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Literature summary extracted from

  • Chang, C.H.; Chen, Y.C.; Tseng, S.W.; Liu, Y.T.; Wen, H.Y.; Li, W.H.; Huang, C.Y.; Ko, C.Y.; Wang, T.T.; Wu, T.K.
    The cysteine 703 to isoleucine or histidine mutation of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae generates an iridal-type triterpenoid (2012), Biochimie, 94, 2376-2381.
    View publication on PubMed

Application

EC Number Application Comment Organism
5.4.99.7 synthesis engineering ERG7 for producing biological active agents is promising Saccharomyces cerevisiae

Protein Variants

EC Number Protein Variants Comment Organism
5.4.99.7 C703D site-directed mutagenesis, the mutant shows unaltered product spectrum compared to the wild-type enzyme Saccharomyces cerevisiae
5.4.99.7 C703G site-directed mutagenesis, the mutant shows altered product spectrum compared to the wild-type enzyme, but not as diverse as mutants C703I and C703H Saccharomyces cerevisiae
5.4.99.7 C703H site-directed mutagenesis, the mutant generates an unusual truncated bicyclic rearranged intermediate, (8R,9R,10R)-polypoda-5,13E,17E,21-tetraen-3beta-ol, related to iridal-skeleton triterpenoid. Numerous oxidosqualene-cyclized truncated intermediates, including tricyclic, unrearranged tetracyclic with 17alpha/beta exocyclic hydrocarbon side chain, rearranged tetracyclic, and chair-chair-chair tricyclic intermediates, are also isolated from the mutant Saccharomyces cerevisiae
5.4.99.7 C703I site-directed mutagenesis, the mutant generates an unusual truncated bicyclic rearranged intermediate, (8R,9R,10R)-polypoda-5,13E,17E,21-tetraen-3beta-ol, related to iridal-skeleton triterpenoid. Numerous oxidosqualene-cyclized truncated intermediates, including tricyclic, unrearranged tetracyclic with 17alpha/beta exocyclic hydrocarbon side chain, rearranged tetracyclic, and chair-chair-chair tricyclic intermediates, are also isolated from the mutant Saccharomyces cerevisiae
5.4.99.7 C703N site-directed mutagenesis, the mutant shows unaltered product spectrum compared to the wild-type enzyme Saccharomyces cerevisiae
5.4.99.7 C703S site-directed mutagenesis, the mutant shows altered product spectrum compared to the wild-type enzyme, but not as diverse as mutants C703I and C703H Saccharomyces cerevisiae
5.4.99.7 C703T site-directed mutagenesis, the mutant shows altered product spectrum compared to the wild-type enzyme, but not as diverse as mutants C703I and C703H Saccharomyces cerevisiae
5.4.99.7 C703V site-directed mutagenesis, the mutant shows altered product spectrum compared to the wild-type enzyme, but not as diverse as mutants C703I and C703H Saccharomyces cerevisiae
5.4.99.7 F699A/C703I site-directed mutagenesis, inactive mutant Saccharomyces cerevisiae
5.4.99.7 F699M/C703I site-directed mutagenesis, inactive mutant Saccharomyces cerevisiae
5.4.99.7 F699T/C703I site-directed mutagenesis, different oxidosqualene-cyclized truncated intermediates, including tricyclic, unrearranged tetracyclic with 17alpha/beta exocyclic hydrocarbon side chain, rearranged tetracyclic, and chair-chair-chair tricyclic intermediates, are isolated from the mutant Saccharomyces cerevisiae

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
5.4.99.7 (3S)-2,3-epoxy-2,3-dihydrosqualene Saccharomyces cerevisiae
-
lanosterol
-
?

Organism

EC Number Organism UniProt Comment Textmining
5.4.99.7 Saccharomyces cerevisiae
-
gene ERG7
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5.4.99.7 (3S)-2,3-epoxy-2,3-dihydrosqualene
-
Saccharomyces cerevisiae lanosterol
-
?

Synonyms

EC Number Synonyms Comment Organism
5.4.99.7 ERG7
-
Saccharomyces cerevisiae
5.4.99.7 OSC
-
Saccharomyces cerevisiae
5.4.99.7 Oxidosqualene-lanosterol cyclase
-
Saccharomyces cerevisiae

General Information

EC Number General Information Comment Organism
5.4.99.7 physiological function functional role of the Cys703 residue in stabilizing the bicyclic C-8 cation and the rearranged intermediate or interacting with Phe699 Saccharomyces cerevisiae