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

7X1C

Crystal structure of peptide VSFIEFVI in complex with HLA-B5801

Summary for 7X1C
Entry DOI10.2210/pdb7x1c/pdb
DescriptorHLA-B, Beta-2-microglobulin, VAL-SER-PHE-ILE-GLU-PHE-VAL-ILE, ... (5 entities in total)
Functional Keywordsimmune system, human leukocyte antigen
Biological sourceHomo sapiens (human)
More
Total number of polymer chains3
Total formula weight44886.83
Authors
Huan, X.,Ren, E.C. (deposition date: 2022-02-23, release date: 2023-05-03, Last modification date: 2024-11-06)
Primary citationHuan, X.,Zhuo, N.,Lee, H.Y.,Ren, E.C.
Allopurinol non-covalently facilitates binding of unconventional peptides to HLA-B*58:01.
Sci Rep, 13:9373-9373, 2023
Cited by
PubMed Abstract: Allopurinol, widely used in gout treatment, is the most common cause of severe cutaneous adverse drug reactions. The risk of developing such life-threatening reactions is increased particularly for HLA-B*58:01 positive individuals. However the mechanism of action between allopurinol and HLA remains unknown. We demonstrate here that a Lamin A/C peptide KAGQVVTI which is unable to bind HLA-B*58:01 on its own, is enabled to form a stable peptide-HLA complex only in the presence of allopurinol. Crystal structure analysis reveal that allopurinol non-covalently facilitated KAGQVVTI to adopt an unusual binding conformation, whereby the C-terminal isoleucine does not engage as a PΩ that typically fit deeply in the binding F-pocket. A similar observation, though to a lesser degree was seen with oxypurinol. Presentation of unconventional peptides by HLA-B*58:01 aided by allopurinol contributes to our fundamental understanding of drug-HLA interactions. The binding of peptides from endogenously available proteins such as self-protein lamin A/C and viral protein EBNA3B suggest that aberrant loading of unconventional peptides in the presence of allopurinol or oxypurinol may be able to trigger anti-self reactions that can lead to Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) and Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS).
PubMed: 37296297
DOI: 10.1038/s41598-023-36293-z
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.409 Å)
Structure validation

237423

PDB entries from 2025-06-11

PDB statisticsPDBj update infoContact PDBjnumon