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Results 1 - 10 of 10
EC Number BRENDA No. Title Journal Volume Pages Year Organism PubMed ID
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47748774 Identification of key amino acid residues determining product specificity of 2,3-oxidosqualene cyclase in Oryza species New Phytol. 218 1076-1088 2018 Oryza sativa Japonica Group 29528490
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47748774 Identification of key amino acid residues determining product specificity of 2,3-oxidosqualene cyclase in Oryza species New Phytol. 218 1076-1088 2018 Oryza sativa Japonica Group Zhonghua 11 29528490
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47653405 Directed evolution experiments reveal mutations at cycloartenol synthase residue His477 that dramatically alter catalysis Org. Lett. 4 4459-4462 2002 Arabidopsis thaliana 12465912
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47715239 Directed evolution to investigate steric control of enzymatic oxidosqualene cyclization. An isoleucine-to-valine mutation in cycloartenol synthase allows lanosterol and parkeol biosynthesis J. Am. Chem. Soc. 121 9887-9888 1999 Saccharomyces cerevisiae -
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47714739 Histidine residue at position 234 of oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae simultaneously influences cyclization, rearrangement, and deprotonation reactions ChemBioChem 6 1177-1181 2005 Saccharomyces cerevisiae 15915534
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47713760 Oxidosqualene Cyclase Residues that Promote Formation of Cycloartenol, Lanosterol, and Parkeol We are grateful to Bridget M. Joubert for advice regarding mutagenesis. We thank Elizabeth A. Hart for an authentic parkeol standard, and for chromatographic and spectroscopic information. This research was funded by the National Institutes of Health (grant no. AI 41598) and the Robert A. Welch Foundation (grant no. C-1323). M.M.M. was an American Society of Pharmacognosy Undergraduate Fellow. M.J.R.S. was a Robert A. Welch Fellow and was supported by an NIH Biotechnology Training Grant (grant no. T32 GM08362). Angew. Chem. 39 4090-4092 2000 Saccharomyces cerevisiae 11093215
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47682344 Plant lanosterol synthase: divergence of the sterol and triterpene biosynthetic pathways in eukaryotes Plant Cell Physiol. 47 673-677 2006 Lotus japonicus 16531457
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47728425 Protein engineering of Saccharomyces cerevisiae oxidosqualene-lanosterol cyclase into parkeol synthase Org. Lett. 14 5222-5225 2012 Saccharomyces cerevisiae 23043506
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47714021 Protostadienol synthase from Aspergillus fumigatus: functional conversion into lanosterol synthase Biochem. Biophys. Res. Commun. 391 899-902 2010 Aspergillus fumigatus 19951700
Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.47716421 Triterpene cyclases from Oryza sativa L.: cycloartenol, parkeol and achilleol B synthases Org. Lett. 13 2678-2681 2011 Oryza sativa 21526825
Results 1 - 10 of 10