Rtt101 and Mms1 in budding yeast form a CUL4DDB1‐like ubiquitin ligase that promotes replication through damaged DNA Mms1 belongs to the DDB1 family of.

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Rtt101 and Mms1 in budding yeast form a CUL4DDB1‐like ubiquitin ligase that promotes replication through damaged DNA Mms1 belongs to the DDB1 family of cullin 4 adaptors. (A) Extracts prepared from wild‐type (−), crt10Δ and mms22Δ cells expressing protein A‐tagged Mms1 and either full‐length (WT) or amino‐terminally truncated (ΔN50) CBP‐9Myc‐Rtt101 were incubated with calmodulin beads, and the total extract (upper panels) and eluate (lower panels) were probed for the presence of bound Rtt101 and Mms1. (B) Three‐dimensional representation of the DDB1 structure adapted from Li et al (2006); PDB accession 2b5m. The three β‐propeller domains are labelled as BPA, BPB and BPC. Each propeller is characterized by seven repeats of antiparallel four‐stranded β‐sheets and can be assigned to distinct functions. BPB has been described to be a cullin‐binding domain, whereas the BPA and BPC domains seem to bind to substrates. Stretches found to be conserved between Mms1 and DDB1 homologues are coloured in orange. (C) Full‐length and the indicated N‐terminal Rtt101 truncation mutants Δ50 and Δ100 were expressed as the only Rtt101 copy from GAL1,10 promoter. An empty vector (Vc) acted as a negative control. (D) Dendrogram of the DDB1/Mms1 homology using the neighbour‐joining algorithm. For the tree construction, only reliable and gap‐free alignment columns were used. Species names: Ag, Anopheles gambiae; At, Arabidopsis thaliana; Br, Brachydanio rerio; Ca, Candida albicans; Dm, Drosophila melanogaster; Eg, Eremothecium gossypii; En, Emericella nidulans; Hs, Homo sapiens; Kw, Kluyveromyces waltii; Mm, Mus musculus; Nc, Neurospora crassa; Sc, Saccharomyces cerevisiae; Sp, Schizosaccharomyces pombe; Xt, Xenopus tropicalis. The principal subfamilies are indicated at the right border of the figure. BPA, β‐propeller A; BPB, β‐propeller B; BPC, β‐propeller C; DDB1, DNA‐damage‐binding protein 1; PDB, Protein Data Bank. IF THIS IMAGE HAS BEEN PROVIDED BY OR IS OWNED BY A THIRD PARTY, AS INDICATED IN THE CAPTION LINE, THEN FURTHER PERMISSION MAY BE NEEDED BEFORE ANY FURTHER USE. PLEASE CONTACT WILEY'S PERMISSIONS DEPARTMENT ON PERMISSIONS@WILEY.COM OR USE THE RIGHTSLINK SERVICE BY CLICKING ON THE 'REQUEST PERMISSIONS' LINK ACCOMPANYING THIS ARTICLE. WILEY OR AUTHOR OWNED IMAGES MAY BE USED FOR NON-COMMERCIAL PURPOSES, SUBJECT TO PROPER CITATION OF THE ARTICLE, AUTHOR, AND PUBLISHER. EMBO Rep, Volume: 9, Issue: 10, Pages: 1034-1040, First published: 15 August 2008, DOI: (10.1038/embor.2008.155)