cysteine-S-conjugate beta-lyase EC#: 4.4.1.13; ChemWhat Code: 1382916

Product Name cysteine-S-conjugate beta-lyase
Example Structure Example Structure of cysteine-S-conjugate beta-lyase EC#: 4.4.1.13
Synonyms beta-cystathionase, beta-lyase, C-DES, C-S lyase, CBL, CBS, CCBL2, Ctl1, Ctl2, cystathionine beta-lyase, cystathionine beta/gamma-lyase, cystathionine lyase, cysteine conjugate beta-lyase, cysteine conjugate. beta.-lyase, cysteine lyase, cysteine S-conjugate beta-lyase, cysteine-S-conjugate beta-lyase, cystine C-S lyase, cystine lyase, glutamine transaminase K, glutamine transaminase K/cysteine conjugate beta-lyase, GTK, Irc7p, KAT, KAT III, KYAT3, kynurenine aminotransferase, kynurenine-oxoglutarate transaminase 3, L-cystine C-S lyase, lyase, cystathionine beta-, lyase, cysteine conjugate.beta., MalY, MetC, More, ORF5, osteotoxin, PatB protein, Str3p, TTHA1620
EC Number 4.4.1.13
CAS Registry Number 68652-57-3
Comments A pyridoxal 5′-phosphate protein. The enzyme is promiscuous regarding the moiety conjugated to L-cysteine, and can accept both aliphatic and aromatic substitutions. The enzyme cleaves a carbon-sulfur bond, releasing a thiol and an unstable enamine product that tautomerizes to an imine form, which undergoes a hydrolytic deamination to form pyruvate and ammonia. While bacteria and plants have dedicated enzymes, all of the animal enzymes discovered thus far are bifunctional, most of which also act as aminotransferases. Formerly EC?4.4.1.6?and EC?4.4.1.8.
Cofactor pyridoxal 5′-phosphate
History
Reactions An L-cysteine-S-conjugate + H(2)O = Rsh + NH(3) + pyruvate.

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