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  2. N-acyl phosphatidylethanolamine-specific phospholipase D

    en.wikipedia.org/wiki/N-acyl_phosphatidyl...

    The NAPEPLD cDNA sequence predicts 396 amino acid sequences in both mice and rats, which are 89% and 90% identical to that of humans. [2] NAPE-PLD was found to have no homology to the known phospholipase D genes, but can be classed by homology to fall into the zinc metallohydrolase family of the beta-lactamase fold.

  3. N-acetylphosphatidylethanolamine-hydrolysing phospholipase D

    en.wikipedia.org/wiki/N-acetylphosphatidyl...

    N-acetylphosphatidylethanolamine-hydrolysing phospholipase D (EC 3.1.4.54, NAPE-PLD, anandamide-generating phospholipase D, N-acyl phosphatidylethanolamine phospholipase D, NAPE-hydrolyzing phospholipase D) is an enzyme with systematic name N-acetylphosphatidylethanolamine phosphatidohydrolase. [1] [2] It catalyses the following chemical reaction

  4. N-Acylphosphatidylethanolamine - Wikipedia

    en.wikipedia.org/wiki/N-Acylphosphatidylethanolamine

    [2] [3] While NAPE-PLD is the enzyme responsible for catalyzing said release of N-acylethanolamine (NAE) from N-acyl-phosphatidylethanolamine (NAPE), this specific subtype of phospholipase D is not responsible for the formation of the anandamide. [4]

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  6. NAPE-PLD - Wikipedia

    en.wikipedia.org/wiki/NAPE-PLD

    NAPE-PLD may refer to: N-acyl-phosphatidylethanolamine-hydrolysing phospholipase D [ wikidata ] N-acyl phosphatidylethanolamine-specific phospholipase D , an enzyme

  7. Disulfur - Wikipedia

    en.wikipedia.org/wiki/Disulfur

    The ground state of S 2 is a triplet: a diradical, with two unpaired electrons like O 2 and SO. [6] It has the S-S bond length of 189 pm, much shorter than the S-S single bonds in S 8, which are 206 pm long. Its Raman spectrum consists of a band at 715 cm −1. [7] The corresponding O-O band for O 2 is found at 1556 cm −1. [8]

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  9. Sulfide - Wikipedia

    en.wikipedia.org/wiki/Sulfide

    The sulfide ion does not exist in aqueous alkaline solutions of Na 2 S. [3] [4] Instead sulfide converts to hydrosulfide: S 2− + H 2 O → SH − + OH −. Upon treatment with an acid, sulfide salts convert to hydrogen sulfide: S 2− + H + → SH − SH − + H + → H 2 S. Oxidation of sulfide is a complicated process.