enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Alanine

    L-alanine is second only to L-leucine in rate of occurrence, accounting for 7.8% of the primary structure in a sample of 1,150 proteins. [5] The right-handed form, D -alanine, occurs in peptides in some bacterial cell walls [ 6 ] : 131 (in peptidoglycan ) and in some peptide antibiotics , and occurs in the tissues of many crustaceans and ...

  3. β-Alanine - Wikipedia

    en.wikipedia.org/wiki/Β-Alanine

    β-Alanine (beta-alanine) is a naturally occurring beta amino acid, which is an amino acid in which the amino group is attached to the β-carbon (i.e. the carbon two carbon atoms away from the carboxylate group) instead of the more usual α-carbon for alanine (α-alanine). The IUPAC name for β-alanine is 3-aminopropanoic acid.

  4. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Amino acids are formally named by the IUPAC-IUBMB Joint Commission on Biochemical Nomenclature in terms of the fictitious "neutral" structure shown in the illustration. For example, the systematic name of alanine is 2-aminopropanoic acid, based on the formula CH 3 −CH(NH 2)−COOH. The Commission justified this approach as follows: [7]

  5. Alanine (data page) - Wikipedia

    en.wikipedia.org/wiki/Alanine_(data_page)

    Chemical formula: C 3 H 7 N O 2 Molar mass: 89.1 g·mol −1 Systematic name: (S)-2-aminopropanoic acid Abbreviations: A, Ala Synonyms: 2-aminopropanoic acid {α/2}-aminopropionic acid AIDS{-}071780 HSDB 1801 NSC 206315

  6. Beta-peptide - Wikipedia

    en.wikipedia.org/wiki/Beta-peptide

    β-alanine, an example of a β-amino acid. The amino group attaches not to the α carbon but to the β-carbon, which in this case is a methylene group.. Beta-peptides (β-peptides) are peptides derived from β-amino acids, in which the amino group is attached to the β-carbon (i.e. the carbon two atoms away from the carboxylate group).

  7. C-terminus - Wikipedia

    en.wikipedia.org/wiki/C-terminus

    A tetrapeptide (example: Val-Gly-Ser-Ala) with green highlighted N-terminal α-amino acid (example: L-valine) and blue marked C-terminal α-amino acid (example: L-alanine). The C-terminus (also known as the carboxyl-terminus , carboxy-terminus , C-terminal tail , carboxy tail , C-terminal end , or COOH-terminus ) is the end of an amino acid ...

  8. Get breaking news and the latest headlines on business, entertainment, politics, world news, tech, sports, videos and much more from AOL

  9. D-Amino acid - Wikipedia

    en.wikipedia.org/wiki/D-Amino_acid

    In this example, alanine is depicted in the zwitterionic form at physiological pH. D-Amino acids are amino acids where the stereogenic carbon alpha to the amino group has the D-configuration. For most naturally-occurring amino acids, this carbon has the L-configuration. D-Amino acids are occasionally found in nature as residues in proteins.