7Y6E
Crystal structure of sDscam FNIII23 domains, isoform Beta2v6
7Y6E の概要
エントリーDOI | 10.2210/pdb7y6e/pdb |
分子名称 | Dscam (2 entities in total) |
機能のキーワード | cell surface receptor, cell adhesion |
由来する生物種 | Chelicerata |
タンパク質・核酸の鎖数 | 7 |
化学式量合計 | 156549.61 |
構造登録者 | |
主引用文献 | Cheng, J.,Yu, Y.,Wang, X.,Zheng, X.,Liu, T.,Hu, D.,Jin, Y.,Lai, Y.,Fu, T.M.,Chen, Q. Structural basis for the self-recognition of sDSCAM in Chelicerata. Nat Commun, 14:2522-2522, 2023 Cited by PubMed Abstract: To create a functional neural circuit, neurons develop a molecular identity to discriminate self from non-self. The invertebrate Dscam family and vertebrate Pcdh family are implicated in determining synaptic specificity. Recently identified in Chelicerata, a shortened Dscam (sDscam) has been shown to resemble the isoform-generating characters of both Dscam and Pcdh and represent an evolutionary transition. Here we presented the molecular details of sDscam self-recognition via both trans and cis interactions using X-ray crystallographic data and functional assays. Based on our results, we proposed a molecular zipper model for the assemblies of sDscam to mediate cell-cell recognition. In this model, sDscam utilized FNIII domain to form side-by-side interactions with neighboring molecules in the same cell while established hand-in-hand interactions via Ig1 domain with molecules from another cell around. Together, our study provided a framework for understanding the assembly, recognition, and evolution of sDscam. PubMed: 37130844DOI: 10.1038/s41467-023-38205-1 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.034 Å) |
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