7NF8
Ovine (b0,+AT-rBAT)2 hetero-tetramer, asymmetric unit, rigid-body fitted
7NF8 の概要
エントリーDOI | 10.2210/pdb7nf8/pdb |
EMDBエントリー | 12298 |
分子名称 | B(0,+)-type amino acid transporter 1, neutral and basic amino acid transport protein rBAT, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total) |
機能のキーワード | transporter, cystinuria, complex, translocase |
由来する生物種 | Ovis aries (Sheep) 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 138379.42 |
構造登録者 | |
主引用文献 | Lee, Y.,Wiriyasermkul, P.,Kongpracha, P.,Moriyama, S.,Mills, D.J.,Kuhlbrandt, W.,Nagamori, S. Ca 2+ -mediated higher-order assembly of heterodimers in amino acid transport system b 0,+ biogenesis and cystinuria. Nat Commun, 13:2708-2708, 2022 Cited by PubMed Abstract: Cystinuria is a genetic disorder characterized by overexcretion of dibasic amino acids and cystine, causing recurrent kidney stones and kidney failure. Mutations of the regulatory glycoprotein rBAT and the amino acid transporter bAT, which constitute system b, are linked to type I and non-type I cystinuria respectively and they exhibit distinct phenotypes due to protein trafficking defects or catalytic inactivation. Here, using electron cryo-microscopy and biochemistry, we discover that Ca mediates higher-order assembly of system b. Ca stabilizes the interface between two rBAT molecules, leading to super-dimerization of bAT-rBAT, which in turn facilitates N-glycan maturation and protein trafficking. A cystinuria mutant T216M and mutations of the Ca site of rBAT cause the loss of higher-order assemblies, resulting in protein trapping at the ER and the loss of function. These results provide the molecular basis of system b biogenesis and type I cystinuria and serve as a guide to develop new therapeutic strategies against it. More broadly, our findings reveal an unprecedented link between transporter oligomeric assembly and protein-trafficking diseases. PubMed: 35577790DOI: 10.1038/s41467-022-30293-9 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (2.83 Å) |
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