Term 1- Lec 11- Enzyme Kinetics Flashcards
Initial rxn rate (Vo or Vi)
Rate of reaction measured over a brief initial period while [S] is till high and [P] is still low
Statin drugs
Are competitive inhibitors of cholesterol synthesis, thus they reduce the amount of cholesterol synthesized and lower plasma cholesterol concentration
Equation for Km
Km is equal to the amount of substrate (y-axis) at (Vmax/2)
The rate of the reaction is:
The value for Vo
Rxn is said to be what order when [S]«<Km
First order. Vo and [S] are proportional, if you double [S] you get double Vo
Rxn is said to be what order when [S]»>Km
Zero order. Enzyme is saturated, all enzyme active sites are filled
Vmax
Vmax is NOT a constant, is dependent on [E]
Kcat
Represents the efficiency of an enzyme. Measures the formation of product per second and per molecule.
Competitive inhibitors
- Have similar structure to the substrate
* Compete with the substrate for the active site
Km
Km IS a constant, thus an intrinsic property of an enzyme. Inversely related to the binding affinity of an enzyme
High Km
Low affinity for the substrate
Low Km
High affinity for the substrate
Isoenzymes
Isoenzymes are different enzymes that catalyze the same reaction, but differ in everything else (gene, 1º sequence, rxn rates)
An example of isoenzymes and what the produce
Glucokinase and hexokinase. They both produce glucose-6-phosphate
Non-competitive inhibitors
bear little resemblance, if any, to the enzyme’s substrate. Bind at a site other than the active site and cause conformational change that still allows the enzyme to bind substrate, but is less eficient.
Is competitive inhibition reversible
Yes
Is non-competitive inhibition reversible
Yes
Example of a competitive inhibitor
Statins—cholesterol, methanol—anti-freeze
Example of a non-competitive inhibitor
Plavix
Example of a suicide substrate
Disulfiram for aldehyde dehydrogenase
What are suicide substrates
Cannot bind the active site of the target enzyme in the form it is digested. Must be modified through several steps before taking the form that irreversibly binds the target enzyme’s active site