Nucleotide Struc/Func Flashcards

1
Q

Name the purines we learned

A

Adenine and Guanine

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2
Q

Name the pyrimidines we learned

A

Cytosine, Thymine, and Uracil

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3
Q

Why are most pyrimidine modifications on the right side?

A

Does not affect Hydrogen Bonding

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4
Q

What are structural isomers that readily convert called

A

Tautomers

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5
Q

Which nitrogenous base tautomerizes most readily?

A

Uracil

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6
Q

Which form of uracil is most prevalent?

A

Keto/lactam form

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7
Q

What makes up the sugar backbone in DNA?

A

2-Deoxyribose

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8
Q

What makes up the sugar backbone in RNA?

A

Ribose

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9
Q

When forming a nucleoside, the nitrogenous base is bound to which carbon on the sugar?

A

Carbon 1

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10
Q

Which stereochemical form predominates in nucleosides?

A

Anti (as opposed to the syn form)

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11
Q

Where do phosphate groups attach to nucleosidic sugars to form a nucleotide?

A

5’ carbon

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12
Q

What is the bond called in DNA?

A

3’-5’ phosphodiester

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13
Q

What is an example of nucleotides carrying specific building blocks in pathways?

A

UDP-glucose, donating glucose to glycogen

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14
Q

What second messengers can be formed from nucleotides?

A

cAMP and cGMP

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15
Q

What does S-adenosyl methionine do?

A

Acts as a methyl group donor

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16
Q

Which enzyme forms S-adenosyl methionine from ATP and methionine?

A

methionine adenosyltransferase

17
Q

How does ATP become involved in NAD+/NADP+ synthesis?

A

NAD+ is phosphorylatesd with a phosphate group on ATP

18
Q

How does ATP become involved in FAD synthesis?

A

Riboflavin has a phosphate group added to become Flavin Mononucletodie (FMN). Then, pyrophosphate is cleaved from another ATP, with the AMP added to become Flavin Adenine Dinucleotide (FAD).

19
Q

What does the synthesis of pantothenic acid into coenzyme A require?

A

ATP

20
Q

Synthetic pyrimidine nucleoside prodrug used in chemotherapy

A

Gemcitabine

21
Q

Thymidine analog which selectively inhibits HIV’s reverse transcriptase

A

Azidothymidine