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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
The library includes a list of the most effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
We use our state-of-the-art dedicated workflow for designing focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
This approach involves comprehensive molecular simulations of the catalytic and allosteric binding pockets and ensemble virtual screening that accounts for their conformational flexibility. In the case of designing modulators, the structural adjustments caused by reaction intermediates are considered to improve activity and selectivity.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q9UPW5
UPID:
CBPC1_HUMAN
Alternative names:
ATP/GTP-binding protein 1; Nervous system nuclear protein induced by axotomy protein 1 homolog; Protein deglutamylase CCP1
Alternative UPACC:
Q9UPW5; B4DIT6; B4DRZ8; Q5VV80; Q63HM7; Q658P5; Q6P9D6; Q9H8U6; Q9H9W8; Q9NVK1
Background:
Cytosolic carboxypeptidase 1 (CCP1), also known as ATP/GTP-binding protein 1 and Nervous system nuclear protein induced by axotomy protein 1 homolog, plays a crucial role in protein deglutamylation. It specifically targets tubulin and non-tubulin proteins, facilitating the removal of polyglutamate side chains. This action is vital for the proper functioning of cellular structures and signaling pathways.
Therapeutic significance:
CCP1's involvement in the neurodegenerative disorder, childhood-onset neurodegeneration with cerebellar atrophy, underscores its therapeutic significance. Understanding CCP1's role could pave the way for innovative treatments targeting this and potentially other neurodegenerative diseases.