| Literature DB >> 21499643 |
Mariana Gutierrez1, Teodor Parella, Jesús Joglar, Jordi Bujons, Pere Clapés.
Abstract
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. © The Royal Society of Chemistry 2011Entities:
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Year: 2011 PMID: 21499643 DOI: 10.1039/c1cc11069a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222