Nucleic Acids (Lecture 29) Flashcards

1
Q

what is a base?

A

aromatic ring that differs in the nucleic acid

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2
Q

what is a nucleoside?

A

base + ribose

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3
Q

what is a nucleotide?

A

base + ribose + phosphate group

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4
Q

what does glutamine amide contribute to the purine structure?

A

N3 N9

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5
Q

what does formate contribute to the purine structure?

A

C2 C8

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6
Q

what does glycine contribute to the purine structure?

A

C4 C5 N7

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7
Q

what does aspartate amine contribute to the purine structure?

A

N1

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8
Q

what does HCO3- contribute to the purine structure?

A

C6

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9
Q

what does aspartate contribute to the pyrimidine structure?

A

N1 C4 C5 C6

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10
Q

what does glutamine amide contribute to the pyrimidine structure?

A

N3

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11
Q

what does HCO3- contribute to the pyrimidine structure?

A

C2

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12
Q

which molecule links to the ribose in a purine?

A

N9

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13
Q

which molecule links to the ribose in a pyrimidine ?

A

N1

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14
Q

which orientation is the base put onto the ribose?

A

beta glycosidic bond (base above)

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15
Q

which stereo conformation re the sugars in nucleic acids

A

D sugars (furganose conformation)

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16
Q

what it the nucleoside and nucleotide for adenine base?

A

nucleoside: adenosine
nucleotide: adenylate (AMP)

17
Q

what it the nucleoside and nucleotide for guanine base?

A

nucleoside: guanosine
nucleotide: guanylate (GMP)

18
Q

what it the nucleoside and nucleotide for cytosine base?

A

nucleoside: cytidine
nucleotide: cytidylate (CMP)

19
Q

what it the nucleoside and nucleotide for uracil base?

A

nucleoside: uridine
nucleotide: uridylate (UMP)

20
Q

what it the nucleoside and nucleotide for thymine base?

A

nucleoside: deoxythymidine
nucleotide: thymidylate deoxythymidylate (dTMP)

21
Q

what it the nucleoside and nucleotide for hypoxanthine base?

A

inosine

inosate (IMP)

22
Q

what it the nucleoside and nucleotide for xantoine base?

A

xanthosine

xanthylate (XMP)

23
Q

what it the nucleoside and nucleotide for orotate (orotic acid) base?

A

orotidine

orotidylate (OMP)

24
Q

what is the first step of de novo synthesis of purines?

A

synthesis of PRPP via alpha-d ribose-5-phosphate and ATP via ribose phosphate pyrophosphokinase (adds 2 phosphates)

25
Q

the de novo synthesis of purines is regulated at which steps?

A

synthesis of PRPP

synthesis of 5-phosphoribosylamine

when the cell needs more purines, the amount of PRPP will increase, thus increasing the amount of 5-phosphoribosylamine

26
Q

what is the committing step in purine de novo synthesis?

A

PRPP –> 5-phosphoribosylamine

27
Q

what is the second step of purine de novo synthesis?

A

PRPP with glutamine form glutamate and beta-5-phosphoribosylamine

pyrophosphate is release, which makes this reaction irreversible

this is done via amidophosphoribosyl transferase

28
Q

what is the N donor in the second step?

A

glutamine

29
Q

why does the release of PPi cause the second step of purine de novo synthesis to be irreversible?

A

low PPi concentration in the cytosol, because it is always converted into 2Pi, thus making the generation of PPi energetically favourable

30
Q

what is the usual pathway to donating an amine group?

A

addition of ATP to a carbonyl group to prime

addition of NH3 and release of Pi

31
Q

where is the N from glutamine derived from?

A

side chain

32
Q

where is the N from aspartic acid derived from?

A

back bone