We have converted the only known true bacterial monoterpene synthase, cineole synthase from Streptomyces clavuligerus (bCinS, C10 substrate), to a highly competent sesquiterpene synthase (C15) with a minimum number of rational mutations. By comparison with diterpene synthases (C20), we were then able to bestow diterpene synthase activity on bCinS. This
Nicole G. H. Leferink +3 more
wiley +1 more source
Three decades of selective product formation <i>via</i> Griesbaum co-ozonolysis: insight and advances (1995-2025). [PDF]
Zain-Ul-Abideen M +4 more
europepmc +1 more source
Effect of Chalcogen Interaction on the Structure of Methine-Bridged Trichalcogenophenes. [PDF]
Nishimura R, Yamashita KI.
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Conformational dynamics and molecular interactions of natural products: unveiling functional structures in biological membranes. [PDF]
Murata M, Satake M, Matsumori N.
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The Mechanism of the Rappe Rearrangement─A Stereochemical Investigation Using Density Functional Theory. [PDF]
Sommer TJ, Rzepa HS.
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SeqForge: a scalable platform for alignment-based searches, motif detection, and sequence curation across meta/genomic datasets. [PDF]
Bring Horvath ER, Winter JM.
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Metal-Mediated Il-8 Binding to Heparan Sulfate Evaluated by Electrochemical Impedance Spectroscopy. [PDF]
Shitrit A +6 more
europepmc +1 more source
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Stroek W +3 more
europepmc +1 more source

