Anontemplate strand of bacterial dna has the base sequence 5′−atgatactaaggccc−3′ determine the amino acids that will be encoded by this sequence. add the amino acids from left to right in the order the amino acids will be translated.

fMet-Ile- Leu-Arg-Pro.

Explanation:

First of all, the DNA sequence will need to be transcribed into its respective mRNA so as to know the codons that will that will translate to each amino acid.

However, for a non-template DNA strand, the DNA sequence is the same as the mRNA sequence except that the thymine base in DNA is replaced with uracil base in the mRNA.

Hence,  5′−ATGATACTAAGGCCC−3′ will become 5'-AUGAUACUAAGGCCC-3'.

The first codon AUG represents the start codon (Methionine) and using the genetic codon table

AUA = isoleusine (Ile)

CUA = leucine (leu)

AGG = Arginine (arg)

CCC = proline (pro)

Adding the amino acids from left to right in order of translation, it becomes fMet-Ile- Leu-Arg-Pro.

sadness is not good

explanation:

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.