259 related articles for article (PubMed ID: 24945931)
1. A conserved type IV pilin signal peptide H-domain is critical for the post-translational regulation of flagella-dependent motility.
Esquivel RN; Pohlschroder M
Mol Microbiol; 2014 Aug; 93(3):494-504. PubMed ID: 24945931
[TBL] [Abstract][Full Text] [Related]
2. Identification of Haloferax volcanii Pilin N-Glycans with Diverse Roles in Pilus Biosynthesis, Adhesion, and Microcolony Formation.
Esquivel RN; Schulze S; Xu R; Hippler M; Pohlschroder M
J Biol Chem; 2016 May; 291(20):10602-14. PubMed ID: 26966177
[TBL] [Abstract][Full Text] [Related]
3. Involvement of ArlI, ArlJ, and CirA in archaeal type IV pilin-mediated motility regulation.
Chatterjee P; Garcia MA; Cote JA; Yun K; Legerme GP; Habib R; Tripepi M; Young C; Kulp D; Dyall-Smith M; Pohlschroder M
J Bacteriol; 2024 Jun; 206(6):e0008924. PubMed ID: 38819156
[TBL] [Abstract][Full Text] [Related]
4. Novel archaeal adhesion pilins with a conserved N terminus.
Esquivel RN; Xu R; Pohlschroder M
J Bacteriol; 2013 Sep; 195(17):3808-18. PubMed ID: 23794623
[TBL] [Abstract][Full Text] [Related]
5. Archaeal flagella, bacterial flagella and type IV pili: a comparison of genes and posttranslational modifications.
Ng SY; Chaban B; Jarrell KF
J Mol Microbiol Biotechnol; 2006; 11(3-5):167-91. PubMed ID: 16983194
[TBL] [Abstract][Full Text] [Related]
6. Haloferax volcanii Immersed Liquid Biofilms Develop Independently of Known Biofilm Machineries and Exhibit Rapid Honeycomb Pattern Formation.
Schiller H; Schulze S; Mutan Z; de Vaulx C; Runcie C; Schwartz J; Rados T; Bisson Filho AW; Pohlschroder M
mSphere; 2020 Dec; 5(6):. PubMed ID: 33328348
[TBL] [Abstract][Full Text] [Related]
7. Pseudomonas aeruginosa minor pilins are incorporated into type IV pili.
Giltner CL; Habash M; Burrows LL
J Mol Biol; 2010 May; 398(3):444-61. PubMed ID: 20338182
[TBL] [Abstract][Full Text] [Related]
8. Neisseria meningitidis Type IV Pili Composed of Sequence Invariable Pilins Are Masked by Multisite Glycosylation.
Gault J; Ferber M; Machata S; Imhaus AF; Malosse C; Charles-Orszag A; Millien C; Bouvier G; Bardiaux B; Péhau-Arnaudet G; Klinge K; Podglajen I; Ploy MC; Seifert HS; Nilges M; Chamot-Rooke J; Duménil G
PLoS Pathog; 2015 Sep; 11(9):e1005162. PubMed ID: 26367394
[TBL] [Abstract][Full Text] [Related]
9. Archaeal type IV pili and their involvement in biofilm formation.
Pohlschroder M; Esquivel RN
Front Microbiol; 2015; 6():190. PubMed ID: 25852657
[TBL] [Abstract][Full Text] [Related]
10. Haloferax volcanii flagella are required for motility but are not involved in PibD-dependent surface adhesion.
Tripepi M; Imam S; Pohlschröder M
J Bacteriol; 2010 Jun; 192(12):3093-102. PubMed ID: 20363933
[TBL] [Abstract][Full Text] [Related]
11. Haloferax volcanii Proteome Response to Deletion of a Rhomboid Protease Gene.
Costa MI; Cerletti M; Paggi RA; Trötschel C; De Castro RE; Poetsch A; Giménez MI
J Proteome Res; 2018 Mar; 17(3):961-977. PubMed ID: 29301397
[TBL] [Abstract][Full Text] [Related]
12. Limited Cross-Complementation Between
Legerme G; Pohlschroder M
Front Microbiol; 2019; 10():700. PubMed ID: 31068907
[TBL] [Abstract][Full Text] [Related]
13. Permuting the PGF Signature Motif Blocks both Archaeosortase-Dependent C-Terminal Cleavage and Prenyl Lipid Attachment for the Haloferax volcanii S-Layer Glycoprotein.
Abdul Halim MF; Karch KR; Zhou Y; Haft DH; Garcia BA; Pohlschroder M
J Bacteriol; 2015 Dec; 198(5):808-15. PubMed ID: 26712937
[TBL] [Abstract][Full Text] [Related]
14. N-glycosylation of Haloferax volcanii flagellins requires known Agl proteins and is essential for biosynthesis of stable flagella.
Tripepi M; You J; Temel S; Önder Ö; Brisson D; Pohlschröder M
J Bacteriol; 2012 Sep; 194(18):4876-87. PubMed ID: 22730124
[TBL] [Abstract][Full Text] [Related]
15. ArtA-Dependent Processing of a Tat Substrate Containing a Conserved Tripartite Structure That Is Not Localized at the C Terminus.
Abdul Halim MF; Stoltzfus JD; Schulze S; Hippler M; Pohlschroder M
J Bacteriol; 2017 Apr; 199(7):. PubMed ID: 28069824
[TBL] [Abstract][Full Text] [Related]
16. Identification of diverse archaeal proteins with class III signal peptides cleaved by distinct archaeal prepilin peptidases.
Szabó Z; Stahl AO; Albers SV; Kissinger JC; Driessen AJ; Pohlschröder M
J Bacteriol; 2007 Feb; 189(3):772-8. PubMed ID: 17114255
[TBL] [Abstract][Full Text] [Related]
17. The Pseudomonas aeruginosa type IV pilin receptor binding domain functions as an adhesin for both biotic and abiotic surfaces.
Giltner CL; van Schaik EJ; Audette GF; Kao D; Hodges RS; Hassett DJ; Irvin RT
Mol Microbiol; 2006 Feb; 59(4):1083-96. PubMed ID: 16430686
[TBL] [Abstract][Full Text] [Related]
18. Archaeal type IV pili stabilize Haloferax volcanii biofilms in flow.
Odermatt PD; Nussbaum P; Monnappa S; Talà L; Li Z; Sivabalasarma S; Albers SV; Persat A
Curr Biol; 2023 Aug; 33(15):3265-3271.e4. PubMed ID: 37473762
[TBL] [Abstract][Full Text] [Related]
19. Evidence for the Sialylation of PilA, the PI-2a Pilus-Associated Adhesin of Streptococcus agalactiae Strain NEM316.
Morello E; Mallet A; Konto-Ghiorghi Y; Chaze T; Mistou MY; Oliva G; Oliveira L; Di Guilmi AM; Trieu-Cuot P; Dramsi S
PLoS One; 2015; 10(9):e0138103. PubMed ID: 26407005
[TBL] [Abstract][Full Text] [Related]
20. Analysis of type IV pilus and its associated motility in Myxococcus xanthus using an antibody reactive with native pilin and pili.
Li Y; Lux R; Pelling AE; Gimzewski JK; Shi W
Microbiology (Reading); 2005 Feb; 151(Pt 2):353-360. PubMed ID: 15699186
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]