EC Number |
Title |
Organism |
---|
1.5.3.13 | Acetylated derivatives of C-methylated analogues of spermidine synthesis and interaction with N1-acetylpolyamine oxidase |
Homo sapiens |
1.5.3.13 | Controlling the regioselectivity and stereospecificity of FAD-dependent polyamine oxidases with the use of amine-attached guide molecules as conformational modulators |
Homo sapiens |
1.5.3.13 | Copper-containing amine oxidases and FAD-dependent polyamine oxidases are key players in plant tissue differentiation and organ development |
Selaginella lepidophylla |
1.5.3.13 | Copper-containing amine oxidases and FAD-dependent polyamine oxidases are key players in plant tissue differentiation and organ development |
Arabidopsis thaliana |
1.5.3.13 | Development of irreversible inactivators of spermine oxidase and N1-acetylpolyamine oxidase |
Homo sapiens |
1.5.3.13 | Exploring the activity of polyamine analogues on polyamine and spermine oxidase methoctramine, a potent and selective inhibitor of polyamine oxidase |
Mus musculus |
1.5.3.13 | Identification and biochemical characterization of polyamine oxidases in amphioxus Implications for emergence of vertebrate-specific spermine and acetylpolyamine oxidases |
Branchiostoma japonicum |
1.5.3.13 | Polyamine oxidase 5 regulates Arabidopsis growth through Thermospermine oxidase activity |
Arabidopsis thaliana |
1.5.3.13 | The polyamine oxidase from lycophyte Selaginella lepidophylla (SelPAO5), unlike that of angiosperms, back-converts thermospermine to norspermidine |
Selaginella lepidophylla |
1.5.3.13 | The structure of murine N1-acetylspermine oxidase reveals molecular details of vertebrate polyamine catabolism |
Mus musculus |