3i7e
From Proteopedia
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| + | {{STRUCTURE_3i7e| PDB=3i7e | SCENE= }} | ||
| - | + | ===Co-crystal structure of HIV-1 protease bound to a mutant resistant inhibitor UIC-98038=== | |
| - | Description: Co-crystal of HIV-protese bound to a mutant resistant inhibitor UIC-98038 | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19746963}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19746963 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19746963}} | ||
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| + | ==About this Structure== | ||
| + | 3I7E 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=3I7E OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19746963</ref><references group="xtra"/> | ||
| + | [[Category: Human immunodeficiency virus 1]] | ||
| + | [[Category: Ghosh, A.]] | ||
| + | [[Category: Hong, L.]] | ||
| + | [[Category: Tang, J.]] | ||
| + | [[Category: Acid protease]] | ||
| + | [[Category: Aid]] | ||
| + | [[Category: Aspartic protease]] | ||
| + | [[Category: Aspartyl protease]] | ||
| + | [[Category: Drug design]] | ||
| + | [[Category: Hiv]] | ||
| + | [[Category: Hiv prtease]] | ||
| + | [[Category: Hiv-protease inhibitor]] | ||
| + | [[Category: Hydrolase]] | ||
| + | [[Category: Protease]] | ||
| + | [[Category: Structure based drug design]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 30 09:17:31 2009'' | ||
Revision as of 07:17, 30 September 2009
Co-crystal structure of HIV-1 protease bound to a mutant resistant inhibitor UIC-98038
Template:ABSTRACT PUBMED 19746963
About this Structure
3I7E is a 2 chains structure of sequences from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Ghosh AK, Kulkarni S, Anderson DD, Hong L, Baldridge A, Wang YF, Chumanevich AA, Kovalevsky AY, Tojo Y, Masayuki A, Koh Y, Tang J, Weber IT, Mitsuya H. Design, Synthesis, Protein-Ligand X-ray Structure, and Biological Evaluation of a Series of Novel Macrocyclic Human Immunodeficiency Virus-1 Protease Inhibitors to Combat Drug Resistance. J Med Chem. 2009 Sep 11. PMID:19746963 doi:10.1021/jm900695w
Page seeded by OCA on Wed Sep 30 09:17:31 2009
