Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
P42701
UPID:
I12R1_HUMAN
Alternative names:
IL-12 receptor beta component
Alternative UPACC:
P42701; A8K308; B2RPF1; B7ZKK3; Q8N6Q7
Background:
The Interleukin-12 receptor subunit beta-1, also known as IL-12 receptor beta component, plays a crucial role in the immune system. It functions as an interleukin receptor that binds interleukin-12 with low affinity and is pivotal in IL12 signal transduction. This receptor, in association with IL12RB2, forms a high affinity receptor for IL12. It also associates with IL23R to form the interleukin-23 receptor, which is essential in IL23 signal transduction, likely through the activation of the Jak-Stat signaling cascade.
Therapeutic significance:
Given its involvement in Immunodeficiency 30, a condition characterized by impaired interferon-gamma mediated immunity leading to susceptibility to mycobacterial diseases, the Interleukin-12 receptor subunit beta-1 represents a potential target for therapeutic intervention. Understanding the role of this protein could open doors to potential therapeutic strategies for managing this immunodeficiency and its associated infections.