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.
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 method includes detailed molecular simulations of the catalytic and allosteric binding pockets, along with ensemble virtual screening that considers their conformational flexibility. In the design of modulators, structural changes induced by reaction intermediates are taken into account to enhance activity and selectivity.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q9UL12
UPID:
SARDH_HUMAN
Alternative names:
BPR-2
Alternative UPACC:
Q9UL12; B2RMR5; B4DPI2; B7ZLT6; Q5SYV0; Q9Y280; Q9Y2Y3
Background:
Sarcosine dehydrogenase, mitochondrial, also known as BPR-2, plays a crucial role in the metabolic pathway, catalyzing the conversion of sarcosine into glycine. This process is vital for the oxidative degradation of choline to glycine, highlighting the enzyme's importance in metabolic regulation.
Therapeutic significance:
Sarcosinemia, a metabolic disorder linked to increased sarcosine levels, implicates BPR-2 in its pathology. Understanding the role of Sarcosine dehydrogenase could open doors to potential therapeutic strategies, offering hope for managing or treating conditions associated with altered sarcosine metabolism.