1992 · 188 citations · 18 references
Life SciencesBiochemistryMolecular BiologyEnzymologyProtein BiochemistryStructural BiologyConjugation ReactionsEnzyme-substrate RecognitionMacromolecular AssemblyProtein StructureStructural EnzymologyE2 Ubiquitin-conjugating EnzymesUbiquitin Chain TopologyUbiquitin System
Covalent ligation of multiubiquitin chains targets eukaryotic proteins for degradation. In such multiubiquitin chains, successive ubiquitins are linked by an isopeptide bond involving the side chain of Lys48 and the carboxyl group of Gly76. The crystal structure of a diubiquitin conjugate has been determined and refined at 2.3-A resolution. The molecule has internal approximate 2-fold symmetry with multiple hydrophobic and hydrophilic contacts along the 2-fold axis. The structure of the diubiquitin conjugate suggests determinants for recognition of multiubiquitin chains. A model for the interaction of diubiquitin and a ubiquitin conjugating enzyme (E2) is proposed.
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Crystallographic <i>R</i> Factor Refinement by Molecular Dynamics
Axel T. Brünger, John Kuriyan, Martin Karplus · Science · 1987 · 2K citations
A Multiubiquitin Chain Is Confined to Specific Lysine in a Targeted Short-Lived Protein
Vincent Chau, John W. Tobias, Andreas Bachmair et al. · Science · 1989 · 1.5K citations