2qhy

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[[Image:2qhy.png|left|200px]]
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{{STRUCTURE_2qhy| PDB=2qhy | SCENE= }}
{{STRUCTURE_2qhy| PDB=2qhy | SCENE= }}
===Crystal Structure of protease inhibitor, MIT-1-AC86 in complex with wild type HIV-1 protease===
===Crystal Structure of protease inhibitor, MIT-1-AC86 in complex with wild type HIV-1 protease===
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{{ABSTRACT_PUBMED_18412349}}
{{ABSTRACT_PUBMED_18412349}}
==About this Structure==
==About this Structure==
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2QHY 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=2QHY OCA].
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[[2qhy]] is a 2 chain structure of [[Beta-lactamase]] 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=2QHY OCA].
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==See Also==
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*[[Beta-lactamase|Beta-lactamase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:18412349</ref><references group="xtra"/>
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<ref group="xtra">PMID:018412349</ref><references group="xtra"/>
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Nalam, M N.L.]]
[[Category: Nalam, M N.L.]]
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[[Category: Hydrolase]]
[[Category: Hydrolase]]
[[Category: Protease inhibitor]]
[[Category: Protease inhibitor]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 08:09:19 2009''
 

Revision as of 11:12, 26 July 2012

Template:STRUCTURE 2qhy

Contents

Crystal Structure of protease inhibitor, MIT-1-AC86 in complex with wild type HIV-1 protease

Template:ABSTRACT PUBMED 18412349

About this Structure

2qhy is a 2 chain structure of Beta-lactamase with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  • Altman MD, Ali A, Reddy GS, Nalam MN, Anjum SG, Cao H, Chellappan S, Kairys V, Fernandes MX, Gilson MK, Schiffer CA, Rana TM, Tidor B. HIV-1 protease inhibitors from inverse design in the substrate envelope exhibit subnanomolar binding to drug-resistant variants. J Am Chem Soc. 2008 May 14;130(19):6099-113. Epub 2008 Apr 16. PMID:18412349 doi:10.1021/ja076558p

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