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3r8d
From Proteopedia
(Difference between revisions)
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| - | + | [[Image:3r8d.jpg|left|200px]] | |
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| + | The line below this paragraph, containing "STRUCTURE_3r8d", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3r8d| PDB=3r8d | SCENE= }} | ||
| - | + | ===Activation of the Human Nuclear Xenobiotic Receptor PXR by the Reverse Transcriptase-Targeted Anti-HIV Drug PNU-142721=== | |
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_21805522}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 21805522 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_21805522}} | ||
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| + | ==About this Structure== | ||
| + | [[3r8d]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3R8D OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:021805522</ref><references group="xtra"/> | ||
| + | [[Category: Histone acetyltransferase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Cheng, Y.]] | ||
| + | [[Category: Redinbo, M R.]] | ||
| + | [[Category: Endobiotic]] | ||
| + | [[Category: Ligand binding domain]] | ||
| + | [[Category: Nuclear receptor]] | ||
| + | [[Category: Pxr]] | ||
| + | [[Category: Transcription]] | ||
| + | [[Category: Transcription regulation]] | ||
| + | [[Category: Xenobiotic]] | ||
| + | [[Category: Xenobiotic]] | ||
Revision as of 06:13, 17 August 2011
Activation of the Human Nuclear Xenobiotic Receptor PXR by the Reverse Transcriptase-Targeted Anti-HIV Drug PNU-142721
Template:ABSTRACT PUBMED 21805522
About this Structure
3r8d is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Cheng Y, Redinbo MR. Activation of the human nuclear xenobiotic receptor PXR by the reverse transcriptase-targeted anti-HIV drug PNU-142721. Protein Sci. 2011 Jul 29. doi: 10.1002/pro.706. PMID:21805522 doi:10.1002/pro.706
