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Bhujel, N.

Publications and source records attributed to Bhujel, N..

2 recordsLinked to original sources

DPI-score: A deep learning-based metric for assessing protein-protein interfaces in cryo-EM derived assemblies

Advances in cryoEM have led to a surge in high-resolution structures; however, model building and refinement at resolutions (>=3 [A]) and in regions with variable local resolution remain challenging, making validation essential. CryoEM derived assemblies often contain extensive protein-protein interfaces, however, most existing validation metrics focus on density fit or overall geometry without directly assessing interface quality. To address this, we present DPI-Score, a deep learning-based metric for assessing protein-protein interfaces in cryoEM derived complexes. The method uses only raw structural coordinates of interface atoms, without requiring engineered features, and achieves 87.53% validation accuracy. DPI-Score was applied to 29,120 interfaces from 6,011 fitted entries with resolutions worse than 3 [A] in the Electron Microscopy Data Bank. Here, we show that DPI-Score provides complementary information to existing validation metrics and can identify interface errors in modelled assemblies that are not detected by density-based scores alone.

bioinformatics↗

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

AbstractCTNND1 encodes the p120-catenin (p120) protein, which has a wide range of functions, including the maintenance of cell-cell junctions, regulation of the epithelial-mesenchymal transition and transcriptional signaling. Due to advances in next generation sequencing, CTNND1 has been implicated in human diseases including cleft palate and blepharocheilodontic syndrome (BCD) albeit only recently. In this study, we identify eight novel protein-truncating variants, six de novo, in thirteen participants presenting with craniofacial dysmorphisms including cleft palate and hypodontia, as well as congenital cardiac anomalies, limb dysmorphologies and neurodevelopmental disorders. Using conditional deletions in mice as well as CRISPR/Cas9 approaches to target CTNND1 in Xenopus, we identified a subset of phenotypes that can be linked to p120-catenin in epithelial integrity and turnover, and additional phenotypes that suggest mesenchymal roles of CTNND1. We propose that CTNND1 variants have a wider developmental role than previously described, and that variations in this gene underlie not only cleft palate and BCD but may be expanded to a broader velocardiofacial-like syndrome.

genetics↗