scholarly article | Q13442814 |
P50 | author | Esam T. Abualrous | Q55506875 |
Miguel Alvaro-Benito | Q81371345 | ||
Marek Wieczorek | Q110028797 | ||
P2093 | author name string | Christian Freund | |
Jana Sticht | |||
Frank Noé | |||
Sebastian Stolzenberg | |||
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Formation of a highly peptide-receptive state of class II MHC. | Q46139976 | ||
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HLA-B27 subtypes differentially associated with disease exhibit conformational differences in solution. | Q52921125 | ||
Sodium dodecyl sulfate stability of HLA-DR1 complexes correlates with burial of hydrophobic residues in pocket 1. | Q54102029 | ||
Empty and peptide-loaded class II major histocompatibility complex proteins produced by expression in Escherichia coli and folding in vitro. | Q54104933 | ||
Allele-specific motifs revealed by sequencing of self-peptides eluted from MHC molecules | Q55042699 | ||
Selective Methyl Group Protonation of Perdeuterated Proteins | Q57851078 | ||
Fast Association Rates Suggest a Conformational Change in the MHC Class I Molecule H-2Dbupon Peptide Binding | Q60311730 | ||
Emerging principles for the recognition of peptide antigens by MHC class I molecules | Q67494475 | ||
Dynamic flexibility of a peptide-binding groove of human HLA-DR1 class II MHC molecules: normal mode analysis of the antigen peptide-class II MHC complex | Q73797302 | ||
Structural characterization of a soluble and partially folded class I major histocompatibility heavy chain/beta 2m heterodimer | Q74546450 | ||
Interactions of HLA-B27 with the peptide loading complex as revealed by heavy chain mutations | Q74582194 | ||
Dynamic characteristics of a peptide-binding groove of human HLA-A2 class I MHC molecules: normal mode analysis of the antigen peptide-class I MHC complex | Q74801820 | ||
Stable peptide binding to MHC class II molecule is rapid and is determined by a receptive conformation shaped by prior association with low affinity peptides | Q77320371 | ||
A conformational change in the human major histocompatibility complex protein HLA-DR1 induced by peptide binding | Q77410886 | ||
Kinetic isomers of a class II MHC-peptide complex | Q77710382 | ||
Differential tapasin dependence of MHC class I molecules correlates with conformational changes upon peptide dissociation: a molecular dynamics simulation study | Q81667466 | ||
Dynamic influence of the two membrane-proximal immunoglobulin-like domains upon the peptide-binding platform domain in class I and class II major histocompatibility complexes: normal mode analysis | Q84827397 | ||
Molecular architecture of the MHC I peptide-loading complex: one tapasin molecule is essential and sufficient for antigen processing | Q84872394 | ||
How T cell receptors interact with peptide-MHCs: a multiple steered molecular dynamics study | Q85076877 | ||
Mechanistic Basis for Epitope Proofreading in the Peptide-Loading Complex | Q86302879 | ||
Recognition of open conformers of classical MHC by chaperones and monoclonal antibodies | Q36266455 | ||
Comparative molecular dynamics analysis of tapasin-dependent and -independent MHC class I alleles | Q36388154 | ||
HLA-DM recognizes the flexible conformation of major histocompatibility complex class II. | Q36404572 | ||
Abundant empty class II MHC molecules on the surface of immature dendritic cells | Q36780413 | ||
NMR paves the way for atomic level descriptions of sparsely populated, transiently formed biomolecular conformers | Q37088583 | ||
Dipeptides promote folding and peptide binding of MHC class I molecules | Q37192020 | ||
The cell biology of major histocompatibility complex class I assembly: towards a molecular understanding. | Q37807059 | ||
Conformational variation in structures of classical and non-classical MHCII proteins and functional implications | Q38050482 | ||
A novel pathway of presentation by class II-MHC molecules involving peptides or denatured proteins important in autoimmunity | Q38064108 | ||
Structural Characteristics of HLA-DQ that May Impact DM Editing and Susceptibility to Type-1 Diabetes | Q38134730 | ||
Molecular mechanisms for contribution of MHC molecules to autoimmune diseases | Q38248679 | ||
Analysis of interactions in a tapasin/class I complex provides a mechanism for peptide selection | Q38304154 | ||
Determinants of immunodominance for CD4 T cells | Q38313559 | ||
Type 1 diabetes associated HLA-DQ2 and DQ8 molecules are relatively resistant to HLA-DM mediated release of invariant chain-derived CLIP peptides | Q38808868 | ||
T-cell responses to oncogenic merkel cell polyomavirus proteins distinguish patients with merkel cell carcinoma from healthy donors | Q38871209 | ||
F pocket flexibility influences the tapasin dependence of two differentially disease-associated MHC Class I proteins | Q38917075 | ||
Predominant naturally processed peptides bound to HLA-DR1 are derived from MHC-related molecules and are heterogeneous in size | Q39229154 | ||
Tapasin dependence of major histocompatibility complex class I molecules correlates with their conformational flexibility. | Q39491424 | ||
Tapasin edits peptides on MHC class I molecules by accelerating peptide exchange. | Q39762120 | ||
3-Layer-based analysis of peptide-MHC interaction: in silico prediction, peptide binding affinity and T cell activation in a relevant allergen-specific model. | Q40001014 | ||
Redox regulation of peptide receptivity of major histocompatibility complex class I molecules by ERp57 and tapasin | Q40113125 | ||
Conformational flexibility of the MHC class I alpha1-alpha2 domain in peptide bound and free states: a molecular dynamics simulation study | Q40298629 | ||
High resolution structures of highly bulged viral epitopes bound to major histocompatibility complex class I. Implications for T-cell receptor engagement and T-cell immunodominance | Q40431345 | ||
The three-dimensional structure of peptide-MHC complexes | Q40444937 | ||
MHC class II complexes sample intermediate states along the peptide exchange pathway. | Q40482918 | ||
Tapasin decreases immune responsiveness to a model tumor antigen | Q40551490 | ||
A single polymorphic residue within the peptide-binding cleft of MHC class I molecules determines spectrum of tapasin dependence | Q40678952 | ||
Molecular mechanism of peptide editing in the tapasin-MHC I complex | Q40837207 | ||
Structural analysis of MHC class I molecules with bound peptide antigens | Q40912854 | ||
Interaction of murine MHC class I molecules with tapasin and TAP enhances peptide loading and involves the heavy chain alpha3 domain. | Q40974100 | ||
Evidence for successive peptide binding and quality control stages during MHC class I assembly. | Q41031373 | ||
Direct binding of peptide to empty MHC class I molecules on intact cells and in vitro. | Q41725161 | ||
Invariant chain association with HLA-DR molecules inhibits immunogenic peptide binding | Q41731115 | ||
Peptide-dependent conformational fluctuation determines the stability of the human leukocyte antigen class I complex. | Q42545343 | ||
Tapasin is a facilitator, not an editor, of class I MHC peptide binding. | Q30311932 | ||
Peptide modulation of class I major histocompatibility complex protein molecular flexibility and the implications for immune recognition. | Q30351955 | ||
Characterization of peptides bound to the class I MHC molecule HLA-A2.1 by mass spectrometry | Q30434686 | ||
Naturally processed peptides longer than nine amino acid residues bind to the class I MHC molecule HLA-A2.1 with high affinity and in different conformations | Q30466462 | ||
Determination of the HLA-DM interaction site on HLA-DR molecules | Q30957797 | ||
Conformational isomers of a class II MHC-peptide complex in solution | Q31916434 | ||
Probing the ligand-induced conformational change in HLA-DR1 by selective chemical modification and mass spectrometric mapping. | Q33225288 | ||
Small organic compounds enhance antigen loading of class II major histocompatibility complex proteins by targeting the polymorphic P1 pocket | Q33258637 | ||
HLA-DM captures partially empty HLA-DR molecules for catalyzed removal of peptide | Q33292091 | ||
Anchor side chains of short peptide fragments trigger ligand-exchange of class II MHC molecules | Q33324394 | ||
Model for the peptide-free conformation of class II MHC proteins | Q33342783 | ||
Differences in the risk of celiac disease associated with HLA-DQ2.5 or HLA-DQ2.2 are related to sustained gluten antigen presentation | Q33498360 | ||
Characterization of structural features controlling the receptiveness of empty class II MHC molecules. | Q33886577 | ||
Energetic asymmetry among hydrogen bonds in MHC class II*peptide complexes | Q33930509 | ||
Diabetogenic T cells recognize insulin bound to IAg7 in an unexpected, weakly binding register | Q33934705 | ||
Cutting edge: HLA-DM functions through a mechanism that does not require specific conserved hydrogen bonds in class II MHC-peptide complexes | Q34028384 | ||
Interaction pattern of Arg 62 in the A-pocket of differentially disease-associated HLA-B27 subtypes suggests distinct TCR binding modes | Q34189720 | ||
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis | Q34250412 | ||
Three-dimensional structure of the human class II histocompatibility antigen HLA-DR1. | Q34350288 | ||
Association of HLA-DR1 with the allergic response to the major mugwort pollen allergen: molecular background. | Q34370060 | ||
The convergent roles of tapasin and HLA-DM in antigen presentation. | Q34784992 | ||
Dipeptides catalyze rapid peptide exchange on MHC class I molecules | Q34925753 | ||
Molecular dynamics simulations to provide insights into epitopes coupled to the soluble and membrane-bound MHC-II complexes | Q34973944 | ||
Evaluating the immunogenicity of protein drugs by applying in vitro MHC binding data and the immune epitope database and analysis resource | Q35039995 | ||
Naturally processed non-canonical HLA-A*02:01 presented peptides | Q35048892 | ||
A subset of HLA-B27 molecules contains peptides much longer than nonamers | Q35056650 | ||
Productive association between MHC class I and tapasin requires the tapasin transmembrane/cytosolic region and the tapasin C-terminal Ig-like domain | Q35645522 | ||
Register shifting of an insulin peptide-MHC complex allows diabetogenic T cells to escape thymic deletion | Q35669113 | ||
The Carboxy Terminus of the Ligand Peptide Determines the Stability of the MHC Class I Molecule H-2Kb: A Combined Molecular Dynamics and Experimental Study | Q35745162 | ||
PyEMMA 2: A Software Package for Estimation, Validation, and Analysis of Markov Models. | Q35843343 | ||
The Thermodynamic Mechanism of Peptide-MHC Class II Complex Formation Is a Determinant of Susceptibility to HLA-DM. | Q35861946 | ||
Tapasin and other chaperones: models of the MHC class I loading complex. | Q35922740 | ||
Stability of empty and peptide-loaded class II major histocompatibility complex molecules at neutral and endosomal pH: comparison to class I proteins | Q36048493 | ||
Empty class II major histocompatibility complex created by peptide photolysis establishes the role of DM in peptide association | Q36189571 | ||
P304 | page(s) | 292 | |
P577 | publication date | 2017-03-17 | |
P1433 | published in | Frontiers in Immunology | Q27723748 |
P1476 | title | Major Histocompatibility Complex (MHC) Class I and MHC Class II Proteins: Conformational Plasticity in Antigen Presentation | |
P478 | volume | 8 |
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