AA Metabolism Khan Flashcards

1
Q
  1. T or F: AA’s maintain blood pH levels
A
  1. True
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2
Q
  1. What are proteins that undergo extensive synthesis and degradation in reticulocytes?
A
  1. Heme Products
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3
Q
  1. T or F: heme has a long half life
A
  1. F
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4
Q
  1. T or F: collagen has a long half life
A
  1. True
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5
Q
  1. What are some factors affecting the rates of protein degradation?
A
  1. Glucocorticoids (increase degradation), thyroid hormones (protein turnover), insulin
    (protein synthesis), lysosomes (proteolysis), denaturation
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6
Q
  1. What are 4 AA’s degraded via the ubiquitin protesome pathway?
A
  1. P,E,S,T
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7
Q
  1. Presence of what AA’s make protein unstable at N terminus?
A
  1. FLDKR
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8
Q
  1. What are the essential AA’s?
A
  1. Arg, His, Ile, Leu, Lys, Met, Phe, Thr, Trp, Val (MILK RH FTW V)
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9
Q
  1. Lack of a single AA can give rise to wasting disease called?
A
  1. Kwashiorkor (causes edema due to increased osmotic pressure in interstitium)
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10
Q
  1. What are 3 ways AA’s are absorbed?
A
  1. Sodium cotransport, facilitated transport, g‐glutamyl cycle
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11
Q
  1. What is re‐converted to GSH in the g‐glutamyl cycle?
A
  1. Oxyproline
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12
Q
  1. What is hartnups disease?
A
  1. Inability to absorb neutral/aromatic AA’s
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13
Q
  1. What are symptoms of hartnups disease?
A
  1. Dermatitis, diarrhea, dementia
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14
Q
  1. Decrease in cysteine uptake can cause?
A
  1. Cystinuria via oxidation to cystine in urine
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15
Q
  1. How does penicillamine alleviate cystinuria?
A
  1. Reacts with one Cys to form cys‐penicillamine
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16
Q
  1. Do pt. with hartnup or cystinuria have hyperamionacidemia?
A
  1. No, they do not absorb them so they are not in excess in serum
17
Q
  1. What genetic defect in AA absorption is linked with cystinuria?
A
  1. Defective Lys, ornithine, cysteine absorption
18
Q
  1. What are the purely ketogenic AA’s?
A
  1. Leuceine, lysine