Protein Transport Flashcards

1
Q

Core of 6-12 hydrophobic AA proceeded by one or more basic AA

A

ER

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2
Q

3-5 non consecutive Arg or Lys . . often contains ser or Thr, amphipathic helix

A

Mitochondria

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3
Q

Ser–Lys–Leu (SKL)

A

Peroxisomes

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4
Q

5 basic AA

A

Nucleus

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5
Q

Nuclear pores . . .

A

Occludes proteins > 60 kd. Hydrophobic (phenylalanine and glycine core). Requires a truck to dump stuff in.

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6
Q

Alpha importin

A

Recognizes the NLS and binds the NLS.

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7
Q

Beta Importin

A

Mediates docking with the outer surface of the nuclear pore in an energy independent fashion.

** Allows the complex to shoot through the nuclear pore (phenylalanine and glycine complex).

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8
Q

Carries the Ran GDP in

A

NTF2

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9
Q

Ran GTP does what?

A

Knocks the cargo off once in the nucleus.

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10
Q

After Ran GTP knocks off the cargo , , , what happens ?

A

Ran GTP binds to alpha importin and the importin/RanGTP complex can leave the nucleus.

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11
Q

RanBP what’s it do

A

Takes RanGTP off of importin complex once it is back in the cytoplasm.

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12
Q

After RanBP takes off the RanGTP from the importin complex in the cytoplasm, what happens to RanBP?

A

RanBP now possesses what it took off from the importin complex (RanGTP). And now. . Ran GAP turns the RanGTP in the cytoplasm to RanGDP so now the GDP can go out into the nucleus for the cycle to repeat.

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13
Q

Ran GEF

A

Turns RanGDP to RanGTP in the nucleus so that RanGTP can unload more cargo.

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14
Q

Ligand induced NLS activation

A

Binding of ligand causes NLS to move to outside.

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15
Q

NLS is only imported when it is

A

Dephosphorylated

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16
Q

At the start of the cell cycle when the lamins become phosphorylated, the 1.?

When de-phos, . . . 2.?

A
  1. Break up

2. Reassemble (GTP dependent)

17
Q

Mitochondrial transport is

A

POST-translational
** ANd requires energy !!

** And nuclear proteins have to be imported into mitochondria.

18
Q

100% required for mitochondrial protein transport

A
  1. Electrochemical gradient
  2. Aliphatic positively charged helix
  3. Chaperones (Hsp-70s)
19
Q

Outer and inner chaperones

A

Outer -unfolds proteins

Inner -ratchets the proteins in.

20
Q

Can the signal sequence be removed in the mitochondria?

A

Yes

21
Q

Big thing about peroxisomes

A

Plasmolegens

22
Q

Main peroxisomal targeting sequence is at which term ?

A

C term . . . SKL

23
Q

Transporter to peroxisomes

A

PEKS 5

24
Q

Substitution of what amino acid leads to what disease regarding peroxisomes . . .

A

Alanine glyoxylate aminotransferase.

Leads to hyperoxaluria.

Results in renal failure.

25
Q

Does peroxisomal transport require ATP or membrane potential?

A

ATP,but no membrane potential.

26
Q

What carries the cargo into the peroxisomes and what does the carrier do?

A

Forms the gate itself.

27
Q

Channel into peroxisomes is recycled how

A

ATP hydrolysis after it becomes ubiquitinated.

28
Q

Zellwegar syndrome

A

Defect in getting many protein to peroxisomes.

AR

Caused by absence of Pex5p receptor.

Enzymes such as catalase will be found in the cytoplasm rather than in peroxisomes.

29
Q

Familial hyper cholesterol is caused by

A

Mutation in LDL receptor

Autosomal Dominant

30
Q

Statins are inhibitors of

A

3-hydroxy-3-methyl-glytaryl-coenzyme A reductase

31
Q

Common ligand that binds to LDL receptor

A

B-100