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Structure of a Complex of the Human α/β T Cell Receptor (TCR) HA1.7, Influenza Hemagglutinin Peptide, and Major Histocompatibility Complex Class II Molecule, HLA-DR4 (DRA0101 and DRB10401)

Language	Label	Description	Also known as
English	No label defined	scientific article	Structure of a Complex of the Human α/β T Cell Receptor (TCR) HA1.7, Influenza Hemagglutinin Peptide, and Major Histocompatibility Complex Class II Molecule, HLA-DR4 (DRA0101 and DRB10401)

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scholarly article

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Structure of a complex of the human alpha/beta T cell receptor (TCR) HA1.7, influenza hemagglutinin peptide, and major histocompatibility complex class II molecule, HLA-DR4 (DRA*0101 and DRB1*0401): insight into TCR cross-restriction and alloreactivity (English)

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author name string

Jens Hennecke

1

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Don C Wiley

2

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language of work or name

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publication date

4 March 2002

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Journal of Experimental Medicine

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195

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5

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571-81

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1 reference

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1 reference

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1 reference

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

T cell receptor antagonism mediated by interaction between T cell receptor junctional residues and peptide antigen analogues

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

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based on heuristic

inferred from PubMed ID database lookup

Reversal of HLA restriction by a point mutation in an antigenic peptide

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA DR4w4-binding motifs illustrate the biochemical basis of degeneracy and specificity in peptide-DR interactions

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human helper T-cell clones that recognize different influenza hemagglutinin determinants are restricted by different HLA-D region epitopes

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single amino acid changes in DR and antigen define residues critical for peptide-MHC binding and T cell recognition

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antigen-specific T cells with monogamous or promiscuous restriction patterns are sensitive to different HLA-DR beta chain substitutions

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

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based on heuristic

inferred from PubMed ID database lookup

High determinant density may explain the phenomenon of alloreactivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

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based on heuristic

inferred from PubMed ID database lookup

Fine specificity of T cell recognition of the same peptide in association with different I-A molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

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based on heuristic

inferred from PubMed ID database lookup

[33] AMoRe: An automated molecular replacement program package

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https://pubmed.ncbi.nlm.nih.gov/11877480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a common docking topology with substantial variation among different TCR-peptide-MHC complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High- and low-potency ligands with similar affinities for the TCR: the importance of kinetics in TCR signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

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based on heuristic

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/11877480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1084/JEM.20011194

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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