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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner 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.
We utilise our cutting-edge, exclusive workflow to develop focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
The procedure entails thorough molecular simulations of the catalytic and allosteric binding pockets, accompanied by ensemble virtual screening that factors in their conformational flexibility. When developing modulators, the structural modifications brought about by reaction intermediates are factored in to optimize activity and selectivity.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q8N653
UPID:
LZTR1_HUMAN
Alternative names:
-
Alternative UPACC:
Q8N653; Q14776; Q20WK0
Background:
Leucine-zipper-like transcriptional regulator 1 plays a pivotal role in the ubiquitination of Ras proteins, including K-Ras, N-Ras, and H-Ras. This process is crucial for the regulation of RAS-MAPK signaling, as it controls Ras levels and reduces its association with membranes, thereby acting as a negative regulator.
Therapeutic significance:
Given its involvement in gliomas, Schwannomatosis 2, and Noonan syndromes 10 and 2, understanding the role of Leucine-zipper-like transcriptional regulator 1 could pave the way for novel therapeutic strategies targeting these conditions. Its function in disease pathogenesis and susceptibility highlights its potential as a therapeutic target.