The codon UGU codes for the amino acid Cysteine. The codon UGG codes for the amino acid Tryptophan.
Therefore the mutation will cause the amino acid Cysteine to be replaced with Tryptophan. These amino acids are quite different, and the final shape of the protein could be changed as a result. This could affect the function of the protein.
A missense mutation is the type that would only affect one amino acid in a protein sequence. This occurs when a single nucleotide change in the DNA sequence results in the substitution of one amino acid for another in the corresponding protein. This alteration can potentially impact the protein's function, depending on the role of the altered amino acid. Other mutations, like silent or nonsense mutations, do not affect the amino acid sequence in the same way.
The amino acid sequence is shifted, and this kind of mutation is called a frame shift mutation. All of the amino acid sequence after the mutation will be changed, which will cause a change in shape of the protein, which will then probably result in a nonfunctional protein, since the shape of a protein determines its function.
A silent mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein. This can happen through a substitution of a nucleotide that still codes for the same amino acid due to the redundancy of the genetic code. For example, if the original sequence is "GAA" (which codes for glutamic acid) and it changes to "GAG," this would represent a silent mutation since both codons code for the same amino acid. Thus, the change in the sequence that doesn't affect the protein's amino acid sequence indicates a silent mutation.
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A mutation that alters the base but not the amino acid is called a "silent mutation." This type of mutation occurs when a change in the DNA sequence does not affect the protein's primary structure due to the redundancy in the genetic code, where multiple codons can code for the same amino acid. Consequently, the resulting protein remains unchanged despite the alteration in the nucleotide sequence.
A missense mutation is the type that would only affect one amino acid in a protein sequence. This occurs when a single nucleotide change in the DNA sequence results in the substitution of one amino acid for another in the corresponding protein. This alteration can potentially impact the protein's function, depending on the role of the altered amino acid. Other mutations, like silent or nonsense mutations, do not affect the amino acid sequence in the same way.
The amino acid sequence is shifted, and this kind of mutation is called a frame shift mutation. All of the amino acid sequence after the mutation will be changed, which will cause a change in shape of the protein, which will then probably result in a nonfunctional protein, since the shape of a protein determines its function.
A silent mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein. This can happen through a substitution of a nucleotide that still codes for the same amino acid due to the redundancy of the genetic code. For example, if the original sequence is "GAA" (which codes for glutamic acid) and it changes to "GAG," this would represent a silent mutation since both codons code for the same amino acid. Thus, the change in the sequence that doesn't affect the protein's amino acid sequence indicates a silent mutation.
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A mutation that alters the base but not the amino acid is called a "silent mutation." This type of mutation occurs when a change in the DNA sequence does not affect the protein's primary structure due to the redundancy in the genetic code, where multiple codons can code for the same amino acid. Consequently, the resulting protein remains unchanged despite the alteration in the nucleotide sequence.
Amino acid order.
Most genetic disorders result from a mutation that changes the amino acid sequence in a protein. This change can lead to altered protein function, which can affect normal cellular processes and result in disease.
Yes, it already has by changing the amino acid you have a mutation. That one amino acid counld be in the active site of an enzyme and that one amino acid being changed could result in loss of function or reduction in function of the enzyme. Sickle cell animea is caused by a single such amino acid substiution.
A mutation can change a codon for one amino acid into a different codon for the same amino acid through a process called silent mutation. This type of mutation occurs when a change in the DNA sequence does not alter the amino acid that is coded for, resulting in the same protein being produced.
a silent mutation.
It is neutral mutation. Codons are made up of 3 base pairs. This gives 64 different combinations, but there are only 20 amino acids, so some different codons will code for the same amino acid. When the base pair that is changed doesn't cause a change in the amino acid it codes for, then ultimately nothing happens
The mutation described is a "silent mutation." This term is used because the change from G to U in the second position of the sequence does not alter the resulting amino acid due to the redundancy in the genetic code. Specifically, both GGU and GGU (the original and mutated sequences) code for the same amino acid, glycine. Therefore, the mutation does not affect the protein's sequence or function.