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3s43
From Proteopedia
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| - | + | [[Image:3s43.jpg|left|200px]] | |
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| + | The line below this paragraph, containing "STRUCTURE_3s43", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3s43| PDB=3s43 | SCENE= }} | ||
| - | + | ===HIV-1 protease triple mutants V32I, I47V, V82I with antiviral drug amprenavir=== | |
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_22238126}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 22238126 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_22238126}} | ||
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| + | ==About this Structure== | ||
| + | [[3s43]] is a 2 chain structure 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=3S43 OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:022238126</ref><references group="xtra"/> | ||
| + | [[Category: HIV-1 retropepsin]] | ||
| + | [[Category: Human immunodeficiency virus 1]] | ||
| + | [[Category: Tie, Y F.]] | ||
| + | [[Category: Wang, Y F.]] | ||
| + | [[Category: Weber, I T.]] | ||
| + | [[Category: Amprenavir]] | ||
| + | [[Category: Aspartic protease]] | ||
| + | [[Category: Drug resistance]] | ||
| + | [[Category: Hiv/aid]] | ||
| + | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
| + | [[Category: Molecular recognition]] | ||
Revision as of 07:38, 21 March 2012
HIV-1 protease triple mutants V32I, I47V, V82I with antiviral drug amprenavir
Template:ABSTRACT PUBMED 22238126
About this Structure
3s43 is a 2 chain structure with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Tie Y, Wang YF, Boross PI, Chiu TY, Ghosh AK, Tozser J, Louis JM, Harrison RW, Weber IT. Critical differences in HIV-1 and HIV-2 protease specificity for clinical inhibitors. Protein Sci. 2012 Mar;21(3):339-50. doi: 10.1002/pro.2019. Epub 2012 Jan 24. PMID:22238126 doi:10.1002/pro.2019
