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Cell bio-
Protein Synthesis
| Question | Answer | |
|---|---|---|
| Myotonic dystrophy gene silencing is | the result of splicing alterations | |
| what is the difference between charged and uncharged tRNAs | charged tRNA has a.a | |
| tRNA binding is parallel and semi-complementary | F : its antiparallel and complementary | |
| mRNA is read __ direction and paired by a tRNA in the __ direction. | 5'- 3' and 3' to 5' | |
| an enzyme that attaches an amino acid to its corresponding tRNA with a covalent bond | aminoacyl-tRNA synthetase : | requires ATP |
| aminoacyl-tRNA sits at | A site | |
| peptidyl tRNA sits at | P site | |
| wobble hypothesis | A tRNA can recognize more than one codon for a specific amino acid. | |
| initiation codon | AUG | |
| translation factors that facilitate initiation | IF-2 in prokaryotes and eIF2 in eukaryotes | |
| on which organism is the initator tRNA binds to an N -formulated methioine | prokaryotes , | not in eukaryotes |
| amino acid is added to what end of the growing polypeptide chain | amino acid | |
| Ribosome moves from___ to __ end of mRNA. | 5’-end to 3’- | |
| Elongation factors ----- facilitate the delivery of the aminoacyl-tRNA to the next corresponding codon on the mRNA | EF-Tu and EF-Ts | they require GTP |
| the peptide bond is catalyzed by | peptidyl transferase ; a reaction facilitated by | 23s rRNA. which is a ribozyme |
| In order for the ribosome to advance 3 nucleotide down on the mRNA , what is required | EF-G and GTP | |
| elongation :: The charged tRNA is released and The peptidyl-tRNA moves from the A site to the P site. | first is false , second it true | |
| termination release factors | RF-1 and Rf-2 ; | RF-3 binds GTP and stimulates the activity of RF-1 and RF-2 |
| high levels could inhibit mitochondrial protein synthesis | chloramphenicol | |
| an enzyme that cleave a portion of the protein to activate it | Endoproteases | |
| in post-translational hydroxylation what a.a are hydroxylated | proline and lysine | |
| example of diseases cause by tandem repeats | huntington ( extraglutamine) fragile X and myotonic dystrophy |