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Volumn 61, Issue 9, 1996, Pages 3127-3137

Synthesis and hydrogen bonding capabilities of biphenyl-based amino acids designed to nucleate β-sheet structure

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000375517     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo952194k     Document Type: Article
Times cited : (24)

References (70)
  • 37
    • 85033868798 scopus 로고    scopus 로고
    • note
    • Several small peptides are capable of populating a β-turn conformation; see: refs 2 and 38-43. However, concensus β-turns do not appear to be sufficient to nucleate folding within sequences which are known to fold when nucleated by unnatural amino acids such as the 4-(2-aminoethyl)-6-dibenzofuranpropionic acid. Unpublished results.
  • 58
    • 85033856337 scopus 로고    scopus 로고
    • note
    • The distances between N(2) and C(15), C(23) and C(13), C(24) and C(14), C(25) and C(15), and O(1) and O(2) were used to calculate the average strand distance in diamide 3.
  • 59
    • 85033839726 scopus 로고    scopus 로고
    • note
    • The distances between N(4) and C(41), N(3) and C(49), N(3) and N(4), and C(42) and C(50) were used to calculate the average strand distance in the R conformer of diamide 4, and the distances between N(2) and C(13), N(1) and N(2), N(1) and C(21), and C(14) and C(22) were used to calculate the average strand distance in the S conformer of diamide 4.
  • 66
    • 85033857357 scopus 로고    scopus 로고
    • note
    • Value calculated by dividing the width of the aromatic signals overlapping the amide proton resonance (0.3 ppm) by the temperature range of the experiment.
  • 70
    • 0001339532 scopus 로고
    • This figure was prepared with MolScript; see: Kraulis, P. T. J. Appl. Crystallogr. 1991, 24, 946-950.
    • (1991) J. Appl. Crystallogr. , vol.24 , pp. 946-950
    • Kraulis, P.T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.