The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Periplasmic Stress and ECF Sigma Factors
Open accessAbstract
▪ Abstract Envelope stress responses play important pysiological roles in a variety of processes, including protein folding, cell wall biosynthesis, and pathogenesis. Many of these responses are controlled by extracytoplasmic function (ECF) sigma factors that respond to external signals by means of a membrane-localized anti–sigma factor. One of the best-characterized, ECF-regulated responses is the σ E envelope stress response of Escherichia coli. The σ E pathway ensures proper assembly of outer-membrane proteins (OMP) by controlling expression of genes involved in OMP folding and degradation in response to envelope stresses that disrupt these processes. Prevailing evidence suggests that, in E. coli, a second envelope stress response controlled by the Cpx two-component system ensures proper pilus assembly. The sensor kinase CpxA recognizes misfolded periplasmic proteins, such as those generated during pilus assembly, and transduces this signal to the response regulator CpxR through conserved phosphotransfer reactions. Phosphorylated CpxR activates transcription of periplasmic factors necessary for pilus assembly.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence
Cole, S. T., Brosch, R., Parkhill, J., Garnier, T., Churcher, C., Harris, D., Gordon, S. V., Eiglmeier, K., Gas, S., Barry, C. E., et al. (1998) · Nature · doi:10.1038/31159 · Cited by 7,847
The Periplasmic Escherichia coli Peptidylprolyl cis,trans-Isomerase FkpA
Bothmann, H., & Plückthun, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m910233199 · Cited by 192
DsbG, a protein disulfide isomerase with chaperone activity
Shao, F., Bader, M. W., Jakob, U., & Bardwell, J. C. A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.18.13349 · Cited by 116
Cited by
Membrane fluidity and its roles in the perception of environmental signals
Los, D. A., & Murata, N. (2004) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2004.08.002 · Cited by 1,020
Defining the roles of the periplasmic chaperones SurA, Skp, and DegP in Escherichia coli
Sklar, J. G., Wu, T., Kahne, D., & Silhavy, T. J. (2007) · Genes & Development · doi:10.1101/gad.1581007 · Cited by 459
Self-citationCao, J., Woodhall, M. R., Alvarez, J., Cartron, M. L., & Andrews, S. C. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05802.x · Cited by 163
Hong, W., Jiao, W., Hu, J., Zhang, J., Liu, C., Fu, X., Shen, D., Xia, B., & Chang, Z. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503934200 · Cited by 132
Karlinsey, J. E., Maguire, M. E., Becker, L. A., Crouch, M. V., & Fang, F. C. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07357.x · Cited by 102
Basics of Stress Adaptation and Implications in New-Generation Foods
Yousef, A., & Courtney, P. (2002) · Microbial Stress Adaptation and Food Safety · doi:10.1201/9781420012828.ch1 · Cited by 100
YfgM is an ancillary subunit of the SecYEG translocon in Escherichia coli.
Götzke, H., Palombo, I., Muheim, C., Perrody, E., Genevaux, P., Kudva, R., Müller, M., & Daley, D. O. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.541672 · Cited by 53
Dynamic interaction of the Sec Translocon with the chaperone PpiD.
Sachelaru, I., Petriman, N.-A., Kudva, R., & Koch, H.-G. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.577916 · Cited by 37
Bioinformatic identification of ClpI, a distinct class of Clp unfoldases in Actinomycetota
Jiang, J., & Schmitz, K. R. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1161764 · Cited by 3
Metadata
- Authors
- Raivio, T. L., & Silhavy, T. J.
- Venue
- Annual Review of Microbiology
- Publisher
- Annual Reviews
- Published
- 2001-10
- Volume
- 55
- Issue
- 1
- Pages
- 591-624
- ISSN
- 0066-4227 (ISSN-L)
- 1545-3251
- OpenAlex
- W2146731040
- Cited by
- 388
- References
- 3
- FWCI
- 1.77
- Type
- journal article
- Language
- en
- Open access
- hybrid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
