Cystathionine gamma-lyase

cystathionine gamma-lyase

Cysteine metabolism. Cystathionase catalyzes the lower reaction.
EC number
CAS number 9012-96-8
IntEnz IntEnz view
ExPASy NiceZyme view
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Gene Ontology AmiGO / EGO
cystathionase (cystathionine gamma-lyase)
Symbol CTH
Entrez 1491
HUGO 2501
OMIM 607657
RefSeq NM_001902
UniProt P32929
Other data
EC number
Locus Chr. 1 p31.1

Cystathionine gamma-lyase (CTH or CSE; also cystathionase) is an enzyme which breaks down cystathionine into cysteine, α-ketobutyrate, and ammonia. Pyridoxal phosphate is a prosthetic group of this enzyme.[1][2][3]

Cystathionine gamma-lyase also catalyses the following elimination reactions:

In some bacteria and mammals, including humans, this enzyme takes part in generating hydrogen sulfide.[2][5] Hydrogen sulfide is one of a few gases that was recently discovered to have a role in cell signaling in the body.[6]

Enzyme Mechanism

Cystathionase uses pyridoxal phosphate to facilitate the cleavage of the sulfur-gamma carbon bond of cystathionine, resulting in the release of cysteine.[3] Afterwards the external ketimine is hydrolyzed, causing the release of α-ketobutyrate. The lysine residue reforms the internal aldimine by kicking off the ammonia leaving group.[7]

The amino group on cystathionine is deprotonated and undergoes a nucleophilic attack of the internal aldimine. An additional deprotonation by a general base results in the formation of the external aldimine and removal of the lysine residue. The basic lysine residue is then able to deprotonate the alpha carbon, pushing electron density into the nitrogen of the pyridine ring.[3] Pyridoxal phosphate is necessary to stabilize this carbanionic intermediate; otherwise the proton's pKa would be too high.[7] The beta carbon is then deprotonated, creating an alpha-beta unsaturation and pushing a lone pair onto the aldimine nitrogen. To reform the aldimine, this lone pair pushes back down, cleaving the sulfur-gamma carbon bond, resulting in the release of cysteine.[3]

A pyridoxamine derivative of vinyl glyoxylate remains after the gamma elimination. The lone pair from the pyridine nitrogen pushes electron density to the gamma carbon, which is protonated by lysine. Lysine then attacks the external aldimine, pushing electron density to the beta carbon, which is protonated by a general acid. The imine is then hydrolyzed to release α-ketobutyrate. Deprotonation of the lysine residue causes ammonia to leave, thus completing the catalytic cycle.[7]

Cystathionine gamma lyase also shows gamma-synthase activity depending on the concentrations of reactants present.[8] The mechanisms are the same until they diverge after formation of the vinyl glyoxylate derivative. In the gamma synthase mechanism, the gamma carbon is attacked by a sulfur nucleophile, resulting in the formation of a new sulfur-gamma carbon bond.[7][8]

The mechanism for cystathionine gamma lyase.

Enzyme Structure

Cystathionine gamma-lyase is a member of the Cys/Met metabolism PLP-dependent enzymes family. Other members include cystathionine gamma synthase, cystathionine beta lyase, and methionine gamma lyase.[8] It is also a member of the broader aspartate aminotransferase family.[1][8] Like many other PLP-dependent enzymes, cystathionine gamma-lyase is a tetramer with D2 symmetry.[8]

Pyridoxal phosphate is bound in the active site by Lys212.[2]

Disease Relevance

Inhibited cystathionase active site.[2] The inhibitor and Tyr114 are in light blue, PLP in purple, and Lys121 in yellow.

Cysteine is the rate-limiting substrate in the synthetic pathway for glutathione in the eye. Glutathione is an antioxidant that protects crystallins in the eye from reactive oxygen species; denatured crystallins can lead to cataracts. Cystathionase is also a target for reactive oxygen species. Thus as cystathionase is oxidized, its activity decreases, causing a decrease in cysteine and, in turn, glutathione in the eye, leading to a decrease in antioxidant availability, causing a further decrease in cystathionase activity. Deficiencies in cystathionase activity have also been shown to contribute to glutathione depletion in patients with cancer and AIDS.[9]

Mutations and deficiencies in cystathionase are associated with cystathioninuria. The mutations T67I and Q240E weaken the enzyme's affinity for pyridoxal phosphate, the co-factor vital to enzymatic function.[2] Low levels of H2S have also been associated with hypertension in mice.[10]

Propargylglycine (acidic beta hydrogen explicitly shown).

Excessive levels of H2S, due to increased activity of cystathionase, are associated with endotoxemia, acute pancreatitis, hemorrhagic shock, and diabetes mellitus.[2]

Propargylglycine and β-cyanoalanine are two irreversible inhibitors of cystathionase used to treat elevated H2S levels. Mechanistically, the amino group of propargylglycine attacks the aldimine to form an external aldimine. The β position of the alkyne is then deprotonated to form the allene, which is then attacked by the phenol of Tyr114. The internal aldimine can regenerate, but the newly created vinyl ether sterically hinders the active site, blocking cysteine from attacking pyridoxal phosphate.[2]


H2S decreases transcription of cystathionase at concentrations between 10 and 80μM. However, transcription is increased by concentrations near 120μM, and inhibited completely at concentrations in excess of 160μM.[6]

See also

External links


  1. 1 2 Berg, J. M.; Tymoczko, J. L.; & Stryer, L. (2012). Biochemistry , (7th ed.). New York: W.H. Freeman Company.
  2. 1 2 3 4 5 6 7 Sun Q, Collins R, Huang S, Holmberg-Schiavone L, Anand GS, Tan CH, van-den-Berg S, Deng LW, Moore PK, Karlberg T, Sivaraman J (2009). "Structural basis for the inhibition mechanism of human cystathionine gamma-lyase, an enzyme responsible for the production of H(2)S". J. Biol. Chem. 284 (5): 3076–85. doi:10.1074/jbc.M805459200. PMID 19019829.
  3. 1 2 3 4 Steegborn C, Clausen T, Sondermann P, Jacob U, Worbs M, Marinkovic S, Huber R, Wahl MC (1999). "Kinetics and inhibition of recombinant human cystathionine gamma-lyase. Toward the rational control of transsulfuration". J. Biol. Chem. 274 (18): 12675–84. doi:10.1074/jbc.274.18.12675. PMID 10212249.
  4. Yamanishi T, Tuboi S (1981). "The mechanism of the L-cystine cleavage reaction catalyzed by rat liver gamma-cystathionase". J. Biochem. 89 (6): 1913–21. PMID 7287665.
  5. Wang R (March 2010). "Toxic Gas, Lifesaver". Scientific American: 52.
  6. 1 2 Wang M, Guo Z, Wang S (2013). "The effect of certain conditions in the regulation of cystathionine γ-lyase by exogenous hydrogen sulfide in mammalian cells". Biochem. Genet. 51 (7-8): 503–13. doi:10.1007/s10528-013-9581-1. PMID 23515848.
  7. 1 2 3 4 Brzovic, Peter; Litzenberger Holbrook, Elizabeth (January 1990). "Reaction mechanism of Escherichia coli cystathionine .gamma.-synthase: direct evidence for a pyridoxamine derivative of vinylgloxylate as a key intermediate in pyridoxal phosphate dependent .gamma.-elimination and .gamma.-replacement reactions". Biochemistry. ACS. 29 (2): 442–451. doi:10.1021/bi00454a020. Retrieved 9 March 2015.
  8. 1 2 3 4 5 Messerschmidt A, Worbs M, Steegborn C, Wahl MC, Huber R, Laber B, Clausen T (2003). "Determinants of enzymatic specificity in the Cys-Met-metabolism PLP-dependent enzymes family: crystal structure of cystathionine gamma-lyase from yeast and intrafamiliar structure comparison". Biol. Chem. 384 (3): 373–86. doi:10.1515/BC.2003.043. PMID 12715888.
  9. Sastre J, Martín JA, Gómez-Cabrera MC, Pereda J, Borrás C, Pallardó FV, Viña J (2005). "Age-associated oxidative damage leads to absence of gamma-cystathionase in over 50% of rat lenses: relevance in cataractogenesis". Free Radic. Biol. Med. 38 (5): 575–82. doi:10.1016/j.freeradbiomed.2004.11.029. PMID 15683713.
  10. Yang G, Wu L, Jiang B, Yang W, Qi J, Cao K, Meng Q, Mustafa AK, Mu W, Zhang S, Snyder SH, Wang R (2008). "H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine gamma-lyase". Science. 322 (5901): 587–90. doi:10.1126/science.1162667. PMC 2749494Freely accessible. PMID 18948540.
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