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The details of FoldDB ID: fd1135
Chemical diagram
molecule

Please see the original reference for structure
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Identification
FoldDB ID

fd1135

Other Name Help Icon Since there is no uniform representation for the non-natural peptides. This is the name as it is mentioned in the original article and/or the external database.

Ac-((3S,4R)-3-aminopyrrolidine-4-carboxylic acid)-Ala-((1S,2S)-2-aminocyclopentanecarboxylic acid)-Arg-((1S,2S)-2-aminocyclopentanecarboxylic acid)-Leu-((1S,2S)-2-aminocyclopentanecarboxylic acid)-Lys-beta3hLeu-Gly-Asp-Ala-Phe-Asn-Arg-NH2

Source

synthetic construct

External ID
Reaxys ID

10770818

Other information
Application

Antagonists of BH3 Domain/Bcl-xL Recognition

Foldamer type

α/β Peptide

Activity
Activity ID Assay name Cell line Target Protein Organism Assay Category Value Unit Type Measurement object
fdact0757

Protein binding Bioassay

Bcl-2 protein

In Vitro (Efficacy)

0.85

µM

IC50

fdact0758

Protein binding Bioassay

Bcl-w protein

In Vitro (Efficacy)

0.041

µM

IC50

fdact0759

Protein binding Bioassay

Bcl-xL protein

In Vitro (Efficacy)

0.029

µM

IC50

fdact0760

Protein binding Bioassay

Bcl-xL protein

In Vitro (Efficacy)

0.018

µM

IC50

fdact0761

Protein binding Bioassay

Mcl-1 protein

In Vitro (Efficacy)

nd

qualitative

fdact0762

cytochrome C release

In Vitro (Efficacy)

nd

qualitative

fdact0763

cytochrome C release

In Vitro (Efficacy)

nd

qualitative

fdact0764

cytochrome C release

In Vitro (Efficacy)

nd

qualitative

Citations
ID Title Year Authors Journal DOI

fdart0145

(α/β+α)-Peptide Antagonists of BH3 Domain/Bcl-xL Recognition:  Toward General Strategies for Foldamer-Based Inhibition of Protein−Protein Interactions

2007

Sadowsky, Jack D., Fairlie, W. Douglas., Hadley, Erik B., Lee, Hee-Seung., Umezawa, Naoki., Nikolovska-Coleska, Zaneta., Wang, Shaomeng., Huang, David C. S., Tomita, York., Gellman, Samuel H.

Journal of the American Chemical Society

..