3djk
From Proteopedia
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{{STRUCTURE_3djk| PDB=3djk | SCENE= }} | {{STRUCTURE_3djk| PDB=3djk | SCENE= }} | ||
===Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A=== | ===Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A=== | ||
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==About this Structure== | ==About this Structure== | ||
| - | + | [[3djk]] 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=3DJK OCA]. | |
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| + | ==See Also== | ||
| + | *[[Virus protease|Virus protease]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:018783203</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: Capsid maturation]] | [[Category: Capsid maturation]] | ||
[[Category: Capsid protein]] | [[Category: Capsid protein]] | ||
| - | [[Category: Cytoplasm]] | ||
[[Category: Dna integration]] | [[Category: Dna integration]] | ||
[[Category: Dna recombination]] | [[Category: Dna recombination]] | ||
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[[Category: Protease]] | [[Category: Protease]] | ||
[[Category: Protease inhibitor]] | [[Category: Protease inhibitor]] | ||
| - | [[Category: Ribosomal frameshifting]] | ||
[[Category: Rna-binding]] | [[Category: Rna-binding]] | ||
[[Category: Rna-directed dna polymerase]] | [[Category: Rna-directed dna polymerase]] | ||
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[[Category: Virion]] | [[Category: Virion]] | ||
[[Category: Wild type protease]] | [[Category: Wild type protease]] | ||
| - | [[Category: Zinc]] | ||
[[Category: Zinc-finger]] | [[Category: Zinc-finger]] | ||
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Revision as of 16:07, 27 July 2012
Contents |
Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A
Template:ABSTRACT PUBMED 18783203
About this Structure
3djk 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, Gemma S, Baldridge A, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H. Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein-Ligand X-ray Studies. J Med Chem. 2008 Sep 11. PMID:18783203 doi:10.1021/jm8004543
Categories: HIV-1 retropepsin | Human immunodeficiency virus 1 | Wang, Y F. | Weber, I T. | Aid | Aspartyl protease | Capsid maturation | Capsid protein | Dna integration | Dna recombination | Dna-directed dna polymerase | Endonuclease | Hiv-1 | Hydrolase | Lipoprotein | Magnesium | Metal-binding | Multifunctional enzyme | Myristate | Nuclease | Nucleotidyltransferase | Nucleus | Phosphoprotein | Protease | Protease inhibitor | Rna-binding | Rna-directed dna polymerase | Transferase | Viral nucleoprotein | Virion | Wild type protease | Zinc-finger
