Structural Basis of Wnt Recognition by Frizzled
Howard Hughes Medical Institute · Stanford University
Abstract
Wnts are lipid-modified morphogens that play critical roles in development principally through engagement of Frizzled receptors. The 3.25 angstrom structure of Xenopus Wnt8 (XWnt8) in complex with mouse Frizzled-8 (Fz8) cysteine-rich domain (CRD) reveals an unusual two-domain Wnt structure, not obviously related to known protein folds, resembling a "hand" with "thumb" and "index" fingers extended to grasp the Fz8-CRD at two distinct binding sites. One site is dominated by a palmitoleic acid lipid group projecting from serine 187 at the tip of Wnt's thumb into a deep groove in the Fz8-CRD. In the second binding site, the conserved tip of Wnt's "index finger" forms hydrophobic amino acid contacts with a…
Citation impact
- FWCI
- 26.60
- Percentile
- 100%
- References
- 60
Authors
5- CYClaudia Y. Janda
Howard Hughes Medical Institute, Stanford University
- DWDeepa Waghray
Howard Hughes Medical Institute, Stanford University
- AMAron M. Levin
Howard Hughes Medical Institute, Stanford University
- CTChristoph Thomas
Howard Hughes Medical Institute, Stanford University
- KCK. Christopher GarcíaCorresponding
Howard Hughes Medical Institute, Stanford University
Topics & keywords
- Wnt signaling pathway
- Frizzled
- Xenopus
- Biology
- LRP6
- Cell biology
- Cysteine
- LRP5