AP-3 complex subunit mu-1 is a protein that in humans is encoded by the AP3M1 gene .[ 5] [ 6]
The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane and may be directly involved in protein sorting to the endosomal /lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3 ), a medium subunit (mu3 ), and a small subunit (sigma 3 ). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome , a genetic disorder characterized by defective lysosome-related organelles . Alternatively spliced transcript variants encoding the same protein have been observed.[ 6]
^ a b c GRCh38: Ensembl release 89: ENSG00000185009 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000021824 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Dell'Angelica EC, Shotelersuk V, Aguilar RC, Gahl WA, Bonifacino JS (Mar 1999). "Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor" . Mol Cell . 3 (1): 11– 21. doi :10.1016/S1097-2765(00)80170-7 . PMID 10024875 . 11- 21&rft.date=1999-03&rft_id=info:doi/10.1016/S1097-2765(00)80170-7&rft_id=info:pmid/10024875&rft.aulast=Dell'Angelica&rft.aufirst=EC&rft.au=Shotelersuk, V&rft.au=Aguilar, RC&rft.au=Gahl, WA&rft.au=Bonifacino, JS&rft_id=https://doi.org/10.1016%2FS1097-2765%2800%2980170-7&rfr_id=info:sid/en.wikipedia.org:AP3M1" class="Z3988">
^ a b "Entrez Gene: AP3M1 adaptor-related protein complex 3, mu 1 subunit" .
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