enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Oligopeptide - Wikipedia

    en.wikipedia.org/wiki/Oligopeptide

    An oligopeptide (oligo-, "a few"), is a peptide consisting of two to twenty amino acids, including dipeptides, tripeptides, tetrapeptides, and other polypeptides. Some of the major classes of naturally occurring oligopeptides include aeruginosins , cyanopeptolins , microcystins , microviridins , microginins , anabaenopeptins , and cyclamides .

  3. Peptide - Wikipedia

    en.wikipedia.org/wiki/Peptide

    A polypeptide is a single linear chain of many amino acids (any length), held together by amide bonds. A protein consists of one or more polypeptides (more than about 50 amino acids long). An oligopeptide consists of only a few amino acids (between two and twenty).

  4. Clicked peptide polymer - Wikipedia

    en.wikipedia.org/wiki/Clicked_peptide_polymer

    The oligopeptide units of a clicked peptide polymer are a different story. The triazole bridges do not confer any stability to oligopeptide. Degradation of the polymer occurs at the peptide bonds linking individual amino acids. The amide bonds can be attacked non-specifically by acid or base catalyzed hydrolysis.

  5. Peptide bond - Wikipedia

    en.wikipedia.org/wiki/Peptide_bond

    Peptide bond formation via dehydration reaction. When two amino acids form a dipeptide through a peptide bond, [1] it is a type of condensation reaction. [2] In this kind of condensation, two amino acids approach each other, with the non-side chain (C1) carboxylic acid moiety of one coming near the non-side chain (N2) amino moiety of the other.

  6. Tetrapeptide - Wikipedia

    en.wikipedia.org/wiki/Tetrapeptide

    A tetrapeptide (example Val-Gly-Ser-Ala) with green marked amino end (L-Valine) and blue marked carboxyl end (L-Alanine). A tetrapeptide is a peptide, classified as an oligopeptide, since it only consists of four amino acids joined by peptide bonds.

  7. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    In this example, the second reactive group (amine/acid) in each of the starting materials bears a protecting group. In organic chemistry , peptide synthesis is the production of peptides , compounds where multiple amino acids are linked via amide bonds, also known as peptide bonds .

  8. Oligopeptidase - Wikipedia

    en.wikipedia.org/wiki/Oligopeptidase

    The prolyl-oligopeptidase or prolyl endopeptidase (POP) is a good example of how an oligopeptidase interacts with and metabolizes an oligopeptide. The peptide has first to penetrate into a 4 Å hole on the surface of the enzyme in order to reach an 8,500Å 3 internal cavity, where the active site is located.

  9. Protein tertiary structure - Wikipedia

    en.wikipedia.org/wiki/Protein_tertiary_structure

    The image above contains clickable links This diagram (which is interactive) of protein structure uses PCNA as an example. (The tertiary structure of a protein consists of the way a polypeptide is formed of a complex molecular shape. This is caused by R-group interactions such as ionic and hydrogen bonds, disulphide bridges, and hydrophobic ...