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3dk1

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{{STRUCTURE_3dk1| PDB=3dk1 | SCENE= }}
{{STRUCTURE_3dk1| PDB=3dk1 | SCENE= }}
===Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0105A===
===Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0105A===
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{{ABSTRACT_PUBMED_18843400}}
{{ABSTRACT_PUBMED_18843400}}
==About this Structure==
==About this Structure==
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3DK1 is a 2 chains 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=3DK1 OCA].
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[[3dk1]] is a 2 chain structure of [[Virus protease]] with sequence 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=3DK1 OCA].
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==See Also==
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*[[Virus protease|Virus protease]]
==Reference==
==Reference==
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<ref group="xtra">PMID:18843400</ref><references group="xtra"/>
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<ref group="xtra">PMID:018843400</ref><references group="xtra"/>
[[Category: HIV-1 retropepsin]]
[[Category: HIV-1 retropepsin]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
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[[Category: Dna integration]]
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[[Category: Protease]]
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[[Category: Ribosomal frameshifting]]
 
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[[Category: Rna-directed dna polymerase]]
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[[Category: Virion]]
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[[Category: Wild type protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May 13 09:57:29 2009''
 

Revision as of 16:23, 26 July 2012

Template:STRUCTURE 3dk1

Contents

Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0105A

Template:ABSTRACT PUBMED 18843400

About this Structure

3dk1 is a 2 chain structure of Virus protease with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  • Ghosh AK, Gemma S, Takayama J, Baldridge A, Leshchenko-Yashchuk S, Miller HB, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H. Potent HIV-1 protease inhibitors incorporating meso-bicyclic urethanes as P2-ligands: structure-based design, synthesis, biological evaluation and protein-ligand X-ray studies. Org Biomol Chem. 2008 Oct 21;6(20):3703-13. Epub 2008 Aug 11. PMID:18843400 doi:10.1039/b809178a

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