Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alican J. Erdogan"'
Autor:
Alican J. Erdogan, Muna Ali, Markus Habich, Silja L. Salscheider, Laura Schu, Carmelina Petrungaro, Luke W. Thomas, Margaret Ashcroft, Lars I. Leichert, Leticia Prates Roma, Jan Riemer
Publikováno v:
Redox Biology, Vol 17, Iss , Pp 200-206 (2018)
Disulfide formation in the mitochondrial intermembrane space is an essential process catalyzed by a disulfide relay machinery. In mammalian cells, the key enzyme in this machinery is the oxidoreductase CHCHD4/Mia40. Here, we determined the in vivo CH
Externí odkaz:
https://doaj.org/article/f2e43501c2324dcab863d4394c5c4fdf
Publikováno v:
Journal of molecular biology. 433(15)
Being essential for oxidative protein folding in the mitochondrial intermembrane space, the mitochondrial disulfide relay relies on the electron transfer (ET) from the sulfhydryl oxidase Erv1 to cytochrome c (Cc). Using solution NMR spectroscopy, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8014200902144530fa61562e8abbb07b
https://pubmed.ncbi.nlm.nih.gov/33971209
https://pubmed.ncbi.nlm.nih.gov/33971209
Autor:
Muna Ali, Jan Riemer, Laura Schu, Carmelina Petrungaro, Lars I. Leichert, Luke W. Thomas, Markus Habich, Alican J. Erdogan, Margaret Ashcroft, Leticia Prates Roma, Silja Lucia Salscheider
Publikováno v:
Redox Biology, Vol 17, Iss, Pp 200-206 (2018)
Disulfide formation in the mitochondrial intermembrane space is an essential process catalyzed by a disulfide relay machinery. In mammalian cells, the key enzyme in this machinery is the oxidoreductase CHCHD4/Mia40. Here, we determined the in vivo CH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af525511d446343381856fcfabae9b2d
https://pubmed.ncbi.nlm.nih.gov/29704824
https://pubmed.ncbi.nlm.nih.gov/29704824
Autor:
Wallace S. Chick, Elaine B. Spector, Mihret T. Elos, Eric P. Wartchow, Mark A. Lovell, Johan L.K. Van Hove, Kathryn C. Chatfield, Jan Riemer, Alican J. Erdogan, Katherine Gowan, Curtis R. Coughlin, Hua Jiang, Courtney P. O’Rourke, Marisa W. Friederich
Publikováno v:
Human molecular genetics. 26(4)
An infant presented with fatal infantile lactic acidosis and cardiomyopathy, and was found to have profoundly decreased activity of respiratory chain complex I in muscle, heart and liver. Exome sequencing revealed compound heterozygous mutations in N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d973fe2c6ce51fe8dba82175fe64157d
https://pubmed.ncbi.nlm.nih.gov/28040730
https://pubmed.ncbi.nlm.nih.gov/28040730