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.
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 employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
P82663
UPID:
RT25_HUMAN
Alternative names:
28S ribosomal protein S25, mitochondrial
Alternative UPACC:
P82663; B4DFJ5; B4DQG6; Q9H7P5
Background:
Small ribosomal subunit protein mS25, also known as 28S ribosomal protein S25, mitochondrial, plays a crucial role in protein synthesis within mitochondria. Its involvement in the mitochondrial ribosome highlights its importance in cellular energy production and overall mitochondrial function.
Therapeutic significance:
The protein is linked to Combined oxidative phosphorylation deficiency 50, a disease characterized by growth retardation, delayed development, and muscle weakness, among other symptoms. Understanding the role of Small ribosomal subunit protein mS25 could open doors to potential therapeutic strategies for this mitochondrial disorder.