Answer:
a) phenylalanine
Explanation:
A triplet codon results into a particular amino acid. mRNA is read in 5' to 3' direction during translation. tRNA carrying an amino acid enters the A site first. Then a peptide bond is formed between the new and old amino acid. The polypeptide along with the tRNA moves to P site while the now empty old tRNA moves from P to E site and exits. Hence a tRNA is first in A site followed by P site and then finally E site.
Here, a tRNA with histidine amino acid is present in the P site. From the given sequence, only CAU codon can result into histidine. So if CAU region is present in P site that means that UUU will be present in A site. UUU codes for phenylalanine amino acid so the tRNA entering the A site will carry phenylalanine.
Answer:
The correct answer is C the extraction of high energy electrons remaining from glycolysis and citric acid cycle .
Explanation:
Electron transport chain(ETC) occur in mitocondria and is the last process of aerobic respiration.ETC deals with the transfer of electron from the reducing equivalent such as NADH,FADH2 thereby oxidising them to their oxidized form NAD+,FAD.
The liberated electron from these equivalents utilizes the proton motive force come from the transport of H+ ion cytosol to mitocondrial matrix and then result in the phosphorylation of ADP to form ATP along with H2O by the reduction O2.
Ansa million. once you're staring at in ordinary terms one technology, it relatively is, all those fruit flies have been produced via 2 mum and dad, then the only plausible parental genotype that provide you a 50/50 ratio is that if the mummy is XwXw and the father is Xry... this gene is carried on the X chromosome, and w represents white eyes and r represents purple eyes. you are able to bypass forward and draw this out in case you like, even yet it provides 50% heterozygous women individuals (with purple eyes, provided that purple is dominant), and 50% white eyed men, who can in ordinary terms inherit Xw from their mom. The Y that they could inherit from the father could have not any effect on their eye shade. it relatively is comparable for women individuals, they are in a position to in ordinary terms inherit Xw from their mom and an Xr from their father, meaning they'll continually be heterozygous for the attention shade gene. 2. returned, set us the genotypes so which you will visualize it; we are going to say that this disease is carried on the X chrmsm (thats whats usually assumed), and the gene for customary creative and prescient is XB, yet for colorblindness its Xb. those are dominant/recessive to boot. So, if the girl is a provider, her genotype is XBXb, and if the male is colorblind, his genotype is XbY. in case you draw this out in a punett sq., you will get 25% heterozygous woman, 25% colorblind woman, 25% well-known male, and 25% colorblind male. so, there's a 50% risk that any baby they have would be colorblind, 50% risk if its a woman, or 50% risk if it relatively is male.wer:
Explanation:
A topographic map I believe would do great.
Answer: fossils provide evidence of the past that shows how species of changed over time.
Explanation:
My teacher said it
