Answer:
The correct answer would be - C) the shape of a molecule determines how it functions in chemical reactions
Explanation:
The molecular shape of the molecules is one of the important characters of the molecules. It is important due to the fact that molecular shape determines how a molecule will react and interact with other molecules.
The shape of the molecules determines boiling point, melting point as well as various chemical reaction by determining the bonds. For instance, H2O or water has a tetrahedral shape which affects its bonding and properties. If molecules were linear in shape there would be no life existed.
Thus, the correct answer would be - C)
Explanation:
A single nucleotide-pair substitution missense mutation causes a change of a single amino acid into another. Aa a result, the produced protein will have an almost normal sequence except for one amino acid.
On the other hand, a frameshift mutation changes the Open Reading Frame (ORF) of the ribosome. The ribosome moves along the mRNA every three nucleotides (codons) and translates them into amino acids that will form the nascent protein. If there is a frameshift mutation (an insertion or deletion of a number of nucleotides not multiple of three) the ribosome will "read" the mRNA differently and will identify different codons than the wild-type sequence, so a large number of amino acids will be different in the mutated protein.
Answer:
where is the picture or what is it talking about?
Answer:
All of the statements are true.
The X chromosome is one of the two sex chromosomes of humans and some animals (the other sex chromosome is the Y chromosome). Men have a single X chromosome and women two X chromosomes.
Diseases whose gene is localized on the X chromosome are most often transmitted in the X-linked recessive mode; some are transmitted on the dominant mode related to the X.
In this mode of inheritance, the morbid allele behaves like a recessive trait.
Women heterozygotes are not affected but can transmit the disease; they are aid to be conductive of the disease.
The disese is only manifested in male subjects (XY) with only one copy of the gene (hemizygous subjects)
