AA degradation and synthesis Flashcards
ketogenic AAs
{LLs - Liver}
Leucine
Lysine
BOTH glucogenic and ketogenic AAs
{Fear I Tripped a Tiger}
Phenylalanine
Isoleucine
Tryptophan
Tyrosine
glucogenic AAs
{Glucogenic GAGA CAMP HAS TV)
Glutamate
Glycinew
Asparagine
Glutamine
Aspartate
Cysteine
Arginine
Methionine
Proline
Histidine
Alanine
Serine
Threonine
Valine
9 essential AAs
{Lucy & Val’s Meth Trip Is Like 3 Fucking Hours}
Leucine
Valine
Methionine
Tryptophan
Isoleucine
Lysine
Threonine
Phenylalanine
Histidine
+ Arginine** only “conditionally essential”
what 3 sources is the amino acid pool supplied by?
dietary intake
protein degradation
de novo amino acid synthesis
what do glucogenic AAs do that ketogenic AAs DO NOT do?
add extra carbons to the TCA cycle
what are the two destinations for carbon skeletons of ketogenic AAs?
converted to Acetyl-CoA
-> enters ketogenesis, FA synthesis, or TCA
converted to acetoacetate
(a ketone body)
-> is oxidized in tissues capable of ketolysis
(NOT liver)
AAs that enter TCA as OAA
Asn
Asp
AAs that enter TCA as pyruvate
{at the “Pyr”, Alan Catches a Glimpse of 3 Trapped Seals}
Ala
Cys
Gly
Thr
Trp
Ser
AAs that enter TCA as alpha-KG
{Professional Hot Glue Gun Art}
Pro
His
Glu
Gln
Arg
AAs that enter TCA as fumarate
{Fuming Tigers}
Phe
Tyr
AAs that enter TCA as succinyl-CoA
{it succs: Val Met 3 Izzys}
Val
Met
Thr
Ile
which AA’s carbon skeleton is converted to Acetyl-CoA?
Ile
AAs whose carbon skeletons are converted to acetoacetate
{La La, Fucking Tripped Tigers}
Leu
Lys
Phe
Trp
Tyr