274 related articles for article (PubMed ID: 17114255)
1. 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]
2. Different minimal signal peptide lengths recognized by the archaeal prepilin-like peptidases FlaK and PibD.
Ng SY; VanDyke DJ; Chaban B; Wu J; Nosaka Y; Aizawa S; Jarrell KF
J Bacteriol; 2009 Nov; 191(21):6732-40. PubMed ID: 19717585
[TBL] [Abstract][Full Text] [Related]
3. Effect of changes at the conserved + 3 position of mature archaellins on in vitro cleavage by the pre-archaellin peptidase FlaK of Methanococcus maripaludis.
Jarrell KF
Arch Microbiol; 2020 Sep; 202(7):1669-1675. PubMed ID: 32285165
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Identification of an additional minor pilin essential for piliation in the archaeon Methanococcus maripaludis.
Nair DB; Chung DK; Schneider J; Uchida K; Aizawa S; Jarrell KF
PLoS One; 2013; 8(12):e83961. PubMed ID: 24386316
[TBL] [Abstract][Full Text] [Related]
6. Cleavage of preflagellins by an aspartic acid signal peptidase is essential for flagellation in the archaeon Methanococcus voltae.
Bardy SL; Jarrell KF
Mol Microbiol; 2003 Nov; 50(4):1339-47. PubMed ID: 14622420
[TBL] [Abstract][Full Text] [Related]
7. Archaeal type IV pilus-like structures--evolutionarily conserved prokaryotic surface organelles.
Pohlschroder M; Ghosh A; Tripepi M; Albers SV
Curr Opin Microbiol; 2011 Jun; 14(3):357-63. PubMed ID: 21482178
[TBL] [Abstract][Full Text] [Related]
8. FlaK of the archaeon Methanococcus maripaludis possesses preflagellin peptidase activity.
Bardy SL; Jarrell KF
FEMS Microbiol Lett; 2002 Feb; 208(1):53-9. PubMed ID: 11934494
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Archaeal signal peptidases.
Ng SY; Chaban B; VanDyke DJ; Jarrell KF
Microbiology (Reading); 2007 Feb; 153(Pt 2):305-14. PubMed ID: 17259602
[TBL] [Abstract][Full Text] [Related]
12. Overexpression of Methanococcus voltae flagellin subunits in Escherichia coli and Pseudomonas aeruginosa: a source of archaeal preflagellin.
Bayley DP; Jarrell KF
J Bacteriol; 1999 Jul; 181(14):4146-53. PubMed ID: 10400569
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genetic and mass spectrometry analyses of the unusual type IV-like pili of the archaeon Methanococcus maripaludis.
Ng SY; Wu J; Nair DB; Logan SM; Robotham A; Tessier L; Kelly JF; Uchida K; Aizawa S; Jarrell KF
J Bacteriol; 2011 Feb; 193(4):804-14. PubMed ID: 21075925
[TBL] [Abstract][Full Text] [Related]
15. Pilin Processing Follows a Different Temporal Route than That of Archaellins in Methanococcus maripaludis.
Nair DB; Jarrell KF
Life (Basel); 2015 Jan; 5(1):85-101. PubMed ID: 25569238
[TBL] [Abstract][Full Text] [Related]
16. Recent advances in the structure and assembly of the archaeal flagellum.
Bardy SL; Ng SY; Jarrell KF
J Mol Microbiol Biotechnol; 2004; 7(1-2):41-51. PubMed ID: 15170402
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Two distinct archaeal type IV pili structures formed by proteins with identical sequence.
Liu J; Eastep GN; Cvirkaite-Krupovic V; Rich-New ST; Kreutzberger MAB; Egelman EH; Krupovic M; Wang F
Nat Commun; 2024 Jun; 15(1):5049. PubMed ID: 38877064
[TBL] [Abstract][Full Text] [Related]
19. Exceptionally widespread nanomachines composed of type IV pilins: the prokaryotic Swiss Army knives.
Berry JL; Pelicic V
FEMS Microbiol Rev; 2015 Jan; 39(1):134-54. PubMed ID: 25793961
[TBL] [Abstract][Full Text] [Related]
20. An Aeromonas salmonicida type IV pilin is required for virulence in rainbow trout Oncorhynchus mykiss.
Masada CL; LaPatra SE; Morton AW; Strom MS
Dis Aquat Organ; 2002 Aug; 51(1):13-25. PubMed ID: 12240967
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
