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3 years ago

What is the function (or role) of ATP in a cell?

Biology

2 answers:

patriot [66]3 years ago

6 0

Answer:

Explanation:

Adenosine triphosphate (ATP), energy-carrying molecule found in the cells of all living things. ATP captures chemical energy obtained from the breakdown of food molecules and releases it to fuel other cellular processes.

Ghella [55]3 years ago

4 0

Answer:

energy

Explanation:

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1. Animals that mostly eat other animals fit into the dietary category called __________.

mezya [45]

Answer:

butt

Explanation:

hahahahahaha

5 0

3 years ago

When nuclear fusion begins, what can be said about the internal processes within that star?

Pie

Hi there! Hopefully this helps!

--------------------------------------------------------------------------------------------------------

The answer to your question is the second sentence:

Atoms in the star begin to combine.

5 0

3 years ago

Read 2 more answers

Comparing DNA Replication and Transcription

ozzi

The missing information has been completed as:

DNA Tempelate complementary DNA mRNA

3' TTACG 5' 5' AATGC 3' 5'UUACG 3'

3' AAUGC 5' 5' TTACG 3' 5'UUACG 3'

3' GGCGG 5' 5' CCGCC3' 5' CCGCC3'

' 3'TGCATCG5' 5' ACGTAGC 3' 5' ACGUAGC 3'

3' AGACTC 5' 5' TCTGAG 3' 5' AGACTC 3'

3'GATAAGA 5' 5' CTATTCT 5' 5' CTAUUCA 3'

3' CTGGCTAC5' 5' GACCGATG 3' 3'CUGGCUAC 5'

Explanation:

Some of the sequence of DNA given is in 3' to 5' direction, mRNA sequence is also given.

The DNA is double stranded helix which replicates by semi conservative mode. The two strands unwind to act as a template for other strands. In transcription the 3' to 5' strand acts as a template because RNA synthesis takes place in 5' to 3' direction. mRNA is single strand. It has nucleotides in it from which 3 base pairs acts as a code for amino acid.

The following table shows DNA strand having complementary sequaence and mRNA synthesized.

DNA Tempelate complementary DNA mRNA

3' TTACG 5' 5' AATGC 3' 5'UUACG 3'

3' AAUGC 5' 5' TTACG 3' 5'UUACG 3'

3' GGCGG 5' 5' CCGCC3' 5' CCGCC3'

' 3'TGCATCG5' 5' ACGTAGC 3' 5' ACGUAGC 3'

3' AGACTC 5' 5' TCTGAG 3' 5' AGACTC 3'

3'GATAAGA 5' 5' CTATTCT 5' 5' CTAUUCA 3'

3' CTGGCTAC5' 5' GACCGATG 3' 3'CUGGCUAC 5'

3 0

3 years ago

the couple is also concerned about their child inheriting hemophilia, another rare disease, which is x-linked. natalie’s brother

IgorC [24]

Hemophilia is a recessive X-linked condition and is inherited from parents. . The probability that Natalie and Daniel’s first child has hemophilia is 1/4, not 1/8. The statement is false.

<h3>What is an X-linked gene?</h3>

When talking about sex-linked genes, we refer to all those genes located in one of the sex-chromosomes and not in the somatic ones.

X-linked genes are the genes located specifically in the X sex chromosome.

Traits coded by these genes are inherited. This is, X-linked genes are transmitted from parents to children through generations.

According to this, X-linked genetic disorders will be inherited as well.

Men have a high probability of being affected since they only have one copy of the X chromosome.

In women, the effect of the mutation might be musk in heterozygous state if the mutation is recessive.

Hemophilia is a recessive X-linked disorder, which means it is coded by the recessive allele.

X+ ⇒ X chrosomosome with Dominant allele

X- ⇒ X chrosomosome with Recessive allele

Genotype Phenotype

X+X+ Healthy woman

X+X- Healthy carrier woman

X-X- Hemophilic woman

X+Y Healthy man

X-Y Hemophilic man

Let us make a pedigree of these families,

Natalie's family:

Mother healthy carrier X+X-

Father healthy X+Y

Brother hemophilic X-Y

Natalie Healthy X+X- or X+X+

Natalie has 1/2 chances of being carrier X+X- and 1/2 of being X+X+.

Daniel's family:

Mother healthy carrier X+X-

Father hemophilic X-Y

Sister hemophilic X-X-

Daniel Healthy X+Y

He has 1/2 chances of being healthy X+Y and 1/2 of being affected X-Y.

According to the product probability rule, if events A and B are independent from each other, the probability of occurrence of both events together is

P(A∩B) = P(A) x P(B)

In this case,

event A is Daniel being affected ⇒ 1/2
event B is Natalie being carrier ⇒ 1/2

P(A∩B) = P(A) x P(B) = 1/2 x 1/2 = 1/4

The probability that Natalie and Daniel’s first child has hemophilia is 1/4, not 1/8. The statement is false.

You can learn more about X-linked genes at

brainly.com/question/12420228

brainly.com/question/14704182

brainly.com/question/1387724

#SPJ1

7 0

1 year ago

Compare CRISPR and miRNA

Zinaida [17]

The miRNA functions as a guide by base-pairing with target mRNA to negatively regulate its expression.
Whereas, CRISPR technology is a simple yet powerful tool for editing genomes. It allows researchers to easily alter DNA sequences and modify gene function. Its many potential applications include correcting genetic defects, treating and preventing the spread of diseases and improving crops.

3 0

3 years ago