hMMS2 serves a redundant role in human PCNA polyubiquitination.

Human SHPRH suppresses genomic instability through proliferating cell nuclear antigen polyubiquitination.

RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO.

Distinct regulation of Ubc13 functions by the two ubiquitin-conjugating enzyme variants Mms2 and Uev1A.

Opposing effects of ubiquitin conjugation and SUMO modification of PCNA on replicational bypass of DNA lesions in Saccharomyces cerevisiae.

UBE2V2 (MMS2) is not required for effective immunoglobulin gene conversion or DNA damage tolerance in DT40.

Human HLTF functions as a ubiquitin ligase for proliferating cell nuclear antigen polyubiquitination.

Human SHPRH is a ubiquitin ligase for Mms2-Ubc13-dependent polyubiquitylation of proliferating cell nuclear antigen.

Ubiquitin binding site of the ubiquitin E2 variant (UEV) protein Mms2 is required for DNA damage tolerance in the yeast RAD6 pathway.

DNA damage-induced ubiquitylation of RFC2 subunit of replication factor C complex.

Neurosprora crassa RAD5 homologue, mus-41, inactivation results in higher sensitivity to mutagens but has little effect on PCNA-ubiquitylation in response to UV-irradiation.

Noncovalent interaction between ubiquitin and the human DNA repair protein Mms2 is required for Ubc13-mediated polyubiquitination.

PCNA modifications for regulation of post-replication repair pathways.

Eukaryotic DNA damage tolerance and translesion synthesis through covalent modifications of PCNA.

Ubiquitylation of yeast proliferating cell nuclear antigen and its implications for translesion DNA synthesis.

Differential regulation of Rad18 through Rad6-dependent mono- and polyubiquitination.

Two different classes of E2 ubiquitin-conjugating enzymes are required for the mono-ubiquitination of proteins and elongation by polyubiquitin chains with a specific topology.

Formation of lysine 63-linked poly-ubiquitin chains protects human lung cells against benzo[a]pyrene-diol-epoxide-induced mutagenicity.