about
Protein-tyrosine phosphorylation interaction network in Bacillus subtilis reveals new substrates, kinase activators and kinase cross-talkThe DNA repair helicase UvrD is essential for replication fork reversal in replication mutantsBuilding the repertoire of dispensable chromosome regions in Bacillus subtilis entails major refinement of cognate large-scale metabolic model.Interaction of bacterial fatty-acid-displaced regulators with DNA is interrupted by tyrosine phosphorylation in the helix-turn-helix domain.Termination factor Rho: From the control of pervasive transcription to cell fate determination in Bacillus subtilis.Transcription termination factor Rho and microbial phenotypic heterogeneity.Genetic engineering of the branched fatty acid metabolic pathway of Bacillus subtilis for the overproduction of surfactin C14 isoform.The Escherichia coli UvrD helicase is essential for Tus removal during recombination-dependent replication restart from Ter sites.RuvAB acts at arrested replication forkssbcB sbcC null mutations allow RecF-mediated repair of arrested replication forks in rep recBC mutantsPhosphorylation of Bacillus subtilis gene regulator AbrB modulates its DNA-binding properties
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-0070-4839
@en
name
Vladimir Bidnenko
@ast
Vladimir Bidnenko
@en
Vladimir Bidnenko
@es
Vladimir Bidnenko
@nl
type
label
Vladimir Bidnenko
@ast
Vladimir Bidnenko
@en
Vladimir Bidnenko
@es
Vladimir Bidnenko
@nl
prefLabel
Vladimir Bidnenko
@ast
Vladimir Bidnenko
@en
Vladimir Bidnenko
@es
Vladimir Bidnenko
@nl
P106
P31
P496
0000-0002-0070-4839