1ec0: Difference between revisions

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{{Seed}}
[[Image:1ec0.png|left|200px]]
[[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==
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].  
[[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].  
 
==See Also==
*[[Virus protease|Virus protease]]


==Reference==
==Reference==
<ref group="xtra">PMID:15560801</ref><references group="xtra"/>
<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]]
[[Category: Hydrolase-hydrolase inhibitor complex]]
[[Category: Protein-inhibitor complex]]
[[Category: Protein-inhibitor complex]]
''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

File:1ec0.png

Template:STRUCTURE 1ec0

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

  1. 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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