AI-ACCELERATED DRUG DISCOVERY
Available from Reaxense
This protein is integrated into the Receptor.AI ecosystem as a prospective target with high therapeutic potential. We performed a comprehensive characterization of Sortilin-related receptor including:
1. LLM-powered literature research
Our custom-tailored LLM extracted and formalized all relevant information about the protein from a large set of structured and unstructured data sources and stored it in the form of a Knowledge Graph. This comprehensive analysis allowed us to gain insight into Sortilin-related receptor therapeutic significance, existing small molecule ligands, relevant off-targets, and protein-protein interactions.
Fig. 1. Preliminary target research workflow
2. AI-Driven Conformational Ensemble Generation
Starting from the initial protein structure, we employed advanced AI algorithms to predict alternative functional states of Sortilin-related receptor, including large-scale conformational changes along "soft" collective coordinates. Through molecular simulations with AI-enhanced sampling and trajectory clustering, we explored the broad conformational space of the protein and identified its representative structures. Utilizing diffusion-based AI models and active learning AutoML, we generated a statistically robust ensemble of equilibrium protein conformations that capture the receptor's full dynamic behavior, providing a robust foundation for accurate structure-based drug design.
Fig. 2. AI-powered molecular dynamics simulations workflow
3. Binding pockets identification and characterization
We employed the AI-based pocket prediction module to discover orthosteric, allosteric, hidden, and cryptic binding pockets on the protein’s surface. Our technique integrates the LLM-driven literature search and structure-aware ensemble-based pocket detection algorithm that utilizes previously established protein dynamics. Tentative pockets are then subject to AI scoring and ranking with simultaneous detection of false positives. In the final step, the AI model assesses the druggability of each pocket enabling a comprehensive selection of the most promising pockets for further targeting.
Fig. 3. AI-based binding pocket detection workflow
4. AI-Powered Virtual Screening
Our ecosystem is equipped to perform AI-driven virtual screening on Sortilin-related receptor. With access to a vast chemical space and cutting-edge AI docking algorithms, we can rapidly and reliably predict the most promising, novel, diverse, potent, and safe small molecule ligands of Sortilin-related receptor. This approach allows us to achieve an excellent hit rate and to identify compounds ready for advanced lead discovery and optimization.
Fig. 4. The screening workflow of Receptor.AI
Receptor.AI, in partnership with Reaxense, developed a next-generation technology for on-demand focused library design to enable extensive target exploration.
The focused library for Sortilin-related receptor includes a list of the most effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
Sortilin-related receptor
partner:
Reaxense
upacc:
Q92673
UPID:
SORL_HUMAN
Alternative names:
Low-density lipoprotein receptor relative with 11 ligand-binding repeats; SorLA-1; Sorting protein-related receptor containing LDLR class A repeats
Alternative UPACC:
Q92673; B2RNX7; Q92856
Background:
The Sortilin-related receptor, also known as SorLA-1, plays a pivotal role in directing proteins to their correct cellular locations. It is crucial in the sorting of the amyloid precursor protein (APP) and its subsequent processing, which is linked to Alzheimer's disease. SorLA-1's involvement in the trafficking of various receptors and enzymes underscores its significance in cellular signaling and homeostasis.
Therapeutic significance:
Given its central role in the processing of APP and the formation of amyloid-beta peptides, SorLA-1 emerges as a promising target in Alzheimer's disease research. Understanding the role of SorLA-1 could open doors to potential therapeutic strategies aimed at mitigating the progression of this debilitating neurodegenerative disorder.
