2.5.1.16: spermidine synthase
This is an abbreviated version!
For detailed information about spermidine synthase, go to the full flat file.
Word Map on EC 2.5.1.16
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2.5.1.16
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polyamine
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spermine
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s-adenosylmethionine
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ornithine
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diamine
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samdc
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dicyclohexylamine
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alpha-difluoromethylornithine
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5'-methylthioadenosine
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cadaverine
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trypanothione
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adometdc
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agmatine
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4.1.1.50
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difluoromethylornithine
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medicine
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drug development
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methylthioadenosine
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thermospermine
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nutrition
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1,3-diaminopropane
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biotechnology
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norspermidine
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multisubstrate
- 2.5.1.16
- polyamine
- spermine
- s-adenosylmethionine
- ornithine
- diamine
- samdc
- dicyclohexylamine
- alpha-difluoromethylornithine
- 5'-methylthioadenosine
- cadaverine
- trypanothione
- adometdc
- agmatine
-
4.1.1.50
- difluoromethylornithine
- medicine
- drug development
- methylthioadenosine
- thermospermine
- nutrition
- 1,3-diaminopropane
- biotechnology
- norspermidine
-
multisubstrate
Reaction
Synonyms
aminopropyltransferase, aminopropyltransferase spermidine synthase, AtSPDS1, AtSPDS2, MdSPDS1, PAPT, PgSPD, putrescine aminopropyltransferase, Spd synthase, SPDS, SPDS2, SPDSYN, spe-sdh, spe3, SpeE, spermidine synthase, spermidine synthase 1, spermidine synthetase, Spm synthase, SpSyn, Synpcc7942_0628, synthase, spermidine
ECTree
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Specific Activity
Specific Activity on EC 2.5.1.16 - spermidine synthase
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additional information
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transgenic plants show 5 to 6fold increase in SPDS activity and 1.3 to 2fold increase in the free spermidine content in leaves over the wild type. Significant increase in activity upon chilling in wild type and transgenics. Slightly higher chill-induced increase in SPDS activity in transgenics. pH 8.0, 37°C
additional information
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higher level of activity in 3 out of 4 transgenic clones. pH 7.5, 37°C
additional information
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development of a high-throughput assay using homogeneous time-resolved fluorescence based on energy transfer from europium cryptate as a donor to crosslinked allophycocyanin XL665 as an acceptor, involving a competitive immunoassay, overview
additional information
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assay method development using micellar electrokinetic chromatography with laser-induced fluorescence detection and 7-fluoro-4-nitrobenzo-2-oxa-1,3-diazole as a fluorescence derivatization reagent