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PDBsum entry 3vxt

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protein Protein-protein interface(s) links
Immune system PDB id
3vxt

 

 

 

 

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Contents
Protein chains
199 a.a.
241 a.a.
Waters ×108
PDB id:
3vxt
Name: Immune system
Title: T36-5 tcr specific for hla-a24-nef134-10
Structure: T36-5 tcr alpha chain. Chain: c, a. Engineered: yes. T36-5 tcr beta chain. Chain: d, b. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.50Å     R-factor:   0.230     R-free:   0.271
Authors: A.Shimizu,S.Fukai,A.Yamagata,A.Iwamoto
Key ref: A.Shimizu et al. (2013). Structure of TCR and antigen complexes at an immunodominant CTL epitope in HIV-1 infection. Sci Rep, 3, 3097. PubMed id: 24192765 DOI: 10.1038/srep03097
Date:
20-Sep-12     Release date:   23-Oct-13    
PROCHECK
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 Headers
 References

Protein chains
No UniProt id for this chain
Struc: 199 a.a.
Protein chains
No UniProt id for this chain
Struc: 241 a.a.
Key:    Secondary structure  CATH domain

 

 
DOI no: 10.1038/srep03097 Sci Rep 3:3097 (2013)
PubMed id: 24192765  
 
 
Structure of TCR and antigen complexes at an immunodominant CTL epitope in HIV-1 infection.
A.Shimizu, A.Kawana-Tachikawa, A.Yamagata, C.Han, D.Zhu, Y.Sato, H.Nakamura, T.Koibuchi, J.Carlson, E.Martin, C.J.Brumme, Y.Shi, G.F.Gao, Z.L.Brumme, S.Fukai, A.Iwamoto.
 
  ABSTRACT  
 
We investigated the crystal structure of an HLA-A*2402-restricted CTL epitope in the HIV-1 nef gene (Nef134-10) before (pHLA) or after TCR docking. The wild type epitope and two escape mutants were included in the study. Y135F was an early-appearing major mutation, while F139L was a late-appearing mutation which was selected in the patients without Y135F. F139 was an eminent feature of the Nef134-10 epitope. Wild type-specific TCR was less fit to F139L mutant suggesting that F139L is an escape from the CTL against the wild type epitope. Although Y135F mutation disrupted the hydrogen bond to HLA-A*2402 His70, newly formed hydrogen bond between T138 and His70 kept the conformation of the epitope in the reconstituted pMHC. TCR from Y135F- or dually-specific CTL had unique mode of binding to the mutant epitope. Y135F has been reported as a processing mutant but CTL carrying structurally adequate TCR can be found in the patients.
 

 

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