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PDBsum entry 2cik
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Immune system/peptide
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PDB id
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2cik
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Contents |
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* Residue conservation analysis
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PDB id:
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Immune system/peptide
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Title:
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Insights into crossreactivity in human allorecognition: the structure of hla-b35011 presenting an epitope derived from cytochrome p450.
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Structure:
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Hla class i histocompatibility antigen b-35 alpha chain. Chain: a. Fragment: residues 25-300. Synonym: hla-b3501, mhc class i antigen b 35, Hla class i histocompatibility antigen b3501 heavy chain, b350101, b35011, b35, b35, b3501. Engineered: yes. Beta-2-microglobulin. Chain: b.
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Expressed in: escherichia coli. Expression_system_taxid: 562. Expression_system_variant: (de3)plyss. Synthetic: yes. Other_details: peptide epitope from human cytochrome p450 isoforms iic8, iic9, iic10 and iic18
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Biol. unit:
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Trimer (from PDB file)
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Resolution:
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1.75Å
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R-factor:
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0.198
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R-free:
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0.227
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Authors:
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C.S.Hourigan,M.Harkiolaki,N.A.Peterson,J.I.Bell,E.Y.Jones, C.A.O'Callaghan
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Key ref:
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C.S.Hourigan
et al.
(2006).
The structure of the human allo-ligand HLA-B*3501 in complex with a cytochrome p450 peptide: steric hindrance influences TCR allo-recognition.
Eur J Immunol,
36,
3288-3293.
PubMed id:
DOI:
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Date:
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22-Mar-06
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Release date:
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25-Oct-06
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PROCHECK
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Headers
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References
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DOI no:
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Eur J Immunol
36:3288-3293
(2006)
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PubMed id:
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The structure of the human allo-ligand HLA-B*3501 in complex with a cytochrome p450 peptide: steric hindrance influences TCR allo-recognition.
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C.S.Hourigan,
M.Harkiolaki,
N.A.Peterson,
J.I.Bell,
E.Y.Jones,
C.A.O'Callaghan.
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ABSTRACT
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Virus-specific T cell populations have been implicated in allo-recognition. The
subdominant T cell receptor JL12 recognizes both HLA-B*0801 presenting the
Epstein-Barr virus-derived peptide FLRGRAYGL and also HLA-B*3501 presenting the
cytochrome p450 self peptide KPIVVLHGY. This cross-reactivity could promote the
rejection of HLA-B*3501-positive cells in Epstein-Barr virus-exposed HLA-B*0801
recipients. LC13, the dominant TCR against the HLA-B*0801:FLRGRAYGL complex,
fails to recognize HLA-B*3501:KPIVVLHGY. We report the 1.75-Angstrom resolution
crystal structure of the human allo-ligand HLA-B*3501:KPIVVLHGY. Similarities
between this structure and that of HLA-B*0801:FLRGRAYGL may facilitate
cross-recognition by JL12. Moreover, the elevated peptide position in
HLA-B*3501:KPIVVLHGY would provide steric hindrance to LC13, preventing it from
interacting in the manner in which it interacts with HLA-B*0801:FLRGRAYGL. These
findings are relevant to understanding the basis of T cell cross-reactivity in
allo-recognition, optimal transplant donor-recipient matching and developing
specific molecular inhibitors of allo-recognition.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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S.Gras,
L.Kedzierski,
S.A.Valkenburg,
K.Laurie,
Y.C.Liu,
J.T.Denholm,
M.J.Richards,
G.F.Rimmelzwaan,
A.Kelso,
P.C.Doherty,
S.J.Turner,
J.Rossjohn,
and
K.Kedzierska
(2010).
Cross-reactive CD8+ T-cell immunity between the pandemic H1N1-2009 and H1N1-1918 influenza A viruses.
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Proc Natl Acad Sci U S A,
107,
12599-12604.
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PDB codes:
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T.G.Tan,
E.Mui,
H.Cong,
W.H.Witola,
A.Montpetit,
S.P.Muench,
J.Sidney,
J.Alexander,
A.Sette,
M.E.Grigg,
A.Maewal,
and
R.McLeod
(2010).
Identification of T. gondii epitopes, adjuvants, and host genetic factors that influence protection of mice and humans.
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Vaccine,
28,
3977-3989.
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A.Wahl,
W.McCoy,
F.Schafer,
W.Bardet,
R.Buchli,
D.H.Fremont,
and
W.H.Hildebrand
(2009).
T-cell tolerance for variability in an HLA class I-presented influenza A virus epitope.
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J Virol,
83,
9206-9214.
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P.Kumar,
A.Vahedi-Faridi,
W.Saenger,
E.Merino,
J.A.López de Castro,
B.Uchanska-Ziegler,
and
A.Ziegler
(2009).
Structural basis for T cell alloreactivity among three HLA-B14 and HLA-B27 antigens.
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J Biol Chem,
284,
29784-29797.
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PDB codes:
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
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