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36 Cards in this Set

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What are the 4 fates of UDP-Glucose?
1) UDP-Glucuronic Acid

2) Glycogen

3) Glycoproteins, Polysaccharides, Gal Metab.

4) Glucose 1 P
What is the net anaerobic glucose reaction?
Glucose + 2P + 2ADP --> 2 Lactate + 2ATP + 2H20
What is the net aerobic glycolysis reaction?
Glucose + 2P + 2ADP +2NAD --> 2 Pyruvate +2ATP +2NADH + 2H+ +2H20
What is the investment phase of glycolysis?
Glucose --> G6P (requires ATP) --> F6P --> F1,6BP (requires ATP)

-need to put in 2 ATP
Why do we use F16BP instead of G16BP?
Because we want to get symmetric products (two 3 carbon molecules)
What is the second phase of glycolysis? How much ATP does it produce?
G3P & DHAP --> 13BPG --> 3PG (generates ATP) --> 2PG --> P-enolpyruvate --> Pyruvate (generates ATP)

-4 ATP made
Red cells lack _______, so they depend on ______ for ATP production?
-mitochondria

-glycolysis
A woman with unstable red blood cells & anemia has a problem with what?
glycolysis
How does glycolysis provide energy for exercise?
-starts with ATP already present --> uses anaerobic glycolysis (2 mins) --> uses aerobic glycolysis + TCA
What are the 3 fates of G6P?
1) Pentose 5-Phosphate (nucleotides & NADPH)

2) Pyruvate (can go to lactate)

3) Glycogen
Dihydroxyacetone phosphate provides intermediates for ________ synthesis
lipid
Dihydroxyacetone phosphate can be converted to phosphatidic acid which is a precursor to ______ & ______
-triacylglycerol

-phospholipids
1,3 BPG generates _________, which regulates hemoglobin. Which enzyme does this conversion?
-2,3 BPG
-bisphosphoglycerate mutase
We can generate ______ from 3 phosphoglycerate?
Serine (amino acids)
What does G3P dehydrogenase catalyze? What does it require?
-G3P --> 1,3BPG

-requires P & NAD+
What does arsenic do?
Targets G3P dehydrogenase and pretends to be phosphate
How do we regenerate NAD+ back from G3P dehydrogenase reaction under anaerobic conditions?
-Conversion of Pyruvate --> Lactate by LDH
G3P dehydrogenase shows ______ cooperativity. What does this mean?
-negative

-means enzyme is less sensitive to changes in substrate concentration --> always wants to do glycolysis
What do oxidizing reactions use ____ and reduce it to _____ to oxidize the substrate
NAD+

NADH
Is there more NAD+ or NADH in the cell?
NAD+ because that is the form it gets used
Pellagra
-Selective deficiency of niacin (nicotinic acid)

-NAD formed from niacin (member of VItamin B familiy)

-D cubed --> Dimentia, Dirreah, Dermetitis
The regulation of glycolysis occurs at steps that are far from _______
equilibrium
Which enzymes are regulated (irreversible) in glycolysis & what regulates them?
1) hexokinase (neg: G6P)

2) PFK-1 (pos: AMP, neg: ATP & citrate)

3) Pyruvate Kinase (pos: F16BP)
What is the key regulatory enzyme/step in glycolysis?
F6P --> F16BP by PFK-1
Under resting conditions, PFK-1 is strongly _________
inhibited
Rate of PFK-1 is determined by amount of ___________ (pos. regulator), especially in liver
Fructose-2,6-Bisphosphate
Fructose-2,6-Bisphosphate is made from ________ by ________
-F6P

-PFK-II
Which phosphatases change F26BP & F16BP back to F6P?
-Phosphatase I & Phosphatase II
How is PFK2 regulated by insulin?
-when PFK2 phosphorylated it goes from kinase --> phosphatase which changes F26BP --> F6P: TURNS OFF PK1

-Insulin activates phosphatase to take phosphate off of PFK2 --> turns it back into kinase --> makes F6P into F26BP: TURNS ON PFK1
Deficiencies in glycolysis mainly affect _____ & _______
-red cells

-skeletal muscle
Pyruvate can be made into lactate, go into TCA or be made into _______
amino acids
2-Deoxyglucose affects _________ by generating neg. feedback inhibition
hexokinase
Fluroide inhibits _______
Enolase
________ is the most common enzyme defect in glycolysis
Pyruvate Kinase
How come pyruvate kinase can be defective in red blood cells & normal in other tissues?
-PK comes in 4 isoenzymes: M1, M2, L & R
Patient has defect in Muscle PFK1, why do they not have anemia?
Because there are 3 PFK enzymes --> Red cells have mix of the 3, so they're ok