Sep 2026· Journal of Chemical Information and Modeling· Vol 66, pp. 12115-12127· 0 citations· 29 references
TL;DR
In a targeted experimental screen for estrogen receptor alpha (ERα) modulators, MoaNet successfully identified both ERα agonists and antagonists, highlighting its practical utility in functional drug discovery.
Abstract
Understanding the functional interactions between molecules and their targets is critical in drug discovery. While current computational approaches achieve high accuracy in predicting drug–target interactions, they often fail to capture the functional consequences of these interactions, such as agonistic or antagonistic effects. Here, we present an end-to-end framework for predicting protein–ligand mechanism of action with transcriptional signature and molecular structural information (MoaNet). Computational evaluations demonstrate that MoaNet outperforms several representative molecular representation architectures adapted for MoA classification on our benchmark data set under scaffold-split evaluation. In a targeted experimental screen for estrogen receptor alpha (ERα) modulators, MoaNet successfully identified both ERα agonists and antagonists, highlighting its practical utility in functional drug discovery.
Two deep learning-based computational protocols designed to address drug mechanisms of action and predicting drug-target interactions are presented, offering scalable, cost-effective tools for accelerating therapeutic development by bridging chemical structure, molecular interactions, and systems-level biological respo...
Y. Sun, Cheng-You Liu, Zi-Hao Jing et al.· Methods in molecular biology· 0 citations
Coumarins are versatile bioactive scaffolds capable of interacting with diverse biomolecules, yet their potential role in modulating protein–protein complexes remains insufficiently characterized. Modern computational biology now enables rational exploration of how small molecules can influence structural coupling, sig...
Yasser Faki Mustafa· Journal of Genetic Engineeri...· 0 citations
Modern drug discovery relies on accurate computational methods for predicting drug-target interactions. When trained on hundreds of millions of protein sequences, transformer-based methods such as ProteinBERT demonstrate high accuracy in predicting protein function and structural properties, including disordered region...
D. Bock, S. Grozdanić, Vladimir Jacimovic et al.· 2026 IEEE 4th Conference on...· 0 citations
HelixDTA is introduced, a deep learning framework featuring a parallel dual-branch architecture that independently learns representations from two distinct but complementary modalities: sequence context and complete target structures that demonstrates significant potential to empower precision drug design and accelerat...
Shang Lou, Xu-Hua Li, Yu-Jie Peng et al.· Journal of Chemical Informat...· 0 citations
Ligand-protein binding prediction remains a central challenge, yet the contribution of ligand-side information to performance is unclear and ligand-only models as interpretable screening tools are established and used as a baseline for assessing the added value of protein representations.
Ananthan Sadagopan, Anurag Sodhi, William J. Gibson· Journal of Medicinal Chemist...· 0 citations
Biological systems are governed by a myriad of molecular interactions, many of which remain poorly recognized. Growing evidence suggests that transient interactions (Kdiss >1 µM) dominate the interactome and are crucial for dynamic molecular networks. By contrast, drug discovery has largely focused on high-affinity com...
S. Ohlson· Drug Discovery Today· 0 citations
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