scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.274.31.21963 |
P698 | PubMed publication ID | 10419519 |
P50 | author | Tamar Ziv | Q47339040 |
Arie Admon | Q63357677 | ||
P2093 | author name string | G N DeMartino | |
I Shaked | |||
Y Reiss | |||
A Komlosh | |||
E Nadav | |||
S Ben-Shahar | |||
P2860 | cites work | Simultaneous binding of PA28 and PA700 activators to 20 S proteasomes | Q24530953 |
Targeting of HIV-1 antigens for rapid intracellular degradation enhances cytotoxic T lymphocyte (CTL) recognition and the induction of de novo CTL responses in vivo after immunization | Q24670153 | ||
A subcomplex of the proteasome regulatory particle required for ubiquitin-conjugate degradation and related to the COP9-signalosome and eIF3. | Q27936509 | ||
Interferon-gamma can stimulate post-proteasomal trimming of the N terminus of an antigenic peptide by inducing leucine aminopeptidase | Q28115538 | ||
Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules | Q28248180 | ||
In vivo assembly of the proteasomal complexes, implications for antigen processing | Q28285019 | ||
ATP-dependent incorporation of 20S protease into the 26S complex that degrades proteins conjugated to ubiquitin | Q34310551 | ||
Defective presentation to class I-restricted cytotoxic T lymphocytes in vaccinia-infected cells is overcome by enhanced degradation of antigen. | Q36355512 | ||
Potential immunocompetence of proteolytic fragments produced by proteasomes before evolution of the vertebrate immune system | Q36380352 | ||
A role for the proteasome regulator PA28alpha in antigen presentation | Q38357921 | ||
Purification by affinity chromatography and preliminary characterization of ornithine decarboxylase from simian virus 40-transformed 3T3 mouse fibroblasts | Q40121557 | ||
Low-Molecular-Weight Enzyme Inhibitors of Microbial Origin | Q40132226 | ||
Generation, translocation, and presentation of MHC class I-restricted peptides | Q40422033 | ||
Rapid and regulated degradation of ornithine decarboxylase | Q40598219 | ||
Genes encoded in the major histocompatibility complex affecting the generation of peptides for TAP transport | Q41371575 | ||
Efficiency of MHC class I antigen processing: a quantitative analysis | Q41446613 | ||
Ornithine decarboxylase is degraded by the 26S proteasome without ubiquitination | Q41589996 | ||
Proteasome subunits encoded by the major histocompatibility complex are not essential for antigen presentation | Q41594408 | ||
Efficient processing of an antigenic sequence for presentation by MHC class I molecules depends on its neighboring residues in the protein | Q41665138 | ||
Empty MHC class I molecules come out in the cold | Q41725383 | ||
The high molecular weight multicatalytic proteinase, macropain, exists in a latent form in human erythrocytes | Q42203334 | ||
The MHC class I ligand-generating system: roles of immunoproteasomes and the interferon-gamma-inducible proteasome activator PA28. | Q47700046 | ||
MHC-linked LMP gene products specifically alter peptidase activities of the proteasome | Q59088266 | ||
Coordinated dual cleavages induced by the proteasome regulator PA28 lead to dominant MHC ligands | Q71254579 | ||
Contribution of proteasome-mediated proteolysis to the hierarchy of epitopes presented by major histocompatibility complex class I molecules | Q71684049 | ||
Localization, quantitation, and in situ detection of specific peptide-MHC class I complexes using a monoclonal antibody | Q73479961 | ||
Production of a specific major histocompatibility complex class I-restricted epitope by ubiquitin-dependent degradation of modified ovalbumin in lymphocyte lysate | Q73596131 | ||
Relative functions of the alpha and beta subunits of the proteasome activator, PA28 | Q73824858 | ||
Double-cleavage production of the CTL epitope by proteasomes and PA28: role of the flanking region | Q74449437 | ||
The sizes of peptides generated from protein by mammalian 26 and 20 S proteasomes. Implications for understanding the degradative mechanism and antigen presentation | Q77911981 | ||
P433 | issue | 31 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 21963-21972 | |
P577 | publication date | 1999-07-01 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | 26 S proteasome-mediated production of an authentic major histocompatibility class I-restricted epitope from an intact protein substrate | |
P478 | volume | 274 |
Q24535312 | 26S proteasomes and immunoproteasomes produce mainly N-extended versions of an antigenic peptide |
Q44323611 | An essential role for tripeptidyl peptidase in the generation of an MHC class I epitope. |
Q47605422 | Association of growth factors, HIF-1 and NF-κB expression with proteasomes in endometrial cancer. |
Q35944320 | Changes in the Proteasome Pool during Malignant Transformation of Mouse Liver Cells |
Q33859470 | Compartmentalized MHC class I antigen processing enhances immunosurveillance by circumventing the law of mass action. |
Q34129301 | Cut and trim: generating MHC class I peptide ligands |
Q36375899 | Efficient generation of a hepatitis B virus cytotoxic T lymphocyte epitope requires the structural features of immunoproteasomes |
Q85793510 | Expression of vascular endothelial growth factor and transcription factors HIF-1, NF-kB expression in squamous cell carcinoma of head and neck; association with proteasome and calpain activities |
Q28363065 | Immunoproteasome assembly and antigen presentation in mice lacking both PA28alpha and PA28beta. |
Q35597106 | Making sense of mass destruction: quantitating MHC class I antigen presentation |
Q34362098 | Proteasome functioning in breast cancer: connection with clinical-pathological factors |
Q34700398 | Protein degradation and the generation of MHC class I-presented peptides. |
Q34348731 | Study of antigen-processing steps reveals preferences explaining differential biological outcomes of two HLA-A2-restricted immunodominant epitopes from human immunodeficiency virus type 1. |
Q39771199 | The tumor suppressor ING3 is degraded by SCF(Skp2)-mediated ubiquitin-proteasome system |
Q24292709 | The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction |
Q29617290 | Ubiquitin ligase activity and tyrosine phosphorylation underlie suppression of growth factor signaling by c-Cbl/Sli-1 |
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