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Results 1 - 10 of 14 for PROLINE OR GLYCINE OR THREONINE OR GLUTAMIC ACID OR HISTIDINE OR VALINE OR ASPARTIC ACID OR LYSINE OR PHENYLALANINE OR LEUCINE OR "N-ACETYLTYROSINE" OR ISOLEUCINE OR TRYPTOPHAN OR METHIONINE OR SERINE OR ALANINE OR ARGININE
Did you mean PROLINE OR GLYCINE OR THREONINE OR glutamine ACID OR HISTIDINE OR VALINE OR ASPARTIC ACID OR LYSINE OR PHENYLALANINE OR LEUCINE OR "N-acetyl tyrosine" OR ISOLEUCINE OR TRYPTOPHAN OR METHIONINE OR SERINE OR ALANINE OR ARGININE?
  1. 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
  2. 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
  3. Arginine:glycine amidinotransferase deficiency 
    ... atoms called a guanidino group from arginine to glycine. Guanidinoacetic acid is converted to creatine in the second step of the process. Creatine is needed for the body to store and use energy ... amidinotransferase enzyme to participate in creatine synthesis, resulting ...
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency - 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. Guanidinoacetate methyltransferase deficiency 
    ... compound creatine from the protein building blocks (amino acids) glycine, arginine, and methionine. Specifically, guanidinoacetate methyltransferase controls the ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
  8. Amish lethal microcephaly 
    ... amino acid) alanine is substituted for the amino acid glycine at position 177 of the SLC25A19 protein, written ...
    https://medlineplus.gov/genetics/condition/amish-lethal-microcephaly - Genetics
  9. Spondyloepimetaphyseal dysplasia, Strudwick type 
    ... G, Cole T, Chapman S, Pope FM. A glycine to aspartic acid substitution of COL2A1 in a family with the ...
    https://medlineplus.gov/...loepimetaphyseal-dysplasia-strudwick-type - Genetics
  10. Multiple mitochondrial dysfunctions syndrome 
    ... that breaks down a protein building block (amino acid) called glycine when levels become too high.Mutations in the ...
    https://medlineplus.gov/...tiple-mitochondrial-dysfunctions-syndrome - Genetics
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