Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher activity, selectivity, and safety.
We pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
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.
Our high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q6QNY0
UPID:
BL1S3_HUMAN
Alternative names:
-
Alternative UPACC:
Q6QNY0; B2RXB8
Background:
Biogenesis of lysosome-related organelles complex 1 subunit 3 plays a crucial role in the formation and function of lysosome-related organelles, such as melanosomes and platelet dense granules. It is part of the BLOC-1 complex, essential for directing membrane protein cargos into vesicles for delivery into neurites and nerve terminals, and is involved in neurite extension.
Therapeutic significance:
The protein is implicated in Hermansky-Pudlak syndrome 8, characterized by oculocutaneous albinism, bleeding disorders, and lysosomal storage defects. Understanding its role could lead to novel therapeutic strategies for this syndrome.