7nf8

Ovine (b0,+AT-rBAT)2 hetero-tetramer, asymmetric unit, rigid-body fitted

spinqualitylabelsall models 7nf8, resolution 2.83Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 7nf8 is a 2 chain structure with sequence from Ovis aries. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Electron Microscopy, Resolution 2.83Å Ligands: CA, CLR, LBN, NAG Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function A0A6P3EL78_SHEEP Publication Abstract from PubMed 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 b(0,+)AT, which constitute system b(0,+), 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(2+) mediates higher-order assembly of system b(0,+). Ca(2+) stabilizes the interface between two rBAT molecules, leading to super-dimerization of b(0,+)AT-rBAT, which in turn facilitates N-glycan maturation and protein trafficking. A cystinuria mutant T216M and mutations of the Ca(2+) 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(0,+) 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. Ca(2+)-mediated higher-order assembly of heterodimers in amino acid transport system b(0,+) biogenesis and cystinuria.,Lee Y, Wiriyasermkul P, Kongpracha P, Moriyama S, Mills DJ, Kuhlbrandt W, Nagamori S Nat Commun. 2022 May 16;13(1):2708. doi: 10.1038/s41467-022-30293-9. PMID:35577790 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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