(Q24676272)

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An N-acetylated natural ligand of human histocompatibility leukocyte antigen (HLA)-B39. Classical major histocompatibility complex class I proteins bind peptides with a blocked NH(2) terminus in vivo

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An N-acetylated natural ligand of human histocompatibility leukocyte antigen (HLA)-B39. Classical major histocompatibility complex class I proteins bind peptides with a blocked NH(2) terminus in vivo (English)

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author name string

J Yagüe

1

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I Alvarez

2

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D Rognan

3

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M Ramos

4

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J Vázquez

5

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J A de Castro

6

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language of work or name

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publication date

19 June 2000

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Journal of Experimental Medicine

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191

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12

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2083-92

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Hepatitis C virus core protein interacts with cellular putative RNA helicase

1 reference

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Functional coherence of the human Y chromosome

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Structure of the human class I histocompatibility antigen, HLA-A2

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7 April 2017

Crystal structures of HLA-A*0201 complexed with antigenic peptides with either the amino- or carboxyl-terminal group substituted by a methyl group

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7 April 2017

Three-dimensional structure of a peptide extending from one end of a class I MHC binding site

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7 April 2017

The antigenic identity of peptide-MHC complexes: a comparison of the conformations of five viral peptides presented by HLA-A2

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7 April 2017

Nonclassical binding of formylated peptide in crystal structure of the MHC class Ib molecule H2-M3

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7 April 2017

Specificity pockets for the side chains of peptide antigens in HLA-Aw68

1 reference

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7 April 2017

Refined structure of the human histocompatibility antigen HLA-A2 at 2.6 A resolution

1 reference

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7 April 2017

Different length peptides bind to HLA-Aw68 similarly at their ends but bulge out in the middle

1 reference

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7 April 2017

Crystal structures of two viral peptides in complex with murine MHC class I H-2Kb

1 reference

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7 April 2017

The ubiquitin system

1 reference

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Proposal for a common nomenclature for sequence ions in mass spectra of peptides

2 references

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The ubiquitin-proteasome proteolytic pathway

1 reference

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Phosphorylated peptides can be transported by TAP molecules, presented by class I MHC molecules, and recognized by phosphopeptide-specific CTL.

1 reference

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Degradation of cell proteins and the generation of MHC class I-presented peptides

1 reference

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28 September 2017

The South Amerindian allotype HLA-B*3909 has the largest known similarity in peptide specificity and common natural ligands with HLA-B27.

1 reference

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28 September 2017

The same natural ligand is involved in allorecognition of multiple HLA-B27 subtypes by a single T cell clone: role of peptide and the MHC molecule in alloreactivity.

1 reference

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28 September 2017

The HLA-A*0201-restricted H-Y antigen contains a posttranslationally modified cysteine that significantly affects T cell recognition

1 reference

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An HLA-A2-restricted tyrosinase antigen on melanoma cells results from posttranslational modification and suggests a novel pathway for processing of membrane proteins

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Protein synthesis elongation factor EF-1 alpha is essential for ubiquitin-dependent degradation of certain N alpha-acetylated proteins and may be substituted for by the bacterial elongation factor EF-Tu

1 reference

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MHC ligands and peptide motifs: first listing

1 reference

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The three-dimensional structure of peptide-MHC complexes

1 reference

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Host resistance directed selectively against H-2-deficient lymphoma variants. Analysis of the mechanism

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Specialized functions of MHC class I molecules. I. An N-formyl peptide receptor is required for construction of the class I antigen Mta.

1 reference

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Specialized functions of major histocompatibility complex class I molecules. II. Hmt binds N-formylated peptides of mitochondrial and prokaryotic origin

1 reference

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28 September 2017

H-2M3 encodes the MHC Class I molecule presenting the maternally transmitted antigen of the mouse

1 reference

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Biochemical specificity of H-2M3a. Stereospecificity and space-filling requirements at position 1 maintain N-formyl peptide binding

1 reference

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28 September 2017

H2-M3, a full-service class Ib histocompatibility antigen

1 reference

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Human cytotoxic T lymphocyte responses to Epstein-Barr virus infection

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T cell allorecognition and endogenous HLA-B27-bound peptides in a cell line with defective HLA-B27-restricted antigen presentation.

1 reference

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Modulation of peptide binding by HLA-B27 polymorphism in pockets A and B, and peptide specificity of B*2703.

1 reference

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Importance of peptide amino and carboxyl termini to the stability of MHC class I molecules

1 reference

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Structural homologies between two HLA B27-restricted peptides suggest residues important for interaction with HLA B27.

1 reference

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In vitro peptide binding to soluble empty class I major histocompatibility complex molecules isolated from transfected Drosophila melanogaster cells.

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Presentation of cytosolic glycosylated peptides by human class I major histocompatibility complex molecules in vivo

1 reference

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21 January 2018

Structures of N-terminally acetylated proteins

1 reference

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High-sensitivity analysis and sequencing of peptides and proteins by quadrupole ion trap mass spectrometry.

1 reference

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The foreign antigen binding site and T cell recognition regions of class I histocompatibility antigens

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Association of class I major histocompatibility heavy and light chains induced by viral peptides

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Identification of self peptides bound to purified HLA-B27

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The three-dimensional structure of HLA-B27 at 2.1 A resolution suggests a general mechanism for tight peptide binding to MHC

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Structural requirements for the peptide-induced conformational change of free major histocompatibility complex class I heavy chains

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Acetylation of protein N-terminal amino groups structural observations on α-amino acetylated proteins

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Recognition of HLA-B27 and related antigen by a monoclonal antibody

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An aminopeptidase occurring in pig kidney. II. A study on the mechanism of the hydrolysis

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Modulation at multiple anchor positions of the peptide specificity of HLA-B27 subtypes differentially associated with ankylosing spondylitis

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Degradation of proteins with acetylated amino termini by the ubiquitin system

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10.1084/JEM.191.12.2083

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