Cysteine

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Identification

Molecular formula
C3H7NO2S
CAS Number
52-90-4
IUPAC Name
2-amino-4-sulfanyl-butanoic acid
Molecular Weight
121.16g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.8580g/cm3
Synonyms
DL-Homocysteine
Interesting facts

Exploring 2-Amino-4-sulfanyl-butanoic Acid

2-Amino-4-sulfanyl-butanoic acid, often referred to as cysteine in biological contexts, is an intriguing compound that plays a vital role in various biochemical processes. Here are some fascinating facts about this amino acid:

  • Essential for Protein Structure: Cysteine contains a thiol group (-SH) that allows for the formation of disulfide bonds. These bonds are crucial for stabilizing the three-dimensional structure of proteins, influencing their functionality and activity.
  • Antioxidant Properties: Cysteine is a precursor to glutathione, one of the body's most potent antioxidants. This makes it essential for protecting cells from oxidative stress and maintaining overall cellular health.
  • Role in Metabolism: Cysteine is involved in the metabolism of sulfur-containing amino acids and is important for the synthesis of coenzymes, which are critical for countless metabolic processes.
  • Behavior in the Body: It can exist in both reduced and oxidized forms, allowing it to participate in redox reactions, a unique feature that enhances its role in cellular signaling and metabolic pathways.
  • Dietary Sources: Natural sources of cysteine include high-protein foods such as poultry, yogurt, and legumes, making it accessible to those with a balanced diet.

In conclusion, 2-amino-4-sulfanyl-butanoic acid is not just a simple amino acid; its multifunctional properties make it a *critical player* in the realm of biochemistry. Understanding its functions can deepen our appreciation for the complexity of biochemical networks in living organisms.

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