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1
The membrane localization domains of two distinct bacterial toxins form a 4-helix-bundle in solution.
Protein Sci. 2017 Mar;26(3):497-504. doi: 10.1002/pro.3097. Epub 2017 Feb 14.
2
Backbone and side-chain assignments of an effector membrane localization domain from Vibrio vulnificus MARTX toxin.
Biomol NMR Assign. 2014 Oct;8(2):225-8. doi: 10.1007/s12104-013-9488-0. Epub 2013 Jun 14.
3
Cytotoxicity of the Vibrio vulnificus MARTX toxin effector DUF5 is linked to the C2A subdomain.
Proteins. 2014 Oct;82(10):2643-56. doi: 10.1002/prot.24628. Epub 2014 Jun 26.
4
Structural basis of inactivation of Ras and Rap1 small GTPases by Ras/Rap1-specific endopeptidase from the sepsis-causing pathogen .
J Biol Chem. 2018 Nov 23;293(47):18110-18122. doi: 10.1074/jbc.RA118.004857. Epub 2018 Oct 3.
5
Backbone and side-chain resonance assignments of the membrane localization domain from Pasteurella multocida toxin.
Biomol NMR Assign. 2014 Apr;8(1):221-4. doi: 10.1007/s12104-013-9487-1. Epub 2013 Jun 14.
6
Identification of a conserved membrane localization domain within numerous large bacterial protein toxins.
Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5581-6. doi: 10.1073/pnas.0908700107. Epub 2010 Mar 8.
7
Characterization of the membrane-targeting C1 domain in Pasteurella multocida toxin.
J Biol Chem. 2010 Aug 13;285(33):25467-75. doi: 10.1074/jbc.M110.102285. Epub 2010 Jun 9.
8
RRSP and RID Effector Domains Dominate the Virulence Impact of Vibrio vulnificus MARTX Toxin.
J Infect Dis. 2019 Feb 23;219(6):889-897. doi: 10.1093/infdis/jiy590.

引用本文的文献

1
α-Helices in the Type III Secretion Effectors: A Prevalent Feature with Versatile Roles.
Int J Mol Sci. 2021 May 21;22(11):5412. doi: 10.3390/ijms22115412.
2
Structural basis of inactivation of Ras and Rap1 small GTPases by Ras/Rap1-specific endopeptidase from the sepsis-causing pathogen .
J Biol Chem. 2018 Nov 23;293(47):18110-18122. doi: 10.1074/jbc.RA118.004857. Epub 2018 Oct 3.
4
Cytosolic Delivery of Multidomain Cargos by the N Terminus of Pasteurella multocida Toxin.
Infect Immun. 2018 Jul 23;86(8). doi: 10.1128/IAI.00248-18. Print 2018 Aug.

本文引用的文献

1
2
Cytotoxicity of the Vibrio vulnificus MARTX toxin effector DUF5 is linked to the C2A subdomain.
Proteins. 2014 Oct;82(10):2643-56. doi: 10.1002/prot.24628. Epub 2014 Jun 26.
3
Backbone and side-chain assignments of an effector membrane localization domain from Vibrio vulnificus MARTX toxin.
Biomol NMR Assign. 2014 Oct;8(2):225-8. doi: 10.1007/s12104-013-9488-0. Epub 2013 Jun 14.
4
Backbone and side-chain resonance assignments of the membrane localization domain from Pasteurella multocida toxin.
Biomol NMR Assign. 2014 Apr;8(1):221-4. doi: 10.1007/s12104-013-9487-1. Epub 2013 Jun 14.
5
Protein backbone and sidechain torsion angles predicted from NMR chemical shifts using artificial neural networks.
J Biomol NMR. 2013 Jul;56(3):227-41. doi: 10.1007/s10858-013-9741-y. Epub 2013 Jun 2.
6
General aspects and recent advances on bacterial protein toxins.
Cold Spring Harb Perspect Med. 2013 Feb 1;3(2):a013573. doi: 10.1101/cshperspect.a013573.
7
Structural determinants of Clostridium difficile toxin A glucosyltransferase activity.
J Biol Chem. 2012 Mar 9;287(11):8013-20. doi: 10.1074/jbc.M111.298414. Epub 2012 Jan 20.
8
Plasma membrane association of three classes of bacterial toxins is mediated by a basic-hydrophobic motif.
Cell Microbiol. 2012 Feb;14(2):286-98. doi: 10.1111/j.1462-5822.2011.01718.x. Epub 2011 Nov 29.
9
Membrane interaction of Pasteurella multocida toxin involves sphingomyelin.
FEBS J. 2011 Dec;278(23):4633-48. doi: 10.1111/j.1742-4658.2011.08365.x. Epub 2011 Oct 20.
10
Characterization of the membrane-targeting C1 domain in Pasteurella multocida toxin.
J Biol Chem. 2010 Aug 13;285(33):25467-75. doi: 10.1074/jbc.M110.102285. Epub 2010 Jun 9.

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