The average height of the oceans surface between high and low tides is called the sea level. It is important to know this measurement because with this it is possible that we can calculate the height of anything on the land. Also, we can <span> calculate the height of anything on the land. Also, we can be able to determine whether the oceans are falling or rising through time.
So the answer is </span><span>Sea level </span>
14: Operons allow prokaryotes to replicate DNA at the appropriate time.
Operons are specific regions of genes that are linked to a singular process. They ensure that the expression of these genes does not go unchecked and only occurs when necessary. Two key examples of this in humans are the lac operon and trp operon.
15. The central dogma of molecular biology is:
DNA to RNA to Proteins
Protein Synthesis occurs in 3 steps.
First our DNA is translated into RNA. Next the RNA is sequenced into Amino Acids by reading the corresponding 3-Base Codons. These Amino Acid sequences form various protein structures.
The phenomenon is called an equinox. More specifically when it is September it is called the autumnal equinox ,and when it is March it is called the vernal equinox. Hope this helped!
Answer:
- Calcium binds to troponin C
- Troponin T moves tropomyosin and unblocks the binding sites
- Myosin heads join to the actin forming cross-bridges
- ATP turns into ADP and inorganic phosphate and releases energy
- The energy is used to impulse myofilaments slide producing a power stroke
- ADP is released and a new ATP joins the myosin heads and breaks the bindings to the actin filament
- ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, starting a new cycle
- Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.
Explanation:
In rest, the tropomyosin inhibits the attraction strengths between myosin and actin filaments. Contraction initiates when an action potential depolarizes the inner portion of the muscle fiber. Calcium channels activate in the T tubules membrane, releasing <u>calcium into the sarcolemma.</u> At this point, tropomyosin is obstructing binding sites for myosin on the thin filament. When calcium binds to troponin C, troponin T alters the tropomyosin position by moving it and unblocking the binding sites. Myosin heads join to the uncovered actin-binding points forming cross-bridges, and while doing so, ATP turns into ADP and inorganic phosphate, which is released. Myofilaments slide impulsed by chemical energy collected in myosin heads, producing a power stroke. The power stroke initiates when the myosin cross-bridge binds to actin. As they slide, ADP molecules are released. A new ATP links to myosin heads and breaks the bindings to the actin filament. Then ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, which starts a new binding cycle to actin. Finally, Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.
