Exam 3 Nucleotide Metabolism (RNA) Flashcards

1
Q

2’ carbon on the 5 membrane ring sugar refers to

A

ribose (OH) or deoxyribose (H)

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2
Q

all nucleoSide X-phosphates are

A

nucleoTides

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3
Q

the precursor for all nucleotides

A

PRPP

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4
Q

-etase signifies

A

require energy in the form of ATP usu

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5
Q

-tase signifies

A

does not use energy

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6
Q

what reactants used to make PRPP

A
  1. ribose-5-phosphate

2. pyrophosphate from ATP required for the synthetase

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7
Q

the pyrophosphate from ATP attaches where on ribose-5-phosphate

A

1’ carbon of ribose-5-phosphate

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8
Q

de novo synthesis of pyrimidines is a _ pathway

A

unidirectional (linear); takes carbamoyl phosphate and PRPP to make UMP then UDP then UTP and then CTP

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9
Q

de novo synthesis of pyrimidines form nitrogenous base _ of PRPP

A

independent of PRPP; slaps the base on PRPP

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10
Q

the precursors to make pyrimidines

A

-NH3 from Gln
-Asp
HCO3-

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11
Q

allosteric regulation of pyrimidines: pyr inhibits

A

C

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12
Q

allosteric regulation of pyrimidines: pur activates

A

A/G

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13
Q

what is CAD

A

eukaryotic protein; a complex that uses of 3 enzymes and occurs in the cytosol for pyrimidines

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14
Q

the C in CAD has a channel where what place

A

CPSII; is a synthetase that modifies HCO3- and the NH3- from Gln as moves down the channel to make carbomyl phosphate

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15
Q

activators of CPSII

A

PRPP and ATP

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16
Q

inhibitors of CPSII

A

UTP

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17
Q

A in CAD has 2 allosteric sites which are

A

ATcase adds Asp to carbamyol phosphate

  1. ATP activates (excess purines into pyrmidines)
  2. CTP inhibits ( endput of pyrmidine)
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18
Q

D in CAD (dihydroorotase)

A

closes the 6 member ring; uses H2O to make pyrimidines

19
Q

DHODH is located where

A

mitochondria

20
Q

FMN is a source of e-s not from

A

carbohydrates

21
Q

what does UMP synthetase do

A

adds orotate (precursor from CAD) adds it to PRPP at the 1’ carbon in ribose backbone then removes carboxyl from Asp to make UMP

22
Q

our energy used for UMP synthetase

A

PRPP

23
Q

what conformation is uracil in after UMP synthetase

A

SYN

24
Q

megalobalstic anemia occurs when

A

cells fail to divide so multi nucleated; b9 or b12 deficiency

25
Q

hereditary orotic aciduria symptoms include

A

excess precursor orotate excreted in the urine

26
Q

why in cases of hereditary orotic aciduria, fails at responding to B9/B12?

A

it has deficiency of UMP synthetase (no de novo synthesis)

27
Q

kinases in prymidines used is for

A

transforming UMP into UTP

28
Q

_ is the only nucleotide to be synthesized directly as a triphosphate

A

CTP

29
Q

CTP synthetase has 2 allosteric regulators:

A
  1. GTP activates (base pairing rxns ie CTP uses GTP and UTP uses ATP)
  2. CTP inhibits both synthetases C and A
30
Q

purines form nitrogenous base _ PRPP

A

on PRPP

31
Q

purines is _ pathway

A

branched pathway; takes aas and PRPP to make IMP and branch to GMP or AMP

32
Q

purine regulation via

A

feedback inhibition by purines

33
Q

precursors for purines

A

same 3 in pyrimidines plus Gly and N10-formyl-THF

34
Q

de novo synthesis of purines happens where

A

cyoplasm

35
Q

precursors use what sources of energy

A

ATP or GTP

36
Q

how do IMP formation occur

A

activation/phosphorylation-replacement

37
Q

making IMP: rxns 1-3 form:

A

the 5 membered ring

38
Q

making IMP: rxns 4-10 form:

A

the 6 membered ring; forming hypoxanthine

39
Q

in vertebrates, purines are made in the

A

purinosome (complex)

40
Q

purinosome: _ enzymes perform 10 reactions

A

6

41
Q

_ facilitates flow in purinosome

A

proximity

42
Q

kinases in purines are used for:

A

making diphosphate and triphosphate

43
Q

precursor IMP to make AMP uses what for energy and is inhibited by

A

GTP; inhibited by AMP

44
Q

precursor IMP to make GMP uses what for energy and is inhibited by

A

ATP; inhibited by GMP