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.
We pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate 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 employ our advanced, specialised process to create targeted 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
Q9Y4W6
UPID:
AFG32_HUMAN
Alternative names:
Paraplegin-like protein
Alternative UPACC:
Q9Y4W6; Q6P1L0
Background:
AFG3-like protein 2, also known as Paraplegin-like protein, plays a pivotal role in axonal and neuron development. It is an ATP-dependent protease essential for the degradation of specific mitochondrial proteins, facilitating neuron health and function. This protein is involved in the maturation of several key proteins within the mitochondria, including paraplegin and PINK1, and regulates mitochondrial dynamics through its interaction with OPA1 and GHITM.
Therapeutic significance:
AFG3-like protein 2 is linked to several neurodegenerative disorders, including Spinocerebellar ataxia 28, Spastic ataxia 5, and Optic atrophy 12. These associations underscore its potential as a target for therapeutic intervention in these diseases. Understanding the role of AFG3-like protein 2 could open doors to potential therapeutic strategies, offering hope for patients suffering from these debilitating conditions.