Lipincott Chapter 31 Flashcards

0
Q

T or F. Huntington’s and Fragile x syndrome are examples of trinucleotide repeat expansion.

A

True. Huntington is CAG repeats (glutamine), and fragile X repeats in the UTR of a gene, decreasing protein produced.

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1
Q

When the genetic code is said to have: specificity, universality, degeneracy and nonoverlapping, what does that mean?

A

Specificity: particular codon always codes for the same AA.
Universality: same code, save for mitochondria
Degeneracy: redundant codes for one AA
Nonoverlapping: code is read from fixed point.

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2
Q

What enzymes are required to attach amino acids to their corresponding tRNAs?

A

Aminoacyl tRNA synthetases.

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3
Q

What does the APE sites in a ribosome do, respectively?

A

A: binds incoming aminoacyl tRNA
P: peptidyl tRNA, this tRNA carries chain of amino acids already synthesized
E: empty tRNA exiting ribosome

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4
Q

T or F. Mitochondria have their own DNA and ribosomes, and make most of their own proteins.

A

False. Most mitochondrial proteins are encoded by nuclear DNA, made by ribosomes in the cytosol and post translationally targeted to mitochondria.

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5
Q

How much energy is required to add one aa to a growing polypeptide chain?

A
  1. two from ATP for the aminoacyl tRNA synthetase reaction

two from GTP for the binding of tRNA to the A site, and the translocation step.

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6
Q

What is the wobble hypothesis?

A

codon anticodon pairing follows the traditional CG AT rule for the first two bases of the codon but can be less stringent for the last base.

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7
Q

What is the Shine Dalgarno sequence?

A

in E. coli mRNA, a purine rich sequence 6-10 bases upstream of AUG where the rRNA component of a ribosomal subunit complements, attaches.

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8
Q

What is the 5’ cap?

A

the eukaryotic equivalent of the shine dalgarno sequence. 5’ cap binds to small 40s subunit and moves down sequence until it hits AUG. scanning process requires ATP.

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9
Q

Describe the process of initiation in translation.

A

AUG recognition is facilitated by (e)IF2-GTP. Initiator tRNA enters P site directly. Large ribosomal subunit joins complex. N terminal Met usually removed before translation completes.

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10
Q

Describe elongation of amino acid chain.

A

tRNAs delivered to A site, facilitated by elongation factors. peptide bond formed by the peptidyltransferase activity of an rRNA of the large ribosomal subunit. the aa on the tRNA in the P site bonds with the aa of the tRNA in the A site. Translocation moves APE down 3 nucleotides (costs GTP to GDP)

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11
Q

Describe aa termination.

A

Termination codons enter A site, recognized by termination factors RF1 and RF2 (eRF). This hydrolyzes the bond between the peptide and tRNA in the P site. RF3 (eRF3) releases RF1/2 (eRF).

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12
Q

eIF, which helps bring initiator tRNA to P site, when phosphorylated, is ______.

A

Inactive.

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13
Q

T or F. NLS and mitochondrial entry sequence are examples of protein targeting sequences.

A

True.

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14
Q

What is protein trimming?

A

many proteins destined for secretion are made as large precursors that are cleaved via endoproteases in the ER, golgi, or secretory vesicle.

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15
Q

Post translational covalent attachments include:

A

Phosphorylation: on Ser, Thre, Tyr by kinases
Glycosylation: for proteins destined to be part of plasma membrane or secreted have carbs added (N linked Asp, or O linked Ser Thre Lys)
Hydroxylation: Proline and lysine, especially in collagen

16
Q

___ of 20 amino acids cannot be synthesized in humans.

A

9.

17
Q

Wheat is lysine deficient, methionine rich. _____ are lysine rich, methionine deficient.

A

BEANS

18
Q

When does positive nitrogen balance occur?

A

childhood, pregnancy, recovery from emaciation

19
Q

Negative nitrogen balance occurs when…

A

inadequate dietary protein, lack of an essential aa, physiologic stresses

20
Q

what is the RDA of protein?

A

0.8 g/kg body weight,