amino acid degradation Flashcards

1
Q

pyruvate family

A

alanine, serine, glycine

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2
Q

alanine breakdown

A

alanine to pyruvate
E: alanine aminotransferase (ALT)
alpha-KG to glutamate

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3
Q

serine breakdown

A
serine to pyruvate
releases unstable aminoacrylate
E: serine dehydratase (SDH)
releases H2O
requires B6 PLP complex (vit B6)
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4
Q

glycine breakdown 2 pathways

A

1) glycine to serine, then to pyruvate

2) glycine degraded directly

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5
Q

glycine to serine

A

glycine to serine
E: serine hydroxymethyltransferase (SHMT)
THF to N5, N10 - Methylene THF + H2O
requires B6

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6
Q

glycine cleavage system

A

Glycine breakdown
E: glycine oxidase in reverse
requires PLP and lipoic acid

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7
Q

what is PLP?

A

active form of vit B6

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8
Q

asparagine breakdown

A
1) asparagine to aspartate
E: asparaginase
releases NH4+
2) aspartate + alpha-KG to glutamate + oxaloacetate
E: aspartate aminotransferase (AST)
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9
Q

which 2 amino acids yield oxaloacetate?

A

Aspartate (Asp-D) and Asparagine (Asn-N)

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10
Q

alpha-KG family

A

glutamate and glutamine

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11
Q

glutamine breakdown

A
1) glutamine to glutamate
E: glutaminase
H2O to NH4+
2) Glutamate to alpha-KG
E: glutamate dehydrogenase (GDH)
NADP+ to NADPH + NH4+
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12
Q

glutamate breakdown

A

glutamate to alpha-KG
E: glutamate dehydrogenase (GDH)
NADP+ to NADPH + NH4+

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13
Q

succinyl-CoA family

A

Methionine, Isoleucine, and Valine

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14
Q

arginine and proline

A

get broken down, they’re being processed

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15
Q

methionine breakdown

A

methionine can produce cysteine then propionyl-CoA

SAM is used as a methyl donor

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16
Q

BCAT

A

branched-chain amino acid aminotransferase

17
Q

leucine breakdown

A
1) leucine to alpha-ketoisocaproate
E: BCAT
alpha-KG to G
2) BCKDH, fatty acid oxidation
to become acetoacetate and acetyl-CoA
18
Q

phenylalanine/tyrosine

A

1) phenylalanine to tyrosine
E: phenylalanine-4-monooxygenase
2) tyrosine to rho-hydroxy-phenylpyruvate
E: tyrosine transaminase
alpha-KG to Glu
then dioxygenases to acetoacetate + fumarate

19
Q

tyrosine synthesis

A

from phenylalanine

20
Q

cysteine synthesis

A

from methionine

21
Q

glutmate

A

from glutamine and vice versa

22
Q

serine and glycine role

A

1 carbon donation (they form pyruvate!)

23
Q

amino acid products

A

1) physiologically active amines
2) glutathione (management of S-S bonds)
3) heme
4) NAD+

24
Q

glutamate produces

A

GABA and Histamine

25
Q

tyrosine produces

A

Catecholamines

EX: Dopa, Dopamine, Norepinephrine –> (uses SAM) Epinephrine

26
Q

glycine produces

A

heme