Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sabrina R. Mackinnon"'
Autor:
Linnea K. M. Blomgren, Melanie Huber, Sabrina R. Mackinnon, Céline Bürer, Arnaud Baslé, Wyatt W. Yue, D. Sean Froese, Thomas J. McCorvie
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract 5,10-methylenetetrahydrofolate reductase (MTHFR) commits folate-derived one-carbon units to generate the methyl-donor s-adenosyl-l-methionine (SAM). Eukaryotic MTHFR appends to the well-conserved catalytic domain (CD) a unique regulatory dom
Externí odkaz:
https://doaj.org/article/5004c4b595224327adf73c6b8e9c3779
Autor:
Sabrina R. Mackinnon, Gustavo A. Bezerra, Tobias Krojer, Tamas Szommer, Frank von Delft, Paul E. Brennan, Wyatt W. Yue
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. A build-up of the enzyme’s substrate, glyoxylate, results in excessive deposition of calcium oxalate c
Externí odkaz:
https://doaj.org/article/dfd6aa5544794ca1b1e7cb0be889d771
Autor:
Sabrina R. Mackinnon, Gustavo A. Bezerra, Tobias Krojer, Tamas Szommer, Frank von Delft, Paul E. Brennan, Wyatt W. Yue
Publikováno v:
Frontiers in chemistry. 10
Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. A build-up of the enzyme’s substrate, glyoxylate, results in excessive deposition of calcium oxalate c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf9b1a061354edcffe29b0b42653014
https://pubmed.ncbi.nlm.nih.gov/35601556
https://pubmed.ncbi.nlm.nih.gov/35601556