Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications

অনুরূপ উপাদানগুলি

• Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation
  অনুযায়ী: Cellini, Barbara, অন্যান্য
  প্রকাশিত: (2009)
• Radiation damage at the active site of human alanine:glyoxylate aminotransferase reveals that the cofactor position is finely tuned during catalysis
  অনুযায়ী: Giardina, Giorgio, অন্যান্য
  প্রকাশিত: (2017)
• Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I()
  অনুযায়ী: Oppici, Elisa, অন্যান্য
  প্রকাশিত: (2012)
• Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I
  অনুযায়ী: Cellini, Barbara, অন্যান্য
  প্রকাশিত: (2010)
• Treponema denticola cystalysin exhibits significant alanine racemase activity accompanied by transamination: mechanistic implications.
  অনুযায়ী: Bertoldi, Mariarita, অন্যান্য
  প্রকাশিত: (2003)