Based on the above information, the mutation type is frameshift mutation.
It is a genetic mutation caused by indels of various nucleotides in a DNA succession that is not detachable by three. The additions and erasures cause an adjustment in the length of a quality, which causes a movement in the codon perusing outline. A frameshift mutation happens when a protein is radically modified as a result of an addition or an erasure. Tay-Sachs illness is a human issue caused by a frameshift change.
A and D are almost entirely solid solid
Answer:
Components of the electron transport chain (ordered by electronegativity from least electronegative to most electronegative):
NADH dehydrogenase >> Coenzyme Q >> Cytochrome b-c1 complex >> Cytochrome c >> Cytochrome oxidase complex > O2
Explanation:
The electron transport chain transfers electrons from donors to acceptors via redox reactions (i.e., where reduction and oxidation occur together), and couples the transfer of electrons with proton transfer (H+ ions) across the membrane. In the electron transport chain, the electrons are transferred from NADH dehydrogenase NADH to oxygen (O2) through a series of transmembrane complexes: NADH-Q oxidoreductase, Q-cytochrome c oxidoreductase and cytochrome c oxidase. In the first place, the reduced form of coenzyme Q (ubiquinone) transports the electrons from the NADH-Q oxidoreductase to the Q-cytochrome c oxidoreductase complex (Cytochrome b-c1 complex). Second, the cytochrome c transports the electrons from this complex (i.e., Cytochrome b-c1 complex) to the Cytochrome oxidase complex, this being the last component in the electron transport chain that is responsible to catalyze the reduction of O2.
I believe it’s a or c. and those links are so annoying i had to start a new account
