3L81
Crystal structure of adaptor protein complex 4 (AP-4) mu4 subunit C-terminal domain, in complex with a sorting peptide from the amyloid precursor protein (APP)
3L81 の概要
エントリーDOI | 10.2210/pdb3l81/pdb |
関連するPDBエントリー | 1BW8 1BXX 3G9H |
分子名称 | AP-4 complex subunit mu-1, Amyloid beta A4 protein, GLYCEROL, ... (4 entities in total) |
機能のキーワード | immunoglobulin-like beta-sandwich, coated pit, golgi apparatus, membrane, phosphoprotein, protein transport, transport, alzheimer disease, amyloid, amyloidosis, transport protein |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Golgi apparatus, trans-Golgi network : O00189 Membrane; Single-pass type I membrane protein: P05067 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 34351.99 |
構造登録者 | Mardones, G.A.,Rojas, A.L.,Burgos, P.V.,Dasilva, L.L.P.,Prabhu, Y.,Bonifacino, J.S.,Hurley, J.H. (登録日: 2009-12-29, 公開日: 2010-06-02, 最終更新日: 2024-02-21) |
主引用文献 | Burgos, P.V.,Mardones, G.A.,Rojas, A.L.,daSilva, L.L.,Prabhu, Y.,Hurley, J.H.,Bonifacino, J.S. Sorting of the Alzheimer's disease amyloid precursor protein mediated by the AP-4 complex. Dev.Cell, 18:425-436, 2010 Cited by PubMed Abstract: Adaptor protein 4 (AP-4) is the most recently discovered and least well-characterized member of the family of heterotetrameric adaptor protein (AP) complexes that mediate sorting of transmembrane cargo in post-Golgi compartments. Herein, we report the interaction of an YKFFE sequence from the cytosolic tail of the Alzheimer's disease amyloid precursor protein (APP) with the mu4 subunit of AP-4. Biochemical and X-ray crystallographic analyses reveal that the properties of the APP sequence and the location of the binding site on mu4 are distinct from those of other signal-adaptor interactions. Disruption of the APP-AP-4 interaction decreases localization of APP to endosomes and enhances gamma-secretase-catalyzed cleavage of APP to the pathogenic amyloid-beta peptide. These findings demonstrate that APP and AP-4 engage in a distinct type of signal-adaptor interaction that mediates transport of APP from the trans-Golgi network (TGN) to endosomes, thereby reducing amyloidogenic processing of the protein. PubMed: 20230749DOI: 10.1016/j.devcel.2010.01.015 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.6 Å) |
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