Step 11 of skeletal muscle contraction:.
A) Inorganic phosphate is released from myosin head pulls actin filaments (power stroke) toward the center of the sarcomere.
B) Phosphate and ADP form to make ATP which binds to the myosin head and causes cross-bridge to detach.
C) ATP breaks down into ADP and inorganic phosphate.
D) Myosin head resets for another cross-bridge cycle Myosin head binds to actin binding site. (Cross-bridge

The suitable option will be - B

B) Phosphate and ADP form to make ATP which binds to the myosin head and causes cross-bridge to detach.

Explanation:

Until step 11, skeletal muscle has already done cross-bridge and power stroke. ADP is released just after the power stroke. After that phosphate and ADP form a new ATP which gets bound to the myosin head.  

Then at step 11, cross-bridge is released as a new ATP is bound to myosin head.  

So, we can say that option B is correct.

hello! if you would like i could share a research essay i did a month or two ago!

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.