EC Number   |
Title |
Organism |
|---|
   2.1.1.72 | A cell cycle-regulated adenine DNA methyltransferase from Caulobacter crescentus processively methylates GANTC sites on hemimethylated DNA |
Caulobacter vibrioides |
| 2.1.1.72 | A distinct class of eukaryotic MT-A70 methyltransferases maintain symmetric DNA N6-adenine methylation at the ApT dinucleotides as an epigenetic mark associated with transcription |
Tetrahymena thermophila |
| 2.1.1.72 | A distinct class of eukaryotic MT-A70 methyltransferases maintain symmetric DNA N6-adenine methylation at the ApT dinucleotides as an epigenetic mark associated with transcription |
Tetrahymena thermophila SB210 |
| 2.1.1.72 | A DNA adenine methyltransferase of Escherichia coli that is cell cycle regulated and essential for viability |
Escherichia coli |
| 2.1.1.72 | A dual role for substrate S-adenosyl-L-methionine in the methylation reaction with bacteriophage T4 Dam DNA-[N6-adenine]-methyltransferase |
Tequatrovirus T4 |
| 2.1.1.72 | A rapid and efficient method for cloning genes of type II restriction-modification systems by use of a killer plasmid |
Geobacillus stearothermophilus |
| 2.1.1.72 | A rapid and efficient method for cloning genes of type II restriction-modification systems by use of a killer plasmid |
Citrobacter sp. |
| 2.1.1.72 | A rapid and efficient method for cloning genes of type II restriction-modification systems by use of a killer plasmid |
Citrobacter sp. RFL231 |
| 2.1.1.72 | A rapid and efficient method for cloning genes of type II restriction-modification systems by use of a killer plasmid |
Geobacillus stearothermophilus 14P |
| 2.1.1.72 | A sequential one-pot approach for rapid and convenient characterization of putative restriction-modification systems |
Nitratiruptor phage NrS-3 |
