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PDBsum entry 2grm
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Transcription
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PDB id
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2grm
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Contents |
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* Residue conservation analysis
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PDB id:
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| Name: |
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Transcription
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Title:
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Crystal structure of prgx/icf10 complex
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Structure:
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Prgx. Chain: a, b, c. Engineered: yes. Mutation: yes. Peptide. Chain: d, e. Engineered: yes
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Source:
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Enterococcus faecalis. Organism_taxid: 1351. Expressed in: escherichia coli. Expression_system_taxid: 562. Synthetic: yes
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Resolution:
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3.00Å
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R-factor:
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0.238
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R-free:
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0.285
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Authors:
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K.Shi,B.K.Kozlowicz,Z.Y.Gu,D.H.Ohlendorf,C.A.Earhart,G.M.Dunny
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Key ref:
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B.K.Kozlowicz
et al.
(2006).
Molecular basis for control of conjugation by bacterial pheromone and inhibitor peptides.
Mol Microbiol,
62,
958-969.
PubMed id:
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Date:
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24-Apr-06
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Release date:
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03-Apr-07
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PROCHECK
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Headers
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References
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Mol Microbiol
62:958-969
(2006)
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PubMed id:
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Molecular basis for control of conjugation by bacterial pheromone and inhibitor peptides.
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B.K.Kozlowicz,
K.Shi,
Z.Y.Gu,
D.H.Ohlendorf,
C.A.Earhart,
G.M.Dunny.
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ABSTRACT
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In many bacteria expression of lateral gene transfer and of virulence factors is
controlled by cell-cell signalling systems. Molecular interactions of microbial
signal molecules with their cognate receptors are not well understood. For the
Enterococcus faecalis conjugative plasmid pCF10, the PrgX protein serves as a
molecular switch controlling expression of conjugation and virulence genes
encoded by the plasmid. The induction state of a pCF10-carrying donor cell is
determined by the ratio of two signalling peptides, cCF10 pheromone and iCF10
inhibitor. Recent analysis of PrgX/cCF10 interactions suggests a mechanism for
conversion to the induced state. However, the means by which iCF10 peptide
antagonizes cCF10 activity is unclear, and it has been suggested that inhibitor
peptides block import of pheromone peptides. We now show that both of these
peptides interact with the same binding pocket of PrgX, but they differentially
alter the conformation of the protein and its oligomerization state, resulting
in opposing biological activities.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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D.J.Rankin,
E.P.Rocha,
and
S.P.Brown
(2011).
What traits are carried on mobile genetic elements, and why?
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Heredity,
106,
1.
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G.M.Dunny,
and
C.M.Johnson
(2011).
Regulatory circuits controlling enterococcal conjugation: lessons for functional genomics.
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Curr Opin Microbiol,
14,
174-180.
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C.M.Johnson,
D.A.Manias,
H.A.Haemig,
S.Shokeen,
K.E.Weaver,
T.M.Henkin,
and
G.M.Dunny
(2010).
Direct evidence for control of the pheromone-inducible prgQ operon of Enterococcus faecalis plasmid pCF10 by a countertranscript-driven attenuation mechanism.
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J Bacteriol,
192,
1634-1642.
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R.J.Bennett,
and
G.M.Dunny
(2010).
Analogous telesensing pathways regulate mating and virulence in two opportunistic human pathogens.
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MBio,
1,
0.
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G.Zhao,
G.Li,
H.Schindelin,
and
W.J.Lennarz
(2009).
An Armadillo motif in Ufd3 interacts with Cdc48 and is involved in ubiquitin homeostasis and protein degradation.
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Proc Natl Acad Sci U S A,
106,
16197-16202.
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PDB code:
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J.R.Chandler,
and
G.M.Dunny
(2008).
Characterization of the sequence specificity determinants required for processing and control of sex pheromone by the intramembrane protease Eep and the plasmid-encoded protein PrgY.
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J Bacteriol,
190,
1172-1183.
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G.M.Dunny
(2007).
The peptide pheromone-inducible conjugation system of Enterococcus faecalis plasmid pCF10: cell-cell signalling, gene transfer, complexity and evolution.
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Philos Trans R Soc Lond B Biol Sci,
362,
1185-1193.
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K.R.Fixen,
J.R.Chandler,
T.Le,
B.K.Kozlowicz,
D.A.Manias,
and
G.M.Dunny
(2007).
Analysis of the amino acid sequence specificity determinants of the enterococcal cCF10 sex pheromone in interactions with the pheromone-sensing machinery.
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J Bacteriol,
189,
1399-1406.
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M.Ibrahim,
A.Guillot,
F.Wessner,
F.Algaron,
C.Besset,
P.Courtin,
R.Gardan,
and
V.Monnet
(2007).
Control of the transcription of a short gene encoding a cyclic peptide in Streptococcus thermophilus: a new quorum-sensing system?
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J Bacteriol,
189,
8844-8854.
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
code is
shown on the right.
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