3i7e

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[[Image:3i7e.png|left|200px]]
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{{STRUCTURE_3i7e| PDB=3i7e | SCENE= }}
{{STRUCTURE_3i7e| PDB=3i7e | SCENE= }}
===Co-crystal structure of HIV-1 protease bound to a mutant resistant inhibitor UIC-98038===
===Co-crystal structure of HIV-1 protease bound to a mutant resistant inhibitor UIC-98038===
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{{ABSTRACT_PUBMED_19746963}}
{{ABSTRACT_PUBMED_19746963}}
==About this Structure==
==About this Structure==
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3I7E 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=3I7E OCA].
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[[3i7e]] 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=3I7E 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: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Ghosh, A.]]
[[Category: Ghosh, A.]]
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[[Category: Protease]]
[[Category: Protease]]
[[Category: Structure based drug design]]
[[Category: Structure based drug design]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 16 11:13:33 2009''
 

Revision as of 03:31, 27 July 2012

Template:STRUCTURE 3i7e

Contents

Co-crystal structure of HIV-1 protease bound to a mutant resistant inhibitor UIC-98038

Template:ABSTRACT PUBMED 19746963

About this Structure

3i7e 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, 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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