Glycine
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Amino Acids
- Serine
- Asparagine
- Alanine
- Valine
- Leucine
- Isoleucine
- Phenylalanine
- Tryptophan
- Methionine
- Proline
- Glycine
- Threonine
- Cysteine
- Tyrosine
- Glutamine
- Aspartate
- Glutamate
- Histidine
- Lysine
- Arginine
Summary
Glycine, which is abbreviated as the 3 letters Gly as well as the single letter G, is one of the 20 amino acids that make up proteins in our body. Glycine’s R-group is a single hydrogen atom, which makes it a non-polar, hydrophobic amino acid. Further, glycine is the only non-chiral amino acid because its alpha carbon is bonded to two identical hydrogens, creating an internal plane of symmetry. Glycine’s small R-group being just a hydrogen allows proteins incorporating it to make very tight turns, giving the polypeptide chain a lot of flexibility to twist and turn.
Key Points
- Glycine
- Abbreviations
- Gly, G
- Chemical Structure
- R-group: -H
- Symmetrical plane around the alpha carbon leads to achirality
- Small R group also allows for conformational and steric flexibility
- Polarity
- Non-polar (lipid soluble/hydrophobic)
- Charge at pH 7
- Neutral (0)
- Other Information
- Only non-chiral amino acid
- Structure can allow for tighter turns in protein structure than other AAs
- Allows for conformational flexibility
- Abbreviations