scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.HUMIMM.2006.08.001 |
P8608 | Fatcat ID | release_zrp5idvcozalrprdt476gxsn5m |
P932 | PMC publication ID | 2169290 |
P698 | PubMed publication ID | 17145365 |
P5875 | ResearchGate publication ID | 6654405 |
P2093 | author name string | Rene J Duquesnoy | |
P2860 | cites work | Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 |
Crystal structure of anti-Hen egg white lysozyme antibody (HyHEL-10) Fv-antigen complex. Local structural changes in the protein antigen and water-mediated interactions of Fv-antigen and light chain-heavy chain interfaces | Q27619619 | ||
Three-dimensional structures of the free and antigen-bound Fab from monoclonal antilysozyme antibody HyHEL-63(,) | Q27622663 | ||
Dissection of binding interactions in the complex between the anti-lysozyme antibody HyHEL-63 and its antigen | Q27640276 | ||
Solution structure and activity of mouse lysozyme M | Q27640600 | ||
High-resolution three-dimensional structure of horse heart cytochrome c | Q27668194 | ||
Structure of an antibody-antigen complex: crystal structure of the HyHEL-10 Fab-lysozyme complex | Q27728062 | ||
Structure of an antibody-lysozyme complex unexpected effect of conservative mutation | Q27729412 | ||
Crystal structure of a cross-reaction complex between Fab F9.13.7 and guinea fowl lysozyme | Q27729792 | ||
Bound water molecules and conformational stabilization help mediate an antigen-antibody association | Q27731557 | ||
Hydrogen bonding and solvent structure in an antigen-antibody interface. Crystal structures and thermodynamic characterization of three Fv mutants complexed with lysozyme | Q27734142 | ||
Neutralizing epitopes on the extracellular interferon gamma receptor (IFNgammaR) alpha-chain characterized by homolog scanning mutagenesis and X-ray crystal structure of the A6 fab-IFNgammaR1-108 complex | Q27747455 | ||
A mutational analysis of binding interactions in an antigen-antibody protein-protein complex | Q27758122 | ||
Structural basis for the binding of an anti-cytochrome c antibody to its antigen: crystal structures of FabE8-cytochrome c complex to 1.8 A resolution and FabE8 to 2.26 A resolution | Q27765034 | ||
Standard conformations for the canonical structures of immunoglobulins | Q28254522 | ||
Conformations of immunoglobulin hypervariable regions | Q28273335 | ||
HLA‐B15: A widespread and diverse family of HLA‐B alleles | Q28286688 | ||
Unraveling hot spots in binding interfaces: progress and challenges | Q29614463 | ||
Anatomy of hot spots in protein interfaces | Q29616238 | ||
Somatic generation of antibody diversity | Q29616439 | ||
On the attribution of binding energy in antigen-antibody complexes McPC 603, D1.3, and HyHEL-5. | Q30195996 | ||
Expressed murine and human CDR-H3 intervals of equal length exhibit distinct repertoires that differ in their amino acid composition and predicted range of structures | Q30746440 | ||
HLAMatchmaker-driven analysis of responses to HLA-typed platelet transfusions in alloimmunized thrombocytopenic patients | Q33369144 | ||
Binding in the growth hormone receptor complex | Q33593803 | ||
Interactions of protein antigens with antibodies | Q33594252 | ||
Anatomy of the antibody molecule | Q34060425 | ||
Differences in electrostatic properties at antibody-antigen binding sites: implications for specificity and cross-reactivity | Q34179284 | ||
Cloning and expression of the cDNA for the murine interferon gamma receptor | Q34317120 | ||
Three-dimensional structure of an antibody-antigen complex | Q34366479 | ||
Energetic and kinetic contributions of contact residues of antibody D1.3 in the interaction with lysozyme | Q34413120 | ||
Reductionism and the search for structure-function relationships in antibody molecules | Q35007284 | ||
Antigen specificity and cross-reactivity of monoclonal anti-lysozyme antibodies | Q69000243 | ||
Site-directed chemical modification of horse cytochrome c results in changes in antigenicity due to local and long-range conformational perturbations | Q69002528 | ||
The expressed lysozyme-specific B cell repertoire. I. Heterogeneity in the monoclonal anti-hen egg white lysozyme specificity repertoire, and its difference from the in situ repertoire | Q71000652 | ||
HLA-DR residues accessible under the peptide-binding groove contribute to polymorphic antibody epitopes | Q71585528 | ||
Comparison of a structural and a functional epitope | Q71601556 | ||
Antigenic regions defined by monoclonal antibodies correspond to structural domains of avian lysozyme | Q72733543 | ||
HLAmatchmaker: a molecularly based algorithm for histocompatibility determination. III. Effect of matching at the HLA-A,B amino acid triplet level on kidney transplant survival | Q73180837 | ||
Systematic exploration of the antigen binding activity of synthetic peptides isolated from the variable regions of immunoglobulins | Q73919852 | ||
Immunological speculations | Q79123866 | ||
The acceptable mismatch program as a fast tool for highly sensitized patients awaiting a cadaveric kidney transplantation: short waiting time and excellent graft outcome | Q80389325 | ||
Is the application of HLAMatchmaker relevant in kidney transplantation? | Q81308319 | ||
HLAMatchmaker-based strategy to identify acceptable HLA class I mismatches for highly sensitized kidney transplant candidates. | Q52009690 | ||
The number of amino acid residues mismatches correlates with flow cytometry crossmatching results in high PRA renal patients. | Q52041496 | ||
HLAMatchmaker: a molecularly based algorithm for histocompatibility determination. II. Verification of the algorithm and determination of the relative immunogenicity of amino acid triplet-defined epitopes. | Q52041499 | ||
HLAMatchmaker: a molecularly based algorithm for histocompatibility determination. I. Description of the algorithm. | Q52041500 | ||
Alloreactive T cell recognition of MHC class I molecules: the T cell receptor interacts with limited regions of the MHC class I long alpha helices. | Q52893012 | ||
A major histocompatibility complex-peptide-restricted antibody and t cell receptor molecules recognize their target by distinct binding modes: crystal structure of human leukocyte antigen (HLA)-A1-MAGE-A1 in complex with FAB-HYB3. | Q52941721 | ||
Serum analysis after transplant nephrectomy reveals restricted antibody specificity patterns against structurally defined HLA class I mismatches | Q61053434 | ||
Protein antigenicity: A thermodynamic approach | Q67687408 | ||
Crystallographic refinement of the three-dimensional structure of the FabD1.3-lysozyme complex at 2.5-A resolution | Q67694554 | ||
Experimental analysis by site-directed mutagenesis of somatic mutation effects on affinity and fine specificity in antibodies specific for lysozyme | Q67723990 | ||
Patterns of antibody specificity during the BALB/c immune response to hen eggwhite lysozyme | Q67927284 | ||
Amino acid residues on HLA molecules critical for alloantibody binding | Q68188123 | ||
Small rearrangements in structures of Fv and Fab fragments of antibody D1.3 on antigen binding | Q68564328 | ||
Amino acid residues 56 to 69 of HLA-A2 specify an antigenic determinant shared by HLA-A2 and HLA-B17 | Q68963626 | ||
Three-dimensional structure of an antigen-antibody complex at 2.8 A resolution | Q68969863 | ||
Extending options for highly sensitized patients to receive a suitable kidney graft | Q36220802 | ||
High-resolution mapping of the HyHEL-10 epitope of chicken lysozyme by site-directed mutagenesis | Q36273475 | ||
Energetic analysis of an antigen/antibody interface: alanine scanning mutagenesis and double mutant cycles on the HyHEL-10/lysozyme interaction | Q36281533 | ||
Purification of human gamma interferon receptors by sequential affinity chromatography on immobilized monoclonal antireceptor antibodies and human gamma interferon | Q36353547 | ||
Epitopes on protein antigens: misconceptions and realities. | Q36576238 | ||
Antibody-antigen complexes | Q37943232 | ||
The atomic mobility component of protein antigenicity | Q38154881 | ||
Structural and functional approaches to the study of protein antigenicity | Q38208203 | ||
HLA-DR and -DQ epitopes and monoclonal antibody specificity | Q38209752 | ||
How do two unrelated antibodies, HyHEL-10 and F9.13.7, recognize the same epitope of hen egg-white lysozyme? | Q38270409 | ||
The contribution of contact and non-contact residues of antibody in the affinity of binding to antigen. The interaction of mutant D1.3 antibodies with lysozyme | Q38313296 | ||
A proposal for the nomenclature of antigenic sites in peptides and proteins | Q39524030 | ||
The chemistry and mechanism of antibody binding to protein antigens. | Q39539172 | ||
Structure of antibody-antigen complexes: implications for immune recognition. | Q39539191 | ||
The structural basis of antibody complementarity | Q39779292 | ||
The antigenic structure of proteins: a reappraisal. | Q40076398 | ||
Impact of peptides on the recognition of HLA class I molecules by human HLA antibodies | Q40360031 | ||
Antibody-antigen interactions: new structures and new conformational changes | Q40399620 | ||
Antibody structure and the evolution of immunoglobulin V gene segments | Q40471075 | ||
Recent origin of the P lysozyme gene in mice | Q40515705 | ||
The humoral immune response against an HLA class I allodeterminant correlates with the HLA-DR phenotype of the responder | Q40802303 | ||
Probing HLA-B7 conformational shifts induced by peptide-binding groove mutations and bound peptide with anti-HLA monoclonal antibodies. | Q41167755 | ||
Role of HLA-B*5101 binding nonamer peptides in formation of the HLA-Bw4 public epitope | Q41188726 | ||
Influence on antibody recognition of amino acid substitutions in the cleft of HLA-DQ2 molecules. Suggestive evidence of peptide-dependent epitopes | Q41285221 | ||
Unusual distributions of amino acids in complementarity-determining (hypervariable) segments of heavy and light chains of immunoglobulins and their possible roles in specificity of antibody-combining sites | Q41295516 | ||
HLA-B16 antigens: sequence of the ST-16 antigen, further definition of two B38 subtypes and evidence for convergent evolution of B*3902. | Q41396339 | ||
Bw4-reactive and Bw6-reactive antibodies recognize multiple distinct HLA structures that partially overlap in the alpha-1 helix | Q41434617 | ||
Amino acids in the peptide-binding groove influence an antibody-defined, disease-associated HLA-DR epitope | Q41466223 | ||
HLA-DRβ chain residues that are predicted to be located in the floor of the peptide-binding groove contribute to antibody-binding epitopes | Q41557902 | ||
Cn3D: a new generation of three-dimensional molecular structure viewer | Q41576502 | ||
HLA-B∗0702 antibody epitopes are affected indirectly by distant antigen residues | Q41577346 | ||
Mutagenesis around residue 176 on HLA-B∗0702 characterizes multiple distinct epitopes for anti-HLA antibodies | Q41602436 | ||
Conformational changes in MHC class I molecules. Antibody, T-cell receptor, and NK cell recognition in an HLA-B7 model system | Q41649533 | ||
Biochemical implications from the variable gene sequences of an anti-cytochrome c antibody and crystallographic characterization of its antigen-binding fragment in free and antigen-complexed forms | Q41665170 | ||
HLAMatchmaker-based analysis of human monoclonal antibody reactivity demonstrates the importance of an additional contact site for specific recognition of triplet-defined epitopes | Q42665365 | ||
Monoclonal antibodies to horse cytochrome c expressing four distinct idiotypes distribute among two sites on the native protein. | Q42800818 | ||
Quantitative estimation of HLA-A and HLA-B antigens carrying the Bw4 supertypic specificity in human peripheral blood lymphocytes | Q44398319 | ||
Monoclonal antibodies as probes of conformational changes in protein-engineered cytochrome c. | Q44839695 | ||
HLA epitope matching. Contribution of matched residues to epitopes recognized by alloantibodies | Q45162670 | ||
Magnitude of the hydrophobic effect at central versus peripheral sites in protein-protein interfaces | Q45255575 | ||
Association of the anti-hen egg lysozyme antibody HyHEL-5 with avian species variant and mutant lysozymes. | Q46017243 | ||
Predictive value of human leucocyte antigen epitope matching using HLAMatchmaker for graft outcomes in a predominantly African-American renal transplant cohort | Q46984237 | ||
Identification of differences in the specificity-determining residues of antibodies that recognize antigens of different size: implications for the rational design of antibody repertoires. | Q47425669 | ||
Antibody-antigen interactions: contact analysis and binding site topography. | Q47628744 | ||
The number of amino acid triplet differences between patient and donor is predictive for the antibody reactivity against mismatched human leukocyte antigens | Q47683551 | ||
Anatomy of an antibody molecule: structure, kinetics, thermodynamics and mutational studies of the antilysozyme antibody D1.3. | Q47700146 | ||
Critical evaluation of the amino acid triplet-epitope matching concept in cadaver kidney transplantation | Q47785748 | ||
Genetic and serological heterogeneity of the supertypic HLA-B locus specificities Bw4 and Bw6. | Q48306828 | ||
Beneficial effect of matching at the HLA-A and -B amino-acid triplet level on rejection-free clear graft survival in penetrating keratoplasty. | Q51034692 | ||
Utility of HLAMatchmaker and single-antigen HLA-antibody detection beads for identification of acceptable mismatches in highly sensitized patients awaiting kidney transplantation. | Q51941761 | ||
HLA class I donor-specific triplet antibodies detected after renal transplantation. | Q51990427 | ||
Humoral sensitization against rejected grafts: specific antibodies to graft immunogenic amino acid triplets. | Q51990430 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 847-862 | |
P577 | publication date | 2006-09-01 | |
P1433 | published in | Human Immunology | Q15709955 |
P1476 | title | A structurally based approach to determine HLA compatibility at the humoral immune level | |
P478 | volume | 67 |
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