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Literature summary for 2.1.1.17 extracted from

  • Gotoh, T.; Ando, N.; Kikuchi, K.
    A novel method for in vitro radiolabeling and testing enveloped viruses by phosphatidylethanolamine N-methyltransferase and host cell-specific binding (2006), Biotechnol. Bioeng., 94, 1017-1024.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
additional information the cell toxicity for Spodoptera frugiperda (SF-9) insect cells of the phosphatidylethanolamine N-methyltransferase preparation dissapears, when the phosphatidylethanolamine N-methyltransferase preparation is treated with 100 mg Bio-Beads SM-2 + 10 mg Butyl Toyopearl or 100 g Bio-Beads SM-2 + 10 mg CM Toyopearl.; treatment of the phosphatidylethanolamine N-methyltransferase preparation with the adsorbent Bio-Beads SM-2 decreases the phosphatidylethanolamine N-methyltransferase activity to: 24.1% with 50 mg and 28.6% with 100 mg. Addition of 1% Trition X-100 restores the activity to 90% in the experiment with 100 mg Bio-Beads SM-2.; treatment of the phosphatidylethanolamine N-methyltransferase preparation with the adsorbent Butyl Toyopearl decreases the phosphatidylethanolamine N-methyltransferase activity to: 0.2% with 10 mg; treatment of the phosphatidylethanolamine N-methyltransferase preparation with the adsorbent CM Toyopearl decreases the phosphatidylethanolamine N-methyltransferase activity to: 0.4% with 10 mg Sus scrofa

Organism

Organism UniProt Comment Textmining
Sus scrofa
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phosphatidylethanolamine N-methyltransferase is used to radioisotopically label the envelope of Autographa californica recombinant strain vGFPuv through the methylation of phosphatidylethanolamine. The modification of envelope phospholipids by phosphatidylethanolamine N-methyltransferase does not affect the infectivity of Autographa californica recombinant strain vGFPuv.
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Purification (Commentary)

Purification (Comment) Organism
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Sus scrofa

Source Tissue

Source Tissue Comment Organism Textmining
liver
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Sus scrofa
-