1DE4
HEMOCHROMATOSIS PROTEIN HFE COMPLEXED WITH TRANSFERRIN RECEPTOR
1DE4 の概要
| エントリーDOI | 10.2210/pdb1de4/pdb |
| 関連するPDBエントリー | 1A6Z 1CX8 |
| 分子名称 | HEMOCHROMATOSIS PROTEIN, BETA-2-MICROGLOBULIN, TRANSFERRIN RECEPTOR, ... (7 entities in total) |
| 機能のキーワード | hfe, hereditary hemochromatosis, mhc class i, transferrin receptor, metal transport inhibitor-receptor complex, metal transport inhibitor/receptor |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 9 |
| 化学式量合計 | 348560.51 |
| 構造登録者 | |
| 主引用文献 | Bennett, M.J.,Lebron, J.A.,Bjorkman, P.J. Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor. Nature, 403:46-53, 2000 Cited by PubMed Abstract: HFE is related to major histocompatibility complex (MHC) class I proteins and is mutated in the iron-overload disease hereditary haemochromatosis. HFE binds to the transferrin receptor (TfR), a receptor by which cells acquire iron-loaded transferrin. The 2.8 A crystal structure of a complex between the extracellular portions of HFE and TfR shows two HFE molecules which grasp each side of a twofold symmetric TfR dimer. On a cell membrane containing both proteins, HFE would 'lie down' parallel to the membrane, such that the HFE helices that delineate the counterpart of the MHC peptide-binding groove make extensive contacts with helices in the TfR dimerization domain. The structures of TfR alone and complexed with HFE differ in their domain arrangement and dimer interfaces, providing a mechanism for communicating binding events between TfR chains. The HFE-TfR complex suggests a binding site for transferrin on TfR and sheds light upon the function of HFE in regulating iron homeostasis. PubMed: 10638746DOI: 10.1038/47417 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.8 Å) |
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