Abstract:
:Siz1 is a founding member of the Siz/PIAS RING family of SUMO E3 ligases. The X-ray structure of an active Siz1 ligase revealed an elongated tripartite architecture comprised of an N-terminal PINIT domain, a central zinc-containing RING-like SP-RING domain, and a C-terminal domain we term the SP-CTD. Structure-based mutational analysis and biochemical studies show that the SP-RING and SP-CTD are required for activation of the E2 approximately SUMO thioester, while the PINIT domain is essential for redirecting SUMO conjugation to the proliferating cell nuclear antigen (PCNA) at lysine 164, a nonconsensus lysine residue that is not modified by the SUMO E2 in the absence of Siz1. Mutational analysis of Siz1 and PCNA revealed surfaces on both proteins that are required for efficient SUMO modification of PCNA in vitro and in vivo.
journal_name
Mol Celljournal_title
Molecular cellauthors
Yunus AA,Lima CDdoi
10.1016/j.molcel.2009.07.013subject
Has Abstractpub_date
2009-09-11 00:00:00pages
669-82issue
5eissn
1097-2765issn
1097-4164pii
S1097-2765(09)00508-5journal_volume
35pub_type
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