defects in pryimidien and purine metabolism Flashcards

1
Q

lesch-nyhan syndrome

A

deficiency in hypoxanthine guanine phosphoribosyltransferase (HGP)

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2
Q

hereditary orotic aciduria

A

deficiency of adenosine deaminase

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3
Q

gout

A

abnormalites of purine metabolizing enzymes

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4
Q

gilbert syndrome

A

decreased bilirubin diglucuronide

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5
Q

5-methyl tetrahydrofolate is required for the

A

conversion of homocysteine to methionine

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6
Q

In the urea cycle, citrulline is formed by the carbamoylation of

A

ornithine

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7
Q

Metabolism of which of the following amino acids would be most likely to raise the level of circulating ketone
bodies in a diabetic animal?

A

leucine and lysine

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8
Q

Aspartate can be synthesized by the amination of

A

oxaloacetate

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9
Q

Which of the following amino acids is formed in the reaction catalyzed by arginase?

A

ornithine

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10
Q

Which of the following options best describes the function of the primase enzyme in eukaryotes?

A

generation of RNA primers for use in replication

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