Protein and Amino Acid Metabolism V Flashcards

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

A

SAM

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

A

tryptophan

20
Q

where is serotonin most abudant

A

platelets and GI tract

21
Q

where is serotonin produced

A

pineal gland

22
Q

what does the melatonin synthesis reaction require

A

SAM

23
Q

what does tryptophan convert to by the liver

A

niacin

24
Q

what converts tryptophan to niacin

A

IDO

25
Q

how is GABA produced

A

decarbozylation of glutamate

26
Q

how do you get histamine

A

decarboxylation of histidine

27
Q

what is glutathione

A

tripeptide with sequence glu-cys-gly

28
Q

what is gamma glutamyl linkage resistant to

A

proteolysis

29
Q

what type of bond holds glutathione together

A

gamma glutamyl

30
Q

what is unique about glutathion

A

does not require mRNA template

31
Q

where is glutathione made principally

A

liver

32
Q

function of glutathione

A

intracecllular reducing agent - specifally peroxidies

33
Q

when glutathione is oxidized what does it form

A

dimer GSSG

34
Q

where is glutathione rich

A

red blood cells

35
Q

why is glutathione high in RBCs

A

maintains plasma membrane integrity by reducing peroxides formed during oxygen transport

36
Q

what are the glutathione s transferases involved in

A

detox process