Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
19 Cards in this Set
- Front
- Back
What does THF do?
|
It acts as a carrier of one-carbon units (e.g. formaldehyde, formate) in a variety of metabolic reactions.
|
|
List the forms of THF.
|
1. N10-formyl-THF
2. N5,N10-methylene -THF 3. N5-formimino-THF 4. Dihydrofolate 5. N5, methyl-THF |
|
What is the only way to convert N5-methyl-THF to a more convenient form?
|
The methionine synthase reaction.
|
|
What is the methyl folate trap?
|
A vitamin B12 deficiency will lead to a build up of N5-methyl-THF, leading to a shortage of other forms of folate and subsequent impairment in processes in which they are involved.
|
|
What is N10-formyl-THF involved in?
|
Purine biosynthesis; contributes C2 and C8 of the purine ring.
|
|
What is N5,N10-methylene-THF involved in?
|
Thymidylate synthase; it methylates dUMP to yield thymidylate.
|
|
Of what are the sulfonamides analogs?
|
They are analogs of p-aminobenzoic acid (PABA)
|
|
What is the mechanism of the sulfonamides?
|
The drug inhibits dihydropteroate synthetase which is a bacterial enzyme that synthesizes folic acid, thus making these and other compounds that inhibit bacterial folate synthesis excellent antibiotics.
|
|
How are the fates of homocysteine, folate, and methionene linked?
|
They are linked in one-carbon metabolism, and with the help of vitamins B6 and B12 participate in a cycle that continually produces donors of one-carbon units for use in essential biochemical reactions.
|
|
How does a folic acid defiency manifest itself?
|
it is manifested as megaloblastic anemia, whih is the insufficient generation of mature red blood cells.
|
|
How is megaloblastic anemia treated?
|
it is treated with vitamin B12 and folate
|
|
a genetic defect in N5, N10-methylene-THF reductase can lead to ?.
|
Hyperhomocyteinemia.
|
|
What is the universal methyl donor?
|
S-adenosylmethionine
|
|
What are the three main one-carbon donors?
|
THF, biotiin (CO2), and SAM (S-adenosylmethionine)
|
|
Levels of ? in the blood mirror the efficiency of ? and is now used as a useful diagnostic target for a variety of disorders associated with methylation.
|
Homocysteine, one-carbon metabolism
|
|
Defects in which enzyme cause homocysteinuria?
|
cystathione-β-synthetase
|
|
Homocystein's reactive thiol group could lead to ?.
|
Protein degradation
|
|
What is another route for homocysteine toxicity?
|
A descrease in the availability of (SAM)
|
|
What are the effects of decrease SAM levels?
|
it can cause hypomethylation and subsequent defects in gene expression, maintenance of DNA integrity and stability, mRNA processing, etc.
|