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