A New Class of Potent Reversible Inhibitors of Metallo-proteinases: C-terminal Thiol-peptides as Zinc-coordinating Ligands-Reference-Cited by-同舟云学术

A New Class of Potent Reversible Inhibitors of Metallo-proteinases: C-terminal Thiol-peptides as Zinc-coordinating Ligands

Published:2001-01 Issue:4 Volume:16 Page:339-350
ISSN:8755-5093
Container-title:Journal of Enzyme Inhibition
language:en
Short-container-title:Journal of Enzyme Inhibition

Author:

Peters Klaus¹,Jahreis GÜNther¹,Kötters Eva-Maria¹

Affiliation:

1. Faculty of Medicine, Institute of Physiological Chemistry, Martin Luther University, Halle-Wittenberg, Hollystraβe 1, D-06097, Halle (Saale), Germany

Publisher

Informa UK Limited

Subject

Molecular Medicine,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756360109162382

Reference56 articles.

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5. Astacins, serralysins, snake venom and matrix metalloproteinases exhibit identical zinc-binding environments (HEXXHXXGXXH and Met-turn) and topologies and should be grouped into a common family, the ‘metzincins’

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5. Chapter 5. Metal Complexes of Amino Acids and Peptides;Amino Acids, Peptides and Proteins