EC Number   |
Title |
Organism |
|---|
    5.4.3.2 | Paramagnetic intermediates generated by radical S-adenosylmethionine (SAM) enzymes |
Escherichia coli |
| 5.4.3.2 | Transcription of the lysine-2,3-aminomutase gene in the kam locus of Bacillus thuringiensis subsp. kurstaki HD73 is controlled by both sigma54 and sigmaK factors |
Bacillus thuringiensis serovar kurstaki |
| 5.4.3.2 | Transcription of the lysine-2,3-aminomutase gene in the kam locus of Bacillus thuringiensis subsp. kurstaki HD73 is controlled by both sigma54 and sigmaK factors |
Bacillus thuringiensis serovar kurstaki HD73 |
| 5.4.3.2 | Travels with carbon-centered radicals. 5'-Deoxyadenosine and 5'-deoxyadenosine-5'-yl in radical enzymology |
Clostridium subterminale |
| 5.4.3.2 | Travels with carbon-centered radicals. 5'-Deoxyadenosine and 5'-deoxyadenosine-5'-yl in radical enzymology |
Clostridium subterminale SB4 |
| 5.4.3.2 | Why nature uses radical SAM enzymes so widely electron nuclear double resonance studies of lysine 2,3-aminomutase show the 5-dAdo? Free radical is never free |
Clostridium subterminale |
| 5.4.3.2 | Why nature uses radical SAM enzymes so widely electron nuclear double resonance studies of lysine 2,3-aminomutase show the 5-dAdo? Free radical is never free |
Clostridium subterminale SB4 |
| 5.4.3.2 | A novel limb in the osmoregulatory network of Methanosarcina mazei Goe1: N(epsilon)-acetyl-beta-lysine can be substituted by glutamate and alanine |
Methanosarcina mazei Go1 |
| 5.4.3.2 | A novel lysine 2,3-aminomutase encoded by the yodO gene of Bacillus subtilis: characterization and the observation of organic radical intermediates |
Bacillus subtilis |
| 5.4.3.2 | Activation of lysine 2,3-aminomutase by S-adenosylmethionine |
Clostridium sp. |
