Binding-site mutations in the alpha1 subunit of the inhibitory glycine receptor convert the inhibitory metal ion Cu2+ into a positive modulator.
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Pulsed electron spin resonance resolves the coordination site of Cu²(+) ions in α1-glycine receptorMicrosecond simulations indicate that ethanol binds between subunits and could stabilize an open-state model of a glycine receptor.Probing the pharmacological properties of distinct subunit interfaces within heteromeric glycine receptors reveals a functional ββ agonist-binding site.
P2860
Binding-site mutations in the alpha1 subunit of the inhibitory glycine receptor convert the inhibitory metal ion Cu2+ into a positive modulator.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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name
Binding-site mutations in the ...... u2+ into a positive modulator.
@en
Binding-site mutations in the ...... u2+ into a positive modulator.
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type
label
Binding-site mutations in the ...... u2+ into a positive modulator.
@en
Binding-site mutations in the ...... u2+ into a positive modulator.
@nl
prefLabel
Binding-site mutations in the ...... u2+ into a positive modulator.
@en
Binding-site mutations in the ...... u2+ into a positive modulator.
@nl
P2093
P1433
P1476
Binding-site mutations in the ...... u2+ into a positive modulator.
@en
P2093
Bodo Laube
Heinrich Betz
Joanna Grudzinska
Tanja Schumann
P304
P356
10.1016/J.NEUROPHARM.2008.08.024
P577
2008-08-28T00:00:00Z