G stands for Guanine, which always pairs with Cytosine. A stands for Adenine, which always pairs with Thymine.
The base sequence for the complementary DNA would be GCA AT. Since DNA strands are complementary, the bases pair as follows: A with T, T with A, C with G, and G with C.
Gca-tat gca ta The answer is AGC CT cat gt
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.
5`... ccagattg ... 3` 3`... ggtctaac ... 5`Remember always A complementarly binds with t with a double bond (hydrogens bonds)(a=t) in the same way g with c by means of 3hydrogen bonds between them.....
To determine the amino acid sequence from mRNA, you would first transcribe the mRNA into a complementary DNA sequence, then translate the DNA sequence into amino acids using the genetic code. Each set of three nucleotides (codon) in the mRNA corresponds to a specific amino acid in the protein.
The complementary DNA strand is formed by pairing adenine (A) with thymine (T) and cytosine (C) with guanine (G). Therefore, if one strand has the sequence gta-gca, the complementary strand would have the sequence cat-cgt.
The sequence of nucleotides that would pair with GCA is CGT. In DNA, guanine (G) pairs with cytosine (C), and adenine (A) pairs with thymine (T). Therefore, for the RNA sequence, GCA would pair with CGU, where uracil (U) replaces thymine.
The base sequence for the complementary DNA would be GCA AT. Since DNA strands are complementary, the bases pair as follows: A with T, T with A, C with G, and G with C.
The strand of mRNA produced from the DNA sequence GCA TTA would be complementary to the DNA template strand. The corresponding mRNA sequence would be CUG AAU, where adenine (A) pairs with uracil (U) in RNA, cytosine (C) pairs with guanine (G), and guanine (G) pairs with cytosine (C).
Gca-tat gca ta The answer is AGC CT cat gt
Gca-tat gca ta The answer is AGC CT cat gt
give the complementary DNA sequence of 5' atg ctt gca cca gtg tga aaa agg gcg?
The sequence "uaa caa gga gca ucc" does not represent any meaningful information on its own. It appears to be a random sequence of nucleotides without any context or indication of what it may represent in terms of genetic information or a specific protein. If you provide more information or context, I may be able to help you interpret it.
During transcription, the DNA sequence is converted into a complementary RNA sequence. For the given DNA base sequence CGT ACG GCT AC, the corresponding RNA sequence would be GCA UGC CGA UG. This involves replacing thymine (T) with uracil (U) in RNA.
The base sequence of RNA is complementary to the DNA from which it is transcribed. This means that RNA contains the same genetic information as the DNA template, with thymine (T) being replaced by uracil (U).
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.
5`... ccagattg ... 3` 3`... ggtctaac ... 5`Remember always A complementarly binds with t with a double bond (hydrogens bonds)(a=t) in the same way g with c by means of 3hydrogen bonds between them.....