| Literature DB >> 25719942 |
Noé Sturm1, Ronald J Quinn1, Esther Kellenberger2.
Abstract
Natural products are made by nature through interaction with biosynthetic enzymes. They also exert their effect as drugs by interaction with proteins. To address the question "Do biosynthetic enzymes and therapeutic targets share common mechanisms for the molecular recognition of natural products?", we compared the active site of five flavonoid biosynthetic enzymes to 8077 ligandable binding sites in the Protein Data Bank using two three-dimensional-based methods (SiteAlign and Shaper). Virtual screenings efficiently retrieved known flavonoid targets, in particular protein kinases. A consistent performance obtained for variable site descriptions (presence/absence of water, variable boundaries, or small structural changes) indicated that the methods are robust and thus well suited for the identification of potential target proteins of natural products. Finally, our results suggested that flavonoid binding is not primarily driven by shape, but rather by the recognition of common anchoring points. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2015 PMID: 25719942 DOI: 10.1055/s-0035-1545697
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352