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  • enzymology
  • In enzymology, a carboxymethyloxysuccinate lyase (EC 4.2.99.12) is an enzyme that catalyzes the chemical reaction carboxymethyloxysuccinate ⇌ {\displaystyle \rightleftharpoons } fumarate + glycolate Hence, this enzyme has one substrate, carboxymethyloxysuccinate, and two products, fumarate and glycolate. (wikipedia.org)
  • In enzymology, a dihydroxyphenylalanine ammonia-lyase (EC 4.3.1.11) is an enzyme that catalyzes the chemical reaction 3,4-dihydroxy-L-phenylalanine ⇌ {\displaystyle \rightleftharpoons } trans-caffeate + NH3 Hence, this enzyme has one substrate, 3,4-dihydroxy-L-phenylalanine (L-DOPA), and two products, trans-caffeate and NH3. (wikipedia.org)
  • In enzymology, an ethanolamine ammonia-lyase (EC 4.3.1.7) is an enzyme that catalyzes the chemical reaction ethanolamine ⇌ {\displaystyle \rightleftharpoons } acetaldehyde + NH3 Hence, this enzyme has one substrate, ethanolamine, and two products, acetaldehyde and NH3. (wikipedia.org)
  • In enzymology, a threo-3-hydroxyaspartate ammonia-lyase (EC 4.3.1.16) is an enzyme that catalyzes the chemical reaction threo-3-hydroxy-L-aspartate ⇌ {\displaystyle \rightleftharpoons } oxaloacetate + NH3 Hence, this enzyme has one substrate, threo-3-hydroxy-L-aspartate, and two products, oxaloacetate and NH3. (wikipedia.org)
  • In enzymology, a 3-ketovalidoxylamine C-N-lyase (EC 4.3.3.1) is an enzyme that catalyzes the chemical reaction 4-nitrophenyl-3-ketovalidamine ⇌ {\displaystyle \rightleftharpoons } 4-nitroaniline + 5-D-(5/6)-5-C-(hydroxymethyl)-2,6-dihydroxycyclohex-2-en-1-one Hence, this enzyme has one substrate, 4-nitrophenyl-3-ketovalidamine, and two products, 4-nitroaniline and 5-D-(5/6)-5-C-(hydroxymethyl)-2,6-dihydroxycyclohex-2-en-1-one. (wikipedia.org)
  • In enzymology, a serine-sulfate ammonia-lyase (EC 4.3.1.10) is an enzyme that catalyzes the chemical reaction L-serine O-sulfate + H2O ⇌ {\displaystyle \rightleftharpoons } pyruvate + NH3 + sulfate Thus, the two substrates of this enzyme are L-serine O-sulfate and H2O, whereas its 3 products are pyruvate, NH3, and sulfate. (wikipedia.org)
  • site
  • APE1 is a gene that codes for DNA AP lyase in humans which binds to AP DNA loops into both the DNA major and minor grooves and binds a flipped-out AP site in a pocket that excludes DNA bases and racemized-anomer AP sites. (wikipedia.org)
  • class
  • Since DNA AP lyase is a class of structures who have numerous target genes that encode for different variations of the enzyme, there is no one single enzyme structure that can be used as an example that encompasses all versions of the enzyme. (wikipedia.org)
  • synthase
  • The formed hydroperoxy fatty acids are highly reactive and dangerous for the plant, and are therefore further metabolized by other enzymes such as allene oxide synthase, hydroperoxide lyase, peroxygenase or divinyl ether synthase. (uu.nl)
  • Methylisocitrate lyase is used in the methylcitrate cycle, a modified version of the Krebs cycle that metabolizes propionyl coenzyme A instead of acetyl coenzyme A. The enzyme 2-methylcitrate synthase adds propionyl coenzyme A to oxaloacetate, yielding methylcitrate instead of citrate. (wikipedia.org)
  • reactive
  • The latter is cleaved by -lyase to form 1,2-dichlorovinylthiol, a reactive intermediate which is implicated in covalent modification of proteins and other cel- lular targets. (wgc2010.sk)
  • make
  • The high expression level, high stability and specificity make the cloned lyases interesting for application in a biocatalytic process. (uu.nl)
  • names
  • Other names in common use include strictosidine synthetase, STR, and 3-alpha(S)-strictosidine tryptamine-lyase. (wikipedia.org)
  • Other names in common use include 2'-carboxybenzalpyruvate aldolase, (3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate, 2-carboxybenzaldehyde-lyase, and (3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate 2-formylbenzoate-lyase. (wikipedia.org)
  • There are several different names for chorismate lyase. (wikipedia.org)
  • group
  • They cleave the C-C bond adjacent to the hydroperoxy group in the lipoxygenase products, resulting in the formation of w-oxo acids and volatile C6- and C9-aldehydes. (uu.nl)