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  2. Category:Amino acid metabolism disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Amino_acid...

    Download as PDF; Printable version; ... Pages in category "Amino acid metabolism disorders" ... Branched-chain keto acid dehydrogenase kinase deficiency;

  3. Organic acidemia - Wikipedia

    en.wikipedia.org/wiki/Organic_acidemia

    The branched-chain amino acids include isoleucine, leucine and valine. [1] Organic acids refer to the amino acids and certain odd-chained fatty acids which are affected by these disorders. The four main types of organic acidemia are: methylmalonic acidemia, propionic acidemia, isovaleric acidemia, and maple syrup urine disease. [1]

  4. File:Aminoacid chain normal Hb and HbE.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Aminoacid_chain...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  5. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Traditionally the inherited metabolic diseases were classified as disorders of carbohydrate metabolism, amino acid metabolism, organic acid metabolism, or lysosomal storage diseases. [4] In recent decades, hundreds of new inherited disorders of metabolism have been discovered and the categories have proliferated.

  6. 10 nutritional deficiencies that can cause depression and ...

    www.aol.com/article/2016/02/05/10-nutritional...

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  7. Protein (nutrient) - Wikipedia

    en.wikipedia.org/wiki/Protein_(nutrient)

    The absorption rates of individual amino acids are highly dependent on the protein source; for example, the digestibilities of many amino acids in humans, the difference between soy and milk proteins [32] and between individual milk proteins, beta-lactoglobulin and casein. [33]

  8. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    The incorporation of these nonstandard amino acids is rare. For example, 25 human proteins include selenocysteine in their primary structure, [64] and the structurally characterized enzymes (selenoenzymes) employ selenocysteine as the catalytic moiety in their active sites. [65] Pyrrolysine and selenocysteine are encoded via variant codons.

  9. Congenital disorders of amino acid metabolism - Wikipedia

    en.wikipedia.org/wiki/Congenital_disorders_of...

    Congenital errors of amino acid metabolism are inherited metabolic disorders that impair the synthesis and degradation of amino acids. [1] This means that the body has trouble breaking down and building some amino acids, the building blocks of protein in the body. [2] The body can also have trouble with cellular update up amino acids.