All categories

3 years ago

Briefly describe an enzyme molecule

Biology

1 answer:

Zielflug [23.3K]3 years ago

7 0

Answer:

Enzymes are biological molecules (typically proteins) that significantly speed up the rate of virtually all of the chemical reactions that take place within cells. ... The molecules that an enzyme works with are called substrates. The substrates bind to a region on the enzyme called the active site.

You might be interested in

The carbohydrates, proteins, and minerals that are vital to an organism’s survival are found in...

Novosadov [1.4K]

3. Food

This is the answer..

4 0

3 years ago

Read 2 more answers

"The ability of an organism to react to an environmental input with a change in form, state, movement, or rate of activity" is a

motikmotik

"The ability of an organism to react to an environmental input with a change in form, state, movement, or rate of activity" is a definition of Phenotypic Plasticity.

Explanation:

The tendency of one genotype when opened to different conditions, to create more than single phenotype is called as "Phenotypic plasticity".It's the secret to studying human behaviour.

It's the key to human conduct study by laying the foundation to take into consideration the concept that the similar genome and the similar neural architecture will lead to human cultural diversity. For plants whose sessile existence needs them to survive with environmental conditions, this capacity is especially important.

3 0

3 years ago

What are the methods of protein structure determination of biomacromolecules?

Alex73 [517]

Answer:

X-ray crystallography diffraction imaging, nuclear magnetic resonance spectroscopy imaging and frozen electron microscopy three-dimensional reconstruction technology.

Explanation:

http://www.creative-biostructure.com/protein-crystallization-and-structure-determination_13.htm

8 0

3 years ago

Help me solve the blank space.

marissa [1.9K]

Answer:

pulse

Explanation:

4 0

3 years ago

Compare each patient's cdna sequence to the wild-type cdna sequence. Each patient has one nucleotide-pair substitution mutation.

Lera25 [3.4K]

The mutation is a change in the nucleotidic sequence. In the exposed example, Patient 1: nucleotide 143, TTC⇒TGC. Patient 2: nucleotide 143, TTC⇒TCC. Patient 3: nucleotide 147, TTC ⇒ TTG.

<h3>What is a mutation?</h3>

A mutation is a change or alteration in DNI sequences that introduce new variants.

Many of these are eliminated, but some of them might succeed and be incorporated into each individual.

These mutations are the ones that have been selected by natural selection.

<h3>Solving the problem</h3>

We know that each sequence initiates with nucleotide number 103 and ends in nucleotide 162.

So first, we will number the nucleotides, from 103 to 162. Each nucleotide has a number in increasing order.

Now, we will identify the mutations in each of the strands by comparing them with the wild-type sequence. The mutation occurs in one of the nucleotides, so we must look for the change in the bases.

Finally, we will identify the nucleotide location of each mutation.

nucleotide wild-type mutated

location nucleotide nucleotide

Patient 1 143 TTC TGC

Patient 2 143 TTC TCC

Patient 3 147 TTC TTG

In the attached files you will find an image for a better understanding.

You will learn more about mutations at

brainly.com/question/4347425

brainly.com/question/17914937