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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
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.
Our top-notch dedicated system is used to design specialised 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
P62854
UPID:
RS26_HUMAN
Alternative names:
40S ribosomal protein S26
Alternative UPACC:
P62854; P02383; P70394; Q06722; Q3MHD8; Q6IRY4
Background:
Small ribosomal subunit protein eS26, also known as 40S ribosomal protein S26, plays a crucial role in the synthesis of proteins within the cell. As a component of the small ribosomal subunit, it is pivotal in translating mRNA into amino acid sequences, thereby facilitating the production of proteins essential for cellular function and growth.
Therapeutic significance:
The protein is linked to Diamond-Blackfan anemia 10, a rare disorder characterized by anemia, congenital anomalies, and an increased risk of malignancy. Understanding the role of Small ribosomal subunit protein eS26 could open doors to potential therapeutic strategies for this condition.