defects in pryimidien and purine metabolism Flashcards
lesch-nyhan syndrome
deficiency in hypoxanthine guanine phosphoribosyltransferase (HGP)
hereditary orotic aciduria
deficiency of adenosine deaminase
gout
abnormalites of purine metabolizing enzymes
gilbert syndrome
decreased bilirubin diglucuronide
5-methyl tetrahydrofolate is required for the
conversion of homocysteine to methionine
In the urea cycle, citrulline is formed by the carbamoylation of
ornithine
Metabolism of which of the following amino acids would be most likely to raise the level of circulating ketone
bodies in a diabetic animal?
leucine and lysine
Aspartate can be synthesized by the amination of
oxaloacetate
Which of the following amino acids is formed in the reaction catalyzed by arginase?
ornithine
Which of the following options best describes the function of the primase enzyme in eukaryotes?
generation of RNA primers for use in replication