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3i6o

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[[Image:3i6o.png|left|200px]]
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{{STRUCTURE_3i6o| PDB=3i6o | SCENE= }}
{{STRUCTURE_3i6o| PDB=3i6o | SCENE= }}
===Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A===
===Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A===
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{{ABSTRACT_PUBMED_19746963}}
{{ABSTRACT_PUBMED_19746963}}
==About this Structure==
==About this Structure==
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3I6O is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_type_1_(bru_isolate) Human immunodeficiency virus type 1 (bru isolate)]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3I6O OCA].
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[[3i6o]] is a 2 chain structure of [[Virus protease]] with sequence from [http://en.wikipedia.org/wiki/Viruses Viruses]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3I6O 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:19746963</ref><references group="xtra"/>
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<ref group="xtra">PMID:019746963</ref><references group="xtra"/>
[[Category: HIV-1 retropepsin]]
[[Category: HIV-1 retropepsin]]
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[[Category: Viruses]]
[[Category: Chumanevich, A A.]]
[[Category: Chumanevich, A A.]]
[[Category: Kovalevsky, A Y.]]
[[Category: Kovalevsky, A Y.]]
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[[Category: Protease inhibitor]]
[[Category: Protease inhibitor]]
[[Category: Wild type protease]]
[[Category: Wild type protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 16 11:49:55 2009''
 

Revision as of 12:50, 27 July 2012

Template:STRUCTURE 3i6o

Contents

Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A

Template:ABSTRACT PUBMED 19746963

About this Structure

3i6o is a 2 chain structure of Virus protease with sequence from Viruses. Full crystallographic information is available from OCA.

See Also

Reference

  • Ghosh AK, Kulkarni S, Anderson DD, Hong L, Baldridge A, Wang YF, Chumanevich AA, Kovalevsky AY, Tojo Y, Masayuki A, Koh Y, Tang J, Weber IT, Mitsuya H. Design, Synthesis, Protein-Ligand X-ray Structure, and Biological Evaluation of a Series of Novel Macrocyclic Human Immunodeficiency Virus-1 Protease Inhibitors to Combat Drug Resistance. J Med Chem. 2009 Sep 11. PMID:19746963 doi:10.1021/jm900695w

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