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 Zinc finger protein ubi-d4 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 Zinc finger protein ubi-d4 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 Zinc finger protein ubi-d4, 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 Zinc finger protein ubi-d4. 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 Zinc finger protein ubi-d4. 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 Zinc finger protein ubi-d4 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.
Zinc finger protein ubi-d4
partner:
Reaxense
upacc:
Q92785
UPID:
REQU_HUMAN
Alternative names:
Apoptosis response zinc finger protein; BRG1-associated factor 45D; D4, zinc and double PHD fingers family 2; Protein requiem
Alternative UPACC:
Q92785; A8K7C9; B4DT58
Background:
Zinc finger protein ubi-d4, also known as Apoptosis response zinc finger protein, BRG1-associated factor 45D, D4, zinc and double PHD fingers family 2, and Protein requiem, plays a pivotal role in transcriptional regulation. It achieves this by binding to modified histones H3 and H4, acting as a negative regulator of myeloid differentiation in hematopoietic progenitor cells, and possibly influencing the development and maturation of lymphoid cells. Additionally, it is involved in the regulation of the non-canonical NF-kappa-B pathway.
Therapeutic significance:
Zinc finger protein ubi-d4 is implicated in Coffin-Siris syndrome 7, a genetic disorder characterized by intellectual disability, coarse facial features, and other systemic malformations. Understanding the role of Zinc finger protein ubi-d4 could open doors to potential therapeutic strategies for this syndrome.
