Biochem exam 2 Flashcards

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1
Q

pyruvate AA (3)

A

alanine (direct transamination)
cysteine (-NH2, - SH)
threonine (thr aldolase–>Co2 + NH4+ and THFA –> serine)

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2
Q

oxaloacetate (2)

A

aspartic acid/asparagine (transamination)

asparagine (-NH3)

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3
Q

alpha ketoglutarate (5)

A

glutamic acid (ox deamination –NADH)
glutamine (-NH4+)
Arginine, proline, histidine (co2 to histamine)

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4
Q

succinyl coA

A

met, thr, valline, methyl malonyl coa (cofactor is b12)

  • ox deamination
  • maple syrup urine disease
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5
Q

phenylalanine and tyrosine

A

p 450 to tyrosine and then fumerate–> acetoacetate

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6
Q

negative nitrogen balance

A

nitrogen excretion through urea > nitrogen uptake through AA

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7
Q

simple feedback

A

linear end product negative

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8
Q

sequential feedback

A

fork products inhibit start of fork

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9
Q

concerted

A

fork products inhibit both fork and pre-fork (need both for pre-fork)

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10
Q

enzyme multiplicity

A

X,y and z inhibit fork and also start of fork

ISOENZYMES

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11
Q

cumulative feedback

A

each enzyme can inhibit first step. each enzyme that binds means more increasing inhibition

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12
Q

glutamine synthetase

A

ATP form is less active, AMP form is active

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13
Q

7 uses for AA synthesis

A

proteins, cofactors, hormones, porphyrins and heme, nucleotides, neurotransmitters, pigments

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14
Q

heme synthesis

A

mt of liver. starts with succinyl coa and glycine condensing by pyrodoxal phosphate. get delta amino then condense using NH4

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15
Q

RBC degraded in

A

spleen, 120 days

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16
Q

bilirubin

A

heme is degraded by mixed function oxidase to add OH to get this. this goes to liver and adds sugar to make bile
- causes jaundice

17
Q

porphyria disease

A

increase levels of delta amino, photosensitivity, red pee, OR enzyme is unstable OR block in enzyme leading to heme so more intermediates (eat liver or blood to get heme)

18
Q

neurotransmitters

A

diffuse between ells to transfer nerve impulse

19
Q

serotonin

A

from tryptophan. nneeds pyrodoxal phosphate. something to do with mushrooms

20
Q

dopamine and norepi

A

tyrosine. using p450 and DOPA and pyrodoxal phosphate and SAM

21
Q

melanin

A

DOPA makes red pigmennt, then quinoline comes in to make melanin, black pigment

22
Q

PKU

A

deficency in thing that converts phenylalanine to tyrosine. phe can be converted to phenylpyruvate

  • more pp in blood and urine
  • pigment issues with no melanin
23
Q

cholesterol cycle

A

don’t forget reductase, mevalonic acid and negative effector cholesterol

24
Q

sphingolipid cycle

A

palmitoyl coa + serine, co2 and nadph. sphingosine, ceramide__> cdp choline and sphingomyelin OR udp sugar and cerebrosie

25
Q

inositol cycle

A

OH and atp

26
Q

neiman pick

A

high sphingomeylin because can’t do to ceramide and phosphophocholine

27
Q

prostaglandin

A

arach and prostagalnndin synth

28
Q

bile salts

A

nadph, p450, co3 and coa

29
Q

FAT and lipid in body

A

chlomicron to liver to lipase to VLDL to serum to LCAT then HDL then IDL then taken up

30
Q

urea cycle

A
glu dehydrogenase (- is GTP and ATP). then take nh4 to carbamoyl phosphate and ornithine make citruline, arginosuccinate, argninie (- fumerate), then ornithine
- urea comes from arginine