Focused On-demand Library for Transcription initiation factor TFIID subunit 10

Focused On-demand Libraries - Reaxense Collaboration

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.

From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.

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 employ our advanced, specialised process to create targeted libraries.

Fig. 1. The sreening workflow of Receptor.AI

Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.

Several key aspects differentiate our library:

Receptor.AI compiles an all-encompassing dataset on the target protein, including historical experiments, literature data, known ligands, and structural insights, maximising the chances of prioritising the most pertinent compounds.
The platform employs state-of-the-art molecular simulations to identify potential binding sites, ensuring the focused library is primed for discovering allosteric inhibitors and binders of concealed pockets.
Over 50 customisable AI models, thoroughly evaluated in various drug discovery endeavours and research projects, make Receptor.AI both efficient and accurate. This technology is integral to the development of our focused libraries.
In addition to generating focused libraries, Receptor.AI offers a full range of services and solutions for every step of preclinical drug discovery, with a pricing model based on success, thereby reducing risk and promoting joint project success.

partner

Reaxense

upacc

Q12962

UPID:

TAF10_HUMAN

Alternative names:

STAF28; Transcription initiation factor TFIID 30 kDa subunit

Alternative UPACC:

Q12962; O00703; Q13175; Q6FH13

Background:

Transcription initiation factor TFIID subunit 10, also known as TAF10, is a pivotal component of the TFIID basal transcription factor complex. This complex is essential for the initiation of RNA polymerase II-dependent transcription, recognizing and binding promoters to facilitate the assembly of the pre-initiation complex. TAF10's involvement extends to the PCAF histone acetylase complex, TFTC, and the STAGA transcription coactivator-HAT complex, highlighting its versatile role in transcription regulation.

Therapeutic significance:

Understanding the role of Transcription initiation factor TFIID subunit 10 could open doors to potential therapeutic strategies.