5NJK
PTB domain of human Numb isoform-1
5NJK の概要
エントリーDOI | 10.2210/pdb5njk/pdb |
分子名称 | Protein numb homolog, ALA-TYR-ILE-GLY-PRO-PTR-LEU, SULFATE ION, ... (4 entities in total) |
機能のキーワード | ptb domain, numb, breast cancer, endocytosis |
由来する生物種 | Homo sapiens (Human) 詳細 |
細胞内の位置 | Membrane; Peripheral membrane protein: P49757 |
タンパク質・核酸の鎖数 | 12 |
化学式量合計 | 113013.58 |
構造登録者 | |
主引用文献 | Colaluca, I.N.,Basile, A.,Freiburger, L.,D'Uva, V.,Disalvatore, D.,Vecchi, M.,Confalonieri, S.,Tosoni, D.,Cecatiello, V.,Malabarba, M.G.,Yang, C.J.,Kainosho, M.,Sattler, M.,Mapelli, M.,Pece, S.,Di Fiore, P.P. A Numb-Mdm2 fuzzy complex reveals an isoform-specific involvement of Numb in breast cancer. J. Cell Biol., 217:745-762, 2018 Cited by PubMed Abstract: Numb functions as an oncosuppressor by inhibiting Notch signaling and stabilizing p53. This latter effect depends on the interaction of Numb with Mdm2, the E3 ligase that ubiquitinates p53 and commits it to degradation. In breast cancer (BC), loss of Numb results in a reduction of p53-mediated responses including sensitivity to genotoxic drugs and maintenance of homeostasis in the stem cell compartment. In this study, we show that the Numb-Mdm2 interaction represents a fuzzy complex mediated by a short Numb sequence encompassing its alternatively spliced exon 3 (Ex3), which is necessary and sufficient to inhibit Mdm2 and prevent p53 degradation. Alterations in the Numb splicing pattern are critical in BC as shown by increased chemoresistance of tumors displaying reduced levels of Ex3-containing isoforms, an effect that could be mechanistically linked to diminished p53 levels. A reduced level of Ex3-less Numb isoforms independently predicts poor outcome in BCs harboring wild-type p53. Thus, we have uncovered an important mechanism of chemoresistance and progression in p53-competent BCs. PubMed: 29269425DOI: 10.1083/jcb.201709092 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.13 Å) |
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