2WII
Complement C3b in complex with factor H domains 1-4
2WII の概要
エントリーDOI | 10.2210/pdb2wii/pdb |
関連するPDBエントリー | 1FHC 1HFH 1OJV 2A73 2A74 2G7I 2ICF 2JGW 2JGX 2RLP 2RLQ 2V8E 2W80 2W81 |
分子名称 | COMPLEMENT C3 BETA CHAIN, COMPLEMENT C3B ALPHA' CHAIN, COMPLEMENT FACTOR H, ... (8 entities in total) |
機能のキーワード | immune system, sushi, secreted, polymorphism, glycoprotein, complement system, complement pathway, immune response, innate immunity, disease mutation, inflammatory response, complement alternate pathway, cleavage on pair of basic residues, age-related macular degeneration, regulator of complement activation, alternative pathway, alternative splicing, phosphoprotein, disulfide bond, thioester bond |
由来する生物種 | HOMO SAPIENS (HUMAN) 詳細 |
細胞内の位置 | Secreted: P01024 P01024 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 209591.19 |
構造登録者 | |
主引用文献 | Wu, J.,Wu, Y.Q.,Ricklin, D.,Janssen, B.J.,Lambris, J.D.,Gros, P. Structure of complement fragment C3b-factor H and implications for host protection by complement regulators. Nat. Immunol., 10:728-733, 2009 Cited by PubMed Abstract: Factor H (FH) is an abundant regulator of complement activation and protects host cells from self-attack by complement. Here we provide insight into the regulatory activity of FH by solving the crystal structure of the first four domains of FH in complex with its target, complement fragment C3b. FH interacted with multiple domains of C3b, covering a large, extended surface area. The structure indicated that FH destabilizes the C3 convertase by competition and electrostatic repulsion and that FH enables proteolytic degradation of C3b by providing a binding platform for protease factor I while stabilizing the overall domain arrangement of C3b. Our results offer general models for complement regulation and provide structural explanations for disease-related mutations in the genes encoding both FH and C3b. PubMed: 19503104DOI: 10.1038/ni.1755 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
構造検証レポート
検証レポート(詳細版)をダウンロード