Answer:
To solve this question, it is necessary to consider the number of protein structures that have been empirically verified and the number of Open reading frames predicted from sequencing data
Explanation:
The most common methodologies used to determine protein 3D structure are nuclear magnetic resonance (NMR) and X-ray crystallography. Although both methods are efficient, the determination of 3D protein structures in physiological conditions is a time and cost-consuming task. Moreover, due to recent advances in bioinformatics and sequencing methodologies, the amount of protein Open Reading Frames predicted from sequencing data (especially obtained from Next Sequencing Generation studies) is many times higher. Indeed, less than 5% of sequenced proteins have an empirically validated 3D structure.
It would be G and H because that is when the nuclear membrane forms and two new cells are formed
hope this helped :3
Answer:
It's too hard
Explanation:
do you go to school. What grade/year are you in?
Answer:
E. Each codon represents a different amino acid.
Explanation:
The genetic code refers to the set of rules guiding the translation of nucleotide bases in DNA or RNA into an amino acid sequence (proteins). The genetic code contains all the codons in the genome, which is a group of three nucleotide base (triplet-based). Each codon species a particular amino acid, however, more than one codon can code for a particular amino acid. This characteristics of the genetic code is called DEGENERACY.
The genetic code is said to be nearly universal because the same codon encodes the same amino acid in almost all living organisms with only few exceptions. The nonoverlapping nature of the genetic code refers to the fact the three bases of a codon are read independently from the bases of another codon i.e. codons do not overlap.
A codon represents one amino acid but more than one codon can represent the same amino acid. Hence, option E is untrue
