Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved 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.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
P36871
UPID:
PGM1_HUMAN
Alternative names:
Glucose phosphomutase 1
Alternative UPACC:
P36871; B2R5N9; B4DPV0; Q16105; Q16106; Q5BKZ9; Q6NW22; Q86U74; Q96J40; Q9NTY4
Background:
Phosphoglucomutase-1 (PGM1), also known as Glucose phosphomutase 1, plays a pivotal role in glucose metabolism by facilitating both the synthesis and breakdown of glucose. This enzyme's versatility underscores its importance in maintaining glucose homeostasis, a critical aspect of cellular energy management.
Therapeutic significance:
PGM1's link to Congenital disorder of glycosylation 1T, a condition marked by a spectrum of clinical features including developmental and immunological deficits, highlights its therapeutic potential. Targeting PGM1-related pathways could offer novel interventions for managing this disorder, emphasizing the enzyme's significance in medical research.