Resum
Structure-guided re-design of the acceptor binding site of d-fructose-6-phosphate aldolase from E. coli leads to the construction of FSA A129S/A165G double mutant with an activity between 5- to >900-fold higher than that of wild-type towards N-Cbz-aminoaldehyde derivatives. © 2011 The Royal Society of Chemistry.
| Idioma original | Anglès |
|---|---|
| Pàgines (de-a) | 5762-5764 |
| Revista | Chemical Communications |
| Volum | 47 |
| Número | 20 |
| DOIs | |
| Estat de la publicació | Publicada - 28 de maig 2011 |