Doc of Prophage P1 Is Inhibited by Its Antitoxin Partner Phd through Fold Complementation (Q27651861)

3

object named as

Lode Wyns

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author name string

Abel Garcia-Pino

1

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Mikkel Christensen-Dalsgaard

2

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Michael Yarmolinsky

4

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Roy David Magnuson

5

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Kenn Gerdes

Journal of Biological Chemistry

6

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language of work or name

English

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publication date

7 November 2008

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published in

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volume

283

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issue

45

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page(s)

30821-7

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cites work

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29 September 2017

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Characterization of the Phd repressor-antitoxin boundary

29 September 2017

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Modular organization of the Phd repressor/antitoxin protein

29 September 2017

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29 September 2017

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MazF Cleaves Cellular mRNAs Specifically at ACA to Block Protein Synthesis in Escherichia coli

29 September 2017

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A novel main-chain anion-binding site in proteins: the nest. A particular combination of phi,psi values in successive residues gives rise to anion-binding sites that occur commonly and are found often at functionally important regions

29 September 2017

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Postsegregational killing mediated by the P1 phage "addiction module" phd-doc requires the Escherichia coli programmed cell death system mazEF.

29 September 2017

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Corepression of the P1 addiction operon by Phd and Doc.

29 September 2017

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29 September 2017

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Plasmid addiction genes of bacteriophage P1: doc, which causes cell death on curing of prophage, and phd, which prevents host death when prophage is retained

29 September 2017

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Programmed cell death in bacterial populations

29 September 2017

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Involvement of cyclic AMP and its receptor protein in filamentation of an Escherichia coli fic mutant

29 September 2017

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29 September 2017

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Rapid induction and reversal of a bacteriostatic condition by controlled expression of toxins and antitoxins.

29 September 2017

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Chromosomal toxin-antitoxin loci can diminish large-scale genome reductions in the absence of selection

21 January 2018

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The Doc toxin and Phd antidote proteins of the bacteriophage P1 plasmid addiction system form a heterotrimeric complex.

21 January 2018

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Stability and DNA binding of the phd protein of the phage P1 plasmid addiction system.

21 January 2018

1 reference

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Processing of X-ray diffraction data collected in oscillation mode

21 January 2018

1 reference

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Partitioning of plasmid R1. Ten direct repeats flanking the parA promoter constitute a centromere-like partition site parC, that expresses incompatibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805654200

Conformational change in the catalytic site of the ribonuclease YoeB toxin by YefM antitoxin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805654200

Crystal structure of archaeal toxin-antitoxin RelE-RelB complex with implications for toxin activity and antitoxin effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805654200

RelE toxins from bacteria and Archaea cleave mRNAs on translating ribosomes, which are rescued by tmRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805654200

Protein sequence alignments: a strategy for the hierarchical analysis of residue conservation.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2576525

27 November 2018

Identifiers

DOI

10.1074/JBC.M805654200

1 reference

release_eovmcqfzv5ckpmktcu2b3obi2i

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/eovmcqfzv5ckpmktcu2b3obi2i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

1 reference

PubMed publication ID

18757857

1 reference