While both will equate changes in a genetic chain, deletion would have more severe consequences. A substitution mutation usually only causes minor disorders and diseases, like sickle cell anemia. Whereas deletion causes much more serious diseases, like cystic fibrosis, and turner syndrome which is where a female is born with only one X chromosome.
Dark reactions<span> make use of these organic energy molecules (ATP and NADPH).</span>
Answer: Holds Genetic Information
Explanation:
Answer:
<h2>Its true!!</h2>
Explanation:
Actually the haemoglobin molecule consists of 2 parts, the haem which is a prosthetic group and the other globin which is a protein. So the haemoglobin as is a protein so, is arranged in quaternary structure of protein which contains 4 subunits. The subunits depend upon the organism whose haemoglobin is being talked about. So the normal haemoglobin found in red blood cells contains 2 alpha subunits + 2 beta subunits. At the centre of each subunit there is the haem part attached. To the centre of haem the Fe3+ ion are present which actually attaches to 1 Oxygen molecule. So as 4 subunits are present and each subunit has 1 Fe3+ ion, so total 4 Oxygen molecules can bind to the 1 Hb molecule!!
