What is the Difference Between Glycine and L Glycine?
🆚 Go to Comparative Table 🆚Glycine is an amino acid that serves as a building block for proteins and is considered the simplest among amino acids due to its single hydrogen atom side chain. Glycine can occur in two isomeric forms: D glycine and L glycine, which are structural isomers of each other. However, the L form of glycine is the most stable and common isomer in biological systems.
The key difference between glycine and L glycine lies in their stereochemistry:
- Glycine: Refers to the amino acid in general, which can manifest in both D and L forms.
- L-Glycine: The most stable and most common isomer found in organisms.
In summary, glycine is an amino acid that makes up proteins, while L-glycine is an isomer of glycine that is more stable and commonly found in biological systems.
Comparative Table: Glycine vs L Glycine
Glycine is an amino acid that serves as a building block for proteins and is classified as a proteinogenic amino acid. It has a single hydrogen atom as its side chain, making it the simplest among amino acids. Glycine can occur in two isomeric forms: D glycine and L glycine, which are structural isomers of each other. Here is a table comparing the differences between glycine and L-glycine:
Characteristic | Glycine | L-Glycine |
---|---|---|
Definition | An amino acid that makes up proteins | An isomer of glycine |
Isomeric Forms | Can occur in two forms: D glycine and L glycine | Only the L form is considered glycine |
Side Chain | Single hydrogen atom | Single hydrogen atom |
Classification | Proteinogenic amino acid | Isomer of a proteinogenic amino acid |
Melting Point | 233 °C | 233 °C (approximately) |
The key difference between glycine and L-glycine is that glycine is an amino acid that makes up proteins, while L-glycine is an isomer of glycine. Both D-glycine and L-glycine are structural isomers, but only the L form is commonly found in organisms.
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