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Results 1 - 4 of 4
EC Number Reaction Commentary Reference
Show all pathways known for 2.2.1.9Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.9isochorismate + 2-oxoglutarate = 5-enolpyruvoyl-6-hydroxy-2-succinyl-cyclohex-3-ene-1-carboxylate + CO2 - -
Show all pathways known for 2.2.1.9Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.9isochorismate + 2-oxoglutarate = 5-enolpyruvoyl-6-hydroxy-2-succinyl-cyclohex-3-ene-1-carboxylate + CO2 proposed mechanism for formation of the tetrahedral intermediate in MenD catalysis. The strong interaction at the terminal carboxylate is proposed to restrict the rotation around C2-C2alpha so that no hydrogen bond is formed between C2alpha-OH and N4' of the cofactor throughout the reaction process. This disables the formation of the enamine intermediate and enables the formation of the tetrahedral intermediate. Modeling, overview 745170
Show all pathways known for 2.2.1.9Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.9isochorismate + 2-oxoglutarate = 5-enolpyruvoyl-6-hydroxy-2-succinyl-cyclohex-3-ene-1-carboxylate + CO2 reaction follows a ping-pong bi-bi mechanism 718915
Show all pathways known for 2.2.1.9Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.9isochorismate + 2-oxoglutarate = 5-enolpyruvoyl-6-hydroxy-2-succinyl-cyclohex-3-ene-1-carboxylate + CO2 two-stage mechanism that is primarily driven by the chemical properties of the cofactor thiamine diphosphate 720243
Results 1 - 4 of 4