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  2. Peptide - Wikipedia

    en.wikipedia.org/wiki/Peptide

    [1] [2] A polypeptide is a longer, continuous, unbranched peptide chain. [3] Polypeptides that have a molecular mass of 10,000 Da or more are called proteins . [ 4 ] Chains of fewer than twenty amino acids are called oligopeptides , and include dipeptides , tripeptides , and tetrapeptides .

  3. Chemotaxonomy - Wikipedia

    en.wikipedia.org/wiki/Chemotaxonomy

    Merriam-Webster defines chemotaxonomy as the method of biological classification based on similarities and dissimilarity in the structure of certain compounds among the organisms being classified. Advocates argue that, as proteins are more closely controlled by genes and less subjected to natural selection than the anatomical features , they ...

  4. Ribosomally synthesized and post-translationally modified ...

    en.wikipedia.org/wiki/Ribosomally_synthesized...

    Ribosomally synthesized and post-translationally modified peptides (RiPPs), also known as ribosomal natural products, are a diverse class of natural products of ribosomal origin. [1] Consisting of more than 20 sub-classes, RiPPs are produced by a variety of organisms , including prokaryotes , eukaryotes , and archaea , and they possess a wide ...

  5. Peptidomimetic - Wikipedia

    en.wikipedia.org/wiki/Peptidomimetic

    Figure 1. Classification of peptidomimetics. [1]A peptidomimetic is a small protein-like chain designed to mimic a peptide. [1] [2] They typically arise either from modification of an existing peptide, or by designing similar systems that mimic peptides, such as peptoids and β-peptides.

  6. Peptoid - Wikipedia

    en.wikipedia.org/wiki/Peptoid

    Like D-Peptides and β peptides, peptoids are completely resistant to proteolysis, [5] and are therefore advantageous for therapeutic applications where proteolysis is a major issue. Since secondary structure in peptoids does not involve hydrogen bonding, it is not typically denatured by solvent, temperature, or chemical denaturants such as ...

  7. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    In chemistry, peptides are synthesized by a variety of reactions. One of the most-used in solid-phase peptide synthesis uses the aromatic oxime derivatives of amino acids as activated units. These are added in sequence onto the growing peptide chain, which is attached to a solid resin support. [ 130 ]

  8. Aminopeptidase - Wikipedia

    en.wikipedia.org/wiki/Aminopeptidase

    Aminopeptidases are a diverse group of enzymes that play crucial roles in various biological processes, including protein digestion, cell growth, and immune response.They are classified based on their substrate specificity (strength of binding) and catalytic mechanism (means of catalyzing their reaction) into two main categories: metalloaminopeptidases and cysteine aminopeptidases.

  9. Glycopeptide - Wikipedia

    en.wikipedia.org/wiki/Glycopeptide

    Glycopeptides are peptides that contain carbohydrate moieties covalently attached to the side chains of the amino acid residues that constitute the peptide.. Over the past few decades it has been recognised that glycans on cell surface (attached to membrane proteins or lipids) and those bound to proteins (glycoproteins) play a critical role in biology.