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.
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 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 is unique due to several crucial aspects:
partner
Reaxense
upacc
Q8NDL9
UPID:
CBPC5_HUMAN
Alternative names:
ATP/GTP-binding protein-like 5; Protein deglutamylase CCP5
Alternative UPACC:
Q8NDL9; A2VDI7; B7WPG9; B7Z7I7; D6W548; Q53SW0; Q53SZ0; Q96IK8; Q9H6V0; Q9H8P8
Background:
Cytosolic carboxypeptidase-like protein 5, also known as Protein deglutamylase CCP5 and ATP/GTP-binding protein-like 5, plays a crucial role in cellular processes by mediating the deglutamylation of tubulin and non-tubulin target proteins. This enzyme is pivotal in the removal of polyglutamate side chains from the C-terminal tail of alpha- and beta-tubulin, facilitating proper cellular function and response.
Therapeutic significance:
The association of Cytosolic carboxypeptidase-like protein 5 with Retinitis pigmentosa 75, a retinal dystrophy, underscores its therapeutic significance. Understanding the role of this protein could open doors to potential therapeutic strategies for treating this and possibly other related diseases.