Gene Ontology annotation through association of InterPro records with GO terms
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 UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
Electronic Gene Ontology annotations created by ARBA machine learning models
Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor.
Integral and associated lysosomal membrane proteins.
Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 function.
BLOC-2, AP-3, and AP-1 proteins function in concert with Rab38 and Rab32 proteins to mediate protein trafficking to lysosome-related organelles.
Cell type-specific Rab32 and Rab38 cooperate with the ubiquitous lysosome biogenesis machinery to synthesize specialized lysosome-related organelles.
A proteome-scale map of the human interactome network.
Architecture of the human interactome defines protein communities and disease networks.
A reference map of the human binary protein interactome.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
The solute carrier superfamily interactome.
Characterization of the adaptor-related protein complex, AP-3.
Association of the AP-3 adaptor complex with clathrin.
AP-3: an adaptor-like protein complex with ubiquitous expression.
The medium subunits of adaptor complexes recognize distinct but overlapping sets of tyrosine-based sorting signals.
Specificity of interaction between adaptor-complex medium chains and the tyrosine-based sorting motifs of TGN38 and lgp120.
Multiple C-terminal motifs of the 46-kDa mannose 6-phosphate receptor tail contribute to efficient binding of medium chains of AP-2 and AP-3.
A structure-based mechanism for initiation of AP-3 coated vesicle formation.
Architecture of clathrin-independent AP3:ARF1-coated carriers.
Flexible open conformation of the AP-3 complex explains its role in cargo recruitment at the Golgi.
Interaction of the Human Respiratory Syncytial Virus matrix protein with cellular adaptor protein complex 3 plays a critical role in trafficking.
The schizophrenia susceptibility factor dysbindin and its associated complex sort cargoes from cell bodies to the synapse.
Upregulation of μ3A Drives Homeostatic Plasticity by Rerouting AMPAR into the Recycling Endosomal Pathway.
Genetic analysis of the neuronal and ubiquitous AP-3 adaptor complexes reveals divergent functions in brain.
Hermansky-Pudlak syndrome protein complexes associate with phosphatidylinositol 4-kinase type II alpha in neuronal and non-neuronal cells.
Widespread Post-transcriptional Attenuation of Genomic Copy-Number Variation in Cancer.
Genomic organization and linkage via a bidirectional promoter of the AP-3 (adaptor protein-3) mu3A and AK (adenosine kinase) genes: deletion mutants of AK in Chinese hamster cells extend into the AP-3 mu3A gene.
Hermansky-Pudlak syndrome: Mutation update.
Sequence requirements for the recognition of tyrosine-based endocytic signals by clathrin AP-2 complexes.
UniProtKB Q9Y2T2 (AP3M1_HUMAN) flat file
AP3M1 bioinformatics: the YxxPhi cargo pocket of the AP-3 mu subunit
Affinage mechanistic annotation for AP3M1 (human)