3 Flashcards
Purine bases. Source of ring atoms: (6)
CO2, Gln, Gly, Asp, N10, THF, PRPP
Pyrimidine bases. Source of ring atoms: (6)
HCO3-, Gln, Asp, N5, N10, methylene THF
Pyrimidine Catabolism
Dietary pyrimidines converted readily to metabolized ketogenic or glucogenic, water soluble compounds such as malonyl CoA, methyl malonyl CoA and succinyl CoA
De Novo Synthesis of Purine Nucleotides
- 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
PRPP (phosphoribosyl pyrophosphate) is made from what 2 things?
ribose phosphate & ATP
Committed step in purine synthesis
Formation of the phosphoribosyl amine (PRA)
Purine ring is synthesized attached to _________
The purine ring is synthesized attached to ribose phosphate. The ribose is initially contributed by Phosphoribosylpyrophosphate (PRPP)
Methotrexate
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
Tetrahydrofolate
FH4 can’t be made in the body. You get it from the folate vitamin
Synthesis of purine nucleotides is controlled by feedback regulation
The pyrimidine ring is synthesized from ______ & _______
The pyrimidine ring is synthesized from CARBAMOYL PHOSPHATE & ASPARTATE by aspartate transcarbamoylase
De Novo Synthesis of Pyrimidine Nucleotides
3 phases:
- Fabrication of orotate ring
- Attach PRPP to form UMP
- Convert UMP to uridine, cytosine, and thymidine (deoxy)nucleotides
The pyrimidine ring is made from carbamoyl phsophate and aspartate by aspartate- transcarbamoylase
The first step and also the COMMITED STEP is the formation of n-carbamoyl aspartate from aspartate and carbamoyl phosphate
When does the ring form in De Novo Synthesis of Pyrimidine Nucleotides?
The ring formes before the reaction with PRPP
Orotic aciduria
A human hereditary disorder involving the synthesis of the pyrimidine nucleotides
Treated w/ oral uridine