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Nucleic Acids Research|April 27, 2021
What makes a type IIA topoisomerase a gyrase or a Topo IV?Jana Hirsch, Dagmar KlostermeierMolecular Pharmaceutics|July 29, 2021
Conjugates of Ciprofloxacin and Amphiphilic Block Copoly(2-alkyl-2-oxazolines)s Overcome Efflux Pumps and Are Active against CIP-Resistant BacteriaAlina Romanovska, Johanna Keil, Jonas Tophoven, et al.Journal of Molecular Biology|April 23, 2013
Mapping the spectrum of conformational states of the DNA- and C-gates in Bacillus subtilis gyraseMarkus G Rudolph, Dagmar KlostermeierBiochemistry|November 27, 2002
Energetics of hydrogen bond networks in RNA: hydrogen bonds surrounding G+1 and U42 are the major determinants for the tertiary structure stability of the hairpin ribozymeDagmar Klostermeier, David P MillarJournal of Molecular Biology|June 15, 2007
Adenosine 5'-O-(3-thio)triphosphate (ATPgammaS) promotes positive supercoiling of DNA by T. maritima reverse gyraseStefan P Jungblut, Dagmar KlostermeierRNA Biology|September 22, 2012
The DEAD-box helicase eIF4A: paradigm or the odd one out?Alexandra Z Andreou, Dagmar KlostermeierNucleic Acids Research|September 15, 2012
The GyrA-box determines the geometry of DNA bound to gyrase and couples DNA binding to the nucleotide cycleMartin A Lanz, Dagmar KlostermeierNucleic Acids Research|May 29, 2009
A conformational change in the helicase core is necessary but not sufficient for RNA unwinding by the DEAD box helicase YxiNAnne R Karow, Dagmar KlostermeierRNA (New York, N.Y.)|August 28, 2009
The Thermus thermophilus DEAD box helicase Hera contains a modified RNA recognition motif domain loosely connected to the helicase coreMarkus G Rudolph, Dagmar KlostermeierThe Journal of Biological Chemistry|July 19, 2025
Conformations of the three gates in Saccharomyces cerevisiae topoisomerase II and their response to DNA, nucleotide, and etoposideJampa Tsedön Stelljes, Dagmar KlostermeierPageof 8