Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Integral and associated lysosomal membrane proteins.

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

The fifth adaptor protein complex.

Adaptor protein complexes AP-4 and AP-5: new players in endosomal trafficking and progressive spastic paraplegia.

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

A proteome-scale map of the human interactome network.

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

Human Immunodeficiency Virus Type 2 (HIV-2) Gag Is Trafficked in an AP-3 and AP-5 Dependent Manner.

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.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

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

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

Bi-allelic variants in AP5Z1 and AP5B1 lead to retinal degeneration.

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

UniProtKB Q2VPB7 (AP5B1_HUMAN) flat file

Affinage mechanistic annotation for AP5B1 (human)

AP5B1 (beta-5 adaptin): does it carry the beta-adaptin clathrin-binding apparatus?