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Results 1 - 10 of 11

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
2.1.1.106	more	no activity with methylcobalamin	Streptomyces laurentii	?	-	?
2.1.1.106	more	TsrM does not catalyse substrate H-atom abstraction but probably exploits a radical-based C-methylation mechanism. TsrM catalyzes methyl transfer to all Trp derivatives tested that are substituted on the indole ring	Streptomyces laurentii	?	-	-
2.1.1.106	S-adenosyl-L-methionine + 3-methylindole	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + ?	-	?
2.1.1.106	S-adenosyl-L-methionine + D,L-tryptophan	significant slower reaction rate with D-tryptophan	Streptomyces laurentii	S-adenosyl-L-homocysteine + D,L-2-methyltryptophan	-	?
2.1.1.106	S-adenosyl-L-methionine + D-tryptophan	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + D-2-methyltryptophan	-	?
2.1.1.106	S-adenosyl-L-methionine + L-5-fluoro-tryptophan	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + L-5-fluoro-2-methyltryptophan	-	?
2.1.1.106	S-adenosyl-L-methionine + L-5-hydroxy-tryptophan	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + L-5-hydroxy-2-methyltryptophan	-	?
2.1.1.106	S-adenosyl-L-methionine + L-5-methyl-tryptophan	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + L-2,5-dimethyltryptophan	-	?
2.1.1.106	S-adenosyl-L-methionine + L-tryptophan	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + L-2-methyltryptophan	-	?
2.1.1.106	S-adenosyl-L-methionine + melatonin	-	Streptomyces laurentii	S-adenosyl-L-homocysteine + ?	-	?

Results 1 - 10 of 11

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Release 2023.1 (January 2023)