Cysteine sulfinic acid

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Cysteine Sulfinic Acid[edit | edit source]

Chemical structure of cysteine sulfinic acid

Cysteine sulfinic acid is a non-proteinogenic amino acid that plays a crucial role in various biological processes. It is derived from the amino acid cysteine through the oxidation of its sulfhydryl group. The chemical formula of cysteine sulfinic acid is C3H7NO5S.

Structure[edit | edit source]

Cysteine sulfinic acid consists of a central carbon atom bonded to an amino group (-NH2), a carboxyl group (-COOH), a sulfonic acid group (-SO3H), and a hydrogen atom (-H). The sulfonic acid group is responsible for the acidic nature of this amino acid.

Biological Significance[edit | edit source]

Cysteine sulfinic acid is a key intermediate in the biosynthesis of taurine, an essential amino acid in humans. It is converted to taurine through the action of the enzyme cysteine dioxygenase. Taurine is involved in various physiological processes, including bile acid conjugation, osmoregulation, and modulation of neuronal activity.

Furthermore, cysteine sulfinic acid is a precursor for the synthesis of hypotaurine, another important metabolite. Hypotaurine is involved in the detoxification of reactive oxygen species and acts as an antioxidant in the body.

Role in Neurotransmission[edit | edit source]

Cysteine sulfinic acid is also a key component in the synthesis of the neurotransmitter glutamate. Glutamate is the most abundant excitatory neurotransmitter in the central nervous system and plays a crucial role in various physiological processes, including learning, memory, and synaptic plasticity.

The enzyme cysteine sulfinic acid decarboxylase converts cysteine sulfinic acid into hypotaurine, which is further converted to pyruvate and ammonia. Pyruvate is then converted to alpha-ketoglutarate, a precursor for the synthesis of glutamate.

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Contributors: Prab R. Tumpati, MD