Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.5.1.1 (asparaginase)
 2,695 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A large portion of mitochondrial asparagine (Asn) is degraded by asparagine amino-transferase to produce alpha-ketosuccinamate (alpha KSA), which is then hydrolized by omega-amidase to produce oxaloacetate (OAA) and ammonia. This is in contrast to the catabolism in the cytosol, where the main catabolic route for Asn occurs initially via asparaginase-catalyzed hydrolysis to form aspartate and ammonia. Mitochondrial production of OAA from Asn was followed by monitoring the decrease in the rate of succinate oxidation (which is inhibited by OAA) in both coupled and uncoupled mitochondria. Rapid OAA production was found to be dependent on the presence of both Asn and glyoxylate, and was eliminated by the aminotransferase inhibitor, aminooxyacetate (AOX). HPLC separation and quantitation of alpha-keto acids and amino acids allowed direct observation of the proposed mitochondrial pathway. Studies using L-[U-14C]Asn in mitochondria yielded labeled carbon in alpha KSA, OAA, and CO2 when either an alpha-keto acid or glyoxylate was provided. The extent of the labeled carbon in these products was greatly influenced by factors that affected the citric acid cycle and oxidative phosphorylation. Carbon dioxide production from Asn alone, even in the presence of AOX, suggested the existence of at least one additional Asn catabolic pathway in the rat liver mitochondria which does not involve alpha KSA as an intermediate.
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PMID:Asparagine catabolism in rat liver mitochondria. 291 80

In higher plants, asparagine (Asn) is a major form of organic nitrogen used for transport and storage. There are two pathways of Asn metabolism, involving asparaginase and Asn aminotransferase. The enzyme serine:glyoxylate aminotransferase encoded by AGT1 has been identified as an asparagine aminotransferase in Arabidopsis. The product of asparagine transamination, alpha-ketosuccinamate, can be hydrolyzed by the enzyme omega-amidase to form oxaloacetate and ammonia. A candidate gene was identified in Arabidopsis based on its sequence similarity with mouse omega-amidase. Recombinant omega-amidase exhibited comparable catalytic activities with alpha-hydroxysuccinamate, alpha-ketosuccinamate and alpha-ketoglutaramate, the product of glutamine transamination. A mutant with a T-DNA inserted in the first exon accumulated alpha-ketosuccinamate and alpha-hydroxysuccinamate as compared with wild-type, both under control conditions and after treatment with Asn. Treatment with Asn led to decreased transcript levels of omega-amidase in root, while transcript levels of AGT1 are increased under these conditions, suggesting that excess Asn may lead to the accumulation of alpha-ketosuccinamate and alpha-hydroxysuccinamate.
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PMID:Identification and characterization of omega-amidase as an enzyme metabolically linked to asparagine transamination in Arabidopsis. 2446 Dec 28