answersLogoWhite

0

What else can I help you with?

Continue Learning about Natural Sciences

If a strand of DNA with the sequence TGA mutated to GCA would it be a silent or missense mutation?

Both a silent and missense mutation is a change in one nucleotide. However, a silent mutation still codes for the same amino acid, but a missense mutation codes for a different amino acid. This means that a silent mutation will have no affect on the resulting protein, but a missense mutation will. Still, it is not guaranteed that a a missense mutation will result in a disfunction of created protein, as long as it is not occurring in the activation site.


What kind of mutation is tag ctt ggc at?

The sequence "tag ctt ggc" provided does not represent a specific mutation. A mutation would involve a change in a specific base or bases within a DNA sequence. Without further context or details, it is not possible to determine the type of mutation.


If a codon is mutated say from GGU to CGU is the same amino acid specified?

Yes. GGU specifies Glycine and CGU specifies Arginine.


Why is point mutation dangerous?

A frame shift mutation destroys the correct sequence of amino acids from the point of the mutation. The protein produced by a frame shift mutation would more than likely be nonfunctional.


How many amino acids would this protein have if a mutation occurred and the 7th dna base pair of the dna strand was changed from a-t to t-a?

This mutation would cause a frameshift mutation, shifting the reading frame of the DNA sequence. Most likely, this would lead to a completely different protein being translated, resulting in a protein with a different sequence of amino acids from the original protein. The number of amino acids would depend on the specific changes in the protein sequence caused by the frameshift mutation.

Related Questions

If a strand of DNA with the sequence TGA mutated to GCA would it be a silent or missense mutation?

Both a silent and missense mutation is a change in one nucleotide. However, a silent mutation still codes for the same amino acid, but a missense mutation codes for a different amino acid. This means that a silent mutation will have no affect on the resulting protein, but a missense mutation will. Still, it is not guaranteed that a a missense mutation will result in a disfunction of created protein, as long as it is not occurring in the activation site.


A part of an mRNA has the sequence CCG. which change to this sequence would indicate a missense mutation?

CGG GAA


What One example of a mutation that would not affect an organisms phenotype?

A silent mutation is an example of a mutation that would not affect an organism's phenotype. This type of mutation occurs in a non-coding region of DNA, such as an intron, and does not change the amino acid sequence of the protein produced. Therefore, it has no impact on the organism's outward appearance or characteristics.


What happens if only one amino acid is coded incorrectly?

If only one amino acid is coded incorrectly in a protein sequence, it may result in a missense mutation. This could potentially lead to a change in the structure and function of the protein. The impact of the mutation would depend on the specific amino acid involved and its location within the protein.


What would have a bigger effect on organism an error during transcription or a missense mutation?

IF only you weren't here for apex! you're welcome for making your day!


Which do you suppose would be more harmful A mutation that changed the nucleotide sequence of an mRNA molecule or a mutation that changed the nucleotide sequence of a DNA molecule?

A mutation in a DNA nucleotide sequence would be more harmful than a mutation in a mRNA nucleotide sequence because it could cause the synthesis of multiple nonfunctional proteins in comparison to a mutation in a mRNA nucleotide sequence that would be less harmful because it would result in a few nonfunctional proteins.


Which mutation would not change the remainder of the reading frame of a gene sequence that follows the mutation?

A silent mutation, where a nucleotide substitution results in a codon that codes for the same amino acid, would not change the remainder of the reading frame of a gene sequence. This is because the amino acid sequence produced by the altered codon remains the same.


What is point mutation substitution?

When a nitrogen base is substituted for a different one so it may code for a different amino acid. Sometimes substitution still codes for a same amino acid, in which case it becomes a silent mutation, but in other times it may alter the protein entirely.


What could happen to DNA that would cause a change in trait or a new trait to be expressed?

That would be a mutation. There are several types of mutations such as silent, nonsense, missense mutations along with inserstions, deletions and amplifications


What kind of mutation is tag ctt ggc at?

The sequence "tag ctt ggc" provided does not represent a specific mutation. A mutation would involve a change in a specific base or bases within a DNA sequence. Without further context or details, it is not possible to determine the type of mutation.


A part of an mRNA has the sequence CAU Use the table below to figure out which amino acid is coded for by CAU then use the table to figure out which change to this sequence would indicate a silent?

AGG-Apex


If a codon is mutated say from GGU to CGU is the same amino acid specified?

Yes. GGU specifies Glycine and CGU specifies Arginine.