156 related articles for article (PubMed ID: 35030303)
1. Chimeric mutants of staphylococcal hemolysin, which act as both one-component and two-component hemolysin, created by grafting the stem domain.
Ghanem N; Kanagami N; Matsui T; Takeda K; Kaneko J; Shiraishi Y; Choe CA; Uchikubo-Kamo T; Shirouzu M; Hashimoto T; Ogawa T; Matsuura T; Huang PS; Yokoyama T; Tanaka Y
FEBS J; 2022 Jun; 289(12):3505-3520. PubMed ID: 35030303
[TBL] [Abstract][Full Text] [Related]
2. Intermolecular ionic interactions serve as a possible switch for stem release in the staphylococcal bi-component toxin for β-barrel pore assembly.
Takeda K; Tanaka Y; Abe N; Kaneko J
Toxicon; 2018 Dec; 155():43-48. PubMed ID: 30312693
[TBL] [Abstract][Full Text] [Related]
3. Controlling pore assembly of staphylococcal gamma-haemolysin by low temperature and by disulphide bond formation in double-cysteine LukF mutants.
Nguyen VT; Higuchi H; Kamio Y
Mol Microbiol; 2002 Sep; 45(6):1485-98. PubMed ID: 12354220
[TBL] [Abstract][Full Text] [Related]
4. Further study on the two pivotal parts of Hlg2 for the full hemolytic activity of staphylococcal gamma-hemolysin.
Yokota K; Sugawara N; Nariya H; Kaneko J; Tomita T; Kamio Y
Biosci Biotechnol Biochem; 1998 Sep; 62(9):1745-50. PubMed ID: 9805375
[TBL] [Abstract][Full Text] [Related]
5. Bacterial two-component and hetero-heptameric pore-forming cytolytic toxins: structures, pore-forming mechanism, and organization of the genes.
Kaneko J; Kamio Y
Biosci Biotechnol Biochem; 2004 May; 68(5):981-1003. PubMed ID: 15170101
[TBL] [Abstract][Full Text] [Related]
6. Stochastic assembly of two-component staphylococcal gamma-hemolysin into heteroheptameric transmembrane pores with alternate subunit arrangements in ratios of 3:4 and 4:3.
Sugawara-Tomita N; Tomita T; Kamio Y
J Bacteriol; 2002 Sep; 184(17):4747-56. PubMed ID: 12169599
[TBL] [Abstract][Full Text] [Related]
7. Subunit composition of a bicomponent toxin: staphylococcal leukocidin forms an octameric transmembrane pore.
Miles G; Movileanu L; Bayley H
Protein Sci; 2002 Apr; 11(4):894-902. PubMed ID: 11910032
[TBL] [Abstract][Full Text] [Related]
8. Crystal structure of the octameric pore of staphylococcal γ-hemolysin reveals the β-barrel pore formation mechanism by two components.
Yamashita K; Kawai Y; Tanaka Y; Hirano N; Kaneko J; Tomita N; Ohta M; Kamio Y; Yao M; Tanaka I
Proc Natl Acad Sci U S A; 2011 Oct; 108(42):17314-9. PubMed ID: 21969538
[TBL] [Abstract][Full Text] [Related]
9. Structural basis for pore-forming mechanism of staphylococcal α-hemolysin.
Sugawara T; Yamashita D; Kato K; Peng Z; Ueda J; Kaneko J; Kamio Y; Tanaka Y; Yao M
Toxicon; 2015 Dec; 108():226-31. PubMed ID: 26428390
[TBL] [Abstract][Full Text] [Related]
10. The N-terminal amino-latch region of Hlg2 component of staphylococcal bi-component γ-haemolysin is dispensable for prestem release to form β-barrel pores.
Takeda K; Tanaka Y; Kaneko J
J Biochem; 2020 Oct; 168(4):349-354. PubMed ID: 32330256
[TBL] [Abstract][Full Text] [Related]
11. Membrane binding of pore-forming γ-hemolysin components studied at different lipid compositions.
Tarenzi T; Lattanzi G; Potestio R
Biochim Biophys Acta Biomembr; 2022 Sep; 1864(9):183970. PubMed ID: 35605647
[TBL] [Abstract][Full Text] [Related]
12. The structure of a Staphylococcus aureus leucocidin component (LukF-PV) reveals the fold of the water-soluble species of a family of transmembrane pore-forming toxins.
Pédelacq JD; Maveyraud L; Prévost G; Baba-Moussa L; González A; Courcelle E; Shepard W; Monteil H; Samama JP; Mourey L
Structure; 1999 Mar; 7(3):277-87. PubMed ID: 10368297
[TBL] [Abstract][Full Text] [Related]
13. Rim domain loops of staphylococcal β-pore forming bi-component toxin S-components recognize target human erythrocytes in a coordinated manner.
Peng Z; Takeshita M; Shibata N; Tada H; Tanaka Y; Kaneko J
J Biochem; 2018 Aug; 164(2):93-102. PubMed ID: 29474554
[TBL] [Abstract][Full Text] [Related]
14. Arresting and releasing Staphylococcal alpha-hemolysin at intermediate stages of pore formation by engineered disulfide bonds.
Kawate T; Gouaux E
Protein Sci; 2003 May; 12(5):997-1006. PubMed ID: 12717022
[TBL] [Abstract][Full Text] [Related]
15. Essential binding of LukF of staphylococcal gamma-hemolysin followed by the binding of H gamma II for the hemolysis of human erythrocytes.
Ozawa T; Kaneko J; Kamio Y
Biosci Biotechnol Biochem; 1995 Jun; 59(6):1181-3. PubMed ID: 7613012
[TBL] [Abstract][Full Text] [Related]
16. Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore.
Song L; Hobaugh MR; Shustak C; Cheley S; Bayley H; Gouaux JE
Science; 1996 Dec; 274(5294):1859-66. PubMed ID: 8943190
[TBL] [Abstract][Full Text] [Related]
17. Cryo-EM-based structural insights into supramolecular assemblies of γ-hemolysin from S. aureus reveal the pore formation mechanism.
Mishra S; Roy A; Dutta S
Structure; 2023 Jun; 31(6):651-667.e5. PubMed ID: 37019111
[TBL] [Abstract][Full Text] [Related]
18. Cluster-forming property correlated with hemolytic activity by staphylococcal γ-hemolysin transmembrane pores.
Tomita N; Abe K; Kamio Y; Ohta M
FEBS Lett; 2011 Nov; 585(21):3452-6. PubMed ID: 22001207
[TBL] [Abstract][Full Text] [Related]
19. Clostridial pore-forming toxins: powerful virulence factors.
Popoff MR
Anaerobe; 2014 Dec; 30():220-38. PubMed ID: 24952276
[TBL] [Abstract][Full Text] [Related]
20. Molecular basis of transmembrane beta-barrel formation of staphylococcal pore-forming toxins.
Yamashita D; Sugawara T; Takeshita M; Kaneko J; Kamio Y; Tanaka I; Tanaka Y; Yao M
Nat Commun; 2014 Sep; 5():4897. PubMed ID: 25263813
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
