Squalene–hopene cyclase: final deprotonation reaction, conformational analysis for the cyclization of (3R,S)-2,3-oxidosqualene and further evidence for the requirement of an isopropylidene moiety both for initiation of the polycyclization cascade and for the formation of the 5-membered E-ring-Reference-Cited by-同舟云学术

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Squalene–hopene cyclase: final deprotonation reaction, conformational analysis for the cyclization of (3R,S)-2,3-oxidosqualene and further evidence for the requirement of an isopropylidene moiety both for initiation of the polycyclization cascade and for the formation of the 5-membered E-ring

Published:2004 Issue:10 Volume:2 Page:1456-1470
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Hoshino Tsutomu,Nakano Schin-ichi,Kondo Tomohiro,Sato Tsutomu,Miyoshi Aya

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2004/OB/B401172D

Reference46 articles.

1. Squalene–hopene cyclase: catalytic mechanism and substrate recognition

2. Hopanoid Biosynthesis and Function in Bacteria

3. Enzyme Mechanisms for Polycyclic Triterpene Formation

4. Enzymatic cyclization of squalene and oxidosqualene to sterols and triterpenes

5. Functional Analysis of the DXDDTA Motif in Squalene-Hopene Cyclase by Site-directed Mutagenesis Experiments: Initiation Site of the Polycyclization Reaction and Stabilization Site of the Carbocation Intermediate of the Initially Cyclized A-Ring

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4. Alternative Active Site Confinement in Squalene–Hopene Cyclase Enforces Substrate Preorganization for Cyclization;ACS Catalysis;2023-03-29

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