The common structural pattern that is a distinguishing characteristic specific to all G-protein-coupled receptors is that they...
A. are transmembrane proteins.
B. have a kinase domain on the intracellular side of the plasma membrane.
C. are only active when pairs of receptors dimerize.
D. contain seven transmembrane helices.

Answers

Answer 1

The common structural pattern that is a distinguishing characteristic specific to all G-protein-coupled receptors is that they contain seven transmembrane helices (Option D). This structural pattern allows them to interact with G proteins and transmit signals across the plasma membrane.

G-protein-coupled receptors (GPCRs) are a class of cell surface receptors that respond to various extracellular signals such as light, odorants, hormones, and neurotransmitters. They are involved in a wide range of physiological and pathological processes, and they are also the targets of many drugs, making them an essential class of receptors to study.

The structural pattern specific to all G-protein-coupled receptors is that they contain seven transmembrane helices, which are arranged in a specific way to form a pocket that binds to extracellular ligands. This structural pattern is also known as the seven-transmembrane domain or 7TM domain. The seven transmembrane helices are arranged in a circular fashion, with the extracellular loops facing outwards and the intracellular loops facing inwards.

Thus, option D- contain seven transmembrane helices is the correct answer.

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Related Questions

16. According to the passage set, which TWO events MOST likely led to the extinction of the dodo?
A. Over time, pigeons evolved into what is known as the dodo.
B. Dodos ate small stones to help with digestion.
New species introduced to the island began hunting the dodo.
D. The dodo laid single eggs in nests on the ground.

Answers

Answer: It's C.

Explanation: The dodo once lived on an uninhabited island where there were no predators, so they evolved and became flightless and slow.

Then one day, the Dutch came and brought dogs with them. The dodos were too slow. The eggs got stolen and eaten, dodos were killed, and the dodos didn't repopulate fast enough, so they went extinct.

In 1981, a couple found a stray kitten whose unusual ears curled up and back from her head. They decided to breed her with their male cat who is homozygous for the allele for normal ears. The first litter of kittens produced two kittens with normal ears and two kittens with curled ears. Subsequent litters with the same parents showed the same ratio of curled ears to normal ears. When curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears. This new trait was determined to be the result of a new and unique mutation in the ear gene of cats, and cats with this trait were named American curl cats.
In American curl cats, the allele that produces the ear-curling trait is which?
The allele that produces normal ears is which?
Dominant
Recessive
Page 120

Answers

In American curl cats, the allele that produces the ear-curling trait is dominant, while the allele that produces normal ears is recessive. This can be determined from the fact that when curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears, indicating that the ear-curling trait is dominant over the normal ear trait.

In American curl cats, the allele that produces the ear-curling trait is dominant. Dominance is a characteristic of an allele that expresses its phenotype in a heterozygote, such that it masks the expression of a recessive allele. When curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears.

The allele that produces normal ears is recessive. Recessive traits are only expressed in a homozygous state, and that are not expressed in a heterozygous state because a dominant allele mask it. The first litter of kittens produced two kittens with normal ears and two kittens with curled ears. The parents were heterozygous, with one carrying the dominant curled allele and the other carrying the recessive normal allele.

In summary, in American curl cats, the allele that produces the ear-curling trait is dominant. The allele that produces normal ears is recessive.

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Subject: Science


1. Approximately how far away would the formation of Earth be if you used the scale from your timeline?


2. Which events helped life develop on Earth? ''Explain''.

Answers

Because several meteorites have been dated, the Earth's age has increased from 4.55 0.3 billion years in 1956 to 4.55 0.02 billion years. I) The synthesis of nucleotides and amino acids.

How did life on Earth start to appear?

In rocks that are 3.7 billion years old, the oldest known life forms, microbes, have left their imprint. The signals were made up of a specific class of carbon molecules produced by living things.

What process created the Earth?

Formation. Over a period of 4.5 billion years, whenever the solar system was still in its current configuration, the second planet from the Sun—Earth—was created when gravity drew spinning gas and dust in. Earth has a solid crust, a high degree of crystallinity, and a central core, just like its sibling terrestrial planets.

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you have discovered a new cell and see that it has a golgi apparatus. it could be a member of

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The cell you discovered with a Golgi apparatus is likely a member of the eukaryotic domain of life.

Eukaryotes are single-celled or multicellular organisms whose cells contain membrane-bound organelles, including a nucleus and Golgi apparatus. These organisms are more complex than prokaryotes and typically contain hundreds of different cell types, including muscles, organs, and nerve cells. All eukaryotic cells also contain DNA and RNA, which allow them to store genetic information and carry out other essential functions.

The Golgi apparatus is an organelle found in eukaryotic cells that are involved in the modification, sorting, and packaging of macromolecules, including proteins and lipids, for export from the cell. It consists of flattened membrane-bound sacs or cisternae and is located near the nucleus. The Golgi apparatus is essential for cell growth and reproduction, as well as the transport of macromolecules throughout the cell.

In summary, the cell you discovered with a Golgi apparatus is likely a eukaryotic cell, as Golgi apparatuses are found only in eukaryotic cells. Other features of eukaryotic cells include a nucleus, mitochondria, and ribosomes.

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growth hormone, secreted by the gland, stimulates growth of bones and muscle by activating intermediary proteins called

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Growth hormone, secreted by the pituitary gland, stimulates the growth of bones and muscle by activating intermediary proteins called growth factors. Growth factors are molecules that bind to receptors on the surface of target cells.


What are growth hormones?

Growth hormone, secreted by the pituitary gland, stimulates the growth of bones and muscle by activating intermediary proteins called STATs (signal transducers and activators of transcription). It has been shown that signaling pathways are crucial to the regulation of growth hormone (GH) in terms of both its secretion and actions.

The signaling pathways used by the GH receptor involve a number of intermediary proteins that interact with the receptor and allow it to carry out its functions. Growth hormone, secreted by the pituitary gland, stimulates the growth of bones and muscle by activating intermediary proteins called STATs (signal transducers and activators of transcription).

These STAT proteins then activate a number of transcription factors that are responsible for the production of various genes that control growth. As a result of this signaling pathway, GH is able to promote growth in both bone and muscle tissues.

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Please help quick!
Which statement can be made about the above passage?
A .Scientists can predict earthquakes, but not tsunamis.
B .Meteorologists can broadcast news quickly about approaching disasters.
C .Shifting of tectonic plates never affects people's lives
D .Tectonic plates have moved and reshaped continents, created and destroyed ocean basins, and caused earthquakes.

Answers

Answer:

The statement that can be made about the above passage is D. Tectonic plates have moved and reshaped continents, created and destroyed ocean basins, and caused earthquakes.

The basic building blocks in a human body are?

Answers

Explanation:

cells bro easy one mark brain list

Answer: CELLS

Explanation: The basic building block of a body is formed by a cell, a tissue, muscle, nerve, skin, blood etc. but billions of cells make up the human body

answer the questions bio 1 honors <3

Answers

Species, Population, and Gene Pool:

Species: a group of organisms that share common characteristics and can interbreed to produce viable offspring.

Population: a group of individuals of the same species living in a specific geographic area.

What is a gene pool?

Gene Pool: the collection of all the genes and their different alleles within a population.

Allele frequency:

Allele frequency: the relative proportion of a particular allele in a population's gene pool.

Genotype vs. Phenotype:

Genotype: an individual's genetic makeup, which determines their inherited traits.

Phenotype: an individual's observable physical or behavioral traits, which result from the interaction between their genotype and environmental factors.

Sources of Genetic Variation:

Mutations: changes in DNA sequences that can result in new alleles.

Genetic Recombination during Sex: the shuffling and recombination of alleles during meiosis, which can generate new combinations of alleles.

Lateral Gene Transfer: the transfer of genetic material between different organisms, which can introduce new genes into a population.

Genes and Traits:

Single-gene Traits: traits that are determined by the expression of a single gene.

Polygenic Traits: traits that are determined by the expression of multiple genes.

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which of the following is not one of the ways of studying and identifying microorganisms?staining culture animal culture human inoculation

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The following is not one of the ways of studying and identifying microorganisms is Animal culture.

Microorganisms can be studied and identified through the following ways:

Staining Culture

Human Inoculation

Animal culture

Staining is a method of dyeing microorganisms to make them visible under a microscope. The process of staining involves the use of chemicals that color certain components of the cell, such as the cell wall, nucleus, or cytoplasm, so that they can be seen more clearly.Culture is a method of growing microorganisms in a lab, usually in a nutrient-rich liquid or solid medium. By observing the growth patterns of the microorganisms, scientists can identify them and determine their properties, such as their size, shape, and metabolic processes.

Human inoculation is the method of studying microorganisms by exposing human subjects to a pathogen under controlled conditions in order to observe how the body responds to the infection. This method is useful in understanding how diseases spread and how they can be treated or prevented.

Animal culture is not a method of studying and identifying microorganisms. However, animal models can be used to study the effects of microorganisms on living organisms, such as the symptoms they cause, the immune response they elicit, and the ways they can be treated.

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In humans, how has that term been historically modified?

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In humans, the term "race" has been historically modified. This term has been used to categorize people into different groups based on their physical characteristics such as skin color, hair texture, and facial features.

However, this categorization has been found to be biologically meaningless as there is more genetic variation within these groups than between them. Additionally, this categorization has been used to justify discriminatory practices such as slavery, segregation, and genocide.

Therefore, it is important to recognize the flawed nature of this term and move towards a more inclusive and equitable understanding of human diversity. This can be achieved through promoting cultural awareness, celebrating differences, and recognizing the humanity of all individuals regardless of their physical characteristics.

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The oxygen consumed during cellular respiration is a DIRECT participant in what process? Exclude the four processes that are indirectly linked to oxygen consumption in cellular respiration A. phosphorylation of ADP to form ATP B. accepting electrons from sugars in glycolysis C. accepting electrons at the end of the mitochondrial electron transport chain D. accepting electrons from the components of the citric acid cycle
E. removing electrons from NADH

Answers

A DIRECT participant in accepting electrons at the conclusion of the mitochondrial electron transport chain is the oxygen used during cellular respiration. So, C is the best choice.

In this procedure, oxygen molecules act as the ultimate electron acceptor by receiving electrons from electron carriers like NADH and FADH2. As a result, water is created and a proton gradient is created, both of which are used to fuel ATP synthase's synthesis of ATP.

Indirect links between oxygen consumption and cellular respiration include the phosphorylation of ADP to form ATP, the uptake of electrons from sugars in glycolysis, the components of the citric acid cycle, and the removal of electrons from NADH.

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why must heat or a surface-active agent be used with application ofthe primary stain during acid-fast staining

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Heat or a surface-active agent must be used with the application of the primary stain during acid-fast staining because the cell wall of acid-fast bacteria is impermeable to stains.

This means that the primary stain is unable to penetrate the cell wall of these bacteria without the aid of heat or a surface-active agent such as carbolfuchsin.

In other words, heat or a surface-active agent is used to help the primary stain penetrate the cell wall of acid-fast bacteria, allowing it to bind to the lipids in their cell walls. This makes the bacteria visible under a microscope and helps to differentiate them from non-acid-fast bacteria, which do not have such impermeable cell walls.

The process of acid-fast staining involves the use of heat or a surface-active agent with the primary stain to help it penetrate the cell wall of acid-fast bacteria. This is necessary because the cell wall of these bacteria is impermeable to stains, making it difficult to visualize them under a microscope. By using heat or a surface-active agent, the primary stain is able to bind to the lipids in the cell wall of these bacteria, making them visible under a microscope. This helps to differentiate them from non-acid-fast bacteria, which do not have such impermeable cell walls.

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which of the following best describes a horticultural or descriptive classification system? group of answer choices organisms are grouped based on linnean classification organisms are grouped based on common ancestry organisms are grouped based on similar characteristics organisms are grouped based on reproductive parts

Answers

Option a. organisms are grouped based on Linnean classification organisms best describe a horticultural or descriptive classification system.

What is a descriptive classification system?

A descriptive classification system is a purely descriptive system based on morphological differences between individuals, which can be used to categorize different species based on these differences but it does not reflect evolutionary relationships between such species in the classification.

Therefore, with this data, we can see that the descriptive classification system is used to categorize species based on their morphological differences regardless of their evolutionary relationships.

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which of the following characteristics apply to all species in kingdom protista? group of answer choices eukaryotic unicellular heterotrophic possess cell walls aquatic

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The following characteristics apply to all species in the kingdom Protista is eukaryotic. All species in Kingdom Protista are eukaryotic, meaning they have a membrane-bound nucleus and other organelles in their cells.

None of the following characteristics apply to all species in the Kingdom Protista:

Heterotrophic: Some protists are heterotrophic (i.e., they obtain their nutrition from other organisms), but some are autotrophic (i.e., they produce their own food through photosynthesis).Possess cell walls: Some protists have cell walls, but not all. Some have cell membranes only.Aquatic: While many protists are aquatic, some are found in soil, or in the bodies of other organisms.

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1. in what kinds of environments would you expect to find the greatest predominance of c3, c4, and cam plants? how can you explain the co-occurrence of 2, or even 3, of these types of photosystems in one area?

Answers

C3 plants are the most common type of plants and are found in moderate temperature environments with average precipitation. Examples of C3 plants include wheat, soybeans, and rice.

C4 plants are better adapted to hot and dry environments, such as tropical and subtropical areas. Examples of C4 plants include corn, sugarcane, and sorghum.

CAM (crassulacean acid metabolism) plants are found in arid environments such as deserts, where they can reduce water loss by opening their stomata at night and closing them during the day. Examples of CAM plants include cacti and succulents.

The co-occurrence of two or even three types of photosynthetic pathways in one area can be explained by the different adaptations of these plants to different environmental conditions. For example, in areas with variable environmental conditions, multiple types of plants may be present, each with different photosynthetic pathways to maximize their ability to survive and thrive in that environment.

Additionally, certain plants may be better adapted to different microclimates within the same general area, leading to the co-occurrence of multiple types of photosystems in the same region.

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albinism is a condition in which pigmentation is lacking. in humans, the result is white hair, nonpigmented skin, and (usually) blue eyes. the trait in humans is caused by recessive alleles. two normal parents have an albino child. what is the probability that their next child will be albino? explain your reasoning.

Answers

If two normal parents have an albino child,  the probability that their next child will be albino is 25%.

If two normal parents have an albino child, this indicates that both parents are carriers of the recessive allele for albinism. In this case, each parent would have one normal allele and one recessive allele for the trait.

The probability that their next child will be albino depends on the genotype of each parent. If both parents are carriers of the recessive allele, then each has a 25% chance of passing on the recessive allele to their offspring, and a 75% chance of passing on a normal allele.

Using a Punnett square to illustrate this, we can see that each parent would have the genotype Aa (where A represents the normal allele and a represents the recessive allele). The Punnett square for a cross between two Aa individuals is shown below:

           A           a

A      AA         Aa

a       Aa         aa

From this Punnett square, we can see that there is a 25% chance (1 out of 4) that the next child of these parents will inherit two copies of the recessive allele (aa) and thus have albinism.

There is also a 50% chance (2 out of 4) that the child will be a carrier like the parents (Aa), and a 25% chance (1 out of 4) that the child will inherit two copies of the normal allele (AA) and will not have albinism.

Therefore, the probability that their next child will be albino is 25%.

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Which best describes a hurricane?
A
a low-pressure weather system
B
a high-pressure weather system
C
a cold front
D
a stationary front

Answers

Answer:

your answer is: A hope this helps

Explanation:

I believe the answer is B

The most superior bone of the vertebral column is the _________. A) coccyx B) vertebra prominens C) axis D) atlas

Answers

The most superior bone of the vertebral column is the atlas, which is denoted as the first cervical vertebra.

The occipital bone of the skull articulates with the atlas, which is situated at the top of the vertebral column and permits head nodding. It is a ring-shaped bone that has no body that helps the head move freely while supporting the weight of the skull.

The most noticeable vertebra in the cervical region is the vertebra prominens, commonly referred to as the seventh cervical vertebra. It is situated close to the base of the neck. The most inferior bone of the vertebral column, commonly referred to as the tailbone, is the coccyx, which is made up of four fused vertebrae.

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during conjugation, the donor cell generally retains a copy of the genetic material being transferred. this is termed a blank process

Answers

Answer:

Conservative

Explanation:

During conjugation, the donor cell generally retains a copy of the genetic material being transferred. This is termed a conservative process.

how is the bulk of carbon dioxide transported in blood?

Answers

The bulk of carbon dioxide (CO2) is transported in blood in three forms:

As bicarbonate ions (HCO3-)

Dissolved in plasma

Bound to hemoglobin

In the blood, CO2 combines with water to generate carbonic acid (H2CO3), which breaks down into bicarbonate ions and hydrogen ions. The major portion of CO2 transport is made up of the bicarbonate ions, which are transported in the blood plasma.

In Plasma-dissolved CO2 A tiny portion of CO2 is directly dissolved in blood plasma and is delivered as a gas.

A little amount of CO2 is bound to the amino acids in hemoglobin molecules in red blood cells and is then transferred to the lungs for exhalation.

The process of carbon dioxide transport in the blood is regulated by a complex system involving the respiratory, circulatory, and nervous systems. The concentration of CO2 in the blood is monitored by chemoreceptors in the brain, which signal the respiratory system to adjust the rate and depth of breathing to maintain normal levels of CO2 in the blood.

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dna is double-stranded, but for each protein, only one of these two strands is used to produce an mrna transcript. what is the coding strand called?

Answers

The coding strand of DNA is also known as the sense strand or the positive strand.

It is called the coding strand because it contains the same sequence of nucleotides as the mRNA molecule that is produced during transcription. In other words, the coding strand has the same sequence as the mRNA, except that it has thymine (T) instead of uracil (U) since mRNA uses uracil instead of thymine.

The other strand of DNA, which is not used as a template for mRNA synthesis, is called the non-coding strand or the antisense strand, as it has a complementary sequence to the coding strand. During transcription, RNA polymerase reads the antisense strand and produces an mRNA molecule that is complementary to it, which is why it is called the template strand.

So, to summarize, the coding strand is the strand of DNA that has the same sequence as the mRNA transcript that is produced during transcription.

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when assessing newborns for chromosomal disorders, which assessment would be most suggestive of a problem?

Answers

when assessing newborns for chromosomal disorders, which assessment would be most suggestive of a problem?

answer:
low set ears

describe how darwins ideas have been updated. be sure to mention the role of natural selection in modern eveolutionary theory

Answers

Darwin's ideas about evolution were based on his observations of plants and animals.

The theory of natural selection is now seen as the cornerstone of evolutionary theory, which explains how populations evolve over time.The following are some of the ways in which Darwin's ideas have been updated:Genetics and Evolutionary Theory: Modern evolutionary theory incorporates genetics, which helps explain how new traits arise in populations and how they are passed down through generations.

The genetic variation that exists within populations provides the raw material for natural selection, which acts on these differences and allows populations to evolve over time. Molecular Biology: In the twentieth century, molecular biology allowed scientists to study the molecular basis of life, including the structure and function of DNA.

This has helped scientists understand how genetic changes occur, and how they are passed down through generations. Genetic drift, which occurs when random events cause changes in the frequency of traits within a population, is another mechanism that can drive evolutionary change.

Natural selection is still the most important mechanism driving evolutionary change, but genetic drift can also play a role. Gene Flow: Gene flow, which occurs when individuals from one population migrate into another and breed with members of that population, can also drive evolutionary change.

This can introduce new traits into a population and increase genetic variation.Natural Selection and Evolutionary Theory: Natural selection is still the most important mechanism driving evolutionary change, but it is now seen as one of several mechanisms that can act on populations.

Other mechanisms, such as genetic drift and gene flow, can also play a role. Overall, modern evolutionary theory has expanded on Darwin's ideas and has incorporated new discoveries in genetics and molecular biology to provide a more comprehensive understanding of how populations evolve over time.

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even though sickle cell confers no advantage in the malaria-free u.s., african americans have a relative high incidence of the gene. this is an example of

Answers

Even though sickle cell confers no advantage in the malaria-free U.S., African Americans have a relatively high incidence of the gene. This is an example of genetic drift.

What is genetic drift?

The phenomenon in which gene frequencies shift randomly in small populations is known as genetic drift. A change in the frequency of a gene in a population due to random sampling is referred to as a genetic drift. The loss of one allele and an increase in another is an example of genetic drift.

What are some examples of genetic drift?

Some examples of genetic drift are as follows:

When a small community splits off from a larger population and forms a new colony, the original gene pool is typically not represented in the new colony's gene pool.

When a tiny group of animals is forced to cross a natural obstacle like a river, the animals that survive are often genetically distinct from the original population.

Generally speaking, genetic drift has a more significant impact on smaller populations than on larger populations. There are two types of genetic drift: founder effects and population bottlenecks.

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during the menstrual cycle, what triggers ovulation to occur? question 23 options: a gradual decrease in estrogen levels. inhibin b sharply spikes. a surge in progesterone occurs. activin is released.

Answers

Ovulation is triggered by a surge in progesterone which occurs during the menstrual cycle.

This surge is caused by the follicle stimulating hormone, which is produced by the pituitary gland. The FSH encourages the growth of follicles in the ovaries, which produce estrogen. As the follicle matures, estrogen levels peak. The peak in estrogen causes the brain to secrete luteinizing hormone, which triggers the follicle to rupture and release an egg (ovulation). Activin, inhibin B, and a gradual decrease in estrogen levels are all part of the process that precedes and follows ovulation. Activin is a hormone secreted by the ovaries, which helps to mature follicles.

Inhibin B is a hormone secreted by the ovaries, which is thought to help control the amount of FSH in the body and in turn the number of follicles that mature. A gradual decrease in estrogen levels occurs as ovulation approaches and during the luteal phase of the menstrual cycle. This decrease in estrogen helps to prepare the body for the next menstrual cycle.

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up to 25% of a cell's atp is used to run sodium-potassium pumps. without the resulting sodium and potassium gradients, neurons and muscles cannot fire properly. if a person is poisoned with cyanide, they cannot generate atp, and die within a few minutes. in relation to the sodium-potassium pump, what specific impact would cyanide have on concentrations across the cell membrane?

Answers

Cyanide depolarizes the peritubular cell layer by +18.8 +/ - 2.3 mV/10 min in the presence and by +4.5 +/ - 0.9 mV/10 min without even a trace of the luminal substrate.

Hydrogen cyanide is a poisonous little nonpolar particle that is delivered by certain plants to discourage herbivores. Cyanide crosses layers and restrains a critical cycle in the breath.

The cyanide particle, CN, ties to the iron molecule in cytochrome C oxidase in the mitochondria of the cells and goes about as an irreversible protein inhibitor. This keeps cytochrome C oxidase from doing what it needs to do, which is to send electrons to oxygen in the electron transport chain of high-impact cell breath.

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what is the role of the 5' cap on a eukaryotic mrna molecule? multiple select question. it facilitates the exit of mrna from the nucleus. it allows the mrna to bind to a ribosome for translation. it is recognized by rna polymerase to allow the initiation of transcription. it enables the spliceosome to identify the first exon.

Answers

The answer to the question is A and B - it facilitates the exit of mRNA from the nucleus and it allows the mRNA to bind to a ribosome for translation.

The role of the 5' cap on a eukaryotic mRNA molecule is to allow the mRNA to bind to a ribosome for translation and it facilitates the exit of mRNA from the nucleus. The 5' cap is a necessary feature of eukaryotic mRNA molecules that aids in their translation. The 5' cap, which is a chemically modified nucleotide added to the 5' end of the mRNA during RNA processing, provides a variety of benefits for the mRNA molecule.

The 5' cap helps to shield the mRNA molecule from RNA-degrading enzymes in the cytoplasm, as well as to promote the ribosome's binding to the mRNA molecule. It also aids in the initiation of protein synthesis by facilitating the formation of a complex between the mRNA, ribosome, and initiator tRNA.

Finally, the 5' cap aids in the process of splicing the mRNA molecule to remove non-coding introns. The 5' cap of eukaryotic mRNA also helps to distinguish between self and non-self RNA. By identifying the 5' cap, host cells may differentiate between their own mRNA and foreign mRNA.

Thus, the 5' cap serves as a molecular "passport" that identifies the mRNA molecule as genuine and necessary for the cell's normal functions.

Therefore, the correct option is A and B.

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Please help quick I’ll mark brainly
Why does the Northern hemisphere produce more CO2 overall? Why does it absorb more CO2 certain times of year?

Answers

Answer:

The Northern Hemisphere produces more CO2 overall for several reasons. One main reason is that it contains more land area and therefore more vegetation that undergoes photosynthesis, which takes in CO2. However, during the winter months, when the temperature drops, the vegetation goes dormant and stops absorbing CO2. At the same time, human activity, such as burning fossil fuels and heating buildings, tends to increase during the winter months, which leads to an increase in CO2 emissions. As a result, the Northern Hemisphere experiences seasonal variations in CO2 levels, with higher levels during the winter months and lower levels during the summer months when vegetation is actively growing and absorbing CO2. Additionally, the Northern Hemisphere experiences more seasonal variation in general, with more extreme temperatures and weather patterns that can affect the balance of CO2 in the atmosphere.

During crossing over, when the invading strand uses the invaded DNA as a _____, this automatically results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected _____ ratio.

Answers

The correct answer is: During crossing over, when the invading strand uses the invaded DNA as a template, this automatically results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected 1:1 ratio of crossing over.

Explanation:

DNA is replicated through the process of crossing over, which involves the exchange of genetic material between two homologous chromosomes. During the process, one of the homologous chromosomes acts as the invading sequence, while the other acts as the invaded DNA. When the invading strand uses the invaded DNA as a template, it results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected 1:1 ratio of crossing over.
What is crossing over?

Crossing over is a process during meiosis where the chromosome arms of maternal and paternal homologous chromosomes swap DNA sections (recombination) to produce new allelic combinations of traits. The crossing-over process starts with the breakage of two homologous chromosomes, the migration of the broken ends toward each other, and the formation of crosslinks by the formation of single crossovers.

These crosslinks are eventually converted to chiasmata that keep the chromosomal arms connected until metaphase I. During this process, one chromosome might lose genetic material while the other might acquire genetic material. This event results in unique combinations of genes that might not be present in either parent. The frequency of crossovers is affected by the distance between the gene and the centromere. Chromosomes that are nearer to the centromere are less likely to cross over than those that are further away. Explaining the departure from the expected Mendelian ratio.

The ratio of offspring created by a cross that exhibits the dominant and recessive traits that Mendel observed is referred to as the Mendelian ratio. Crossing over might result in new allelic combinations of genes that deviate from the Mendelian ratios. This is because the transmission of genes is no longer controlled by a single gene pair on a chromosome. Chromosome segregation is disturbed in one way or another by crossovers.

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leucine aminopeptidases (laps) are found in all living organisms and have been associated with the response of the marine mussel, mytilus edulis, to changes in salinity. laps are enzymes that remove n-terminal amino acids from protein

Answers

Leucine aminopeptidases (LAPs) are a group of enzymes found in all living organisms, including the marine mussel Mytilus edulis. These enzymes play a crucial role in protein metabolism by catalyzing the cleavage of N-terminal amino acids from protein substrates.

LAPs have been implicated in a variety of physiological processes, including protein turnover, regulation of peptide hormone levels, and immune system function. In Mytilus edulis, LAPs have been shown to play a role in the organism's response to changes in salinity. When the salinity of their environment changes,

Mytilus edulis utilizes LAPs to modify the composition of proteins in their cells, allowing them to better adapt to the changing conditions. This adaptation is important for the organism's survival, as changes in salinity can significantly affect the functioning of cells and tissues.

Overall, LAPs are versatile enzymes that play a critical role in protein metabolism and are found in a wide range of living organisms, including the marine mussel Mytilus edulis. Their ability to modify protein substrates makes them important players in many physiological processes, including adaptation to changing environmental conditions.

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