Back to search

Substrate binding and sequence preference of the proteasome revealed by active-site-directed affinity probes

Data up to Jan 2025

Published1998
Citations179
References23

Total Citations Per Year

Abstract

References (23)

Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules

1994 • 2,480 citations

STRUCTURE AND FUNCTIONS OF THE 20S AND 26S PROTEASOMES

1996 • 2,408 citations

Structure of 20S proteasome from yeast at 2.4Å resolution

1997 • 2,211 citations

Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin

1995 • 1,601 citations

Crystal Structure of the 20 S Proteasome from the Archaeon T. acidophilum at 3.4 Å Resolution

1995 • 1,513 citations

The Human Cytomegalovirus US11 Gene Product Dislocates MHC Class I Heavy Chains from the Endoplasmic Reticulum to the Cytosol

1996 • 1,083 citations

The Behavior and Significance of Slow‐Binding Enzyme Inhibitors

1988 • 828 citations

Current protocols in protein science

1996 • 473 citations

Covalent modification of the active site threonine of proteasomal β subunits and theEscherichia colihomolog HslV by a new class of inhibitors

1997 • 441 citations

Mechanistic Studies on the Inactivation of the Proteasome by Lactacystin

1996 • 370 citations

Regel zur Abschätzung der chemischen Verschiebung von Protonen an einer Doppelbindung

1966 • 292 citations

Human cytomegalovirus down-regulates HLA class I expression by reducing the stability of class I H chains.

1993 • 215 citations

Peptidyl vinyl sulphones: a new class of potent and selective cysteine protease inhibitors: S2P2 specificity of human cathepsin O2 in comparison with cathepsins S and L

1996 • 139 citations

Novel dipeptide aldehydes are proteasome inhibitors and block the MHC-I antigen-processing pathway.

1995 • 99 citations

The LMP antigens: A stable MHC-controlled multisubunit protein complex

1986 • 93 citations

Design and synthesis of novel protease inhibitors. Tripeptide α′,β′-epoxyketones as nanomolar inactivators of the proteasome

1996 • 50 citations

A 3,4-dichloroisocoumarin-resistant component of the multicatalytic proteinase complex

1992 • 50 citations

Kinetic Studies of the Branched Chain Amino Acid Preferring Peptidase Activity of the 20S Proteasome: Development of a Continuous Assay and Inhibition by Tripeptide Aldehydes and clasto-Lactacystin β-Lactone

1998 • 47 citations

Potent α-ketocarbonyl and boronic ester derived inhibitors of proteasome

1996 • 45 citations

Reactions of [14C]-3,4-Dichloroisocoumarin with Subunits of Pituitary and Spleen Multicatalytic Proteinase Complexes (Proteasomes)

1997 • 37 citations

A comparative study of the chymotrypsin-like activity of the rat liver multicatalytic proteinase and the ClpP from Escherichia coli.

1993 • 35 citations

Structure and Function of the 20S Proteasome and of Its Regulatory Complexes

1995 • 31 citations

ChemInform Abstract: Design and Synthesis of Novel Protease Inhibitors. Tripeptide α′, β′‐Epoxyketones as Nanomolar Inactivators of the Proteasome.

1996 • 13 citations

Cited By (0)

Loading...
Substrate binding and sequence preference of the proteasome revealed by… (1998) – Chemistry & Biology | Metascience Observatory Explorer