9M3N: Human TRIM21 PRYSPRY

Crystal structure of human TRIM21 PRYSPRY in complex with T-02. Determined by X-ray diffraction at 2.08 Å resolution. Released 16 Jul 2025.

Method
X-ray diffraction
Resolution
2.08 Å
Organism
Homo sapiens
Chains
1
Atoms
1,516
Mol. weight
20.82 kDa
Ligands
A1EMT
Released
16 Jul 2025

Explore 9M3N in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

9M3N contains 2 α-helices and 17 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 2 helices, 17 β-strands

ElementResiduesLengthSheet
β-strand28611
β-strand29112
β-strand300-30231
β-strand308-31141
β-strand331-33223
β-strand33312
β-strand33713
β-strand341-34771
β-strand354-36073
α-helix373-3753
β-strand377-38373
β-strand387-39043
β-strand396-39833
β-strand406-41271
β-strand417-42261
β-strand428-43361
β-strand442-44763
α-helix458-4592
β-strand460-46231

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
E3 ubiquitin-protein ligase TRIM21Aprotein180Homo sapiensP19474 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>9M3N_1 E3 ubiquitin-protein ligase TRIM21 (chains A)
CAVHITLDPDTANPWLILSEDRRQVRLGDTQQSIPGNEERFDSYPMVLGAQHFHSGKHYW
EVDVTGKEAWDLGVCRDSVRRKGHFLLSSKSGFWTIWLWNKQKYEAGTYPQTPLHLQVPP
CQVGIFLDYEAGMVSFYNITDHGSLIYSFSECAFTGPLRPFFSPGFNDGGKNTAPLTLCP

Ligands and cofactors

IDNameFormulaCopies
A1EMT1-ethyl-~{N}-methyl-5-phenyl-~{N}-[3-[3-(trifluoromethyl)phenyl]cyclobutyl]pyra…C24 H24 F3 N3 O1

Primary citation

TRIM21-Driven Degradation of BRD4: Development of Heterobifunctional Degraders and Investigation of Recruitment and Selectivity Mechanisms. Zhang, L., Wang, Q., Li, X. et al. J Chem Inf Model (2025) 65:7584-7604. DOI 10.1021/acs.jcim.5c00473 · PubMed

Other PDB entries of the same protein (UniProt P19474 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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