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  2. Proline - Wikipedia

    en.wikipedia.org/wiki/Proline

    Proline (symbol Pro or P) [4] is an organic acid classed as a proteinogenic amino acid (used in the biosynthesis of proteins), although it does not contain the amino ...

  3. Stachydrine - Wikipedia

    en.wikipedia.org/wiki/Stachydrine

    Stachydrine, also known as proline betaine, is a naturally occurring alkaloid found in citrus, caper, chestnuts, alfalfa, Leonurus japonicus, Maclura tricuspidata, Stachys arvensis and Arisaema heterophyllum. It has been studied for its potential health benefits.

  4. Colostrinin - Wikipedia

    en.wikipedia.org/wiki/Colostrinin

    Colostrinin (also known as CLN, proline-rich polypeptides or PRP) is a naturally occurring mixture of proline-rich polypeptides derived from colostrum. Early work on Colostrinin [ edit ]

  5. Hydroxyproline - Wikipedia

    en.wikipedia.org/wiki/Hydroxyproline

    Hydroxyproline and proline play key roles for collagen stability. [4] They permit the sharp twisting of the collagen helix. [5] In the canonical collagen Xaa-Yaa-Gly triad (where Xaa and Yaa are any amino acid), a proline occupying the Yaa position is hydroxylated to give a Xaa-Hyp-Gly sequence.

  6. Essential amino acid - Wikipedia

    en.wikipedia.org/wiki/Essential_amino_acid

    Proline and arginine are both derived from glutamate. Serine , formed from 3-phosphoglycerate , which comes from glycolysis , is the precursor of glycine and cysteine . Tyrosine is synthesized by the hydroxylation of phenylalanine , which is an essential amino acid.

  7. Arginine and proline metabolism - Wikipedia

    en.wikipedia.org/wiki/Arginine_and_proline...

    Arginine and proline metabolism is one of the central pathways for the biosynthesis of the amino acids arginine and proline from glutamate. The pathways linking arginine, glutamate, and proline are bidirectional. Thus, the net utilization or production of these amino acids is highly dependent on cell type and developmental stage.

  8. Secondary amino acid - Wikipedia

    en.wikipedia.org/wiki/Secondary_amino_acid

    Proline and its higher homolog pipecolic acid affect the secondary structure of protein. D-alpha-amino acid - L-alpha-amino acid sequence can induce beta hairpin. [1] It suggested that acyclic secondary amino acids are more flexible than cyclic secondary amino acids in protein by replacement of pipecolic acid by N-methyl-L-alanine in efrapeptin C.

  9. Insulin lispro - Wikipedia

    en.wikipedia.org/wiki/Insulin_lispro

    It is a manufactured form of human insulin where the amino acids lysine and proline have been switched at the end of the B chain of the insulin molecule. [10] This switch of amino acids mimics Insulin-like growth factor 1 which also has lysine (K) and proline (P) in that order at positions 28 and 29. [14]