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Results: 1 to 20 of 96

1.

A protein sequence that can encode native structure by disfavoring alternate conformations.

Wigley WC, Corboy MJ, Cutler TD, Thibodeau PH, Oldan J, Lee MG, Rizo J, Hunt JF, Thomas PJ.

Nat Struct Biol. 2002 May;9(5):381-8.

PMID:
11938353
[PubMed - indexed for MEDLINE]
2.

Transmembrane domain of cystic fibrosis transmembrane conductance regulator: design, characterization, and secondary structure of synthetic peptides m1-m6.

Wigley WC, Vijayakumar S, Jones JD, Slaughter C, Thomas PJ.

Biochemistry. 1998 Jan 20;37(3):844-53.

PMID:
9454574
[PubMed - indexed for MEDLINE]
3.

Positional dependence of non-native polar mutations on folding of CFTR helical hairpins.

Wehbi H, Gasmi-Seabrook G, Choi MY, Deber CM.

Biochim Biophys Acta. 2008 Jan;1778(1):79-87. Epub 2007 Sep 15.

PMID:
17949679
[PubMed - indexed for MEDLINE]
Free Article
4.

Alteration of the cystic fibrosis transmembrane conductance regulator folding pathway.

Qu BH, Thomas PJ.

J Biol Chem. 1996 Mar 29;271(13):7261-4.

PMID:
8631737
[PubMed - indexed for MEDLINE]
Free Article
5.

Non-native interhelical hydrogen bonds in the cystic fibrosis transmembrane conductance regulator domain modulated by polar mutations.

Choi MY, Cardarelli L, Therien AG, Deber CM.

Biochemistry. 2004 Jun 29;43(25):8077-83.

PMID:
15209503
[PubMed - indexed for MEDLINE]
6.

Destabilization of the transmembrane domain induces misfolding in a phenotypic mutant of cystic fibrosis transmembrane conductance regulator.

Choi MY, Partridge AW, Daniels C, Du K, Lukacs GL, Deber CM.

J Biol Chem. 2005 Feb 11;280(6):4968-74. Epub 2004 Nov 10.

PMID:
15537638
[PubMed - indexed for MEDLINE]
Free Article
7.

A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator.

Annereau JP, Wulbrand U, Vankeerberghen A, Cuppens H, Bontems F, Tümmler B, Cassiman JJ, Stoven V.

FEBS Lett. 1997 May 5;407(3):303-8.

PMID:
9175873
[PubMed - indexed for MEDLINE]
Free Article
8.

Role of the extracellular loop in the folding of a CFTR transmembrane helical hairpin.

Wehbi H, Rath A, Glibowicka M, Deber CM.

Biochemistry. 2007 Jun 19;46(24):7099-106. Epub 2007 May 22.

PMID:
17516627
[PubMed - indexed for MEDLINE]
9.

Structural analysis of the PsbQ protein of photosystem II by Fourier transform infrared and circular dichroic spectroscopy and by bioinformatic methods.

Balsera M, Arellano JB, Gutiérrez JR, Heredia P, Revuelta JL, De Las Rivas J.

Biochemistry. 2003 Feb 4;42(4):1000-7.

PMID:
12549920
[PubMed - indexed for MEDLINE]
10.

Cooperativity and flexibility of cystic fibrosis transmembrane conductance regulator transmembrane segments participate in membrane localization of a charged residue.

Carveth K, Buck T, Anthony V, Skach WR.

J Biol Chem. 2002 Oct 18;277(42):39507-14. Epub 2002 Aug 18.

PMID:
12186867
[PubMed - indexed for MEDLINE]
Free Article
11.

Interhelical hydrogen bonds in the CFTR membrane domain.

Therien AG, Grant FE, Deber CM.

Nat Struct Biol. 2001 Jul;8(7):597-601.

PMID:
11427889
[PubMed - indexed for MEDLINE]
12.

Loop sequence dictates the secondary structure of a human membrane protein hairpin.

Nadeau VG, Deber CM.

Biochemistry. 2013 Apr 9;52(14):2419-26. doi: 10.1021/bi400187w. Epub 2013 Mar 29.

PMID:
23488803
[PubMed - indexed for MEDLINE]
13.

Interhelical packing in detergent micelles. Folding of a cystic fibrosis transmembrane conductance regulator construct.

Therien AG, Deber CM.

J Biol Chem. 2002 Feb 22;277(8):6067-72. Epub 2001 Dec 17.

PMID:
11748233
[PubMed - indexed for MEDLINE]
Free Article
14.

Polar residues in membrane domains of proteins: molecular basis for helix-helix association in a mutant CFTR transmembrane segment.

Partridge AW, Melnyk RA, Deber CM.

Biochemistry. 2002 Mar 19;41(11):3647-53.

PMID:
11888281
[PubMed - indexed for MEDLINE]
15.

Proline residues in transmembrane alpha helices affect the folding of bacteriorhodopsin.

Lu H, Marti T, Booth PJ.

J Mol Biol. 2001 Apr 27;308(2):437-46.

PMID:
11327778
[PubMed - indexed for MEDLINE]
16.

Impact of the deltaF508 mutation in first nucleotide-binding domain of human cystic fibrosis transmembrane conductance regulator on domain folding and structure.

Lewis HA, Zhao X, Wang C, Sauder JM, Rooney I, Noland BW, Lorimer D, Kearins MC, Conners K, Condon B, Maloney PC, Guggino WB, Hunt JF, Emtage S.

J Biol Chem. 2005 Jan 14;280(2):1346-53. Epub 2004 Nov 3.

PMID:
15528182
[PubMed - indexed for MEDLINE]
Free Article
17.

A short segment of the R domain of cystic fibrosis transmembrane conductance regulator contains channel stimulatory and inhibitory activities that are separable by sequence modification.

Xie J, Adams LM, Zhao J, Gerken TA, Davis PB, Ma J.

J Biol Chem. 2002 Jun 21;277(25):23019-27. Epub 2002 Apr 11.

PMID:
11950844
[PubMed - indexed for MEDLINE]
Free Article
18.

The PEST sequence does not contribute to the stability of the cystic fibrosis transmembrane conductance regulator.

Chen EY, Clarke DM.

BMC Biochem. 2002 Oct 2;3:29. Epub 2002 Oct 2.

PMID:
12361483
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Prediction of the antigenic sites of the cystic fibrosis transmembrane conductance regulator protein by molecular modelling.

Gallet X, Benhabiles N, Lewin M, Brasseur R, Thomas-Soumarmon A.

Protein Eng. 1995 Aug;8(8):829-34.

PMID:
8637853
[PubMed - indexed for MEDLINE]
20.

Expression and purification of two hydrophobic double-spanning membrane proteins derived from the cystic fibrosis transmembrane conductance regulator.

Therien AG, Glibowicka M, Deber CM.

Protein Expr Purif. 2002 Jun;25(1):81-6.

PMID:
12071702
[PubMed - indexed for MEDLINE]

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