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Pathways of ubiquitin conjugation
Author(s) -
Haas Arthur L.,
Siepmann Thomas J.
Publication year - 1997
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.11.14.9409544
Subject(s) - ubiquitin , ubiquitin ligase , biology , proteasome , isozyme , ubiquitin protein ligases , ubiquitin conjugating enzyme , biochemistry , microbiology and biotechnology , function (biology) , dna ligase , f box protein , deubiquitinating enzyme , computational biology , peptide sequence , genetics , enzyme , gene
The covalent attachment of the polypeptide ubiquitin to proteins marks them for degradation by the ubiquitin/26S proteasome‐dependent degradation pathway. This pathway functions in regulating many fundamental processes required for cell viability. Phylogenetic analysis of ubiquitin sequences reveals greater variability among lower eukaryotes and defines essential residues, many of which are conserved among the three ubiquitin‐like proteins known to undergo parallel ligation pathways. The hierarchical design of the ubiquitin conjugation mechanism provides great flexibility for the divergent evolution of new functions mediated by this posttranslational modification. Within this hierarchy, a single ubiquitin‐activating enzyme provides charged intermediates to multiple targeting pathways defined by cognate ubiquitin carrier protein (E2)/ligase (E3) pairs. Sequence analysis of E2 isozymes shows that the E2 superfamily is composed of distinct function‐specific families. The apparent lack of E2/E3 specificity suggested in the literature results from the presence of multiple isozymes within many E2 families and erroneous family assignments based on incomplete data sets. Other apparent inconsistencies are explained by interfamily sequence relationships among some E2 isoforms.—Haas, A. L., Siepmann, T.J. Pathways of ubiquitin conjugation. FASEB J. 11, 1257–1268 (1997)