SummaryThe Type I R–M system EcoR124I is encoded by three genes. HsdM is responsible for modification (DNA methylation), HsdS for DNA sequence specificity and HsdR for restriction endonuclease activity. The trimeric methyltransferase (M2S) recognises the asymmetric sequence (GAAN6RTCG). An engineered R–M system, denoted EcoR124INT, has two copies of the N-terminal domain of the HsdS subunit of EcoR124I, instead of a single S subunit with two domains, and recognises the symmetrical sequence GAAN7TTC. We investigate the methyltransferase activity of EcoR124INT, characterise the enzyme and its subunits by analytical ultracentrifugation and obtain low-resolution structural models from small-angle neutron scattering experiments using contrast va...
Although EcoR124 is one of the better-studied Type I restriction-modification enzymes, it still pres...
Type I DNA restriction/modification (RM) enzymes are molecular machines found in the majority of bac...
Type I restriction-modification enzymes are oligomeric proteins composed of methylation (M), DNA seq...
SummaryThe Type I R–M system EcoR124I is encoded by three genes. HsdM is responsible for modificatio...
Type I restriction-modification (RM) systems are comprised of two multi-subunit enzymes, the methylt...
The EcoR124INT restriction-modification (R-M) system contains the genes HsdS3, HsdM and HsdR. S3 enc...
AbstractType I restriction-modification (R-M) systems encode multisubunit/multidomain enzymes. Two g...
Type I restriction-modification (RM) systems are comprised of two multi-subunit enzymes, the methylt...
<div><p>Type I restriction-modification (RM) systems are comprised of two multi-subunit enzymes, the...
AbstractType I restriction-modification (RM) systems are large, multifunctional enzymes composed of ...
AbstractWe describe the fusion of enhanced green fluorescent protein to the C-terminus of the HsdS D...
Type I restriction-modification (R-M) enzymes recognize specific sequences on foreign DNA invading t...
Biophysics Laboratories The type IC methyltransferase M.EcoR124I consists of a specificity subunit (...
DNA methyltransferases (MTases) are a group of enzymes that catalyze the methyl group transfer from ...
AbstractBackground: Methyltransferases (Mtases) catalyze the transfer of methyl groups from S-adenos...
Although EcoR124 is one of the better-studied Type I restriction-modification enzymes, it still pres...
Type I DNA restriction/modification (RM) enzymes are molecular machines found in the majority of bac...
Type I restriction-modification enzymes are oligomeric proteins composed of methylation (M), DNA seq...
SummaryThe Type I R–M system EcoR124I is encoded by three genes. HsdM is responsible for modificatio...
Type I restriction-modification (RM) systems are comprised of two multi-subunit enzymes, the methylt...
The EcoR124INT restriction-modification (R-M) system contains the genes HsdS3, HsdM and HsdR. S3 enc...
AbstractType I restriction-modification (R-M) systems encode multisubunit/multidomain enzymes. Two g...
Type I restriction-modification (RM) systems are comprised of two multi-subunit enzymes, the methylt...
<div><p>Type I restriction-modification (RM) systems are comprised of two multi-subunit enzymes, the...
AbstractType I restriction-modification (RM) systems are large, multifunctional enzymes composed of ...
AbstractWe describe the fusion of enhanced green fluorescent protein to the C-terminus of the HsdS D...
Type I restriction-modification (R-M) enzymes recognize specific sequences on foreign DNA invading t...
Biophysics Laboratories The type IC methyltransferase M.EcoR124I consists of a specificity subunit (...
DNA methyltransferases (MTases) are a group of enzymes that catalyze the methyl group transfer from ...
AbstractBackground: Methyltransferases (Mtases) catalyze the transfer of methyl groups from S-adenos...
Although EcoR124 is one of the better-studied Type I restriction-modification enzymes, it still pres...
Type I DNA restriction/modification (RM) enzymes are molecular machines found in the majority of bac...
Type I restriction-modification enzymes are oligomeric proteins composed of methylation (M), DNA seq...