A frame shift mutation is the shift of the genetics of an object.
This type of mutation os caused by the insertion or deletion of nucleotides in a DNA sequence that is not divisible by three.
Answer:
Its a substitution mutation because one of the specific base, G is replaced by A.
This is a Point Mutation because Point mutation brings changes in the structure of a gene because of the substitutions with another base pair. Like in this case, G is substituted by A. In case of frameshift mutations, there is a change in the number of nucleotides due to either insertions or deletions of the nucleotides, which is not in this case.
Answer:
because it is hard to breakdown fat in a very short time while ATP can be broken down in a very short time.Fats have a very strong bond of molecular chains and this makes it hard to breakdown quickly
Answer:
A) they help transport some substances through the membrane.
Explanation:
The membrane proteins that span the bilayer of phospholipids help in the transport of polar, large and charged substances across the membrane. The nonpolar core of the membrane does not allow these charged and polar substances to pass through. Proteins serving as channels form pores to allow movement of the specific substances.
On the other hand, carrier transport proteins of the membrane bind to the substances present at one side of the membrane and deliver them to the opposite side.
