Authors: | Wombacher, R.; Keiper, S.; Suhm, S.; Serganov, A.; Patel, D. J.; Jäschke, A. |
Article Title: | Control of stereoselectivity in an enzymatic reaction by backdoor access |
Abstract: | (Figure Presented) Sneaking in: The active site of a Diels-Alder ribozyme features two different "doors" through which the diene may enter. Depending on which door is used, either of the two enantiomeric Diels-Alder products is synthesized selectively. Enantioselectivity can be modulated by controlling access to the ribozyme's active site. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA. |
Keywords: | metabolism; chemistry; substrate specificity; models, molecular; protein structure, tertiary; chemical structure; catalysis; enzyme specificity; protein tertiary structure; olefins; synthesis (chemical); stereoisomerism; cycloaddition; enantioselectivity; ribozyme; reaction kinetics; rna, catalytic; enzyme immobilization; enzyme catalysis; ribozymes; aromatic compounds |
Journal Title: | Angewandte Chemie - International Edition |
Volume: | 45 |
Issue: | 15 |
ISSN: | 1433-7851 |
Publisher: | Wiley Blackwell |
Date Published: | 2006-04-03 |
Start Page: | 2469 |
End Page: | 2472 |
Language: | English |
DOI: | 10.1002/anie.200503280 |
PUBMED: | 16528762 |
PROVIDER: | scopus |
PMCID: | PMC4693636 |
DOI/URL: | |
Notes: | --- - "Cited By (since 1996): 11" - "Export Date: 4 June 2012" - "CODEN: ACIEA" - "Source: Scopus" |