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andrew-mc [135]
3 years ago
5

What galaxy do we belong to

Biology
2 answers:
Yuki888 [10]3 years ago
7 0
We belon to the Milky Way (not the candy bar)
Rudiy273 years ago
3 0
We belong to the Milky Way Galaxy
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How does the structure of an amino acid replicate to its function in cellular processes? Use the role of amino acids in the stru
Alona [7]

A protein's shape directly affects how well it works. For instance, a protein works as a protective protein or a structural protein if its structure is fibrous, as is the case with proteins like collagen and keratin. The protein becomes denatured and ceases to serve its intended purpose if the structure of the amino acids is altered in any way.

<h3>What are amino acids?</h3>

Organic substances known as amino acids have both functional groups for amino and carboxylic acids. Alpha-amino acids, which make up proteins, are by far the most significant amino acids in nature, despite the fact that there are hundreds of other types. The genetic coding only contains 22 alpha amino acids. An organic compound is an amino acid. Carbon-hydrogen bonds are present in organic compounds. All amino acids share a similar fundamental structure. Each molecule has a core carbon atom that is joined to a hydrogen atom, a basic amino group, a carboxylic acid group, and an R-group, also known as a side-chain group.

To know more about amino acids ,visit:

brainly.com/question/28409615

#SPJ9

3 0
1 year ago
Two organisms, AABBCCDDEE and aabbccddee, are mated to produce an F1 that is self-fertilized to produce F2. If the capital lette
Galina-37 [17]

Answer:

a) How many genotypes will occur in F2

--The genotypes would be- AA Aa aa BB Bb bb CC Cc cc DD Dd dd EE Ee ee (15 genotypes)

Reason-

This is because, after crossing the parents, the F1 generation would all be Heterozygous dominant since one parent is homozygous dominant, while the other is homozygous recessive.

b) 25% of all F2 genotypes would be recessive across the 5 loci

Reason-

This is because each loci would produce only a 25% chance for a recessive trait, which would results to a general probability of 25% also.

c) Yes i would change my answer in A and B if the parent cross was- AABBCCDDEE X aaBBccDDEE

d) Yes i would change my answer in A and B if the parent cross was- AABBCCDDEE X aabbccddEE

4 0
3 years ago
Cancer is a disease that usually results when A. a person has limited exposure to sunlight. B. mutations cause a person's body c
Elena-2011 [213]
B. Mutations cause a person's body cells to divide uncontrollably. There isn't a signal for cells to stop dividing, so this can cause cancer because cancer cells won't stop dividing without this signal. 
7 0
3 years ago
Explain Gynecomastia in males.
PolarNik [594]

Gynecomastia is an increase in the size of the mammary gland in men. The condition can occur in one or both breasts. It starts as a small mass under the nipple, which can be sensitive. One breast can be bigger than the other. Its cause is an imbalance between the stimulatory effects of estrogen (female sex hormones) and the inhibitory effects of androgens (male sex hormones) in the breast tissue, when the first ones increase, or the second ones descend.

Gynecomastia is a problem relatively common in the population, and there are three prevalence peaks throughout life:

Newborns: Between 60 and 90% of newborns have gynecomastia, produced by the passage of maternal estrogens through the placenta. It is a transient gynecomastia that disappears in about 2-3 weeks.

Puberty: Gynecomastia in puberty affects mainly young people aged between 10 and 14 years, and is due to the transient and physiological increase in estrogen that occurs at this age.

Elderly: Is due to an increase in fatty tissue with a greater peripheral aromatization ( a process that occurs in adipose tissue and that involves the conversion of androgens into estrogens), a decrease in the production of testosterone by the testes and the use of drugs.

8 0
3 years ago
What would be the most likely effect on the transcription of the trp structural genes for the mutation scenarios provided? mutat
blagie [28]

Answer:

I've responded to each scenario individually, please see below:

1. mutation that prevents ribosome binding to the mRNA

No transcription occurs

2. 5' UTR mutation that changes region 1 tryptophan codons into alanine codons

Transcription when alanine is low

3. mutation that creates a stop codon in region 1 of mRNA 5' UTR

Transcription occurs, a truncated protein will be made during translation

4. deletions in region 2 of the mRNA 5' UTR

Transcription occurs, region 1 and 2 might get paired together

5. deletions in region 3 of the mRNA 5' UTR

Transcription occurs, region 3 and 4 could combine to form a hairpin loop structure

6. deletions in region 4 of the mRNA 5' UTR

Transcription occurs, region 3 and 4 could combine to form a hairpin loop structure

7. deletion of the string of adenine after region 4 of the mRNA 5' UTR

Transcription occurs, however, it will not be as stable a molecule because of losing its polyA tail

Hope that answers the question, have a great day!

6 0
3 years ago
Read 2 more answers
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