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  2. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Structure of a typical L-alpha-amino acid in the "neutral" form. Amino acids are organic compounds that contain both amino and carboxylic acid functional groups. [1] Although over 500 amino acids exist in nature, by far the most important are the 22 α-amino acids incorporated into proteins. [2]

  3. List of macronutrients - Wikipedia

    en.wikipedia.org/wiki/List_of_macronutrients

    There are three principal classes of macronutrients: carbohydrate, protein and fat. [1] Macronutrients are defined as a class of chemical compounds which humans consume in relatively large quantities compared to vitamins and minerals which provide humans with energy.

  4. Biomolecule - Wikipedia

    en.wikipedia.org/wiki/Biomolecule

    Covalent bond name between monomers Amino acids: Oligopeptides: Polypeptides, proteins ... Lignin is a complex polyphenolic macromolecule composed mainly of beta-O4 ...

  5. List of amino acids - Wikipedia

    en.wikipedia.org/wiki/List_of_amino_acids

    Amino acids are listed by type: Proteinogenic amino acid; Non-proteinogenic amino acids This page was last edited on 5 January 2020, at 17:16 (UTC). Text is ...

  6. Macromolecule - Wikipedia

    en.wikipedia.org/wiki/Macromolecule

    A macromolecule is a very large molecule important to biological processes, such as a protein or nucleic acid. ... (4 nucleotides vs >20 amino acids in proteins), ...

  7. Protein - Wikipedia

    en.wikipedia.org/wiki/Protein

    The amino acids in a polypeptide chain are linked by peptide bonds between amino and carboxyl group. An individual amino acid in a chain is called a residue, and the linked series of carbon, nitrogen, and oxygen atoms are known as the main chain or protein backbone.

  8. 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).

  9. Arginine - Wikipedia

    en.wikipedia.org/wiki/Arginine

    Arginine is the amino acid with the formula (H 2 N)(HN)CN(H)(CH 2) 3 CH(NH 2)CO 2 H. The molecule features a guanidino group appended to a standard amino acid framework. At physiological pH, the carboxylic acid is deprotonated (−CO 2 −) and both the amino and guanidino groups are protonated, resulting in a cation.