2BZ8
N-terminal Sh3 domain of CIN85 bound to Cbl-b peptide
2BZ8 の概要
エントリーDOI | 10.2210/pdb2bz8/pdb |
分子名称 | SH3-DOMAIN KINASE BINDING PROTEIN 1, SIGNAL TRANSDUCTION PROTEIN CBL-B SH3-BINDING PROTEIN CBL-B, RING FINGER PROTEIN 56, CBL-B, SODIUM ION, ... (4 entities in total) |
機能のキーワード | sh3 domain, cin85 adaptor protein, cbl ubiquitin ligase, endocytosis |
由来する生物種 | HOMO SAPIENS (HUMAN) 詳細 |
細胞内の位置 | Cytoplasm : Q96B97 Q13191 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 14923.65 |
構造登録者 | |
主引用文献 | Jozic, D.,Cardenes, N.,Lissanu-Deribe, Y.,Moncalian, G.,Hoeller, D.,Groemping, Y.,Dikic, I.,Rittinger, K.,Bravo, J. Cbl Promotes Clustering of Endocytic Adaptor Proteins Nat.Struct.Mol.Biol., 12:972-, 2005 Cited by PubMed Abstract: The ubiquitin ligases c-Cbl and Cbl-b play a crucial role in receptor downregulation by mediating multiple monoubiquitination of receptors and promoting their sorting for lysosomal degradation. Their function is modulated through interactions with regulatory proteins including CIN85 and PIX, which recognize a proline-arginine motif in Cbl and thus promote or inhibit receptor endocytosis. We report the structures of SH3 domains of CIN85 and beta-PIX in complex with a proline-arginine peptide from Cbl-b. Both structures reveal a heterotrimeric complex containing two SH3 domains held together by a single peptide. Trimerization also occurs in solution and is facilitated by the pseudo-symmetrical peptide sequence. Moreover, ternary complexes of CIN85 and Cbl are formed in vivo and are important for the ability of Cbl to promote epidermal growth factor receptor (EGFR) downregulation. These results provide molecular explanations for a novel mechanism by which Cbl controls receptor downregulation. PubMed: 16228008DOI: 10.1038/NSMB1000 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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