Protein: GID4
PDB ID: 8V1P
Deposition Date: Tuesday 21st November 2023
Authors: Dong, C., Dong, A., Calabrese, M., Wang, F., Owen, D., Arrowsmith, C.H., Edwards, A.M., Min, J.

SGC in the Open

Our blog posts are home to inspiring stories, insights, and updates from the forefront of our research. 

Within these pages, you will discover articles that showcase our latest discoveries, collaborative projects, and the impact of our open-access approach. This section offers a behind-the-scenes look at the innovative work unfolding at the SGC, featuring contributions from our scientists, partners, and community members. Interested in getting first the latest news from SGC?

 
13.03.2024

Structural Genomics Consortium Principal Investigators Receive $4.3 Million Infrastructure Award to Transform Early Drug Discovery at the University of Toronto

by: SGC

Toronto, March 13, 2024 – The Structural Genomics Consortium’s (SGC) Principal Investigators at the University of Toronto have been awarded a $4.3-million infrastructure award from the Canada Foundation for Innovation (CFI) and the Ontario Research Fund (ORF) through the 2023 Innovation Fund competition.

12.03.2024

Insights and Lessons Learned: Highlights from the CACHE Symposium

by: SGC

Last week, the inaugural CACHE Symposium brought together leading experts in the field of computational chemistry and artificial intelligence to share their insights and experiences on advancing the field of computational hit finding and collaborating through open science.

07.03.2024

Shaping Tomorrow: The Women Leading Open Science Advancements at the Structural Genomics Consortium [Part 2]

by: SGC

Imagine being part of a world that shapes the future yet feeling invisible within it. This is the reality for women in STEM, who are nearly twice as likely as those in other fields to contemplate leaving their careers behind. The culprits? Overwhelming burnout, overlooked achievements, wage disparities, and a yearning for work that resonates on a deeper level.

To celebrate the International Day of Women and Girls in STEM earlier this year, I had the chance to interview a dynamic and global network of female scientists, who actively work to accelerate early drug discovery.

04.03.2024

Structural Genomics Principal Investigators to receive more than $3 million from CIHR’s Fall 2023 Project Grant competition.

by: SGC

SGC's CIHR Award recipients. (L-R): Drs. Cheryl Arrowsmith, Matthieu Schapira, and Dalia Barsyte-Lovejoy.

The Canadian Institutes of Health Research (CIHR) has recently released the results of its Fall 2023 Project Grant funding competition. This competition aims to provide financial support to projects that will advance knowledge, research methodologies, patient care, and overall health outcomes.

TP-061 A chemical probe to Brr2.

The probe and control may be requested here.

overview
Probe Negative control
 

TP-061

 

TP-061N

Bad response to refrigeration 2 (Brr2) is a 200 kDa protein and a member of DEXD/H-box helicase constituting a part of U5 snRNP. Brr2 catalyzes an ATP-dependent unwinding of the U4/U6 RNA duplex, which is a critical step in the activation of spliceosome.

 

Takeda in collaboration with the University of Oxford and OICR has developed TP-061 as a potent inhibitor of Brr2. TP-061 exhibits IC50 of 21 nM in the ADP-Glo ATPase assay and 480 nM in the unwinding assay. Target binding is confirmed by SPR with Kd of 22 nM. The enantiomer, TP-061N, serves as an ideal negative control with IC50 of 84 mM in the ATPase assay.

 

properties
selectivity profile

TP-061 shows excellent selectivity over closely-related helicases, with no inhibition of eIF4A1, eIF4A3 and DHX29 up to 100 mM.

 

Additional selectivity over 300 kinases using in-house assay showed none with inhibition > 50% when tested at 1 mM.

in vitro potency
cell based assay data

 

 

references

Ito et. al. Discovery of spiro[indole-3,20-pyrrolidin]-2(1H)-one based inhibitors targeting Brr2, a core component of the U5 snRNP. Bioorg Med Chem., 2017, 25, 4753-4767, https://doi.org/10.1016/j.bmc.2017.07.017.

pk properties
co-crystal structures
synthetic schemes
materials and methods

SGC-UBD1031 A probe with dual USP16-HDAC6 activity.

The probe and control may be requested here.

overview
Probe Negative control

 

SGC-UBD1031

 

SGC-UBD1031N

SGC in collaboration with Dr Mark Lautens’ at the University of Toronto’s Department of Chemistry has developed the first chemical probe SGC-UBD1031 for the ubiquitin binding domain (UBD) of USP16. SGC-UBD1031 has equipotent affinity to HDAC6 UBD and it is recommended to be used in parallel with SGC-UBD253.

SGC-UBD1031 binds potently to USP16 UBD with KD = 48 nM (SPR), and in cells it inhibits the USP16-ISG15 interaction with EC50 = 1.7 micromolar (nanoBRET). 

SGC-UBD1031N is a closely related negative control with no activity in the nanoBRET assay up to 30 micromolar. 

properties
selectivity profile
in vitro potency
cell based assay data
references
pk properties
co-crystal structures
synthetic schemes
materials and methods

An Overview of SGC Initiatives

The SGC has dedicated the past twenty years to advancing scientific knowledge by freely distributing research tools, data, and technologies. With over half of human genes and their corresponding proteins still largely unexplored, and many diseases poorly understood, SGC focuses on increasing research into these understudied areas – but can’t do it alone! Our mission involves a global call to action, encouraging collaboration across continents and sectors to address critical challenges in drug discovery and biological research.