Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The energetic state of mitochondria modulates complex III biogenesis through the ATP-dependent activity of Bcs1.

Cell metabolism - 1 Oct 2013

Ostojić Jelena, Panozzo Cristina, Lasserre Jean-Paul, Nouet Cécile, Courtin Florence, Blancard Corinne, di Rago Jean-Paul, Dujardin Geneviève

Abstract excerpt

Our understanding of the mechanisms involved in mitochondrial biogenesis has continuously expanded during the last decades, yet little is known about how they are modulated to optimize the functioning of mitochondria. Here, we show that mutations in the ATP binding domain of Bcs1, a chaperone involved in the assembly of complex III, can be rescued by mutations that decrease the ATP hydrolytic activity of the ATP...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenosine Triphosphate
Share to ATPases Associated with Diverse Cellular Activities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electron Transport Complex III

Share to Mitochondria

Share to Mitochondrial Membranes

Share to Mitochondrial Proteins

Share to Molecular Chaperones

Share to Saccharomyces cerevisiae Proteins

Source

Identifiers

PMID: 24055101
DOI: 10.1016/j.cmet.2013.08.017

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The energetic state of mitochondria modulates complex III biogenesis through the ATP-dependent activity of Bcs1.PMID 24055101Read ↗

Mitochondrial ATP synthase disorders: molecular mechanisms and the quest for curative therapeutic approaches.Semantic proximity Read ↗

Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects.Semantic proximity Read ↗

The role of mitochondrial ATP synthase in cancer.Semantic proximity Read ↗

Molecular Insights into Mitochondrial Protein Translocation and Human Disease.Semantic proximity Read ↗

Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase.Semantic proximity Read ↗

Studies of the assembly pathway of human ATP synthaseSemantic proximity Read ↗

The mitochondrial ADP/ATP carrier: functional and structural studies in the route of elucidating pathophysiological aspects.Semantic proximity Read ↗

Molecular mechanism of mitochondrial respiratory chain assembly and its relation to mitochondrial diseases.Semantic proximity Read ↗

Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency.Semantic proximity Read ↗

Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster.Semantic proximity Read ↗

The INA complex facilitates assembly of the peripheral stalk of the mitochondrial F1Fo-ATP synthase.Semantic proximity Read ↗

Human diseases associated with defects in assembly of OXPHOS complexes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.