Mootha Vamsi K VK

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Proteomics (3)
Unknown (1)

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Chaetomium globosum (2)
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Petunia integrifolia subsp. inflata (2)
Naja naja (2)
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NEWT:502780 (2)
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bacterium BzS1 (2)
NEWT:479249 (2)
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environmental samples (2)
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Clavibacter michiganensis subsp. michiganensis NCPPB 382 (2)
Human respiratory syncytial virus A (2)
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pride (2)
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Acute leukemia (1)

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Mass Spectrometry (2)
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2015 (1)
2026 (1)
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2016 (1)

Lab affiliation

1.Department of Molecular Biology and Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114, USA, 2.Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA, 3.Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. (1)
HHMI and Department of Molecular Biology, Mass General Hospital Department of Systems Biology, Harvard Medical School Broad Institute of MIT & Harvard (1)

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METTL17 is an Fe-S cluster checkpoint for mitochondrial translation

Friedreich’s ataxia (FA) is the most common monogenic mitochondrial disease. FA is caused by a depletion of the mitochondrial protein frataxin (FXN), an iron-sulfur (Fe-S) cluster biogenesis factor. To better understand the cellular consequences of FA, we performed quantitative proteome profiling of...

ORGANISM(S): Homo sapiens (Human)

2023-12-27 | PXD045443 | Pride

Mitochondrial depolarization stabilizes the vitamin B12 chaperone MMADHC in the cytosol to increase MTR activity

Of the ~1100 mitochondrial proteins, only a handful like PINK1 and ATFS-1 are known to stabilize and relocalize upon collapse of the proton motive force (PMF) to execute signaling roles. To systematically identify genes that increase exclusively at the protein level upon PMF collapse, we performed a...

ORGANISM(S): Homo sapiens (Human)

2026-08-24 | PXD079746 | Pride

Proton motive force Mmadhc Vitamin b12 One carbon metabolism Metabolic compartmentalization

EMRE is an Essential Component of the Mitochondrial Calcium Uniporter Complex

Not available

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2015-04-03 | MSV000079095 | MassIVE

Hypoxia as a therapy for mitochondrial disease.