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.
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
Q9Y2M5
UPID:
KLH20_HUMAN
Alternative names:
Kelch-like ECT2-interacting protein; Kelch-like protein X
Alternative UPACC:
Q9Y2M5; B3KMA0; B4DUR0; Q5TZF2; Q5ZF45; Q9H457
Background:
Kelch-like protein 20, also known as Kelch-like ECT2-interacting protein, plays a pivotal role in various cellular processes. It acts as a substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex, influencing interferon response, anterograde Golgi to endosome transport, apoptosis regulation, angiogenesis, and neurite outgrowth. This protein mediates the ubiquitination of DAPK1, leading to its degradation, and is involved in 'Lys-33'-linked ubiquitination of CORO7 and PDZ-RhoGEF/ARHGEF11.
Therapeutic significance:
Understanding the role of Kelch-like protein 20 could open doors to potential therapeutic strategies.