Search Results - "Käshammer, Lisa"

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  1. 1
    Mechanism of DNA End Sensing and Processing by the Mre11-Rad50 Complex

    Mechanism of DNA End Sensing and Processing by the Mre11-Rad50 Complex by Käshammer, Lisa, Saathoff, Jan-Hinnerk, Lammens, Katja, Gut, Fabian, Bartho, Joseph, Alt, Aaron, Kessler, Brigitte, Hopfner, Karl-Peter

    Published in Molecular cell (07-11-2019)
    “…DNA double-strand breaks (DSBs) threaten genome stability throughout life and are linked to tumorigenesis in humans. To initiate DSB repair by end joining or…”
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  2. 2
    The bacterial Mre11-Rad50 homolog SbcCD cleaves opposing strands of DNA by two chemically distinct nuclease reactions

    The bacterial Mre11-Rad50 homolog SbcCD cleaves opposing strands of DNA by two chemically distinct nuclease reactions by Saathoff, Jan-Hinnerk, Käshammer, Lisa, Lammens, Katja, Byrne, Robert Thomas, Hopfner, Karl-Peter

    Published in Nucleic acids research (30-11-2018)
    “…Abstract The Mre11-Rad50 complex is a DNA double-strand break sensor that cleaves blocked DNA ends and hairpins by an ATP-dependent endo/exonuclease activity…”
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  3. 3
    Cryo-EM structure of the bacterial divisome core complex and antibiotic target FtsWIQBL

    Cryo-EM structure of the bacterial divisome core complex and antibiotic target FtsWIQBL by Käshammer, Lisa, van den Ent, Fusinita, Jeffery, Magnus, Jean, Nicolas L., Hale, Victoria L., Löwe, Jan

    Published in Nature microbiology (01-06-2023)
    “…In most bacteria, cell division relies on the synthesis of new cell wall material by the multiprotein divisome complex. Thus, at the core of the divisome are…”
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  4. 4
    Structural mechanism of endonucleolytic processing of blocked DNA ends and hairpins by Mre11-Rad50

    Structural mechanism of endonucleolytic processing of blocked DNA ends and hairpins by Mre11-Rad50 by Gut, Fabian, Käshammer, Lisa, Lammens, Katja, Bartho, Joseph D., Boggusch, Anna-Maria, van de Logt, Erik, Kessler, Brigitte, Hopfner, Karl-Peter

    Published in Molecular cell (15-09-2022)
    “…DNA double-strand breaks (DSBs) threaten genome stability and are linked to tumorigenesis in humans. Repair of DSBs requires the removal of attached proteins…”
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