原创力文档a strategy using nmr peptide structures of thromboxane a2 receptor as templates to construct ligand-recognition pocket of prostacyclin receptor策略使用核磁共振血栓素a2受体肽结构作为模板来构建ligand-recognition口袋环前列腺素受体.pdfVIP
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a strategy using nmr peptide structures of thromboxane a2 receptor as templates to construct ligand-recognition pocket of prostacyclin receptor策略使用核磁共振血栓素a2受体肽结构作为模板来构建ligand-recognition口袋环前列腺素受体
BMC Biochemistry BioMed Central
Research article Open Access
A strategy using NMR peptide structures of thromboxane A2
receptor as templates to construct ligand-recognition pocket of
prostacyclin receptor
Cheng-Huai Ruan, Jaixin Wu and Ke-He Ruan*
Address: From the Vascular Biology Research Center and Division of Hematology, Department of Internal Medicine, The University of Texas Health
Science Center, Houston, 6431 Fannin St., Houston, Texas 77030, USA
Email: Cheng-Huai Ruan - chengruan@; Jaixin Wu - jaixin.wu@; Ke-He Ruan* - kruan@
* Corresponding author
Published: 04 November 2005 Received: 19 May 2005
Accepted: 04 November 2005
BMC Biochemistry 2005, 6:23 doi:10.1186/1471-2091-6-23
This article is available from: /1471-2091/6/23
© 2005 Ruan et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
thetic peptide.G protein-coupled receptorGPCRprostacyclin (prostaglandin I (PGI ) receptorprotein modelingthromboxane A receptorNMR structuresyn-
2 2 2
Abstract
Background: Prostacyclin receptor (IP) and thromboxane A2 receptor (TP) belong to rhodopsin-
type G protein-coupling receptors and respectively bind to prostacyclin and thromboxane A2
derived from arachidonic acid.
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