5.4.99.17: squalene-hopene cyclase
This is an abbreviated version!
For detailed information about squalene-hopene cyclase, go to the full flat file.
Word Map on EC 5.4.99.17
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5.4.99.17
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cyclization
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alicyclobacillus
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acidocaldarius
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hopanoids
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cyclases
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oxidosqualene
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pentacyclic
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triterpene
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2,3-oxidosqualene
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tetracyclic
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tetrahymanol
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carbocation
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polyolefinic
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5.4.99.7
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lanosterol
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aspartate-rich
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synthesis
- 5.4.99.17
-
cyclization
- alicyclobacillus
- acidocaldarius
-
hopanoids
- cyclases
- oxidosqualene
-
pentacyclic
-
triterpene
- 2,3-oxidosqualene
-
tetracyclic
- tetrahymanol
-
carbocation
-
polyolefinic
-
5.4.99.7
- lanosterol
-
aspartate-rich
- synthesis
Reaction
Synonyms
AacSHC, cyclase, squalene-hopanoid, SHC, SHC1, SHC2, Spterp25, SQ-hopene cyclase, squalene hopene cyclase, squalene-hopene cyclase, ZmoSHC1, ZmSHC1
ECTree
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Application
Application on EC 5.4.99.17 - squalene-hopene cyclase
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synthesis
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production of unnatural polyprenoids and supranatural steroids by manipulation of the enzyme reaction by combination of substrate analogues
synthesis
cyclization of homofarnesol to ambroxan as well as the conversion of citronellal to 2-isopropenyl-5-methyl-cyclohexanol bythe isozyme SHC1 can be economically attractive, as both products are used in the flavour and fragrance industry
synthesis
it is possible to use the cyanobacterium Synechocystis to generate squalene, a hydrocarbon of commercial interest and a potential biofuel
synthesis
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cyclization of homofarnesol to ambroxan as well as the conversion of citronellal to 2-isopropenyl-5-methyl-cyclohexanol bythe isozyme SHC1 can be economically attractive, as both products are used in the flavour and fragrance industry
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