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Title:
Docking simulations suggest that all-trans retinoic acid could bind to retinoid X receptors | Journal of Computer-Aided Molecular Design
Description:
Retinoid X receptors (RXRs) are ligand-controlled transcription factors which heterodimerize with other nuclear receptors to regulate gene transcriptions associated with crucial biological events. 9-cis retinoic acid (9cRA), which transactivates RXRs, is believed to be an endogenous RXR ligand. All-trans retinoic acid (ATRA) is a natural ligand for retinoic acid receptors (RARs), which heterodimerize with RXRs. Although the concentration of 9cRA in tissues is very low, ATRA is relatively abundant and some reports show that ATRA activates RXRs. We computationally studied the possibility of ATRA binding to RXRs using two different docking methods with our developed programs to assess the binding affinities of naturally occurring retinoids. The simulations showed good correlations to the reported binding affinities of these molecules for RXRs and RARs.
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article, acid, google, scholar, cas, retinoic, retinoid, receptors, tsuji, receptor, chem, docking, shudo, molecular, kagechika, cis, alltrans, nuclear, cell, rxrs, biol, gronemeyer, pharm, bull, japan, privacy, cookies, function, content, data, journal, simulations, ligand, atra, binding, access, effects, fukasawa, kawachi, mol, information, publish, search, design, cra, human, structure, ligandbinding, domain, med,
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month download article/chapter trans-retinoic acid metabolites ligand-flexible docking simulations differential cytosolic/nuclear localization ligand-controlled transcription factors receptor-mediated transdifferentiation cascade docking simulations suggest rxrΞ² ligand-binding domain 9-cis retinoic acid 9-cis-retinoic acid related subjects receptor-antagonistic diazepinylbenzoic acids retinoic acid receptors trans retinoic acid trans-retinoic acid retinoic acid receptor ligand-binding domain privacy choices/manage cookies full article pdf mammalian nuclear receptors protein data bank nuclear receptor superfamily retinoic acid synthesis author information authors docosahexaenoic acid rar/rxr modulators rxr-rar heterodimers high affinity ligand silico ligand screening endogenous rxr ligand human endothelial cells hormone binding european economic area regulate gene transcriptions crucial biological events local motifs involved rescue lethal defect cultured hippocampal neurons embryonic subcellular distribution polyenylidene thiazolidine derivatives dicarba-closo-dodecaboranes diarylamines incorporating hexahydrophenalene fully agonistic conformation homology modeling professional seitaikoubunnsi niokeru sougosayoubui electronic supplementary material check access instant access de lera ar pdf receptor-rigid
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headline:Docking simulations suggest that all-trans retinoic acid could bind to retinoid X receptors
description:Retinoid X receptors (RXRs) are ligand-controlled transcription factors which heterodimerize with other nuclear receptors to regulate gene transcriptions associated with crucial biological events. 9-cis retinoic acid (9cRA), which transactivates RXRs, is believed to be an endogenous RXR ligand. All-trans retinoic acid (ATRA) is a natural ligand for retinoic acid receptors (RARs), which heterodimerize with RXRs. Although the concentration of 9cRA in tissues is very low, ATRA is relatively abundant and some reports show that ATRA activates RXRs. We computationally studied the possibility of ATRA binding to RXRs using two different docking methods with our developed programs to assess the binding affinities of naturally occurring retinoids. The simulations showed good correlations to the reported binding affinities of these molecules for RXRs and RARs.
datePublished:2015-09-18T00:00:00Z
dateModified:2015-09-18T00:00:00Z
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keywords:
Retinoid X receptors
Retinoic acid receptors
All-trans retinoic acid
9-cis retinoic acid
13-cis retinoic acid
Docking simulation
Physical Chemistry
Computer Applications in Chemistry
Animal Anatomy / Morphology / Histology
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headline:Docking simulations suggest that all-trans retinoic acid could bind to retinoid X receptors
description:Retinoid X receptors (RXRs) are ligand-controlled transcription factors which heterodimerize with other nuclear receptors to regulate gene transcriptions associated with crucial biological events. 9-cis retinoic acid (9cRA), which transactivates RXRs, is believed to be an endogenous RXR ligand. All-trans retinoic acid (ATRA) is a natural ligand for retinoic acid receptors (RARs), which heterodimerize with RXRs. Although the concentration of 9cRA in tissues is very low, ATRA is relatively abundant and some reports show that ATRA activates RXRs. We computationally studied the possibility of ATRA binding to RXRs using two different docking methods with our developed programs to assess the binding affinities of naturally occurring retinoids. The simulations showed good correlations to the reported binding affinities of these molecules for RXRs and RARs.
datePublished:2015-09-18T00:00:00Z
dateModified:2015-09-18T00:00:00Z
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Retinoid X receptors
Retinoic acid receptors
All-trans retinoic acid
9-cis retinoic acid
13-cis retinoic acid
Docking simulation
Physical Chemistry
Computer Applications in Chemistry
Animal Anatomy / Morphology / Histology
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