Carbohydrates Flashcards

1
Q

Glucose transporter found in the brain

A

GLUT 1 and GLUT 3

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2
Q

Glucose transporter found in RBCs

A

GLUT 1

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3
Q

Glucose transporter with dual function (uptake and release)

A

GLUT 2

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4
Q

Glucose transporter found in heart and skeletal muscle

A

GLUT 4

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5
Q

Glucose transporter found in SI and aids in absorption of fructose

A

GLUT 5

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6
Q

Major pathway for glucose metab that converts glucose into 3 carbon compounds to provide energy

A

Glycolysis

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7
Q

Major pathway for formation of ATP

A

Citric acid cycle | TCA | Kreb’s Cycle

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8
Q

Process of synthesizing glucose from non-carbohydrate precursors in order to prevent hypoglycemia

A

Gluconeogenesis

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9
Q

Pathway that produces ribose-5-phosphate required for biosynthesis of nucleotides

A

Pentose Phosphate Pathway | HMP shunt

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10
Q

Pathways (3) that occur both in Cytosol and Mitochondria

A

Heme Synthesis
Urea cycle
Gluconeogenesis

(HUG takes TWO)

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11
Q

Pathways (5) that occur in Mitochondria only

A
Ketogenesis
Oxidative phosphorylation
B-oxidation
Acetyl CoA production
TCA cycle
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12
Q

Pathways (2) that occur in Cytosol only

A

Glycolysis

HMP shunt

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13
Q

End products of glycolysis.

A

2 molecules of either pyruvate or lactate

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14
Q

Rate limiting step and enzyme of glycolysis

A

Fructose 6-phosphate → Fructose 1,6-biphosphate

Phosphofructokinase-1

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15
Q

Inhibited by Glucose-6-P

A

Hexokinase

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16
Q

Inhibited by Fructose-6-P

A

Glucokinase

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17
Q

Picture of Hexokinase:

___ Km ; ____ Vmax ; _____ Affinity

A

Low Km ; Low Vmax

High Affinity

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18
Q

Picture of Glucokinase:

___ Km ; ____ Vmax ; _____ Affinity

A

High Km ; High Vmax

Low Affinity

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19
Q

Net ATP from Glycolysis using Malate aspartate shuttle

A

7 ATPs

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20
Q

Net ATP from Glycolysis using Glycerophosphate Shuttle

A

5 ATPs

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21
Q

(3) Irreversible steps of Glycolysis

A

Step 1. Glucose phosphorylation
Step 3. Fructose-6-Phosphate phosphorylation
Step 10. Pyruvate formation

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22
Q

Most important activator of PFK 1

A

Fructose 2,6 biphosphate

A product of PFK 2, feed forward regulation

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23
Q

Conversion of Pyruvate to Lactate during Anaerobic glycolysis uses what enzyme?

A

Lactate dehydrogenase

24
Q

Conversion of Pyruvate to Acetyl CoA in Kreb’s cycle uses what enzyme?

A

Pyruvate dehydrogenase

25
Conversion of Pyruvate to Oxaloacetate in Gluconeogenesis uses what enzyme?
Pyruvate Carboxylase | Addition of Carbon
26
Most common cause of congenital lactic acidosis
Pyruvate dehydrogenase deficiency
27
Most common enzyme defect in glycolysis
Pyruvate kinase deficiency
28
Products of Citric Acid cycle
1 FADH2 1 GTP 2 CO2 3 NADH
29
Rate limiting step and enzyme in Citric Acid Cycle
Isocitrate → a-ketoglutarate Isocitrate dehydrogenase
30
Process of synthesizing glucose from non-carbohydrate precursors in order to prevent hypoglycemia
Gluconeogenesis
31
Substrate(s) of Gluconeogenesis
Intermediates of glycolysis and TCA except Acetyl CoA Glycerol and Propionyl CoA Lactate Glucogenic Amino acids
32
Rate limiting step and enzyme of Gluconeogenesis?
Fructose 1,6 biphosphate → Fructose 6-phosphate Fructose 1,6 biphosphatase (vs. glycolysis: Phosphofructokinase-1)
33
An inhibitor of Fructose 1,6 biphosphatase
Fructose 2,6 biphosphatase
34
Energy required in gluconeogenesis: | ____ ATP ____ GTP ____ NADH ____ FADH
4 ATP 2 GTP 2 NADH 0 FADH
35
Primary glycosidic bond is at
alpha ( 1→4)
36
Branched points occur at
alpha ( 1 → 6 )
37
Rate limiting step and enzyme of glycogenolysis
Shortening of glycogen chains Glycogen phosphorylase and debranching enzyme
38
Rate limiting step and enzyme of glycogenesis
Elongation of glycogen chains Glycogen synthase Branching enzyme
39
Glycogen storage disease that presents with ↑ glycogen in lysosomes due to deficient ______ enzyme
Pompe disease | Lysosomal acid maltase
40
Glycogen storage disease that presents with ↑ glycogen in liver and renal tubule due to deficient ______ enzyme
Von Gierke disease | Glucose-6-phosphatase
41
Glycogen storage disease that presents with ↑ limit dextrin, hepatomegaly and hypoglycemia due to deficient ______ enzyme
Cori disease | Debranching enzyme
42
Glycogen storage disease that presents with ↑ polysaccharide with few branch points due to deficient ______ enzyme
Andersen disease | Branching enzyme
43
Glycogen storage disease that presents with ↑ muscle glycogen due to deficient ______ enzyme
McArdle syndrome | Muscle phosphorylase
44
Glycogen storage disease that presents with mild hypoglycemia and hepatomegaly due to deficient ______ enzyme
Hers disease | Liver phosphorylase
45
(4) Hexoses
Glucose Galactose Mannose Fructose
46
(3) Pentoses
Ribose Ribulose Xylulose
47
(3) Disaccharides
Sucrose Lactose Maltose
48
Galactose metab disease that presents with galactosemia, diarrhea, vomiting, mental retardation, and premature ovarian failure due to deficient ______ enzyme
Classic galactosemia | Galactose 1 phosphate uridyl transferase deficiency (GALT)
49
Enzyme used in conversion of Glucose to sorbitol
Aldolase reductase
50
What pathway is affected in Essential pentosuria?
Uronic Acid Pathway
51
What enzyme is deficient in Essential pentosuria?
Xylulose Reductase deficiency
52
Substrate of pentose phosphate pathway
GLucose 6 phosphate
53
Rate limiting enzyme in HMP shunt?
Glucose 6 phosphate dehydrogenase
54
(2) products of PPP?
NADPH | Ribose-5-phosphate
55
What phase in HMP shunt is NADPH produced?
First Phase. | Oxidative and irreversible
56
(3) amino acids that composed Glutathione
Glycine Cysteine Glutamate