3 Flashcards

1
Q

Purine bases. Source of ring atoms: (6)

A

CO2, Gln, Gly, Asp, N10, THF, PRPP

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2
Q

Pyrimidine bases. Source of ring atoms: (6)

A

HCO3-, Gln, Asp, N5, N10, methylene THF

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3
Q

Pyrimidine Catabolism

A

Dietary pyrimidines converted readily to metabolized ketogenic or glucogenic, water soluble compounds such as malonyl CoA, methyl malonyl CoA and succinyl CoA

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4
Q

De Novo Synthesis of Purine Nucleotides

A
  1. PRPP reacts w/ Glutamine and forms –> PRA (PRPP activates the C-1’ ribosyl carbon for the formation of an N-glycosidic bond-“NH2 gets added onto C-1” ** Stimulates: PRPP Inhibits: GMP, AMP, IMP 2. Glycine molecule (along w/ more things) is added to the growing purine precursor (9 steps) and makes IMP **Inhibits: Methotrexate 3. IMP is precursor for both AMP & GMP **Feedback inhibition (AMP prevents more AMP and GPM prevents more GMP) 4. AMP/GMP are phosphorylated –> ADP/GDP (they can go to the ATP/GTP level as well, if so they are used for energy or for RNA synthesis) 5. ADP/GDP are reduced to deoxyribose (dADP & dGDP) and then to dATP/dGTP(used for DNA synthesis) or just from the original ADP/GDP to ATP/GTP
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5
Q

PRPP (phosphoribosyl pyrophosphate) is made from what 2 things?

A

ribose phosphate & ATP

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6
Q

Committed step in purine synthesis

A

Formation of the phosphoribosyl amine (PRA)

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7
Q

Purine ring is synthesized attached to _________

A

The purine ring is synthesized attached to ribose phosphate. The ribose is initially contributed by Phosphoribosylpyrophosphate (PRPP)

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8
Q

Methotrexate

A

An antineoplastic agent that targets dihydrofolate reductase that converts in the liver (cancer drug) This inhibition disrupts DNA replication in rapidly dividing cells (inhibitor of DNA synthesis) It binds dihydrofolate reductase 100x more tightly Inhibits the metabolism of folic acid

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9
Q

Tetrahydrofolate

A

FH4 can’t be made in the body. You get it from the folate vitamin

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10
Q

Synthesis of purine nucleotides is controlled by feedback regulation

A
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11
Q

The pyrimidine ring is synthesized from ______ & _______

A

The pyrimidine ring is synthesized from CARBAMOYL PHOSPHATE & ASPARTATE by aspartate transcarbamoylase

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12
Q

De Novo Synthesis of Pyrimidine Nucleotides

A

3 phases:

  1. Fabrication of orotate ring
  2. Attach PRPP to form UMP
  3. Convert UMP to uridine, cytosine, and thymidine (deoxy)nucleotides
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13
Q

The pyrimidine ring is made from carbamoyl phsophate and aspartate by aspartate- transcarbamoylase

A

The first step and also the COMMITED STEP is the formation of n-carbamoyl aspartate from aspartate and carbamoyl phosphate

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14
Q

When does the ring form in De Novo Synthesis of Pyrimidine Nucleotides?

A

The ring formes before the reaction with PRPP

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15
Q

Orotic aciduria

A

A human hereditary disorder involving the synthesis of the pyrimidine nucleotides

Treated w/ oral uridine

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16
Q

After pyrimidine biosynthesis, DNA is then synthesized from dATP, dCTP, dGTP and dTTP. The concentration of _____ is the limiting factor

A

dTTP

17
Q

Sulfa drugs

A
  • Antibacterial agents that act as competitive inhibitors of the bacterial enzyme that incorporates p-aminobenzoic acid (PABA) into folate
  • This inhibition disrupts DNA replication in bacteria
  • Humans acquire folate as a vitamin from the diet, sulfa drugs selectively affect bacteria
18
Q
A