis experiments, demonstrated that the toxicity of PezT is dependent on a highly conserved, phosphoryltransferase active site and an ATP/GTP nucleotide binding site., In the PezA(2)PezT(2) complex, PezA neutralizes the toxicity of PezT by, blocking the nucleotide binding site through steric hindrance.
<StructureSection load='2p5t' size='340' side='right'caption='[[2p5t]], [[Resolution|resolution]] 3.20&Aring;' scene=''>
 
== Structural highlights ==
==About this Structure==
<table><tr><td colspan='2'>[[2p5t]] is a 9 chain structure with sequence from [https://en.wikipedia.org/wiki/Streptococcus_pneumoniae Streptococcus pneumoniae] and [https://en.wikipedia.org/wiki/Streptococcus_pneumoniae_TIGR4 Streptococcus pneumoniae TIGR4]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2P5T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2P5T FirstGlance]. <br>
2P5T is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Streptococcus_pneumoniae Streptococcus pneumoniae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2P5T OCA].  
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.2&#8491;</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=2p5t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2p5t OCA], [https://pdbe.org/2p5t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2p5t RCSB], [https://www.ebi.ac.uk/pdbsum/2p5t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2p5t ProSAT]</span></td></tr>
==Reference==
</table>
Molecular and structural characterization of the PezAT chromosomal toxin-antitoxin system of the human pathogen Streptococcus pneumoniae., Khoo SK, Loll B, Chan WT, Shoeman RL, Ngoo L, Yeo CC, Meinhart A, J Biol Chem. 2007 Jul 6;282(27):19606-18. Epub 2007 May 8. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17488720 17488720]
== Function ==
[[Category: Protein complex]]
[https://www.uniprot.org/uniprot/PEZA_STRPN PEZA_STRPN] Antitoxin component of a toxin-antitoxin (TA) module. Upon expression in E.coli neutralizes the toxic effect of cognate toxin PezT. Represses transcription of its own operon, PezT acts as a corepressor, considerably increasing repression.<ref>PMID:17488720</ref> <ref>PMID:21445328</ref>
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/p5/2p5t_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2p5t ConSurf].
<div style="clear:both"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Streptococcus pneumoniae]]
[[Category: Streptococcus pneumoniae]]
[[Category: Loll, B.]]
[[Category: Streptococcus pneumoniae TIGR4]]
[[Category: Meinhart, A.]]
[[Category: Loll B]]
[[Category: helix-turn-helix motif]]
[[Category: Meinhart A]]
[[Category: phosphoryltransferase]]
[[Category: postsegregational killing system]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:19:22 2008''

Latest revision as of 09:08, 21 February 2024

Molecular and structural characterization of the PezAT chromosomal toxin-antitoxin system of the human pathogen Streptococcus pneumoniae

2p5t, resolution 3.20Å

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