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  2. Alanine - Wikipedia

    en.wikipedia.org/wiki/Alanine

    S)-Alanine (left) and (R)-alanine (right) in zwitterionic form at neutral pH. Alanine is useful in loss of function experiments with respect to phosphorylation. Some techniques involve creating a library of genes, each of which has a point mutation at a different position in the area of interest, sometimes even every position in the whole gene ...

  3. Zwitterion - Wikipedia

    en.wikipedia.org/wiki/Zwitterion

    In chemistry, a zwitterion (/ ˈ t s v ɪ t ə ˌ r aɪ ə n / TSVIT-ə-ry-ən; from German Zwitter ' hermaphrodite '), also called an inner salt or dipolar ion, [1] is a molecule that contains an equal number of positively and negatively charged functional groups. [2] 1,2-dipolar compounds, such as ylides, are sometimes excluded from the ...

  4. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Amino acids with the structure NH + 3 −CXY−CXY−CO − 2, such as β-alanine, a component of carnosine and a few other peptides, are β-amino acids. Ones with the structure NH + 3 −CXY−CXY−CXY−CO − 2 are γ-amino acids, and so on, where X and Y are two substituents (one of which is normally H). [7]

  5. 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.

  6. D-Amino acid - Wikipedia

    en.wikipedia.org/wiki/D-Amino_acid

    D-Amino acids are used in racemic crystallography to create centrosymmetric crystals, which, depending on the protein, may allow for easier and more robust protein structure determination. [9] Gramicidin is a polypeptide made up from mixture of D- and L-amino acids. [10] Other compounds containing D-amino acids are tyrocidine and valinomycin.

  7. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    Phenylalanine ball and stick model spinning. Phenylalanine (symbol Phe or F) [3] is an essential α-amino acid with the formula C 9 H 11 NO 2.It can be viewed as a benzyl group substituted for the methyl group of alanine, or a phenyl group in place of a terminal hydrogen of alanine.

  8. 4 High-Protein Ingredients to Add to Your Smoothie That Aren ...

    www.aol.com/4-high-protein-ingredients-add...

    Estrogen is essential for maintaining bone structure and, interestingly, phytoestrogens mimic the beneficial effects estrogen has in the body. “Tofu would be great in a smoothie with cinnamon ...

  9. Proteinogenic amino acid - Wikipedia

    en.wikipedia.org/wiki/Proteinogenic_amino_acid

    The structures given below are standard chemical structures, not the typical zwitterion forms that exist in aqueous solutions. Structure of the 21 proteinogenic amino acids with 3 and 1 letters codes, grouped by side chain functionality