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We are analyzing https://link.springer.com/article/10.1007/s10822-015-9869-9.

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.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Environment
  • Education
  • Science

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {πŸ’Έ}

We can't see how the site brings in money.

While profit motivates many websites, others exist to inspire, entertain, or provide valuable resources. Websites have a variety of goals. And this might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {πŸ”}

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,

Topics {βœ’οΈ}

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

Schema {πŸ—ΊοΈ}

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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
         pageStart:975
         pageEnd:988
         sameAs:https://doi.org/10.1007/s10822-015-9869-9
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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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      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
      pageStart:975
      pageEnd:988
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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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