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The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide.
Thomas PJ, Shenbagamurthi P, Sondek J, Hullihen JM, Pedersen PL. Thomas PJ, et al. J Biol Chem. 1992 Mar 25;267(9):5727-30. J Biol Chem. 1992. PMID: 1372891
This residue lies in a region of the protein that we have synthesized chemically and shown to bind adenine nucleotides (Thomas, P. ...
This residue lies in a region of the protein that we have synthesized chemically and shown to bind adenine nucleotides (Thomas, P. .. …
The BiP molecular chaperone plays multiple roles during the biogenesis of torsinA, an AAA+ ATPase associated with the neurological disease early-onset torsion dystonia.
Zacchi LF, Wu HC, Bell SL, Millen L, Paton AW, Paton JC, Thomas PJ, Zolkiewski M, Brodsky JL. Zacchi LF, et al. Among authors: thomas pj. J Biol Chem. 2014 May 2;289(18):12727-47. doi: 10.1074/jbc.M113.529123. Epub 2014 Mar 13. J Biol Chem. 2014. PMID: 24627482 Free PMC article.
The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein.
Ko YH, Thomas PJ, Delannoy MR, Pedersen PL. Ko YH, et al. Among authors: thomas pj. J Biol Chem. 1993 Nov 15;268(32):24330-8. J Biol Chem. 1993. PMID: 7693699
Effects of the delta F508 mutation on the structure, function, and folding of the first nucleotide-binding domain of CFTR.
Thomas PJ, Pedersen PL. Thomas PJ, et al. J Bioenerg Biomembr. 1993 Feb;25(1):11-9. doi: 10.1007/BF00768063. J Bioenerg Biomembr. 1993. PMID: 7680027
Nucleotide domains in transport ATPases: structure-function and relationship to disease.
Thomas PJ, Ko YH, Shenbagamurthi P, Pedersen PL. Thomas PJ, et al. Soc Gen Physiol Ser. 1995;50:17-28. Soc Gen Physiol Ser. 1995. PMID: 7676321 Review. No abstract available.
The cystic fibrosis transmembrane conductance regulator. Nucleotide binding to a synthetic peptide segment from the second predicted nucleotide binding fold.
Ko YH, Thomas PJ, Pedersen PL. Ko YH, et al. Among authors: thomas pj. J Biol Chem. 1994 May 20;269(20):14584-8. J Biol Chem. 1994. PMID: 7514174
Previous studies from this laboratory with a 67-amino acid synthetic peptide (P-67) demonstrated directly that the first predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator (CFTR) binds ATP (Thomas, P.J, Shenbagamurthi, P., Ysern, S …
Previous studies from this laboratory with a 67-amino acid synthetic peptide (P-67) demonstrated directly that the first predicted nucleotid …
Rat liver mitochondrial ATP synthase. Effects of mutations in the glycine-rich region of a beta subunit peptide on its interaction with adenine nucleotides.
Garboczi DN, Thomas PJ, Pedersen PL. Garboczi DN, et al. Among authors: thomas pj. J Biol Chem. 1990 Aug 25;265(24):14632-7. J Biol Chem. 1990. PMID: 2143765
Mitochondrial ATP synthase. cDNA cloning, amino acid sequence, overexpression, and properties of the rat liver alpha subunit.
Lee JH, Garboczi DN, Thomas PJ, Pedersen PL. Lee JH, et al. Among authors: thomas pj. J Biol Chem. 1990 Mar 15;265(8):4664-9. J Biol Chem. 1990. PMID: 2137825
Cystic fibrosis transmembrane conductance regulator: nucleotide binding to a synthetic peptide.
Thomas PJ, Shenbagamurthi P, Ysern X, Pedersen PL. Thomas PJ, et al. Science. 1991 Feb 1;251(4993):555-7. doi: 10.1126/science.1703660. Science. 1991. PMID: 1703660
Mutational analysis of the consensus nucleotide binding sequences in the rat liver mitochondrial ATP synthase beta-subunit.
Thomas PJ, Garboczi DN, Pedersen PL. Thomas PJ, et al. J Biol Chem. 1992 Oct 5;267(28):20331-8. J Biol Chem. 1992. PMID: 1400352
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