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.
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 use our state-of-the-art dedicated workflow for designing focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
It includes comprehensive molecular simulations of the catalytic and allosteric binding pockets and the ensemble virtual screening accounting for their conformational mobility. In the case of designing modulators, the structural changes induced by reaction intermediates are taken into account to leverage activity and selectivity.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P15086
UPID:
CBPB1_HUMAN
Alternative names:
Pancreas-specific protein
Alternative UPACC:
P15086; O60834; Q53XJ0; Q96BQ8
Background:
Carboxypeptidase B, also known as Pancreas-specific protein, plays a crucial role in protein digestion by removing terminal amino acids from the peptide chain. This enzyme, encoded by the gene with the accession number P15086, is predominantly expressed in the pancreas and is essential for the proper breakdown and absorption of dietary proteins.
Therapeutic significance:
Understanding the role of Carboxypeptidase B could open doors to potential therapeutic strategies. Its pivotal function in protein metabolism suggests that modulating its activity could have implications for conditions related to protein digestion and absorption.