Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

8PD4

Crystal structure of TRIM58 PRY-SPRY domain

Summary for 8PD4
Entry DOI10.2210/pdb8pd4/pdb
DescriptorE3 ubiquitin-protein ligase TRIM58 (2 entities in total)
Functional Keywordse3 ligase, trim58, pry-spry, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight48469.13
Authors
Renatus, M.,Schroeder, M. (deposition date: 2023-06-11, release date: 2024-01-31, Last modification date: 2024-02-07)
Primary citationHoegenauer, K.,An, S.,Axford, J.,Benander, C.,Bergsdorf, C.,Botsch, J.,Chau, S.,Fernandez, C.,Gleim, S.,Hassiepen, U.,Hunziker, J.,Joly, E.,Keller, A.,Lopez Romero, S.,Maher, R.,Mangold, A.S.,Mickanin, C.,Mihalic, M.,Neuner, P.,Patterson, A.W.,Perruccio, F.,Roggo, S.,Scesa, J.,Schroder, M.,Shkoza, D.,Thai, B.,Vulpetti, A.,Renatus, M.,Reece-Hoyes, J.S.
Discovery of Ligands for TRIM58, a Novel Tissue-Selective E3 Ligase.
Acs Med.Chem.Lett., 14:1631-1639, 2023
Cited by
PubMed Abstract: Redirecting E3 ligases to neo-substrates, leading to their proteasomal disassembly, known as targeted protein degradation (TPD), has emerged as a promising alternative to traditional, occupancy-driven pharmacology. Although the field has expanded tremendously over the past years, the choice of E3 ligases remains limited, with an almost exclusive focus on CRBN and VHL. Here, we report the discovery of novel ligands to the PRY-SPRY domain of TRIM58, a RING ligase that is specifically expressed in erythroid precursor cells. A DSF screen, followed by validation using additional biophysical methods, led to the identification of TRIM58 ligand . A basic SAR around the chemotype was established by utilizing a competitive binding assay employing a short FP peptide probe derived from an endogenous TRIM58 substrate. The X-ray co-crystal structure of TRIM58 in complex with gave insights into the binding mode and potential exit vectors for bifunctional degrader design.
PubMed: 38116426
DOI: 10.1021/acsmedchemlett.3c00259
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.714 Å)
Structure validation

238895

数据于2025-07-16公开中

PDB statisticsPDBj update infoContact PDBjnumon