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2,648 Possible Causes for Glycine,, N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)

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  • Influenza

    For example, the first row shows that the amino acid in position 5 of HA1 mutated from glycine (G, shown in light green) to valine (V, shown in burgundy) in November 1999,[dx.doi.org] The high proton selectivity of the channel is lost when transmembrane domain His 37 is replaced with glycine, alanine, glutamic acid, serine, or threonine ( 22 , 23 ), making[doi.org] […] and then back to glycine in November 2001 and afterwards, except for three isolates in January to February 2002 that show a glutamic acid (E, shown in pink) at that position[dx.doi.org]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Connective Tissue Disease

    ) Glycine cleavage enzyme system Biochemical profile: Elevated plasma and CSF glycine Clinical features: In fetuses, severe hiccups In neonatal form, severe hiccups, hypotonia[merck.com] Glycine Metabolism Disorders Disease (OMIM Number) Defective Proteins or Enzymes Defective Gene or Genes (Chromosomal Location) Comments Nonketotic hyperglycinemia (605899[merck.com] Not determined Biochemical profile: Elevated urinary proline, hydroxyproline, and glycine but normal plasma levels Clinical features: Probably benign Treatment: None needed[merck.com]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Infectious Mononucleosis

    […] antigen-1 through Epstein-Barr nuclear antigen-1's glycine/alanine repeat.[dx.doi.org] During infectious mononucleosis, IgM autoantibodies are generated to a protein, p542, which contains a glycine-rich 28-mer epitope cross-reactive with the Epstein-Barr nuclear[dx.doi.org] The reactive epitopes on p542 were mapped with deletion mutants, which indicated that the glycine-rich 28-mer was the major antigenic determinant, with lesser antibody responses[dx.doi.org]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Meningitis

    The possibility that this type of DIAM is caused by sensitivity to the stabilizing agents of the commercial preparations, such as polyethylene glycol, maltose, sucrose, or glycine[dx.doi.org]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Idiopathic Pulmonary Fibrosis

    Glutathione (L-gamma-glutamyl-L-cysteinyl-glycine, GSH), a sulfhydryl-containing tripeptide produced by most mammalian cells, is an efficient scavenger of toxic oxidants,[doai.io]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Tuberculosis

    Ramakrishnan L, Federspiel NA, Falkow S (2000) Granuloma-specific expression of Mycobacterium virulence proteins from the glycine-rich PE-PGRS family.[springerlink.com]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Nonketotic Hyperglycinemia

    The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism.[en.wikipedia.org] […] hyperglycinemia Non-ketotic hyperglycinemia (disorder) nonketotic hyperglycinemia Glycine synthase deficiency Hyperglycinemia, Transient Neonatal GLYCINE ENCEPHALOPATHY GLYCINE[wikidata.org] Glycine encephalopathy is caused by the shortage of an enzyme that normally breaks down glycine in the body.[ghr.nlm.nih.gov]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Atypical Glycine Encephalopathy

    Glycine encephalopathy is caused by the shortage of an enzyme that normally breaks down glycine in the body.[ghr.nlm.nih.gov] The disease is caused by defects in the glycine cleavage system , an enzyme responsible for glycine catabolism.[en.wikipedia.org] Hyperglycinemia nonketotic; Glycine encephalopathy (Glycine encephalopathy) - Genes and GLDC AMT.[ivami.com]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Hereditary Hyperekplexia

    In contrast, the ability of the competitive antagonist strychnine to block glycine-induced currents was similar in all cases.[ncbi.nlm.nih.gov] The human neurological disorder hyperekplexia is frequently caused by recessive and dominant mutations of the glycine receptor alpha1 subunit gene, GLRA1.[ncbi.nlm.nih.gov] Abstract The human neurological disorder hyperekplexia is frequently caused by recessive and dominant mutations of the glycine receptor α1 subunit gene, GLRA1 .[doi.org]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)
  • Iminoglycinuria

    Iminoglycinuria (IG) is an autosomal recessive abnormality of renal transport of glycine and the imino acids proline and hydroxyproline, but the specific genetic defect(s)[ncbi.nlm.nih.gov] […] rate) (Fig. 3), and elevated renal clearance of proline and glycine (Table 2).[ncbi.nlm.nih.gov] Abstract Summary: Seven infants (two French Canadian, four Ashkenazi Jewish, and one Greek) with massive selective hyperiminoglycinuria (proline, hydroxyproline, and glycine[doi.org]

    Missing: N (N (N2 (N (N (N L methionyl L alpha glutamyl) L histidyl) D phenylalanyl) L arginyl) L tryptophyl)

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