2026· ITM Web of Conferences· Vol 88, pp. 01021· 0 citations· 11 references
TL;DR
This paper discusses graph embedding-based approaches with the focus on their strategies of feature representation and integration with multi-source data and clustering algorithms, and a summary of graph neural network-based approaches, and their benefits in nonlinear feature learning, as well as multi-modal information fusion.
Abstract
Protein complexes are fundamental structural elements in cells, which perform vital biological roles and are central to mechanisms such as signal transduction, metabolic control and gene expression. As high-throughput experimental technologies have developed, extensive data on protein-protein interactions have been collected and often in the form of complex networks. These datasets are, however, usually marred by problems of noise and incompleteness and these present serious problems in the identification of protein complexes. In recent years, AI techniques have provided new ways to solve this issue. With the identification of protein complexes in the spotlight, the paper will provide a systematic review of two main dimensions: First, it discusses graph embedding-based approaches with the focus on their strategies of feature representation and integration with multi-source data and clustering algorithms. Second, it is a summary of graph neural network-based approaches, and their benefits in nonlinear feature learning, as well as multi-modal information fusion. Moreover, the paper types and classifies popular datasets, and provides detailed analysis of the existing studies under the prism of data quality, multi-source fusion approaches and model complexity. Studies show that graph neural networks are better at expressing relationships of complexity; they are however, not without problems of being costly to compute, and highly dependent on data.
This review systematically summarizes the latest research progress in druggable protein prediction algorithms, providing a comprehensive analysis across three dimensions: data resources, feature engineering, and predictive models.
Hong-Qi Zhang, Hong-Ling Wang, Shang-Hua Liu et al.· Current Drug Targets· 0 citations
Accurate identification of protein-protein interactions (PPIs) is fundamental for understanding cellular mechanisms and facilitating drug discovery. Although high-throughput experimental methods have expanded the known interactome, they remain resourceintensive and prone to noise. Consequently, computational approaches...
Pantelis Makrygiannis, Nikitas-Rigas Kalogeropoulos, Agorakis Bompotas et al.· International journal on art...· 0 citations
This article systematically reviews the technical architecture and core algorithm modules of AlphaFold3, and looks forward to the application progress in the construction of protein-ligand complex structures, including the improvement in the confidence of pocket-type ligands paired with G protein-coupled receptors comp...
K. Tang· Theoretical and Natural Scie...· 0 citations
Abstract For more than 50 years, the linear sequence and the multiple sequence alignment have been the foundational data structures of protein science, and they remain central to homology search, phylogenetic inference, covariance-based contact prediction, and modern protein language models. However, relational and gra...
Dana S. Matthews, S. B. Pulsford, Anthony Barancewicz et al.· Biochemical Journal· 0 citations
Protein–protein interactions (PPIs) play a crucial role in enabling proteins to carry out their functions within various biological processes (Hui et al., 2003). Since the introduction of the yeast two-hybrid (Y2H) method for PPI detection in 1989 (Fields and Song, 1989), the identification of PPIs has become a signifi...