Homology modeling of the serotonin transporter: Insights into the primary escitalopram-binding site

被引:37
作者
Jorgensen, Anne Marie
Tagmose, Lena
Jorgensen, Anne Marie M.
Topiol, Sid
Sabio, Michael
Gundertofte, Klaus
Bogeso, Klaus P.
Peters, Guenther H.
机构
[1] MEMPHYS-Center for Biomembrane Physics, Department of Chemistry, Technical University of Denmark
[2] Department of Computational Chemistry, H. Lundbeck A/S, 2500 Valby
[3] Department of Computational Chemistry, Lundbeck Research USA, Inc., Paramus, NJ 07652
[4] Lundbeck Research Denmark, H. Lundbeck A/S, 2500 Valby
关键词
D O I
10.1002/cmdc.200600242
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The serotonin transporter (SERT) is one of the neuro transmitter transporters that plays a critical role in the regulation of endogenous amine concentrations and therefore is an important target for therapeutic agents affecting the central nervous system. The recently published, high resolution X-ray structure of the closely related amino acid transporter, Aquifex aeolicus leucine transporter (LeuT), provides on opportunity to develop a three-dimensional model of the structure of SERT We present herein a homology model of SERT using LeuT as the template and containing escitoloprom as a bound ligand. Our model explains selectivities known from mutational studies and varying ligand data, which are discussed and illustrated in the paper.
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收藏
页码:815 / 826
页数:12
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