(Q50206502)

English

Analysis of the Catalytic Mechanism of Bifunctional Triterpene/Sesquarterpene Cyclase: Tyr167 Functions To Terminate Cyclization of Squalene at the Bicyclic Step

scientific article published on 7 September 2017

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Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

Analysis of the Catalytic Mechanism of Bifunctional Triterpene/Sesquarterpene Cyclase: Tyr167 Functions To Terminate Cyclization of Squalene at the Bicyclic Step (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

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Liudmila Tenkovskaia

1

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

Mizuki Murakami

2

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

Kotone Okuno

3

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

Daijiro Ueda

4

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

Tsutomu Sato

5

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

publication date

7 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

18

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

19

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

1910-1913

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

Cyclization of squalene from both termini: identification of an onoceroid synthase and enzymatic synthesis of ambrein.

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Sesquarterpenes (C35 terpenes) biosynthesized via the cyclization of a linear C35 isoprenoid by a tetraprenyl-β-curcumene synthase and a tetraprenyl-β-curcumene cyclase: identification of a new terpene cyclase

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Identification of novel sesterterpene/triterpene synthase from Bacillus clausii

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Squalene-hopene cyclase: catalytic mechanism and substrate recognition

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

On the origins of triterpenoid skeletal diversity

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Enzyme mechanisms for triterpene cyclization: new pieces of the puzzle

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Enzymatic synthesis of cyclic triterpenes

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Squalene-hopene cyclases

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Squalene hopene cyclases: highly promiscuous and evolvable catalysts for stereoselective CC and CX bond formation

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

A new triterpene synthase from Arabidopsis thaliana produces a tricyclic triterpene with two hydroxyl groups

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Deletion of the Gly600 residue of Alicyclobacillus acidocaldarius squalene cyclase alters the substrate specificity into that of the eukaryotic-type cyclase specific to (3S)-2,3-oxidosqualene

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

A polycyclic terpenoid that alleviates oxidative stress

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Onocerin Biosynthesis Requires Two Highly Dedicated Triterpene Cyclases in a Fern Lycopodium clavatum.

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Identification of Serratane Synthase Gene from the Fern Lycopodium clavatum.

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.201700329

21 January 2018

Identifiers

10.1002/CBIC.201700329

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 February 2018

http://europepmc.org/abstract/MED/28881085

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