enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 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.

  3. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    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. Peptides are chemically synthesized by the condensation reaction of the carboxyl group of one amino acid to the amino group of another.

  4. Peptide - Wikipedia

    en.wikipedia.org/wiki/Peptide

    Amino acids that have been incorporated into peptides are termed residues. A water molecule is released during formation of each amide bond. [ 6 ] All peptides except cyclic peptides have an N-terminal (amine group) and C-terminal (carboxyl group) residue at the end of the peptide (as shown for the tetrapeptide in the image).

  5. Protein structure - Wikipedia

    en.wikipedia.org/wiki/Protein_structure

    A single amino acid monomer may also be called a residue, which indicates a repeating unit of a polymer. Proteins form by amino acids undergoing condensation reactions, in which the amino acids lose one water molecule per reaction in order to attach to one another with a peptide bond.

  6. N-terminus - Wikipedia

    en.wikipedia.org/wiki/N-terminus

    Each amino acid has an amine group and a carboxylic group.Amino acids link to one another by peptide bonds which form through a dehydration reaction that joins the carboxyl group of one amino acid to the amine group of the next in a head-to-tail manner to form a polypeptide chain.

  7. Protein primary structure - Wikipedia

    en.wikipedia.org/wiki/Protein_primary_structure

    Amino acids are polymerised via peptide bonds to form a long backbone, with the different amino acid side chains protruding along it.In biological systems, proteins are produced during translation by a cell's ribosomes.

  8. Proteolysis - Wikipedia

    en.wikipedia.org/wiki/Proteolysis

    Strong mineral acids can readily hydrolyse the peptide bonds in a protein (acid hydrolysis). The standard way to hydrolyze a protein or peptide into its constituent amino acids for analysis is to heat it to 105 °C for around 24 hours in 6M hydrochloric acid. [27] However, some proteins are resistant to acid hydrolysis.

  9. Beta turn - Wikipedia

    en.wikipedia.org/wiki/Beta_turn

    Carbon atoms grey, oxygen atoms red and nitrogen atoms blue. The defining hydrogen bond is shown as a magenta line. The hydrogen bond criterion for beta turns, applied to polypeptides whose amino acids are linked by trans peptide bonds, gives rise to just four categories, as shown by Venkatachalam in 1968. They are called types I, II, I’ and ...