scholarly journals PTK7/Otk interacts with Wnts and inhibits canonical Wnt signalling

2011 ◽  
Vol 30 (18) ◽  
pp. 3729-3740 ◽  
Author(s):  
Hanna Peradziryi ◽  
Nicole A Kaplan ◽  
Martina Podleschny ◽  
Xiaoping Liu ◽  
Peter Wehner ◽  
...  
Keyword(s):  
2019 ◽  
Vol 2019 ◽  
pp. 1-1
Author(s):  
Chenyang Zhao ◽  
Jinlan Gao ◽  
Sen Li ◽  
Qi Liu ◽  
Xiaoyu Hou ◽  
...  

genesis ◽  
2017 ◽  
Vol 55 (10) ◽  
pp. e23068 ◽  
Author(s):  
Jolanda. J. D. de Roo ◽  
Cor Breukel ◽  
Amiet R. Chhatta ◽  
Margot M. Linssen ◽  
Sandra A. Vloemans ◽  
...  

2014 ◽  
Vol 16 (11) ◽  
pp. 1126-1126 ◽  
Author(s):  
Ichiro Takada ◽  
Masatomo Mihara ◽  
Miyuki Suzawa ◽  
Fumiaki Ohtake ◽  
Shinji Kobayashi ◽  
...  

2019 ◽  
Vol 20 (17) ◽  
pp. 4168 ◽  
Author(s):  
Mark Agostino ◽  
Sebastian Öther-Gee Pohl

Several proteins other than the frizzled receptors (Fzd) and the secreted Frizzled-related proteins (sFRP) contain Fzd-type cysteine-rich domains (CRD). We have termed these domains “putative Fzd-type CRDs”, as the relevance of Wnt signalling in the majority of these is unknown; the RORs, an exception to this, are well known for mediating non-canonical Wnt signalling. In this study, we have predicted the likely binding affinity of all Wnts for all putative Fzd-type CRDs. We applied both our previously determined Wnt‒Fzd CRD binding affinity prediction model, as well as a newly devised model wherein the lipid term was forced to contribute favourably to the predicted binding energy. The results obtained from our new model indicate that certain putative Fzd CRDs are much more likely to bind Wnts, in some cases exhibiting selectivity for specific Wnts. The results of this study inform the investigation of Wnt signalling modulation beyond Fzds and sFRPs.


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