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PDBsum entry 6f8s
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PDB id:
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Toxin
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Title:
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Toxin-antitoxin complex grata
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Structure:
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Xre family transcriptional regulator. Chain: a, c. Engineered: yes. Other_details: antitoxin graa. Putative killer protein. Chain: b, d. Engineered: yes. Other_details: toxin grat
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Source:
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Pseudomonas putida. Arthrobacter siderocapsulatus. Organism_taxid: 303. Gene: ayo08_18510. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008. Pseudomonas putida (strain atcc 47054 / dsm 6125 / ncimb 11950 / kt2440). Organism_taxid: 160488.
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Resolution:
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2.50Å
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R-factor:
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0.180
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R-free:
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0.212
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Authors:
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A.Talavera,R.Loris
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Key ref:
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A.Talavera
et al.
(2019).
A dual role in regulation and toxicity for the disordered N-terminus of the toxin GraT.
Nat Commun,
10,
972.
PubMed id:
DOI:
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Date:
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13-Dec-17
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Release date:
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11-Jul-18
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PROCHECK
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Headers
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References
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Q88MI6
(Q88MI6_PSEPK) -
Antidote protein from Pseudomonas putida (strain ATCC 47054 / DSM 6125 / CFBP 8728 / NCIMB 11950 / KT2440)
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Seq: Struc:
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99 a.a.
94 a.a.
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Enzyme class:
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Chains A, B, C, D:
E.C.?
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DOI no:
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Nat Commun
10:972
(2019)
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PubMed id:
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A dual role in regulation and toxicity for the disordered N-terminus of the toxin GraT.
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A.Talavera,
H.Tamman,
A.Ainelo,
A.Konijnenberg,
S.Hadži,
F.Sobott,
A.Garcia-Pino,
R.Hõrak,
R.Loris.
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ABSTRACT
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Bacterial toxin-antitoxin (TA) modules are tightly regulated to maintain growth
in favorable conditions or growth arrest during stress. A typical regulatory
strategy involves the antitoxin binding and repressing its own promoter while
the toxin often acts as a co-repressor. Here we show that Pseudomonas putida
graTA-encoded antitoxin GraA and toxin GraT differ from other TA proteins in the
sense that not the antitoxin but the toxin possesses a flexible region. GraA
auto-represses the graTA promoter: two GraA dimers bind cooperatively at
opposite sides of the operator sequence. Contrary to other TA modules, GraT is a
de-repressor of the graTA promoter as its N-terminal disordered segment prevents
the binding of the GraT2A2 complex to the operator.
Removal of this region restores operator binding and abrogates Gr aT toxicity.
GraTA represents a TA module where a flexible region in the toxin rather than in
the antitoxin controls operon expression and toxin activity.
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');
}
}
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