21. Movement problems typically become apparent by age 2 in people with triosephosphate isomerase deficiency. 22. The protein encoded by this gene belongs to the aconitase / IPM isomerase family. 23. The deficiency of phosphohexose isomerase can lead to a condition referred to as hemolytic syndrome. 24. If it gives off one product, it is solely enoyl Co-Al isomerase . 25. It is formed through the conversion of maleylacetoacetate into fumarylacetoacetate by the enzyme maleylacetoacetate isomerase . 26. People with triosephosphate isomerase deficiency often do not survive past childhood due to respiratory failure. 27. IPP is isomerized to the allylic ester dimethylallyl pyrophosphate ( DMAPP ) by IPP isomerase . 28. We chose the article Isomerase for review. 29. Methylmalonyl-CoA mutase is a member of the isomerase subfamily of adensylcobalamin-dependent enzymes. 30. Prolyl isomerase folding can be autocatalytic and therefore the speed of folding depends on reactant concentration.
