Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better activity, selectivity, and safety.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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 employ our advanced, specialised process to create 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.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q8WXW3
UPID:
PIBF1_HUMAN
Alternative names:
Centrosomal protein of 90 kDa
Alternative UPACC:
Q8WXW3; O95664; Q6U9V2; Q6UG50; Q86V07; Q96SF4
Background:
Progesterone-induced-blocking factor 1, also known as Centrosomal protein of 90 kDa, is pivotal in ciliogenesis and maintaining mitotic spindle pole integrity. It facilitates the centrosomal accumulation of PCM1, aiding in primary cilia formation and centriole duplication. Its secreted form acts as a mediator of progesterone, influencing arachidonic acid metabolism and promoting a Th2 biased immune response.
Therapeutic significance:
Linked to Joubert syndrome 33, a disorder characterized by cerebellar ataxia and psychomotor delay, understanding the role of Progesterone-induced-blocking factor 1 could open doors to potential therapeutic strategies.