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40 Cards in this Set

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What are the essential amino acids?
PVT TIM HALL
Phenylalanine, Valine, Tryptophan
Threonine, Isoleucine, Methionine
Histadine, Arginine, Leucine, Lysine
What essential amino acid can for a nonessential amino acid
Phenylalanine to tyrosine via phenylalanine hydroylase within the kidneys
transaminates to hydroxyphenylpyruvate
Tyrosine
is a non essential amino acid made from phenylalanine (phenylalanine hydroxylase)
Partially ketogenic: fumerate (TCA), acetoacetate (to ketones)
transaminated to make neurotransmitters dopamine, norepinephrine, and epinephrine, melanine, and thyroid hormones
Serine
Non essential amino acid synthesized from glycine and the coenzyme folic acid within the kidneys
Serine transamination creates pyruvate as its carbon skeleton
100% glucogenic
PKU
phenylketonuria
Metabolic disorder, inherited deficiency of phenylalanine hydroxylase. Cannot convert Phe to Tyr. Phe builds up and is excreted as phenylpyruvate.
Which amino acids are 100% ketogenic?
Lysine, Leucine
What amino acids are 100% glycogenic?
Upon deamination/transamination, their carbon skeletons enter the TCA cycle
Everything that is not 100% or partially ketogenic
Which amino acids are partially ketogenic?
Phe-Fumerate, Acetoacetate
Ile- Succinyl CoA, Acetyl CoA
Threonine-Pyruvate, Succinyl CoA, Acetyl CoA
Trp- Pyruvate, Acetyl CoA
Tyr-Fumerate, Acetoacetate
Name the BCAA
(branched chain amino acids)
Leucine
Isoleucine
Valine
Leu, 100% ketogenic (acetoacetate)
Ile- partially ketogenic
Valine-100% glucogenic (Succinyl CoA)
Lysine
Essential amino acid
100% ketogenic (acetoacetate)
Lysine + SAM = carnitine
Carnitine
Involved in FA transport.
Made in the liver, stored in the muscle.
Formed from methylated lysine
(Lys + SAM)
Methionine
Essential amino acid
100% glucogenic (succinyl CoA)
S-adenylsyl methionine (SAM) is a principle methyl donor
-DNA, RNA, N-containing compounds
SAM
S-adenylsyl methionine
principal methyl donor
Homocysteine
remove methyl from SAM to create S-adenosyl homocysteine (SAH) to yield Homocysteine
Name the aromatic amino acids
Pheylalanine, Tyrosine, Tryptophan
Partially ketogenic
Phe: fumerate, acetoacetate
Tyr: Fumerate, acetoacetate
Trp: pyruvate, acetyl CoA
Tryptophan
Essential amino acid
Partially ketogenic (Pyruvate, acetyl CoA)
Metabolized to melatonin and serotonine
Sleepy turkey
Cori cycle
occurs in the liver, allow that transport of muscle glycogen to serum glucose.
alanine can travel from muscle to liver, transaminate to pyruvate to undergo gluconeogenesis
Alanine
Nonessential amino acid
100% glucogenic
Released from muscles with glutamate, they transaminate with each other. (pyruvate/a-KG)
Glutamine
Nonessential amino acid
100% glucogenic, a-KG
Major ammonia carrier
Player in the Cori and Urea cycle and Arg synthesis (citrulline)
Glutamine fxn
ammonia carrier
released from MM with alanine during fast
component stress and HSP protein
levels increase during trauma
Liver
Principle organ that metabolizes dietary AA, except BCAA (MM).
Houses the Urea Cycle and Stage 2 of Cori.
Basic amino acids
Lys, Arg, His

all essential
POLAR, positively charged
Polar amino acids
Can be charged or neutral
Basic aa are positively charged (lys, arg, his)
Dicarboxylic aa are negatively charged (Asp, Glu)(acids)
Neutral/polar (Asn, Cys, Gln, Ser Thr)
Dicarboxylic amino acids are ACIDS
Neutral aa may be polar and non polar
Dicarboxylic amino acids
Glutamic acid (Glu)
Aspartic acid (Asp)
Negatively charged acids
Polar, charged
Positively charges amino acids
Are basic amino acids, also polar
Lys, His, Arg
Negatively charged amino acids
Are acidic and polar
Glutamic acid
Aspartic acid
Pepsin
Pepsinogen, a zymogen, is released into the STOMACH and is activated by HCl, and hydrolyses peptide bonds
creating large polypeptides, oligopeptides, and free aa
Gastrin
HORMONE that stimulates HCl release into the stomach
Hydrochloric acid
Denatures proteins in the stomach, by unfolding the secondary, tertiary, and quaternary structures (NOT, peptide bonds (primary)
Activates pepsinogen to pepsin
transferases
move functional groups
hydrolases
cleave compounds
Arginine
essential amino acid
(+) polar
Metabolised in intestinal cells to yield citrulline and urea.
Citrulline
made from Arginine in enterocytes is released into blood to the kidneys to make Arg for tissues.
Also key to Urea cycle in liver (with Arg)
Which 3 amino acids do not dominate or transaminate?
Lysine, Histadine, Threonine
This makes them indispensable(essential) because they cannot synthesized
Glutathione
Antioxidant and aa transporter

reacts with H2O2, prostaglandin
Carnitine
FA transport, made from methylated Lysine (lys + SAM)
Creatine
Made in liver/kidney, stored in skeletal MM (95%) Replenishes ATP in rapidly contracting MM
Urinary levels an indicator of muscle mass
Choline
methyl donor, acetylcholine (neurotransmitter), lecithin, sphingomyelin
Leucine
100% ketogenic (acetyl CoA, Acetoacetate)
Essential, BCAA
Cholesterol syn
Stimulates Insulin
Limiting amino acid
The essential amino acid that is present in the lowest amount