Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced 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.
The library 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.
Our high-tech, dedicated method is applied to construct targeted 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 distinguishes itself through several key 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.