Benzodiazepine agonists protect a histidine residue from modification by diethyl pyrocarbonate whereas propyl β-carboline does not
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(87)80240-5/fullpdf
Reference12 articles.
1. Histidine modification with diethyl pyrocarbonate shows heterogeneity of benzodiazepine receptors.
2. Involvement of tyrosyl residues in the binding of benzodiazepines to their brain receptors
3. Characterization of ?-Aminobutyric Acid-Benzodiazepine Receptor Complexes by Protection Against Inactivation by Group-Specific Reagents
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4. The Major Site of Photoaffinity Labeling of the γ-Aminobutyric Acid Type A Receptor by [3H]Flunitrazepam Is Histidine 102 of the α Subunit;Journal of Biological Chemistry;1996-04
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