Inhibition of Prohormone Convertases PC1/3 and PC2 by 2,5-Dideoxystreptamine Derivatives-Reference-Cited by-同舟云学术

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Inhibition of Prohormone Convertases PC1/3 and PC2 by 2,5-Dideoxystreptamine Derivatives

Published:2011-12-14 Issue:3 Volume:81 Page:440-454
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Vivoli Mirella,Caulfield Thomas R.,Martínez-Mayorga Karina,Johnson Alan T.,Jiao Guan-Sheng,Lindberg Iris

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference60 articles.

1. The synthesis of inhibitors for processing proteinases and their action on the Kex2 proteinase of yeast

2. Identification of Inhibitors of Prohormone Convertases 1 and 2 Using a Peptide Combinatorial Library

3. Structure–Function Analysis of the 7B2 CT Peptide

4. Mutations in the Catalytic Domain of Prohormone Convertase 2 Result in Decreased Binding to 7B2 and Loss of Inhibition with 7B2 C-terminal Peptide

5. The Prohormone Processing Enzyme PC3 Is a Lipid Raft-Associated Transmembrane Protein

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