Amino Acids and Sickle Cell Disease

Amino Acids and Sickle Cell Disease

Assessment

Interactive Video

Created by

Emma Peterson

Biology, Chemistry, Science

10th Grade - University

Hard

The video introduces amino acids, explaining their structure and role in biochemistry. It covers macromolecules like carbohydrates, proteins, and fats, and their digestion into monomers. The structure of amino acids, including the alpha carbon and side chains, is detailed. The video distinguishes between proteogenic and non-proteogenic amino acids, highlighting their roles in protein synthesis. Sickle cell disease is discussed, focusing on its genetic mutation and impact on hemoglobin. The video concludes with a preview of stereochemistry and future topics.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What are the monomers of carbohydrates after digestion?

Triglycerides

Monosaccharides

Disaccharides

Polysaccharides

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which group is attached to the alpha carbon in an amino acid?

Hydroxyl group

Phosphate group

Methyl group

Amino group

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the significance of the order of amino and carboxyl groups in amino acids?

It changes the amino acid's color.

It is crucial for protein synthesis.

It affects the amino acid's taste.

It determines the amino acid's solubility.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of methionine in the body?

It acts as a neurotransmitter.

It donates a methyl group.

It stores energy.

It forms cell membranes.

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which amino acid is not coded by a genetic codon?

Ornithine

Alanine

Glycine

Valine

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which amino acid is replaced in sickle cell disease?

Lysine

Valine

Alanine

Glutamic acid

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the genetic nature of sickle cell disease?

Autosomal dominant

Autosomal recessive

Y-linked

X-linked recessive

8.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary structural difference in hemoglobin in sickle cell disease?

Globin is replaced by another protein.

Glutamic acid is replaced by valine.

Iron is replaced by copper.

Heme is absent.

9.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main advantage of sickle cell trait in certain populations?

Resistance to malaria

Increased oxygen capacity

Improved athletic performance

Faster blood clotting

10.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What will be discussed in the next video?

Lipid digestion

Protein synthesis

Stereochemistry

Carbohydrate metabolism

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