Thompson 2 Flashcards

0
Q

Glucokinase has a _____ Km. _____ Vmax.

A

High. High.

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1
Q

Glucokinase is located in the _______.

A

Liver and beta cells.

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2
Q

T or F. Phosphorylating metabolic intermediates helps trap shit inside cells.

A

True.

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3
Q

1-3 bpg turns into 2-3 bpg by what enzyme?

A

Mutase.

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4
Q

What inhibits glucokinase?

A

G6P

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5
Q

What activates/inhibites PFK1?

A

Activates: AMP, F26BP
Inhibits: ATP, citrate

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6
Q

What activates/inhibits pyruvate kinase?

A

Activates: F16BP
Inhibits: (phosphorylation) cAMP, alanine

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7
Q

Describe cAMP initiation starting from signal and ending with cAMP activity.

A

Hormone binds with receptor.
Alpha subunit binds with GTP, actives adenylyl cyclasE
Adenylyl cyclase converts atp to camp,
cAMP activates protein kinases

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8
Q

Insulin opposes the _____ cascade. How?

A

insulin inhibits cAMP cascade. insulin binds receptor, receptor gets phosphorylated, which phosphorylates protein kinases with a variety of effects (reversal of glucagon stimulated phosphorylation)

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9
Q

How is PFK1 regulated?

A

High glucagon, high cAMP, high protein kinase A, P inactivates PFK2, FBP2 active, cleaves F16BP to F6P (GNG)

High insulin, low cAMP, active PFK2, makes F26BP, activates PK1, glycolysis

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10
Q

Pyruvate can turn into:
Lactate via __________ (enzyme)
Acetyl CoA via _________
oxaloacetate via ________

A

lactate dehydrogenase
pyruvate dehydrogenase complex
pyruvate carboxylase

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11
Q

Pyruvate to lactate yields ______

A

NAD+.

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12
Q

What is net yield of NADH when glucose to lactate? Net ATP?

A
  1. 2.
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13
Q

Pyruvate –> Acetyl CoA, ____, _____

A

CO2, NADH

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14
Q

What cofactors does PDH complex require?

A
COA
TPP
Lipoic Acid
FAD
NAD+
nad's fad was to tp, and get barbaCOA on his lip.
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15
Q

Describe the tight regulation of PDH complex. Is it cAMP dependent or independent?

A

ACoA and NADH activate a kinase, which phosphorylates PDH, inactivating it.
ADP inhibits the kinase. Or phosphatase comes. PDH not phosphorylated. Thus PDH active.
cAMP independent.

16
Q

Glucose to G6P.

A

hexokinase or glucokinase (liver)

17
Q

G6P to F6P

A

phosphoglucose isomerase

18
Q

F6P to F16BP.

A

phosphofructokinase 1 PFK1

19
Q

F16BP to G3P and DHAP.

A

aldolase.

20
Q

DHAP to G3P.

A

Triose phosphate isomerase

21
Q

F6P to F26BP. What does F26BP upregulate?

A

PFK2. upregulates PK1.

22
Q

G3P to 1,3 Bisphosphoglycerate.

A

G3P dehydrogenase.

23
Q

1,3 BPG to 2,3 BPG.

A

Mutase.

24
Q

1,3 BPG to 3 Phosphoglycerate.

A

Phosphoglycerate kinase.

25
Q

3 Phosphoglycerate to 2 phosphoglycerate.

A

phosphoglycero mutase.

26
Q

2 phosphoglycerate to phosphoenolpyruvate (PEP).

A

Enolase.

27
Q

PEP to pyruvate.

A

pyruvate kinase 1.

28
Q

What is the net gain of one ACoA into TCA?

A

3 NADH
1 FADH2
1 GTP

29
Q

What is the net gain of pyruvate to ACoA?

A

NADH.

30
Q

Citrate is a precursor for ______.

A

FA, cholesterol. (anapleurotic).

31
Q

Citrate inhibits what enzyme in glycolysis?

A

PFK1.

32
Q

What inhibits isocitrate dehydrogenase? Activates it.

A

inhibits: high energy shit, NADH and ATP.
activates: ADP, Ca2+

33
Q

What inhibits alphaketoglutarate dehydrogenase complex?

A

NADH, succinyl coa

34
Q

What are the cofactors of PDH and aketoglutarate DH complex?

A

nad’s fad was tp’ing and barbaCOA on his Lips.

35
Q

T or F. Amino acids can be building blocks for aketoglutarate, succinyl coa, fumarate, OAA and pyruvate.

A

True.