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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
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
Q8N9W5
UPID:
DAAF3_HUMAN
Alternative names:
-
Alternative UPACC:
Q8N9W5; A8MUY0; E3W9A1; E9PAX5; Q6P4F6; Q8N9W0; Q96AR2
Background:
Dynein axonemal assembly factor 3 plays a crucial role in the assembly of axonemal inner and outer dynein arms, essential for ciliary function. This protein is pivotal in the preassembly of dyneins into complexes, facilitating their transport into cilia, thereby ensuring proper ciliary motility and structure.
Therapeutic significance:
Given its fundamental role in ciliary function, Dynein axonemal assembly factor 3 is directly linked to Primary Ciliary Dyskinesia, particularly type 2, characterized by motile cilia abnormalities. Understanding the role of Dynein axonemal assembly factor 3 could open doors to potential therapeutic strategies for treating or managing this condition.