Mutations in theEscherichia coli surEgene increase isoaspartyl accumulation in a strain lacking thepcmrepair methyltransferase but suppress stress-survival phenotypes
Open Access
- 1 October 1998
- journal article
- Published by Oxford University Press (OUP) in FEMS Microbiology Letters
- Vol. 167 (1) , 19-25
- https://doi.org/10.1111/j.1574-6968.1998.tb13202.x
Abstract
The Escherichia coli surE gene is co-transcribed with pcm, encoding the l-isoaspartyl protein repair methyltransferase, and is highly conserved amongKeywords
This publication has 17 references indexed in Scilit:
- Analysis of 1.9 Mb of contiguous sequence from chromosome 4 of Arabidopsis thalianaNature, 1998
- Targeted Gene Disruption of theCaenorhabditis elegansl-Isoaspartyl Protein Repair Methyltransferase Impairs Survival of Dauer Stage NematodesArchives of Biochemistry and Biophysics, 1997
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- RpoS- and OxyR-independent induction of HPI catalase at stationary phase in Escherichia coli and identification of rpoS mutations in common laboratory strainsJournal of Bacteriology, 1997
- Deamidation in Proteins: The Crystal Structure of Bovine Pancreatic Ribonuclease with an Isoaspartyl Residue at Position 67Journal of Molecular Biology, 1996
- Positive selection vectors for allelic exchangeGene, 1996
- Repair, refold, recycle: how bacteria can deal with spontaneous and environmental damage to proteinsMolecular Microbiology, 1995
- A protein methyltransferase specific for altered aspartyl residues is important in Escherichia coli stationary-phase survival and heat-shock resistance.Proceedings of the National Academy of Sciences, 1992
- Direct clone characterization from plaques and colonies by the polymerase chain reactionNucleic Acids Research, 1989
- Conversion of isoaspartyl peptides to normal peptides: implications for the cellular repair of damaged proteins.Proceedings of the National Academy of Sciences, 1987