Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Automatic Gene Ontology annotation based on Rhea mapping
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Peroxisomes in human and mouse testis: differential expression of peroxisomal proteins in germ cells and distinct somatic cell types of the testis.
Contribution of peroxisome-specific isoform of Lon protease in sorting PTS1 proteins to peroxisomes.
Peroxisomal acyl-CoA-oxidase deficiency: two new cases.
Defining the membrane proteome of NK cells.
KIF14 negatively regulates Rap1a-Radil signaling during breast cancer progression.
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms.
Overexpression and characterization of the human peroxisomal acyl-CoA oxidase in insect cells.
Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase.
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome.
UniProtKB Q15067 (ACOX1_HUMAN) record
Oxidation of tetracosapentaenoyl-CoA to delta2-tetracosaheptaenoyl-CoA
Cargo of PEX5S,L translocates from the cytosol to the peroxisomal matrix
PEX5S,L:Cargo binds PEX13:PEX14:PEX2:PEX10:PEX12 (Docking and Translocation Module)
Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid.
Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of long-chain dicarboxylic acids.
Three-dimensional structure of rat-liver acyl-CoA oxidase in complex with a fatty acid: insights into substrate-recognition and reactivity toward molecular oxygen.
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Rat ACOX1 crystal structure 2DDH contains a free fatty-acid ligand in the substrate channel after thioester hydrolysis, with carboxyl oxygen contacts to the enzyme/FAD environment. This supports binding under crystallization conditions, without establishing a human physiological carrier function.