2.5.1.22: spermine synthase
This is an abbreviated version!
For detailed information about spermine synthase, go to the full flat file.
Word Map on EC 2.5.1.22
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2.5.1.22
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polyamine
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putrescine
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s-adenosylmethionine
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ornithine
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aminopropyltransferases
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snyder-robinson
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alpha-difluoromethylornithine
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acaulis5
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thermospermine
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trans-4-methylcyclohexylamine
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gyro
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kyphoscoliosis
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agriculture
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adometdc
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2.5.1.16
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medicine
- 2.5.1.22
- polyamine
- putrescine
- s-adenosylmethionine
- ornithine
- aminopropyltransferases
-
snyder-robinson
- alpha-difluoromethylornithine
- acaulis5
- thermospermine
- trans-4-methylcyclohexylamine
-
gyro
-
kyphoscoliosis
- agriculture
- adometdc
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2.5.1.16
- medicine
Reaction
Synonyms
ACL5, aminopropyltransferase, spermidine, OsSPMS1, SMS, spermidine aminopropyltransferase, spermine synthase, spermine synthase 1, spermine synthetase, Spm synthase, SpmS, SPMS1, SpmSyn, synthase, spermine
ECTree
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General Information
General Information on EC 2.5.1.22 - spermine synthase
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drug target
spermine synthase and MYC cooperate to maintain colorectal cancer cell survival by repressing Bim expression. Combined inhibition of spermine synthase and MYC signaling may be an effective therapy for colorectal cancer
malfunction
metabolism
physiological function
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cells derived from patients with Snyder-Robinson syndrome, a rare X-linked recessive human disease caused by SMS gene mutations that greatly reduce the content of spermine synthase, show an increase in decarboxylated S-adenosylmethionine
malfunction
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in Gy mice, which lack spermine synthase activity, the content of dcAdoMet is significantly increased by 10-30fold in liver, brain and kidney and by 150fold in heart. Transgenic expression of spermine synthase in the Gy mice reverses all of the increases in dcAdoMet content and AdoMetDC, phenotypes, overview
malfunction
SMS single missense mutations cause the Snyder-Robinson Syndrome, SRS. Concerning mutability depending on structural micro-environment and involvement in the function and structural integrity of the SMS, the I150 site does not tolerate any mutation, while V132, despite its key position at the interface of SMS dimer, is quite mutable. The G56 site is still quite sensitive to charge residue replacement
malfunction
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spermine and thermospermine synthesis mutants accumulate more Na+ and show decreased survival under salt stress compared to wild-type plants
malfunction
mutations in the spermine synthase gene are associated with Snyder Robinson mental retardation syndrome
malfunction
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OsSPMS1 knockout mutant show an increase in grain yield per plant in a high-yield variety, Suken118 suggesting that OsSPMS1 is an important target for yield enhancement in rice
spermine synthase and MYC cooperate to maintain colorectal cancer cell survival by repressing Bim expression
metabolism
the enzyme is critical for maintaining the balance of spermine/spermidine in the cell
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inverse relationship between the amount of spermine synthase protein and the content of decarboxylated S-adenosylmethionine. In mice lacking spermine synthase occurs a large increase in decarboxylated S-adenosylmethionine, dcAdoMet, overexpression of human spermine synthase reduces the amount of this nucleoside, Content of AdoMet and dcAdoMet in cultured lymphoblasts from control and Snyder-Robinson syndrome patients
physiological function
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spermine accumulation is involved in long-term salt stress. Induction of polyamine metabolism is a SOS-independent response to salinity
physiological function
spermine synthase is a key enzyme controlling the concentration of spermidine and spermine in the cell
physiological function
the enzyme exerts a positive effect on antioxidant systems
physiological function
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the enzyme (OsSPMS1) negatively regulates seed germination, grain size, and grain yield per plant. OsSPMS1 affects ethylene synthesis and may regulate seed germination and plant growth by affecting the 1-aminocyclopropane-1-carboxylic acid and ethylene pathways