Search Results - "Šišáková, Eva"

DNA cleavage by Type ISP Restriction-Modification enzymes is initially targeted to the 3'-5' strand by van Aelst, Kara, Šišáková, Eva, Szczelkun, Mark D

“…The mechanism by which a double-stranded DNA break is produced following collision of two translocating Type I Restriction-Modification enzymes is not fully…”
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RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I by Šišáková, Eva, Stanley, Louise K, Weiserová, Marie, Szczelkun, Mark D

“…The Type I restriction-modification enzyme EcoR124I is an ATP-dependent endonuclease that uses dsDNA translocation to locate and cleave distant non-specific…”
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The Type ISP Restriction-Modification enzymes LlaBIII and LlaGI use a translocation-collision mechanism to cleave non-specific DNA distant from their recognition sites by Šišáková, Eva, van Aelst, Kara, Diffin, Fiona M, Szczelkun, Mark D

“…The Type ISP Restriction-Modification (RM) enzyme LlaBIII is encoded on plasmid pJW566 and can protect Lactococcus lactis strains against bacteriophage…”
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Phosphorylation of Type IA restriction-modification complex enzyme EcoKI on the HsdR subunit by Cajthamlová, Kamila, Šišáková, Eva, Weiser, Jaroslav, Weiserová, Marie

“…Abstract Phosphorylation of Type I restriction-modification (R-M) enzymes EcoKI, EcoAI, and EcoR124I – representatives of IA, IB, and IC families, respectively…”
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The Interrelationship of Helicase and Nuclease Domains during DNA Translocation by the Molecular Motor EcoR124I by Šišáková, Eva, Weiserová, Marie, Dekker, Cees, Seidel, Ralf, Szczelkun, Mark D.

“…The type I restriction–modification enzyme EcoR124I comprises three subunits with the stoichiometry HsdR2/HsdM2/HsdS1. The HsdR subunits are archetypical…”
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Structural model for the multisubunit Type IC restriction–modification DNA methyltransferase M.EcoR124I in complex with DNA by Obarska, Agnieszka, Blundell, Alex, Feder, Marcin, Vejsadová, Štěpánka, Šišáková, Eva, Weiserová, Marie, Bujnicki, Janusz M., Firman, Keith

“…Recent publication of crystal structures for the putative DNA-binding subunits (HsdS) of the functionally uncharacterized Type I restriction–modification (R-M)…”
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