1a30

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{{STRUCTURE_1a30| PDB=1a30 | SCENE= }}
{{STRUCTURE_1a30| PDB=1a30 | SCENE= }}
===HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR===
===HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR===
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{{ABSTRACT_PUBMED_9485357}}
{{ABSTRACT_PUBMED_9485357}}
==About this Structure==
==About this Structure==
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1A30 is a 3 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=1A30 OCA].
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[[1a30]] is a 3 chain structure of [[Hemoglobin]] and [[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=1A30 OCA].
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==See Also==
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*[[Hemoglobin|Hemoglobin]]
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*[[Virus protease|Virus protease]]
==Reference==
==Reference==
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<ref group="xtra">PMID:9485357</ref><references group="xtra"/>
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<ref group="xtra">PMID:009485357</ref><ref group="xtra">PMID:015298055</ref><ref group="xtra">PMID:015382890</ref><references group="xtra"/>
[[Category: HIV-1 retropepsin]]
[[Category: HIV-1 retropepsin]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
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[[Category: Aspartic protease]]
[[Category: Aspartic protease]]
[[Category: Hiv protease]]
[[Category: Hiv protease]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 22:04:17 2009''
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Revision as of 06:05, 27 July 2012

Template:STRUCTURE 1a30

Contents

HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR

Template:ABSTRACT PUBMED 9485357

About this Structure

1a30 is a 3 chain structure of Hemoglobin and Virus protease with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  • Louis JM, Dyda F, Nashed NT, Kimmel AR, Davies DR. Hydrophilic peptides derived from the transframe region of Gag-Pol inhibit the HIV-1 protease. Biochemistry. 1998 Feb 24;37(8):2105-10. PMID:9485357 doi:10.1021/bi972059x
  • Veit M. [New strategies for drug development]. Berl Munch Tierarztl Wochenschr. 2004 Jul-Aug;117(7-8):276-87. PMID:15298055
  • Spyrakis F, Fornabaio M, Cozzini P, Mozzarelli A, Abraham DJ, Kellogg GE. Computational titration analysis of a multiprotic HIV-1 protease-ligand complex. J Am Chem Soc. 2004 Sep 29;126(38):11764-5. PMID:15382890 doi:10.1021/ja0465754

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