Cysteine metabolism

Cysteine metabolism refers to the biological pathways that consume or create cysteine. The pathways of different amino acids and other metabolites interweave and overlap to creating complex systems.

Human cysteine metabolism

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In human cysteine metabolism,[citation needed] L-cysteine is consumed in several ways as shown below. L-Cysteine is also consumed in pantothenate/coenzyme A biosynthesis.

L-Cysteine consumption pathways
EnzymeProductsCofactor/Additional Reactant
cysteine dioxygenase[1]cysteine sulfinic acidiron
serine racemase[2]D-cysteinepyridoxal phosphate
cysteine lyase[3]L-cysteate/hydrogen sulfidepyridoxal phosphate/sulfite
cystathionine γ-lyase[4]pyruvate/NH3/H2Spyridoxal phosphate
cysteine—tRNA ligase[5]L-cysteinyl-tRNACys
cystine reductase[6]L-cystine/NADH and H+NAD+
cysteine transaminase[7]3-mercapto-pyruvate/L-glutamatepyridoxal phosphate/alpha-ketoglutaric acid
glutamate–cysteine ligase[8]γ-glutamyl cysteine/ADP and PiATP

L-Cysteine is the product of several processes as well. In addition to the reactions below, L-cysteine is also a product of glycine, serine, and threonine metabolism.

L-cysteine production pathways
ReactantsEnzymeCofactorsNotes
O-acetyl-L-serine/hydrogen sulfidecysteine synthase[9]pyridoxal phosphatenot present in humans
L-cystine/2 glutathioneglutathione-cystine transhydrogenase[10]
cystathioninecystathionine γ-lyase[4]pyridoxal phosphate
3-mercapto-pyruvatecysteine transaminase[7]pyridoxal phosphate

References

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See also

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