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.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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.
We use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q96DU3
UPID:
SLAF6_HUMAN
Alternative names:
Activating NK receptor; NK-T-B-antigen
Alternative UPACC:
Q96DU3; A6NMW2; B2R8X8; Q14CF0; Q5TAS4; Q5TAS6; Q5TAT3; Q96DV0
Background:
SLAM family member 6, also known as Activating NK receptor or NK-T-B-antigen, plays a pivotal role in immune regulation. It modulates the activation and differentiation of various immune cells, contributing to both innate and adaptive immune responses. This protein's function is influenced by the presence of adapter proteins SH2D1A/SAP and SH2D1B/EAT-2, which control its signaling pathways. It is particularly crucial in natural killer (NK) cell activation, T-cell differentiation into Th17 phenotype, and the regulation of germinal center formation.
Therapeutic significance:
Understanding the role of SLAM family member 6 could open doors to potential therapeutic strategies. Its involvement in key immune processes suggests its potential as a target in modulating immune responses, offering avenues for the development of treatments for immune-related disorders.