AI-ACCELERATED DRUG DISCOVERY

Protein sprouty homolog 4

Explore its Potential with AI-Driven Innovation
Predicted by Alphafold

Protein sprouty homolog 4 - Focused Library Design

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 Protein sprouty homolog 4 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 Protein sprouty homolog 4 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 Protein sprouty homolog 4, 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 Protein sprouty homolog 4. 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 Protein sprouty homolog 4. 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 Protein sprouty homolog 4 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.

Protein sprouty homolog 4

partner:

Reaxense

upacc:

Q9C004

UPID:

SPY4_HUMAN

Alternative names:

-

Alternative UPACC:

Q9C004; A4FVB2; A4FVB3; Q6QIX2; Q9C003

Background:

Protein sprouty homolog 4 plays a pivotal role in suppressing the insulin receptor and EGFR-transduced MAPK signaling pathways, crucial for cell growth and differentiation. It uniquely inhibits MAPK activation by a constitutively active mutant Ras, highlighting its specificity in cellular signaling modulation. Additionally, it represses integrin-mediated cell spreading, underscoring its importance in cell migration and adhesion processes.

Therapeutic significance:

Given its involvement in Hypogonadotropic hypogonadism 17 with or without anosmia, a disorder linked to impaired sexual maturation and sensory deficits, Protein sprouty homolog 4 presents a promising target for therapeutic intervention. Understanding its role could open doors to potential therapeutic strategies, especially considering its regulatory impact on critical signaling pathways and cell behavior.

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