212 related articles for article (PubMed ID: 22556361)
1. The VC1777-VC1779 proteins are members of a sialic acid-specific subfamily of TRAP transporters (SiaPQM) and constitute the sole route of sialic acid uptake in the human pathogen Vibrio cholerae.
Chowdhury N; Norris J; McAlister E; Lau SYK; Thomas GH; Boyd EF
Microbiology (Reading); 2012 Aug; 158(Pt 8):2158-2167. PubMed ID: 22556361
[TBL] [Abstract][Full Text] [Related]
2. The membrane proteins SiaQ and SiaM form an essential stoichiometric complex in the sialic acid tripartite ATP-independent periplasmic (TRAP) transporter SiaPQM (VC1777-1779) from Vibrio cholerae.
Mulligan C; Leech AP; Kelly DJ; Thomas GH
J Biol Chem; 2012 Jan; 287(5):3598-608. PubMed ID: 22167185
[TBL] [Abstract][Full Text] [Related]
3. Sialic acid catabolism and transport gene clusters are lineage specific in Vibrio vulnificus.
Lubin JB; Kingston JJ; Chowdhury N; Boyd EF
Appl Environ Microbiol; 2012 May; 78(9):3407-15. PubMed ID: 22344665
[TBL] [Abstract][Full Text] [Related]
4. Sialic acid catabolism confers a competitive advantage to pathogenic vibrio cholerae in the mouse intestine.
Almagro-Moreno S; Boyd EF
Infect Immun; 2009 Sep; 77(9):3807-16. PubMed ID: 19564383
[TBL] [Abstract][Full Text] [Related]
5. Host-Derived Sialic Acids Are an Important Nutrient Source Required for Optimal Bacterial Fitness In Vivo.
McDonald ND; Lubin JB; Chowdhury N; Boyd EF
mBio; 2016 Apr; 7(2):e02237-15. PubMed ID: 27073099
[TBL] [Abstract][Full Text] [Related]
6. Insights into the evolution of sialic acid catabolism among bacteria.
Almagro-Moreno S; Boyd EF
BMC Evol Biol; 2009 May; 9():118. PubMed ID: 19470179
[TBL] [Abstract][Full Text] [Related]
7. Functional characterization of VC1929 of Vibrio cholerae El Tor: role in mannose-sensitive haemagglutination, virulence and utilization of sialic acid.
Sharma SK; Moe TS; Srivastava R; Chandra D; Srivastava BS
Microbiology (Reading); 2011 Nov; 157(Pt 11):3180-3186. PubMed ID: 21873407
[TBL] [Abstract][Full Text] [Related]
8. Sialic acid transport in Haemophilus influenzae is essential for lipopolysaccharide sialylation and serum resistance and is dependent on a novel tripartite ATP-independent periplasmic transporter.
Severi E; Randle G; Kivlin P; Whitfield K; Young R; Moxon R; Kelly D; Hood D; Thomas GH
Mol Microbiol; 2005 Nov; 58(4):1173-85. PubMed ID: 16262798
[TBL] [Abstract][Full Text] [Related]
9. Excision dynamics of Vibrio pathogenicity island-2 from Vibrio cholerae: role of a recombination directionality factor VefA.
Almagro-Moreno S; Napolitano MG; Boyd EF
BMC Microbiol; 2010 Nov; 10():306. PubMed ID: 21118541
[TBL] [Abstract][Full Text] [Related]
10. The substrate-binding protein imposes directionality on an electrochemical sodium gradient-driven TRAP transporter.
Mulligan C; Geertsma ER; Severi E; Kelly DJ; Poolman B; Thomas GH
Proc Natl Acad Sci U S A; 2009 Feb; 106(6):1778-83. PubMed ID: 19179287
[TBL] [Abstract][Full Text] [Related]
11. Tripartite ATP-Independent Periplasmic (TRAP) Transporters and Tripartite Tricarboxylate Transporters (TTT): From Uptake to Pathogenicity.
Rosa LT; Bianconi ME; Thomas GH; Kelly DJ
Front Cell Infect Microbiol; 2018; 8():33. PubMed ID: 29479520
[TBL] [Abstract][Full Text] [Related]
12. Tripartite ATP-independent Periplasmic (TRAP) Transporters Use an Arginine-mediated Selectivity Filter for High Affinity Substrate Binding.
Fischer M; Hopkins AP; Severi E; Hawkhead J; Bawdon D; Watts AG; Hubbard RE; Thomas GH
J Biol Chem; 2015 Nov; 290(45):27113-27123. PubMed ID: 26342690
[TBL] [Abstract][Full Text] [Related]
13. Sialic acid utilization by the soil bacterium Corynebacterium glutamicum.
Gruteser N; Marin K; Krämer R; Thomas GH
FEMS Microbiol Lett; 2012 Nov; 336(2):131-8. PubMed ID: 22924979
[TBL] [Abstract][Full Text] [Related]
14. Bacterial periplasmic sialic acid-binding proteins exhibit a conserved binding site.
Gangi Setty T; Cho C; Govindappa S; Apicella MA; Ramaswamy S
Acta Crystallogr D Biol Crystallogr; 2014 Jul; 70(Pt 7):1801-11. PubMed ID: 25004958
[TBL] [Abstract][Full Text] [Related]
15. Characterization of ferric and ferrous iron transport systems in Vibrio cholerae.
Wyckoff EE; Mey AR; Leimbach A; Fisher CF; Payne SM
J Bacteriol; 2006 Sep; 188(18):6515-23. PubMed ID: 16952942
[TBL] [Abstract][Full Text] [Related]
16. Transport and catabolism of the sialic acids N-glycolylneuraminic acid and 3-keto-3-deoxy-D-glycero-D-galactonononic acid by Escherichia coli K-12.
Hopkins AP; Hawkhead JA; Thomas GH
FEMS Microbiol Lett; 2013 Oct; 347(1):14-22. PubMed ID: 23848303
[TBL] [Abstract][Full Text] [Related]
17. Sialic acid catabolism in Staphylococcus aureus.
Olson ME; King JM; Yahr TL; Horswill AR
J Bacteriol; 2013 Apr; 195(8):1779-88. PubMed ID: 23396916
[TBL] [Abstract][Full Text] [Related]
18. Haem utilization in Vibrio cholerae involves multiple TonB-dependent haem receptors.
Mey AR; Payne SM
Mol Microbiol; 2001 Nov; 42(3):835-49. PubMed ID: 11722746
[TBL] [Abstract][Full Text] [Related]
19. Molecular evolution of Vibrio pathogenicity island-2 (VPI-2): mosaic structure among Vibrio cholerae and Vibrio mimicus natural isolates.
Jermyn WS; Boyd EF
Microbiology (Reading); 2005 Jan; 151(Pt 1):311-322. PubMed ID: 15632448
[TBL] [Abstract][Full Text] [Related]
20. Characterization of a novel sialic acid transporter of the sodium solute symporter (SSS) family and in vivo comparison with known bacterial sialic acid transporters.
Severi E; Hosie AH; Hawkhead JA; Thomas GH
FEMS Microbiol Lett; 2010 Mar; 304(1):47-54. PubMed ID: 20100283
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]