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Results 1 - 8 of 8 for HISTIDINE OR PROLINE OR THREONINE OR GLUTAMIC ACID OR GLYCINE OR ASPARTIC ACID OR VALINE OR LYSINE OR PHENYLALANINE OR LEUCINE OR TRYPTOPHAN OR TYROSINE OR ISOLEUCINE OR TAURINE OR METHIONINE OR CYSTEINE OR ARGININE OR ALANINE OR SERINE
Did you mean HISTIDINE OR PROLINE OR THREONINE OR glutamine ACID OR GLYCINE OR ASPARTIC ACID OR VALINE OR LYSINE OR PHENYLALANINE OR LEUCINE OR TRYPTOPHAN OR TYROSINE OR ISOLEUCINE OR TAURINE OR METHIONINE OR CYSTEINE OR ARGININE OR ALANINE OR SERINE?
  1. Histidinemia 
    ... characterized by elevated blood levels of the amino acid histidine, a building block of most proteins. Histidinemia is ... making an enzyme called histidase. Histidase breaks down histidine to a molecule called urocanic acid. Histidase is active (expressed) primarily in the liver ...
    https://medlineplus.gov/genetics/condition/histidinemia - Genetics
  2. Maternally inherited diabetes and deafness 
    ... gene, called tRNAGlu, attaches to the amino acid glutamic acid (Glu) and adds it to growing proteins.These ...
    https://medlineplus.gov/...aternally-inherited-diabetes-and-deafness - Genetics
  3. Hyperprolinemia 
    ... excess of a particular protein building block (amino acid), called proline, in the blood. This condition generally occurs when ... the previous reaction, converting it to the amino acid glutamate. The conversion of proline to glutamate (and the conversion of glutamate to ...
    https://medlineplus.gov/genetics/condition/hyperprolinemia - Genetics
  4. Epidermolytic hyperkeratosis 
    ... Wu K, Lee ES, Steinert PM. A novel glutamic acid to aspartic acid mutation near the end of ...
    https://medlineplus.gov/.../condition/epidermolytic-hyperkeratosis - Genetics
  5. Prolidase deficiency 
    ... acids). Specifically, prolidase divides dipeptides containing the amino acids proline or hydroxyproline. By freeing these amino acids, prolidase helps make them available for use in ...
    https://medlineplus.gov/genetics/condition/prolidase-deficiency - Genetics
  6. Cutis laxa 
    ... the formation of the protein building block (amino acid) proline, which is a key component of elastic fiber ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics
  7. Glutamate formiminotransferase deficiency 
    ... steps in the breakdown (metabolism) of the amino acid histidine, a building block of most proteins. It also ...
    https://medlineplus.gov/...glutamate-formiminotransferase-deficiency - Genetics
  8. Gyrate atrophy of the choroid and retina 
    ... P5C). P5C can be converted into the amino acids glutamate and proline.OAT gene mutations that cause gyrate atrophy result ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics