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 F-box only protein 11 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 F-box only protein 11 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 F-box only protein 11, 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 F-box only protein 11. 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 F-box only protein 11. 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 F-box only protein 11 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.
F-box only protein 11
partner:
Reaxense
upacc:
Q86XK2
UPID:
FBX11_HUMAN
Alternative names:
Protein arginine N-methyltransferase 9; Vitiligo-associated protein 1
Alternative UPACC:
Q86XK2; A1L491; Q52ZP1; Q53EP7; Q53RT5; Q8IXG3; Q96E90; Q9H6V8; Q9H9L1; Q9NR14; Q9UFK1; Q9UHI1; Q9UKC2
Background:
F-box only protein 11, also known as Protein arginine N-methyltransferase 9 and Vitiligo-associated protein 1, plays a crucial role in cellular processes. It acts as a substrate recognition component of the SCF E3 ubiquitin-protein ligase complex, targeting proteins like DTL/CDT2, BCL6, and PRDM1/BLIMP1 for ubiquitination and proteasomal degradation. This protein is pivotal in TGF-beta signaling, cell migration, cell-cycle progression, and the neddylating of phosphorylated p53/TP53, inhibiting its transcriptional activity.
Therapeutic significance:
F-box only protein 11's involvement in Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities highlights its potential as a therapeutic target. Understanding its role could open doors to novel strategies for treating this developmental disorder and possibly other related conditions.
