Protein and Amino Acid Metabolism V Flashcards

(36 cards)

1
Q

what do you need for the synthesis of cretine

A

glycine, arginine, SAM

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2
Q

when is the phosphorylation of creatine favored

A

when ATP conc in muscle is high

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3
Q

is the phophate group transfer potential of creatine phosphater higher or lower than that of ATP

A

higher

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4
Q

what happens allows for continued muscle contraction during an intense burst o faerobic activity

A

regen of ATP from creatine phospahte and ADP

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5
Q

what releases creatinine

A

muscel cells

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6
Q

how is creatinine excreted

A

urine

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7
Q

amount of creatinine excreted each day is propertion to waht

A

muscle mass

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8
Q

creatinine is an indicator of what

A

kidney function

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9
Q

symptoms of children suffering from defect of enzyme of creatine synthesis/uptake

A

hypotonia, neurlogical symtoms

little skeletal/cardiac muscle pathology

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10
Q

how do you treat children with creatine synthesis problem

A

dietary supplementation of creatine

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11
Q

what catecholamine signaling molcules are derived from tyroosine

A

dopamine
norepinephrine
epinephrine

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12
Q

how do you get from tyrosin to epinephrine

A

tyrosine –> DOPA —> dopamine —> NE —-> epinerphee

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13
Q

what are tyrosines contained in

A

thryoglubulin

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14
Q

what is thyrglobin degreated in

A

lysosomes

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15
Q

where does synthesis of melanin take place

A

melanocytes

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16
Q

how do you get synthesis melanin

A

tyrosine —-> DOPA —–> dopaquinone —–>melanin

17
Q

what is required for the conversion of NO to epinephrine

18
Q

what casues oculocuaneous albinism type 1

A

loss of function of tyrosinase due to mutation in TYR gene

19
Q

what is serotonin derived from

20
Q

where is serotonin most abudant

A

platelets and GI tract

21
Q

where is serotonin produced

22
Q

what does the melatonin synthesis reaction require

23
Q

what does tryptophan convert to by the liver

24
Q

what converts tryptophan to niacin

25
how is GABA produced
decarbozylation of glutamate
26
how do you get histamine
decarboxylation of histidine
27
what is glutathione
tripeptide with sequence glu-cys-gly
28
what is gamma glutamyl linkage resistant to
proteolysis
29
what type of bond holds glutathione together
gamma glutamyl
30
what is unique about glutathion
does not require mRNA template
31
where is glutathione made principally
liver
32
function of glutathione
intracecllular reducing agent - specifally peroxidies
33
when glutathione is oxidized what does it form
dimer GSSG
34
where is glutathione rich
red blood cells
35
why is glutathione high in RBCs
maintains plasma membrane integrity by reducing peroxides formed during oxygen transport
36
what are the glutathione s transferases involved in
detox process