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  2. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    The 21 proteinogenic α-amino acids found in eukaryotes, grouped according to their side chains' pK a values and charges carried at physiological pH (7.4) 2-, alpha-, or α-amino acids [21] have the generic formula H 2 NCHRCOOH in most cases, [b] where R is an organic substituent known as a "side chain". [22]

  3. Acidaminococcus - Wikipedia

    en.wikipedia.org/wiki/Acidaminococcus

    Acidaminococcus is a genus in the phylum Bacillota , whose members are anaerobic diplococci that can use amino acids as the sole energy source for growth. [1] Like other members of the class Negativicutes , they are gram-negative , despite being Bacillota , which are normally gram-positive .

  4. Animal nutrition - Wikipedia

    en.wikipedia.org/wiki/Animal_nutrition

    As there is no protein or amino acid storage provision, amino acids must be present in the diet. Excess amino acids are discarded, typically in the urine. For all animals, some amino acids are essential (an animal cannot produce them internally) and some are non-essential (the animal can produce them from other nitrogen-containing compounds). A ...

  5. Heterotroph - Wikipedia

    en.wikipedia.org/wiki/Heterotroph

    Bases, amino acids, and ribose are considered to be the first fermentation substrates. [33] Heterotrophs are currently found in each domain of life: Bacteria, Archaea, and Eukarya. [34] Domain Bacteria includes a variety of metabolic activity including photoheterotrophs, chemoheterotrophs, organotrophs, and heterolithotrophs. [34]

  6. Peptidoglycan - Wikipedia

    en.wikipedia.org/wiki/Peptidoglycan

    Cross-linking between amino acids in different linear amino sugar chains occurs with the help of the enzyme DD-transpeptidase and results in a 3-dimensional structure that is strong and rigid. The specific amino acid sequence and molecular structure vary with the bacterial species. [10]

  7. Histidine - Wikipedia

    en.wikipedia.org/wiki/Histidine

    Histidine ball and stick model spinning. Histidine (symbol His or H) [2] is an essential amino acid that is used in the biosynthesis of proteins.It contains an α-amino group (which is in the protonated –NH 3 + form under biological conditions), a carboxylic acid group (which is in the deprotonated –COO − form under biological conditions), and an imidazole side chain (which is partially ...

  8. Aromatic amino acid - Wikipedia

    en.wikipedia.org/wiki/Aromatic_amino_acid

    Animals obtain aromatic amino acids from their diet, but nearly [a] all plants and some micro-organisms must synthesize their aromatic amino acids through the metabolically costly shikimate pathway in order to make them. Histidine, phenylalanine, tryptophan, are essential amino acids for animals. Since they are not synthesized in the human body ...

  9. Proteasome - Wikipedia

    en.wikipedia.org/wiki/Proteasome

    The degradation process yields peptides of about seven to eight amino acids long, which can then be further degraded into shorter amino acid sequences and used in synthesizing new proteins. [1] Proteasomes are found inside all eukaryotes and archaea, and in some bacteria. In eukaryotes, proteasomes are located both in the nucleus and in the ...