The effect of the mutation is; there would be another amino acid that may form due to the change in sequence of the anticodon. change in the sequence of anticodon may result to different amino acid that may form.
In a point mutation, a change in a single nucleotide can lead to a specific mutation. For example, a substitution mutation occurs when one nucleotide is swapped for another, such as A to T or C to G. This change can result in different amino acids being coded for in the protein sequence.
This is a substitution mutation where the nucleotide "c" is replaced with "g" at the beginning of the sequence.
The most common type of mutation is a point mutation, where a single nucleotide base is changed, inserted, or deleted in the DNA sequence. This can result in a different amino acid being incorporated into the protein during translation, leading to potential changes in the protein's function.
An example for this is, cytidine deaminases (AID and APOBEC proteins), they can convert C in to U, there by make G--A mutation in double stranded DNA.
The effect of the mutation is; there would be another amino acid that may form due to the change in sequence of the anticodon. change in the sequence of anticodon may result to different amino acid that may form.
The tRNA anticodon for TAC would be AUG. However, tRNA does not transcribe DNA and would not come in contact with the nitrogen base thymine. A better question would be what is the tRNA anticodon for the mRNA codon UAC.
A pairs with T so the anticodon would be TTT
In a point mutation, a change in a single nucleotide can lead to a specific mutation. For example, a substitution mutation occurs when one nucleotide is swapped for another, such as A to T or C to G. This change can result in different amino acids being coded for in the protein sequence.
please chose one of the choices below 1) the mrna will be changed from U-A-C tp U-A-G 2)the trna will be changed from U-A-C to T-A-C 3) the mrna will be changed from T-U-C to T-U-G 4) The trna willbe changed from C-A-U to C-A-C choice one of them 1)
the corresponding anticodon will be GAT because the C transfers to G, the U transfers to A and the A transfers to T----- DR. Mohamed AK-47
UUGCodon-AnticodonA - UT - AC - GG - C
The matching anticodon for GCA would be CGU.
The sequence TGA-GCC-ATG-A is changed in 2 places to become TGA-GCA-CAT-GA.When one base is changed, it is called a point mutation.In this case, a GCC in the DNA has been changed to a GCA. This would mean the mRNA codon (coded for by this DNA) would change from CGG to CGU.Both of these codons code for the same amino acid - Arginine. Therefore this type of point mutation is known as a silent mutation.The extra C that appears would be called an addition mutation, which is a type of frameshift mutation.
The only base-pairs that are possible are: Adenine - Uracil (for RNA, since the question refers to codon and anticodon) Guanine - Cytosine The reason for this particular base pairing is that it is the only possible combination for the hydrogen bonds between the bases to be effectively made.
The sequence TGA-GCC-ATG-A is changed in 2 places to become TGA-GCA-CAT-GA.When one base is changed, it is called a point mutation.In this case, a GCC in the DNA has been changed to a GCA. This would mean the mRNA codon (coded for by this DNA) would change from CGG to CGU.Both of these codons code for the same amino acid - Arginine. Therefore this type of point mutation is known as a silent mutation.The extra C that appears would be called an addition mutation, which is a type of frameshift mutation.
The anticodon of a tRNA molecule has only three nitrogen bases. The anticodon is complementary to a codon of mRNA at the ribosome. The tRNA molecule carries a specific amino acid from the cytoplasm to its complementary mRNA codon, where it will be incorporated into the new protein being made.