Metabolism Reactions Flashcards

(38 cards)

1
Q

Glucose –> Phosphoenolpyruvate (What process is this?)

A

Initial steps of Glycolysis

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2
Q

Phosphoenolpyruvate –> Pyruvate (Enzyme)

A

Pyruvate Kinase

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3
Q

Pyruvate –> Oxaloacetate (Enzyme)

A

Pyruvate Carboxylase

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4
Q

Pyruvate –> Lactic acid (Enzyme)

A

Lactate Dehydrogenase

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5
Q

Pyruvate –> Acetyl CoA, which enters TCA cycle (Enzyme)

A

Pyruvate Dehydrogenase

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6
Q

Galactose –> Galactose 1-Phosphate

A

Galactokinase (defiency = mild galactosemia)

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7
Q

Galactose -1-Phosphate –> Glucose 1-phosphate

A

Galactose 1-phosphate uridyltransferase (defiency severe galactosemia)

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8
Q

Glucose –> Glucose 6-Phosphate (Liver, Beta cells of pancreas)

A

Glucokinase

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9
Q

Glucose-6-phosphate –> Glucose

A

Glucose-6-phosphatase (Von Gierke’s)

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10
Q

Glucose-6-phosphate –> 6-phosphogluconate/6phosphogluconolactone

A

Glucose 6-phosphate dehydrogenaase (G6PD) (Deficiency = no HMP shunt)

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11
Q

Fructose -6phosphate –> Fructose 1,6, bisphosphate

A

Phosphofructokinase -1 (Defiency= no glycolysis)

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12
Q

Fructose 1,6, bisphosphate –> Fructose 6-phosphate

A

Fructose 1,6, bisphosphatase

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13
Q

Fructose –> Fructose 1-phosphate

A

Fructokinase (deficiency = essential fructosuria)

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14
Q

Fructose 1-phosphate –> Glyceraldehyde/DHAP

A

Aldolase B

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15
Q

HMG CoA –> Mevalonate –> Cholesterol

A

HMG CoA reductase

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16
Q

Oxaloacetate –> Phosphoenolpyruvate (PEP)

A

PEP Carboxykinase

17
Q

Isocitrate –> alpha-ketoglutarate (Within TCA cycle)

A

Isocitrate Dehydrogenase

18
Q

Oxaloacetate –> Citrate (TCA Cycle)

A

Citrate Synthase

19
Q

Alpha-ketoglutarate –> Succinyl Co-A

A

Alpha ketoglutrate Dehydrogenase

20
Q

Ornithine –> Citrulline (Urea Cycle)

A

Ornithine Transcarbamylase

21
Q

Glucose –> Glucose 6-Phosphate (Tissues, NOT liver/beta cells of pancreas)

22
Q

What are the enzymes and end product when the body is in a FASTING state

A

Increased glucagon, CAMP, Protein Kinase A, FBPase-2 –> More Gluconeogenesis

23
Q

What are the enzymes and end product when the body is in a FED state

A

Increased insulin, Decreased CAMP, PKA, FBPase-2 –> More Glycolysis

24
Q

Pyruvate –> Alanine

25
O2 --> O2* (reactive species, superoxide)
NADPH
26
O2* --> H2O2
Superoxide dismutase
27
H2O2 --> HOCL
Myeloperoxidase
28
Glucose --> Sorbitol
Aldose Reductase
29
Sorbitol --> Fructose
Sorbitol Dehydrogenase
30
Ornithine + Carbamoyl Phosphate --> Citrulline
Ornithine Transcarbamylase
31
CO2 + NH3 --> Carbamoyl Phosphate
Carbamoyl Phosphate Synthetase I (rate-limiting of urea cycle)
32
Homocysteine + B6 --> Cystathionine --> Cysteine
Cystathionine Synthase
33
Homocysteine + B12 --> Methionine
Homocysteine Methyltransferase
34
Blocked degradation of branched amino acids (Isoleucine, Leucine, Valine)
Maple Syrup Urine Disease, increased alpha-ketoacids in blood. Sxn: CNS defects, intellectual disability, death, urine smells like maple syrup/burnt sugar. Tx: Restrict isoleucine, leucine, valine, supplement with thiamine
35
Glycogen --> Glucose
Glycogen Phosphorylase (upregulated by Glucagon, Calcium, Calcium-calmodulin in muscle during contraction)
36
Glucose --> Glycogen
Glycogen Synthase (Upregulated by Insulin)
37
Fed State (Insulin release)
Glycolysis and aerobic respiration
38
Fasting State (Glucagon release) or Adrenaline
Hepatic glycogenolysis (major), Hepatic Gluconeogenesis, Adipose release of free fatty acids