SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease

Philipp Gut, Sanna Matilainen, Jesse G. Meyer, Pieti Pallijeff, Joy Richard, Christopher J. Carroll, Liliya Euro, Christopher B. Jackson, Pirjo Isohanni, Berge A. Minassian, Reem A. Alkhater, Elsebet Ostergaard, Gabriele Civiletto, Alice Parisi, Jonathan Thevenet, Matthew J. Rardin, Wenjuan He, Yuya Nishida, John C. Newman, Xiaojing LiuStefan Christen, Sofia Moco, Jason W. Locasale, Birgit Schilling, Anu Suomalainen, Eric Verdin

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
Article number5927
JournalNature Communications
Volume11
Issue number1
Number of pages14
ISSN2041-1723
DOIs
Publication statusPublished - 23 Nov 2020
MoE publication typeA1 Journal article-refereed

Fields of Science

  • HIGH-RESOLUTION METABOLOMICS
  • DATA-INDEPENDENT ACQUISITION
  • QUANTITATIVE PROTEOMICS
  • ACETYLATION
  • ENCEPHALOMYOPATHY
  • DEFICIENCY
  • ACYLATION
  • SIRT5
  • METABOLISM
  • DESUCCINYLATION
  • 3111 Biomedicine

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