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Hypothetical bi-grain with microelectrodes . Parameters used in the finite element calculations

Hypothetical binary complex formed between dihydroxyacetone phosphate and triose-phosphate isomerase constructed from published X-ray coordinates for the chicken muscle enzyme

Hypothetical binding isotherm .

Hypothetical binding mode of demethylated methoxychlor metabolites.

Hypothetical binding of .

Hypothetical binding site model for GABA-antagonistic insecticides established by Ozoe et al, reproduced with permission from the author 165 . The picture .

Hypothetical binding sites between

Hypothetical biogenesis of fawcettimine

Hypothetical biogenesis of illudinine.

Hypothetical biogenesis of lycodine and phlegmarine-type alkalooids

Hypothetical biogenesis of quassinoids References, pp. 93—102

Hypothetical biogenetic relationships of the bisindolylmaleimides

Hypothetical biogetetic route of Lycopodium alkaloids

Hypothetical biological binding site.

Hypothetical biosynthesis and reactions of dregeanin

Hypothetical biosynthesis of -dicarboxyaziridine.

Hypothetical biosynthesis of anabasine and anabatine.

Hypothetical biosynthesis of calystegine A5.

Hypothetical biosynthesis of Carapa lactones

Hypothetical biosynthesis of lycopodine.

Hypothetical biosynthesis of nimbin derivatives References, pp. 93—102

Hypothetical biosynthesis of phragmalin References, pp. 93—102

Hypothetical Biosynthesis of Retronecine via a Dimer

Hypothetical Biosynthesis ofGinsenosideAglycones. The biosynthesis of ginsenoside aglycones begins with the formation of squalene-2,3-oxide by a flavoprotein-containing epoxide synthase .

Hypothetical biosynthetic example of how reversibility of the acylation step and high specificity of the condensation stage promotes elongettion of the correct acyl intermediate. Here, incomplete reductive processing by the previous module results in acylation of the downstream KS with a substrate incapable of being elongated. However, the reversible nature of the acylation allows complete reductive processing to be conducted, ultimately yielding an a, P-unsaturated intermediate—the correct substrate of KS domains in clade IX—which can be successfully elongated



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