GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000024
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000052
Gene Ontology annotation based on curation of immunofluorescence data
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000108
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
GO_REF:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:10926541
Role of adenine nucleotide translocator 1 in mtDNA maintenance.
PMID:16507998
Inhibition of ADP/ATP exchange in receptor-interacting protein-mediated necrosis.
PMID:20833797
Phosphoproteome analysis of functional mitochondria isolated from resting human muscle reveals extensive phosphorylation of inner membrane protein complexes and enzymes.
PMID:21370995
Expression of leucine-rich repeat kinase 2 (LRRK2) inhibits the processing of uMtCK to induce cell death in a cell culture model system.
PMID:21586654
adPEO mutations in ANT1 impair ADP-ATP translocation in muscle mitochondria.
PMID:23173940
The substrate specificity of the human ADP/ATP carrier AAC1.
PMID:24316735
Orphan nuclear receptor TR3 acts in autophagic cell death via mitochondrial signaling pathway.
PMID:24725412
Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in Parkinson's disease.
PMID:27641616
TSPO ligands stimulate ZnPPIX transport and ROS accumulation leading to the inhibition of P. falciparum growth in human blood.
PMID:27693233
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number.
PMID:2823266
cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes.
PMID:30046662
Expanding the phenotype of de novo SLC25A4-linked mitochondrial disease to include mild myopathy.
PMID:31883789
Human-Specific ARHGAP11B Acts in Mitochondria to Expand Neocortical Progenitors by Glutaminolysis.
PMID:33961781
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
PMID:34800366
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
PMID:37278158
Human mitochondrial ADP/ATP carrier SLC25A4 operates with a ping-pong kinetic mechanism.
PMID:40355756
The solute carrier superfamily interactome.
Reactome:R-HSA-166187
Mitochondrial Uncoupling
Reactome:R-HSA-180905
Association of Vpr with ANT1
Reactome:R-HSA-5250209
ARL2:GTP:ARL2BP binds SLC25A4
Reactome:R-HSA-5672027
ARL2:GTP:ARL2BP:SLC25A4 dimer exchanges ATP for ADP across the mitochondrial inner membrane
Reactome:R-HSA-9864415
AAC1 imports a proton