Gene Ontology annotation through association of InterPro records with GO terms

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

Gene Ontology annotation based on curation of immunofluorescence data

A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia.

The fifth adaptor protein complex.

Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15.

Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease.

Role of the AP-5 adaptor protein complex in late endosome-to-Golgi retrieval.

Rag GTPases and phosphatidylinositol 3-phosphate mediate recruitment of the AP-5/SPG11/SPG15 complex.

Structural basis for membrane remodeling by the AP5-SPG11-SPG15 complex.

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy.

A structural explanation for the binding of endocytic dileucine motifs by the AP2 complex.

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.

AP5S1 (sigma-5): what the AP-5 structure says the subunit does

UniProtKB entry Q9NUS5 (AP5S1_HUMAN)

Affinage mechanistic annotation for AP5S1 (human)