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.
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.
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 top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
P54845
UPID:
NRL_HUMAN
Alternative names:
-
Alternative UPACC:
P54845; A8MX14; Q53XD0
Background:
The Neural retina-specific leucine zipper protein, identified by the accession number P54845, plays a pivotal role in the visual system. It acts as a transcriptional activator, regulating the expression of rod-specific genes such as RHO and PDE6B, and functions as a coactivator for CRX and NR2E3. Its binding to the rhodopsin promoter is sequence-specific, highlighting its importance in vision.
Therapeutic significance:
Linked to Retinitis pigmentosa 27 and Retinal degeneration autosomal recessive clumped pigment type, this protein's dysfunction underscores its therapeutic potential. Understanding its role could lead to breakthroughs in treating these retinal dystrophies, offering hope for restoring vision or halting disease progression.