Exam 4 Quiz 4 Flashcards

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1
Q

do all proteins need to be constitutive?

A

No! They only make the proteins that they need at that time

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2
Q

post-translational control

A

the protein is already made, how the function is limited after its made

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3
Q

regulating enzyme activity post-translationally

A

feedback inhibition

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4
Q

feedback inhibition

A

where you have a series of enzymes that go onto make an end product.
-the end product of a pathway typically interrupts the function of the first enzyme in the pathway

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5
Q

first enzyme in the pathway

A

allosteric enzyme

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6
Q

allosteric enzyme

A

-have a second, important site (allosteric site) along with the active site (the main site)

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7
Q

allosteric site

A

where the end product binds when it is in excess which then goes onto disrupt the active site inhibiting the process from continuing (saves energy)

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8
Q

is Feeback reversible

A

yes

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9
Q

concerted feedback inhibition

A

-involves the use of isoenzymes which are different proteins that catalyze the same reaction but are under different regulatory controls

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10
Q

example of concerted feedback inhibition

A

aromatic AA synthesis, each have a different regulatory control but working towards the same product

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11
Q

if more than one end product

A

all end products must be in excess in order for synthesis to be completely inhibited

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12
Q

covalent modification of enzymes

A

occurs throughout the addition and removal of a particular group/model

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13
Q

main groups used to modify enzymes

A

-Adenosine monophosphate
-Adenosine diphospahte
-inorganic phosphate
-methyl groups

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14
Q

Glutamine synthetase

A

making glutamine, when glutamine levels are staying high AMP is added on which causes the glutamine to reduce

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15
Q

regulation of translation at translation level

A

regulating enzyme synthesis vis:
-riboswitches
-regulatory RNA/small RNA

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16
Q

riboswitches

A

-mRNA contains binding site for specific metabolite
-when metabolite bound it alters folding of mRNA hiding the Shane-Dalgarno sequence

17
Q

aptamer region

A

specific secondary structure that allows for metabolite bonding

18
Q

when specific metabolite is bound

A

-translation is blocked
-inhibits the Shine dalgarno sequence from being recognized

19
Q

when no metabolite is bound

A

shine dalgarno sequence is seen by 30S or 16S rRNA to continue with the process

20
Q

Regulatory RNA/small RNA

A

binding to an mRNA molecule due to complimentary base pairing

21
Q

small RNA

A

-40-400 nucleotide bases
-act as regulatory
-exert control through base pairing

22
Q

regulation through 4 different mechanisms

A

-hides shine dalgarno
-opens shine dalgarno
-increases stability
-decreases stability

23
Q

Regulation of transcription

A

-at transcription level (only prokaryotes)
-regulating enzyme synthesis
-attenuation

24
Q

regulating enzyme synthesis only occurs in prokaryotes because

A

transcription and translation need to be occurring at the same time, only seen in prokaryotes bc no nucleus

25
Q

Attenuation

A

at leader sequence there are tandem tryptophan residues (or whatever AA you need) right next to one another in the N terminal

26
Q

what does the rest of the leading sequence form?

A

secondary structures

27
Q

leader sequence can fall inot different scenarios based on

A

what is happening in the cell

28
Q

if tryptophan is plentiful

A

ribosome will translate leader sequence and inhibit further transcription

29
Q

if tryptophan is in short supply

A

ribosome will be stalled during translation but transcription will continue

30
Q

when there is excess tryptophan (explain)

A

-want to turn off transcription
-base pairing is done close to the leader sequence
-RNA polymerase terminates because of the stem loop structure

31
Q

when there is not enough tryptophan

A

-ribosome gets stopped because there is not enough tryptophan
-secondary structure forms earlier because ribosome takes longer to move
-RNA polymerase can continue because the stem loop structure is further away from the leader sequence