Abstract
Several mechanisms have been proposed for the synthesis of substrate-linked ubiquitin chains. HECT ligases directly catalyse protein ubiquitination and have been found to non-covalently interact with ubiquitin. We report crystal structures of the Nedd4 HECT domain, alone and in complex with ubiquitin, which show a new binding mode involving two surfaces on ubiquitin and both subdomains of the HECT N-lobe. The structures suggest a model for HECT-to-substrate ubiquitin transfer, in which the growing chain on the substrate is kept close to the catalytic cysteine to promote processivity. Mutational analysis highlights differences between the processes of substrate polyubiquitination and self-ubiquitination.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Endosomal Sorting Complexes Required for Transport / chemistry*
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Endosomal Sorting Complexes Required for Transport / genetics
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Endosomal Sorting Complexes Required for Transport / metabolism*
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Humans
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Molecular Sequence Data
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Nedd4 Ubiquitin Protein Ligases
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Protein Binding
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Sequence Homology, Amino Acid
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Ubiquitin / metabolism*
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Ubiquitin-Protein Ligases / chemistry*
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Ubiquitin-Protein Ligases / genetics
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Ubiquitin-Protein Ligases / metabolism*
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Ubiquitination
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X-Ray Diffraction
Substances
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Endosomal Sorting Complexes Required for Transport
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Ubiquitin
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Nedd4 Ubiquitin Protein Ligases
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Nedd4 protein, human
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Ubiquitin-Protein Ligases