Identification of an inhibitory Zn 2+ binding site on the human glycine receptor α1 subunit
Author:
Affiliation:
1. Department of Pharmacology, The School of Pharmacy, 29–39 Brunswick Square, London WC1N 1AX, UK
2. Department of Pharmaceutical Chemistry, The School of Pharmacy, 29–39 Brunswick Square, London WC1N 1AX, UK
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-7793.1999.00053.x
Reference29 articles.
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4. Identification and Mechanism of Action of Two Histidine Residues Underlying High-Affinity Zn2+ Inhibition of the NMDA Receptor
5. The role of an α subtype M2‐M3 His in regulating inhibition of GABAA receptor current by Zn2+ and other divalent cations;Fisher J. L.;Journal of Neuroscience,1998
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