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Results 1 - 4 of 4

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
1.1.1.B66	(4E)-5-carbamimidamido-2-iminopent-4-enoic acid + NADPH + H+	-	Bacillus sp. 5mfcol3.1	D-2-dehydroarginine + NADP+	-	?
1.1.1.B66	5-carbamimidamido-2-iminopentanoic acid + NADPH + H+	Bsp5 shows poor activity in the reverse reaction direction	Bacillus sp. 5mfcol3.1	D-arginine + NADP+	-	?
1.1.1.B66	more	enzyme Bsp5 reduces acyclic imino acids produced in situ by a partner oxidase	Bacillus sp. 5mfcol3.1	?	-	-
1.1.1.B66	more	the asymmetric reductase intercepts acyclic imino acids produced in situ by a partner oxidase (Ind4 from Paenibacillus sp.) in a coupled assay, overview. Nonenzymatic hydrolysis of acyclic imino acids gives compounds (4E)-5-carbamimidamido-2-oxopent-4-enoic acid and 5-carbamimidamido-2-oxopentanoic acid. Bsp5 fails to reduce 5-carbamimidamido-2-oxopentanoic acid, and incubation of Bsp5 with 2-methylpyrroline also results in no reaction. Bsp5 lacks imine reducing activity on cyclic substrates. LC-MS analysis of the molecules	Bacillus sp. 5mfcol3.1	?	-	-

Results 1 - 4 of 4

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Release 2023.1 (January 2023)