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.
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.
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.
Our high-tech, dedicated method is applied to construct targeted 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 stands out due to several important features:
partner
Reaxense
upacc
Q8NFJ9
UPID:
BBS1_HUMAN
Alternative names:
BBS2-like protein 2
Alternative UPACC:
Q8NFJ9; Q32MM9; Q32MN0; Q96SN4
Background:
The Bardet-Biedl syndrome 1 protein, also known as BBS2-like protein 2, plays a pivotal role in ciliogenesis and the sorting of specific membrane proteins to the primary cilia. It is part of the BBSome complex, essential for the formation of cilia and for the sonic hedgehog (SHH) pathway regulation. This protein's function is crucial in olfactory cilium biogenesis and maintenance.
Therapeutic significance:
Given its involvement in Bardet-Biedl syndrome 1, characterized by severe pigmentary retinopathy, obesity, and other systemic manifestations, understanding the Bardet-Biedl syndrome 1 protein could open doors to potential therapeutic strategies for this autosomal recessive disorder.