7Y8H
Crystal structure of sDscam FNIII1 domain, isoform alpha7
Summary for 7Y8H
Entry DOI | 10.2210/pdb7y8h/pdb |
Descriptor | Down Syndrome Cell Adhesion Molecules, SULFATE ION (3 entities in total) |
Functional Keywords | cell surface receptor, cell adhesion |
Biological source | Chelicerata |
Total number of polymer chains | 2 |
Total formula weight | 22504.81 |
Authors | |
Primary citation | 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 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
Download full validation report