These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 11257515)

  • 1. Structural and functional studies of alpha-helix 5 region from Bacillus thuringiensis Cry1Ab delta-endotoxin.
    Nuñez-Valdez M; Sánchez J; Lina L; Güereca L; Bravo A
    Biochim Biophys Acta; 2001 Mar; 1546(1):122-31. PubMed ID: 11257515
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of mutations in the pore-forming region essential for insecticidal activity of a Bacillus thuringiensis delta-endotoxin.
    Kumar AS; Aronson AI
    J Bacteriol; 1999 Oct; 181(19):6103-7. PubMed ID: 10498724
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bacillus thuringiensis Cry1Ab mutants affecting oligomer formation are non-toxic to Manduca sexta larvae.
    Jiménez-Juárez N; Muñoz-Garay C; Gómez I; Saab-Rincon G; Damian-Almazo JY; Gill SS; Soberón M; Bravo A
    J Biol Chem; 2007 Jul; 282(29):21222-9. PubMed ID: 17537728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Helix 4 mutants of the Bacillus thuringiensis insecticidal toxin Cry1Aa display altered pore-forming abilities.
    Vachon V; Préfontaine G; Rang C; Coux F; Juteau M; Schwartz JL; Brousseau R; Frutos R; Laprade R; Masson L
    Appl Environ Microbiol; 2004 Oct; 70(10):6123-30. PubMed ID: 15466558
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Importance of polarity of the α4-α5 loop residue-Asn(166) in the pore-forming domain of the Bacillus thuringiensis Cry4Ba toxin: implications for ion permeation and pore opening.
    Juntadech T; Kanintronkul Y; Kanchanawarin C; Katzenmeier G; Angsuthanasombat C
    Biochim Biophys Acta; 2014 Jan; 1838(1 Pt B):319-27. PubMed ID: 24120447
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The alpha-helix 4 residue, Asn135, is involved in the oligomerization of Cry1Ac1 and Cry1Ab5 Bacillus thuringiensis toxins.
    Tigue NJ; Jacoby J; Ellar DJ
    Appl Environ Microbiol; 2001 Dec; 67(12):5715-20. PubMed ID: 11722927
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Role of alpha-helix seven of Bacillus thuringiensis Cry1Ab delta-endotoxin in membrane insertion, structural stability, and ion channel activity.
    Alcantara EP; Alzate O; Lee MK; Curtiss A; Dean DH
    Biochemistry; 2001 Feb; 40(8):2540-7. PubMed ID: 11327876
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Role of tryptophan residues in toxicity of Cry1Ab toxin from Bacillus thuringiensis.
    Padilla C; Pardo-López L; de la Riva G; Gómez I; Sánchez J; Hernandez G; Nuñez ME; Carey MP; Dean DH; Alzate O; Soberón M; Bravo A
    Appl Environ Microbiol; 2006 Jan; 72(1):901-7. PubMed ID: 16391132
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutagenesis of three surface-exposed loops of a Bacillus thuringiensis insecticidal toxin reveals residues important for toxicity, receptor recognition and possibly membrane insertion.
    Smedley DP; Ellar DJ
    Microbiology (Reading); 1996 Jul; 142 ( Pt 7)():1617-24. PubMed ID: 8757726
    [TBL] [Abstract][Full Text] [Related]  

  • 10. N-acetylgalactosamine on the putative insect receptor aminopeptidase N is recognised by a site on the domain III lectin-like fold of a Bacillus thuringiensis insecticidal toxin.
    Burton SL; Ellar DJ; Li J; Derbyshire DJ
    J Mol Biol; 1999 Apr; 287(5):1011-22. PubMed ID: 10222207
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dominant negative phenotype of Bacillus thuringiensis Cry1Ab, Cry11Aa and Cry4Ba mutants suggest hetero-oligomer formation among different Cry toxins.
    Carmona D; Rodríguez-Almazán C; Muñoz-Garay C; Portugal L; Pérez C; de Maagd RA; Bakker P; Soberón M; Bravo A
    PLoS One; 2011; 6(5):e19952. PubMed ID: 21603577
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single amino acid changes in domain II of Bacillus thuringiensis CryIAb delta-endotoxin affect irreversible binding to Manduca sexta midgut membrane vesicles.
    Rajamohan F; Alcantara E; Lee MK; Chen XJ; Curtiss A; Dean DH
    J Bacteriol; 1995 May; 177(9):2276-82. PubMed ID: 7730254
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bacillus thuringiensis Cry4Aa insecticidal protein: functional importance of the intrinsic stability of the unique α4-α5 loop comprising the Pro-rich sequence.
    Imtong C; Kanchanawarin C; Katzenmeier G; Angsuthanasombat C
    Biochim Biophys Acta; 2014 Jun; 1844(6):1111-8. PubMed ID: 24632526
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Asn183 in alpha5 is essential for oligomerisation and toxicity of the Bacillus thuringiensis Cry4Ba toxin.
    Likitvivatanavong S; Katzenmeier G; Angsuthanasombat C
    Arch Biochem Biophys; 2006 Jan; 445(1):46-55. PubMed ID: 16356469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Specific epitopes of domains II and III of Bacillus thuringiensis Cry1Ab toxin involved in the sequential interaction with cadherin and aminopeptidase-N receptors in Manduca sexta.
    Gómez I; Arenas I; Benitez I; Miranda-Ríos J; Becerril B; Grande R; Almagro JC; Bravo A; Soberón M
    J Biol Chem; 2006 Nov; 281(45):34032-9. PubMed ID: 16968705
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structural changes of the Cry1Ac oligomeric pre-pore from bacillus thuringiensis induced by N-acetylgalactosamine facilitates toxin membrane insertion.
    Pardo-López L; Gómez I; Rausell C; Sanchez J; Soberón M; Bravo A
    Biochemistry; 2006 Aug; 45(34):10329-36. PubMed ID: 16922508
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Domains II and III of Bacillus thuringiensis Cry1Ab toxin remain exposed to the solvent after insertion of part of domain I into the membrane.
    Zavala LE; Pardo-López L; Cantón PE; Gómez I; Soberón M; Bravo A
    J Biol Chem; 2011 May; 286(21):19109-17. PubMed ID: 21464133
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Enhancement of Bacillus thuringiensis Cry1Ab and Cry1Fa Toxicity to Spodoptera frugiperda by Domain III Mutations Indicates There Are Two Limiting Steps in Toxicity as Defined by Receptor Binding and Protein Stability.
    Gómez I; Ocelotl J; Sánchez J; Lima C; Martins E; Rosales-Juárez A; Aguilar-Medel S; Abad A; Dong H; Monnerat R; Peña G; Zhang J; Nelson M; Wu G; Bravo A; Soberón M
    Appl Environ Microbiol; 2018 Oct; 84(20):. PubMed ID: 30097439
    [No Abstract]   [Full Text] [Related]  

  • 19. Mutations in domain I interhelical loops affect the rate of pore formation by the Bacillus thuringiensis Cry1Aa toxin in insect midgut brush border membrane vesicles.
    Lebel G; Vachon V; Préfontaine G; Girard F; Masson L; Juteau M; Bah A; Larouche G; Vincent C; Laprade R; Schwartz JL
    Appl Environ Microbiol; 2009 Jun; 75(12):3842-50. PubMed ID: 19376918
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Role of alkaline phosphatase from Manduca sexta in the mechanism of action of Bacillus thuringiensis Cry1Ab toxin.
    Arenas I; Bravo A; Soberón M; Gómez I
    J Biol Chem; 2010 Apr; 285(17):12497-503. PubMed ID: 20177063
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.