Metabolism Reactions Flashcards

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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)

A

Hexokinase

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

A

ALT

25
Q

O2 –> O2* (reactive species, superoxide)

A

NADPH

26
Q

O2* –> H2O2

A

Superoxide dismutase

27
Q

H2O2 –> HOCL

A

Myeloperoxidase

28
Q

Glucose –> Sorbitol

A

Aldose Reductase

29
Q

Sorbitol –> Fructose

A

Sorbitol Dehydrogenase

30
Q

Ornithine + Carbamoyl Phosphate –> Citrulline

A

Ornithine Transcarbamylase

31
Q

CO2 + NH3 –> Carbamoyl Phosphate

A

Carbamoyl Phosphate Synthetase I (rate-limiting of urea cycle)

32
Q

Homocysteine + B6 –> Cystathionine –> Cysteine

A

Cystathionine Synthase

33
Q

Homocysteine + B12 –> Methionine

A

Homocysteine Methyltransferase

34
Q

Blocked degradation of branched amino acids (Isoleucine, Leucine, Valine)

A

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
Q

Glycogen –> Glucose

A

Glycogen Phosphorylase (upregulated by Glucagon, Calcium, Calcium-calmodulin in muscle during contraction)

36
Q

Glucose –> Glycogen

A

Glycogen Synthase (Upregulated by Insulin)

37
Q

Fed State (Insulin release)

A

Glycolysis and aerobic respiration

38
Q

Fasting State (Glucagon release) or Adrenaline

A

Hepatic glycogenolysis (major), Hepatic Gluconeogenesis, Adipose release of free fatty acids