Chaparral Labs
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protein

AP-3 complex subunit mu-1

AP3M1
protein:Q9Y2T2disease:adad:direction:down

Gene

AP3M1

Organism

Homo sapiens(9606)

Length

418 aa

Mass

46,939 Da

AI summarysource-grounded · cited inline
claude-haiku-4-5-20251001

AP-3 complex subunit mu-1 (AP3M1) is a component of the AP-3 adaptor complex, which mediates vesicle budding from the Golgi membrane and trafficking to lysosomes (UniProt: Q9Y2T2). In neurons, the AP-3 complex works with BLOC-1 to direct cargo into vesicles at cell bodies for delivery to neurites and nerve terminals, linking it to synaptic function and neuronal trafficking pathways.

AP3M1 is downregulated in Alzheimer's disease brain tissue relative to age-matched controls, with a mean log2 fold-change of −0.97 across subcellular fractions in post-mortem TMT proteomics (Chaparral AD proteomics). This reduction may impair vesicle trafficking and lysosomal delivery, processes increasingly recognized as disrupted in AD pathology. The direction tag indicates consistent downregulation in the analyzed brain fractions (down). No SFARI curation is available for this protein.

Generated from the curated entity record below. May contain errors — verify against source links.

Proteomics Evidence · AD

↓ Down in AD

P3

not detected

P2

not detected

S2

-0.969

S3

not detected

Mean log₂FC across detected fractions: -0.9686 (1 of 4 fractions detected)

Human post-mortem AD brain vs age-matched controls, TMT-labeled, 4 subcellular fractions (P2, P3, S2, S3), DDA proteomics.

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Function

Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane and may be directly involved in trafficking to lysosomes. In concert with the BLOC-1 complex, AP-3 is required to target cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals

Sources

Last updated 5/8/2026, 6:32:14 AM