2b6a: Difference between revisions

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[[Image:2b6a.jpg|left|200px]]<br /><applet load="2b6a" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:2b6a.jpg|left|200px]]
caption="2b6a, resolution 2.650&Aring;" />
 
'''Crystal structure of HIV-1 reverse transcriptase (RT) in complex with THR-50'''<br />
{{Structure
|PDB= 2b6a |SIZE=350|CAPTION= <scene name='initialview01'>2b6a</scene>, resolution 2.650&Aring;
|SITE=
|LIGAND= <scene name='pdbligand=T50:1-(2,6-DIFLUOROBENZYL)-2-(2,6-DIFLUOROPHENYL)-4-METHYL-1H-BENZIMIDAZOLE'>T50</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/RNA-directed_DNA_polymerase RNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.49 2.7.7.49]
|GENE= POL ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=11676 Human immunodeficiency virus 1])
}}
 
'''Crystal structure of HIV-1 reverse transcriptase (RT) in complex with THR-50'''
 


==Overview==
==Overview==
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==About this Structure==
==About this Structure==
2B6A is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1] with <scene name='pdbligand=T50:'>T50</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/RNA-directed_DNA_polymerase RNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.49 2.7.7.49] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B6A OCA].  
2B6A is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B6A OCA].  


==Reference==
==Reference==
Synthesis and biological activity of novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 2-Aryl-substituted benzimidazoles., Roth T, Morningstar ML, Boyer PL, Hughes SH, Buckheit RW Jr, Michejda CJ, J Med Chem. 1997 Dec 19;40(26):4199-207. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9435891 9435891]
Synthesis and biological activity of novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 2-Aryl-substituted benzimidazoles., Roth T, Morningstar ML, Boyer PL, Hughes SH, Buckheit RW Jr, Michejda CJ, J Med Chem. 1997 Dec 19;40(26):4199-207. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9435891 9435891]
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Zhang, W.]]
[[Category: Zhang, W.]]
[[Category: T50]]
[[Category: T50]]
[[Category: aids]]
[[Category: aid]]
[[Category: drug design]]
[[Category: drug design]]
[[Category: hiv]]
[[Category: hiv]]
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[[Category: rt]]
[[Category: rt]]


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