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Results 1 - 10 of 126

EC Number	Substrates	Commentary Substrates	Products	Commentary (Products)	Reversibility
2.3.1.74	(2RS)-methylmalonyl-CoA + n-hexanoyl-CoA	-	triketide lactone + 6-ethyl-4-hydroxy-3,5-dimethyl-2-pyrone	-	?
2.3.1.74	2 malonyl-CoA + 2 stearoyl-CoA	-	6-heptadecyl-4-hydroxy-2H-pyran-2-one + 4-hydroxy-6-(2-oxononadecyl)-2H-pyran-2-one + 2 CoA + 2 CO2	-	?
2.3.1.74	2 malonyl-CoA + acetyl-CoA	poor substrate	4-hydroxy-6-methyl-2-pyrone + 3 CoA + 2 CO2	i.e. triacetic acid lactone	?
2.3.1.74	2 malonyl-CoA + acetyl-CoA	-	4-hydroxy-6-methyl-2-pyrone + 3 CoA + 2 CO2	-	?
2.3.1.74	3 malonyl-CoA + 4-cinnamoyl-CoA	-	4 CoA + pinocembrin chalcone + 3 CO2	-	?
2.3.1.74	3 malonyl-CoA + 4-coumaroyl-CoA	-	4 CoA + naringenin chalcone + 3 CO2	-	?
2.3.1.74	3 malonyl-CoA + 4-coumaroyl-CoA	100% activity	4 CoA + naringenin chalcone + 3 CO2	-	?
2.3.1.74	3 malonyl-CoA + 4-coumaroyl-CoA	the enzyme effectively yields naringenin as a dominant product at pH 7.5	4 CoA + naringenin chalcone + 3 CO2	-	?
2.3.1.74	3 malonyl-CoA + 4-coumaroyl-CoA	the reaction has highest efficiency with isoform CHS1. 4-coumaroyl-CoA is the best substrate for isoform CHS1	4 CoA + naringenin chalcone + 3 CO2	-	?
2.3.1.74	3 malonyl-CoA + 4-coumaroyl-CoA	when incubated with 4-coumaroyl-CoA and malonyl-CoA as substrates at pH 7.5, the enzyme catalyzes the formation of naringeninchalcone as a major product, along with 4-hydroxybenzalacetone. At pH 9.5, the enzyme effectively yields 4-hydroxybenzalacetone as a dominant product, along with naringenin chalcone	4 CoA + naringenin chalcone + 3 CO2	-	?

Results 1 - 10 of 126