BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 20345660)

  • 1. Role of Escherichia coli FtsN protein in the assembly and stability of the cell division ring.
    Rico AI; García-Ovalle M; Palacios P; Casanova M; Vicente M
    Mol Microbiol; 2010 May; 76(3):760-71. PubMed ID: 20345660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Role of two essential domains of Escherichia coli FtsA in localization and progression of the division ring.
    Rico AI; García-Ovalle M; Mingorance J; Vicente M
    Mol Microbiol; 2004 Sep; 53(5):1359-71. PubMed ID: 15387815
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Coordinated disassembly of the divisome complex in Escherichia coli.
    Söderström B; Mirzadeh K; Toddo S; von Heijne G; Skoglund U; Daley DO
    Mol Microbiol; 2016 Aug; 101(3):425-38. PubMed ID: 27096604
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The bypass of ZipA by overexpression of FtsN requires a previously unknown conserved FtsN motif essential for FtsA-FtsN interaction supporting a model in which FtsA monomers recruit late cell division proteins to the Z ring.
    Pichoff S; Du S; Lutkenhaus J
    Mol Microbiol; 2015 Mar; 95(6):971-87. PubMed ID: 25496259
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The order of the ring: assembly of Escherichia coli cell division components.
    Vicente M; Rico AI
    Mol Microbiol; 2006 Jul; 61(1):5-8. PubMed ID: 16824090
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cell Cycle-Dependent Recruitment of FtsN to the Divisome in Escherichia coli.
    Männik J; Pichoff S; Lutkenhaus J; Männik J
    mBio; 2022 Aug; 13(4):e0201722. PubMed ID: 35968943
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The hypermorph FtsA* protein has an in vivo role in relieving the Escherichia coli proto-ring block caused by excess ZapC.
    Ortiz C; Casanova M; Palacios P; Vicente M
    PLoS One; 2017; 12(9):e0184184. PubMed ID: 28877250
    [TBL] [Abstract][Full Text] [Related]  

  • 8. FtsQ, FtsL and FtsI require FtsK, but not FtsN, for co-localization with FtsZ during Escherichia coli cell division.
    Chen JC; Beckwith J
    Mol Microbiol; 2001 Oct; 42(2):395-413. PubMed ID: 11703663
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disruption of divisome assembly rescued by FtsN-FtsA interaction in
    Pichoff S; Du S; Lutkenhaus J
    Proc Natl Acad Sci U S A; 2018 Jul; 115(29):E6855-E6862. PubMed ID: 29967164
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An altered FtsA can compensate for the loss of essential cell division protein FtsN in Escherichia coli.
    Bernard CS; Sadasivam M; Shiomi D; Margolin W
    Mol Microbiol; 2007 Jun; 64(5):1289-305. PubMed ID: 17542921
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Escherichia coli FtsK functional domains involved in its interaction with its divisome protein partners.
    Grenga L; Luzi G; Paolozzi L; Ghelardini P
    FEMS Microbiol Lett; 2008 Oct; 287(2):163-7. PubMed ID: 18759781
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A deficiency in S-adenosylmethionine synthetase interrupts assembly of the septal ring in Escherichia coli K-12.
    Wang S; Arends SJ; Weiss DS; Newman EB
    Mol Microbiol; 2005 Nov; 58(3):791-9. PubMed ID: 16238627
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ZipA is required for recruitment of FtsK, FtsQ, FtsL, and FtsN to the septal ring in Escherichia coli.
    Hale CA; de Boer PA
    J Bacteriol; 2002 May; 184(9):2552-6. PubMed ID: 11948172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The early divisome protein FtsA interacts directly through its 1c subdomain with the cytoplasmic domain of the late divisome protein FtsN.
    Busiek KK; Eraso JM; Wang Y; Margolin W
    J Bacteriol; 2012 Apr; 194(8):1989-2000. PubMed ID: 22328664
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A mutation in Escherichia coli ftsZ bypasses the requirement for the essential division gene zipA and confers resistance to FtsZ assembly inhibitors by stabilizing protofilament bundling.
    Haeusser DP; Rowlett VW; Margolin W
    Mol Microbiol; 2015 Sep; 97(5):988-1005. PubMed ID: 26046682
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Direct interactions of early and late assembling division proteins in Escherichia coli cells resolved by FRET.
    Alexeeva S; Gadella TW; Verheul J; Verhoeven GS; den Blaauwen T
    Mol Microbiol; 2010 Jul; 77(2):384-98. PubMed ID: 20497333
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FtsN-like proteins are conserved components of the cell division machinery in proteobacteria.
    Möll A; Thanbichler M
    Mol Microbiol; 2009 May; 72(4):1037-53. PubMed ID: 19400794
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FtsN, a late recruit to the septum in Escherichia coli.
    Addinall SG; Cao C; Lutkenhaus J
    Mol Microbiol; 1997 Jul; 25(2):303-9. PubMed ID: 9282742
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Examination of the interaction between FtsZ and MinCN in E. coli suggests how MinC disrupts Z rings.
    Shen B; Lutkenhaus J
    Mol Microbiol; 2010 Mar; 75(5):1285-98. PubMed ID: 20132438
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Premature targeting of a cell division protein to midcell allows dissection of divisome assembly in Escherichia coli.
    Goehring NW; Gueiros-Filho F; Beckwith J
    Genes Dev; 2005 Jan; 19(1):127-37. PubMed ID: 15630023
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.