Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nna‐Emeka Ejimogu"'
Autor:
Verna Van, Janae B. Brown, Corin R. O’Shea, Hannah Rosenbach, Ijaz Mohamed, Nna-Emeka Ejimogu, Toan S. Bui, Veronika A. Szalai, Kelly N. Chacón, Ingrid Span, Fangliang Zhang, Aaron T. Smith
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
The enzyme ATE1 catalyzes eukaryotic post-translation arginylation, a key protein modification necessary for cellular homeostasis. Here, the authors show that ATE1s are previously unrealized iron-sulfur proteins that use this oxygen-sensitive inorgan
Externí odkaz:
https://doaj.org/article/9c8010dbcbf942c7aaba88c2aec4f3c9
Autor:
Mariah L Hoye, Lorenzo Calviello, Abigail J Poff, Nna-Emeka Ejimogu, Carly R Newman, Maya D Montgomery, Jianhong Ou, Stephen N Floor, Debra L Silver
Publikováno v:
eLife, Vol 11 (2022)
Mutations in the RNA helicase, DDX3X, are a leading cause of Intellectual Disability and present as DDX3X syndrome, a neurodevelopmental disorder associated with cortical malformations and autism. Yet, the cellular and molecular mechanisms by which D
Externí odkaz:
https://doaj.org/article/c52d1cf713ca4d10bb32efe06bea8b74
Publikováno v:
Journal of molecular biology. 434(21)
Eukaryotic post-translational arginylation, mediated by the family of enzymes known as the arginyltransferases (ATE1s), is an important post-translational modification that can alter protein function and even dictate cellular protein half-life. Multi
Autor:
Mariah L Hoye, Lorenzo Calviello, Abigail J Poff, Nna-Emeka Ejimogu, Carly R Newman, Maya D Montgomery, Jianhong Ou, Stephen N Floor, Debra L Silver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77618de9353ab3eb5d6f072e637b443d
https://doi.org/10.7554/elife.78203.sa2
https://doi.org/10.7554/elife.78203.sa2
Publikováno v:
The FASEB Journal. 36
Autor:
Abigail Poff, Debra Silver, Mariah Hoye, Jianhong Ou, Stephen Floor, Carly Newman, Lorenzo Calviello, Nna-Emeka Ejimogu
Mutations in the RNA helicase, DDX3X, are a leading cause of Intellectual Disability and present as DDX3X syndrome, a neurodevelopmental disorder associated with cortical malformations and autism. Yet the cellular and molecular mechanisms by which DD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d3ee4a9ffd829f280fa205d6460ef91
https://doi.org/10.1101/2022.02.21.481343
https://doi.org/10.1101/2022.02.21.481343
Publikováno v:
Acta Crystallographica Section A Foundations and Advances. 78:a236-a236
Publikováno v:
The FASEB Journal. 35
Autor:
Ingrid Span, Hannah Rosenbach, Kelly N. Chacón, Nna-Emeka Ejimogu, Toan S. Bui, Veronika A. Szalai, Ijaz Mohamed, Janae B. Brown, Aaron T. Smith, Verna Van
Eukaryotic arginylation is an essential post-translational modification that both modulates protein stability and regulates protein half-life through the N-degron pathway. Arginylation is catalyzed by a family of enzymes known as the arginyl-tRNA tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c661c9b26eb14d9dc5e0d885c5350e98
https://doi.org/10.1101/2021.04.13.439645
https://doi.org/10.1101/2021.04.13.439645