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Volumn 7, Issue 8, 2006, Pages 1251-1257

Stabilization of bzip peptides through incorporation of fluorinated aliphatic residues

Author keywords

Amino acids; Fluorine; Leucine zipper; Protein engineering; Stabilization

Indexed keywords

4,4,4 TRIFLUOROVALINE; 5,5,5 TRIFLUOROISOLEUCINE; ISOLEUCINE; LEUCINE ZIPPER PROTEIN; MUTANT PROTEIN; PROTEIN BZIP; UNCLASSIFIED DRUG; VALINE;

EID: 33747179843     PISSN: 14394227     EISSN: 14397633     Source Type: Journal    
DOI: 10.1002/cbic.200500420     Document Type: Article
Times cited : (65)

References (59)
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    • note
    • WinReedit and Win Match were written by J. W. Lary and D. A. Yphantis and are available on the National Analytical Ultracentrifugation Facility (NAUF) FTP site.
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    • note
    • Winnl106 was written by M. L. Johnson, J. W. Lary, and D. A. Yphantis and is available on the National Analytical Ultracentrifugation Facility (NAUF) FTP site.
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    • Sednterp was written by D. T. Hayes, T. M. Laue, and J. Philo and is available on the Reversible Associations in Structural and Molecular Biology anonymous FTP site.
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    • note
    • Since the N-terminal leader sequence, including the 6xHis tag, was fused to the peptides, we wanted to determine the effect of this sequence, if any, on the DNA-binding activity and specificity of the proteins. Therefore, a control peptide was expressed and purified that consists of the wild-type sequence of 56 residues, which encoded the DNA-binding and leucine zipper regions from GCN4, fused to the same N-terminal leader sequence.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.