Chapter 33 Quiz Flashcards

1
Q
  1. What groups provide the various atoms in a purine molecule?
A

Carbon dioxide, aspartate, glutamine, glycine and tetrahydrofolate

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2
Q
  1. What drugs block purine nucleotide biosynthesis?
A

Antifolate dugs and glutamine analogs

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3
Q
  1. What nucleotides can be synthesized from IMP?
A

Guanine and Adenine

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4
Q
  1. What amino acids are required for their synthesis from IMP?
A

Glutamine to have it converted to guanine and Aspartate to convert it to Adenine

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5
Q
  1. Why is hepatic purine biosynthesis stringently regulated?
A

it is energetically expensive; ATP, glycine , glutamine, partake and reduced tetrahydrofolate is all consumed; it is thus necessary to closely regulate purine biosynthesis.

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6
Q
  1. How is AMP and GMP biosynthesis from IMP regulated?
A

feedback system

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7
Q
  1. What molecules including amino acids are required for the biosynthesis of pyrimidine nucleotides?
A

Carbamoyl Phosphate and Aspartate

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8
Q
  1. Human catabolize purines to what molecule?
A

Uric Acid

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9
Q
  1. Starting with Adenosine, what is the first reaction in metabolism of adenosine? What is the name of the molecule?
A

Oxidation the amino group is replaced with an Oxo group. INOSINE

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10
Q
  1. What is the second reaction in the metabolism of adenosine? What is the name of this molecule?
A

The hydration of the sugar from the Adenosine base is now called HYPOXANTHINE

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11
Q
  1. What is the 3rd reaction in the metabolism of adenosine? What is the name of the molecule?
A

Another oxidation at carbon number #2. Xanthine.

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12
Q
  1. What is the action of or role of Xanthine Oxidase?
A

to oxidize the xanthine molecule at the number 8 carbon to uric acid

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13
Q
  1. What are the disorders of purine catabolism? Know the name as well as the enzyme that is deficient.
A

Gout - PRPP synthase (increasing ribose affinity and resistance to feedback inhibition)
Lesch-Nyhan Syndrome - Hypoxanthine-guanine phosphoribosyl transferase
von Gierke - glucose-6-phosphatase
Hypouricemia - xanthine oxidase
Adenosine Deaminase Deficiency
Nucleoside Phosphorylase Deficiency

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14
Q
  1. What is the name of the final metabolic product of Cytosine and Uracil?
A

Beta-Alanine

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15
Q
  1. What is the name of the final metabolic product of Thymine?
A

Beta-AminoButyrate

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16
Q
  1. What is orotic aciduria and what enzyme is it caused by?
A

types and is basically the inability of mitochondria being able to utilize carbamoyl phosphate, this then leads to the overproduction of Orotic Acid
Type I has the absence of both orotate phosphoribosyl transferase and orotidylate decarboxylase
Type II is due to the absence of orotidylate decarboxylase only