Target type: biologicalprocess
The chemical reactions and pathways resulting in the breakdown of L-cysteine, the L-enantiomer of 2-amino-3-mercaptopropanoic acid, i.e. (2R)-2-amino-3-mercaptopropanoic acid. [GOC:jsg, GOC:mah]
L-cysteine catabolism is a fundamental metabolic pathway responsible for the breakdown of the sulfur-containing amino acid L-cysteine. This process plays a vital role in cellular metabolism, detoxification, and the biosynthesis of essential molecules. The catabolism of L-cysteine proceeds through two main pathways: the transsulfuration pathway and the cysteine dioxygenase pathway.
**1. Transsulfuration Pathway:**
* **Step 1: Conversion to cystathionine:** L-cysteine reacts with α-ketoglutarate in a reaction catalyzed by the enzyme cystathionine β-synthase. This reaction produces cystathionine, a sulfur-containing amino acid.
* **Step 2: Conversion to homocysteine:** Cystathionine is then cleaved by cystathionine γ-lyase, releasing homocysteine, α-ketobutyrate, and hydrogen sulfide (H2S).
* **Step 3: Conversion to methionine:** Homocysteine can be remethylated to methionine, another essential amino acid. This reaction requires the enzyme tetrahydrofolate reductase (THF reductase) and the coenzyme tetrahydrofolate (THF).
**2. Cysteine Dioxygenase Pathway:**
* **Step 1: Oxidation to cysteine sulfinate:** L-cysteine is oxidized to cysteine sulfinate by the enzyme cysteine dioxygenase. This reaction requires molecular oxygen (O2) and generates hydrogen peroxide (H2O2).
* **Step 2: Conversion to sulfite:** Cysteine sulfinate is then decarboxylated by the enzyme cysteine sulfinate decarboxylase, producing sulfite and pyruvate.
* **Step 3: Sulfite oxidation:** Sulfite is further oxidized to sulfate by the enzyme sulfite oxidase. This reaction also requires molecular oxygen and generates hydrogen peroxide.
**Overall, the catabolism of L-cysteine results in the production of various metabolic intermediates, including α-ketobutyrate, homocysteine, methionine, pyruvate, and sulfate. These products play essential roles in various cellular processes:**
* **Sulfur metabolism:** Cysteine catabolism provides sulfur for the biosynthesis of essential sulfur-containing molecules, such as glutathione, coenzyme A, and various proteins.
* **Amino acid metabolism:** L-cysteine catabolism is interconnected with the metabolism of other amino acids, including methionine, homocysteine, and serine.
* **Redox balance:** The catabolism of L-cysteine generates reducing equivalents, which contribute to maintaining redox homeostasis in the cell.
* **Detoxification:** The transsulfuration pathway is involved in the detoxification of various xenobiotics and reactive oxygen species.
* **H2S production:** The transsulfuration pathway produces hydrogen sulfide (H2S), a signaling molecule with diverse physiological effects.
L-cysteine catabolism is a highly regulated process that is influenced by various factors, including dietary intake, hormonal signals, and cellular stress. Dysregulation of this pathway can lead to various metabolic disorders and disease states.
'"
Protein | Definition | Taxonomy |
---|---|---|
Cystathionine beta-synthase | A cystathionine beta-synthase that is encoded in the genome of human. [PRO:DNx, UniProtKB:P35520] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
aminooxyacetic acid | (aminooxy)acetic acid : A member of the class of hydroxylamines that is acetic acid substituted at postion 2 by an aminooxy group. It is a compound which inhibits aminobutyrate aminotransferase activity in vivo, resulting in increased levels of gamma-aminobutyric acid in tissues. Aminooxyacetic Acid: A compound that inhibits aminobutyrate aminotransferase activity in vivo, thereby raising the level of gamma-aminobutyric acid in tissues. | amino acid; hydroxylamines; monocarboxylic acid | anticonvulsant; EC 2.6.1.19 (4-aminobutyrate--2-oxoglutarate transaminase) inhibitor; EC 4.2.1.22 (cystathionine beta-synthase) inhibitor; nootropic agent |
aurintricarboxylic acid | aurintricarboxylic acid : A member of the class of quinomethanes that is 3-methylidene-6-oxocyclohexa-1,4-diene-1-carboxylic acid in which the methylidene hydrogens are replaced by 4-carboxy-3-hydroxyphenyl groups. The trisodium salt is the biological stain 'chrome violet CG' while the triammonium salt is 'aluminon'. Aurintricarboxylic Acid: A dye which inhibits protein biosynthesis at the initial stages. The ammonium salt (aluminon) is a reagent for the colorimetric estimation of aluminum in water, foods, and tissues. | monohydroxybenzoic acid; quinomethanes; tricarboxylic acid | fluorochrome; histological dye; insulin-like growth factor receptor 1 antagonist |
hypericin | |||
agathisflavone | agathisflavone : A biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-6 and C-8 of the two chromene rings. agathisflavone: bis-apigenin coupled at 6 and 8 positions; isolated from the plant Canarium manii; has hepatoprotective activity against carbon tetrachloride-induced hepatotoxicity | biaryl; biflavonoid; hydroxyflavone | antineoplastic agent; antiviral agent; hepatoprotective agent; metabolite |
cupressuflavone | cupressuflavone : A biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-8 of the two chromene rings respectively. Isolated from Cupressus sempervirens and Juniperus occidentalis, it exhibits free radical scavenging and antielastase activities. cupressuflavone: from Cupressus macrocarpa; structure in first source | biflavonoid; hydroxyflavone; ring assembly | EC 3.4.21.37 (leukocyte elastase) inhibitor; metabolite; radical scavenger |
myricetin | 7-hydroxyflavonol; hexahydroxyflavone | antineoplastic agent; antioxidant; cyclooxygenase 1 inhibitor; food component; geroprotector; hypoglycemic agent; plant metabolite | |
podocarpusflavone a | podocarpusflavone A: isolated from Podocarpus imbricatus | flavonoid oligomer | |
rubrolide a | rubrolide A: from Synoicum prunum; structure in first source |