Lecture 32: Amino Acid Metabolism II Flashcards

1
Q

3 intermediate molecules from Glycolysis used to synthesize amino acids

A

3-PG
PEP
Pyruvate

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2
Q

Intermediate molecules from TCA cycle used to synthesize amino acids

A

a-ketoglutarate

Oxaloacetate

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3
Q

Intermediate molecules from pentose phosphate pathway used to synthesize amino acids

A

Ribose-5-phosphate

Erythrose-4-phosphate

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4
Q

Non essential amino acids include

A
Cysteine C
Alanine A
Asparagine N
Aspartic acid D
Tyrosine Y
Proline P
Glutamic acid E
Glycine G
Serine S
Glutamine Q
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5
Q

Essential amino acids include

A
Histidine
Isoleucine
Leucine
Lysine
Phenylalanine
Threonine
Tryptophan
Valine
(Arginine)
(Methionine)
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6
Q

Oxaloacetate gives rise to ____, which gives rise to what other AAs

A

Aspartate

  • Asparagine
  • Methionine
  • Threonine
  • Lysine
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7
Q

Threonine gives rise to

A

Isoleucine

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8
Q

PEP + Erythrose 4-phosphate give rise to

A

Phenylalanine
Tyrosine
Tryptophan

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9
Q

Phenylalanine gives rise to

A

Tyrosine

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10
Q

Pyruvate gives rise to

A

Alanine
Valine
Leucine

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11
Q

Ribose-5-phosphate gives rise to

A

Histidine

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12
Q

a-ketoglutarate gives rise to ___, which gives rise to

A

Glutamate

  • Glutamine
  • Proline
  • Arginine
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13
Q

3-PG gives rise to ___, which gives rise to

A

Serine

  • Cysteine
  • Glycine
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14
Q

_____ Donates an NH3 to ______ to form Asparagine

A

Glutamine donates NH3 to Aspartate

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15
Q

Aspartate can be used to synthesize Asparagine, lysine, threonine or methionine. Which AA is formed in the normal pathway without tight regulation

A

Asparagine is normally formed
Other organisms can modify aspartate to form lysine, methionine and threonine, and it is tightly regulated by feedback inhibition

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16
Q

Synthetases vs synthases and ATP

A

Synthetases use ATP, synthases do not

17
Q

Glutamine is formed in cells as a way to transfer ___ to the liver

A

NH4+ ammonia

18
Q

Which amino acid pathways use transamination reactions, what are the enzymes, and what do the enzymes depend on

A

Pyruvate–> Alanine by SGPT
OAA–> Aspartate by SGOT
a-Ketoglutarate–> Glutamate by Glutamate dehydrogenase
-All these enzymes are dependent on pyridoxal phosphate

19
Q

Adenylylation and glutamine synthetase

A

Adenylylation (addition of an AMP ribonucleotide) inactivates glutamine synthetase

20
Q

Regulation of glutamine synthetase with PII

A
  • Glutamine maintains PII in its inhibitory form, so it can adenylylate glutamine synthetase to inactivate it.
  • a-ketoglutarate and ATP maintain PII in its activating form, so it can deadenylate and activate glutamine synthetase
21
Q

Glutamate fates–
After a couple reductions and a cyclization, ____ is formed.
After one reduction and a transamination, ____ is formed. This molecule is actually _____ minus urea

A

Proline

Ornithine, which is arginine minus urea

22
Q

Tyrosine is a catabolic intermediate of

A

Phenylalanine

23
Q

Aromatic amino acids are derived from intermediates originating in what pathway

A

Pentose phosphate pathway

24
Q

What is the intermediate made from PEP and Erythrose 4-phosphate before being converted to Tryptophan, Phenylalanine or tyrosine

A

Chorismate

25
Q

Name the two central amino acids

A

Glycine

Serine

26
Q

What amino acid is Heme a derivative of

A

Glycine

27
Q

Glutamate derived molecules include (not talking about other AAs)

A

Glutathione
Polyamines
GABA

28
Q

Arginine derived molecules include

A

NO

Creatine phosphate

29
Q

Methionine derived molecules include

A

SAM

30
Q

Histidine derived molecules include

A

Histimine

31
Q

Tryptophan derived molecules include

A

Serotonin

32
Q

Tyrosine derived molecules include

A

Epinephrine/norepinephrine
Dopamine
Melanins