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Difference Between Nucleotide and Nucleoside

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Introduction to Nucleotide and Nucleoside

Nucleotides and nucleosides are fundamental building blocks of nucleic acids. A nucleotide consists of a nucleoside attached to one or more phosphate groups, while a nucleoside is made up of a nitrogenous base linked to a sugar molecule without any phosphate groups.


Comparison Between Nucleotide and Nucleoside

Characteristic

Nucleoside

Nucleotide

Basic Composition

Consists of a nitrogenous base (purine or pyrimidine) linked to a sugar (ribose or deoxyribose)

Consists of a nucleoside with one or more phosphate groups attached

Phosphate Group

Absent

Present

Role in Nucleic Acids

Serves as a building block for nucleotide synthesis

Directly incorporated into DNA and RNA as the structural backbone

Examples

Adenosine, Guanosine, Cytidine, Uridine, Thymidine

Adenosine monophosphate (AMP), Guanosine triphosphate (GTP), etc.

Function

Involved in cellular signaling and energy transfer when phosphorylated

Essential for encoding genetic information and energy metabolism

Energy Storage

Can be converted into nucleotides which are used in energy transfer reactions

ATP, a nucleotide, is the primary energy carrier in cells

Molecular Weight

Generally lower due to absence of phosphate groups

Higher due to the additional phosphate group(s)

Enzymatic Interactions

Intermediates in the formation of nucleotides by enzymes

Substrates and cofactors for many enzymatic reactions, including DNA/RNA synthesis


Essential Study Materials for NEET UG Success

FAQs on Difference Between Nucleotide and Nucleoside

1. What is the difference between a nucleotide and a nucleoside inhibitor?

Nucleoside inhibitors mimic natural nucleosides but lack phosphate groups and must be phosphorylated inside the cell to become active. In contrast, nucleotide inhibitors already include one or more phosphate groups, meaning they are closer to the active form required for incorporation into viral DNA or RNA.

2. What is an example of a nucleoside?

A common example of a nucleoside is adenosine, which consists of the adenine base linked to a ribose sugar.

3. What is an example of a non-nucleoside?

Efavirenz is an example of a non-nucleoside reverse transcriptase inhibitor (NNRTI), used in antiviral therapy without mimicking the natural nucleoside structure.

4. What is a nucleoside difference from a nucleotide is not having?

A nucleoside does not have any phosphate groups attached, whereas a nucleotide includes one or more phosphate groups.

5. What is the main difference between nucleoside and nucleotide?

The main difference is that a nucleoside is composed of a nitrogenous base linked to a sugar, while a nucleotide consists of a nucleoside plus one or more phosphate groups.

6. What is the difference between nucleoside and non-nucleoside?

Nucleosides are the basic building blocks of nucleic acids, composed of a sugar and a base, whereas non-nucleosides typically refer to compounds (often inhibitors) that do not mimic the nucleoside structure and do not participate directly in forming nucleic acids.

7. What is the difference between a nucleotide and a nucleobase?

A nucleotide comprises a nucleobase, a sugar, and one or more phosphate groups, whereas a nucleobase is just the nitrogen-containing compound (such as adenine, thymine, cytosine, guanine, or uracil) without the sugar or phosphate.

8. Is sugar a nucleoside?

No, sugar by itself is not a nucleoside. A nucleoside is formed when a sugar molecule is bonded to a nucleobase.

9. Why is it called nucleoside?

It is called a nucleoside because it consists of a nucleobase linked to a sugar, forming the core unit from which nucleotides—and ultimately nucleic acids—are built.

10. Are nucleosides in DNA or RNA?

Nucleosides are found in both DNA and RNA. In DNA, they are present as deoxyribonucleosides, and in RNA, they appear as ribonucleosides.