Geometric Deep Learning for Structure-Based Drug Design: A Survey
Zaixi Zhang, Jiaxian Yan, Yining Huang, Qi Liu, Enhong Chen, Mengdi, Wang, and Marinka Zitnik

TL;DR
This survey reviews recent advances in geometric deep learning applied to structure-based drug design, highlighting key tasks, models, datasets, challenges, and future directions in the field.
Contribution
It provides a comprehensive overview of state-of-the-art methods, formal problem definitions, and benchmarks in geometric deep learning for SBDD, along with insights into challenges and opportunities.
Findings
Significant progress in binding site prediction and molecule generation.
Identification of key challenges like generalization and evaluation metrics.
Curated datasets and benchmarks for future research.
Abstract
Structure-based drug design (SBDD) leverages the three-dimensional geometry of proteins to identify potential drug candidates. Traditional approaches, rooted in physicochemical modeling and domain expertise, are often resource-intensive. Recent advancements in geometric deep learning, which effectively integrate and process 3D geometric data, alongside breakthroughs in accurate protein structure predictions from tools like AlphaFold, have significantly propelled the field forward. This paper systematically reviews the state-of-the-art in geometric deep learning for SBDD. We begin by outlining foundational tasks in SBDD, discussing prevalent 3D protein representations, and highlighting representative predictive and generative models. Next, we provide an in-depth review of key tasks, including binding site prediction, binding pose generation, de novo molecule generation, linker design,…
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Taxonomy
TopicsComputational Drug Discovery Methods · Microbial Natural Products and Biosynthesis · Protein Structure and Dynamics
MethodsAlphaFold
