AA catabolism -Brar Flashcards
What is required for ubiquitin tagging of proteins?
E1: ubiquitin activating enzyme
E2: ubiquitin-conjugating enzyme
E3: Ubiquitin-protein ligase
ATP is also required
Steps of AA degradation
- removal of nitrogen (liver is major site of protein degradation in mammals)–> producing alpha-keto-acids
- alpha-amino groups are converted to ammonium ions by the oxidative deamination of glutamate
* ammonium=toxic, most urea in blood is in the form of non-toxic glutamate - amino groups funneled into alpha-ketoglutarate via aspartate transaminase and alpine transaminase (ALT and AST)
* elevation in these enzymes=hepatic damage = in LFT’s (liver functioning test) and are easily elevated - deamination : takes place in the mitochondria via glutamate dehydrogenase (uses NAD or NADP)
- carbon of degraded AA emerge as major metabolic intermediated
5. ammonium is converted to urea, creating NADH–> urea=water soluble =excreted in urine
urea H2N-C=O-NH2
Which AA are degraded to pyruvate?
Serine and threonine degradation can be directly deaminated to pyruvate –>glucagonic AAs enter the TCA cycle
glycine–> serine–> pyruvate
tryptophan–> alanine–> pyruvate
cysteine–> pyruvate
threonine–> amino acetone–>pyruvate
7 major metabolic intermediates created by degradation of AA
Acetyl–CoA Acetoacetyl–CoA Pyruvate α-Ketoglutarate Succinyl–CoA Fumarate Oxaoloacetate
Which AA are degraded to oxaloacetate?
aspartate
asparagine: hydrolysis to aspartate + NH4+ –>oxaloacetate
Which AA are degraded to alpha-ketoglutarate?
glutamine + proline + arginine + histidine
all form glutamate –> alpha-ketoglutarate
*histidine has two pathways to get here–> many steps
Which AA are degraded to succinyl-CoA?
Methionine, Valine, and Isoleucine
form propionyl CoA–> methylmalonyl CoA–> succinyl CoA
*methionine forms S-adenosylmethionine (SAM) –>
Which AA are degraded to fumarate?
phenylalanine, tyrosine
phenylalanine (requires tetrahydrobiopterin)–> tyrosine–> fumarate and acetoacetate