6RLR
Crystal structure of CD9 large extracellular loop
6RLR の概要
| エントリーDOI | 10.2210/pdb6rlr/pdb |
| 分子名称 | CD9 antigen (2 entities in total) |
| 機能のキーワード | cd9 antigen, tetraspanin, immune system |
| 由来する生物種 | Homo sapiens (Human) |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 41042.52 |
| 構造登録者 | Neviani, V.,Kroon-Batenburg, L.,Lutz, M.,Pearce, N.M.,Pos, W.,Schotte, R.,Spits, H.,Gros, P. (登録日: 2019-05-02, 公開日: 2020-09-23, 最終更新日: 2024-11-06) |
| 主引用文献 | Oosterheert, W.,Xenaki, K.T.,Neviani, V.,Pos, W.,Doulkeridou, S.,Manshande, J.,Pearce, N.M.,Kroon-Batenburg, L.M.,Lutz, M.,van Bergen En Henegouwen, P.M.,Gros, P. Implications for tetraspanin-enriched microdomain assembly based on structures of CD9 with EWI-F. Life Sci Alliance, 3:-, 2020 Cited by PubMed Abstract: Tetraspanins are eukaryotic membrane proteins that contribute to a variety of signaling processes by organizing partner-receptor molecules in the plasma membrane. How tetraspanins bind and cluster partner receptors into tetraspanin-enriched microdomains is unknown. Here, we present crystal structures of the large extracellular loop of CD9 bound to nanobodies 4C8 and 4E8 and, the cryo-EM structure of 4C8-bound CD9 in complex with its partner EWI-F. CD9-EWI-F displays a tetrameric arrangement with two central EWI-F molecules, dimerized through their ectodomains, and two CD9 molecules, one bound to each EWI-F transmembrane helix through CD9-helices h3 and h4. In the crystal structures, nanobodies 4C8 and 4E8 bind CD9 at loops C and D, which is in agreement with the 4C8 conformation in the CD9-EWI-F complex. The complex varies from nearly twofold symmetric (with the two CD9 copies nearly anti-parallel) to ca. 50° bent arrangements. This flexible arrangement of CD9-EWI-F with potential CD9 homo-dimerization at either end provides a "concatenation model" for forming short linear or circular assemblies, which may explain the occurrence of tetraspanin-enriched microdomains. PubMed: 32958604DOI: 10.26508/lsa.202000883 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2 Å) |
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