Anagrammen & Informatie over | Engels woord LYASE

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Voorbeelden van het gebruik van LYASE in een zin

• coli, generate PABA from chorismate by the combined action of the enzymes 4-amino-4-deoxychorismate synthase and 4-amino-4-deoxychorismate lyase.
• 0, the citrate lyase and phosphoribosyl pyrophosphate synthetase, two enzymes controlling anabolic (ATP-demanding) pathways are activated, while the phosphofructokinase and the pyruvate dehydrogenase, two enzymes controlling amphibolic pathways (supplying ATP as well as important biosynthetic intermediates) are inhibited He concluded that control of these pathways has evolved to maintain the energy charge within rather narrow limits - in other words, that the energy charge, like the pH of a cell, must be buffered at all times.
• These enzymes include amygdalin beta-glucosidase, prunasin beta-glucosidase and mandelonitrile lyase.
• 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency, (HMGCLD) also known as HMGCL deficiency, HMG-CoA lyase deficiency, or hydroxymethylglutaric aciduria, is an uncommon autosomal recessive inborn error in ketone body production and leucine breakdown caused by HMGCL gene mutations.
• Monofunctional glycosylases have only glycosylase activity, whereas bifunctional glycosylases also possess AP lyase activity.
• Besides peroxisomal functions, glyoxysomes possess additionally the key enzymes of the glyoxylate cycle (isocitrate lyase and malate synthase) which accomplish the glyoxylate cycle bypass.
• Enzymes with single-substrate mechanisms include isomerases such as triosephosphateisomerase or bisphosphoglycerate mutase, intramolecular lyases such as adenylate cyclase and the hammerhead ribozyme, an RNA lyase.
• The glyoxylate cycle bypasses the two oxidative decarboxylation reactions of the TCA cycle and directly converts isocitrate through isocitrate lyase and malate synthase into malate and succinate.
• In argininosuccinic aciduria, the enzyme argininosuccinate lyase, involved in the conversion of arginino succinate to arginine within the urea cycle, is damaged or missing.
• gov/pmc/articles/PMC213756/ Characterization of the Erwinia carotovora pelB gene and its product pectate lyase.
• Adenylosuccinate lyase deficiency is a rare autosomal recessive metabolic disorder characterized by the appearance of succinylaminoimidazolecarboxamide riboside (SAICA riboside) and succinyladenosine (S-Ado) in cerebrospinal fluid, urine.
• Both pectate lyase and P22 tailspike protein contain right-handed helices; left-handed versions have been observed in enzymes such as UDP-N-acetylglucosamine acyltransferase and archaeal carbonic anhydrase.
• After citrate enters a cell through citrate permeases, citrate lyase cleaves it into acetate and oxaloacetate, which is further broken down into carbon dioxide and pyruvate.
• Phenylalanine ammonia lyase facilitates the deamination of L-phenylalanine to (E)-cinnamate, which is then oxidized by cinnamate 4-hydroxylase to yield p-Coumaric acid.
• Petiveriin also serves as precursor to phenylmethanethial S-oxide, a lachrymatory agent structurally similar to syn-propanethial-S-oxide from onion, but whose formation requires novel cysteine sulfoxide lyase and lachrymatory factor synthase enzymes differing from those found in onion.
• S1P can be dephosphorylated to sphingosine by sphingosine phosphatases and can be irreversibly degraded by an enzyme, sphingosine phosphate lyase.
• Five missense mutations (A287P, R457H, V492E, C569Y, and V608F) and a splicing mutation in the POR genes have been found in patients who had hormonal evidence for combined deficiencies of two steroidogenic cytochrome P450 enzymes - P450c17 CYP17A1, which catalyzes steroid 17α-hydroxylation and 17,20 lyase reaction, and P450c21 21-hydroxylase, which catalyzes steroid 21-hydroxylation.
• Adenylosuccinate lyase (or adenylosuccinase) is an enzyme that in humans is encoded by the ADSL gene.
• Biochemically, 1-octen-3-ol is generated from the peroxidation of linoleic acid, catalyzed by a lipoxygenase, followed by cleavage of the resulting hydroperoxide with the help of a hydroperoxide lyase.
• Other names in common use include myo-inositol-1-phosphate synthase, D-glucose 6-phosphate cycloaldolase, inositol 1-phosphate synthatase, glucose 6-phosphate cyclase, inositol 1-phosphate synthetase, glucose-6-phosphate inositol monophosphate cycloaldolase, glucocycloaldolase, and 1L-myo-inositol-1-phosphate lyase (isomerizing).

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