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Literature summary for 2.6.1.44 extracted from

  • Kawai, C.; Minatogawa, Y.; Akiyoshi, H.; Hirose, S.; Suehiro, T.; Tone, S.
    A novel mutation of human liver alanine:glyoxylate aminotransferase causes primary hyperoxaluria type 1: immunohistochemical quantification and subcellular distribution (2012), Acta Histochem. Cytochem., 45, 121-129.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
for sequence determination, GFP-fusion proteins used in localization experiments Homo sapiens

Protein Variants

Protein Variants Comment Organism
additional information after random mutagenesis the subcellular distribution of mutant proteins (GFP-fusion proteins) is analyzed Homo sapiens
W251K naturally occuring mutation, mutant protein localized in peroxisome and cytosol Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
peroxisome
-
Homo sapiens 5777
-

Organism

Organism UniProt Comment Textmining
Homo sapiens A2V838
-
-

Source Tissue

Source Tissue Comment Organism Textmining
liver
-
Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
L-alanine + glyoxylate
-
Homo sapiens pyruvate + glycine
-
?

Synonyms

Synonyms Comment Organism
alanine:glyoxylate aminotransferase
-
Homo sapiens

General Information

General Information Comment Organism
malfunction mutation W251K involved in primary hyperoxaluria type 1 Homo sapiens