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

9EK7

Crystal structure of MAIT TCR in complex with MR1-5FdU

Summary for 9EK7
Entry DOI10.2210/pdb9ek7/pdb
DescriptorMajor histocompatibility complex class I-related gene protein, SODIUM ION, TCR alpha, ... (11 entities in total)
Functional Keywordsreceptor, immune system
Biological sourceHomo sapiens (human)
More
Total number of polymer chains8
Total formula weight189619.86
Authors
Awad, W.,Rossjohn, J. (deposition date: 2024-12-01, release date: 2025-05-07, Last modification date: 2025-05-21)
Primary citationProta, G.,Berloffa, G.,Awad, W.,Vacchini, A.,Chancellor, A.,Schaefer, V.,Constantin, D.,Littler, D.R.,Colombo, R.,Nosi, V.,Mori, L.,Rossjohn, J.,De Libero, G.
Mitochondria regulate MR1 protein expression and produce self-metabolites that activate MR1-restricted T cells.
Proc.Natl.Acad.Sci.USA, 122:e2418525122-e2418525122, 2025
Cited by
PubMed Abstract: Mitochondria coordinate several metabolic pathways, producing metabolites that influence the immune response in various ways. It remains unclear whether mitochondria impact antigen presentation by the MHC-class-I-related antigen-presenting molecule, MR1, which presents small molecules to MR1-restricted T-lymphocytes. Here, we demonstrate that mitochondrial complex III and the enzyme dihydroorotate dehydrogenase are essential for the cell-surface expression of MR1 and for generating uridine- and thymidine-related compounds that bind to MR1 and are produced upon oxidation by reactive oxygen species. One mitochondria-derived immunogenic formylated metabolite we identified is 5-formyl-deoxyuridine (5-FdU). Structural studies indicate that 5-FdU binds in the A'-antigen-binding pocket of MR1, positioning the deoxyribose toward the surface of MR1 for TCR interaction. 5-FdU stimulates specific T cells and detects circulating T cells when loaded onto MR1-tetramers. 5-FdU-reactive cells resemble adaptive T cells and express the phenotypes of naïve, memory, and effector cells, indicating prior in vivo stimulation. These findings suggest that mitochondria may play a role in MR1-mediated immune surveillance.
PubMed: 40354545
DOI: 10.1073/pnas.2418525122
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.15 Å)
Structure validation

247536

PDB entries from 2026-01-14

PDB statisticsPDBj update infoContact PDBjnumon