amino acid metabolism I - Breakdown Flashcards

1
Q

protein sources:

  • stomach- ____ pH denatures proteins and activates ____
  • small intestine
    • ____ in the duodenum cleaves trypsinogen
    • ____ are exopeptidases (chew from N-term)
    • ____ break apart dipeptides
  • ____ ____ , ____ , and ____ can be transported into cells
A
  • low, pepsin
    • enteropeptidase
      • aminopeptidases
      • dipeptidases
  • amino acids, dipeptides, and tripeptides
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2
Q

protein sources: intracellular:

  • the ____
  • the ____
    • N-end rule: N-terminal amino acid identity dermines:
      • polar/charged amino acids have the ____ half-life
A
  • lysosome
  • proteasome
    • rate of ubiquitination
      • shortest
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3
Q

what can we do with individual amino acids:

A

REDUCE - remove nitrogen through the urea cycle

REUSE - make new proteins

RECYCLE - repurpose the carbon skeleton

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4
Q

____ ____ is always the coenzyme for deaminatio

A

pyridoxal phosphate

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5
Q

direction deamination by serine dehydratase:

  • remove H2O = ____
  • add H2O back to remove NH4+ = ____
  • serine is deaminated to form ____
A
  • dehyration
  • deamination
  • pryuvate
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6
Q

most amino acids follow a 2 enzyme mechanism of deamination:

  • step 1: aminotransferases make ____
    • using ____
  • step 2: ____ ____ releases an ____ ion
    • and rengerates ____
A
  • glutamate
    • alpha-ketoglutarate
  • glutamate dehydrogenase, ammonium
    • alpha-ketoglutarate
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7
Q

Aspartate Aminotransferase (AST) - in ____

Serum Glutamate-Oxaloacetate Transaminase (SGOT) - in ____

catalyzes the interconversion of ____ and ____

A

cells

serum

aspartate and oxaloacetate

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8
Q

Alanine Aminotransferase (ALT) - in ____

Serum Glutamate-Pyruvate Transaminase (SGPT) - in ____

catalyzes the interconversion of ____ and ____

A

cells

serum

alanine and pyruvate

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9
Q

urea cycle:

  • NH4+ is a toxic byproduct of amino acid ____
  • NH4+ can be converted to urea in the ____
  • urea is transported to the ____ to be excreted from the body
  • muscle cells transport their NH4+ to the liver via ____ and the action of ____
  • all other cells transport their NH4+ to the liver via ____
    • ____ ____ adds an amine to Glu to make Gln
    • ____ in the liver removes an amine from Gln to make Glu
A
  • catabolism
  • liver
  • kidneys
  • alanine, ALT
  • glutamine
    • glutamine synthetase
    • glutaminase
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10
Q

urea is composed of 4 pieces

A

NH2 from glutamate

carbonyl from water

central carbon from HCO3

NH2 from aspartate

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11
Q

urea cycle step 1:

  • ____ ____ ____ ____ (CPSI) combines NH3 and CO2 to make ____ ____ using 2 ATP
    • creation of carbamoyl phosphate is the ____ step in urea cycle
    • ____ is an allosteric activator of CPSI
A
  • carbamoyl phosphate synthetase I, carbamoyl phosphate
    • committed
    • NAG
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12
Q

urea cycle step 2:

  • ____ + ____ ⇒ citrulline
    • ornithine and citrulline are ____ amino acids
    • ornithine msut move into the ____ to combine with carbamoyl phosphate
    • citrulline is exported to the ____
A
  • ornithine + carbamoyl phosphate
    • nonproteinogenic
    • mitochondira
    • cytoplasm
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13
Q

urea cycle step 3:

  • citrulline + ____ → ____
    • ____ donates NH3
    • rest of aspartate is ____
    • ____ is created
A
  • aspartate → argininosuccinate
    • asparate
    • fumarate
    • arginine
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14
Q

urea cycle step 4:

  • arginine → ____
    • releases ____
    • addition of water when cleaving arginine adds the final ____ of urea
  • ornithine enters into the ____ and continues the cycle
A
  • ornithine
    • urea
    • oxygen
  • mitochondria
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15
Q

urea cycle extra step:

  • fumarate → → OAA uses ____ cycle
  • OAA → Asparate is performed by ____
A
  • TCA
  • AST
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16
Q

which amino acids are glycogenic?

A

glycine, alanine, valine, proline, methionine, serine, cysteine, asparagine, glutamine, arginine, histidine, aspartate, glutamine

17
Q

which amino acids are ketogenic

A

leucine

lysine

18
Q

which amino acids are both glucogenic and ketogenic

A

phenylalanine

isoleucine

threonine

tryptophan

tyrosine

19
Q

amino acids are glucogenic if they are degraded into intermediate molecules that can feed through ____ to reform ____

A

gluconeogenesis

glucose

20
Q

amino acids are ketogenic if they are degraded into intermediate molecules that can

A

be used to create ketone bodies