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  2. Phenylglycine - Wikipedia

    en.wikipedia.org/wiki/Phenylglycine

    Phenylglycine is the organic compound with the formula C 6 H 5 CH(NH 2)CO 2 H. It is a non-proteinogenic alpha amino acid related to alanine, but with a phenyl group in place of the methyl group. It is a white solid. The compound exhibits some biological activity. [1]

  3. 4-Hydroxyphenylglycine - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxyphenylglycine

    Biosynthesis of HPG. HPG is synthesized from prephenate, an intermediate in the shikimic acid pathway and also a precursor to tyrosine.Prephenate is aromatized by prephenate dehydrogenase (Pdh) using NAD + as a cofactor to produce 4-hydroxyphenylpyruvate. 4-Hydroxyphenylpyruvate is then oxidized by 4-hydroxymandelate synthase (4HmaS) using oxygen to form 4-hydroxymandelate and hydrogen ...

  4. N-Phenylglycine - Wikipedia

    en.wikipedia.org/wiki/N-Phenylglycine

    N-Phenylglycine is an organic compound with the formula C 6 H 5 NHCH 2 CO 2 H. This white solid achieved fame as the industrial precursor to indigo dye . [ 1 ] It is a non-proteinogenic alpha amino acid related to sarcosine , but with an N - phenyl group in place of N - methyl .

  5. Dihydroxyphenylglycine - Wikipedia

    en.wikipedia.org/wiki/Dihydroxyphenylglycine

    When synthesized in bacteria, DHPG requires 5 enzymes, DpgA-D and 4-hydroxyphenylglycine transferase (Pgat), in order to be synthesized. [4] DpgA is a type III polyketide synthase and initiates the synthesis by condensing acetyl-CoA with three molecules of malonyl-CoA.

  6. Protein primary structure - Wikipedia

    en.wikipedia.org/wiki/Protein_primary_structure

    Knowing the structure of a similar homologous sequence (for example a member of the same protein family) allows highly accurate prediction of the tertiary structure by homology modeling. If the full-length protein sequence is available, it is possible to estimate its general biophysical properties, such as its isoelectric point.

  7. Damage-associated molecular pattern - Wikipedia

    en.wikipedia.org/wiki/Damage-associated...

    SYR1/2 (S. lycopersicum) Some Solanaceae species HypSys 15-, 18-, or 20-aa peptides Apoplastic or cytoplasmic preproHypSys Unknown Some Solanaceae species Peps 23~36-aa peptides (A. thaliana) Cytosolic and vacuolar PROPEPs PEPR1/2 (A. thaliana) A. thaliana, Zea mays, S. lycopersicum, Oryza sativa: PIP1/2 11-aa peptides Apoplastic preproPIP1/2 RLK7

  8. Chemosynthesis - Wikipedia

    en.wikipedia.org/wiki/Chemosynthesis

    Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...

  9. Diglyceride - Wikipedia

    en.wikipedia.org/wiki/Diglyceride

    General chemical structures of 1,2-diacylglycerols (top) and 1,3-diacylglycerols (bottom), where R 1 and R 2 are fatty acid side chains A diglyceride , or diacylglycerol ( DAG ), is a glyceride consisting of two fatty acid chains covalently bonded to a glycerol molecule through ester linkages. [ 1 ]