1YWH
crystal structure of urokinase plasminogen activator receptor
1YWH の概要
エントリーDOI | 10.2210/pdb1ywh/pdb |
分子名称 | Urokinase plasminogen activator surface receptor, antagonist peptide, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... (9 entities in total) |
機能のキーワード | upar, three-finger fold, protein-peptide complex, hydrolase receptor |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 16 |
化学式量合計 | 304707.61 |
構造登録者 | Llinas, P.,Le Du, M.H.,Gardsvoll, H.,Dano, K.,Ploug, M.,Gilquin, B.,Stura, E.A.,Menez, A. (登録日: 2005-02-18, 公開日: 2005-05-10, 最終更新日: 2024-10-30) |
主引用文献 | Llinas, P.,Le Du, M.H.,Gardsvoll, H.,Dano, K.,Ploug, M.,Gilquin, B.,Stura, E.A.,Menez, A. Crystal structure of the human urokinase plasminogen activator receptor bound to an antagonist peptide EMBO J., 24:1655-1663, 2005 Cited by PubMed Abstract: We report the crystal structure of a soluble form of human urokinase-type plasminogen activator receptor (uPAR/CD87), which is expressed at the invasive areas of the tumor-stromal microenvironment in many human cancers. The structure was solved at 2.7 A in association with a competitive peptide inhibitor of the urokinase-type plasminogen activator (uPA)-uPAR interaction. uPAR is composed of three consecutive three-finger domains organized in an almost circular manner, which generates both a deep internal cavity where the peptide binds in a helical conformation, and a large external surface. This knowledge combined with the discovery of a convergent binding motif shared by the antagonist peptide and uPA allowed us to build a model of the human uPA-uPAR complex. This model reveals that the receptor-binding module of uPA engages the uPAR central cavity, thus leaving the external receptor surface accessible for other protein interactions (vitronectin and integrins). By this unique structural assembly, uPAR can orchestrate the fine interplay with the partners that are required to guide uPA-focalized proteolysis on the cell surface and control cell adhesion and migration. PubMed: 15861141DOI: 10.1038/sj.emboj.7600635 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
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