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PDBsum entry 5dfl
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Ligase/signaling protein
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PDB id
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5dfl
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References listed in PDB file
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Key reference
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Title
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The molecular basis of lysine 48 ubiquitin chain synthesis by ube2k.
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Authors
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A.J.Middleton,
C.L.Day.
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Ref.
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Sci Rep, 2015,
5,
16793.
[DOI no: ]
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PubMed id
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Abstract
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The post-translational modification of proteins by ubiquitin is central to the
regulation of eukaryotic cells. Substrate-bound ubiquitin chains linked by
lysine 11 and 48 target proteins to the proteasome for degradation and determine
protein abundance in cells, while other ubiquitin chain linkages regulate
protein interactions. The specificity of chain-linkage type is usually
determined by ubiquitin-conjugating enzymes (E2s). The degradative E2, Ube2K,
preferentially catalyses formation of Lys48-linked chains, but like most E2s,
the molecular basis for chain formation is not well understood. Here we report
the crystal structure of a Ube2K~ubiquitin conjugate and demonstrate that even
though it is monomeric, Ube2K can synthesize Lys48-linked ubiquitin chains.
Using site-directed mutagenesis and modelling, our studies reveal a molecular
understanding of the catalytic complex and identify key features required for
synthesis of degradative Lys48-linked chains. The position of the acceptor
ubiquitin described here is likely conserved in other E2s that catalyse
Lys48-linked ubiquitin chain synthesis.
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