Kandpal - Translation 1 Flashcards
What is the start codon?
AUG = Met
Since there are 3 stop codons what are they?
UAA, UAG, UGA
What is the terminus for amino acids sequence in a protein?
N terminus to C terminus
Since the genetic code is commaless and nonoverlapping. What does that mean?
Since there is no comma this causes potential changes in in the sequence.
Note: There are exceptions, AUG for N-formyl methoinine and methionine. UGA: stop codon and selenocysteine. UAG: Stop codon and oyrrolysin
What are the 3 type of mutations?
- Silent - change in nucleotide but does not change in the amino acid sequence (Mutattion in the 3rd position of a codon)
- Missense - substitution of one amino acid for another
- Nonsense - replacement of a sense codon with a stop codon
How many consecutive bases in an mRNA can be read in a sequence?
3 frames for one strand
For tRNA, what attaches the amino acid and a protein?
An adaptor.
Note: tRNA is a secondary and tertiary structure
Modifications provides stability for tRNA’s against regeneration or degradation?
Degradation.
At the 5’ end, what does it end with?
“G”
AT the 3’ end, what does it end with?
CCA-3’
Note: the 3’ end is an amino acid attachment site
If you have fewer than 61 codons it is a problem, what is the solution and how is this recognized?
The Wobble effect, an alternate base pairing, which it is a base pairing where it can understand where there is a non paired hydrogen bonding.
What type of modified is especially promiscuous in non stranded base pairing?
Inosine, only found in tRNA
The adaptor of the amino acid attached at what junction?
3’ OH of tRNA and is carried out by aminoacyl tRNA synthetase
What is the intermediate where ATP is used for amino acid activation?
AMP. ATP is hydrolyzed and becomes AMP
What are the 2 pockets for that scrutinize an amino acid?
Editing site and Synthesis site. This allows for proper sequence to be added.
What are the 2 ways an enzyme recognizes t-RNA?
- binding of anticodon to a 3- nucleotide binding pocket on the enzyme.
- making contact with the sequence in the acceptor stem.
What may be a cause when selenoprotein N mutation?
Different forms of autosomal recessive muscle disorders
ie. Congenital muscular dystrophy with spinal rigidity (RSMD1)
What are ribosomes?
Ribonucleoproteins with large “surface” and catalytic activity for protein synthesis
What are the 3 sites on the large ribosome?
E-site: Exit of deacylated tRNA
P-site; Most recently added amino acid (Peptidyl tRNA)
A-site:incoming Aminoacyl tRNA
Since there are 50s subunits and 30s subunits, how many assembled ribosomes are there?
70s, don’t do the math. lol
What type of AA will cause non watson/crick base pairing?
Inosine