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.
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.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We utilise our cutting-edge, exclusive workflow to develop focused 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 is unique due to several crucial aspects:
partner
Reaxense
upacc
O60343
UPID:
TBCD4_HUMAN
Alternative names:
Akt substrate of 160 kDa
Alternative UPACC:
O60343; A7E2X8; B4DU25; B4E235; B6ETN8; B6ETN9; Q5W0B9; Q68D14
Background:
TBC1 domain family member 4, also known as Akt substrate of 160 kDa, plays a crucial role in cellular processes by acting as a GTPase-activating protein for RAB2A, RAB8A, RAB10, and RAB14. Its involvement in insulin-induced glucose transporter SLC2A4/GLUT4 translocation highlights its significance in glucose uptake mechanisms.
Therapeutic significance:
The protein's association with Type 2 diabetes mellitus 5, a disorder characterized by insulin resistance and metabolic syndrome, underscores its therapeutic potential. Targeting this protein could lead to innovative treatments for managing diabetes and its complications, improving patient outcomes.