answersLogoWhite

0

A wobble base pair is a type of non-standard pairing between nucleotides in DNA or RNA. It occurs when the third base in a codon can pair with multiple different bases in the anticodon during translation. This flexibility allows for some variation in the genetic code without changing the amino acid sequence of a protein. Wobble base pairing helps to increase the efficiency and accuracy of protein synthesis by reducing the likelihood of errors during translation.

User Avatar

AnswerBot

6mo ago

What else can I help you with?

Related Questions

Is "AUG" a start codon in genetic coding?

Yes, "AUG" is a start codon in genetic coding.


What is the function of most of the DNA in the body?

Most of the DNA in humans appears to have no genetic function.


Is ATG a start codon in genetic coding?

No, ATG is not a start codon in genetic coding. The start codon is typically AUG.


What is the function of introns in genetic material?

Introns are non-coding sections of DNA that are removed during the process of gene expression. They help regulate gene expression and can also contribute to genetic diversity through alternative splicing.


Why is AUG called the start codon in genetic coding?

The codon AUG is called the start codon in genetic coding because it signals the beginning of protein synthesis in a gene. It initiates the process of translating the genetic information into a protein.


Genetic codes contain what?

the contain what you look like and mabye what your kids will look like but i might be wrong


When eukaryotic cell part contains directions for cell growth and reproduction?

The nucleus contains the genetic material (DNA) that carries the instructions for cell growth and reproduction in eukaryotic cells. This genetic material is organized into chromosomes and is responsible for coding various proteins that regulate the processes of cell division and growth.


Why do multiple sequences code for the same amino acid in genetic coding?

Multiple sequences code for the same amino acid in genetic coding because of redundancy in the genetic code. This redundancy allows for errors in DNA replication or mutations to occur without affecting the final protein structure and function.


What is the genetic coding?

The genetic code is the set of rules by which information encoded in genetic material (DNA or RNA sequences) is translated into proteins (amino acid sequences) by living cells.


What is the coding mechanism for heredity?

The coding mechanism for heredity is primarily based on DNA, which consists of sequences of nucleotides that encode genetic information. Genes, which are specific sequences of DNA, provide instructions for synthesizing proteins that influence traits and functions in an organism. During reproduction, genetic information is passed from parents to offspring through the processes of meiosis and fertilization, ensuring the continuity of hereditary traits. This molecular blueprint is central to inheritance and variation in living organisms.


How point mutation frame shift mutation and meiosis contribute to genetic variation?

Point mutations introduce single nucleotide changes in the DNA sequence, leading to variations in protein coding sequences. Frame shift mutations result from insertions or deletions of nucleotides, altering the reading frame and causing significant changes in protein sequences. Meiosis, through the processes of crossing over and independent assortment, shuffles genetic material between homologous chromosomes, generating new combinations of alleles and increasing genetic variation among offspring.


Can coding DNA type of genetic material be used for DNA fingerprinting?

Yes, coding DNA can be used for DNA fingerprinting. Coding DNA, which contains genes that encode for proteins, can contain genetic variations that are unique to each individual. These variations can be used as markers in DNA fingerprinting to identify individuals or determine relationships between individuals.