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Volumn 3, Issue 22, 2005, Pages 4038-4039

Probing dipeptide trans/cis stereochemistry using pH control of thiopeptide analogues, and application to the PepT1 transporter

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; PH EFFECTS; STEREOCHEMISTRY;

EID: 28444494458     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b513274f     Document Type: Article
Times cited : (14)

References (12)
  • 8
    • 0030255292 scopus 로고    scopus 로고
    • i values. Numerous low energy conformations for each compound are then superimposed, so that the potential binding to common features (charge, hydrogen bonding, hydrophobic regions) can be identified in three dimensions. More than one hypothesis often results, and these can then be analyzed against a wider range of substrates. As with the simple mechanics based calculations on isolated dipeptides, cis amides often arose in Catalyst and this led to one of our early ideas that a cis amide bond might be favoured for transport by PepT1.
    • (1996) J. Comput. Aided Mol. Des. , vol.10 , pp. 417
    • Vinter, J.G.1
  • 11
    • 28444477251 scopus 로고    scopus 로고
    • note
    • 3H]-D-Phe-L-Gln with or without the test compound at the appropriate concentration. After incubation for one hour, the oocytes were washed sequentially five times in 1 mL of ice-cold uptake medium, then lysed individually with 100 μL 2% (w/v) SDS in vials, and liquid scintillation counted.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.