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 features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q86YV9
UPID:
HPS6_HUMAN
Alternative names:
Hermansky-Pudlak syndrome 6 protein; Ruby-eye protein homolog
Alternative UPACC:
Q86YV9; Q5VV69; Q9H685
Background:
The BLOC-2 complex member HPS6, also known as Hermansky-Pudlak syndrome 6 protein or Ruby-eye protein homolog, plays a pivotal role in cellular organelle function. It is instrumental in regulating lysosome synthesis and function, as well as the function of specialized organelles like melanosomes and platelet dense granules. HPS6 facilitates the transport of lysosomes within cells, ensuring their proper positioning, which is crucial for lysosome maturation and function.
Therapeutic significance:
HPS6 is directly linked to Hermansky-Pudlak syndrome 6, a disorder characterized by oculocutaneous albinism, bleeding issues, and lysosomal storage defects, leading to conditions such as pulmonary fibrosis. Understanding the role of HPS6 could open doors to potential therapeutic strategies for treating or managing this syndrome.