Control of stereoselectivity in an enzymatic reaction by backdoor access Journal Article


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"
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  1. Dinshaw J Patel
    478 Patel