866 related articles for article (PubMed ID: 14640699)
1. Lipid-protein interactions studied by introduction of a tryptophan residue: the mechanosensitive channel MscL.
Powl AM; East JM; Lee AG
Biochemistry; 2003 Dec; 42(48):14306-17. PubMed ID: 14640699
[TBL] [Abstract][Full Text] [Related]
2. Heterogeneity in the binding of lipid molecules to the surface of a membrane protein: hot spots for anionic lipids on the mechanosensitive channel of large conductance MscL and effects on conformation.
Powl AM; East JM; Lee AG
Biochemistry; 2005 Apr; 44(15):5873-83. PubMed ID: 15823046
[TBL] [Abstract][Full Text] [Related]
3. The role of tryptophan residues in an integral membrane protein: diacylglycerol kinase.
Clark EH; East JM; Lee AG
Biochemistry; 2003 Sep; 42(37):11065-73. PubMed ID: 12974643
[TBL] [Abstract][Full Text] [Related]
4. Identification of the hydrophobic thickness of a membrane protein using fluorescence spectroscopy: studies with the mechanosensitive channel MscL.
Powl AM; Wright JN; East JM; Lee AG
Biochemistry; 2005 Apr; 44(15):5713-21. PubMed ID: 15823029
[TBL] [Abstract][Full Text] [Related]
5. A fluorescence method to define transmembrane alpha-helices in membrane proteins: studies with bacterial diacylglycerol kinase.
Jittikoon J; East JM; Lee AG
Biochemistry; 2007 Sep; 46(38):10950-9. PubMed ID: 17722884
[TBL] [Abstract][Full Text] [Related]
6. Orientation of LamB signal peptides in bilayers: influence of lipid probes on peptide binding and interpretation of fluorescence quenching data.
Voglino L; Simon SA; McIntosh TJ
Biochemistry; 1999 Jun; 38(23):7509-16. PubMed ID: 10360948
[TBL] [Abstract][Full Text] [Related]
7. Tryptophan spectroscopy studies and black lipid bilayer analysis indicate that the oligomeric structure of Cry1Ab toxin from Bacillus thuringiensis is the membrane-insertion intermediate.
Rausell C; Muñoz-Garay C; Miranda-CassoLuengo R; Gómez I; Rudiño-Piñera E; Soberón M; Bravo A
Biochemistry; 2004 Jan; 43(1):166-74. PubMed ID: 14705942
[TBL] [Abstract][Full Text] [Related]
8. Interaction of C-terminal loop 13 of sodium-glucose cotransporter SGLT1 with lipid bilayers.
Raja MM; Kinne RK
Biochemistry; 2005 Jun; 44(25):9123-9. PubMed ID: 15966736
[TBL] [Abstract][Full Text] [Related]
9. Identification of a chameleon-like pH-sensitive segment within the colicin E1 channel domain that may serve as the pH-activated trigger for membrane bilayer association.
Merrill AR; Steer BA; Prentice GA; Weller MJ; Szabo AG
Biochemistry; 1997 Jun; 36(23):6874-84. PubMed ID: 9188682
[TBL] [Abstract][Full Text] [Related]
10. Control of the transmembrane orientation and interhelical interactions within membranes by hydrophobic helix length.
Ren J; Lew S; Wang J; London E
Biochemistry; 1999 May; 38(18):5905-12. PubMed ID: 10231543
[TBL] [Abstract][Full Text] [Related]
11. Importance of direct interactions with lipids for the function of the mechanosensitive channel MscL.
Powl AM; East JM; Lee AG
Biochemistry; 2008 Nov; 47(46):12175-84. PubMed ID: 18950196
[TBL] [Abstract][Full Text] [Related]
12. Interactions of phospholipids with the potassium channel KcsA.
Williamson IM; Alvis SJ; East JM; Lee AG
Biophys J; 2002 Oct; 83(4):2026-38. PubMed ID: 12324421
[TBL] [Abstract][Full Text] [Related]
13. Capping transmembrane helices of MscL with aromatic residues changes channel response to membrane stretch.
Chiang CS; Shirinian L; Sukharev S
Biochemistry; 2005 Sep; 44(37):12589-97. PubMed ID: 16156671
[TBL] [Abstract][Full Text] [Related]
14. Mechanosensitive channel of Thermoplasma, the cell wall-less archaea: cloning and molecular characterization.
Kloda A; Martinac B
Cell Biochem Biophys; 2001; 34(3):321-47. PubMed ID: 11898860
[TBL] [Abstract][Full Text] [Related]
15. Site-directed mutagenesis of the greasy slide aromatic residues within the LamB (maltoporin) channel of Escherichia coli: effect on ion and maltopentaose transport.
Denker K; Orlik F; Schiffler B; Benz R
J Mol Biol; 2005 Sep; 352(3):534-50. PubMed ID: 16095613
[TBL] [Abstract][Full Text] [Related]
16. Different effects of lipid chain length on the two sides of a membrane and the lipid annulus of MscL.
Powl AM; East JM; Lee AG
Biophys J; 2007 Jul; 93(1):113-22. PubMed ID: 17416625
[TBL] [Abstract][Full Text] [Related]
17. Binding regions of outer membrane protein A in complexes with the periplasmic chaperone Skp. A site-directed fluorescence study.
Qu J; Behrens-Kneip S; Holst O; Kleinschmidt JH
Biochemistry; 2009 Jun; 48(22):4926-36. PubMed ID: 19382746
[TBL] [Abstract][Full Text] [Related]
18. Modulation of the binding of signal peptides to lipid bilayers by dipoles near the hydrocarbon-water interface.
Voglino L; McIntosh TJ; Simon SA
Biochemistry; 1998 Sep; 37(35):12241-52. PubMed ID: 9724538
[TBL] [Abstract][Full Text] [Related]
19. Trp2063 and Trp2064 in the factor Va C2 domain are required for high-affinity binding to phospholipid membranes but not for assembly of the prothrombinase complex.
Peng W; Quinn-Allen MA; Kim SW; Alexander KA; Kane WH
Biochemistry; 2004 Apr; 43(14):4385-93. PubMed ID: 15065883
[TBL] [Abstract][Full Text] [Related]
20. Effect of variations in the structure of a polyleucine-based alpha-helical transmembrane peptide on its interaction with phosphatidylglycerol bilayers.
Liu F; Lewis RN; Hodges RS; McElhaney RN
Biochemistry; 2004 Mar; 43(12):3679-87. PubMed ID: 15035638
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
