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Results 1 - 5 of 5
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EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.304CoA - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.304CoA very effective competitive inhibitor for the polymerization of 3-hydroxypropionyl-CoA Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.304HBCH2CoA substrate analogue, in which the S-atom in hydroxybutanoyl-CoA is replaced with a CH2 group. HBCH2CoA is a competitive inhibitor of class I and class III PHB synthases. Upon incubation with a synthase acylated with a [3H]-saturated trimer-CoA, i.e. sTCoA, products are the methylene analogue of [3H]-sTCoA, [3H]-sT-CH2-CoA, saturated dimer-[3H]-sD-CO2H, and trimer-acid [3H]-sT-CO2H. HBCH2CoA may be reporting on the termination and repriming process of the synthases, rather than elongation Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.304more no inhibition by bovine serum albumin Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.304N-ethyl-maleimide 1 mM N-ethyl-maleimide for 15 min inhibits the enzyme by 56% Go to the Ligand Summary Page
Results 1 - 5 of 5
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