9FSE
Human ROR2 cysteine-rich domain (CRD) and Kringle domain
9FSE の概要
| エントリーDOI | 10.2210/pdb9fse/pdb |
| 分子名称 | Tyrosine-protein kinase transmembrane receptor ROR2, SULFATE ION (3 entities in total) |
| 機能のキーワード | ror2, wnt, wnt5a, frizzled, signalling, secreted, signalling protein, receptor tyrosine kinase, ror, signaling protein |
| 由来する生物種 | Homo sapiens (human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 27046.47 |
| 構造登録者 | Griffiths, S.C.,Tan, J.,Wagner, A.,Blazer, L.L.,Adams, J.J.,Srinivasan, S.,Moghisaei, S.,Sidhu, S.S.,Siebold, C.,Ho, H.H. (登録日: 2024-06-20, 公開日: 2024-07-10, 最終更新日: 2024-11-13) |
| 主引用文献 | Griffiths, S.C.,Tan, J.,Wagner, A.,Blazer, L.L.,Adams, J.J.,Srinivasan, S.,Moghisaei, S.,Sidhu, S.S.,Siebold, C.,Ho, H.H. Structure and function of the ROR2 cysteine-rich domain in vertebrate noncanonical WNT5A signaling. Elife, 13:-, 2024 Cited by PubMed Abstract: The receptor tyrosine kinase ROR2 mediates noncanonical WNT5A signaling to orchestrate tissue morphogenetic processes, and dysfunction of the pathway causes Robinow syndrome, brachydactyly B, and metastatic diseases. The domain(s) and mechanisms required for ROR2 function, however, remain unclear. We solved the crystal structure of the extracellular cysteine-rich (CRD) and Kringle (Kr) domains of ROR2 and found that, unlike other CRDs, the ROR2 CRD lacks the signature hydrophobic pocket that binds lipids/lipid-modified proteins, such as WNTs, suggesting a novel mechanism of ligand reception. Functionally, we showed that the ROR2 CRD, but not other domains, is required and minimally sufficient to promote WNT5A signaling, and Robinow mutations in the CRD and the adjacent Kr impair ROR2 secretion and function. Moreover, using function-activating and -perturbing antibodies against the Frizzled (FZ) family of WNT receptors, we demonstrate the involvement of FZ in WNT5A-ROR signaling. Thus, ROR2 acts via its CRD to potentiate the function of a receptor super-complex that includes FZ to transduce WNT5A signals. PubMed: 38780011DOI: 10.7554/eLife.71980 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.48 Å) |
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