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. © 2011 The Royal Society of Chemistry.
Original language | English |
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Pages (from-to) | 5762-5764 |
Journal | Chemical Communications |
Volume | 47 |
Issue number | 20 |
DOIs | |
Publication status | Published - 28 May 2011 |