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30 Cards in this Set

  • Front
  • Back
Give 3 different examples of enzyme regulating mechanisms
Allosteric Regulation, Product Inhibition and Isozyme Expression
What is Allosteric Regulation?
It is conformational changes induced or stabalised by allosteric effectors which alter enzyme activty
Allosteric inhibitors modify the active site of the enzymes so that substrate binding is ??
Reduced and Prevented
What do allosteric activators do?
They modify active site of the enzyme so that the affinity for the substrate is increased
AMP-activated kinase is a 'master' regulator' of fat metabolism. True or False?
False. It is a master regulator of energy metabolism
AMPK is an example of what type of allosteric effector?
Allosteric Activator. It is activated by AMP
Give an example of allosteric inhibition
Phosphofructokinase (PFK)
PFK is inhibited by high [ATP] i.e. at a high energy charge. True or False?
True
Give an example of Product Inhibition
Hexokinase
Hexokinase is inhibited by glucose-6-phosphate. True or False
True
Hexokinase isozymes dont have different kinetic properties. True or False?
False. They do have different kinetic properties
What is the minimal metabolic system?
Two enzymes that communicate via a single intermediate
Control by enzymes over a global steady state. Global steady state is quantified by _________________ __________________.
Control coefficients
What are the control coefficients?
Metabolite control (X) and Pathway flux (J)
Control by metabolites over _______________ _________________ ___________________________
Local system properties
Local steady state is quantifies by ??
Elasticity coefficients
Control by effectors over ___________ _________________ ________________________
Any system property
System sensitivity to effectors is quantified by regulation coefficient. True or False?
False. Quantified by response coefficients
What are the 'main laws' of Metabolic Control Analysis?
Summation and Connectivity Theorems
Control over metabolic flux resides in a single step. True or False?
False. Control over metabolic flux does not reside in a single step but is generally shared between all enzymes in a system
Which enzymes should be manipulated to optimise metabolic fluxes to yield desirable products?
Flux Control
Where should therapeutic drugs be targeted to maintain or restore homeostasis?
Concentration control
Negative Feedback ______________________metabolic systems and Positive feedback _____________________ metabolic systems
inhibits
reinforces
Stable flux or (dampened oscillations) are associated with _________________ feedback while turbo design (explosion or block) is associated with _______________________ feed back
Negative
Positive
Positive feed-forward _______________________ metabolic systems and is associated with __________________ _____________________
Activates
Spike Filter
Glucokinase kinetics allow ________________ ___________________
Glucose sensing
State the differences in substate affinity, dependency and product inhibition between hexokinase and glucokinase
Substrate affinity:
Hexokinase Km=0.1mM Glucokinase K0.5=5mM
Substrate dependency:
Hexokinase= Saturating Glucokinase= Cooperative
Product Inhibition:
Hexokinase= Yes Glucokinase= No
Specific isozyme expression regulates ____________________ reaction and thus influences control of ________________________ _________________________
Hexokinase
Energy Metabolism
Describe glucokinase kinetics in the pancreatic B cell
Blood glucose >5mM , glucose catabolism increases, ATP/ADP increases and insulin release increases
Descibe hexokinase kinetics in the muscle cell
Muscle contraction, ATP/ADP decreases, glucose catabolism increases, ATP/ADP increases