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1ec0

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[[Image:1ec0.png|left|200px]]
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{{STRUCTURE_1ec0| PDB=1ec0 | SCENE= }}
{{STRUCTURE_1ec0| PDB=1ec0 | SCENE= }}
===HIV-1 protease in complex with the inhibitor bea403===
===HIV-1 protease in complex with the inhibitor bea403===
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{{ABSTRACT_PUBMED_15560801}}
{{ABSTRACT_PUBMED_15560801}}
==About this Structure==
==About this Structure==
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1EC0 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=1EC0 OCA].
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[[1ec0]] 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=1EC0 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:15560801</ref><references group="xtra"/>
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<ref group="xtra">PMID:015560801</ref><references group="xtra"/>
[[Category: HIV-1 retropepsin]]
[[Category: HIV-1 retropepsin]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Unge, T.]]
[[Category: Unge, T.]]
[[Category: Dimer]]
[[Category: Dimer]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
[[Category: Protein-inhibitor complex]]
[[Category: Protein-inhibitor complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 12:22:11 2009''
 

Revision as of 16:51, 26 July 2012

Template:STRUCTURE 1ec0

Contents

HIV-1 protease in complex with the inhibitor bea403

Template:ABSTRACT PUBMED 15560801

About this Structure

1ec0 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

  • Lindberg J, Pyring D, Lowgren S, Rosenquist A, Zuccarello G, Kvarnstrom I, Zhang H, Vrang L, Classon B, Hallberg A, Samuelsson B, Unge T. Symmetric fluoro-substituted diol-based HIV protease inhibitors. Ortho-fluorinated and meta-fluorinated P1/P1'-benzyloxy side groups significantly improve the antiviral activity and preserve binding efficacy. Eur J Biochem. 2004 Nov;271(22):4594-602. PMID:15560801 doi:10.1111/j.1432-1033.2004.04431.x

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