Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
Molecular chaperones Hsp90 and Hsp70 deliver preproteins to the mitochondrial import receptor Tom70.
Dissection of the mitochondrial import and assembly pathway for human Tom40.
Identification of Tom5 and Tom6 in the preprotein translocase complex of human mitochondrial outer membrane.
Proteomic analysis of exosomes from human neural stem cells by flow field-flow fractionation and nanoflow liquid chromatography-tandem mass spectrometry.
Defining the membrane proteome of NK cells.
Suppression of the novel ER protein Maxer by mutant ataxin-1 in Bergman glia contributes to non-cell-autonomous toxicity.
Tom70 mediates activation of interferon regulatory factor 3 on mitochondria.
Cytoplasmic ribosomal protein S3 (rpS3) plays a pivotal role in mitochondrial DNA damage surveillance.
Tom70 mediates Sendai virus-induced apoptosis on mitochondria.
A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.
SARS-CoV-2 Orf9b suppresses type I interferon responses by targeting TOM70.
Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.
Toxoplasma gondii association with host mitochondria requires key mitochondrial protein import machinery.
Multilevel proteomics reveals host perturbations by SARS-CoV-2 and SARS-CoV.
Crystal structure of SARS-CoV-2 Orf9b in complex with human TOM70 suggests unusual virus-host interactions.
Interactomes of SARS-CoV-2 and human coronaviruses reveal host factors potentially affecting pathogenesis.
Phosphorylation of SARS-CoV-2 Orf9b Regulates Its Targeting to Two Binding Sites in TOM70 and Recruitment of Hsp90.
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
Evolution of enhanced innate immune evasion by SARS-CoV-2.
The role of the individual TOM subunits in the association of PINK1 with depolarized mitochondria.
A comprehensive SARS-CoV-2-human protein-protein interactome reveals COVID-19 pathobiology and potential host therapeutic targets.
Pink1 is recruited from the cytoplasm to the mitochondria
SARS-CoV-1 3a binds TRAF3 within NLRP3 inflammasome
SARS-CoV-2 9b binds TOMM70
SARS-CoV-1 9b binds TOMM70
MAVS:TOMM70 recruits HSP90:TBK1:IRF3
Falcon deep research report for human TOMM70