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Svet_ta [14]
3 years ago
13

The ATP molecule used in biochemical reactions is most similar in function to which of the following a house key be shipping cra

te see rechargeable battery or D copy machine
Biology
2 answers:
mezya [45]3 years ago
7 0
<span>shipping crate

ATP usually releases energy by breaking down the weak phosphate cell present.  The energy released due to the breaking down of the phosphate cell is then utilized. The ATP is converted to ADP. Whenever a cell feels the necessity for energy it releases a phosphate to gather the energy. It is an automatic and ongoing process. The weak bond between the second and the third phosphate is always targeted for turning ATP to ADP. This is the reason ATP is considered the main energy currency for the cell.<span>
</span></span>
tino4ka555 [31]3 years ago
7 0

The right answer is rechargeable battery.

ATP is the energy unit of the cell. The mechanical energy of muscle contraction comes directly from chemical energy (ATP). During muscle activity, the regeneration of ATP is done in 3 ways:

* by interaction of ADP with creatine phosphate,

* by anaerobic cellular respiration

* and by aerobic cellular respiration.

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It’s D

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A plant TT for tall height is crossed with a plant tt
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the phenotype of the height of the plants would be all tall since there is a dominant allele in every genotype

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A child is born to parents that both have hypophosphatemic rickets, a disease that is caused by a sex-linked dominant trait. Wha
Sati [7]

Answer:

75%

Explanation:

Hypophosphatemic rickets is a disorder characterized by hypophosphatemia (low level of phosphate in the blood), defective intestinal absorption of calcium, and rickets (impaired mineralization of cartilaginous growth plates)  or osteomalacia (impaired mineralization of the osteoid) unresponsive to vitamin D. It can be inherited or acquired.

When it comes to inheritable hypophosphatemic rickets, the disorder is most often inherited in an X-linked dominant manner. This means that the gene is inherited through the X chromosome and that one dominant allele is enough to cause it.

As the mother is heterozygous for the trait, she has one dominant and one recessive allele (XHXh). The father has one X chromosome, which he inherited from his mother, and as he has the condition, the dominant allele will be present on it (XHY).

This means that, if the child is a girl, she will definitely have the disorder. Girls inherit one X chromosome from each of their parents. Even if she inherited the one with the recessive allele from her mother, she would get the one with the dominant allele from her father.

If the child is a boy, he has a 50% chance to inherit the condition. Boys inherit the Y chromosome from their father and the X chromosome from their mother. As the mother is heterozygous, he can either get the chromosome without the dominant allele or the one with it. This means that there is a 50% chance of inheriting the disorder.

If we say that there are equal chances of this couple having female and male children, when we combine these results, we get a 75% chance of them inheriting hypophosphatemic rickets.

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