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Results 1 - 10 of 13

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
5.4.99.4	2-Methyleneglutarate	-	Eubacterium barkeri	2-Methylene-3-methylsuccinate	-	?
5.4.99.4	2-Methyleneglutarate	-	Eubacterium barkeri	2-Methylene-3-methylsuccinate	i.e methylitaconate	?
5.4.99.4	2-Methyleneglutarate	r	Eubacterium barkeri	2-Methylene-3-methylsuccinate	-	?
5.4.99.4	2-Methyleneglutarate	r	Eubacterium barkeri	2-Methylene-3-methylsuccinate	i.e methylitaconate	?
5.4.99.4	2-Methyleneglutarate	the equilibrium favours the formation of 2-methyleneglutarate	Eubacterium barkeri	2-Methylene-3-methylsuccinate	i.e methylitaconate	?
5.4.99.4	more	inducible enzyme, participates in the anaerobic conversion of nicotinic acid to equimolar amounts of propionate	Eubacterium barkeri	?	-	?
5.4.99.4	more	enzyme is induced by growth on nicotinic acid and is not detectable in cells grown on glucose	Eubacterium barkeri	?	-	?
5.4.99.4	more	carbon-skeleton rearrangement mechanism. Adenosylcobalamin acts as a carrier for the hydrogen atom that is abstracted from alpha-methyleneglutarate and replaced by the acrylyl group of 2-methyleneglutarate	Eubacterium barkeri	?	-	?
5.4.99.4	(R)-3-[methyl-H3]methylitaconate	-	Eubacterium barkeri	2-methyleneglutarate	-	r
5.4.99.4	(R,Z)-3-methyl[2'-H1]itaconate	-	Eubacterium barkeri	2-methyleneglutarate	-	r

Results 1 - 10 of 13

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Release 2023.1 (January 2023)