Literature DB >> 17544304

Exploring ligand recognition and ion flow in comparative models of the human GABA type A receptor.

Younes Mokrab1, Vassiliy N Bavro, Kenji Mizuguchi, N P Todorov, Ian L Martin, Susan M J Dunn, S L Chan, P-L Chau.   

Abstract

We present two comparative models of the GABA(A) receptor. Model 1 is based on the 4-A resolution structure of the nicotinic acetylcholine receptor from Torpedo marmorata and represents the unliganded receptor. Two agonists, GABA and muscimol, two benzodiazepines, flunitrazepam and alprazolam, together with the general anaesthetic halothane, have been docked to this model. The ion flow is also explored in model 1 by evaluating the interaction energy of a chloride ion as it traverses the extracellular, transmembrane and intracellular domains of the protein. Model 2 differs from model 1 only in the extracellular domain and represents the liganded receptor. Comparison between the two models not only allows us to explore commonalities and differences with comparative models of the nicotinic acetylcholine receptor, but also suggests possible protein sub-domain interactions with the GABA(A) receptor not previously addressed.

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Year:  2007        PMID: 17544304     DOI: 10.1016/j.jmgm.2007.04.012

Source DB:  PubMed          Journal:  J Mol Graph Model        ISSN: 1093-3263            Impact factor:   2.518


  11 in total

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10.  Different Benzodiazepines Bind with Distinct Binding Modes to GABAA Receptors.

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