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47 Cards in this Set

  • Front
  • Back
plot out how different animals get rid of ammonia
draw the Urea cycle
fill in the blanks
formation of carbamoyl phosphate
structure of ornithine
what's this?
Draw out citruline
What's this?
draw out aspartate
What's this?
aspartate
draw out argininsuccinate
draw out argininsuccinate
what's this?
argininosuccinate
draw fumarate
what's this?
fumarate
draw arginine
what's this?
arginine
draw urea
what's this?
urea
how many phosphate anhydride bonds does the formation of urea take up?
takes up 4 phosphate anhydride bonds
2 for making carbamoyl phosphate
1 in making argininosuccinate
1 for hydrolyzing argininosuccinate
draw out simply how aspartate is regenerated from fumarate
complex urea cycle + oxidation in mitochondria
complex urea cycle + oxidation in mitochondria
example of proton gradient in urea cycle transport, and what disease it may cause if not working correctly
NADH cycles and transport
model for small-molecule transporters?
E. coli lactose permease
transports TDG
most abundant protein in the mitochondrial inner membrane?
ATP/ADP exchanger (translocase)
exports ATP
carries a proton into the matrix w/ each ATP/ADP exchange
Urea regulation
Urea cycle disorders
defect in carbamylphosphate synthetase I creates what disorder?
lethargy, convulsions, early death
defect in argininosuccinate lyase creates what disorder?
argininosuccinic acidemia, vomiting, convulsions
defect in arginase creates what disorder?
arginemia, intellectual disability
pharmacological treatment for some urea cycle defects
urea cycle defect that can also lead to autism?
single-nucleotide polymorphisms in the gene for mitochondrial, Ca2+ dependent Asp/Glu exchanger
main transporter in the brain
what is Arginine also a precursor for that seemingly has nothing to do with urea cycle?
arginine is a precursor of nitric oxide (NO)
What is the role of NO?
short-lived messenger that controls blood pressure, clotting, and neurotransmission. Binds guanylyl cyclase and activates production of c-GMP
amino acids feeding in to the TCA cycle
AA that are neither glucogenic or ketogenic
Glutamate
AA that lead to oxaloacetate
asparagine
aspartate
AA that lead to pyruvate
alanine
cysteine
glycine
serine
threonine
tryptophan
AA that lead into fumarate
phenylalanine
tyrosine
AA that lead into succinyl-CoA
isoleucine
methionine
threonine
valine
AA that lead to glutamate then alphaketoglutarate
arginine
glutamine
histidine
proline
AA that run into acetyl CoA
isoleucine
leucine
threonine
tryptophan
AA that lead into acetoacetyl-CoA
leucine
lysine
phenylalanine
tryptophan
tyrosine
Essential amino acids
Arginine
Histidine
Isoleucine
Leucine
Lysine
Methionine
Phenylalanine
Threonine
Tryptophan
Valine
(RHVMILKFTW)
Really HeaV MILK For The Win
What is serine formed from? draw it out