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Mice21 [21]
2 years ago
13

Help

Biology
1 answer:
Arlecino [84]2 years ago
6 0
It’s number 5 cause it sound right
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When calcium ions are released into muscle fibers, what happens along the actin filament? Multiple Choice The position of the tr
zimovet [89]

Answer:

The correct answer will be options

1. The position of the tropomyosin threads shift

2. Exposing myosin binding sites

3. Allowing the myosin head to attach to the actin filament

Explanation:

Calcium plays an important role in the contraction of muscles especially in the formation of the cross-bridge between myosin and actin filaments.

In the presence of calcium, myosin head binds the actin filament as calcium binds to the troponin which changes the configuration of the troponin which releases the tropomyosin from the myosin-binding site on actin.

Once the myosin binding site is freed, myosin binds the site and causes muscle contraction due to ATP hydrolysis.

Thus, the selected options are the correct answer.

5 0
3 years ago
The mayas used……………………to build structures.<br><br><br> A) stone <br><br> B)wood
LenaWriter [7]

A) Stone

They used materials they were available to them which was majorly limestone which is a type of stone.

5 0
3 years ago
Explain how DNA is used to make a protein.
Nookie1986 [14]
DNA starts off on the nucleus where it then gets separated into DRNA so that it can travel to other parts of the cell. It is the. Carried by vehicle to the rough ER where ribosomes are added to it then it goes to the smooth ER where waste is expelled. Finally, it goes to the Golgi apparatus where it is either stored or carried to a part of the cell.
6 0
3 years ago
Read 2 more answers
Another mutation in the MYBPC3 gene that can cause HCM is a change from an arginine at position 403 of the protein to a glutamin
Darina [25.2K]

The position within the original arginine codon where the point mutation most likely occurred was the second nucleotide. In this case, the mutation was CGA  >> CAA.

<h3>Mutations and codons</h3>

A mutation is any alteration in the nucleotide sequence of an organism.

A point mutation is a single base substitution that doesn't change the open reading frame of a given protein.

In this case, the CGA codon encodes for Arginine, whereas the CAA codon encodes for Glutamine, thereby the mutation likely occurred in the second base (C<u>G</u>A  >> C<u>A</u>A)

Learn more about mutation here:

brainly.com/question/17031191

3 0
2 years ago
Pea plants usually reproduce by
tester [92]
The answer is A 100%
3 0
3 years ago
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