4kk2: Difference between revisions
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[[Category: Bhosle, R]] | [[Category: Bhosle, R]] | ||
[[Category: Chowdhury, S]] | [[Category: Chowdhury, S]] | ||
[[Category: EFI, Enzyme Function Initiative]] | |||
[[Category: Evans, B]] | [[Category: Evans, B]] | ||
[[Category: Gerlt, J A]] | [[Category: Gerlt, J A]] | ||
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[[Category: Hillerich, B]] | [[Category: Hillerich, B]] | ||
[[Category: Imker, H J]] | [[Category: Imker, H J]] | ||
[[Category: Love, J]] | [[Category: Love, J]] | ||
[[Category: Obaidi, N F.Al]] | [[Category: Obaidi, N F.Al]] |
Revision as of 09:47, 31 January 2018
Crystal structure of a chimeric FPP/GFPP synthase (TARGET EFI-502313c) from Artemisia spiciformiS (1-72:GI751454468,73-346:GI75233326), apo structureCrystal structure of a chimeric FPP/GFPP synthase (TARGET EFI-502313c) from Artemisia spiciformiS (1-72:GI751454468,73-346:GI75233326), apo structure
Structural highlights
Function[CHRDS_ARTSI] Condenses two molecules of dimethylallyl diphosphate (DMAPP) to produce mainly an irregular monoterpene, chrysanthemyl diphosphate (CPP) and lower amounts of a branched monoterpene, lavandulyl diphosphate (LPP). CPP is a precursor of the pyrethrin insecticides. When incubated with isopentenyl diphosphate (IPP) and DMAPP, catalyzes three competing isoprenoid condensation reactions, a chain elongation to give geranyl diphosphate (GPP), a cyclopropanation to give CPP and a branching to give LPP.[1] References
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