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The Ubp6 family of deubiquitinating enzymes contains a ubiquitin‐like domain: SUb
Author(s) -
Wyndham Allison M.,
Baker Rohan T.,
Chelvanayagam Gareth
Publication year - 1999
Publication title -
protein science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.353
H-Index - 175
eISSN - 1469-896X
pISSN - 0961-8368
DOI - 10.1110/ps.8.6.1268
Subject(s) - deubiquitinating enzyme , ubiquitin , saccharomyces cerevisiae , biology , peptide sequence , sequence alignment , conserved sequence , homology (biology) , ubiquitin conjugating enzyme , biochemistry , ubiquitin ligase , amino acid , microbiology and biotechnology , genetics , yeast , gene
A sequence motif that is S imilar to Ub iquitin (SUb) has been identified in the Saccharomyces cerevisiae ubiquitin‐specific protease Ubp6. SUb is conserved in all known Ubp6 homologues from a spectrum of eukaryotic species and is also present in a group of hypothetical proteins of unknown function (Unk1–3) present in sequence databases. An N‐terminal deletion mutant of Ubp6 that lacks SUb is still capable of cleaving α‐linked ubiquitin fusions, suggesting that SUb forms a separate domain to the catalytic core of Ubp6 and demonstrating that it is not required for in vitro cleavage activity. A homology model of the 78 N‐terminal amino acids of human Ubp6, based on the known fold of ubiquitin, is presented. In human Ubp6, SUb shares only 20% sequence identity with ubiquitin. Even weaker similarity occurs between S. cerevisiae SUb and ubiquitin. The homology model supports a ubiquitin‐like fold for SUb and suggests that two conserved Lys residues, corresponding to Lys48 and Lys63 of ubiquitin, are functionally important.