7MO8
Cryo-EM structure of 1:1 c-MET I/HGF I complex after focused 3D refinement of holo-complex
7MO8 の概要
| エントリーDOI | 10.2210/pdb7mo8/pdb |
| EMDBエントリー | 23920 |
| 分子名称 | Hepatocyte growth factor, Hepatocyte growth factor receptor, 2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose (3 entities in total) |
| 機能のキーワード | c-met, hgf, receptor tyrosine kinase, signaling protein |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 240720.88 |
| 構造登録者 | Uchikawa, E.,Chen, Z.M.,Xiao, G.Y.,Zhang, X.W.,Bai, X.C. (登録日: 2021-05-01, 公開日: 2021-06-09, 最終更新日: 2024-10-16) |
| 主引用文献 | Uchikawa, E.,Chen, Z.,Xiao, G.Y.,Zhang, X.,Bai, X.C. Structural basis of the activation of c-MET receptor. Nat Commun, 12:4074-4074, 2021 Cited by PubMed Abstract: The c-MET receptor is a receptor tyrosine kinase (RTK) that plays essential roles in normal cell development and motility. Aberrant activation of c-MET can lead to both tumors growth and metastatic progression of cancer cells. C-MET can be activated by either hepatocyte growth factor (HGF), or its natural isoform NK1. Here, we report the cryo-EM structures of c-MET/HGF and c-MET/NK1 complexes in the active state. The c-MET/HGF complex structure reveals that, by utilizing two distinct interfaces, one HGF molecule is sufficient to induce a specific dimerization mode of c-MET for receptor activation. The binding of heparin as well as a second HGF to the 2:1 c-MET:HGF complex further stabilize this active conformation. Distinct to HGF, NK1 forms a stable dimer, and bridges two c-METs in a symmetrical manner for activation. Collectively, our studies provide structural insights into the activation mechanisms of c-MET, and reveal how two isoforms of the same ligand use dramatically different mechanisms to activate the receptor. PubMed: 34210960DOI: 10.1038/s41467-021-24367-3 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (4.5 Å) |
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