Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search General Information

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search

Search term:

Results 1 - 10 of 10
EC Number General Information Commentary Reference
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5malfunction allantoin accumulation is mediated by allantoinase downregulation. Knockout, knockdown, and stress-inducible mutants of AtALN reveal that allantoin accumulation is essential for salt stress tolerance, phenotypes, overview -, 758020
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5malfunction ALN-overexpressing (ALNox) lines. in ALNox lines the ALN gene expression increase leads to increased enzyme activity and suppressed allantoin accumulation. Therefore, ALNox Arabidopsis thaliana lines exhibit the opposite phenotype in comparison with aln-3 mutants, namely sensitivity sto abiotic stress. The aln-3 enzyme-deficient mutant lines exhibit increased Cd tolerance -, 758067
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5malfunction T-DNA insertions in allantoinase cause the constitutive accumulation of allantoin resulting in plant resistance to different abiotic stresses such as drought, salinity (NaCl), and heavy metal cadmium toxicity. High concentration of allantoin in allantoinase-negative mutant (aln-3) leaves alleviates cadmium toxicity via inducing antioxidant mechanisms in these plants. In contrast with wild-type leaves, high levels of Cd in Col-0 roots reduces transcript abundance of uricase, leading to a significant decline in allantoin level of treated roots at 1000 and 1500 mM CdCl2, molecular mechanism underlying allantoin content of root in response to Cd stress, overview. Root elongation is reduced in Cd-treated wild-type but not enzyme-deficient plants. Despite higher Cd content, aln-3 roots contain lower reactive oxygen species concentrations. Antioxidant enzymes are more active in aln-3 roots following Cd treatment -, 758060
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5metabolism allantoin treatment of wild-type Col-0 seeds increases superoxide dismutase activity causing an enhanced seed germination and seedling growth following Cd exposure. Allantoinase-overexpressing (ALNox) lines with lower levels of allantoin exhibit more susceptibility to Cd treatment than wild-type Arabidopsis thaliana, implying that there is a positive correlation between allantoin concentration and Cd resistance in plants. The potential regulatory function of allantoin does not require abscisic acid (ABA) at germination but may be ABA-dependent at later stages of seedling growth, suggesting a potential crosstalk between allantoin-mediated stress response and ABA signalling pathway in plants. Protective role for allantoin at early stages of seedling growth. Increased allantoin concentration (both in vivo and in vitro) causes Cd-tolerance in plants -, 758067
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5metabolism Cd tolerance and the role allantoin plays in plant abiotic stress response are linked -, 758060
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5metabolism expression of genes for allantoin synthesis and degradation are oppositely regulated during salt stress. The AtALN promoter activity is present in specific plant tissues during plant development and is strongly repressed by salt stress. Allantoin transport mediated by ureide permease 5 (AtUPS5) is an important event in salt stress alleviation -, 758020
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5metabolism the rice genome is predicted to contain singles gene for each of the allantoin-catabolic enzymes: allantoinase (OsALN), allantoate amidohydrolase (OsAAH), ureidoglycine aminohydrolase (OsUGlyAH), and ureidoglycolate amidohydrolase (OsUAH), analysis of transcriptional regulation of these allantoin-catabolic genes in response to the N status, quantitative expression analysis, and production of allantoin-derived metabolites in response to changes in exogenous N status, overview 756836
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5more residue Ser292 is likely implicated in the binding of the allantoin ring through the carbonyl group of the polypeptide main chain, which is the common mechanism observed in other members of the amidohydrolase family. Modeling and docking studies -, 733438
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5physiological function allantoin accumulation is essential for salt stress tolerance. The regulation of the enzyme-encoding gene is mainly responsible for allantoin accumulation observed under salt stress. Possible roles of allantoin as a protectant compound in oxidative events or signaling, overview -, 758020
Show all pathways known for 3.5.2.5Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.5physiological function allantoin is used as an N source in rice plants, allantoin-derived metabolites following the up-regulation of OsALN and OsAAH expression, under N starvation conditions 756836
Results 1 - 10 of 10